BindingDB logo
myBDB logout

PubMed code 22041172

Compile data set for download or QSAR
Found 41 hits of Enzyme Inhibition Constant Data   
Target/Host
(Institution)		LigandTarget/Host
Links		Ligand
Links		Trg + Lig
Links		Ki
nM		ΔG°
kJ/mole		IC50
nM		Kd
nM		EC50/IC50
nM		koff
s-1		kon
M-1s-1		pHTemp
°C
Acetylcholinesterase


(Electrophorus electricus (Electric eel))		BDBM50310278
PNG
(9-O-[4-(Phenylol-1-yloxy)butyl]berberine bromide |...)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCCCOc1ccccc1
Show InChI InChI=1S/C29H28NO5/c1-31-26-10-9-20-15-25-23-17-28-27(34-19-35-28)16-21(23)11-12-30(25)18-24(20)29(26)33-14-6-5-13-32-22-7-3-2-4-8-22/h2-4,7-10,15-18H,5-6,11-14,19H2,1H3/q+1
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 97n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of electric eel AChE using acetylcholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))		BDBM50359508
PNG
(CHEMBL1927128)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCCCOc1ccccc1O
Show InChI InChI=1S/C29H27NO6/c1-32-26-9-8-19-14-23-21-16-28-27(35-18-36-28)15-20(21)10-11-30(23)17-22(19)29(26)34-13-5-4-12-33-25-7-3-2-6-24(25)31/h2-3,6-9,14-17H,4-5,10-13,18H2,1H3/p+1
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 123n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of electric eel AChE using acetylcholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))		BDBM50359513
PNG
(CHEMBL1927133)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCCCOc1ccc(O)cc1
Show InChI InChI=1S/C29H27NO6/c1-32-26-9-4-19-14-25-23-16-28-27(35-18-36-28)15-20(23)10-11-30(25)17-24(19)29(26)34-13-3-2-12-33-22-7-5-21(31)6-8-22/h4-9,14-17H,2-3,10-13,18H2,1H3/p+1
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 304n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of electric eel AChE using acetylcholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))		BDBM50203126
PNG
(3,4-dimethoxy-6,7-dihydro-[1,3]dioxolo[4,5-g]pyrid...)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OC
Show InChI InChI=1S/C20H18NO4/c1-22-17-4-3-12-7-16-14-9-19-18(24-11-25-19)8-13(14)5-6-21(16)10-15(12)20(17)23-2/h3-4,7-10H,5-6,11H2,1-2H3/q+1
UniProtKB/SwissProt

GoogleScholar
AffyNet 
Purchase

CHEMBL
DrugBank
MCE
KEGG
PC cid
PC sid
PDB
UniChem

Similars
Article
PubMed
n/an/a 374n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of electric eel AChE using acetylcholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))		BDBM50359509
PNG
(CHEMBL1927129)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCc1cccc(O)c1
Show InChI InChI=1S/C27H23NO5/c1-30-24-6-5-18-12-23-21-14-26-25(32-16-33-26)13-19(21)7-9-28(23)15-22(18)27(24)31-10-8-17-3-2-4-20(29)11-17/h2-6,11-15H,7-10,16H2,1H3/p+1
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 422n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of electric eel AChE using acetylcholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))		BDBM50359512
PNG
(CHEMBL1927132)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCCOc1ccc(O)cc1
Show InChI InChI=1S/C28H25NO6/c1-31-25-8-3-18-13-24-22-15-27-26(34-17-35-27)14-19(22)9-10-29(24)16-23(18)28(25)33-12-2-11-32-21-6-4-20(30)5-7-21/h3-8,13-16H,2,9-12,17H2,1H3/p+1
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 460n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of electric eel AChE using acetylcholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))		BDBM50359507
PNG
(CHEMBL1927127)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCCOc1ccccc1O
Show InChI InChI=1S/C28H25NO6/c1-31-25-8-7-18-13-22-20-15-27-26(34-17-35-27)14-19(20)9-10-29(22)16-21(18)28(25)33-12-4-11-32-24-6-3-2-5-23(24)30/h2-3,5-8,13-16H,4,9-12,17H2,1H3/p+1
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 490n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of electric eel AChE using acetylcholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))		BDBM50359511
PNG
(CHEMBL1927131)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCCCOc1cccc(O)c1
Show InChI InChI=1S/C29H27NO6/c1-32-26-8-7-19-13-25-23-16-28-27(35-18-36-28)14-20(23)9-10-30(25)17-24(19)29(26)34-12-3-2-11-33-22-6-4-5-21(31)15-22/h4-8,13-17H,2-3,9-12,18H2,1H3/p+1
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 547n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of electric eel AChE using acetylcholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))		BDBM10404
PNG
((1S,12S,14R)-9-methoxy-4-methyl-11-oxa-4-azatetrac...)
Show SMILES COc1ccc2CN(C)CC[C@@]34C=C[C@H](O)C[C@@H]3Oc1c24 |r,c:12|
Show InChI InChI=1S/C17H21NO3/c1-18-8-7-17-6-5-12(19)9-14(17)21-16-13(20-2)4-3-11(10-18)15(16)17/h3-6,12,14,19H,7-10H2,1-2H3/t12-,14-,17-/m0/s1
UniProtKB/SwissProt

