Discovery of New Schiff Bases Tethered Pyrazole Moiety: Design, Synthesis, Biological Evaluation, and Molecular Docking Study as Dual Targeting DHFR/DNA Gyrase Inhibitors with Immunomodulatory Activity.

A series of Bis-pyrazole Schiff bases (6a-d and 7a-d) and mono-pyrazole Schiff bases (8a-d and 9a-d) were designed and synthesized through the reaction of 5-aminopyrazoles 1a-d with aldehydes 2-5 using mild reaction condition with a good yield percentage. The chemical structure of newly formed Schiff bases tethered pyrazole core was confirmed based on spectral and experimental data. All the newly formed pyrazole Schiff bases were evaluated against eight pathogens (Gram-positive, Gram-negative, and fungi). The result exhibited that, most of them have good and broad activities. Among those, only six Schiff bases (6b, 7b, 7c, 8a, 8d, and 9b) displayed MIC values (0.97-62.5 µg/mL) compared to Tetracycline (15.62-62.5 µg/mL) and Amphotericin B (15.62-31.25 µg/mL), MBC values (1.94-87.5 µg/mL) and selectivity to tumor cell than normal cells. Immunomodulatory activities showed that the promising Schiff bases increase the immunomodulator effect of defense cell and the Schiff base 8a is the highest one by (Intra. killing activity = 136.5 ± 0.3%) having a pyrazole moiety as well as amide function (O=C-NH2) and piperidinyl core. Furthermore, the most potent one exhibited broad activity depending on both MIC and MBC values. Moreover, to study the mechanism of these pyrazole Schiff bases, two active Schiff bases 8a and 9b from six derivatives were introduced to study the enzyme assay as dihydrofolate reductase (DHFR) on E. coli organism and DNA gyrase with two different organisms, S. aureus and B. subtilis, to determine the inhibitory activities with lower values in the case of DNA gyrase (8a and 9b) or nearly as DHFR compound 9b, while pyrazole 8a showed excellent inhibitory against all enzyme assay. The molecular docking study against dihydrofolate reductase and DNA gyrase were performed to study the binding between active site in the pocket with the two Schiff bases (8a and 9b) that exhibited good binding affinity with different bond types as H-bonding, aren-aren, and arene-cation interaction as well as study the physicochemical and pharmacokinetic properties of the two active Schiff bases 8a and 9b.

1. Introduction

One of the mopan class="Species">st common ecies">pan class="Species">causes of death all over the world is the microbial infections and multidrug-resistant bacteria. According to the World Health Organization (WHO), the resistance of microbes to antibiotics drugs is one of the dangerous health problems that threaten humans. Therefore, the production of novel bioactive compounds acting as antimicrobial agents for overcoming the resistance problem is an urgent topic that configures interest between the organic and medicinal chemistry researchers and is considered one of the greatest achievements over time [1,2,3]. Antibiotic-resistant infection problem arises from the broad use and abuse of conventional antibiotics, already, every year an estimated 700,000 people around the world die of drug-resistant diseases, 10 million people could die each year from diseases that have grown resistant [4,5,6].

pan class="Chemical">Schiff bases (–CH=N– function) have the biologiecies">pan class="Species">cal and pharmacological applications [7,8,9]. Schiff base (I), 4-chloro-2-((4-fluorobenzyl imino)methyl)phenol, showed antibacterial activity against E. coli and P. fluorescence [10], as well as Schiff base (II), bearing 2-(piperazin-1-yl)ethan-amine derivative, exhibited good anticancer activity against lung (NCI H-522) cells [11]. Moreover, Schiff base (III) with quinoline derivative as an active core demonstrated in vitro anti-inflammatory activity [12]. One of the most wide pharmacophore cores is pyrazole derivatives, and our study involves the design and synthesis of new pyrazole derivatives.

Besides, literature displayed many pan class="Chemical">pyrazoles that have a wide array of biologiecies">pan class="Species">cal activities such as neuraminidase inhibitors against influenza H1N1 virus [13], apoptotic inducers [14], antimicrobial, cytotoxic [15], and antimalarial [16] activities. Pyrazole moiety attached to enaminonitrile pyridine derivative (IV) showed anticancer activity against both HePG-2 and MCF-7 lines [17]. Also, pyrazole with N-(4-phenyl)sulfonylacetamide derivative (V) exhibited good activity and selectivity toward the COX-2 enzyme [18]. On the other hand, pyrazole moiety containing both N-(4-chlorophenyl) and (2-fluorophenyl)acrylamide derivative (VI) produced potent antifungal activity [19]. Recently, there is a growing interest in the synthesis of Schiff bases tethered pyrazole ring because of their importance in biological activities [20,21,22]. For example, Schiff base (VII), bearing imidazole and pyrazole nucleus, showed potency against E. coli [23]. While, Schiff base (VIII), derived from N-phenyl-pyrazole derivative with 2-aminophenol, reveled promising anticancer activity close to doxorubicin [24]. Furthermore, we have reported the synthesis of Schiff base bearing pyrazole moiety (IX), 5-(benzylideneamino)-3-(4-methoxyphenylamino)-N-(4-methylphenyl)-1H-pyrazole-4-carboxamide, displayed a potent antitumor agent against MCF-7 lines [25] (Figure 1).

Figure 1

Structures of bioactive Schiff bases and pyrazole compounds I–IX.

pan class="Gene">Dihydrofolate reductase (ecies">pan class="Gene">DHFR) enzyme is a target for several anticancer and antibacterial drugs and of high importance in medicinal chemistry [26,27] because of its function as a cofactor in the biosynthesis of nucleic acids and amino acids. Mechanism of action for DHFR is blocking the synthesis of DNA, RNA, and proteins, causing cell growth arrest [28,29]. Also, DNA gyrase is an enzyme that belongs to type II topoisomerases and catalyzes changes in DNA topology [30]. In addition, it is composed of two chains GyrA and GyrB subunits that are responsible for the transient break of two strands of DNA, as well as introducing negative supercoils in DNA during replication. Drugs that target DNA gyrase exhibited their antibacterial activity by two mechanisms as gyrase poisoning as in Ciprofloxacin or by blocking the ATP binding site as in Novobiocin [31] and depending on the previous important function, it has become an attractive target for the development of antibacterial drug [32]. Therefore, DHFR and DNA topoisomerases have a proven track record in supporting their role in microbial diseases and cancer chemotherapy [33,34]. The immune system is a remarkably advanced vertebrate defense system and its main function is defense against invaders by producing cell and molecular varieties that can recognize and thus eliminate unlimited varieties of foreign and harmful agents [35,36]. In general, immunomodulators can be classified as two different types depending on their effects: immunosuppressants and Immunostimulants, and both could mount an immune response or defend against pathogens or tumors [37]. Immunomodulation is the process produced by the administration of a drug or compound to alter an immune response positive or negative. A number of proteins, amino acids, and natural compounds showed an important ability to regulate immune responses, including interferon-γ (IFN–γ) steroids [38].

pan class="Species">For the aecies">pan class="Species">forementioned reasons biological activities of Schiff bases, pyrazole moiety and Schiff bases tethered pyrazole ring and in continuation of our research program [39,40,41,42,43,44,45,46,47,48,49,50], in this work, we have synthesized a new series of bis-pyrazole Schiff bases (6a–d and 7a–d) and mono-Schiff bases tethered pyrazole moiety (8a–d and 9a–d) for the examination of their in vitro antimicrobial, antiproliferative, immunomodulatory activities and extend our work to drug resistance activity (MDRB), enzymes assessment (dihydrofolate reductase and DNA gyrase), as well as some of in silico studies as physicochemical properties, structure-activity relationship, and the molecular docking hoping to find new pyrazole derivatives as dual-targeting DHFR and DNA gyrase inhibitors.

2. Results and Discussion

2.1. Chemistry

The pan class="Species">starting material, ecies">pan class="Chemical">5-amino-N-aryl-3-(4-methoxyphenylamino)-1H-pyrazole-4-carboxamide 1a–d, was prepared according to the reported method [51,52,53]. New Schiff bases with hybrid active core pyrazole derivatives were synthetized by the reaction of pyrazole derivatives 1a–d with different aldehyde containing different pharmacophore atoms or groups that are represented in Scheme 1 namely 1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carbaldehyde (2), 5-chloro-3-methyl-1-phenyl-1H-pyrazole-4-carbaldehyde (3), 4-(piperidin-1-yl)benzaldehyde (4), and 3,4,5-trimethoxybenzaldehyde (5) hoping to be effective as antimicrobial and anticancer activities.

Scheme 1

The synthesis of starting materials (1a–d, 3 and 4) and the structure of (2 and 5).

The newly designed pan class="Chemical">bis-pyrazole Schiff bases ecies">pan class="Chemical">6a–d or 7a-d were prepared via the condensation of 5-aminopyrazole derivatives 1a–d with 1,5-dimethyl-3-oxo-2-phenyl-2, 3-dihydro-1H-pyrazole-4-carbaldehyde (2) or 5-chloro-3-methyl-1-phenyl-1H-pyrazole-4-carbaldehyde (3), respectively (Scheme 2). The structures of bis-pyrazole Schiff bases 6 and 7 were proved on the basis of analytical and spectral data. IR spectrum of 5-((1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)methylene-amino)-3-(4-methoxyphenylamino)-1H-pyrazole-4-carboxamide (6a) confirmed the presence of absorption bands at 3359, 3165, 1675, and 1654 cm−1 for NH, NH2, C=O (antipyrine) and C=O (amide) groups, respectively. Its 1H NMR (400 MHz) spectrum showed singlet signals attributable to the protons of -CH=N- and 2NH at δ 8.68, 8.85, and 12.37 ppm, respectively. In addition to three singlet signal related to -CH3, -N-CH3, and -OCH3 protons appeared at δ 2.61, 3.37, and 3.70 ppm, respectively. The protons of aromatic rings appear as two doublet at δ 6.85 and 7.37 ppm for four aromatic protons with coupling constant (J) 8.2 and 7.4 Hz, as well as, the five protons that exist as multiplet in region δ 7.45–7.48 ppm for three protons and triplet signal at 7.56 ppm for the last two protons. Furthermore, two singlet singlets at δ 7.19 and 7.80 ppm for NH2-amide function.

