Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Protein kinase C beta type' and Ligand = 'BDBM50052038'   

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
Protein kinase C beta type (Homo sapiens (Human))	BDBM50052038 (18-tetrahydro-1H-1-pyrrolylmethyl-(18S)-17-oxa-4,1...) Show SMILES O=C1NC(=O)C2=C1c1cn(CCO[C@H](CN3CCCC3)CCn3cc2c2ccccc32)c2ccccc12 |c:5| Show InChI InChI=1S/C30H30N4O3/c35-29-27-23-18-33(25-9-3-1-7-21(23)25)14-11-20(17-32-12-5-6-13-32)37-16-15-34-19-24(28(27)30(36)31-29)22-8-2-4-10-26(22)34/h1-4,7-10,18-20H,5-6,11-17H2,(H,31,35,36)/t20-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	44	n/a	n/a	n/a	n/a	n/a	n/a
Lilly Research Laboratories Curated by ChEMBL					Assay Description Inhibition of Protein kinase C beta 2				J Med Chem 39: 2664-71 (1996) Article DOI: 10.1021/jm950588y BindingDB Entry DOI: 10.7270/Q25H7FBV
					More data for this Ligand-Target Pair
Protein kinase C beta type (Homo sapiens (Human))	BDBM50052038 (18-tetrahydro-1H-1-pyrrolylmethyl-(18S)-17-oxa-4,1...) Show SMILES O=C1NC(=O)C2=C1c1cn(CCO[C@H](CN3CCCC3)CCn3cc2c2ccccc32)c2ccccc12 |c:5| Show InChI InChI=1S/C30H30N4O3/c35-29-27-23-18-33(25-9-3-1-7-21(23)25)14-11-20(17-32-12-5-6-13-32)37-16-15-34-19-24(28(27)30(36)31-29)22-8-2-4-10-26(22)34/h1-4,7-10,18-20H,5-6,11-17H2,(H,31,35,36)/t20-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	44	n/a	n/a	n/a	n/a	n/a	n/a
Lilly Research Laboratories Curated by ChEMBL					Assay Description Inhibition of Protein kinase C beta 2				J Med Chem 39: 2664-71 (1996) Article DOI: 10.1021/jm950588y BindingDB Entry DOI: 10.7270/Q25H7FBV
					More data for this Ligand-Target Pair