Compile Data Set for Download or QSAR

Found 79 hits of ki for UniProtKB: P13444   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50228186 (CHEMBL3706404) Show SMILES [H][C@@]1(O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)[C@@H](CCSCCC(N)C(O)=O)OP(O)(=O)OP(O)(=O)NP(O)(O)=O |r| Show InChI InChI=1S/C16H28N7O14P3S/c17-7(16(26)27)1-3-41-4-2-8(36-40(33,34)37-39(31,32)22-38(28,29)30)12-10(24)11(25)15(35-12)23-6-21-9-13(18)19-5-20-14(9)23/h5-8,10-12,15,24-25H,1-4,17H2,(H,26,27)(H,33,34)(H2,18,19,20)(H4,22,28,29,30,31,32)/t7?,8-,10+,11-,12-,15-/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	110	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Compound was tested for inhibition constant with kidney form of M-2 variants of Rat methionine adenosyltransferase when ATP was the variable substrat...				J Med Chem 32: 885-90 (1989) BindingDB Entry DOI: 10.7270/Q2K939Q8
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50226974 (CHEMBL603986) Show SMILES [H][C@@]1(OC([C@H](O)[C@@H]1O)n1cnc2C(N)N=CNc12)[C@@H](CSCCC(N)C(O)=O)OP(O)(=O)OP(O)(=O)ONP(O)(O)=O |r,c:15| Show InChI InChI=1S/C15H28N7O15P3S/c16-6(15(25)26)1-2-41-3-7(35-39(30,31)37-40(32,33)36-21-38(27,28)29)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-12,14,23-24H,1-3,16-17H2,(H,18,19)(H,25,26)(H,30,31)(H,32,33)(H3,21,27,28,29)/t6?,7-,9+,10-,11-,12?,14?/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	PubMed	130	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition constants of M-2 Forms of rat methionine adenosyltransferase using ATP as the variable substrate; Inhibition is competitive type				J Med Chem 30: 1599-603 (1987) BindingDB Entry DOI: 10.7270/Q2CV4KZR
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50227269 (CHEMBL3706402) Show SMILES [H][C@@]1(O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)[C@H](CSCCC(N)C(O)=O)OP(O)(=O)OP(O)(=O)NP(O)(O)=O |r| Show InChI InChI=1S/C15H26N7O14P3S/c16-6(15(25)26)1-2-40-3-7(35-39(32,33)36-38(30,31)21-37(27,28)29)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-11,14,23-24H,1-3,16H2,(H,25,26)(H,32,33)(H2,17,18,19)(H4,21,27,28,29,30,31)/t6?,7-,9-,10+,11+,14+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	130	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Inhibition constant of ATP varied compound was measured on M-2 variate Methionine adenosyltransferase in rat kidney				J Med Chem 31: 384-9 (1988) BindingDB Entry DOI: 10.7270/Q2736T3C
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50227269 (CHEMBL3706402) Show SMILES [H][C@@]1(O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)[C@H](CSCCC(N)C(O)=O)OP(O)(=O)OP(O)(=O)NP(O)(O)=O |r| Show InChI InChI=1S/C15H26N7O14P3S/c16-6(15(25)26)1-2-40-3-7(35-39(32,33)36-38(30,31)21-37(27,28)29)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-11,14,23-24H,1-3,16H2,(H,25,26)(H,32,33)(H2,17,18,19)(H4,21,27,28,29,30,31)/t6?,7-,9-,10+,11+,14+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	130	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Compound was tested for inhibition constant with kidney form of M-2 variants of Rat methionine adenosyltransferase when ATP was the variable substrat...				J Med Chem 32: 885-90 (1989) BindingDB Entry DOI: 10.7270/Q2K939Q8
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50228186 (CHEMBL3706404) Show SMILES [H][C@@]1(O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)[C@@H](CCSCCC(N)C(O)=O)OP(O)(=O)OP(O)(=O)NP(O)(O)=O |r| Show InChI InChI=1S/C16H28N7O14P3S/c17-7(16(26)27)1-3-41-4-2-8(36-40(33,34)37-39(31,32)22-38(28,29)30)12-10(24)11(25)15(35-12)23-6-21-9-13(18)19-5-20-14(9)23/h5-8,10-12,15,24-25H,1-4,17H2,(H,26,27)(H,33,34)(H2,18,19,20)(H4,22,28,29,30,31,32)/t7?,8-,10+,11-,12-,15-/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	160	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Compound was tested for inhibition constant with kidney form of M-T variants of Rat methionine adenosyltransferase when ATP was the variable substrat...				J Med Chem 32: 885-90 (1989) BindingDB Entry DOI: 10.7270/Q2K939Q8
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50227269 (CHEMBL3706402) Show SMILES [H][C@@]1(O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)[C@H](CSCCC(N)C(O)=O)OP(O)(=O)OP(O)(=O)NP(O)(O)=O |r| Show InChI InChI=1S/C15H26N7O14P3S/c16-6(15(25)26)1-2-40-3-7(35-39(32,33)36-38(30,31)21-37(27,28)29)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-11,14,23-24H,1-3,16H2,(H,25,26)(H,32,33)(H2,17,18,19)(H4,21,27,28,29,30,31)/t6?,7-,9-,10+,11+,14+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	210	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Compound was tested for inhibition constant with kidney form of M-T variants of Rat methionine adenosyltransferase when ATP was the variable substrat...				J Med Chem 32: 885-90 (1989) BindingDB Entry DOI: 10.7270/Q2K939Q8
