Compile Data Set for Download or QSAR

Found 2944 hits with Last Name = 'son' and Initial = 'jb'   

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
Dihydrofolate reductase (Escherichia coli)	BDBM18050 (2-[(4-{[(2,4-diaminopteridin-6-yl)methyl](methyl)a...) Show SMILES CN(Cc1cnc2nc(N)nc(N)c2n1)c1ccc(cc1)C(=O)N[C@@H](CCC(O)=O)C(O)=O |r| Show InChI InChI=1S/C20H22N8O5/c1-28(9-11-8-23-17-15(24-11)16(21)26-20(22)27-17)12-4-2-10(3-5-12)18(31)25-13(19(32)33)6-7-14(29)30/h2-5,8,13H,6-7,9H2,1H3,(H,25,31)(H,29,30)(H,32,33)(H4,21,22,23,26,27)/t13-/m0/s1	MMDB NCI pathway Reactome pathway KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	0.00100	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Connecticut Curated by ChEMBL					Assay Description Inhibition of recombinant Escherichia coli DHFR				ACS Med Chem Lett 7: 692-6 (2016) Article DOI: 10.1021/acsmedchemlett.6b00120 BindingDB Entry DOI: 10.7270/Q2DJ5HKK
					More data for this Ligand-Target Pair
Dihydrofolate reductase (Homo sapiens (Human))	BDBM18050 (2-[(4-{[(2,4-diaminopteridin-6-yl)methyl](methyl)a...) Show SMILES CN(Cc1cnc2nc(N)nc(N)c2n1)c1ccc(cc1)C(=O)N[C@@H](CCC(O)=O)C(O)=O |r| Show InChI InChI=1S/C20H22N8O5/c1-28(9-11-8-23-17-15(24-11)16(21)26-20(22)27-17)12-4-2-10(3-5-12)18(31)25-13(19(32)33)6-7-14(29)30/h2-5,8,13H,6-7,9H2,1H3,(H,25,31)(H,29,30)(H,32,33)(H4,21,22,23,26,27)/t13-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	DrugBank MMDB PDB Article PubMed	0.00300	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Connecticut Curated by ChEMBL					Assay Description Inhibition of recombinant human DHFR assessed as reduction in NADPH oxidation using dihydrofolate as substrate by fluorescence spectrophotometric ana...				ACS Med Chem Lett 7: 692-6 (2016) Article DOI: 10.1021/acsmedchemlett.6b00120 BindingDB Entry DOI: 10.7270/Q2DJ5HKK
					More data for this Ligand-Target Pair				3D Structure (crystal)
Enteropeptidase (Homo sapiens (Human))	BDBM571836 ((Z)-3-((6-((4-Carbamimidoyl-2-fluorophenoxy)carbon...) Show SMILES CCn1c2ccc(cc2s\c1=N/CC(C)(C)C(O)=O)C(=O)Oc1ccc(cc1F)C(N)=N Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	0.160	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Dihydrofolate reductase (Escherichia coli)	BDBM18069 (5-[(3,4,5-trimethoxyphenyl)methyl]pyrimidine-2,4-d...) Show SMILES COc1cc(Cc2cnc(N)nc2N)cc(OC)c1OC Show InChI InChI=1S/C14H18N4O3/c1-19-10-5-8(6-11(20-2)12(10)21-3)4-9-7-17-14(16)18-13(9)15/h5-7H,4H2,1-3H3,(H4,15,16,17,18)	MMDB NCI pathway Reactome pathway KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	0.220	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Connecticut Curated by ChEMBL					Assay Description Inhibition of recombinant Escherichia coli DHFR expressed in Escherichia coli BL21(DE3) cells assessed as reduction in NADPH oxidation using dihydrof...				ACS Med Chem Lett 7: 692-6 (2016) Article DOI: 10.1021/acsmedchemlett.6b00120 BindingDB Entry DOI: 10.7270/Q2DJ5HKK
