Literature DB >> 19616956

Design, synthesis, and structure-activity relationships of 1,3-dihydrobenzimidazol-2-one analogues as anti-HIV agents.

Anna-Maria Monforte1, Patrizia Logoteta, Stefania Ferro, Laura De Luca, Nunzio Iraci, Giovanni Maga, Erik De Clercq, Christophe Pannecouque, Alba Chimirri.   

Abstract

Non-nucleoside reverse transcriptase inhibitors (NNRTIs) have become very important components in the antiretroviral combination therapies used to treat HIV. Recently, our group identified some 1,3-dihydrobenzimidazol-2-one derivatives and their sulfones as a potent and novel class of NNRTIs. We herein report the synthesis and biological evaluation of the new compounds in which different structural modifications have been introduced in order to investigate their effects on RT inhibition.

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Year:  2009        PMID: 19616956     DOI: 10.1016/j.bmc.2009.06.068

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  8 in total

1.  Chemically modified peptides targeting the PDZ domain of GIPC as a therapeutic approach for cancer.

Authors:  Chitta Ranjan Patra; Chamila N Rupasinghe; Shamit K Dutta; Santanu Bhattacharya; Enfeng Wang; Mark R Spaller; Debabrata Mukhopadhyay
Journal:  ACS Chem Biol       Date:  2012-02-15       Impact factor: 5.100

2.  Discovery of Thiophene[3,2-d]pyrimidine Derivatives as Potent HIV-1 NNRTIs Targeting the Tolerant Region I of NNIBP.

Authors:  Dongwei Kang; Xiao Ding; Gaochan Wu; Zhipeng Huo; Zhongxia Zhou; Tong Zhao; Da Feng; Zhao Wang; Ye Tian; Dirk Daelemans; Erik De Clercq; Christophe Pannecouque; Peng Zhan; Xinyong Liu
Journal:  ACS Med Chem Lett       Date:  2017-10-19       Impact factor: 4.345

3.  Synthesis of quinolin-2-one alkaloid derivatives and their inhibitory activities against HIV-1 reverse transcriptase.

Authors:  Pi Cheng; Qiong Gu; Wei Liu; Jian-Feng Zou; Yang-Yong Ou; Zhong-Yong Luo; Jian-Guo Zeng
Journal:  Molecules       Date:  2011-09-07       Impact factor: 4.411

4.  Route to Benzimidazol-2-ones via Decarbonylative Ring Contraction of Quinoxalinediones: Application to the Synthesis of Flibanserin, A Drug for Treating Hypoactive Sexual Desire Disorder in Women and Marine Natural Product Hunanamycin Analogue.

Authors:  Rahul D Shingare; Akshay S Kulkarni; Revannath L Sutar; D Srinivasa Reddy
Journal:  ACS Omega       Date:  2017-08-29

5.  Synthesis of Multisubstituted Benzimidazolones via Copper-Catalyzed Oxidative Tandem C-H Aminations and Alkyl Deconstructive Carbofunctionalization.

Authors:  Taoyuan Liang; He Zhao; Lingzhen Gong; Huanfeng Jiang; Min Zhang
Journal:  iScience       Date:  2019-04-19

6.  Reaction of Papaverine with Baran DiversinatesTM.

Authors:  Folake A Egbewande; Mark J Coster; Ian D Jenkins; Rohan A Davis
Journal:  Molecules       Date:  2019-10-31       Impact factor: 4.411

7.  Alkylated benzimidazoles: Design, synthesis, docking, DFT analysis, ADMET property, molecular dynamics and activity against HIV and YFV.

Authors:  Ritika Srivastava; Sunil K Gupta; Farha Naaz; Parth Sarthi Sen Gupta; Madhu Yadav; Vishal Kumar Singh; Anuradha Singh; Malay Kumar Rana; Satish Kumar Gupta; Dominique Schols; Ramendra K Singh
Journal:  Comput Biol Chem       Date:  2020-10-06       Impact factor: 2.877

8.  Regioselective synthesis of benzimidazolones via cascade C-N coupling of monosubstituted ureas.

Authors:  Johannes B Ernst; Nicholas E S Tay; Nathan T Jui; Stephen L Buchwald
Journal:  Org Lett       Date:  2014-06-27       Impact factor: 6.005

  8 in total

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