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50226974 (CHEMBL603986) Show SMILES [H][C@@]1(OC([C@H](O)[C@@H]1O)n1cnc2C(N)N=CNc12)[C@@H](CSCCC(N)C(O)=O)OP(O)(=O)OP(O)(=O)ONP(O)(O)=O |r,c:15| Show InChI InChI=1S/C15H28N7O15P3S/c16-6(15(25)26)1-2-41-3-7(35-39(30,31)37-40(32,33)36-21-38(27,28)29)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-12,14,23-24H,1-3,16-17H2,(H,18,19)(H,25,26)(H,30,31)(H,32,33)(H3,21,27,28,29)/t6?,7-,9+,10-,11-,12?,14?/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	PubMed	210	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition constants of MT Forms of rat Novikoff Ascitic Hepatomae using ATP as the variable substrate; Inhibition is competitive type				J Med Chem 30: 1599-603 (1987) BindingDB Entry DOI: 10.7270/Q2CV4KZR
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50227269 (CHEMBL3706402) Show SMILES [H][C@@]1(O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)[C@H](CSCCC(N)C(O)=O)OP(O)(=O)OP(O)(=O)NP(O)(O)=O |r| Show InChI InChI=1S/C15H26N7O14P3S/c16-6(15(25)26)1-2-40-3-7(35-39(32,33)36-38(30,31)21-37(27,28)29)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-11,14,23-24H,1-3,16H2,(H,25,26)(H,32,33)(H2,17,18,19)(H4,21,27,28,29,30,31)/t6?,7-,9-,10+,11+,14+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	210	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Inhibition constant of ATP varied compound was measured on MT variant methionine adenosyltransferase in rat ascitic hepatoma cells				J Med Chem 31: 384-9 (1988) BindingDB Entry DOI: 10.7270/Q2736T3C
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50226768 (CHEMBL1791426) Show SMILES [H][C@](CNP(O)(=O)OP(O)(=O)OP(O)(O)=O)(SCCC(N)C(O)=O)[C@@]1([H])O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12 |r| Show InChI InChI=1S/C15H26N7O14P3S/c16-6(15(25)26)1-2-40-7(3-21-37(27,28)35-39(32,33)36-38(29,30)31)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-11,14,23-24H,1-3,16H2,(H,25,26)(H,32,33)(H2,17,18,19)(H2,21,27,28)(H2,29,30,31)/t6?,7-,9+,10-,11-,14-/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	PubMed	270	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Inhibition constant of ATP varied compound was measured on MT variant methionine adenosyltransferase in rat ascitic hepatoma cells				J Med Chem 31: 384-9 (1988) BindingDB Entry DOI: 10.7270/Q2736T3C
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50228185 (CHEMBL3706405) Show SMILES [H][C@@]1(O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)[C@H](CCSCCC(N)C(O)=O)OP(O)(=O)OP(O)(=O)NP(O)(O)=O |r| Show InChI InChI=1S/C16H28N7O14P3S/c17-7(16(26)27)1-3-41-4-2-8(36-40(33,34)37-39(31,32)22-38(28,29)30)12-10(24)11(25)15(35-12)23-6-21-9-13(18)19-5-20-14(9)23/h5-8,10-12,15,24-25H,1-4,17H2,(H,26,27)(H,33,34)(H2,18,19,20)(H4,22,28,29,30,31,32)/t7?,8-,10-,11+,12+,15+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	270	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Compound was tested for inhibition constant with kidney form of M-2 variants of Rat methionine adenosyltransferase when ATP was the variable substrat...				J Med Chem 32: 885-90 (1989) BindingDB Entry DOI: 10.7270/Q2K939Q8
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50226972 (CHEMBL606493) Show SMILES [H][C@@]1(OC([C@H](O)[C@@H]1O)n1cnc2C(N)N=CNc12)[C@H](CNP(O)(=O)OP(O)(=O)OP(O)(O)=O)SCCC(N)C(O)=O |r,c:15| Show InChI InChI=1S/C15H28N7O14P3S/c16-6(15(25)26)1-2-40-7(3-21-37(27,28)35-39(32,33)36-38(29,30)31)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-12,14,23-24H,1-3,16-17H2,(H,18,19)(H,25,26)(H,32,33)(H2,21,27,28)(H2,29,30,31)/t6?,7-,9-,10+,11+,12?,14?/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	PubMed	270	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition constants of MT Forms of rat Novikoff Ascitic Hepatomae using ATP as the variable substrate; Inhibition is competitive type				J Med Chem 30: 1599-603 (1987) BindingDB Entry DOI: 10.7270/Q2CV4KZR
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50226770 (CHEMBL609078) Show SMILES [H][C@@]1(OC([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)[C@H](CNP(O)(=O)OP(O)(=O)OP(O)(O)=O)SCCC(N)C(O)=O |r| Show InChI InChI=1S/C15H26N7O14P3S/c16-6(15(25)26)1-2-40-7(3-21-37(27,28)35-39(32,33)36-38(29,30)31)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-11,14,23-24H,1-3,16H2,(H,25,26)(H,32,33)(H2,17,18,19)(H2,21,27,28)(H2,29,30,31)/t6?,7-,9-,10+,11+,14?/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	270	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition constant of compound with Novikoff ascitic hepatoma (M-T) form of rat methionine adenosyltransferase when ATP was used as variable substra...				J Med Chem 30: 888-94 (1987) BindingDB Entry DOI: 10.7270/Q22J6F29
