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Compile Data Set for Download or QSAR

Found 120 hits with Last Name = 'mingardi' 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
Metabotropic glutamate receptor 1


(RAT)
BDBM50204428
PNG
((S)-4-(3,3-dimethylbutan-2-yl) 2-propyl 3,5-dimeth...)
Show SMILES CCCOC(=O)c1[nH]c(C)c(C(=O)O[C@@H](C)C(C)(C)C)c1C
Show InChI InChI=1S/C17H27NO4/c1-8-9-21-16(20)14-10(2)13(11(3)18-14)15(19)22-12(4)17(5,6)7/h12,18H,8-9H2,1-7H3/t12-/m0/s1
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n/an/a 16n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
Corticotropin-releasing factor receptor 1


(Homo sapiens (Human))
BDBM50116105
PNG
(3-(6-(dimethylamino)-4-methylpyridin-3-yl)-2,5-dim...)
Show SMILES CCCN(CCC)c1cc(C)nc2c(c(C)nn12)-c1cnc(cc1C)N(C)C |(-1.91,-13.39,;-3.24,-14.16,;-4.58,-13.4,;-5.91,-14.18,;-7.24,-13.41,;-8.57,-14.19,;-9.91,-13.42,;-5.9,-15.72,;-7.22,-16.49,;-7.23,-18.03,;-8.56,-18.8,;-5.9,-18.8,;-4.55,-18.03,;-3.07,-18.5,;-2.16,-17.24,;-.62,-17.23,;-3.09,-15.99,;-4.56,-16.48,;-2.58,-19.96,;-3.61,-21.11,;-3.13,-22.57,;-1.62,-22.88,;-.59,-21.72,;-1.08,-20.27,;-.06,-19.11,;-1.13,-24.34,;.38,-24.65,;-2.15,-25.5,)|
Show InChI InChI=1S/C22H32N6/c1-8-10-27(11-9-2)20-13-16(4)24-22-21(17(5)25-28(20)22)18-14-23-19(26(6)7)12-15(18)3/h12-14H,8-11H2,1-7H3
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n/an/a 28.2n/an/an/an/an/an/a



GlaxoSmithKline Medicines Research Centre

Curated by ChEMBL


Assay Description
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells


J Med Chem 51: 7370-9 (2009)


Article DOI: 10.1021/jm800744m
BindingDB Entry DOI: 10.7270/Q2N87C1X
More data for this
Ligand-Target Pair
Corticotropin-releasing factor receptor 1


(Homo sapiens (Human))
BDBM50412811
PNG
(CHEMBL458810)
Show SMILES Cc1cc(c2CCN(c2n1)c1ccc(cc1C(F)(F)F)C#N)-n1ccc(n1)N1CCNC1=O
Show InChI InChI=1S/C22H18F3N7O/c1-13-10-18(32-8-5-19(29-32)31-9-6-27-21(31)33)15-4-7-30(20(15)28-13)17-3-2-14(12-26)11-16(17)22(23,24)25/h2-3,5,8,10-11H,4,6-7,9H2,1H3,(H,27,33)
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n/an/a 32.4n/an/an/an/an/an/a



GlaxoSmithKline Medicines Research Centre

Curated by ChEMBL


Assay Description
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells


J Med Chem 51: 7370-9 (2009)


Article DOI: 10.1021/jm800744m
BindingDB Entry DOI: 10.7270/Q2N87C1X
More data for this
Ligand-Target Pair
Corticotropin-releasing factor receptor 1


(Homo sapiens (Human))
BDBM50084875
PNG
(8-(2,4-dichlorophenyl)-N-(1,3-dimethoxypropan-2-yl...)
Show SMILES COCC(COC)Nc1nc(C)nc2c(c(C)nn12)-c1ccc(Cl)cc1Cl |(-3.04,-6.69,;-3.03,-8.23,;-4.37,-9,;-4.37,-10.54,;-3.03,-11.31,;-1.7,-10.54,;-1.7,-9.01,;-5.7,-11.31,;-5.7,-12.85,;-7.03,-13.63,;-7.03,-15.17,;-8.36,-15.94,;-5.7,-15.93,;-4.37,-15.17,;-2.91,-15.64,;-2,-14.4,;-.46,-14.4,;-2.91,-13.15,;-4.37,-13.63,;-2.18,-17.01,;-3.01,-18.3,;-2.29,-19.67,;-.75,-19.73,;-.03,-21.08,;.06,-18.41,;-.65,-17.05,;.16,-15.75,)|
Show InChI InChI=1S/C18H21Cl2N5O2/c1-10-16(14-6-5-12(19)7-15(14)20)17-21-11(2)22-18(25(17)24-10)23-13(8-26-3)9-27-4/h5-7,13H,8-9H2,1-4H3,(H,21,22,23)
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n/an/a 39.8n/an/an/an/an/an/a



GlaxoSmithKline Medicines Research Centre

Curated by ChEMBL


Assay Description
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells


J Med Chem 51: 7370-9 (2009)


Article DOI: 10.1021/jm800744m
BindingDB Entry DOI: 10.7270/Q2N87C1X
More data for this
Ligand-Target Pair
Corticotropin-releasing factor receptor 1


