Reaction Details |
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Target | Reverse transcriptase/RNaseH |
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Ligand | BDBM1287 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_196348 (CHEMBL802044) |
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IC50 | 347±n/a nM |
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Citation | Gibson, S; McGuire, R; Rees, DC Principal components describing biological activities and molecular diversity of heterocyclic aromatic ring fragments. J Med Chem39:4065-72 (1996) [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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BDBM1287 |
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n/a |
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Name | BDBM1287 |
Synonyms: | 3-Aminopyridin-2(1H)-one analogue 7 | 3-[(1,3-benzothiazol-2-ylmethyl)amino]-5-ethyl-6-methyl-1,2-dihydropyridin-2-one | CHEMBL431274 | Pyridinone deriv. 4 |
Type | Small organic molecule |
Emp. Form. | C16H17N3OS |
Mol. Mass. | 299.391 |
SMILES | CCc1cc(NCc2nc3ccccc3s2)c(=O)[nH]c1C |
Structure |
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