Compile Data Set for Download or QSAR

Found 36 hits with Last Name = 'bramanti' and Initial = 'g'   

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 (Rattus norvegicus)	BDBM21642 ((2S)-1-[(2S)-2-methyl-3-sulfanylpropanoyl]pyrrolid...) Show SMILES C[C@H](CS)C(=O)N1CCC[C@H]1C(O)=O Show InChI InChI=1S/C9H15NO3S/c1-6(5-14)8(11)10-4-2-3-7(10)9(12)13/h6-7,14H,2-5H2,1H3,(H,12,13)/t6-,7+/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046641 (1R,2R-trans-2-(Ethyl-hydroxycarbamoylmethyl-carbam...) Show SMILES CCN(CC(=O)NO)C(=O)C1CCCCC1C(O)=O Show InChI InChI=1S/C12H20N2O5/c1-2-14(7-10(15)13-19)11(16)8-5-3-4-6-9(8)12(17)18/h8-9,19H,2-7H2,1H3,(H,13,15)(H,17,18)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	14	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046633 (1R,2R-trans-2-(Hydroxycarbamoylmethyl-methyl-carba...) Show SMILES CN(CC(=O)NO)C(=O)C1CCCCC1C(O)=O Show InChI InChI=1S/C11H18N2O5/c1-13(6-9(14)12-18)10(15)7-4-2-3-5-8(7)11(16)17/h7-8,18H,2-6H2,1H3,(H,12,14)(H,16,17)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	45	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046633 (1R,2R-trans-2-(Hydroxycarbamoylmethyl-methyl-carba...) Show SMILES CN(CC(=O)NO)C(=O)C1CCCCC1C(O)=O Show InChI InChI=1S/C11H18N2O5/c1-13(6-9(14)12-18)10(15)7-4-2-3-5-8(7)11(16)17/h7-8,18H,2-6H2,1H3,(H,12,14)(H,16,17)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	45	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046632 (CHEMBL159829 | Cis-2-(Hydroxycarbamoylmethyl-propy...) Show SMILES CCCN(CC(=O)NO)C(=O)C1CCCCC1C(O)=O Show InChI InChI=1S/C13H22N2O5/c1-2-7-15(8-11(16)14-20)12(17)9-5-3-4-6-10(9)13(18)19/h9-10,20H,2-8H2,1H3,(H,14,16)(H,18,19)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	400	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046632 (CHEMBL159829 | Cis-2-(Hydroxycarbamoylmethyl-propy...) Show SMILES CCCN(CC(=O)NO)C(=O)C1CCCCC1C(O)=O Show InChI InChI=1S/C13H22N2O5/c1-2-7-15(8-11(16)14-20)12(17)9-5-3-4-6-10(9)13(18)19/h9-10,20H,2-8H2,1H3,(H,14,16)(H,18,19)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	400	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046621 (CHEMBL352453 | Trans-2-(Hydroxycarbamoylmethyl-iso...) Show SMILES CC(C)N(CC(=O)NO)C(=O)C1CCCCC1C(O)=O Show InChI InChI=1S/C13H22N2O5/c1-8(2)15(7-11(16)14-20)12(17)9-5-3-4-6-10(9)13(18)19/h8-10,20H,3-7H2,1-2H3,(H,14,16)(H,18,19)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	500	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046629 (1-(3-Hydroxycarbamoyl-2-methyl-propionyl)-pyrrolid...) Show SMILES CC(CC(=O)NO)C(=O)N1CCC[C@H]1C(O)=O Show InChI InChI=1S/C10H16N2O5/c1-6(5-8(13)11-17)9(14)12-4-2-3-7(12)10(15)16/h6-7,17H,2-5H2,1H3,(H,11,13)(H,15,16)/t6?,7-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	600	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046628 (CHEMBL434293 | Trans-2-(Hydroxycarbamoylmethyl-met...) Show SMILES