Literature DB >> 20598531

Synthesis and in vitro evaluation of N-alkyl-3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)indolin-2-one analogs as potential anticancer agents.

Narsimha Reddy Penthala1, Thirupathi Reddy Yerramreddy, Nikhil Reddy Madadi, Peter A Crooks.   

Abstract

A series of novel 3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)indolin-2-one analogs (3) have been synthesized under microwave irradiation and conventional heating methods. These analogs were evaluated for in vitro cytotoxicity against a panel of 57 human tumor cell lines. Compound 3o had GI(50) values of 190 nM and 750 nM against A549/ATTC non-small cell lung cancer and LOX IMVI melanoma cell lines, respectively, and both 3n and 3o exhibited GI(50) values ranging from 2 to 5 microM against CCRF-CEM, HL-60(TB), K-562, MOLT-4, and RPMI-8226 leukemia cell lines. These results indicate that N-4-methoxybenzyl-3-hydroxy-(2-imino-3-methyl-5-oxo-4-yl)indolin-2-one analogs may be useful leads for anticancer drug development. Copyright 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20598531      PMCID: PMC3725999          DOI: 10.1016/j.bmcl.2010.06.042

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


  13 in total

1.  An investigation into the cytotoxicity and mode of action of some novel N-alkyl-substituted isatins.

Authors:  Kara L Vine; Julie M Locke; Marie Ranson; Stephen G Pyne; John B Bremner
Journal:  J Med Chem       Date:  2007-09-21       Impact factor: 7.446

2.  In vitro cytotoxicity evaluation of some substituted isatin derivatives.

Authors:  Kara L Vine; Julie M Locke; Marie Ranson; Kirsten Benkendorff; Stephen G Pyne; John B Bremner
Journal:  Bioorg Med Chem       Date:  2006-10-20       Impact factor: 3.641

3.  Novel substituted (Z)-5-((N-benzyl-1H-indol-3-yl)methylene)imidazolidine-2,4-diones and 5-((N-benzyl-1H-indol-3-yl)methylene)pyrimidine-2,4,6(1H,3H,5H)-triones as potent radio-sensitizing agents.

Authors:  Y Thirupathi Reddy; Konjeti R Sekhar; Nidhish Sasi; P Narsimha Reddy; Michael L Freeman; Peter A Crooks
Journal:  Bioorg Med Chem Lett       Date:  2009-11-22       Impact factor: 2.823

4.  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

5.  Novel substituted (Z)-2-(N-benzylindol-3-ylmethylene)quinuclidin-3-one and (Z)-(+/-)-2-(N-benzylindol-3-ylmethylene)quinuclidin-3-ol derivatives as potent thermal sensitizing agents.

Authors:  Vijayakumar N Sonar; Y Thirupathi Reddy; Konjeti R Sekhar; Soumya Sasi; Michael L Freeman; Peter A Crooks
Journal:  Bioorg Med Chem Lett       Date:  2007-10-17       Impact factor: 2.823

6.  Comparison of in vitro anticancer-drug-screening data generated with a tetrazolium assay versus a protein assay against a diverse panel of human tumor cell lines.

Authors:  L V Rubinstein; R H Shoemaker; K D Paull; R M Simon; S Tosini; P Skehan; D A Scudiero; A Monks; M R Boyd
Journal:  J Natl Cancer Inst       Date:  1990-07-04       Impact factor: 13.506

7.  3-(2-Amino-1-methyl-4-oxo-4,5-dihydro-1H-imidazol-5-yl)-5-fluoro-3-hydr-oxy-1-methyl-indolin-2-one methanol hemisolvate.

Authors:  Narsimha Reddy Penthala; Thirupathi Reddy Yerram Reddy; Sean Parkin; Peter A Crooks
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2009-10-31

8.  3-(2-Amino-1-methyl-4-oxo-4,5-dihydro-1H-imidazol-5-yl)-3-hydr-oxy-1-phenyl-indolin-2-one ethanol solvate.

Authors:  Narsimha Reddy Penthala; Thirupathi Reddy Yerram Reddy; Sean Parkin; Peter A Crooks
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2009-09-12

9.  3-(2-Amino-1-methyl-4-oxo-4,5-dihydro-1H-imidazol-5-yl)-3-hydroxy-indolin-2-one monohydrate.

Authors:  Narsimha Reddy Penthala; Thirupathi Reddy Yerram Reddy; Sean Parkin; Peter A Crooks
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2009-02-21

10.  N-phenethyl and N-naphthylmethyl isatins and analogues as in vitro cytotoxic agents.

Authors:  Lidia Matesic; Julie M Locke; John B Bremner; Stephen G Pyne; Danielle Skropeta; Marie Ranson; Kara L Vine
Journal:  Bioorg Med Chem       Date:  2008-01-07       Impact factor: 3.641

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  7 in total

1.  Dioxol and dihydrodioxin analogs of 2- and 3-phenylacetonitriles as potent anti-cancer agents with nanomolar activity against a variety of human cancer cells.

Authors:  Nikhil R Madadi; Amit Ketkar; Narsimha R Penthala; April C L Bostian; Robert L Eoff; Peter A Crooks
Journal:  Bioorg Med Chem Lett       Date:  2016-03-17       Impact factor: 2.823

2.  Synthesis and anti-proliferative activity of aromatic substituted 5-((1-benzyl-1H-indol-3-yl)methylene)-1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-trione analogs against human tumor cell lines.

Authors:  Nikhil Reddy Madadi; Narsimha Reddy Penthala; Venumadhav Janganati; Peter A Crooks
Journal:  Bioorg Med Chem Lett       Date:  2013-12-09       Impact factor: 2.823

3.  5-Chloro-1-(4-meth-oxy-benz-yl)indoline-2,3-dione.

Authors:  Weiyao Wu; Tingting Zheng; Shengli Cao; Zhichang Xiao
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-01-08

4.  5-Fluoro-1-(4-meth-oxy-benz-yl)indoline-2,3-dione.

Authors:  Weiyao Wu; Huihui Lin; Chong-Qing Wan; Sheng-Li Cao
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-06-30

5.  rac-N-Benzyl-isatincreatinine (unknown solvate).

Authors:  Narsimha Reddy Penthala; Peter A Crooks
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2013-01-26

6.  Design, synthesis and biological evaluation of novel bromophenol derivatives incorporating indolin-2-one moiety as potential anticancer agents.

Authors:  Li-Jun Wang; Shuai-Yu Wang; Bo Jiang; Ning Wu; Xiang-Qian Li; Bao-Cheng Wang; Jiao Luo; Meng Yang; Shui-Hua Jin; Da-Yong Shi
Journal:  Mar Drugs       Date:  2015-02-02       Impact factor: 5.118

7.  Synthesis and characterisation of thiobarbituric acid enamine derivatives, and evaluation of their α-glucosidase inhibitory and anti-glycation activity.

Authors:  M Ali; Assem Barakat; Ayman El-Faham; Hessa H Al-Rasheed; Kholoud Dahlous; Abdullah Mohammed Al-Majid; Anamika Sharma; Sammer Yousuf; Mehar Sanam; Zaheer Ul-Haq; M Iqbal Choudhary; Beatriz G de la Torre; Fernando Albericio
Journal:  J Enzyme Inhib Med Chem       Date:  2020-12       Impact factor: 5.051

  7 in total

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