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34 条记录 (耗时 0.039 秒)

    5,7-disubstituted[1.3]thiazolo [4,5-D] pyrimidin-2(3H)-amine derivatives and their use in therapy
    21.
    发明授权
    5,7-disubstituted[1.3]thiazolo [4,5-D] pyrimidin-2(3H)-amine derivatives and their use in therapy 失效
    5,7-二取代[1.3]噻唑并[4,5-D]嘧啶-2（3H） - 胺衍生物及其在治疗中的用途

    公开(公告)号：US08158785B2

    公开(公告)日：2012-04-17

    申请号：US12442831

    申请日：2007-09-27

    申请人： Rolf Johansson ,  Sofia Karlstrom ,  Annika Kers ,  Gunnar Nordvall ,  Tobias Rein ,  Can Slivo

    发明人： Rolf Johansson ,  Sofia Karlstrom ,  Annika Kers ,  Gunnar Nordvall ,  Tobias Rein ,  Can Slivo

    IPC分类号： A61K31/519 ,  A61P9/10 ,  A61P25/00 ,  C07D417/14

    CPC分类号： C07D513/04

    摘要： There are disclosed novel 5-substituted 7-amino-[1,3]thiazolo[4,5-d]pyrimidine derivatives of formula (I) wherein R1, R2, R3, R4 and n are as defined in the specification, and pharmaceutically acceptable salts thereof, together with processes for their preparation, pharmaceutical compositions comprising them and their use in therapy. The compounds of formula (I) are CX3CR1 receptor antagonists and are thereby particularly useful in the treatment or prophylaxis of neurodegenerative disorders, demyelinating disease, cardio- and cerebrovascular atherosclerotic disorders, peripheral artery disease, rheumatoid arthritis, pulmonary diseases such as COPD, asthma or pain.

    摘要翻译： 公开了式（I）的新的5-取代的7-取代的7-氨基 - [1,3]噻唑并[4,5-d]嘧啶衍生物，其中R 1，R 2，R 3，R 4和n如说明书中所定义， 其可接受的盐及其制备方法，包含它们的药物组合物及其在治疗中的用途。 式（I）化合物是CX3CR1受体拮抗剂，因此特别可用于治疗或预防神经变性疾病，脱髓鞘疾病，心血管和脑血管动脉粥样硬化疾病，外周动脉疾病，类风湿性关节炎，肺疾病如COPD，哮喘或 疼痛。

    5,7-disubstituted thiazolo[4,5-d]pyrimidines for the selective inhibition of chemokine receptors
    22.
    发明授权
    5,7-disubstituted thiazolo[4,5-d]pyrimidines for the selective inhibition of chemokine receptors 有权
    5,7-二取代噻唑并[4,5-d]嘧啶，用于选择性抑制趋化因子受体

    公开(公告)号：US07960395B2

    公开(公告)日：2011-06-14

    申请号：US11862743

    申请日：2007-09-27

    申请人： Rolf Johansson ,  Sofia Karlström ,  Annika Kers ,  Gunnar Nordvall ,  Tobias Rein ,  Can Slivo

    发明人： Rolf Johansson ,  Sofia Karlström ,  Annika Kers ,  Gunnar Nordvall ,  Tobias Rein ,  Can Slivo

    IPC分类号： C07D487/04 ,  A61K31/519 ,  A61P11/06 ,  A61P9/10 ,  A61P37/06

    CPC分类号： C07D513/04

    摘要： There are disclosed novel 5,7-disubstituted [1,3]thiazolo[4,5-d]pyrimidin-2(3H)-one derivatives of formula (I) wherein R1, R2, R3, R4 and n are as defined in the specification, and pharmaceutically acceptable salts thereof, together with processes for their preparation, pharmaceutical compositions comprising them and their use in therapy. The compounds of formula (I) are CX3CR1 receptor antagonists and are thereby particularly useful in the treatment or prophylaxis of neurodegenerative disorders, demyelinating disease, cardio- and cerebrovascular atherosclerotic disorders, peripheral artery disease, rheumatoid arthritis, pulmonary diseases such as COPD, asthma or pain.

