BindingDB logo
myBDB logout

12 similar compounds to monomer 50008547

Compile data set for download or QSAR
Wt: 192.2
BDBM50008539
Wt: 234.2
BDBM50008542
Wt: 176.2
BDBM50008552
Purchase
Wt: 192.2
BDBM50008561
Wt: 206.2
BDBM50008565
Purchase
Wt: 192.2
BDBM50304446
Purchase
Wt: 326.3
BDBM50310594
Wt: 296.3
BDBM50310597
Wt: 356.3
BDBM50310598
Wt: 386.3
BDBM50310599
Wt: 321.3
BDBM50310606
Wt: 178.1
BDBM50386066
Purchase

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 18 hits for monomerid = 50008539,50008542,50008552,50008561,50008565,50304446,50310594,50310597,50310598,50310599,50310606,50386066   
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
Cholinesterases; ACHE & BCHE


(Homo sapiens (Human))
BDBM50008542
PNG
(5,6-Diethoxy-2-methyl-indan-1-one | CHEMBL158242)
Show SMILES CCOc1cc2CC(C)C(=O)c2cc1OCC
Show InChI InChI=1S/C14H18O3/c1-4-16-12-7-10-6-9(3)14(15)11(10)8-13(12)17-5-2/h7-9H,4-6H2,1-3H3
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 380n/an/an/an/an/an/a



University of Illinois

Curated by ChEMBL


Assay Description
IC50 against acetylcholinesterase; value ranges from 1.3-380 nM.


J Med Chem 35: 584-9 (1992)


Article DOI: 10.1021/jm00081a022
BindingDB Entry DOI: 10.7270/Q20G3J3J
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50386066
PNG
(CHEMBL2043047)
Show SMILES COc1cc2CCC(=O)c2cc1O
Show InChI InChI=1S/C10H10O3/c1-13-10-4-6-2-3-8(11)7(6)5-9(10)12/h4-5,12H,2-3H2,1H3
UniProtKB/SwissProt

GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 9.20E+4n/an/an/an/an/an/a



Sun Yat-sen University

Curated by ChEMBL


Assay Description
Inhibition of electric eel acetylcholine esterase using acetylcholine chloride as substrate incubated for 15 mins prior to substrate addition measure...


Bioorg Med Chem Lett 22: 4462-6 (2012)


Article DOI: 10.1016/j.bmcl.2012.04.029
BindingDB Entry DOI: 10.7270/Q2PC33DC
More data for this
Ligand-Target Pair
Cholinesterases; ACHE & BCHE


(Homo sapiens (Human))
BDBM50008565
PNG
(5,6-Dimethoxy-2-methyl-indan-1-one | CHEMBL154848)
Show SMILES COc1cc2CC(C)C(=O)c2cc1OC
Show InChI InChI=1S/C12H14O3/c1-7-4-8-5-10(14-2)11(15-3)6-9(8)12(7)13/h5-7H,4H2,1-3H3
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 5.20n/an/an/an/an/an/a



University of Illinois

Curated by ChEMBL


Assay Description
Inhibition of acetylcholinesterase.


J Med Chem 35: 584-9 (1992)


Article DOI: 10.1021/jm00081a022
BindingDB Entry DOI: 10.7270/Q20G3J3J
More data for this
Ligand-Target Pair
Cholinesterases; ACHE & BCHE


(Homo sapiens (Human))
BDBM50008552
PNG
(4-Methoxy-2-methyl-indan-1-one | CHEMBL422338)
Show SMILES COc1cccc2C(=O)C(C)Cc12
Show InChI InChI=1S/C11H12O2/c1-7-6-9-8(11(7)12)4-3-5-10(9)13-2/h3-5,7H,6H2,1-2H3
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 380n/an/an/an/an/an/a



University of Illinois

Curated by ChEMBL


Assay Description
Inhibition of acetylcholinesterase.


J Med Chem 35: 584-9 (1992)


Article DOI: 10.1021/jm00081a022
BindingDB Entry DOI: 10.7270/Q20G3J3J
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50008539
PNG
(5-Hydroxy-6-methoxy-2-methyl-indan-1-one | CHEMBL1...)
Show SMILES COc1cc2C(=O)C(C)Cc2cc1O
Show InChI InChI=1S/C11H12O3/c1-6-3-7-4-9(12)10(14-2)5-8(7)11(6)13/h4-6,12H,3H2,1-2H3
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 380n/an/an/an/an/an/a



University of Illinois

Curated by ChEMBL


Assay Description
IC50 against acetylcholinesterase; value ranges from 1.3-380 nM.


J Med Chem 35: 584-9 (1992)


Article DOI: 10.1021/jm00081a022
BindingDB Entry DOI: 10.7270/Q20G3J3J
More data for this
Ligand-Target Pair
Cholinesterases; ACHE & BCHE


(Homo sapiens (Human))
BDBM50008539
PNG
(5-Hydroxy-6-methoxy-2-methyl-indan-1-one | CHEMBL1...)
Show SMILES COc1cc2C(=O)C(C)Cc2cc1O
Show InChI InChI=1S/C11H12O3/c1-6-3-7-4-9(12)10(14-2)5-8(7)11(6)13/h4-6,12H,3H2,1-2H3
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 380n/an/an/an/an/an/a



University of Illinois

Curated by ChEMBL


Assay Description
Inhibition of acetylcholinesterase.


