Treatment for renal fibrosis
    2.
    发明申请
    Treatment for renal fibrosis 审中-公开
    治疗肾纤维化

    公开(公告)号:US20060194822A1

    公开(公告)日:2006-08-31

    申请号:US11262317

    申请日:2005-10-28

    IPC分类号: A61K31/517

    CPC分类号: A61K31/495

    摘要: The present invention relates to compositions containing quinazolinones. More particularly, the present invention relates to a composition for treatment renal fibrosis, comprising as active ingredient a quinazolinone derivative as herein defined. The currently preferred embodiment is halofuginone, which is now show to slow or prevent progression of renal fibrosis in vivo, thereby preventing end-stage renal failure.

    摘要翻译: 本发明涉及含有喹唑啉酮的组合物。 更具体地,本发明涉及用于治疗肾纤维化的组合物,其包含作为本文定义的喹唑啉酮衍生物的活性成分。 目前优选的实施方案是卤夫酮,其现在显示为缓慢或预防体内肾纤维化的进展,从而防止终末期肾衰竭。

    COMPOSITION AND METHOD FOR TREATING OR PREVENTING SKELETAL MUSCLE FIBROSIS
    3.
    发明申请
    COMPOSITION AND METHOD FOR TREATING OR PREVENTING SKELETAL MUSCLE FIBROSIS 有权
    用于治疗或预防骨骼肌肉纤维化的组合物和方法

    公开(公告)号:US20130281472A1

    公开(公告)日:2013-10-24

    申请号:US13782325

    申请日:2013-03-01

    IPC分类号: A61K31/517

    CPC分类号: A61K31/517

    摘要: A compound in combination with a pharmaceutically acceptable carrier, the compound having a formula: wherein: R1 is a member of the group consisting of hydrogen, halogen, nitro, benzo, lower alkyl, phenyl, and lower alkoxy; R2 is a member of the group consisting of hydroxy, acetoxy, and lower alkoxy; and R3 is a member of the group consisting of hydrogen and lower alkenoxy-carbonyl; and n is either 1 or 2; and pharmaceutically acceptable salts thereof; for use in treatment of or prevention of skeletal muscle fibrosis and/or for inducing skeletal muscle regeneration.

    摘要翻译: 化合物与药学上可接受的载体组合,所述化合物具有下式:其中:R 1是氢,卤素,硝基,苯并,低级烷基,苯基和低级烷氧基的成员; R2是由羟基,乙酰氧基和低级烷氧基组成的组的成员; 并且R 3是由氢和低级链烯氧基 - 羰基组成的组的成员; n为1或2; 及其药学上可接受的盐; 用于治疗或预防骨骼肌纤维化和/或用于诱导骨骼肌再生。

    Quinazolinone-containing pharmaceutical compositions for prevention of neovascularization and for treating malignancies
    4.
    发明授权
    Quinazolinone-containing pharmaceutical compositions for prevention of neovascularization and for treating malignancies 失效
    含喹唑啉酮的药物组合物,用于预防新血管形成和治疗恶性肿瘤

    公开(公告)号:US06420371B1

    公开(公告)日:2002-07-16

    申请号:US09479660

    申请日:2000-01-10

    IPC分类号: A61K31505

    CPC分类号: A61K31/517

    摘要: The invention provides a composition for attenuating neovascularization and treating malignancies, including a pharmaceutically effective amount of a compound having a formula: wherein: R1 is a number of the group consisting of hydrogen, halogen, nitro, benzo, lower alkyl, phenyl and lower alkoxy, R2 is a member of the group consisting of hydroxy, acetoxy, and lower alkoxy, and R3 is a member of the group consisting of hydrogen and lower alkenoxy carbonyl, as active ingredient therein, in combination with a pharmaceutically acceptable carrier.

