Non-peptidic anti-AIDS agents: inhibition of HIV-1 proteinase by disulfonates
- PMID: 1445307
- DOI: 10.1016/0006-291x(92)91102-v
Non-peptidic anti-AIDS agents: inhibition of HIV-1 proteinase by disulfonates
Abstract
Based upon an earlier observation that sodium docosanedioate (NaO2C-(CH2)20-CO2NA) weakly inhibits HIV-1 proteinase (IC50 12 microM), we have identified a class of more potent inhibitors (sulfonic acids) of this enzyme which are likewise dianionic at pH 5-6.5. Many of the compounds were moderately strong inhibitors of the enzyme (IC50 40nM-10 microM) and some have previously been shown to have anti-HIV activity in lymphocytes. Proteinase inhibition was dependent on the separation between sulfonate/carboxylate substituents, consistent with the hypothesis that negative charged ends of an inhibitor might form ionic bonds with Arg 8 and Arg 108 located at either end of the substrate-binding groove of the enzyme. The binding mode remains to be established by structure elucidation. Results for enzyme inhibition are presented along with structure-activity relationships and evidence for pH dependent inhibition. The general observations reported here may be useful for developing more potent and selective non-peptidic proteinase inhibitors.
Similar articles
-
Hydroxyquinones are competitive non-peptide inhibitors of HIV-1 proteinase.Biochim Biophys Acta. 1995 Nov 15;1253(1):5-8. doi: 10.1016/0167-4838(95)00183-u. Biochim Biophys Acta. 1995. PMID: 7492599
-
Flavones are inhibitors of HIV-1 proteinase.Biochem Biophys Res Commun. 1992 Oct 30;188(2):631-7. doi: 10.1016/0006-291x(92)91103-w. Biochem Biophys Res Commun. 1992. PMID: 1445308
-
Inhibition of HIV-1 proteinase by non-peptide carboxylates.Biochem Biophys Res Commun. 1991 Apr 15;176(1):241-6. doi: 10.1016/0006-291x(91)90915-t. Biochem Biophys Res Commun. 1991. PMID: 2018518
-
Human immunodeficiency virus type 1 protease inhibitors.Arch Intern Med. 1997 May 12;157(9):951-9. Arch Intern Med. 1997. PMID: 9140265 Review.
-
Resilience to resistance of HIV-1 protease inhibitors: profile of darunavir.AIDS Rev. 2008 Jul-Sep;10(3):131-42. AIDS Rev. 2008. PMID: 18820715 Free PMC article. Review.
Cited by
-
Biologically active metabolite(s) from haemolymph of red-headed centipede Scolopendra subspinipes possess broad spectrum antibacterial activity.AMB Express. 2019 Jun 28;9(1):95. doi: 10.1186/s13568-019-0816-3. AMB Express. 2019. PMID: 31254123 Free PMC article.
-
Dicaffeoylquinic and dicaffeoyltartaric acids are selective inhibitors of human immunodeficiency virus type 1 integrase.Antimicrob Agents Chemother. 1998 Jan;42(1):140-6. doi: 10.1128/AAC.42.1.140. Antimicrob Agents Chemother. 1998. PMID: 9449274 Free PMC article.
-
Secretion of Ipa proteins by Shigella flexneri: inducer molecules and kinetics of activation.Infect Immun. 1997 Oct;65(10):4005-10. doi: 10.1128/iai.65.10.4005-4010.1997. Infect Immun. 1997. PMID: 9316999 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources