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    • 2. 发明申请
    • Heterocyclic boronic acid compounds
    • 杂环硼酸化合物
    • US20070060547A1
    • 2007-03-15
    • US10514575
    • 2004-11-12
    • David CampbellDavid WinnJuan Betancort
    • David CampbellDavid WinnJuan Betancort
    • C07F5/02A61K31/69
    • C07F5/025
    • Dipeptidyl peptidase IV (DPP-IV)-inhibiting compounds are provided that have formula I: wherein n is 1 to 3; X is CH2; S; O; CF2 or C(CH3)2; Z is H; halogen; hydroxyl; (C1-6)alkoxy; (C1-12)alkyl; (C3-12)cycloalkyl; phenyl; or heteroaryl; where the phenyl and heteroaryl groups are optionally mono- or independently plurisubstituted with R7; optionally, X together with an adjacent ring carbon and Z form a fused cyclopropyl; and optionally, one of the bonds in the ring containing X is a double bond; and CriRii, R1, R1, R3, R4 and R5 are as described herein. Methods for preparing these compounds, and methods for treating diabetes, especially Type II diabetes, and other related diseases are described using the compounds of formula I in pharmaceutical compositions which contain these compounds. Pharmaceutical compositions which contain combinations of these compounds with other antidiabetic agents are also described herein.
    • 提供二肽基肽酶IV(DPP-IV)抑制化合物,其具有式I:其中n为1至3; X是CH 2 2; S; O; CF 2或C(CH 3)2)2。 Z是H; 卤素; 羟; (C 1-6)烷氧基; (C 1-12)烷基; (C 3-12)环烷基; 苯基; 或杂芳基; 其中苯基和杂芳基任选被R7单取代或独立地被二取代; 任选地,X与相邻的环碳一起形成稠合的环丙基; 并且任选地,含有X的环中的一个键是双键; 和R i,R i,R i,R i,R i,R i,R i, R 4和R 5如本文所述。 使用含有这些化合物的药物组合物中的式I化合物来描述制备这些化合物的方法,以及治疗糖尿病,特别是II型糖尿病和其它相关疾病的方法。 含有这些化合物与其它抗糖尿病药物的组合的药物组合物也在本文中描述。
    • 4. 发明授权
    • Activity-based probes and methods of their preparation and use
    • 基于活性的探针及其制备和使用方法
    • US07923433B2
    • 2011-04-12
    • US10530646
    • 2003-10-08
    • David WinnDavid Alan Campbell
    • David WinnDavid Alan Campbell
    • A61K38/05
    • C07D311/90C07D311/82C12Q1/37
    • The present invention provides compositions and methods for assessing profiles of catalytically active enzymes in compositions containing a plurality of proteins. In preferred embodiments, the enzyme is a hydrolase, most preferably a cysteine protease. The methods described herein use activity based probes (“ABPs”) that have an affinity moiety for directing the binding of the ABP to one or more catalytically active target enzymes, a reactive group for forming a covalent bond at an active site of the target enzyme(s), and a TAG (e.g., a detectable label, preferably a fluorophore). One or more ABPs may be combined with a protein-containing sample under conditions for binding and reaction of the ABP(s) with target enzyme(s) that are present in the sample. The resulting products may then be used to assess the active enzyme profile of the sample, and can be correlated to the presence, amount, or activity of one or more target enzyme(s) present in the original complex protein mixture.
    • 本发明提供了用于在含有多种蛋白质的组合物中评估催化活性酶的谱的组合物和方法。 在优选的实施方案中,酶是水解酶,最优选半胱氨酸蛋白酶。 本文描述的方法使用具有亲和部分的活性基探针(“ABP”),该亲和部分用于引导ABP与一种或多种催化活性靶酶的结合,用于在靶酶的活性位点形成共价键的反应性基团 (例如,可检测标记,优选荧光团)。 可以在ABP与样品中存在的目标酶的结合和反应的条件下,将一种或多种ABP与含蛋白质的样品组合。 然后可以将所得产物用于评估样品的活性酶谱,并且可与存在于原始复合蛋白​​混合物中的一种或多种目标酶的存在,量或活性相关。