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    • 3. 发明授权
    • Certain unsymmetrical quinolinyl ethers having anti-inflammatory and
anti-allergic activity
    • 某些具有抗炎和抗过敏活性的不对称喹啉基醚
    • US4794188A
    • 1988-12-27
    • US810868
    • 1985-12-19
    • John H. MusserUtpal R. Chakraborty
    • John H. MusserUtpal R. Chakraborty
    • C07C29/40C07C33/20C07C37/11C07C39/11C07C43/23C07C45/30C07C45/44C07C45/67C07C45/71C07C47/575C07C49/782C07C49/796C07C49/825C07C49/84C07C50/32C07C59/68C07C65/24C07C229/38C07D213/30C07D213/79C07D213/84C07D215/14C07D215/22C07D215/227C07D307/42C07D333/16C07D333/56C07D217/24
    • C07D213/30C07C229/38C07C255/00C07C29/40C07C309/00C07C37/20C07C41/30C07C45/305C07C45/44C07C45/673C07C45/71C07C47/575C07C49/782C07C49/796C07C49/825C07C49/84C07C50/32C07C59/68C07C65/24C07D213/79C07D213/84C07D215/14C07D215/227C07D307/42C07D333/16C07D333/56
    • Compounds of the formula:Ar.sub.1 -X-Ar-Z-(R).sub.n'and salts thereof, whereinAr.sub.1 is a nitrogen, sulfur or oxygen heterocyclic ring;Ar is a phenyl ring or a nitrogen, oxygen or sulfur heterocyclic ring;Ar and Ar.sub.1 may be fully substituted or less than fully substituted with H, CH.sub.3, lower alkyl, aryl, aralkyl, halo, hydroxy, lower alkoxy, CF.sub.3, carboxy, alkylcarboxy, arylcarboxy, alkylcarbalkoxy, alkanoyl, formyl, oxo, nitrilo, amino, aminoalkyl, alkylamine, carboxamide, aryloxy, nitro, sulfonyl, sulfonamide, thio, alkylthio, hydroxyalkyl or oxyalkylcarbalkoxy;X= ##STR1## of up to 2 carbon atoms in the principal chain and up to a total of 4 carbon atoms, ##STR2## Z is an alkylene chain containing up to 10 carbon atoms in the principal chain and a total of up to 12 carbon atoms and from 0 to 2 double bonds and the said alkylene chain may be attached to Ar through an oxygen, sulfur or amino nitrogen atom, and when n'=2, one of the R substituents may be halogen on an omega carbon of the alkylene chain Z;when n'=1, R is a substituent attached to one of the carbon atoms of Z selected from the group consisting of .dbd.O, OR.sub.3, SR.sub.3, N(R.sub.2).sub.2 and R.sub.1, --COR.sub.4 and when n'=2 one R is previously defined and the additional R is a substituent attached to one of the carbon atoms of Z selected from the group consisting of .dbd.O, OR.sub.3, SR.sub.3, N(R.sub.2).sub.2, --COR.sub.4, lactone and halo;R.sub.1 is H or CH.sub.3 ;R.sub.2 is H, lower alkyl, aryl or aralkyl;R.sub.3 is H, lower alkyl, lower alkanoyl, aryl, aralkyl or substituted aryl in which the substituent is halo, lower alkyl or lower alkoxy;R.sub.4 is OR.sub.2 or N(R.sub.2).sub.2 ;n=0 or 1;n'=1 to 7; andn"=0, 1 or 2.
