Reaction Details |
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Target | Reverse transcriptase |
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Ligand | BDBM2325 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_450291 (CHEMBL900572) |
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Ki | 1400±n/a nM |
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Citation | Mai, A; Artico, M; Rotili, D; Tarantino, D; Clotet-Codina, I; Armand-Ugón, M; Ragno, R; Simeoni, S; Sbardella, G; Nawrozkij, MB; Samuele, A; Maga, G; Esté, JA Synthesis and biological properties of novel 2-aminopyrimidin-4(3H)-ones highly potent against HIV-1 mutant strains. J Med Chem50:5412-24 (2007) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Reverse transcriptase |
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Name: | Reverse transcriptase |
Synonyms: | n/a |
Type: | Protein |
Mol. Mass.: | 29598.37 |
Organism: | Human immunodeficiency virus 1 |
Description: | Q9WKE8 |
Residue: | 254 |
Sequence: | PISPITVPVKLKPGMDGPKVKQWPLTEEKIKALTEICTEMEKEGKIEKIGPENPYNTPVF
AIKKKDSTKWRKVVDFRELNKRTQDFWEVQLGIPHPAGLKKKKSVTVLDVGDAYFSVPLD
KDFRKYTAFTIPSINNETPGIRYQYNVLPQGWKGSPAIFQSSMTKILEPFRKQNPDIVIY
QYMDDLYVGSDLEIEQHRAKIEELRQHLLRWGFTTPDKKHQKEPPFLWMGYELHPDKWTV
QPIVLPEKDSWTVN
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BDBM2325 |
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n/a |
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Name | BDBM2325 |
Synonyms: | 2-(cyclopentylsulfanyl)-6-[1-(2,6-difluorophenyl)ethyl]-5-methyl-3,4-dihydropyrimidin-4-one | S-DABO | thio-DABO 3w |
Type | Small organic molecule |
Emp. Form. | C18H20F2N2OS |
Mol. Mass. | 350.426 |
SMILES | CC(c1nc(SC2CCCC2)[nH]c(=O)c1C)c1c(F)cccc1F |
Structure |
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