| Reaction Details |
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 | Report a problem with these data |
| Target | Reverse transcriptase |
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| Ligand | BDBM50484284 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_768443 (CHEMBL1832162) |
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| IC50 | 13900±n/a nM |
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| Citation |  Barral, K; Weck, C; Payrot, N; Roux, L; Durafour, C; Zoulim, F; Neyts, J; Balzarini, J; Canard, B; Priet, S; Alvarez, K Acyclic nucleoside thiophosphonates as potent inhibitors of HIV and HBV replication. Eur J Med Chem46:4281-8 (2011) [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 |
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| Synonyms: | n/a |
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| Type: | Protein |
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| Mol. Mass.: | 29598.37 |
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| Organism: | Human immunodeficiency virus 1 |
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| Description: | Q9WKE8 |
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| Residue: | 254 |
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| Sequence: | PISPITVPVKLKPGMDGPKVKQWPLTEEKIKALTEICTEMEKEGKIEKIGPENPYNTPVF
AIKKKDSTKWRKVVDFRELNKRTQDFWEVQLGIPHPAGLKKKKSVTVLDVGDAYFSVPLD
KDFRKYTAFTIPSINNETPGIRYQYNVLPQGWKGSPAIFQSSMTKILEPFRKQNPDIVIY
QYMDDLYVGSDLEIEQHRAKIEELRQHLLRWGFTTPDKKHQKEPPFLWMGYELHPDKWTV
QPIVLPEKDSWTVN
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| BDBM50484284 |
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| n/a |
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| Name | BDBM50484284 |
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| Synonyms: | CHEMBL1830072 |
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| Type | Small organic molecule |
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| Emp. Form. | C9H12N5Na4O9P3S |
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| Mol. Mass. | 551.165 |
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| SMILES | [Na;v0+].[Na;v0+].[Na;v0+].[Na;v0+].[#6]-[#6@H](-[#6]-n1cnc2c(-[#7])ncnc12)-[#8]-[#6]P([#16-])(=O)[#8]P([#8-])(=O)[#8]P([#8-])([#8-])=O |r| |
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| Structure | 
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