Compile Data Set for Download or QSAR

Found 36 hits with Last Name = 'iijima' and Initial = 'y'   

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
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50024714 (2-(4-Carboxymethyl-5-oxo-3-thiophen-2-yl-[1,4]thia...) Show SMILES OC(=O)CN1C(CSC[C@H](N[C@@H](CCc2ccccc2)C(O)=O)C1=O)c1cccs1 Show InChI InChI=1S/C21H24N2O5S2/c24-19(25)11-23-17(18-7-4-10-30-18)13-29-12-16(20(23)26)22-15(21(27)28)9-8-14-5-2-1-3-6-14/h1-7,10,15-17,22H,8-9,11-13H2,(H,24,25)(H,27,28)/t15-,16-,17?/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	2.80	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co., Ltd. Curated by ChEMBL					Assay Description Inhibitory activity against rabbit lung Angiotensin I converting enzyme with 5 mM hippurylhistidylleucine as substrate				J Med Chem 30: 1984-91 (1987) BindingDB Entry DOI: 10.7270/Q2Q52NMJ
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50023299 (2-(1-Carboxymethyl-2-oxo-6-phenyl-azepan-3-ylamino...) Show SMILES OC(=O)CN1C[C@H](CC[C@H](N[C@@H](CCc2ccccc2)C(O)=O)C1=O)c1ccccc1 Show InChI InChI=1S/C24H28N2O5/c27-22(28)16-26-15-19(18-9-5-2-6-10-18)12-14-20(23(26)29)25-21(24(30)31)13-11-17-7-3-1-4-8-17/h1-10,19-21,25H,11-16H2,(H,27,28)(H,30,31)/t19-,20-,21-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.10	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co., Ltd. Curated by ChEMBL					Assay Description Concentration required for 50% inhibition of rabbit lung Angiotensin I converting enzyme with 5 mM hippuryl-histidyl-leucine as substrate				J Med Chem 31: 422-8 (1988) BindingDB Entry DOI: 10.7270/Q2S75GWH
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50023298 (2-(4-Carboxymethyl-5-oxo-3-phenyl-[1,4]thiazepan-6...) Show SMILES OC(=O)CN1[C@@H](CSC[C@H](N[C@@H](CCc2ccccc2)C(O)=O)C1=O)c1ccccc1 Show InChI InChI=1S/C23H26N2O5S/c26-21(27)13-25-20(17-9-5-2-6-10-17)15-31-14-19(22(25)28)24-18(23(29)30)12-11-16-7-3-1-4-8-16/h1-10,18-20,24H,11-15H2,(H,26,27)(H,29,30)/t18-,19-,20-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.40	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co., Ltd. Curated by ChEMBL					Assay Description Inhibitory activity against rabbit lung Angiotensin I converting enzyme with 5 mM hippurylhistidylleucine as substrate				J Med Chem 30: 1984-91 (1987) BindingDB Entry DOI: 10.7270/Q2Q52NMJ
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50023298 (2-(4-Carboxymethyl-5-oxo-3-phenyl-[1,4]thiazepan-6...) Show SMILES OC(=O)CN1[C@@H](CSC[C@H](N[C@@H](CCc2ccccc2)C(O)=O)C1=O)c1ccccc1 Show InChI InChI=1S/C23H26N2O5S/c26-21(27)13-25-20(17-9-5-2-6-10-17)15-31-14-19(22(25)28)24-18(23(29)30)12-11-16-7-3-1-4-8-16/h1-10,18-20,24H,11-15H2,(H,26,27)(H,29,30)/t18-,19-,20-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.40	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co., Ltd. Curated by ChEMBL					Assay Description Concentration required for 50% inhibition of rabbit lung Angiotensin I converting enzyme with 5 mM hippuryl-histidyl-leucine as substrate				J Med Chem 31: 422-8 (1988) BindingDB Entry DOI: 10.7270/Q2S75GWH
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50024710 (2-(4-Carboxymethyl-5-oxo-2-thiophen-2-yl-[1,4]thia...) Show SMILES OC(=O)CN1C[C@H](SC[C@H](N[C@@H](CCc2ccccc2)C(O)=O)C1=O)c1cccs1 Show InChI InChI=1S/C21H24N2O5S2/c24-19(25)12-23-11-18(17-7-4-10-29-17)30-13-16(20(23)26)22-15(21(27)28)9-8-14-5-2-1-3-6-14/h1-7,10,15-16,18,22H,8-9,11-13H2,(H,24,25)(H,27,28)/t15-,16-,18-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.60	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co., Ltd. Curated by ChEMBL					Assay Description Inhibitory activity against rabbit lung Angiotensin I converting enzyme with 5 mM hippurylhistidylleucine as substrate				J Med Chem 30: 1984-91 (1987) BindingDB Entry DOI: 10.7270/Q2Q52NMJ
