Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Safiye Emirdağ Öztürk"'
Autor:
Mikako Fujita, Safiye Emirdağ Öztürk, Nurettin Yayli, Halil I. Ciftci, N. Gokce Ulusoy, Mustafa Can, Masami Otsuka, Doha El-Sayed Ellakwa, Howaida I. Abd-Alla, Taha F.S. Ali, Hiroshi Tateishi, Ece Sozer, Zeynep Ocak, Mohamed O. Radwan
Publikováno v:
Molecules
Molecules, Vol 24, Iss 19, p 3535 (2019)
Volume 24
Issue 19
Molecules, Vol 24, Iss 19, p 3535 (2019)
Volume 24
Issue 19
Fujita, Mikako/0000-0001-6705-4052; , Mohamed/0000-0002-9220-2659; Ali, Taha/0000-0002-8881-0408; Abd-Alla, Howaida I./0000-0001-9638-8481
WOS: 000496242300120
PubMed: 31574910
Imatinib, an Abelson (ABL) tyrosine kinase inhibitor, is a
WOS: 000496242300120
PubMed: 31574910
Imatinib, an Abelson (ABL) tyrosine kinase inhibitor, is a
Autor:
Taha F.S. Ali, Ryoko Koga, Mikako Fujita, Mohamed O. Radwan, Safiye Emirdağ Öztürk, Masami Otsuka, Halil I. Ciftci, Hiroshi Tateishi, Zeynep Ocak, Mustafa Can
Publikováno v:
Biologicalpharmaceutical bulletin. 41(4)
The discovery of the chimeric tyrosine kinase breakpoint cluster region kinase-Abelson kinase (BCR-ABL)-targeted drug imatinib conceptually changed the treatment of chronic myelogenous leukemia (CML). However, some CML patients show drug resistance t
Publikováno v:
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 141:300-306
A novel ligand, vicinal dioxime ligand (egonol-hydrazone glyoxime) (LH2) was synthesized and characterized using (1)H NMR, (13)C NMR, MS, AAS, infrared spectroscopy, and magnetic susceptibility measurements. Mononuclear nickel (II), copper (II) and c
Publikováno v:
Bioorganic Chemistry. 53:15-23
Gypsogenin ( L 1 ; 3 - hydroxy - 23 - oxoolean - 12 - en - 28 - oic acid ), a natural saponin, was isolated from the boiling water extract of Gypsophila arrostii roots. In addition, the derivatives gypsogenin thiosemicarbazone ( L 2 ; 23 - [(aminocar
Publikováno v:
Tetrahedron. 69:3664-3668
The laccase-catalyzed reaction of 3-tert-butyl-1H-pyrazol-5(4H)-one with a number of catechols and aerial oxygen as an oxidant selectively affords 4-substituted 3-tert-butyl-1H-pyrazol-5-ol derivatives with yields ranging from 77 to 99%.
Publikováno v:
Volume: 38, Issue: 3 168-178
Cumhuriyet Medical Journal
Cumhuriyet Medical Journal
Bu çalışmada; Styrax officinalis L. tohumlarından izole edilen egonolün, insan eritrositleri antioksidan savunma sistemi üzerine etkisinin araştırılması amaçlanmıştır. Yöntem: Egonolün deney ortamındaki son derişimleri 0.2, 0.4, 0.6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f7cc7935f4c133851abfe1839215f59
https://dergipark.org.tr/tr/pub/cmj/issue/25161/265800
https://dergipark.org.tr/tr/pub/cmj/issue/25161/265800
Publikováno v:
Bioorganic & Medicinal Chemistry. 16:4431-4437
Synthesis of egonol derivatives, 5-(3''-chloropropyl)-7-methoxy-2-(3',4'-methylenedioxyphenyl)benzofuran 1, 5-(3''-bromopropyl)-7-methoxy-2-(3',4'-methylenedioxyphenyl)benzofuran 2, 3-[2-(1,3-benzodioxol-5-yl)-7-methoxy-1-benzofuran-5-yl]propanal 3,
Autor:
Aysun Çapcı-Karagöz, Tamer Karayildirim, Ali Özmen, Esin Poyrazoğlu-Çoban, Safiye Emirdağ-Öztürk, Özgen Alankuş-Çalışkan
Publikováno v:
European journal of medicinal chemistry. 82
A series of gypsogenin ( 1 ) derivatives ( 1a – i ) was synthesized in good yields, and the derivatives’ structures were established using UV, IR, 1 H NMR, 13 C NMR, and LCMS spectroscopic data. Among the tested compounds, 1a , 1b , 1d , 1e , and
Autor:
Benjamin Mordmüller, Aysun Çapcı Karagöz, Safiye Emirdağ Öztürk, Tony Fröhlich, Christoph Reiter, Jana Held, Volker Klein, Maen Zeino, Katrin Viertel, Hüseyin Anil, Svetlana B. Tsogoeva, Thomas Efferth
Publikováno v:
European journal of medicinal chemistry. 75
Malaria and cancer cause the death of millions of people every year. To combat these two diseases, it is important that new pharmaceutically active compounds have the ability to overcome multidrug resistance in cancer and Plasmodium falciparum strain
Publikováno v:
Bioorganicmedicinal chemistry. 19(3)
Eighteen derivatives of egonol (A-R) were synthesized and evaluated for their antimicrobial activities against Staphylococcus aureus ATCC 29213, Bacillus subtilis ATCC 6633, Candida albicans ATCC 10231 and Escherichia coli ATCC 8739 microorganisms co