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Compile Data Set for Download or QSAR

Found 31 hits with Last Name = 'davis-taber' and Initial = 'r'   
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
Calcium-activated potassium channel subunit beta


(GUINEA PIG)
BDBM86244
PNG
(A-312110)
Show SMILES Fc1ccc(cc1I)[C@@H]1C2C(=O)COCC2=NC2=C1S(=O)(=O)CC2 |r,c:17,19|
Show InChI InChI=1S/C16H13FINO4S/c17-9-2-1-8(5-10(9)18)14-15-12(6-23-7-13(15)20)19-11-3-4-24(21,22)16(11)14/h1-2,5,14-15H,3-4,6-7H2/t14-,15?/m1/s1
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4.90n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by PDSP Ki Database




Mol Pharmacol 64: 143-53 (2003)


Article DOI: 10.1124/mol.64.1.143
BindingDB Entry DOI: 10.7270/Q22B8WMJ
More data for this
Ligand-Target Pair
Calcium-activated potassium channel subunit beta


(GUINEA PIG)
BDBM86250
PNG
(CAS_60559-98-0 | NSC_43345 | P1075)
Show SMILES CCC(C)(C)N=C(NC#N)Nc1cccnc1 |w:5.4|
Show InChI InChI=1S/C12H17N5/c1-4-12(2,3)17-11(15-9-13)16-10-6-5-7-14-8-10/h5-8H,4H2,1-3H3,(H2,15,16,17)
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10.5n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by PDSP Ki Database




Mol Pharmacol 64: 143-53 (2003)


Article DOI: 10.1124/mol.64.1.143
BindingDB Entry DOI: 10.7270/Q22B8WMJ
More data for this
Ligand-Target Pair
Calcium-activated potassium channel subunit beta


(GUINEA PIG)
BDBM86250
PNG
(CAS_60559-98-0 | NSC_43345 | P1075)
Show SMILES CCC(C)(C)N=C(NC#N)Nc1cccnc1 |w:5.4|
Show InChI InChI=1S/C12H17N5/c1-4-12(2,3)17-11(15-9-13)16-10-6-5-7-14-8-10/h5-8H,4H2,1-3H3,(H2,15,16,17)
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10.7n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by PDSP Ki Database




Br J Pharmacol 143: 81-90 (2004)


Article DOI: 10.1038/sj.bjp.0705908
BindingDB Entry DOI: 10.7270/Q2QR4VQ0
More data for this
Ligand-Target Pair
Calcium-activated potassium channel subunit beta


(GUINEA PIG)
BDBM86247
PNG
(BAY X 9228 | CAS_3038059 | NSC_3038059)
Show SMILES CCOc1ccccc1N=C(C[N+]([O-])=O)NC(C)C(C)(C)C |w:9.9|
Show InChI InChI=1S/C16H25N3O3/c1-6-22-14-10-8-7-9-13(14)18-15(11-19(20)21)17-12(2)16(3,4)5/h7-10,12H,6,11H2,1-5H3,(H,17,18)
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16n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by PDSP Ki Database




Mol Pharmacol 64: 143-53 (2003)


Article DOI: 10.1124/mol.64.1.143
BindingDB Entry DOI: 10.7270/Q22B8WMJ
More data for this
Ligand-Target Pair
Calcium-activated potassium channel subunit beta


(GUINEA PIG)
BDBM86250
PNG
(CAS_60559-98-0 | NSC_43345 | P1075)
Show SMILES CCC(C)(C)N=C(NC#N)Nc1cccnc1 |w:5.4|
Show InChI InChI=1S/C12H17N5/c1-4-12(2,3)17-11(15-9-13)16-10-6-5-7-14-8-10/h5-8H,4H2,1-3H3,(H2,15,16,17)
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20.6n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by PDSP Ki Database




Mol Pharmacol 64: 143-53 (2003)


