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Compile Data Set for Download or QSAR

Found 61 hits with Last Name = 'brufani' and Initial = 'm'   
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


(Tetronarce californica (Pacific electric ray) (Tor...)
BDBM50069245
PNG
(CHEMBL157336 | N-[12-(Adamantan-1-ylamino)-dodecyl...)
Show SMILES CN(C)c1ccc(CC(=O)NCCCCCCCCCCCCNC23CC4CC(CC(C4)C2)C3)cc1 |TLB:33:24:31:28.27.29,THB:33:28:24.25.32:31,23:24:31:28.27.29,29:28:25:30.32.31,29:30:25:28.33.27|
Show InChI InChI=1S/C32H53N3O/c1-35(2)30-15-13-26(14-16-30)22-31(36)33-17-11-9-7-5-3-4-6-8-10-12-18-34-32-23-27-19-28(24-32)21-29(20-27)25-32/h13-16,27-29,34H,3-12,17-25H2,1-2H3,(H,33,36)
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1.80E+3n/an/an/an/an/an/an/an/a



Istituto di Strutturistica Chimica G. Giacomello

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase (AChE) in bovine brain


Bioorg Med Chem Lett 8: 575-80 (1999)


BindingDB Entry DOI: 10.7270/Q2S181N2
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)
BDBM50069248
PNG
(CHEMBL421974 | N-[11-(Adamantan-1-ylamino)-undecyl...)
Show SMILES CN(C)c1ccc(CC(=O)NCCCCCCCCCCCNC23CC4CC(CC(C4)C2)C3)cc1 |TLB:32:23:30:27.26.28,THB:32:27:23.24.31:30,22:23:30:27.26.28,28:27:24:29.31.30,28:29:24:27.32.26|
Show InChI InChI=1S/C31H51N3O/c1-34(2)29-14-12-25(13-15-29)21-30(35)32-16-10-8-6-4-3-5-7-9-11-17-33-31-22-26-18-27(23-31)20-28(19-26)24-31/h12-15,26-28,33H,3-11,16-24H2,1-2H3,(H,32,35)
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2.10E+3n/an/an/an/an/an/an/an/a



Istituto di Strutturistica Chimica G. Giacomello

Curated by ChEMBL


Assay Description
Compound was evaluated for competitive inhibition constant of acetylcholinesterase (AChE) from Torpedo californica


Bioorg Med Chem Lett 8: 575-80 (1999)


BindingDB Entry DOI: 10.7270/Q2S181N2
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)
BDBM50069243
PNG
(CHEMBL153934 | N-[10-(Adamantan-1-ylamino)-decyl]-...)
Show SMILES CN(C)c1ccc(CC(=O)NCCCCCCCCCCNC23CC4CC(CC(C4)C2)C3)cc1 |TLB:31:22:29:26.25.27,THB:31:26:22.23.30:29,21:22:29:26.25.27,27:26:23:28.30.29,27:28:23:26.31.25|
Show InChI InChI=1S/C30H49N3O/c1-33(2)28-13-11-24(12-14-28)20-29(34)31-15-9-7-5-3-4-6-8-10-16-32-30-21-25-17-26(22-30)19-27(18-25)23-30/h11-14,25-27,32H,3-10,15-23H2,1-2H3,(H,31,34)
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2.50E+3n/an/an/an/an/an/an/an/a



Istituto di Strutturistica Chimica G. Giacomello

Curated by ChEMBL


Assay Description
Compound was evaluated for competitive inhibition constant of acetylcholinesterase (AChE) from Torpedo californica


Bioorg Med Chem Lett 8: 575-80 (1999)


BindingDB Entry DOI: 10.7270/Q2S181N2
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)
BDBM50069247
PNG
(CHEMBL157429 | N-[9-(Adamantan-1-ylamino)-nonyl]-2...)
Show SMILES CN(C)c1ccc(CC(=O)NCCCCCCCCCNC23CC4CC(CC(C4)C2)C3)cc1 |TLB:30:21:28:25.24.26,THB:30:25:21.22.29:28,20:21:28:25.24.26,26:25:22:27.29.28,26:27:22:25.30.24|
Show InChI InChI=1S/C29H47N3O/c1-32(2)27-12-10-23(11-13-27)19-28(33)30-14-8-6-4-3-5-7-9-15-31-29-20-24-16-25(21-29)18-26(17-24)22-29/h10-13,24-26,31H,3-9,14-22H2,1-2H3,(H,30,33)
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3.40E+3n/an/an/an/an/an/an/an/a



Istituto di Strutturistica Chimica G. Giacomello

Curated by ChEMBL


Assay Description
Compound was evaluated for competitive inhibition constant of acetylcholinesterase (AChE) from Torpedo californica


Bioorg Med Chem Lett 8: 575-80 (1999)


BindingDB Entry DOI: 10.7270/Q2S181N2
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)
BDBM50069244
PNG
(CHEMBL357551 | N-[8-(Adamantan-1-ylamino)-octyl]-2...)
Show SMILES CN(C)c1ccc(CC(=O)NCCCCCCCCNC23CC4CC(CC(C4)C2)C3)cc1 |TLB:29:20:27:24.23.25,THB:29:24:20.21.28:27,19:20:27:24.23.25,25:24:21:26.28.27,25:26:21:24.29.23|
Show InChI InChI=1S/C28H45N3O/c1-31(2)26-11-9-22(10-12-26)18-27(32)29-13-7-5-3-4-6-8-14-30-28-19-23-15-24(20-28)17-25(16-23)21-28/h9-12,23-25,30H,3-8,13-21H2,1-2H3,(H,29,32)
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5.50E+3n/an/an/an/an/an/an/an/a



