BindingDB logo
myBDB logout

PubMed code 2374147

Compile data set for download or QSAR
Found 16 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
Glutamate receptor ionotropic, NMDA 2C


(Rattus norvegicus (Rat))
BDBM50015743
PNG
(Acetic acid 3-[1-(3,6-dihydro-2H-pyridin-1-yl)-cyc...)
Show SMILES CC(=O)Oc1cccc(c1)C1(CCCCC1)N1CCC=CC1 |c:21|
Show InChI InChI=1S/C19H25NO2/c1-16(21)22-18-10-8-9-17(15-18)19(11-4-2-5-12-19)20-13-6-3-7-14-20/h3,6,8-10,15H,2,4-5,7,11-14H2,1H3
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
6n/an/an/an/an/an/an/an/a



National Institute of Diabetes

Curated by ChEMBL


Assay Description
Ability to displace [3H]- TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.


J Med Chem 33: 2211-5 (1990)


BindingDB Entry DOI: 10.7270/Q2BZ6515
More data for this
Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C


(Rattus norvegicus (Rat))
BDBM50015738
PNG
(3-[1-(3,6-Dihydro-2H-pyridin-1-yl)-cyclohexyl]-phe...)
Show SMILES Oc1cccc(c1)C1(CCCCC1)N1CCC=CC1 |c:18|
Show InChI InChI=1S/C17H23NO/c19-16-9-7-8-15(14-16)17(10-3-1-4-11-17)18-12-5-2-6-13-18/h2,5,7-9,14,19H,1,3-4,6,10-13H2
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
7n/an/an/an/an/an/an/an/a



National Institute of Diabetes

Curated by ChEMBL


Assay Description
Ability to displace [3H]-TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.


J Med Chem 33: 2211-5 (1990)


BindingDB Entry DOI: 10.7270/Q2BZ6515
More data for this
Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C


(Rattus norvegicus (Rat))
BDBM50015734
PNG
(1-(1-Thiophen-2-yl-cyclohexyl)-1,2,3,6-tetrahydro-...)
Show SMILES C1CCC(CC1)(N1CCC=CC1)c1cccs1 |c:10|
Show InChI InChI=1S/C15H21NS/c1-3-9-15(10-4-1,14-8-7-13-17-14)16-11-5-2-6-12-16/h2,5,7-8,13H,1,3-4,6,9-12H2
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

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



National Institute of Diabetes

Curated by ChEMBL


Assay Description
Ability to displace [3H]-TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.


J Med Chem 33: 2211-5 (1990)


BindingDB Entry DOI: 10.7270/Q2BZ6515
More data for this
Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C


(Rattus norvegicus (Rat))
BDBM50015741
PNG
(1-[1-(3-Methoxy-phenyl)-cyclohexyl]-1,2,3,6-tetrah...)
Show SMILES COc1cccc(c1)C1(CCCCC1)N1CCC=CC1 |c:19|
Show InChI InChI=1S/C18H25NO/c1-20-17-10-8-9-16(15-17)18(11-4-2-5-12-18)19-13-6-3-7-14-19/h3,6,8-10,15H,2,4-5,7,11-14H2,1H3
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
33n/an/an/an/an/an/an/an/a



National Institute of Diabetes

Curated by ChEMBL


Assay Description
Ability to displace [3H]-TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.


J Med Chem 33: 2211-5 (1990)


BindingDB Entry DOI: 10.7270/Q2BZ6515
More data for this
Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C


(Rattus norvegicus (Rat))
BDBM50015732
PNG
(1-(1-Phenyl-cyclohexyl)-1,2,3,6-tetrahydro-pyridin...)
Show SMILES C1CCC(CC1)(N1CCC=CC1)c1ccccc1 |c:10|
Show InChI InChI=1S/C17H23N/c1-4-10-16(11-5-1)17(12-6-2-7-13-17)18-14-8-3-9-15-18/h1,3-5,8,10-11H,2,6-7,9,12-15H2
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
37n/an/an/an/an/an/an/an/a



National Institute of Diabetes

Curated by ChEMBL


Assay Description
Ability to displace [3H]- TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.


J Med Chem 33: 2211-5 (1990)


BindingDB Entry DOI: 10.7270/Q2BZ6515
More data for this
Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C


(Rattus norvegicus (Rat))
BDBM50015733
PNG
(3-[1-(3,6-Dihydro-2H-pyridin-1-yl)-cyclohexyl]-ben...)
Show SMILES O=NCc1cccc(c1)C1(CCCCC1)N1CCC=CC1 |c:20|
Show InChI InChI=1S/C18H24N2O/c21-19-15-16-8-7-9-17(14-16)18(10-3-1-4-11-18)20-12-5-2-6-13-20/h2,5,7-9,14H,1,3-4,6,10-13,15H2
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
56n/an/an/an/an/an/an/an/a



National Institute of Diabetes

Curated by ChEMBL


Assay Description
Ability to displace [3H]-TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.


J Med Chem 33: 2211-5 (1990)


BindingDB Entry DOI: 10.7270/Q2BZ6515
More data for this
Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C


(Rattus norvegicus (Rat))
BDBM50015735
PNG
(1-(1-m-Tolyl-cyclohexyl)-1,2,3,6-tetrahydro-pyridi...)
Show SMILES Cc1cccc(c1)C1(CCCCC1)N1CCC=CC1 |c:18|
Show InChI InChI=1S/C18H25N/c1-16-9-8-10-17(15-16)18(11-4-2-5-12-18)19-13-6-3-7-14-19/h3,6,8-10,15H,2,4-5,7,11-14H2,1H3
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
81n/an/an/an/an/an/an/an/a



National Institute of Diabetes

Curated by ChEMBL


Assay Description
Ability to displace [3H]- TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.


J Med Chem 33: 2211-5 (1990)


BindingDB Entry DOI: 10.7270/Q2BZ6515
More data for this
Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C


(Rattus norvegicus (Rat))
BDBM50015744
PNG
(1-[1-(3-Methoxymethoxy-phenyl)-cyclohexyl]-1,2,3,6...)
Show SMILES COCOc1cccc(c1)C1(CCCCC1)N1CCC=CC1 |c:21|
Show InChI InChI=1S/C19H27NO2/c1-21-16-22-18-10-8-9-17(15-18)19(11-4-2-5-12-19)20-13-6-3-7-14-20/h3,6,8-10,15H,2,4-5,7,11-14,16H2,1H3
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
92n/an/an/an/an/an/an/an/a



National Institute of Diabetes

Curated by ChEMBL


Assay Description
Ability to displace [3H]- TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.


J Med Chem 33: 2211-5 (1990)


BindingDB Entry DOI: 10.7270/Q2BZ6515
More data for this
Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C


(Rattus norvegicus (Rat))
BDBM50015740
PNG
(1-[1-(3-Vinyl-phenyl)-cyclohexyl]-1,2,3,6-tetrahyd...)
Show SMILES C=Cc1cccc(c1)C1(CCCCC1)N1CCC=CC1 |c:19|
Show InChI InChI=1S/C19H25N/c1-2-17-10-9-11-18(16-17)19(12-5-3-6-13-19)20-14-7-4-8-15-20/h2,4,7,9-11,16H,1,3,5-6,8,12-15H2
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
114n/an/an/an/an/an/an/an/a



National Institute of Diabetes

Curated by ChEMBL


Assay Description
Ability to displace [3H]- TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.


J Med Chem 33: 2211-5 (1990)


BindingDB Entry DOI: 10.7270/Q2BZ6515
More data for this
Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C


(Rattus norvegicus (Rat))
BDBM50015731
PNG
(1-[1-(3-Methylsulfanyl-phenyl)-cyclohexyl]-1,2,3,6...)
Show SMILES CSc1cccc(c1)C1(CCCCC1)N1CCC=CC1 |c:19|
Show InChI InChI=1S/C18H25NS/c1-20-17-10-8-9-16(15-17)18(11-4-2-5-12-18)19-13-6-3-7-14-19/h3,6,8-10,15H,2,4-5,7,11-14H2,1H3
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
PubMed
231n/an/an/an/an/an/an/an/a



National Institute of Diabetes

Curated by ChEMBL


Assay Description
Ability to displace [3H]- TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.


J Med Chem 33: 2211-5 (1990)


BindingDB Entry DOI: 10.7270/Q2BZ6515
More data for this
Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C


(Rattus norvegicus (Rat))
BDBM50015736
PNG
(1-[1-(3-Fluoro-phenyl)-cyclohexyl]-1,2,3,6-tetrahy...)
Show SMILES Fc1cccc(c1)C1(CCCCC1)N1CCC=CC1 |c:18|
Show InChI InChI=1S/C17H22FN/c18-16-9-7-8-15(14-16)17(10-3-1-4-11-17)19-12-5-2-6-13-19/h2,5,7-9,14H,1,3-4,6,10-13H2
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
281n/an/an/an/an/an/an/an/a



National Institute of Diabetes

Curated by ChEMBL


Assay Description
Ability to displace [3H]- TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.


