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TargetGag-Pol polyprotein [489-587]
LigandBDBM50055593
Substrate/Competitorn/a
Meas. Tech.ChEMBL_157575 (CHEMBL763326)
Ki 0.033±n/a nM
Citation Jadhav, PKAla, PWoerner, FJChang, CHGarber, SSAnton, EDBacheler, LT Cyclic urea amides: HIV-1 protease inhibitors with low nanomolar potency against both wild type and protease inhibitor resistant mutants of HIV. J Med Chem40:181-91 (1997) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Gag-Pol polyprotein [489-587]
Name:Gag-Pol polyprotein [489-587]
Synonyms:Human immunodeficiency virus type 1 protease | POL_HV1H2 | Pol polyprotein | gag-pol
Type:Enzyme Subunit
Mol. Mass.:10781.16
Organism:Human immunodeficiency virus type 1
Description:P04585[489-587]
Residue:99
Sequence:
PQVTLWQRPLVTIKIGGQLKEALLDTGADDTVLEEMSLPGRWKPKMIGGIGGFIKVRQYD
QILIEICGHKAIGTVLVGPTPVNIIGRNLLTQIGCTLNF
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  Blast E-value cutoff:
BDBM50055593
n/a
NameBDBM50055593
Synonyms:CHEMBL292905 | N-(1H-Imidazol-2-yl)-3-((4R,5S,6S,7R)-3,4,7-tribenzyl-5,6-dihydroxy-2-oxo-[1,3]diazepan-1-ylmethyl)-benzamide
TypeSmall organic molecule
Emp. Form.C37H37N5O4
Mol. Mass.615.7208
SMILESO[C@@H]1[C@@H](O)[C@@H](Cc2ccccc2)N(Cc2cccc(c2)C(=O)Nc2ncc[nH]2)C(=O)N(Cc2ccccc2)[C@@H]1Cc1ccccc1
Structure
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