Reaction Details |
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Target | Reverse transcriptase/RNaseH |
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Ligand | BDBM50030543 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_195358 (CHEMBL802598) |
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IC50 | >100000±n/a nM |
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Citation | Maruenda, H; Johnson, F Design and synthesis of novel inhibitors of HIV-1 reverse transcriptase. J Med Chem38:2145-51 (1995) [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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BDBM50030543 |
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n/a |
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Name | BDBM50030543 |
Synonyms: | Acetic acid 2-(1,3,11-trioxo-2,3,10,11-tetrahydro-1H-5-thia-2,4,10-triaza-dibenzo[a,d]cyclohepten-4-ylmethoxy)-ethyl ester | CHEMBL68530 |
Type | Small organic molecule |
Emp. Form. | C16H15N3O6S |
Mol. Mass. | 377.372 |
SMILES | CC(=O)OCCOCn1c2Sc3ccccc3NC(=O)c2c(=O)[nH]c1=O |
Structure |
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