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571793 ((3-((5-((4-Carbamimidoyl-2-fluorophenoxy)carbonyl)...) Show SMILES CCN(CCC(=O)N[C@@H](CC(O)=O)C(O)=O)c1ncc(s1)C(=O)Oc1ccc(cc1F)C(N)=N |r| Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	0.520	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571830 (3-((6-((4-Carbamimidoyl-2-fluorophenoxy)carbonyl)b...) Show SMILES CCN(CCC(O)=O)c1nc2ccc(cc2s1)C(=O)Oc1ccc(cc1F)C(N)=N Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	0.550	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571817 (3-((6-((4-Carbamimidoyl-2-fluorophenoxy)carbonyl)b...) Show SMILES CN(CCC(O)=O)c1nc2ccc(cc2s1)C(=O)Oc1ccc(cc1F)C(N)=N Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	0.570	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571815 (4-((6-((4-Carbamimidoyl-2-fluorophenoxy)carbonyl)b...) Show SMILES CN(CCCC(O)=O)c1nc2ccc(cc2s1)C(=O)Oc1ccc(cc1F)C(N)=N Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	0.570	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571802 (4-((5-((4-Carbamimidoyl-2-fluorophenoxy)carbonyl)t...) Show SMILES CN(CCCC(O)=O)c1ncc(s1)C(=O)Oc1ccc(cc1F)C(N)=N Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	0.570	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571797 ((3-((5-((4-Carbamimidoyl-2-fluorophenoxy)carbonyl)...) Show SMILES CCN(CCC(=O)N[C@H](CCC(O)=O)C(O)=O)c1ncc(s1)C(=O)Oc1ccc(cc1F)C(N)=N |r| Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	0.570	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571814 (3-((6-((4-Carbamimidoyl-2-fluorophenoxy)carbonyl)b...) Show SMILES CC(C)(CNc1nc2ccc(cc2s1)C(=O)Oc1ccc(cc1F)C(N)=N)C(O)=O Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	0.590	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571772 (1-(5-((4-Carbamimidoyl-2-fluorophenoxy)carbonyl)th...) Show SMILES NC(=N)c1ccc(OC(=O)c2cnc(s2)N2CCC(CC2)C(O)=O)c(F)c1 Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	0.600	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571760 (3-((5-((4-carbamimidoyl-2-fluorophenoxy)carbonyl)t...) Show SMILES CCN(CCC(O)=O)c1ncc(s1)C(=O)Oc1ccc(cc1F)C(N)=N Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	0.680	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571843 (3-((6-((4-Carbamimidoyl-2-fluorophenoxy)carbonyl)b...) Show SMILES CCN(CC(C)(C)C(O)=O)c1nc2ccc(cc2s1)C(=O)Oc1ccc(cc1F)C(N)=N Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	0.700	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571841 (3-((6-((4-Carbamimidoylphenoxy)carbonyl)benzo[d]th...) Show SMILES CC(C)(CNc1nc2ccc(cc2s1)C(=O)Oc1ccc(cc1)C(N)=N)C(O)=O Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	0.890	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Dihydrofolate reductase (Escherichia coli)	BDBM210930 (UCP1173) Show SMILES CCc1nc(N)nc(N)c1C#C[C@H](C)c1cc(OC)cc(c1)-c1ccc(cc1)C(O)=O |r| Show InChI InChI=1S/C24H24N4O3/c1-4-21-20(22(25)28-24(26)27-21)10-5-14(2)17-11-18(13-19(12-17)31-3)15-6-8-16(9-7-15)23(29)30/h6-9,11-14H,4H2,1-3H3,(H,29,30)(H4,25,26,27,28)/t14-/m0/s1	MMDB NCI pathway Reactome pathway KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid PDB UniChem	Article PubMed	0.910	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Connecticut Curated by ChEMBL					Assay Description Inhibition of recombinant Escherichia coli DHFR expressed in Escherichia coli BL21(DE3) cells assessed as reduction in NADPH oxidation using dihydrof...				ACS Med Chem Lett 7: 692-6 (2016) Article DOI: 10.1021/acsmedchemlett.6b00120 BindingDB Entry DOI: 10.7270/Q2DJ5HKK
