Reaction Details |
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Target | Reverse transcriptase/RNaseH |
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Ligand | BDBM50193520 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_385312 (CHEMBL869229) |
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IC50 | 7600±n/a nM |
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Citation | Deng, BL; Hartman, TL; Buckheit, RW; Pannecouque, C; De Clercq, E; Cushman, M Replacement of the metabolically labile methyl esters in the alkenyldiarylmethane series of non-nucleoside reverse transcriptase inhibitors with isoxazolone, isoxazole, oxazolone, or cyano substituents. J Med Chem49:5316-23 (2006) [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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BDBM50193520 |
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n/a |
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Name | BDBM50193520 |
Synonyms: | (E)-5-[1-(3-methoxy-7-methyl-benzo[d]isoxazol-5-yl)-4-(2-oxooxazolidin-3-yl)but-1-enyl]-2,7-dimethylbenzo[d]isoxazol-3-one | CHEMBL387003 |
Type | Small organic molecule |
Emp. Form. | C25H25N3O6 |
Mol. Mass. | 463.4825 |
SMILES | COc1noc2c(C)cc(cc12)C(=C/CCN1CCOC1=O)\c1cc(C)c2on(C)c(=O)c2c1 |
Structure |
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