Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Gunes Coban"'
Publikováno v:
Process Biochemistry. 116:49-59
Allium ampeloprasum L., elephant garlic, is a plant that is cultivated and notable for its usage for medical and nutritional purposes. From this point, the present work presents the phenolic profiles of methanol extracts from the flowers, leaves, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58acbb40cb534385a41311f4878e4e41
https://doi.org/10.1016/j.procbio.2022.03.002
https://doi.org/10.1016/j.procbio.2022.03.002
This study was aimed to develop novel compounds to combat antimicrobial resistance, which is one of the biggest threats to global health. For this purpose, compounds bearing triazolopyrimidinone ring and N-(methylnaphthalene)piperazine (NMP) hybrids
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8f5b4ef8c4a2c117706a23f9e51d64a
https://hdl.handle.net/11454/78354
https://hdl.handle.net/11454/78354
Autor:
Fadime Aydın Köse, Gunes Coban
Publikováno v:
Saudi Pharmaceutical Journal, Vol 27, Iss 7, Pp 952-967 (2019)
Saudi Pharmaceutical Journal : SPJ
Saudi Pharmaceutical Journal : SPJ
Aydin Kose, Fadime/0000-0001-5222-7555
WOS: 000498856700007
PubMed: 31997902
A series of novel 3,5-disubstituted indolin-2-ones were designed and synthesized as selective FGFR inhibitors. in the design process of 3,5-disubstituted indo
WOS: 000498856700007
PubMed: 31997902
A series of novel 3,5-disubstituted indolin-2-ones were designed and synthesized as selective FGFR inhibitors. in the design process of 3,5-disubstituted indo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::985fe86f5f3f25f141d21d7516d5edd3
http://www.sciencedirect.com/science/article/pii/S1319016419300982
http://www.sciencedirect.com/science/article/pii/S1319016419300982
Autor:
Gulsah Bayraktar, Ali Ahmet Kilimcioğlu, Hasan Akbaba, Huseyin Istanbullu, Bilge Debeleç Bütüner, İbrahim Çavuş, Ercin Erciyas, Gunes Coban, Ahmet Özbilgin, Vildan Alptüzün
A series of thiazolopyrimidine derivatives was designed and synthesized as aLeishmania majorpteridine reductase 1 (LmPTR1) enzyme inhibitor. TheirLmPTR1 inhibitor activities were evaluated using the enzyme produced byEscherichia coliin a recombinant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17c9faef18e6006989175189b33db0a8
http://hdl.handle.net/20.500.12481/11319
http://hdl.handle.net/20.500.12481/11319
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. 24:3710-3729
In this study, non-rigid analogs of thalidomide have been designed in order to develop potentially active, more effective and safer lead molecules for disorders caused or contributed by inflammation. Five different series of acylaminoacetamide compou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80f0d13f7db3b128e9af47276dc4ab4c
https://doi.org/10.1007/s00044-015-1419-4
https://doi.org/10.1007/s00044-015-1419-4
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
Publikováno v:
European Journal of Medicinal Chemistry. 44:2280-2285
Benzimidazoles are important compounds because of their antibacterial, antifungal, antimicrobial, antiprotozoal and antihelmintic activities. Some benzimidazole derivatives also interfere with the reactions of DNA topoisomerases, enzymes functioning
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ea8aff2969e219df6f80c248b718c39
https://doi.org/10.1016/j.ejmech.2008.06.018
https://doi.org/10.1016/j.ejmech.2008.06.018
Autor:
Guliz Armagan, Gunes Coban, Görkem Sarıkaya, Vildan Alptüzün, Ayşe Selcen Alpan, Sülünay Parlar
Publikováno v:
Archiv der Pharmazie. 350:e1600351
A series of Mannich bases of benzimidazole derivatives having a phenolic group were designed to assess their anticholinesterase and antioxidant activities. The acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) inhibitory activities were e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55c573d896bff11c4978db94c52d0520
https://doi.org/10.1002/ardp.201600351
https://doi.org/10.1002/ardp.201600351
Autor:
ISTANBULLU, Huseyin1 huseyin.istanbullu@ikc.edu.tr, BAYRAKTAR, Gulsah2, OZTURK, Ismail3, COBAN, Gunes2, SAYLAM, Merve1
Publikováno v:
Journal of Research in Pharmacy. 2022, Vol. 26 Issue 1, p231-242. 12p.