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TargetGag-Pol polyprotein [489-587]
LigandBDBM50124719
Substrate/Competitorn/a
Meas. Tech.ChEBML_157538
Ki 0.190000±n/a nM
Citation Kaltenbach, RFPatel, MWaltermire, REHarris, GDStone, BRKlabe, RMGarber, SBacheler, LTCordova, BCLogue, KWright, MRErickson-Viitanen, STrainor, GL Synthesis, antiviral activity and pharmacokinetics of P1/P1' substituted 3-aminoindazole cyclic urea HIV protease inhibitors. Bioorg Med Chem Lett13:605-8 (2003) [PubMed]
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:
BDBM50124719
n/a
NameBDBM50124719
Synonyms:(4R,5S,6S,7R)-1-(3-Amino-1H-indazol-5-ylmethyl)-3-butyl-4,7-bis-(3,5-dimethyl-benzyl)-5,6-dihydroxy-[1,3]diazepan-2-one | CHEMBL442770
TypeSmall organic molecule
Emp. Form.C35H45N5O3
Mol. Mass.583.7635
SMILESCCCCN1[C@H](Cc2cc(C)cc(C)c2)[C@H](O)[C@@H](O)[C@@H](Cc2cc(C)cc(C)c2)N(Cc2ccc3[nH]nc(N)c3c2)C1=O
Structure
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