Modified corticotropin releasing factor peptides and uses thereof
    1.
    发明授权
    Modified corticotropin releasing factor peptides and uses thereof 失效
    修饰的促肾上腺皮质激素释放因子肽及其用途

    公开(公告)号:US07982018B2

    公开(公告)日:2011-07-19

    申请号:US11873291

    申请日:2007-10-16

    摘要: The present invention relates to compounds comprising modified corticotrophin releasing factor peptide and specifically urocortin and urocortin-related peptides, modified derivatives thereof, and conjugates of such modified peptides and derivatives to serum components, preferably serum proteins or peptides. The compounds and conjugates of the invention comprise a reactive group, which is covalently attached to a modified peptide or derivative, optionally through a linking group. The present invention also provides methods for the covalent attachment of a modified peptide or derivative to a serum protein or peptide to form a conjugate of the invention. The conjugates of the invention preferably exhibit a longer in vivo circulating half-life compared to the corresponding unconjugated peptides. The conjugates of the invention also retain at least some of the biological activity of the unconjugated peptides, and preferably exhibit increased biological activity compared to the unconjugated peptides. The present invention also provides methods for the treatment and prevention of a disease or disorder comprising the administration of one or more of the compounds or conjugates of the invention to a subject in need of such treatment or prevention.

    摘要翻译: 本发明涉及包含修饰的促肾上腺皮质激素释放因子肽,特别是尿皮质素和尿皮质素相关肽,其修饰的衍生物,以及这些修饰肽和衍生物与血清成分,优选血清蛋白或肽的缀合物的化合物。 本发明的化合物和缀合物包含反应性基团,其任选地通过连接基团共价连接到修饰的肽或衍生物上。 本发明还提供了将修饰的肽或衍生物共价连接到血清蛋白或肽以形成本发明的缀合物的方法。 与相应的未结合的肽相比,本发明的缀合物优选表现出更长的体内循环半衰期。 本发明的缀合物还保留非共轭肽的至少一些生物活性,并且与非共轭多肽相比优​​选表现出增加的生物学活性。 本发明还提供了治疗和预防疾病或病症的方法,包括将本发明的一种或多种化合物或缀合物施用于需要这种治疗或预​​防的受试者。

    Modified Corticotropin Releasing Factor Peptides and Uses Thereof
    2.
    发明申请
    Modified Corticotropin Releasing Factor Peptides and Uses Thereof 失效
    改性促肾上腺皮质激素释放因子肽及其用途

    公开(公告)号:US20080167231A1

    公开(公告)日:2008-07-10

    申请号:US11873291

    申请日:2007-10-16

    IPC分类号: A61K38/00 C07K16/00

    摘要: The present invention relates to compounds comprising modified corticotrophin releasing factor peptide and specifically urocortin and urocortin-related peptides, modified derivatives thereof, and conjugates of such modified peptides and derivatives to serum components, preferably serum proteins or peptides. The compounds and conjugates of the invention comprise a reactive group, which is covalently attached to a modified peptide or derivative, optionally through a linking group. The present invention also provides methods for the covalent attachment of a modified peptide or derivative to a serum protein or peptide to form a conjugate of the invention. The conjugates of the invention preferably exhibit a longer in vivo circulating half-life compared to the corresponding unconjugated peptides. The conjugates of the invention also retain at least some of the biological activity of the unconjugated peptides, and preferably exhibit increased biological activity compared to the unconjugated peptides. The present invention also provides methods for the treatment and prevention of a disease or disorder comprising the administration of one or more of the compounds or conjugates of the invention to a subject in need of such treatment or prevention.

