Method for synthesis of &agr;-sulfonamido amide, carboxylic acid and hydroxamic acid derivatives
    1.
    发明授权
    Method for synthesis of &agr;-sulfonamido amide, carboxylic acid and hydroxamic acid derivatives 失效
    α-亚磺酰氨基酰胺,羧酸和异羟肟酸衍生物的合成方法

    公开(公告)号:US06583318B2

    公开(公告)日:2003-06-24

    申请号:US10146713

    申请日:2002-05-15

    CPC classification number: C07C303/40 C07C311/19 C07C311/29

    Abstract: A method of synthesizing &agr;-sulfonamido amide, carboxylic acid or hydroxamic acid derivatives comprising providing a set of polymer-bound reactant(s) (sulfonamide, aldehyde or ketone, isocyanide or acid) to react with three sets of the other three reactants to form an array of polymer-bound &agr;-sulfonamido amide-type intermediates and use of such intermediates for the preparation of combinatorial libraries.

    Abstract translation: 一种合成α-亚磺酰氨基酰胺,羧酸或异羟肟酸衍生物的方法,包括提供一组聚合物结合的反应物(磺酰胺,醛或酮,异氰化物或酸)与三组其他三种反应物反应形成 聚合物结合的α-亚磺酰氨基酰胺型中间体阵列以及这种中间体用于制备组合文库的用途。

    Heterocycle derivatives as PPAR-gamma agonists
    9.
    发明授权
    Heterocycle derivatives as PPAR-gamma agonists 失效
    杂环衍生物作为PPAR-γ激动剂

    公开(公告)号:US06462046B2

    公开(公告)日:2002-10-08

    申请号:US09734458

    申请日:2000-12-11

    CPC classification number: C07D401/06 C07D241/04 C07D241/08 C07D405/12

    Abstract: Compounds having the structure are peroxisome proliferator-activated receptor-gamma (PPAR-gamma) selective agonists and as such are useful in the modulation of blood glucose and the increase of insulin sensitivity in mammals. This activity of the piperazine derivatives of the invention make them particularly useful in the treatment of those conditions selected from the group consisting of diabetes, atherosclerosis, hyperglycemia, hyperlipidemia, obesity, syndrome X, insulin resistance, hypertension, heart failure and cardiovascular disease in mammals.

    Abstract translation: 具有结构的化合物是过氧化物酶体增殖物激活受体-γ(PPAR-γ)选择性激动剂,因此可用于调节血糖和哺乳动物胰岛素敏感性的增加。 本发明的哌嗪衍生物的这种活性使得它们特别可用于治疗选自以下的那些病症:糖尿病,动脉粥样硬化,高血糖症,高脂血症,肥胖症,综合征X,胰岛素抵抗,高血压,心力衰竭和哺乳动物心血管疾病 。

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