J Med Chem 33: 2211-5 (1990)


BindingDB Entry DOI: 10.7270/Q2BZ6515
More data for this
Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C


(Rattus norvegicus (Rat))
BDBM50015739
PNG
(3-[1-(3,6-Dihydro-2H-pyridin-1-yl)-cyclohexyl]-ben...)
Show SMILES O=Cc1cccc(c1)C1(CCCCC1)N1CCC=CC1 |c:19|
Show InChI InChI=1S/C18H23NO/c20-15-16-8-7-9-17(14-16)18(10-3-1-4-11-18)19-12-5-2-6-13-19/h2,5,7-9,14-15H,1,3-4,6,10-13H2
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
324n/an/an/an/an/an/an/an/a



National Institute of Diabetes

Curated by ChEMBL


Assay Description
Ability to displace [3H]- TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.


J Med Chem 33: 2211-5 (1990)


BindingDB Entry DOI: 10.7270/Q2BZ6515
More data for this
Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C


(Rattus norvegicus (Rat))
BDBM50015730
PNG
(1-[1-(3-Trifluoromethyl-phenyl)-cyclohexyl]-1,2,3,...)
Show SMILES FC(F)(F)c1cccc(c1)C1(CCCCC1)N1CCC=CC1 |c:21|
Show InChI InChI=1S/C18H22F3N/c19-18(20,21)16-9-7-8-15(14-16)17(10-3-1-4-11-17)22-12-5-2-6-13-22/h2,5,7-9,14H,1,3-4,6,10-13H2
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
422n/an/an/an/an/an/an/an/a



National Institute of Diabetes

Curated by ChEMBL


Assay Description
Ability to displace [3H]- TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.


J Med Chem 33: 2211-5 (1990)


BindingDB Entry DOI: 10.7270/Q2BZ6515
More data for this
Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C


(Rattus norvegicus (Rat))
BDBM50015742
PNG
(1-[1-(3-[1,3]Dioxolan-2-yl-phenyl)-cyclohexyl]-1,2...)
Show SMILES C1COC(O1)c1cccc(c1)C1(CCCCC1)N1CCC=CC1 |c:23|
Show InChI InChI=1S/C20H27NO2/c1-3-10-20(11-4-1,21-12-5-2-6-13-21)18-9-7-8-17(16-18)19-22-14-15-23-19/h2,5,7-9,16,19H,1,3-4,6,10-15H2
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
PubMed
601n/an/an/an/an/an/an/an/a



National Institute of Diabetes

Curated by ChEMBL


Assay Description
Ability to displace [3H]-TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.


J Med Chem 33: 2211-5 (1990)


BindingDB Entry DOI: 10.7270/Q2BZ6515
More data for this
Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C


(Rattus norvegicus (Rat))
BDBM50015745
PNG
(1-[1-(3-Benzyloxy-phenyl)-cyclohexyl]-1,2,3,6-tetr...)
Show SMILES C(Oc1cccc(c1)C1(CCCCC1)N1CCC=CC1)c1ccccc1 |c:19|
Show InChI InChI=1S/C24H29NO/c1-4-11-21(12-5-1)20-26-23-14-10-13-22(19-23)24(15-6-2-7-16-24)25-17-8-3-9-18-25/h1,3-5,8,10-14,19H,2,6-7,9,15-18,20H2
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
733n/an/an/an/an/an/an/an/a



National Institute of Diabetes

Curated by ChEMBL


Assay Description
Ability to displace [3H]-TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.


J Med Chem 33: 2211-5 (1990)


BindingDB Entry DOI: 10.7270/Q2BZ6515
More data for this
Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C


(Rattus norvegicus (Rat))
BDBM50015737
PNG
(1-[1-(3,5-Dimethoxy-phenyl)-cyclohexyl]-1,2,3,6-te...)
Show SMILES COc1cc(OC)cc(c1)C1(CCCCC1)N1CCC=CC1 |c:21|
Show InChI InChI=1S/C19H27NO2/c1-21-17-13-16(14-18(15-17)22-2)19(9-5-3-6-10-19)20-11-7-4-8-12-20/h4,7,13-15H,3,5-6,8-12H2,1-2H3
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
8.60E+3n/an/an/an/an/an/an/an/a



National Institute of Diabetes

Curated by ChEMBL


Assay Description
Ability to displace [3H]-TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.


J Med Chem 33: 2211-5 (1990)


BindingDB Entry DOI: 10.7270/Q2BZ6515
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%