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TargetGag-Pol polyprotein [489-587]
LigandBDBM50037838
Substrate/Competitorn/a
Meas. Tech.ChEMBL_159307 (CHEMBL769360)
IC50>35000±n/a nM
Citation Kitchin, JBethell, RCCammack, NDolan, SEvans, DNHolman, SHolmes, DSMcMeekin, PMo, CLNieland, N Synthesis and structure-activity relationships of a series of penicillin-derived HIV proteinase inhibitors: heterocyclic ring systems containing P1' and P2' substituents. J Med Chem37:3707-16 (1994) [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:
BDBM50037838
n/a
NameBDBM50037838
Synonyms:(2R,4S)-2-[Benzylcarbamoyl-((S)-phenylacetylamino)-methyl]-5,5-dimethyl-thiazolidine-4-carboxylic acid [(S)-3-((2S,4R)-2-tert-butylcarbamoyl-4-ethoxy-pyrrolidin-1-yl)-2-hydroxy-propyl]-amide | CHEMBL332736
TypeSmall organic molecule
Emp. Form.C37H54N6O6S
Mol. Mass.710.926
SMILESCCO[C@@H]1C[C@H](N(C[C@@H](O)CNC(=O)[C@@H]2N[C@H](SC2(C)C)C(NC(=O)Cc2ccccc2)C(=O)NCc2ccccc2)C1)C(=O)NC(C)(C)C
Structure
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