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TargetGag-Pol polyprotein [489-587]
LigandBDBM175
Substrate/Competitorn/a
Meas. Tech.ChEMBL_157717 (CHEMBL763391)
Ki 0.037±n/a nM
Citation Han, QChang, CHLi, RRu, YJadhav, PKLam, PY Cyclic HIV protease inhibitors: design and synthesis of orally bioavailable, pyrazole P2/P2' cyclic ureas with improved potency. J Med Chem41:2019-28 (1998) [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:
BDBM175
n/a
NameBDBM175
Synonyms:(4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1,3-bis({[3-(2,2,2-trifluoroacetyl)phenyl]methyl})-1,3-diazepan-2-one | (4R,5S,6S,7R)-Hexahydro-5,6-dihydroxy-1,3-bis[[3-(trifluoroacetyl)phenyl]methyl]-4,7-bis(phenylmethyl)-2H-1,3-diazepin-2-one | CHEMBL292631 | Cyclic Urea
Typen/a
Emp. Form.C37H32F6N2O5
Mol. Mass.698.6508
SMILESO[C@@H]1[C@@H](O)[C@@H](Cc2ccccc2)N(Cc2cccc(c2)C(=O)C(F)(F)F)C(=O)N(Cc2cccc(c2)C(=O)C(F)(F)F)[C@@H]1Cc1ccccc1
Structure
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