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50023296 (2-(1-Carboxymethyl-2-oxo-7-phenyl-azepan-3-ylamino...) Show SMILES OC(=O)CN1[C@@H](CCC[C@H](N[C@@H](CCc2ccccc2)C(O)=O)C1=O)c1ccccc1 Show InChI InChI=1S/C24H28N2O5/c27-22(28)16-26-21(18-10-5-2-6-11-18)13-7-12-19(23(26)29)25-20(24(30)31)15-14-17-8-3-1-4-9-17/h1-6,8-11,19-21,25H,7,12-16H2,(H,27,28)(H,30,31)/t19-,20-,21-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.60	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co., Ltd. Curated by ChEMBL					Assay Description Concentration required for 50% inhibition of rabbit lung Angiotensin I converting enzyme with 5 mM hippuryl-histidyl-leucine as substrate				J Med Chem 31: 422-8 (1988) BindingDB Entry DOI: 10.7270/Q2S75GWH
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50023295 (2-(4-Carboxymethyl-5-oxo-2-phenyl-[1,4]thiazepan-6...) Show SMILES OC(=O)CN1C[C@H](SC[C@H](N[C@@H](CCc2ccccc2)C(O)=O)C1=O)c1ccccc1 Show InChI InChI=1S/C23H26N2O5S/c26-21(27)14-25-13-20(17-9-5-2-6-10-17)31-15-19(22(25)28)24-18(23(29)30)12-11-16-7-3-1-4-8-16/h1-10,18-20,24H,11-15H2,(H,26,27)(H,29,30)/t18-,19-,20-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.70	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co., Ltd. Curated by ChEMBL					Assay Description Concentration required for 50% inhibition of rabbit lung Angiotensin I converting enzyme with 5 mM hippuryl-histidyl-leucine as substrate				J Med Chem 31: 422-8 (1988) BindingDB Entry DOI: 10.7270/Q2S75GWH
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50023295 (2-(4-Carboxymethyl-5-oxo-2-phenyl-[1,4]thiazepan-6...) Show SMILES OC(=O)CN1C[C@H](SC[C@H](N[C@@H](CCc2ccccc2)C(O)=O)C1=O)c1ccccc1 Show InChI InChI=1S/C23H26N2O5S/c26-21(27)14-25-13-20(17-9-5-2-6-10-17)31-15-19(22(25)28)24-18(23(29)30)12-11-16-7-3-1-4-8-16/h1-10,18-20,24H,11-15H2,(H,26,27)(H,29,30)/t18-,19-,20-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.70	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co., Ltd. Curated by ChEMBL					Assay Description Inhibitory activity against rabbit lung Angiotensin I converting enzyme with 5 mM hippurylhistidylleucine as substrate				J Med Chem 30: 1984-91 (1987) BindingDB Entry DOI: 10.7270/Q2Q52NMJ
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50024713 (2-(4-Carboxymethyl-5-oxo-2-thiophen-3-yl-[1,4]thia...) Show SMILES OC(=O)CN1C[C@H](SC[C@H](N[C@@H](CCc2ccccc2)C(O)=O)C1=O)c1ccsc1 Show InChI InChI=1S/C21H24N2O5S2/c24-19(25)11-23-10-18(15-8-9-29-12-15)30-13-17(20(23)26)22-16(21(27)28)7-6-14-4-2-1-3-5-14/h1-5,8-9,12,16-18,22H,6-7,10-11,13H2,(H,24,25)(H,27,28)/t16-,17-,18-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	4.10	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co., Ltd. Curated by ChEMBL					Assay Description Inhibitory activity against rabbit lung Angiotensin I converting enzyme with 5 mM hippurylhistidylleucine as substrate				J Med Chem 30: 1984-91 (1987) BindingDB Entry DOI: 10.7270/Q2Q52NMJ
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50023300 (2-(1-Carboxymethyl-2-oxo-6-phenyl-azepan-3-ylamino...) Show SMILES OC(=O)CN1C[C@@H](CC[C@H](N[C@@H](CCc2ccccc2)C(O)=O)C1=O)c1ccccc1 Show InChI InChI=1S/C24H28N2O5/c27-22(28)16-26-15-19(18-9-5-2-6-10-18)12-14-20(23(26)29)25-21(24(30)31)13-11-17-7-3-1-4-8-17/h1-10,19-21,25H,11-16H2,(H,27,28)(H,30,31)/t19-,20+,21+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	4.30	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co., Ltd. Curated by ChEMBL					Assay Description Concentration required for 50% inhibition of rabbit lung Angiotensin I converting enzyme with 5 mM hippuryl-histidyl-leucine as substrate				J Med Chem 31: 422-8 (1988) BindingDB Entry DOI: 10.7270/Q2S75GWH
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50367254 (ENALAPRILAT) Show SMILES C[C@H](N[C@@H](CCc1ccccc1)C(O)=O)C(=O)N1CCC[C@H]1C(O)=O |r| Show InChI InChI=1S/C18H24N2O5/c1-12(16(21)20-11-5-8-15(20)18(24)25)19-14(17(22)23)10-9-13-6-3-2-4-7-13/h2-4,6-7,12,14-15,19H,5,8-11H2,1H3,(H,22,23)(H,24,25)/t12-,14-,15-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase MCE KEGG MMDB PC cid PC sid PDB UniChem Similars	PubMed	n/a	n/a	5.70	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co., Ltd. Curated by ChEMBL					Assay Description Concentration required for 50% inhibition of rabbit lung Angiotensin I converting enzyme with 5 mM hippuryl-histidyl-leucine as substrate				J Med Chem 31: 422-8 (1988) BindingDB Entry DOI: 10.7270/Q2S75GWH
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50011192 ((R)-1-[(S)-2-((S)-1-Carboxy-3-phenyl-propylamino)-...) Show SMILES CC(NC(CCc1ccccc1)C(O)=O)C(=O)N1CCC[C@H]1C(O)=O Show InChI InChI=1S/C18H24N2O5/c1-12(16(21)20-11-5-8-15(20)18(24)25)19-14(17(22)23)10-9-13-6-3-2-4-7-13/h2-4,6-7,12,14-15,19H,5,8-11H2,1H3,(H,22,23)(H,24,25)/t12?,14?,15-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL MMDB PC cid PC sid UniChem Similars	PubMed	n/a	n/a	5.70	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co., Ltd. Curated by ChEMBL					Assay Description Inhibitory activity against rabbit lung Angiotensin I converting enzyme with 5 mM hippurylhistidylleucine as substrate				J Med Chem 30: 1984-91 (1987) BindingDB Entry DOI: 10.7270/Q2Q52NMJ
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50023302 (2-(1-Carboxymethyl-2-oxo-7-phenyl-azepan-3-ylamino...) Show SMILES OC(=O)CN1[C@H](CCC[C@H](N[C@@H](CCc2ccccc2)C(O)=O)C1=O)c1ccccc1 Show InChI InChI=1S/C24H28N2O5/c27-22(28)16-26-21(18-10-5-2-6-11-18)13-7-12-19(23(26)29)25-20(24(30)31)15-14-17-8-3-1-4-9-17/h1-6,8-11,19-21,25H,7,12-16H2,(H,27,28)(H,30,31)/t19-,20-,21+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	16	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co., Ltd. Curated by ChEMBL					Assay Description Concentration required for 50% inhibition of rabbit lung Angiotensin I converting enzyme with 5 mM hippuryl-histidyl-leucine as substrate				J Med Chem 31: 422-8 (1988) BindingDB Entry DOI: 10.7270/Q2S75GWH
					More data for this Ligand-Target Pair
Platelet-activating factor receptor (Cavia porcellus)	BDBM50366241 (CHEMBL297624 | L-652731) Show SMILES COc1cc(cc(OC)c1OC)[C@H]1CC[C@@H](O1)c1cc(OC)c(OC)c(OC)c1 Show InChI InChI=1S/C22H28O7/c1-23-17-9-13(10-18(24-2)21(17)27-5)15-7-8-16(29-15)14-11-19(25-3)22(28-6)20(12-14)26-4/h9-12,15-16H,7-8H2,1-6H3/t15-,16-/m1/s1	MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	24	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co. Ltd Curated by ChEMBL					Assay Description Inhibiting Platelet activating factor receptor by radioreceptor binding assay using rabbit platelets and [3H]-PAF				J Med Chem 39: 5281-4 (1997) Article DOI: 10.1021/jm950640q BindingDB Entry DOI: 10.7270/Q2FF3T06
					More data for this Ligand-Target Pair
Platelet-activating factor receptor (Cavia porcellus)	BDBM50055488 (CHEMBL148491 | Carbonic acid methyl ester (E)-(1R,...) Show SMILES COC(=O)OC[C@H]1[C@H]2CC[C@@H](C)[C@]1(C)CC\C(C)=C\CC[C@@]1(C)O[C@@H]1C2=O |t:18| Show InChI InChI=1S/C22H34O5/c1-14-7-6-11-22(4)19(27-22)18(23)16-9-8-15(2)21(3,12-10-14)17(16)13-26-20(24)25-5/h7,15-17,19H,6,8-13H2,1-5H3/b14-7+/t15-,16-,17+,19-,21+,22-/m1/s1	MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	26	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co. Ltd Curated by ChEMBL					Assay Description Inhibiting Platelet activating factor receptor by radioreceptor binding assay using rabbit platelets and [3H]-PAF				J Med Chem 39: 5281-4 (1997) Article DOI: 10.1021/jm950640q BindingDB Entry DOI: 10.7270/Q2FF3T06
					More data for this Ligand-Target Pair
Platelet-activating factor receptor (Cavia porcellus)	BDBM50055491 ((E)-(1R,2R,3R,5R,12S,13R,16S)-16-(Isoxazol-3-yloxy...) Show SMILES C[C@@H]1CC[C@@H]2[C@H](COc3ccon3)[C@@]1(C)CC\C(C)=C\CC[C@@]1(C)O[C@@H]1[C@@H]2O |t:20| Show InChI InChI=1S/C23H35NO4/c1-15-6-5-11-23(4)21(28-23)20(25)17-8-7-16(2)22(3,12-9-15)18(17)14-26-19-10-13-27-24-19/h6,10,13,16-18,20-21,25H,5,7-9,11-12,14H2,1-4H3/b15-6+/t16-,17-,18+,20-,21-,22+,23-/m1/s1	MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	31	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co. Ltd Curated by ChEMBL					Assay Description Inhibiting Platelet activating factor receptor by radioreceptor binding assay using rabbit platelets and [3H]-PAF				J Med Chem 39: 5281-4 (1997) Article DOI: 10.1021/jm950640q BindingDB Entry DOI: 10.7270/Q2FF3T06
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50023303 (2-(4-Carboxymethyl-5-oxo-2-phenyl-[1,4]thiazepan-6...) Show SMILES OC(=O)CN1C[C@@H](SC[C@H](N[C@@H](CCc2ccccc2)C(O)=O)C1=O)c1ccccc1 Show InChI InChI=1S/C23H26N2O5S/c26-21(27)14-25-13-20(17-9-5-2-6-10-17)31-15-19(22(25)28)24-18(23(29)30)12-11-16-7-3-1-4-8-16/h1-10,18-20,24H,11-15H2,(H,26,27)(H,29,30)/t18-,19-,20+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	36	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co., Ltd. Curated by ChEMBL					Assay Description Inhibitory activity against rabbit lung Angiotensin I converting enzyme with 5 mM hippurylhistidylleucine as substrate				J Med Chem 30: 1984-91 (1987) BindingDB Entry DOI: 10.7270/Q2Q52NMJ
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50023303 (2-(4-Carboxymethyl-5-oxo-2-phenyl-[1,4]thiazepan-6...) Show SMILES OC(=O)CN1C[C@@H](SC[C@H](N[C@@H](CCc2ccccc2)C(O)=O)C1=O)c1ccccc1 Show InChI InChI=1S/C23H26N2O5S/c26-21(27)14-25-13-20(17-9-5-2-6-10-17)31-15-19(22(25)28)24-18(23(29)30)12-11-16-7-3-1-4-8-16/h1-10,18-20,24H,11-15H2,(H,26,27)(H,29,30)/t18-,19-,20+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	36	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co., Ltd. Curated by ChEMBL					Assay Description Concentration required for 50% inhibition of rabbit lung Angiotensin I converting enzyme with 5 mM hippuryl-histidyl-leucine as substrate				J Med Chem 31: 422-8 (1988) BindingDB Entry DOI: 10.7270/Q2S75GWH
					More data for this Ligand-Target Pair
Platelet-activating factor receptor (Cavia porcellus)	BDBM50055482 ((E)-(1R,3S,5R,12S,13R,16S)-16-(Isoxazol-3-yloxymet...) Show SMILES C[C@@H]1CC[C@@H]2[C@H](COc3ccon3)[C@@]1(C)CC\C(C)=C\CC[C@@]1(C)O[C@@H]1C2=O |t:20| Show InChI InChI=1S/C23H33NO4/c1-15-6-5-11-23(4)21(28-23)20(25)17-8-7-16(2)22(3,12-9-15)18(17)14-26-19-10-13-27-24-19/h6,10,13,16-18,21H,5,7-9,11-12,14H2,1-4H3/b15-6+/t16-,17-,18+,21-,22+,23-/m1/s1	MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	50	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co. Ltd Curated by ChEMBL					Assay Description Inhibiting Platelet activating factor receptor by radioreceptor binding assay using rabbit platelets and [3H]-PAF				J Med Chem 39: 5281-4 (1997) Article DOI: 10.1021/jm950640q BindingDB Entry DOI: 10.7270/Q2FF3T06
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50024712 (2-(4-Carboxymethyl-5-oxo-2-thiophen-2-yl-[1,4]thia...) Show SMILES OC(=O)CN1C[C@@H](SC[C@H](N[C@@H](CCc2ccccc2)C(O)=O)C1=O)c1cccs1 Show InChI InChI=1S/C21H24N2O5S2/c24-19(25)12-23-11-18(17-7-4-10-29-17)30-13-16(20(23)26)22-15(21(27)28)9-8-14-5-2-1-3-6-14/h1-7,10,15-16,18,22H,8-9,11-13H2,(H,24,25)(H,27,28)/t15-,16-,18+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	65	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co., Ltd. Curated by ChEMBL					Assay Description Inhibitory activity against rabbit lung Angiotensin I converting enzyme with 5 mM hippurylhistidylleucine as substrate				J Med Chem 30: 1984-91 (1987) BindingDB Entry DOI: 10.7270/Q2Q52NMJ
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50023301 (2-(4-Carboxymethyl-5-oxo-3-phenyl-[1,4]thiazepan-6...) Show SMILES OC(=O)CN1[C@H](CSC[C@H](N[C@@H](CCc2ccccc2)C(O)=O)C1=O)c1ccccc1 Show InChI InChI=1S/C23H26N2O5S/c26-21(27)13-25-20(17-9-5-2-6-10-17)15-31-14-19(22(25)28)24-18(23(29)30)12-11-16-7-3-1-4-8-16/h1-10,18-20,24H,11-15H2,(H,26,27)(H,29,30)/t18-,19-,20+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	78	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co., Ltd. Curated by ChEMBL					Assay Description Concentration required for 50% inhibition of rabbit lung Angiotensin I converting enzyme with 5 mM hippuryl-histidyl-leucine as substrate				J Med Chem 31: 422-8 (1988) BindingDB Entry DOI: 10.7270/Q2S75GWH
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50023301 (2-(4-Carboxymethyl-5-oxo-3-phenyl-[1,4]thiazepan-6...) Show SMILES OC(=O)CN1[C@H](CSC[C@H](N[C@@H](CCc2ccccc2)C(O)=O)C1=O)c1ccccc1 Show InChI InChI=1S/C23H26N2O5S/c26-21(27)13-25-20(17-9-5-2-6-10-17)15-31-14-19(22(25)28)24-18(23(29)30)12-11-16-7-3-1-4-8-16/h1-10,18-20,24H,11-15H2,(H,26,27)(H,29,30)/t18-,19-,20+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	78	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co., Ltd. Curated by ChEMBL					Assay Description Inhibitory activity against rabbit lung Angiotensin I converting enzyme with 5 mM hippurylhistidylleucine as substrate				J Med Chem 30: 1984-91 (1987) BindingDB Entry DOI: 10.7270/Q2Q52NMJ
					More data for this Ligand-Target Pair
Platelet-activating factor receptor (Cavia porcellus)	BDBM50055479 (Acetic acid (E)-(1R,2R,3R,5R,12S,13R,16S)-2-hydrox...) Show SMILES C[C@@H]1CC[C@@H]2[C@H](COC(C)=O)[C@@]1(C)CC\C(C)=C\CC[C@@]1(C)O[C@@H]1[C@@H]2O |t:17| Show InChI InChI=1S/C22H36O4/c1-14-7-6-11-22(5)20(26-22)19(24)17-9-8-15(2)21(4,12-10-14)18(17)13-25-16(3)23/h7,15,17-20,24H,6,8-13H2,1-5H3/b14-7+/t15-,17-,18+,19-,20-,21+,22-/m1/s1	MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	80	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co. Ltd Curated by ChEMBL					Assay Description Inhibiting Platelet activating factor receptor by radioreceptor binding assay using rabbit platelets and [3H]-PAF				J Med Chem 39: 5281-4 (1997) Article DOI: 10.1021/jm950640q BindingDB Entry DOI: 10.7270/Q2FF3T06