Scheme 2

The synthesis of Bis-pyrazole Schiff bases (6a–d and 7a–d).

Also, its pan class="Chemical">13C NMR (101 MHz) spectrum showed the characteriecies">pan class="Species">stic signals for CH3, -N-CH3 and OCH3 at δ 11.50, 33.93, and 55.21 ppm, respectively. The carbons for the carbonyl groups of amide function and antipyrine moiety appeared at δ 162.54 and 166.76 ppm, respectively. The mass spectrum showed its [M+] peak (m/z 445) corresponding to C23H23N7O3 (molecular formula) with the relative intensity = 13.44%.

Also, the synthesis of pan class="Chemical">Schiff bases tethered ecies">pan class="Chemical">pyrazole moiety 8a–d or 9a–d were performed by the condensation of 5-aminopyrazole derivatives 1a–d with 4-(piperidin-1-yl) benzaldehyde (4) or 3, 4, 5-trimethoxybenzaldehyde (5), respectively, in good yield (Scheme 3). The 1H NMR spectrum of compound 8b revealed four singlet signals at δ 8.71, 8.77, 10.14, and 12.56 ppm for the protons of -CH=N- and 3NH groups, respectively. The protons of the methoxy group appeared at δ 3.72 ppm as a singlet signal. Moreover, the piperidine moiety protons appeared at δ 1.60 ppm for six protons as a broad signal and 3.43 ppm for four protons. The aromatic protons appear in region δ 6.89–7.85 ppm for thirteen protons and represented as three doublet, one triplet, and one multiplet signals at δ 6.89(d), 7.68(d), 7.85(d), 7.08 (t), and 7.35–7.48 (m) ppm respectively, with coupling constant (J) ranging between 8.1–8.3 Hz. Its 13C NMR spectrum showed three characteristic signals at δ 23.95, 24.93, and 47.65 ppm referred to as the carbons of piperidinyl moiety. In addition, two signals at δ 55.20 and 163.06 ppm for the carbons of -OCH3 and C=O, respectively, as well as aromatic carbons and C=N appeared from δ 92.57 to 160.09 ppm. The mass spectrum exhibited the molecular ion peak at m/z = 494 [M+, 32.82%] corresponding to C29H30N6O2 (molecular formula).

Scheme 3

The synthesis of Schiff bases tethered mono-pyrazole moiety (8a–d and 9a–d).

In the same way, treatment of pan class="Chemical">5-aminopyrazole derivative 1c with ecies">pan class="Chemical">3,4,5-trimethoxybenzaldehyde (5) afforded 3-(p-methoxyphenylamino)-N-p-tolyl-5-(3,4,5-trimethoxybenzylideneamino)-1H-pyrazole-4-carboxamide (9c) having four methoxy groups, as well as N-p-tolyl 4-carboxamide based on elemental analysis and spectral data. IR spectrum of Schiff base 9c showed characteristic bands related to NH and carbonyl groups at 3437, 3285, and 1655 cm−1, respectively. The 1H NMR spectrum of Schiff base 9c exhibited four singlet signals at δ 2.27, 3.73, 3.79, and 3.92 ppm for one methyl and four methoxy groups. Furthermore, four singlet signals at upfield can be classified as the signal at δ 8.70 ppm related to -CH=N and three singlet signals at δ 8.96, 9.95, and 12.64 ppm for three NH protons as well as ten aromatic protons between δ 6.91 to 7.59 ppm. The 13C NMR spectrum of 9c displayed a singlet signal at 21.31 ppm for methyl group and three singlet signals at 55.04, 56.79, and 60.65 related to four methoxy groups as well as one signal at 162.88 for carbonyl group beside aromatic carbons that appeared in region 91.93–161.74 ppm.

2.2. Biological Evaluation

2.2.1. In Vitro Antimicrobial Activities

Antimicrobial activities of the newly pan class="Species">formed ecies">pan class="Chemical">Schiff bases (6a–d, 7a–d, 8a–d, and 9a–d) and reference drugs were evaluated against three Gram-positive, three Gram-negative, and two fungi strain at Al-Azhar University, Cairo, Egypt. The inhibition zones (IZ, in mm ± standard deviation) and the minimal inhibitory concentration (MIC) (μg/mL) were determined by the conventional paper disk diffusion method [54,55]. The broad-spectrum antibiotics, Tetracycline and Amphotericin B were used as positive controls. The results are presented in Table 1, Table 2 and Table 3.

Table 1

Inhibition zone (IZ) in mm ± standard deviation of Schiff bases (6a–d, 7a–d, 8a–d, and 9a–d) and reference drugs against pathogenic microbes.

Schiff Bases and References Drugs	Gram-Positive Bacteria			Gram-Negative Bacteria			Fungi
	Bs	Sa	Ef	Ec	Pa	St	Ca	Fo
6a	21 ± 0.4	25 ± 0.31	21 ± 0.11	24 ± 0.2	20 ± 0.15	18 ± 0.16	22 ± 0.35	13 ± 0.3
6b	30 ± 0.5	24 ± 0.12	29 ± 0.55	25 ± 0.81	24 ± 0.2	20 ± 0.16	22 ± 0.56	18 ± 0.15
6c	20 ± 0.11	23 ± 0.29	21 ± 0.54	22 ± 0.43	NA	15 ± 0.36	17 ± 0.21	9 ± 0.35
6d	13 ± 0.41	NA	14 ± 0.47	19 ± 0.33	12 ± 0.63	NA	13.0 ± 0.2	NA
7a	20 ± 0.4	19 ± 0.31	21 ± 0.11	18 ± 0.2	20 ± 0.15	18 ± 0.16	13 ± 0.35	15 ± 0.3
7b	28 ± 0.16	23 ± 0.55	25 ± 0.3	21 ± 0.14	24 ± 0.78	22 ± 0.12	21 ± 0.2	17 ± 0.45
7c	32 ± 0.22	33 ± 0.53	29 ± 0.17	30 ± 0.29	27 ± 0.73	29 ± 0.2	27 ± 0.5	22 ± 0.11
7d	23 ± 0.22	24 ± 0.33	22 ± 0.35	27 ± 0.3	17 ± 0.74	17 ± 0.12	20 ± 0.5	15 ± 0.14
8a	27 ± 0.5	26 ± 0.14	25 ± 0.33	23 ± 0.14	25 ± 0.85	23 ± 0.11	24 ± 0.3	20 ± 0.82
8b	15 ± 0.45	NA	12 ± 0.74	14 ± 0.21	NA	15 ± 0.2	12 ± 0.65	NA
8c	22 ± 0.41	17 ± 0.78	25 ± 0.14	18 ± 0.3	NA	14 ± 0.52	19 ± 0.65	NA
8d	24 ± 0.5	25 ± 0.77	23 ± 0.65	26 ± 0.11	21±0.2	23 ± 0.65	25 ± 0.33	21 ± 0.16
9a	25 ± 0.21	21 ± 0.17	19 ± 0.14	22 ± 0.18	17 ± 0.2	20 ± 0.33	22 ± 0.19	19 ± 0.55
9b	25 ± 0.87	21 ± 0.3	24 ± 0.35	23 ± 0.2	21 ± 0.55	23 ± 0.4	19 ± 0.25	17 ± 0.5
9c	22 ± 0.18	22 ± 0.34	21 ± 0.72	23 ± 0.44	NA	23 ± 0.33	21 ± 0.5	19 ± 0.28
9d	18 ± 0.12	16 ± 0.54	NA	15 ± 0.96	NA	12 ± 0.61	18 ± 0.2	14 ± 0.38
Tetracycline	25 ± 0.22	25 ± 0.11	22 ± 0.25	23 ± 0.2	20 ± 0.5	21 ± 0.55	NA	NA
Amphotericin B	NA	NA	NA	NA	NA	NA	22 ± 0.2	18 ± 0.32

NA: no activity (8 mm), weak activity (8–12 mm), moderate activity (12–15 mm), strong activity (>15 mm), solvent (8 mm), and Bacillus subtilis (Bs), Staphylococcus aureus (Sa), Enterococcus faecalis (Ef), Escherichia coli (Ec), Pseudomonas aeruginosa (Pa), Salmonella typhi (St), Candida albicans (Ca), and Fusarium oxysporum (Fo).

Table 2

Minimal inhibitory concentrations (MIC, µg/mL) and the minimum bactericidal concentrations (MBC, µg/mL) of the potent Schiff bases against bacterial pathogens.

The Potent Schiff Bases	Gram-Positive						Gram-Negative
	B.s		S.a		E.f		E.c		P.a		S.t
	MIC	MBC	MIC	MBC	MIC	MBC	MIC	MBC	MIC	MBC	MIC	MBC
6b	7.81	14.05	15.62	31.25	9.25	18.5	62.5	87.5	31.25	53.12	15.62	28.11
7b	5.57	10.58	1.95	3.7	3.9	6.63	7.81	12.49	31.25	59.37	3.9	6.63
7c	9.25	18.5	31.25	53.12	7.81	15.62	18.51	36.5	55.5	88.8	31.25	56.25
8a	1.95	3.9	5.57	5.57	3.9	6.63	0.97	1.94	5.57	10.58	7.81	12.49
8d	3.9	6.63	7.81	15.62	15.62	31.25	7.81	15.62	27.77	55.54	18.51	36.5
9b	4.5	9.2	7.81	15.62	3.9	7.41	7.81	14.05	15.62	31.25	5.57	10.58
Tetracycline	31.25	40.62	62.5	87.5	62.5	93.75	15.62	18.74	62.5	87.5	31.25	43.75

Bacillus subtilis (Bs), Staphylococcus aureus (Sa), Enterococcus faecalis (Ef), Escherichia coli (Ec), Pseudomonas aeruginosa (Pa), and Salmonella typhi (St).

