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Methods for treating or reducing the risk of pain and inflammatory disorders by administering inhibitors of activated thrombin activatable fibrinolysis inhibitor

机译:通过施用活化的凝血酶可活化的纤溶抑制剂的抑制剂来治疗或降低疼痛和炎性疾病风险的方法

摘要

The invention includes methods for treating or reducing the risk of inflammation in a patient which comprises treating the patient with an inhibitor of activated thrombin activatable fibrinolysis inhibitor. Such diseases include but are not limited to nephritis, systemic lupus erythematosus, rheumatoid arthritis, glomerulonephritis, and sacoidosis. The invention includes methods for treating or reducing the risk of pain in a patient which comprises treating the patient with an inhibitor of activated thrombin activatable fibrinolysis inhibitor. In one class of these methods, the inhibitor of activated thrombin activatable fibrinolysis inhibitor is selected from the group consisting of 2-(6-amino-pyridin-3-ylmethyl)-3-butyl-succinic acid, 2-(6-amino-pyridin-3-ylmethyl)-3-phenethyl-succinic acid, 2-(6-amino-pyridin-3-ylmethyl)-3-methyl-succinic acid, 2-(6-amino-5-methyl-pyridin-3-ylmethyl)-3-[(1-benzyloxycarbonylamino-2-methyl-propyl)hydroxy-phosphinoyl]-propionic acid, 2-(6-amino-pyridin-3-ylmethyl)-3-[hydroxy-(3-phenyl-propyl)-phosphinoyl]-propionic acid, 2-(amino-pyridin-3-ylmethyl)-N-hydroxy-succinamic acid, 3-(6-amino-pyridin-3-yl)-2-mercaptomethyl-propionic acid, 2-(2-amino-pyridin-4-ylmethyl)-3-mercapto-propionic acid, 2-(6-amino-pyridin-3-ylmethyl)-2-mercaptomethyl-butyric acid, 3-(6-amino-5-methyl-pyridin-3-yl)-2-mercaptomethyl-2-methyl-propionic acid, 3-(6-amino-5-methyl-pyridin-3-yl)-2-mercaptomethyl-propionic acid, 3-(6-amino-4-methyl-pyridin-3-yl)-2-mercaptomethyl-propionic acid, and 3-(6-amino-pyridin-3-yl)-2-mercaptomethyl-butyric acid or a pharmaceutically acceptable salt thereof. ;The invention is also a method for treating or reducing the risk of inflammation in a patient, or treating or reducing the risk of pain, which comprises treating the patient with a composition comprising an inhibitor of activated thrombin activatable fibrinolysis inhibitor and an NSAID, e.g., a COX-2 inhibitor. Such diseases include but are not limited to nephritis, systemic lupus, erythematosus, rheumatoid arthritis, glomerulonephritis, and sacoidosis.
机译:本发明包括治疗或降低患者发炎风险的方法,该方法包括用活化的凝血酶可活化的纤维蛋白溶解抑制剂的抑制剂治疗患者。此类疾病包括但不限于肾炎,系统性红斑狼疮,类风湿性关节炎,肾小球肾炎和囊肿。本发明包括治疗或减轻患者疼痛风险的方法,该方法包括用活化的凝血酶可活化的纤维蛋白溶解抑制剂的抑制剂治疗患者。在这些方法的一类中,活化的凝血酶可活化的纤维蛋白溶解抑制剂的抑制剂选自2-(6-氨基-吡啶-3-基甲基)-3-丁基-琥珀酸,2-(6-氨基-吡啶-3-基甲基)-3-苯乙基琥珀酸,2-(6-氨基吡啶-3-基甲基)-3-甲基琥珀酸,2-(6-氨基-5-甲基-吡啶-3- ylmethyl)-3-[(1-苄氧基羰基氨基-2-甲基-丙基)羟基膦酰基-丙酸,2-(6-氨基-吡啶-3-ylmethyl)-3-[羟基-(3-苯基-丙基)-膦酰基&-丙酸,2-(氨基-吡啶-3-基甲基)-N-羟基琥珀酸,3-(6-氨基-吡啶-3-基)-2-巯基甲基-丙酸, 2-(2-氨基-吡啶-4-基甲基)-3-巯基丙酸,2-(6-氨基-吡啶-3-基甲基)-2-巯基甲基丁酸,3-(6-氨基-5 -甲基-吡啶-3-基)-2-巯基甲基-2-甲基-丙酸,3-(6-氨基-5-甲基-吡啶-3-基)-2-巯基甲基-丙酸,3-(6 -氨基-4-甲基吡啶-3-基)-2-巯基甲基丙酸和3-(6-氨基-吡啶-3-基)-2-巯基甲基丁酸或其药学上可接受的盐。本发明还是用于治疗或降低患者发炎的风险,或治疗或降低疼痛的风险的方法,其包括用包含活化的凝血酶可活化的纤溶抑制剂和NSAID的抑制剂的组合物治疗患者。 ,一种COX-2抑制剂。此类疾病包括但不限于肾炎,系统性狼疮,红斑,类风湿性关节炎,肾小球肾炎和囊肿。

著录项

  • 公开/公告号US2003035795A1

    专利类型

  • 公开/公告日2003-02-20

    原文格式PDF

  • 申请/专利权人 GARDELL STEPHEN J.;MAO SHI-SHAN;

    申请/专利号US20020120323

  • 发明设计人 STEPHEN J. GARDELL;SHI-SHAN MAO;

    申请日2002-04-11

  • 分类号A61K38/55;

  • 国家 US

  • 入库时间 2022-08-22 00:10:23

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