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Compile Data Set for Download or QSAR

Found 305 hits with Last Name = 'achab' and Initial = 'a'   
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


(Bos taurus (bovine))
BDBM10592
PNG
(7-chloro-15-methyl-10-azatetracyclo[11.3.1.0^{2,11...)
Show SMILES CC1=CC2CC(C1)c1c(C2)nc2cc(Cl)ccc2c1N
Show InChI InChI=1S/C17H17ClN2/c1-9-4-10-6-11(5-9)16-15(7-10)20-14-8-12(18)2-3-13(14)17(16)19/h2-4,8,10-11H,5-7H2,1H3,(H2,19,20)
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n/an/a 0.0245n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase activity from bovine erythrocytes after 30 minutes of incubation


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM50369748
PNG
(CHEMBL208599)
Show SMILES CCC1=CC2C[C@H](C1)c1c(C2)nc2cc(Cl)ccc2c1N
Show InChI InChI=1S/C18H19ClN2/c1-2-10-5-11-7-12(6-10)17-16(8-11)21-15-9-13(19)3-4-14(15)18(17)20/h3-5,9,11-12H,2,6-8H2,1H3,(H2,20,21)/t11?,12-/m0/s1
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n/an/a 0.0674n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase activity from bovine erythrocytes after 30 minutes of incubation


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM50369748
PNG
(CHEMBL208599)
Show SMILES CCC1=CC2C[C@H](C1)c1c(C2)nc2cc(Cl)ccc2c1N
Show InChI InChI=1S/C18H19ClN2/c1-2-10-5-11-7-12(6-10)17-16(8-11)21-15-9-13(19)3-4-14(15)18(17)20/h3-5,9,11-12H,2,6-8H2,1H3,(H2,20,21)/t11?,12-/m0/s1
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n/an/a 0.230n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase activity from bovine erythrocytes after 30 minutes of incubation


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (human))
BDBM10592
PNG
(7-chloro-15-methyl-10-azatetracyclo[11.3.1.0^{2,11...)
Show SMILES CC1=CC2CC(C1)c1c(C2)nc2cc(Cl)ccc2c1N
Show InChI InChI=1S/C17H17ClN2/c1-9-4-10-6-11(5-9)16-15(7-10)20-14-8-12(18)2-3-13(14)17(16)19/h2-4,8,10-11H,5-7H2,1H3,(H2,19,20)
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n/an/a 0.320n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Inhibition of acetylcholinesterase isolated from Human erythrocytes.


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (human))
BDBM50369748
PNG
(CHEMBL208599)
Show SMILES CCC1=CC2C[C@H](C1)c1c(C2)nc2cc(Cl)ccc2c1N
Show InChI InChI=1S/C18H19ClN2/c1-2-10-5-11-7-12(6-10)17-16(8-11)21-15-9-13(19)3-4-14(15)18(17)20/h3-5,9,11-12H,2,6-8H2,1H3,(H2,20,21)/t11?,12-/m0/s1
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n/an/a 0.320n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Inhibition of acetylcholinesterase isolated from Human erythrocytes.


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM50094626
PNG
((+)-15-ethyl-7-fluoro-10-azatetracyclo[11.3.1.02,1...)
Show SMILES CCC1=CC2CC(C1)c1c(C2)nc2cc(F)ccc2c1N
Show InChI InChI=1S/C18H19FN2/c1-2-10-5-11-7-12(6-10)17-16(8-11)21-15-9-13(19)3-4-14(15)18(17)20/h3-5,9,11-12H,2,6-8H2,1H3,(H2,20,21)
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n/an/a 0.5n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase activity from bovine erythrocytes after 30 minutes of incubation


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM10592
PNG
(7-chloro-15-methyl-10-azatetracyclo[11.3.1.0^{2,11...)
Show SMILES CC1=CC2CC(C1)c1c(C2)nc2cc(Cl)ccc2c1N
Show InChI InChI=1S/C17H17ClN2/c1-9-4-10-6-11(5-9)16-15(7-10)20-14-8-12(18)2-3-13(14)17(16)19/h2-4,8,10-11H,5-7H2,1H3,(H2,19,20)
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n/an/a 0.640n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase activity from bovine erythrocytes after 30 minutes of incubation


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (human))
BDBM50369748
PNG
(CHEMBL208599)
Show SMILES CCC1=CC2C[C@H](C1)c1c(C2)nc2cc(Cl)ccc2c1N
Show InChI InChI=1S/C18H19ClN2/c1-2-10-5-11-7-12(6-10)17-16(8-11)21-15-9-13(19)3-4-14(15)18(17)20/h3-5,9,11-12H,2,6-8H2,1H3,(H2,20,21)/t11?,12-/m0/s1
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n/an/a 0.75n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Inhibition of acetylcholinesterase isolated from Human erythrocytes.