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571766 (4-Carbamimidoyl-2-fluorophenyl 2-(4-(methoxycarbon...) Show SMILES COC(=O)C1CCN(CC1)c1ncc(s1)C(=O)Oc1ccc(cc1F)C(N)=N Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	0.920	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Dihydrofolate reductase (Escherichia coli)	BDBM50190621 (CHEMBL3827532 | US10870625, Compound 15) Show SMILES CCc1nc(N)nc(N)c1C#CCc1cc(ccc1OC)-c1ccc(cc1)C(O)=O Show InChI InChI=1S/C23H22N4O3/c1-3-19-18(21(24)27-23(25)26-19)6-4-5-17-13-16(11-12-20(17)30-2)14-7-9-15(10-8-14)22(28)29/h7-13H,3,5H2,1-2H3,(H,28,29)(H4,24,25,26,27)	MMDB NCI pathway Reactome pathway KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Similars	Article PubMed	0.980	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Connecticut Curated by ChEMBL					Assay Description Inhibition of recombinant Escherichia coli DHFR expressed in Escherichia coli BL21(DE3) cells assessed as reduction in NADPH oxidation using dihydrof...				ACS Med Chem Lett 7: 692-6 (2016) Article DOI: 10.1021/acsmedchemlett.6b00120 BindingDB Entry DOI: 10.7270/Q2DJ5HKK
					More data for this Ligand-Target Pair
Integrin alpha-IIb/beta-3 (Homo sapiens (Human))	BDBM50264380 (CHEMBL4078717) Show SMILES NC(=N)c1ccc(cc1)C(=O)N[C@@H](Cc1ccc(cc1)[N+]([O-])=O)C(=O)N1CCc2nn(CC(O)=O)cc2C1 |r| Show InChI InChI=1S/C25H25N7O6/c26-23(27)16-3-5-17(6-4-16)24(35)28-21(11-15-1-7-19(8-2-15)32(37)38)25(36)30-10-9-20-18(12-30)13-31(29-20)14-22(33)34/h1-8,13,21H,9-12,14H2,(H3,26,27)(H,28,35)(H,33,34)/t21-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid PDB UniChem Similars	PDB Article PubMed	<1	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Strathclyde Curated by ChEMBL					Assay Description Displacement of [3H]UR-3189 from integrin alpha2b beta3 receptor in resting human platelet				J Med Chem 60: 3241-3251 (2017) Article DOI: 10.1021/acs.jmedchem.6b01711 BindingDB Entry DOI: 10.7270/Q29W0HZ4
					More data for this Ligand-Target Pair				3D Structure (crystal)
Enteropeptidase (Homo sapiens (Human))	BDBM571783 ((1-(5-((4-Carbamimidoyl-2-fluorophenoxy)carbonyl)t...) Show SMILES NC(=N)c1ccc(OC(=O)c2cnc(s2)N2CCC(CC2)C(=O)NCC(O)=O)c(F)c1 Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	1	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Dihydrofolate reductase (Staphylococcus aureus)	BDBM18050 (2-[(4-{[(2,4-diaminopteridin-6-yl)methyl](methyl)a...) Show SMILES CN(Cc1cnc2nc(N)nc(N)c2n1)c1ccc(cc1)C(=O)N[C@@H](CCC(O)=O)C(O)=O |r| Show InChI InChI=1S/C20H22N8O5/c1-28(9-11-8-23-17-15(24-11)16(21)26-20(22)27-17)12-4-2-10(3-5-12)18(31)25-13(19(32)33)6-7-14(29)30/h2-5,8,13H,6-7,9H2,1H3,(H,25,31)(H,29,30)(H,32,33)(H4,21,22,23,26,27)/t13-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	1	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Connecticut Curated by ChEMBL					Assay Description Inhibition of Staphylococcus aureus DHFR				ACS Med Chem Lett 7: 692-6 (2016) Article DOI: 10.1021/acsmedchemlett.6b00120 BindingDB Entry DOI: 10.7270/Q2DJ5HKK
					More data for this Ligand-Target Pair				3D Structure (crystal)
