Compile Data Set for Download or QSAR

Found 181 hits with Last Name = 'butov' and Initial = 'gm'   

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
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50012059 (CHEMBL3263302) Show SMILES O=C(NCCCCCCCCNC(=O)NC1C2CC3CC(C2)CC1C3)NC1C2CC3CC(C2)CC1C3 |TLB:24:23:21:17.19.18,25:26:28:31.30.32,14:15:21.20.22:17.18.24,THB:24:18:21:15.23.22,33:34:28:31.30.32,33:31:28:34.35.26,26:34:30:28.27.32,26:27:30:34.35.33,14:15:21:17.19.18,19:20:15:17.18.24,19:18:15:21.20.22,(30.44,-12.61,;30.47,-11.07,;29.15,-10.27,;27.82,-11.05,;26.49,-10.27,;25.16,-11.05,;23.82,-10.27,;22.48,-11.05,;21.15,-10.27,;19.82,-11.05,;18.49,-10.27,;17.16,-11.04,;15.82,-10.28,;15.82,-8.74,;14.49,-11.05,;13.15,-10.29,;11.96,-11.24,;10.81,-10.38,;10.36,-9.04,;8.61,-8.92,;9.88,-9.82,;10.33,-11.27,;11.11,-8.82,;12.72,-8.84,;11.51,-8.1,;31.81,-10.33,;33.12,-11.12,;33.1,-12.63,;32.15,-13.86,;33.78,-13.24,;35.15,-13.82,;36.1,-12.76,;34.56,-13.25,;36.1,-11.25,;34.69,-10.68,;33.83,-11.83,)| Show InChI InChI=1S/C30H50N4O2/c35-29(33-27-23-11-19-9-20(13-23)14-24(27)12-19)31-7-5-3-1-2-4-6-8-32-30(36)34-28-25-15-21-10-22(17-25)18-26(28)16-21/h19-28H,1-18H2,(H2,31,33,35)(H2,32,34,36)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Volzhsky Polytechnic Institute (branch) Volgograd State Technical University Curated by ChEMBL					Assay Description Displacement of ACPU from recombinant human soluble epoxide hydrolase after 1.5 hrs by FRET assay				Bioorg Med Chem Lett 24: 2193-7 (2014) Article DOI: 10.1016/j.bmcl.2014.03.016 BindingDB Entry DOI: 10.7270/Q2PR7XHZ
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50012016 (CHEMBL3263294) Show SMILES CC(NC(=O)NCCCCNC(=O)NC(C)C12CC3CC(CC(C3)C1)C2)C12CC3CC(CC(C3)C1)C2 |TLB:33:32:35:27.29.28,33:28:35:31.32.34,19:20:17.18.23:24,THB:21:20:17:23.22.24,21:22:17:19.20.25,19:18:21.20.25:24,31:30:27:33.32.34,31:32:27:30.35.29| Show InChI InChI=1S/C30H50N4O2/c1-19(29-13-21-7-22(14-29)9-23(8-21)15-29)33-27(35)31-5-3-4-6-32-28(36)34-20(2)30-16-24-10-25(17-30)12-26(11-24)18-30/h19-26H,3-18H2,1-2H3,(H2,31,33,35)(H2,32,34,36)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	2.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Volzhsky Polytechnic Institute (branch) Volgograd State Technical University Curated by ChEMBL					Assay Description Displacement of ACPU from recombinant human soluble epoxide hydrolase after 1.5 hrs by FRET assay				Bioorg Med Chem Lett 24: 2193-7 (2014) Article DOI: 10.1016/j.bmcl.2014.03.016 BindingDB Entry DOI: 10.7270/Q2PR7XHZ
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50012054 (CHEMBL3263297) Show SMILES CC(NC(=O)NCCCCCCCCNC(=O)NC(C)C12CC3CC(CC(C3)C1)C2)C12CC3CC(CC(C3)C1)C2 |TLB:18:20:23:26.27.25,29:20:27:23.24.25,33:34:38:31.32.37,THB:29:24:27:20.21.28,35:36:31:39.33.34,35:34:31:38.36.37,33:32:38:39.34.35,28:20:23:26.27.25,28:26:23:20.21.29| Show InChI InChI=1S/C34H58N4O2/c1-23(33-17-25-11-26(18-33)13-27(12-25)19-33)37-31(39)35-9-7-5-3-4-6-8-10-36-32(40)38-24(2)34-20-28-14-29(21-34)16-30(15-28)22-34/h23-30H,3-22H2,1-2H3,(H2,35,37,39)(H2,36,38,40)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Volzhsky Polytechnic Institute (branch) Volgograd State Technical University Curated by ChEMBL					Assay Description Displacement of ACPU from recombinant human soluble epoxide hydrolase after 1.5 hrs by FRET assay				Bioorg Med Chem Lett 24: 2193-7 (2014) Article DOI: 10.1016/j.bmcl.2014.03.016 BindingDB Entry DOI: 10.7270/Q2PR7XHZ
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50012011 (CHEMBL3263289) Show SMILES O=C(NCCCCCCNC(=O)NCC12CC3CC(CC(C3)C1)C2)NCC12CC3CC(CC(C3)C1)C2 |TLB:13:14:17:21.20.19,25:26:29:33.32.31,THB:15:16:19:23.14.22,15:14:17.16.21:19,27:28:31:35.26.34,27:26:29.28.33:31,22:14:17:21.20.19,22:20:17:23.15.14,34:26:29:33.32.31,34:32:29:35.27.26| Show InChI InChI=1S/C30H50N4O2/c35-27(33-19-29-13-21-7-22(14-29)9-23(8-21)15-29)31-5-3-1-2-4-6-32-28(36)34-20-30-16-24-10-25(17-30)12-26(11-24)18-30/h21-26H,1-20H2,(H2,31,33,35)(H2,32,34,36)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	3.40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Volzhsky Polytechnic Institute (branch) Volgograd State Technical University Curated by ChEMBL					Assay Description Displacement of ACPU from recombinant human soluble epoxide hydrolase after 1.5 hrs by FRET assay				Bioorg Med Chem Lett 24: 2193-7 (2014) Article DOI: 10.1016/j.bmcl.2014.03.016 BindingDB Entry DOI: 10.7270/Q2PR7XHZ
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50546459 (CHEMBL4759033) Show SMILES O=C(NCCCCCCCCNC(=O)NC1CC2CCC1C2)NC1CC2CCC1C2 Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.400	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human soluble epoxide hydrolase by kinetic fluorescent assay				Citation and Details Article DOI: 10.1016/j.bmcl.2020.127430 BindingDB Entry DOI: 10.7270/Q2WQ07D6
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50546457 (CHEMBL4786305) Show SMILES O=C(NCCCCCCCCCCNC(=O)NC1CC2CC1C=C2)NC1CC2CC1C=C2 |c:23,33| Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.400	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human soluble epoxide hydrolase by kinetic fluorescent assay				Citation and Details Article DOI: 10.1016/j.bmcl.2020.127430 BindingDB Entry DOI: 10.7270/Q2WQ07D6
