Found 5 hits for monomerid = 50327478 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 |
Histamine H3 receptor
(Homo sapiens (Human)) | BDBM50327478
((S)-7-bromo-8-(1-isopropylpiperidin-4-yloxy)-4-met...)Show SMILES CC(C)N1CCC(CC1)Oc1cc2cc3C(=O)NC[C@H](C)n3c2cc1Br |r| Show InChI InChI=1S/C20H26BrN3O2/c1-12(2)23-6-4-15(5-7-23)26-19-9-14-8-18-20(25)22-11-13(3)24(18)17(14)10-16(19)21/h8-10,12-13,15H,4-7,11H2,1-3H3,(H,22,25)/t13-/m0/s1 | Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
F Hoffmann-La Roche Ltd
Curated by ChEMBL
| Assay Description Displacement of [3H]-RAMH from human histamine H3 receptor |
Bioorg Med Chem Lett 20: 5713-7 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.009 BindingDB Entry DOI: 10.7270/Q2571C7N |
More data for this Ligand-Target Pair | |
Cytochrome P450 2C9
(Homo sapiens (Human)) | BDBM50327478
((S)-7-bromo-8-(1-isopropylpiperidin-4-yloxy)-4-met...)Show SMILES CC(C)N1CCC(CC1)Oc1cc2cc3C(=O)NC[C@H](C)n3c2cc1Br |r| Show InChI InChI=1S/C20H26BrN3O2/c1-12(2)23-6-4-15(5-7-23)26-19-9-14-8-18-20(25)22-11-13(3)24(18)17(14)10-16(19)21/h8-10,12-13,15H,4-7,11H2,1-3H3,(H,22,25)/t13-/m0/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 | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
F Hoffmann-La Roche Ltd
Curated by ChEMBL
| Assay Description Inhibition of CYP2C9 |
Bioorg Med Chem Lett 20: 5713-7 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.009 BindingDB Entry DOI: 10.7270/Q2571C7N |
More data for this Ligand-Target Pair | |
Histamine H3 receptor
(Homo sapiens (Human)) | BDBM50327478
((S)-7-bromo-8-(1-isopropylpiperidin-4-yloxy)-4-met...)Show SMILES CC(C)N1CCC(CC1)Oc1cc2cc3C(=O)NC[C@H](C)n3c2cc1Br |r| Show InChI InChI=1S/C20H26BrN3O2/c1-12(2)23-6-4-15(5-7-23)26-19-9-14-8-18-20(25)22-11-13(3)24(18)17(14)10-16(19)21/h8-10,12-13,15H,4-7,11H2,1-3H3,(H,22,25)/t13-/m0/s1 | Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 4 | n/a | n/a | n/a | n/a |
F Hoffmann-La Roche Ltd
Curated by ChEMBL
| Assay Description Inverse agonist activity at human recombinant histamine H3 receptor assessed as effect on [35S]GTPgammaS binding |
Bioorg Med Chem Lett 20: 5713-7 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.009 BindingDB Entry DOI: 10.7270/Q2571C7N |
More data for this Ligand-Target Pair | |
Cytochrome P450 2D6
(Homo sapiens (Human)) | BDBM50327478
((S)-7-bromo-8-(1-isopropylpiperidin-4-yloxy)-4-met...)Show SMILES CC(C)N1CCC(CC1)Oc1cc2cc3C(=O)NC[C@H](C)n3c2cc1Br |r| Show InChI InChI=1S/C20H26BrN3O2/c1-12(2)23-6-4-15(5-7-23)26-19-9-14-8-18-20(25)22-11-13(3)24(18)17(14)10-16(19)21/h8-10,12-13,15H,4-7,11H2,1-3H3,(H,22,25)/t13-/m0/s1 | PDB
UniProtKB/SwissProt UniProtKB/TrEMBL
GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
F Hoffmann-La Roche Ltd
Curated by ChEMBL
| Assay Description Inhibition of CYP2D6 |
Bioorg Med Chem Lett 20: 5713-7 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.009 BindingDB Entry DOI: 10.7270/Q2571C7N |
More data for this Ligand-Target Pair | |
Cytochrome P450 3A4
(Homo sapiens (Human)) | BDBM50327478
((S)-7-bromo-8-(1-isopropylpiperidin-4-yloxy)-4-met...)Show SMILES CC(C)N1CCC(CC1)Oc1cc2cc3C(=O)NC[C@H](C)n3c2cc1Br |r| Show InChI InChI=1S/C20H26BrN3O2/c1-12(2)23-6-4-15(5-7-23)26-19-9-14-8-18-20(25)22-11-13(3)24(18)17(14)10-16(19)21/h8-10,12-13,15H,4-7,11H2,1-3H3,(H,22,25)/t13-/m0/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 | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
F Hoffmann-La Roche Ltd
Curated by ChEMBL
| Assay Description Inhibition of CYP3A4 |
Bioorg Med Chem Lett 20: 5713-7 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.009 BindingDB Entry DOI: 10.7270/Q2571C7N |
More data for this Ligand-Target Pair | |