GoogleScholar
AffyNet 
Purchase

CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
UniChem

Patents

Similars
Article
PubMed
n/an/a 623n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of electric eel AChE using acetylcholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))		BDBM50359510
PNG
(CHEMBL1927130)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCCOc1cccc(O)c1
Show InChI InChI=1S/C28H25NO6/c1-31-25-7-6-18-12-24-22-15-27-26(34-17-35-27)13-19(22)8-9-29(24)16-23(18)28(25)33-11-3-10-32-21-5-2-4-20(30)14-21/h2,4-7,12-16H,3,8-11,17H2,1H3/p+1
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 628n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of electric eel AChE using acetylcholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM50359510
PNG
(CHEMBL1927130)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCCOc1cccc(O)c1
Show InChI InChI=1S/C28H25NO6/c1-31-25-7-6-18-12-24-22-15-27-26(34-17-35-27)13-19(22)8-9-29(24)16-23(18)28(25)33-11-3-10-32-21-5-2-4-20(30)14-21/h2,4-7,12-16H,3,8-11,17H2,1H3/p+1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 898n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using acetylcholine as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM50359513
PNG
(CHEMBL1927133)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCCCOc1ccc(O)cc1
Show InChI InChI=1S/C29H27NO6/c1-32-26-9-4-19-14-25-23-16-28-27(35-18-36-28)15-20(23)10-11-30(25)17-24(19)29(26)34-13-3-2-12-33-22-7-5-21(31)6-8-22/h4-9,14-17H,2-3,10-13,18H2,1H3/p+1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 950n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using acetylcholine as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM50359513
PNG
(CHEMBL1927133)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCCCOc1ccc(O)cc1
Show InChI InChI=1S/C29H27NO6/c1-32-26-9-4-19-14-25-23-16-28-27(35-18-36-28)15-20(23)10-11-30(25)17-24(19)29(26)34-13-3-2-12-33-22-7-5-21(31)6-8-22/h4-9,14-17H,2-3,10-13,18H2,1H3/p+1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 1.04E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using butylthiocholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))		BDBM50359514
PNG
(CHEMBL1927134)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCC(=O)NCCc1c[nH]c2ccccc12
Show InChI InChI=1S/C32H29N3O5/c1-37-28-7-6-20-14-27-24-16-30-29(39-19-40-30)15-21(24)9-12-35(27)18-25(20)32(28)38-13-10-31(36)33-11-8-22-17-34-26-5-3-2-4-23(22)26/h2-7,14-18,34H,8-13,19H2,1H3/p+1
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 1.11E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of electric eel AChE using acetylcholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM50359510
PNG
(CHEMBL1927130)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCCOc1cccc(O)c1
Show InChI InChI=1S/C28H25NO6/c1-31-25-7-6-18-12-24-22-15-27-26(34-17-35-27)13-19(22)8-9-29(24)16-23(18)28(25)33-11-3-10-32-21-5-2-4-20(30)14-21/h2,4-7,12-16H,3,8-11,17H2,1H3/p+1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 1.13E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using butylthiocholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM50359507
PNG
(CHEMBL1927127)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCCOc1ccccc1O
Show InChI InChI=1S/C28H25NO6/c1-31-25-8-7-18-13-22-20-15-27-26(34-17-35-27)14-19(20)9-10-29(22)16-21(18)28(25)33-12-4-11-32-24-6-3-2-5-23(24)30/h2-3,5-8,13-16H,4,9-12,17H2,1H3/p+1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 1.30E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using acetylcholine as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))		BDBM50359515
PNG
(CHEMBL1927135)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCC(=O)NCCc1c[nH]c2ccc(C)cc12
Show InChI InChI=1S/C33H31N3O5/c1-20-3-5-27-24(13-20)23(17-35-27)7-10-34-32(37)9-12-39-33-26-18-36-11-8-22-15-30-31(41-19-40-30)16-25(22)28(36)14-21(26)4-6-29(33)38-2/h3-6,13-18,35H,7-12,19H2,1-2H3/p+1
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 1.42E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of electric eel AChE using acetylcholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))		BDBM50359516
PNG
(CHEMBL1927136)
Show SMILES COc1ccc2[nH]cc(CCNC(=O)CCOc3c(OC)ccc4cc5-c6cc7OCOc7cc6CC[n+]5cc34)c2c1
Show InChI InChI=1S/C33H31N3O6/c1-38-23-4-5-27-24(15-23)22(17-35-27)7-10-34-32(37)9-12-40-33-26-18-36-11-8-21-14-30-31(42-19-41-30)16-25(21)28(36)13-20(26)3-6-29(33)39-2/h3-6,13-18,35H,7-12,19H2,1-2H3/p+1
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 1.44E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of electric eel AChE using acetylcholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM50359514
PNG
(CHEMBL1927134)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCC(=O)NCCc1c[nH]c2ccccc12
