Use of N1,N4-bis[3-(Ethylamino)Propyl]-2-Butene-1,4-Diamine Compounds in Combination with Epigenetic-Acting Pharmaceuticals for Enhanced Cancer Therapy
    8.
    发明申请
    Use of N1,N4-bis[3-(Ethylamino)Propyl]-2-Butene-1,4-Diamine Compounds in Combination with Epigenetic-Acting Pharmaceuticals for Enhanced Cancer Therapy 审中-公开
    使用N1,N4-双[3-(乙基氨基)丙基] -2-丁烯-1,4-二胺化合物与表观遗传学作用药物联合用于增强癌症治疗

    公开(公告)号:US20130102556A1

    公开(公告)日:2013-04-25

    申请号:US13576692

    申请日:2011-02-02

    摘要: Combination methods for treatment of cancer and of blood disorders, using PG-11047 ((2Z)-N1,N4-bis[3-(ethy-lammo) propyl]-2-butene-1,4-diamine) and PG-11048 ((2E)-N1,N4-bis[3-(ethylamino)propyl]-2-butene-1,4-diamine) in combination with DNA methyltransferase (DNMT) inhibitors, histone deacetylase (HDAC) inhibitors, or both DNA methyltransferase inhibitors and histone deacetylase inhibitors, are disclosed. Hematopoietic cancers, lung cancers, mesothelioma, cutaneous T-cell lymphoma (CTCL), multiple myeloma, solid tumors, and blood disorders such as myelodysplastic syndromes can be treated using the methods of the invention.

    摘要翻译: 使用PG-11047((2Z)-N1,N4-双[3-(乙基 - 氨基)丙基] -2-丁烯-1,4-二胺)和PG-11048(+)的治疗癌症和血液病症的组合方法 ((2E)-N1,N4-双[3-(乙基氨基)丙基] -2-丁烯-1,4-二胺)与DNA甲基转移酶(DNMT)抑制剂,组蛋白脱乙酰酶(HDAC)抑制剂或DNA甲基转移酶 抑制剂和组蛋白脱乙酰酶抑制剂。 造血癌,肺癌,间皮瘤,皮肤T细胞淋巴瘤(CTCL),多发性骨髓瘤,实体瘤和血液病症如骨髓增生异常综合征均可使用本发明的方法治疗。

    Treatment and prevention of vascular hyperplasia using polyamine and polyamine analog compounds
    9.
    发明申请
    Treatment and prevention of vascular hyperplasia using polyamine and polyamine analog compounds 审中-公开
    使用多胺和多胺类似物化合物治疗和预防血管增生

    公开(公告)号:US20070232677A1

    公开(公告)日:2007-10-04

    申请号:US11724521

    申请日:2007-03-14

    IPC分类号: A61K31/409 A61K31/13

    CPC分类号: A61K31/13 A61K31/409

    摘要: This disclosure relates to methods of inhibiting vascular hyperplasia using polyamines, polyamine analogs, and conformationally restricted polyamine analogs, or a conjugate of a polyamine, polyamine analog, or conformationally restricted polyamine analog. Polyamines, polyamine analogs, conformationally restricted polyamine analogs, and conjugates thereof are useful in reducing stenosis and restenosis of blood vessels and grafts.

    摘要翻译: 本公开涉及使用多胺,多胺类似物和构象限制性多胺类似物或多胺,多胺类似物或构象限制性多胺类似物的缀合物来抑制血管增生的方法。 多胺,多胺类似物,构象限制性多胺类似物及其缀合物可用于减少血管和移植物的狭窄和再狭窄。

    Polyamine analogs as therapeutic agents for ocular diseases
    10.
    发明申请
    Polyamine analogs as therapeutic agents for ocular diseases 审中-公开
    多胺类似物作为眼部疾病的治疗剂

    公开(公告)号:US20060160906A1

    公开(公告)日:2006-07-20

    申请号:US11244095

    申请日:2005-10-04

    IPC分类号: A61K31/13

    摘要: This disclosure relates to methods of treating ocular diseases using polyamine analogs, particularly conformationally restricted polyamine analogs. The ocular diseases to be treated include a variety of ophthalmic disorders characterized by angiogenesis and/or neovascularization, including macular degeneration. Both wet macular degeneration and dry macular degeneration can be treated using the methods of the invention. The invention also provides ophthalmic formulations, including sustained release formulations and sustained release devices.

    摘要翻译: 本公开涉及使用多胺类似物,特别是构象限制的多胺类似物治疗眼部疾病的方法。 待治疗的眼部疾病包括以血管生成和/或新血管形成为特征的各种眼科疾病,包括黄斑变性。 可以使用本发明的方法治疗湿性黄斑变性和干性黄斑变性。 本发明还提供眼用制剂,包括缓释制剂和持续释放装置。