Literature DB >> 24113364

Synthesis and evaluation of (Z)-2,3-diphenylacrylonitrile analogs as anti-cancer and anti-microbial agents.

Mohammad Sayed Alam1, Young-Joo Nam, Dong-Ung Lee.   

Abstract

In the present study, a series of (Z)-2,3-diphenylacrylonitrile analogs were synthesized and then evaluated in terms of their cytotoxic activities against four human cancer cell lines, e.g. lung cancer (A549), ovarian cancer (SK-OV-3), skin cancer (SK-MEL-2), and colon cancer (HCT15), as well as anti-microbial activities against three microbes, e.g. Staphylococcus aureus, Salmonella typhi, and Aspergillus niger. The title compounds were synthesized by Knoevenagel condensation reaction of benzyl cyanide or p-nitrobenzyl cyanide with substituted benzaldehydes in good yields. Most of the compounds exhibited significant suppressive activities against the growth of all cancer cell lines. Compound 3c was most active in inhibiting the growth of A549, SK-OV-3, SK-MEL-2, and HCT15 cells lines with IC50 values of 0.57, 0.14, 0.65, and 0.34 mg/mL, respectively, followed by compounds 3f, 3i, and 3h. Compound 3c exhibited 2.4 times greater cytotoxic activity against HCT15 cells, whereas it showed similar potency against SK-OV-3 cells to that of the standard anti-cancer agent doxorubicin. Structure-activity relationship study revealed that electron-donating groups at the para-position of phenyl ring B were more favorable for improved cytotoxic activity, whereas the presence of electron-withdrawing groups was unfavorable compare to unsubstituted acrylonitrile. An optimal electron density on phenyl ring A of (Z)-2,3-diphenylacrylonitrile analogs was crucial for their cytotoxic activities against human cancer cell lines used in the present study. Qualitative structure-cytotoxic activity relationships were studied using physicochemical parameters; a good correlation between calculated polar surface area (PSA), a lipophobic parameter, and cytotoxic activity was found. Moreover, all compounds showed significant anti-bacterial activities against S. typhi, whereas compound 3k showed potent inhibition against both S. aureus and S. typhi bacterial strains.
Copyright © 2013 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  Acrylonitriles; Antimicrobial activity; Cytotoxicity; Human cancer cell line

Mesh:

Substances:

Year:  2013        PMID: 24113364     DOI: 10.1016/j.ejmech.2013.08.031

Source DB:  PubMed          Journal:  Eur J Med Chem        ISSN: 0223-5234            Impact factor:   6.514


  4 in total

1.  Synthesis and evaluation of bile acid amides of [Formula: see text]-cyanostilbenes as anticancer agents.

Authors:  Devesh S Agarwal; Rajnish Prakash Singh; K Lohitesh; Prabhat N Jha; Rajdeep Chowdhury; Rajeev Sakhuja
Journal:  Mol Divers       Date:  2017-12-13       Impact factor: 2.943

2.  Identification of (Z)-2,3-Diphenylacrylonitrileas Anti-Cancer Molecule in Persian Gulf Sea Cucumber Holothuria parva.

Authors:  Salimeh Amidi; Zahra Hashemi; Abbasali Motallebi; Melika Nazemi; Hoda Farrokhpayam; Enayatollah Seydi; Jalal Pourahmad
Journal:  Mar Drugs       Date:  2017-10-16       Impact factor: 5.118

3.  New 3-Aryl-2-(2-thienyl)acrylonitriles with High Activity Against Hepatoma Cells.

Authors:  Eva Schaller; Andi Ma; Lisa Chiara Gosch; Adrian Klefenz; David Schaller; Nils Goehringer; Leonard Kaps; Detlef Schuppan; Andrea Volkamer; Rainer Schobert; Bernhard Biersack; Bianca Nitzsche; Michael Höpfner
Journal:  Int J Mol Sci       Date:  2021-02-24       Impact factor: 5.923

4.  Biological and quantitative-SAR evaluations, and docking studies of (E)-N -benzylidenebenzohydrazide analogues as potential antibacterial agents.

Authors:  Mohammad Sayed Alam; Sefat Jebin; M Mostafizur Rahman; Md Latiful Bari; Dong-Ung Lee
Journal:  EXCLI J       Date:  2016-06-17       Impact factor: 4.068

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.