Polycationic calcium modulator peptides for the treatment of hyperparathyroidism and hypercalcemic disorders
    4.
    发明授权
    Polycationic calcium modulator peptides for the treatment of hyperparathyroidism and hypercalcemic disorders 有权
    用于治疗甲状旁腺功能亢进和高钙血症的多阳离子钙调节肽

    公开(公告)号:US08987200B2

    公开(公告)日:2015-03-24

    申请号:US11941857

    申请日:2007-11-16

    CPC分类号: A61K38/17

    摘要: The present invention provides methods and kits for treating hyperparathyroidism, bone disease and/or hypercalcemic disorders. In particular, methods for lowering serum PTH and serum calcium using polycationic calcium modulator peptides are provided. The calcium modulator peptides can be used to treat subjects having, for example: primary, secondary or tertiary hyperparathyroidism; hypercalcemia of malignancy; metastatic bone disease; or osteoporosis.

    摘要翻译: 本发明提供了用于治疗甲状旁腺功能亢进,骨疾病和/或高钙血症的方法和试剂盒。 特别地,提供了使用聚阳离子钙调节剂肽降低血清PTH和血清钙的方法。 钙调节肽可用于治疗患有例如:原发性,继发性或次级甲状旁腺功能亢进的受试者; 恶性高钙血症; 转移性骨病; 或骨质疏松。

    Therapeutic agents for reducing parathyroid hormone levels
    5.
    发明授权
    Therapeutic agents for reducing parathyroid hormone levels 有权
    降低甲状旁腺激素水平的治疗剂

    公开(公告)号:US08377880B2

    公开(公告)日:2013-02-19

    申请号:US13365213

    申请日:2012-02-02

    摘要: Compounds having activity for lowering parathyroid hormone levels are described. In one embodiment, the compounds are comprised of a contiguous sequence of subunits, X1—X2—X3—X4—X5—X6—X7, wherein the X1 subunit comprises a thiol-containing moiety and the distribution of charge on the X2—X7 subunits provides the desired activity. Methods of using the compounds for treating hyperparathyroidism, bone disease and/or hypercalcemic disorders are also described, and in particular, methods for lowering plasma PTH and serum calcium are provided. The compounds can be used to treat subjects having, for example: primary, secondary or tertiary hyperparathyroidism; hypercalcemia of malignancy; metastatic bone disease; or osteoporosis.

    摘要翻译: 描述了具有降低甲状旁腺激素水平的活性的化合物。 在一个实施方案中,化合物由亚单位X1-X2-X3-X4-X5-X6-X7的连续序列组成,其中X1亚基包含含巯基的部分,并且X2-X7亚基上的电荷分布 提供所需的活动。 还描述了使用该化合物治疗甲状旁腺功能亢进,骨疾病和/或高钙血症的方法,特别是提供降低血浆PTH和血清钙的方法。 这些化合物可用于治疗患有例如:原发性,继发性或甲状腺功能亢进的受试者; 恶性高钙血症; 转移性骨病; 或骨质疏松。

    POLYCATIONIC CALCIUM MODULATOR PEPTIDES FOR THE TREATMENT OF HYPERPARATHYROIDISM AND HYPERCALCEMIC DISORDERS
    7.
    发明申请
    POLYCATIONIC CALCIUM MODULATOR PEPTIDES FOR THE TREATMENT OF HYPERPARATHYROIDISM AND HYPERCALCEMIC DISORDERS 有权
    用于治疗高尿酸血症和高血压疾病的聚合钙调节剂

    公开(公告)号:US20090023652A1

    公开(公告)日:2009-01-22

    申请号:US11941857

    申请日:2007-11-16

    CPC分类号: A61K38/17

    摘要: The present invention provides methods and kits for treating hyperparathyroidism, bone disease and/or hypercalcemic disorders. In particular, methods for lowering serum PTH and serum calcium using polycationic calcium modulator peptides are provided. The calcium modulator peptides can be used to treat subjects having, for example: primary, secondary or tertiary hyperparathyroidism; hypercalcemia of malignancy; metastatic bone disease; or osteoporosis.

