Compile Data Set for Download or QSAR

Found 39 hits with Last Name = 'guo' and Initial = 'jq'   

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
S-adenosylmethionine decarboxylase proenzyme (Homo sapiens (Human))	BDBM50403124 (CHEMBL2115571) Show SMILES C[S+](CCC(N)C(O)=O)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12 Show InChI InChI=1S/C15H22N6O5S/c1-27(3-2-7(16)15(24)25)4-8-10(22)11(23)14(26-8)21-6-20-9-12(17)18-5-19-13(9)21/h5-8,10-11,14,22-23H,2-4,16H2,1H3,(H2-,17,18,19,24,25)/p+1/t7?,8-,10-,11-,14-,27?/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article	3.80E+3	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 to inactivate the bacterial AdoMet-DC; value ranges from 3.8 to 39.6 uM				Bioorg Med Chem Lett 3: 2811-2816 (1993) Article DOI: 10.1016/S0960-894X(01)80770-8 BindingDB Entry DOI: 10.7270/Q2TH8N6T
					More data for this Ligand-Target Pair
S-adenosylmethionine decarboxylase proenzyme (Homo sapiens (Human))	BDBM50281293 (2-amino-5-({[(2S,3S,4R)-5-(6-amino-9H-purin-9-yl)-...) Show SMILES Br.[Br-].C[S+](CCCC(N)C#N)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12 Show InChI InChI=1S/C16H24N7O3S/c1-27(4-2-3-9(18)5-17)6-10-12(24)13(25)16(26-10)23-8-22-11-14(19)20-7-21-15(11)23/h7-10,12-13,16,24-25H,2-4,6,18H2,1H3,(H2,19,20,21)/q+1/p+1/t9?,10-,12-,13-,16?,27?/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	7.20E+3	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 to inactivate the human AdoMet-DC				Bioorg Med Chem Lett 3: 2811-2816 (1993) Article DOI: 10.1016/S0960-894X(01)80770-8 BindingDB Entry DOI: 10.7270/Q2TH8N6T
					More data for this Ligand-Target Pair
S-adenosylmethionine decarboxylase proenzyme (Homo sapiens (Human))	BDBM50403124 (CHEMBL2115571) Show SMILES C[S+](CCC(N)C(O)=O)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12 Show InChI InChI=1S/C15H22N6O5S/c1-27(3-2-7(16)15(24)25)4-8-10(22)11(23)14(26-8)21-6-20-9-12(17)18-5-19-13(9)21/h5-8,10-11,14,22-23H,2-4,16H2,1H3,(H2-,17,18,19,24,25)/p+1/t7?,8-,10-,11-,14-,27?/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article	1.07E+4	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 to inactivate the human AdoMet-DC; value ranges from 10.7 to 62.7 uM				Bioorg Med Chem Lett 3: 2811-2816 (1993) Article DOI: 10.1016/S0960-894X(01)80770-8 BindingDB Entry DOI: 10.7270/Q2TH8N6T
					More data for this Ligand-Target Pair
S-adenosylmethionine decarboxylase proenzyme (Homo sapiens (Human))	BDBM50403124 (CHEMBL2115571) Show SMILES C[S+](CCC(N)C(O)=O)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12 Show InChI InChI=1S/C15H22N6O5S/c1-27(3-2-7(16)15(24)25)4-8-10(22)11(23)14(26-8)21-6-20-9-12(17)18-5-19-13(9)21/h5-8,10-11,14,22-23H,2-4,16H2,1H3,(H2-,17,18,19,24,25)/p+1/t7?,8-,10-,11-,14-,27?/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article	1.07E+4	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 to inactivate the bacterial AdoMet-DC; value ranges from 3.8 to 39.6 uM				Bioorg Med Chem Lett 3: 2811-2816 (1993) Article DOI: 10.1016/S0960-894X(01)80770-8 BindingDB Entry DOI: 10.7270/Q2TH8N6T
					More data for this Ligand-Target Pair
S-adenosylmethionine decarboxylase proenzyme (Homo sapiens (Human))	BDBM50366321 (CHEMBL3392203 | CHEMBL606101) Show SMILES OS(O)(=O)=O.OS([O-])(=O)=O.C[S+](C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)C1C[C@@H](N)C=C1 |r,c:35| Show InChI InChI=1S/C16H23N6O3S/c1-26(9-3-2-8(17)4-9)5-10-12(23)13(24)16(25-10)22-7-21-11-14(18)19-6-20-15(11)22/h2-3,6-10,12-13,16,23-24H,4-5,17H2,1H3,(H2,18,19,20)/q+1/p+1/t8-,9?,10+,12+,13+,16?,26?/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	1.80E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Tested for irreversible inhibitory activity against AdoMet-DC (S-adenosyl-methionine decarboxylase-) isolated from Escherichia coli				Bioorg Med Chem Lett 3: 147-152 (1993) Article DOI: 10.1016/S0960-894X(01)80865-9 BindingDB Entry DOI: 10.7270/Q2PR7WG3
