首页> 外国专利> PREVENTION AND TREATMENT OF A PULMONARY BACTERIAL INFECTION OR A SYMPTOMATIC PULMONARY EXPOSURE TO ENDOTOXIN BY INHALATION OF ANTIENDOTOXINIC PHARMACOS.

PREVENTION AND TREATMENT OF A PULMONARY BACTERIAL INFECTION OR A SYMPTOMATIC PULMONARY EXPOSURE TO ENDOTOXIN BY INHALATION OF ANTIENDOTOXINIC PHARMACOS.

机译:吸入抗毒素药可预防和治疗肺内细菌感染或有症状的内毒素性肺暴露。

摘要

Use of an antiendotoxin compound for the preparation of a pharmaceutical composition intended for the prevention and treatment of pulmonary bacterial infection or symptomatic pulmonary exposure to endotoxin, in a patient, wherein said pharmaceutical composition is administered to said patient by inhalation, in wherein said antiendotoxin compound is a Lipid A analogue, and wherein said Lipid A analogue has the formula: wherein R1 is selected from the group consisting of each one of J, K and Q, independently, it is linear or branched C1 to C15 alkyl; L is O, NH, or CH2; M is O or NH; and G is NH, O, S, SO, or SO2; R2 is linear or branched C5 to C15 alkyl; R3 is selected from the group consisting of linear or branched C5 to C18 alkyl, and in which E is NH, O, S, SO, or SO2; each of A, B and D, independently, is linear or branched C1 to C15 alkyl; R4 is selected from the group consisting of C4 to C20 linear or branched alkyl, and in which each of U and V, independently, is linear or branched C2 to C15 alkyl, and W is hydrogen or C1 to C alkyl C5 linear or branched; RA is R5 or R5-O-CH2-, R5 being selected from the group consisting of hydrogen, J¿, -J¿-OH, -J¿-OK¿, -J¿-OK¿-OH, and ¿J ¿-O-PO (OH) 2, in which each of J¿ and K¿, independently, is C1 to C5 alkyl linear or branched; R6 is selected from the group consisting of hydroxy, halogen, C1 to C5 alkoxy, and C1 to C5 acyloxy; A1 and A2, independently, are selected from the group consisting of OH, in which Z is linear or branched C1 to C10 alkyl; or pharmaceutically acceptable salts thereof.
机译:抗内毒素化合物在制备用于预防和治疗患者的肺细菌感染或有症状的肺内毒素的药物组合物中的用途,其中所述药物组合物通过吸入给予所述患者,其中所述抗内毒素化合物R 1是脂质A类似物,并且其中所述脂质A类似物具有下式:其中R 1选自J,K和Q中的每一个,独立地是直链或支链的C 1 -C 15烷基; L为O,NH或CH 2; M为O或NH; G为NH,O,S,SO或SO 2; R2为直链或支链的C5至C15烷基; R3选自由直链或支链的C5至C18烷基组成的组,并且其中E为NH,O,S,SO或SO2; A,B和D各自独立地为直链或支链的C1至C15烷基; R4选自由C4至C20的直链或支链的烷基组成的组,其中U和V各自独立地为直链或支链的C2至C15的烷基,并且W为氢或C1至C6的直链或支链的烷基; RA是R5或R5-O-CH2-,R5选自氢,J¿,-J¿-OH,-J¿-OK¿,-J¿-OK¿-OH和¿J¿ -O-PO(OH)2,其中,J′和K′各自独立地为直链或支链的C1至C5烷基; R6选自羟基,卤素,C1-C5烷氧基和C1-C5酰氧基。 A1和A2独立地选自OH,其中Z是直链或支链的C1-C10烷基;或其药学上可接受的盐。

著录项

  • 公开/公告号ES2237475T3

    专利类型

  • 公开/公告日2005-08-01

    原文格式PDF

  • 申请/专利权人 EISAI CO. LTD;

    申请/专利号ES20000980723T

  • 发明设计人 ROSSIGNOL DANIEL P.;VERMEULEN MARY W.;

    申请日2000-11-22

  • 分类号A61K31/70;A61K31/7016;A61K9/00;

  • 国家 ES

  • 入库时间 2022-08-21 22:14:39

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