Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Nalan GÜNDOĞDU-KARABURUN"'
Autor:
Derya Osmani̇ye, Begüm Nurpelin Sağlik, Serkan Levent, Ulviye ACAR Çevi̇k, Sinem Ilgin, Leyla Yurttaş, Yusuf Özkay, Ahmet Cagri Karaburun, Zafer Asım Kaplancikli, Nalan Gundogdu-Karaburun
Publikováno v:
ACS Omega, Vol 9, Iss 10, Pp 11388-11397 (2024)
Externí odkaz:
https://doaj.org/article/d4a9628db6714277af3a724ab7e07d7a
Autor:
Shoruq Ahmed Naji, Begüm Nurpelin Sağlik, Mariangela Agamennone, Asaf Evrim Evren, Nalan Gundogdu-Karaburun, Ahmet Çagrı Karaburun
Publikováno v:
ACS Omega, Vol 8, Iss 51, Pp 48884-48903 (2023)
Externí odkaz:
https://doaj.org/article/0a0c73bb2d754168ab55c25e59a8185b
Autor:
Gülhan TURAN-ZITOUNI, Zafer Asım KAPLANCIKLI, Ahmet ÖZDEMİR, Şeref DEMIRAYAK, Ümit UÇUCU, Asiye MERİÇ, Nalan GÜNDOĞDU-KARABURUN, Ahmet Çağrı KARABURUN, Yağmur TUNALI
Publikováno v:
Turkish Journal of Pharmaceutical Sciences, Vol 8, Iss 1, Pp 31-42 (2011)
Triazole derivatives are the major chemical group of antifungal azole derivatives. Nowadays, the most frequently used triazoles are fluconazole and itraconazole. They posses a broad spectrum of antifungal activity and reduced toxicity when compared w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::57ce4fbaa66adbe44b7c17652184d28a
http://www.turkjps.org/archives/archive-detail/article-preview/synthess-of-some-4-phenyl-cyclohexyl-5-l-phenoxyet/12466
http://www.turkjps.org/archives/archive-detail/article-preview/synthess-of-some-4-phenyl-cyclohexyl-5-l-phenoxyet/12466
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 56(4)
PubMed: 11421256
In this study, derivatives of 1-benzyl-2-substituted-4,5-diphenyl-1H-imidazole were synthesized and their analgesic activity assayed in two tests. 1,2,4,5-Tetrasubstituted imidazole compounds were obtained by the treatment of pu
In this study, derivatives of 1-benzyl-2-substituted-4,5-diphenyl-1H-imidazole were synthesized and their analgesic activity assayed in two tests. 1,2,4,5-Tetrasubstituted imidazole compounds were obtained by the treatment of pu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a73687831156148641b5fbf711b0ecb7
https://pubmed.ncbi.nlm.nih.gov/11421256
https://pubmed.ncbi.nlm.nih.gov/11421256
Autor:
Seref Demirayak, Leyla Yurttas, Nalan Gundogdu-Karaburun, Ahmet Cagri Karaburun, Ismail Kayagil
Publikováno v:
Saudi Pharmaceutical Journal, Vol 25, Iss 7, Pp 1063-1072 (2017)
The synthesis of 3-[3/4-(2-aryl-2-oxoethoxy)arylidene]chroman/thiochroman-4-one derivatives (1–34) and evaluation of their anticancer activities were aimed in this work. Final compounds were obtained in multistep synthesis reactions using phenol/th
Externí odkaz:
https://doaj.org/article/e3642fec8f414af9be05909b11903815