Compile Data Set for Download or QSAR

Found 126 hits with Last Name = 'medapati' and Initial = 'rb'   

Target/Host (Institution)	Ligand	Target/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	pH	Temp °C
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM50403292 (CHEMBL5285364) Show SMILES OC(=O)CN1[C@H](SC[C@H](NC(=O)[C@@H](S)Cc2ccccc2)C1=O)c1ccccc1 Show InChI InChI=1S/C21H22N2O4S2/c24-18(25)12-23-20(27)16(13-29-21(23)15-9-5-2-6-10-15)22-19(26)17(28)11-14-7-3-1-4-8-14/h1-10,16-17,21,28H,11-13H2,(H,22,26)(H,24,25)/t16-,17-,21+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars		n/a	n/a	950	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM50391288 (CHEMBL5288438) Show SMILES CS(=O)(=O)Nc1cccc(c1)-c1ccc(COC2CC[C@@H]([C@H]2OC\C=C/CCC(O)=O)N2CCCCCC2)cc1 Show InChI InChI=1S/C31H42N2O6S/c1-40(36,37)32-27-11-9-10-26(22-27)25-15-13-24(14-16-25)23-39-29-18-17-28(33-19-6-2-3-7-20-33)31(29)38-21-8-4-5-12-30(34)35/h4,8-11,13-16,22,28-29,31-32H,2-3,5-7,12,17-21,23H2,1H3,(H,34,35)/b8-4-/t28-,29?,31+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	1.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM50456116 (Prx-03140) Show SMILES CC(C)n1c2sccc2c(O)c(C(=O)NCCCN2CCCCC2)c1=O Show InChI InChI=1S/C19H27N3O3S/c1-13(2)22-18(25)15(16(23)14-7-12-26-19(14)22)17(24)20-8-6-11-21-9-4-3-5-10-21/h7,12-13,23H,3-6,8-11H2,1-2H3,(H,20,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	1.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibitory activity against Dihydrofolate reductase in rat liver				Citation and Details
					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM50391287 (CHEMBL5278176) Show SMILES CNS(=O)(=O)Cc1ccccc1-c1ccc(COC2CC[C@@H]([C@H]2OC\C=C/CCC(O)=O)N2CCCCCC2)cc1 Show InChI InChI=1S/C32H44N2O6S/c1-33-41(37,38)24-27-11-6-7-12-28(27)26-16-14-25(15-17-26)23-40-30-19-18-29(34-20-8-2-3-9-21-34)32(30)39-22-10-4-5-13-31(35)36/h4,6-7,10-12,14-17,29-30,32-33H,2-3,5,8-9,13,18-24H2,1H3,(H,35,36)/b10-4-/t29-,30?,32+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	1.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM50391258 (CHEMBL5286257) Show SMILES Nc1ncc(OCc2ccc(OCCCN3C(=O)c4ccccc4C3=O)cc2)c(N)n1 Show InChI InChI=1S/C22H21N5O4/c23-19-18(12-25-22(24)26-19)31-13-14-6-8-15(9-7-14)30-11-3-10-27-20(28)16-4-1-2-5-17(16)21(27)29/h1-2,4-9,12H,3,10-11,13H2,(H4,23,24,25,26)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	1.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM325596 (3-[5-(1-Cyclobutyl-piperidin-4-yl)-[1,3,4]oxadiazo...) Show SMILES CC(C)n1nc(-c2nnc(o2)C2CCN(CC2)C2CCC2)c2ccccc12 Show InChI InChI=1S/C21H27N5O/c1-14(2)26-18-9-4-3-8-17(18)19(24-26)21-23-22-20(27-21)15-10-12-25(13-11-15)16-6-5-7-16/h3-4,8-9,14-16H,5-7,10-13H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	2.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM50391288 (CHEMBL5288438) Show SMILES CS(=O)(=O)Nc1cccc(c1)-c1ccc(COC2CC[C@@H]([C@H]2OC\C=C/CCC(O)=O)N2CCCCCC2)cc1 Show InChI InChI=1S/C31H42N2O6S/c1-40(36,37)32-27-11-9-10-26(22-27)25-15-13-24(14-16-25)23-39-29-18-17-28(33-19-6-2-3-7-20-33)31(29)38-21-8-4-5-12-30(34)35/h4,8-11,13-16,22,28-29,31-32H,2-3,5-7,12,17-21,23H2,1H3,(H,34,35)/b8-4-/t28-,29?,31+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	2.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The compound was tested for beta-adrenergic activity against Beta-1 adrenergic receptor from guinea pig left atria				Citation and Details