Enteropeptidase (Homo sapiens (Human))	BDBM571839 (4-Carbamimidoyl-2-fluorophenyl 2-((4-methoxy-4-oxo...) Show SMILES COC(=O)CCCN(C)c1nc2ccc(cc2s1)C(=O)Oc1ccc(cc1F)C(N)=N Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	1.10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Delta-type opioid receptor/Kappa-type opioid receptor/Mu-type opioid receptor/Sigma non-opioid intracellular receptor 1 (Rattus norvegicus (rat)-RAT)	BDBM50223637 (Alphacemethadone | Alphacetylmethadol) Show SMILES CC[C@@H](OC(C)=O)C(C[C@@H](C)N(C)C)(c1ccccc1)c1ccccc1 |r| Show InChI InChI=1S/C23H31NO2/c1-6-22(26-19(3)25)23(17-18(2)24(4)5,20-13-9-7-10-14-20)21-15-11-8-12-16-21/h7-16,18,22H,6,17H2,1-5H3/t18-,22-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Patents	PubMed	1.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of [3H]- naloxone binding to Opioid receptors in rat brain membrane in the absence of Na				J Med Chem 24: 903-6 (1981) BindingDB Entry DOI: 10.7270/Q26W9D8D
					More data for this Ligand-Target Pair
Dihydrofolate reductase (Staphylococcus aureus)	BDBM210930 (UCP1173) Show SMILES CCc1nc(N)nc(N)c1C#C[C@H](C)c1cc(OC)cc(c1)-c1ccc(cc1)C(O)=O |r| Show InChI InChI=1S/C24H24N4O3/c1-4-21-20(22(25)28-24(26)27-21)10-5-14(2)17-11-18(13-19(12-17)31-3)15-6-8-16(9-7-15)23(29)30/h6-9,11-14H,4H2,1-3H3,(H,29,30)(H4,25,26,27,28)/t14-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid PDB UniChem	Article PubMed	1.30	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Connecticut Curated by ChEMBL					Assay Description Inhibition of recombinant Staphylococcus aureus DHFR expressed in Escherichia coli BL21(DE3) cells assessed as reduction in NADPH oxidation using dih...				ACS Med Chem Lett 7: 692-6 (2016) Article DOI: 10.1021/acsmedchemlett.6b00120 BindingDB Entry DOI: 10.7270/Q2DJ5HKK
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571840 (4-Carbamimidoyl-2-fluorophenyl 2-((3-methoxy-3-oxo...) Show SMILES COC(=O)CCN(C)c1nc2ccc(cc2s1)C(=O)Oc1ccc(cc1F)C(N)=N Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	1.30	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571789 (3-(1-(5-((4-Carbamimidoyl-2-fluorophenoxy)carbonyl...) Show SMILES CC(C)(CNC(=O)C1CCN(CC1)c1ncc(s1)C(=O)Oc1ccc(cc1F)C(N)=N)C(O)=O Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	1.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571787 (4-(1-(5-((4-carbamimidoyl-2-fluorophenoxy)carbonyl...) Show SMILES CN(CCCC(O)=O)C(=O)C1CCN(CC1)c1ncc(s1)C(=O)Oc1ccc(cc1F)C(N)=N Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	1.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Dihydrofolate reductase (Staphylococcus aureus)	BDBM210931 (UCP1175) Show SMILES CCc1nc(N)nc(N)c1C#CCc1cc(OC)cc(c1)-c1ccc(cc1)C(O)=O Show InChI InChI=1S/C23H22N4O3/c1-3-20-19(21(24)27-23(25)26-20)6-4-5-14-11-17(13-18(12-14)30-2)15-7-9-16(10-8-15)22(28)29/h7-13H,3,5H2,1-2H3,(H,28,29)(H4,24,25,26,27)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid PDB UniChem	PDB Article PubMed	1.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Connecticut Curated by ChEMBL					Assay Description Inhibition of recombinant Staphylococcus aureus DHFR expressed in Escherichia coli BL21(DE3) cells assessed as reduction in NADPH oxidation using dih...				ACS Med Chem Lett 7: 692-6 (2016) Article DOI: 10.1021/acsmedchemlett.6b00120 BindingDB Entry DOI: 10.7270/Q2DJ5HKK
					More data for this Ligand-Target Pair				3D Structure (crystal)
