会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 1. 发明申请
    • ALPHA-FETOPROTEIN PEPTIDES AND USES THEREOF
    • ALPHA-FETOPROTEIN PEPTIDES及其用途
    • US20110269692A1
    • 2011-11-03
    • US13108923
    • 2011-05-16
    • Thomas T. AndersenJames A. BennettHerbert I. JacobsonFassil B. Mesfin
    • Thomas T. AndersenJames A. BennettHerbert I. JacobsonFassil B. Mesfin
    • A61K38/08A61K38/12A61P35/00
    • A61K38/1709A61K31/138A61K38/12A61K45/06A61K49/0002C07K14/4715C07K2319/00G01N33/57415A61K2300/00
    • Therapeutic compounds which are cell proliferation modulators, preferably inhibitors. These modulators contain amino acid structures that are arranged as a hydrophilic analog of an alpha-fetoprotein. The modulator may be a peptide itself, e.g., an octapeptide like that of SEQ ID NO: 5; a peptidomimetic; or may be in the form of a pharmaceutically acceptable scaffold, such as a polycyclic hydrocarbon to which is attached the necessary amino acid structures for biological and/or chemical activity. The modulators of the invention are distinguished in one aspect over previous compounds in that they are orally active, and therefore do not have to be injected into the patient. The compositions and methods are useful for reducing estrogen-dependent and estrogen-independent growth of cells, and treating or preventing cancer, such as breast cancer, brain cancer, head-and-neck cancer, thyroid cancer, lung cancer, colon cancer, ovarian cancer, prostate cancer, cervical cancer, and skin cancer. The treatment or prevention methods can include the use of tamoxifen therapy in combination with the peptide therapy.
    • 作为细胞增殖调节剂的治疗化合物,优选抑制剂。 这些调节剂含有排列成甲胎蛋白的亲水类似物的氨基酸结构。 调节剂可以是肽本身,例如像SEQ ID NO:5那样的八肽; 一个拟人的 或者可以是药学上可接受的支架的形式,例如连接有用于生物和/或化学活性的必需氨基酸结构的多环烃。 本发明的调节剂在一个方面与先前化合物的区别在于它们是口服活性的,因此不必将其注入患者体内。 组合物和方法可用于减少细胞的雌激素依赖性和雌激素非依赖性生长,以及治疗或预防癌症,如乳腺癌,脑癌,头颈癌,甲状腺癌,肺癌,结肠癌,卵巢癌 癌症,前列腺癌,子宫颈癌和皮肤癌。 治疗或预防方法可以包括与肽疗法组合使用他莫昔芬治疗。
    • 4. 发明授权
    • Alpha-fetoprotein peptides and uses thereof
    • 甲胎蛋白肽及其用途
    • US07122522B2
    • 2006-10-17
    • US10300530
    • 2002-11-20
    • Thomas T. AndersenJames A. BennettHerbert I. JacobsonFassil B. Mesfin
    • Thomas T. AndersenJames A. BennettHerbert I. JacobsonFassil B. Mesfin
    • A61K38/00
    • A61K49/0002A61K38/1709C07K14/4715C07K2319/00G01N33/57415
    • Therapeutic compounds which are cell proliferation modulators, preferably inhibitors. These modulators contain amino acid structures that are arranged as a hydrophilic analog of an alpha-fetoprotein. The modulator may be a peptide itself, e.g., an octapeptide like that of SEQ ID NO: 5; a peptidomimetic; or may be in the form of a pharmaceutically acceptable scaffold, such as a polycyclic hydrocarbon to which is attached the necessary amino acid structures for biological and/or chemical activity. The modulators of the invention are distinguished in one aspect over previous compounds in that they are orally active, and therefore do not have to be injected into the patient. The compositions and methods are useful for reducing estrogen-stimulated growth of cells, and treating or preventing cancer, such as breast cancer. The treatment or prevention methods can include the use of tamoxifen therapy in combination with the peptide therapy.
    • 作为细胞增殖调节剂的治疗化合物,优选抑制剂。 这些调节剂含有排列成甲胎蛋白的亲水类似物的氨基酸结构。 调节剂可以是肽本身,例如像SEQ ID NO:5那样的八肽; 一个拟人的 或者可以是药学上可接受的支架的形式,例如连接有用于生物和/或化学活性的必需氨基酸结构的多环烃。 本发明的调节剂在一个方面与先前化合物的区别在于它们是口服活性的,因此不必将其注入患者体内。 组合物和方法可用于减少雌激素刺激的细胞生长,以及治疗或预防癌症,例如乳腺癌。 治疗或预防方法可以包括与肽疗法组合使用他莫昔芬治疗。
    • 5. 发明授权
    • Alpha-fetoprotein peptides and uses thereof
    • 甲胎蛋白肽及其用途
    • US07943577B2
    • 2011-05-17
    • US11582629
    • 2006-10-17
    • Thomas T. AndersenJames A. BennettHerbert I. JacobsonFassil B. Mesfin
    • Thomas T. AndersenJames A. BennettHerbert I. JacobsonFassil B. Mesfin
    • A61K38/00
    • A61K38/1709A61K31/138A61K38/12A61K45/06A61K49/0002C07K14/4715C07K2319/00G01N33/57415A61K2300/00
    • Therapeutic compounds which are cell proliferation modulators, preferably inhibitors. These modulators contain amino acid structures that are arranged as a hydrophilic analog of an alpha-fetoprotein. The modulator may be a peptide itself, e.g., an octapeptide like that of SEQ ID NO: 5; a peptidomimetic; or may be in the form of a pharmaceutically acceptable scaffold, such as a polycyclic hydrocarbon to which is attached the necessary amino acid structures for biological and/or chemical activity. The modulators of the invention are distinguished in one aspect over previous compounds in that they are orally active, and therefore do not have to be injected into the patient. The compositions and methods are useful for reducing estrogen-dependent and estrogen-independent growth of cells, and treating or preventing cancer, such as breast cancer, brain cancer, head-and-neck cancer, thyroid cancer, lung cancer, colon cancer, ovarian cancer, prostate cancer, cervical cancer, and skin cancer. The treatment or prevention methods can include the use of tamoxifen therapy in combination with the peptide therapy.
    • 作为细胞增殖调节剂的治疗化合物,优选抑制剂。 这些调节剂含有排列成甲胎蛋白的亲水类似物的氨基酸结构。 调节剂可以是肽本身,例如像SEQ ID NO:5那样的八肽; 一个拟人的 或者可以是药学上可接受的支架的形式,例如连接有用于生物和/或化学活性的必需氨基酸结构的多环烃。 本发明的调节剂在一个方面与先前化合物的区别在于它们是口服活性的,因此不必将其注入患者体内。 组合物和方法可用于减少细胞的雌激素依赖性和雌激素非依赖性生长,以及治疗或预防癌症,如乳腺癌,脑癌,头颈癌,甲状腺癌,肺癌,结肠癌,卵巢癌 癌症,前列腺癌,子宫颈癌和皮肤癌。 治疗或预防方法可以包括与肽疗法组合使用他莫昔芬治疗。
    • 6. 发明申请
    • Alpha-fetoprotein peptides and uses thereof
    • 甲胎蛋白肽及其用途
    • US20100249040A1
    • 2010-09-30
    • US11582629
    • 2006-10-17
    • Thomas T. AndersenJames A. BennettHerbert I. JacobsonFassil B. Mesfin
    • Thomas T. AndersenJames A. BennettHerbert I. JacobsonFassil B. Mesfin
    • A61K38/08A61P35/00
    • A61K38/1709A61K31/138A61K38/12A61K45/06A61K49/0002C07K14/4715C07K2319/00G01N33/57415A61K2300/00
    • Therapeutic compounds which are cell proliferation modulators, preferably inhibitors. These modulators contain amino acid structures that are arranged as a hydrophilic analog of an alpha-fetoprotein. The modulator may be a peptide itself, e.g., an octapeptide like that of SEQ ID NO: 5; a peptidomimetic; or may be in the form of a pharmaceutically acceptable scaffold, such as a polycyclic hydrocarbon to which is attached the necessary amino acid structures for biological and/or chemical activity. The modulators of the invention are distinguished in one aspect over previous compounds in that they are orally active, and therefore do not have to be injected into the patient. The compositions and methods are useful for reducing estrogen-dependent and estrogen-independent growth of cells, and treating or preventing cancer, such as breast cancer, brain cancer, head-and-neck cancer, thyroid cancer, lung cancer, colon cancer, ovarian cancer, prostate cancer, cervical cancer, and skin cancer. The treatment or prevention methods can include the use of tamoxifen therapy in combination with the peptide therapy.
    • 作为细胞增殖调节剂的治疗化合物,优选抑制剂。 这些调节剂含有排列成甲胎蛋白的亲水类似物的氨基酸结构。 调节剂可以是肽本身,例如像SEQ ID NO:5那样的八肽; 一个拟人的 或者可以是药学上可接受的支架的形式,例如连接有用于生物和/或化学活性的必需氨基酸结构的多环烃。 本发明的调节剂在一个方面与先前化合物的区别在于它们是口服活性的,因此不必将其注入患者体内。 组合物和方法可用于减少细胞的雌激素依赖性和雌激素非依赖性生长,以及治疗或预防癌症,如乳腺癌,脑癌,头颈癌,甲状腺癌,肺癌,结肠癌,卵巢癌 癌症,前列腺癌,子宫颈癌和皮肤癌。 治疗或预防方法可以包括与肽疗法组合使用他莫昔芬治疗。