Article DOI: 10.1124/mol.64.1.143
BindingDB Entry DOI: 10.7270/Q22B8WMJ
More data for this
Ligand-Target Pair
Calcium-activated potassium channel subunit beta


(GUINEA PIG)
BDBM86247
PNG
(BAY X 9228 | CAS_3038059 | NSC_3038059)
Show SMILES CCOc1ccccc1N=C(C[N+]([O-])=O)NC(C)C(C)(C)C |w:9.9|
Show InChI InChI=1S/C16H25N3O3/c1-6-22-14-10-8-7-9-13(14)18-15(11-19(20)21)17-12(2)16(3,4)5/h7-10,12H,6,11H2,1-5H3,(H,17,18)
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41.3n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by PDSP Ki Database




Mol Pharmacol 64: 143-53 (2003)


Article DOI: 10.1124/mol.64.1.143
BindingDB Entry DOI: 10.7270/Q22B8WMJ
More data for this
Ligand-Target Pair
Pituitary adenylate cyclase-activating polypeptide type I receptor


(Homo sapiens (Human))
BDBM50110068
PNG
(3-Chloro-4-hydroxy-benzoic acid [1-[4-(4-isopropyl...)
Show SMILES COc1cc(\C=N\NC(=O)c2ccc(O)c(Cl)c2)cc(OC)c1OCc1ccc(cc1)C(C)C
Show InChI InChI=1S/C26H27ClN2O5/c1-16(2)19-7-5-17(6-8-19)15-34-25-23(32-3)11-18(12-24(25)33-4)14-28-29-26(31)20-9-10-22(30)21(27)13-20/h5-14,16,30H,15H2,1-4H3,(H,29,31)/b28-14+
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56n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Displacement of [125I]PACAP27 from PAC1R expressed in HEK293f cells


Bioorg Med Chem Lett 18: 2162-6 (2008)


Article DOI: 10.1016/j.bmcl.2008.01.052
BindingDB Entry DOI: 10.7270/Q22J6CQ0
More data for this
Ligand-Target Pair
Pituitary adenylate cyclase-activating polypeptide type I receptor


(Homo sapiens (Human))
BDBM50122102
PNG
(3-Cyano-4-hydroxy-benzoic acid [1-(2,3,5,6-tetrame...)
Show SMILES Cc1cc(C)c(C)c(Cn2ccc3c(\C=N\NC(=O)c4ccc(O)c(c4)C#N)cccc23)c1C
Show InChI InChI=1S/C28H26N4O2/c1-17-12-18(2)20(4)25(19(17)3)16-32-11-10-24-22(6-5-7-26(24)32)15-30-31-28(34)21-8-9-27(33)23(13-21)14-29/h5-13,15,33H,16H2,1-4H3,(H,31,34)/b30-15+
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72n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Displacement of [125I]PACAP27 from PAC1R expressed in HEK293f cells


Bioorg Med Chem Lett 18: 2162-6 (2008)


Article DOI: 10.1016/j.bmcl.2008.01.052
BindingDB Entry DOI: 10.7270/Q22J6CQ0
More data for this
Ligand-Target Pair
Pituitary adenylate cyclase-activating polypeptide type I receptor


(Homo sapiens (Human))
BDBM50374178
PNG
(CHEMBL411120)
Show SMILES Oc1ccc(cc1Cl)C(=O)N\N=C\c1cccc2n(Cc3cccc(c3)C(F)(F)F)ccc12
Show InChI InChI=1S/C24H17ClF3N3O2/c25-20-12-16(7-8-22(20)32)23(33)30-29-13-17-4-2-6-21-19(17)9-10-31(21)14-15-3-1-5-18(11-15)24(26,27)28/h1-13,32H,14H2,(H,30,33)/b29-13+
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85n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Displacement of [125I]PACAP27 from PAC1R expressed in HEK293f cells


Bioorg Med Chem Lett 18: 2162-6 (2008)