J Med Chem 35: 584-9 (1992)


Article DOI: 10.1021/jm00081a022
BindingDB Entry DOI: 10.7270/Q20G3J3J
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50008561
PNG
(6-Hydroxy-5-methoxy-2-methyl-indan-1-one | CHEMBL3...)
Show SMILES COc1cc2CC(C)C(=O)c2cc1O
Show InChI InChI=1S/C11H12O3/c1-6-3-7-4-10(14-2)9(12)5-8(7)11(6)13/h4-6,12H,3H2,1-2H3
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 380n/an/an/an/an/an/a



University of Illinois

Curated by ChEMBL


Assay Description
IC50 against acetylcholinesterase; value ranges from 1.3-380 nM.


J Med Chem 35: 584-9 (1992)


Article DOI: 10.1021/jm00081a022
BindingDB Entry DOI: 10.7270/Q20G3J3J
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50008565
PNG
(5,6-Dimethoxy-2-methyl-indan-1-one | CHEMBL154848)
Show SMILES COc1cc2CC(C)C(=O)c2cc1OC
Show InChI InChI=1S/C12H14O3/c1-7-4-8-5-10(14-2)11(15-3)6-9(8)12(7)13/h5-7H,4H2,1-3H3
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 380n/an/an/an/an/an/a



University of Illinois

Curated by ChEMBL


Assay Description
IC50 against acetylcholinesterase; value ranges from 1.3-380 nM.


J Med Chem 35: 584-9 (1992)


Article DOI: 10.1021/jm00081a022
BindingDB Entry DOI: 10.7270/Q20G3J3J
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50008542
PNG
(5,6-Diethoxy-2-methyl-indan-1-one | CHEMBL158242)
Show SMILES CCOc1cc2CC(C)C(=O)c2cc1OCC
Show InChI InChI=1S/C14H18O3/c1-4-16-12-7-10-6-9(3)14(15)11(10)8-13(12)17-5-2/h7-9H,4-6H2,1-3H3
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 6.30n/an/an/an/an/an/a



University of Illinois

Curated by ChEMBL


Assay Description
Inhibition of acetylcholinesterase.


J Med Chem 35: 584-9 (1992)


Article DOI: 10.1021/jm00081a022
BindingDB Entry DOI: 10.7270/Q20G3J3J
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50008552
PNG
(4-Methoxy-2-methyl-indan-1-one | CHEMBL422338)
Show SMILES COc1cccc2C(=O)C(C)Cc12
Show InChI InChI=1S/C11H12O2/c1-7-6-9-8(11(7)12)4-3-5-10(9)13-2/h3-5,7H,6H2,1-2H3
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 12n/an/an/an/an/an/a



University of Illinois

Curated by ChEMBL


Assay Description
Inhibition of acetylcholinesterase.


J Med Chem 35: 584-9 (1992)


Article DOI: 10.1021/jm00081a022
BindingDB Entry DOI: 10.7270/Q20G3J3J
More data for this
Ligand-Target Pair
Glycogen synthase kinase-3 beta


(Homo sapiens (Human))
BDBM50304446
PNG
(5,6-dimethoxy-2,3-dihydro-1H-inden-1-one | CHEMBL6...)
Show SMILES COc1cc2CCC(=O)c2cc1OC
Show InChI InChI=1S/C11H12O3/c1-13-10-5-7-3-4-9(12)8(7)6-11(10)14-2/h5-6H,3-4H2,1-2H3
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

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



Instituto de Qu£mica M£dica-CSIC

Curated by ChEMBL


Assay Description
Inhibition of GSK3beta by liquid scintillation counting


Bioorg Med Chem 17: 6914-25 (2009)


Article DOI: 10.1016/j.bmc.2009.08.042
BindingDB Entry DOI: 10.7270/Q2N29X2P
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50310594
PNG
(5,6-dimethoxy-2-(4-methoxybenzoyl)-2,3-dihydro-1H-...)
Show SMILES COc1ccc(cc1)C(=O)C1Cc2cc(OC)c(OC)cc2C1=O
Show InChI InChI=1S/C19H18O5/c1-22-13-6-4-11(5-7-13)18(20)15-8-12-9-16(23-2)17(24-3)10-14(12)19(15)21/h4-7,9-10,15H,8H2,1-3H3
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 6.20n/an/an/an/an/an/a



Alwar Pharmacy College

Curated by ChEMBL


Assay Description
Inhibition of Electrophorus electricus AChE by Ellman's method


Bioorg Med Chem Lett 19: 5075-7 (2009)