					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM50391298 (CHEMBL5275605) Show SMILES CC(=O)NCc1ccc(cc1)-c1ccc(COC2CC[C@@H]([C@H]2OC\C=C/CCC(O)=O)N2CCCCCC2)cc1 Show InChI InChI=1S/C33H44N2O5/c1-25(36)34-23-26-10-14-28(15-11-26)29-16-12-27(13-17-29)24-40-31-19-18-30(35-20-6-2-3-7-21-35)33(31)39-22-8-4-5-9-32(37)38/h4,8,10-17,30-31,33H,2-3,5-7,9,18-24H2,1H3,(H,34,36)(H,37,38)/b8-4-/t30-,31?,33+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	2.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM325561 (1-Isopropyl-3-{5-[1-(3-methoxy propyl) piperidin-4...) Show SMILES COCCCN1CCC(CC1)c1nnc(o1)-c1nn(C(C)C)c2ccccc12 Show InChI InChI=1S/C21H29N5O2/c1-15(2)26-18-8-5-4-7-17(18)19(24-26)21-23-22-20(28-21)16-9-12-25(13-10-16)11-6-14-27-3/h4-5,7-8,15-16H,6,9-14H2,1-3H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem		n/a	n/a	3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM325602 (1-Isopropyl-3-{5-[1-(tetrahydro-pyran-4-ylmethyl)-...) Show SMILES CC(C)n1nc(-c2nnc(o2)C2CCN(CC3CCOCC3)CC2)c2ccccc12 Show InChI InChI=1S/C23H31N5O2/c1-16(2)28-20-6-4-3-5-19(20)21(26-28)23-25-24-22(30-23)18-7-11-27(12-8-18)15-17-9-13-29-14-10-17/h3-6,16-18H,7-15H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	8.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50391267 (CHEMBL5289747) Show SMILES CC(=O)Nc1ccc(cc1)S(=O)(=O)c1ccc(N)cc1 Show InChI InChI=1S/C14H14N2O3S/c1-10(17)16-12-4-8-14(9-5-12)20(18,19)13-6-2-11(15)3-7-13/h2-9H,15H2,1H3,(H,16,17)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars		n/a	n/a	9.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM325561 (1-Isopropyl-3-{5-[1-(3-methoxy propyl) piperidin-4...) Show SMILES COCCCN1CCC(CC1)c1nnc(o1)-c1nn(C(C)C)c2ccccc12 Show InChI InChI=1S/C21H29N5O2/c1-15(2)26-18-8-5-4-7-17(18)19(24-26)21-23-22-20(28-21)16-9-12-25(13-10-16)11-6-14-27-3/h4-5,7-8,15-16H,6,9-14H2,1-3H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem		n/a	n/a	9.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM50391246 (CHEMBL5275895) Show SMILES COc1ccc(CNc2cnc(N)nc2N)cc1 Show InChI InChI=1S/C12H15N5O/c1-18-9-4-2-8(3-5-9)6-15-10-7-16-12(14)17-11(10)13/h2-5,7,15H,6H2,1H3,(H4,13,14,16,17)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rat microsomal HMG-CoA reductase activity by 50%				Citation and Details
					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM50391283 (CHEMBL5268064) Show SMILES OC(=O)CC\C=C/CO[C@H]1C(CC[C@@H]1N1CCCCCC1)OCc1ccc(cc1)-c1ccc(O)cc1 Show InChI InChI=1S/C30H39NO5/c32-26-15-13-25(14-16-26)24-11-9-23(10-12-24)22-36-28-18-17-27(31-19-5-1-2-6-20-31)30(28)35-21-7-3-4-8-29(33)34/h3,7,9-16,27-28,30,32H,1-2,4-6,8,17-22H2,(H,33,34)/b7-3-/t27-,28?,30+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Evaluated for inhibitory activity against rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50391281 (CHEMBL5286642) Show SMILES OCc1ccccc1-c1ccc(CO[C@H]2CC[C@@H]([C@H]2OC\C=C/CCC(O)=O)N2CCCCCC2)cc1 Show InChI InChI=1S/C31H41NO5/c33-22-26-10-5-6-11-27(26)25-15-13-24(14-16-25)23-37-29-18-17-28(32-19-7-1-2-8-20-32)31(29)36-21-9-3-4-12-30(34)35/h3,5-6,9-11,13-16,28-29,31,33H,1-2,4,7-8,12,17-23H2,(H,34,35)/b9-3-/t28-,29-,31+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	