Compile Data Set for Download or QSAR

Found 3 hits of ic50 for monomerid = 50301106   

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
Receptor tyrosine-protein kinase erbB-2 (Homo sapiens (Human))	BDBM50301106 ((2S,3S)-N-hydroxy-5-(N-methylbenzamido)-2-(4-pheny...) Show SMILES CN(C1CN[C@@H]([C@H](C1)C(=O)NO)C(=O)N1CCC(=CC1)c1ccccc1)C(=O)c1ccccc1 |r,c:18| Show InChI InChI=1S/C26H30N4O4/c1-29(25(32)20-10-6-3-7-11-20)21-16-22(24(31)28-34)23(27-17-21)26(33)30-14-12-19(13-15-30)18-8-4-2-5-9-18/h2-12,21-23,27,34H,13-17H2,1H3,(H,28,31)/t21?,22-,23-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
Incyte Corporation Curated by ChEMBL					Assay Description Inhibition of HER-2				Bioorg Med Chem Lett 19: 5037-42 (2009) Article DOI: 10.1016/j.bmcl.2009.07.052 BindingDB Entry DOI: 10.7270/Q2154J0S
					More data for this Ligand-Target Pair
Disintegrin and metalloproteinase domain-containing protein 10 (Homo sapiens (Human))	BDBM50301106 ((2S,3S)-N-hydroxy-5-(N-methylbenzamido)-2-(4-pheny...) Show SMILES CN(C1CN[C@@H]([C@H](C1)C(=O)NO)C(=O)N1CCC(=CC1)c1ccccc1)C(=O)c1ccccc1 |r,c:18| Show InChI InChI=1S/C26H30N4O4/c1-29(25(32)20-10-6-3-7-11-20)21-16-22(24(31)28-34)23(27-17-21)26(33)30-14-12-19(13-15-30)18-8-4-2-5-9-18/h2-12,21-23,27,34H,13-17H2,1H3,(H,28,31)/t21?,22-,23-/m0/s1	PDB UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	12	n/a	n/a	n/a	n/a	n/a	n/a
Incyte Corporation Curated by ChEMBL					Assay Description Inhibition of ADAM-10				Bioorg Med Chem Lett 19: 5037-42 (2009) Article DOI: 10.1016/j.bmcl.2009.07.052 BindingDB Entry DOI: 10.7270/Q2154J0S
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50301106 ((2S,3S)-N-hydroxy-5-(N-methylbenzamido)-2-(4-pheny...) Show SMILES CN(C1CN[C@@H]([C@H](C1)C(=O)NO)C(=O)N1CCC(=CC1)c1ccccc1)C(=O)c1ccccc1 |r,c:18| Show InChI InChI=1S/C26H30N4O4/c1-29(25(32)20-10-6-3-7-11-20)21-16-22(24(31)28-34)23(27-17-21)26(33)30-14-12-19(13-15-30)18-8-4-2-5-9-18/h2-12,21-23,27,34H,13-17H2,1H3,(H,28,31)/t21?,22-,23-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	12	n/a	n/a	n/a	n/a	n/a	n/a
Incyte Corporation Curated by ChEMBL					Assay Description Inhibition of MMP-2				Bioorg Med Chem Lett 19: 5037-42 (2009) Article DOI: 10.1016/j.bmcl.2009.07.052 BindingDB Entry DOI: 10.7270/Q2154J0S
					More data for this Ligand-Target Pair