Article DOI: 10.1016/j.bmcl.2009.07.042
BindingDB Entry DOI: 10.7270/Q2Z0389S
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50310597
PNG
(2-benzoyl-5,6-dimethoxy-2,3-dihydro-1H-inden-1-one...)
Show SMILES COc1cc2CC(C(=O)c3ccccc3)C(=O)c2cc1OC
Show InChI InChI=1S/C18H16O4/c1-21-15-9-12-8-14(17(19)11-6-4-3-5-7-11)18(20)13(12)10-16(15)22-2/h3-7,9-10,14H,8H2,1-2H3
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 21n/an/an/an/an/an/a



Alwar Pharmacy College

Curated by ChEMBL


Assay Description
Inhibition of Electrophorus electricus AChE by Ellman's method


Bioorg Med Chem Lett 19: 5075-7 (2009)


Article DOI: 10.1016/j.bmcl.2009.07.042
BindingDB Entry DOI: 10.7270/Q2Z0389S
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50310598
PNG
(2-(3,4-dimethoxybenzoyl)-5,6-dimethoxy-2,3-dihydro...)
Show SMILES COc1ccc(cc1OC)C(=O)C1Cc2cc(OC)c(OC)cc2C1=O
Show InChI InChI=1S/C20H20O6/c1-23-15-6-5-11(8-16(15)24-2)19(21)14-7-12-9-17(25-3)18(26-4)10-13(12)20(14)22/h5-6,8-10,14H,7H2,1-4H3
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 4.30n/an/an/an/an/an/a



Alwar Pharmacy College

Curated by ChEMBL


Assay Description
Inhibition of Electrophorus electricus AChE by Ellman's method


Bioorg Med Chem Lett 19: 5075-7 (2009)


Article DOI: 10.1016/j.bmcl.2009.07.042
BindingDB Entry DOI: 10.7270/Q2Z0389S
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50310599
PNG
(5,6-dimethoxy-1-oxo-2,3-dihydro-1H-2-indenyl-3,4,5...)
Show SMILES COc1cc2CC(C(=O)c3cc(OC)c(OC)c(OC)c3)C(=O)c2cc1OC
Show InChI InChI=1S/C21H22O7/c1-24-15-7-11-6-14(20(23)13(11)10-16(15)25-2)19(22)12-8-17(26-3)21(28-5)18(9-12)27-4/h7-10,14H,6H2,1-5H3
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 2.70n/an/an/an/an/an/a



Alwar Pharmacy College

Curated by ChEMBL


Assay Description
Inhibition of Electrophorus electricus AChE by Ellman's method


Bioorg Med Chem Lett 19: 5075-7 (2009)


Article DOI: 10.1016/j.bmcl.2009.07.042
BindingDB Entry DOI: 10.7270/Q2Z0389S
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50310606
PNG
(4-(5,6-dimethoxy-1-oxo-2,3-dihydro-1H-indene-2-car...)
Show SMILES COc1cc2CC(C(=O)c3ccc(cc3)C#N)C(=O)c2cc1OC
Show InChI InChI=1S/C19H15NO4/c1-23-16-8-13-7-15(19(22)14(13)9-17(16)24-2)18(21)12-5-3-11(10-20)4-6-12/h3-6,8-9,15H,7H2,1-2H3
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 53n/an/an/an/an/an/a



Alwar Pharmacy College

Curated by ChEMBL


Assay Description
Inhibition of Electrophorus electricus AChE by Ellman's method


Bioorg Med Chem Lett 19: 5075-7 (2009)


Article DOI: 10.1016/j.bmcl.2009.07.042
BindingDB Entry DOI: 10.7270/Q2Z0389S
More data for this
Ligand-Target Pair
Butyrylcholinesterase (BuChE)


(Equus caballus (Horse))
BDBM50386066
PNG
(CHEMBL2043047)
Show SMILES COc1cc2CCC(=O)c2cc1O
Show InChI InChI=1S/C10H10O3/c1-13-10-4-6-2-3-8(11)7(6)5-9(10)12/h4-5,12H,2-3H2,1H3
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 2.58E+5n/an/an/an/an/an/a



Sun Yat-sen University

Curated by ChEMBL


Assay Description
Inhibition of equine serum butyrylcholinesterase using butylthiocholine chloride as substrate incubated for 15 mins prior to substrate addition measu...


Bioorg Med Chem Lett 22: 4462-6 (2012)


Article DOI: 10.1016/j.bmcl.2012.04.029
BindingDB Entry DOI: 10.7270/Q2PC33DC
More data for this
Ligand-Target Pair
Cholinesterases; ACHE & BCHE


(Homo sapiens (Human))
BDBM50008561
PNG
(6-Hydroxy-5-methoxy-2-methyl-indan-1-one | CHEMBL3...)
Show SMILES COc1cc2CC(C)C(=O)c2cc1O
Show InChI InChI=1S/C11H12O3/c1-6-3-7-4-10(14-2)9(12)5-8(7)11(6)13/h4-6,12H,3H2,1-2H3
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 1.30n/an/an/an/an/an/a



University of Illinois

Curated by ChEMBL


Assay Description
Inhibition of acetylcholinesterase.


J Med Chem 35: 584-9 (1992)


Article DOI: 10.1021/jm00081a022
BindingDB Entry DOI: 10.7270/Q20G3J3J
More data for this
Ligand-Target Pair