BDBM77617 4-methyl-2-(1-piperidinyl)quinoline::4-methyl-2-piperidin-1-yl-quinoline::4-methyl-2-piperidin-1-ylquinoline::4-methyl-2-piperidino-quinoline::ML204::VU0024172-3::cid_230710
SMILES Cc1cc(nc2ccccc12)N1CCCCC1
InChI Key InChIKey=USYRQXDHKXGTCK-UHFFFAOYSA-N
Data 5 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 5 hits for monomerid = 77617
TargetShort transient receptor potential channel 4(Mus musculus)
Johns Hopkins Ion Channel Center
Curated by PubChem BioAssay
Johns Hopkins Ion Channel Center
Curated by PubChem BioAssay
Affinity DataIC50: 2.63E+3nMAssay Description:Data Source: Johns Hopkins Ion Channel Center BioAssay Type: Confirmatory, Concentration-Response Relationship Observed Source (MLPCN Center Name): ...More data for this Ligand-Target Pair
TargetShort transient receptor potential channel 4(Mus musculus)
Johns Hopkins Ion Channel Center
Curated by PubChem BioAssay
Johns Hopkins Ion Channel Center
Curated by PubChem BioAssay
Affinity DataIC50: 960nMAssay Description:Inhibition of mouse TRPC4 beta expressed in HEK293 cells co-expressing mu-opioid receptor assessed as reduction in DAMGO-induced intracellular calciu...More data for this Ligand-Target Pair
TargetShort transient receptor potential channel 6(Mus musculus)
University Of Nebraska Medical Center
Curated by ChEMBL
University Of Nebraska Medical Center
Curated by ChEMBL
Affinity DataIC50: 1.79E+4nMAssay Description:Inhibition of HA-tagged mouse TRPC6 expressed in HEK293 cells assessed as reduction in acetylcholine-induced membrane potential by FLIPR membrane pot...More data for this Ligand-Target Pair
TargetShort transient receptor potential channel 4(Mus musculus)
Johns Hopkins Ion Channel Center
Curated by PubChem BioAssay
Johns Hopkins Ion Channel Center
Curated by PubChem BioAssay
Affinity DataIC50: 2.60E+3nMAssay Description:Inhibition of mouse TRPC4 beta expressed in HEK293 cells co-expressing mu-opioid receptor assessed as reduction in DAMGO-induced current by QPatch cl...More data for this Ligand-Target Pair
TargetAcetylcholinesterase(Homo sapiens (Human))
University Of Nebraska Medical Center
Curated by ChEMBL
University Of Nebraska Medical Center
Curated by ChEMBL
Affinity DataIC50: 840nMAssay Description:Inhibition of human recombinant acetylcholinesterase expressed in HEK-293 cells using AMTch as substrate after 30 mins by spectrophotometric methodMore data for this Ligand-Target Pair