    摘要翻译： 公开了式（I）的新的5,7-二取代[1,3]噻唑并[4,5-d]嘧啶-2（3H） - 酮衍生物，其中R 1，R 2，R 3，R 4和n如 说明书及其药学上可接受的盐以及其制备方法，包含它们的药物组合物及其在治疗中的用途。 式（I）化合物是CX3CR1受体拮抗剂，因此特别可用于治疗或预防神经变性疾病，脱髓鞘疾病，心血管和脑血管动脉粥样硬化疾病，外周动脉疾病，类风湿性关节炎，肺疾病如COPD，哮喘或 疼痛。

    5,7-disubstituted thiazolo[4,5-D]pyrimidines as chemokine inhibitors
    23.
    发明授权
    5,7-disubstituted thiazolo[4,5-D]pyrimidines as chemokine inhibitors 有权
    5,7-二取代噻唑并[4,5-D]嘧啶作为趋化因子抑制剂

    公开(公告)号：US07947693B2

    公开(公告)日：2011-05-24

    申请号：US11910780

    申请日：2006-04-03

    申请人： Gunnar Nordvall ,  Colin Ray ,  Tobias Rein ,  Daniel Sohn

    发明人： Gunnar Nordvall ,  Colin Ray ,  Tobias Rein ,  Daniel Sohn

    IPC分类号： C07D487/04 ,  A61K31/519 ,  A61P11/06 ,  A61P9/10 ,  A61P37/06

    CPC分类号： C07D513/04

    摘要： There are disclosed novel 5-substituted 7-amino-[1,3]thiazolo[4,5-d]pyrimidine derivatives of formula (I) wherein R1, R2, R3, R4 and R5 are as defined in the specification, and pharmaceutically acceptable salts thereof, together with processes for their preparation, pharmaceutical compositions comprising them and their use in therapy. The compounds of formula (I) are CX3CR1 receptor antagonists and are thereby particularly useful in the treatment or prophylaxis of neurodegenerative disorders, demyelinating disease, cardio- and cerebrovascular atherosclerotic disorders, peripheral artery disease, rheumatoid arthritis, pulmonary diseases such as COPD, asthma or pain.

    摘要翻译： 公开了式（I）的新的5-取代的7-取代的7-氨基 - [1,3]噻唑并[4,5-d]嘧啶衍生物，其中R 1，R 2，R 3，R 4和R 5如说明书中所定义， 其可接受的盐及其制备方法，包含它们的药物组合物及其在治疗中的用途。 式（I）化合物是CX3CR1受体拮抗剂，因此特别可用于治疗或预防神经变性疾病，脱髓鞘疾病，心血管和脑血管动脉粥样硬化疾病，外周动脉疾病，类风湿性关节炎，肺疾病如COPD，哮喘或 疼痛。

    Novel Heteroaryl Substituted Benzothiazoles
    26.
    发明申请
    Novel Heteroaryl Substituted Benzothiazoles 失效
    新型杂芳基取代苯并噻唑

    公开(公告)号：US20090028787A1

    公开(公告)日：2009-01-29

    申请号：US12162255

    申请日：2007-01-25

    申请人： Ylva Gravenfors ,  Catrin Jonasson ,  Jonas Malmstrom ,  Gunnar Nordvall ,  David Pyring ,  Can Slivo ,  Daniel Sohn ,  Peter Strom ,  David Wensbo

    发明人： Ylva Gravenfors ,  Catrin Jonasson ,  Jonas Malmstrom ,  Gunnar Nordvall ,  David Pyring ,  Can Slivo ,  Daniel Sohn ,  Peter Strom ,  David Wensbo