					More data for this Ligand-Target Pair
S-adenosylmethionine decarboxylase proenzyme (Homo sapiens (Human))	BDBM50281292 (2-amino-4-({[(2S,3S,4R)-5-(6-amino-9H-purin-9-yl)-...) Show SMILES Br.[Br-].C[S+](CCC(N)C#N)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12 Show InChI InChI=1S/C15H22N7O3S/c1-26(3-2-8(17)4-16)5-9-11(23)12(24)15(25-9)22-7-21-10-13(18)19-6-20-14(10)22/h6-9,11-12,15,23-24H,2-3,5,17H2,1H3,(H2,18,19,20)/q+1/p+1/t8?,9-,11-,12-,15?,26?/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	3.11E+4	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 to inactivate the bacterial AdoMet-DC				Bioorg Med Chem Lett 3: 2811-2816 (1993) Article DOI: 10.1016/S0960-894X(01)80770-8 BindingDB Entry DOI: 10.7270/Q2TH8N6T
					More data for this Ligand-Target Pair
S-adenosylmethionine decarboxylase proenzyme (Homo sapiens (Human))	BDBM50281292 (2-amino-4-({[(2S,3S,4R)-5-(6-amino-9H-purin-9-yl)-...) Show SMILES Br.[Br-].C[S+](CCC(N)C#N)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12 Show InChI InChI=1S/C15H22N7O3S/c1-26(3-2-8(17)4-16)5-9-11(23)12(24)15(25-9)22-7-21-10-13(18)19-6-20-14(10)22/h6-9,11-12,15,23-24H,2-3,5,17H2,1H3,(H2,18,19,20)/q+1/p+1/t8?,9-,11-,12-,15?,26?/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	2.47E+5	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 to inactivate the human AdoMet-DC				Bioorg Med Chem Lett 3: 2811-2816 (1993) Article DOI: 10.1016/S0960-894X(01)80770-8 BindingDB Entry DOI: 10.7270/Q2TH8N6T
					More data for this Ligand-Target Pair
S-adenosylmethionine decarboxylase proenzyme (Homo sapiens (Human))	BDBM50366318 (CHEMBL3392208 | CHEMBL605698) Show SMILES OS(O)(=O)=O.Nc1ncnc2n(cnc12)[C@@H]1O[C@H](CSC2CCNC2)[C@@H](O)[C@H]1O |r| Show InChI InChI=1S/C14H20N6O3S/c15-12-9-13(18-5-17-12)20(6-19-9)14-11(22)10(21)8(23-14)4-24-7-1-2-16-3-7/h5-8,10-11,14,16,21-22H,1-4H2,(H2,15,17,18)/t7?,8-,10-,11-,14?/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	4.15E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Tested for irreversible inhibitory activity against AdoMet-DC (S-adenosyl-methionine decarboxylase-) isolated from Escherichia coli				Bioorg Med Chem Lett 3: 147-152 (1993) Article DOI: 10.1016/S0960-894X(01)80865-9 BindingDB Entry DOI: 10.7270/Q2PR7WG3
					More data for this Ligand-Target Pair
S-adenosylmethionine decarboxylase proenzyme (Homo sapiens (Human))	BDBM50366320 (CHEMBL3392206 | CHEMBL605899) Show SMILES OS(O)(=O)=O.Nc1ncnc2n(cnc12)[C@@H]1O[C@H](CS[C@@H]2CN[C@@H](C2)C(O)=O)[C@@H](O)[C@H]1O |r| Show InChI InChI=1S/C15H20N6O5S/c16-12-9-13(19-4-18-12)21(5-20-9)14-11(23)10(22)8(26-14)3-27-6-1-7(15(24)25)17-2-6/h4-8,10-11,14,17,22-23H,1-3H2,(H,24,25)(H2,16,18,19)/t6-,7+,8-,10-,11-,14?/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	4.78E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Tested for irreversible inhibitory activity against AdoMet-DC (S-adenosyl-methionine decarboxylase-) isolated from Escherichia coli				Bioorg Med Chem Lett 3: 147-152 (1993) Article DOI: 10.1016/S0960-894X(01)80865-9 BindingDB Entry DOI: 10.7270/Q2PR7WG3
					More data for this Ligand-Target Pair
S-adenosylmethionine decarboxylase proenzyme (Homo sapiens (Human))	BDBM50366317 (CHEMBL3392204 | CHEMBL606102) Show SMILES OS(O)(=O)=O.OS([O-])(=O)=O.C[S+](C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)C1CCNC1 |r| Show InChI InChI=1S/C15H23N6O3S/c1-25(8-2-3-17-4-8)5-9-11(22)12(23)15(24-9)21-7-20-10-13(16)18-6-19-14(10)21/h6-9,11-12,15,17,22-23H,2-5H2,1H3,(H2,16,18,19)/q+1/p+1/t8?,9-,11-,12-,15?,25?/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	6.69E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Tested for irreversible inhibitory activity against AdoMet-DC (S-adenosyl-methionine decarboxylase-) isolated from Escherichia coli				Bioorg Med Chem Lett 3: 147-152 (1993) Article DOI: 10.1016/S0960-894X(01)80865-9 BindingDB Entry DOI: 10.7270/Q2PR7WG3