Enteropeptidase (Homo sapiens (Human))	BDBM571785 (3-(1-(5-((4-Carbamimidoyl-2-fluorophenoxy)carbonyl...) Show SMILES NC(=N)c1ccc(OC(=O)c2cnc(s2)N2CCC(CC2)C(=O)NCCC(O)=O)c(F)c1 Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	1.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571781 (4-Carbamimidoyl-2-fluorophenyl 2-(4-((4-methoxy-4-...) Show SMILES COC(=O)CCCN(C)C(=O)C1CCN(CC1)c1ncc(s1)C(=O)Oc1ccc(cc1F)C(N)=N Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	1.80	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Dihydrofolate reductase (Escherichia coli)	BDBM210929 (UCP1172) Show SMILES CCc1nc(N)nc(N)c1C#C[C@@H](C)c1cc(OC)cc(c1)-c1ccc(cc1)C(O)=O |r| Show InChI InChI=1S/C24H24N4O3/c1-4-21-20(22(25)28-24(26)27-21)10-5-14(2)17-11-18(13-19(12-17)31-3)15-6-8-16(9-7-15)23(29)30/h6-9,11-14H,4H2,1-3H3,(H,29,30)(H4,25,26,27,28)/t14-/m1/s1	MMDB NCI pathway Reactome pathway KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.80	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Connecticut Curated by ChEMBL					Assay Description Inhibition of recombinant Escherichia coli DHFR expressed in Escherichia coli BL21(DE3) cells assessed as reduction in NADPH oxidation using dihydrof...				ACS Med Chem Lett 7: 692-6 (2016) Article DOI: 10.1021/acsmedchemlett.6b00120 BindingDB Entry DOI: 10.7270/Q2DJ5HKK
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571773 (4-Carbamimidoyl-2-fluorophenyl 2-(4-((2-methoxy-2-...) Show SMILES COC(=O)CNC(=O)C1CCN(CC1)c1ncc(s1)C(=O)Oc1ccc(cc1F)C(N)=N Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	1.80	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Dihydrofolate reductase (Escherichia coli)	BDBM50190622 (CHEMBL3827326) Show SMILES CC(O)=O.CCc1nc(N)nc(N)c1C#C[C@H](C)c1cc(ccc1OC)-c1ccc(cc1)C(O)=O |r| Show InChI InChI=1S/C24H24N4O3.C2H4O2/c1-4-20-18(22(25)28-24(26)27-20)11-5-14(2)19-13-17(10-12-21(19)31-3)15-6-8-16(9-7-15)23(29)30;1-2(3)4/h6-10,12-14H,4H2,1-3H3,(H,29,30)(H4,25,26,27,28);1H3,(H,3,4)/t14-;/m0./s1	MMDB NCI pathway Reactome pathway KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.90	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Connecticut Curated by ChEMBL					Assay Description Inhibition of recombinant Escherichia coli DHFR expressed in Escherichia coli BL21(DE3) cells assessed as reduction in NADPH oxidation using dihydrof...				ACS Med Chem Lett 7: 692-6 (2016) Article DOI: 10.1021/acsmedchemlett.6b00120 BindingDB Entry DOI: 10.7270/Q2DJ5HKK
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571824 (4-Carbamimidoyl-2-fluorophenyl 2-(4-benzoamidopipe...) Show SMILES NC(=N)c1ccc(OC(=O)c2ccc3nc(sc3c2)N2CCC(CC2)NC(=O)c2ccccc2)c(F)c1 Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	1.90	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Delta-type opioid receptor/Kappa-type opioid receptor/Mu-type opioid receptor/Sigma non-opioid intracellular receptor 1 (Rattus norvegicus (rat)-RAT)	BDBM50223633 (Levomethadone) Show SMILES CCC(=O)C(C[C@@H](C)N(C)C)(c1ccccc1)c1ccccc1 Show InChI InChI=1S/C21H27NO/c1-5-20(23)21(16-17(2)22(3)4,18-12-8-6-9-13-18)19-14-10-7-11-15-19/h6-15,17H,5,16H2,1-4H3/t17-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase KEGG PC cid PC sid UniChem Similars	PubMed	2	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of [3H]- naloxone binding to Opioid receptors in rat brain membrane in the absence of Na				J Med Chem 24: 903-6 (1981) BindingDB Entry DOI: 10.7270/Q26W9D8D
					More data for this Ligand-Target Pair
