BDBM50401756 CHEMBL2207143

SMILES: CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@@H](N)CSSC[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCC(N)=O)NC1=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)OCC(O)=O

InChI Key: InChIKey=WJUBUQDSQKKTFJ-GIISNQDKSA-N

Data: 2 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50401756   

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
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401756 (CHEMBL2207143) Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@@H](N)CSSC[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCC(N)=O)NC1=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)OCC(O)=O |r| Show InChI InChI=1S/C45H67N11O15S2/c1-5-23(4)37-44(69)50-27(12-13-33(47)58)40(65)52-30(17-34(48)59)41(66)54-31(21-73-72-20-26(46)38(63)51-29(42(67)55-37)16-24-8-10-25(57)11-9-24)45(70)56-14-6-7-32(56)43(68)53-28(15-22(2)3)39(64)49-18-36(62)71-19-35(60)61/h8-11,22-23,26-32,37,57H,5-7,12-21,46H2,1-4H3,(H2,47,58)(H2,48,59)(H,49,64)(H,50,69)(H,51,63)(H,52,65)(H,53,68)(H,54,66)(H,55,67)(H,60,61)/t23-,26-,27-,28-,29-,30-,31-,32-,37-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of PAM in human DMS53 cells using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair
Peptidyl-glycine alpha-amidating monooxygenase (Homo sapiens (Human))	BDBM50401756 (CHEMBL2207143) Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@@H](N)CSSC[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCC(N)=O)NC1=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)OCC(O)=O |r| Show InChI InChI=1S/C45H67N11O15S2/c1-5-23(4)37-44(69)50-27(12-13-33(47)58)40(65)52-30(17-34(48)59)41(66)54-31(21-73-72-20-26(46)38(63)51-29(42(67)55-37)16-24-8-10-25(57)11-9-24)45(70)56-14-6-7-32(56)43(68)53-28(15-22(2)3)39(64)49-18-36(62)71-19-35(60)61/h8-11,22-23,26-32,37,57H,5-7,12-21,46H2,1-4H3,(H2,47,58)(H2,48,59)(H,49,64)(H,50,69)(H,51,63)(H,52,65)(H,53,68)(H,54,66)(H,55,67)(H,60,61)/t23-,26-,27-,28-,29-,30-,31-,32-,37-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
Australian National University Curated by ChEMBL					Assay Description Competitive inhibition of secreted PAM in human DMS53 cell culture medium using as(R)-Tyr-(S)-Val-Gly as substrate after 2 hrs by HPLC analysis				Bioorg Med Chem Lett 22: 7015-8 (2012) Article DOI: 10.1016/j.bmcl.2012.10.004 BindingDB Entry DOI: 10.7270/Q2VT1T73
					More data for this Ligand-Target Pair