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50024711 (2-(4-Carboxymethyl-5-oxo-2-thiophen-3-yl-[1,4]thia...) Show SMILES OC(=O)CN1C[C@@H](SC[C@H](N[C@@H](CCc2ccccc2)C(O)=O)C1=O)c1ccsc1 Show InChI InChI=1S/C21H24N2O5S2/c24-19(25)11-23-10-18(15-8-9-29-12-15)30-13-17(20(23)26)22-16(21(27)28)7-6-14-4-2-1-3-5-14/h1-5,8-9,12,16-18,22H,6-7,10-11,13H2,(H,24,25)(H,27,28)/t16-,17-,18+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	87	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co., Ltd. Curated by ChEMBL					Assay Description Inhibitory activity against rabbit lung Angiotensin I converting enzyme with 5 mM hippurylhistidylleucine as substrate				J Med Chem 30: 1984-91 (1987) BindingDB Entry DOI: 10.7270/Q2Q52NMJ
					More data for this Ligand-Target Pair
Platelet-activating factor receptor (Cavia porcellus)	BDBM50055489 ((E)-(1R,3S,5R,12S,13R,16S)-5,9,12,13-Tetramethyl-2...) Show SMILES C[C@@H]1CC[C@@H]2[C@H](C=O)[C@@]1(C)CC\C(C)=C\CC[C@@]1(C)O[C@@H]1C2=O |t:14| Show InChI InChI=1S/C20H30O3/c1-13-6-5-10-20(4)18(23-20)17(22)15-8-7-14(2)19(3,11-9-13)16(15)12-21/h6,12,14-16,18H,5,7-11H2,1-4H3/b13-6+/t14-,15-,16+,18-,19+,20-/m1/s1	MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	120	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co. Ltd Curated by ChEMBL					Assay Description Inhibiting Platelet activating factor receptor by radioreceptor binding assay using rabbit platelets and [3H]-PAF				J Med Chem 39: 5281-4 (1997) Article DOI: 10.1021/jm950640q BindingDB Entry DOI: 10.7270/Q2FF3T06
					More data for this Ligand-Target Pair
Platelet-activating factor receptor (Cavia porcellus)	BDBM50055493 (CHEMBL148549 | Carbonic acid (E)-(1R,2R,3R,5R,12S,...) Show SMILES COC(=O)OC[C@H]1[C@H]2CC[C@@H](C)[C@]1(C)CC\C(C)=C\CC[C@@]1(C)O[C@@H]1[C@@H]2O |t:18| Show InChI InChI=1S/C22H36O5/c1-14-7-6-11-22(4)19(27-22)18(23)16-9-8-15(2)21(3,12-10-14)17(16)13-26-20(24)25-5/h7,15-19,23H,6,8-13H2,1-5H3/b14-7+/t15-,16-,17+,18-,19-,21+,22-/m1/s1	MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	130	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co. Ltd Curated by ChEMBL					Assay Description Inhibiting Platelet activating factor receptor by radioreceptor binding assay using rabbit platelets and [3H]-PAF				J Med Chem 39: 5281-4 (1997) Article DOI: 10.1021/jm950640q BindingDB Entry DOI: 10.7270/Q2FF3T06
					More data for this Ligand-Target Pair
Platelet-activating factor receptor (Cavia porcellus)	BDBM50055495 (CHEMBL151075 | Dimethyl-carbamic acid (E)-(1R,2R,3...) Show SMILES C[C@@H]1CC[C@@H]2[C@H](COC(=O)N(C)C)[C@@]1(C)CC\C(C)=C\CC[C@@]1(C)O[C@@H]1[C@@H]2O |t:19| Show InChI InChI=1S/C23H39NO4/c1-15-8-7-12-23(4)20(28-23)19(25)17-10-9-16(2)22(3,13-11-15)18(17)14-27-21(26)24(5)6/h8,16-20,25H,7,9-14H2,1-6H3/b15-8+/t16-,17-,18+,19-,20-,22+,23-/m1/s1	MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	180	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co. Ltd Curated by ChEMBL					Assay Description Inhibiting Platelet activating factor receptor by radioreceptor binding assay using rabbit platelets and [3H]-PAF				J Med Chem 39: 5281-4 (1997) Article DOI: 10.1021/jm950640q BindingDB Entry DOI: 10.7270/Q2FF3T06
					More data for this Ligand-Target Pair