Istituto di Strutturistica Chimica G. Giacomello

Curated by ChEMBL


Assay Description
Compound was evaluated for competitive inhibition constant of acetylcholinesterase (AChE) from Torpedo californica


Bioorg Med Chem Lett 8: 575-80 (1999)


BindingDB Entry DOI: 10.7270/Q2S181N2
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)
BDBM50069246
PNG
(CHEMBL152361 | N-[7-(Adamantan-1-ylamino)-heptyl]-...)
Show SMILES CN(C)c1ccc(CC(=O)NCCCCCCCNC23CC4CC(CC(C4)C2)C3)cc1 |TLB:28:19:26:23.22.24,THB:28:23:19.20.27:26,18:19:26:23.22.24,24:23:20:25.27.26,24:25:20:23.28.22|
Show InChI InChI=1S/C27H43N3O/c1-30(2)25-10-8-21(9-11-25)17-26(31)28-12-6-4-3-5-7-13-29-27-18-22-14-23(19-27)16-24(15-22)20-27/h8-11,22-24,29H,3-7,12-20H2,1-2H3,(H,28,31)
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7.00E+3n/an/an/an/an/an/an/an/a



Istituto di Strutturistica Chimica G. Giacomello

Curated by ChEMBL


Assay Description
Compound was evaluated for competitive inhibition constant of acetylcholinesterase (AChE) from Torpedo californica


Bioorg Med Chem Lett 8: 575-80 (1999)


BindingDB Entry DOI: 10.7270/Q2S181N2
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM8960
PNG
((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)
Show SMILES COc1cc2CC(CC3CCN(Cc4ccccc4)CC3)C(=O)c2cc1OC
Show InChI InChI=1S/C24H29NO3/c1-27-22-14-19-13-20(24(26)21(19)15-23(22)28-2)12-17-8-10-25(11-9-17)16-18-6-4-3-5-7-18/h3-7,14-15,17,20H,8-13,16H2,1-2H3
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n/an/a 6n/an/an/an/an/an/a



Istituto di Strutturistica Chimica G. Giacomello

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase (AChE) in bovine brain


Bioorg Med Chem Lett 8: 575-80 (1999)


BindingDB Entry DOI: 10.7270/Q2S181N2
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Cholinesterases


(Homo sapiens (Human))
BDBM8960
PNG
((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)
Show SMILES COc1cc2CC(CC3CCN(Cc4ccccc4)CC3)C(=O)c2cc1OC
Show InChI InChI=1S/C24H29NO3/c1-27-22-14-19-13-20(24(26)21(19)15-23(22)28-2)12-17-8-10-25(11-9-17)16-18-6-4-3-5-7-18/h3-7,14-15,17,20H,8-13,16H2,1-2H3
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n/an/a 8n/an/an/an/an/an/a



Istituto di Strutturistica Chimica G. Giacomello

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase (AChE) in human erythrocytes


Bioorg Med Chem Lett 8: 575-80 (1999)


BindingDB Entry DOI: 10.7270/Q2S181N2
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Acetylcholinesterase


(Bos taurus (bovine))
BDBM8960
PNG
((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)
Show SMILES COc1cc2CC(CC3CCN(Cc4ccccc4)CC3)C(=O)c2cc1OC
Show InChI InChI=1S/C24H29NO3/c1-27-22-14-19-13-20(24(26)21(19)15-23(22)28-2)12-17-8-10-25(11-9-17)16-18-6-4-3-5-7-18/h3-7,14-15,17,20H,8-13,16H2,1-2H3
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n/an/a 8n/an/an/an/an/an/a



Istituto di Strutturistica Chimica G. Giacomello

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase in Torpedo californica


Bioorg Med Chem Lett 8: 575-80 (1999)


BindingDB Entry DOI: 10.7270/Q2S181N2
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)
BDBM8960
PNG
((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)
Show SMILES COc1cc2CC(CC3CCN(Cc4ccccc4)CC3)C(=O)c2cc1OC
Show InChI InChI=1S/C24H29NO3/c1-27-22-14-19-13-20(24(26)21(19)15-23(22)28-2)12-17-8-10-25(11-9-17)16-18-6-4-3-5-7-18/h3-7,14-15,17,20H,8-13,16H2,1-2H3
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n/an/a 12n/an/an/an/an/an/a



Istituto di Strutturistica Chimica G. Giacomello

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase (AChE) in Torpedo californica


Bioorg Med Chem Lett 8: 575-80 (1999)


BindingDB Entry DOI: 10.7270/Q2S181N2
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM8960
PNG
((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)
Show SMILES COc1cc2CC(CC3CCN(Cc4ccccc4)CC3)C(=O)c2cc1OC
Show InChI InChI=1S/C24H29NO3/c1-27-22-14-19-13-20(24(26)21(19)15-23(22)28-2)12-17-8-10-25(11-9-17)16-18-6-4-3-5-7-18/h3-7,14-15,17,20H,8-13,16H2,1-2H3
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n/an/a 17n/an/an/an/an/an/a



