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Reaction Details
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TargetHuman immunodeficiency virus type 1 protease
LigandBDBM50005695
Substrate/Competitorn/a
Meas. Tech.ChEMBL_159480
IC50 1.9±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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BDBM50005695
NameBDBM50005695
Synonyms:1-(2-Hydroxy-3-{3-methyl-2-[2-(naphthalen-1-yloxy)-acetylamino]-butyrylamino}-4-phenyl-butyryl)-pyrrolidine-2-carboxylic acid tert-butylamide | BDBM50407028 | CHEMBL283522 | CHEMBL335391
TypeSmall organic molecule
Emp. Form.C36H46N4O6
Mol. Mass.630.7736
SMILESCC(C)[C@H](NC(=O)COc1cccc2ccccc12)C(=O)N[C@@H](Cc1ccccc1)[C@H](O)C(=O)N1CCC[C@H]1C(=O)NC(C)(C)C
Structure
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