Platelet-activating factor receptor (Cavia porcellus)	BDBM50055483 (CHEMBL151310 | Dimethyl-carbamic acid (E)-(1R,3S,5...) Show SMILES C[C@@H]1CC[C@@H]2[C@H](COC(=O)N(C)C)[C@@]1(C)CC\C(C)=C\CC[C@@]1(C)O[C@@H]1C2=O |t:19| Show InChI InChI=1S/C23H37NO4/c1-15-8-7-12-23(4)20(28-23)19(25)17-10-9-16(2)22(3,13-11-15)18(17)14-27-21(26)24(5)6/h8,16-18,20H,7,9-14H2,1-6H3/b15-8+/t16-,17-,18+,20-,22+,23-/m1/s1	MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	180	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co. Ltd Curated by ChEMBL					Assay Description Inhibiting Platelet activating factor receptor by radioreceptor binding assay using rabbit platelets and [3H]-PAF				J Med Chem 39: 5281-4 (1997) Article DOI: 10.1021/jm950640q BindingDB Entry DOI: 10.7270/Q2FF3T06
					More data for this Ligand-Target Pair
Platelet-activating factor receptor (Cavia porcellus)	BDBM50055492 (CHEMBL147337 | Propionic acid (E)-(1R,2R,3R,5R,12S...) Show SMILES CCC(=O)OC[C@H]1[C@H]2CC[C@@H](C)[C@]1(C)CC\C(C)=C\CC[C@@]1(C)O[C@@H]1[C@@H]2O |t:18| Show InChI InChI=1S/C23H38O4/c1-6-19(24)26-14-18-17-10-9-16(3)22(18,4)13-11-15(2)8-7-12-23(5)21(27-23)20(17)25/h8,16-18,20-21,25H,6-7,9-14H2,1-5H3/b15-8+/t16-,17-,18+,20-,21-,22+,23-/m1/s1	MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	340	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co. Ltd Curated by ChEMBL					Assay Description Inhibiting Platelet activating factor receptor by radioreceptor binding assay using rabbit platelets and [3H]-PAF				J Med Chem 39: 5281-4 (1997) Article DOI: 10.1021/jm950640q BindingDB Entry DOI: 10.7270/Q2FF3T06
					More data for this Ligand-Target Pair
Platelet-activating factor receptor (Cavia porcellus)	BDBM50055487 (Acetic acid (E)-(1R,3S,5R,12S,13R,16S)-5,9,12,13-t...) Show SMILES C[C@@H]1CC[C@@H]2[C@H](COC(C)=O)[C@@]1(C)CC\C(C)=C\CC[C@@]1(C)O[C@@H]1C2=O |t:17| Show InChI InChI=1S/C22H34O4/c1-14-7-6-11-22(5)20(26-22)19(24)17-9-8-15(2)21(4,12-10-14)18(17)13-25-16(3)23/h7,15,17-18,20H,6,8-13H2,1-5H3/b14-7+/t15-,17-,18+,20-,21+,22-/m1/s1	MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	410	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co. Ltd Curated by ChEMBL					Assay Description Inhibiting Platelet activating factor receptor by radioreceptor binding assay using rabbit platelets and [3H]-PAF				J Med Chem 39: 5281-4 (1997) Article DOI: 10.1021/jm950640q BindingDB Entry DOI: 10.7270/Q2FF3T06
					More data for this Ligand-Target Pair
Platelet-activating factor receptor (Cavia porcellus)	BDBM50055484 (CHEMBL421954 | Carbonic acid phenyl ester (E)-(1R,...) Show SMILES C[C@@H]1CC[C@@H]2[C@H](COC(=O)Oc3ccccc3)[C@@]1(C)CC\C(C)=C\CC[C@@]1(C)O[C@@H]1C2=O |t:24| Show InChI InChI=1S/C27H36O5/c1-18-9-8-15-27(4)24(32-27)23(28)21-13-12-19(2)26(3,16-14-18)22(21)17-30-25(29)31-20-10-6-5-7-11-20/h5-7,9-11,19,21-22,24H,8,12-17H2,1-4H3/b18-9+/t19-,21-,22+,24-,26+,27-/m1/s1	MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	550	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co. Ltd Curated by ChEMBL					Assay Description Inhibiting Platelet activating factor receptor by radioreceptor binding assay using rabbit platelets and [3H]-PAF				J Med Chem 39: 5281-4 (1997) Article DOI: 10.1021/jm950640q BindingDB Entry DOI: 10.7270/Q2FF3T06
					More data for this Ligand-Target Pair
Platelet-activating factor receptor (Cavia porcellus)	BDBM50055494 (CHEMBL147079 | Propionic acid (E)-(1R,3S,5R,12S,13...) Show SMILES CCC(=O)OC[C@H]1[C@H]2CC[C@@H](C)[C@]1(C)CC\C(C)=C\CC[C@@]1(C)O[C@@H]1C2=O |t:18| Show InChI InChI=1S/C23H36O4/c1-6-19(24)26-14-18-17-10-9-16(3)22(18,4)13-11-15(2)8-7-12-23(5)21(27-23)20(17)25/h8,16-18,21H,6-7,9-14H2,1-5H3/b15-8+/t16-,17-,18+,21-,22+,23-/m1/s1	MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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