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (human))
BDBM10592
PNG
(7-chloro-15-methyl-10-azatetracyclo[11.3.1.0^{2,11...)
Show SMILES CC1=CC2CC(C1)c1c(C2)nc2cc(Cl)ccc2c1N
Show InChI InChI=1S/C17H17ClN2/c1-9-4-10-6-11(5-9)16-15(7-10)20-14-8-12(18)2-3-13(14)17(16)19/h2-4,8,10-11H,5-7H2,1H3,(H2,19,20)
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n/an/a 0.780n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Inhibition of acetylcholinesterase isolated from Human erythrocytes.


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM10592
PNG
(7-chloro-15-methyl-10-azatetracyclo[11.3.1.0^{2,11...)
Show SMILES CC1=CC2CC(C1)c1c(C2)nc2cc(Cl)ccc2c1N
Show InChI InChI=1S/C17H17ClN2/c1-9-4-10-6-11(5-9)16-15(7-10)20-14-8-12(18)2-3-13(14)17(16)19/h2-4,8,10-11H,5-7H2,1H3,(H2,19,20)
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n/an/a 1.15n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase of bovine erythrocytes


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM50369748
PNG
(CHEMBL208599)
Show SMILES CCC1=CC2C[C@H](C1)c1c(C2)nc2cc(Cl)ccc2c1N
Show InChI InChI=1S/C18H19ClN2/c1-2-10-5-11-7-12(6-10)17-16(8-11)21-15-9-13(19)3-4-14(15)18(17)20/h3-5,9,11-12H,2,6-8H2,1H3,(H2,20,21)/t11?,12-/m0/s1
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n/an/a 1.30n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase of bovine erythrocytes


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (human))
BDBM50094630
PNG
(5,7-dichloro-15-ethyl-10-azatetracyclo[11.3.1.02,1...)
Show SMILES CCC1=CC2CC(C1)c1c(C2)nc2cc(Cl)cc(Cl)c2c1N
Show InChI InChI=1S/C18H18Cl2N2/c1-2-9-3-10-5-11(4-9)16-14(6-10)22-15-8-12(19)7-13(20)17(15)18(16)21/h3,7-8,10-11H,2,4-6H2,1H3,(H2,21,22)
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n/an/a 1.39n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Inhibition of acetylcholinesterase isolated from Human erythrocytes.


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (human))
BDBM50094631
PNG
(15-ethyl-5,7-difluoro-10-azatetracyclo[11.3.1.02,1...)
Show SMILES CCC1=CC2CC(C1)c1c(C2)nc2cc(F)cc(F)c2c1N
Show InChI InChI=1S/C18H18F2N2/c1-2-9-3-10-5-11(4-9)16-14(6-10)22-15-8-12(19)7-13(20)17(15)18(16)21/h3,7-8,10-11H,2,4-6H2,1H3,(H2,21,22)
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n/an/a 1.76n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Inhibition of acetylcholinesterase isolated from Human erythrocytes.


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM50094626
PNG
((+)-15-ethyl-7-fluoro-10-azatetracyclo[11.3.1.02,1...)
Show SMILES CCC1=CC2CC(C1)c1c(C2)nc2cc(F)ccc2c1N
Show InChI InChI=1S/C18H19FN2/c1-2-10-5-11-7-12(6-10)17-16(8-11)21-15-9-13(19)3-4-14(15)18(17)20/h3-5,9,11-12H,2,6-8H2,1H3,(H2,20,21)
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n/an/a 1.91n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase activity from bovine erythrocytes after 0 minutes of incubation


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 1


(Mus musculus (Mouse))
BDBM233415
PNG
(US9351965, 22)
Show SMILES COc1cccc(F)c1C[C@@]1(O)CCC[C@H](C1)NC(=O)c1ccc2[nH]nc(-c3ccnc(C)c3)c2c1
Show InChI InChI=1S/C28H29FN4O3/c1-17-13-18(10-12-30-17)26-21-14-19(8-9-24(21)32-33-26)27(34)31-20-5-4-11-28(35,15-20)16-22-23(29)6-3-7-25(22)36-2/h3,6-10,12-14,20,35H,4-5,11,15-16H2,1-2H3,(H,31,34)(H,32,33)/t20-,28-/m1/s1
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n/an/a 2n/an/an/an/an/an/a



Merck Sharp & Dohme Corp.

