首页> 外国专利> Carbamiloxi compound that inhibit leukocyte adhesion mediated by vla-4, compounds that are prodrugs of the compounds, composicionfarmaceutica,Method for setting vla-4 in a Biological Sample, method for treating an inflammatory condition.

Carbamiloxi compound that inhibit leukocyte adhesion mediated by vla-4, compounds that are prodrugs of the compounds, composicionfarmaceutica,Method for setting vla-4 in a Biological Sample, method for treating an inflammatory condition.

机译:抑制由vla-4介导的白细胞粘附的卡巴莫西化合物,作为该化合物的前药的化合物,composicionfarmaceutica,将vla-4设置在生物样品中的方法,治疗炎性疾病的方法。

摘要

The compound described is VLA-4. Some of these compounds also inhibit leukocyte binders, particularly as measured by VLA-4. These compounds can be used in the treatment of human and other mammalian inflammation, such as asthma, Alzheimer's disease, anorexia, AIDS dementia, diabetes, intestinal inflammation, rheumatoid arthritis.Tissue transplantation, tumor metastasis and thoracic ischemia. These compounds can also be used to treat inflammation of the brain, such as multiple sclerosis. The compound can be a formula in which R1 is selected from a group, including asphalt, alternative asphalt, arilo, alternative arilo, cyclopentadiene, alternative cyclopentadiene, heterocycle, alternative hetereocycleo, isomerization and isomerization; R2 is selected from a group, including hydrogen, tar. Cyclopentyl, cyclopentyl, cyclopentyl, cyclopentyl, cyclopentylArilo, substituting arilo, heteromorphic, substituting heteromorphic, R1 and R2 together with nitrogenound atom to R2 yel S0 (2) group,In combination with R1, they can form an isomerization group or an alternative heterocycle group; R3 is selected from a group, including hydrogen, tar, alternative tar, cyclopropyl, alternative cyclopropyl, alternative arilo, isomerization, alternative isomerization, and alternative. When R2 does not form a heterocycle group containing R1, R2 and R3, the alternative heterocycle. R5 es - (CH2) x-ar-r5, wherein R5 is selected from the group consisting of - o-z-nr8r8 and - o-z-r12 in lacual R8 and R8, independent of the hydrogen tar group.Replaced tar, rotary, rotary, acyclic, substituted
机译:所述化合物是VLA-4。这些化合物中的一些还抑制白细胞结合,特别是通过VLA-4测定。这些化合物可用于治疗人类和其他哺乳动物的炎症,例如哮喘,阿尔茨海默氏病,厌食症,艾滋病痴呆,糖尿病,肠道炎症,类风湿关节炎,组织移植,肿瘤转移和胸腔缺血。这些化合物还可用于治疗脑部炎症,例如多发性硬化症。该化合物可以是其中R 1选自以下的分子式:沥青,替代沥青,芳基,替代芳基,环戊二烯,替代环戊二​​烯,杂环,替代杂环,异构化和异构化; R 2选自氢,焦油。环戊基,环戊基,环戊基,环戊基,环状戊基; R 3选自氢,焦油,备选焦油,环丙基,备选环丙基,备选芳基,异构化,备选异构化和备选。当R 2不形成包含R 1,R 2和R 3的杂环基时,则为杂环。 R 5为-(CH 2)x-ar-r 5,其中R 5选自在惰性R 8和R 8中的-oz-nr8r8和-oz-r12,独立于氢焦油基团。无环的,取代的

著录项

  • 公开/公告号AR016133A1

    专利类型

  • 公开/公告日2001-06-20

    原文格式PDF

  • 申请/专利权人 WYETH;ATHENA NEUROSCIENCES INC.;

    申请/专利号AR1998P103779

  • 发明设计人

    申请日1998-07-30

  • 分类号C07C311/19;C07D207/48;C07D277/06;C07D295/14;A61K31/10;A61K31/195;A61K31/395;

  • 国家 AR

  • 入库时间 2022-08-22 01:26:20

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