Reaction Details |
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Target | Reverse transcriptase |
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Ligand | BDBM50482144 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_629799 (CHEMBL1115617) |
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IC50 | 1900±n/a nM |
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Citation | Mackman, RL; Ray, AS; Hui, HC; Zhang, L; Birkus, G; Boojamra, CG; Desai, MC; Douglas, JL; Gao, Y; Grant, D; Laflamme, G; Lin, KY; Markevitch, DY; Mishra, R; McDermott, M; Pakdaman, R; Petrakovsky, OV; Vela, JE; Cihlar, T Discovery of GS-9131: Design, synthesis and optimization of amidate prodrugs of the novel nucleoside phosphonate HIV reverse transcriptase (RT) inhibitor GS-9148. Bioorg Med Chem18:3606-17 (2010) [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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BDBM50482144 |
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n/a |
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Name | BDBM50482144 |
Synonyms: | CHEMBL1098407 |
Type | Small organic molecule |
Emp. Form. | C10H13FN5O11P3 |
Mol. Mass. | 491.1568 |
SMILES | Nc1ncnc2n(cnc12)[C@@H]1O[C@H](OCP(O)(=O)OP(O)(=O)OP(O)(O)=O)C=C1F |r,c:29| |
Structure |
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