US Patent


Assay Description
Activated ERK2 activity was also determined in the IMAP assay format using the procedure outlined above. 1 μl of 25× compound was added to 1...


US Patent US9351965 (2016)


BindingDB Entry DOI: 10.7270/Q2GT5M11
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (human))
BDBM50094626
PNG
((+)-15-ethyl-7-fluoro-10-azatetracyclo[11.3.1.02,1...)
Show SMILES CCC1=CC2CC(C1)c1c(C2)nc2cc(F)ccc2c1N
Show InChI InChI=1S/C18H19FN2/c1-2-10-5-11-7-12(6-10)17-16(8-11)21-15-9-13(19)3-4-14(15)18(17)20/h3-5,9,11-12H,2,6-8H2,1H3,(H2,20,21)
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n/an/a 2.11n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Inhibition of acetylcholinesterase isolated from Human erythrocytes.


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 1


(Mus musculus (Mouse))
BDBM233416
PNG
(US9351965, 23)
Show SMILES COc1cccc(F)c1C[C@@]1(O)CCC[C@H](C1)NC(=O)c1ccc2[nH]nc(-c3ccc4nccn4c3)c2c1
Show InChI InChI=1S/C29H28FN5O3/c1-38-25-6-2-5-23(30)22(25)16-29(37)11-3-4-20(15-29)32-28(36)18-7-9-24-21(14-18)27(34-33-24)19-8-10-26-31-12-13-35(26)17-19/h2,5-10,12-14,17,20,37H,3-4,11,15-16H2,1H3,(H,32,36)(H,33,34)/t20-,29-/m1/s1
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n/an/a 2.20n/an/an/an/an/an/a



Merck Sharp & Dohme Corp.

US Patent


Assay Description
Activated ERK2 activity was also determined in the IMAP assay format using the procedure outlined above. 1 μl of 25× compound was added to 1...


US Patent US9351965 (2016)


BindingDB Entry DOI: 10.7270/Q2GT5M11
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (human))
BDBM50094633
PNG
(5,7-difluoro-15-methyl-10-azatetracyclo[11.3.1.02,...)
Show SMILES CC1=CC2CC(C1)c1c(C2)nc2cc(F)cc(F)c2c1N
Show InChI InChI=1S/C17H16F2N2/c1-8-2-9-4-10(3-8)15-13(5-9)21-14-7-11(18)6-12(19)16(14)17(15)20/h2,6-7,9-10H,3-5H2,1H3,(H2,20,21)
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n/an/a 2.20n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Inhibition of acetylcholinesterase isolated from Human erythrocytes.


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM50369748
PNG
(CHEMBL208599)
Show SMILES CCC1=CC2C[C@H](C1)c1c(C2)nc2cc(Cl)ccc2c1N
Show InChI InChI=1S/C18H19ClN2/c1-2-10-5-11-7-12(6-10)17-16(8-11)21-15-9-13(19)3-4-14(15)18(17)20/h3-5,9,11-12H,2,6-8H2,1H3,(H2,20,21)/t11?,12-/m0/s1
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n/an/a 2.31n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase activity from bovine erythrocytes after 0 minutes of incubation


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM50094633
PNG
(5,7-difluoro-15-methyl-10-azatetracyclo[11.3.1.02,...)
Show SMILES CC1=CC2CC(C1)c1c(C2)nc2cc(F)cc(F)c2c1N
Show InChI InChI=1S/C17H16F2N2/c1-8-2-9-4-10(3-8)15-13(5-9)21-14-7-11(18)6-12(19)16(14)17(15)20/h2,6-7,9-10H,3-5H2,1H3,(H2,20,21)
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PubMed
n/an/a 2.43n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase of bovine erythrocytes


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM50094631
PNG
(15-ethyl-5,7-difluoro-10-azatetracyclo[11.3.1.02,1...)
Show SMILES CCC1=CC2CC(C1)c1c(C2)nc2cc(F)cc(F)c2c1N
Show InChI InChI=1S/C18H18F2N2/c1-2-9-3-10-5-11(4-9)16-14(6-10)22-15-8-12(19)7-13(20)17(15)18(16)21/h3,7-8,10-11H,2,4-6H2,1H3,(H2,21,22)
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n/an/a 2.62n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase of bovine erythrocytes