(Homo sapiens (Human))
BDBM50412814
PNG
(CHEMBL456660)
Show SMILES CCc1cc(ccc1N1CCc2c1nc(C)cc2-n1ccc(n1)N1CCNC1=O)C#N
Show InChI InChI=1S/C23H23N7O/c1-3-17-13-16(14-24)4-5-19(17)28-9-6-18-20(12-15(2)26-22(18)28)30-10-7-21(27-30)29-11-8-25-23(29)31/h4-5,7,10,12-13H,3,6,8-9,11H2,1-2H3,(H,25,31)
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n/an/a 50.1n/an/an/an/an/an/a



GlaxoSmithKline Medicines Research Centre

Curated by ChEMBL


Assay Description
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells


J Med Chem 51: 7370-9 (2009)


Article DOI: 10.1021/jm800744m
BindingDB Entry DOI: 10.7270/Q2N87C1X
More data for this
Ligand-Target Pair
Corticotropin-releasing factor receptor 1


(Homo sapiens (Human))
BDBM50412812
PNG
(CHEMBL459173)
Show SMILES COc1ccc(N2CCc3c2nc(C)cc3-n2ccc(n2)N2CCNC2=O)c(c1)C(F)F
Show InChI InChI=1S/C22H22F2N6O2/c1-13-11-18(30-9-6-19(27-30)29-10-7-25-22(29)31)15-5-8-28(21(15)26-13)17-4-3-14(32-2)12-16(17)20(23)24/h3-4,6,9,11-12,20H,5,7-8,10H2,1-2H3,(H,25,31)
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n/an/a 56.2n/an/an/an/an/an/a



GlaxoSmithKline Medicines Research Centre

Curated by ChEMBL


Assay Description
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells


J Med Chem 51: 7370-9 (2009)


Article DOI: 10.1021/jm800744m
BindingDB Entry DOI: 10.7270/Q2N87C1X
More data for this
Ligand-Target Pair
Corticotropin-releasing factor receptor 1


(Homo sapiens (Human))
BDBM50412798
PNG
(EMICERFONT)
Show SMILES COc1ccc(N2CCc3c2nc(C)cc3-n2ccc(n2)N2CCNC2=O)c(C)c1
Show InChI InChI=1S/C22H24N6O2/c1-14-12-16(30-3)4-5-18(14)26-9-6-17-19(13-15(2)24-21(17)26)28-10-7-20(25-28)27-11-8-23-22(27)29/h4-5,7,10,12-13H,6,8-9,11H2,1-3H3,(H,23,29)
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n/an/a 66.1n/an/an/an/an/an/a



GlaxoSmithKline Medicines Research Centre

Curated by ChEMBL


Assay Description
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells


J Med Chem 51: 7370-9 (2009)


Article DOI: 10.1021/jm800744m
BindingDB Entry DOI: 10.7270/Q2N87C1X
More data for this
Ligand-Target Pair
Corticotropin-releasing factor receptor 1


(Homo sapiens (Human))
BDBM50412808
PNG
(CHEMBL456640)
Show SMILES Cc1cc(c2CCN(c2n1)c1ccc(OC(F)(F)F)cc1C)-n1ccc(n1)N1CCNC1=O
Show InChI InChI=1S/C22H21F3N6O2/c1-13-11-15(33-22(23,24)25)3-4-17(13)29-8-5-16-18(12-14(2)27-20(16)29)31-9-6-19(28-31)30-10-7-26-21(30)32/h3-4,6,9,11-12H,5,7-8,10H2,1-2H3,(H,26,32)
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n/an/a 67.6n/an/an/an/an/an/a



GlaxoSmithKline Medicines Research Centre

Curated by ChEMBL


Assay Description
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells


J Med Chem 51: 7370-9 (2009)


Article DOI: 10.1021/jm800744m
BindingDB Entry DOI: 10.7270/Q2N87C1X
More data for this
Ligand-Target Pair
Corticotropin-releasing factor receptor 1


(Homo sapiens (Human))
BDBM50412809
PNG
(CHEMBL516170)
Show SMILES Cc1cc(c2CCN(c2n1)c1ccc(cc1C)C#N)-n1ccc(n1)N1CCNC1=O
Show InChI InChI=1S/C22H21N7O/c1-14-11-16(13-23)3-4-18(14)27-8-5-17-19(12-15(2)25-21(17)27)29-9-6-20(26-29)28-10-7-24-22(28)30/h3-4,6,9,11-12H,5,7-8,10H2,1-2H3,(H,24,30)
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n/an/a 67.6n/an/an/an/an/an/a



GlaxoSmithKline Medicines Research Centre

Curated by ChEMBL


Assay Description
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells


J Med Chem 51: 7370-9 (2009)


Article DOI: 10.1021/jm800744m
BindingDB Entry DOI: 10.7270/Q2N87C1X
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 1


(RAT)
BDBM50204429
PNG
(CHEMBL388669 | adamantane-1-carboxylic acid (1-oxo...)
Show SMILES O=C(Nc1ccc2[nH]c3c(CCNC3=O)c2c1)C12CC3CC(CC(C3)C1)C2 |TLB:20:21:25:19.24.18,THB:18:19:22:25.26.17,18:17:20.19.24:22,20:19:25:21.22.26|
Show InChI InChI=1S/C22H25N3O2/c26-20-19-16(3-4-23-20)17-8-15(1-2-18(17)25-19)24-21(27)22-9-12-5-13(10-22)7-14(6-12)11-22/h1-2,8,12-14,25H,3-7,9-11H2,(H,23,26)(H,24,27)
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n/an/a 71n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 1


(RAT)
BDBM50204434
PNG
(1-oxo-2,3,4,9-tetrahydro-1H-beta-carboline-6-carbo...)
Show SMILES O=C(NC12CC3CC(CC(C3)C1)C2)c1ccc2[nH]c3c(CCNC3=O)c2c1 |THB:2:3:6:10.8.9,8:7:4:10.9.11,8:9:6.7.12:4,11:9:6:12.3.4,11:3:6:10.8.9|
Show InChI InChI=1S/C22H25N3O2/c26-20(25-22-9-12-5-13(10-22)7-14(6-12)11-22)15-1-2-18-17(8-15)16-3-4-23-21(27)19(16)24-18/h1-2,8,12-14,24H,3-7,9-11H2,(H,23,27)(H,25,26)
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n/an/a 71n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
Corticotropin-releasing factor receptor 1


(Homo sapiens (Human))
BDBM50412817
PNG
(CHEMBL464185)
Show SMILES Cc1cc(c2CCN(c2n1)c1ccc(cc1C(F)(F)F)C(F)(F)F)-n1ccc(n1)-n1cc[nH]c1=O
Show InChI InChI=1S/C22H16F6N6O/c1-12-10-17(34-8-5-18(31-34)33-9-6-29-20(33)35)14-4-7-32(19(14)30-12)16-3-2-13(21(23,24)25)11-15(16)22(26,27)28/h2-3,5-6,8-11H,4,7H2,1H3,(H,29,35)
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n/an/a 89.1n/an/an/an/an/an/a



GlaxoSmithKline Medicines Research Centre

Curated by ChEMBL


Assay Description
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells


J Med Chem 51: 7370-9 (2009)


Article DOI: 10.1021/jm800744m
BindingDB Entry DOI: 10.7270/Q2N87C1X
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 1


(RAT)
BDBM50204446
PNG
(1-oxo-2,3,4,9-tetrahydro-1H-beta-carboline-6-carbo...)
Show SMILES O=C(NC1C2CC3CC(C2)CC1C3)c1ccc2[nH]c3c(CCNC3=O)c2c1 |TLB:9:8:12:5.4.3,9:4:7.8.10:12,THB:3:4:7:10.11.12,3:11:7:5.9.4,2:3:7.8.10:12,(-2.07,-19.86,;-2.06,-21.41,;-3.4,-22.18,;-4.74,-21.42,;-6.1,-22.09,;-7.03,-21,;-7.2,-19.6,;-8.87,-19.1,;-7.82,-20.25,;-7.69,-21.76,;-6.41,-19.53,;-4.85,-19.91,;-5.88,-18.92,;-.72,-22.17,;-.72,-23.71,;.62,-24.48,;1.95,-23.69,;3.42,-24.16,;4.28,-22.89,;3.41,-21.67,;4.03,-20.27,;5.56,-20.09,;6.46,-21.34,;5.85,-22.75,;6.76,-23.99,;1.94,-22.16,;.6,-21.39,)|
Show InChI InChI=1S/C22H25N3O2/c26-21(25-19-14-6-11-5-12(8-14)9-15(19)7-11)13-1-2-18-17(10-13)16-3-4-23-22(27)20(16)24-18/h1-2,10-12,14-15,19,24H,3-9H2,(H,23,27)(H,25,26)
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n/an/a 93n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 1


(RAT)
BDBM50204435
PNG
(6-(benzyloxy)-3,4-dihydro-2H-pyrido[3,4-b]indol-1(...)
Show SMILES O=C1NCCc2c1[nH]c1ccc(OCc3ccccc3)cc21
Show InChI InChI=1S/C18H16N2O2/c21-18-17-14(8-9-19-18)15-10-13(6-7-16(15)20-17)22-11-12-4-2-1-3-5-12/h1-7,10,20H,8-9,11H2,(H,19,21)
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n/an/a 104n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 1


(RAT)
BDBM50204445
PNG
(CHEMBL234960 | N-(3,3-dimethylbutan-2-yl)-N-methyl...)
Show SMILES CC(N(C)C(=O)c1ccc2[nH]c3c(CCNC3=O)c2c1)C(C)(C)C |w:1.0|
Show InChI InChI=1S/C19H25N3O2/c1-11(19(2,3)4)22(5)18(24)12-6-7-15-14(10-12)13-8-9-20-17(23)16(13)21-15/h6-7,10-11,21H,8-9H2,1-5H3,(H,20,23)
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n/an/a 120n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
Corticotropin-releasing factor receptor 1