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50546461 (CHEMBL4750771) Show SMILES CC1(C)C2CCC1(C)C(C2)NC(=O)NCCCCCCCCNC(=O)NC1CC2CCC1(C)C2(C)C Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.400	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human soluble epoxide hydrolase by kinetic fluorescent assay				Citation and Details Article DOI: 10.1016/j.bmcl.2020.127430 BindingDB Entry DOI: 10.7270/Q2WQ07D6
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50546449 (CHEMBL4746902) Show SMILES FC(F)(F)Oc1ccc(NC(=O)NC2CC3CCC2C3)cc1 Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.400	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human soluble epoxide hydrolase by kinetic fluorescent assay				Citation and Details Article DOI: 10.1016/j.bmcl.2020.127430 BindingDB Entry DOI: 10.7270/Q2WQ07D6
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50012011 (CHEMBL3263289) Show SMILES O=C(NCCCCCCNC(=O)NCC12CC3CC(CC(C3)C1)C2)NCC12CC3CC(CC(C3)C1)C2 |TLB:13:14:17:21.20.19,25:26:29:33.32.31,THB:15:16:19:23.14.22,15:14:17.16.21:19,27:28:31:35.26.34,27:26:29.28.33:31,22:14:17:21.20.19,22:20:17:23.15.14,34:26:29:33.32.31,34:32:29:35.27.26| Show InChI InChI=1S/C30H50N4O2/c35-27(33-19-29-13-21-7-22(14-29)9-23(8-21)15-29)31-5-3-1-2-4-6-32-28(36)34-20-30-16-24-10-25(17-30)12-26(11-24)18-30/h21-26H,1-20H2,(H2,31,33,35)(H2,32,34,36)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	0.400	n/a	n/a	n/a	n/a	n/a	n/a
Volzhsky Polytechnic Institute (branch) Volgograd State Technical University Curated by ChEMBL					Assay Description Inhibition of recombinant human soluble epoxide hydrolase using CMNPC as substrate preincubated for 5 mins followed by substrate addition measured at...				Bioorg Med Chem Lett 24: 2193-7 (2014) Article DOI: 10.1016/j.bmcl.2014.03.016 BindingDB Entry DOI: 10.7270/Q2PR7XHZ
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50539380 (CHEMBL4643551) Show SMILES OC(=O)c1ccc(O[C@H]2CC[C@@H](CC2)NC(=O)NC23CC4CC(CC(Cl)(C4)C2)C3)cc1 |r,wU:8.7,wD:11.14,TLB:21:22:26.20.19:27,28:18:26:23.21.22,THB:17:18:26:23.21.22,21:20:27:23.22.28,28:22:26:19.18.27,(68.54,-12.24,;67.2,-11.47,;67.19,-9.93,;65.85,-12.25,;64.52,-11.49,;63.2,-12.26,;63.19,-13.8,;61.86,-14.59,;60.5,-13.83,;59.18,-14.61,;57.83,-13.86,;57.8,-12.32,;59.16,-11.51,;60.49,-12.28,;56.43,-11.59,;55.12,-12.42,;55.19,-13.97,;53.75,-11.71,;52.39,-12.42,;50.86,-11.93,;49.4,-12.53,;49.41,-14.04,;50.97,-14.5,;50.12,-13.34,;50.07,-11.93,;49.76,-10.42,;48.44,-11.3,;51.44,-11.36,;52.38,-13.93,;64.53,-14.57,;65.86,-13.8,)| Show InChI InChI=1S/C24H31ClN2O4/c25-23-10-15-9-16(11-23)13-24(12-15,14-23)27-22(30)26-18-3-7-20(8-4-18)31-19-5-1-17(2-6-19)21(28)29/h1-2,5-6,15-16,18,20H,3-4,7-14H2,(H,28,29)(H2,26,27,30)/t15?,16?,18-,20-,23?,24?	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.400	n/a	n/a	n/a	n/a	n/a	n/a
University of California Davis Curated by ChEMBL					Assay Description Inhibition of human soluble epoxide hydrolase using cyano(2methoxy naphthalen-6-yl)methyl trans-(3-phenyloxyran-2-yl)methylcarbonate as substrate pre...				Bioorg Med Chem Lett 30: (2020) Article DOI: 10.1016/j.bmcl.2019.126908 BindingDB Entry DOI: 10.7270/Q2M0490F
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50539356 (CHEMBL4641404) Show SMILES OC(=O)c1ccc(O[C@H]2CC[C@@H](CC2)N2C(=O)N(C(=O)C2=O)C23CC4CC(CC(Cl)(C4)C2)C3)cc1 |r,wU:8.7,wD:11.14,TLB:32:22:30:27.25.26,25:26:30.24.23:31,THB:32:26:30:23.22.31,17:22:30:27.25.26,25:24:31:27.26.32,(46.15,-13.46,;44.82,-12.69,;44.81,-11.15,;43.49,-13.47,;42.15,-12.71,;40.82,-13.48,;40.82,-15.02,;39.49,-15.79,;38.15,-15.02,;36.83,-15.78,;35.49,-15,;35.5,-13.46,;36.84,-12.7,;38.16,-13.47,;34.17,-12.69,;32.76,-13.3,;32.44,-14.81,;31.74,-12.16,;32.51,-10.83,;31.89,-9.42,;34.02,-11.15,;35.17,-10.13,;30.2,-12.19,;29.04,-11.06,;27.46,-10.95,;26.79,-12.31,;27.99,-13.42,;27.75,-12,;28.34,-10.71,;28.73,-9.22,;27.15,-9.42,;29.82,-10.81,;29.52,-13.54,;42.16,-15.79,;43.49,-15.02,)| Show InChI InChI=1S/C26H29ClN2O6/c27-25-10-15-9-16(11-25)13-26(12-15,14-25)29-22(31)21(30)28(24(29)34)18-3-7-20(8-4-18)35-19-5-1-17(2-6-19)23(32)33/h1-2,5-6,15-16,18,20H,3-4,7-14H2,(H,32,33)/t15?,16?,18-,20-,25?,26?	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.400	n/a	n/a	n/a	n/a	n/a	n/a
University of California Davis Curated by ChEMBL					Assay Description Inhibition of human soluble epoxide hydrolase by kinetic fluorescent assay				Bioorg Med Chem Lett 30: (2020) Article DOI: 10.1016/j.bmcl.2019.126908 BindingDB Entry DOI: 10.7270/Q2M0490F
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50012054 (CHEMBL3263297) Show SMILES CC(NC(=O)NCCCCCCCCNC(=O)NC(C)C12CC3CC(CC(C3)C1)C2)C12CC3CC(CC(C3)C1)C2 |TLB:18:20:23:26.27.25,29:20:27:23.24.25,33:34:38:31.32.37,THB:29:24:27:20.21.28,35:36:31:39.33.34,35:34:31:38.36.37,33:32:38:39.34.35,28:20:23:26.27.25,28:26:23:20.21.29| Show InChI InChI=1S/C34H58N4O2/c1-23(33-17-25-11-26(18-33)13-27(12-25)19-33)37-31(39)35-9-7-5-3-4-6-8-10-36-32(40)38-24(2)34-20-28-14-29(21-34)16-30(15-28)22-34/h23-30H,3-22H2,1-2H3,(H2,35,37,39)(H2,36,38,40)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	0.5	n/a	n/a	n/a	n/a	n/a	n/a
Volzhsky Polytechnic Institute (branch) Volgograd State Technical University Curated by ChEMBL					Assay Description Inhibition of recombinant human soluble epoxide hydrolase using CMNPC as substrate preincubated for 5 mins followed by substrate addition measured at...				Bioorg Med Chem Lett 24: 2193-7 (2014) Article DOI: 10.1016/j.bmcl.2014.03.016 BindingDB Entry DOI: 10.7270/Q2PR7XHZ