Table 3

Minimal inhibitory concentrations (MIC, µg/mL) and the minimum fungicidal concentrations (MFC, µg/mL) of the potent Schiff bases against fungi pathogen.

The Potent Schiff Bases	Fungi
	C.a		F.o
	MIC	MFC	MIC	MFC
6b	31.25	53.12	55.5	88.8
7b	15.62	28.11	31.25	46.87
7c	31.25	41.65	55.54	87.5
8a	7.81	15.62	15.62	27.77
8d	9.25	17.57	31.25	56.25
9b	7.81	12.49	15.62	26.55
Amphotericin B	15.62	34.62	31.25	65.62

Candida albicans (Ca) and Fusarium oxysporum (Fo).

From the inhibition zone measurements (IZ, Table 1), we pan class="Species">can conclude that there are six ecies">pan class="Chemical">Schiff bases (6b, 7b, 7c, 8a, 8d, and 9b) that displayed inhibition zone more than or near to the reference drugs (Tetracycline and Amphotericin B) against pathogenic microbes. For Gram positive and Gram negative, it was found that most of the Schiff bases exhibited moderate to potent anti-bacterial activities with inhibition zone (IZ) ranging between 12 and 33 mm for all pathogen tested in this study compared to Tetracycline that have IZ ranging between 20 and 25 mm. Moreover, most of the newly synthesized Schiff bases showed IZ between 9 and 27 mm, in comparison to Amphotericin B as a therapeutic abroad anti-fungal agent (18–22 mm). This result encouraged us to complete the study and measure the minimal inhibitory concentrations (MIC, µg/mL) of the potent Schiff bases (6b, 7b, 7c, 8a, 8d, and 9b). The results are represented in Table 2 and Table 3.

From Table 2 and Table 3, the six mopan class="Species">st potent ecies">pan class="Chemical">Schiff bases demonstrated broad, potent, and excellent activities against B. subtilis (Bs), where 6b (7.81 µg/mL, 4-fold), 7b (5.57 µg/mL, 5-folds), 7c (9.25 µg/mL, 3-folds) 8a (1.92 µg/mL, 16-folds), 8d (3.9 µg/mL, 8-folds), and 9b (4.5 µg/mL, 6-folds) were more potent compared to Tetracycline (31.25 µg/mL, standard antibacterial drug). The two Bis-pyrazole Schiff bases (7b and 7c) have only one difference in their structure by replacing phenyl (C6H5-) with 4-methylphenyl (4-CH3-C6H4-). The result showed good activities in comparison to standard drugs against both Gram positive and negative strains. The presence of phenyl ring in 7b makes it more effective than 7c (4-methyl phenyl ring), where a Schiff base 7b exhibited 32-folds (1.95 µg/mL), 16-fold (3.9 µg/mL), and 8-folds (3.9 µg/mL) more potent activity than that of Tetracycline (62.5, 62.5, and 31.25 µg/mL) against S. aureus (Sa), E. faecalis (Ef), and S. typhi (St), respectively. Furthermore, Schiff base 7b showed comparable activities toward both fungal strains used in this study with MIC values (15.62, 31.25 µg/mL) against C. albicans (Ca) and F. oxysporum (Fo), respectively, with two-folds higher than Schiff base 7c.

pan class="Chemical">Schiff base ecies">pan class="Chemical">8a bearing amide group in position four of pyrazole moiety exhibited minimal inhibitory concentrations (0.97 and 5.57 µg/mL) with 16 and 11.2-folds more than Tetracycline (15.62 and 62.5 µg/mL) against E. coli (Ec) and P. aeruginosa (Pa), respectively. From Table 3, among the tested pyrazole Schiff bases that exhibited anti-fungal activities, the two Schiff bases 8a and 9b revealed the best antifungal results with MIC values (7.81 and 15.62 µg/mL) against C. albicans (Ca) and F. oxysporum (Fo), respectively, that reveled 2-fold activity in comparison with Amphotericin B (15.62, 31.25 µg/mL).

2.2.2. Minimal Bactericidal Concentration (MBC) and Minimum Fungicidal Concentration (MFC)

The pan class="Disease">MBC is complementary to the MIC; whereas the MIC teecies">pan class="Species">st demonstrates the lowest level of antimicrobial agent that greatly inhibits growth, but the MBC determines the lowest level of antimicrobial agent that leads to the death of microbial organisms. In other words, if a MIC shows inhibition only, i.e., the antimicrobial activity does not cause death, in contrast to MBC that causes death [56]. MBC is usually presented as MBC50, which means the drug concentration kills 50% of the initial bacterial population [57]. The promising pyrazole Schiff bases 6b, 7b, 7c, 8a, 8d, and 9b showed bactericidal activities in general. For Gram positive bacteria, MBC values ranged between (3.7 and 53.12 µg/mL) compared to Tetracycline (40.62 and 93.75 µg/mL), and the most active Schiff base 8a exhibited bactericidal activity (3.9, 5.57, 6.63 µg/mL) for B. subtilis (Bs), S. aureus (Sa), E. faecalis (Ef) compared to Tetracycline (40.62, 87.5, 93.75 µg/mL) respectively, followed by 9b and 7c that showed MBC values (9.2, 15.62, 7.41 µg/mL) and (10.58, 3.7, 6.63 µg/mL). Also, three Schiff bases 8a, 9b, and 7c revealed MBC values (1.94, 14.05, 12.49 µg/mL) and (10.58, 31.25, 59.37 µg/mL) for both E. coli (Ec) and P. aeruginosa (Pa), respectively.

On the other hand, pan class="Species">for Gram negative bacteria, ecies">pan class="Chemical">Schiff base 7b showed the best MBC value among the six Schiff bases (6.63 µg/mL with nearly 6.6 folds potent than the standard drug) against S. typhi (St). But, Schiff base 7c exhibited the worst results to Gram negative bacterial strains. In the same way, four from six of the promising Schiff bases known as 7b, 8a, 8d, and 9b showed a good fungicidal activity with MFC values ranging from (12.94–56.25 µg/mL) in comparison with Amphotericin B (34.62–65.62 µg/mL). However, both 6b and 7c showed slightly increased activity than reference drug.

Previous pan class="Species">studies reported that there is a relation between the MIC and ecies">pan class="Disease">MBC to decide whether the newly designed compounds have cidal or statical activities for bacteria and fungi [58]; antibacterial agent that has MBC/MIC ratios higher than or equal to 8 is considered as a bacteriostatic agent, and by contrast, the MBC/MIC ratio between 1 and 2 is regarded as bactericidal agent according to Clinical and Laboratory Standards Institute (CLSI) standards [59,60]. As shown in Table 2 and Table 3 and by applying MBC/MIC and MFC/MIC ratios, the values obtained ranged between one and nearly two and that expressed all the promising compounds show bactericidal and fungicidal activities with lower concentration depending on MBC, MFC, and MIC values.

2.2.3. In Vitro Antiproliferative Activities

Our work is extended to pan class="Species">study in vitro antiecies">pan class="Chemical">proliferative activities (IC50, µM) of the most potent Schiff bases 6b, 7b, 7c, 8a, 8d, and 9b that are tested against two human cancer cell lines namely hepatocellular carcinoma cell line (HepG2) and mammary gland breast cancer cell line (MCF-7) as well as normal, non-cancer cells (Vero cells, ATCC CCL-81) according to the 3-[4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) protocol [61,62,63], in comparison with that of doxorubicin as a well-known chemotherapeutic agent (positive control) and the results are shown in Table 4 and Figure 2.

Table 4

The IC50 (µM) of Schiff bases (6b, 7b, 7c, 8a, 8d, and 9b) against the two cancer cell lines HepG-2 and MCF-7 as well as Vero cells (ATCC CCL-81) cell lines.

The Potent Schiff Bases	IC50 (µM)
	HepG-2	MCF-7	Vero
6b	3.42 ± 0.17	5.09 ± 0.52	343.89 ± 0.49
7b	7.18 ± 0.49	4.81 ± 0.25	361.22 ± 0.23
7c	1.22 ± 0.23	3.24 ± 0.41	213.45 ± 0.57
8a	2.25 ± 0.85	1.98 ± 1.55	120.55 ± 0.34
8d	2.63 ± 0.44	3.69 ± 0.22	241.19 ± 1.55
9b	1.92 ± 0.49	2.21 ± 0.36	195.94 ± 0.57
Doxorubicin	3.92 ± 0.50	1.94 ± 0.80	ND

** ND meaning not determined.

Figure 2

The antiproliferative activities (IC50, µM) of the Schiff bases and doxorubicin against HepG-2 and MCF-7 cell lines.

From Table 4 and Figure 2 results, it was obpan class="Chemical">served that moecies">pan class="Species">st of the Schiff bases displayed potent cytotoxicity with low micromolar (µM) concentration. For HepG-2 lines, five Schiff bases 6b, 7c, 8a, 8d, and 9b expressed IC50 lower than doxorubicin and their cytotoxicity ranged between (1.22 ± 0.23 and 3.42 ± 0.17 µM) in comparison to reference drug (3.92 ± 0.50 µM), only Schiff base 7b showed lower toxicity with (0.54-fold) against doxorubicin. Notably, three Schiff bases 7c, 8a, and 9b exhibited remarkable antitumor activities with IC50 values 1.22 ± 0.23, 2.25 ± 0.85, and 1.92 ± 0.49, respectively.

