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TargetReverse transcriptase/RNaseH
LigandBDBM50121351
Substrate/Competitorn/a
Meas. Tech.ChEMBL_195204 (CHEMBL798996)
IC50 56600±n/a nM
Citation Barreca, MLBalzarini, JChimirri, ADe Clercq, EDe Luca, LHöltje, HDHöltje, MMonforte, AMMonforte, PPannecouque, CRao, AZappalà, 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]
More Info.:Get all data from this article,  Assay Method
 
Reverse transcriptase/RNaseH
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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  Blast E-value cutoff:
BDBM50121351
n/a
NameBDBM50121351
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
TypeSmall organic molecule
Emp. Form.C14H9BrCl2N2OS
Mol. Mass.404.109
SMILESClc1cccc(Cl)c1C1SCC(=O)N1c1ccc(Br)cn1
Structure
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