1.12E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM50391281 (CHEMBL5286642) Show SMILES OCc1ccccc1-c1ccc(CO[C@H]2CC[C@@H]([C@H]2OC\C=C/CCC(O)=O)N2CCCCCC2)cc1 Show InChI InChI=1S/C31H41NO5/c33-22-26-10-5-6-11-27(26)25-15-13-24(14-16-25)23-37-29-18-17-28(32-19-7-1-2-8-20-32)31(29)36-21-9-3-4-12-30(34)35/h3,5-6,9-11,13-16,28-29,31,33H,1-2,4,7-8,12,17-23H2,(H,34,35)/b9-3-/t28-,29-,31+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	1.39E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The compound was tested for beta-adrenergic activity against Beta-1 adrenergic receptor from guinea pig right atria				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50391266 (CHEMBL5271080) Show SMILES Nc1ccc(cc1)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C12H11NO2S/c13-10-6-8-12(9-7-10)16(14,15)11-4-2-1-3-5-11/h1-9H,13H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	2.04E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50391278 (CHEMBL5274204) Show SMILES OC(=O)CC\C=C/CO[C@H]1[C@H](CC[C@@H]1N1CCCCC1)OCc1ccc(cc1)-c1ccccc1 Show InChI InChI=1S/C29H37NO4/c31-28(32)12-6-2-9-21-33-29-26(30-19-7-3-8-20-30)17-18-27(29)34-22-23-13-15-25(16-14-23)24-10-4-1-5-11-24/h1-2,4-5,9-11,13-16,26-27,29H,3,6-8,12,17-22H2,(H,31,32)/b9-2-/t26-,27-,29+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	2.67E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM325598 (3-[5-(1-Cyclopropylmethyl-piperidin-4-yl)-[1,3,4]o...) Show SMILES CC(C)n1nc(-c2nnc(o2)C2CCN(CC3CC3)CC2)c2ccccc12 Show InChI InChI=1S/C21H27N5O/c1-14(2)26-18-6-4-3-5-17(18)19(24-26)21-23-22-20(27-21)16-9-11-25(12-10-16)13-15-7-8-15/h3-6,14-16H,7-13H2,1-2H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	3.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The compound was tested for beta-adrenergic activity against Beta-1 adrenergic receptor from guinea pig left atria				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50391265 (CHEMBL5276171) Show SMILES COc1cc(Cc2cnc(N)nc2N)cc(OC)c1OCCCNc1ccc(cc1)N(C)C Show InChI InChI=1S/C24H32N6O3/c1-30(2)19-8-6-18(7-9-19)27-10-5-11-33-22-20(31-3)13-16(14-21(22)32-4)12-17-15-28-24(26)29-23(17)25/h6-9,13-15,27H,5,10-12H2,1-4H3,(H4,25,26,28,29)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	3.64E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM325596 (3-[5-(1-Cyclobutyl-piperidin-4-yl)-[1,3,4]oxadiazo...) Show SMILES CC(C)n1nc(-c2nnc(o2)C2CCN(CC2)C2CCC2)c2ccccc12 Show InChI InChI=1S/C21H27N5O/c1-14(2)26-18-9-4-3-8-17(18)19(24-26)21-23-22-20(27-21)15-10-12-25(13-11-15)16-6-5-7-16/h3-4,8-9,14-16H,5-7,10-13H2,1-2H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	3.70E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The compound was tested for beta-adrenergic activity against Beta-1 adrenergic receptor from guinea pig right atria				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM50403292 (CHEMBL5285364) Show SMILES OC(=O)CN1[C@H](SC[C@H](NC(=O)[C@@H](S)Cc2ccccc2)C1=O)c1ccccc1 Show InChI InChI=1S/C21H22N2O4S2/c24-18(25)12-23-20(27)16(13-29-21(23)15-9-5-2-6-10-15)22-19(26)17(28)11-14-7-3-1-4-8-14/h1-10,16-17,21,28H,11-13H2,(H,22,26)(H,24,25)/t16-,17-,21+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars		n/a	n/a	3.77E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The compound was tested for beta-adrenergic activity against Beta-2 adrenergic receptor from guinea pig trachea.				