Reaction Details |
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Target | Reverse transcriptase/RNaseH |
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Ligand | BDBM50121351 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_195204 (CHEMBL798996) |
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IC50 | 56600±n/a nM |
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Citation | Barreca, ML; Balzarini, J; Chimirri, A; De Clercq, E; De Luca, L; Höltje, HD; Höltje, M; Monforte, AM; Monforte, P; Pannecouque, C; Rao, A; Zappalà, M Design, synthesis, structure-activity relationships, and molecular modeling studies of 2,3-diaryl-1,3-thiazolidin-4-ones as potent anti-HIV agents. J Med Chem45:5410-3 (2002) [PubMed] |
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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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BDBM50121351 |
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n/a |
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Name | BDBM50121351 |
Synonyms: | 3-(5-Bromo-pyridin-2-yl)-2-(2,6-dichloro-phenyl)-thiazolidin-4-one | 3-(5-Bromopyridin-2-yl)-2-(2,6-dichlorophenyl)-l,3-thiazolidin-4-one | 3-(5-bromopyridin-2-yl)-2-(2,6-dichlorophenyl)thiazolidin-4-one | CHEMBL357261 |
Type | Small organic molecule |
Emp. Form. | C14H9BrCl2N2OS |
Mol. Mass. | 404.109 |
SMILES | Clc1cccc(Cl)c1C1SCC(=O)N1c1ccc(Br)cn1 |
Structure |
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