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4 similar compounds to monomer 50405739

Compile data set for download or QSAR
Wt: 310.4
BDBM86162
Wt: 352.5
BDBM86166
Wt: 522.8
BDBM50405743
Wt: 550.9
BDBM50405747

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 6 hits for monomerid = 86162,86166,50405743,50405747   
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
Glutamate delta 2


(Xenopus)
BDBM86166
PNG
(DB-10)
Show SMILES C(CCCCCNCc1ccccc1)CCCCNCc1ccccc1
Show InChI InChI=1S/C24H36N2/c1(3-5-13-19-25-21-23-15-9-7-10-16-23)2-4-6-14-20-26-22-24-17-11-8-12-18-24/h7-12,15-18,25-26H,1-6,13-14,19-22H2
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
PC cid
PC sid
UniChem

Similars

Article
PubMed
>1.00E+4n/an/an/an/an/an/an/an/a



State University of New York

Curated by PDSP Ki Database




J Pharmacol Exp Ther 305: 740-8 (2003)


Article DOI: 10.1124/jpet.102.045799
BindingDB Entry DOI: 10.7270/Q2N878C5
More data for this
Ligand-Target Pair
Glutamate delta 2


(Xenopus)
BDBM86162
PNG
(DB-7)
Show SMILES C(CCCNCc1ccccc1)CCCNCc1ccccc1
Show InChI InChI=1S/C21H30N2/c1(2-10-16-22-18-20-12-6-4-7-13-20)3-11-17-23-19-21-14-8-5-9-15-21/h4-9,12-15,22-23H,1-3,10-11,16-19H2
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
>1.00E+4n/an/an/an/an/an/an/an/a



State University of New York

Curated by PDSP Ki Database




J Pharmacol Exp Ther 305: 740-8 (2003)


Article DOI: 10.1124/jpet.102.045799
BindingDB Entry DOI: 10.7270/Q2N878C5
More data for this
Ligand-Target Pair
Muscarinic acetylcholine receptor M2


(Homo sapiens (Human))
BDBM50405743
PNG
(CHEMBL166232)
Show SMILES C(CCCCNCCCCCCNCc1ccccc1)CCCNCCCCCCNCc1ccccc1
Show InChI InChI=1S/C34H58N4/c1(3-15-25-35-27-17-5-7-19-29-37-31-33-21-11-9-12-22-33)2-4-16-26-36-28-18-6-8-20-30-38-32-34-23-13-10-14-24-34/h9-14,21-24,35-38H,1-8,15-20,25-32H2
PDB

UniProtKB/SwissProt

GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/a 83.2n/an/an/an/an/a



University of Camerino

Curated by ChEMBL


Assay Description
Antagonist potency against carbachol induced inhibition of electrically stimulated guinea pig atria Muscarinic acetylcholine receptor


J Med Chem 32: 79-84 (1989)


Article DOI: 10.1021/jm00121a017
BindingDB Entry DOI: 10.7270/Q2N017RN
More data for this
Ligand-Target Pair
Muscarinic acetylcholine receptor M3


(Cavia porcellus)
BDBM50405747
PNG
(CHEMBL168304)
Show SMILES Cc1ccc(CNCCCCCCNCCCCCCCCNCCCCCCNCc2ccc(C)cc2)cc1
Show InChI InChI=1S/C36H62N4/c1-33-17-21-35(22-18-33)31-39-29-15-9-7-13-27-37-25-11-5-3-4-6-12-26-38-28-14-8-10-16-30-40-32-36-23-19-34(2)20-24-36/h17-24,37-40H,3-16,25-32H2,1-2H3
MMDB

Reactome pathway
KEGG

UniProtKB/TrEMBL

B.MOAD
DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/a 2.34E+3n/an/an/an/an/a



University of Camerino

Curated by ChEMBL


Assay Description
Antagonist potency against carbachol induced contractions of isolated guinea pig ileum Muscarinic acetylcholine receptor


J Med Chem 32: 79-84 (1989)


Article DOI: 10.1021/jm00121a017
BindingDB Entry DOI: 10.7270/Q2N017RN
More data for this
Ligand-Target Pair
Muscarinic acetylcholine receptor M2


(Homo sapiens (Human))
BDBM50405747
PNG
(CHEMBL168304)
Show SMILES Cc1ccc(CNCCCCCCNCCCCCCCCNCCCCCCNCc2ccc(C)cc2)cc1
Show InChI InChI=1S/C36H62N4/c1-33-17-21-35(22-18-33)31-39-29-15-9-7-13-27-37-25-11-5-3-4-6-12-26-38-28-14-8-10-16-30-40-32-36-23-19-34(2)20-24-36/h17-24,37-40H,3-16,25-32H2,1-2H3
PDB

UniProtKB/SwissProt

GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/a 166n/an/an/an/an/a



University of Camerino

Curated by ChEMBL


Assay Description
Antagonist potency against carbachol induced inhibition of electrically stimulated guinea pig atria Muscarinic acetylcholine receptor


J Med Chem 32: 79-84 (1989)


Article DOI: 10.1021/jm00121a017
BindingDB Entry DOI: 10.7270/Q2N017RN
More data for this
Ligand-Target Pair
Muscarinic acetylcholine receptor M3


(Cavia porcellus)
BDBM50405743
PNG
(CHEMBL166232)
Show SMILES C(CCCCNCCCCCCNCc1ccccc1)CCCNCCCCCCNCc1ccccc1
Show InChI InChI=1S/C34H58N4/c1(3-15-25-35-27-17-5-7-19-29-37-31-33-21-11-9-12-22-33)2-4-16-26-36-28-18-6-8-20-30-38-32-34-23-13-10-14-24-34/h9-14,21-24,35-38H,1-8,15-20,25-32H2
MMDB

Reactome pathway
KEGG

UniProtKB/TrEMBL

B.MOAD
DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/a 2.19E+3n/an/an/an/an/a



University of Camerino

Curated by ChEMBL


Assay Description
Antagonist potency against carbachol induced contractions of isolated guinea pig ileum Muscarinic acetylcholine receptor


J Med Chem 32: 79-84 (1989)


Article DOI: 10.1021/jm00121a017
BindingDB Entry DOI: 10.7270/Q2N017RN
More data for this
Ligand-Target Pair