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    • 1. 发明申请
    • Pyranopyranone derivatives as antimicrobial agents
    • US20110224170A1
    • 2011-09-15
    • US13028576
    • 2011-02-16
    • Barbara WagnerJanina PurschwitzKarin Bieler
    • Barbara WagnerJanina PurschwitzKarin Bieler
    • A61K31/366A61K31/695A01N43/90A01N55/10C07D493/04A61P31/00A01P1/00
    • A61K31/366A01N43/90A01N55/00C07D493/04C07D493/08C07D493/10C07D493/20C07F7/0812A01N2300/00
    • Disclosed is the use of pyranopyranone derivatives of formula wherein R1, R2, R3, R4 and R5 independently of one another are hydrogen; C1-C30alkyl, C2-C30alkenyl, or C3-C12cycloalkyl, which may be substituted by one or more E and/or interrupted by one or more D; C6-C20aryl, which may be substituted by one or more G; C4-C20heteroaryl, which may be substituted by one or more G, C2-C18alkenyl, C2-C18alkynyl, C7-C25aralkyl, or —CO—R6; —SiR8R9R10; or R4 and R5 together form a five or six membered ring; or R3 and R4 together form a five or six membered ring; D is —CO—; —COO—; —S—; —SO—; —SO2—; —O—; —NR7—; —SiR8R9—; —POR10—; —CR12═CR13—; or —C≡C—; and E is —OR6; —SR6; —NR14R15; —NR14COR15; —COR6; —COOR6; —CONR14R15; —CN; halogen; or OSO3R11; SO3R11; SO2R11; PO3(R11)2; OPO3(R11)2; G is E; C1-C18alkyl, which is optionally interrupted by D; C1-C18 perfluoroalkyl; C1-C18alkoxy, which is optionally substituted by E and/or interrupted by D; wherein R6 is H; C6-C18aryl which is optionally substituted by OH, C1-C30alkyl or C1-C30alkoxy; or C1-C30alkyl which is optionally interrupted by —O—; R7 is H; C6-C18aryl which is optionally substituted by OH, C1-C30alkyl or C1-C30alkoxy; or C1-C30alkyl which is optionally interrupted by —O—; R8, R9 and R10 independently of each other are hydrogen; C1-C30alkyl; C6-C18aryl which is optionally substituted by C1-C30alkyl; and R11 is hydrogen; C6-C18aryl, which is optionally substituted by OH, C1-C30alkyl or C1-C30alkoxy; or C1-C30alkyl, which is optionally interrupted by —O—; R12, R13, R14 and R15 independently of each other are hydrogen; C6-C18aryl which is optionally substituted by OH, C1-C30alkyl or C1-C30alkoxy; C1-C30alkyl, which is optionally interrupted by —O—; or R14 and R15 together form a five or six membered ring; as antimicrobial and/or preserving agents.
    • 2. 发明申请
    • ANTIMICROBIAL AMINO-SALICYLIC ACID DERIVATIVES
    • 抗微生物氨基磺酸衍生物
    • US20120189568A1
    • 2012-07-26
    • US13391671
    • 2010-08-13
    • Werner HölzlJanina Purschwitz
    • Werner HölzlJanina Purschwitz
    • A01N37/46A61P31/04A61K8/42A01P1/00A01P3/00A61L9/01A61K31/606A61P31/10
    • C11D3/48A61K8/42A61Q5/02A61Q11/02A61Q15/00A61Q17/005C11D3/32
    • Disclosed is a novel method for achieving an antimicrobial, preservative and/or microorganism adhesion inhibiting effect, for the protection within an article and/or material or on the surface of an article and/or material. The novel method comprises application of a salicylic compound of the formula (I) wherein one of A and A is a residue of the formula (I′): —NH—CO—R1 while the other is hydrogen; R1 is C1-C22alkyl, C3-C12cycloalkyl, C3-C12cycloalkyl interrupted by O and/or NR5, C4-C12aryl, C5-C18arylalkyl; R2 is OR3 or NHR4; R3 and R4 are selected from H, C1-C22alkyl, C3-C12cycloalkyl, C3-C12cycloalkyl interrupted by O and/or NR5, C4-C12aryl, C5-C18arylalkyl; R5 is H or C1-C8alkyl; wherein each aryl moiety is unsubstituted or substituted by C1-C4alkyl, C1-C4alkoxy, C1-C4acyl, C1-C4acyloxy, C1-C4acylamino, CF3, OH, amino, halogen; or an adduct or salt thereof; to said article and/or material.
    • 公开了一种用于在制品和/或材料内或制品和/或材料的表面上实现抗微生物,防腐和/或微生物粘附抑制作用的新颖方法。 该新方法包括施用式(I)的水杨酸化合物,其中A和A之一是式(I')的残基:-NH-CO-R 1,而另一个是氢; R1是C1-C22烷基,C3-C12环烷基,被O和/或NR5,C4-C12芳基,C5-C18芳烷基中断的C3-C12环烷基; R2是OR3或NHR4; R 3和R 4选自H,C 1 -C 22烷基,C 3 -C 12环烷基,被O和/或NR 5,C 4 -C 12芳基,C 5 -C 18芳烷基间隔的C 3 -C 12环烷基; R5是H或C1-C8烷基; 其中每个芳基部分是未取代的或被C 1 -C 4烷基,C 1 -C 4烷氧基,C 1 -C 4酰基,C 1 -C 4酰氧基,C 1 -C 4酰氨基,CF 3,OH,氨基,卤素取代。 或其加合物或其盐; 对所述物品和/或材料。