Formulations containing cynara scolymus and phaseolus vulgaris extracts which are useful in the treatment of obesity
    31.
    发明公开
    Formulations containing cynara scolymus and phaseolus vulgaris extracts which are useful in the treatment of obesity 有权
    Formulierungen mit Extrakten aus Cynara scolymus und Phaseolus vulgaris zur Behandlung von Adipositas

    公开(公告)号:EP1967198A1

    公开(公告)日:2008-09-10

    申请号:EP07425132.3

    申请日:2007-03-07

    申请人: Indena S.p.A.

    摘要: The present invention relates to a Cynara scolymus extract with a high content of caffeoylquinic acids, and a composition containing said Cynara scolymus extract with a Phaseolus vulgaris extract.
    Said composition is useful in reducing obesity as it reduces cholesterol, triglycerides and blood glucose by sensitising the cells to insulin. This combination, when taken before meals, reduces the appetite, leading to a reduction in body weight. The extracts are preferably formulated in Oenothera biennis oil, fish oil, or oils rich in unsaturated ω-3 fatty acids.

    摘要翻译: 本发明涉及具有高含量咖啡酰奎宁酸的Cynara scolymus提取物,以及含有所述Cynara scolymus提取物与菜豆提取物的组合物。 所述组合物可用于减少肥胖症,因为其通过使细胞对胰岛素敏感而降低胆固醇,甘油三酯和血糖。 这种组合在饭前服用时会降低食欲,导致体重下降。 提取物优选配制在含有不饱和É-3脂肪酸的欧烯二酸油,鱼油或油中。

    Process for the preparation of a taxane derivative
    36.
    发明公开
    Process for the preparation of a taxane derivative 有权
    韦尔法罕zur Herstellung eines Taxanderivats

    公开(公告)号:EP1854799A1

    公开(公告)日:2007-11-14

    申请号:EP06009813.4

    申请日:2006-05-12

    申请人: INDENA S.p.A.

    CPC分类号: C07D493/10

    摘要: The invention relates to an improved process for the synthesis of 13-(N-Boc-β-isobutylserinyl)-14-β-hydroxybaccatin III-1,14-carbonate (I), wherein carbonation of the 1,14-hydroxy groups of the baccatin skeleton is carried out with bis(trichloromethylcarbonate and the 7-hydroxy group is protected with a trichloroacetyl group.

    摘要翻译: 本发明涉及13-(N-Boc-2-异丁基丝氨酰基)-14-羟基浆果赤霉素III-11,14-碳酸酯(I)的合成方法,其中1,14-羟基的碳酸化为 浆果赤霉素骨架用双(三氯甲基碳酸酯)和7-羟基用三氯乙酰基保护进行。

    Semisynthesis process for the preparation of 10-deacetyl-n-debenzoyl-paclitaxel
    40.
    发明公开
    Semisynthesis process for the preparation of 10-deacetyl-n-debenzoyl-paclitaxel 审中-公开
    用于制备10-脱乙酰-n-脱苯甲酰基 - 紫杉醇的半合成方法

    公开(公告)号:EP1712552A1

    公开(公告)日:2006-10-18

    申请号:EP05007888.0

    申请日:2005-04-11

    申请人: INDENA S.p.A.

    IPC分类号: C07D305/14

    CPC分类号: C07D305/14

    摘要: The invention relates to a process for the preparation of 10-deacetyl-N-debenzoyl-paclitaxel (I)

    a synthon useful for the preparation of taxanes with antitumour activity, and intermediates for the preparation thereof.
    The invention also discloses a process for the preparation of Docetaxel starting from said compound of formula (I).

    摘要翻译: 本发明涉及制备10-去乙酰基-N-脱苯甲酰基 - 紫杉醇(I)合成子的方法,该合成子可用于制备具有抗肿瘤活性的紫杉烷类化合物,以及用于其制备的中间体。 本发明还公开了从所述式(I)化合物开始制备多西紫杉醇的方法。