BDBM50498572 CHEMBL3609616

SMILES: C[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)OCc1cc(cc(c1)C(F)(F)F)C(F)(F)F

InChI Key: InChIKey=IQGTUPXJLRMAOA-OHQNULFHSA-N

Data: 4 KI  2 IC50  2 EC50

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 8 hits for monomerid = 50498572   

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
Neurokinin 1 receptor (Homo sapiens (Human))	BDBM50498572 (CHEMBL3609616) Show SMILES C[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)OCc1cc(cc(c1)C(F)(F)F)C(F)(F)F |r| Show InChI InChI=1S/C43H42F6N6O7/c1-24(53-39(59)33(50)17-26-11-13-31(56)14-12-26)38(58)52-22-37(57)54-35(18-25-7-3-2-4-8-25)40(60)55-36(19-28-21-51-34-10-6-5-9-32(28)34)41(61)62-23-27-15-29(42(44,45)46)20-30(16-27)43(47,48)49/h2-16,20-21,24,33,35-36,51,56H,17-19,22-23,50H2,1H3,(H,52,58)(H,53,59)(H,54,57)(H,55,60)/t24-,33+,35+,36+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	0.120	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Arizona Curated by ChEMBL					Assay Description Displacement of [3H]-substance P from human NK1 receptor transfected in CHO cells				Bioorg Med Chem Lett 25: 3716-20 (2015) Article DOI: 10.1016/j.bmcl.2015.06.030 BindingDB Entry DOI: 10.7270/Q2R78J7N
					More data for this Ligand-Target Pair
Neurokinin 1 receptor (Rattus norvegicus (rat))	BDBM50498572 (CHEMBL3609616) Show SMILES C[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)OCc1cc(cc(c1)C(F)(F)F)C(F)(F)F |r| Show InChI InChI=1S/C43H42F6N6O7/c1-24(53-39(59)33(50)17-26-11-13-31(56)14-12-26)38(58)52-22-37(57)54-35(18-25-7-3-2-4-8-25)40(60)55-36(19-28-21-51-34-10-6-5-9-32(28)34)41(61)62-23-27-15-29(42(44,45)46)20-30(16-27)43(47,48)49/h2-16,20-21,24,33,35-36,51,56H,17-19,22-23,50H2,1H3,(H,52,58)(H,53,59)(H,54,57)(H,55,60)/t24-,33+,35+,36+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	0.150	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Arizona Curated by ChEMBL					Assay Description Displacement of [3H]-substance P from rat NK1 receptor transfected in CHO cells				Bioorg Med Chem Lett 25: 3716-20 (2015) Article DOI: 10.1016/j.bmcl.2015.06.030 BindingDB Entry DOI: 10.7270/Q2R78J7N
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50498572 (CHEMBL3609616) Show SMILES C[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)OCc1cc(cc(c1)C(F)(F)F)C(F)(F)F |r| Show InChI InChI=1S/C43H42F6N6O7/c1-24(53-39(59)33(50)17-26-11-13-31(56)14-12-26)38(58)52-22-37(57)54-35(18-25-7-3-2-4-8-25)40(60)55-36(19-28-21-51-34-10-6-5-9-32(28)34)41(61)62-23-27-15-29(42(44,45)46)20-30(16-27)43(47,48)49/h2-16,20-21,24,33,35-36,51,56H,17-19,22-23,50H2,1H3,(H,52,58)(H,53,59)(H,54,57)(H,55,60)/t24-,33+,35+,36+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	35	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Arizona Curated by ChEMBL					Assay Description Displacement of [3H]-DPDPE from human delta opioid receptor transfected in HN9.10 cells				Bioorg Med Chem Lett 25: 3716-20 (2015) Article DOI: 10.1016/j.bmcl.2015.06.030 BindingDB Entry DOI: 10.7270/Q2R78J7N
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM50498572 (CHEMBL3609616) Show SMILES C[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)OCc1cc(cc(c1)C(F)(F)F)C(F)(F)F |r| Show InChI InChI=1S/C43H42F6N6O7/c1-24(53-39(59)33(50)17-26-11-13-31(56)14-12-26)38(58)52-22-37(57)54-35(18-25-7-3-2-4-8-25)40(60)55-36(19-28-21-51-34-10-6-5-9-32(28)34)41(61)62-23-27-15-29(42(44,45)46)20-30(16-27)43(47,48)49/h2-16,20-21,24,33,35-36,51,56H,17-19,22-23,50H2,1H3,(H,52,58)(H,53,59)(H,54,57)(H,55,60)/t24-,33+,35+,36+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	37	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Arizona Curated by ChEMBL					Assay Description Displacement of [3H]-DAMGO from rat mu opioid receptor transfected in HN9.10 cells				Bioorg Med Chem Lett 25: 3716-20 (2015) Article DOI: 10.1016/j.bmcl.2015.06.030 BindingDB Entry DOI: 10.7270/Q2R78J7N
					More data for this Ligand-Target Pair
Opioid receptors; mu and delta (MOUSE)	BDBM50498572 (CHEMBL3609616) Show SMILES C[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)OCc1cc(cc(c1)C(F)(F)F)C(F)(F)F |r| Show InChI InChI=1S/C43H42F6N6O7/c1-24(53-39(59)33(50)17-26-11-13-31(56)14-12-26)38(58)52-22-37(57)54-35(18-25-7-3-2-4-8-25)40(60)55-36(19-28-21-51-34-10-6-5-9-32(28)34)41(61)62-23-27-15-29(42(44,45)46)20-30(16-27)43(47,48)49/h2-16,20-21,24,33,35-36,51,56H,17-19,22-23,50H2,1H3,(H,52,58)(H,53,59)(H,54,57)(H,55,60)/t24-,33+,35+,36+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	43	n/a	n/a	n/a	n/a	n/a	n/a
University of Arizona Curated by ChEMBL					Assay Description Agonist activity at delta opioid receptor in mouse vas deferens assessed as inhibition of electrically-stimulated muscle contraction				Bioorg Med Chem Lett 25: 3716-20 (2015) Article DOI: 10.1016/j.bmcl.2015.06.030 BindingDB Entry DOI: 10.7270/Q2R78J7N
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50498572 (CHEMBL3609616) Show SMILES C[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)OCc1cc(cc(c1)C(F)(F)F)C(F)(F)F |r| Show InChI InChI=1S/C43H42F6N6O7/c1-24(53-39(59)33(50)17-26-11-13-31(56)14-12-26)38(58)52-22-37(57)54-35(18-25-7-3-2-4-8-25)40(60)55-36(19-28-21-51-34-10-6-5-9-32(28)34)41(61)62-23-27-15-29(42(44,45)46)20-30(16-27)43(47,48)49/h2-16,20-21,24,33,35-36,51,56H,17-19,22-23,50H2,1H3,(H,52,58)(H,53,59)(H,54,57)(H,55,60)/t24-,33+,35+,36+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	150	n/a	n/a	n/a	n/a
University of Arizona Curated by ChEMBL					Assay Description Agonist activity at human delta opioid receptor transfected in HN9.10 cells by [35S]GTPgammaS binding assay				Bioorg Med Chem Lett 25: 3716-20 (2015) Article DOI: 10.1016/j.bmcl.2015.06.030 BindingDB Entry DOI: 10.7270/Q2R78J7N
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM50498572 (CHEMBL3609616) Show SMILES C[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)OCc1cc(cc(c1)C(F)(F)F)C(F)(F)F |r| Show InChI InChI=1S/C43H42F6N6O7/c1-24(53-39(59)33(50)17-26-11-13-31(56)14-12-26)38(58)52-22-37(57)54-35(18-25-7-3-2-4-8-25)40(60)55-36(19-28-21-51-34-10-6-5-9-32(28)34)41(61)62-23-27-15-29(42(44,45)46)20-30(16-27)43(47,48)49/h2-16,20-21,24,33,35-36,51,56H,17-19,22-23,50H2,1H3,(H,52,58)(H,53,59)(H,54,57)(H,55,60)/t24-,33+,35+,36+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	100	n/a	n/a	n/a	n/a
University of Arizona Curated by ChEMBL					Assay Description Agonist activity at rat mu opioid receptor transfected in HN9.10 cells by [35S]GTPgammaS binding assay				Bioorg Med Chem Lett 25: 3716-20 (2015) Article DOI: 10.1016/j.bmcl.2015.06.030 BindingDB Entry DOI: 10.7270/Q2R78J7N
					More data for this Ligand-Target Pair
Mu-type opioid receptor (GUINEA PIG)	BDBM50498572 (CHEMBL3609616) Show SMILES C[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)OCc1cc(cc(c1)C(F)(F)F)C(F)(F)F |r| Show InChI InChI=1S/C43H42F6N6O7/c1-24(53-39(59)33(50)17-26-11-13-31(56)14-12-26)38(58)52-22-37(57)54-35(18-25-7-3-2-4-8-25)40(60)55-36(19-28-21-51-34-10-6-5-9-32(28)34)41(61)62-23-27-15-29(42(44,45)46)20-30(16-27)43(47,48)49/h2-16,20-21,24,33,35-36,51,56H,17-19,22-23,50H2,1H3,(H,52,58)(H,53,59)(H,54,57)(H,55,60)/t24-,33+,35+,36+/m1/s1	UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	520	n/a	n/a	n/a	n/a	n/a	n/a
University of Arizona Curated by ChEMBL					Assay Description Agonist activity at mu opioid receptor in guinea pig ileum assessed as inhibition of electrically-stimulated muscle contraction				Bioorg Med Chem Lett 25: 3716-20 (2015) Article DOI: 10.1016/j.bmcl.2015.06.030 BindingDB Entry DOI: 10.7270/Q2R78J7N
					More data for this Ligand-Target Pair