(Homo sapiens (Human))
BDBM50412802
PNG
(CHEMBL515363)
Show SMILES COc1ccc(N2CCc3c2nc(C)cc3-n2ccc(n2)-n2cc[nH]c2=O)c(C)c1
Show InChI InChI=1S/C22H22N6O2/c1-14-12-16(30-3)4-5-18(14)26-9-6-17-19(13-15(2)24-21(17)26)28-10-7-20(25-28)27-11-8-23-22(27)29/h4-5,7-8,10-13H,6,9H2,1-3H3,(H,23,29)
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n/an/a 120n/an/an/an/an/an/a



GlaxoSmithKline Medicines Research Centre

Curated by ChEMBL


Assay Description
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells


J Med Chem 51: 7370-9 (2009)


Article DOI: 10.1021/jm800744m
BindingDB Entry DOI: 10.7270/Q2N87C1X
More data for this
Ligand-Target Pair
Corticotropin-releasing factor receptor 1


(Homo sapiens (Human))
BDBM50412813
PNG
(CHEMBL513937)
Show SMILES Cc1cc(c2CCN(c2n1)c1ccc(cc1OC(F)(F)F)C#N)-n1ccc(n1)N1CCNC1=O
Show InChI InChI=1S/C22H18F3N7O2/c1-13-10-17(32-8-5-19(29-32)31-9-6-27-21(31)33)15-4-7-30(20(15)28-13)16-3-2-14(12-26)11-18(16)34-22(23,24)25/h2-3,5,8,10-11H,4,6-7,9H2,1H3,(H,27,33)
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n/an/a 120n/an/an/an/an/an/a



GlaxoSmithKline Medicines Research Centre

Curated by ChEMBL


Assay Description
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells


J Med Chem 51: 7370-9 (2009)


Article DOI: 10.1021/jm800744m
BindingDB Entry DOI: 10.7270/Q2N87C1X
More data for this
Ligand-Target Pair
Corticotropin-releasing factor receptor 1


(Homo sapiens (Human))
BDBM50412799
PNG
(CHEMBL458599)
Show SMILES COc1ccc(N2CCc3c2nc(C)cc3-n2ccc(n2)N2CCCC2=O)c(C)c1
Show InChI InChI=1S/C23H25N5O2/c1-15-13-17(30-3)6-7-19(15)26-11-8-18-20(14-16(2)24-23(18)26)28-12-9-21(25-28)27-10-4-5-22(27)29/h6-7,9,12-14H,4-5,8,10-11H2,1-3H3
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n/an/a 123n/an/an/an/an/an/a



GlaxoSmithKline Medicines Research Centre

Curated by ChEMBL


Assay Description
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells


J Med Chem 51: 7370-9 (2009)


Article DOI: 10.1021/jm800744m
BindingDB Entry DOI: 10.7270/Q2N87C1X
More data for this
Ligand-Target Pair
Corticotropin-releasing factor receptor 1


(Homo sapiens (Human))
BDBM50412803
PNG
(CHEMBL456448)
Show SMILES COc1ccc(N2CCc3c2nc(C)cc3-n2ccc(n2)N2CCCNC2=O)c(C)c1
Show InChI InChI=1S/C23H26N6O2/c1-15-13-17(31-3)5-6-19(15)27-11-7-18-20(14-16(2)25-22(18)27)29-12-8-21(26-29)28-10-4-9-24-23(28)30/h5-6,8,12-14H,4,7,9-11H2,1-3H3,(H,24,30)
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n/an/a 145n/an/an/an/an/an/a



GlaxoSmithKline Medicines Research Centre

Curated by ChEMBL


Assay Description
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells


J Med Chem 51: 7370-9 (2009)


Article DOI: 10.1021/jm800744m
BindingDB Entry DOI: 10.7270/Q2N87C1X
More data for this
Ligand-Target Pair
Corticotropin-releasing factor receptor 1


(Homo sapiens (Human))
BDBM50412816
PNG
(CHEMBL464184)
Show SMILES Cc1cc(c2CCN(c2n1)c1ccc(Cl)cc1Cl)-n1ccc(n1)-n1cc[nH]c1=O
Show InChI InChI=1S/C20H16Cl2N6O/c1-12-10-17(28-8-5-18(25-28)27-9-6-23-20(27)29)14-4-7-26(19(14)24-12)16-3-2-13(21)11-15(16)22/h2-3,5-6,8-11H,4,7H2,1H3,(H,23,29)
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n/an/a 158n/an/an/an/an/an/a



GlaxoSmithKline Medicines Research Centre

Curated by ChEMBL


Assay Description
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells


J Med Chem 51: 7370-9 (2009)


Article DOI: 10.1021/jm800744m
BindingDB Entry DOI: 10.7270/Q2N87C1X
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 1


(RAT)
BDBM50204433
PNG
(6-(benzyloxy)-7-methyl-3,4-dihydro-2H-pyrido[3,4-b...)
Show SMILES Cc1cc2[nH]c3c(CCNC3=O)c2cc1OCc1ccccc1
Show InChI InChI=1S/C19H18N2O2/c1-12-9-16-15(14-7-8-20-19(22)18(14)21-16)10-17(12)23-11-13-5-3-2-4-6-13/h2-6,9-10,21H,7-8,11H2,1H3,(H,20,22)
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n/an/a 167n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 1


