BDBM50395013 CHEMBL2163455::US9708370, 59 CP-3(iii)

SMILES: C[C@@H](NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](C)C(=O)NN(Cc1ccccc1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O

InChI Key: InChIKey=FMGHKOGJNJIMBB-YOENNBKZSA-N

Data: 3 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 3 hits for monomerid = 50395013   

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
Growth hormone secretagogue receptor type 1 (Homo sapiens (Human))	BDBM50395013 (CHEMBL2163455 | US9708370, 59 CP-3(iii)) Show SMILES C[C@@H](NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](C)C(=O)NN(Cc1ccccc1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r| Show InChI InChI=1S/C35H49N11O6/c1-22(42-33(50)27(37)18-26-19-39-21-40-26)31(48)41-23(2)32(49)45-46(20-25-13-7-4-8-14-25)35(52)44-29(17-24-11-5-3-6-12-24)34(51)43-28(30(38)47)15-9-10-16-36/h3-8,11-14,19,21-23,27-29H,9-10,15-18,20,36-37H2,1-2H3,(H2,38,47)(H,39,40)(H,41,48)(H,42,50)(H,43,51)(H,44,52)(H,45,49)/t22-,23+,27+,28+,29-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Montr£al Curated by ChEMBL					Assay Description Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method				J Med Chem 55: 6502-11 (2012) Article DOI: 10.1021/jm300557t BindingDB Entry DOI: 10.7270/Q22J6D00
					More data for this Ligand-Target Pair
Estrogen receptor [D538G] (Homo sapiens (Human))	BDBM50395013 (CHEMBL2163455 | US9708370, 59 CP-3(iii)) Show SMILES C[C@@H](NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](C)C(=O)NN(Cc1ccccc1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r| Show InChI InChI=1S/C35H49N11O6/c1-22(42-33(50)27(37)18-26-19-39-21-40-26)31(48)41-23(2)32(49)45-46(20-25-13-7-4-8-14-25)35(52)44-29(17-24-11-5-3-6-12-24)34(51)43-28(30(38)47)15-9-10-16-36/h3-8,11-14,19,21-23,27-29H,9-10,15-18,20,36-37H2,1-2H3,(H2,38,47)(H,39,40)(H,41,48)(H,42,50)(H,43,51)(H,44,52)(H,45,49)/t22-,23+,27+,28+,29-/m1/s1	PDB GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
VALORISATION-RECHERCHE, LIMITED PARTNERSHIP; VALORISATION HSJ, LIMITED PARTNERSHIP US Patent					Assay Description GHS-R1a radioreceptor assay using LLCPK-1 membranes overexpressing GSH-R1a and radioiodinated (1-28) rat ghrelin as tracer.				US Patent US9708370 (2017) BindingDB Entry DOI: 10.7270/Q2XP76ZK
					More data for this Ligand-Target Pair
Platelet glycoprotein 4 (Rattus norvegicus)	BDBM50395013 (CHEMBL2163455 | US9708370, 59 CP-3(iii)) Show SMILES C[C@@H](NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](C)C(=O)NN(Cc1ccccc1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r| Show InChI InChI=1S/C35H49N11O6/c1-22(42-33(50)27(37)18-26-19-39-21-40-26)31(48)41-23(2)32(49)45-46(20-25-13-7-4-8-14-25)35(52)44-29(17-24-11-5-3-6-12-24)34(51)43-28(30(38)47)15-9-10-16-36/h3-8,11-14,19,21-23,27-29H,9-10,15-18,20,36-37H2,1-2H3,(H2,38,47)(H,39,40)(H,41,48)(H,42,50)(H,43,51)(H,44,52)(H,45,49)/t22-,23+,27+,28+,29-/m1/s1	PDB Reactome pathway UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Montr£al Curated by ChEMBL					Assay Description Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry				J Med Chem 55: 6502-11 (2012) Article DOI: 10.1021/jm300557t BindingDB Entry DOI: 10.7270/Q22J6D00
					More data for this Ligand-Target Pair