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM50369748
PNG
(CHEMBL208599)
Show SMILES CCC1=CC2C[C@H](C1)c1c(C2)nc2cc(Cl)ccc2c1N
Show InChI InChI=1S/C18H19ClN2/c1-2-10-5-11-7-12(6-10)17-16(8-11)21-15-9-13(19)3-4-14(15)18(17)20/h3-5,9,11-12H,2,6-8H2,1H3,(H2,20,21)/t11?,12-/m0/s1
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n/an/a 2.77n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase of bovine erythrocytes


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM10592
PNG
(7-chloro-15-methyl-10-azatetracyclo[11.3.1.0^{2,11...)
Show SMILES CC1=CC2CC(C1)c1c(C2)nc2cc(Cl)ccc2c1N
Show InChI InChI=1S/C17H17ClN2/c1-9-4-10-6-11(5-9)16-15(7-10)20-14-8-12(18)2-3-13(14)17(16)19/h2-4,8,10-11H,5-7H2,1H3,(H2,19,20)
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n/an/a 3.03n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase activity from bovine erythrocytes after 0 minutes of incubation


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM10592
PNG
(7-chloro-15-methyl-10-azatetracyclo[11.3.1.0^{2,11...)
Show SMILES CC1=CC2CC(C1)c1c(C2)nc2cc(Cl)ccc2c1N
Show InChI InChI=1S/C17H17ClN2/c1-9-4-10-6-11(5-9)16-15(7-10)20-14-8-12(18)2-3-13(14)17(16)19/h2-4,8,10-11H,5-7H2,1H3,(H2,19,20)
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n/an/a 3.10n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase activity from bovine erythrocytes after 0 minutes of incubation


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM50094628
PNG
(15-ethyl-5-fluoro-10-azatetracyclo[11.3.1.02,11.04...)
Show SMILES CCC1=CC2CC(C1)c1c(C2)nc2cccc(F)c2c1N
Show InChI InChI=1S/C18H19FN2/c1-2-10-6-11-8-12(7-10)16-15(9-11)21-14-5-3-4-13(19)17(14)18(16)20/h3-6,11-12H,2,7-9H2,1H3,(H2,20,21)
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n/an/a 3.20n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase activity from bovine erythrocytes after 0 minutes of incubation


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM50369748
PNG
(CHEMBL208599)
Show SMILES CCC1=CC2C[C@H](C1)c1c(C2)nc2cc(Cl)ccc2c1N
Show InChI InChI=1S/C18H19ClN2/c1-2-10-5-11-7-12(6-10)17-16(8-11)21-15-9-13(19)3-4-14(15)18(17)20/h3-5,9,11-12H,2,6-8H2,1H3,(H2,20,21)/t11?,12-/m0/s1
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n/an/a 3.34n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase activity from bovine erythrocytes after 0 minutes of incubation


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM50094628
PNG
(15-ethyl-5-fluoro-10-azatetracyclo[11.3.1.02,11.04...)
Show SMILES CCC1=CC2CC(C1)c1c(C2)nc2cccc(F)c2c1N
Show InChI InChI=1S/C18H19FN2/c1-2-10-6-11-8-12(7-10)16-15(9-11)21-14-5-3-4-13(19)17(14)18(16)20/h3-6,11-12H,2,7-9H2,1H3,(H2,20,21)
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n/an/a 3.58n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase activity from bovine erythrocytes after 30 minutes of incubation


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM50094625
PNG
(15-ethyl-5,7-dimethyl-10-azatetracyclo[11.3.1.02,1...)
Show SMILES CCC1=CC2CC(C1)c1c(C2)nc2cc(C)cc(C)c2c1N
Show InChI InChI=1S/C20H24N2/c1-4-13-7-14-9-15(8-13)19-17(10-14)22-16-6-11(2)5-12(3)18(16)20(19)21/h5-7,14-15H,4,8-10H2,1-3H3,(H2,21,22)
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n/an/a 3.59n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase of bovine erythrocytes


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (human))
BDBM50094626
PNG
((+)-15-ethyl-7-fluoro-10-azatetracyclo[11.3.1.02,1...)
Show SMILES CCC1=CC2CC(C1)c1c(C2)nc2cc(F)ccc2c1N
Show InChI InChI=1S/C18H19FN2/c1-2-10-5-11-7-12(6-10)17-16(8-11)21-15-9-13(19)3-4-14(15)18(17)20/h3-5,9,11-12H,2,6-8H2,1H3,(H2,20,21)
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n/an/a 3.79n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Inhibition of acetylcholinesterase isolated from Human erythrocytes.