On the other hand, the antipan class="Chemical">proliferative activities of the ecies">pan class="Chemical">Schiff bases against MCF-7 lines showed moderate activities except for the two Schiff bases 8a (1.98 ± 1.55 µM, 0.979 fold) and 9b (2.21 ± 0.36 µM, 0.877 fold) which showed values near to doxorubicin (1.94 ± 0.80 µM). Nevertheless, other derivatives exhibited only moderate activities.

To determine the safety and selectivity of the mopan class="Species">st potent ecies">pan class="Chemical">Schiff bases 6b, 7b, 7c, 8a, 8d, and 9b, the cytotoxicity of promising compounds was determined on healthy non-cancer cells (Vero cells, ATCC CCL-81) from an African green monkey kidney continuous cell by colorimetric MTT assay. The new Schiff bases showed very lower toxicity on healthy non-cancer cells Vero cells with (IC50 > 120), and that proved that these new Schiff bases 6b, 7b, 7c, 8a, 8d, and 9b displayed safety and revealed selectivity toward cancerous cells.

Finally, from all the previously pan class="Species">studied and beecies">pan class="Species">cause of the efficiency of the promising six Schiff bases as antimicrobial and antiproliferative potential agents, these derivatives were chosen for further investigation.

2.2.4. Immunomodulatory Activity

In this section, we gain insight into the in vitro immunomodulatory potential of the active compounds. Innate immunity is the firpan class="Species">st line of defense againecies">pan class="Species">st pathogens present in our environment such as fungi, bacteria, and viruses and eliminates damaged cells and tumor cells characterized by rapid response, infection halting. The innate immunity system may include macrophage, mast cells, dendritic cells (DCs), eosinophils, basophils, neutrophils as well as invariant natural killer cells (NK cells) [64]. The neutrophil can cause microorganisms intracellular killing [65]. The immunomodulatory activity expressed by percentage (%) values for the intracellular killing was performed using nitro blue tetrazolium (NBT) reductase assay, where the increasing percentage is related to improvement in the killing ability of the neutrophils, and was performed according to the reported method [66]. The results are represented in Table 5.

Table 5

Intracellular killing activities of Schiff bases.

The Potent Schiff Bases (at 15.62 µg/mL)	Intracellular Killing Activity %
6b	88.7 ± 0.19
7b	95.4 ± 0.98
7c	72.8 ± 0.37
8a	136.5 ± 0.3
8d	49.6 ± 0.14
9b	115.2 ± 0.5

The potent pan class="Chemical">Schiff bases 6b, ecies">pan class="Chemical">7b, 7c, 8a, 8d, and 9b were evaluated as immunomodulatory agents by percentage values that ranged between (49.6 ± 0.14%) and (136.5 ± 0.3%) and depending on the obtained results the pyrazole derivatives generally induced the immune system to defend against pathogens or tumors by variable percentage. The highest immunostimulatory action was shown by compound 8a (136.5 ± 0.3%) that has a pyrazole moiety as well as amide function (O=C-NH2) and piperidinyl core followed by compound 9b with a ratio (115.2 ± 0.5%) having pyrazole and benzamide (Ph-NH-C=O) in position four in addition to three methoxy groups.

2.2.5. Drug Resistance

The synthesized pan class="Chemical">pyrazole Schiff bases 6b, ecies">pan class="Chemical">7b, 7c, 8a, 8d, and 9b were tested for their in vitro antibacterial activity against a panel of multidrug-resistant bacteria (MDRB) classified as one clinical strain S. aureus (ATCC 43300) (MRSA) with three standard strain S. aureus (ATCC 33591), E. coli (ATCC BAA-196), and P. aeruginosa (ATCC BAA-2111). The broad-spectrum antibiotic Norfloxacin was used as a positive control. The obtained results from Table 6 revealed that the synthesized pyrazole Schiff bases showed varying degrees of activities with strong activities (inhibition zone higher than 15 mm) against the tested microorganisms and therefore, MIC and MBC were performed and are shown in Table 7.

Table 6

In vitro antimicrobial activities of the most promising Schiff bases against multidrug-resistant bacteria (MDRB).

The Potent Schiff Bases	Mean Diameter of Inhibition Zone (mm) against MDRB.
	S. aureusATCC 43300	S. aureusATCC 33591	E. coliATCC BAA-196	P. aeruginosaATCC BAA-2111
6b	21 ± 0.21	20 ±0. 35	25 ± 0.15	21 ± 0.66
7b	18 ± 0.11	15 ± 0.41	20 ± 0.44	21 ± 0.33
7c	17 ± 0.37	21 ± 0.19	21 ± 0.3	22 ± 0.5
8a	26 ± 0.15	24 ± 0.12	25 ± 0.46	27 ± 0.54
8d	18 ± 0.5	21 ± 0.23	16 ± 0.11	25 ± 0.99
9b	24 ± 0.65	25 ± 0.12	22 ± 0.2	24 ± 0.88
Norfloxacin	25 ± 0.50	26 ± 0.5	27 ± 0.98	24 ± 0.47

Table 7

Minimal inhibitory concentrations (MIC, µg/mL) and minimum bactericidal concentrations (MBC, µg/mL) of the most potent Schiff bases against MDRB.

The Potent Schiff Bases	S. aureus ATCC 43300		S. aureus ATCC 33591		E. coliATCC BAA-196		P. aeruginosaATCC BAA-2111
	MIC	MBC	MIC	MBC	MIC	MBC	MIC	MBC
6b	6.25	11.87	7.81	15.62	3.9	7.41	7.81	15.98
7b	7.81	15.62	8.88	15.98	9.25	18.5	7.81	15.62
7c	7.81	14.83	5.55	11.1	7.81	14.83	4.44	6.66
8a	1.95	3.9	3.9	7.8	1.95	3.9	3.9	7.8
8d	15.62	31.25	3.9	7.41	15.62	31.25	6.25	11.87
9b	2.5	4.5	1.95	3.31	6.25	11.87	5.2	9.88
Norfloxacin	1.25	2.81	0.78	1.56	1.57	3.53	3.13	4.69

From Table 7, it is obpan class="Chemical">served that the MIC values range, ecies">pan class="Species">for the most promising six Schiff bases 6b, 7b, 7c, 8a, 8d, and 9b, between 1.95 and 15.62 µg/mL as well as MBC values between 3.31 and 31.25 µg/mL against MDRB strains compared with Norfloxacin MIC (0.78–3.13 µg/mL) and MBC (1.56–4.69 µg/mL). Most of the tested pyrazole Schiff bases 6b, 7b, 7c, 8a, 8d, and 9b showed remarkable broad-spectrum activities against both Gram-positive and Gram-negative bacteria for inhibitory or bactericidal activity and among them Schiff bases 8a and 9b showed the highest activities in comparison with other derivatives; compound 8a with mono-pyrazole, piperidinyl, and p-tolyl-amide derivative demonstrated MIC values ranging between (1.95 and 7.8 µg/mL). Besides, Schiff base 9b having a mono pyrazole nucleus and benzamide in position four also showed MIC values (1.95–6.25 µg/mL) and MBC values (3.31–11.87 µg/mL). According to the Clinical and Laboratory Standards Institute (CLSI) standards and by applying the MBC/MIC ratio, we found that all the tested pyrazole Schiff bases exhibited values less than two, meaning bactericidal property.

2.2.6. Enzyme Assessment of Dihydrofolate Reductase (DHFR) and DNA Gyrase

In continuation of our previous efpan class="Species">forts, we tecies">pan class="Chemical">argeted the most two active Schiff bases (8a and 9b) depending on previous studies as antimicrobial and anticancer agents from the previous results to evaluate their activities and mechanism against DHFR and DNA gyrase enzymes. The two active Schiff bases (8a and 9b) were introduced to enzyme assay against dihydrofolate reductase (DHFR) on E. coli organism and DNA gyrase with two different organisms as S. aureus and B. subtilis to determine the inhibitory activities expressed as IC50 (µM), using Trimethoprim and Ciprofloxacin, respectively, as the reference drugs. The result is shown in Table 8 and Figure 3.

Table 8

Determination of the DNA gyrase and DHFR inhibitory activities of the most promising two Schiff bases 8a and 9b.

Schiff Bases	IC50 (Mean ± SEM, µM)
	S. aureus DNA Gyrase	B. subtilis DNA Gyrase	DHFR E. coli
8a	7.69 ± 0.23	15.27 ± 0.50	3.98 ± 0.61
9b	10.47 ± 0.55	14.25 ± 0.42	6.48 ± 0.33
Ciprofloxacin	26.31 ± 1.64	29.72 ± 1.32	---
Trimethoprim	---	---	5.17 ± 0.12

Figure 3

The inhibitory activities (IC50, µM) of the two Schiff bases (8a and 9b) and reference drugs against DNA gyrase and dihydrofolate reductase (DHFR).

The results show that, both pan class="Chemical">Schiff bases ecies">pan class="Chemical">8a and 9b have an inhibitory property against two different types of DNA gyrase, where IC50 values of Schiff base 8a demonstrated (7.69 ± 0.23 and 15.27 ± 0.50 µM) for S. aureus DNA gyrase, and Schiff base 9b revealed (10.47 ± 0.55 and 14.25 ± 0.42 µM) for B. subtilis DNA gyrase and both 8a and 9b exhibited inhibitory stronger activities than Ciprofloxacin (26.31 ± 1.64 and 29.72 ± 1.32 µM). Moreover, Schiff base 8a (3.98 ± 0.61 µM) with pyrazole core and piperidinyl pharmacophore showed DHFR enzyme with 1.3-fold higher potential than the positive control (Trimethoprim, 5.17 ± 0.12 µM) while the Schiff base 9b with one pyrazole moiety showed IC50 value (6.48 ± 0.33 µM) with (0.80 fold), respectively.

