Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Ayse Hande Tarikogullari"'
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 32, Iss 1, Pp 13-19 (2017)
A series of 4-phthalimidobenzenesulfonamide derivatives were designed, synthesized and evaluated for the inhibitory activities against acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE). Structures of the title compounds were confirmed by
Externí odkaz:
https://doaj.org/article/4ea03bcd7b954ee28da24436fb4f7c31
Publikováno v:
Bioorganic and Medicinal Chemistry Reports. :1-5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9bc645e2cbf66bd5a8f1e216341d2f34
https://doi.org/10.25135/acg.bmcr.26.2111.2255
https://doi.org/10.25135/acg.bmcr.26.2111.2255
Autor:
Ayse Hande Tarikogullari, Ercin Erciyas, Sumru Sozer Karadagli, Ulrike Holzgrabe, Vildan Alptüzün, Sülünay Parlar, Gozde Sayar
Publikováno v:
Bioorganic Chemistry. 87:888-900
A group of N-benzylpiperidine-3/4-carbohydrazide-hydrazones were designed, synthesized and evaluated for acetylcholinesterase (AChE), butyrylcholinesterase (BuChE) activities, Aβ42 self-aggregation inhibitory potentials, and antioxidant capacities,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0395daac2e63e5dd7eb17d8a91be5d2e
https://doi.org/10.1016/j.bioorg.2018.11.051
https://doi.org/10.1016/j.bioorg.2018.11.051
Autor:
Petek Ballar Kirmizibayrak, Sirin Uysal, Merve Saylam, Zeynep Soyer, Sinem Yilmaz, Ayse Hande Tarikogullari
A series of novel 4-aminobenzensulfonamide/carboxamide derivatives bearing naphthoquinone pharmacophore were designed, sythesized and evaluated for their proteasome inhibitory and anti-proliferative activities against human breast cancer cell line (M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4ceea7676ef3cc921102a373ac35001
https://hdl.handle.net/11454/61492
https://hdl.handle.net/11454/61492
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 32, Iss 1, Pp 13-19 (2017)
Journal of Enzyme Inhibition and Medicinal Chemistry
Journal of Enzyme Inhibition and Medicinal Chemistry
WOS: 000392591100005
PubMed ID: 27766908
A series of 4-phthalimidobenzenesulfonamide derivatives were designed, synthesized and evaluated for the inhibitory activities against acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE). S
PubMed ID: 27766908
A series of 4-phthalimidobenzenesulfonamide derivatives were designed, synthesized and evaluated for the inhibitory activities against acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE). S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfd7c57c39c340bc6abaf17fa17ec34b
https://doaj.org/article/4ea03bcd7b954ee28da24436fb4f7c31
https://doaj.org/article/4ea03bcd7b954ee28da24436fb4f7c31
Autor:
Hasan Semih Güneş, Gunes Coban, Luca Carlino, Ayse Hande Tarikogullari, Sülünay Parlar, Görkem Sarıkaya, Vildan Alptüzün, Ayşe Selcen Alpan, Ercin Erciyas
Publikováno v:
Medicinal Chemistry Research. 25:2005-2014
A series of N-{2-[2-(1H-benzimidazole-2-yl)phenoxy]ethyl} substituted amine derivatives were synthesized and tested for their cholinesterase inhibitor activity. Acetylcholinesterase and butyrylcholinesterase inhibitor activities were evaluated in vit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9534471be6032022ae8855f8e818f699
https://doi.org/10.1007/s00044-016-1648-1
https://doi.org/10.1007/s00044-016-1648-1
Publikováno v:
Medicinal Chemistry Research. 22:4708-4714
Glycine is a major inhibitory neurotransmitter and recent studies have shown that certain lipophilic glycine derivatives demonstrate anticonvulsant activity in animal epilepsy models. On the other hand, anilide is another fruitful structure for desig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35cfb5939056d3e791a0f01f2af63729
https://doi.org/10.1007/s00044-013-0474-y
https://doi.org/10.1007/s00044-013-0474-y
Publikováno v:
Chemicalpharmaceutical bulletin. 64(9)
WOS: 000382352700006
PubMed ID: 27581632
A series of pyridinium salts bearing alkylphenyl groups at 1 position and hydrazone structure at 4 position of the pyridinium ring were synthesized and evaluated for the inhibition of both acetylchol
PubMed ID: 27581632
A series of pyridinium salts bearing alkylphenyl groups at 1 position and hydrazone structure at 4 position of the pyridinium ring were synthesized and evaluated for the inhibition of both acetylchol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a4be91a5ccfd00800a070ae67302c0b
https://pubmed.ncbi.nlm.nih.gov/27581632
https://pubmed.ncbi.nlm.nih.gov/27581632
Autor:
Ayse Hande Tarikogullari, Guliz Armagan, Vildan Alptüzün, Görkem Sarıkaya, Ayşe Selcen Alpan, Gunes Coban, Mumin Alper Erdogan, Sülünay Parlar
Publikováno v:
Archiv der Pharmazie. 351:1800076
This study indicates the synthesis, cholinesterase (ChE) inhibitory activity, and molecular modeling studies of 48 compounds as o- and p-(3-substitutedethoxyphenyl)-1H-benzimidazole derivatives. According to the ChE inhibitor activity results, genera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93f88e7209c4c3df610d5be996332430
https://doi.org/10.1002/ardp.201800076
https://doi.org/10.1002/ardp.201800076
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