(RAT)
BDBM50204427
PNG
(CHEMBL243020 | N-(bicyclo[2.2.1]heptan-2-yl)-1-oxo...)
Show SMILES O=C(NC1CC2CCC1C2)c1ccc2[nH]c3c(CCNC3=O)c2c1 |w:8.7,5.5,3.2,TEB:2:3:6.7:9|
Show InChI InChI=1S/C19H21N3O2/c23-18(22-16-8-10-1-2-11(16)7-10)12-3-4-15-14(9-12)13-5-6-20-19(24)17(13)21-15/h3-4,9-11,16,21H,1-2,5-8H2,(H,20,24)(H,22,23)
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n/an/a 226n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 1


(RAT)
BDBM50204439
PNG
(6-(3,3-dimethylbutan-2-yloxy)-3,4-dihydro-2H-pyrid...)
Show SMILES CC(Oc1ccc2[nH]c3c(CCNC3=O)c2c1)C(C)(C)C |w:1.0|
Show InChI InChI=1S/C17H22N2O2/c1-10(17(2,3)4)21-11-5-6-14-13(9-11)12-7-8-18-16(20)15(12)19-14/h5-6,9-10,19H,7-8H2,1-4H3,(H,18,20)
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n/an/a 239n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
Corticotropin-releasing factor receptor 1


(Homo sapiens (Human))
BDBM50412804
PNG
(CHEMBL456449)
Show SMILES COc1ccc(N2CCc3c2nc(C)cc3-n2ccc(n2)N2CCNS2(=O)=O)c(C)c1
Show InChI InChI=1S/C21H24N6O3S/c1-14-12-16(30-3)4-5-18(14)25-9-6-17-19(13-15(2)23-21(17)25)26-10-7-20(24-26)27-11-8-22-31(27,28)29/h4-5,7,10,12-13,22H,6,8-9,11H2,1-3H3
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n/an/a 309n/an/an/an/an/an/a



GlaxoSmithKline Medicines Research Centre

Curated by ChEMBL


Assay Description
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells


J Med Chem 51: 7370-9 (2009)


Article DOI: 10.1021/jm800744m
BindingDB Entry DOI: 10.7270/Q2N87C1X
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 1


(RAT)
BDBM50204444
PNG
(1-oxo-2,3,4,9-tetrahydro-1H-beta-carboline-6-carbo...)
Show SMILES O=C(NCC12CC3CC(CC(C3)C1)C2)c1ccc2[nH]c3c(CCNC3=O)c2c1 |TLB:3:4:7:11.9.10,THB:9:8:5:11.10.12,9:10:7.8.13:5,12:10:7:13.4.5,12:4:7:11.9.10|
Show InChI InChI=1S/C23H27N3O2/c27-21(25-12-23-9-13-5-14(10-23)7-15(6-13)11-23)16-1-2-19-18(8-16)17-3-4-24-22(28)20(17)26-19/h1-2,8,13-15,26H,3-7,9-12H2,(H,24,28)(H,25,27)
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n/an/a 312n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
Corticotropin-releasing factor receptor 1


(Homo sapiens (Human))
BDBM50412806
PNG
(CHEMBL457710)
Show SMILES CCOc1ccc(N2CCc3c2nc(C)cc3-n2ccc(n2)N2CCNC2=O)c(C)c1
Show InChI InChI=1S/C23H26N6O2/c1-4-31-17-5-6-19(15(2)13-17)27-10-7-18-20(14-16(3)25-22(18)27)29-11-8-21(26-29)28-12-9-24-23(28)30/h5-6,8,11,13-14H,4,7,9-10,12H2,1-3H3,(H,24,30)
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n/an/a 316n/an/an/an/an/an/a



GlaxoSmithKline Medicines Research Centre

Curated by ChEMBL


Assay Description
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells


J Med Chem 51: 7370-9 (2009)


Article DOI: 10.1021/jm800744m
BindingDB Entry DOI: 10.7270/Q2N87C1X
More data for this
Ligand-Target Pair
Corticotropin-releasing factor receptor 1


(Homo sapiens (Human))
BDBM50412815
PNG
(CHEMBL457742)
Show SMILES COc1cc(ccc1N1CCc2c1nc(C)cc2-n1ccc(n1)-n1cc[nH]c1=O)-n1cccn1
Show InChI InChI=1S/C24H22N8O2/c1-16-14-20(32-12-7-22(28-32)30-13-9-25-24(30)33)18-6-11-29(23(18)27-16)19-5-4-17(15-21(19)34-2)31-10-3-8-26-31/h3-5,7-10,12-15H,6,11H2,1-2H3,(H,25,33)
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n/an/a 363n/an/an/an/an/an/a



GlaxoSmithKline Medicines Research Centre

Curated by ChEMBL


Assay Description
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells


J Med Chem 51: 7370-9 (2009)


Article DOI: 10.1021/jm800744m
BindingDB Entry DOI: 10.7270/Q2N87C1X
More data for this
Ligand-Target Pair
Corticotropin-releasing factor receptor 1


