Reaction Details |
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Target | Reverse transcriptase/RNaseH |
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Ligand | BDBM50169066 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_310383 (CHEMBL833564) |
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EC50 | 2300±n/a nM |
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Citation | De Martino, G; La Regina, G; Di Pasquali, A; Ragno, R; Bergamini, A; Ciaprini, C; Sinistro, A; Maga, G; Crespan, E; Artico, M; Silvestri, R Novel 1-[2-(diarylmethoxy)ethyl]-2-methyl-5-nitroimidazoles as HIV-1 non-nucleoside reverse transcriptase inhibitors. A structure-activity relationship investigation. J Med Chem48:4378-88 (2005) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Reverse transcriptase/RNaseH |
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Name: | Reverse transcriptase/RNaseH |
Synonyms: | HIV-1 Reverse Transcriptase RNase H | Human immunodeficiency virus type 1 reverse transcriptase | Reverse transcriptase/RNaseH |
Type: | PROTEIN |
Mol. Mass.: | 65229.15 |
Organism: | Human immunodeficiency virus 1 |
Description: | ChEMBL_1473730 |
Residue: | 566 |
Sequence: | PISPIETVPVKLKPGMDGPKVKQWPLTEEKIKALVEICTEMEKEGKISKIGPENPYNTPV
FAIKKKDSTKWRKLVDFRELNKRTQDFWEVQLGIPHPAGLKKRKSVTVLDVGDAYFSVPL
DEDFRKYTAFTIPSINNETPGIRYQYNVLPQGWKGSPAIFQSSMTKILEPFRKQNPDIVI
YQYMDDLYVGSDLEIGQHRTKIEELRQHLLRWGLTTPDKKHQKEPPFLWMGYELHPDKWT
VQPIVLPEKDSWTVNDIQKLVGKLNWASQIYPGIRVRQLCKLLRGTKALTEVIPLTEEAE
LELAENREILKEPVHGVYYDPSKDLIAEIQKQGQGQWTYQIYQEPFKNLRTGKYARMRGA
HTNDVKQLTEAVQKITTESIVIWGKTPKFKLPIQKETWETWWTEYWQATWIPEWEFVNTP
PLVKLWYQLEKEPIVGAETFYVDGAANRETKLGKAGYVTNRGRQKVVTLTDTTNQKTELQ
AIYLALQDSGLEVNIVTDSQYALGIIQAQPDQSESELVNQIIEQLIKKEKVYLAWVPAHK
GIGGNEQVDKLVSAGIRKVLFLDGID
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BDBM50169066 |
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n/a |
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Name | BDBM50169066 |
Synonyms: | 1-(2-Benzhydrylsulfanyl-ethyl)-2-methyl-5-nitro-1H-imidazole | CHEMBL191155 |
Type | Small organic molecule |
Emp. Form. | C19H19N3O2S |
Mol. Mass. | 353.438 |
SMILES | Cc1ncc(n1CCSC(c1ccccc1)c1ccccc1)[N+]([O-])=O |
Structure |
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