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1Author    M. Manzoor-I-Khuda, Gerhard HabermehlRequires cookie*
 Title    Chemical Constituents of Cor chorus capsularis and C.olitorius (Jute Plant), Part IV* Isolation of Corosolic Acid, Ursolic Acid and corosin and Correlation of Corosin with Tormentic Acid  
 Abstract    Three triterpenoids have for the first time been isolated from fresh undried jute root, ursolic acid as its acetate, corosolic acid as its acetate and indicated to be urs-2a,2/?-diol-12-en-28-oic-acid and oxo-corosin isolated as its acetate-methyl-ester, C36H54O10, m.p. 160 °C, aD-15° (c 0.435%). The 24-carboxyl in corosin-anhydro-lactone-acetate has been reduced to the methyl group and the resultant lactone on acetylation indicated to be identical with tormentic acid lactone acetate. 
  Reference    Z. Naturforsch. 34b, 1320—1325 (1979); received May 14 1979 
  Published    1979 
  Keywords    Triterpenoids, Jute Root, Corchorus capsularis, Corchorus olitorius 
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 TEI-XML for    default:Reihe_B/34/ZNB-1979-34b-1320.pdf 
 Identifier    ZNB-1979-34b-1320 
 Volume    34 
2Author    Z. Afar Iqbalc, H.E JRequires cookie*
 Title    Isoperadione: A New Triterpenoid from Salvia bucharica  
 Abstract    V iqar U d d in A h m a d 3 *, M uham m ad Z ah id c, M uham m ad Shaiq A li3, Z ulfiqar A li3, N aseer A lam 3, R asool B akhsh T areenb, M uham m ad A new isomer of peradione (2) named as isoperadione (1) has been isolated along with peradione (2) and perovskone (3) from the hexane soluble part of Salvia bucharica. The structures of 1 -3 were elucidated with the aid of modern spectroscopic techniques. 
  Reference    Z. Naturforsch. 54b, 415—418 (1999); received September 8 1998 
  Published    1999 
  Keywords    Salvia bucharica, Lamiaceae, Triterpenoids, Isoperadione, NMR Data 
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 TEI-XML for    default:Reihe_B/54/ZNB-1999-54b-0415.pdf 
 Identifier    ZNB-1999-54b-0415 
 Volume    54 
3Author    A. M. Rizk, A. M. Youssef, M. A. Diab, H. M. SalemRequires cookie*
 Title    Triterpenoids and Related Substances of Euphorbia paralias  
 Abstract    The study of the triterpenoids and their related substances of E uphorbia paralias resulted in isolation of ursolic acid, cycloartenol, 24-methylenecycloartenol, uvaol, a hydrocarbon fraction (/1-C29 71-C35), alcohol fraction (hexacosanol and octacosanol) and a sterol fraction (/?-sitosterol, stigmasterol, campesterol and cholesterol). Constituents of Egyptian Euphorbiaceae, I 
  Reference    (Z. Naturforsch. 29c, 529 [1974]; received June 10 1974) 
  Published    1974 
  Keywords    E uphorbia paralias, Triterpenoids, Sterols, Alcohols, ra-Alkanes 
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 TEI-XML for    default:Reihe_C/29/ZNC-1974-29c-0529.pdf 
 Identifier    ZNC-1974-29c-0529 
 Volume    29 
4Author    Jürgen Lücke, MohammadAttaulah Khan, Wolfgang VoelterRequires cookie*
 Title    Isolation and Structure Identification of a Triterpenoid with a Cyclopropane Moiety from Euphorbia lactae  
 Abstract    4-Methylcyclo-art-22-ene-3,25-diol was isolated from Euphorbia lactae and its structure identified by elemental analysis, mass spectrometry and proton NMR spectroscopy. 
  Reference    Z. Naturforsch. 40b, 702—703 (1985); eingegangen am 9. August 1984 
  Published    1985 
  Keywords    Triterpenoids, Cycloartenols, Cyclopropane-Containing Triterpenoid, 4-Methylcycloart-22-ene-3, 25-diol 
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 TEI-XML for    default:Reihe_B/40/ZNB-1985-40b-0702_n.pdf 
 Identifier    ZNB-1985-40b-0702_n 
 Volume    40 
5Author    GerardJ. Niem, WimJ. Baas, Elisabeth Besson, JeanC. HopinRequires cookie*
 Title    Investigations on Hoya Species. III. Leaf Phenolics and Latex Lipids of Hoya lacunosa Bl.  