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM10592
PNG
(7-chloro-15-methyl-10-azatetracyclo[11.3.1.0^{2,11...)
Show SMILES CC1=CC2CC(C1)c1c(C2)nc2cc(Cl)ccc2c1N
Show InChI InChI=1S/C17H17ClN2/c1-9-4-10-6-11(5-9)16-15(7-10)20-14-8-12(18)2-3-13(14)17(16)19/h2-4,8,10-11H,5-7H2,1H3,(H2,19,20)
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n/an/a 4.23n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase of bovine erythrocytes


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (human))
BDBM50079861
PNG
((+)-7-fluoro-15-methyl-10-azatetracyclo[11.3.1.02,...)
Show SMILES CC1=CC2CC(C1)c1c(C2)nc2cc(F)ccc2c1N
Show InChI InChI=1S/C17H17FN2/c1-9-4-10-6-11(5-9)16-15(7-10)20-14-8-12(18)2-3-13(14)17(16)19/h2-4,8,10-11H,5-7H2,1H3,(H2,19,20)
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n/an/a 4.58n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Inhibition of acetylcholinesterase isolated from Human erythrocytes.


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (human))
BDBM50094625
PNG
(15-ethyl-5,7-dimethyl-10-azatetracyclo[11.3.1.02,1...)
Show SMILES CCC1=CC2CC(C1)c1c(C2)nc2cc(C)cc(C)c2c1N
Show InChI InChI=1S/C20H24N2/c1-4-13-7-14-9-15(8-13)19-17(10-14)22-16-6-11(2)5-12(3)18(16)20(19)21/h5-7,14-15H,4,8-10H2,1-3H3,(H2,21,22)
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n/an/a 4.96n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Inhibition of acetylcholinesterase isolated from Human erythrocytes.


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM50094626
PNG
((+)-15-ethyl-7-fluoro-10-azatetracyclo[11.3.1.02,1...)
Show SMILES CCC1=CC2CC(C1)c1c(C2)nc2cc(F)ccc2c1N
Show InChI InChI=1S/C18H19FN2/c1-2-10-5-11-7-12(6-10)17-16(8-11)21-15-9-13(19)3-4-14(15)18(17)20/h3-5,9,11-12H,2,6-8H2,1H3,(H2,20,21)
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n/an/a 6.73n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase of bovine erythrocytes


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 1


(Mus musculus (Mouse))
BDBM233459
PNG
(US9351965, 66)
Show SMILES Cc1cc(ccn1)-c1n[nH]c2ccc(cc12)C(=O)N[C@@H]1CCC[C@@](O)(Cn2ncc3ccccc23)C1
Show InChI InChI=1S/C28H28N6O2/c1-18-13-19(10-12-29-18)26-23-14-20(8-9-24(23)32-33-26)27(35)31-22-6-4-11-28(36,15-22)17-34-25-7-3-2-5-21(25)16-30-34/h2-3,5,7-10,12-14,16,22,36H,4,6,11,15,17H2,1H3,(H,31,35)(H,32,33)/t22-,28+/m1/s1
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n/an/a 7n/an/an/an/an/an/a



Merck Sharp & Dohme Corp.

US Patent


Assay Description
Activated ERK2 activity was also determined in the IMAP assay format using the procedure outlined above. 1 μl of 25× compound was added to 1...


US Patent US9351965 (2016)


BindingDB Entry DOI: 10.7270/Q2GT5M11
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM50094626
PNG
((+)-15-ethyl-7-fluoro-10-azatetracyclo[11.3.1.02,1...)
Show SMILES CCC1=CC2CC(C1)c1c(C2)nc2cc(F)ccc2c1N
Show InChI InChI=1S/C18H19FN2/c1-2-10-5-11-7-12(6-10)17-16(8-11)21-15-9-13(19)3-4-14(15)18(17)20/h3-5,9,11-12H,2,6-8H2,1H3,(H2,20,21)
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n/an/a 7.40n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase of bovine erythrocytes


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 1


(Mus musculus (Mouse))
BDBM233394
PNG
(US9351965, 1 | US9351965, 2 | US9351965, 3 | US935...)
Show SMILES Cc1cc(ccn1)-c1n[nH]c2ccc(cc12)C(=O)NC1CCCC(O)(Cc2ccccc2F)C1
Show InChI InChI=1S/C27H27FN4O2/c1-17-13-18(10-12-29-17)25-22-14-19(8-9-24(22)31-32-25)26(33)30-21-6-4-11-27(34,16-21)15-20-5-2-3-7-23(20)28/h2-3,5,7-10,12-14,21,34H,4,6,11,15-16H2,1H3,(H,30,33)(H,31,32)
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n/an/a 7.60n/an/an/an/an/an/a



Merck Sharp & Dohme Corp.