					More data for this Ligand-Target Pair
S-adenosylmethionine decarboxylase proenzyme (Homo sapiens (Human))	BDBM50366316 (CHEMBL3392209 | CHEMBL605267) Show SMILES OS(O)(=O)=O.Nc1ncnc2n(cnc12)[C@@H]1O[C@H](CS[C@H]2CN[C@@H](C2)C(O)=O)[C@@H](O)[C@H]1O |r| Show InChI InChI=1S/C15H20N6O5S/c16-12-9-13(19-4-18-12)21(5-20-9)14-11(23)10(22)8(26-14)3-27-6-1-7(15(24)25)17-2-6/h4-8,10-11,14,17,22-23H,1-3H2,(H,24,25)(H2,16,18,19)/t6-,7-,8+,10+,11+,14?/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	9.60E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Tested for irreversible inhibitory activity against AdoMet-DC (S-adenosyl-methionine decarboxylase-) isolated from Escherichia coli				Bioorg Med Chem Lett 3: 147-152 (1993) Article DOI: 10.1016/S0960-894X(01)80865-9 BindingDB Entry DOI: 10.7270/Q2PR7WG3
					More data for this Ligand-Target Pair
S-adenosylmethionine decarboxylase proenzyme (Homo sapiens (Human))	BDBM50366319 (CHEMBL1791405 | CHEMBL3392205) Show SMILES OS(O)(=O)=O.OS([O-])(=O)=O.C[S+](C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)C1CN[C@@H](C1)C(O)=O |r| Show InChI InChI=1S/C16H22N6O5S/c1-28(7-2-8(16(25)26)18-3-7)4-9-11(23)12(24)15(27-9)22-6-21-10-13(17)19-5-20-14(10)22/h5-9,11-12,15,18,23-24H,2-4H2,1H3,(H2-,17,19,20,25,26)/p+2/t7-,8+,9-,11-,12-,15-,28?/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	1.07E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Tested for irreversible inhibitory activity against AdoMet-DC (S-adenosyl-methionine decarboxylase-) isolated from Escherichia coli				Bioorg Med Chem Lett 3: 147-152 (1993) Article DOI: 10.1016/S0960-894X(01)80865-9 BindingDB Entry DOI: 10.7270/Q2PR7WG3
					More data for this Ligand-Target Pair
S-adenosylmethionine decarboxylase proenzyme (Homo sapiens (Human))	BDBM50366319 (CHEMBL1791405 | CHEMBL3392205) Show SMILES OS(O)(=O)=O.OS([O-])(=O)=O.C[S+](C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)C1CN[C@@H](C1)C(O)=O |r| Show InChI InChI=1S/C16H22N6O5S/c1-28(7-2-8(16(25)26)18-3-7)4-9-11(23)12(24)15(27-9)22-6-21-10-13(17)19-5-20-14(10)22/h5-9,11-12,15,18,23-24H,2-4H2,1H3,(H2-,17,19,20,25,26)/p+2/t7-,8+,9-,11-,12-,15-,28?/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	1.07E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Tested for irreversible inhibitory activity against AdoMet-DC (S-adenosyl-methionine decarboxylase-) isolated from Escherichia coli				Bioorg Med Chem Lett 3: 147-152 (1993) Article DOI: 10.1016/S0960-894X(01)80865-9 BindingDB Entry DOI: 10.7270/Q2PR7WG3
					More data for this Ligand-Target Pair
Sodium channel protein type 2 subunit alpha (Rattus norvegicus)	BDBM50344821 (10-hydroxymethyl-5-imino-(2S)-12,13-dioxa-4,6-diaz...) Show SMILES NC1=N[C@H](O)[C@H]2[C@H]3O[C@]4(O)O[C@@H]([C@@H](O)[C@@]2(N1)[C@@H]4O)[C@]3(O)CO |r,t:1,TLB:13:12:16:6.7.5,18:11:16:6.7.5,18:6:16:11.10.12,19:18:7:16.14.5,20:18:7:16.14.5,THB:12:11:7:16.14.5,3:5:16:11.10.12| Show InChI InChI=1S/C11H17N3O8/c12-8-13-6(17)2-4-9(19,1-15)5-3(16)10(2,14-8)7(18)11(20,21-4)22-5/h2-7,15-20H,1H2,(H3,12,13,14)/t2-,3-,4-,5+,6-,7+,9+,10-,11+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid PDB UniChem Similars	Article PubMed	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
Cambridge NeuroScience Inc. Curated by ChEMBL					Assay Description In vitro inhibition of [14C]- guanidinium influx in Chinese hamster ovary (CHO) cells expressing rat brain sodium channel type IIA (CNaIIA-1)				J Med Chem 41: 3048-61 (1998) Article DOI: 10.1021/jm980124a BindingDB Entry DOI: 10.7270/Q2R49RF5