Finally, it is noticed that designing new pan class="Chemical">Schiff bases with ecies">pan class="Chemical">pyrazole moiety (mono or Bis) with different amide and aniline derivatives in position four and three respectively, based on pyrazole nucleus prepared from cyan-acetanilide derivatives, and the reaction of amino pyrazole obtained with different aldehyde may improve the antimicrobial activity (MIC, MBC, MDRB); therefore, the enzyme inhibitory activity (DNA gyrase) and dihydrofolate reductase (DHFR) and anticancer activity against the two different cell lines, HepG-2 and MCF-7, determine the safety and selectivity on Vero cell line.

2.3. In Silico Studies

2.3.1. Docking and Molecular Modeling Study

In recent years, molecular modeling pan class="Species">study is considered as an important ecies">pan class="Species">study because it provides a more accurate picture of biologically active molecules at the atomic level and plays a major role in the drug designing process [67]. Docking process was performed using Molecular Operating Environment software 10.2008 (MOE), Chemical Computing Group Inc., Montreal, Quebec, Canada. Two proteins were obtained from the protein data bank (https://www.rcsb.org/) for this purpose. First one (PDB: 1DLS) for dihydrofolate reductase enzyme (DHFR) that co-crystallized with Methotrexate (MTX) [68], and another one is S. aureus DNA gyrase enzyme (PDB: 2XCT) and Ciprofloxacin was found co-crystallized inside the pocket [57,60]. The docking results involving all energy score (S) (Kcal/mol), binding of amino acids inside pocket with interacting groups of the ligand in docking compounds, and lengths of the bond are summarized in Table 9 and represented in Figure 4a–d.

Table 9

Docking results of the promising pyrazole Schiff bases inside 1DLS and 2XCT active site.

The Promising Compounds	Energy Score(S) (Kcal/mol)	Amino Acids	Interacting Groups	Length (Å)
MTX (1DLS)	−27.31	Ile 7Glu 30Arg 70Asn 64Phe 34	NH2 of pyrimidine ringNH2 of pyrimidine ringTwo oxygen of carboxylateCarbonyl of amidePyrazine ring	2.892.733.12 & 2.682.64--
8a (1DLS)	−18.96	Asp 21Lys 55	NH of pyrazoleOxygen of methoxy group	3.103.33
9b (1DLS)	−26.13	Arg 28Ars 64Phe 34Phe 31	Two oxygen of two methoxy group in tri methoxy phenylMethoxy of tri methoxy ald.Ph of tri methoxy aldehydePh of amide derivatives	2.843.073.00----
Cip. (2XCT)	−11.87	Ser 1084Ser 1084	CO of COOHOH of COOH	2.492.60
8a (2XCT)	−19.09	Asp 508Pro 1080	NH of pyrazoleNH2 of amide	2.512.69
9b (2XCT)	−21.74	Lys 1043Ser 1085Lys 460Lys 460	Oxygen of methoxy groupNH of pyrazolePh of tri methyl aldehydePh of amide derivatives	3.002.98--
(-) indicate arene-cation interaction; (--)indicate arene-arene interaction

Figure 4

(a) 2D and 3D interactions of compound 8a in the active site of 1DLS. (b) 2D and 3D interactions of compound 9b in the active site of 1DLS. (c) 2D and 3D interactions of compound 8a in the active site of 2XCT. (d) 2D and 3D interactions of compound 9b in the active site of 2XCT.

Docking of the pan class="Chemical">promising compounds ecies">pan class="Chemical">8a, 9b inside the active site of (PDB: 1DLS) for the dihydrofolate reductase enzyme (DHFR) revealed that compounds 8a, 9b provide a docking pose with an energy score (S= −18.96 and −26.13 Kcal/mol) compared to Methotrexate (MTX) (S = −27.31 Kcal/mol) that forms five hydrogen bonds, two hydrogen bond donor with Ile 7 and Glu 30 two amino of pyrimidine, and three hydrogen bond acceptor two with Arg 70 and the third one with Asn 64 with bond length (3.12, 2.68 and 2.64 Å). It was observed that the two Schiff bases 8a and 9b (Figure 4a,b) mainly interacts with the target enzyme by showing hydrogen bonding interaction for example, Schiff base 8a with IC50 values (3.98 ± 0.61 µM) showed two hydrogen bonds with one hydrogen bond donor between Asp 21 and NH of pyrazole nucleus and another hydrogen bond acceptor between Lys 55 and the oxygen atom of the methoxy group of the p-anisidine amine with bond length 3.10 and 3.33 Å respectively. On the other hand, compound 9b showed energy score near to Methotrexate (MTX), with three hydrogen bond acceptor between Arg 28 and two oxygen of methoxy groups of tri-methoxy benzaldehyde derivatives with (2.84 and 3.07 Å), and the third methoxy group forms a bond with Ars 64 with bond length (3.00 Å) as well as two arene-arene interaction with two amino acids Phe 34 and Phe 31, beside hydrophobic interaction.

While pan class="Species">for ecies">pan class="Species">S. aureus DNA gyrase enzyme (PDB: 2XCT), the natural ligand 1-cyclopropyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid (Ciprofloxacin) advertised two hydrogen bond interactions with Ser 1084 amino acid with bond length 2.49, 2.60 Å via carboxylate ion and self-docking process showed that Ciprofloxacin binds with the pocket with an energy score (S) = −11.87 kcal/mol. Both Schiff bases 8a and 9b with S. aureus DNA gyrase IC50 values (7.69 ± 0.23 and 10.47 ± 0.55 µM) showed score energy (S = −19.09, −21.74 Kcal/mol) higher than Ciprofloxacin (S = −11.87 Kcal/mol), respectively (see Table 9) [57,60]. As for amino acid interactions, Schiff base 8a showed two hydrogen bond donors with Asp 508 through the NH of pyrazole, in addition to hydrogen bond between Pro 1080 and amino of amide group (Figure 4c). Schiff base 9b formed two hydrogen bonds (Figure 4d) Lys 1043 and Ser 1085 through the oxygen of methoxy group and NH of pyrazole as well as two arene-cation interactions between phenyl derivatives of tri-substituted aldehyde and amide derivatives with Lys 460.

Finally, all the docked compounds showed desirable interaction, especially pan class="Chemical">hydrogen bond and ecies">pan class="Chemical">arene-cation or arene-arene interaction with two protein targets, and that proceeds mainly through NH of pyrazole or oxygen of methoxy groups, present in our new promising compounds. It can be concluded that the newly designed pyrazole Schiff bases, mainly mono pyrazole Schiff bases 8a and 9b could exert their antimicrobial, anticancer activity with selectivity to the cancer cell and induced increased immunity against pathogen and tumor via two different mechanisms as DHFR and DNA gyrase inhibitors.

2.3.2. Predication of the Physicochemical and Pharmacokinetics Properties

The physicochemipan class="Species">cal ecies">pan class="Chemical">properties to evaluate the drug-likeness of the two pyrazole Schiff bases (8a and 9b) were generated in silico using Swiss ADME (http://swissadme.ch/index.php#undefined). Also, the reference drugs (Norfloxacin, Ciprofloxacin, and Trimethoprim) were generated, and the results are shown in Table 10.

Table 10

In silico the physicochemical properties of the two pyrazole Schiff bases (8a and 9b) and the reference drugs for Lipinski’s rule of five and Veber filter:-.

Schiff Bases and the Reference	MW	MLogP	nHBA	nHBD	nRB	TPSA	Violations fromLipinski’s Rule	Violations from Veber Filter
Rule	<500	≤4.15	≤10	≤5	≤10	≤140 Å2	Yes; 0 or 1 violation	Yes; 0 violation
8a	418.49	2.86	4	3	7	108.63	Yes; 0 violation	Yes; 0 violation
9b	501.53	2.73	7	3	11	119.09	Yes; 1 violation:MW > 500	No; 1 violation: Rotors > 10
Norfloxacin	319.33	1.04	5	2	3	74.57	Yes; 0 violation	Yes; 0 violation
Ciprofloxacin	331.34	1.28	5	2	3	74.57	Yes; 0 violation	Yes; 0 violation
Trimethoprim	290.32	0.41	5	2	5	105.51	Yes; 0 violation	Yes; 0 violation

The Lipinski rule-of-five (Ro5) include pan class="Species">four ecies">parameters: (a) MW ≤ 500 as molecular weight, (b) MLogP ≤ 4.15 as lipophilicity, (c) N or O ≤ 10 as ecies">pan class="Chemical">hydrogen bond acceptors, (d) NH or OH ≤ 5 as hydrogen bond donors [69].

From Table 10, the number of pan class="Chemical">hydrogen bond acceptors (nHBA), donors (nHBD), and lipophilicity ecies">pan class="Chemical">property for the two pyrazole Schiff bases were in agreement with the Lipinski’s rule of five (Ro5). The molecular weight of the Schiff base (9b) is more than 500 g/mol. The pyrazole Schiff bases must not be violated more than one parameter to become an oral drug concerning bioavailability [70]. Therefore, the two pyrazole Schiff bases (8a and 9b) may become an oral drug.

Veber (GSK) filter includes two parameters: (a) nRB ≤ 10 as rotatable bonds, (b) TPSA ≤ 140 as topologipan class="Species">cal polar surface area [71]. According to this rule, the ecies">pan class="Chemical">pyrazole Schiff base 8a is in agreement with Veber filter.

The pharmacokinetics pan class="Chemical">properties of the two ecies">pan class="Chemical">pyrazole Schiff bases (8a and 9b), and the reference drugs (Norfloxacin, Ciprofloxacin, and Trimethoprim) were generated in silico using Swiss ADME (http://swissadme.ch/index.php#undefined), shown in Table 11 and we can deduce that:

Table 11

In silico the pharmacokinetics properties of the two pyrazole Schiff bases (8a and 9b) and the reference drugs:-.