Istituto di Strutturistica Chimica G. Giacomello

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase (AChE) in electric eel


Bioorg Med Chem Lett 8: 575-80 (1999)


BindingDB Entry DOI: 10.7270/Q2S181N2
More data for this
Ligand-Target Pair
Cholinesterases


(Homo sapiens (Human))
BDBM50004000
PNG
((3aS,8aR)-1,3a,8-trimethyl-1,2,3,3a,8,8a-hexahydro...)
Show SMILES CNC(=O)Oc1ccc2N(C)[C@H]3N(C)CC[C@@]3(C)c2c1 |r|
Show InChI InChI=1S/C15H21N3O2/c1-15-7-8-17(3)13(15)18(4)12-6-5-10(9-11(12)15)20-14(19)16-2/h5-6,9,13H,7-8H2,1-4H3,(H,16,19)/t13-,15+/m1/s1
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n/an/a 30n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of Acetylcholinesterase(AChE) from human RBC


Bioorg Med Chem Lett 5: 2077-2080 (1995)


Article DOI: 10.1016/0960-894X(95)00371-Y
BindingDB Entry DOI: 10.7270/Q2NP24CR
More data for this
Ligand-Target Pair
Cholinesterases


(Homo sapiens (Human))
BDBM50285179
PNG
((11-Morpholin-4-yl-undecyl)-carbamic acid (3aS,8aR...)
Show SMILES CN1CC[C@]2(C)[C@H]1N(C)c1ccc(OC(=O)NCCCCCCCCCCCN3CCOCC3)cc21
Show InChI InChI=1S/C29H48N4O3/c1-29-15-18-31(2)27(29)32(3)26-14-13-24(23-25(26)29)36-28(34)30-16-11-9-7-5-4-6-8-10-12-17-33-19-21-35-22-20-33/h13-14,23,27H,4-12,15-22H2,1-3H3,(H,30,34)/t27-,29+/m1/s1
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n/an/a 40n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of Acetylcholinesterase(AChE) from human RBC


Bioorg Med Chem Lett 5: 2077-2080 (1995)


Article DOI: 10.1016/0960-894X(95)00371-Y
BindingDB Entry DOI: 10.7270/Q2NP24CR
More data for this
Ligand-Target Pair
Cholinesterases


(Homo sapiens (Human))
BDBM50285184
PNG
((10-Morpholin-4-yl-decyl)-carbamic acid (3aS,8aR)-...)
Show SMILES CN1CC[C@]2(C)[C@H]1N(C)c1ccc(OC(=O)NCCCCCCCCCCN3CCOCC3)cc21
Show InChI InChI=1S/C28H46N4O3/c1-28-14-17-30(2)26(28)31(3)25-13-12-23(22-24(25)28)35-27(33)29-15-10-8-6-4-5-7-9-11-16-32-18-20-34-21-19-32/h12-13,22,26H,4-11,14-21H2,1-3H3,(H,29,33)/t26-,28+/m1/s1
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n/an/a 40n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of Acetylcholinesterase(AChE) from human RBC


Bioorg Med Chem Lett 5: 2077-2080 (1995)


Article DOI: 10.1016/0960-894X(95)00371-Y
BindingDB Entry DOI: 10.7270/Q2NP24CR
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)
BDBM50004000
PNG
((3aS,8aR)-1,3a,8-trimethyl-1,2,3,3a,8,8a-hexahydro...)
Show SMILES CNC(=O)Oc1ccc2N(C)[C@H]3N(C)CC[C@@]3(C)c2c1 |r|
Show InChI InChI=1S/C15H21N3O2/c1-15-7-8-17(3)13(15)18(4)12-6-5-10(9-11(12)15)20-14(19)16-2/h5-6,9,13H,7-8H2,1-4H3,(H,16,19)/t13-,15+/m1/s1
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n/an/a 46n/an/an/an/an/an/a



Istituto di Strutturistica Chimica G. Giacomello

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase (AChE) in Torpedo californica


Bioorg Med Chem Lett 8: 575-80 (1999)


BindingDB Entry DOI: 10.7270/Q2S181N2
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50004000
PNG
((3aS,8aR)-1,3a,8-trimethyl-1,2,3,3a,8,8a-hexahydro...)
Show SMILES CNC(=O)Oc1ccc2N(C)[C@H]3N(C)CC[C@@]3(C)c2c1 |r|
Show InChI InChI=1S/C15H21N3O2/c1-15-7-8-17(3)13(15)18(4)12-6-5-10(9-11(12)15)20-14(19)16-2/h5-6,9,13H,7-8H2,1-4H3,(H,16,19)/t13-,15+/m1/s1
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n/an/a 46n/an/an/an/an/an/a



Istituto di Strutturistica Chimica G. Giacomello

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase (AChE) in electric eel


Bioorg Med Chem Lett 8: 575-80 (1999)


BindingDB Entry DOI: 10.7270/Q2S181N2
More data for this
Ligand-Target Pair
Cholinesterases


