Zobrazeno 1 - 10
of 122
pro vyhledávání: '"Cavit Kazaz"'
Publikováno v:
Molecules, Vol 29, Iss 13, p 3017 (2024)
In this study, the isolation of compounds from the aerial parts of Morina persica L. and the antimicrobial, antioxidant and antityrosinase activities of various polarity extracts and isolated compounds were investigated. Column chromatography methods
Externí odkaz:
https://doaj.org/article/438159d582fc4378aa44b7a94d481ed1
Autor:
Demet Demirci Gültekin, Arif Daştan, Yavuz Taşkesenligil, Cavit Kazaz, Yunus Zorlu, Metin Balci
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 19, Iss 1, Pp 764-770 (2023)
Previously we reported on the bromination of endo-7-bromonorbornene at different temperatures yielding mixtures of addition products. The structural elucidations of the formed compounds were achieved by NMR spectroscopy. Particularly, the γ-gauche e
Externí odkaz:
https://doaj.org/article/1a3f061d12cf4d0982d634bdd733f1bf
Autor:
Benan Kalaycı, Nihal Şimşek Özek, Ferhunde Aysin, Hilal Özbek, Cavit Kazaz, Mehmet Önal, Zühal Güvenalp
Publikováno v:
Saudi Pharmaceutical Journal, Vol 31, Iss 8, Pp 101682- (2023)
Astragalus L. is a genus member of the Fabaceae family, representing about 3,000 species all over the world and 380 species in Turkey. Astragalus species have been used in traditional medicine for many years. Astragalus globosus Vahl, known as “top
Externí odkaz:
https://doaj.org/article/b7cbcf97f5ae4e51a499a2192e85c38e
Autor:
Esen Sezen Karaoglan, Yasin Bayir, Abdulmecit Albayrak, Erdem Toktay, Ufuk Ozgen, Cavit Kazaz
Publikováno v:
Eurasian Journal of Medicine, Vol 52, Iss 3, Pp 249-253 (2020)
Externí odkaz:
https://doaj.org/article/0731eddaed0d4356a60f02001a8a6d3b
Publikováno v:
Applied Sciences, Vol 13, Iss 3, p 1503 (2023)
In this study, we aimed to isolate compounds from Stachys lavandulifolia (Lamiaceae) by chromatographic methods and perform tyrosinase, acetylcholinesterase, butyrylcholinesterase enzyme-inhibition and antimicrobial activity studies of these compound
Externí odkaz:
https://doaj.org/article/dd9d9e9c7d794d90a87f644fc468bd71
Autor:
Songül Karakaya, Sefa Gözcü, Zühal Güvenalp, Hilal Özbek, Hafize Yuca, Benan Dursunoğlu, Cavit Kazaz, Ceyda Sibel Kılıç
Publikováno v:
Pharmaceutical Biology, Vol 56, Iss 1, Pp 18-24 (2018)
Context: Ferulago (Apiaceae) species have been used since ancient times for the treatment of intestinal worms, hemorrhoids, and as a tonic, digestive, aphrodisiac, or sedative, as well as in salads or as a spice due to their special odors. Objectives
Externí odkaz:
https://doaj.org/article/a9e8092ae6424ad88a445db6e73e3b0d
Autor:
Songül Karakaya, Hilal Özbek, Sefa Gözcü, Zühal Güvenalp, Hafize Yuca, Hayri Duman, Cavit Kazaz, Ceyda Sibel Kiliç
Publikováno v:
Bangladesh Journal of Pharmacology, Vol 13, Iss 1 (2018)
Eleven coumarins named osthole (1), imperatorin (2), bergapten (3), prantschimgin (4), grandivitinol (5), suberosin (6), xanthotoxin (7), felamidin (8), marmesin (9), umbelliferone (10), ulopterol (11), and a sterol mixture consisted of stigmasterol
Externí odkaz:
https://doaj.org/article/4d395db697894e7380557032fe53f529
Publikováno v:
Bangladesh Journal of Pharmacology, Vol 12, Iss 4 (2017)
Externí odkaz:
https://doaj.org/article/102dc0e213b74e8eb9e3a5f853ae02f8
Autor:
Mehmet Emin Topaloglu, Medine Gulluce, Oztekin Algul, Ebru Mete, Halise Inci Gul, Cavit Kazaz, Sinan Bilginer
Publikováno v:
Molecules, Vol 16, Iss 6, Pp 4660-4671 (2011)
The development of resistance to current antifungal therapeutics drives the search for new effective agents. The fact that several acetophenone-derived Mannich bases had shown remarkable antifungal activities in our previous studies led us to design
Externí odkaz:
https://doaj.org/article/7b16f98269464cfabff5a541995f5b66
Publikováno v:
Journal of the Serbian Chemical Society, Vol 75, Iss 12, Pp 1625-1635 (2010)
1-(3-Aminophenyl)-4-benzoyl-5-phenyl-1H-pyrazole-3-carboxylic acid (1) was synthesized according to the literature. 2-(3-Aminophenyl)-2,6-dihydro-3,4-diphenyl-7H-pyrazolo[3,4-d]pyridazin-7-one (5) was obtained by the cyclocondensation reaction of 1 w
Externí odkaz:
https://doaj.org/article/daf287e5dbdb4e559db1feeb70be63cc