Schiff Basesand the Reference.	GIAbsorption	BBB Permeant	P-gp Substrate	CYP1A2 Inhibitor	CYP2C19 Inhibitor	CYP2C9 Inhibitor	CYP2D6 Inhibitor	CYP3A4 Inhibitor	Log Kp (cm/s)
8a	High	No	No	No	Yes	Yes	No	Yes	−5.95
9b	Low	No	No	No	Yes	Yes	Yes	Yes	−5.81
Norfloxacin	High	No	Yes	No	No	No	No	No	−8.98
Ciprofloxacin	High	No	Yes	No	No	No	No	No	−9.09
Trimethoprim	High	No	Yes	No	No	No	No	No	−7.42

pan class="Chemical">Schiff base ecies">pan class="Chemical">8a and the three reference drugs show a high gastrointestinal absorption (GI).

The two pan class="Chemical">pyrazole Schiff bases (ecies">pan class="Chemical">8a and 9b) and the reference drugs did not show any effect on the central nervous system as none of the Schiff bases show blood-brain barrier (BBB) permeation.

None of the pan class="Chemical">Schiff bases are predicted as non-subecies">pan class="Species">strate for the permeability of glycoprotein (P-gp). Where P-glycoprotein is appraising active efflux by biological membranes and protects the central nervous system.

The two pan class="Chemical">Schiff bases (ecies">pan class="Chemical">8a and 9b) are predicted as inhibitors of CYP2C19, CYP2C9, CYP2D6, and CYP3A4 enzymes excluding 8a as a non-inhibitor of CYP2D6 enzyme. Also, the two Schiff bases are predicted as non-inhibitors of CYP1A2 enzyme. The reference drugs are predicted as non- inhibitors of five enzymes.

The log of skin permeability coefficient (log Kp) is predicted pan class="Species">for the two ecies">pan class="Chemical">Schiff bases 8a and 9b as −5.95 and −5.81 cm/s, respectively. The log Kp of the reference drugs ranged from −7.42 to −9.09 cm/s.

3. Experimental Section

3.1. Chemistry

Melting points were recorded on a Gallenkamp apparatus. The IR spectra were perpan class="Species">formed (KBr) on a 1650 FT-IR inecies">pan class="Species">strument. NMR spectra (DMSO-d6) were recorded on a Varian spectrometer (1H-NMR: 300/400 MHz and 13C-NMR: 76/101 MHz). Mass spectra and elemental analyses were determined at the Microanalytical Center, Cairo University, Egypt.

Compounds, {pan class="Chemical">5-amino-N-aryl-3-(4-methoxyphenylamino)-1H-pyrazole-4-carboxamide 1a–d [51,52,53], ecies">pan class="Chemical">5-chloro-3-methyl-1-phenyl-1H-pyrazole-4-carbaldehyde (3) [72] and 4-(piperidin-1-yl)benzaldehyde (4) [73]}, were prepared according to the reported procedure.

pan class="Chemical">1,5-Dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carbaldehyde (ecies">pan class="Chemical">4-antipyrinecarboxaldehyde) (2) and 3,4,5-trimethoxybenzaldehyde (5) were of Merck AR grade, Germany.

General method pan class="Species">for synthesis of double ecies">pan class="Chemical">pyrazole Schiff bases (

Compounds 1a–d (0.01 mol) were mixed with pan class="Chemical">1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carbaldehyde (2), ecies">pan class="Chemical">5-chloro-3-methyl-1-phenyl-1H-pyrazole-4-carbaldehyde (3), 4-(piperidin-1-yl)benzaldehyde (4), or 3,4,5-trimethoxybenzaldehyde (5) in absolute EtOH (25 mL) and a catalytic amount of glacial acetic acid (1 mL). The reaction mixture was refluxed for one hour; the solid product obtained on hot was filtered off and recrystallized from EtOH to afford the corresponding new bis-pyrazole Schiff bases 6a–d, 7a–d or mono-pyrazole Schiff bases 8a–d and 9a–d, respectively.

5-((1,5-Dimethyl-3-oxo-2-pan class="Chemical">phenyl-2,3-dihydro-ecies">pan class="Chemical">1H-pyrazol-4-yl)methyleneamino)-3-(p-methoxyphenylamino)-1H-pyrazole-4-carboxamide (6a): Yellow crystals; melting point: 274–276 °C; yield: 79%. IR (KBr) νmax/cm−1 3359, 3165 (NH, NH2), 1675, 1654 (2C=O). 1H-NMR (400 MHz) δ ppm: 2.61 (s, 3H, CH3), 3.37 (s, 3H, NCH3), 3.70 (s, 3H, OCH3), 6.85 (d, 2H, J = 8.2 Hz, ArH), 7.19 (s, 1H, NH2-amide, exchangeable with D2O), 7.37 (d, 2H, J = 7.4 Hz, ArH), 7.45–7.48 (m, 3H, ArH), 7.56 (t, 2H, ArH), 7.80 (s, 1H, NH2-amide, exchangeable with D2O), 8.68 (s, 1H, -CH=N-), 8.85, 12.37 (2s, 2H, 2NH, exchangeable with D2O). 13C-NMR (101 MHz) δ ppm: 11.50 (CH3), 33.93 (NCH3), 55.21 (OCH3), 101.94, 105.97, 114.24, 117.08, 126.85, 128.42, 129.38, 133.70, 135.49, 144.36, 148.19, 153.38, 154.30, 156.79 (18C), 162.54 (C=O, amide), 166.76 (C=O, antipyrine). MS (m/z, %): 445 (M+, 13.44). Anal. Calcd. (%) for C23H23N7O3 (445.47): C, 62.01; H, 5.20; N, 22.01. Found: C, 62.23; H, 5.07; N, 22.16.

5-((1,5-Dimethyl-3-oxo-2-pan class="Chemical">phenyl-2,3-dihydro-ecies">pan class="Chemical">1H-pyrazol-4-yl)methyleneamino)-3-(p-methoxyphenylamino)-N-phenyl-1H-pyrazole-4-carboxamide (6b): Yellow crystals; melting point: 241–243 °C; yield: 82%. IR (KBr) νmax/cm−1 3427, 3249 (NH), 1672, 1655 (2C=O). 1H-NMR (400 MHz) δ ppm: 2.64 (s, 3H, CH3), 3.39 (s, 3H, NCH3), 3.72 (s, 3H, OCH3), 6.88 (d, 2H, J = 9.0 Hz, ArH), 7.01 (t, 1H, ArH), 7.27 (t, 2H, ArH), 7.42–7.52 (m, 5H, ArH), 7.60 (t, 2H, ArH), 7.88 (d, 2H, J = 7.6 Hz, ArH), 8.77 (s, 1H, -CH=N-), 8.79, 10.43, 12.44 (3s, 3H, 3NH, exchangeable with D2O). 13C-NMR (101 MHz) δ ppm: 11.53 (CH3), 33.91 (NCH3), 55.29 (OCH3), 102.01, 105.94, 114.24, 121.47, 123.52, 125.27, 128.39, 129.35, 133.71, 133.84, 135.41, 144.64, 148.13, 153.60, 154.32, 156.81 (24C), 162.36 (C=O, amide), 166.71 (C=O, antipyrine). MS (m/z, %): 521 (M+, 28.63). Anal. Calcd. (%) for C29H27N7O3 (521.57): C, 66.78; H, 5.22; N, 18.80. Found: C, 66.61; H, 5.37; N, 18.73.

5-((1,5-Dimethyl-3-oxo-2-pan class="Chemical">phenyl-2,3-dihydro-ecies">pan class="Chemical">1H-pyrazol-4-yl)methyleneamino)-3-(p-methoxyphenylamino)-N-p-tolyl-1H-pyrazole-4-carboxamide (6c): Yellow crystals; melting point: 126–128 °C; yield: 87%. IR (KBr) νmax/cm−1 3432, 3290 (NH), 1669, 1652 (2C=O). 1H-NMR (400 MHz) δ ppm: 2.24 (s, 3H, CH3), 2.62 (s, 3H, CH3), 3.38 (s, 3H, NCH3), 3.71 (s, 3H, OCH3), 6.88 (d, 2H, J = 8.7 Hz, ArH), 7.07 (d, 2H, J = 8.0 Hz, ArH), 7.42 (d, 2H, J = 7.6 Hz, ArH), 7.47–7.61 (m, 5H, ArH), 7.76 (d, 2H, J = 8.1 Hz, ArH), 8.79 (s, 2H, -CH=N- & NH exchangeable with D2O), 10.38, 12.23 (2s, 2H, 2NH, exchangeable with D2O). 13C-NMR (101 MHz) δ ppm: 11.56 (CH3), 21.29 (CH3), 33.87 (NCH3), 55.31 (OCH3), 102.04, 105.96, 114.19, 121.52, 123.49, 125.25, 128.37, 129.31, 133.73, 133.80, 135.39, 144.61, 148.11, 153.59, 154.34, 156.82 (24C), 162.34 (C=O, amide), 166.69 (C=O, antipyrine). MS (m/z, %): 535 (M+, 35.07). Anal. Calcd. (%) for C30H29N7O3 (535.60): C, 67.27; H, 5.46; N, 18.31. Found: C, 67.09; H, 5.38; N, 18.47.

pan class="Chemical">N-(4-Chlorophenyl)-5-((1,5-dimethyl-3-oxo-2-ecies">pan class="Chemical">phenyl-2,3-dihydro-1H-pyrazol-4-yl)methyleneamino)-3-(p-methoxyphenylamino)-1H-pyrazole-4-carboxamide (6d): Orange crystals; melting point: 200–202 °C; yield: 82%. IR (KBr) νmax/cm−1 3424, 3281 (NH), 1670, 1654 (2C=O). 1H-NMR (400 MHz) δ ppm: 2.61 (s, 3H, CH3), 3.39 (s, 3H, N-CH3), 3.72 (s, 3H, OCH3), 6.88 (d, 2H, J = 9.1 Hz, ArH), 7.30 (d, 2H, J = 8.9 Hz, ArH), 7.42–7.52 (m, 5H, ArH), 7.60 (t, 2H, ArH), 7.96 (d, 2H, J = 8.9 Hz, ArH), 8.71 (s, 1H, -CH=N-), 8.81, 10.66, 12.59 (3s, 3H, 3NH, exchangeable with D2O). 13C-NMR (101 MHz) δ ppm: 11.52 (CH3), 33.86 (N-CH3), 55.59 (OCH3), 102.08, 105.92, 114.20, 121.58, 123.51, 125.26, 128.41, 129.28, 133.71, 133.78, 135.43, 144.60, 148.14, 153.61, 154.36, 156.88 (24C), 162.36 (C=O, amide), 166.72 (C=O, antipyrine). MS (m/z, %): 556 (M+, 14.46). Anal. Calcd. (%) for C29H26ClN7O3 (556.01): C, 62.64; H, 4.71; N, 17.63. Found: C, 62.76; H, 4.61; N, 17.69.