(Homo sapiens (Human))
BDBM50004000
PNG
((3aS,8aR)-1,3a,8-trimethyl-1,2,3,3a,8,8a-hexahydro...)
Show SMILES CNC(=O)Oc1ccc2N(C)[C@H]3N(C)CC[C@@]3(C)c2c1 |r|
Show InChI InChI=1S/C15H21N3O2/c1-15-7-8-17(3)13(15)18(4)12-6-5-10(9-11(12)15)20-14(19)16-2/h5-6,9,13H,7-8H2,1-4H3,(H,16,19)/t13-,15+/m1/s1
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n/an/a 47n/an/an/an/an/an/a



Istituto di Strutturistica Chimica G. Giacomello

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase (AChE) in Torpedo californica


Bioorg Med Chem Lett 8: 575-80 (1999)


BindingDB Entry DOI: 10.7270/Q2S181N2
More data for this
Ligand-Target Pair
Cholinesterases


(Homo sapiens (Human))
BDBM50285188
PNG
((9-Morpholin-4-yl-nonyl)-carbamic acid (3aS,8aR)-1...)
Show SMILES CN1CC[C@]2(C)[C@H]1N(C)c1ccc(OC(=O)NCCCCCCCCCN3CCOCC3)cc21
Show InChI InChI=1S/C27H44N4O3/c1-27-13-16-29(2)25(27)30(3)24-12-11-22(21-23(24)27)34-26(32)28-14-9-7-5-4-6-8-10-15-31-17-19-33-20-18-31/h11-12,21,25H,4-10,13-20H2,1-3H3,(H,28,32)/t25-,27+/m1/s1
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n/an/a 60n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of Acetylcholinesterase(AChE) from human RBC


Bioorg Med Chem Lett 5: 2077-2080 (1995)


Article DOI: 10.1016/0960-894X(95)00371-Y
BindingDB Entry DOI: 10.7270/Q2NP24CR
More data for this
Ligand-Target Pair
Cholinesterases


(Homo sapiens (Human))
BDBM50285180
PNG
((12-Morpholin-4-yl-dodecyl)-carbamic acid (3aS,8aR...)
Show SMILES CN1CC[C@]2(C)[C@H]1N(C)c1ccc(OC(=O)NCCCCCCCCCCCCN3CCOCC3)cc21
Show InChI InChI=1S/C30H50N4O3/c1-30-16-19-32(2)28(30)33(3)27-15-14-25(24-26(27)30)37-29(35)31-17-12-10-8-6-4-5-7-9-11-13-18-34-20-22-36-23-21-34/h14-15,24,28H,4-13,16-23H2,1-3H3,(H,31,35)/t28-,30+/m1/s1
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n/an/a 70n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of Acetylcholinesterase(AChE) from human RBC


Bioorg Med Chem Lett 5: 2077-2080 (1995)


Article DOI: 10.1016/0960-894X(95)00371-Y
BindingDB Entry DOI: 10.7270/Q2NP24CR
More data for this
Ligand-Target Pair
Cholinesterases


(Homo sapiens (Human))
BDBM50285182
PNG
((8-Morpholin-4-yl-octyl)-carbamic acid (3aS,8aR)-1...)
Show SMILES CN1CC[C@]2(C)[C@H]1N(C)c1ccc(OC(=O)NCCCCCCCCN3CCOCC3)cc21
Show InChI InChI=1S/C26H42N4O3/c1-26-12-15-28(2)24(26)29(3)23-11-10-21(20-22(23)26)33-25(31)27-13-8-6-4-5-7-9-14-30-16-18-32-19-17-30/h10-11,20,24H,4-9,12-19H2,1-3H3,(H,27,31)/t24-,26+/m1/s1
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n/an/a 80n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of Acetylcholinesterase(AChE) from human RBC


Bioorg Med Chem Lett 5: 2077-2080 (1995)


Article DOI: 10.1016/0960-894X(95)00371-Y
BindingDB Entry DOI: 10.7270/Q2NP24CR
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM50004000
PNG
((3aS,8aR)-1,3a,8-trimethyl-1,2,3,3a,8,8a-hexahydro...)
Show SMILES CNC(=O)Oc1ccc2N(C)[C@H]3N(C)CC[C@@]3(C)c2c1 |r|
Show InChI InChI=1S/C15H21N3O2/c1-15-7-8-17(3)13(15)18(4)12-6-5-10(9-11(12)15)20-14(19)16-2/h5-6,9,13H,7-8H2,1-4H3,(H,16,19)/t13-,15+/m1/s1
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n/an/a 123n/an/an/an/an/an/a



Istituto di Strutturistica Chimica G. Giacomello

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase in Torpedo californica


Bioorg Med Chem Lett 8: 575-80 (1999)


BindingDB Entry DOI: 10.7270/Q2S181N2
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM50004000
PNG
((3aS,8aR)-1,3a,8-trimethyl-1,2,3,3a,8,8a-hexahydro...)
Show SMILES CNC(=O)Oc1ccc2N(C)[C@H]3N(C)CC[C@@]3(C)c2c1 |r|
Show InChI InChI=1S/C15H21N3O2/c1-15-7-8-17(3)13(15)18(4)12-6-5-10(9-11(12)15)20-14(19)16-2/h5-6,9,13H,7-8H2,1-4H3,(H,16,19)/t13-,15+/m1/s1
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n/an/a 146n/an/an/an/an/an/a