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM50391298 (CHEMBL5275605) Show SMILES CC(=O)NCc1ccc(cc1)-c1ccc(COC2CC[C@@H]([C@H]2OC\C=C/CCC(O)=O)N2CCCCCC2)cc1 Show InChI InChI=1S/C33H44N2O5/c1-25(36)34-23-26-10-14-28(15-11-26)29-16-12-27(13-17-29)24-40-31-19-18-30(35-20-6-2-3-7-21-35)33(31)39-22-8-4-5-9-32(37)38/h4,8,10-17,30-31,33H,2-3,5-7,9,18-24H2,1H3,(H,34,36)(H,37,38)/b8-4-/t30-,31?,33+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	>4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The compound was tested for alpha-adrenergic activity against Alpha-1 adrenergic receptor from rat aorta.				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM325602 (1-Isopropyl-3-{5-[1-(tetrahydro-pyran-4-ylmethyl)-...) Show SMILES CC(C)n1nc(-c2nnc(o2)C2CCN(CC3CCOCC3)CC2)c2ccccc12 Show InChI InChI=1S/C23H31N5O2/c1-16(2)28-20-6-4-3-5-19(20)21(26-28)23-25-24-22(30-23)18-7-11-27(12-8-18)15-17-9-13-29-14-10-17/h3-6,16-18H,7-15H2,1-2H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	>4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The compound was tested for beta-adrenergic activity against Beta-1 adrenergic receptor from guinea pig left atria				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM325561 (1-Isopropyl-3-{5-[1-(3-methoxy propyl) piperidin-4...) Show SMILES COCCCN1CCC(CC1)c1nnc(o1)-c1nn(C(C)C)c2ccccc12 Show InChI InChI=1S/C21H29N5O2/c1-15(2)26-18-8-5-4-7-17(18)19(24-26)21-23-22-20(28-21)16-9-12-25(13-10-16)11-6-14-27-3/h4-5,7-8,15-16H,6,9-14H2,1-3H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem		n/a	n/a	>4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The compound was tested for beta-adrenergic activity against Beta-1 adrenergic receptor from guinea pig right atria				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM50391283 (CHEMBL5268064) Show SMILES OC(=O)CC\C=C/CO[C@H]1C(CC[C@@H]1N1CCCCCC1)OCc1ccc(cc1)-c1ccc(O)cc1 Show InChI InChI=1S/C30H39NO5/c32-26-15-13-25(14-16-26)24-11-9-23(10-12-24)22-36-28-18-17-27(31-19-5-1-2-6-20-31)30(28)35-21-7-3-4-8-29(33)34/h3,7,9-16,27-28,30,32H,1-2,4-6,8,17-22H2,(H,33,34)/b7-3-/t27-,28?,30+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	>4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The compound was tested for beta-adrenergic activity against Beta-1 adrenergic receptor from guinea pig left atria				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM325594 (3-[5-(1-Cyclobutylmethyl-piperidin-4-yl)-[1,3,4]ox...) Show SMILES CC(C)n1nc(-c2nnc(o2)C2CCN(CC3CCC3)CC2)c2ccccc12 Show InChI InChI=1S/C22H29N5O/c1-15(2)27-19-9-4-3-8-18(19)20(25-27)22-24-23-21(28-22)17-10-12-26(13-11-17)14-16-6-5-7-16/h3-4,8-9,15-17H,5-7,10-14H2,1-2H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	>4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The compound was tested for beta-adrenergic activity against Beta-1 adrenergic receptor from guinea pig left atria				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM325597 (1-Isopropyl-3-[5-(1-isopropyl-piperidin-4-yl)-[1,3...) Show SMILES CC(C)N1CCC(CC1)c1nnc(o1)-c1nn(C(C)C)c2ccccc12 Show InChI InChI=1S/C20H27N5O/c1-13(2)24-11-9-15(10-12-24)19-21-22-20(26-19)18-16-7-5-6-8-17(16)25(23-18)14(3)4/h5-8,13-15H,9-12H2,1-4H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	