    摘要翻译: 本发明提供一种用于减毒新生血管形成和治疗恶性肿瘤的组合物,包括药学有效量的具有下式的化合物:其中:R1是氢,卤素,硝基,苯并,低级烷基,苯基和低级烷氧基 R2是羟基,乙酰氧基和低级烷氧基的成员,R 3是作为活性成分的氢和低级链烯氧基羰基的组成与药学上可接受的载体的组合。

    Treatment of skin disorders
    5.
    发明授权
    Treatment of skin disorders 失效
    治疗皮肤病

    公开(公告)号:US06211188B1

    公开(公告)日:2001-04-03

    申请号:US08797702

    申请日:1997-02-11

    IPC分类号: A61K31505

    CPC分类号: A61K31/517 Y10S514/863

    摘要: An effective treatment for skin disorders characterized by abnormal skin cell behavior, including a pharmaceutically effective amount of Halofuginone. Skin disorders which can be treated include keloids, hypertrophic scars, psoriasis, acne, seborrhea and alopecia. Halofuginone can reduce or eliminate clinical symptoms of these disorders, as well as substantially prevent the formation of keloids and hypertrophic scars.

    摘要翻译: 特征在于皮肤细胞行为异常的皮肤病症的有效治疗,包括药学上有效量的卤夫酮。 可以治疗的皮肤疾病包括瘢痕疙瘩,肥大性瘢痕,牛皮癣,痤疮,皮脂溢和脱发。 卤夫酮可以减少或消除这些疾病的临床症状,并且基本上防止瘢痕疙瘩和肥厚性瘢痕的形成。

    Quinazolinone containing pharmaceutical compositions for prevention of
neovascularization and for treating malignancies
    6.
    发明授权
    Quinazolinone containing pharmaceutical compositions for prevention of neovascularization and for treating malignancies 失效
    含喹唑啉酮的药物组合物,用于预防新血管形成和治疗恶性肿瘤

    公开(公告)号:US6028075A

    公开(公告)日:2000-02-22

    申请号:US797703

    申请日:1997-02-11

    CPC分类号: A61K31/517

    摘要: The invention provides a composition for attenuating neovascularization and treating malignancies, including a pharmaceutically effective amount of a compound having a formula: ##STR1## wherein: R.sub.1 is a member of the group consisting of hydrogen, halogen, nitro, benzo, lower alkyl, phenyl and lower alkoxy;R.sub.2 is a member of the group consisting of hydroxy, acetoxy, and lower alkoxy, andR.sub.3 is a member of the group consisting of hydrogen and lower alkenoxy carbonyl;as active ingredient therein, in combination with a pharmaceutically acceptable carrier.

    摘要翻译: 本发明提供用于减毒新生血管形成和治疗恶性肿瘤的组合物,包括药学有效量的具有下式的化合物:其中:R 1是氢,卤素,硝基,苯并,低级烷基,苯基和低级烷氧基 ; R2是由羟基,乙酰氧基和低级烷氧基组成的组的成员,R3是由氢和低级链烯氧基羰基组成的组的成员; 作为其中的活性成分,与药学上可接受的载体组合。

    COMPOSITION AND METHOD FOR TREATING OR PREVENTING SKELETAL MUSCLE FIBROSIS

    公开(公告)号:US20160030429A1

    公开(公告)日:2016-02-04

    申请号:US14679650

    申请日:2015-04-06

    IPC分类号: A61K31/517

    CPC分类号: A61K31/517

    摘要: A compound in combination with a pharmaceutically acceptable carrier, the compound having a formula: wherein: R1 is a member of the group consisting of hydrogen, halogen, nitro, benzo, lower alkyl, phenyl, and lower alkoxy; R2 is a member of the group consisting of hydroxy, acetoxy, and lower alkoxy; and R3 is a member of the group consisting of hydrogen and lower alkenoxy-carbonyl; and n is either 1 or 2; and pharmaceutically acceptable salts thereof; for use in treatment of or prevention of skeletal muscle fibrosis and/or for inducing skeletal muscle regeneration.

    Composition and method for treating or preventing skeletal muscle fibrosis
    8.
    发明授权
    Composition and method for treating or preventing skeletal muscle fibrosis 有权
    用于治疗或预防骨骼肌纤维化的组合物和方法

    公开(公告)号:US09023859B2

    公开(公告)日:2015-05-05

    申请号:US13782325

    申请日:2013-03-01

    IPC分类号: A61K31/505 A61K31/517

    CPC分类号: A61K31/517

    摘要: A compound in combination with a pharmaceutically acceptable carrier, the compound having a formula: wherein: R1 is a member of the group consisting of hydrogen, halogen, nitro, benzo, lower alkyl, phenyl, and lower alkoxy; R2 is a member of the group consisting of hydroxy, acetoxy, and lower alkoxy; and R3 is a member of the group consisting of hydrogen and lower alkenoxy-carbonyl; and n is either 1 or 2; and pharmaceutically acceptable salts thereof; for use in treatment of or prevention of skeletal muscle fibrosis and/or for inducing skeletal muscle regeneration.

