Literature DB >> 20673723

Conjugates of betulin derivatives with AZT as potent anti-HIV agents.

Juan Xiong1, Yoshiki Kashiwada, Chin-Ho Chen, Keduo Qian, Susan L Morris-Natschke, Kuo-Hsiung Lee, Yoshihisa Takaishi.   

Abstract

Fourteen novel conjugates of 3,28-di-O-acylbetulins with AZT were prepared as anti-HIV agents, based on our previously reported potent anti-HIV triterpene leads, including 3-O-acyl and 3,28-di-O-acylbetulins. Nine of the conjugates (49-53, 55, 56, 59, and 60) exhibited potent anti-HIV activity at the submicromolar level, with EC(50) values ranging from 0.040 to 0.098muM in HIV-1(NL4-3) infected MT-4 cells. These compounds were equipotent or more potent than 3-O-(3',3'-dimethylsuccinyl)betulinic acid (2), which is currently in Phase IIb anti-AIDS clinical trial. Copyright 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20673723      PMCID: PMC3016297          DOI: 10.1016/j.bmc.2010.06.092

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


  21 in total

Review 1.  From magic bullets to designed multiple ligands.

Authors:  Richard Morphy; Corinne Kay; Zoran Rankovic
Journal:  Drug Discov Today       Date:  2004-08-01       Impact factor: 7.851

2.  Anti-AIDS agents. 32. Synthesis and anti-HIV activity of betulin derivatives.

Authors:  I C Sun; J K Shen; H K Wang; L M Cosentino; K H Lee
Journal:  Bioorg Med Chem Lett       Date:  1998-05-19       Impact factor: 2.823

3.  Betulinic acid and dihydrobetulinic acid derivatives as potent anti-HIV agents.

Authors:  Y Kashiwada; F Hashimoto; L M Cosentino; C H Chen; P E Garrett; K H Lee
Journal:  J Med Chem       Date:  1996-03-01       Impact factor: 7.446

4.  3,28-Di-O-(dimethylsuccinyl)-betulin isomers as anti-HIV agents.

Authors:  Y Kashiwada; J Chiyo; Y Ikeshiro; T Nagao; H Okabe; L M Cosentino; K Fowke; K H Lee
Journal:  Bioorg Med Chem Lett       Date:  2001-01-22       Impact factor: 2.823

5.  Anti-AIDS agents--XXVII. Synthesis and anti-HIV activity of betulinic acid and dihydrobetulinic acid derivatives.

Authors:  F Hashimoto; Y Kashiwada; L M Cosentino; C H Chen; P E Garrett; K H Lee
Journal:  Bioorg Med Chem       Date:  1997-12       Impact factor: 3.641

6.  3-O-Glutaryl-dihydrobetulin and related monoacyl derivatives as potent anti-HIV agents.

Authors:  Yoshiki Kashiwada; Michiko Sekiya; Yasumasa Ikeshiro; Toshihiro Fujioka; Nicole R Kilgore; Carl T Wild; Graham P Allaway; Kuo-Hsiung Lee
Journal:  Bioorg Med Chem Lett       Date:  2004-12-06       Impact factor: 2.823

Review 7.  Chemistry, biological activity, and chemotherapeutic potential of betulinic acid for the prevention and treatment of cancer and HIV infection.

Authors:  Robert H Cichewicz; Samir A Kouzi
Journal:  Med Res Rev       Date:  2004-01       Impact factor: 12.944

8.  PA-457: a potent HIV inhibitor that disrupts core condensation by targeting a late step in Gag processing.

Authors:  F Li; R Goila-Gaur; K Salzwedel; N R Kilgore; M Reddick; C Matallana; A Castillo; D Zoumplis; D E Martin; J M Orenstein; G P Allaway; E O Freed; C T Wild
Journal:  Proc Natl Acad Sci U S A       Date:  2003-10-22       Impact factor: 11.205

9.  Anti-AIDS agents. 34. Synthesis and structure-activity relationships of betulin derivatives as anti-HIV agents.

Authors:  I C Sun; H K Wang; Y Kashiwada; J K Shen; L M Cosentino; C H Chen; L M Yang; K H Lee
Journal:  J Med Chem       Date:  1998-11-05       Impact factor: 7.446

10.  3'-Azido-3'-deoxythymidine (BW A509U): an antiviral agent that inhibits the infectivity and cytopathic effect of human T-lymphotropic virus type III/lymphadenopathy-associated virus in vitro.

Authors:  H Mitsuya; K J Weinhold; P A Furman; M H St Clair; S N Lehrman; R C Gallo; D Bolognesi; D W Barry; S Broder
Journal:  Proc Natl Acad Sci U S A       Date:  1985-10       Impact factor: 11.205

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  8 in total

Review 1.  Recent advances in natural anti-HIV triterpenoids and analogs.

Authors:  Hai-Feng Wu; Susan L Morris-Natschke; Xu-Dong Xu; Mei-Hua Yang; Yung-Yi Cheng; Shi-Shan Yu; Kuo-Hsiung Lee
Journal:  Med Res Rev       Date:  2020-07-14       Impact factor: 12.944

2.  Anti-AIDS agents 88. Anti-HIV conjugates of betulin and betulinic acid with AZT prepared via click chemistry.

Authors:  Ibrahim D Bori; Hsin-Yi Hung; Keduo Qian; Chin-Ho Chen; Susan L Morris-Natschke; Kuo-Hsiung Lee
Journal:  Tetrahedron Lett       Date:  2012-04-11       Impact factor: 2.415

Review 3.  Structure and Anti-HIV Activity of Betulinic Acid Analogues.

Authors:  Qiu-Xia Huang; Hong-Fei Chen; Xing-Rui Luo; Yin-Xiang Zhang; Xu Yao; Xing Zheng
Journal:  Curr Med Sci       Date:  2018-06-22

4.  Design and Synthesis of Novel Betulin Derivatives Containing Thio-/Semicarbazone Moieties as Apoptotic Inducers through Mitochindria-Related Pathways.

Authors:  Jiafeng Wang; Jiale Wu; Yinglong Han; Jie Zhang; Yu Lin; Haijun Wang; Jing Wang; Jicheng Liu; Ming Bu
Journal:  Molecules       Date:  2021-10-21       Impact factor: 4.411

Review 5.  Cytochrome P450 monooxygenase-mediated tailoring of triterpenoids and steroids in plants.

Authors:  Karan Malhotra; Jakob Franke
Journal:  Beilstein J Org Chem       Date:  2022-09-21       Impact factor: 2.544

6.  Antileishmanial activity of semisynthetic lupane triterpenoids betulin and betulinic acid derivatives: synergistic effects with miltefosine.

Authors:  Maria C Sousa; Raquel Varandas; Rita C Santos; Manuel Santos-Rosa; Vera Alves; Jorge A R Salvador
Journal:  PLoS One       Date:  2014-03-18       Impact factor: 3.240

7.  Antineoplastic agents. 595. Structural modifications of betulin and the X-ray crystal structure of an unusual betulin amine dimer.

Authors:  George R Pettit; Noeleen Melody; Frank Hempenstall; Jean-Charles Chapuis; Thomas L Groy; Lee Williams
Journal:  J Nat Prod       Date:  2014-04-02       Impact factor: 4.050

Review 8.  Metabolic and functional diversity of saponins, biosynthetic intermediates and semi-synthetic derivatives.

Authors:  Tessa Moses; Kalliope K Papadopoulou; Anne Osbourn
Journal:  Crit Rev Biochem Mol Biol       Date:  2014-10-06       Impact factor: 8.250

  8 in total

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