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TargetIntegrase
LigandBDBM50157832
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1720244 (CHEMBL4135244)
IC50 35000±n/a nM
Citation Kankanala, JKirby, KAHuber, ADCasey, MCWilson, DJSarafianos, SGWang, Z Design, synthesis and biological evaluations of N-Hydroxy thienopyrimidine-2,4-diones as inhibitors of HIV reverse transcriptase-associated RNase H. Eur J Med Chem141:149-161 (2017) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Integrase
Name:Integrase
Synonyms:pol
Type:PROTEIN
Mol. Mass.:32203.43
Organism:Human immunodeficiency virus 1
Description:ChEMBL_106649
Residue:288
Sequence:
FLDGIDKAQEEHEKYHSNWRAMASDFNLPPVVAKEIVASCDKCQLKGEAMHGQVDCSPGI
WQLDCTHLEGKVILVAVHVASGYIEAEVIPAETGQETAYFLLKLAGRWPVKTVHTDNGSN
FTSTTVKAACWWAGIKQEFGIPYNPQSQGVIESMNKELKKIIGQVRDQAEHLKTAVQMAV
FIHNFKRKGGIGGYSAGERIVDIIATDIQTKELQKQITKIQNFRVYYRDSRDPVWKGPAK
LLWKGEGAVVIQDNSDIKVVPRRKAKIIRDYGKQMAGDDCVASRQDED
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  Blast E-value cutoff:
BDBM50157832
n/a
NameBDBM50157832
Synonyms:3-Hydroxy-4a,7a-dihydro-1H-thieno[2,3-d]pyrimidine-2,4-dione | CHEMBL361350
TypeSmall organic molecule
Emp. Form.C6H4N2O3S
Mol. Mass.184.173
SMILESOn1c(=O)[nH]c2sccc2c1=O
Structure
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