Sankyo Co. Ltd Curated by ChEMBL					Assay Description Inhibiting Platelet activating factor receptor by radioreceptor binding assay using rabbit platelets and [3H]-PAF				J Med Chem 39: 5281-4 (1997) Article DOI: 10.1021/jm950640q BindingDB Entry DOI: 10.7270/Q2FF3T06
					More data for this Ligand-Target Pair
Platelet-activating factor receptor (Cavia porcellus)	BDBM50055480 ((E)-(1R,3S,5R,12S,13R,16S)-16-Hydroxymethyl-5,9,12...) Show SMILES C[C@@H]1CC[C@@H]2[C@H](CO)[C@@]1(C)CC\C(C)=C\CC[C@@]1(C)O[C@@H]1C2=O |t:14| Show InChI InChI=1S/C20H32O3/c1-13-6-5-10-20(4)18(23-20)17(22)15-8-7-14(2)19(3,11-9-13)16(15)12-21/h6,14-16,18,21H,5,7-12H2,1-4H3/b13-6+/t14-,15-,16+,18-,19+,20-/m1/s1	MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co. Ltd Curated by ChEMBL					Assay Description Inhibiting Platelet activating factor receptor by radioreceptor binding assay using rabbit platelets and [3H]-PAF				J Med Chem 39: 5281-4 (1997) Article DOI: 10.1021/jm950640q BindingDB Entry DOI: 10.7270/Q2FF3T06
					More data for this Ligand-Target Pair
Platelet-activating factor receptor (Cavia porcellus)	BDBM50055485 (16-(Isoxazol-3-yloxymethyl)-5,9,12,13-tetramethyl-...) Show SMILES C[C@@H]1CC[C@@H]2[C@H](C=O)[C@@]1(C)CC[C@]1(C)O[C@H]1CC[C@@]1(C)O[C@@H]1C2=O Show InChI InChI=1S/C20H30O4/c1-12-5-6-13-14(11-21)18(12,2)9-10-19(3)15(23-19)7-8-20(4)17(24-20)16(13)22/h11-15,17H,5-10H2,1-4H3/t12-,13-,14+,15+,17-,18+,19+,20-/m1/s1	MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.70E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co. Ltd Curated by ChEMBL					Assay Description Inhibiting Platelet activating factor receptor by radioreceptor binding assay using rabbit platelets and [3H]-PAF				J Med Chem 39: 5281-4 (1997) Article DOI: 10.1021/jm950640q BindingDB Entry DOI: 10.7270/Q2FF3T06
					More data for this Ligand-Target Pair
Platelet-activating factor receptor (Cavia porcellus)	BDBM50055481 (16-(Isoxazol-3-yloxymethyl)-5,9,12,13-tetramethyl-...) Show SMILES C[C@@H]1CC[C@@H]2[C@H](CO)[C@@]1(C)CC[C@]1(C)O[C@H]1CC[C@@]1(C)O[C@@H]1C2=O Show InChI InChI=1S/C20H32O4/c1-12-5-6-13-14(11-21)18(12,2)9-10-19(3)15(23-19)7-8-20(4)17(24-20)16(13)22/h12-15,17,21H,5-11H2,1-4H3/t12-,13-,14+,15+,17-,18+,19+,20-/m1/s1	MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co. Ltd Curated by ChEMBL					Assay Description Inhibiting Platelet activating factor receptor by radioreceptor binding assay using rabbit platelets and [3H]-PAF				J Med Chem 39: 5281-4 (1997) Article DOI: 10.1021/jm950640q BindingDB Entry DOI: 10.7270/Q2FF3T06
					More data for this Ligand-Target Pair
Platelet-activating factor receptor (Cavia porcellus)	BDBM50055486 ((1R,3S,5R,8S,9S,12S,13R,16S)-8,9-Dihydroxy-16-hydr...) Show SMILES C[C@@H]1CC[C@@H]2[C@H](CO)[C@@]1(C)CC[C@](C)(O)[C@@H](O)CC[C@@]1(C)O[C@@H]1C2=O Show InChI InChI=1S/C20H34O5/c1-12-5-6-13-14(11-21)18(12,2)9-10-19(3,24)15(22)7-8-20(4)17(25-20)16(13)23/h12-15,17,21-22,24H,5-11H2,1-4H3/t12-,13-,14+,15+,17-,18+,19+,20-/m1/s1	MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.80E+5	n/a	n/a	n/a	n/a	n/a	n/a
Sankyo Co. Ltd Curated by ChEMBL					Assay Description Inhibiting Platelet activating factor receptor by radioreceptor binding assay using rabbit platelets and [3H]-PAF				J Med Chem 39: 5281-4 (1997) Article DOI: 10.1021/jm950640q BindingDB Entry DOI: 10.7270/Q2FF3T06
					More data for this Ligand-Target Pair