Target
Gag-Pol polyprotein [489-587]
Ligand
BDBM50147191
Substrate
n/a
Meas. Tech.
ChEMBL_158990 (CHEMBL763756)
IC50
1300±n/a nM
Citation
 Yehia, NAAntuch, WBeck, BHess, SSchauer-Vukasinovic, VAlmstetter, MFurer, PHerdtweck, EDömling, A Novel nonpeptidic inhibitors of HIV-1 protease obtained via a new multicomponent chemistry strategy. Bioorg Med Chem Lett 14:3121-5 (2004) [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:
BDBM50147191
Synonyms:
4-(1,5-Dimethyl-hex-4-enyl)-3-hydroxy-5-oxo-2-phenethyl-2,5-dihydro-furan-2-carboxylic acid tert-butylamide | CHEMBL104471
Type:
Small organic molecule
Emp. Form.:
C25H35NO4
Mol. Mass.:
413.5497
SMILES:
[#6]-[#6](-[#6]-[#6]\[#6]=[#6](\[#6])-[#6])-[#6]-1-[#6](=O)-[#8]C([#6]-[#6]-c2ccccc2)([#6](=O)-[#7]C([#6])([#6])[#6])[#6]-1=O
Structure:
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