Literature DB >> 18308566

Indole- and indolizine-glyoxylamides displaying cytotoxicity against multidrug resistant cancer cell lines.

David A James1, Keizo Koya, Hao Li, Guiqing Liang, Zhiqiang Xia, Weiwen Ying, Yaming Wu, Lijun Sun.   

Abstract

We report herein the SAR studies of a series of indole- and indolizine-glyoxylamides that demonstrate substantial in vitro anti-proliferative activities against cancer cell lines, including multidrug resistance (MDR) phenotypes. The in vitro cytotoxic effects have been demonstrated across a wide array of tumor types of various origins (e.g., breast, colon, uterine).

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18308566     DOI: 10.1016/j.bmcl.2008.02.029

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  14 in total

1.  One-pot synthesis of highly substituted N-fused heteroaromatic bicycles from azole aldehydes.

Authors:  Victor K Outlaw; Felipe B d'Andrea; Craig A Townsend
Journal:  Org Lett       Date:  2015-03-27       Impact factor: 6.005

2.  Photochemical synthesis and anticancer activity of barbituric acid, thiobarbituric acid, thiosemicarbazide, and isoniazid linked to 2-phenyl indole derivatives.

Authors:  S Vijaya Laxmi; G Rajitha; B Rajitha; Asha Jyothi Rao
Journal:  J Chem Biol       Date:  2015-11-17

3.  Novel synthetic chalcones induce apoptosis in the A549 non-small cell lung cancer cells harboring a KRAS mutation.

Authors:  Yiqiang Wang; Andreas Hedblom; Steffi K Koerner; Mailin Li; Finith E Jernigan; Barbara Wegiel; Lijun Sun
Journal:  Bioorg Med Chem Lett       Date:  2016-10-24       Impact factor: 2.823

4.  Synthesis and in vitro screening of novel N-benzyl aplysinopsin analogs as potential anticancer agents.

Authors:  Narsimha Reddy Penthala; Thirupathi Reddy Yerramreddy; Peter A Crooks
Journal:  Bioorg Med Chem Lett       Date:  2011-01-11       Impact factor: 2.823

5.  Aplysinopsin analogs: Synthesis and anti-proliferative activity of substituted (Z)-5-(N-benzylindol-3-ylmethylene)imidazolidine-2,4-diones.

Authors:  Y Thirupathi Reddy; P Narsimha Reddy; Srinivas Koduru; Chendil Damodaran; Peter A Crooks
Journal:  Bioorg Med Chem       Date:  2010-03-27       Impact factor: 3.641

6.  Microwave assisted synthesis and in vitro cytotoxicities of substituted (Z)-2-amino-5-(1-benzyl-1H-indol-3-yl)methylene-1-methyl-1H-imidazol-4(5H)-ones against human tumor cell lines.

Authors:  Narsimha Reddy Penthala; Thirupathi Reddy Yerramreddy; Peter A Crooks
Journal:  Bioorg Med Chem Lett       Date:  2009-11-22       Impact factor: 2.823

7.  Diethyl indolizine-1,3-dicarboxyl-ate.

Authors:  Wei-Jin Gu; Jin Zhuang; Yu-Liang Jiang; Bing-Xiang Wang
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-12-15

8.  Investigation of Antifungal Properties of Synthetic Dimethyl-4-Bromo-1-(Substituted Benzoyl) Pyrrolo[1,2-a] Quinoline-2,3-Dicarboxylates Analogues: Molecular Docking Studies and Conceptual DFT-Based Chemical Reactivity Descriptors and Pharmacokinetics Evaluation.

Authors:  Vijayakumar Uppar; Sandeep Chandrashekharappa; Chandan Shivamallu; Sushma P; Shiva Prasad Kollur; Joaquín Ortega-Castro; Juan Frau; Norma Flores-Holguín; Atiyaparveen I Basarikatti; Mallikarjun Chougala; Mrudula Mohan M; Govindappa Banuprakash; Katharigatta N Venugopala; Belakatte P Nandeshwarappa; Ravindra Veerapur; Abdulaziz A Al-Kheraif; Abdallah M Elgorban; Asad Syed; Kiran K Mudnakudu-Nagaraju; Basavaraj Padmashali; Daniel Glossman-Mitnik
Journal:  Molecules       Date:  2021-05-06       Impact factor: 4.411

9.  1-[(3,5-Dimethyl-1H-pyrazol-1-yl)carbon-yl]-5-methyl-indolizine-3-carbo-nitrile.

Authors:  Wei-Jin Gu; Wen-Li Xie; Ting-Ting Wang
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-11-24

10.  (3,5-Dimethyl-1H-pyrazol-1-yl){3-[(3,5-dimethyl-1H-pyrazol-1-yl)carbon-yl]-5-methyl-indolizin-1-yl}methanone.

Authors:  Xiang-Yun Song; Wei-Jin Gu; Yu-Liang Jiang; Bing-Xiang Wang
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2013-02-28
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.