Article DOI: 10.1016/j.bmcl.2008.01.052
BindingDB Entry DOI: 10.7270/Q22J6CQ0
More data for this
Ligand-Target Pair
Calcium-activated potassium channel subunit beta


(GUINEA PIG)
BDBM86245
PNG
(CAS_85371-64-8 | NSC_4826 | PINACIDIL)
Show SMILES CC(N=C(NC#N)Nc1ccncc1)C(C)(C)C |w:2.1|
Show InChI InChI=1S/C13H19N5/c1-10(13(2,3)4)17-12(16-9-14)18-11-5-7-15-8-6-11/h5-8,10H,1-4H3,(H2,15,16,17,18)
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104n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by PDSP Ki Database




Mol Pharmacol 64: 143-53 (2003)


Article DOI: 10.1124/mol.64.1.143
BindingDB Entry DOI: 10.7270/Q22B8WMJ
More data for this
Ligand-Target Pair
Pituitary adenylate cyclase-activating polypeptide type I receptor


(Homo sapiens (Human))
BDBM50374184
PNG
(CHEMBL270677)
Show SMILES COc1cc(\C=N\NC(=O)c2ccc(O)c(Cl)c2)cc(OC)c1OCc1ccc(cc1)C(F)(F)F
Show InChI InChI=1S/C24H20ClF3N2O5/c1-33-20-9-15(12-29-30-23(32)16-5-8-19(31)18(25)11-16)10-21(34-2)22(20)35-13-14-3-6-17(7-4-14)24(26,27)28/h3-12,31H,13H2,1-2H3,(H,30,32)/b29-12+
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140n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Displacement of [125I]PACAP27 from PAC1R expressed in HEK293f cells


Bioorg Med Chem Lett 18: 2162-6 (2008)


Article DOI: 10.1016/j.bmcl.2008.01.052
BindingDB Entry DOI: 10.7270/Q22J6CQ0
More data for this
Ligand-Target Pair
Pituitary adenylate cyclase-activating polypeptide type I receptor


(Homo sapiens (Human))
BDBM50374179
PNG
(CHEMBL409325)
Show SMILES COc1cc(\C=N\NC(=O)c2ccc(O)c(Cl)c2)cc(OCc2ccc(cc2)C(C)C)c1OC
Show InChI InChI=1S/C26H27ClN2O5/c1-16(2)19-7-5-17(6-8-19)15-34-24-12-18(11-23(32-3)25(24)33-4)14-28-29-26(31)20-9-10-22(30)21(27)13-20/h5-14,16,30H,15H2,1-4H3,(H,29,31)/b28-14+
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152n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Displacement of [125I]PACAP27 from PAC1R expressed in HEK293f cells


Bioorg Med Chem Lett 18: 2162-6 (2008)


Article DOI: 10.1016/j.bmcl.2008.01.052
BindingDB Entry DOI: 10.7270/Q22J6CQ0
More data for this
Ligand-Target Pair
Calcium-activated potassium channel subunit beta


(GUINEA PIG)
BDBM86251
PNG
(CAS_94535-50-9 | CROMAKALIM (-) | NSC_93504)
Show SMILES CC1(C)Oc2ccc(cc2C(C1O)N1CCCC1=O)C#N
Show InChI InChI=1S/C16H18N2O3/c1-16(2)15(20)14(18-7-3-4-13(18)19)11-8-10(9-17)5-6-12(11)21-16/h5-6,8,14-15,20H,3-4,7H2,1-2H3
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157n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by PDSP Ki Database




Mol Pharmacol 64: 143-53 (2003)


Article DOI: 10.1124/mol.64.1.143
BindingDB Entry DOI: 10.7270/Q22B8WMJ
More data for this
Ligand-Target Pair
Pituitary adenylate cyclase-activating polypeptide type I receptor


