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TargetHuman immunodeficiency virus type 1 reverse transcriptase
LigandBDBM50082057
Substrate/Competitorn/a
Meas. Tech.ChEMBL_196180
Ki 100±n/a nM
Citation Campiani GMorelli EFabbrini MNacci VGreco GNovellino ERamunno AMaga GSpadari SCaliendo GBergamini AFaggioli EUccella IBolacchi FMarini SColetta MNacca ACaccia S Pyrrolobenzoxazepinone derivatives as non-nucleoside HIV-1 RT inhibitors: further structure-activity relationship studies and identification of more potent broad-spectrum HIV-1 RT inhibitors with antiviral activity. J Med Chem 42:4462-70 (1999) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Human immunodeficiency virus type 1 reverse transcriptase
Name:Human immunodeficiency virus type 1 reverse transcriptase
Synonyms: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:
BDBM50082057
n/a
NameBDBM50082057
Synonyms:(+/-)-5-ethyl-5-m-tolyl-6-oxa-10b-aza-benzo[e]azulen-4-one | 5-Ethyl-5-m-tolyl-6-oxa-10b-aza-benzo[e]azulen-4-one | CHEMBL139532
TypeSmall organic molecule
Emp. Form.C21H19NO2
Mol. Mass.317.3811
SMILESCCC1(Oc2ccccc2-n2cccc2C1=O)c1cccc(C)c1
Structure
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