Istituto di Strutturistica Chimica G. Giacomello

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase (AChE) in bovine brain


Bioorg Med Chem Lett 8: 575-80 (1999)


BindingDB Entry DOI: 10.7270/Q2S181N2
More data for this
Ligand-Target Pair
Carbonic anhydrase


(Homo sapiens (Human))
BDBM50229834
PNG
(CHEMBL328270)
Show SMILES COC(=O)CCCCC(=O)Nc1nnc(s1)S(N)(=O)=O
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n/an/a 230n/an/an/an/an/an/a



Istituto Chimico Internazionale Dr. G. Rende

Curated by ChEMBL




J Med Chem 35: 2697-703 (1992)


BindingDB Entry DOI: 10.7270/Q2K076G9
More data for this
Ligand-Target Pair
Cholinesterases


(Homo sapiens (Human))
BDBM10972
PNG
((3aS,8aR)-1,3a,8-trimethyl-1H,2H,3H,3aH,8H,8aH-pyr...)
Show SMILES [H][C@]12N(C)CC[C@@]1(C)c1cc(OC(=O)NCCCCCCC)ccc1N2C
Show InChI InChI=1S/C21H33N3O2/c1-5-6-7-8-9-13-22-20(25)26-16-10-11-18-17(15-16)21(2)12-14-23(3)19(21)24(18)4/h10-11,15,19H,5-9,12-14H2,1-4H3,(H,22,25)/t19-,21+/m1/s1
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n/an/a 290n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of Acetylcholinesterase(AChE) from human RBC


Bioorg Med Chem Lett 5: 2077-2080 (1995)


Article DOI: 10.1016/0960-894X(95)00371-Y
BindingDB Entry DOI: 10.7270/Q2NP24CR
More data for this
Ligand-Target Pair
Carbonic anhydrase


(Homo sapiens (Human))
BDBM50229838
PNG
(CHEMBL88183)
Show SMILES CCCCCOC(=O)CCC(=O)\N=c1\sc(nn1C)S(N)(=O)=O
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n/an/a 310n/an/an/an/an/an/a



Istituto Chimico Internazionale Dr. G. Rende

Curated by ChEMBL




J Med Chem 35: 2697-703 (1992)


BindingDB Entry DOI: 10.7270/Q2K076G9
More data for this
Ligand-Target Pair
Carbonic anhydrase


(Homo sapiens (Human))
BDBM50229841
PNG
(CHEMBL420799)
Show SMILES CCC(C)OC(=O)CCC(=O)Nc1nnc(s1)S(N)(=O)=O
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n/an/a 370n/an/an/an/an/an/a



Istituto Chimico Internazionale Dr. G. Rende

Curated by ChEMBL




J Med Chem 35: 2697-703 (1992)


BindingDB Entry DOI: 10.7270/Q2K076G9
More data for this
Ligand-Target Pair
Cholinesterases


(Homo sapiens (Human))
BDBM50285185
PNG
((7-Morpholin-4-yl-heptyl)-carbamic acid (3aS,8aR)-...)
Show SMILES CN1CC[C@]2(C)[C@H]1N(C)c1ccc(OC(=O)NCCCCCCCN3CCOCC3)cc21
Show InChI InChI=1S/C25H40N4O3/c1-25-11-14-27(2)23(25)28(3)22-10-9-20(19-21(22)25)32-24(30)26-12-7-5-4-6-8-13-29-15-17-31-18-16-29/h9-10,19,23H,4-8,11-18H2,1-3H3,(H,26,30)/t23-,25+/m1/s1
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n/an/a 380n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of Acetylcholinesterase(AChE) from human RBC


Bioorg Med Chem Lett 5: 2077-2080 (1995)


Article DOI: 10.1016/0960-894X(95)00371-Y
BindingDB Entry DOI: 10.7270/Q2NP24CR
More data for this
Ligand-Target Pair
Carbonic anhydrase


(Homo sapiens (Human))
BDBM50229842
PNG
(CHEMBL90119)
Show SMILES CCCCCOC(=O)CCC(=O)Nc1nnc(s1)S(N)(=O)=O
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n/an/a 390n/an/an/an/an/an/a



Istituto Chimico Internazionale Dr. G. Rende

Curated by ChEMBL




J Med Chem 35: 2697-703 (1992)


BindingDB Entry DOI: 10.7270/Q2K076G9
More data for this
Ligand-Target Pair
Carbonic anhydrase


(Homo sapiens (Human))
BDBM50212309
PNG
(CHEMBL91302)
Show SMILES NCCCCC(=O)Nc1nnc(s1)S(N)(=O)=O
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n/an/a 440n/an/an/an/an/an/a



Istituto Chimico Internazionale Dr. G. Rende

Curated by ChEMBL




J Med Chem 35: 2697-703 (1992)


BindingDB Entry DOI: 10.7270/Q2K076G9
More data for this
Ligand-Target Pair
Carbonic anhydrase


(Homo sapiens (Human))
BDBM10880
PNG
(AZA | AZA2 | AZM acetazolamide | Acerazolamide, AA...)
Show SMILES CC(=O)Nc1nnc(s1)S(N)(=O)=O
Show InChI InChI=1S/C4H6N4O3S2/c1-2(9)6-3-7-8-4(12-3)13(5,10)11/h1H3,(H2,5,10,11)(H,6,7,9)
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n/an/a 440n/an/an/an/an/an/a