(Homo sapiens (Human))
BDBM50374188
PNG
(CHEMBL270226)
Show SMILES COc1cc(\C=N\NC(=O)c2ccc(O)c(Cl)c2)cc(OCc2c(C)c(C)cc(C)c2C)c1OC
Show InChI InChI=1S/C27H29ClN2O5/c1-15-9-16(2)18(4)21(17(15)3)14-35-25-11-19(10-24(33-5)26(25)34-6)13-29-30-27(32)20-7-8-23(31)22(28)12-20/h7-13,31H,14H2,1-6H3,(H,30,32)/b29-13+
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167n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Displacement of [125I]PACAP27 from PAC1R expressed in HEK293f cells


Bioorg Med Chem Lett 18: 2162-6 (2008)


Article DOI: 10.1016/j.bmcl.2008.01.052
BindingDB Entry DOI: 10.7270/Q22J6CQ0
More data for this
Ligand-Target Pair
Pituitary adenylate cyclase-activating polypeptide type I receptor


(Homo sapiens (Human))
BDBM50374187
PNG
(CHEMBL256379)
Show SMILES COc1cc(\C=N\NC(=O)c2ccc(O)c(Cl)c2)cc(OC)c1OCc1ccccc1
Show InChI InChI=1S/C23H21ClN2O5/c1-29-20-10-16(13-25-26-23(28)17-8-9-19(27)18(24)12-17)11-21(30-2)22(20)31-14-15-6-4-3-5-7-15/h3-13,27H,14H2,1-2H3,(H,26,28)/b25-13+
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185n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Displacement of [125I]PACAP27 from PAC1R expressed in HEK293f cells


Bioorg Med Chem Lett 18: 2162-6 (2008)


Article DOI: 10.1016/j.bmcl.2008.01.052
BindingDB Entry DOI: 10.7270/Q22J6CQ0
More data for this
Ligand-Target Pair
Pituitary adenylate cyclase-activating polypeptide type I receptor


(Homo sapiens (Human))
BDBM50374177
PNG
(CHEMBL409729)
Show SMILES COc1cc(\C=N\NC(=O)c2ccc(O)c(Cl)c2)cc(OC)c1OCc1cccc(c1)C(F)(F)F
Show InChI InChI=1S/C24H20ClF3N2O5/c1-33-20-9-15(12-29-30-23(32)16-6-7-19(31)18(25)11-16)10-21(34-2)22(20)35-13-14-4-3-5-17(8-14)24(26,27)28/h3-12,31H,13H2,1-2H3,(H,30,32)/b29-12+
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204n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Displacement of [125I]PACAP27 from PAC1R expressed in HEK293f cells


Bioorg Med Chem Lett 18: 2162-6 (2008)


Article DOI: 10.1016/j.bmcl.2008.01.052
BindingDB Entry DOI: 10.7270/Q22J6CQ0
More data for this
Ligand-Target Pair
Pituitary adenylate cyclase-activating polypeptide type I receptor


(Homo sapiens (Human))
BDBM50374180
PNG
(CHEMBL404071)
Show SMILES Oc1ccc(cc1Cl)C(=O)N\N=C\c1cccc(COc2ccc(cc2)C(F)(F)F)c1
Show InChI InChI=1S/C22H16ClF3N2O3/c23-19-11-16(4-9-20(19)29)21(30)28-27-12-14-2-1-3-15(10-14)13-31-18-7-5-17(6-8-18)22(24,25)26/h1-12,29H,13H2,(H,28,30)/b27-12+
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241n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Displacement of [125I]PACAP27 from PAC1R expressed in HEK293f cells


Bioorg Med Chem Lett 18: 2162-6 (2008)


Article DOI: 10.1016/j.bmcl.2008.01.052
BindingDB Entry DOI: 10.7270/Q22J6CQ0
More data for this
Ligand-Target Pair
Calcium-activated potassium channel subunit beta


