null

SMILES: Cc1cc(O)cc(C)c1C[C@H](N)C(=O)N[C@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H](CC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O)Cc1ccccc1

InChI Key: InChIKey=IBMDHHYVXFARQY-JPBAFFISSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50469381   

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
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50469381 (CHEMBL4277122) Show SMILES Cc1cc(O)cc(C)c1C[C@H](N)C(=O)N[C@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H](CC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O)Cc1ccccc1 |r| Show InChI InChI=1S/C79H103N17O13/c1-48-39-56(97)40-49(2)57(48)47-58(81)71(102)91-60(32-20-38-87-79(85)86)73(104)94-66(45-54-29-16-7-17-30-54)78(109)96-65(44-53-27-14-6-15-28-53)77(108)92-61(33-35-67(82)98)72(103)88-55(41-50-21-8-3-9-22-50)46-69(100)89-63(42-51-23-10-4-11-24-51)75(106)93-62(34-36-68(83)99)74(105)95-64(43-52-25-12-5-13-26-52)76(107)90-59(70(84)101)31-18-19-37-80/h3-17,21-30,39-40,55,58-66,97H,18-20,31-38,41-47,80-81H2,1-2H3,(H2,82,98)(H2,83,99)(H2,84,101)(H,88,103)(H,89,100)(H,90,107)(H,91,102)(H,92,108)(H,93,106)(H,94,104)(H,95,105)(H,96,109)(H4,85,86,87)/t55-,58-,59-,60+,61-,62-,63-,64-,65-,66-/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Vrije Universiteit Brussel Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from human MOR expressed in CHO cell membranes after 60 mins by liquid scintillation counting				J Med Chem 61: 9784-9789 (2018) Article DOI: 10.1021/acs.jmedchem.8b01282 BindingDB Entry DOI: 10.7270/Q2F76G8Q
					More data for this Ligand-Target Pair