CN(CC(=O)NO)C(=O)C1CCCC1C(O)=O Show InChI InChI=1S/C10H16N2O5/c1-12(5-8(13)11-17)9(14)6-3-2-4-7(6)10(15)16/h6-7,17H,2-5H2,1H3,(H,11,13)(H,15,16)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046631 (CHEMBL159791 | Cis-2-(3-Mercapto-propionyl)-cycloh...) Show SMILES OC(=O)C1CCCCC1C(=O)CCS Show InChI InChI=1S/C10H16O3S/c11-9(5-6-14)7-3-1-2-4-8(7)10(12)13/h7-8,14H,1-6H2,(H,12,13)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046631 (CHEMBL159791 | Cis-2-(3-Mercapto-propionyl)-cycloh...) Show SMILES OC(=O)C1CCCCC1C(=O)CCS Show InChI InChI=1S/C10H16O3S/c11-9(5-6-14)7-3-1-2-4-8(7)10(12)13/h7-8,14H,1-6H2,(H,12,13)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046641 (1R,2R-trans-2-(Ethyl-hydroxycarbamoylmethyl-carbam...) Show SMILES CCN(CC(=O)NO)C(=O)C1CCCCC1C(O)=O Show InChI InChI=1S/C12H20N2O5/c1-2-14(7-10(15)13-19)11(16)8-5-3-4-6-9(8)12(17)18/h8-9,19H,2-7H2,1H3,(H,13,15)(H,17,18)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	2.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046634 (CHEMBL161968 | Cis-2-(Hydroxycarbamoylmethyl-carba...) Show SMILES ONC(=O)CNC(=O)C1CCCCC1C(O)=O Show InChI InChI=1S/C10H16N2O5/c13-8(12-17)5-11-9(14)6-3-1-2-4-7(6)10(15)16/h6-7,17H,1-5H2,(H,11,14)(H,12,13)(H,15,16)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046634 (CHEMBL161968 | Cis-2-(Hydroxycarbamoylmethyl-carba...) Show SMILES ONC(=O)CNC(=O)C1CCCCC1C(O)=O Show InChI InChI=1S/C10H16N2O5/c13-8(12-17)5-11-9(14)6-3-1-2-4-7(6)10(15)16/h6-7,17H,1-5H2,(H,11,14)(H,12,13)(H,15,16)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046638 (CHEMBL163601 | Cis-2-(2-Mercapto-ethylcarbamoyl)-c...) Show SMILES OC(=O)C1CCCC1C(=O)NCCS Show InChI InChI=1S/C9H15NO3S/c11-8(10-4-5-14)6-2-1-3-7(6)9(12)13/h6-7,14H,1-5H2,(H,10,11)(H,12,13)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046630 (1-(3-Carboxy-butyryl)-pyrrolidine-2-carboxylic aci...) Show SMILES C[C@H](CC(=O)N1CCCC1C(O)=O)C(O)=O Show InChI InChI=1S/C10H15NO5/c1-6(9(13)14)5-8(12)11-4-2-3-7(11)10(15)16/h6-7H,2-5H2,1H3,(H,13,14)(H,15,16)/t6-,7?/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	5.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046626 (CHEMBL163568 | Cis-2-(Carboxymethyl-ethyl-carbamoy...) Show SMILES CCN(CC(O)=O)C(=O)C1CCCCC1C(O)=O Show InChI InChI=1S/C12H19NO5/c1-2-13(7-10(14)15)11(16)8-5-3-4-6-9(8)12(17)18/h8-9H,2-7H2,1H3,(H,14,15)(H,17,18)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	7.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046626 (CHEMBL163568 | Cis-2-(Carboxymethyl-ethyl-carbamoy...) Show SMILES CCN(CC(O)=O)C(=O)C1CCCCC1C(O)=O Show InChI InChI=1S/C12H19NO5/c1-2-13(7-10(14)15)11(16)8-5-3-4-6-9(8)12(17)18/h8-9H,2-7H2,1H3,(H,14,15)(H,17,18)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	7.