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50226770 (CHEMBL609078) Show SMILES [H][C@@]1(OC([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)[C@H](CNP(O)(=O)OP(O)(=O)OP(O)(O)=O)SCCC(N)C(O)=O |r| Show InChI InChI=1S/C15H26N7O14P3S/c16-6(15(25)26)1-2-40-7(3-21-37(27,28)35-39(32,33)36-38(29,30)31)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-11,14,23-24H,1-3,16H2,(H,25,26)(H,32,33)(H2,17,18,19)(H2,21,27,28)(H2,29,30,31)/t6?,7-,9-,10+,11+,14?/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	360	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition constant of compound with kidney (M-2) form of rat methionine adenosyltransferase when ATP was used as variable substrate;Competitive type...				J Med Chem 30: 888-94 (1987) BindingDB Entry DOI: 10.7270/Q22J6F29
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50226972 (CHEMBL606493) Show SMILES [H][C@@]1(OC([C@H](O)[C@@H]1O)n1cnc2C(N)N=CNc12)[C@H](CNP(O)(=O)OP(O)(=O)OP(O)(O)=O)SCCC(N)C(O)=O |r,c:15| Show InChI InChI=1S/C15H28N7O14P3S/c16-6(15(25)26)1-2-40-7(3-21-37(27,28)35-39(32,33)36-38(29,30)31)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-12,14,23-24H,1-3,16-17H2,(H,18,19)(H,25,26)(H,32,33)(H2,21,27,28)(H2,29,30,31)/t6?,7-,9-,10+,11+,12?,14?/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	PubMed	360	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition constants of M-2 Forms of rat methionine adenosyltransferase using ATP as the variable substrate; Inhibition is competitive type				J Med Chem 30: 1599-603 (1987) BindingDB Entry DOI: 10.7270/Q2CV4KZR
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50226768 (CHEMBL1791426) Show SMILES [H][C@](CNP(O)(=O)OP(O)(=O)OP(O)(O)=O)(SCCC(N)C(O)=O)[C@@]1([H])O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12 |r| Show InChI InChI=1S/C15H26N7O14P3S/c16-6(15(25)26)1-2-40-7(3-21-37(27,28)35-39(32,33)36-38(29,30)31)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-11,14,23-24H,1-3,16H2,(H,25,26)(H,32,33)(H2,17,18,19)(H2,21,27,28)(H2,29,30,31)/t6?,7-,9+,10-,11-,14-/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	PubMed	360	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Inhibition constant of ATP varied compound was measured on M-2 variate methionine adenosyltransferase in rat kidney				J Med Chem 31: 384-9 (1988) BindingDB Entry DOI: 10.7270/Q2736T3C
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50227270 (CHEMBL3706403) Show SMILES N[C@@H](CCSCC(C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)OP(O)(=O)OP(O)(=O)NP(O)(O)=O)C(O)=O |r| Show InChI InChI=1S/C16H28N7O14P3S/c17-8(16(26)27)1-2-41-4-7(36-40(33,34)37-39(31,32)22-38(28,29)30)3-9-11(24)12(25)15(35-9)23-6-21-10-13(18)19-5-20-14(10)23/h5-9,11-12,15,24-25H,1-4,17H2,(H,26,27)(H,33,34)(H2,18,19,20)(H4,22,28,29,30,31,32)/t7?,8-,9+,11+,12+,15+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	390	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Inhibition constant of ATP varied compound was measured on M-2 variate methionine adenosyltransferase in rat kidney				J Med Chem 31: 384-9 (1988) BindingDB Entry DOI: 10.7270/Q2736T3C
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50228185 (CHEMBL3706405) Show SMILES [H][C@@]1(O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)[C@H](CCSCCC(N)C(O)=O)OP(O)(=O)OP(O)(=O)NP(O)(O)=O |r| Show InChI InChI=1S/C16H28N7O14P3S/c17-7(16(26)27)1-3-41-4-2-8(36-40(33,34)37-39(31,32)22-38(28,29)30)12-10(24)11(25)15(35-12)23-6-21-9-13(18)19-5-20-14(9)23/h5-8,10-12,15,24-25H,1-4,17H2,(H,26,27)(H,33,34)(H2,18,19,20)(H4,22,28,29,30,31,32)/t7?,8-,10-,11+,12+,15+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	410	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Compound was tested for inhibition constant with kidney form of M-T variants of Rat methionine adenosyltransferase when ATP was the variable substrat...				J Med Chem 32: 885-90 (1989) BindingDB Entry DOI: 10.7270/Q2K939Q8
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50227271 (CHEMBL1791425) Show SMILES NC(CCSC(CCOP(O)(=O)OP(O)(=O)NP(O)(O)=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)C(O)=O |r| Show InChI InChI=1S/C16H28N7O14P3S/c17-7(16(26)27)2-4-41-8(1-3-35-40(33,34)37-39(31,32)22-38(28,29)30)12-10(24)11(25)15(36-12)23-6-21-9-13(18)19-5-20-14(9)23/h5-8,10-12,15,24-25H,1-4,17H2,(H,26,27)(H,33,34)(H2,18,19,20)(H4,22,28,29,30,31,32)/t7?,8?,10-,11+,12+,15+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	440	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Inhibition constant of ATP varied compound was measured on M-2 variate methionine adenosyltransferase in rat kidney				J Med Chem 31: 384-9 (1988) BindingDB Entry DOI: 10.7270/Q2736T3C
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50227270 (CHEMBL3706403) Show SMILES N[C@@H](CCSCC(C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)OP(O)(=O)OP(O)(=O)NP(O)(O)=O)C(O)=O |r| Show InChI InChI=1S/C16H28N7O14P3S/c17-8(16(26)27)1-2-41-4-7(36-40(33,34)37-39(31,32)22-38(28,29)30)3-9-11(24)12(25)15(35-9)23-6-21-10-13(18)19-5-20-14(10)23/h5-9,11-12,15,24-25H,1-4,17H2,(H,26,27)(H,33,34)(H2,18,19,20)(H4,22,28,29,30,31,32)/t7?,8-,9+,11+,12+,15+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	630	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Inhibition constant of ATP varied compound was measured on MT variant methionine adenosyltransferase in rat ascitic hepatoma cells				J Med Chem 31: 384-9 (1988) BindingDB Entry DOI: 10.7270/Q2736T3C
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50226974 (CHEMBL603986) Show SMILES [H][C@@]1(OC([C@H](O)[C@@H]1O)n1cnc2C(N)N=CNc12)[C@@H](CSCCC(N)C(O)=O)OP(O)(=O)OP(O)(=O)ONP(O)(O)=O |r,c:15| Show InChI InChI=1S/C15H28N7O15P3S/c16-6(15(25)26)1-2-41-3-7(35-39(30,31)37-40(32,33)36-21-38(27,28)29)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-12,14,23-24H,1-3,16-17H2,(H,18,19)(H,25,26)(H,30,31)(H,32,33)(H3,21,27,28,29)/t6?,7-,9+,10-,11-,12?,14?/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	PubMed	650	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition constants of M-2 Forms of rat methionine adenosyltransferase using Methionine as the variable substrate; Inhibition is non competitive typ...				J Med Chem 30: 1599-603 (1987) BindingDB Entry DOI: 10.7270/Q2CV4KZR
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50227269 (CHEMBL3706402) Show SMILES [H][C@@]1(O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)[C@H](CSCCC(N)C(O)=O)OP(O)(=O)OP(O)(=O)NP(O)(O)=O |r| Show InChI InChI=1S/C15H26N7O14P3S/c16-6(15(25)26)1-2-40-3-7(35-39(32,33)36-38(30,31)21-37(27,28)29)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-11,14,23-24H,1-3,16H2,(H,25,26)(H,32,33)(H2,17,18,19)(H4,21,27,28,29,30,31)/t6?,7-,9-,10+,11+,14+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	650	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Compound was tested for inhibition constant with kidney form of M-2 variants of Rat methionine adenosyltransferase when Methionine was the variable s...				J Med Chem 32: 885-90 (1989) BindingDB Entry DOI: 10.7270/Q2K939Q8
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50227269 (CHEMBL3706402) Show SMILES [H][C@@]1(O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)[C@H](CSCCC(N)C(O)=O)OP(O)(=O)OP(O)(=O)NP(O)(O)=O |r| Show InChI InChI=1S/C15H26N7O14P3S/c16-6(15(25)26)1-2-40-3-7(35-39(32,33)36-38(30,31)21-37(27,28)29)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-11,14,23-24H,1-3,16H2,(H,25,26)(H,32,33)(H2,17,18,19)(H4,21,27,28,29,30,31)/t6?,7-,9-,10+,11+,14+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	650	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Inhibition constant of Met varied compound was measured on M-2 variant Methionine adenosyltransferase in rat kidney				J Med Chem 31: 384-9 (1988) BindingDB Entry DOI: 10.7270/Q2736T3C
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50227269 (CHEMBL3706402) Show SMILES [H][C@@]1(O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)[C@H](CSCCC(N)C(O)=O)OP(O)(=O)OP(O)(=O)NP(O)(O)=O |r| Show InChI InChI=1S/C15H26N7O14P3S/c16-6(15(25)26)1-2-40-3-7(35-39(32,33)36-38(30,31)21-37(27,28)29)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-11,14,23-24H,1-3,16H2,(H,25,26)(H,32,33)(H2,17,18,19)(H4,21,27,28,29,30,31)/t6?,7-,9-,10+,11+,14+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	670	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Inhibition constant of Met varied compound was measured on MT variant methionine adenosyltransferase in rat ascitic hepatoma cells				J Med Chem 31: 384-9 (1988) BindingDB Entry DOI: 10.7270/Q2736T3C
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50227269 (CHEMBL3706402) Show SMILES [H][C@@]1(O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)[C@H](CSCCC(N)C(O)=O)OP(O)(=O)OP(O)(=O)NP(O)(O)=O |r| Show InChI InChI=1S/C15H26N7O14P3S/c16-6(15(25)26)1-2-40-3-7(35-39(32,33)36-38(30,31)21-37(27,28)29)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-11,14,23-24H,1-3,16H2,(H,25,26)(H,32,33)(H2,17,18,19)(H4,21,27,28,29,30,31)/t6?,7-,9-,10+,11+,14+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	670	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Compound was tested for inhibition constant with kidney form of M-T variants of Rat methionine adenosyltransferase when Methionine was the variable s...				J Med Chem 32: 885-90 (1989) BindingDB Entry DOI: 10.7270/Q2K939Q8
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50226974 (CHEMBL603986) Show SMILES [H][C@@]1(OC([C@H](O)[C@@H]1O)n1cnc2C(N)N=CNc12)[C@@H](CSCCC(N)C(O)=O)OP(O)(=O)OP(O)(=O)ONP(O)(O)=O |r,c:15| Show InChI InChI=1S/C15H28N7O15P3S/c16-6(15(25)26)1-2-41-3-7(35-39(30,31)37-40(32,33)36-21-38(27,28)29)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-12,14,23-24H,1-3,16-17H2,(H,18,19)(H,25,26)(H,30,31)(H,32,33)(H3,21,27,28,29)/t6?,7-,9+,10-,11-,12?,14?/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	PubMed	670	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition constants of MT Forms of rat Novikoff Ascitic Hepatomae using Methionine as the variable substrate; Inhibition is non competitive type				J Med Chem 30: 1599-603 (1987) BindingDB Entry DOI: 10.7270/Q2CV4KZR