					More data for this Ligand-Target Pair
Sodium channel protein type 2 subunit alpha (Rattus norvegicus)	BDBM50066062 (1,3-Bis-(4-sec-butyl-phenyl)-imidazolidin-2-yliden...) Show SMILES CCC(C)c1ccc(cc1)N1CCN(C1=N)c1ccc(cc1)C(C)CC Show InChI InChI=1S/C23H31N3/c1-5-17(3)19-7-11-21(12-8-19)25-15-16-26(23(25)24)22-13-9-20(10-14-22)18(4)6-2/h7-14,17-18,24H,5-6,15-16H2,1-4H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	60	n/a	n/a	n/a	n/a	n/a	n/a
Cambridge NeuroScience Inc. Curated by ChEMBL					Assay Description In vitro inhibition of [14C]- guanidinium influx in Chinese hamster ovary (CHO) cells expressing rat brain sodium channel type IIA (CNaIIA-1)				J Med Chem 41: 3048-61 (1998) Article DOI: 10.1021/jm980124a BindingDB Entry DOI: 10.7270/Q2R49RF5
					More data for this Ligand-Target Pair
Sodium channel protein type 2 subunit alpha (Rattus norvegicus)	BDBM50066059 (1,3-Bis-(4-sec-butyl-phenyl)-tetrahydro-pyrimidin-...) Show SMILES CCC(C)c1ccc(cc1)N1CCCN(C1=N)c1ccc(cc1)C(C)CC Show InChI InChI=1S/C24H33N3/c1-5-18(3)20-8-12-22(13-9-20)26-16-7-17-27(24(26)25)23-14-10-21(11-15-23)19(4)6-2/h8-15,18-19,25H,5-7,16-17H2,1-4H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	60	n/a	n/a	n/a	n/a	n/a	n/a
Cambridge NeuroScience Inc. Curated by ChEMBL					Assay Description In vitro inhibition of [14C]- guanidinium influx in Chinese hamster ovary (CHO) cells expressing rat brain sodium channel type IIA (CNaIIA-1)				J Med Chem 41: 3048-61 (1998) Article DOI: 10.1021/jm980124a BindingDB Entry DOI: 10.7270/Q2R49RF5
					More data for this Ligand-Target Pair
Sodium channel protein type 2 subunit alpha (Rattus norvegicus)	BDBM50066066 ((S)-1-[4-(Benzothiazol-2-yl-methyl-amino)-piperidi...) Show SMILES CN(C1CCN(C[C@H](O)COc2ccc(F)c(F)c2)CC1)c1nc2ccccc2s1 Show InChI InChI=1S/C22H25F2N3O2S/c1-26(22-25-20-4-2-3-5-21(20)30-22)15-8-10-27(11-9-15)13-16(28)14-29-17-6-7-18(23)19(24)12-17/h2-7,12,15-16,28H,8-11,13-14H2,1H3/t16-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	260	n/a	n/a	n/a	n/a	n/a	n/a
Cambridge NeuroScience Inc. Curated by ChEMBL					Assay Description In vitro inhibition of [14C]- guanidinium influx in Chinese hamster ovary (CHO) cells expressing rat brain sodium channel type IIA (CNaIIA-1)				J Med Chem 41: 3048-61 (1998) Article DOI: 10.1021/jm980124a BindingDB Entry DOI: 10.7270/Q2R49RF5
					More data for this Ligand-Target Pair
Sodium channel protein type 2 subunit alpha (Rattus norvegicus)	BDBM50066067 (2-(4-tert-Butyl-phenyl)-6-isopropyl-3,4-dihydro-2H...) Show SMILES CC(C)c1ccc2N(C(CCc2c1)c1ccc(cc1)C(C)(C)C)C(N)=N Show InChI InChI=1S/C23H31N3/c1-15(2)17-8-12-21-18(14-17)9-13-20(26(21)22(24)25)16-6-10-19(11-7-16)23(3,4)5/h6-8,10-12,14-15,20H,9,13H2,1-5H3,(H3,24,25)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	460	n/a	n/a	n/a	n/a	n/a	n/a
Cambridge NeuroScience Inc. Curated by ChEMBL					Assay Description In vitro inhibition of [14C]- guanidinium influx in Chinese hamster ovary (CHO) cells expressing rat brain sodium channel type IIA (CNaIIA-1)				J Med Chem 41: 3048-61 (1998) Article DOI: 10.1021/jm980124a BindingDB Entry DOI: 10.7270/Q2R49RF5
					More data for this Ligand-Target Pair
Sodium channel protein type 2 subunit alpha (Rattus norvegicus)	BDBM50066069 (CHEMBL103284 | N-(4-tert-Butyl-benzyl)-N-(4-sec-bu...) Show SMILES CCC(C)c1ccc(cc1)N(Cc1ccc(cc1)C(C)(C)C)C(N)=N Show InChI InChI=1S/C22H31N3/c1-6-16(2)18-9-13-20(14-10-18)25(21(23)24)15-17-7-11-19(12-8-17)22(3,4)5/h7-14,16H,6,15H2,1-5H3,(H3,23,24)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	620	n/a	n/a	n/a	n/a	n/a	n/a