    IPC分类号： A61K31/496 ,  C07D417/14 ,  C07D417/04 ,  A61K31/5377 ,  A61P25/28 ,  A61K49/00 ,  A61K31/4439 ,  C07D413/14

    CPC分类号： C07D417/04 ,  C07B59/002 ,  C07D513/04

    摘要： The present invention relates to novel heteroaryl substituted benzothiazole derivatives, precursors thereof, and therapeutic uses for such compounds, having the structural formula (I) below: [Chemical formula should be inserted here. Please see paper copy] and to their pharmaceutically acceptable salt, compositions and methods of use. Furthermore, the invention relates to novel heteroaryl substituted benzothiazole derivatives that are suitable for imaging amyloid deposits in living patients, their compositions, methods of use and processes to make such compounds. More specifically, the present invention relates to a method of imaging amyloid deposits in brain in vivo to allow antemortem diagnosis of Alzheimer's disease as well as measuring clinical efficacy of Alzheimer's disease therapeutic agents.

    摘要翻译： 本发明涉及新颖的杂芳基取代的苯并噻唑衍生物，其前体，以及具有以下结构式（I）的化合物的治疗用途：[化学式应在此插入。 请参阅纸本]及其药学上可接受的盐，组合物和使用方法。 此外，本发明涉及适用于在活体患者中成像淀粉样蛋白沉积物的新型杂芳基取代的苯并噻唑衍生物，其组合物，使用方法和制备此类化合物的方法。 更具体地说，本发明涉及一种在体内淀粉样蛋白沉积物在体内成像以使阿尔茨海默病的止血诊断成为可能并测量阿尔茨海默病治疗剂的临床疗效的方法。

    Novel Compounds 480
    27.
    发明申请
    Novel Compounds 480 有权
    新型化合物480

    公开(公告)号：US20080318981A1

    公开(公告)日：2008-12-25

    申请号：US11862743

    申请日：2007-09-27

    申请人： Rolf Johansson ,  Sofia Karlstrom ,  Annika Kers ,  Gunnar Nordvall ,  Tobias Rein ,  Can Slivo

    发明人： Rolf Johansson ,  Sofia Karlstrom ,  Annika Kers ,  Gunnar Nordvall ,  Tobias Rein ,  Can Slivo

    IPC分类号： A61K31/519 ,  A61P25/00 ,  A61P9/00 ,  A61P11/00 ,  C07D513/04

    CPC分类号： C07D513/04

    摘要： There are disclosed novel 5,7-disubstituted [1,3]thiazolo[4,5-d]pyrimidin-2(3H)-one derivatives of formula (I) wherein R1, R2, R3, R4 and n are as defined in the specification, and pharmaceutically acceptable salts thereof, together with processes for their preparation, pharmaceutical compositions comprising them and their use in therapy. The compounds of formula (I) are CX3CR1 receptor antagonists and are thereby particularly useful in the treatment or prophylaxis of neurodegenerative disorders, demyelinating disease, cardio- and cerebrovascular atherosclerotic disorders, peripheral artery disease, rheumatoid arthritis, pulmonary diseases such as COPD, asthma or pain.

    摘要翻译： 公开了式（I）的新的5,7-二取代[1,3]噻唑并[4,5-d]嘧啶-2（3H） - 酮衍生物，其中R 1，R 2，R 3，R 4和n如 说明书及其药学上可接受的盐以及其制备方法，包含它们的药物组合物及其在治疗中的用途。 式（I）化合物是CX3CR1受体拮抗剂，因此特别可用于治疗或预防神经变性疾病，脱髓鞘疾病，心血管和脑血管动脉粥样硬化疾病，外周动脉疾病，类风湿性关节炎，肺疾病如COPD，哮喘或 疼痛。

    Heteroaryl substituted benzothiazoles
    28.
    发明授权
    Heteroaryl substituted benzothiazoles 失效
    杂芳基取代的苯并噻唑

    公开(公告)号：US08163928B2

    公开(公告)日：2012-04-24

    申请号：US12162255

    申请日：2007-01-25

    申请人： Ylva Gravenfors ,  Catrin Jonasson ,  Jonas Malmstrom ,  Gunnar Nordvall ,  David Pyring ,  Can Slivo ,  Daniel Sohn ,  Peter Strom ,  David Wensbo

