Reaction Details |
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Target | Reverse transcriptase/RNaseH |
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Ligand | BDBM50070537 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_80270 (CHEMBL686917) |
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IC50 | 420±n/a nM |
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Citation | Sahlberg, C; Noréen, R; Engelhardt, P; Högberg, M; Kangasmetsä, J; Vrang, L; Zhang, H Synthesis and anti-HIV activities of urea-PETT analogs belonging to a new class of potent non-nucleoside HIV-1 reverse transcriptase inhibitors. Bioorg Med Chem Lett8:1511-6 (1999) [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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BDBM50070537 |
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n/a |
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Name | BDBM50070537 |
Synonyms: | 1-(5-Chloro-pyridin-2-yl)-3-[2-(2,6-difluoro-phenyl)-ethyl]-urea | CHEMBL36930 |
Type | Small organic molecule |
Emp. Form. | C14H12ClF2N3O |
Mol. Mass. | 311.714 |
SMILES | Fc1cccc(F)c1CCNC(=O)Nc1ccc(Cl)cn1 |
Structure |
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