会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 4. 发明申请
    • ANTI-VIRAL CNIDARINS
    • 反传染媒介
    • US20160333060A1
    • 2016-11-17
    • US15110156
    • 2015-01-09
    • THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SER . . .
    • Barry R. O'KeefeJames B. McMahonKoreen RamessarChang-yun Xiong
    • C07K14/435C07K16/18A61K38/17
    • C07K14/43595A61K38/00A61K38/1767A61K48/00C07K14/435C07K16/18
    • An isolated and purified nucleic acid molecule that encodes a polypeptide comprising at least eight contiguous amino acids of SEQ ID NO: 1, 2, or 3, wherein the at least eight contiguous amino acids have anti-viral activity, as well as an isolated and purified nucleic acid molecule that encodes a polypeptide comprising at least eight contiguous amino acids of SEQ ID NO: 1, 2, or 3, wherein the at least eight contiguous amino acids have anti-viral activity, a vector comprising such an isolated and purified nucleic acid molecule, a host cell comprising the nucleic acid molecule, optionally in the form of a vector, a method of producing an antiviral polypeptide or conjugate thereof, the anti-viral polypeptide itself, a conjugate or fusion protein comprising the anti-viral polypeptide, and compositions comprising an effective amount of the anti-viral polypeptide or conjugate or fusion protein thereof. Further provided are methods of inhibiting prophylactically or therapeutically a viral infection of a host.
    • 分离和纯化的核酸分子,其编码包含SEQ ID NO:1,2或3的至少8个连续氨基酸的多肽,其中所述至少8个连续氨基酸具有抗病毒活性,以及​​分离和 纯化的核酸分子,其编码包含SEQ ID NO:1,2或3的至少8个连续氨基酸的多肽,其中所述至少8个连续氨基酸具有抗病毒活性,包含这种分离和纯化的核酸的载体 酸分子,包含核酸分子的宿主细胞,任选以载体的形式,产生抗病毒多肽或其缀合物的方法,抗病毒多肽本身,包含抗病毒多肽的缀合物或融合蛋白, 以及包含有效量的抗病毒多肽或其结合物或其融合蛋白的组合物。 还提供了预防性或治疗性地抑制宿主的病毒感染的方法。
    • 7. 发明申请
    • COMPOSITIONS AND METHODS TO TREAT CARDIAC DISEASES
    • 组合物和治疗心脏病的方法
    • US20150038463A1
    • 2015-02-05
    • US14338987
    • 2014-07-23
    • University of ConnecticutThe United States of America, as represented by the Secretary, Department of Health and Human Ser
    • Bruce LiangKenneth A. Jacobson
    • C07F9/6561
    • A61K31/675A61K31/683C07F9/65616
    • Phosphonate and phosphinate N-methanocarba derivatives of AMP including their prodrug analogs are described. MRS2339, a 2-chloro-AMP derivative containing a (N)-methanocarba(bicyclo[3.1.0]hexane) ring system in place of ribose, activates P2X receptors, ligand-gated ion channels. Phosphonate analogues of MRS2339 were synthesized using Michaelis-Arbuzov and Wittig reactions, based on the expectation of increased half-life in vivo due to the stability of the C—P bond. When administered to calsequestrin-overexpressing mice (a genetic model of heart failure) via a mini-osmotic pump (Alzet), some analogues significantly increased intact heart contractile function in vivo, as assessed by echocardiography-derived fractional shortening (FS) as compared to vehicle-infused mice. The range of carbocyclic nucleotide analogues for treatment of heart failure has been expanded.
    • 描述了膦酸盐和次膦酸盐,其包括其前体药物类似物的N-甲基碳酰胺衍生物。 含有(N) - 甲烷卡巴(双环[3.1.0]己烷)环体系的代替核糖的2-氯-AMP衍生物MRS2339激活P2X受体,配体门控离子通道。 基于由于C-P键的稳定性而增加的体内半衰期的期望,使用Michaelis-Arbuzov和Wittig反应合成MRS2339的膦酸酯类似物。 当通过小型渗透泵(Alzet)将氯雷斯特林过度表达的小鼠(心力衰竭的遗传模型)施用时,一些类似物显着增加体内完整的心脏收缩功能,如通过超声心动图来源的分数缩短(FS)评估的,与 车辆输注小鼠。 用于治疗心力衰竭的碳环核苷酸类似物的范围已经扩大。