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Inhibitor Report for: Tacrine-Melatonin-Feruloyl-5c

Permeable agent with antioxidant properties,cholinesterase inhibitory activity, less hepatotoxicity than tacrine, and neuroprotective capacity, able to activate the Nrf2 transcriptional pathway


General
Type Derivative of Tacrine, Derivative of Tryptamine, Multitarget, Feruloyl, Acrylate, Antioxidant, Hydroxycinnamic-ester, Alkyl linked bis-ligand
Chemical_Nomenclature
Canonical SMILES O=C(C(=C(C1=CC(=C(O)C=C1)OC)[H])[H])N(CCCCCCCNC3=C2C=C(OC)C=CC2=NC4=C3CCCC4)CC(NCCC5=C[N]C6=C5C=C(OC)C=C6)=O
InChI InChI=1S/C44H53N5O6/c1-53-32-15-17-37-35(26-32)31(28-47-37)21-23-45-42(51)29-49(43(52)20-14-30-13-19-40(50)41(25-30)55-3)24-10-6-4-5-9-22-46-44-34-11-7-8-12-38(34)48-39-18-16-33(54-2)27-36(39)44/h13-20,25-28,47,50H,4-12,21-24,29H2,1-3H3,(H,45,51)(H,46,48)/b20-14+
InChIKey BCHYGDBEGKZQHD-XSFVSMFZSA-N
Other name(s)
________________________________________________________________________________________________
MW|747.93
Formula|C44H53N5O6
CAS_number|
PubChem|
UniChem|BCHYGDBEGKZQHD-XSFVSMFZSA-N
IUPHAR|
Wikipedia|

Target
Families | Tacrine-Melatonin-Feruloyl-5c ligand of proteins in family: BCHE

References:
Search PubMed for references concerning: Tacrine-Melatonin-Feruloyl-5c
    Title: The Antioxidant Additive Approach for Alzheimer's Disease Therapy: New Ferulic (Lipoic) Acid Plus Melatonin Modified Tacrines as Cholinesterases Inhibitors, Direct Antioxidants, and Nuclear Factor (Erythroid-Derived 2)-Like 2 Activators
    Benchekroun M, Romero A, Egea J, Leon R, Michalska P, Buendia I, Jimeno ML, Jun D, Janockova J and Ismaili L <6 more author(s)>
    Ref: Journal of Medicinal Chemistry, 59:9967, 2016 : PubMed