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Ecdisterona de Pfaffia tuberosa (Spreng. ) Hicken / Ecdysterone from Pfaffia tuberosa (Spreng. ) Hicken
Nishimoto, Nobushigue; Shiobara, Yoshinori; Inoue, Shun-suke; Fujino, Masumi; Takemoto, Tsunematsu; Yeoh, Cheow Lin; Hashimoto, Goro.
Affiliation
  • Nishimoto, Nobushigue; Tokushima Bunri University. Faculty of Pharmaceutical Sciences. Ya­mashirocho. JP
  • Shiobara, Yoshinori; Tokushima Bunri University. Faculty of Pharmaceutical Sciences. Ya­mashirocho. JP
  • Inoue, Shun-suke; Tokushima Bunri University. Faculty of Pharmaceutical Sciences. Ya­mashirocho. JP
  • Fujino, Masumi; Tokushima Bunri University. Faculty of Pharmaceutical Sciences. Ya­mashirocho. JP
  • Takemoto, Tsunematsu; Tokushima Bunri University. Faculty of Pharmaceutical Sciences. Ya­mashirocho. JP
  • Yeoh, Cheow Lin; Japan Bio Institute Co., Ltd. Tokyo. JP
  • Hashimoto, Goro; Centro de Pesquisas de História Natural. São Paulo. BR
Rev. bras. farmacogn ; 1(2): 188-191, dez. 1986.
Article in Portuguese | LILACS | ID: lil-545556
Responsible library: BR1.1
RESUMO
As raízes secas da espécie brasileira Pfaffia tuberosa (Spreng.) Hicken foram submetidas a extração com metanol. Deste extrato metanólico foram isolados a ecdisterona e o ácido oleanólico, através de processos de separação por HPLC e cromatografia em coluna. Tanto a ecdisterona como o ácido oleanólico foram identificados comparativamenve com os respec­tivos padrões. Análise quantitativa por HPLC mostrou 0,23 por cento de ecdisterona. Este teor foi considerado baixo em relação a outra espécie, também brasileira, a Pfaffia iresinoides.
ABSTRACT
In this paper, we wish to report the isolation and identification of ecdysterone from Pfaffia tuberosa (Spreng.) Hicken. The roots of Pfaffia tuberosa (Spreng.) Hicken were colected in the Mato Grosso State - Brazil. The dried and sliced roots (197g) were extracted with hot MeOH. A suspension of the resulting MeOH extract in the water was treated with n-BuOH. The n-BuOH layer was concentrated in vacuo to give a brown viscous oil (5g), wich was chromatographed on silicagel (65g) using CHCl3 - MeOH - H2O (802010) lower phase, and 15ml fractions were collected. Fractions 11-13 were concentrated and the residual solid was recrystallized from EtOH to afford oleanolic acid (65mg). The crystalline residue obtained from fractions 44-56 was recrystallized from EtOAC-MeOH to give ecdysterone (87mg). Each compound was identified by direct comparison with an authentic sample. Further HPLC quantitative analysis showed lower content of ecdysterone (0,23 percent) compared with that of Pfaffia iresinoides Spreng.

Full text: Available Collection: International databases Database: LILACS Language: Portuguese Journal: Rev. bras. farmacogn Journal subject: Pharmacy Year: 1986 Document type: Article Affiliation country: Brazil / Japan Institution/Affiliation country: Centro de Pesquisas de História Natural/BR / Japan Bio Institute Co., Ltd/JP / Tokushima Bunri University/JP
Full text: Available Collection: International databases Database: LILACS Language: Portuguese Journal: Rev. bras. farmacogn Journal subject: Pharmacy Year: 1986 Document type: Article Affiliation country: Brazil / Japan Institution/Affiliation country: Centro de Pesquisas de História Natural/BR / Japan Bio Institute Co., Ltd/JP / Tokushima Bunri University/JP
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