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    Histone deacetylase inhibitor prodrugs
    22.
    发明授权
    Histone deacetylase inhibitor prodrugs 有权
    组蛋白脱乙酰酶抑制剂前药

    公开(公告)号：US08227636B2

    公开(公告)日：2012-07-24

    申请号：US10594483

    申请日：2005-04-05

    申请人： Thomas A. Miller ,  David J. Witter ,  Sandro Belvedere

    发明人： Thomas A. Miller ,  David J. Witter ,  Sandro Belvedere

    IPC分类号： C07C69/02 ,  A61K31/22

    CPC分类号： C07D213/80 ,  C07C259/06 ,  C07C271/22 ,  C07D213/82 ,  C07D215/38 ,  C07D215/40 ,  C07D215/42

    摘要： The present invention is directed to prodrugs of hydroxamic acid based histone deacetylase (HDAC) inhibitors, e.g., suberoylanilide hydroxamic acid (SAHA). The prodrugs are acylated derivatives having increased aqueous solubility and cellular permeability as compared with the free hydroxamic acid, and are useful for inhibiting HDACs, and for selectively inducing terminal differentiation, cell growth arrest and/or apoptosis of neoplastic cells, thereby inhibiting proliferation of such cells. Thus, the prodrugs of the present invention are useful in treating a patient having a tumor characterized by proliferation of neoplastic cells. The prodrugs of the invention are also useful in the prevention and treatment of thioredoxin (TRX)-mediated diseases, such as autoimmune, allergic and inflammatory diseases, and in the prevention and/or treatment of diseases of the central nervous system (CNS), such as neurodegenerative diseases.

    摘要翻译： 本发明涉及基于异羟肟酸的组蛋白脱乙酰酶（HDAC）抑制剂例如辛二酰苯胺异羟肟酸（SAHA）的前药。 前药是与游离异羟肟酸相比具有增加的水溶性和细胞渗透性的酰化衍生物，并且可用于抑制HDAC，并且用于选择性诱导肿瘤细胞的终末分化，细胞生长停滞和/或凋亡，由此抑制这些 细胞。 因此，本发明的前药可用于治疗具有以肿瘤细胞增殖为特征的肿瘤的患者。 本发明的前药还可用于预防和治疗硫氧还蛋白（TRX）介导的疾病，如自身免疫，过敏和炎性疾病，以及预防和/或治疗中枢神经系统疾病（CNS）， 如神经退行性疾病。

    Thiophene and benzothiophene hydroxamic acid derivatives
    23.
    发明授权
    Thiophene and benzothiophene hydroxamic acid derivatives 有权
    噻吩和苯并噻吩异羟肟酸衍生物

    公开(公告)号：US07935724B2

    公开(公告)日：2011-05-03

    申请号：US10574992

    申请日：2004-10-08

    申请人： Thomas A. Miller ,  David J. Witter ,  Sandro Belvedere

    发明人： Thomas A. Miller ,  David J. Witter ,  Sandro Belvedere

    IPC分类号： A61K31/381 ,  C07D333/70

    CPC分类号： C07D333/66 ,  C07C259/08 ,  C07C2602/08 ,  C07D333/38 ,  C07D333/70 ,  C07D409/12 ,  C07D409/14 ,  C07D413/12 ,  C07D417/12

    摘要： The present invention relates to a novel class of hydroxamic acid derivatives having a benzothiophene or thiophene backbone. The hydroxamic acid compounds can be used to treat cancer. The hydroxamic acid compounds can also inhibit historic deacetylase and are suitable for use in selectively inducing terminal differentiation, and arresting cell growth and/or apoptosis of neoplastic cells, thereby inhibiting proliferation of such cells. Thus, the compounds of the present invention are useful in treating a patient having a tumor characterized by proliferation of neoplastic cells. The compounds of the invention are also useful in the prevention and treatment of TRX-mediated diseases, such as autoimmune, allergic and inflammatory diseases, and in the prevention and/or treatment of diseases of the central nervous system (CNS), such as neurodegenerative diseases, The present invention further provides pharmaceutical compositions comprising the hydroxamic acid derivatives and safe dosing regimens of these pharmaceutical compositions, which are easy to follow, and which result in a therapeutically effective amount of the hydroxamic acid derivatives in vivo.

    摘要翻译： 本发明涉及具有苯并噻吩或噻吩主链的新一类异羟肟酸衍生物。 异羟肟酸化合物可用于治疗癌症。 异羟肟酸化合物还可以抑制历史的脱乙酰酶，并且适用于选择性诱导末端分化，并阻止肿瘤细胞的细胞生长和/或凋亡，从而抑制这些细胞的增殖。 因此，本发明的化合物可用于治疗具有以肿瘤细胞增殖为特征的肿瘤的患者。 本发明的化合物还可用于预防和治疗TRX介导的疾病，例如自身免疫性，过敏性和炎性疾病，以及预防和/或治疗中枢神经系统（CNS）的疾病，例如神经变性 疾病，本发明进一步提供包含异羟肟酸衍生物和这些药物组合物的安全投药方案的药物组合物，其易于遵循，并且其在体内导致治疗有效量的异羟肟酸衍生物。

    Histone Deacetylase Inhibitor Prodrugs
    24.
    发明申请
    Histone Deacetylase Inhibitor Prodrugs 有权
    组蛋白脱乙酰酶抑制剂前药

    公开(公告)号：US20090023786A1

    公开(公告)日：2009-01-22

    申请号：US10594483

    申请日：2005-04-05

    申请人： Thomas A. Miller ,  David J. Witter ,  Sandro Belvedere

    发明人： Thomas A. Miller ,  David J. Witter ,  Sandro Belvedere

    IPC分类号： A61K31/4406 ,  C07C229/40 ,  A61K31/216 ,  A61P35/00 ,  C07D213/80

    CPC分类号： C07D213/80 ,  C07C259/06 ,  C07C271/22 ,  C07D213/82 ,  C07D215/38 ,  C07D215/40 ,  C07D215/42

    摘要： The present invention is directed to prodrugs of hydroxamic acid based histone deacetylase (HDAC) inhibitors, e.g., suberoylanilide hydroxamic acid (SAHA). The prodrugs are acylated derivatives having increased aqueous solubility and cellular permeability as compared with the free hydroxamic acid, and are useful for inhibiting HDACs, and for selectively inducing terminal differentiation, cell growth arrest and/or apoptosis of neoplastic cells, thereby inhibiting proliferation of such cells. Thus, the prodrugs of the present invention are useful in treating a patient having a tumor characterized by proliferation of neoplastic cells. The prodrugs of the invention are also useful in the prevention and treatment of thioredoxin (TRX)-mediated diseases, such as autoimmune, allergic and inflammatory diseases, and in the prevention and/or treatment of diseases of the central nervous system (CNS), such as neurodegenerative diseases.

    摘要翻译： 本发明涉及基于异羟肟酸的组蛋白脱乙酰酶（HDAC）抑制剂例如辛二酰苯胺异羟肟酸（SAHA）的前药。 前药是与游离异羟肟酸相比具有增加的水溶性和细胞渗透性的酰化衍生物，并且可用于抑制HDAC，并且用于选择性诱导肿瘤细胞的终末分化，细胞生长停滞和/或凋亡，由此抑制这些 细胞。 因此，本发明的前药可用于治疗具有以肿瘤细胞增殖为特征的肿瘤的患者。 本发明的前药还可用于预防和治疗硫氧还蛋白（TRX）介导的疾病，如自身免疫，过敏和炎性疾病，以及预防和/或治疗中枢神经系统疾病（CNS）， 如神经退行性疾病。

    Histone deacetylase inhibitors
    27.
    发明授权
    Histone deacetylase inhibitors 有权
    组蛋白脱乙酰酶抑制剂

    公开(公告)号：US07507858B2

    公开(公告)日：2009-03-24

    申请号：US11629448

    申请日：2005-07-15

    申请人： Sandro Belvedere ,  Thomas A. Miller ,  David J. Witter

    发明人： Sandro Belvedere ,  Thomas A. Miller ,  David J. Witter

    IPC分类号： C07C259/04

    CPC分类号： C07C259/06 ,  A61K31/16 ,  A61K31/185 ,  A61K31/426 ,  A61K31/47 ,  C07D215/40 ,  C07D277/82

    摘要： This invention relates to iminodiacetic acid and diamine hydroxamic acid derivatives, that are inhibitors of histone deacetylase (HDAC), and are useful in the prevention and/or treatment of cellular proliferative diseases, for example cancer, autoimmune, allergic and inflammatory diseases, diseases of the central nervous system (CNS) such as neurodegenerative diseases, and in the prevention and/or treatment of restenosis.

