Reaction Details |
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Target | Gag-Pol polyprotein [489-587] |
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Ligand | BDBM151 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_80092 |
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Ki | 0.280000±n/a nM |
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Citation | Patel, M; Bacheler, LT; Rayner, MM; Cordova, BC; Klabe, RM; Erickson-Viitanen, S; Seitz, SP The synthesis and evaluation of cyclic ureas as HIV protease inhibitors: modifications of the P1/P1' residues. Bioorg Med Chem Lett8:823-8 (1999) [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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BDBM151 |
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n/a |
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Name | BDBM151 |
Synonyms: | (4R,5S,6S,7R)-1,3-bis[(3-aminophenyl)methyl]-4,7-dibenzyl-5,6-dihydroxy-1,3-diazepan-2-one | CHEMBL223824 | DMP450 |
Type | n/a |
Emp. Form. | C33H36N4O3 |
Mol. Mass. | 536.6639 |
SMILES | Nc1cccc(CN2[C@H](Cc3ccccc3)[C@H](O)[C@@H](O)[C@@H](Cc3ccccc3)N(Cc3cccc(N)c3)C2=O)c1 |
Structure |
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