Reaction Details |
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Target | Reverse transcriptase/RNaseH |
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Ligand | BDBM50172745 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_321416 (CHEMBL881947) |
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IC50 | 11200±n/a nM |
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Citation | Bedoya, LM; Beltrán, M; Sancho, R; Olmedo, DA; Sánchez-Palomino, S; del Olmo, E; López-Pérez, JL; Muñoz, E; San Feliciano, A; Alcamí, J 4-Phenylcoumarins as HIV transcription inhibitors. Bioorg Med Chem Lett15:4447-50 (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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BDBM50172745 |
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n/a |
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Name | BDBM50172745 |
Synonyms: | 5,7-Dihydroxy-8-(3-methyl-but-2-enyl)-4-phenyl-chromen-2-one | 5,7-dihydroxy-8-(3-methylbut-2-enyl)-4-phenylchromen-2-one | CHEMBL363624 |
Type | Small organic molecule |
Emp. Form. | C20H18O4 |
Mol. Mass. | 322.3545 |
SMILES | [#6]\[#6](-[#6])=[#6]\[#6]-c1c(-[#8])cc(-[#8])c2c(cc(=O)oc12)-c1ccccc1 |
Structure |
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