Dihydrofolate reductase (Escherichia coli)	BDBM50190619 (CHEMBL3827086 | US10870625, Compound 14) Show SMILES CCc1nc(N)nc(N)c1C#CCc1cc(ccc1OC)-c1ccccc1C(O)=O Show InChI InChI=1S/C23H22N4O3/c1-3-19-18(21(24)27-23(25)26-19)10-6-7-15-13-14(11-12-20(15)30-2)16-8-4-5-9-17(16)22(28)29/h4-5,8-9,11-13H,3,7H2,1-2H3,(H,28,29)(H4,24,25,26,27)	MMDB NCI pathway Reactome pathway KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Connecticut Curated by ChEMBL					Assay Description Inhibition of recombinant Escherichia coli DHFR expressed in Escherichia coli BL21(DE3) cells assessed as reduction in NADPH oxidation using dihydrof...				ACS Med Chem Lett 7: 692-6 (2016) Article DOI: 10.1021/acsmedchemlett.6b00120 BindingDB Entry DOI: 10.7270/Q2DJ5HKK
					More data for this Ligand-Target Pair
Dihydrofolate reductase (Staphylococcus aureus)	BDBM210929 (UCP1172) Show SMILES CCc1nc(N)nc(N)c1C#C[C@@H](C)c1cc(OC)cc(c1)-c1ccc(cc1)C(O)=O |r| Show InChI InChI=1S/C24H24N4O3/c1-4-21-20(22(25)28-24(26)27-21)10-5-14(2)17-11-18(13-19(12-17)31-3)15-6-8-16(9-7-15)23(29)30/h6-9,11-14H,4H2,1-3H3,(H,29,30)(H4,25,26,27,28)/t14-/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	2.10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Connecticut Curated by ChEMBL					Assay Description Inhibition of recombinant Staphylococcus aureus DHFR expressed in Escherichia coli BL21(DE3) cells assessed as reduction in NADPH oxidation using dih...				ACS Med Chem Lett 7: 692-6 (2016) Article DOI: 10.1021/acsmedchemlett.6b00120 BindingDB Entry DOI: 10.7270/Q2DJ5HKK
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571828 (4-Carbamimidoyl-2-fluorophenyl 2-(ethyl(3-methoxy-...) Show SMILES CCN(CCC(=O)OC)c1nc2ccc(cc2s1)C(=O)Oc1ccc(cc1F)C(N)=N Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	2.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571806 (3-(3-((5-((4-Carbamimidoyl-2-fluorophenoxy)carbony...) Show SMILES CCN(CCC(=O)Nc1cccc(c1)C(O)=O)c1ncc(s1)C(=O)Oc1ccc(cc1F)C(N)=N Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	2.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571798 (4-Carbamimidoyl-2-fluorophenyl 2-(ethyl(3-methoxy-...) Show SMILES CCN(CCC(=O)OC)c1ncc(s1)C(=O)Oc1ccc(cc1F)C(N)=N Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	2.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571777 (4-Carbamimidoyl-2-fluorophenyl 2-(4-((3-methoxy-2,...) Show SMILES COC(=O)C(C)(C)CNC(=O)C1CCN(CC1)c1ncc(s1)C(=O)Oc1ccc(cc1F)C(N)=N Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	2.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571775 (4-Carbamimidoyl-2-fluorophenyl 2-(4-((3-methoxy-3-...) Show SMILES COC(=O)CCNC(=O)C1CCN(CC1)c1ncc(s1)C(=O)Oc1ccc(cc1F)C(N)=N Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	2.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571800 (4-Carbamimidoyl-2-fluorophenyl 2-((4-methoxy-4-oxo...) Show SMILES COC(=O)CCCN(C)c1ncc(s1)C(=O)Oc1ccc(cc1F)C(N)=N Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Dihydrofolate reductase (Escherichia coli)	BDBM210928 (UCP1164) Show SMILES CCc1nc(N)nc(N)c1C#C[C@@H](C)c1cc(ccc1OC)-c1ccc(cc1)C(O)=O |r| Show InChI InChI=1S/C24H24N4O3/c1-4-20-18(22(25)28-24(26)27-20)11-5-14(2)19-13-17(10-12-21(19)31-3)15-6-8-16(9-7-15)23(29)30/h6-10,12-14H,4H2,1-3H3,(H,29,30)(H4,25,26,27,28)/t14-/m1/s1	MMDB NCI pathway Reactome pathway KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	3.10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Connecticut Curated by ChEMBL					Assay Description Inhibition of recombinant Escherichia coli DHFR expressed in Escherichia coli BL21(DE3) cells assessed as reduction in NADPH oxidation using dihydrof...				ACS Med Chem Lett 7: 692-6 (2016) Article DOI: 10.1021/acsmedchemlett.6b00120 BindingDB Entry DOI: 10.7270/Q2DJ5HKK