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50227271 (CHEMBL1791425) Show SMILES NC(CCSC(CCOP(O)(=O)OP(O)(=O)NP(O)(O)=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)C(O)=O |r| Show InChI InChI=1S/C16H28N7O14P3S/c17-7(16(26)27)2-4-41-8(1-3-35-40(33,34)37-39(31,32)22-38(28,29)30)12-10(24)11(25)15(36-12)23-6-21-9-13(18)19-5-20-14(9)23/h5-8,10-12,15,24-25H,1-4,17H2,(H,26,27)(H,33,34)(H2,18,19,20)(H4,22,28,29,30,31,32)/t7?,8?,10-,11+,12+,15+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	810	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Inhibition constant of ATP varied compound was measured on MT variant methionine adenosyltransferase in rat ascitic hepatoma cells				J Med Chem 31: 384-9 (1988) BindingDB Entry DOI: 10.7270/Q2736T3C
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50228186 (CHEMBL3706404) Show SMILES [H][C@@]1(O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)[C@@H](CCSCCC(N)C(O)=O)OP(O)(=O)OP(O)(=O)NP(O)(O)=O |r| Show InChI InChI=1S/C16H28N7O14P3S/c17-7(16(26)27)1-3-41-4-2-8(36-40(33,34)37-39(31,32)22-38(28,29)30)12-10(24)11(25)15(35-12)23-6-21-9-13(18)19-5-20-14(9)23/h5-8,10-12,15,24-25H,1-4,17H2,(H,26,27)(H,33,34)(H2,18,19,20)(H4,22,28,29,30,31,32)/t7?,8-,10+,11-,12-,15-/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	1.10E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Compound was tested for inhibition constant with kidney form of M-T variants of Rat methionine adenosyltransferase when Methionine was the variable s...				J Med Chem 32: 885-90 (1989) BindingDB Entry DOI: 10.7270/Q2K939Q8
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50227271 (CHEMBL1791425) Show SMILES NC(CCSC(CCOP(O)(=O)OP(O)(=O)NP(O)(O)=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)C(O)=O |r| Show InChI InChI=1S/C16H28N7O14P3S/c17-7(16(26)27)2-4-41-8(1-3-35-40(33,34)37-39(31,32)22-38(28,29)30)12-10(24)11(25)15(36-12)23-6-21-9-13(18)19-5-20-14(9)23/h5-8,10-12,15,24-25H,1-4,17H2,(H,26,27)(H,33,34)(H2,18,19,20)(H4,22,28,29,30,31,32)/t7?,8?,10-,11+,12+,15+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	1.50E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Inhibition constant of Met varied compound was measured on MT variant methionine adenosyltransferase in rat ascitic hepatoma cells				J Med Chem 31: 384-9 (1988) BindingDB Entry DOI: 10.7270/Q2736T3C
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50227271 (CHEMBL1791425) Show SMILES NC(CCSC(CCOP(O)(=O)OP(O)(=O)NP(O)(O)=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)C(O)=O |r| Show InChI InChI=1S/C16H28N7O14P3S/c17-7(16(26)27)2-4-41-8(1-3-35-40(33,34)37-39(31,32)22-38(28,29)30)12-10(24)11(25)15(36-12)23-6-21-9-13(18)19-5-20-14(9)23/h5-8,10-12,15,24-25H,1-4,17H2,(H,26,27)(H,33,34)(H2,18,19,20)(H4,22,28,29,30,31,32)/t7?,8?,10-,11+,12+,15+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	2.10E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Inhibition constant of Met varied compound was measured on M-2 variant methionine adenosyltransferase in rat kidney				J Med Chem 31: 384-9 (1988) BindingDB Entry DOI: 10.7270/Q2736T3C
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50228186 (CHEMBL3706404) Show SMILES [H][C@@]1(O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)[C@@H](CCSCCC(N)C(O)=O)OP(O)(=O)OP(O)(=O)NP(O)(O)=O |r| Show InChI InChI=1S/C16H28N7O14P3S/c17-7(16(26)27)1-3-41-4-2-8(36-40(33,34)37-39(31,32)22-38(28,29)30)12-10(24)11(25)15(35-12)23-6-21-9-13(18)19-5-20-14(9)23/h5-8,10-12,15,24-25H,1-4,17H2,(H,26,27)(H,33,34)(H2,18,19,20)(H4,22,28,29,30,31,32)/t7?,8-,10+,11-,12-,15-/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	2.10E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Compound was tested for inhibition constant with kidney form of M-2 variants of Rat methionine adenosyltransferase when Methionine was the variable s...				J Med Chem 32: 885-90 (1989) BindingDB Entry DOI: 10.7270/Q2K939Q8
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50227270 (CHEMBL3706403) Show SMILES N[C@@H](CCSCC(C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)OP(O)(=O)OP(O)(=O)NP(O)(O)=O)C(O)=O |r| Show InChI InChI=1S/C16H28N7O14P3S/c17-8(16(26)27)1-2-41-4-7(36-40(33,34)37-39(31,32)22-38(28,29)30)3-9-11(24)12(25)15(35-9)23-6-21-10-13(18)19-5-20-14(10)23/h5-9,11-12,15,24-25H,1-4,17H2,(H,26,27)(H,33,34)(H2,18,19,20)(H4,22,28,29,30,31,32)/t7?,8-,9+,11+,12+,15+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	2.20E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Inhibition constant of Met varied compound was measured on M-2 variant methionine adenosyltransferase in rat kidney				J Med Chem 31: 384-9 (1988) BindingDB Entry DOI: 10.7270/Q2736T3C