US Patent


Assay Description
Activated ERK2 activity was also determined in the IMAP assay format using the procedure outlined above. 1 μl of 25× compound was added to 1...


US Patent US9351965 (2016)


BindingDB Entry DOI: 10.7270/Q2GT5M11
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM50079861
PNG
((+)-7-fluoro-15-methyl-10-azatetracyclo[11.3.1.02,...)
Show SMILES CC1=CC2CC(C1)c1c(C2)nc2cc(F)ccc2c1N
Show InChI InChI=1S/C17H17FN2/c1-9-4-10-6-11(5-9)16-15(7-10)20-14-8-12(18)2-3-13(14)17(16)19/h2-4,8,10-11H,5-7H2,1H3,(H2,19,20)
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n/an/a 8.5n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase of bovine erythrocytes


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 1


(Mus musculus (Mouse))
BDBM233472
PNG
(US9351965, 79)
Show SMILES Cc1cc(ccn1)-c1n[nH]c2ccc(cc12)C(=O)N[C@@H]1CCC[C@@](O)(Cn2ncc3cccnc23)C1
Show InChI InChI=1S/C27H27N7O2/c1-17-12-18(8-11-28-17)24-22-13-19(6-7-23(22)32-33-24)26(35)31-21-5-2-9-27(36,14-21)16-34-25-20(15-30-34)4-3-10-29-25/h3-4,6-8,10-13,15,21,36H,2,5,9,14,16H2,1H3,(H,31,35)(H,32,33)/t21-,27+/m1/s1
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n/an/a 8.60n/an/an/an/an/an/a



Merck Sharp & Dohme Corp.

US Patent


Assay Description
Activated ERK2 activity was also determined in the IMAP assay format using the procedure outlined above. 1 μl of 25× compound was added to 1...


US Patent US9351965 (2016)


BindingDB Entry DOI: 10.7270/Q2GT5M11
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 1


(Mus musculus (Mouse))
BDBM233408
PNG
(US9351965, 15)
Show SMILES O[C@]1(Cc2ccccc2F)CCC[C@H](C1)NC(=O)c1ccc2[nH]nc(-c3ccc4nccn4c3)c2c1
Show InChI InChI=1S/C28H26FN5O2/c29-23-6-2-1-4-19(23)15-28(36)11-3-5-21(16-28)31-27(35)18-7-9-24-22(14-18)26(33-32-24)20-8-10-25-30-12-13-34(25)17-20/h1-2,4,6-10,12-14,17,21,36H,3,5,11,15-16H2,(H,31,35)(H,32,33)/t21-,28+/m1/s1
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n/an/a 8.60n/an/an/an/an/an/a



Merck Sharp & Dohme Corp.

US Patent


Assay Description
Activated ERK2 activity was also determined in the IMAP assay format using the procedure outlined above. 1 μl of 25× compound was added to 1...


US Patent US9351965 (2016)


BindingDB Entry DOI: 10.7270/Q2GT5M11
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 1


(Mus musculus (Mouse))
BDBM233417
PNG
(US9351965, 24)
Show SMILES COc1cccc(F)c1C[C@@]1(O)CCC[C@H](C1)NC(=O)c1ccc2[nH]nc(-c3ccc4nc(C)sc4c3)c2c1
Show InChI InChI=1S/C30H29FN4O3S/c1-17-32-25-11-8-18(14-27(25)39-17)28-21-13-19(9-10-24(21)34-35-28)29(36)33-20-5-4-12-30(37,15-20)16-22-23(31)6-3-7-26(22)38-2/h3,6-11,13-14,20,37H,4-5,12,15-16H2,1-2H3,(H,33,36)(H,34,35)/t20-,30-/m1/s1
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n/an/a 8.90n/an/an/an/an/an/a



Merck Sharp & Dohme Corp.

US Patent


Assay Description
Activated ERK2 activity was also determined in the IMAP assay format using the procedure outlined above. 1 μl of 25× compound was added to 1...


