CHEMBL459756
hH3R Ki 2.0 nM, AChE IC50 1096 nm
General
Type : Histamine-Receptor3-H3-Antagonist,Multitarget,Piperidine
Chemical_Nomenclature : 1-[[4-[4-(2-piperidin-1-ylethyl)phenyl]phenyl]methyl]piperidine
Canonical SMILES : C1CCN(CC1)CCC2=CC=C(C=C2)C3=CC=C(C=C3)CN4CCCCC4
InChI : InChI=1S\/C25H34N2\/c1-3-16-26(17-4-1)20-15-22-7-11-24(12-8-22)25-13-9-23(10-14-25)21-27-18-5-2-6-19-27\/h7-14H,1-6,15-21H2
InChIKey : IPENPJGNQLBYMT-UHFFFAOYSA-N
Other name(s) : BDBM50412469,Compound 12
MW : 362.5
Formula : C25H34N2
CAS_number :
PubChem : 25147728
UniChem : IPENPJGNQLBYMT-UHFFFAOYSA-N
IUPHAR :
Wikipedia :
Target
Families : CHEMBL459756 ligand of proteins in family: ACHE || BCHE
Stucture :
Protein : human-ACHE || human-BCHE
References (1)
| Title : Synthesis and structure-activity relationships for biphenyl H3 receptor antagonists with moderate anti-cholinesterase activity - Morini_2008_Bioorg.Med.Chem_16_9911 |
| Author(s) : Morini G , Comini M , Rivara M , Rivara S , Bordi F , Plazzi PV , Flammini L , Saccani F , Bertoni S , Ballabeni V , Barocelli E , Mor M |
| Ref : Bioorganic & Medicinal Chemistry , 16 :9911 , 2008 |
| Abstract : Morini_2008_Bioorg.Med.Chem_16_9911 |
| ESTHER : Morini_2008_Bioorg.Med.Chem_16_9911 |
| PubMedSearch : Morini_2008_Bioorg.Med.Chem_16_9911 |
| PubMedID: 18976927 |