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50546453 (CHEMBL4800466) Show SMILES O=C(NCC12CC3CC(CC(C3)C1)C2)NC1CC2CC1C=C2 |c:24,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	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.700	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human soluble epoxide hydrolase by kinetic fluorescent assay				Citation and Details Article DOI: 10.1016/j.bmcl.2020.127430 BindingDB Entry DOI: 10.7270/Q2WQ07D6
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50012011 (CHEMBL3263289) Show SMILES O=C(NCCCCCCNC(=O)NCC12CC3CC(CC(C3)C1)C2)NCC12CC3CC(CC(C3)C1)C2 |TLB:13:14:17:21.20.19,25:26:29:33.32.31,THB:15:16:19:23.14.22,15:14:17.16.21:19,27:28:31:35.26.34,27:26:29.28.33:31,22:14:17:21.20.19,22:20:17:23.15.14,34:26:29:33.32.31,34:32:29:35.27.26| Show InChI InChI=1S/C30H50N4O2/c35-27(33-19-29-13-21-7-22(14-29)9-23(8-21)15-29)31-5-3-1-2-4-6-32-28(36)34-20-30-16-24-10-25(17-30)12-26(11-24)18-30/h21-26H,1-20H2,(H2,31,33,35)(H2,32,34,36)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	0.700	n/a	n/a	n/a	n/a	n/a	n/a
Volzhsky Polytechnic Institute (branch) Volgograd State Technical University Curated by ChEMBL					Assay Description Inhibition of recombinant human soluble epoxide hydrolase using CMNPC as substrate preincubated for 5 mins followed by substrate addition measured at...				Bioorg Med Chem Lett 24: 2193-7 (2014) Article DOI: 10.1016/j.bmcl.2014.03.016 BindingDB Entry DOI: 10.7270/Q2PR7XHZ
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50539360 (CHEMBL4633887) Show SMILES Fc1ccccc1NC(=O)NCC12CC3CC(CC(C3)C1)C2 |TLB:11:12:15:19.18.17,THB:20:12:15:19.18.17,20:18:15:21.13.12,13:14:17:21.12.20,13:12:15.14.19:17| Show InChI InChI=1S/C18H23FN2O/c19-15-3-1-2-4-16(15)21-17(22)20-11-18-8-12-5-13(9-18)7-14(6-12)10-18/h1-4,12-14H,5-11H2,(H2,20,21,22)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.700	n/a	n/a	n/a	n/a	n/a	n/a
University of California Davis Curated by ChEMBL					Assay Description Inhibition of human soluble epoxide hydrolase by kinetic fluorescent assay				Bioorg Med Chem Lett 30: (2020) Article DOI: 10.1016/j.bmcl.2019.126908 BindingDB Entry DOI: 10.7270/Q2M0490F
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50539384 (CHEMBL4645669) Show SMILES O=C(NCCCCCCNC(=O)NCCC12CC3CC(CC(C3)C1)C2)NCCC12CC3CC(CC(C3)C1)C2 |TLB:27:28:31:35.34.33,14:15:18:22.21.20,THB:33:34:31.32.37:29,33:32:29:35.34.36,20:21:18.19.24:16,20:19:16:22.21.23,36:34:31:37.28.29,36:28:31:35.34.33,23:21:18:24.15.16,23:15:18:22.21.20| Show InChI InChI=1S/C32H54N4O2/c37-29(35-9-5-31-17-23-11-24(18-31)13-25(12-23)19-31)33-7-3-1-2-4-8-34-30(38)36-10-6-32-20-26-14-27(21-32)16-28(15-26)22-32/h23-28H,1-22H2,(H2,33,35,37)(H2,34,36,38)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.800	n/a	n/a	n/a	n/a	n/a	n/a
University of California Davis Curated by ChEMBL					Assay Description Inhibition of human soluble epoxide hydrolase using cyano(2methoxy naphthalen-6-yl)methyl trans-(3-phenyloxyran-2-yl)methylcarbonate as substrate pre...				Bioorg Med Chem Lett 30: (2020) Article DOI: 10.1016/j.bmcl.2019.126908 BindingDB Entry DOI: 10.7270/Q2M0490F
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50012054 (CHEMBL3263297) Show SMILES CC(NC(=O)NCCCCCCCCNC(=O)NC(C)C12CC3CC(CC(C3)C1)C2)C12CC3CC(CC(C3)C1)C2 |TLB:18:20:23:26.27.25,29:20:27:23.24.25,33:34:38:31.32.37,THB:29:24:27:20.21.28,35:36:31:39.33.34,35:34:31:38.36.37,33:32:38:39.34.35,28:20:23:26.27.25,28:26:23:20.21.29| Show InChI InChI=1S/C34H58N4O2/c1-23(33-17-25-11-26(18-33)13-27(12-25)19-33)37-31(39)35-9-7-5-3-4-6-8-10-36-32(40)38-24(2)34-20-28-14-29(21-34)16-30(15-28)22-34/h23-30H,3-22H2,1-2H3,(H2,35,37,39)(H2,36,38,40)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	0.800	n/a	n/a	n/a	n/a	n/a	n/a
Volzhsky Polytechnic Institute (branch) Volgograd State Technical University Curated by ChEMBL					Assay Description Inhibition of recombinant human soluble epoxide hydrolase using CMNPC as substrate preincubated for 5 mins followed by substrate addition measured at...				Bioorg Med Chem Lett 24: 2193-7 (2014) Article DOI: 10.1016/j.bmcl.2014.03.016 BindingDB Entry DOI: 10.7270/Q2PR7XHZ
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50546454 (CHEMBL4776297) Show SMILES O=C(NC1CC2CC1C=C2)NC1C2CC3CC(C2)CC1C3 |c:9,TLB:10:11:13:17.15.16,THB:18:16:13:20.19.11,18:19:13:17.15.16,15:14:11:17.16.18,15:16:13.14.20:11,(12.51,-54.37,;12.51,-52.8,;11.16,-52.02,;9.8,-52.8,;9.8,-54.33,;8.47,-55.09,;9.3,-53.54,;8.48,-52.02,;7.14,-52.77,;7.13,-54.3,;13.87,-52.02,;15.23,-52.81,;15.25,-54.32,;14.04,-55.61,;15.56,-55.18,;16.99,-55.73,;18.01,-54.43,;16.6,-54.79,;18.01,-52.88,;16.59,-52.32,;15.54,-53.57,)| Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.900	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human soluble epoxide hydrolase by kinetic fluorescent assay				Citation and Details Article DOI: 10.1016/j.bmcl.2020.127430 BindingDB Entry DOI: 10.7270/Q2WQ07D6
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50539358 (CHEMBL4637039) Show SMILES Fc1ccccc1NC(=O)NC1C2CC3CC(C2)CC1C3 |TLB:17:16:20:13.12.11,17:12:15.16.18:20,THB:11:12:15:18.19.20,11:19:15:13.17.12,10:11:15.16.18:20,(27.35,-19.37,;27.82,-20.84,;29.32,-21.17,;29.78,-22.65,;28.74,-23.78,;27.23,-23.45,;26.78,-21.97,;25.28,-21.63,;24.12,-22.65,;24.54,-24.13,;22.68,-22.12,;21.4,-22.97,;21.39,-24.5,;19.99,-24.85,;18.66,-24.37,;17.46,-25.64,;18.97,-25.22,;20.37,-25.78,;18.96,-23.63,;20,-22.4,;18.65,-22.87,)| Show InChI InChI=1S/C17H21FN2O/c18-14-3-1-2-4-15(14)19-17(21)20-16-12-6-10-5-11(8-12)9-13(16)7-10/h1-4,10-13,16H,5-9H2,(H2,19,20,21)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	Article PubMed	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
