Version 1
: Received: 5 November 2016 / Approved: 7 November 2016 / Online: 7 November 2016 (08:30:12 CET)
How to cite:
Shaik, A. B.; Prasad, Y. R.; Shahanaaz, S. Design, Synthesis, Characterization and Computational Evaluation of Novel Isobutychalcones as Cytotoxic Agents: Part-A. Preprints2016, 2016110043. https://doi.org/10.20944/preprints201611.0043.v1
Shaik, A. B.; Prasad, Y. R.; Shahanaaz, S. Design, Synthesis, Characterization and Computational Evaluation of Novel Isobutychalcones as Cytotoxic Agents: Part-A. Preprints 2016, 2016110043. https://doi.org/10.20944/preprints201611.0043.v1
Shaik, A. B.; Prasad, Y. R.; Shahanaaz, S. Design, Synthesis, Characterization and Computational Evaluation of Novel Isobutychalcones as Cytotoxic Agents: Part-A. Preprints2016, 2016110043. https://doi.org/10.20944/preprints201611.0043.v1
APA Style
Shaik, A. B., Prasad, Y. R., & Shahanaaz, S. (2016). Design, Synthesis, Characterization and Computational Evaluation of Novel Isobutychalcones as Cytotoxic Agents: Part-A. Preprints. https://doi.org/10.20944/preprints201611.0043.v1
Chicago/Turabian Style
Shaik, A. B., Yejella Rajendra Prasad and Shaik Shahanaaz. 2016 "Design, Synthesis, Characterization and Computational Evaluation of Novel Isobutychalcones as Cytotoxic Agents: Part-A" Preprints. https://doi.org/10.20944/preprints201611.0043.v1
Abstract
A series of novel isobutylchalcones (A1-A20) were prepared, evaluated for their cytotoxic activity and characterized by FTIR, 1H NMR, 13C NMR, and elemental analysis data. The logic behind the design is to synthesize and compare chalcones containing electron releasing lipophilic isobutyl substituent on aromatic ring A and the B ring with aromatic ring containing a range of electron releasing and electron withdrawing groups as well as heteroaromatic rings for their cytotoxic activity. The compounds were tested against HT-29 (colon cancer), MCF-7 (breast cancer) and DU-145 (prostate cancer) cell lines using methotrexate (IC50 12 ± 1 (HT-29), 9 ±1 (MCF-7) 5 ± 1 (DU-145)) as reference standard. Compound A6 having 2,4-difluorphenyl moiety was most potent of the series against all the three cell lines and notably A6 was mainly effective against DU-145 cell lines with an IC50 value of 18 µg/mL. The critical structural features required for the activity against all the cell lines were identified through pharmacophore model using PHASETM which has recognised a 5 point AHHRR model and is consistent with the cytotoxic activity of the tested compounds.
Keywords
chalcone; cytotoxic activity; pharmacophore model
Subject
Chemistry and Materials Science, Medicinal Chemistry
Copyright:
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.