Amidines, preparation process and therapeutical application thereof
    1.
    发明授权
    Amidines, preparation process and therapeutical application thereof 失效
    脒,其制备方法及其治疗应用

    公开(公告)号:US4665085A

    公开(公告)日:1987-05-12

    申请号:US717185

    申请日:1985-03-12

    摘要: Compounds having the formula (I) wherein R.sub.1 and R.sub.2 are a hydrogen atom, an alkyl group or a hydroxy group, or else R.sub.1 and R.sub.2 form together a bivalent ethylene or trimethylene radical; R.sub.3 is a halogen atom, an alkyl group, an alkoxy group, a mono- or polyhydroxylated alkyl group, an amino group, a mono- or di-alkyl amino group, an acetamido or sulfonamido group; R.sub.1 is a hydroxy group, a mono- or polyhydroxylated alkyl group, an amino group, a mono- or dialkyl amino group, an acetamido or sulfonamido group; R.sub.4 being in the position 3, 4 or 5 and A is a bridge having from 1 to 3 links selected among the groups having the formula (II), --NH--,--N.dbd.--O-- and --S--. R.sub.5 represents an hydrogen atom, an alkyl group, a hydroxy group or an alkoxy group as well as the addition salts thereof with pharmaceutically acceptable acids. Said compound may be used in therapeutical treatment as antihypertensive agents, particularly in the ocular field. ##STR1##

    摘要翻译: PCT No.PCT / FR84 / 00170 Sec。 371日期1985年3月12日 102(e)1985年3月12日PCT PCT。1984年7月6日PCT公布。 公开号WO85 / 00366 1985年1月31日。具有式(I)的化合物,其中R 1和R 2是氢原子,烷基或羟基,或者R 1和R 2一起形成二价乙烯或三亚甲基; R3是卤素原子,烷基,烷氧基,单羟基或多羟基化烷基,氨基,一或二烷基氨基,乙酰氨基或亚磺酰氨基; R1是羟基,单羟基烷基或多羟基化烷基,氨基,一或二烷基氨基,乙酰氨基或亚磺酰氨基; R4为位置3,4或5,A为选自具有式(II)的基团,-NH - , - N = -O-和-S-的1至3个连接的桥。 R5表示氢原子,烷基,羟基或烷氧基,以及其与药学上可接受的酸的加成盐。 所述化合物可用作治疗性治疗作为抗高血压药,特别是在眼部。 (I)(II)

    Ready-to-use indomethacin-based eye lotion
    2.
    发明授权
    Ready-to-use indomethacin-based eye lotion 失效
    即食用基于吲哚美辛的眼液

    公开(公告)号:US5744154A

    公开(公告)日:1998-04-28

    申请号:US706268

    申请日:1996-09-04

    CPC分类号: A61K9/0048 A61K31/405

    摘要: The present invention relates to a ready-to-use indomethacin eye lotion comprising, in aqueous solution: indomethacin, a .beta.- or .gamma.-cyclodextrin etherified with C.sub.1 -C.sub.4 alkyl or C.sub.1 -C.sub.4 hydroxyalkyl groups, the cyclodextrin being present in a molar ratio with respect to the indomethacin of at least 10/1, and the pH of the solution being from 4.0 to 6.0.

    摘要翻译: 本发明涉及即用型吲哚美辛眼液,其包含在水溶液中:吲哚美辛,用C 1 -C 4烷基或C 1 -C 4羟烷基醚化的β-或γ-环糊精,所述环糊精以摩尔比 相对于吲哚美辛至少为10/1,溶液的pH为4.0-6.0。

    Pyrazolo-quinolines, compositions and pharmaceutical preparations
    5.
    发明授权
    Pyrazolo-quinolines, compositions and pharmaceutical preparations 失效
    吡唑并喹啉,组合物和药物制剂

    公开(公告)号:US4190661A

    公开(公告)日:1980-02-26

    申请号:US906410

    申请日:1978-05-16

    摘要: This invention relates to compounds having the formula: ##STR1## in which: R represents a C.sub.1-6 alkyl radical or a C.sub.1-6 alkenyl radical; A represents an indazol-2,3- or 4,5- or 6,7-diyl radical, which indazoldiyl radical may be substituted on the nitrogen atoms at 1- or 2-position with C.sub.1-6 alkyl or phenyl-(C.sub.1-6) alkyl radicals, and their salts with pharmaceutically acceptable bases.Said compounds are therapeutically useful as antibacterial agents.

    摘要翻译: 本发明涉及具有下式的化合物:其中:R表示C 1-6烷基或C 1-6烯基; A表示吲唑-2,3-或4,5-或6,7-二基,其吲哚二基可以在1-或2-位的氮原子上被C 1-6烷基或苯基 - (C1- 6)烷基,及其与药学上可接受的碱的盐。 所述化合物在治疗上用作抗菌剂。