Istituto Chimico Internazionale Dr. G. Rende

Curated by ChEMBL




J Med Chem 35: 2697-703 (1992)


BindingDB Entry DOI: 10.7270/Q2K076G9
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Carbonic anhydrase


(Homo sapiens (Human))
BDBM50229847
PNG
(CHEMBL91512)
Show SMILES COC(=O)CCC(=O)\N=c1\sc(nn1C)S(N)(=O)=O
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n/an/a 450n/an/an/an/an/an/a



Istituto Chimico Internazionale Dr. G. Rende

Curated by ChEMBL




J Med Chem 35: 2697-703 (1992)


BindingDB Entry DOI: 10.7270/Q2K076G9
More data for this
Ligand-Target Pair
Carbonic anhydrase


(Homo sapiens (Human))
BDBM50229846
PNG
(CHEMBL264307)
Show SMILES NS(=O)(=O)c1nnc(NC(=O)CCCCCCCC(O)=O)s1
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n/an/a 480n/an/an/an/an/an/a



Istituto Chimico Internazionale Dr. G. Rende

Curated by ChEMBL




J Med Chem 35: 2697-703 (1992)


BindingDB Entry DOI: 10.7270/Q2K076G9
More data for this
Ligand-Target Pair
Carbonic anhydrase


(Homo sapiens (Human))
BDBM50229835
PNG
(CHEMBL90857)
Show SMILES NS(=O)(=O)c1nnc(NC(=O)CCCCC(O)=O)s1
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n/an/a 520n/an/an/an/an/an/a



Istituto Chimico Internazionale Dr. G. Rende

Curated by ChEMBL




J Med Chem 35: 2697-703 (1992)


BindingDB Entry DOI: 10.7270/Q2K076G9
More data for this
Ligand-Target Pair
Carbonic anhydrase


(Homo sapiens (Human))
BDBM50229839
PNG
(CHEMBL91622)
Show SMILES CCCCCCCCCCCCOC(=O)CCC(=O)Nc1nnc(s1)S(N)(=O)=O
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n/an/a 520n/an/an/an/an/an/a



Istituto Chimico Internazionale Dr. G. Rende

Curated by ChEMBL




J Med Chem 35: 2697-703 (1992)


BindingDB Entry DOI: 10.7270/Q2K076G9
More data for this
Ligand-Target Pair
Carbonic anhydrase


(Homo sapiens (Human))
BDBM50229845
PNG
(CHEMBL91517)
Show SMILES NS(=O)(=O)c1nnc(NC(=O)CCCC(O)=O)s1
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n/an/a 520n/an/an/an/an/an/a



Istituto Chimico Internazionale Dr. G. Rende

Curated by ChEMBL




J Med Chem 35: 2697-703 (1992)


BindingDB Entry DOI: 10.7270/Q2K076G9
More data for this
Ligand-Target Pair
Carbonic anhydrase


(Homo sapiens (Human))
BDBM50229836
PNG
(CHEMBL92500)
Show SMILES COC(=O)CCC(=O)Nc1nnc(s1)S(N)(=O)=O
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n/an/a 550n/an/an/an/an/an/a



Istituto Chimico Internazionale Dr. G. Rende

Curated by ChEMBL




J Med Chem 35: 2697-703 (1992)


BindingDB Entry DOI: 10.7270/Q2K076G9
More data for this
Ligand-Target Pair
Carbonic anhydrase


(Homo sapiens (Human))
BDBM50185303
PNG
(CHEMBL88115)
Show SMILES NS(=O)(=O)c1nnc(NC(=O)CCC(O)=O)s1
Show InChI InChI=1S/C6H8N4O5S2/c7-17(14,15)6-10-9-5(16-6)8-3(11)1-2-4(12)13/h1-2H2,(H,12,13)(H2,7,14,15)(H,8,9,11)
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n/an/a 550n/an/an/an/an/an/a



Istituto Chimico Internazionale Dr. G. Rende

Curated by ChEMBL




J Med Chem 35: 2697-703 (1992)


BindingDB Entry DOI: 10.7270/Q2K076G9
More data for this
Ligand-Target Pair
Cholinesterases


(Homo sapiens (Human))
BDBM50285183
PNG
((2-Morpholin-4-yl-ethyl)-carbamic acid (3aS,8aR)-1...)
Show SMILES CN1CC[C@]2(C)[C@H]1N(C)c1ccc(OC(=O)NCCN3CCOCC3)cc21
Show InChI InChI=1S/C20H30N4O3/c1-20-6-8-22(2)18(20)23(3)17-5-4-15(14-16(17)20)27-19(25)21-7-9-24-10-12-26-13-11-24/h4-5,14,18H,6-13H2,1-3H3,(H,21,25)/t18-,20+/m1/s1
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n/an/a 700n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against Acetylcholinesterase from human RBC


Bioorg Med Chem Lett 5: 2077-2080 (1995)


Article DOI: 10.1016/0960-894X(95)00371-Y
BindingDB Entry DOI: 10.7270/Q2NP24CR
More data for this
Ligand-Target Pair
Carbonic anhydrase


