Compile Data Set for Download or QSAR

Found 3 hits of ec50 for UniProtKB: P12821   

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
Angiotensin-converting enzyme (Homo sapiens (Human))	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 MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	DrugBank PDB Article PubMed	n/a	n/a	n/a	n/a	1.85E+4	n/a	n/a	n/a	n/a
MRC Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 2QH, UK. Curated by ChEMBL					Assay Description Inhibition of human ACE K1087A mutant				Bioorg Med Chem Lett 16: 5084-7 (2006) Article DOI: 10.1016/j.bmcl.2006.07.034 BindingDB Entry DOI: 10.7270/Q2T72M6C
					More data for this Ligand-Target Pair				3D Structure (crystal)
Angiotensin-converting enzyme (Homo sapiens (Human))	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 MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	DrugBank PDB Article PubMed	n/a	n/a	n/a	n/a	2.12E+4	n/a	n/a	n/a	n/a
MRC Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 2QH, UK. Curated by ChEMBL					Assay Description Inhibition of human ACE C domain				Bioorg Med Chem Lett 16: 5084-7 (2006) Article DOI: 10.1016/j.bmcl.2006.07.034 BindingDB Entry DOI: 10.7270/Q2T72M6C
					More data for this Ligand-Target Pair				3D Structure (crystal)
Angiotensin-converting enzyme (Homo sapiens (Human))	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 MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	DrugBank PDB Article PubMed	n/a	n/a	n/a	n/a	1.42E+6	n/a	n/a	n/a	n/a
MRC Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 2QH, UK. Curated by ChEMBL					Assay Description Inhibition of human ACE Y1096F mutant				Bioorg Med Chem Lett 16: 5084-7 (2006) Article DOI: 10.1016/j.bmcl.2006.07.034 BindingDB Entry DOI: 10.7270/Q2T72M6C
					More data for this Ligand-Target Pair				3D Structure (crystal)