US Patent US9351965 (2016)


BindingDB Entry DOI: 10.7270/Q2GT5M11
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 1


(Mus musculus (Mouse))
BDBM233516
PNG
(US9351965, 123)
Show SMILES Cc1cc(ccn1)-c1n[nH]c2ccc(cc12)C(=O)NC1CCCC(Cn2ncc3ccccc23)C1
Show InChI InChI=1S/C28H28N6O/c1-18-13-20(11-12-29-18)27-24-15-21(9-10-25(24)32-33-27)28(35)31-23-7-4-5-19(14-23)17-34-26-8-3-2-6-22(26)16-30-34/h2-3,6,8-13,15-16,19,23H,4-5,7,14,17H2,1H3,(H,31,35)(H,32,33)
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n/an/a 10.7n/an/an/an/an/an/a



Merck Sharp & Dohme Corp.

US Patent


Assay Description
Activated ERK2 activity was also determined in the IMAP assay format using the procedure outlined above. 1 μl of 25× compound was added to 1...


US Patent US9351965 (2016)


BindingDB Entry DOI: 10.7270/Q2GT5M11
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 1


(Mus musculus (Mouse))
BDBM233485
PNG
(US9351965, 92)
Show SMILES Cc1cc(ccn1)-c1n[nH]c2ccc(cc12)C(=O)N[C@@H]1CCC[C@@](O)(CN2C(=O)Cc3ccccc23)C1
Show InChI InChI=1S/C29H29N5O3/c1-18-13-20(10-12-30-18)27-23-14-21(8-9-24(23)32-33-27)28(36)31-22-6-4-11-29(37,16-22)17-34-25-7-3-2-5-19(25)15-26(34)35/h2-3,5,7-10,12-14,22,37H,4,6,11,15-17H2,1H3,(H,31,36)(H,32,33)/t22-,29+/m1/s1
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n/an/a 10.8n/an/an/an/an/an/a



Merck Sharp & Dohme Corp.

US Patent


Assay Description
Activated ERK2 activity was also determined in the IMAP assay format using the procedure outlined above. 1 μl of 25× compound was added to 1...


US Patent US9351965 (2016)


BindingDB Entry DOI: 10.7270/Q2GT5M11
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 1


(Mus musculus (Mouse))
BDBM233435
PNG
(US9351965, 42)
Show SMILES Cc1cc(ccn1)-c1n[nH]c2ccc(cc12)C(=O)NC1CCCC(C1)(Oc1cccc(F)c1)C(N)=O
Show InChI InChI=1S/C27H26FN5O3/c1-16-12-17(9-11-30-16)24-22-13-18(7-8-23(22)32-33-24)25(34)31-20-5-3-10-27(15-20,26(29)35)36-21-6-2-4-19(28)14-21/h2,4,6-9,11-14,20H,3,5,10,15H2,1H3,(H2,29,35)(H,31,34)(H,32,33)
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n/an/a 11.2n/an/an/an/an/an/a



Merck Sharp & Dohme Corp.

US Patent


Assay Description
Activated ERK2 activity was also determined in the IMAP assay format using the procedure outlined above. 1 μl of 25× compound was added to 1...


US Patent US9351965 (2016)


BindingDB Entry DOI: 10.7270/Q2GT5M11
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (human))
BDBM50094629
PNG
(5-chloro-15-ethyl-10-azatetracyclo[11.3.1.02,11.04...)
Show SMILES CCC1=CC2CC(C1)c1c(C2)nc2cccc(Cl)c2c1N
Show InChI InChI=1S/C18H19ClN2/c1-2-10-6-11-8-12(7-10)16-15(9-11)21-14-5-3-4-13(19)17(14)18(16)20/h3-6,11-12H,2,7-9H2,1H3,(H2,20,21)
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Article
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n/an/a 11.7n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Inhibition of acetylcholinesterase isolated from Human erythrocytes.


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM50079866
PNG
((+)-15-ethyl-7-methyl-10-azatetracyclo[11.3.1.02,1...)
Show SMILES CCC1=CC2CC(C1)c1c(C2)nc2cc(C)ccc2c1N
Show InChI InChI=1S/C19H22N2/c1-3-12-7-13-9-14(8-12)18-17(10-13)21-16-6-11(2)4-5-15(16)19(18)20/h4-7,13-14H,3,8-10H2,1-2H3,(H2,20,21)
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n/an/a 12n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase of bovine erythrocytes


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 1


(Mus musculus (Mouse))
BDBM233412
PNG
(US9351965, 19)
Show SMILES Cn1cc2cc(ccc2n1)-c1n[nH]c2ccc(cc12)C(=O)N[C@@H]1CCC[C@](O)(Cc2c(F)cccc2F)C1
Show InChI InChI=1S/C29H27F2N5O2/c1-36-16-19-12-17(7-9-25(19)35-36)27-21-13-18(8-10-26(21)33-34-27)28(37)32-20-4-3-11-29(38,14-20)15-22-23(30)5-2-6-24(22)31/h2,5-10,12-13,16,20,38H,3-4,11,14-15H2,1H3,(H,32,37)(H,33,34)/t20-,29-/m1/s1
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n/an/a 12.1n/an/an/an/an/an/a



Merck Sharp & Dohme Corp.

