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TargetReverse transcriptase/RNaseH
LigandBDBM50168060
Substrate/Competitorn/a
Meas. Tech.ChEMBL_305566 (CHEMBL827160)
IC50 4800±n/a nM
Citation Ranise, ASpallarossa, ACesarini, SBondavalli, FSchenone, SBruno, OMenozzi, GFossa, PMosti, LLa Colla, MSanna, GMurreddu, MCollu, GBusonera, BMarongiu, MEPani, ALa Colla, PLoddo, R Structure-based design, parallel synthesis, structure-activity relationship, and molecular modeling studies of thiocarbamates, new potent non-nucleoside HIV-1 reverse transcriptase inhibitor isosteres of phenethylthiazolylthiourea derivatives. J Med Chem48:3858-73 (2005) [PubMed]  Article
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
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  Blast E-value cutoff:
BDBM50168060
n/a
NameBDBM50168060
Synonyms:CHEMBL195108 | N-[2-(4-Iodo-phenylthiocarbamoyloxy)-ethyl]-phthalamic acid
TypeSmall organic molecule
Emp. Form.C17H15IN2O4S
Mol. Mass.470.281
SMILESOC(=O)c1ccccc1C(=O)NCCOC(=S)Nc1ccc(I)cc1
Structure
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