Pentacyclic triterpene distribution in various plants - rich sources for a new group of multi-potent plant extracts.

نویسندگان

  • Sebastian Jäger
  • Holger Trojan
  • Thomas Kopp
  • Melanie N Laszczyk
  • Armin Scheffler
چکیده

Pentacyclic triterpenes are secondary plant metabolites widespread in fruit peel, leaves and stem bark. In particular the lupane-, oleanane-, and ursane triterpenes display various pharmacological effects while being devoid of prominent toxicity. Therefore, these triterpenes are promising leading compounds for the development of new multi-targeting bioactive agents. Screening of 39 plant materials identified triterpene rich (> 0.1% dry matter) plant parts. Plant materials with high triterpene concentrations were then used to obtain dry extracts by accelerated solvent extraction resulting in a triterpene content of 50 - 90%. Depending on the plant material, betulin (birch bark), betulinic acid (plane bark), oleanolic acid (olive leaves, olive pomace, mistletoe sprouts, clove flowers), ursolic acid (apple pomace) or an equal mixture of the three triterpene acids (rosemary leaves) are the main components of these dry extracts. They are quantitatively characterised plant extracts supplying a high concentration of actives and therefore can be used for development of phytopharmaceutical formulations.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Bioavailability and metabolism of maslinic acid, a natural pentacyclic triterpene

Maslinic acid is a pentacyclic triterpene found in plants used in traditional medicine with antidiabetic, antitumor, antioxidant and parasitostatic activities. A diet rich in foods of plant origin could provide a regular supply of this bioactive compound since it has been detected in olives, spinaches, eggplants, chickpeas and pomegranates. The multiple biological effects elicited by maslinic a...

متن کامل

Cytotoxic activity of ursolic acid derivatives obtained by isolation and oxidative derivatization.

Structure-activity relationships of ursane-type pentacyclic triterpenes obtained from natural sources and by chemical derivatization are reviewed. Ursolic acid, corosolic acid, and a new ursane-type pentacyclic triterpene, 7,24-dihydroxyursolic acid, were isolated from the methanolic extract of the leaves of the Bangladeshi medicinal plant, Saurauja roxburghii. Derivatization of ursolic acid by...

متن کامل

Pentacyclic Triterpene Bioavailability: An Overview of In Vitro and In Vivo Studies.

Pentacyclic triterpenes are naturally found in a great variety of fruits, vegetables and medicinal plants and are therefore part of the human diet. The beneficial health effects of edible and medicinal plants have partly been associated with their triterpene content, but the in vivo efficacy in humans depends on many factors, including absorption and metabolism. This review presents an overview...

متن کامل

Biosynthesis of p-Sitosterol and Pentacyclic Triterpenes of Salvia oficinaZk*

As Heftmann, Bennett, and Bonner have indicated (l), considerable information has accumulated concerning the biosynthesis of sterols in animals (2) and fungi (3), yet practically nothing is known about the biogenesis of typically higher plant sterols or the numerous pentacyclic triterpenes that are widely distributed throughout the plant kingdom. As yet, it cannot be assumed that the over-all b...

متن کامل

New Hopane Triterpene from Eleocharis sellowiana (Cyperaceae)

The genus Eleocharis R. Br. (Cyperaceae, Cyperoideae, Scirpeae) includes about 200 species, occurring in wet environments like swamps, lakes and rivers margins. Their aerial parts are formed by simple, not ramified stalks that end in a spiciform inflorescence formed by numerous very inconspicuous flowers. Their subterraneous parts are formed by roots and stem (called rhizome or stolon, dependin...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Molecules

دوره 14 6  شماره 

صفحات  -

تاریخ انتشار 2009