(GUINEA PIG)
BDBM86245
PNG
(CAS_85371-64-8 | NSC_4826 | PINACIDIL)
Show SMILES CC(N=C(NC#N)Nc1ccncc1)C(C)(C)C |w:2.1|
Show InChI InChI=1S/C13H19N5/c1-10(13(2,3)4)17-12(16-9-14)18-11-5-7-15-8-6-11/h5-8,10H,1-4H3,(H2,15,16,17,18)
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251n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by PDSP Ki Database




Mol Pharmacol 64: 143-53 (2003)


Article DOI: 10.1124/mol.64.1.143
BindingDB Entry DOI: 10.7270/Q22B8WMJ
More data for this
Ligand-Target Pair
Pituitary adenylate cyclase-activating polypeptide type I receptor


(Homo sapiens (Human))
BDBM50374186
PNG
(CHEMBL272122)
Show SMILES Oc1ccc(cc1Cl)C(=O)N\N=C\c1cccc(COc2cccc(c2)C(F)(F)F)c1
Show InChI InChI=1S/C22H16ClF3N2O3/c23-19-10-16(7-8-20(19)29)21(30)28-27-12-14-3-1-4-15(9-14)13-31-18-6-2-5-17(11-18)22(24,25)26/h1-12,29H,13H2,(H,28,30)/b27-12+
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274n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Displacement of [125I]PACAP27 from PAC1R expressed in HEK293f cells


Bioorg Med Chem Lett 18: 2162-6 (2008)


Article DOI: 10.1016/j.bmcl.2008.01.052
BindingDB Entry DOI: 10.7270/Q22J6CQ0
More data for this
Ligand-Target Pair
Pituitary adenylate cyclase-activating polypeptide type I receptor


(Homo sapiens (Human))
BDBM50374183
PNG
(CHEMBL269990)
Show SMILES COc1cc(\C=N\NC(=O)c2ccc(O)c(Cl)c2)ccc1OCc1cccc(c1)C(F)(F)F
Show InChI InChI=1S/C23H18ClF3N2O4/c1-32-21-10-14(12-28-29-22(31)16-6-7-19(30)18(24)11-16)5-8-20(21)33-13-15-3-2-4-17(9-15)23(25,26)27/h2-12,30H,13H2,1H3,(H,29,31)/b28-12+
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404n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Displacement of [125I]PACAP27 from PAC1R expressed in HEK293f cells


Bioorg Med Chem Lett 18: 2162-6 (2008)


Article DOI: 10.1016/j.bmcl.2008.01.052
BindingDB Entry DOI: 10.7270/Q22J6CQ0
More data for this
Ligand-Target Pair
Calcium-activated potassium channel subunit beta


(GUINEA PIG)
BDBM86249
PNG
(ZD 6169 | ZD-6169)
Show SMILES C[C@](O)(C(=O)Nc1ccc(cc1)C(=O)c1ccccc1)C(F)(F)F
Show InChI InChI=1S/C17H14F3NO3/c1-16(24,17(18,19)20)15(23)21-13-9-7-12(8-10-13)14(22)11-5-3-2-4-6-11/h2-10,24H,1H3,(H,21,23)/t16-/m0/s1
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451n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by PDSP Ki Database




Mol Pharmacol 64: 143-53 (2003)


Article DOI: 10.1124/mol.64.1.143
BindingDB Entry DOI: 10.7270/Q22B8WMJ
More data for this
Ligand-Target Pair
Pituitary adenylate cyclase-activating polypeptide type I receptor


(Homo sapiens (Human))
BDBM50374182
PNG
(CHEMBL272118)
Show SMILES Oc1ccc(cc1Cl)C(=O)N\N=C\c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C21H17ClN2O3/c22-19-12-17(8-11-20(19)25)21(26)24-23-13-15-6-9-18(10-7-15)27-14-16-4-2-1-3-5-16/h1-13,25H,14H2,(H,24,26)/b23-13+
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522n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Displacement of [125I]PACAP27 from PAC1R expressed in HEK293f cells


Bioorg Med Chem Lett 18: 2162-6 (2008)