(Homo sapiens (Human))
BDBM50229843
PNG
(CHEMBL91131)
Show SMILES CCOC(=O)CCC(=O)Nc1nnc(s1)S(N)(=O)=O
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n/an/a 730n/an/an/an/an/an/a



Istituto Chimico Internazionale Dr. G. Rende

Curated by ChEMBL




J Med Chem 35: 2697-703 (1992)


BindingDB Entry DOI: 10.7270/Q2K076G9
More data for this
Ligand-Target Pair
Carbonic anhydrase


(Homo sapiens (Human))
BDBM50229844
PNG
(CHEMBL328566)
Show SMILES COC(=O)CCCCCCCC(=O)Nc1nnc(s1)S(N)(=O)=O
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n/an/a 910n/an/an/an/an/an/a



Istituto Chimico Internazionale Dr. G. Rende

Curated by ChEMBL




J Med Chem 35: 2697-703 (1992)


BindingDB Entry DOI: 10.7270/Q2K076G9
More data for this
Ligand-Target Pair
Carbonic anhydrase


(Homo sapiens (Human))
BDBM50229837
PNG
(CHEMBL89489)
Show SMILES COC(=O)CCCC(=O)Nc1nnc(s1)S(N)(=O)=O
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n/an/a 910n/an/an/an/an/an/a



Istituto Chimico Internazionale Dr. G. Rende

Curated by ChEMBL




J Med Chem 35: 2697-703 (1992)


BindingDB Entry DOI: 10.7270/Q2K076G9
More data for this
Ligand-Target Pair
Cholinesterases


(Homo sapiens (Human))
BDBM50285178
PNG
((6-Morpholin-4-yl-hexyl)-carbamic acid (3aS,8aR)-1...)
Show SMILES CN1CC[C@]2(C)[C@H]1N(C)c1ccc(OC(=O)NCCCCCCN3CCOCC3)cc21
Show InChI InChI=1S/C24H38N4O3/c1-24-10-13-26(2)22(24)27(3)21-9-8-19(18-20(21)24)31-23(29)25-11-6-4-5-7-12-28-14-16-30-17-15-28/h8-9,18,22H,4-7,10-17H2,1-3H3,(H,25,29)/t22-,24+/m1/s1
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n/an/a 930n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of Acetylcholinesterase(AChE) from human RBC


Bioorg Med Chem Lett 5: 2077-2080 (1995)


Article DOI: 10.1016/0960-894X(95)00371-Y
BindingDB Entry DOI: 10.7270/Q2NP24CR
More data for this
Ligand-Target Pair
Carbonic anhydrase


(Homo sapiens (Human))
BDBM50229840
PNG
(CHEMBL329625)
Show SMILES COC(=O)CC(=O)Nc1nnc(s1)S(N)(=O)=O
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n/an/a 940n/an/an/an/an/an/a



Istituto Chimico Internazionale Dr. G. Rende

Curated by ChEMBL




J Med Chem 35: 2697-703 (1992)


BindingDB Entry DOI: 10.7270/Q2K076G9
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)
BDBM50069245
PNG
(CHEMBL157336 | N-[12-(Adamantan-1-ylamino)-dodecyl...)
Show SMILES CN(C)c1ccc(CC(=O)NCCCCCCCCCCCCNC23CC4CC(CC(C4)C2)C3)cc1 |TLB:33:24:31:28.27.29,THB:33:28:24.25.32:31,23:24:31:28.27.29,29:28:25:30.32.31,29:30:25:28.33.27|
Show InChI InChI=1S/C32H53N3O/c1-35(2)30-15-13-26(14-16-30)22-31(36)33-17-11-9-7-5-3-4-6-8-10-12-18-34-32-23-27-19-28(24-32)21-29(20-27)25-32/h13-16,27-29,34H,3-12,17-25H2,1-2H3,(H,33,36)
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n/an/a 3.30E+3n/an/an/an/an/an/a



Istituto di Strutturistica Chimica G. Giacomello

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase (AChE) in Torpedo californica


Bioorg Med Chem Lett 8: 575-80 (1999)


BindingDB Entry DOI: 10.7270/Q2S181N2
More data for this
Ligand-Target Pair
Cholinesterases


(Homo sapiens (Human))
BDBM50285186
PNG
((3-Morpholin-4-yl-propyl)-carbamic acid (3aS,8aR)-...)
Show SMILES CN1CC[C@]2(C)[C@H]1N(C)c1ccc(OC(=O)NCCCN3CCOCC3)cc21
Show InChI InChI=1S/C21H32N4O3/c1-21-7-10-23(2)19(21)24(3)18-6-5-16(15-17(18)21)28-20(26)22-8-4-9-25-11-13-27-14-12-25/h5-6,15,19H,4,7-14H2,1-3H3,(H,22,26)/t19-,21+/m1/s1
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n/an/a 3.80E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of Acetylcholinesterase(AChE) from human RBC


Bioorg Med Chem Lett 5: 2077-2080 (1995)