    发明人： Ylva Gravenfors ,  Catrin Jonasson ,  Jonas Malmstrom ,  Gunnar Nordvall ,  David Pyring ,  Can Slivo ,  Daniel Sohn ,  Peter Strom ,  David Wensbo

    IPC分类号： A61K51/00 ,  A61K51/04

    CPC分类号： C07D417/04 ,  C07B59/002 ,  C07D513/04

    摘要： The present invention relates to novel heteroaryl substituted benzothiazole derivatives, precursors thereof, and therapeutic uses for such compounds, having the structural formula (I) below: [Chemical formula should be inserted here. Please see paper copy] and to their pharmaceutically acceptable salt, compositions and methods of use. Furthermore, the invention relates to novel heteroaryl substituted benzothiazole derivatives that are suitable for imaging amyloid deposits in living patients, their compositions, methods of use and processes to make such compounds. More specifically, the present invention relates to a method of imaging amyloid deposits in brain in vivo to allow antemortem diagnosis of Alzheimer's disease as well as measuring clinical efficacy of Alzheimer's disease therapeutic agents.

    摘要翻译： 本发明涉及新颖的杂芳基取代的苯并噻唑衍生物，其前体，以及具有以下结构式（I）的化合物的治疗用途：[化学式应在此插入。 请参阅纸本]及其药学上可接受的盐，组合物和使用方法。 此外，本发明涉及适用于在活体患者中成像淀粉样蛋白沉积物的新型杂芳基取代的苯并噻唑衍生物，其组合物，使用方法和制备此类化合物的方法。 更具体地说，本发明涉及一种在体内淀粉样蛋白沉积物在体内成像以使阿尔茨海默病的止血诊断成为可能并测量阿尔茨海默病治疗剂的临床疗效的方法。

    5,7-disubstituted thiazolo[4,5-D]pyrimidines for the selective inhibition of chemokine receptors
    29.
    发明授权
    5,7-disubstituted thiazolo[4,5-D]pyrimidines for the selective inhibition of chemokine receptors 失效
    5,7-二取代噻唑并[4,5-D]嘧啶，用于选择性抑制趋化因子受体

    公开(公告)号：US08088780B2

    公开(公告)日：2012-01-03

    申请号：US11910781

    申请日：2006-04-03

    申请人： Gunnar Nordvall ,  Colin Ray ,  Tobias Rein ,  Daniel Sohn

    发明人： Gunnar Nordvall ,  Colin Ray ,  Tobias Rein ,  Daniel Sohn

    IPC分类号： C07D487/04 ,  A61K31/519 ,  A61P11/06 ,  A61P9/10 ,  A61P37/06

    CPC分类号： C07D413/04

    摘要： There are disclosed novel 5,7-disubstituted [1,3]thiazolo[4,5-d]pyrimidin-2(3H)-one derivatives of formula (I) wherein R1, R2, R3, R4 and R5 are as defined in the specification, and pharmaceutically acceptable salts thereof, together with processes for their preparation, pharmaceutical compositions comprising them and their use in therapy. The compounds of formula (I) are CX3CR1 receptor antagonists and are thereby particularly useful in the treatment or prophylaxis of neurodegenerative disorders, demyelinating disease, cardio- and cerebrovascular atherosclerotic disorders, peripheral artery disease, rheumatoid arthritis, pulmonary diseases such as COPD, asthma or pain.

    摘要翻译： 公开了式（I）的新的5,7-二取代[1,3]噻唑并[4,5-d]嘧啶-2（3H） - 酮衍生物，其中R 1，R 2，R 3，R 4和R 5如 说明书及其药学上可接受的盐以及其制备方法，包含它们的药物组合物及其在治疗中的用途。 式（I）化合物是CX3CR1受体拮抗剂，因此特别可用于治疗或预防神经变性疾病，脱髓鞘疾病，心脑血管动脉粥样硬化性疾病，外周动脉疾病，类风湿性关节炎，肺疾病如COPD，哮喘或 疼痛。