    • 式:Ar1-X-Ar-Z-(R)n'的化合物及其盐,其中Ar 1是氮,硫或氧杂环; Ar是苯环或氮,氧或硫杂环; Ar和Ar 1可以被完全取代或少于完全被H,CH 3,低级烷基,芳基,芳烷基,卤素,羟基,低级烷氧基,CF 3,羧基,烷基羧基,芳基羧基,烷基烷氧基,烷酰基,甲酰基,氧代,次氮基,氨基 ,氨基烷基,烷基胺,甲酰胺,芳氧基,硝基,磺酰基,磺酰胺,硫代,烷硫基,羟基烷基或氧烷基碳烷氧基; 在主链中最多2个碳原子的X = ,最多总共4个碳原子,Z是在主链中含有至多10个碳原子的亚烷基链, 总共多达12个碳原子和0至2个双键,并且所述亚烷基链可以通过氧,硫或氨基氮原子连接到Ar上,当n'= 2时,R取代基之一可以是卤素 亚烷基链Z的ω碳; 当n'= 1时,R是与选自= O,OR 3,SR 3,N(R 2)2和R 1,-COR 4的Z的一个碳原子连接的取代基,当n'= 2时,R 并且附加的R是与选自= O,OR 3,SR 3,N(R 2)2,-COR 4,内酯和卤素的Z的一个碳原子连接的取代基。 R1是H或CH3; R2是H,低级烷基,芳基或芳烷基; R3是H,低级烷基,低级烷酰基,芳基,芳烷基或取代芳基,其中取代基是卤素,低级烷基或低级烷氧基; R4是OR2或N(R2)2; n = 0或1; n'= 1至7; 和n“= 0,1或2。
    • 7. 发明授权
    • Cell fixative and method of analyzing virally infected cells
    • 细胞固定剂和分析病毒感染细胞的方法
    • US5597688A
    • 1997-01-28
    • US467799
    • 1995-06-06
    • Mark C. ConnellyUtpal R. ChakrabortyHouston G. Brooks, Jr.
    • Mark C. ConnellyUtpal R. ChakrabortyHouston G. Brooks, Jr.
    • C12Q1/00G01N1/30G01N15/14G01N33/48G01N33/533G01N33/545G01N33/569C12Q1/70G01N33/53
    • G01N33/56988G01N1/30G01N33/56972G01N33/56983G01N2001/305Y10S435/975Y10S436/805Y10T436/10Y10T436/101666Y10T436/108331Y10T436/25
    • The present invention provides a novel cellular fixative composition and method of cellular fixing and cellular analysis wherein cells may be fixed for further analysis without destroying the cell's surface markers, cellular morphology, and the cell's light scattering properties. Treatment of cells with the fixative as described herein also allows antibodies or .other desired components to enter the cell through the cellular membrane, without allowing important contents of the cell to escape. As an added benefit, the fixative composition of the invention may also kill or at least inactivate or reduce the activity of deadly virus contained in the cell. In its broadest aspect, the presently claimed fixative composition comprises at least three components, and in more preferred embodiments, four components. In a particularly preferred embodiment, the fixative composition described herein comprises at least one compound suitable for increasing the permeability of a cellular membrane, at least one compound that facilitates transportation of components across cellular membranes, at least one detergent, and at least one compound having the structure:R.sub.1 R.sub.2 R.sub.3 R.sub.4 R.sub.5 --Ar--X
    • 本发明提供了一种新的细胞固定组合物和细胞固定和细胞分析方法,其中细胞可以固定用于进一步分析,而不破坏细胞的表面标志物,细胞形态和细胞的光散射性质。 用本文所述的固定剂处理细胞还允许抗体或其它所需组分通过细胞膜进入细胞,而不允许细胞的重要内容物逸出。 作为额外的益处,本发明的固定组合物还可以杀死或至少灭活或降低细胞中包含的致命病毒的活性。 在其最广泛的方面,目前要求的固定剂组合物包含至少三种组分,在更优选的实施方案中包含四种组分。 在一个特别优选的实施方案中,本文描述的固定剂组合物包含至少一种适合于增加细胞膜的渗透性的化合物,至少一种促进组分跨细胞膜运输的化合物,至少一种洗涤剂和至少一种具有 结构:R1R2R3R4R5-Ar-X