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    • 5. 发明授权
    • Helium-neon excitable reticulocyte dyes derivable from halolepidines
    • 氙 - 氖可激发的网织红细胞染料衍生自卤代哌啶
    • US06495692B1
    • 2002-12-17
    • US08763022
    • 1996-12-10
    • Nai-Yi WangAlex W. C. Yem
    • Nai-Yi WangAlex W. C. Yem
    • C07D21700
    • G01N1/30C09B23/02Y10S436/80Y10T436/117497
    • A method for synthesizing dyes excitable by a helium-neon laser (excitable at 633 nm) from hololepidines, e. G., 7-halolepidine, which dyes are suitable for the detection and enumeration of reticulocytes in human blood samples. In another aspect, this invention provides a method for immunotyping phenocytes. The method is based on the phenomenon that when dyes of certain structure intercalate into DNA or RNA, the intensity of the dyes increases. The general structure of dyes suitable for use in this invention is shown below: wherein: R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R11, R12, R13, Y, and n are as defined in the specification.
    • 通过氦 - 氖激光(可在633nm激发的)从全萜类可兴奋的染料的方法, G.,7-卤代脒,这些染料适用于人血液样品中网织红细胞的检测和计数。 另一方面,本发明提供了一种用于免疫分型的肝细胞的方法。 该方法基于当某些结构的染料插入DNA或RNA时,染料的强度增加。适用于本发明的染料的一般结构如下所示:其中:R1,R2,R3,R4 ,R5,R6,R7,R8,R9,R10,R11,R12,R13,Y和n如说明书中所定义。
    • 7. 发明授权
    • Method of using phenyl-alkylene-2-pyridyl derivatives to increase
cardiac contractility in a mammal
    • 使用苯基 - 亚烷基-2-吡啶基衍生物增加哺乳动物心脏收缩力的方法
    • US4569941A
    • 1986-02-11
    • US692602
    • 1985-01-17
    • John T. SuhRack H. Chung, deceasedNai-Yi WangJeffrey N. Barton
    • John T. SuhRack H. Chung, deceasedNai-Yi WangJeffrey N. Barton
    • C07D207/08C07D211/22A61K31/445
    • C07D207/08C07D211/22
    • Compounds of the formulae: ##STR1## wherein, Z and Y are each alkylene or oxy-alkylene containing one to about five carbon atoms in the principal chain or said alkylene substituted with OH, alkanoyloxy, alkoxy, mercapto or alkylmercapto;each of R.sub.1, R.sub.2 and R.sub.3 is independently H, alkyl, aryl, halo, alkoxy, alkenyloxy, alkylsulfinyl, alkylsulfonyl, alkylmercapto, cyano, carboxy, carbalkoxy, carboxamido, sulfamoyl, trifluoromethyl, hydroxy, hydroxyalkyl, acyloxy, alkylamino, sulfonylamino, or acylamino; or R.sub.1 and R.sub.2, when taken together, form a methylenedioxy or --O--CO--O--;Ar is heteroaryl, cycloalkyl or ##STR2## wherein, R.sub.1, R.sub.2 and R.sub.3 are as hereindescribed; andR is H, alkyl, cycloalkyl, aryl, aralkyl, alkenyl, alkynyl, carboalkoxy, or CONR.sub.4 R.sub.5 wherein each of R.sub.4 and R.sub.5 is H or alkyl; wherein the total number of carbon atoms in each hydrocarbyl group is up to 10; and ##STR3## wherein, each of R.sub.1 and R.sub.2 is independently H, alkyl, aryl, halo, alkoxy, alkenyloxy, alkylsulfinyl, alkylsulfonyl, alkylmercapto, cyano, carboxy, carbalkoxy, carboxamido, sulfamoyl, trifluoromethyl, hydroxy, hydroxyalkyl, acyloxy, alkylamino, sulfonylamino, or acylamino; or R.sub.1 and R.sub.2, when taken together, form a methylenedioxy, or --O--CO--O--; R.sub.6 is H, alkyl, aryl, halo, alkoxy, alkenyloxy, alkylsulfonyl, alkylmercapto, cyano, carboxy, carbalkoxy, carboxamido, sulfamoyl, trifluoromethyl, hydroxy, hydroxyalkyl, acyloxy, alkylamino, sulfonylamino or acylamino; wherein the total number of carbon atoms in each hydrocarbyl group is up to 10; and acid addition salts thereof have selective cardiotonic, antihypertensive and antiallergic activity.