					More data for this Ligand-Target Pair
Delta-type opioid receptor/Kappa-type opioid receptor/Mu-type opioid receptor/Sigma non-opioid intracellular receptor 1 (Rattus norvegicus (rat)-RAT)	BDBM50223637 (Alphacemethadone | Alphacetylmethadol) Show SMILES CC[C@@H](OC(C)=O)C(C[C@@H](C)N(C)C)(c1ccccc1)c1ccccc1 |r| Show InChI InChI=1S/C23H31NO2/c1-6-22(26-19(3)25)23(17-18(2)24(4)5,20-13-9-7-10-14-20)21-15-11-8-12-16-21/h7-16,18,22H,6,17H2,1-5H3/t18-,22-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Patents	PubMed	3.40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was evaluated for the inhibition of [3H]- naloxone binding to Opioid receptors in rat brain membrane in the presence of Na				J Med Chem 24: 903-6 (1981) BindingDB Entry DOI: 10.7270/Q26W9D8D
					More data for this Ligand-Target Pair
Dihydrofolate reductase (Staphylococcus aureus)	BDBM18069 (5-[(3,4,5-trimethoxyphenyl)methyl]pyrimidine-2,4-d...) Show SMILES COc1cc(Cc2cnc(N)nc2N)cc(OC)c1OC Show InChI InChI=1S/C14H18N4O3/c1-19-10-5-8(6-11(20-2)12(10)21-3)4-9-7-17-14(16)18-13(9)15/h5-7H,4H2,1-3H3,(H4,15,16,17,18)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	3.40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Connecticut Curated by ChEMBL					Assay Description Inhibition of recombinant Staphylococcus aureus DHFR expressed in Escherichia coli BL21(DE3) cells assessed as reduction in NADPH oxidation using dih...				ACS Med Chem Lett 7: 692-6 (2016) Article DOI: 10.1021/acsmedchemlett.6b00120 BindingDB Entry DOI: 10.7270/Q2DJ5HKK
					More data for this Ligand-Target Pair				3D Structure (crystal)
Enteropeptidase (Homo sapiens (Human))	BDBM571838 (4-Carbamimidoyl-2-fluorophenyl 2-(ethyl(3-methoxy-...) Show SMILES CCN(CC(C)(C)C(=O)OC)c1nc2ccc(cc2s1)C(=O)Oc1ccc(cc1F)C(N)=N Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	3.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571834 (4-Carbamimidoyl-2-fluorophenyl (Z)-3-ethyl-2-((3-m...) Show SMILES CCn1c2ccc(cc2s\c1=N/CC(C)(C)C(=O)OC)C(=O)Oc1ccc(cc1F)C(N)=N Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571823 (3-((6-((4-Carbamimidoylphenoxy)carbonyl)benzo[d]th...) Show SMILES CN(CCC(O)=O)c1nc2ccc(cc2s1)C(=O)Oc1ccc(cc1)C(N)=N Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	4.30	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair
Enteropeptidase (Homo sapiens (Human))	BDBM571807 ((1-(5-((4-Carbamimidoyl)phenoxy)carbonyl)thiazol-2...) Show SMILES NC(=N)c1ccc(OC(=O)c2cnc(s2)N2CCC(CC2)C(=O)N[C@@H](CC(O)=O)C(O)=O)cc1 |r| Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	4.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory activity of the enteropeptidase inhibitor synthesized using the purified Recombinant Human Enteropeptidase and the substrate Acetyl-As...				Citation and Details BindingDB Entry DOI: 10.7270/Q2WD43TB
					More data for this Ligand-Target Pair

Displayed 1 to 50 (of 2944 total )  |  Next  |  Last  >>

Jump to: