Found 5 hits for monomerid = 50220121 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)) | BDBM50220121
((3R,4S)-N-(2-(3,5-bis(trifluoromethyl)phenyl)propa...)Show SMILES CN(C(=O)[C@H]1CN(C[C@@H]1c1ccc(F)cc1C)C(=O)C1CCN(CC1)C(C)=O)C(C)(C)c1cc(cc(c1)C(F)(F)F)C(F)(F)F Show InChI InChI=1S/C32H36F7N3O3/c1-18-12-24(33)6-7-25(18)26-16-42(28(44)20-8-10-41(11-9-20)19(2)43)17-27(26)29(45)40(5)30(3,4)21-13-22(31(34,35)36)15-23(14-21)32(37,38)39/h6-7,12-15,20,26-27H,8-11,16-17H2,1-5H3/t26-,27+/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 0.0500 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Displacement of [125I]SP from human NK1 receptor expressed in CHO cells |
Bioorg Med Chem Lett 17: 5310-5 (2007)
Article DOI: 10.1016/j.bmcl.2007.08.028 BindingDB Entry DOI: 10.7270/Q2DR2V75 |
More data for this Ligand-Target Pair | |
Cytochrome P450 3A4
(Homo sapiens (Human)) | BDBM50220121
((3R,4S)-N-(2-(3,5-bis(trifluoromethyl)phenyl)propa...)Show SMILES CN(C(=O)[C@H]1CN(C[C@@H]1c1ccc(F)cc1C)C(=O)C1CCN(CC1)C(C)=O)C(C)(C)c1cc(cc(c1)C(F)(F)F)C(F)(F)F Show InChI InChI=1S/C32H36F7N3O3/c1-18-12-24(33)6-7-25(18)26-16-42(28(44)20-8-10-41(11-9-20)19(2)43)17-27(26)29(45)40(5)30(3,4)21-13-22(31(34,35)36)15-23(14-21)32(37,38)39/h6-7,12-15,20,26-27H,8-11,16-17H2,1-5H3/t26-,27+/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 4.90E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human CYP3A4 |
Bioorg Med Chem Lett 17: 5310-5 (2007)
Article DOI: 10.1016/j.bmcl.2007.08.028 BindingDB Entry DOI: 10.7270/Q2DR2V75 |
More data for this Ligand-Target Pair | |
Cytochrome P450 2D6
(Homo sapiens (Human)) | BDBM50220121
((3R,4S)-N-(2-(3,5-bis(trifluoromethyl)phenyl)propa...)Show SMILES CN(C(=O)[C@H]1CN(C[C@@H]1c1ccc(F)cc1C)C(=O)C1CCN(CC1)C(C)=O)C(C)(C)c1cc(cc(c1)C(F)(F)F)C(F)(F)F Show InChI InChI=1S/C32H36F7N3O3/c1-18-12-24(33)6-7-25(18)26-16-42(28(44)20-8-10-41(11-9-20)19(2)43)17-27(26)29(45)40(5)30(3,4)21-13-22(31(34,35)36)15-23(14-21)32(37,38)39/h6-7,12-15,20,26-27H,8-11,16-17H2,1-5H3/t26-,27+/m1/s1 | PDB
UniProtKB/SwissProt UniProtKB/TrEMBL
GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 5.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human CYP2D6 |
Bioorg Med Chem Lett 17: 5310-5 (2007)
Article DOI: 10.1016/j.bmcl.2007.08.028 BindingDB Entry DOI: 10.7270/Q2DR2V75 |
More data for this Ligand-Target Pair | |
Neurokinin 1 receptor
(Homo sapiens (Human)) | BDBM50220121
((3R,4S)-N-(2-(3,5-bis(trifluoromethyl)phenyl)propa...)Show SMILES CN(C(=O)[C@H]1CN(C[C@@H]1c1ccc(F)cc1C)C(=O)C1CCN(CC1)C(C)=O)C(C)(C)c1cc(cc(c1)C(F)(F)F)C(F)(F)F Show InChI InChI=1S/C32H36F7N3O3/c1-18-12-24(33)6-7-25(18)26-16-42(28(44)20-8-10-41(11-9-20)19(2)43)17-27(26)29(45)40(5)30(3,4)21-13-22(31(34,35)36)15-23(14-21)32(37,38)39/h6-7,12-15,20,26-27H,8-11,16-17H2,1-5H3/t26-,27+/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 0.510 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Displacement of [125I]SP from human NK1 receptor expressed in CHO cells in presence of 50% human serum |
Bioorg Med Chem Lett 17: 5310-5 (2007)
Article DOI: 10.1016/j.bmcl.2007.08.028 BindingDB Entry DOI: 10.7270/Q2DR2V75 |
More data for this Ligand-Target Pair | |
Cytochrome P450 2C9
(Homo sapiens (Human)) | BDBM50220121
((3R,4S)-N-(2-(3,5-bis(trifluoromethyl)phenyl)propa...)Show SMILES CN(C(=O)[C@H]1CN(C[C@@H]1c1ccc(F)cc1C)C(=O)C1CCN(CC1)C(C)=O)C(C)(C)c1cc(cc(c1)C(F)(F)F)C(F)(F)F Show InChI InChI=1S/C32H36F7N3O3/c1-18-12-24(33)6-7-25(18)26-16-42(28(44)20-8-10-41(11-9-20)19(2)43)17-27(26)29(45)40(5)30(3,4)21-13-22(31(34,35)36)15-23(14-21)32(37,38)39/h6-7,12-15,20,26-27H,8-11,16-17H2,1-5H3/t26-,27+/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human CYP2C9 |
Bioorg Med Chem Lett 17: 5310-5 (2007)
Article DOI: 10.1016/j.bmcl.2007.08.028 BindingDB Entry DOI: 10.7270/Q2DR2V75 |
More data for this Ligand-Target Pair | |