Reaction Details |
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Target | Gag-Pol polyprotein [489-587] |
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Ligand | BDBM1144 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_36514 |
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Ki | 0.080168±n/a nM |
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Citation | Katritzky, AR; Oliferenko, A; Lomaka, A; Karelson, M Six-membered cyclic ureas as HIV-1 protease inhibitors: a QSAR study based on CODESSA PRO approach. Quantitative structure-activity relationships. Bioorg Med Chem Lett12:3453-7 (2002) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Gag-Pol polyprotein [489-587] |
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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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BDBM1144 |
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n/a |
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Name | BDBM1144 |
Synonyms: | (4R,5R,6R)-1-[(3-aminophenyl)methyl]-4-benzyl-5-hydroxy-3-(1H-indazol-5-ylmethyl)-6-(2-phenylethyl)-1,3-diazinan-2-one | (4R,5R,6R)-Tetrahydro-1-[1H-indazol-5-ylmethyl]-3-(3-aminophenyl-methyl)-4-(2-phenylethyl)-5-hydroxy)-6-(phenylmethyl)-2(1H)-pyrimidinone | Tetrahydropyrimidinone deriv. 92 |
Type | Small organic molecule |
Emp. Form. | C34H35N5O2 |
Mol. Mass. | 545.674 |
SMILES | Nc1cccc(CN2[C@H](CCc3ccccc3)[C@@H](O)[C@@H](Cc3ccccc3)N(Cc3ccc4[nH]ncc4c3)C2=O)c1 |r| |
Structure |
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