>4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The compound was tested for beta-adrenergic activity against Beta-1 adrenergic receptor from guinea pig right atria				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM50391278 (CHEMBL5274204) Show SMILES OC(=O)CC\C=C/CO[C@H]1[C@H](CC[C@@H]1N1CCCCC1)OCc1ccc(cc1)-c1ccccc1 Show InChI InChI=1S/C29H37NO4/c31-28(32)12-6-2-9-21-33-29-26(30-19-7-3-8-20-30)17-18-27(29)34-22-23-13-15-25(16-14-23)24-10-4-1-5-11-24/h1-2,4-5,9-11,13-16,26-27,29H,3,6-8,12,17-22H2,(H,31,32)/b9-2-/t26-,27-,29+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	>4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The compound was tested for beta-adrenergic activity against Beta-1 adrenergic receptor from guinea pig right atria				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM50391267 (CHEMBL5289747) Show SMILES CC(=O)Nc1ccc(cc1)S(=O)(=O)c1ccc(N)cc1 Show InChI InChI=1S/C14H14N2O3S/c1-10(17)16-12-4-8-14(9-5-12)20(18,19)13-6-2-11(15)3-7-13/h2-9H,15H2,1H3,(H,16,17)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars		n/a	n/a	>4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Antagonistic activity against Thromboxane A2 receptor in guinea pig trachea in the presence of 11,9-epoxymethano-PGH2				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM50391266 (CHEMBL5271080) Show SMILES Nc1ccc(cc1)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C12H11NO2S/c13-10-6-8-12(9-7-10)16(14,15)11-4-2-1-3-5-11/h1-9H,13H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	>4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM50391265 (CHEMBL5276171) Show SMILES COc1cc(Cc2cnc(N)nc2N)cc(OC)c1OCCCNc1ccc(cc1)N(C)C Show InChI InChI=1S/C24H32N6O3/c1-30(2)19-8-6-18(7-9-19)27-10-5-11-33-22-20(31-3)13-16(14-21(22)32-4)12-17-15-28-24(26)29-23(17)25/h6-9,13-15,27H,5,10-12H2,1-4H3,(H4,25,26,28,29)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	>4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM50391248 (CHEMBL5284140) Show SMILES COc1cc(COc2cnc(N)nc2N)ccc1OCCCNS(=O)(=O)c1ccc(C)cc1 Show InChI InChI=1S/C22H27N5O5S/c1-15-4-7-17(8-5-15)33(28,29)26-10-3-11-31-18-9-6-16(12-19(18)30-2)14-32-20-13-25-22(24)27-21(20)23/h4-9,12-13,26H,3,10-11,14H2,1-2H3,(H4,23,24,25,27)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	>4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Evaluated for inhibitory activity against rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM50391246 (CHEMBL5275895) Show SMILES COc1ccc(CNc2cnc(N)nc2N)cc1 Show InChI InChI=1S/C12H15N5O/c1-18-9-4-2-8(3-5-9)6-15-10-7-16-12(14)17-11(10)13/h2-5,7,15H,6H2,1H3,(H4,13,14,16,17)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	>4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50403292 (CHEMBL5285364) Show SMILES OC(=O)CN1[C@H](SC[C@H](NC(=O)[C@@H](S)Cc2ccccc2)C1=O)c1ccccc1 Show InChI InChI=1S/C21H22N2O4S2/c24-18(25)12-23-20(27)16(13-29-21(23)15-9-5-2-6-10-15)22-19(26)17(28)11-14-7-3-1-4-8-14/h1-10,16-17,21,28H,11-13H2,(H,22,26)(H,24,25)/t16-,17-,21+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars		n/a	n/a	>4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50391298 (CHEMBL5275605) Show SMILES CC(=O)NCc1ccc(cc1)-c1ccc(COC2CC[C@@H]([C@H]2OC\C=C/CCC(O)=O)N2CCCCCC2)cc1 