BDBM50073520 (S)-3-((S)-2-{(R)-2-[(S)-2-Amino-3-(4-hydroxy-phenyl)-propionylamino]-propionylamino}-3-phenyl-propionylamino)-N-{(S)-1-[(S)-1-((R)-1-carbamoyl-ethylcarbamoyl)-2-methyl-propylcarbamoyl]-2-methyl-propyl}-succinamic acid::CHEMBL134186

SMILES: CC(C)[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](C)NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)N[C@@H](C(C)C)C(=O)N[C@H](C)C(N)=O

InChI Key: InChIKey=LISMJSZLMCGABX-WTMJUUSGSA-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 = 50073520   

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
Delta-type opioid receptor (MOUSE)	BDBM50073520 ((S)-3-((S)-2-{(R)-2-[(S)-2-Amino-3-(4-hydroxy-phen...) Show SMILES CC(C)[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](C)NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)N[C@@H](C(C)C)C(=O)N[C@H](C)C(N)=O Show InChI InChI=1S/C38H54N8O10/c1-19(2)30(37(55)41-21(5)32(40)50)46-38(56)31(20(3)4)45-36(54)28(18-29(48)49)44-35(53)27(17-23-10-8-7-9-11-23)43-33(51)22(6)42-34(52)26(39)16-24-12-14-25(47)15-13-24/h7-15,19-22,26-28,30-31,47H,16-18,39H2,1-6H3,(H2,40,50)(H,41,55)(H,42,52)(H,43,51)(H,44,53)(H,45,54)(H,46,56)(H,48,49)/t21-,22-,26+,27+,28+,30+,31+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University "La Sapienza" of Rome Curated by ChEMBL					Assay Description Displacement of [3H]-NLT from Opioid receptor delta 1 of adult male mouse brain.				J Med Chem 42: 400-4 (1999) Article DOI: 10.1021/jm9810699 BindingDB Entry DOI: 10.7270/Q2KD1X2G
					More data for this Ligand-Target Pair
Mu-type opioid receptor (MOUSE)	BDBM50073520 ((S)-3-((S)-2-{(R)-2-[(S)-2-Amino-3-(4-hydroxy-phen...) Show SMILES CC(C)[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](C)NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)N[C@@H](C(C)C)C(=O)N[C@H](C)C(N)=O Show InChI InChI=1S/C38H54N8O10/c1-19(2)30(37(55)41-21(5)32(40)50)46-38(56)31(20(3)4)45-36(54)28(18-29(48)49)44-35(53)27(17-23-10-8-7-9-11-23)43-33(51)22(6)42-34(52)26(39)16-24-12-14-25(47)15-13-24/h7-15,19-22,26-28,30-31,47H,16-18,39H2,1-6H3,(H2,40,50)(H,41,55)(H,42,52)(H,43,51)(H,44,53)(H,45,54)(H,46,56)(H,48,49)/t21-,22-,26+,27+,28+,30+,31+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.90E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University "La Sapienza" of Rome Curated by ChEMBL					Assay Description Displacement of [3H]-DAGO from Opioid receptor mu 1 of adult male mouse brain.				J Med Chem 42: 400-4 (1999) Article DOI: 10.1021/jm9810699 BindingDB Entry DOI: 10.7270/Q2KD1X2G
					More data for this Ligand-Target Pair