Show InChI InChI=1S/C32H29N3O5/c1-37-28-7-6-20-14-27-24-16-30-29(39-19-40-30)15-21(24)9-12-35(27)18-25(20)32(28)38-13-10-31(36)33-11-8-22-17-34-26-5-3-2-4-23(22)26/h2-7,14-18,34H,8-13,19H2,1H3/p+1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 1.46E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using acetylcholine as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM50359514
PNG
(CHEMBL1927134)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCC(=O)NCCc1c[nH]c2ccccc12
Show InChI InChI=1S/C32H29N3O5/c1-37-28-7-6-20-14-27-24-16-30-29(39-19-40-30)15-21(24)9-12-35(27)18-25(20)32(28)38-13-10-31(36)33-11-8-22-17-34-26-5-3-2-4-23(22)26/h2-7,14-18,34H,8-13,19H2,1H3/p+1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 1.64E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using butylthiocholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM50359512
PNG
(CHEMBL1927132)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCCOc1ccc(O)cc1
Show InChI InChI=1S/C28H25NO6/c1-31-25-8-3-18-13-24-22-15-27-26(34-17-35-27)14-19(22)9-10-29(24)16-23(18)28(25)33-12-2-11-32-21-6-4-20(30)5-7-21/h3-8,13-16H,2,9-12,17H2,1H3/p+1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 1.66E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using acetylcholine as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM50359508
PNG
(CHEMBL1927128)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCCCOc1ccccc1O
Show InChI InChI=1S/C29H27NO6/c1-32-26-9-8-19-14-23-21-16-28-27(35-18-36-28)15-20(21)10-11-30(23)17-22(19)29(26)34-13-5-4-12-33-25-7-3-2-6-24(25)31/h2-3,6-9,14-17H,4-5,10-13,18H2,1H3/p+1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 1.74E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using acetylcholine as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM50359507
PNG
(CHEMBL1927127)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCCOc1ccccc1O
Show InChI InChI=1S/C28H25NO6/c1-31-25-8-7-18-13-22-20-15-27-26(34-17-35-27)14-19(20)9-10-29(22)16-21(18)28(25)33-12-4-11-32-24-6-3-2-5-23(24)30/h2-3,5-8,13-16H,4,9-12,17H2,1H3/p+1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 1.74E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using butylthiocholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM50359515
PNG
(CHEMBL1927135)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCC(=O)NCCc1c[nH]c2ccc(C)cc12
Show InChI InChI=1S/C33H31N3O5/c1-20-3-5-27-24(13-20)23(17-35-27)7-10-34-32(37)9-12-39-33-26-18-36-11-8-22-15-30-31(41-19-40-30)16-25(22)28(36)14-21(26)4-6-29(33)38-2/h3-6,13-18,35H,7-12,19H2,1-2H3/p+1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 1.79E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using acetylcholine as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM50359511
PNG
(CHEMBL1927131)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCCCOc1cccc(O)c1
Show InChI InChI=1S/C29H27NO6/c1-32-26-8-7-19-13-25-23-16-28-27(35-18-36-28)14-20(23)9-10-30(25)17-24(19)29(26)34-12-3-2-11-33-22-6-4-5-21(31)15-22/h4-8,13-17H,2-3,9-12,18H2,1H3/p+1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 1.92E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using acetylcholine as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM50359515
PNG
(CHEMBL1927135)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCC(=O)NCCc1c[nH]c2ccc(C)cc12
Show InChI InChI=1S/C33H31N3O5/c1-20-3-5-27-24(13-20)23(17-35-27)7-10-34-32(37)9-12-39-33-26-18-36-11-8-22-15-30-31(41-19-40-30)16-25(22)28(36)14-21(26)4-6-29(33)38-2/h3-6,13-18,35H,7-12,19H2,1-2H3/p+1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 1.96E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using butylthiocholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM50359512
PNG
(CHEMBL1927132)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCCOc1ccc(O)cc1
Show InChI InChI=1S/C28H25NO6/c1-31-25-8-3-18-13-24-22-15-27-26(34-17-35-27)14-19(22)9-10-29(24)16-23(18)28(25)33-12-2-11-32-21-6-4-20(30)5-7-21/h3-8,13-16H,2,9-12,17H2,1H3/p+1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 2.06E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using butylthiocholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM50359508
PNG
(CHEMBL1927128)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCCCOc1ccccc1O
Show InChI InChI=1S/C29H27NO6/c1-32-26-9-8-19-14-23-21-16-28-27(35-18-36-28)15-20(21)10-11-30(23)17-22(19)29(26)34-13-5-4-12-33-25-7-3-2-6-24(25)31/h2-3,6-9,14-17H,4-5,10-13,18H2,1H3/p+1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 2.09E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using butylthiocholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM50359517
PNG
