BDBM65595 MLS001204096::N-[(3-methoxyphenyl)-(8-oxidanylquinolin-7-yl)methyl]ethanamide::N-[(8-Hydroxy-quinolin-7-yl)-(3-methoxy-phenyl)-methyl]-acetamide::N-[(8-hydroxy-7-quinolinyl)-(3-methoxyphenyl)methyl]acetamide::N-[(8-hydroxy-7-quinolyl)-(3-methoxyphenyl)methyl]acetamide::N-[(8-hydroxyquinolin-7-yl)-(3-methoxyphenyl)methyl]acetamide::SMR000516877::cid_3132202
SMILES COc1cccc(c1)C(NC(C)=O)c1ccc2cccnc2c1O
InChI Key InChIKey=XNISVWUYQDHGJO-UHFFFAOYSA-N
Data 3 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 65595
TargetBotulinum neurotoxin type A(Clostridium botulinum)
The Scripps Research Institute
Curated by ChEMBL
The Scripps Research Institute
Curated by ChEMBL
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of Clostridium botulinum BoNT/A LC expressed in Escherichia coli assessed as cleavage of SNAPtide preincubated for 5 mins followed by SNAP...More data for this Ligand-Target Pair
TargetIntegrase(Human immunodeficiency virus type 1)
University of Southern California
Curated by ChEMBL
University of Southern California
Curated by ChEMBL
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of HIV-1 integrase 3'-processing activityMore data for this Ligand-Target Pair
TargetIntegrase(Human immunodeficiency virus type 1)
University of Southern California
Curated by ChEMBL
University of Southern California
Curated by ChEMBL
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of HIV-1 integrase strand transfer activityMore data for this Ligand-Target Pair