(Homo sapiens (Human))
BDBM50412810
PNG
(CHEMBL458626)
Show SMILES Cc1cc(c2CCN(c2n1)c1ccc(cc1C)-n1cccn1)-n1ccc(n1)N1CCNC1=O
Show InChI InChI=1S/C24H24N8O/c1-16-14-18(31-10-3-8-26-31)4-5-20(16)29-11-6-19-21(15-17(2)27-23(19)29)32-12-7-22(28-32)30-13-9-25-24(30)33/h3-5,7-8,10,12,14-15H,6,9,11,13H2,1-2H3,(H,25,33)
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n/an/a 372n/an/an/an/an/an/a



GlaxoSmithKline Medicines Research Centre

Curated by ChEMBL


Assay Description
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells


J Med Chem 51: 7370-9 (2009)


Article DOI: 10.1021/jm800744m
BindingDB Entry DOI: 10.7270/Q2N87C1X
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 1


(RAT)
BDBM50204443
PNG
(6-(1-phenylethoxy)-3,4-dihydro-2H-pyrido[3,4-b]ind...)
Show SMILES CC(Oc1ccc2[nH]c3c(CCNC3=O)c2c1)c1ccccc1 |w:1.0|
Show InChI InChI=1S/C19H18N2O2/c1-12(13-5-3-2-4-6-13)23-14-7-8-17-16(11-14)15-9-10-20-19(22)18(15)21-17/h2-8,11-12,21H,9-10H2,1H3,(H,20,22)
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n/an/a 380n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
Cytochrome P450 1A2


(Homo sapiens (Human))
BDBM50323798
PNG
(CHEMBL1214336 | N-[5-(3-pyridinyl)-2,3-dihydro-1H-...)
Show SMILES CC(C)S(=O)(=O)NC1Cc2ccc(cc2C1)-c1cccnc1
Show InChI InChI=1S/C17H20N2O2S/c1-12(2)22(20,21)19-17-9-14-6-5-13(8-16(14)10-17)15-4-3-7-18-11-15/h3-8,11-12,17,19H,9-10H2,1-2H3
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n/an/a 600n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibition of human CYP1A2 after 10 mins


J Med Chem 53: 5801-12 (2010)


Article DOI: 10.1021/jm1005429
BindingDB Entry DOI: 10.7270/Q2FT8N0T
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 1


(RAT)
BDBM50204442
PNG
(7-(benzyloxy)-1,2-dihydropyrrolo[3,4-b]indol-3(4H)...)
Show SMILES O=C1NCc2c1[nH]c1ccc(OCc3ccccc3)cc21
Show InChI InChI=1S/C17H14N2O2/c20-17-16-14(9-18-17)13-8-12(6-7-15(13)19-16)21-10-11-4-2-1-3-5-11/h1-8,19H,9-10H2,(H,18,20)
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n/an/a 683n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
Corticotropin-releasing factor receptor 1


(Homo sapiens (Human))
BDBM50412800
PNG
(CHEMBL515532)
Show SMILES COc1ccc(N2CCc3c2nc(C)cc3-n2ccc(n2)N2CCN(C)C2=O)c(C)c1
Show InChI InChI=1S/C23H26N6O2/c1-15-13-17(31-4)5-6-19(15)27-9-7-18-20(14-16(2)24-22(18)27)29-10-8-21(25-29)28-12-11-26(3)23(28)30/h5-6,8,10,13-14H,7,9,11-12H2,1-4H3
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n/an/a 794n/an/an/an/an/an/a



GlaxoSmithKline Medicines Research Centre

Curated by ChEMBL


Assay Description
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells


J Med Chem 51: 7370-9 (2009)


Article DOI: 10.1021/jm800744m
BindingDB Entry DOI: 10.7270/Q2N87C1X
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 1


(RAT)
BDBM50204431
PNG
(8-benzyloxy-3,4a,5,9b-tetrahydro-pyridazino[4,5-b]...)
Show SMILES O=C1NNCc2c1[nH]c1ccc(OCc3ccccc3)cc21
Show InChI InChI=1S/C17H15N3O2/c21-17-16-14(9-18-20-17)13-8-12(6-7-15(13)19-16)22-10-11-4-2-1-3-5-11/h1-8,18-19H,9-10H2,(H,20,21)
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n/an/a 1.02E+3n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 1


(RAT)
BDBM50204430
PNG
(1-oxo-N-phenyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]...)
Show SMILES O=C(Nc1ccccc1)c1ccc2[nH]c3c(CCNC3=O)c2c1
Show InChI InChI=1S/C18H15N3O2/c22-17(20-12-4-2-1-3-5-12)11-6-7-15-14(10-11)13-8-9-19-18(23)16(13)21-15/h1-7,10,21H,8-9H2,(H,19,23)(H,20,22)
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n/an/a 1.04E+3n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
Corticotropin-releasing factor receptor 1


(Homo sapiens (Human))
BDBM50412807
PNG
(CHEMBL457975)
Show SMILES CC(C)Oc1ccc(N2CCc3c2nc(C)cc3-n2ccc(n2)N2CCNC2=O)c(C)c1
Show InChI InChI=1S/C24H28N6O2/c1-15(2)32-18-5-6-20(16(3)13-18)28-10-7-19-21(14-17(4)26-23(19)28)30-11-8-22(27-30)29-12-9-25-24(29)31/h5-6,8,11,13-15H,7,9-10,12H2,1-4H3,(H,25,31)
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n/an/a 1.23E+3n/an/an/an/an/an/a