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50226972 (CHEMBL606493) Show SMILES [H][C@@]1(OC([C@H](O)[C@@H]1O)n1cnc2C(N)N=CNc12)[C@H](CNP(O)(=O)OP(O)(=O)OP(O)(O)=O)SCCC(N)C(O)=O |r,c:15| Show InChI InChI=1S/C15H28N7O14P3S/c16-6(15(25)26)1-2-40-7(3-21-37(27,28)35-39(32,33)36-38(29,30)31)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-12,14,23-24H,1-3,16-17H2,(H,18,19)(H,25,26)(H,32,33)(H2,21,27,28)(H2,29,30,31)/t6?,7-,9-,10+,11+,12?,14?/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	PubMed	2.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition constants of MT Forms of rat Novikoff Ascitic Hepatomae using Methionine as the variable substrate; Inhibition is non competitive type				J Med Chem 30: 1599-603 (1987) BindingDB Entry DOI: 10.7270/Q2CV4KZR
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50226768 (CHEMBL1791426) Show SMILES [H][C@](CNP(O)(=O)OP(O)(=O)OP(O)(O)=O)(SCCC(N)C(O)=O)[C@@]1([H])O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12 |r| Show InChI InChI=1S/C15H26N7O14P3S/c16-6(15(25)26)1-2-40-7(3-21-37(27,28)35-39(32,33)36-38(29,30)31)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-11,14,23-24H,1-3,16H2,(H,25,26)(H,32,33)(H2,17,18,19)(H2,21,27,28)(H2,29,30,31)/t6?,7-,9+,10-,11-,14-/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	PubMed	2.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Inhibition constant of Met varied compound was measured on MT variant methionine adenosyltransferase in rat ascitic hepatoma cells				J Med Chem 31: 384-9 (1988) BindingDB Entry DOI: 10.7270/Q2736T3C
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50226770 (CHEMBL609078) Show SMILES [H][C@@]1(OC([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)[C@H](CNP(O)(=O)OP(O)(=O)OP(O)(O)=O)SCCC(N)C(O)=O |r| Show InChI InChI=1S/C15H26N7O14P3S/c16-6(15(25)26)1-2-40-7(3-21-37(27,28)35-39(32,33)36-38(29,30)31)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-11,14,23-24H,1-3,16H2,(H,25,26)(H,32,33)(H2,17,18,19)(H2,21,27,28)(H2,29,30,31)/t6?,7-,9-,10+,11+,14?/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	2.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition constant of compound with Novikoff ascitic hepatoma (M-T) form of rat methionine adenosyltransferase when methionine was used as variable ...				J Med Chem 30: 888-94 (1987) BindingDB Entry DOI: 10.7270/Q22J6F29
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50228185 (CHEMBL3706405) Show SMILES [H][C@@]1(O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)[C@H](CCSCCC(N)C(O)=O)OP(O)(=O)OP(O)(=O)NP(O)(O)=O |r| Show InChI InChI=1S/C16H28N7O14P3S/c17-7(16(26)27)1-3-41-4-2-8(36-40(33,34)37-39(31,32)22-38(28,29)30)12-10(24)11(25)15(35-12)23-6-21-9-13(18)19-5-20-14(9)23/h5-8,10-12,15,24-25H,1-4,17H2,(H,26,27)(H,33,34)(H2,18,19,20)(H4,22,28,29,30,31,32)/t7?,8-,10-,11+,12+,15+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	2.70E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Compound was tested for inhibition constant with kidney form of M-T variants of Rat methionine adenosyltransferase when Methionine was the variable s...				J Med Chem 32: 885-90 (1989) BindingDB Entry DOI: 10.7270/Q2K939Q8
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50227270 (CHEMBL3706403) Show SMILES N[C@@H](CCSCC(C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)OP(O)(=O)OP(O)(=O)NP(O)(O)=O)C(O)=O |r| Show InChI InChI=1S/C16H28N7O14P3S/c17-8(16(26)27)1-2-41-4-7(36-40(33,34)37-39(31,32)22-38(28,29)30)3-9-11(24)12(25)15(35-9)23-6-21-10-13(18)19-5-20-14(10)23/h5-9,11-12,15,24-25H,1-4,17H2,(H,26,27)(H,33,34)(H2,18,19,20)(H4,22,28,29,30,31,32)/t7?,8-,9+,11+,12+,15+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	2.70E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Inhibition constant of Met varied compound was measured on MT variant methionine adenosyltransferase in rat ascitic hepatoma cells				J Med Chem 31: 384-9 (1988) BindingDB Entry DOI: 10.7270/Q2736T3C
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50226768 (CHEMBL1791426) Show SMILES [H][C@](CNP(O)(=O)OP(O)(=O)OP(O)(O)=O)(SCCC(N)C(O)=O)[C@@]1([H])O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12 |r| Show InChI InChI=1S/C15H26N7O14P3S/c16-6(15(25)26)1-2-40-7(3-21-37(27,28)35-39(32,33)36-38(29,30)31)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-11,14,23-24H,1-3,16H2,(H,25,26)(H,32,33)(H2,17,18,19)(H2,21,27,28)(H2,29,30,31)/t6?,7-,9+,10-,11-,14-/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	PubMed	3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Inhibition constant of Met varied compound was measured on M-2 variant methionine adenosyltransferase in rat kidney				J Med Chem 31: 384-9 (1988) BindingDB Entry DOI: 10.7270/Q2736T3C
