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Target
Gag-Pol polyprotein [489-587]
Ligand
BDBM50124721
Substrate
n/a
Meas. Tech.
ChEBML_157538
Ki
0.031000±n/a nM
Citation
 Kaltenbach, RF; Patel, M; Waltermire, RE; Harris, GD; Stone, BR; Klabe, RM; Garber, S; Bacheler, LT; Cordova, BC; Logue, K; Wright, MR; Erickson-Viitanen, S; Trainor, GL Synthesis, antiviral activity and pharmacokinetics of P1/P1' substituted 3-aminoindazole cyclic urea HIV protease inhibitors. Bioorg Med Chem Lett 13:605-8 (2003) [PubMed]  Article 
Target
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:
PQVTLWQRPLVTIKIGGQLKEALLDTGADDTVLEEMSLPGRWKPKMIGGIGGFIKVRQYDQILIEICGHKAIGTVLVGPTPVNIIGRNLLTQIGCTLNF
  
Inhibitor
Name:
BDBM50124721
Synonyms:
(4R,5S,6S,7R)-1-(3-Amino-1H-indazol-5-ylmethyl)-3,4,7-tribenzyl-5,6-dihydroxy-[1,3]diazepan-2-one | CHEMBL346818 | DMP-850
Type:
Small organic molecule
Emp. Form.:
C34H35N5O3
Mol. Mass.:
561.6734
SMILES:
Nc1[nH]nc2ccc(CN3[C@H](Cc4ccccc4)[C@H](O)[C@@H](O)[C@@H](Cc4ccccc4)N(Cc4ccccc4)C3=O)cc12
Structure:
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