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BDBM50161480 CHEMBL3786937

SMILES: CN(C)C(=O)N[C@H]1CCc2c(O)cccc2C1

InChI Key: InChIKey=SGLUQONQBJDTLQ-UHFFFAOYSA-N

Data: 3 KI  3 IC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 6 hits for monomerid = 50161480   
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
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50161480
PNG
(CHEMBL3786937)
Show SMILES CN(C)C(=O)N[C@H]1CCc2c(O)cccc2C1 |r|
Show InChI InChI=1S/C24H24N2O4S/c1-29-21-7-5-6-19(16-21)18-25-13-15-30-22-11-10-20-12-14-26(24(20)17-22)31(27,28)23-8-3-2-4-9-23/h2-12,14,16-17,25H,13,15,18H2,1H3
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1.60n/an/an/an/an/an/an/an/a



Erzurum Technical University

Curated by ChEMBL


Assay Description
Inhibition of AChE (unknown origin) using acetylcholine iodate as substrate preincubated for 10 mins followed by substrate addition by Lineweaver-Bur...


Bioorg Med Chem 24: 2318-29 (2016)

More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50161480
PNG
(CHEMBL3786937)
Show SMILES CN(C)C(=O)N[C@H]1CCc2c(O)cccc2C1 |r|
Show InChI InChI=1S/C24H24N2O4S/c1-29-21-7-5-6-19(16-21)18-25-13-15-30-22-11-10-20-12-14-26(24(20)17-22)31(27,28)23-8-3-2-4-9-23/h2-12,14,16-17,25H,13,15,18H2,1H3
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2.80n/an/an/an/an/an/an/an/a



Erzurum Technical University

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 2 using 4-nitrophenylacetate as substrate by Lineweaver-Burk plot analysis


Bioorg Med Chem 24: 2318-29 (2016)

More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50161480
PNG
(CHEMBL3786937)
Show SMILES CN(C)C(=O)N[C@H]1CCc2c(O)cccc2C1 |r|
Show InChI InChI=1S/C24H24N2O4S/c1-29-21-7-5-6-19(16-21)18-25-13-15-30-22-11-10-20-12-14-26(24(20)17-22)31(27,28)23-8-3-2-4-9-23/h2-12,14,16-17,25H,13,15,18H2,1H3
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3.60n/an/an/an/an/an/an/an/a



Erzurum Technical University

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 1 using 4-nitrophenylacetate as substrate by Lineweaver-Burk plot analysis


Bioorg Med Chem 24: 2318-29 (2016)

More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50161480
PNG
(CHEMBL3786937)
Show SMILES CN(C)C(=O)N[C@H]1CCc2c(O)cccc2C1 |r|
Show InChI InChI=1S/C24H24N2O4S/c1-29-21-7-5-6-19(16-21)18-25-13-15-30-22-11-10-20-12-14-26(24(20)17-22)31(27,28)23-8-3-2-4-9-23/h2-12,14,16-17,25H,13,15,18H2,1H3
PDB
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n/an/a 132n/an/an/an/an/an/a



Erzurum Technical University

Curated by ChEMBL


Assay Description
Inhibition of AChE (unknown origin) using acetylcholine iodate as substrate preincubated for 10 mins followed by substrate addition by Ellman's metho...


Bioorg Med Chem 24: 2318-29 (2016)

More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50161480
PNG
(CHEMBL3786937)
Show SMILES CN(C)C(=O)N[C@H]1CCc2c(O)cccc2C1 |r|
Show InChI InChI=1S/C24H24N2O4S/c1-29-21-7-5-6-19(16-21)18-25-13-15-30-22-11-10-20-12-14-26(24(20)17-22)31(27,28)23-8-3-2-4-9-23/h2-12,14,16-17,25H,13,15,18H2,1H3
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n/an/a 75n/an/an/an/an/an/a



Erzurum Technical University

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 2 using 4-nitrophenylacetate as substrate by spectrophotometric analysis


Bioorg Med Chem 24: 2318-29 (2016)

More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50161480
PNG
(CHEMBL3786937)
Show SMILES CN(C)C(=O)N[C@H]1CCc2c(O)cccc2C1 |r|
Show InChI InChI=1S/C24H24N2O4S/c1-29-21-7-5-6-19(16-21)18-25-13-15-30-22-11-10-20-12-14-26(24(20)17-22)31(27,28)23-8-3-2-4-9-23/h2-12,14,16-17,25H,13,15,18H2,1H3
PDB
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NCI pathway
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n/an/a 9.70n/an/an/an/an/an/a



Erzurum Technical University

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 1 using 4-nitrophenylacetate as substrate by spectrophotometric analysis


Bioorg Med Chem 24: 2318-29 (2016)

More data for this
Ligand-Target Pair