Reaction Details |
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Target | Reverse transcriptase |
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Ligand | BDBM2955 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1548831 (CHEMBL3755387) |
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IC50 | 45±n/a nM |
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Citation | Bastos, MM; Costa, CC; Bezerra, TC; da Silva, Fde C; Boechat, N Efavirenz a nonnucleoside reverse transcriptase inhibitor of first-generation: Approaches based on its medicinal chemistry. Eur J Med Chem108:455-65 (2016) [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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BDBM2955 |
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n/a |
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Name | BDBM2955 |
Synonyms: | GW420867X | HBY1293 | propan-2-yl (2S)-2-ethyl-7-fluoro-3-oxo-1,2,3,4-tetrahydroquinoxaline-1-carboxylate |
Type | Small organic molecule |
Emp. Form. | C14H17FN2O3 |
Mol. Mass. | 280.2948 |
SMILES | CC[C@@H]1N(C(=O)OC(C)C)c2cc(F)ccc2NC1=O |r| |
Structure |
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