Pregled bibliografske jedinice broj: 524569
Evaluation of Biological Activity of New Guanidinium Based Adamantane Compounds Novel Adamantane Derivatives as Potent Butyrylcholinesterase Inhibitors
Evaluation of Biological Activity of New Guanidinium Based Adamantane Compounds Novel Adamantane Derivatives as Potent Butyrylcholinesterase Inhibitors // 4th European Conference on Chemistry for Life Sciences / 4ECCLS
Budimpešta, Mađarska, 2011. str. 224-224 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 524569 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Evaluation of Biological Activity of New
Guanidinium Based Adamantane Compounds Novel
Adamantane Derivatives as Potent
Butyrylcholinesterase Inhibitors
Autori
Šekutor, Marina ; Mlinarić-Majerski, Kata ; Primožič, Ines ; Hrenar, Tomica ; Tomić- Pisarović, Srđanka
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
4th European Conference on Chemistry for Life Sciences / 4ECCLS
/ - , 2011, 224-224
Skup
4th European Conference on Chemistry for Life Sciences / 4ECCLS
Mjesto i datum
Budimpešta, Mađarska, 31.08.2011. - 03.09.2011
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
adamantane ; inhibitors ; butyrylcholinesterase ; kinetic and docking studies
Sažetak
It is known that the adamantane moiety plays an important biological role in various types of compounds due to its lipophilicity and bulkiness.[1] These findings suggest the importance of the adamantane substructure to reach and interact with the site of activity. On the other hand, the compounds with an incorporated guanidinium moiety are also known to act as pharmacologically active substrates with antimicrobial [2], antiviral [3] and anti- cancer action [4]. Polycyclic guanylhydrazones have recently found application as nitric oxide synthase (NOS) inhibitors.[5] In our recent study we have tried to combine the effects of these two subunits hoping for a synergic result. We have successfully synthesized adamantane guanylhydrazones 1-5 and have tested them as butyrylcholinesterase inhibitors. The inhibition of liophylized horse serum butyrylcholinesterase by compounds 1-5 was measured with acetylthiocholine as substrate. The Ellman's method [6] for cholinesterase activity determination was used and the inhibition constants were determined using the Hunter and Downs diagrams. The obtained results were supported with docking studies.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
MZOS-098-0982933-2911 - Kavezasti spojevi: ugradbene jedinice u molekularnim sustavima (Majerski, Kata, MZOS ) ( CroRIS)
MZOS-119-1191344-3121 - Sinteze i enzimske transformacije biološki aktivnih spojeva (Tomić-Pisarović, Srđanka, MZOS ) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb,
Prirodoslovno-matematički fakultet, Zagreb
Profili:
Kata Majerski (autor)
Srđanka Tomić-Pisarović (autor)
Ines Primožič (autor)
Marina Šekutor (autor)
Tomica Hrenar (autor)