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046642 (CHEMBL159987 | Cis-2-(Carboxymethyl-propyl-carbamo...) Show SMILES CCCN(CC(O)=O)C(=O)C1CCCCC1C(O)=O Show InChI InChI=1S/C13H21NO5/c1-2-7-14(8-11(15)16)12(17)9-5-3-4-6-10(9)13(18)19/h9-10H,2-8H2,1H3,(H,15,16)(H,18,19)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046639 (CHEMBL159330 | Cis-2-(Carboxymethyl-methyl-carbamo...) Show SMILES CN(CC(O)=O)C(=O)C1CCCCC1C(O)=O Show InChI InChI=1S/C11H17NO5/c1-12(6-9(13)14)10(15)7-4-2-3-5-8(7)11(16)17/h7-8H,2-6H2,1H3,(H,13,14)(H,16,17)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046637 (CHEMBL351263 | Cis-2-(Carboxymethyl-ethyl-carbamoy...) Show SMILES CCN(CC(O)=O)C(=O)C1CCCC1C(O)=O Show InChI InChI=1S/C11H17NO5/c1-2-12(6-9(13)14)10(15)7-4-3-5-8(7)11(16)17/h7-8H,2-6H2,1H3,(H,13,14)(H,16,17)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046635 (CHEMBL159973 | Cis-2-(Carboxymethyl-carbamoyl)-cyc...) Show SMILES OC(=O)CNC(=O)C1CCCCC1C(O)=O Show InChI InChI=1S/C10H15NO5/c12-8(13)5-11-9(14)6-3-1-2-4-7(6)10(15)16/h6-7H,1-5H2,(H,11,14)(H,12,13)(H,15,16)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046622 (CHEMBL159995 | Trans-2-[(Benzyloxycarbamoyl-methyl...) Show SMILES CN(CC(=O)NOCc1ccccc1)C(=O)C1CCCC1C(O)=O Show InChI InChI=1S/C17H22N2O5/c1-19(16(21)13-8-5-9-14(13)17(22)23)10-15(20)18-24-11-12-6-3-2-4-7-12/h2-4,6-7,13-14H,5,8-11H2,1H3,(H,18,20)(H,22,23)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046625 (1R,2R-trans-2-[(Benzoyloxycarbamoyl-methyl)-carbam...) Show SMILES CN(CC(=O)NOC(=O)c1ccccc1)C(=O)[C@@H]1CCCC[C@@H]1C(O)=O Show InChI InChI=1S/C18H22N2O6/c1-20(16(22)13-9-5-6-10-14(13)17(23)24)11-15(21)19-26-18(25)12-7-3-2-4-8-12/h2-4,7-8,13-14H,5-6,9-11H2,1H3,(H,19,21)(H,23,24)/t13-,14+/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046620 (CHEMBL159956 | Cis-2-[(Benzyloxycarbamoyl-methyl)-...) Show SMILES CN(CC(=O)NOCc1ccccc1)C(=O)C1CCCCC1C(O)=O Show InChI InChI=1S/C18H24N2O5/c1-20(17(22)14-9-5-6-10-15(14)18(23)24)11-16(21)19-25-12-13-7-3-2-4-8-13/h2-4,7-8,14-15H,5-6,9-12H2,1H3,(H,19,21)(H,23,24)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046624 (1R,2R-trans-2-[(Benzoyloxycarbamoyl-methyl)-ethyl-...) Show SMILES CCN(CC(=O)NOC(=O)c1ccccc1)C(=O)[C@@H]1CCCC[C@@H]1C(O)=O Show InChI InChI=1S/C19H24N2O6/c1-2-21(17(23)14-10-6-7-11-15(14)18(24)25)12-16(22)20-27-19(26)13-8-4-3-5-9-13/h3-5,8-9,14-15H,2,6-7,10-12H2,1H3,(H,20,22)(H,24,25)/t14-,15+/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046627 (CHEMBL161552 | Cis-2-[(Benzyloxycarbamoyl-methyl)-...) Show SMILES CCN(CC(=O)NOCc1ccccc1)C(=O)C1CCCCC1C(O)=O Show InChI InChI=1S/C19H26N2O5/c1-2-21(18(23)15-10-6-7-11-16(15)19(24)25)12-17(22)20-26-13-14-8-4-3-5-9-14/h3-5,8-9,15-16H,2,6-7,10-13H2,1H3,(H,20,22)(H,24,25)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046640 (CHEMBL163549 | Cis-2-(2-Mercapto-ethylcarbamoyl)-c...) Show SMILES OC(=O)C1CCCCC1C(=O)NCCS Show InChI InChI=1S/C10H17NO3S/c12-9(11-5-6-15)7-3-1-2-4-8(7)10(13)14/h7-8,15H,1-6H2,(H,11,12)(H,13,14)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	>1.