Reaction Details |
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Target | Reverse transcriptase/RNaseH |
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Ligand | BDBM50030550 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_195358 (CHEMBL802598) |
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IC50 | 640±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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BDBM50030550 |
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n/a |
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Name | BDBM50030550 |
Synonyms: | 4-(2-Ethoxy-ethoxymethyl)-10,11-dihydro-4H-5-thia-2,4,10-triaza-dibenzo[a,d]cycloheptene-1,3-dione | CHEMBL69657 |
Type | Small organic molecule |
Emp. Form. | C16H19N3O4S |
Mol. Mass. | 349.405 |
SMILES | CCOCCOCn1c2Sc3ccccc3NCc2c(=O)[nH]c1=O |
Structure |
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