Cambridge NeuroScience Inc. Curated by ChEMBL					Assay Description In vitro inhibition of [14C]- guanidinium influx in Chinese hamster ovary (CHO) cells expressing rat brain sodium channel type IIA (CNaIIA-1)				J Med Chem 41: 3048-61 (1998) Article DOI: 10.1021/jm980124a BindingDB Entry DOI: 10.7270/Q2R49RF5
					More data for this Ligand-Target Pair
Sodium channel protein type 2 subunit alpha (Rattus norvegicus)	BDBM50066052 ((3-sec-Butyl-phenyl)-[1-(4-sec-butyl-phenyl)-imida...) Show SMILES CCC(C)c1ccc(cc1)N1CCNC1=Nc1cccc(c1)C(C)CC |w:15.17| Show InChI InChI=1S/C23H31N3/c1-5-17(3)19-10-12-22(13-11-19)26-15-14-24-23(26)25-21-9-7-8-20(16-21)18(4)6-2/h7-13,16-18H,5-6,14-15H2,1-4H3,(H,24,25)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	780	n/a	n/a	n/a	n/a	n/a	n/a
Cambridge NeuroScience Inc. Curated by ChEMBL					Assay Description In vitro inhibition of [14C]- guanidinium influx in Chinese hamster ovary (CHO) cells expressing rat brain sodium channel type IIA (CNaIIA-1)				J Med Chem 41: 3048-61 (1998) Article DOI: 10.1021/jm980124a BindingDB Entry DOI: 10.7270/Q2R49RF5
					More data for this Ligand-Target Pair
Sodium channel protein type 2 subunit alpha (Rattus norvegicus)	BDBM50066057 (CHEMBL110909 | CHEMBL320199 | N,N'-Bis-(4-sec-buty...) Show SMILES CCC(C)c1ccc(NC(N)=Nc2ccc(cc2)C(C)CC)cc1 |w:11.11| Show InChI InChI=1S/C21H29N3/c1-5-15(3)17-7-11-19(12-8-17)23-21(22)24-20-13-9-18(10-14-20)16(4)6-2/h7-16H,5-6H2,1-4H3,(H3,22,23,24)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	800	n/a	n/a	n/a	n/a	n/a	n/a
Cambridge NeuroScience Inc. Curated by ChEMBL					Assay Description In vitro inhibition of [14C]- guanidinium influx in Chinese hamster ovary (CHO) cells expressing rat brain sodium channel type IIA (CNaIIA-1)				J Med Chem 41: 3048-61 (1998) Article DOI: 10.1021/jm980124a BindingDB Entry DOI: 10.7270/Q2R49RF5
					More data for this Ligand-Target Pair
Sodium channel protein type 2 subunit alpha (Rattus norvegicus)	BDBM50066060 (CHEMBL545504 | N,N'-Bis-(4-sec-butyl-phenyl)-N,N'-...) Show SMILES CCC(C)c1ccc(cc1)N(C)C(=N)N(C)c1ccc(cc1)C(C)CC Show InChI InChI=1S/C23H33N3/c1-7-17(3)19-9-13-21(14-10-19)25(5)23(24)26(6)22-15-11-20(12-16-22)18(4)8-2/h9-18,24H,7-8H2,1-6H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Cambridge NeuroScience Inc. Curated by ChEMBL					Assay Description In vitro inhibition of [14C]- guanidinium influx in Chinese hamster ovary (CHO) cells expressing rat brain sodium channel type IIA (CNaIIA-1)				J Med Chem 41: 3048-61 (1998) Article DOI: 10.1021/jm980124a BindingDB Entry DOI: 10.7270/Q2R49RF5
					More data for this Ligand-Target Pair
Sodium channel protein type 2 subunit alpha (Rattus norvegicus)	BDBM50066068 (CHEMBL28853 | N-Acenaphthen-5-yl-N'-(4-methoxy-nap...) Show SMILES COc1ccc(N=C(N)Nc2ccc3CCc4cccc2c34)c2ccccc12 |w:6.5| Show InChI InChI=1S/C24H21N3O/c1-28-22-14-13-20(17-6-2-3-7-18(17)22)26-24(25)27-21-12-11-16-10-9-15-5-4-8-19(21)23(15)16/h2-8,11-14H,9-10H2,1H3,(H3,25,26,27)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	1.64E+3	n/a	n/a	n/a	n/a	n/a	n/a
Cambridge NeuroScience Inc. Curated by ChEMBL					Assay Description In vitro inhibition of [14C]- guanidinium influx in Chinese hamster ovary (CHO) cells expressing rat brain sodium channel type IIA (CNaIIA-1)				J Med Chem 41: 3048-61 (1998) Article DOI: 10.1021/jm980124a BindingDB Entry DOI: 10.7270/Q2R49RF5
					More data for this Ligand-Target Pair