5-((5-Chloro-3-methyl-1-pan class="Chemical">phenyl-ecies">pan class="Chemical">1H-pyrazol-4-yl)methyleneamino)-3-(p-methoxyphenylamino)-1H-pyrazole-4-carboxamide (7a): Yellow crystals; melting point: 270–272 °C; yield: 74%. IR (KBr) νmax/cm−1 3342, 3166 (NH, NH2), 1655 (C=O). 1H-NMR (300 MHz) δ ppm: 2.52 (s, 3H, CH3), 3.72 (s, 3H, OCH3), 6.87 (d, 2H, J = 8.0 Hz, ArH), 7.35–7.66 (m, 9H, 7H of ArH & 2H of NH2-amide exchangeable with D2O), 8.83 (s, 1H, -CH=N-), 8.88, 12.69 (2s, 2H, 2NH, exchangeable with D2O). Anal. Calcd. (%) for C22H20ClN7O2 (449.89): C, 58.73; H, 4.48; N, 21.79. Found: C, 58.90; H, 4.51; N, 21.64.

5-((5-Chloro-3-methyl-1-pan class="Chemical">phenyl-ecies">pan class="Chemical">1H-pyrazol-4-yl)methyleneamino)-3-(p-methoxyphenylamino)-N-phenyl-1H-pyrazole-4-carboxamide (7b): Yellow crystals; melting point: 228–230 °C; yield: 79%. IR (KBr) νmax/cm−1 3345 (NH), 1657 (C=O). 1H-NMR (300 MHz) δ ppm: 2.59 (s, 3H, CH3), 3.73 (s, 3H, OCH3), 6.90 (d, 2H, J = 7.5 Hz, ArH), 7.09 (t, 1H, ArH), 7.35 (t, 2H, ArH), 7.53–7.67 (m, 9H, ArH), 8.76 (s, 1H, -CH=N-), 8.91, 9.53, 12.87 (3s, 3H, 3NH, exchangeable with D2O). MS (m/z, %): 525 (M+, 23.62). Anal. Calcd. (%) for C28H24ClN7O2 (525.99): C, 63.94; H, 4.60; N, 18.64. Found: C, 64.07; H, 4.51; N, 18.69.

5-((5-Chloro-3-methyl-1-pan class="Chemical">phenyl-ecies">pan class="Chemical">1H-pyrazol-4-yl)methyleneamino)-3-(p-methoxyphenylamino)-N-p-tolyl-1H-pyrazole-4-carboxamide (7c): Yellow crystals; melting point: 264–266 °C; yield: 77%. IR (KBr) νmax/cm−1 3339 (NH), 1652 (C=O). 1H-NMR (300 MHz) δ ppm: 2.27 (s, 3H, CH3), 2.58 (s, 3H, CH3), 3.72 (s, 3H, OCH3), 6.89 (t, 1H, ArH), 7.16 (d, 2H, J = 8.3 Hz, ArH), 7.46 (d, 2H, J = 8.4 Hz, ArH), 7.52–7.67 (m, 8H, ArH), 8.78 (s, 1H, -CH=N-), 8.90, 9.46, 12.86 (3s, 3H, 3NH, exchangeable with D2O). Anal. Calcd. (%) for C29H26ClN7O2 (540.02): C, 64.50; H, 4.85; N, 18.16. Found: C, 64.45; H, 4.90; N, 18.10.

5-((5-Chloro-3-methyl-1-pan class="Chemical">phenyl-ecies">pan class="Chemical">1H-pyrazol-4-yl)methyleneamino)-N-(p-chlorophenyl)-3-(p-methoxyphenylamino)-1H-pyrazole-4-carboxamide (7d): Yellow crystals; melting point: 269–270 °C; yield: 70%. IR (KBr) νmax/cm−1 3354 (NH), 1659 (C=O). 1H-NMR (300 MHz) δ ppm: 2.58 (s, 3H, CH3), 3.73 (s, 3H, OCH3), 6.75 (t, 1H, ArH), 6.90 (d, 2H, J = 8.8 Hz, ArH), 7.34 (d, 2H, J = 9.0 Hz, ArH), 7.41 (t, 2H, ArH), 7.63–7.67 (m, 4H, ArH), 7.75 (d, 2H, J = 8.9 Hz, ArH), 8.69 (s, 1H, -CH=N-), 9.19, 10.26, 12.73 (3s, 3H, 3NH, exchangeable with D2O). MS (m/z, %): 560 (M+, 9.06). Anal. Calcd. (%) for C28H23Cl2N7O2 (560.43): C, 60.01; H, 4.14; N, 17.49. Found: C, 59.95; H, 4.20; N, 17.44.

pan class="Chemical">3-(p-Methoxyphenylamino)-5-(4-(piperidin-1-yl)benzylideneamino)-1H-pyrazole-4-carboxamide (ecies">pan class="Chemical">8a): Orange crystals; melting point: 225–227 °C; yield: 74%. IR (KBr) νmax/cm−1 3346, 3160 (NH, NH2), 1654 (C=O). 1H-NMR (300 MHz) δ ppm: 1.60 (s, 6H, piperidine moiety), 3.41 (s, 4H, piperidine moiety), 3.71 (s, 3H, OCH3), 6.85 (d, 2H, J = 8.6 Hz, ArH), 7.04 (d, 2H, J = 8.9 Hz, ArH), 7.25 (s, 1H, NH2-amide exchangeable with D2O), 7.32–7.44 (m, 3H, 2H of ArH & 1H of NH2-amide exchangeable with D2O), 7.75 (d, 2H, J = 8.9 Hz, ArH), 8.66 (s, 1H, -CH=N-), 8.84, 12.36 (2s, 2H, 2NH, exchangeable with D2O). Anal. Calcd. (%) for C23H26N6O2 (418.49): C, 66.01; H, 6.26; N, 20.08. Found: C, 66.16; H, 6.17; N, 20.00.

pan class="Chemical">3-(p-Methoxyphenylamino)-N-phenyl-5-(4-(piperidin-1-yl)benzylideneamino)-1H-pyrazole-4-carboxamide (8b): Yellow cryecies">pan class="Species">stals; melting point: 219–220 °C; yield: 87%. IR (KBr) νmax/cm−1 3350 (NH), 1655 (C=O). 1H-NMR (300 MHz) δ ppm: 1.60 (s, 6H, piperidine moiety), 3.43 (s, 4H, piperidine moiety), 3.72 (s, 3H, OCH3), 6.89 (d, 2H, J = 8.1 Hz, ArH), 7.08 (t, 3H, ArH), 7.35–7.48 (m, 4H, ArH), 7.68 (d, 2H, J = 8.2 Hz, ArH), 7.85 (d, 2H, J = 8.3 Hz, ArH), 8.71 (s, 1H, -CH=N-), 8.77, 10.14, 12.56 (3s, 3H, 3NH, exchangeable with D2O). 13C-NMR (76 MHz) δ ppm: 23.95, 24.93, 47.65 (5C, piperidine moiety), 55.20 (-OCH3), 92.57, 113.73, 114.30, 117.38, 118.81, 123.10, 125.43, 129.11, 131.36, 135.13, 138.68, 151.93, 153.89, 155.91, 160.09 (22C), 163.06 (C=O). MS (m/z, %): 494 (M+, 32.82). Anal. Calcd. (%) for C29H30N6O2 (494.59): C, 70.42; H, 6.11; N, 16.99. Found: C, 70.50; H, 6.05; N, 17.00.

pan class="Chemical">3-(p-Methoxyphenylamino)-5-(4-(piperidin-1-yl)benzylideneamino)-N-p-tolyl-1H-pyrazole-4-carboxamide (8c): Yellow cryecies">pan class="Species">stals; melting point: 230–232 °C; yield: 82 %. IR (KBr) νmax/cm−1 3352 (NH), 1660 (C=O). 1H-NMR (300 MHz) δ ppm: 1.62 (s, 6H, piperidine moiety), 2.28 (s, 3H, CH3), 3.46 (s, 4H, piperidine moiety), 3.72 (s, 3H, OCH3), 6.88 (d, 2H, J = 8.6 Hz, ArH), 7.11 (d, 2H, J = 8.9 Hz, ArH), 7.19 (d, 2H, J = 8.1 Hz, ArH), 7.47–7.59 (m, 4H, ArH), 7.85 (d, 2H, J = 8.9 Hz, ArH), 8.71 (s, 1H, -CH=N-), 8.77, 10.06 (2s, 2H, 2NH, exchangeable with D2O), 12.56 (s, 1H, NH). Anal. Calcd. (%) for C30H32N6O2 (508.61): C, 70.84; H, 6.34; N, 16.52. Found: C, 70.90; H, 6.25; N, 16.43.

