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SMILES: O=C(CN1CCN(CCCCCCN2C(=O)c3ccccc3C2=O)CC1)N1c2ccccc2C(=O)Nc2cccnc12

InChI Key: InChIKey=DOPNDYBRRJTHNC-UHFFFAOYSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50012348   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Muscarinic acetylcholine receptor M2


(RAT)
BDBM50012348
PNG
(2-(6-{4-[2-Oxo-2-(6-oxo-5,6-dihydro-benzo[e]pyrido...)
Show SMILES O=C(CN1CCN(CCCCCCN2C(=O)c3ccccc3C2=O)CC1)N1c2ccccc2C(=O)Nc2cccnc12
Show InChI InChI=1S/C32H34N6O4/c39-28(38-27-14-6-5-12-25(27)30(40)34-26-13-9-15-33-29(26)38)22-36-20-18-35(19-21-36)16-7-1-2-8-17-37-31(41)23-10-3-4-11-24(23)32(37)42/h3-6,9-15H,1-2,7-8,16-22H2,(H,34,40)
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CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
18n/an/an/an/an/an/an/an/a



NIDDK

Curated by ChEMBL


Assay Description
Inhibition of binding of [3H]-N-Methyl-scopolamine to Muscarinic acetylcholine receptor M2 of rat heart tissue membranes.


J Med Chem 34: 2133-45 (1991)


BindingDB Entry DOI: 10.7270/Q2SJ1JKW
More data for this
Ligand-Target Pair
Muscarinic acetylcholine receptor M1


(RAT)
BDBM50012348
PNG
(2-(6-{4-[2-Oxo-2-(6-oxo-5,6-dihydro-benzo[e]pyrido...)
Show SMILES O=C(CN1CCN(CCCCCCN2C(=O)c3ccccc3C2=O)CC1)N1c2ccccc2C(=O)Nc2cccnc12
Show InChI InChI=1S/C32H34N6O4/c39-28(38-27-14-6-5-12-25(27)30(40)34-26-13-9-15-33-29(26)38)22-36-20-18-35(19-21-36)16-7-1-2-8-17-37-31(41)23-10-3-4-11-24(23)32(37)42/h3-6,9-15H,1-2,7-8,16-22H2,(H,34,40)
Reactome pathway
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
18n/an/an/an/an/an/an/an/a



NIDDK

Curated by ChEMBL


Assay Description
Inhibition of binding of [3H]-N-Methyl-scopolamine to Muscarinic acetylcholine receptor M1 of transfected A9L cells.


J Med Chem 34: 2133-45 (1991)


BindingDB Entry DOI: 10.7270/Q2SJ1JKW
More data for this
Ligand-Target Pair