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TargetHuman immunodeficiency virus type 1 protease
LigandBDBM50005705
Substrate/Competitorn/a
Meas. Tech.ChEBML_159481
IC50 6500±n/a nM
Citation Tam, TFCarrière, JMacDonald, DCastelhano, ALPliura, DHDewdney, NJThomas, EMBach, CBarnett, JChan, H Intriguing structure-activity relations underlie the potent inhibition of HIV protease by norstatine-based peptides. J Med Chem35:1318-20 (1992) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Human immunodeficiency virus type 1 protease
Name:Human immunodeficiency virus type 1 protease
Synonyms:Pol polyprotein
Type:Enzyme Subunit
Mol. Mass.:10781.16
Organism:Human immunodeficiency virus type 1
Description:n/a
Residue:99
Sequence:
PQVTLWQRPLVTIKIGGQLKEALLDTGADDTVLEEMSLPGRWKPKMIGGIGGFIKVRQYD
QILIEICGHKAIGTVLVGPTPVNIIGRNLLTQIGCTLNF
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BDBM50005705
NameBDBM50005705
Synonyms:1-(3-Benzyloxycarbonylamino-2-hydroxy-4-phenyl-butyl)-pyrrolidine-2-carboxylic acid tert-butyl ester | CHEMBL25119 | CHEMBL3349992
TypeSmall organic molecule
Emp. Form.C27H36N2O5
Mol. Mass.468.5851
SMILESCC(C)(C)OC(=O)[C@@H]1CCCN1C[C@@H](O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1
Structure
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