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TargetGag-Pol polyprotein [489-587]
LigandBDBM50070299
Substrate/Competitorn/a
Meas. Tech.ChEMBL_157555 (CHEMBL763307)
Ki 4.7±n/a nM
Citation Janakiraman, MNWatenpaugh, KDTomich, PKChong, KTTurner, SRTommasi, RAThaisrivongs, SStrohbach, JW Non-peptidic HIV protease inhibitors: C2-symmetry-based design of bis-sulfonamide dihydropyrones. Bioorg Med Chem Lett8:1237-42 (1999) [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:
BDBM50070299
n/a
NameBDBM50070299
Synonyms:4N-[3-(1-{2-ethyl-4-hydroxy-2-[3-(1-methyl-1H-4-imidazolylsulfonamido)phenyl]-6-oxo-3,6-dihydro-2H-5-pyranyl}propyl)phenyl]-1-methyl-1H-4-imidazolesulfonamide | CHEMBL20565
TypeSmall organic molecule
Emp. Form.C30H34N6O7S2
Mol. Mass.654.757
SMILESCCC(C1C(=O)CC(CC)(OC1=O)c1cccc(NS(=O)(=O)c2cn(C)cn2)c1)c1cccc(NS(=O)(=O)c2cn(C)cn2)c1
Structure
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