Reaction Details |
| Report a problem with these data |
Target | Reverse transcriptase/RNaseH |
---|
Ligand | BDBM50097038 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_140625 (CHEMBL752870) |
---|
IC50 | 1300±n/a nM |
---|
Citation | Venkatachalam, TK; Sudbeck, EA; Mao, C; Uckun, FM Anti-HIV activity of aromatic and heterocyclic thiazolyl thiourea compounds. Bioorg Med Chem Lett11:523-8 (2001) [PubMed] |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
Reverse transcriptase/RNaseH |
---|
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
|
|
|
BDBM50097038 |
---|
n/a |
---|
Name | BDBM50097038 |
Synonyms: | 1-Adamantan-1-ylmethyl-3-thiazol-2-yl-thiourea | CHEMBL149161 |
Type | Small organic molecule |
Emp. Form. | C15H21N3S2 |
Mol. Mass. | 307.477 |
SMILES | S=C(NCC12CC3CC(CC(C3)C1)C2)Nc1nccs1 |TLB:7:8:12:6.5.11,THB:7:6:12:8.13.9,9:8:5:10.12.11,9:10:5:8.13.7| |
Structure |
|