Sodium channel protein type 2 subunit alpha (Rattus norvegicus)	BDBM50066061 (1-(4-sec-Butyl-phenyl)-5-(4-isopropyl-phenyl)-imid...) Show SMILES CCC(C)c1ccc(cc1)N1C(CN=C1N)c1ccc(cc1)C(C)C |c:14| Show InChI InChI=1S/C22H29N3/c1-5-16(4)18-10-12-20(13-11-18)25-21(14-24-22(25)23)19-8-6-17(7-9-19)15(2)3/h6-13,15-16,21H,5,14H2,1-4H3,(H2,23,24)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Cambridge NeuroScience Inc. Curated by ChEMBL					Assay Description In vitro inhibition of [14C]- guanidinium influx in Chinese hamster ovary (CHO) cells expressing rat brain sodium channel type IIA (CNaIIA-1)				J Med Chem 41: 3048-61 (1998) Article DOI: 10.1021/jm980124a BindingDB Entry DOI: 10.7270/Q2R49RF5
					More data for this Ligand-Target Pair
Sodium channel protein type 2 subunit alpha (Rattus norvegicus)	BDBM50066063 (9,15-Dioxa-2,4-diaza-tricyclo[14.2.2.2*5,8*]docosa...) Show SMILES NC1=Nc2ccc(OCCCCCOc3ccc(N1)cc3)cc2 |w:2.2| Show InChI InChI=1S/C18H21N3O2/c19-18-20-14-4-8-16(9-5-14)22-12-2-1-3-13-23-17-10-6-15(21-18)7-11-17/h4-11H,1-3,12-13H2,(H3,19,20,21)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
Cambridge NeuroScience Inc. Curated by ChEMBL					Assay Description In vitro inhibition of [14C]- guanidinium influx in Chinese hamster ovary (CHO) cells expressing rat brain sodium channel type IIA (CNaIIA-1)				J Med Chem 41: 3048-61 (1998) Article DOI: 10.1021/jm980124a BindingDB Entry DOI: 10.7270/Q2R49RF5
					More data for this Ligand-Target Pair
Sodium channel protein type 2 subunit alpha (Rattus norvegicus)	BDBM50066053 (CHEMBL544569 | N,N'-Bis-(4-ethoxy-phenyl)-guanidin...) Show SMILES CCOc1ccc(NC(N)=Nc2ccc(OCC)cc2)cc1 |w:10.10| Show InChI InChI=1S/C17H21N3O2/c1-3-21-15-9-5-13(6-10-15)19-17(18)20-14-7-11-16(12-8-14)22-4-2/h5-12H,3-4H2,1-2H3,(H3,18,19,20)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.28E+3	n/a	n/a	n/a	n/a	n/a	n/a
Cambridge NeuroScience Inc. Curated by ChEMBL					Assay Description In vitro inhibition of [14C]- guanidinium influx in Chinese hamster ovary (CHO) cells expressing rat brain sodium channel type IIA (CNaIIA-1)				J Med Chem 41: 3048-61 (1998) Article DOI: 10.1021/jm980124a BindingDB Entry DOI: 10.7270/Q2R49RF5
					More data for this Ligand-Target Pair
S-adenosylmethionine decarboxylase proenzyme (Homo sapiens (Human))	BDBM50281292 (2-amino-4-({[(2S,3S,4R)-5-(6-amino-9H-purin-9-yl)-...) Show SMILES Br.[Br-].C[S+](CCC(N)C#N)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12 Show InChI InChI=1S/C15H22N7O3S/c1-26(3-2-8(17)4-16)5-9-11(23)12(24)15(25-9)22-7-21-10-13(18)19-6-20-14(10)22/h6-9,11-12,15,23-24H,2-3,5,17H2,1H3,(H2,18,19,20)/q+1/p+1/t8?,9-,11-,12-,15?,26?/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	9.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against AdoMet-DC from Escherichia coli				Bioorg Med Chem Lett 3: 2811-2816 (1993) Article DOI: 10.1016/S0960-894X(01)80770-8 BindingDB Entry DOI: 10.7270/Q2TH8N6T
					More data for this Ligand-Target Pair
Sodium channel protein type 2 subunit alpha (Rattus norvegicus)	BDBM50066055 (3-Phenyl-1,2,3,4-tetrahydro-quinazolin-2-ylamine; ...) Show SMILES NC1Nc2ccccc2CN1c1ccccc1 Show InChI InChI=1S/C14H15N3/c15-14-16-13-9-5-4-6-11(13)10-17(14)12-7-2-1-3-8-12/h1-9,14,16H,10,15H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	9.95E+3	n/a	n/a	n/a	n/a	n/a	n/a
Cambridge NeuroScience Inc. Curated by ChEMBL					Assay Description In vitro inhibition of [14C]- guanidinium influx in Chinese hamster ovary (CHO) cells expressing rat brain sodium channel type IIA (CNaIIA-1)				J Med Chem 41: 3048-61 (1998) Article DOI: 10.1021/jm980124a BindingDB Entry DOI: 10.7270/Q2R49RF5
					More data for this Ligand-Target Pair
Sodium channel protein type 2 subunit alpha (Rattus norvegicus)	BDBM50010769 (CHEMBL556117 | CHEMBL77675 | N,N'-Diphenyl-guanidi...) Show SMILES NC(Nc1ccccc1)=Nc1ccccc1 |w:9.10| Show InChI InChI=1S/C13H13N3/c14-13(15-11-7-3-1-4-8-11)16-12-9-5-2-6-10-12/h1-10H,(H3,14,15,16)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>1.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
