Reaction Details |
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Target | Reverse transcriptase/RNaseH |
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Ligand | BDBM50368502 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_196932 (CHEMBL803949) |
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IC50 | 125000±n/a nM |
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Citation | Tan, GT; Wickramasinghe, A; Baba, M; Hughes, SH; Mohan, P; Pezzuto, JM; Singh, R; Verma, S Potential anti-AIDS naphthalenesulfonic acid derivatives. Synthesis and inhibition of HIV-1 induced cytopathogenesis and HIV-1 and HIV-2 reverse transcriptase activities. J Med Chem35:4846-53 (1992) [PubMed] |
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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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BDBM50368502 |
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n/a |
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Name | BDBM50368502 |
Synonyms: | CHEMBL1788183 |
Type | Small organic molecule |
Emp. Form. | C32H20N2O16S6 |
Mol. Mass. | 880.897 |
SMILES | [O-]S(=O)(=O)c1cc(c2cc(NS(=O)(=O)c3ccc(cc3)-c3ccc(cc3)S(=O)(=O)Nc3ccc4cc(cc(c4c3)S([O-])(=O)=O)S([O-])(=O)=O)ccc2c1)S([O-])(=O)=O |
Structure |
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