Preparation and in vitro screening of novel heterocyclic glycoconjugate cholinesterase inhibitors (CROSBI ID 649768)
Prilog sa skupa u zborniku | sažetak izlaganja sa skupa
Podaci o odgovornosti
Baumann, Krešimir ; Šinko, Goran ; Tomić, Srđanka
engleski
Preparation and in vitro screening of novel heterocyclic glycoconjugate cholinesterase inhibitors
Compounds containing a heterocyclic moiety attached to a carbohydrate system are important biologicaly active compounds. Pyridinium, imidazolium and benzimidazolium derivatives, among others, have been used in natural product chemistry and organic synthesis. Furthermore, they exibit a wide variety of biological activities. It is well established that the cholinesterases (ChE), particularly butyrylcholinesterase (BChE), are associated with te patogenesis and progression of Alzheimer's and Parkinson's disease.1 Cholinesterase inhibitors (ChEI) have been widely recognized as an effective palliative treatment for Alzheimer's and Parkinson's disease, preventing the breakdown of neurotrasmitter acetylcholine (ACh) by inhibiting ChE in the brain regions relevant for the above mentioned diseases.1 Many heterocyclic glycoconjugates have received a great deal of attention in this field of research. A series of novel heterocyclic β-D-gluco-, β-D- galacto- and α-D-mannopyranoside derivatives was synthesised as potential BChE inhibitors. Synthesis of target molecules was conducted in four steps: protection of sugar hydroxyl groups by peracetylation, O-glycosylation of the anomeric C-atom with 2-bromoethanol leading to the introduction of two C-atoms spacer followed by condensation with pyridine, imidazole and benzimidazole derivatives and the final removal of acetyls as protecting groups. All compounds were prepared in good yields and were characterized by standard analytical methods (1D NMR, IR, MS) and optical rotation measurements. Inhibitory properties of all synthesized compounds towards BChE were studied by applying Ellman's method.2, 3 Kinetic parameters (Km, Vm) and the inhibition constant (Ki) were determined.
gycoconjugate, heterocycle, butyrylcholinesterase, inhibitors
Rad u okviru projekta Hrvatska zaklade za znanost (PEPTGLYCOSAR, IP 2014-09-7899)
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
Podaci o prilogu
2017.
objavljeno
Podaci o matičnoj publikaciji
18th Tetrahedron Symposium - New Developments in Organic Chemistry, Programme Book
Budimpešta: Elsevier
Podaci o skupu
18th Tetrahedron Symposium - New Developments in Organic Chemistry
poster
27.06.2017-30.06.2017
Budimpešta, Mađarska