Show InChI InChI=1S/C33H44N2O5/c1-25(36)34-23-26-10-14-28(15-11-26)29-16-12-27(13-17-29)24-40-31-19-18-30(35-20-6-2-3-7-21-35)33(31)39-22-8-4-5-9-32(37)38/h4,8,10-17,30-31,33H,2-3,5-7,9,18-24H2,1H3,(H,34,36)(H,37,38)/b8-4-/t30-,31?,33+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	>4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50391288 (CHEMBL5288438) Show SMILES CS(=O)(=O)Nc1cccc(c1)-c1ccc(COC2CC[C@@H]([C@H]2OC\C=C/CCC(O)=O)N2CCCCCC2)cc1 Show InChI InChI=1S/C31H42N2O6S/c1-40(36,37)32-27-11-9-10-26(22-27)25-15-13-24(14-16-25)23-39-29-18-17-28(33-19-6-2-3-7-20-33)31(29)38-21-8-4-5-12-30(34)35/h4,8-11,13-16,22,28-29,31-32H,2-3,5-7,12,17-21,23H2,1H3,(H,34,35)/b8-4-/t28-,29?,31+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	>4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM325602 (1-Isopropyl-3-{5-[1-(tetrahydro-pyran-4-ylmethyl)-...) Show SMILES CC(C)n1nc(-c2nnc(o2)C2CCN(CC3CCOCC3)CC2)c2ccccc12 Show InChI InChI=1S/C23H31N5O2/c1-16(2)28-20-6-4-3-5-19(20)21(26-28)23-25-24-22(30-23)18-7-11-27(12-8-18)15-17-9-13-29-14-10-17/h3-6,16-18H,7-15H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	>4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM325596 (3-[5-(1-Cyclobutyl-piperidin-4-yl)-[1,3,4]oxadiazo...) Show SMILES CC(C)n1nc(-c2nnc(o2)C2CCN(CC2)C2CCC2)c2ccccc12 Show InChI InChI=1S/C21H27N5O/c1-14(2)26-18-9-4-3-8-17(18)19(24-26)21-23-22-20(27-21)15-10-12-25(13-11-15)16-6-5-7-16/h3-4,8-9,14-16H,5-7,10-13H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	>4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM325598 (3-[5-(1-Cyclopropylmethyl-piperidin-4-yl)-[1,3,4]o...) Show SMILES CC(C)n1nc(-c2nnc(o2)C2CCN(CC3CC3)CC2)c2ccccc12 Show InChI InChI=1S/C21H27N5O/c1-14(2)26-18-6-4-3-5-17(18)19(24-26)21-23-22-20(27-21)16-9-11-25(12-10-16)13-15-7-8-15/h3-6,14-16H,7-13H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	>4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM325594 (3-[5-(1-Cyclobutylmethyl-piperidin-4-yl)-[1,3,4]ox...) Show SMILES CC(C)n1nc(-c2nnc(o2)C2CCN(CC3CCC3)CC2)c2ccccc12 Show InChI InChI=1S/C22H29N5O/c1-15(2)27-19-9-4-3-8-18(19)20(25-27)22-24-23-21(28-22)17-10-12-26(13-11-17)14-16-6-5-7-16/h3-4,8-9,15-17H,5-7,10-14H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	>4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM325597 (1-Isopropyl-3-[5-(1-isopropyl-piperidin-4-yl)-[1,3...) Show SMILES CC(C)N1CCC(CC1)c1nnc(o1)-c1nn(C(C)C)c2ccccc12 Show InChI InChI=1S/C20H27N5O/c1-13(2)24-11-9-15(10-12-24)19-21-22-20(26-19)18-16-7-5-6-8-17(16)25(23-18)14(3)4/h5-8,13-15H,9-12H2,1-4H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	>4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50391248 (CHEMBL5284140) Show SMILES COc1cc(COc2cnc(N)nc2N)ccc1OCCCNS(=O)(=O)c1ccc(C)cc1 Show InChI InChI=1S/C22H27N5O5S/c1-15-4-7-17(8-5-15)33(28,29)26-10-3-11-31-18-9-6-16(12-19(18)30-2)14-32-20-13-25-22(24)27-21(20)23/h4-9,12-13,26H,3,10-11,14H2,1-2H3,(H4,23,24,25,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	>4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50391246 (CHEMBL5275895) Show SMILES COc1ccc(CNc2cnc(N)nc2N)cc1 Show InChI InChI=1S/C12H15N5O/c1-18-9-4-2-8(3-5-9)6-15-10-7-16-12(14)17-11(10)13/h2-5,7,15H,6H2,1H3,(H4,13,14,16,17)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	>4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50391283 (CHEMBL5268064) Show SMILES OC(=O)CC\C=C/CO[C@H]1C(CC[C@@H]1N1CCCCCC1)OCc1ccc(cc1)-c1ccc(O)cc1 Show InChI InChI=1S/C30H39NO5/c32-26-15-13-25(14-16-26)24-11-9-23(10-12-24)22-36-28-18-17-27(31-19-5-1-2-6-20-31)30(28)35-21-7-3-4-8-29(33)34/h3,7,9-16,27-28,30,32H,1-2,4-6,8,17-22H2,(H,33,34)/b7-3-/t27-,28?,30+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	>4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				Citation and Details
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 4 (Homo sapiens (Human))	BDBM50391258 (CHEMBL5286257) Show SMILES Nc1ncc(OCc2ccc(OCCCN3C(=O)c4ccccc4C3=O)cc2)c(N)n1 Show InChI InChI=1S/C22H21N5O4/c23-19-18(12-25-22(24)26-19)31-13-14-6-8-15(9-7-14)30-11-3-10-27-20(28)16-4-1-2-5-17(16)21(27)29/h1-2,4-9,12H,3,10-11,13H2,(H4,23,24,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	n/a	n/a	22	n/a	n/a	n/a	n/a
TBA					Assay Description Beta-1 adrenergic receptor activitation measured by isoprenaline-induced positive inotropic effect in guinea pig left atrium				Citation and Details
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 4 (Homo sapiens (Human))	BDBM50391255 (CHEMBL5283568) Show SMILES Nc1ncc(OCc2cccc3ccccc23)c(N)n1 Show InChI InChI=1S/C15H14N4O/c16-14-13(8-18-15(17)19-14)20-9-11-6-3-5-10-4-1-2-7-12(10)11/h1-8H,9H2,(H4,16,17,18,19)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	n/a	n/a	10	n/a	n/a	n/a	n/a
TBA					Assay Description Beta-1 adrenergic receptor activitation measured by isoprenaline-induced positive inotropic effect in guinea pig left atrium				Citation and Details
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 4 (Homo sapiens (Human))	BDBM50391256 (CHEMBL5271303) Show SMILES Nc1ncc(NCc2cccc3ccccc23)c(N)n1 Show InChI InChI=1S/C15H15N5/c16-14-13(9-19-15(17)20-14)18-8-11-6-3-5-10-4-1-2-7-12(10)11/h1-7,9,18H,8H2,(H4,16,17,19,20)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a
TBA					Assay Description Beta-1 adrenergic receptor activitation measured by isoprenaline-induced positive inotropic effect in guinea pig left atrium				Citation and Details
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 4 (Homo sapiens (Human))	BDBM50391259 (CHEMBL5290222) Show SMILES Nc1ncc(OCc2c(Cl)cccc2Cl)c(N)n1 Show InChI InChI=1S/C11H10Cl2N4O/c12-7-2-1-3-8(13)6(7)5-18-9-4-16-11(15)17-10(9)14/h1-4H,5H2,(H4,14,15,16,17)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	n/a	n/a	25	n/a	n/a	n/a	n/a
TBA					Assay Description Beta-1 adrenergic receptor activitation measured by isoprenaline-induced positive inotropic effect in guinea pig left atrium				Citation and Details
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 4 (Homo sapiens (Human))	BDBM50391260 (CHEMBL5288891) Show SMILES Nc1ncc(Cc2cccc3ccccc23)c(N)n1 Show InChI InChI=1S/C15H14N4/c16-14-12(9-18-15(17)19-14)8-11-6-3-5-10-4-1-2-7-13(10)11/h1-7,9H,8H2,(H4,16,17,18,19)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars		n/a	n/a	n/a	n/a	49	n/a	n/a	n/a	n/a
TBA					Assay Description Beta-1 adrenergic receptor activitation measured by isoprenaline-induced positive inotropic effect in guinea pig left atrium				Citation and Details
					More data for this Ligand-Target Pair

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