US Patent


Assay Description
Activated ERK2 activity was also determined in the IMAP assay format using the procedure outlined above. 1 μl of 25× compound was added to 1...


US Patent US9351965 (2016)


BindingDB Entry DOI: 10.7270/Q2GT5M11
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM50079871
PNG
((rac)7,15-dimethyl-10-azatetracyclo[11.3.1.02,11.0...)
Show SMILES CC1=CC2CC(C1)c1c(C2)nc2cc(C)ccc2c1N
Show InChI InChI=1S/C18H20N2/c1-10-3-4-14-15(7-10)20-16-9-12-5-11(2)6-13(8-12)17(16)18(14)19/h3-5,7,12-13H,6,8-9H2,1-2H3,(H2,19,20)
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n/an/a 12.4n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase of bovine erythrocytes


J Med Chem 43: 4657-66 (2001)


Article DOI: 10.1021/jm000980y
BindingDB Entry DOI: 10.7270/Q2Q52Q9B
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 1


(Mus musculus (Mouse))
BDBM233436
PNG
(US9351965, 43 | US9351965, 44 | US9351965, 45)
Show SMILES Cc1cc(ccn1)-c1n[nH]c2ccc(cc12)C(=O)NC1CCCC(CO)(C1)Oc1cccc(F)c1
Show InChI InChI=1S/C27H27FN4O3/c1-17-12-18(9-11-29-17)25-23-13-19(7-8-24(23)31-32-25)26(34)30-21-5-3-10-27(15-21,16-33)35-22-6-2-4-20(28)14-22/h2,4,6-9,11-14,21,33H,3,5,10,15-16H2,1H3,(H,30,34)(H,31,32)
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n/an/a 13.4n/an/an/an/an/an/a



Merck Sharp & Dohme Corp.

US Patent


Assay Description
Activated ERK2 activity was also determined in the IMAP assay format using the procedure outlined above. 1 μl of 25× compound was added to 1...


US Patent US9351965 (2016)


BindingDB Entry DOI: 10.7270/Q2GT5M11
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 1


(Mus musculus (Mouse))
BDBM233515
PNG
(US9351965, 122)
Show SMILES Cc1cc(ccn1)-c1n[nH]c2ccc(cc12)C(=O)NC1CCCC(Cn2cc3ccccc3n2)C1
Show InChI InChI=1S/C28H28N6O/c1-18-13-20(11-12-29-18)27-24-15-21(9-10-26(24)31-32-27)28(35)30-23-7-4-5-19(14-23)16-34-17-22-6-2-3-8-25(22)33-34/h2-3,6,8-13,15,17,19,23H,4-5,7,14,16H2,1H3,(H,30,35)(H,31,32)
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n/an/a 14.3n/an/an/an/an/an/a



Merck Sharp & Dohme Corp.

US Patent


Assay Description
Activated ERK2 activity was also determined in the IMAP assay format using the procedure outlined above. 1 μl of 25× compound was added to 1...


US Patent US9351965 (2016)


BindingDB Entry DOI: 10.7270/Q2GT5M11
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 1


(Mus musculus (Mouse))
BDBM233405
PNG
(US9351965, 12)
Show SMILES Cc1nc2ccc(cn2n1)-c1n[nH]c2ccc(cc12)C(=O)N[C@@H]1CCC[C@](O)(Cc2ccccc2F)C1
Show InChI InChI=1S/C28H27FN6O2/c1-17-30-25-11-9-20(16-35(25)34-17)26-22-13-18(8-10-24(22)32-33-26)27(36)31-21-6-4-12-28(37,15-21)14-19-5-2-3-7-23(19)29/h2-3,5,7-11,13,16,21,37H,4,6,12,14-15H2,1H3,(H,31,36)(H,32,33)/t21-,28+/m1/s1
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Merck Sharp & Dohme Corp.

US Patent


Assay Description
Activated ERK2 activity was also determined in the IMAP assay format using the procedure outlined above. 1 μl of 25× compound was added to 1...


US Patent US9351965 (2016)


BindingDB Entry DOI: 10.7270/Q2GT5M11
More data for this
Ligand-Target Pair
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