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Pregled bibliografske jedinice broj: 954584

4-aminoquinilines as reversible inhibitors of human cholinesterase activity


Bosak, Anita; Opsenica, Dejan M.; Šinko, Goran; Zlatar, Matija; Kovarik, Zrinka
4-aminoquinilines as reversible inhibitors of human cholinesterase activity // Programme and Abstract Book, Military Medical Science Letters - Special Issue on the occasion of the 13th International Meeting on Cholinesterases and the 7th International Conference on Paraoxonases, Hradec Králové, Republika Češka, 2018 / Korábečný, Jan ; Soukup, Ondrej (ur.).
Hradec Kralove: University of Defence, Faculty of Military Health Sciences, Czech Republic, 2018. str. 73-73 (poster, međunarodna recenzija, sažetak, znanstveni)


CROSBI ID: 954584 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
4-aminoquinilines as reversible inhibitors of human cholinesterase activity

Autori
Bosak, Anita ; Opsenica, Dejan M. ; Šinko, Goran ; Zlatar, Matija ; Kovarik, Zrinka

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni

Izvornik
Programme and Abstract Book, Military Medical Science Letters - Special Issue on the occasion of the 13th International Meeting on Cholinesterases and the 7th International Conference on Paraoxonases, Hradec Králové, Republika Češka, 2018 / Korábečný, Jan ; Soukup, Ondrej - Hradec Kralove : University of Defence, Faculty of Military Health Sciences, Czech Republic, 2018, 73-73

Skup
13th International Meeting on Cholinesterases ; 7th International Conference on Paraoxonases

Mjesto i datum
Hradec Králové, Češka Republika, 09.09.2018. - 14.09.2018

Vrsta sudjelovanja
Poster

Vrsta recenzije
Međunarodna recenzija

Ključne riječi
acetylcholinesterase, butyrylcholinesterase, treatment, 4-aminoquinoline, Alzheimer’s disease

Sažetak
We synthesised eight derivatives of 4-aminoquinolines differing in the substituents attached to the C(4)-amino group and C(7) carbon of 4-aminoquinoline, and tested their potency to inhibit human AChE and BChE. All of the compounds reversibly inhibited both enzymes with dissociation inhibition (Ki) constants from 0.50 to 50 µM exhibiting selectivity. In other words, for all compounds, AChE exhibited higher affinity than BChE. The most potent inhibitors of AChE were compounds with an octyl chain or adamantane, regardless of the group in position C(7). The shortening of the chain length caused the AChE inhibition decrease by 5-20 times. Docking studies made it clear that the high AChE affinity resulted from simultaneous interactions of the quinoline group with aromatic residues of both the catalytic active site and the peripheral site. In conclusion, the inhibition potency and selectivity classify several novel compounds as leads for further modification and optimization towards the development of new inhibitors of AChE and potential drugs for treatment of neurodegenerative diseases. Key words: acetylcholinesterase, butyrylcholinesterase, treatment, 4-aminoquinoline, Alzheimer’s disease Acknowledgment: this study was financed by the Croatian Science Foundation (Grant. No. 4307) and Ministry of Science and Technological Development of Serbia (Grants no. 172008 and 172035)

Izvorni jezik
Engleski

Znanstvena područja
Kemija, Javno zdravstvo i zdravstvena zaštita, Farmacija, Biotehnologija u biomedicini (prirodno područje, biomedicina i zdravstvo, biotehničko područje)

Napomena
This study was financed by the Croatian Science Foundation (Grant. No. 4307) and Ministry of Science and Technological Development of Serbia (Grants no. 172008 and 172035)



POVEZANOST RADA


Projekti:
HRZZ-IP-2013-11-4307 - Dizajn, sinteza i evaluacija novih protuotrova kod trovanja živčanim bojnim otrovima i pesticidima (CHOLINESTERASE) (Kovarik, Zrinka, HRZZ - 2013-11) ( CroRIS)

Ustanove:
Institut za medicinska istraživanja i medicinu rada, Zagreb

Profili:

Avatar Url Zrinka Kovarik (autor)

Avatar Url Goran Šinko (autor)

Avatar Url Anita Bosak (autor)

Citiraj ovu publikaciju:

Bosak, Anita; Opsenica, Dejan M.; Šinko, Goran; Zlatar, Matija; Kovarik, Zrinka
4-aminoquinilines as reversible inhibitors of human cholinesterase activity // Programme and Abstract Book, Military Medical Science Letters - Special Issue on the occasion of the 13th International Meeting on Cholinesterases and the 7th International Conference on Paraoxonases, Hradec Králové, Republika Češka, 2018 / Korábečný, Jan ; Soukup, Ondrej (ur.).
Hradec Kralove: University of Defence, Faculty of Military Health Sciences, Czech Republic, 2018. str. 73-73 (poster, međunarodna recenzija, sažetak, znanstveni)
Bosak, A., Opsenica, D., Šinko, G., Zlatar, M. & Kovarik, Z. (2018) 4-aminoquinilines as reversible inhibitors of human cholinesterase activity. U: Korábečný, J. & Soukup, O. (ur.)Programme and Abstract Book, Military Medical Science Letters - Special Issue on the occasion of the 13th International Meeting on Cholinesterases and the 7th International Conference on Paraoxonases, Hradec Králové, Republika Češka, 2018.
@article{article, author = {Bosak, Anita and Opsenica, Dejan M. and \v{S}inko, Goran and Zlatar, Matija and Kovarik, Zrinka}, year = {2018}, pages = {73-73}, keywords = {acetylcholinesterase, butyrylcholinesterase, treatment, 4-aminoquinoline, Alzheimer’s disease}, title = {4-aminoquinilines as reversible inhibitors of human cholinesterase activity}, keyword = {acetylcholinesterase, butyrylcholinesterase, treatment, 4-aminoquinoline, Alzheimer’s disease}, publisher = {University of Defence, Faculty of Military Health Sciences, Czech Republic}, publisherplace = {Hradec Kr\'{a}lov\'{e}, \v{C}e\v{s}ka Republika} }
@article{article, author = {Bosak, Anita and Opsenica, Dejan M. and \v{S}inko, Goran and Zlatar, Matija and Kovarik, Zrinka}, year = {2018}, pages = {73-73}, keywords = {acetylcholinesterase, butyrylcholinesterase, treatment, 4-aminoquinoline, Alzheimer’s disease}, title = {4-aminoquinilines as reversible inhibitors of human cholinesterase activity}, keyword = {acetylcholinesterase, butyrylcholinesterase, treatment, 4-aminoquinoline, Alzheimer’s disease}, publisher = {University of Defence, Faculty of Military Health Sciences, Czech Republic}, publisherplace = {Hradec Kr\'{a}lov\'{e}, \v{C}e\v{s}ka Republika} }




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