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TargetGag-Pol polyprotein [489-587]
LigandBDBM50121731
Substrate/Competitorn/a
Meas. Tech.ChEMBL_79946 (CHEMBL689317)
IC50 5000±n/a nM
Citation Hidaka, KKimura, THayashi, YMcDaniel, KFDekhtyar, TColletti, LKiso, Y Design and synthesis of pseudo-symmetric HIV protease inhibitors containing a novel hydroxymethylcarbonyl (HMC)-hydrazide isostere. Bioorg Med Chem Lett13:93-6 (2002) [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:
BDBM50121731
n/a
NameBDBM50121731
Synonyms:CHEMBL177918 | KNI-1278 | N-[(S)-3-{N-Benzyl-N'-[2-(2,6-dimethyl-phenoxy)-acetyl]-hydrazino}-2-hydroxy-3-oxo-1-((S)-phenylmethyl)-propyl]-2-(2,6-dimethyl-phenoxy)-acetamide
TypeSmall organic molecule
Emp. Form.C37H41N3O6
Mol. Mass.623.7379
SMILESCc1cccc(C)c1OCC(=O)N[C@@H](Cc1ccccc1)[C@H](O)C(=O)N(Cc1ccccc1)NC(=O)COc1c(C)cccc1C
Structure
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