N-(p-Chloropan class="Chemical">phenyl)-ecies">pan class="Chemical">3-(p-methoxyphenylamino)-5-(4-(piperidin-1-yl)benzylideneamino)-1H-pyrazole-4-carboxamide (8d): Yellow crystals; melting point: 268–270 °C; yield: 81 %. IR (KBr) νmax/cm−1 3365 (NH), 1657 (C=O). 1H-NMR (300 MHz) δ ppm: 1.62 (s, 6H, piperidine moiety), 3.45 (s, 4H, piperidine moiety), 3.72 (s, 3H, OCH3), 6.89 (d, 2H, J = 9.0 Hz, ArH), 7.11 (d, 2H, J = 9.2 Hz, ArH), 7.42 (d, 2H, J = 8.9 Hz, ArH), 7.46 (d, 2H, J = 9.3 Hz, ArH), 7.70 (d, 2H, J = 8.9 Hz, ArH), 7.85 (d, 2H, J = 8.9 Hz, ArH), 8.64 (s, 1H, -CH=N-), 8.80, 10.24 (2s, 2H, 2NH, exchangeable with D2O), 12.30 (s, 1H, NH). Anal. Calcd. (%) for C29H29ClN6O2 (529.03): C, 65.84; H, 5.53; N, 15.89. Found: C, 65.65; H, 5.48; N, 15.71.

pan class="Chemical">3-(p-Methoxyphenylamino)-5-(3,4,5-trimethoxybenzylideneamino)-1H-pyrazole-4-carboxamide (ecies">pan class="Chemical">9a): Yellow crystals; Melting point: 222–224 °C; Yield: 73 %. IR (KBr) νmax/cm−1 3373, 3142 (NH, NH2), 1654 (C=O). 1H-NMR (300 MHz) δ ppm: 3.72, 3.77, 3.87 (3s, 12H, 4OCH3), 6.82 (d, 2H, J = 9.0 Hz, ArH), 6.89 (d, 2H, J = 8.9 Hz, ArH), 7.25–7.46 (m, 4H, 2H of ArH & 2H of NH2-amide exchangeable with D2O), 8.85 (s, 2H, -CH=N- & NH exchangeable with D2O), 12.12 (s, 1H, NH, exchangeable with D2O). 13C-NMR (76 MHz) δ ppm: 55.04, 56.11, 60.28 (4C, 4OCH3), 92.17, 104.26, 115.34, 121.14, 133.85, 141.73, 153.43, 154.64, 160.12 (16C), 162.51 (C=O). MS (m/z, %): 425 (M+, 46.11). Anal. Calcd. (%) for C21H23N5O5 (425.44): C, 59.29; H, 5.45; N, 16.46. Found: C, 59.25; H, 5.59; N, 16.54.

pan class="Chemical">3-(p-Methoxyphenylamino)-N-phenyl-5-(3,4,5-trimethoxybenzylideneamino)-1H-pyrazole-4-carboxamide (9b): Yellow cryecies">pan class="Species">stals; melting point: 221–223 °C; yield: 72 %. IR (KBr) νmax/cm−1 3446, 3294 (NH), 1652 (C=O). 1H-NMR (300 MHz) δ ppm: 3.74, 3.79, 3.92 (3s, 12H, 4OCH3), 6.91 (d, 2H, J = 9.0 Hz, ArH), 7.07 (t, 1H, ArH), 7.32–7.42 (m, 6H, ArH), 7.68 (d, 2H, J = 7.5 Hz, ArH), 8.69 (s, 1H, -CH=N-), 9.01, 10.05, 12.64 (3s, 3H, 3NH, exchangeable with D2O). 13C-NMR (76 MHz) δ ppm: 55.09, 56.81, 60.62 (4C, 4OCH3), 92.37, 104.42, 114.19, 121.09, 126.37, 128.04, 129.28, 132.58, 137.04, 141.55, 153.73, 154.68, 161.80 (22C), 162.90 (C=O). MS (m/z, %): 500 (M+-1, 15.28). Anal. Calcd. (%) for C27H27N5O5 (501.53): C, 64.66; H, 5.43; N, 13.96. Found: C, 64.42; H, 5.58; N, 14.12.

pan class="Chemical">3-(p-Methoxyphenylamino)-N-p-tolyl-5-(3,4,5-trimethoxybenzylideneamino)-1H-pyrazole-4-carboxamide (9c): Yellow cryecies">pan class="Species">stals, melting point: 234–236 °C; yield: 79%. IR (KBr) νmax/cm−1 3437, 3285 (NH), 1655 (C=O). 1H-NMR (300 MHz) δ ppm: 2.27 (s, 3H, CH3), 3.73, 3.79, 3.92 (3s, 12H, 4OCH3), 6.91 (d, 2H, J = 8.1 Hz, ArH), 7.15 (d, 2H, J = 8.3 Hz, ArH), 7.40–7.59 (m, 6H, ArH), 8.70 (s, 1H, -CH=N-), 8.96, 9.95, 12.64 (3s, 3H, 3NH, exchangeable with D2O). 13C-NMR (76 MHz) δ ppm: 21.31 (CH3), 55.04, 56.79, 60.65 (4C, 4OCH3), 91.93, 104.26, 114.17, 121.14, 126.46, 129.37, 132.54, 136.85, 141.57, 153.74, 154.40, 161.74 (22C), 162.88 (C=O). MS (m/z, %): 515 (M+, 24.80). Anal. Calcd. (%) for C28H29N5O5 (515.56): C, 65.23; H, 5.67; N, 13.58. Found: C, 65.15; H, 5.79; N, 13.51.

N-(p-Chloropan class="Chemical">phenyl)-ecies">pan class="Chemical">3-(p-methoxyphenylamino)-5-(3,4,5-trimethoxybenzylideneamino)-1H-pyrazole-4-carboxamide (9d): Orange crystals; melting point: 213–215 °C; yield: 87%. IR (KBr) νmax/cm−1 3441, 3289 (NH), 1650 (C=O). 1H-NMR (400 MHz) δ ppm: 3.73, 3.78, 3.90 (3s, 12H, 4OCH3), 6.90 (d, 2H, J = 8.9 Hz, ArH), 7.40–7.41 (m, 6H, ArH), 7.71 (d, 2H, J = 8.9 Hz, ArH), 8.65 (s, 1H, -CH=N-), 9.00, 10.10, 12.75 (3s, 3H, 3NH, exchangeable with D2O). 13C-NMR (101 MHz) δ ppm: 55.26, 56.06, 60.31 (4C, 4OCH3), 92.30, 106.51, 114.45, 120.55, 126.68, 128.86, 130.21, 137.56, 141.64, 153.37, 154.07, 161.91 (22C), 162.72 (C=O). MS (m/z, %): 535 (M+, 19.89). Anal. Calcd. (%) for C27H26ClN5O5 (535.98): C, 60.50; H, 4.89; N, 13.07. Found: C, 60.37; H, 4.99; N, 12.91.

3.2. Biological Evaluation (See Supplementary Material)

The inhibition zones of pan class="Chemical">pyrazole Schiff bases (ecies">pan class="Chemical">6a–d, 7a–d, 8a–d, and 9a–d) and the minimal inhibitory concentrations (MIC) of the potent Schiff bases (6b, 7b, 7c, 8a, 8d, and 9b) were performed according to the conventional paper disk diffusion method [54,55,74].

The antipan class="Chemical">proliferative activities (IC50, µM) of the moecies">pan class="Species">st potent Schiff bases (6b, 7b, 7c, 8a, 8d, and 9b) were performed according to the 3-[4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) protocol [61,62,63].

The immunomodulatory activity of the potent pan class="Chemical">Schiff bases (6b, ecies">pan class="Chemical">7b, 7c, 8a, 8d, and 9b) was evaluated according to previous work [57,66].

The in vitro enzyme assay of the mopan class="Species">st ecies">pan class="Chemical">promising compounds 8a and 9b was carried out against DNA gyrase and dihydrofolate reductase (DHFR) enzymes using Ciprofloxacin and Trimethoprim as reference drugs according to previous work [68].

3.3. Molecular Docking Study

Docking simulations were perpan class="Species">formed using Molecular Operating Environment (MOE) software version 2008.10, Chemiecies">pan class="Species">cal Computing Group Inc., Montreal, Quebec, Canada. The docking process methodology of new compounds was performed according to previous work [57,58,68].

4. Conclusions

In conclusion, a new pan class="Chemical">series of mono and ecies">pan class="Chemical">bis-pyrazole Schiff bases 6a–d-9a–d were synthesized successfully and evaluated preliminary for their in vitro antimicrobial activities. From inhibition zones values, it was found that six Schiff bases (6b, 7b, 7c, 8a, 8d, and 9b) displayed more than or near to the reference drugs (Tetracycline and Amphotericin B). Therefore, Schiff bases (6b, 7b, 7c, 8a, 8d, and 9b) were evaluated for their minimal inhibitory, minimal bactericidal concentrations, antiproliferative activities against two cell lines (HepG-2 and MCF-7), immunomodulatory and drug resistance properties as well as antiproliferative activity against healthy non-cancer Vero cells that exhibited IC50 values (≥120 µM). The results of evaluation exhibited that, the two Schiff bases containing mono-pyrazole 8a and 9b were more potent among the Schiff bases (6b, 7b, 7c, 8a, 8d and 9b) in this study. The results of enzyme assay for the two Schiff bases 8a and 9b against dihydrofolate reductase (DHFR) and DNA gyrase exhibited that IC50 values of the both Schiff bases 8a and 9b were stronger than Trimethoprim and Ciprofloxacin drugs, respectively. The molecular docking revealed that the two Schiff bases 8a and 9b showed desirable interaction, especially hydrogen bond and arene-cation or arene-arene interaction with the two protein targets 1DLS and 2XCT. Finally, the physicochemical and pharmacokinetic properties predication displayed that the two pyrazole Schiff bases may show drug-likeness and considered as candidates for the discovery or development of new drugs.