Reaction Details |
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Target | Reverse transcriptase/RNaseH |
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Ligand | BDBM50008335 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_197283 (CHEMBL804270) |
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EC50 | 2700±n/a nM |
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Citation | Kireev, DB; Chrétien, JR; Grierson, DS; Monneret, C A 3D QSAR study of a series of HEPT analogues: the influence of conformational mobility on HIV-1 reverse transcriptase inhibition. J Med Chem40:4257-64 (1998) [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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BDBM50008335 |
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n/a |
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Name | BDBM50008335 |
Synonyms: | 6-(3-Ethyl-phenylsulfanyl)-1-(2-hydroxy-ethoxymethyl)-5-methyl-1H-pyrimidine-2,4-dione | CHEMBL417626 |
Type | Small organic molecule |
Emp. Form. | C16H20N2O4S |
Mol. Mass. | 336.406 |
SMILES | CCc1cccc(Sc2c(C)c(=O)[nH]c(=O)n2COCCO)c1 |
Structure |
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