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Physical Sciences and Mathematics

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TÜBİTAK

2006

Lamiaceae

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Gc-Ms Analysis And Antibacterial Activity Of Cultivated Satureja Cuneifolia Ten. Essential Oil, Yüksel Kan, Uçkun Sai̇t Uçan, Murat Kartal, M. Levent Altun, Si̇nem Aslan, Esi̇n Sayar, Ti̇murhan Ceyhan Jan 2006

Gc-Ms Analysis And Antibacterial Activity Of Cultivated Satureja Cuneifolia Ten. Essential Oil, Yüksel Kan, Uçkun Sai̇t Uçan, Murat Kartal, M. Levent Altun, Si̇nem Aslan, Esi̇n Sayar, Ti̇murhan Ceyhan

Turkish Journal of Chemistry

The composition of the essential oil of Satureja cuneifolia Ten. cultivated in Konya, Turkey, was investigated by capillary GC-MS. The compounds were characterized by comparison with library searches. Six main compounds were identified. Carvacrol was the dominant component, comprising 59.28% of the essential oil. The oil also contained 15.72% thymol, 9.69% p-cymene, 4.16% \gamma -terpinene, 1.70% linalool and 1.25% borneol. The antibacterial activity of the essential oil of S. cuneifolia and its components was determined by a semiquantative disc-diffusion method, and the minimum inhibitory concentration (MIC) was determined based on a micro-well dilution method against strains of Pseudomonas aeruginosa, Bacillus …


Secondary Metabolites From Phlomis Syriaca And Their Antioxidant Activities, Ü. Şebnem Harput, İhsan Çaliş, İclal Saracoğlu, Ali̇ Arslan Dönmez, Akito Nagatsu Jan 2006

Secondary Metabolites From Phlomis Syriaca And Their Antioxidant Activities, Ü. Şebnem Harput, İhsan Çaliş, İclal Saracoğlu, Ali̇ Arslan Dönmez, Akito Nagatsu

Turkish Journal of Chemistry

An iridoid glucoside, lamiide (1); 4 phenylethanoid glycosides, acteoside (2), \beta-OH acteoside (3), leucosceptoside A (4) and samioside (5); a caffeic acid ester, chlorogenic acid (6); 2 flavone glucosides, luteolin-7-O-glucopyranoside (7) and chrysoeriol-7-O-glucopyranoside (8); and a flavanone aglycone, naringenin (9), were isolated from the aerial parts of Phlomis syriaca. The structures of the isolated compounds were elucidated by means of spectroscopic (UV, IR, 1D- and 2D-NMR, and FAB-MS) methods. Free radical scavenging activity of the isolated compounds was determined using the radical 2,2-diphenyl-1-picrylhydrazyl (DPPH), spectroscopically.


Iridoid, Flavonoid, And Phenylethanoid Glycosides From Wiedemannia Orientalis, Zühal Güvenalp, Hi̇lal Özbek, Türesi̇n Ünsalar, Cavi̇t Kazaz, L. Ömür Demi̇rezer Jan 2006

Iridoid, Flavonoid, And Phenylethanoid Glycosides From Wiedemannia Orientalis, Zühal Güvenalp, Hi̇lal Özbek, Türesi̇n Ünsalar, Cavi̇t Kazaz, L. Ömür Demi̇rezer

Turkish Journal of Chemistry

Five iridoid glycosides, lamiide, ipolamiide, ipolamiidoside, 6\beta-hydroxyipolamiide, and 5-hydroxy-8-epi-loganin; 5 flavonoid glycosides, apigenin 7-O-\beta-glucopyranoside, luteolin 5-O-\beta- glucopyranoside, isorhamnetin 3-O-rutinoside, quercetin 3-O-rutinoside, and apigenin 7-O-(6''-O-trans-p-coumaroyl) \beta-glucopyranoside; and a phenylethanoid glycoside, acteoside (= verbascoside), were isolated from the aerial parts of Wiedemannia orientalis (Lamiaceae). Their structures were identified using spectral methods (UV, 1D- and 2D-NMR, and EI-MS).