Article DOI: 10.1016/j.bmcl.2008.01.052
BindingDB Entry DOI: 10.7270/Q22J6CQ0
More data for this
Ligand-Target Pair
Pituitary adenylate cyclase-activating polypeptide type I receptor


(Homo sapiens (Human))
BDBM50374181
PNG
(CHEMBL256837)
Show SMILES Oc1ccc(cc1Cl)C(=O)N\N=C\c1ccc(OCc2cccc(c2)C(F)(F)F)cc1
Show InChI InChI=1S/C22H16ClF3N2O3/c23-19-11-16(6-9-20(19)29)21(30)28-27-12-14-4-7-18(8-5-14)31-13-15-2-1-3-17(10-15)22(24,25)26/h1-12,29H,13H2,(H,28,30)/b27-12+
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537n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Displacement of [125I]PACAP27 from PAC1R expressed in HEK293f cells


Bioorg Med Chem Lett 18: 2162-6 (2008)


Article DOI: 10.1016/j.bmcl.2008.01.052
BindingDB Entry DOI: 10.7270/Q22J6CQ0
More data for this
Ligand-Target Pair
Calcium-activated potassium channel subunit beta


(GUINEA PIG)
BDBM86251
PNG
(CAS_94535-50-9 | CROMAKALIM (-) | NSC_93504)
Show SMILES CC1(C)Oc2ccc(cc2C(C1O)N1CCCC1=O)C#N
Show InChI InChI=1S/C16H18N2O3/c1-16(2)15(20)14(18-7-3-4-13(18)19)11-8-10(9-17)5-6-12(11)21-16/h5-6,8,14-15,20H,3-4,7H2,1-2H3
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542n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by PDSP Ki Database




Mol Pharmacol 64: 143-53 (2003)


Article DOI: 10.1124/mol.64.1.143
BindingDB Entry DOI: 10.7270/Q22B8WMJ
More data for this
Ligand-Target Pair
Pituitary adenylate cyclase-activating polypeptide type I receptor


(Homo sapiens (Human))
BDBM50374185
PNG
(CHEMBL255824)
Show SMILES Oc1ccc(cc1Cl)C(=O)N\N=C\c1cccc(OCc2cccc(c2)C(F)(F)F)c1
Show InChI InChI=1S/C22H16ClF3N2O3/c23-19-11-16(7-8-20(19)29)21(30)28-27-12-14-3-2-6-18(10-14)31-13-15-4-1-5-17(9-15)22(24,25)26/h1-12,29H,13H2,(H,28,30)/b27-12+
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554n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Displacement of [125I]PACAP27 from PAC1R expressed in HEK293f cells


Bioorg Med Chem Lett 18: 2162-6 (2008)


Article DOI: 10.1016/j.bmcl.2008.01.052
BindingDB Entry DOI: 10.7270/Q22J6CQ0
More data for this
Ligand-Target Pair
Pituitary adenylate cyclase-activating polypeptide type I receptor


(Homo sapiens (Human))
BDBM50110055
PNG
(3-Chloro-4-hydroxy-benzoic acid [1-(4-isopropyl-be...)
Show SMILES CC(C)c1ccc(Cn2ccc3c(\C=N\NC(=O)c4ccc(O)c(Cl)c4)cccc23)cc1
Show InChI InChI=1S/C26H24ClN3O2/c1-17(2)19-8-6-18(7-9-19)16-30-13-12-22-21(4-3-5-24(22)30)15-28-29-26(32)20-10-11-25(31)23(27)14-20/h3-15,17,31H,16H2,1-2H3,(H,29,32)/b28-15+
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604n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Displacement of [125I]PACAP27 from PAC1R expressed in HEK293f cells


Bioorg Med Chem Lett 18: 2162-6 (2008)


Article DOI: 10.1016/j.bmcl.2008.01.052
BindingDB Entry DOI: 10.7270/Q22J6CQ0
More data for this
Ligand-Target Pair
Calcium-activated potassium channel subunit beta


