Found 7 hits for monomerid = 50498573 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)) | BDBM50498573
(CHEMBL3609620)Show SMILES C[C@@H](NC(=O)[C@@H](N)Cc1c(C)cc(O)cc1C)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/C34H34F6N4O5/c1-17-8-24(45)9-18(2)26(17)14-27(41)31(47)43-19(3)30(46)44-29(12-21-15-42-28-7-5-4-6-25(21)28)32(48)49-16-20-10-22(33(35,36)37)13-23(11-20)34(38,39)40/h4-11,13,15,19,27,29,42,45H,12,14,16,41H2,1-3H3,(H,43,47)(H,44,46)/t19-,27+,29+/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| 0.0160 | 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)) | BDBM50498573
(CHEMBL3609620)Show SMILES C[C@@H](NC(=O)[C@@H](N)Cc1c(C)cc(O)cc1C)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/C34H34F6N4O5/c1-17-8-24(45)9-18(2)26(17)14-27(41)31(47)43-19(3)30(46)44-29(12-21-15-42-28-7-5-4-6-25(21)28)32(48)49-16-20-10-22(33(35,36)37)13-23(11-20)34(38,39)40/h4-11,13,15,19,27,29,42,45H,12,14,16,41H2,1-3H3,(H,43,47)(H,44,46)/t19-,27+,29+/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| 0.280 | 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 | |
Mu-type opioid receptor
(Rattus norvegicus (rat)) | BDBM50498573
(CHEMBL3609620)Show SMILES C[C@@H](NC(=O)[C@@H](N)Cc1c(C)cc(O)cc1C)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/C34H34F6N4O5/c1-17-8-24(45)9-18(2)26(17)14-27(41)31(47)43-19(3)30(46)44-29(12-21-15-42-28-7-5-4-6-25(21)28)32(48)49-16-20-10-22(33(35,36)37)13-23(11-20)34(38,39)40/h4-11,13,15,19,27,29,42,45H,12,14,16,41H2,1-3H3,(H,43,47)(H,44,46)/t19-,27+,29+/m1/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| 0.300 | 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 | |
Delta-type opioid receptor
(Homo sapiens (Human)) | BDBM50498573
(CHEMBL3609620)Show SMILES C[C@@H](NC(=O)[C@@H](N)Cc1c(C)cc(O)cc1C)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/C34H34F6N4O5/c1-17-8-24(45)9-18(2)26(17)14-27(41)31(47)43-19(3)30(46)44-29(12-21-15-42-28-7-5-4-6-25(21)28)32(48)49-16-20-10-22(33(35,36)37)13-23(11-20)34(38,39)40/h4-11,13,15,19,27,29,42,45H,12,14,16,41H2,1-3H3,(H,43,47)(H,44,46)/t19-,27+,29+/m1/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| 0.800 | 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)) | BDBM50498573
(CHEMBL3609620)Show SMILES C[C@@H](NC(=O)[C@@H](N)Cc1c(C)cc(O)cc1C)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/C34H34F6N4O5/c1-17-8-24(45)9-18(2)26(17)14-27(41)31(47)43-19(3)30(46)44-29(12-21-15-42-28-7-5-4-6-25(21)28)32(48)49-16-20-10-22(33(35,36)37)13-23(11-20)34(38,39)40/h4-11,13,15,19,27,29,42,45H,12,14,16,41H2,1-3H3,(H,43,47)(H,44,46)/t19-,27+,29+/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 | 1.60 | 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 | |
Delta-type opioid receptor
(Homo sapiens (Human)) | BDBM50498573
(CHEMBL3609620)Show SMILES C[C@@H](NC(=O)[C@@H](N)Cc1c(C)cc(O)cc1C)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/C34H34F6N4O5/c1-17-8-24(45)9-18(2)26(17)14-27(41)31(47)43-19(3)30(46)44-29(12-21-15-42-28-7-5-4-6-25(21)28)32(48)49-16-20-10-22(33(35,36)37)13-23(11-20)34(38,39)40/h4-11,13,15,19,27,29,42,45H,12,14,16,41H2,1-3H3,(H,43,47)(H,44,46)/t19-,27+,29+/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 | 12 | 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 | |
Opioid receptors; mu and delta
(MOUSE) | BDBM50498573
(CHEMBL3609620)Show SMILES C[C@@H](NC(=O)[C@@H](N)Cc1c(C)cc(O)cc1C)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/C34H34F6N4O5/c1-17-8-24(45)9-18(2)26(17)14-27(41)31(47)43-19(3)30(46)44-29(12-21-15-42-28-7-5-4-6-25(21)28)32(48)49-16-20-10-22(33(35,36)37)13-23(11-20)34(38,39)40/h4-11,13,15,19,27,29,42,45H,12,14,16,41H2,1-3H3,(H,43,47)(H,44,46)/t19-,27+,29+/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 | 400 | 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 | |