GlaxoSmithKline Medicines Research Centre

Curated by ChEMBL


Assay Description
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells


J Med Chem 51: 7370-9 (2009)


Article DOI: 10.1021/jm800744m
BindingDB Entry DOI: 10.7270/Q2N87C1X
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 1


(RAT)
BDBM50204432
PNG
(6-benzyloxy-2,3,4,4a,9,9a-hexahydro-beta-carbolin-...)
Show SMILES O=C1NCCC2C1Nc1ccc(OCc3ccccc3)cc21 |w:5.4,6.7|
Show InChI InChI=1S/C18H18N2O2/c21-18-17-14(8-9-19-18)15-10-13(6-7-16(15)20-17)22-11-12-4-2-1-3-5-12/h1-7,10,14,17,20H,8-9,11H2,(H,19,21)
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n/an/a 1.67E+3n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
Corticotropin-releasing factor receptor 1


(Homo sapiens (Human))
BDBM50412801
PNG
(CHEMBL458600)
Show SMILES COc1ccc(N2CCc3c2nc(C)cc3-n2ccc(n2)N2CCOC2=O)c(C)c1
Show InChI InChI=1S/C22H23N5O3/c1-14-12-16(29-3)4-5-18(14)25-8-6-17-19(13-15(2)23-21(17)25)27-9-7-20(24-27)26-10-11-30-22(26)28/h4-5,7,9,12-13H,6,8,10-11H2,1-3H3
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n/an/a 1.95E+3n/an/an/an/an/an/a



GlaxoSmithKline Medicines Research Centre

Curated by ChEMBL


Assay Description
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells


J Med Chem 51: 7370-9 (2009)


Article DOI: 10.1021/jm800744m
BindingDB Entry DOI: 10.7270/Q2N87C1X
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 1


(RAT)
BDBM50204437
PNG
(7-(benzyloxy)-3,4-dihydro-2H-pyrido[3,4-b]indol-1(...)
Show SMILES O=C1NCCc2c1[nH]c1cc(OCc3ccccc3)ccc21
Show InChI InChI=1S/C18H16N2O2/c21-18-17-15(8-9-19-18)14-7-6-13(10-16(14)20-17)22-11-12-4-2-1-3-5-12/h1-7,10,20H,8-9,11H2,(H,19,21)
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n/an/a 2.85E+3n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
Corticotropin-releasing factor receptor 1


(Homo sapiens (Human))
BDBM50412805
PNG
(CHEMBL515503)
Show SMILES COc1ccc(N2CCc3c2nc(C)cc3-n2ccc(n2)N2CCCS2(=O)=O)c(C)c1
Show InChI InChI=1S/C22H25N5O3S/c1-15-13-17(30-3)5-6-19(15)25-10-7-18-20(14-16(2)23-22(18)25)26-11-8-21(24-26)27-9-4-12-31(27,28)29/h5-6,8,11,13-14H,4,7,9-10,12H2,1-3H3
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n/an/a 3.24E+3n/an/an/an/an/an/a



GlaxoSmithKline Medicines Research Centre

Curated by ChEMBL


Assay Description
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells


J Med Chem 51: 7370-9 (2009)


Article DOI: 10.1021/jm800744m
BindingDB Entry DOI: 10.7270/Q2N87C1X
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 1


(RAT)
BDBM50204441
PNG
(5-(benzyloxy)-3,4-dihydro-2H-pyrido[3,4-b]indol-1(...)
Show SMILES O=C1NCCc2c1[nH]c1cccc(OCc3ccccc3)c21
Show InChI InChI=1S/C18H16N2O2/c21-18-17-13(9-10-19-18)16-14(20-17)7-4-8-15(16)22-11-12-5-2-1-3-6-12/h1-8,20H,9-11H2,(H,19,21)
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n/an/a 3.98E+3n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 1


(RAT)
BDBM50204447
PNG
(6-phenoxy-3,4-dihydro-2H-pyrido[3,4-b]indol-1(9H)-...)
Show SMILES O=C1NCCc2c1[nH]c1ccc(Oc3ccccc3)cc21
Show InChI InChI=1S/C17H14N2O2/c20-17-16-13(8-9-18-17)14-10-12(6-7-15(14)19-16)21-11-4-2-1-3-5-11/h1-7,10,19H,8-9H2,(H,18,20)
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n/an/a 4.07E+3n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 1


(RAT)
BDBM50204436
PNG
(1-adamantan-1-yl-3-(1-oxo-2,3,4,9-tetrahydro-1H-be...)
Show SMILES O=C(Nc1ccc2[nH]c3c(CCNC3=O)c2c1)NC12CC3CC(CC(C3)C1)C2 |TLB:21:22:26:20.25.19,THB:21:20:26:22.23.27,23:22:26.25.24:19,23:24:21.22.27:19|
Show InChI InChI=1S/C22H26N4O2/c27-20-19-16(3-4-23-20)17-8-15(1-2-18(17)25-19)24-21(28)26-22-9-12-5-13(10-22)7-14(6-12)11-22/h1-2,8,12-14,25H,3-7,9-11H2,(H,23,27)(H2,24,26,28)
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n/an/a 4.66E+3n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 1


