BDBM50542855 CHEMBL4641329

SMILES: CC(=O)N[C@@H](CCCNC(N)=N)C(=O)NC(CCCN)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O

InChI Key: InChIKey=AZHOIVYVBSUFPP-VSGQZEEBSA-N

Data: 2 KI

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 = 50542855   

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
Neuropeptide Y receptor type 4 (Homo sapiens (Human))	BDBM50542855 (CHEMBL4641329) Show SMILES CC(=O)N[C@@H](CCCNC(N)=N)C(=O)NC(CCCN)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |r| Show InChI InChI=1S/C54H79N19O10/c1-30(74)67-38(11-5-23-63-52(57)58)46(78)68-39(10-4-22-55)48(80)72-43(27-32-16-20-35(76)21-17-32)50(82)69-41(13-7-25-65-54(61)62)49(81)73-44(28-33-29-66-37-9-3-2-8-36(33)37)51(83)70-40(12-6-24-64-53(59)60)47(79)71-42(45(56)77)26-31-14-18-34(75)19-15-31/h2-3,8-9,14-21,29,38-44,66,75-76H,4-7,10-13,22-28,55H2,1H3,(H2,56,77)(H,67,74)(H,68,78)(H,69,82)(H,70,83)(H,71,79)(H,72,80)(H,73,81)(H4,57,58,63)(H4,59,60,64)(H4,61,62,65)/t38-,39?,40-,41-,42-,43-,44-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	PubMed	155	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Regensburg Curated by ChEMBL					Assay Description Displacement of [3H]UR-KK200 from human Y4 receptor expressed in CHO cells co-expressing Gqi5-mtAEQ measured after 90 mins by scintillation counting ...				J Med Chem 63: 8198-8215 (2020)
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 4 (Homo sapiens (Human))	BDBM50542855 (CHEMBL4641329) Show SMILES CC(=O)N[C@@H](CCCNC(N)=N)C(=O)NC(CCCN)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |r| Show InChI InChI=1S/C54H79N19O10/c1-30(74)67-38(11-5-23-63-52(57)58)46(78)68-39(10-4-22-55)48(80)72-43(27-32-16-20-35(76)21-17-32)50(82)69-41(13-7-25-65-54(61)62)49(81)73-44(28-33-29-66-37-9-3-2-8-36(33)37)51(83)70-40(12-6-24-64-53(59)60)47(79)71-42(45(56)77)26-31-14-18-34(75)19-15-31/h2-3,8-9,14-21,29,38-44,66,75-76H,4-7,10-13,22-28,55H2,1H3,(H2,56,77)(H,67,74)(H,68,78)(H,69,82)(H,70,83)(H,71,79)(H,72,80)(H,73,81)(H4,57,58,63)(H4,59,60,64)(H4,61,62,65)/t38-,39?,40-,41-,42-,43-,44-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	PubMed	160	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Regensburg Curated by ChEMBL					Assay Description Displacement of [3H]UR-KK200 from human Y4 receptor expressed in CHO cells co-expressing Gqi5-mtAEQ measured after 90 mins by scintillation counting ...				J Med Chem 63: 8198-8215 (2020)
					More data for this Ligand-Target Pair