    摘要翻译: 化合物与药学上可接受的载体组合,所述化合物具有下式:其中:R 1是氢,卤素,硝基,苯并,低级烷基,苯基和低级烷氧基的成员; R2是由羟基,乙酰氧基和低级烷氧基组成的组的成员; 并且R 3是由氢和低级链烯氧基 - 羰基组成的组的成员; n为1或2; 及其药学上可接受的盐; 用于治疗或预防骨骼肌纤维化和/或用于诱导骨骼肌再生。

    Inhibition of pathogenic processes related to tissue trauma
    9.
    发明申请
    Inhibition of pathogenic processes related to tissue trauma 审中-公开
    抑制与组织创伤相关的致病过程

    公开(公告)号:US20070010538A1

    公开(公告)日:2007-01-11

    申请号:US11402638

    申请日:2006-04-11

    IPC分类号: A61K31/517

    CPC分类号: A61K31/517

    摘要: According to the present invention compositions and methods are provided to prevent the pathogenic aspects of tissue trauma while preserving normal tissue repair mechanisms, based on the fact that these molecules abrogate the cascade of damage initiated by tissue trauma, while maintaining this the requisite healthy extracellular matrix economy. The composition for regulating the extracellular matrix economy, comprise a pharmaceutically effective amount of an effector in combination with a pharmaceutically acceptable carrier. Preferably, the effector is a quinazolinone derivative. More preferably, the quinazolinone derivative is a member of a group having formula (I), wherein R1 is a member of the group consisting of hydrogen, halogen, nitro, benzo, lower alkyl, phenyl, and lower alkoxy; R2 is a member of the group consisting of hydroxy, acetoxy, and lower alkoxy, and R3 is a member of the group consisting of hydrogen and lower alkenoxy; and pharmaceutically acceptable salts thereof; and n is either 1 or 2. Most preferably, the effector is Halofuginone and pharmaceutically acceptable salts thereof.

    摘要翻译: 根据本发明,提供了组合物和方法,以防止组织创伤的病态方面,同时保持正常组织修复机制,这是基于这些分子消除由组织创伤引起的损伤级联的事实,同时保持必需的健康细胞外基质 经济。 用于调节细胞外基质经济性的组合物包含与药学上可接受的载体组合的药学有效量的效应物。 优选地,效应子是喹唑啉酮衍生物。 更优选地,喹唑啉酮衍生物是具有式(I)的基团的成员,其中R 1是由氢,卤素,硝基,苯并,低级烷基,苯基和 低级烷氧基 R 2是由羟基,乙酰氧基和低级烷氧基组成的组中的成员,R 3 3是氢和低级链烯氧基的成员; 及其药学上可接受的盐; 并且n为1或2.最优选地,效应物是卤代酮及其药学上可接受的盐。

    Treatment of skin disorders
    10.
    再颁专利
    Treatment of skin disorders 失效
    治疗皮肤病

    公开(公告)号:USRE39096E1

    公开(公告)日:2006-05-16

    申请号:US10408788

    申请日:2003-04-03

    IPC分类号: A61K31/519 A61K31/517

    CPC分类号: A61K31/517 Y10S514/863

    摘要: An effective treatment for skin disorders characterized by abnormal skin cell behavior, including a pharmaceutically effective amount of Halofuginone. Skin disorders which can be treated include keloids, hypertrophic scars, psoriasis, acne, seborrhea and alopecia. Halofuginone can reduce or eliminate clinical symptoms of these disorders, as well as substantially prevent the formation of keloids and hypertrophic scars.

    摘要翻译: 特征在于皮肤细胞行为异常的皮肤病症的有效治疗,包括药学上有效量的卤夫酮。 可以治疗的皮肤疾病包括瘢痕疙瘩,肥大性瘢痕,牛皮癣,痤疮,皮脂溢和脱发。 卤夫酮可以减少或消除这些疾病的临床症状,并且基本上防止瘢痕疙瘩和肥厚性瘢痕的形成。