    摘要翻译: 本发明提供了用于治疗甲状旁腺功能亢进,骨疾病和/或高钙血症的方法和试剂盒。 特别地,提供了使用聚阳离子钙调节剂肽降低血清PTH和血清钙的方法。 钙调节肽可用于治疗患有例如:原发性,继发性或次级甲状旁腺功能亢进的受试者; 恶性高钙血症; 转移性骨病; 或骨质疏松。

    Therapeutic agents for reducing parathyroid hormone levels
    8.
    发明授权
    Therapeutic agents for reducing parathyroid hormone levels 有权
    降低甲状旁腺激素水平的治疗剂

    公开(公告)号:US08999932B2

    公开(公告)日:2015-04-07

    申请号:US12846724

    申请日:2010-07-29

    摘要: Compounds having activity for lowering parathyroid hormone levels are described. In one embodiment, the compounds are comprised of a contiguous sequence of subunits, X1-X2-X3-X4-X5-X6-X7, wherein the X1 subunit comprises a thiol-containing moiety and the distribution of charge on the X2-X7 subunits provides the desired activity. Methods of using the compounds for treating hyperparathyroidism, bone disease and/or hypercalcemic disorders are also described, and in particular, methods for lowering plasma PTH and serum calcium are provided. The compounds can be used to treat subjects having, for example: primary, secondary or tertiary hyperparathyroidism; hypercalcemia of malignancy; metastatic bone disease; or osteoporosis.

    摘要翻译: 描述了具有降低甲状旁腺激素水平的活性的化合物。 在一个实施方案中,化合物由亚单位X1-X2-X3-X4-X5-X6-X7的连续序列组成,其中X1亚基包含含巯基的部分,并且X2-X7亚基上的电荷分布 提供所需的活动。 还描述了使用该化合物治疗甲状旁腺功能亢进,骨疾病和/或高钙血症的方法,特别是提供降低血浆PTH和血清钙的方法。 这些化合物可用于治疗患有例如:原发性,继发性或甲状腺功能亢进的受试者; 恶性高钙血症; 转移性骨病; 或骨质疏松。

    Protein kinase required for Ras signal transduction
    9.
    发明授权
    Protein kinase required for Ras signal transduction 失效
    Ras信号转导所需的蛋白激酶

    公开(公告)号:US5747288A

    公开(公告)日:1998-05-05

    申请号:US909983

    申请日:1997-06-12

    CPC分类号: C12N9/1205 A61K38/00

    摘要: The kinase suppressor of Ras (Ksr), a novel protein kinase involved in the regulation of cell growth and differentiation, provides an important target for therapeutic intervention. The subject compositions also include nucleic acids which encode a Ksr kinase, and hybridization probes and primers capable of hybridizing with a Ksr gene. Such probes are used to identify mutant Ksr alleles associated with disease. The invention includes methods, including phosphorylation and binding assays, for screening chemical libraries for lead compounds for a pharmacological agent useful in the diagnosis or treatment of disease associated Ksr activity or Ksr-dependent signal transduction.

    摘要翻译: 参与调节细胞生长和分化的新蛋白激酶Ras(Ksr)的激酶抑制剂为治疗干预提供了重要的靶标。 主题组合物还包括编码Ksr激酶的核酸,以及能够与Ksr基因杂交的杂交探针和引物。 这样的探针用于鉴定与疾病相关的突变体Ksr等位基因。 本发明包括用于筛选用于诊断或治疗与疾病相关的Ksr活性或Ksr依赖性信号转导的药理学试剂的化合物的化学文库的方法,包括磷酸化和结合测定。

    Protein kinase required for Ras signal transduction
    10.
    发明授权
    Protein kinase required for Ras signal transduction 失效
    Ras信号转导所需的蛋白激酶

    公开(公告)号:US5700675A

    公开(公告)日:1997-12-23

    申请号:US571758

    申请日:1995-12-13

    CPC分类号: C12N9/1205 A61K38/00

    摘要: The kinase suppressor of Ras (Ksr), a novel protein kinase involved in the regulation of cell growth and differentiation, provides an important target for therapeutic intervention. The subject compositions also include nucleic acids which encode a Ksr kinase, and hybridization probes and primers capable of hybridizing with a Ksr gene. Such probes are used to identify mutant Ksr alleles associated with disease. The invention includes methods, including phosphorylation and binding assays, for screening chemical libraries for lead compounds for a pharmacological agent useful in the diagnosis or treatment of disease associated Ksr activity or Ksr-dependent signal transduction.

    摘要翻译: 参与调节细胞生长和分化的新蛋白激酶Ras(Ksr)的激酶抑制剂为治疗干预提供了重要的靶标。 主题组合物还包括编码Ksr激酶的核酸,以及能够与Ksr基因杂交的杂交探针和引物。 这样的探针用于鉴定与疾病相关的突变体Ksr等位基因。 本发明包括用于筛选用于诊断或治疗与疾病相关的Ksr活性或Ksr依赖性信号转导的药理学试剂的化合物的化学文库的方法,包括磷酸化和结合测定。