    • 下式的化合物:其中Z和Y分别是在主链中含有一至五个碳原子的亚烷基或氧代 - 亚烷基或被OH,烷酰氧基,烷氧基,巯基或烷基巯基取代的所述亚烷基; R 1,R 2和R 3各自独立地是H,烷基,芳基,卤素,烷氧基,烯氧基,烷基亚磺酰基,烷基磺酰基,烷基巯基,氰基,羧基,烷氧基,甲酰胺基,氨磺酰基,三氟甲基,羟基,羟基烷基,酰氧基,烷基氨基,磺酰基氨基或 酰氨基; 当R 1和R 2一起形成亚甲二氧基或-O-CO-O-时; Ar是杂芳基,环烷基或者其中R 1,R 2和R 3如以下所示: 并且R为H,烷基,环烷基,芳基,芳烷基,烯基,炔基,烷氧羰基或CONR4R5,其中R4和R5各自为H或烷基; 其中每个烃基中的碳原子总数最多为10; 其中,R1和R2各自独立地为H,烷基,芳基,卤素,烷氧基,烯氧基,烷基亚磺酰基,烷基磺酰基,烷基巯基,氰基,羧基,烷氧基,甲酰氨基,氨磺酰基,三氟甲基,羟基, ,酰氧基,烷基氨基,磺酰基氨基或酰基氨基; 当R 1和R 2一起形成亚甲二氧基或-O-CO-O-时; R 6是H,烷基,芳基,卤素,烷氧基,烯氧基,烷基磺酰基,烷基巯基,氰基,羧基,烷氧基,甲酰胺基,氨磺酰基,三氟甲基,羟基,羟基烷基,酰氧基,烷基氨基,磺酰基氨基或酰基氨基; 其中每个烃基中的碳原子总数最多为10; 其酸加成盐具有选择性强心药,抗高血压药和抗过敏活性。
    • 10. 发明授权
    • Method of hypertensive treatment using phenyl-alkylene-2-pyridyl
derivatives
    • 使用苯基 - 亚烷基-2-吡啶基衍生物的高血压治疗方法
    • US4632929A
    • 1986-12-30
    • US788175
    • 1985-09-23
    • John T. SuhRack H. Chung, deceasedNai-Yi WangJeffrey N. Barton
    • John T. SuhRack H. Chung, deceasedNai-Yi WangJeffrey N. Barton
    • C07D207/08C07D211/22A61K31/445
    • C07D207/08C07D211/22
    • Compounds of the formulae: ##STR1## wherein, Z and Y are each alkylene or oxy-alkylene containing one to about five carbon atoms in the principal chain or said alkylene substituted with OH, alkanoyloxy, alkoxy, mercapto or alkylmercapto;each of R.sub.1, R.sub.2 and R.sub.3 is independently H, alkyl, aryl, halo, alkoxy, alkenyloxy, alkylsulfinyl, alkylsulfonyl, alkylmercapto, cyano, carboxy, carbalkoxy, carboxamido, sulfamoyl, trifluoromethyl, hydroxy, hydroxyalkyl, acyloxy, alkylamino, sulfonylamino, or acylamino; or R.sub.1 and R.sub.2, when taken together, form a methylenedioxy or --O--CO--O--;Ar is heteroaryl, cycloalkyl or ##STR2## wherein, R.sub.1, R.sub.2 and R.sub.3 are as hereindescribed; and R is H, alkyl, cycloalkyl, aryl, aralkyl, alkenyl, alkynyl, carboalkoxy, or CONR.sub.4 R.sub.5 wherein each of R.sub.4 and R.sub.5 is H or alkyl; wherein the total number of carbon atoms in each hydrocarbyl group is up to 10; and ##STR3## wherein, each of R.sub.1 and R.sub.2 is independently H, alkyl, aryl, halo, alkoxy, alkenyloxy, alkylsulfinyl, alkylsulfonyl, alkylmercapto, cyano, carboxy, carbalkoxy, carboxamido, sulfamoyl, trifluoromethyl, hydroxy, hydroxyalkyl, acyloxy, alkylamino, sulfonylamino, or acylamino; or R.sub.1 and R.sub.2, when taken together, form a methylenedioxy, or --O--CO--O--; R.sub.6 is H, alkyl, aryl, halo, alkoxy, alkenyloxy, alkylsulfonyl, alkylmercapto, cyano, carboxy, carbalkoxy, carboxamido, sulfamoyl, trifluoromethyl, hydroxy, hydroxyalkyl, acyloxy, alkylamino, sulfonylamino or acylamino; wherein the total number of carbon atoms in each hydrocarbyl group is up to 10; and acid addition salts thereof have selective cardiotonic, antihypertensive and antiallergic activity.
    • 下式的化合物:其中Z和Y分别是在主链中含有一至五个碳原子的亚烷基或氧代 - 亚烷基或被OH,烷酰氧基,烷氧基,巯基或烷基巯基取代的所述亚烷基; R 1,R 2和R 3各自独立地是H,烷基,芳基,卤素,烷氧基,烯氧基,烷基亚磺酰基,烷基磺酰基,烷基巯基,氰基,羧基,烷氧基,甲酰胺基,氨磺酰基,三氟甲基,羟基,羟基烷基,酰氧基,烷基氨基,磺酰基氨基或 酰氨基; 当R 1和R 2一起形成亚甲二氧基或-O-CO-O-时; Ar是杂芳基,环烷基或者其中R 1,R 2和R 3如以下所示: 并且R为H,烷基,环烷基,芳基,芳烷基,烯基,炔基,烷氧羰基或CONR4R5,其中R4和R5各自为H或烷基; 其中每个烃基中的碳原子总数最多为10; 其中,R1和R2各自独立地为H,烷基,芳基,卤素,烷氧基,烯氧基,烷基亚磺酰基,烷基磺酰基,烷基巯基,氰基,羧基,烷氧基,甲酰氨基,氨磺酰基,三氟甲基,羟基, ,酰氧基,烷基氨基,磺酰基氨基或酰基氨基; 当R 1和R 2一起形成亚甲二氧基或-O-CO-O-时; R 6是H,烷基,芳基,卤素,烷氧基,烯氧基,烷基磺酰基,烷基巯基,氰基,羧基,烷氧基,甲酰胺基,氨磺酰基,三氟甲基,羟基,羟基烷基,酰氧基,烷基氨基,磺酰基氨基或酰基氨基; 其中每个烃基中的碳原子总数最多为10; 其酸加成盐具有选择性强心药,抗高血压药和抗过敏活性。