Literature DB >> 30429967

Medicinal chemistry of acridine and its analogues.

Parteek Prasher1,2, Mousmee Sharma1.   

Abstract

'Acridine' along with its functional analogue 'Acridone' is the most privileged pharmacophore in medicinal chemistry with diverse applications ranging from DNA intercalators, endonuclease mimics, ratiometric selective ion sensors, and P-glycoprotein inhibitors in countering the multi-drug resistance, enzyme inhibitors, and reversals of neurodegenerative disorders. Their interaction with DNA and ability of selectively identifying numerous biologically useful ions has cemented exploitability of the acridone nucleus in modern day therapeutics. Additionally, most derivatives and salts of acridine are planar, crystalline, and stable displaying a strong fluorescence which, when coupled with their marked bio selectivity and low cytotoxicity, enables the studying and monitoring of several biochemical, metabolic, and pharmacological processes. In this review, a detailed picture covering the important therapeutic aspects of the acridone nucleus and its functional analogues is discussed.

Entities:  

Year:  2018        PMID: 30429967      PMCID: PMC6195008          DOI: 10.1039/c8md00384j

Source DB:  PubMed          Journal:  Medchemcomm        ISSN: 2040-2503            Impact factor:   3.597


  138 in total

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2.  The structure of the DNA-acridine complex.

Authors:  L S LERMAN
Journal:  Proc Natl Acad Sci U S A       Date:  1963-01-15       Impact factor: 11.205

3.  A multimeric quinacrine conjugate as a potential inhibitor of Alzheimer's beta-amyloid fibril formation.

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4.  Novel multi-substituted benzyl acridone derivatives as survivin inhibitors for hepatocellular carcinoma treatment.

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Review 5.  New agents for the treatment of drug-resistant Mycobacterium tuberculosis.

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Review 6.  The role of a Schiff base scaffold, N-(2-hydroxy acetophenone) glycinate-in overcoming multidrug resistance in cancer.

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Journal:  Eur J Pharm Sci       Date:  2013-09-14       Impact factor: 4.384

7.  Potential antitumor agents. 19. Multiply substituted 4'-(9-acridinylamino)methanesulfonanilides.

Authors:  B F Cain; G Atwell
Journal:  J Med Chem       Date:  1976-09       Impact factor: 7.446

8.  Effects of DNA charge and length on the electrophoretic mobility of intercalated DNA.

Authors:  H R Reese
Journal:  Biopolymers       Date:  1994-10       Impact factor: 2.505

9.  Chloro acridone derivatives as cytotoxic agents active on multidrug-resistant cell lines and their duplex DNA complex studies by electrospray ionization mass spectrometry.

Authors:  V V S Rajendra Prasad; J Venkat Rao; R S Giri; N K Sathish; S M Shanta Kumar; Y C Mayur
Journal:  Chem Biol Interact       Date:  2008-06-27       Impact factor: 5.192

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  15 in total

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2.  Thermal stabilisation of the short DNA duplexes by acridine-4-carboxamide derivatives.

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Review 3.  Tailored therapeutics based on 1,2,3-1H-triazoles: a mini review.

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Journal:  Bioorg Med Chem       Date:  2020-10-26       Impact factor: 3.641

5.  Antifungal Activity of Capridine β as a Consequence of Its Biotransformation into Metabolite Affecting Yeast Topoisomerase II Activity.

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6.  Grindstone Chemistry: Design, One-Pot Synthesis, and Promising Anticancer Activity of Spiro[acridine-9,2'-indoline]-1,3,8-trione Derivatives against the MCF-7 Cancer Cell Line.

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Review 7.  Acridine-Based Antimalarials-From the Very First Synthetic Antimalarial to Recent Developments.

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Review 8.  'Acridines' as New Horizons in Antifungal Treatment.

Authors:  Iwona Gabriel
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9.  Synthesis of novel cytotoxic tetracyclic acridone derivatives and study of their molecular docking, ADMET, QSAR, bioactivity and protein binding properties.

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Journal:  Sci Rep       Date:  2020-11-26       Impact factor: 4.379

10.  19 F NMR-Based Fragment Screening for 14 Different Biologically Active RNAs and 10 DNA and Protein Counter-Screens.

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Journal:  Chembiochem       Date:  2020-09-25       Impact factor: 3.461

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