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Synthesis and biological evaluation of water-soluble derivatives of chiral gossypol as HIV fusion inhibitors targeting gp41.
- Source :
-
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2018 Jan 01; Vol. 28 (1), pp. 49-52. Date of Electronic Publication: 2017 Aug 24. - Publication Year :
- 2018
-
Abstract
- A series of novel or known water-soluble derivatives of chiral gossypol were synthesized and screened in vitro for their anti-HIV-1 activity. (-)-gossypol derivative was more active against HIV-1 than the corresponding (+)-gossypol derivative, respectively. Among these derivatives, d-glucosamine derivative of (-)-gossypol, oligopeptide derivative of (-)-gossypol and taurine derivative of (-)-gossypol, such as compounds 1a, 3a and 14a, showed significant inhibitory activities against HIV-1 replication, HIV-1 mediated cell-cell fusion and HIV gp41 6-helix bundle formation as some amino acid derivatives of (-)-gossypol.<br /> (Copyright © 2017 Elsevier Ltd. All rights reserved.)
- Subjects :
- Binding Sites
Drug Design
Gossypol metabolism
Gossypol pharmacology
HIV Envelope Protein gp41 metabolism
HIV Fusion Inhibitors metabolism
HIV Fusion Inhibitors pharmacology
Humans
Hydrogen Bonding
Inhibitory Concentration 50
Molecular Docking Simulation
Protein Structure, Tertiary
Solubility
Stereoisomerism
Virus Replication drug effects
Water chemistry
Gossypol chemistry
HIV Envelope Protein gp41 antagonists & inhibitors
HIV Fusion Inhibitors chemical synthesis
HIV-1 physiology
Subjects
Details
- Language :
- English
- ISSN :
- 1464-3405
- Volume :
- 28
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry letters
- Publication Type :
- Academic Journal
- Accession number :
- 29162455
- Full Text :
- https://doi.org/10.1016/j.bmcl.2017.08.049