Article DOI: 10.1016/0960-894X(95)00371-Y
BindingDB Entry DOI: 10.7270/Q2NP24CR
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)
BDBM50069243
PNG
(CHEMBL153934 | N-[10-(Adamantan-1-ylamino)-decyl]-...)
Show SMILES CN(C)c1ccc(CC(=O)NCCCCCCCCCCNC23CC4CC(CC(C4)C2)C3)cc1 |TLB:31:22:29:26.25.27,THB:31:26:22.23.30:29,21:22:29:26.25.27,27:26:23:28.30.29,27:28:23:26.31.25|
Show InChI InChI=1S/C30H49N3O/c1-33(2)28-13-11-24(12-14-28)20-29(34)31-15-9-7-5-3-4-6-8-10-16-32-30-21-25-17-26(22-30)19-27(18-25)23-30/h11-14,25-27,32H,3-10,15-23H2,1-2H3,(H,31,34)
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n/an/a 5.30E+3n/an/an/an/an/an/a



Istituto di Strutturistica Chimica G. Giacomello

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase (AChE) in bovine erythrocytes


Bioorg Med Chem Lett 8: 575-80 (1999)


BindingDB Entry DOI: 10.7270/Q2S181N2
More data for this
Ligand-Target Pair
Cholinesterases


(Homo sapiens (Human))
BDBM50285181
PNG
((5-Morpholin-4-yl-pentyl)-carbamic acid (3aS,8aR)-...)
Show SMILES CN1CC[C@]2(C)[C@H]1N(C)c1ccc(OC(=O)NCCCCCN3CCOCC3)cc21
Show InChI InChI=1S/C23H36N4O3/c1-23-9-12-25(2)21(23)26(3)20-8-7-18(17-19(20)23)30-22(28)24-10-5-4-6-11-27-13-15-29-16-14-27/h7-8,17,21H,4-6,9-16H2,1-3H3,(H,24,28)/t21-,23+/m1/s1
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n/an/a 7.60E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of Acetylcholinesterase(AChE) from human RBC


Bioorg Med Chem Lett 5: 2077-2080 (1995)


Article DOI: 10.1016/0960-894X(95)00371-Y
BindingDB Entry DOI: 10.7270/Q2NP24CR
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50069245
PNG
(CHEMBL157336 | N-[12-(Adamantan-1-ylamino)-dodecyl...)
Show SMILES CN(C)c1ccc(CC(=O)NCCCCCCCCCCCCNC23CC4CC(CC(C4)C2)C3)cc1 |TLB:33:24:31:28.27.29,THB:33:28:24.25.32:31,23:24:31:28.27.29,29:28:25:30.32.31,29:30:25:28.33.27|
Show InChI InChI=1S/C32H53N3O/c1-35(2)30-15-13-26(14-16-30)22-31(36)33-17-11-9-7-5-3-4-6-8-10-12-18-34-32-23-27-19-28(24-32)21-29(20-27)25-32/h13-16,27-29,34H,3-12,17-25H2,1-2H3,(H,33,36)
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n/an/a 8.90E+3n/an/an/an/an/an/a



Istituto di Strutturistica Chimica G. Giacomello

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase (AChE) in electric eel


Bioorg Med Chem Lett 8: 575-80 (1999)


BindingDB Entry DOI: 10.7270/Q2S181N2
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)
BDBM50069244
PNG
(CHEMBL357551 | N-[8-(Adamantan-1-ylamino)-octyl]-2...)
Show SMILES CN(C)c1ccc(CC(=O)NCCCCCCCCNC23CC4CC(CC(C4)C2)C3)cc1 |TLB:29:20:27:24.23.25,THB:29:24:20.21.28:27,19:20:27:24.23.25,25:24:21:26.28.27,25:26:21:24.29.23|
Show InChI InChI=1S/C28H45N3O/c1-31(2)26-11-9-22(10-12-26)18-27(32)29-13-7-5-3-4-6-8-14-30-28-19-23-15-24(20-28)17-25(16-23)21-28/h9-12,23-25,30H,3-8,13-21H2,1-2H3,(H,29,32)
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n/an/a 1.00E+4n/an/an/an/an/an/a



Istituto di Strutturistica Chimica G. Giacomello

Curated by ChEMBL


Assay Description
Compound was evaluated for competitive inhibition constant of acetylcholinesterase (AChE) from Torpedo californica


Bioorg Med Chem Lett 8: 575-80 (1999)


BindingDB Entry DOI: 10.7270/Q2S181N2
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50069243
PNG
(CHEMBL153934 | N-[10-(Adamantan-1-ylamino)-decyl]-...)
Show SMILES CN(C)c1ccc(CC(=O)NCCCCCCCCCCNC23CC4CC(CC(C4)C2)C3)cc1 |TLB:31:22:29:26.25.27,THB:31:26:22.23.30:29,21:22:29:26.25.27,27:26:23:28.30.29,27:28:23:26.31.25|
Show InChI InChI=1S/C30H49N3O/c1-33(2)28-13-11-24(12-14-28)20-29(34)31-15-9-7-5-3-4-6-8-10-16-32-30-21-25-17-26(22-30)19-27(18-25)23-30/h11-14,25-27,32H,3-10,15-23H2,1-2H3,(H,31,34)
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n/an/a 1.40E+4n/an/an/an/an/an/a



Istituto di Strutturistica Chimica G. Giacomello

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of acetylcholinesterase in electric eel


Bioorg Med Chem Lett 8: 575-80 (1999)


BindingDB Entry DOI: 10.7270/Q2S181N2
More data for this
Ligand-Target Pair
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