Reaction Details |
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Target | Reverse transcriptase/RNaseH |
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Ligand | BDBM50184078 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_364650 (CHEMBL854191) |
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IC50 | 11000±n/a nM |
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Citation | Krajewski, K; Zhang, Y; Parrish, D; Deschamps, J; Roller, PP; Pathak, VK New HIV-1 reverse transcriptase inhibitors based on a tricyclic benzothiophene scaffold: synthesis, resolution, and inhibitory activity. Bioorg Med Chem Lett16:3034-8 (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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BDBM50184078 |
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n/a |
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Name | BDBM50184078 |
Synonyms: | (2aS,7aS)-2-((R)-2-methyl-pyrrolidin-1-yl)-2aH-7-thia-cyclobuta[a]indene-1,7a-dicarboxylic acid dimethyl ester | CHEMBL383271 |
Type | Small organic molecule |
Emp. Form. | C19H21NO4S |
Mol. Mass. | 359.439 |
SMILES | COC(=O)C1=C([C@@H]2c3ccccc3S[C@]12C(=O)OC)N1CCC[C@H]1C |t:4| |
Structure |
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