(RAT)
BDBM50204426
PNG
(6-(cyclohexylmethoxy)-3,4-dihydro-2H-pyrido[3,4-b]...)
Show SMILES O=C1NCCc2c1[nH]c1ccc(OCC3CCCCC3)cc21
Show InChI InChI=1S/C18H22N2O2/c21-18-17-14(8-9-19-18)15-10-13(6-7-16(15)20-17)22-11-12-4-2-1-3-5-12/h6-7,10,12,20H,1-5,8-9,11H2,(H,19,21)
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n/an/a 5.56E+3n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM50323794
PNG
(CHEMBL1214396 | N-[5-(4-methyl-3-pyridinyl)-2,3-di...)
Show SMILES CC(C)S(=O)(=O)NC1Cc2ccc(cc2C1)-c1cnccc1C
Show InChI InChI=1S/C18H22N2O2S/c1-12(2)23(21,22)20-17-9-14-4-5-15(8-16(14)10-17)18-11-19-7-6-13(18)3/h4-8,11-12,17,20H,9-10H2,1-3H3
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n/an/a>9.00E+3n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibition of human CYP3A4 after 10 mins


J Med Chem 53: 5801-12 (2010)


Article DOI: 10.1021/jm1005429
BindingDB Entry DOI: 10.7270/Q2FT8N0T
More data for this
Ligand-Target Pair
Cytochrome P450 2C19


(Homo sapiens (Human))
BDBM50323797
PNG
(CHEMBL1214337 | N-[5-(2-fluoro-3-pyridinyl)-2,3-di...)
Show SMILES CC(C)S(=O)(=O)NC1Cc2ccc(cc2C1)-c1cccnc1F
Show InChI InChI=1S/C17H19FN2O2S/c1-11(2)23(21,22)20-15-9-12-5-6-13(8-14(12)10-15)16-4-3-7-19-17(16)18/h3-8,11,15,20H,9-10H2,1-2H3
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n/an/a 9.00E+3n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibition of human CYP2C19 after 10 mins


J Med Chem 53: 5801-12 (2010)


Article DOI: 10.1021/jm1005429
BindingDB Entry DOI: 10.7270/Q2FT8N0T
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 1


(RAT)
BDBM50204448
PNG
(6-(benzyloxy)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]i...)
Show SMILES C(Oc1ccc2[nH]c3CNCCc3c2c1)c1ccccc1
Show InChI InChI=1S/C18H18N2O/c1-2-4-13(5-3-1)12-21-14-6-7-17-16(10-14)15-8-9-19-11-18(15)20-17/h1-7,10,19-20H,8-9,11-12H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 1


(RAT)
BDBM50204424
PNG
(6-benzyloxy-2,3,4,4a,9,9a-hexahydro-1H-beta-carbol...)
Show SMILES C(Oc1ccc2NC3CNCCC3c2c1)c1ccccc1 |w:12.11,7.7|
Show InChI InChI=1S/C18H20N2O/c1-2-4-13(5-3-1)12-21-14-6-7-17-16(10-14)15-8-9-19-11-18(15)20-17/h1-7,10,15,18-20H,8-9,11-12H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 1


(RAT)
BDBM50204425
PNG
(CHEMBL234959 | N-(3,3-dimethylbutan-2-yl)-1-oxo-2,...)
Show SMILES CC(NC(=O)c1ccc2[nH]c3c(CCNC3=O)c2c1)C(C)(C)C |w:1.0|
Show InChI InChI=1S/C18H23N3O2/c1-10(18(2,3)4)20-16(22)11-5-6-14-13(9-11)12-7-8-19-17(23)15(12)21-14/h5-6,9-10,21H,7-8H2,1-4H3,(H,19,23)(H,20,22)
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n/an/a>1.00E+4n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 1


(RAT)
BDBM50058672
PNG
(6-Methoxy-2,3,4,9-tetrahydro-beta-carbolin-1-one |...)
Show SMILES COc1ccc2[nH]c3c(CCNC3=O)c2c1
Show InChI InChI=1S/C12H12N2O2/c1-16-7-2-3-10-9(6-7)8-4-5-13-12(15)11(8)14-10/h2-3,6,14H,4-5H2,1H3,(H,13,15)
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n/an/a>1.00E+4n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 1


(RAT)
BDBM50204438
PNG
(6-hydroxy-3,4-dihydro-1-oxo-beta-carboline | 6-hyd...)
Show SMILES Oc1ccc2[nH]c3c(CCNC3=O)c2c1
Show InChI InChI=1S/C11H10N2O2/c14-6-1-2-9-8(5-6)7-3-4-12-11(15)10(7)13-9/h1-2,5,13-14H,3-4H2,(H,12,15)
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n/an/a>1.00E+4n/an/an/an/an/an/a



GlaxoSmithKline Medicine Research Centre

Curated by ChEMBL


Assay Description
Antagonist activity at rat mGluR1a expressed in CHO cells assessed as inhibition of intracellular calcium ion mobilization by FLIPR assay


Bioorg Med Chem Lett 17: 2254-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.055
BindingDB Entry DOI: 10.7270/Q2FT8KPZ
More data for this
Ligand-Target Pair
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