Reaction Details |
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Target | Reverse transcriptase/RNaseH |
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Ligand | BDBM50158726 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_306176 (CHEMBL830970) |
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IC50 | 97000±n/a nM |
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Citation | Dayam, R; Sanchez, T; Clement, O; Shoemaker, R; Sei, S; Neamati, N Beta-diketo acid pharmacophore hypothesis. 1. Discovery of a novel class of HIV-1 integrase inhibitors. J Med Chem48:111-20 (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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BDBM50158726 |
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n/a |
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Name | BDBM50158726 |
Synonyms: | CHEMBL175563 | N-Benzo[1,3]dioxol-5-yl-3-{5-[1-benzo[1,3]dioxol-5-yl-meth-(Z)-ylidene]-4-oxo-2-thioxo-thiazolidin-3-yl}-propionamide |
Type | Small organic molecule |
Emp. Form. | C21H16N2O6S2 |
Mol. Mass. | 456.492 |
SMILES | O=C(CCN1C(=S)S\C(=C/c2ccc3OCOc3c2)C1=O)Nc1ccc2OCOc2c1 |
Structure |
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