BDBM23302 4-amino-7-chloroquinoline (ACQ)-based compound, 7::N-(3-aminopropyl)-7-chloroquinolin-4-amine
SMILES NCCCNc1ccnc2cc(Cl)ccc12
InChI Key InChIKey=YXPOTYIIRALLPH-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 23302
TargetBotulinum neurotoxin type A2 [1-425](Clostridium botulinum)
National Cancer Institute At Frederick
National Cancer Institute At Frederick
Affinity DatapH: 7.3 T: 2°CAssay Description:Botox A catalyzed the hydrolysis of substrate peptide between residues 11 (glutamine) and 12 (arginine), corresponding to residues 197 and 198 of SNA...More data for this Ligand-Target Pair
Affinity DataIC50: 2.50E+6nMAssay Description:Inhibition of His6-tagged KIND1 (unknown origin) expressed in Escherichia coli BL21(DE3) by fluorescence polarization methodMore data for this Ligand-Target Pair
Affinity DataIC50: 5.65E+5nMAssay Description:Inhibition of His6-tagged KIND2 (unknown origin) expressed in Escherichia coli BL21(DE3) by fluorescence polarization methodMore data for this Ligand-Target Pair