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046636 (CHEMBL159996 | Cis-2-[(Benzyloxycarbamoyl-methyl)-...) Show SMILES OC(=O)C1CCCCC1C(=O)NCC(=O)NOCc1ccccc1 Show InChI InChI=1S/C17H22N2O5/c20-15(19-24-11-12-6-2-1-3-7-12)10-18-16(21)13-8-4-5-9-14(13)17(22)23/h1-3,6-7,13-14H,4-5,8-11H2,(H,18,21)(H,19,20)(H,22,23)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046627 (CHEMBL161552 | Cis-2-[(Benzyloxycarbamoyl-methyl)-...) Show SMILES CCN(CC(=O)NOCc1ccccc1)C(=O)C1CCCCC1C(O)=O Show InChI InChI=1S/C19H26N2O5/c1-2-21(18(23)15-10-6-7-11-16(15)19(24)25)12-17(22)20-26-13-14-8-4-3-5-9-14/h3-5,8-9,15-16H,2,6-7,10-13H2,1H3,(H,20,22)(H,24,25)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046640 (CHEMBL163549 | Cis-2-(2-Mercapto-ethylcarbamoyl)-c...) Show SMILES OC(=O)C1CCCCC1C(=O)NCCS Show InChI InChI=1S/C10H17NO3S/c12-9(11-5-6-15)7-3-1-2-4-8(7)10(13)14/h7-8,15H,1-6H2,(H,11,12)(H,13,14)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	>1.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046625 (1R,2R-trans-2-[(Benzoyloxycarbamoyl-methyl)-carbam...) Show SMILES CN(CC(=O)NOC(=O)c1ccccc1)C(=O)[C@@H]1CCCC[C@@H]1C(O)=O Show InChI InChI=1S/C18H22N2O6/c1-20(16(22)13-9-5-6-10-14(13)17(23)24)11-15(21)19-26-18(25)12-7-3-2-4-8-12/h2-4,7-8,13-14H,5-6,9-11H2,1H3,(H,19,21)(H,23,24)/t13-,14+/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046636 (CHEMBL159996 | Cis-2-[(Benzyloxycarbamoyl-methyl)-...) Show SMILES OC(=O)C1CCCCC1C(=O)NCC(=O)NOCc1ccccc1 Show InChI InChI=1S/C17H22N2O5/c20-15(19-24-11-12-6-2-1-3-7-12)10-18-16(21)13-8-4-5-9-14(13)17(22)23/h1-3,6-7,13-14H,4-5,8-11H2,(H,18,21)(H,19,20)(H,22,23)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046620 (CHEMBL159956 | Cis-2-[(Benzyloxycarbamoyl-methyl)-...) Show SMILES CN(CC(=O)NOCc1ccccc1)C(=O)C1CCCCC1C(O)=O Show InChI InChI=1S/C18H24N2O5/c1-20(17(22)14-9-5-6-10-15(14)18(23)24)11-16(21)19-25-12-13-7-3-2-4-8-13/h2-4,7-8,14-15H,5-6,9-12H2,1H3,(H,19,21)(H,23,24)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046624 (1R,2R-trans-2-[(Benzoyloxycarbamoyl-methyl)-ethyl-...) Show SMILES CCN(CC(=O)NOC(=O)c1ccccc1)C(=O)[C@@H]1CCCC[C@@H]1C(O)=O Show InChI InChI=1S/C19H24N2O6/c1-2-21(17(23)14-10-6-7-11-15(14)18(24)25)12-16(22)20-27-19(26)13-8-4-3-5-9-13/h3-5,8-9,14-15H,2,6-7,10-12H2,1H3,(H,20,22)(H,24,25)/t14-,15+/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50046623 (1-(3-Carboxy-propionyl)-pyrrolidine-2-carboxylic a...) Show SMILES OC(=O)CCC(=O)N1CCCC1C(O)=O Show InChI InChI=1S/C9H13NO5/c11-7(3-4-8(12)13)10-5-1-2-6(10)9(14)15/h6H,1-5H2,(H,12,13)(H,14,15)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	6.24E+5	n/a	n/a	n/a	n/a	n/a	n/a
Laboratori Guidotti S.p.A. Curated by ChEMBL					Assay Description In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrate				J Med Chem 36: 699-707 (1993) BindingDB Entry DOI: 10.7270/Q21N81RS
					More data for this Ligand-Target Pair