(CHEMBL1927137)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCCOC(=O)\C=C\c1ccc(O)c(OC)c1
Show InChI InChI=1S/C32H29NO8/c1-36-27-8-6-21-15-25-23-17-30-29(40-19-41-30)16-22(23)10-11-33(25)18-24(21)32(27)39-13-3-12-38-31(35)9-5-20-4-7-26(34)28(14-20)37-2/h4-9,14-18H,3,10-13,19H2,1-2H3/p+1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 2.25E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using acetylcholine as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM50359509
PNG
(CHEMBL1927129)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCc1cccc(O)c1
Show InChI InChI=1S/C27H23NO5/c1-30-24-6-5-18-12-23-21-14-26-25(32-16-33-26)13-19(21)7-9-28(23)15-22(18)27(24)31-10-8-17-3-2-4-20(29)11-17/h2-6,11-15H,7-10,16H2,1H3/p+1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 2.26E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using acetylcholine as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM50359511
PNG
(CHEMBL1927131)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCCCOc1cccc(O)c1
Show InChI InChI=1S/C29H27NO6/c1-32-26-8-7-19-13-25-23-16-28-27(35-18-36-28)14-20(23)9-10-30(25)17-24(19)29(26)34-12-3-2-11-33-22-6-4-5-21(31)15-22/h4-8,13-17H,2-3,9-12,18H2,1H3/p+1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 2.40E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using butylthiocholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM50359517
PNG
(CHEMBL1927137)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCCOC(=O)\C=C\c1ccc(O)c(OC)c1
Show InChI InChI=1S/C32H29NO8/c1-36-27-8-6-21-15-25-23-17-30-29(40-19-41-30)16-22(23)10-11-33(25)18-24(21)32(27)39-13-3-12-38-31(35)9-5-20-4-7-26(34)28(14-20)37-2/h4-9,14-18H,3,10-13,19H2,1-2H3/p+1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 2.40E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using butylthiocholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM50359516
PNG
(CHEMBL1927136)
Show SMILES COc1ccc2[nH]cc(CCNC(=O)CCOc3c(OC)ccc4cc5-c6cc7OCOc7cc6CC[n+]5cc34)c2c1
Show InChI InChI=1S/C33H31N3O6/c1-38-23-4-5-27-24(15-23)22(17-35-27)7-10-34-32(37)9-12-40-33-26-18-36-11-8-21-14-30-31(42-19-41-30)16-25(21)28(36)13-20(26)3-6-29(33)39-2/h3-6,13-18,35H,7-12,19H2,1-2H3/p+1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 2.49E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using acetylcholine as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM50359509
PNG
(CHEMBL1927129)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCc1cccc(O)c1
Show InChI InChI=1S/C27H23NO5/c1-30-24-6-5-18-12-23-21-14-26-25(32-16-33-26)13-19(21)7-9-28(23)15-22(18)27(24)31-10-8-17-3-2-4-20(29)11-17/h2-6,11-15H,7-10,16H2,1H3/p+1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 2.64E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using butylthiocholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM50359516
PNG
(CHEMBL1927136)
Show SMILES COc1ccc2[nH]cc(CCNC(=O)CCOc3c(OC)ccc4cc5-c6cc7OCOc7cc6CC[n+]5cc34)c2c1
Show InChI InChI=1S/C33H31N3O6/c1-38-23-4-5-27-24(15-23)22(17-35-27)7-10-34-32(37)9-12-40-33-26-18-36-11-8-21-14-30-31(42-19-41-30)16-25(21)28(36)13-20(26)3-6-29(33)39-2/h3-6,13-18,35H,7-12,19H2,1-2H3/p+1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 2.72E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using butylthiocholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))		BDBM50359517
PNG
(CHEMBL1927137)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCCOC(=O)\C=C\c1ccc(O)c(OC)c1
Show InChI InChI=1S/C32H29NO8/c1-36-27-8-6-21-15-25-23-17-30-29(40-19-41-30)16-22(23)10-11-33(25)18-24(21)32(27)39-13-3-12-38-31(35)9-5-20-4-7-26(34)28(14-20)37-2/h4-9,14-18H,3,10-13,19H2,1-2H3/p+1
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 3.21E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of electric eel AChE using acetylcholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM50310278
PNG
(9-O-[4-(Phenylol-1-yloxy)butyl]berberine bromide |...)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OCCCCOc1ccccc1
Show InChI InChI=1S/C29H28NO5/c1-31-26-10-9-20-15-25-23-17-28-27(34-19-35-28)16-21(23)11-12-30(25)18-24(20)29(26)33-14-6-5-13-32-22-7-3-2-4-8-22/h2-4,7-10,15-18H,5-6,11-14,19H2,1H3/q+1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 4.89E+3n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using butylthiocholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM10404
PNG
((1S,12S,14R)-9-methoxy-4-methyl-11-oxa-4-azatetrac...)
Show SMILES COc1ccc2CN(C)CC[C@@]34C=C[C@H](O)C[C@@H]3Oc1c24 |r,c:12|
Show InChI InChI=1S/C17H21NO3/c1-18-8-7-17-6-5-12(19)9-14(17)21-16-13(20-2)4-3-11(10-18)15(16)17/h3-6,12,14,19H,7-10H2,1-2H3/t12-,14-,17-/m0/s1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
Purchase

CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
UniChem

Patents

Similars
Article
PubMed
n/an/a 1.57E+4n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using butylthiocholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))		BDBM50203126
PNG
(3,4-dimethoxy-6,7-dihydro-[1,3]dioxolo[4,5-g]pyrid...)
Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CC[n+]3cc2c1OC
Show InChI InChI=1S/C20H18NO4/c1-22-17-4-3-12-7-16-14-9-19-18(24-11-25-19)8-13(14)5-6-21(16)10-15(12)20(17)23-2/h3-4,7-10H,5-6,11H2,1-2H3/q+1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
Purchase

CHEMBL
DrugBank
MCE
KEGG
PC cid
PC sid
PDB
UniChem

Similars
Article
PubMed
n/an/a 1.82E+4n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using butylthiocholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))		BDBM50214744
PNG
((2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoic aci...)
Show SMILES COc1cc(\C=C\C(O)=O)ccc1O
Show InChI InChI=1S/C10H10O4/c1-14-9-6-7(2-4-8(9)11)3-5-10(12)13/h2-6,11H,1H3,(H,12,13)/b5-3+
UniProtKB/SwissProt

GoogleScholar
AffyNet 
Purchase

CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
UniChem

Patents

Similars
Article
PubMed
n/an/a>1.00E+5n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of electric eel AChE using acetylcholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))		BDBM50067040
PNG
(((E,E)-1,7-bis(4-hydroxy-3-methoxyphenyl)-1,6-hept...)
Show SMILES COc1cc(C=CC(=O)CC(=O)C=Cc2ccc(O)c(OC)c2)ccc1O |w:12.11,5.4|
Show InChI InChI=1S/C21H20O6/c1-26-20-11-14(5-9-18(20)24)3-7-16(22)13-17(23)8-4-15-6-10-19(25)21(12-15)27-2/h3-12,24-25H,13H2,1-2H3
UniProtKB/SwissProt

GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
PDB
UniChem

Patents

Similars
Article
PubMed
n/an/a>1.00E+5n/an/an/an/an/an/a



Guangzhou Institute of Biomedicine and Health

Curated by ChEMBL


Assay Description
Inhibition of electric eel AChE using acetylcholine chloride as substrate preincubated for 15 mins by Ellman's method

Bioorg Med Chem 19: 7228-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.040
BindingDB Entry DOI: 10.7270/Q23F4Q3K
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%