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TargetGag-Pol polyprotein [489-587]
LigandBDBM50037842
Substrate/Competitorn/a
Meas. Tech.ChEMBL_159307 (CHEMBL769360)
IC50 21±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:
BDBM50037842
n/a
NameBDBM50037842
Synonyms:4N-(tert-butyl)-3-{3-[2-benzylcarbamoyl(benzylcarboxamido)methyl-5,5-dimethyl-(2R,4S)-1,3-thiazolan-4-ylcarboxamido]-2-hydroxypropyl}-5,5-dimethyl-(4R)-1,3-thiazolane-4-carboxamide | CHEMBL122402
TypeSmall organic molecule
Emp. Form.C36H52N6O5S2
Mol. Mass.712.965
SMILESCC(C)(C)NC(=O)[C@H]1N(CC(O)CNC(=O)[C@@H]2N[C@H](SC2(C)C)[C@H](NC(=O)Cc2ccccc2)C(=O)NCc2ccccc2)CSC1(C)C
Structure
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