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TÜBİTAK

Journal

Diterpenoids

Publication Year

Articles 1 - 5 of 5

Full-Text Articles in Physical Sciences and Mathematics

New Antimicrobial Biscembrane Hydrocarbon And Cembranoid Diterpenes From The Soft Coral Sarcophyton Trocheliophorum, Muhammad Zubair, Walied Alarif, Khalid Al-Footy, Mohamed Ph, Magda Ali, Salim Basaif, Sultan Al-Lihaibi, Seif-Eldin Ayyad Jan 2016

New Antimicrobial Biscembrane Hydrocarbon And Cembranoid Diterpenes From The Soft Coral Sarcophyton Trocheliophorum, Muhammad Zubair, Walied Alarif, Khalid Al-Footy, Mohamed Ph, Magda Ali, Salim Basaif, Sultan Al-Lihaibi, Seif-Eldin Ayyad

Turkish Journal of Chemistry

A new tetracyclic biscembrane hydrocarbon, trocheliane (1), along with two new cembranoid diterpenes, sarcotrocheldiol A (2) and B (3), and the known diterpene cembrene-C (4), were isolated from the Red Sea soft coral Sarcophyton trocheliophorum. The structures and relative stereochemistry of the compounds were elucidated by interpretation of MS, 1 D NMR, and 2 D NMR experiments. The sensitivity of some pathogenic bacteria used as test organisms to the new compounds 1-3 was determined. 1 showed appreciable antimicrobial activity with the diameter of inhibition zones ranging from 11 to 18 mm. 1 was active against the two multidrug resistant bacteria …


Terpenic And Phenolic Compounds From Sideritis Stricta, F. Pinar Şahi̇n, Nurten Ezer, İhsan Çaliş Jan 2006

Terpenic And Phenolic Compounds From Sideritis Stricta, F. Pinar Şahi̇n, Nurten Ezer, İhsan Çaliş

Turkish Journal of Chemistry

From the overground parts of an endemic Sideritis species, S. stricta, 4 diterpenes, sideridiol (1), isosidol (2), isolinearol (3), and linearol (4); 2 flavonoid glycosides, isoscutellarein 7-O-[6'''-O-acetyl-\beta -D-allopyranosyl-(1 \to 2)]-\beta -D-glucopyranoside (5), and isoscutellarein 7-O-[6'''-O-acetyl-\beta -D-allopyranosyl-(1 \to 2)]-6''-O-acetyl-\beta -D-glucopyranoside (6); a methoxyflavone, xanthomicrol (7); and a phenylethanoid glycoside, verbascoside (=acteoside) (8) were isolated. The structures of the isolated compounds were established based on spectroscopic evidence (UV, IR, 1D- and 2D-NMR, MS).


Terpenoids And Steroids From The Roots Of Salvia Blepharochlaena, Ufuk Kolak, Gülaçti Topçu, Seher Bi̇rteksöz, Gülten Ötük, Ayhan Ulubelen Jan 2005

Terpenoids And Steroids From The Roots Of Salvia Blepharochlaena, Ufuk Kolak, Gülaçti Topçu, Seher Bi̇rteksöz, Gülten Ötük, Ayhan Ulubelen

Turkish Journal of Chemistry

From the roots of Salvia blepharochlaena Hedge and Hub. Mor. 4 triterpenoids, 4 steroids, 6 diterpenoids, and an aromatic ester were isolated. The structures of these compounds were established by spectroscopic methods. Formosanolide was isolated for the first time from the genus Salvia.


Kaurane Diterpenoids From Three Sideritis Species, Maurizio Bruno, Franco Piozzi, Nelly Apostolides Arnold, K. Hüsnü Can Başer, Nurhayat Tabanca, Neşe Kirimer Jan 2005

Kaurane Diterpenoids From Three Sideritis Species, Maurizio Bruno, Franco Piozzi, Nelly Apostolides Arnold, K. Hüsnü Can Başer, Nurhayat Tabanca, Neşe Kirimer

Turkish Journal of Chemistry

Some kaurane diterpenoids were isolated from 3 species of the genus Sideritis (Lamiaceae) growing in the Eastern Mediterranean region. Sideritis libanotica subsp. libanotica contained siderol 2 and sideridiol 3. Sideritis erythrantha var. erythrantha yielded sideridiol 3. Sideritis perfoliata gave siderol 2, sideridiol 3 and sideritriol 4. The products are known as they occur in another species of Sideritis growing in Italy and in other species growing also in Turkey. The products are isolated for the first time from these 3 species. The taxonomic significance of these results is discussed.


Diterpenes From Sideritis Sipylea And S. Dichotoma, Gülaçti Topçu, Ahmet C. Gören, Turgut Kiliç, Y. Kemal Yildiz, Gülendam Tümen Jan 2002

Diterpenes From Sideritis Sipylea And S. Dichotoma, Gülaçti Topçu, Ahmet C. Gören, Turgut Kiliç, Y. Kemal Yildiz, Gülendam Tümen

Turkish Journal of Chemistry

Two Sideritis species afforded eleven kaurene and one beyerene diterpenes. Structures of the compounds from Sideritis sipylea} were elucidated as linearol (1), 7-epicandicandiol (2), sideridiol (3), siderol (4), isolinearol (5), isosidol (6) and epoxyisolinearol (7). Linearol was treated with m -chloroperbenzoic to afford its analogues ent-3\beta ,7\alpha ,17-trihydroxy-18-acetoxykaur-15-ene (1a) and ent}-7\alpha ,17,18-trihydroxy-3\beta -acetoxykaur-15-ene (1b) as new compounds. From the second species, Sideritis dichotoma, the kaurenes sideridiol (3) siderol (4), ent-7\alpha ,18-dihydroxy-15\beta ,16\beta -epoxykaurane (8)}, ent}-7\alpha -acetoxy,18-hydroxy-15\beta ,16\beta -epoxykaurane (9), ent-7\alpha -acetoxy-15,18-dihydroxy-kaur-16-ene (10), ent-7\alpha ,15,18-trihydroxykaur-16-ene (11) and the beyerene ent-7\alpha ,18-dihydroxybeyer-15-ene (12) were isolated. Structural elucidation is based on NMR techniques …