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50226770 (CHEMBL609078) Show SMILES [H][C@@]1(OC([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)[C@H](CNP(O)(=O)OP(O)(=O)OP(O)(O)=O)SCCC(N)C(O)=O |r| Show InChI InChI=1S/C15H26N7O14P3S/c16-6(15(25)26)1-2-40-7(3-21-37(27,28)35-39(32,33)36-38(29,30)31)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-11,14,23-24H,1-3,16H2,(H,25,26)(H,32,33)(H2,17,18,19)(H2,21,27,28)(H2,29,30,31)/t6?,7-,9-,10+,11+,14?/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition constant of compound with kidney (M-2) form of rat methionine adenosyltransferase when methionine was used as variable substrate;Simple no...				J Med Chem 30: 888-94 (1987) BindingDB Entry DOI: 10.7270/Q22J6F29
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50226972 (CHEMBL606493) Show SMILES [H][C@@]1(OC([C@H](O)[C@@H]1O)n1cnc2C(N)N=CNc12)[C@H](CNP(O)(=O)OP(O)(=O)OP(O)(O)=O)SCCC(N)C(O)=O |r,c:15| Show InChI InChI=1S/C15H28N7O14P3S/c16-6(15(25)26)1-2-40-7(3-21-37(27,28)35-39(32,33)36-38(29,30)31)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-12,14,23-24H,1-3,16-17H2,(H,18,19)(H,25,26)(H,32,33)(H2,21,27,28)(H2,29,30,31)/t6?,7-,9-,10+,11+,12?,14?/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	PubMed	3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition constants of M-2 Forms of rat methionine adenosyltransferase using Methionine as the variable substrate; Inhibition is non competitive typ...				J Med Chem 30: 1599-603 (1987) BindingDB Entry DOI: 10.7270/Q2CV4KZR
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM18134 (({[({[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-...) Show SMILES Nc1ncnc2n(cnc12)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)NP(O)(O)=O)[C@@H](O)[C@H]1O |r| Show InChI InChI=1S/C10H17N6O12P3/c11-8-5-9(13-2-12-8)16(3-14-5)10-7(18)6(17)4(27-10)1-26-31(24,25)28-30(22,23)15-29(19,20)21/h2-4,6-7,10,17-18H,1H2,(H,24,25)(H2,11,12,13)(H4,15,19,20,21,22,23)/t4-,6-,7-,10-/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	PubMed	4.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory constant against rat Methionine adenosyltransferase was reported				J Med Chem 29: 318-22 (1986) BindingDB Entry DOI: 10.7270/Q2DF6RSH
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50228185 (CHEMBL3706405) Show SMILES [H][C@@]1(O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)[C@H](CCSCCC(N)C(O)=O)OP(O)(=O)OP(O)(=O)NP(O)(O)=O |r| Show InChI InChI=1S/C16H28N7O14P3S/c17-7(16(26)27)1-3-41-4-2-8(36-40(33,34)37-39(31,32)22-38(28,29)30)12-10(24)11(25)15(35-12)23-6-21-9-13(18)19-5-20-14(9)23/h5-8,10-12,15,24-25H,1-4,17H2,(H,26,27)(H,33,34)(H2,18,19,20)(H4,22,28,29,30,31,32)/t7?,8-,10-,11+,12+,15+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	5.40E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Fox Chase Cancer Center Curated by ChEMBL					Assay Description Compound was tested for inhibition constant with kidney form of M-2 variants of Rat methionine adenosyltransferase when Methionine was the variable s...				J Med Chem 32: 885-90 (1989) BindingDB Entry DOI: 10.7270/Q2K939Q8
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50226973 (CHEMBL1791411) Show SMILES NC(CCSC(CP(O)(=O)OP(O)(=O)NP(O)(O)=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2C(N)N=CNc12)C(O)=O |r,c:33| Show InChI InChI=1S/C15H28N7O13P3S/c16-6(15(25)26)1-2-39-7(3-36(27,28)35-38(32,33)21-37(29,30)31)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-12,14,23-24H,1-3,16-17H2,(H,18,19)(H,25,26)(H,27,28)(H4,21,29,30,31,32,33)/t6?,7?,9-,10+,11+,12?,14+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition constants of MT Forms of rat Novikoff Ascitic Hepatomae using ATP as the variable substrate; Inhibition is competitive type				J Med Chem 30: 1599-603 (1987) BindingDB Entry DOI: 10.7270/Q2CV4KZR
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50367328 (CHEMBL1791415) Show SMILES NC(CCSC(CP(O)(=O)OP(O)(=O)NP(O)(O)=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)C(O)=O |r| Show InChI InChI=1S/C15H26N7O13P3S/c16-6(15(25)26)1-2-39-7(3-36(27,28)35-38(32,33)21-37(29,30)31)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-11,14,23-24H,1-3,16H2,(H,25,26)(H,27,28)(H2,17,18,19)(H4,21,29,30,31,32,33)/t6?,7?,9-,10+,11+,14+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition constant was evaluated on novikoff hepatoma (MAT-T) form of rat methionine adenosyltransferase, when ATP was the variable substrate (60 uM...				J Med Chem 29: 1030-8 (1986) BindingDB Entry DOI: 10.7270/Q2CF9QN4
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50226769 (CHEMBL607665) Show SMILES Nc1ncnc2n(cnc12)C1O[C@H](CCNP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O |r| Show InChI InChI=1S/C11H19N6O12P3/c12-9-6-10(14-3-13-9)17(4-15-6)11-8(19)7(18)5(27-11)1-2-16-30(20,21)28-32(25,26)29-31(22,23)24/h3-5,7-8,11,18-19H,1-2H2,(H,25,26)(H2,12,13,14)(H2,16,20,21)(H2,22,23,24)/t5-,7-,8-,11?/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	PubMed	1.40E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition constant of compound with kidney (M-2) form of rat methionine adenosyltransferase when ATP was used as variable substrate;Competitive type...				J Med Chem 30: 888-94 (1987) BindingDB Entry DOI: 10.7270/Q22J6F29
