CHEMBL440526
General
Type : Multitarget,Carbamate,Coumarin
Chemical_Nomenclature : [3-[[methyl-[3-(2-oxochromen-7-yl)oxypropyl]amino]methyl]phenyl] N-heptylcarbamate
Canonical SMILES : CCCCCCCNC(=O)OC1=CC=CC(=C1)CN(C)CCCOC2=CC3=C(C=C2)C=CC(=O)O3
InChI : InChI=1S\/C28H36N2O5\/c1-3-4-5-6-7-16-29-28(32)34-25-11-8-10-22(19-25)21-30(2)17-9-18-33-24-14-12-23-13-15-27(31)35-26(23)20-24\/h8,10-15,19-20H,3-7,9,16-18,21H2,1-2H3,(H,29,32)
InChIKey : FTRXEEOTFGUKHN-UHFFFAOYSA-N
Other name(s) : aminoalkoxyheteroaryl deriv. 18,BDBM10925,3-{[methyl({3-[(2-oxo-2H-chromen-7-yl)oxy]propyl})amino]methyl}phenyl N-heptylcarbamate hydrochloride,Heptylcarbamic acid 3-[methyl[3-[(2-oxo-2H-1-benzopyran-7-yl)oxy]propyl]aminomethyl]phenyl ester
MW : 480.6
Formula : C28H36N2O5
CAS_number :
PubChem : 11800047
UniChem : FTRXEEOTFGUKHN-UHFFFAOYSA-N
IUPHAR :
Wikipedia :
Target
References (3)
| Title : New Coumarin Derivatives as Cholinergic and Cannabinoid System Modulators - Montanari_2021_Molecules_26_3254 |
| Author(s) : Montanari S , Allara M , Scalvini L , Kostrzewa M , Belluti F , Gobbi S , Naldi M , Rivara S , Bartolini M , Ligresti A , Bisi A , Rampa A |
| Ref : Molecules , 26 :3254 , 2021 |
| Abstract : Montanari_2021_Molecules_26_3254 |
| ESTHER : Montanari_2021_Molecules_26_3254 |
| PubMedSearch : Montanari_2021_Molecules_26_3254 |
| PubMedID: 34071439 |
| Title : Fatty Acid Amide Hydrolase (FAAH), Acetylcholinesterase (AChE), and Butyrylcholinesterase (BuChE): Networked Targets for the Development of Carbamates as Potential Anti-Alzheimer's Disease Agents - Montanari_2016_J.Med.Chem_59_6387 |
| Author(s) : Montanari S , Scalvini L , Bartolini M , Belluti F , Gobbi S , Andrisano V , Ligresti A , Di Marzo V , Rivara S , Mor M , Bisi A , Rampa A |
| Ref : Journal of Medicinal Chemistry , 59 :6387 , 2016 |
| Abstract : Montanari_2016_J.Med.Chem_59_6387 |
| ESTHER : Montanari_2016_J.Med.Chem_59_6387 |
| PubMedSearch : Montanari_2016_J.Med.Chem_59_6387 |
| PubMedID: 27309570 |
| Title : The First Dual ChE\/FAAH Inhibitors: New Perspectives for Alzheimer's Disease? - Rampa_2012_ACS.Med.Chem.Lett_3_182 |
| Author(s) : Rampa A , Bartolini M , Bisi A , Belluti F , Gobbi S , Andrisano V , Ligresti A , Di Marzo V |
| Ref : ACS Med Chem Lett , 3 :182 , 2012 |
| Abstract : Rampa_2012_ACS.Med.Chem.Lett_3_182 |
| ESTHER : Rampa_2012_ACS.Med.Chem.Lett_3_182 |
| PubMedSearch : Rampa_2012_ACS.Med.Chem.Lett_3_182 |
| PubMedID: 24900454 |