    摘要翻译: 本发明涉及包含修饰的促肾上腺皮质激素释放因子肽,特别是尿皮质素和尿皮质素相关肽,其修饰的衍生物,以及这些修饰肽和衍生物与血清成分,优选血清蛋白或肽的缀合物的化合物。 本发明的化合物和缀合物包含反应性基团,其任选地通过连接基团共价连接到修饰的肽或衍生物上。 本发明还提供了将修饰的肽或衍生物共价连接到血清蛋白或肽以形成本发明的缀合物的方法。 与相应的未结合的肽相比,本发明的缀合物优选表现出更长的体内循环半衰期。 本发明的缀合物还保留非共轭肽的至少一些生物活性,并且与非共轭多肽相比优​​选表现出增加的生物学活性。 本发明还提供了治疗和预防疾病或病症的方法,包括将本发明的一种或多种化合物或缀合物施用于需要这种治疗或预​​防的受试者。

    Composition and method for treating inflammation
    4.
    发明授权
    Composition and method for treating inflammation 失效
    用于治疗炎症的组合物和方法

    公开(公告)号:US5300292A

    公开(公告)日:1994-04-05

    申请号:US989959

    申请日:1992-12-10

    申请人: Thomas R. Ulich

    发明人: Thomas R. Ulich

    IPC分类号: A61K38/20 C07G7/00 A61K37/02

    CPC分类号: A61K38/204

    摘要: A method for treatment of inflammation, comprising the step of administering to a patient in need thereof an effective, inflammation-inhibiting amount of a composition comprising IL-6, or IL-6 and TGF.beta. together in a weight ratio of from about 5:95 to 95:5, preferably from about 20:80 to 80:20. Also disclosed is a composition for treatment of inflammation, comprising as active ingredients IL-6 and TGF.beta. in a weight ratio of from about 5:95 to about 95:5, optionally comprising a carrier in combination with the active ingredients, and a method of reducing migration of neutrophils into tissue of an animal which has received an inflammatory stimulus, comprising the step of administering to the tissue an effective neutrophil-migration-inhibiting amount of a composition as defined above.

    摘要翻译: 一种治疗炎症的方法,包括以下步骤:向有需要的患者施用有效的炎症抑制量的包含IL-6或IL-6和TGF(β)的组合物,其重量比为约 5:95至95:5,优选约20:80至80:20。 还公开了用于治疗炎症的组合物,其包含重量比为约5:95至约95:5的活性成分IL-6和TGF(β),任选地包含与活性成分组合的载体,以及 一种减少嗜中性粒细胞向接受炎性刺激的动物组织中的迁移的方法,包括向组织施用有效的中性粒细胞迁移抑制量的上述组合物的步骤。

    Composition and method for treating inflammation
    5.
    发明授权
    Composition and method for treating inflammation 失效
    用于治疗炎症的组合物和方法

    公开(公告)号:US5376368A

    公开(公告)日:1994-12-27

    申请号:US186762

    申请日:1994-01-25

    申请人: Thomas R. Ulich

    发明人: Thomas R. Ulich

    IPC分类号: A61K38/20 A61K37/02 C07G7/00

    CPC分类号: A61K38/204

    摘要: A method for treatment of inflammation, comprising the step of administering to a patient in need thereof an effective, inflammation-inhibiting amount of a composition comprising IL-6, or IL-6 and TGF.beta. together in a weight ratio of from about 5:95 to 95:5, preferably from about 20:80 to 80:20. Also disclosed is a composition for treatment of inflammation, comprising as active ingredients IL-6 and TGF.beta. in a weight ratio of from about 5:95 to about 95:5, optionally comprising a carrier in combination with the active ingredients, and a method of reducing migration of neutrophils into tissue of an animal which has received an inflammatory stimulus, comprising the step of administering to the tissue an effective neutrophil-migration-inhibiting amount of a composition as defined above.

    摘要翻译: 一种用于治疗炎症的方法,包括以下步骤:向有需要的患者施用有效的炎症抑制量的包含IL-6或IL-6和TGFβ的组合物,其重量比为约5: 95至95:5,优选约20:80至80:20。 还公开了用于治疗炎症的组合物,其包含重量比为约5:95至约95:5的活性成分IL-6和TGFβ,任选地包含与活性成分组合的载体,以及方法 减少嗜中性粒细胞迁移到已经接受炎症刺激的动物的组织中,包括向组织施用有效的中性粒细胞迁移抑制量的上述组合物的步骤。