 Abstract    Hoya lacunosa leaves contain some main C-glycosylflavonoids, which were identified as: 6-C-arabinosyl 8-C-glucosylapigenin (isoschaftoside), 6-C-glucosyl 8-C-arabinosylapigenin (schaftosi-de) and 6,8-di-C-arabinosylapigenin. In the latex triterpenols were found, often both free and in ester form, of which /?-amyrin, a-amyrin, lupeol, 24-methylenecycloartanol, obtusifoliol and cyclo-eucalenol were identified in the free alcohol fraction. The esters, forming the m ajor part o f the to­ tal lipid fraction, were solely acetates o f some of the above mentioned alcohols. 
  Reference    Z. Naturforsch. 34c, 1125—1128 (1979); received August 31 1979 
  Published    1979 
  Keywords    Hoya lacunosa, Asclepiadaceae, C-Glycosylflavonoids, Latex, Triterpenoids, 4-ar-Methylsterols 
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 TEI-XML for    default:Reihe_C/34/ZNC-1979-34c-1125.pdf 
 Identifier    ZNC-1979-34c-1125 
 Volume    34 
6Author    F. Ran, Z-Jo Sef, M. Arner, BiancaK. ErpRequires cookie*
 Title    Composition of Iridals, Unusual Triterpenoids from Sword-Lilies, and the Seasonal Dependence of Their Content in Various Parts of Different Iris Species  
 Abstract    The com position o f iridals, new triterpenoids from sword-lilies, and their fatty acid esters in roots, rhizomes and leaves o f I. germ anica Linn., I. pseudacorus Linn, and two different varie­ ties o f I. pallida Lam. was determined. Quantitative analysis o f their total content in the var­ ious parts o f the plants in the course o f the year showed specific seasonal changes in rhizomes and leaves. Based on these results the possible significance o f these com pounds for the plants is discussed. 
  Reference    Z. Naturforsch. 47c, 21 (1992); received M ay 21/August 29 1991 
  Published    1992 
  Keywords    Iridals, Triterpenoids, Iris pallida Lam, Iris germ anica Linn, Iris pseudacorus Linn 
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 TEI-XML for    default:Reihe_C/47/ZNC-1992-47c-0021.pdf 
 Identifier    ZNC-1992-47c-0021 
 Volume    47 
7Author    ViqarUddin Ahmad, Q. Najmus-Saqib, K. Usmanghani, W. Fuchs, W. VoelterRequires cookie*
 Title    New Triterpenoid from Primula denticulata  
 Abstract    From the alcoholic extract of the plant Primula denticulata four main compounds could be isolated by column chromatography: Pri-dentigenin A, B, C and D. Several spectroscopic methods and the synthesis of several derivatives allow to determine the structure of Pridenti-genin B. 
  Reference    Z. Naturforsch. 35b, 511—512 (1980); eingegangen am 27. Dezember 1979 
  Published    1980 
  Keywords    Triterpenoids, Primula denticulata, Structure Elucidation, X H NMR Spectra, 13 C NMR Spectra 
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 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0511_n.pdf 
 Identifier    ZNB-1980-35b-0511_n 
 Volume    35 
8Author    Christine Kamperdick3, Günter Adam3, NguyenHong Vanb, TranVan SungbRequires cookie*
 Title    Chemical Constituents of Madhuca pasquiery  
 Abstract    Four triterpenoids, the scarce nortriterpenoid platanic acid, two flavonoids and 2,4-dihy-droxy phenylacetic acid methyl ester, hitherto unknown as a natural product, were isolated from Madhuca pasquiery. The structures were established by means of mass and NMR spectroscopy. 
  Reference    Z. Naturforsch. 52c, 295 (1997); received D ecem ber 12 1996/February 12 1997 
  Published    1997 
  Keywords    Madhuca pasquiery, 2, 4-Dihydroxy Phenylacetic Acid Methyl E ster, Platanic Acid, Triterpenoids, Flavonoids 
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 TEI-XML for    default:Reihe_C/52/ZNC-1997-52c-0295.pdf 
 Identifier    ZNC-1997-52c-0295 
 Volume    52