(GUINEA PIG)
BDBM86249
PNG
(ZD 6169 | ZD-6169)
Show SMILES C[C@](O)(C(=O)Nc1ccc(cc1)C(=O)c1ccccc1)C(F)(F)F
Show InChI InChI=1S/C17H14F3NO3/c1-16(24,17(18,19)20)15(23)21-13-9-7-12(8-10-13)14(22)11-5-3-2-4-6-11/h2-10,24H,1H3,(H,21,23)/t16-/m0/s1
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630n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by PDSP Ki Database




Mol Pharmacol 64: 143-53 (2003)


Article DOI: 10.1124/mol.64.1.143
BindingDB Entry DOI: 10.7270/Q22B8WMJ
More data for this
Ligand-Target Pair
Calcium-activated potassium channel subunit beta


(GUINEA PIG)
BDBM86246
PNG
(zm244085)
Show SMILES O=C1CCCC2=NC3=C(C(C12)c1cccc(c1)C#N)C(=O)CCC3 |c:7,t:5|
Show InChI InChI=1S/C20H18N2O2/c21-11-12-4-1-5-13(10-12)18-19-14(6-2-8-16(19)23)22-15-7-3-9-17(24)20(15)18/h1,4-5,10,18-19H,2-3,6-9H2
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671n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by PDSP Ki Database




Mol Pharmacol 64: 143-53 (2003)


Article DOI: 10.1124/mol.64.1.143
BindingDB Entry DOI: 10.7270/Q22B8WMJ
More data for this
Ligand-Target Pair
Calcium-activated potassium channel subunit beta


(GUINEA PIG)
BDBM86246
PNG
(zm244085)
Show SMILES O=C1CCCC2=NC3=C(C(C12)c1cccc(c1)C#N)C(=O)CCC3 |c:7,t:5|
Show InChI InChI=1S/C20H18N2O2/c21-11-12-4-1-5-13(10-12)18-19-14(6-2-8-16(19)23)22-15-7-3-9-17(24)20(15)18/h1,4-5,10,18-19H,2-3,6-9H2
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2.77E+3n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by PDSP Ki Database




Mol Pharmacol 64: 143-53 (2003)


Article DOI: 10.1124/mol.64.1.143
BindingDB Entry DOI: 10.7270/Q22B8WMJ
More data for this
Ligand-Target Pair
Calcium-activated potassium channel subunit beta


(GUINEA PIG)
BDBM86248
PNG
(CAS_364-98-7 | NSC_3019 | diazoxide)
Show SMILES CC1=Nc2ccc(Cl)cc2S(=O)(=O)N1 |t:1|
Show InChI InChI=1S/C8H7ClN2O2S/c1-5-10-7-3-2-6(9)4-8(7)14(12,13)11-5/h2-4H,1H3,(H,10,11)
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>1.00E+4n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by PDSP Ki Database




Mol Pharmacol 64: 143-53 (2003)


Article DOI: 10.1124/mol.64.1.143
BindingDB Entry DOI: 10.7270/Q22B8WMJ
More data for this
Ligand-Target Pair
Calcium-activated potassium channel subunit beta


(GUINEA PIG)
BDBM86248
PNG
(CAS_364-98-7 | NSC_3019 | diazoxide)
Show SMILES CC1=Nc2ccc(Cl)cc2S(=O)(=O)N1 |t:1|
Show InChI InChI=1S/C8H7ClN2O2S/c1-5-10-7-3-2-6(9)4-8(7)14(12,13)11-5/h2-4H,1H3,(H,10,11)
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>1.00E+4n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by PDSP Ki Database




Mol Pharmacol 64: 143-53 (2003)


Article DOI: 10.1124/mol.64.1.143
BindingDB Entry DOI: 10.7270/Q22B8WMJ
More data for this
Ligand-Target Pair