Cambridge NeuroScience Inc. Curated by ChEMBL					Assay Description In vitro inhibition of [14C]- guanidinium influx in Chinese hamster ovary (CHO) cells expressing rat brain sodium channel type IIA (CNaIIA-1)				J Med Chem 41: 3048-61 (1998) Article DOI: 10.1021/jm980124a BindingDB Entry DOI: 10.7270/Q2R49RF5
					More data for this Ligand-Target Pair
Sodium channel protein type 2 subunit alpha (Rattus norvegicus)	BDBM50010804 (1,3-Diphenyl-imidazolidin-2-ylideneamine | CHEMBL5...) Show SMILES N=C1N(CCN1c1ccccc1)c1ccccc1 Show InChI InChI=1S/C15H15N3/c16-15-17(13-7-3-1-4-8-13)11-12-18(15)14-9-5-2-6-10-14/h1-10,16H,11-12H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.47E+4	n/a	n/a	n/a	n/a	n/a	n/a
Cambridge NeuroScience Inc. Curated by ChEMBL					Assay Description In vitro inhibition of [14C]- guanidinium influx in Chinese hamster ovary (CHO) cells expressing rat brain sodium channel type IIA (CNaIIA-1)				J Med Chem 41: 3048-61 (1998) Article DOI: 10.1021/jm980124a BindingDB Entry DOI: 10.7270/Q2R49RF5
					More data for this Ligand-Target Pair
Sodium channel protein type 2 subunit alpha (Rattus norvegicus)	BDBM50066070 (2-Phenyl-3,4-dihydro-2H-quinoline-1-carboxamidine;...) Show SMILES NC(=N)N1C(CCc2ccccc12)c1ccccc1 Show InChI InChI=1S/C16H17N3/c17-16(18)19-14-9-5-4-8-13(14)10-11-15(19)12-6-2-1-3-7-12/h1-9,15H,10-11H2,(H3,17,18)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.76E+4	n/a	n/a	n/a	n/a	n/a	n/a
Cambridge NeuroScience Inc. Curated by ChEMBL					Assay Description In vitro inhibition of [14C]- guanidinium influx in Chinese hamster ovary (CHO) cells expressing rat brain sodium channel type IIA (CNaIIA-1)				J Med Chem 41: 3048-61 (1998) Article DOI: 10.1021/jm980124a BindingDB Entry DOI: 10.7270/Q2R49RF5
					More data for this Ligand-Target Pair
Sodium channel protein type 2 subunit alpha (Rattus norvegicus)	BDBM50066056 (1,5-Diphenyl-imidazolidin-(2Z)-ylideneamine; hydro...) Show SMILES NC1=NCC(N1c1ccccc1)c1ccccc1 |t:1| Show InChI InChI=1S/C15H15N3/c16-15-17-11-14(12-7-3-1-4-8-12)18(15)13-9-5-2-6-10-13/h1-10,14H,11H2,(H2,16,17)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
Cambridge NeuroScience Inc. Curated by ChEMBL					Assay Description In vitro inhibition of [14C]- guanidinium influx in Chinese hamster ovary (CHO) cells expressing rat brain sodium channel type IIA (CNaIIA-1)				J Med Chem 41: 3048-61 (1998) Article DOI: 10.1021/jm980124a BindingDB Entry DOI: 10.7270/Q2R49RF5
					More data for this Ligand-Target Pair
Sodium channel protein type 2 subunit alpha (Rattus norvegicus)	BDBM50066064 (CHEMBL103505 | Phenyl-[1-phenyl-imidazolidin-(2E)-...) Show SMILES C1CN(C(N1)=Nc1ccccc1)c1ccccc1 |w:5.6| Show InChI InChI=1S/C15H15N3/c1-3-7-13(8-4-1)17-15-16-11-12-18(15)14-9-5-2-6-10-14/h1-10H,11-12H2,(H,16,17)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	>2.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
Cambridge NeuroScience Inc. Curated by ChEMBL					Assay Description In vitro inhibition of [14C]- guanidinium influx in Chinese hamster ovary (CHO) cells expressing rat brain sodium channel type IIA (CNaIIA-1)				J Med Chem 41: 3048-61 (1998) Article DOI: 10.1021/jm980124a BindingDB Entry DOI: 10.7270/Q2R49RF5
					More data for this Ligand-Target Pair
Sodium channel protein type 2 subunit alpha (Rattus norvegicus)	BDBM50066065 (1,3-Diphenyl-tetrahydro-pyrimidin-2-ylideneamine; ...) Show SMILES N=C1N(CCCN1c1ccccc1)c1ccccc1 Show InChI InChI=1S/C16H17N3/c17-16-18(14-8-3-1-4-9-14)12-7-13-19(16)15-10-5-2-6-11-15/h1-6,8-11,17H,7,12-13H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	>2.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