University of California Davis Curated by ChEMBL					Assay Description Inhibition of human soluble epoxide hydrolase by kinetic fluorescent assay				Bioorg Med Chem Lett 30: (2020) Article DOI: 10.1016/j.bmcl.2019.126908 BindingDB Entry DOI: 10.7270/Q2M0490F
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM158481 (US9029401, 1728 (t-TUCB)) Show SMILES OC(=O)c1ccc(O[C@H]2CC[C@@H](CC2)NC(=O)Nc2ccc(OC(F)(F)F)cc2)cc1 |r,wU:8.7,wD:11.14,(10,,;8.67,-.77,;8.67,-2.31,;7.34,,;6,-.77,;4.67,,;4.67,1.54,;3.33,2.31,;2,1.54,;2,,;.67,-.77,;-.67,,;-.67,1.54,;.67,2.31,;-2,-.77,;-3.33,,;-3.33,1.54,;-4.67,-.77,;-6,,;-6,1.54,;-7.34,2.31,;-8.67,1.54,;-10,2.31,;-10,3.85,;-10,5.39,;-8.67,4.62,;-11.34,4.62,;-8.67,,;-7.34,-.77,;6,2.31,;7.34,1.54,)| Show InChI InChI=1S/C21H21F3N2O5/c22-21(23,24)31-18-11-5-15(6-12-18)26-20(29)25-14-3-9-17(10-4-14)30-16-7-1-13(2-8-16)19(27)28/h1-2,5-8,11-12,14,17H,3-4,9-10H2,(H,27,28)(H2,25,26,29)/t14-,17-	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid PDB UniChem Similars	PDB Article PubMed	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
University of California Davis Curated by ChEMBL					Assay Description Inhibition of human soluble epoxide hydrolase using CMNPC as substrate by fluorescence based assay				Bioorg Med Chem Lett 30: (2020) Article DOI: 10.1016/j.bmcl.2019.126908 BindingDB Entry DOI: 10.7270/Q2M0490F
					More data for this Ligand-Target Pair				3D Structure (crystal)
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM158481 (US9029401, 1728 (t-TUCB)) Show SMILES OC(=O)c1ccc(O[C@H]2CC[C@@H](CC2)NC(=O)Nc2ccc(OC(F)(F)F)cc2)cc1 |r,wU:8.7,wD:11.14,(10,,;8.67,-.77,;8.67,-2.31,;7.34,,;6,-.77,;4.67,,;4.67,1.54,;3.33,2.31,;2,1.54,;2,,;.67,-.77,;-.67,,;-.67,1.54,;.67,2.31,;-2,-.77,;-3.33,,;-3.33,1.54,;-4.67,-.77,;-6,,;-6,1.54,;-7.34,2.31,;-8.67,1.54,;-10,2.31,;-10,3.85,;-10,5.39,;-8.67,4.62,;-11.34,4.62,;-8.67,,;-7.34,-.77,;6,2.31,;7.34,1.54,)| Show InChI InChI=1S/C21H21F3N2O5/c22-21(23,24)31-18-11-5-15(6-12-18)26-20(29)25-14-3-9-17(10-4-14)30-16-7-1-13(2-8-16)19(27)28/h1-2,5-8,11-12,14,17H,3-4,9-10H2,(H,27,28)(H2,25,26,29)/t14-,17-	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid PDB UniChem Similars	PDB Article PubMed	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of recombinant human soluble epoxide hydrolase using CMNPC as fluorescent substrate				Citation and Details Article DOI: 10.1016/j.bmcl.2020.127430 BindingDB Entry DOI: 10.7270/Q2WQ07D6
					More data for this Ligand-Target Pair				3D Structure (crystal)
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50012016 (CHEMBL3263294) Show SMILES CC(NC(=O)NCCCCNC(=O)NC(C)C12CC3CC(CC(C3)C1)C2)C12CC3CC(CC(C3)C1)C2 |TLB:33:32:35:27.29.28,33:28:35:31.32.34,19:20:17.18.23:24,THB:21:20:17:23.22.24,21:22:17:19.20.25,19:18:21.20.25:24,31:30:27:33.32.34,31:32:27:30.35.29| Show InChI InChI=1S/C30H50N4O2/c1-19(29-13-21-7-22(14-29)9-23(8-21)15-29)33-27(35)31-5-3-4-6-32-28(36)34-20(2)30-16-24-10-25(17-30)12-26(11-24)18-30/h19-26H,3-18H2,1-2H3,(H2,31,33,35)(H2,32,34,36)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.20	n/a	n/a	n/a	n/a	n/a	n/a
Volzhsky Polytechnic Institute (branch) Volgograd State Technical University Curated by ChEMBL					Assay Description Inhibition of recombinant human soluble epoxide hydrolase using CMNPC as substrate preincubated for 5 mins followed by substrate addition measured at...				Bioorg Med Chem Lett 24: 2193-7 (2014) Article DOI: 10.1016/j.bmcl.2014.03.016 BindingDB Entry DOI: 10.7270/Q2PR7XHZ
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM129310 (US8815951, 411) Show SMILES O=C(NC12CC3CC(CC(C3)C1)C2)NC12CC3CC(CC(C3)C1)C2 |TLB:23:14:21:17.18.19,13:14:17:21.20.19,2:3:6:10.9.8,12:3:10:6.7.8,THB:23:18:21:14.22.15,22:14:17:21.20.19,22:20:17:14.23.15,12:7:10:3.11.4,11:3:6:10.9.8,11:9:6:3.12.4| Show InChI InChI=1S/C21H32N2O/c24-19(22-20-7-13-1-14(8-20)3-15(2-13)9-20)23-21-10-16-4-17(11-21)6-18(5-16)12-21/h13-18H,1-12H2,(H2,22,23,24)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.20	n/a	n/a	n/a	n/a	n/a	n/a
University of California Davis Curated by ChEMBL					Assay Description Inhibition of recombinant human sEH expressed in baculovirus expression system using CMNPC as substrate preincubated for 5 mins followed by substrate...				Bioorg Med Chem Lett 28: 2302-2313 (2018) Article DOI: 10.1016/j.bmcl.2018.05.024 BindingDB Entry DOI: 10.7270/Q2222X8F
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM129310 (US8815951, 411) Show SMILES O=C(NC12CC3CC(CC(C3)C1)C2)NC12CC3CC(CC(C3)C1)C2 |TLB:23:14:21:17.18.19,13:14:17:21.20.19,2:3:6:10.9.8,12:3:10:6.7.8,THB:23:18:21:14.22.15,22:14:17:21.20.19,22:20:17:14.23.15,12:7:10:3.11.4,11:3:6:10.9.8,11:9:6:3.12.4| Show InChI InChI=1S/C21H32N2O/c24-19(22-20-7-13-1-14(8-20)3-15(2-13)9-20)23-21-10-16-4-17(11-21)6-18(5-16)12-21/h13-18H,1-12H2,(H2,22,23,24)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.20	n/a	n/a	n/a	n/a	n/a	n/a
Volzhsky Polytechnic Institute (branch) Volgograd State Technical University Curated by ChEMBL					Assay Description Inhibition of recombinant human soluble epoxide hydrolase using CMNPC as substrate preincubated for 5 mins followed by substrate addition measured at...				Bioorg Med Chem Lett 24: 2193-7 (2014) Article DOI: 10.1016/j.bmcl.2014.03.016 BindingDB Entry DOI: 10.7270/Q2PR7XHZ
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM129310 (US8815951, 411) Show SMILES O=C(NC12CC3CC(CC(C3)C1)C2)NC12CC3CC(CC(C3)C1)C2 |TLB:23:14:21:17.18.19,13:14:17:21.20.19,2:3:6:10.9.8,12:3:10:6.7.8,THB:23:18:21:14.22.15,22:14:17:21.20.19,22:20:17:14.23.15,12:7:10:3.11.4,11:3:6:10.9.8,11:9:6:3.12.4| Show InChI InChI=1S/C21H32N2O/c24-19(22-20-7-13-1-14(8-20)3-15(2-13)9-20)23-21-10-16-4-17(11-21)6-18(5-16)12-21/h13-18H,1-12H2,(H2,22,23,24)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.30	n/a	n/a	n/a	n/a	n/a	n/a
Volzhsky Polytechnic Institute (branch) Volgograd State Technical University Curated by ChEMBL					Assay Description Inhibition of recombinant human soluble epoxide hydrolase using CMNPC as substrate preincubated for 5 mins followed by substrate addition measured at...				Bioorg Med Chem Lett 24: 2193-7 (2014) Article DOI: 10.1016/j.bmcl.2014.03.016 BindingDB Entry DOI: 10.7270/Q2PR7XHZ
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50546447 (CHEMBL4755752) Show SMILES OC(=O)c1ccc(O[C@H]2CC[C@@H](CC2)NC(=O)NC2CC3CC2C=C3)cc1 |r,wU:8.7,wD:11.14,c:25,(22.5,-4.71,;21.17,-5.48,;21.17,-7.02,;19.83,-4.72,;18.49,-5.49,;17.16,-4.72,;17.16,-3.17,;15.83,-2.4,;14.49,-3.17,;14.5,-4.71,;13.16,-5.48,;11.83,-4.71,;11.83,-3.17,;13.16,-2.4,;10.49,-5.48,;9.16,-4.72,;9.16,-3.18,;7.83,-5.49,;6.49,-4.72,;6.5,-3.17,;5.17,-2.4,;4.65,-3.99,;5.16,-5.48,;3.83,-4.7,;3.83,-3.16,;18.49,-2.4,;19.83,-3.17,)| Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human soluble epoxide hydrolase by kinetic fluorescent assay				Citation and Details Article DOI: 10.1016/j.bmcl.2020.127430 BindingDB Entry DOI: 10.7270/Q2WQ07D6
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50539385 (CHEMBL4641883) Show SMILES O=C(NCCCCCCCCNC(=O)NCCC12CC3CC(CC(C3)C1)C2)NCCC12CC3CC(CC(C3)C1)C2 |TLB:29:30:33:37.36.35,16:17:20:24.23.22,THB:35:36:33.34.39:31,35:34:31:37.36.38,22:23:20.21.26:18,22:21:18:24.23.25,38:36:33:39.30.31,38:30:33:37.36.35,25:23:20:26.17.18,25:17:20:24.23.22| Show InChI InChI=1S/C34H58N4O2/c39-31(37-11-7-33-19-25-13-26(20-33)15-27(14-25)21-33)35-9-5-3-1-2-4-6-10-36-32(40)38-12-8-34-22-28-16-29(23-34)18-30(17-28)24-34/h25-30H,1-24H2,(H2,35,37,39)(H2,36,38,40)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.5	n/a	n/a	n/a	n/a	n/a	n/a
University of California Davis Curated by ChEMBL					Assay Description Inhibition of human soluble epoxide hydrolase using cyano(2methoxy naphthalen-6-yl)methyl trans-(3-phenyloxyran-2-yl)methylcarbonate as substrate pre...				Bioorg Med Chem Lett 30: (2020) Article DOI: 10.1016/j.bmcl.2019.126908 BindingDB Entry DOI: 10.7270/Q2M0490F
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50539371 (CHEMBL4642121) Show SMILES O=C1N(CCCCCCN2C(=O)N(C(=O)C2=O)C23CC4CC(CC(C4)C2)C3)C(=O)C(=O)N1C12CC3CC(CC(C3)C1)C2 |TLB:31:32:35:39.38.37,12:17:20:24.23.22,THB:33:34:37:41.32.40,33:32:35.34.39:37,18:19:22:26.17.25,18:17:20.19.24:22,40:32:35:39.38.37,40:38:35:41.33.32,25:17:20:24.23.22,25:23:20:26.18.17| Show InChI InChI=1S/C32H42N4O6/c37-25-27(39)35(31-13-19-7-20(14-31)9-21(8-19)15-31)29(41)33(25)5-3-1-2-4-6-34-26(38)28(40)36(30(34)42)32-16-22-10-23(17-32)12-24(11-22)18-32/h19-24H,1-18H2	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.60	n/a	n/a	n/a	n/a	n/a	n/a
University of California Davis Curated by ChEMBL					Assay Description Inhibition of human soluble epoxide hydrolase by kinetic fluorescent assay				Bioorg Med Chem Lett 30: (2020) Article DOI: 10.1016/j.bmcl.2019.126908 BindingDB Entry DOI: 10.7270/Q2M0490F
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50012017 (CHEMBL3263295) Show SMILES CCC(CNC(=O)NCCCCNC(=O)NCC(CC)C12CC3CC(CC(C3)C1)C2)C12CC3CC(CC(C3)C1)C2 |TLB:33:34:38:31.37.32,37:36:33.31.32:39,37:32:39:38.36.35,17:20:22.23.27:25,THB:33:32:38:34.39.35,21:20:22.23.27:25,21:22:25:20.28.29,28:26:23:21.20.29,28:20:23:26.27.25,17:20:23:26.27.25| Show InChI InChI=1S/C34H58N4O2/c1-3-29(33-15-23-9-24(16-33)11-25(10-23)17-33)21-37-31(39)35-7-5-6-8-36-32(40)38-22-30(4-2)34-18-26-12-27(19-34)14-28(13-26)20-34/h23-30H,3-22H2,1-2H3,(H2,35,37,39)(H2,36,38,40)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.30	n/a	n/a	n/a	n/a	n/a	n/a
Volzhsky Polytechnic Institute (branch) Volgograd State Technical University Curated by ChEMBL					Assay Description Inhibition of recombinant human soluble epoxide hydrolase using CMNPC as substrate preincubated for 5 mins followed by substrate addition measured at...				Bioorg Med Chem Lett 24: 2193-7 (2014) Article DOI: 10.1016/j.bmcl.2014.03.016 BindingDB Entry DOI: 10.7270/Q2PR7XHZ
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50546460 (CHEMBL4762498) Show SMILES CC1(C)C2CCC1(C)C(C2)NC(=O)NCCCCNC(=O)NC1CC2CCC1(C)C2(C)C Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.30	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human soluble epoxide hydrolase by kinetic fluorescent assay				Citation and Details Article DOI: 10.1016/j.bmcl.2020.127430 BindingDB Entry DOI: 10.7270/Q2WQ07D6
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50546450 (CHEMBL4790175) Show SMILES CC1(C)C2CCC1(C)C(C2)NC(=O)Nc1ccc(OC(F)(F)F)cc1 Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human soluble epoxide hydrolase by kinetic fluorescent assay				Citation and Details Article DOI: 10.1016/j.bmcl.2020.127430 BindingDB Entry DOI: 10.7270/Q2WQ07D6
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50012016 (CHEMBL3263294) Show SMILES CC(NC(=O)NCCCCNC(=O)NC(C)C12CC3CC(CC(C3)C1)C2)C12CC3CC(CC(C3)C1)C2 |TLB:33:32:35:27.29.28,33:28:35:31.32.34,19:20:17.18.23:24,THB:21:20:17:23.22.24,21:22:17:19.20.25,19:18:21.20.25:24,31:30:27:33.32.34,31:32:27:30.35.29| Show InChI InChI=1S/C30H50N4O2/c1-19(29-13-21-7-22(14-29)9-23(8-21)15-29)33-27(35)31-5-3-4-6-32-28(36)34-20(2)30-16-24-10-25(17-30)12-26(11-24)18-30/h19-26H,3-18H2,1-2H3,(H2,31,33,35)(H2,32,34,36)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.5	n/a	n/a	n/a	n/a	n/a	n/a
Volzhsky Polytechnic Institute (branch) Volgograd State Technical University Curated by ChEMBL					Assay Description Inhibition of recombinant human soluble epoxide hydrolase using CMNPC as substrate preincubated for 5 mins followed by substrate addition measured at...				Bioorg Med Chem Lett 24: 2193-7 (2014) Article DOI: 10.1016/j.bmcl.2014.03.016 BindingDB Entry DOI: 10.7270/Q2PR7XHZ
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50012059 (CHEMBL3263302) Show SMILES O=C(NCCCCCCCCNC(=O)NC1C2CC3CC(C2)CC1C3)NC1C2CC3CC(C2)CC1C3 |TLB:24:23:21:17.19.18,25:26:28:31.30.32,14:15:21.20.22:17.18.24,THB:24:18:21:15.23.22,33:34:28:31.30.32,33:31:28:34.35.26,26:34:30:28.27.32,26:27:30:34.35.33,14:15:21:17.19.18,19:20:15:17.18.24,19:18:15:21.20.22,(30.44,-12.61,;30.47,-11.07,;29.15,-10.27,;27.82,-11.05,;26.49,-10.27,;25.16,-11.05,;23.82,-10.27,;22.48,-11.05,;21.15,-10.27,;19.82,-11.05,;18.49,-10.27,;17.16,-11.04,;15.82,-10.28,;15.82,-8.74,;14.49,-11.05,;13.15,-10.29,;11.96,-11.24,;10.81,-10.38,;10.36,-9.04,;8.61,-8.92,;9.88,-9.82,;10.33,-11.27,;11.11,-8.82,;12.72,-8.84,;11.51,-8.1,;31.81,-10.33,;33.12,-11.12,;33.1,-12.63,;32.15,-13.86,;33.78,-13.24,;35.15,-13.82,;36.1,-12.76,;34.56,-13.25,;36.1,-11.25,;34.69,-10.68,;33.83,-11.83,)| Show InChI InChI=1S/C30H50N4O2/c35-29(33-27-23-11-19-9-20(13-23)14-24(27)12-19)31-7-5-3-1-2-4-6-8-32-30(36)34-28-25-15-21-10-22(17-25)18-26(28)16-21/h19-28H,1-18H2,(H2,31,33,35)(H2,32,34,36)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.60	n/a	n/a	n/a	n/a	n/a	n/a
Volzhsky Polytechnic Institute (branch) Volgograd State Technical University Curated by ChEMBL					Assay Description Inhibition of recombinant human soluble epoxide hydrolase using CMNPC as substrate preincubated for 5 mins followed by substrate addition measured at...				Bioorg Med Chem Lett 24: 2193-7 (2014) Article DOI: 10.1016/j.bmcl.2014.03.016 BindingDB Entry DOI: 10.7270/Q2PR7XHZ
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM25731 (1,3-dicyclohexylurea | CHEMBL1458 | US8815951, 1,3...) Show SMILES O=C(NC1CCCCC1)NC1CCCCC1 Show InChI InChI=1S/C13H24N2O/c16-13(14-11-7-3-1-4-8-11)15-12-9-5-2-6-10-12/h11-12H,1-10H2,(H2,14,15,16)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
Volzhsky Polytechnic Institute (branch) Volgograd State Technical University Curated by ChEMBL					Assay Description Inhibition of recombinant human soluble epoxide hydrolase using CMNPC as substrate preincubated for 5 mins followed by substrate addition measured at...				Bioorg Med Chem Lett 24: 2193-7 (2014) Article DOI: 10.1016/j.bmcl.2014.03.016 BindingDB Entry DOI: 10.7270/Q2PR7XHZ
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50539383 (CHEMBL4644608) Show SMILES O=C(NCCCCNC(=O)NCCC12CC3CC(CC(C3)C1)C2)NCCC12CC3CC(CC(C3)C1)C2 |TLB:12:13:16:20.19.18,25:26:29:33.32.31,THB:18:19:16.17.22:14,18:17:14:20.19.21,31:32:29.30.35:27,31:30:27:33.32.34,21:19:16:22.13.14,21:13:16:20.19.18,34:32:29:35.26.27,34:26:29:33.32.31| Show InChI InChI=1S/C30H50N4O2/c35-27(33-7-3-29-15-21-9-22(16-29)11-23(10-21)17-29)31-5-1-2-6-32-28(36)34-8-4-30-18-24-12-25(19-30)14-26(13-24)20-30/h21-26H,1-20H2,(H2,31,33,35)(H2,32,34,36)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.40	n/a	n/a	n/a	n/a	n/a	n/a
University of California Davis Curated by ChEMBL					Assay Description Inhibition of human soluble epoxide hydrolase using cyano(2methoxy naphthalen-6-yl)methyl trans-(3-phenyloxyran-2-yl)methylcarbonate as substrate pre...				Bioorg Med Chem Lett 30: (2020) Article DOI: 10.1016/j.bmcl.2019.126908 BindingDB Entry DOI: 10.7270/Q2M0490F
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50539364 (CHEMBL4649528) Show SMILES CC12CC3CC(C)(C1)CC(C3)(C2)NC(=O)Nc1ccccc1F |TLB:4:5:11:2.3.10,4:3:7.5.8:11,10:9:7:2.4.3,THB:12:9:7:2.4.3,10:3:7:8.9.11| Show InChI InChI=1S/C19H25FN2O/c1-17-7-13-8-18(2,10-17)12-19(9-13,11-17)22-16(23)21-15-6-4-3-5-14(15)20/h3-6,13H,7-12H2,1-2H3,(H2,21,22,23)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.60	n/a	n/a	n/a	n/a	n/a	n/a
University of California Davis Curated by ChEMBL					Assay Description Inhibition of human soluble epoxide hydrolase by kinetic fluorescent assay				Bioorg Med Chem Lett 30: (2020) Article DOI: 10.1016/j.bmcl.2019.126908 BindingDB Entry DOI: 10.7270/Q2M0490F
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50546441 (CHEMBL4778603) Show SMILES [H][C@]12CC[C@](C)(C(C1)NC(=O)Nc1ccccc1F)C2(C)C |r| Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.70	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human soluble epoxide hydrolase by kinetic fluorescent assay				Citation and Details Article DOI: 10.1016/j.bmcl.2020.127430 BindingDB Entry DOI: 10.7270/Q2WQ07D6
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50539372 (CHEMBL4644920) Show SMILES O=C1N(CCCCCCCCN2C(=O)N(C(=O)C2=O)C23CC4CC(CC(C4)C2)C3)C(=O)C(=O)N1C12CC3CC(CC(C3)C1)C2 |TLB:14:19:22:26.25.24,33:34:37:41.40.39,THB:35:36:39:43.34.42,35:34:37.36.41:39,42:34:37:41.40.39,42:40:37:43.35.34,20:21:24:28.19.27,20:19:22.21.26:24,27:19:22:26.25.24,27:25:22:28.20.19| Show InChI InChI=1S/C34H46N4O6/c39-27-29(41)37(33-15-21-9-22(16-33)11-23(10-21)17-33)31(43)35(27)7-5-3-1-2-4-6-8-36-28(40)30(42)38(32(36)44)34-18-24-12-25(19-34)14-26(13-24)20-34/h21-26H,1-20H2	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.80	n/a	n/a	n/a	n/a	n/a	n/a
University of California Davis Curated by ChEMBL					Assay Description Inhibition of human soluble epoxide hydrolase by kinetic fluorescent assay				Bioorg Med Chem Lett 30: (2020) Article DOI: 10.1016/j.bmcl.2019.126908 BindingDB Entry DOI: 10.7270/Q2M0490F
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50012059 (CHEMBL3263302) Show SMILES O=C(NCCCCCCCCNC(=O)NC1C2CC3CC(C2)CC1C3)NC1C2CC3CC(C2)CC1C3 |TLB:24:23:21:17.19.18,25:26:28:31.30.32,14:15:21.20.22:17.18.24,THB:24:18:21:15.23.22,33:34:28:31.30.32,33:31:28:34.35.26,26:34:30:28.27.32,26:27:30:34.35.33,14:15:21:17.19.18,19:20:15:17.18.24,19:18:15:21.20.22,(30.44,-12.61,;30.47,-11.07,;29.15,-10.27,;27.82,-11.05,;26.49,-10.27,;25.16,-11.05,;23.82,-10.27,;22.48,-11.05,;21.15,-10.27,;19.82,-11.05,;18.49,-10.27,;17.16,-11.04,;15.82,-10.28,;15.82,-8.74,;14.49,-11.05,;13.15,-10.29,;11.96,-11.24,;10.81,-10.38,;10.36,-9.04,;8.61,-8.92,;9.88,-9.82,;10.33,-11.27,;11.11,-8.82,;12.72,-8.84,;11.51,-8.1,;31.81,-10.33,;33.12,-11.12,;33.1,-12.63,;32.15,-13.86,;33.78,-13.24,;35.15,-13.82,;36.1,-12.76,;34.56,-13.25,;36.1,-11.25,;34.69,-10.68,;33.83,-11.83,)| Show InChI InChI=1S/C30H50N4O2/c35-29(33-27-23-11-19-9-20(13-23)14-24(27)12-19)31-7-5-3-1-2-4-6-8-32-30(36)34-28-25-15-21-10-22(17-25)18-26(28)16-21/h19-28H,1-18H2,(H2,31,33,35)(H2,32,34,36)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.10	n/a	n/a	n/a	n/a	n/a	n/a
Volzhsky Polytechnic Institute (branch) Volgograd State Technical University Curated by ChEMBL					Assay Description Inhibition of recombinant human soluble epoxide hydrolase using CMNPC as substrate preincubated for 5 mins followed by substrate addition measured at...				Bioorg Med Chem Lett 24: 2193-7 (2014) Article DOI: 10.1016/j.bmcl.2014.03.016 BindingDB Entry DOI: 10.7270/Q2PR7XHZ
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50133707 (CHEMBL3633681) Show SMILES CC12CC3CC(C)(C1)CC(C3)(C2)NC(=O)NCc1cc(on1)-c1ccco1 |TLB:4:5:11:3.2.10,4:3:11:7.5.8,6:5:11:3.2.10,6:5:1.11.2:10,7:1:5.8.4:10,THB:0:1:5.8.4:10,7:5:1.11.2:10| Show InChI InChI=1S/C21H27N3O3/c1-19-7-14-8-20(2,11-19)13-21(9-14,12-19)23-18(25)22-10-15-6-17(27-24-15)16-4-3-5-26-16/h3-6,14H,7-13H2,1-2H3,(H2,22,23,25)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.10	n/a	n/a	n/a	n/a	n/a	n/a
University of California at Davis Curated by ChEMBL					Assay Description Inhibition of recombinant human soluble epoxide hydrolase using CMNPC as substrate by kinetic fluorescent assay				Bioorg Med Chem Lett 25: 5514-9 (2015) Article DOI: 10.1016/j.bmcl.2015.10.066 BindingDB Entry DOI: 10.7270/Q28P62C1
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50539354 (CHEMBL4642519) Show SMILES OC(=O)c1ccc(O[C@H]2CC[C@@H](CC2)NC(=O)NC2CCCCCC2)cc1 |r,wU:8.7,wD:11.14,(43.15,-3.99,;41.8,-3.22,;41.8,-1.68,;40.46,-4,;39.13,-3.23,;37.8,-4,;37.8,-5.54,;36.46,-6.33,;35.11,-5.57,;33.79,-6.36,;32.43,-5.6,;32.41,-4.07,;33.77,-3.26,;35.1,-4.03,;31.03,-3.34,;29.73,-4.17,;29.8,-5.71,;28.36,-3.45,;27.06,-4.29,;27.37,-5.8,;26.38,-6.96,;24.86,-6.92,;23.91,-5.72,;24.29,-4.22,;25.69,-3.58,;39.13,-6.31,;40.47,-5.54,)| Show InChI InChI=1S/C21H30N2O4/c24-20(25)15-7-11-18(12-8-15)27-19-13-9-17(10-14-19)23-21(26)22-16-5-3-1-2-4-6-16/h7-8,11-12,16-17,19H,1-6,9-10,13-14H2,(H,24,25)(H2,22,23,26)/t17-,19-	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.5	n/a	n/a	n/a	n/a	n/a	n/a
University of California Davis Curated by ChEMBL					Assay Description Inhibition of human soluble epoxide hydrolase by kinetic fluorescent assay				Bioorg Med Chem Lett 30: (2020) Article DOI: 10.1016/j.bmcl.2019.126908 BindingDB Entry DOI: 10.7270/Q2M0490F
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50133694 (CHEMBL3633668) Show SMILES O=C(NCc1cc(on1)-c1ccco1)NCC12CC3CC(CC(C3)C1)C2 |TLB:23:18:25:22.21.24,23:22:25:19.18.17,THB:21:20:17:23.22.24,21:22:19.20.25:17| Show InChI InChI=1S/C20H25N3O3/c24-19(21-11-16-7-18(26-23-16)17-2-1-3-25-17)22-12-20-8-13-4-14(9-20)6-15(5-13)10-20/h1-3,7,13-15H,4-6,8-12H2,(H2,21,22,24)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.90	n/a	n/a	n/a	n/a	n/a	n/a
University of California at Davis Curated by ChEMBL					Assay Description Inhibition of recombinant human soluble epoxide hydrolase using CMNPC as substrate by kinetic fluorescent assay				Bioorg Med Chem Lett 25: 5514-9 (2015) Article DOI: 10.1016/j.bmcl.2015.10.066 BindingDB Entry DOI: 10.7270/Q28P62C1
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM25731 (1,3-dicyclohexylurea | CHEMBL1458 | US8815951, 1,3...) Show SMILES O=C(NC1CCCCC1)NC1CCCCC1 Show InChI InChI=1S/C13H24N2O/c16-13(14-11-7-3-1-4-8-11)15-12-9-5-2-6-10-12/h11-12H,1-10H2,(H2,14,15,16)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	5.10	n/a	n/a	n/a	n/a	n/a	n/a
Volzhsky Polytechnic Institute (branch) Volgograd State Technical University Curated by ChEMBL					Assay Description Inhibition of recombinant human soluble epoxide hydrolase using CMNPC as substrate preincubated for 5 mins followed by substrate addition measured at...				Bioorg Med Chem Lett 24: 2193-7 (2014) Article DOI: 10.1016/j.bmcl.2014.03.016 BindingDB Entry DOI: 10.7270/Q2PR7XHZ
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50546452 (CHEMBL4799688) Show SMILES CCCCCCCCNC(=O)NC1CC2CCC1(C)C2(C)C Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human soluble epoxide hydrolase by kinetic fluorescent assay				Citation and Details Article DOI: 10.1016/j.bmcl.2020.127430 BindingDB Entry DOI: 10.7270/Q2WQ07D6
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50539379 (CHEMBL4646845) Show SMILES O=C(NCCN(CCNC(=O)NCC12CC3CC(CC(C3)C1)C2)CCNC(=O)NCC12CC3CC(CC(C3)C1)C2)NCC12CC3CC(CC(C3)C1)C2 |TLB:12:13:16:20.19.18,29:30:33:37.36.35,41:42:45:49.48.47,THB:14:15:18:22.13.21,14:13:16.15.20:18,31:32:35:39.30.38,31:30:33.32.37:35,43:44:47:51.42.50,43:42:45.44.49:47,21:13:16:20.19.18,21:19:16:22.14.13,38:30:33:37.36.35,38:36:33:39.31.30,50:42:45:49.48.47,50:48:45:51.43.42| Show InChI InChI=1S/C42H69N7O3/c50-37(46-25-40-16-28-7-29(17-40)9-30(8-28)18-40)43-1-4-49(5-2-44-38(51)47-26-41-19-31-10-32(20-41)12-33(11-31)21-41)6-3-45-39(52)48-27-42-22-34-13-35(23-42)15-36(14-34)24-42/h28-36H,1-27H2,(H2,43,46,50)(H2,44,47,51)(H2,45,48,52)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.70	n/a	n/a	n/a	n/a	n/a	n/a
University of California Davis Curated by ChEMBL					Assay Description Inhibition of human soluble epoxide hydrolase by kinetic fluorescent assay				Bioorg Med Chem Lett 30: (2020) Article DOI: 10.1016/j.bmcl.2019.126908 BindingDB Entry DOI: 10.7270/Q2M0490F
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50133695 (CHEMBL3633669) Show SMILES Cc1cc(CNC(=O)NCC23CC4CC(CC(C4)C2)C3)on1 |TLB:17:12:19:16.15.18,17:16:19:13.12.11,THB:15:14:11:17.16.18,15:16:13.14.19:11| Show InChI InChI=1S/C17H25N3O2/c1-11-2-15(22-20-11)9-18-16(21)19-10-17-6-12-3-13(7-17)5-14(4-12)8-17/h2,12-14H,3-10H2,1H3,(H2,18,19,21)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.70	n/a	n/a	n/a	n/a	n/a	n/a
University of California at Davis Curated by ChEMBL					Assay Description Inhibition of recombinant human soluble epoxide hydrolase using CMNPC as substrate by kinetic fluorescent assay				Bioorg Med Chem Lett 25: 5514-9 (2015) Article DOI: 10.1016/j.bmcl.2015.10.066 BindingDB Entry DOI: 10.7270/Q28P62C1
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50546445 (CHEMBL4748031) Show SMILES Fc1ccccc1NC(=O)NC1CC2CCC1C2 Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.80	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human soluble epoxide hydrolase by kinetic fluorescent assay				Citation and Details Article DOI: 10.1016/j.bmcl.2020.127430 BindingDB Entry DOI: 10.7270/Q2WQ07D6
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50274193 (CHEMBL4128873) Show SMILES S=C(NCCCCCCCNC(=S)NC12CC3CC(CC(C3)C1)C2)NC12CC3CC(CC(C3)C1)C2 |TLB:13:14:17:21.20.19,24:25:28:32.31.30,THB:33:25:28:32.31.30,33:31:28:34.26.25,15:14:17.16.21:19,15:16:19:23.14.22,22:14:17:21.20.19,22:20:17:23.14.15,26:27:30:34.25.33,26:25:28.27.32:30| Show InChI InChI=1S/C29H48N4S2/c34-26(32-28-14-20-8-21(15-28)10-22(9-20)16-28)30-6-4-2-1-3-5-7-31-27(35)33-29-17-23-11-24(18-29)13-25(12-23)19-29/h20-25H,1-19H2,(H2,30,32,34)(H2,31,33,35)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	7.20	n/a	n/a	n/a	n/a	n/a	n/a
University of California Davis Curated by ChEMBL					Assay Description Inhibition of recombinant human sEH expressed in baculovirus expression system using CMNPC as substrate preincubated for 5 mins followed by substrate...				Bioorg Med Chem Lett 28: 2302-2313 (2018) Article DOI: 10.1016/j.bmcl.2018.05.024 BindingDB Entry DOI: 10.7270/Q2222X8F
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50012015 (CHEMBL3263293) Show SMILES O=C(NCCCCNC(=O)NC12CC3CC(CC(C3)C1)C2)NC12CC3CC(CC(C3)C1)C2 |TLB:20:11:18:14.16.15,31:22:29:26.25.27,THB:20:15:12.11.19:18,21:22:29:26.25.27,16:17:12:20.14.15,16:15:12:17.19.18,23:22:25.29.24:27,23:24:31.30.22:27,10:11:18:14.16.15,31:26:23.30.22:29| Show InChI InChI=1S/C26H42N4O2/c31-23(29-25-11-17-5-18(12-25)7-19(6-17)13-25)27-3-1-2-4-28-24(32)30-26-14-20-8-21(15-26)10-22(9-20)16-26/h17-22H,1-16H2,(H2,27,29,31)(H2,28,30,32)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	7.20	n/a	n/a	n/a	n/a	n/a	n/a
Volzhsky Polytechnic Institute (branch) Volgograd State Technical University Curated by ChEMBL					Assay Description Inhibition of recombinant human soluble epoxide hydrolase using CMNPC as substrate preincubated for 5 mins followed by substrate addition measured at...				Bioorg Med Chem Lett 24: 2193-7 (2014) Article DOI: 10.1016/j.bmcl.2014.03.016 BindingDB Entry DOI: 10.7270/Q2PR7XHZ
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50012012 (CHEMBL3263290) Show SMILES O=C(NCCCCCCCCNC(=O)NCC12CC3CC(CC(C3)C1)C2)NCC12CC3CC(CC(C3)C1)C2 |TLB:15:16:19:23.22.21,27:28:31:35.34.33,THB:17:18:21:25.16.24,17:16:19.18.23:21,29:30:33:37.28.36,29:28:31.30.35:33,24:16:19:23.22.21,24:22:19:25.17.16,36:28:31:35.34.33,36:34:31:37.29.28| Show InChI InChI=1S/C32H54N4O2/c37-29(35-21-31-15-23-9-24(16-31)11-25(10-23)17-31)33-7-5-3-1-2-4-6-8-34-30(38)36-22-32-18-26-12-27(19-32)14-28(13-26)20-32/h23-28H,1-22H2,(H2,33,35,37)(H2,34,36,38)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	7.30	n/a	n/a	n/a	n/a	n/a	n/a
Volzhsky Polytechnic Institute (branch) Volgograd State Technical University Curated by ChEMBL					Assay Description Inhibition of recombinant human soluble epoxide hydrolase using CMNPC as substrate preincubated for 5 mins followed by substrate addition measured at...				Bioorg Med Chem Lett 24: 2193-7 (2014) Article DOI: 10.1016/j.bmcl.2014.03.016 BindingDB Entry DOI: 10.7270/Q2PR7XHZ
					More data for this Ligand-Target Pair

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