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50226973 (CHEMBL1791411) Show SMILES NC(CCSC(CP(O)(=O)OP(O)(=O)NP(O)(O)=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2C(N)N=CNc12)C(O)=O |r,c:33| Show InChI InChI=1S/C15H28N7O13P3S/c16-6(15(25)26)1-2-39-7(3-36(27,28)35-38(32,33)21-37(29,30)31)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-12,14,23-24H,1-3,16-17H2,(H,18,19)(H,25,26)(H,27,28)(H4,21,29,30,31,32,33)/t6?,7?,9-,10+,11+,12?,14+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	1.60E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition constants of M-2 Forms of rat methionine adenosyltransferase using ATP as the variable substrate; Inhibition is competitive type				J Med Chem 30: 1599-603 (1987) BindingDB Entry DOI: 10.7270/Q2CV4KZR
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50226768 (CHEMBL1791426) Show SMILES [H][C@](CNP(O)(=O)OP(O)(=O)OP(O)(O)=O)(SCCC(N)C(O)=O)[C@@]1([H])O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12 |r| Show InChI InChI=1S/C15H26N7O14P3S/c16-6(15(25)26)1-2-40-7(3-21-37(27,28)35-39(32,33)36-38(29,30)31)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-11,14,23-24H,1-3,16H2,(H,25,26)(H,32,33)(H2,17,18,19)(H2,21,27,28)(H2,29,30,31)/t6?,7-,9+,10-,11-,14-/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	PubMed	2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition constant of compound with Novikoff ascitic hepatoma (M-T) form of rat methionine adenosyltransferase when ATP was used as variable substra...				J Med Chem 30: 888-94 (1987) BindingDB Entry DOI: 10.7270/Q22J6F29
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50226973 (CHEMBL1791411) Show SMILES NC(CCSC(CP(O)(=O)OP(O)(=O)NP(O)(O)=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2C(N)N=CNc12)C(O)=O |r,c:33| Show InChI InChI=1S/C15H28N7O13P3S/c16-6(15(25)26)1-2-39-7(3-36(27,28)35-38(32,33)21-37(29,30)31)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-12,14,23-24H,1-3,16-17H2,(H,18,19)(H,25,26)(H,27,28)(H4,21,29,30,31,32,33)/t6?,7?,9-,10+,11+,12?,14+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	2.60E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition constants of M-2 Forms of rat methionine adenosyltransferase using Methionine as the variable substrate; Inhibition is competitive type				J Med Chem 30: 1599-603 (1987) BindingDB Entry DOI: 10.7270/Q2CV4KZR
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50367328 (CHEMBL1791415) Show SMILES NC(CCSC(CP(O)(=O)OP(O)(=O)NP(O)(O)=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)C(O)=O |r| Show InChI InChI=1S/C15H26N7O13P3S/c16-6(15(25)26)1-2-39-7(3-36(27,28)35-38(32,33)21-37(29,30)31)11-9(23)10(24)14(34-11)22-5-20-8-12(17)18-4-19-13(8)22/h4-7,9-11,14,23-24H,1-3,16H2,(H,25,26)(H,27,28)(H2,17,18,19)(H4,21,29,30,31,32,33)/t6?,7?,9-,10+,11+,14+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	2.60E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition constant was evaluated with kidney (MAT-2) form of rat methionine adenosyltransferase, when methionine was the variable substrate (2 mM)				J Med Chem 29: 1030-8 (1986) BindingDB Entry DOI: 10.7270/Q2CF9QN4
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50367329 (CHEMBL1791416) Show SMILES NC(CCSC(CP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)C(O)=O |r| Show InChI InChI=1S/C15H25N6O14P3S/c16-6(15(24)25)1-2-39-7(3-36(26,27)34-38(31,32)35-37(28,29)30)11-9(22)10(23)14(33-11)21-5-20-8-12(17)18-4-19-13(8)21/h4-7,9-11,14,22-23H,1-3,16H2,(H,24,25)(H,26,27)(H,31,32)(H2,17,18,19)(H2,28,29,30)/t6?,7?,9-,10+,11+,14+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	3.20E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition constant was evaluated on novikoff hepatoma (MAT-T) form of rat methionine adenosyltransferase, when ATP was the variable substrate (60 uM...				J Med Chem 29: 1030-8 (1986) BindingDB Entry DOI: 10.7270/Q2CF9QN4
					More data for this Ligand-Target Pair
S-adenosylmethionine synthase isoform type-1/type-2 (Rattus norvegicus)	BDBM50367329 (CHEMBL1791416) Show SMILES NC(CCSC(CP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)C(O)=O |r| Show InChI InChI=1S/C15H25N6O14P3S/c16-6(15(24)25)1-2-39-7(3-36(26,27)34-38(31,32)35-37(28,29)30)11-9(22)10(23)14(33-11)21-5-20-8-12(17)18-4-19-13(8)21/h4-7,9-11,14,22-23H,1-3,16H2,(H,24,25)(H,26,27)(H,31,32)(H2,17,18,19)(H2,28,29,30)/t6?,7?,9-,10+,11+,14+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	3.20E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition constant of compound with Novikoff ascitic hepatoma (M-T) form of rat methionine adenosyltransferase when ATP was used as variable substra...				J Med Chem 30: 888-94 (1987) BindingDB Entry DOI: 10.7270/Q22J6F29
					More data for this Ligand-Target Pair

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