New developments in natural products-based anti-AIDS research
This review discusses anti‐HIV natural products from several compound classes, including terpenoids, coumarins, alkaloids, polyphenols, tannins, and flavonoids. Natural products can provide novel anti‐AIDS chemotherapeutic leads that are structurally unique or have new mechanisms of action. The drug...
Saved in:
Published in | Medicinal research reviews Vol. 27; no. 1; pp. 108 - 132 |
---|---|
Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01.01.2007
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | This review discusses anti‐HIV natural products from several compound classes, including terpenoids, coumarins, alkaloids, polyphenols, tannins, and flavonoids. Natural products can provide novel anti‐AIDS chemotherapeutic leads that are structurally unique or have new mechanisms of action. The drug discovery and development process proceeds from bioactivity‐directed isolation and identification of a promising lead natural product, followed by rational design‐based structural modification and structure–activity relationship analyses to optimize the lead compound as a drug candidate. This process is notably exemplified by the discovery of the modified betulinic acid derivative, DSB [PA‐457], which is currently in Phase II clinical trial and is the first‐in‐class HIV maturation inhibitor (MI). © 2006 Wiley Periodicals, Inc. Med Res Rev, 27, No. 1, 108–132, 2007 |
---|---|
Bibliography: | istex:CE86A8D68039BF6A434753C1CBFB92D3E904E7D1 ark:/67375/WNG-7K1N9XJT-Z Anti-AIDS Agents 67. For part 66, see M. Suzuki, P.C. Smith, S.L. Morris-Natschke, K.H. Lee, Syntheses, anti-HIV activity, and in vitro metabolic stability of 3′,4′-di-O-(−)-camphanoyl-(+)-cis-khellactone (DCK) derivatives, Bioorg. Med. Chem. Lett., submitted. ArticleID:MED20075 khellactone (DCK) derivatives, Bioorg. Med. Chem. Lett., submitted. in vitro (−)‐camphanoyl‐(+) cis metabolic stability of 3′,4′‐di Anti‐AIDS Agents 67. For part 66, see M. Suzuki, P.C. Smith, S.L. Morris‐Natschke, K.H. Lee, Syntheses, anti‐HIV activity, and O ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Article-2 ObjectType-Feature-3 ObjectType-Review-1 |
ISSN: | 0198-6325 1098-1128 |
DOI: | 10.1002/med.20075 |