Cambridge NeuroScience Inc. Curated by ChEMBL					Assay Description In vitro inhibition of [14C]- guanidinium influx in Chinese hamster ovary (CHO) cells expressing rat brain sodium channel type IIA (CNaIIA-1)				J Med Chem 41: 3048-61 (1998) Article DOI: 10.1021/jm980124a BindingDB Entry DOI: 10.7270/Q2R49RF5
					More data for this Ligand-Target Pair
Sodium channel protein type 2 subunit alpha (Rattus norvegicus)	BDBM50066054 (11,12-Dihydro-6H-dibenzo[b,f]azocine-5-carboxamidi...) Show SMILES NC(=N)N1Cc2ccccc2CCc2ccccc12 Show InChI InChI=1S/C16H17N3/c17-16(18)19-11-14-7-2-1-5-12(14)9-10-13-6-3-4-8-15(13)19/h1-8H,9-11H2,(H3,17,18)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.80E+4	n/a	n/a	n/a	n/a	n/a	n/a
Cambridge NeuroScience Inc. Curated by ChEMBL					Assay Description In vitro inhibition of [14C]- guanidinium influx in Chinese hamster ovary (CHO) cells expressing rat brain sodium channel type IIA (CNaIIA-1)				J Med Chem 41: 3048-61 (1998) Article DOI: 10.1021/jm980124a BindingDB Entry DOI: 10.7270/Q2R49RF5
					More data for this Ligand-Target Pair
S-adenosylmethionine decarboxylase proenzyme (Homo sapiens (Human))	BDBM50281293 (2-amino-5-({[(2S,3S,4R)-5-(6-amino-9H-purin-9-yl)-...) Show SMILES Br.[Br-].C[S+](CCCC(N)C#N)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12 Show InChI InChI=1S/C16H24N7O3S/c1-27(4-2-3-9(18)5-17)6-10-12(24)13(25)16(26-10)23-8-22-11-14(19)20-7-21-15(11)23/h7-10,12-13,16,24-25H,2-4,6,18H2,1H3,(H2,19,20,21)/q+1/p+1/t9?,10-,12-,13-,16?,27?/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was evaluated to inactivate the bacterial AdoMet-DC				Bioorg Med Chem Lett 3: 2811-2816 (1993) Article DOI: 10.1016/S0960-894X(01)80770-8 BindingDB Entry DOI: 10.7270/Q2TH8N6T
					More data for this Ligand-Target Pair
Sodium channel protein type 2 subunit alpha (Rattus norvegicus)	BDBM50066071 (CHEMBL543152 | N-Benzyl-N-phenyl-guanidine; hydroc...) Show SMILES NC(=N)N(Cc1ccccc1)c1ccccc1 Show InChI InChI=1S/C14H15N3/c15-14(16)17(13-9-5-2-6-10-13)11-12-7-3-1-4-8-12/h1-10H,11H2,(H3,15,16)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
Cambridge NeuroScience Inc. Curated by ChEMBL					Assay Description In vitro inhibition of [14C]- guanidinium influx in Chinese hamster ovary (CHO) cells expressing rat brain sodium channel type IIA (CNaIIA-1)				J Med Chem 41: 3048-61 (1998) Article DOI: 10.1021/jm980124a BindingDB Entry DOI: 10.7270/Q2R49RF5
					More data for this Ligand-Target Pair
S-adenosylmethionine decarboxylase proenzyme (Homo sapiens (Human))	BDBM50366314 (CHEMBL3392211 | CHEMBL607699) Show SMILES NC(CCSC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)C#N |r| Show InChI InChI=1S/C14H19N7O3S/c15-3-7(16)1-2-25-4-8-10(22)11(23)14(24-8)21-6-20-9-12(17)18-5-19-13(9)21/h5-8,10-11,14,22-23H,1-2,4,16H2,(H2,17,18,19)/t7?,8-,10-,11-,14?/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	1.79E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against AdoMet-DC from Escherichia coli				Bioorg Med Chem Lett 3: 2811-2816 (1993) Article DOI: 10.1016/S0960-894X(01)80770-8 BindingDB Entry DOI: 10.7270/Q2TH8N6T
					More data for this Ligand-Target Pair
S-adenosylmethionine decarboxylase proenzyme (Homo sapiens (Human))	BDBM50366315 (CHEMBL1163096 | CHEMBL3392218) Show SMILES NC(CCCSC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)C#N |r| Show InChI InChI=1S/C15H21N7O3S/c16-4-8(17)2-1-3-26-5-9-11(23)12(24)15(25-9)22-7-21-10-13(18)19-6-20-14(10)22/h6-9,11-12,15,23-24H,1-3,5,17H2,(H2,18,19,20)/t8?,9-,11-,12-,15?/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	2.05E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against AdoMet-DC from Escherichia coli				Bioorg Med Chem Lett 3: 2811-2816 (1993) Article DOI: 10.1016/S0960-894X(01)80770-8 BindingDB Entry DOI: 10.7270/Q2TH8N6T
					More data for this Ligand-Target Pair