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TargetIntegrase
LigandBDBM50174222
Substrate/Competitorn/a
Meas. Tech.ChEMBL_321235 (CHEMBL881770)
IC50 1000±n/a nM
Citation Bailly, FQueffelec, CMbemba, GMouscadet, JFCotelle, P Synthesis and HIV-1 integrase inhibitory activities of caffeic acid dimers derived from Salvia officinalis. Bioorg Med Chem Lett15:5053-6 (2005) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Integrase
Name:Integrase
Synonyms:Human immunodeficiency virus type 1 integrase
Type:PROTEIN
Mol. Mass.:32231.48
Organism:Human immunodeficiency virus 1
Description:ChEMBL_90865
Residue:288
Sequence:
FLDGIDKAQDEHEKYHSNWRAMASDFNLPPVVAKEIVASCDKCQLKGEAMHGQVDCSPGI
WQLDCTHLEGKVILVAVHVASGYIEAEVIPAETGQETAYFLLKLAGRWPVKTIHTDNGSN
FTSTTVKAACWWAGIKQEFGIPYNPQSQGVVESMNKELKKIIGQVRDQAEHLKTAVQMAV
FIHNFKRKGGIGGYSAGERIVDIIATDIQTKELQKQITKIQNFRVYYRDSRDPLWKGPAK
LLWKGEGAVVIQDNSDIKVVPRRKVKIIRDYGKQMAGDDCVASRQDED
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  Blast E-value cutoff:
BDBM50174222
n/a
NameBDBM50174222
Synonyms:3-[3-(6,7-Dihydroxy-2-oxo-2H-chromen-3-yloxy)-4-hydroxy-phenyl]-acrylic acid | CHEMBL196272
TypeSmall organic molecule
Emp. Form.C18H12O8
Mol. Mass.356.2831
SMILESOC(=O)\C=C\c1ccc(O)c(Oc2cc3cc(O)c(O)cc3oc2=O)c1
Structure
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