null

SMILES: C[C@H](NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](C)NC(=O)N(Cc1ccc(O)cc1)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(N)=O

InChI Key: InChIKey=OZAFXYOETBBYKW-HDSXGYDGSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50395025   

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))	BDBM50395025 (CHEMBL2163443 | US9708370, CP-1B(i)) Show SMILES C[C@H](NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](C)NC(=O)N(Cc1ccc(O)cc1)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(N)=O |r| Show InChI InChI=1S/C40H47N11O7/c1-23(35(42)53)46-38(56)33(16-25-8-4-3-5-9-25)49-39(57)34(17-27-19-44-32-11-7-6-10-30(27)32)48-36(54)24(2)47-40(58)51(21-26-12-14-29(52)15-13-26)50-37(55)31(41)18-28-20-43-22-45-28/h3-15,19-20,22-24,31,33-34,44,52H,16-18,21,41H2,1-2H3,(H2,42,53)(H,43,45)(H,46,56)(H,47,58)(H,48,54)(H,49,57)(H,50,55)/t23-,24-,31-,33+,34-/m0/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
Platelet glycoprotein 4 (Rattus norvegicus)	BDBM50395025 (CHEMBL2163443 | US9708370, CP-1B(i)) Show SMILES C[C@H](NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](C)NC(=O)N(Cc1ccc(O)cc1)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(N)=O |r| Show InChI InChI=1S/C40H47N11O7/c1-23(35(42)53)46-38(56)33(16-25-8-4-3-5-9-25)49-39(57)34(17-27-19-44-32-11-7-6-10-30(27)32)48-36(54)24(2)47-40(58)51(21-26-12-14-29(52)15-13-26)50-37(55)31(41)18-28-20-43-22-45-28/h3-15,19-20,22-24,31,33-34,44,52H,16-18,21,41H2,1-2H3,(H2,42,53)(H,43,45)(H,46,56)(H,47,58)(H,48,54)(H,49,57)(H,50,55)/t23-,24-,31-,33+,34-/m0/s1	PDB Reactome pathway UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	7.22E+4	n/a	n/a	n/a	n/a	7.3	n/a
VALORISATION-RECHERCHE, LIMITED PARTNERSHIP; VALORISATION HSJ, LIMITED PARTNERSHIP US Patent					Assay Description Competition experiments were performed by incubating 50 μg of LLC-PK1 membranes expressing human GHS-R1a with 15 fmol of 125I-Ghrelin and increa...				US Patent US9708370 (2017) BindingDB Entry DOI: 10.7270/Q2XP76ZK
					More data for this Ligand-Target Pair
Estrogen receptor [D538G] (Homo sapiens (Human))	BDBM50395025 (CHEMBL2163443 | US9708370, CP-1B(i)) Show SMILES C[C@H](NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](C)NC(=O)N(Cc1ccc(O)cc1)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(N)=O |r| Show InChI InChI=1S/C40H47N11O7/c1-23(35(42)53)46-38(56)33(16-25-8-4-3-5-9-25)49-39(57)34(17-27-19-44-32-11-7-6-10-30(27)32)48-36(54)24(2)47-40(58)51(21-26-12-14-29(52)15-13-26)50-37(55)31(41)18-28-20-43-22-45-28/h3-15,19-20,22-24,31,33-34,44,52H,16-18,21,41H2,1-2H3,(H2,42,53)(H,43,45)(H,46,56)(H,47,58)(H,48,54)(H,49,57)(H,50,55)/t23-,24-,31-,33+,34-/m0/s1	PDB UniProtKB/SwissProt 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)	BDBM50395025 (CHEMBL2163443 | US9708370, CP-1B(i)) Show SMILES C[C@H](NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](C)NC(=O)N(Cc1ccc(O)cc1)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(N)=O |r| Show InChI InChI=1S/C40H47N11O7/c1-23(35(42)53)46-38(56)33(16-25-8-4-3-5-9-25)49-39(57)34(17-27-19-44-32-11-7-6-10-30(27)32)48-36(54)24(2)47-40(58)51(21-26-12-14-29(52)15-13-26)50-37(55)31(41)18-28-20-43-22-45-28/h3-15,19-20,22-24,31,33-34,44,52H,16-18,21,41H2,1-2H3,(H2,42,53)(H,43,45)(H,46,56)(H,47,58)(H,48,54)(H,49,57)(H,50,55)/t23-,24-,31-,33+,34-/m0/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