    摘要翻译： 本发明涉及亚氨基二乙酸和二胺异羟肟酸衍生物，其是组蛋白脱乙酰酶（HDAC）的抑制剂，可用于预防和/或治疗细胞增殖性疾病，例如癌症，自身免疫性，过敏性和炎性疾病， 中枢神经系统（CNS）如神经变性疾病，以及预防和/或治疗再狭窄。

    Hydroxyalkylarylamide Derivatives
    28.
    发明申请
    Hydroxyalkylarylamide Derivatives 审中-公开
    羟烷基芳基酰胺衍生物

    公开(公告)号：US20090062297A1

    公开(公告)日：2009-03-05

    申请号：US12087623

    申请日：2007-01-08

    申请人： Richard W. Heidebrecht ,  Thomas A. Miller ,  Kevin J. Wilson ,  David J. Witter ,  Jonathan Grimm

    发明人： Richard W. Heidebrecht ,  Thomas A. Miller ,  Kevin J. Wilson ,  David J. Witter ,  Jonathan Grimm

    IPC分类号： A61K31/496 ,  C07D333/24 ,  A61K31/381 ,  A61K31/422 ,  C07D413/12 ,  C07D333/70

    CPC分类号： C07D333/70 ,  C07D333/20 ,  C07D413/12

    摘要： The present invention relates to a novel class of hydroxyalkylarylamide derivatives. The instant compounds can be used to treat cancer. The fluorinated arylamide derivatives can also inhibit histone deacetylase and are suitable for use in selectively inducing terminal differentiation, and arresting cell growth and/or apoptosis of neoplastic cells, thereby inhibiting proliferation of such cells. Thus, the compounds of the present invention are useful in treating a patient having a tumor characterized by proliferation of neoplastic cells. The compounds of the invention may also be useful in the prevention and treatment of TRX-mediated diseases, such as autoimmune, allergic and inflammatory diseases, and in the prevention and/or treatment of diseases of the central nervous system (CNS), such as neurodegenerative diseases. The present invention further provides pharmaceutical compositions comprising the hydroxamic acid derivatives and safe dosing regimens of these pharmaceutical compositions, which are easy to follow, and which result in a therapeutically effective amount of the hydroxamic acid derivatives in vivo.

    摘要翻译： 本发明涉及一类新的羟烷基芳基酰胺衍生物。 本发明化合物可用于治疗癌症。 氟化芳基酰胺衍生物还可以抑制组蛋白脱乙酰酶，并且适用于选择性诱导终末分化，并阻止肿瘤细胞的细胞生长和/或凋亡，从而抑制这些细胞的增殖。 因此，本发明的化合物可用于治疗具有以肿瘤细胞增殖为特征的肿瘤的患者。 本发明的化合物还可用于预防和治疗TRX介导的疾病，例如自身免疫性，过敏性和炎性疾病，以及预防和/或治疗中枢神经系统（CNS）的疾病，例如 神经退行性疾病 本发明进一步提供包含异羟肟酸衍生物和这些药物组合物的安全投药方案的药物组合物，它们易于遵循，并且其在体内导致治疗有效量的异羟肟酸衍生物。

    ACTUATABLE PLOW BLADE GROUND SUPPORT METHOD AND APPARATUS
    29.
    发明申请
    ACTUATABLE PLOW BLADE GROUND SUPPORT METHOD AND APPARATUS 审中-公开

    公开(公告)号：US20170328021A1

    公开(公告)日：2017-11-16

    申请号：US15592465

    申请日：2017-05-11

    申请人： Thomas A. Miller

    发明人： Thomas A. Miller

    IPC分类号： E01H5/06 ,  E02F9/22 ,  E01H5/09

    摘要： A ground support apparatus for a material moving implement configured for moving a material from a surface. The material moving implement has a front surface and a rear surface. The ground support apparatus includes an actuating system that has at least one skid shoe actuator attached to the rear surface of the material moving implement, and at least one skid shoe operably coupled to the at least one skid shoe actuator. The skid shoe includes a first end configured for coupling to the at least one skid shoe actuator and a second end configured for contacting the surface. The ground support apparatus also includes manually-operated skid shoe controls operably connected to the actuating system and operable to actuate the at least one skid shoe actuator.