JP2014525464A5 - - Google Patents

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JP2014525464A5
JP2014525464A5 JP2014528675A JP2014528675A JP2014525464A5 JP 2014525464 A5 JP2014525464 A5 JP 2014525464A5 JP 2014528675 A JP2014528675 A JP 2014528675A JP 2014528675 A JP2014528675 A JP 2014528675A JP 2014525464 A5 JP2014525464 A5 JP 2014525464A5
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compound
cancer
pharmaceutical composition
nhc
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JP6342805B2 (ja
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Claims (56)

  1. 下記式:
    を有する化合物であって、式中、
    1およびR2は独立して水素または置換もしくは非置換アルキルであり;
    3は独立して置換または非置換アルキルであり;
    5は独立してハロゲン、−CN、−CXa 3、−S(O)2H、−NO、−NO2、−C(O)H、−C(O)NH2、−S(O)2NH2、−OH、−SH、−SO2Cl、−SO3H、−SO4H、−NHNH2、−ONH2、−NHC=(O)NHNH2、−NHC=(O)NH2、−NHSO2H、−NHC=(O)H、−NHC(O)−OH、−NHOH、−OCF3、−OCHF2、−CO2H、または置換もしくは非置換(C1−C6)アルキルであり;
    6は独立してハロゲン、−CN、−CXb 3、−S(O)2H、−NO、−NO2、−C(O)H、−C(O)NH2、−S(O)2NH2、−OH、−SH、−SO2Cl、−SO3H、−SO4H、−NHNH2、−ONH2、−NHC=(O)NHNH2、−NHC=(O)NH2、−NHSO2H、−NHC=(O)H、−NHC(O)−OH、−NHOH、−OCF3、−OCHF2、または−CO2Hであり;
    1は独立して結合または置換もしくは非置換アルキレンであり;
    z1は独立して0から4の整数であり;
    z2は独立して0から5の整数であり;
    aおよびXbは独立して−F、−Cl、−Br、または−Iである、
    上記化合物。
  2. 1が水素である、請求項1に記載の化合物。
  3. 1が非置換(C1−C6)アルキルである、請求項1に記載の化合物。
  4. 2が水素である、請求項1に記載の化合物。
  5. 2が非置換(C1−C6)アルキルである、請求項1に記載の化合物。
  6. 1が結合である、請求項1に記載の化合物。
  7. 1が非置換(C1−C6)アルキレンである、請求項1に記載の化合物。
  8. 1がメチレンである、請求項7に記載の化合物。
  9. 3が置換または非置換アルキルである、請求項1に記載の化合物。
  10. 3が非置換(C1−C6)アルキルである、請求項9に記載の化合物。
  11. 3がイソプロピルである、請求項10に記載の化合物。
  12. 5がハロゲン、−CN、−CXa 3、−NO、−NO2、−C(O)H、または−CO2Hである、請求項1に記載の化合物。
  13. 5がハロゲンまたは−CXa 3である、請求項12に記載の化合物。
  14. 5が−CXa 3である、請求項13に記載の化合物。
  15. aが−Fである、請求項14に記載の化合物。
  16. 5がハロゲンである、請求項13に記載の化合物。
  17. 5が−Fである、請求項16に記載の化合物。
  18. 5が−Clである、請求項16に記載の化合物。
  19. 6がハロゲン、−CN、−CXb 3、−NO、−NO2、−C(O)H、または−CO2
    Hである、請求項1に記載の化合物。
  20. 6がハロゲンまたは−CXb 3である、請求項19に記載の化合物。
  21. 6が−CXb 3である、請求項20に記載の化合物。
  22. bが−Fである、請求項21に記載の化合物。
  23. 6がハロゲンである、請求項1に記載の化合物。
  24. 6が−Fである、請求項23に記載の化合物。
  25. z1が0である、請求項1に記載の化合物。
  26. z1が1である、請求項1に記載の化合物。
  27. z2が2である、請求項1に記載の化合物。
  28. 下記式:
    を有し、式中
    4は独立してハロゲン、−CN、−CX3、−S(O)2H、−NO、−NO2、−C(O)H、−C(O)NH2、−S(O)2NH2、−OH、−SH、−SO2Cl、−SO3H、−SO4H、−NHNH2、−ONH2、−NHC=(O)NHNH2、−NHC=(O)NH2、−NHSO2H、−NHC=(O)H、−NHC(O)−OH、−NHOH、−OCF3、−OCHF2、−CO2H、または置換もしくは非置換(C1−C6)アルキルであ
    り;
    yは独立して0から4の整数であり;
    Xは独立して−F、−Cl、−Br、または−Iである、
    請求項1に記載の化合物。
  29. 4がハロゲン、−CN、−CX3、−NO、−NO2、−C(O)H、または−CO2Hである、請求項28に記載の化合物。
  30. 4がハロゲンまたは−CX3である、請求項29に記載の化合物。
  31. 4が−CX3である、請求項30に記載の化合物。
  32. Xが−Fである、請求項31に記載の化合物。
  33. yが1である、請求項28に記載の化合物。
  34. 下記式:
    からなる群から選択される式を有する、請求項1に記載の化合物。
  35. 下記式:
    からなる群から選択される式を有する、請求項33に記載の化合物。
  36. 薬剤的に許容できる賦形剤および請求項1〜35のうちのいずれか1項に記載の化合物を含んでなる、医薬組成物。
  37. 抗がん剤をさらに含んでなる、請求項36に記載の医薬組成物。
  38. 前記抗がん剤がEGFRを標的とする治療法または治療剤である、請求項37に記載の医薬組成物。
  39. 前記EGFRを標的とする治療法または治療剤がエルロチニブまたはゲフィチニブである、請求項38に記載の医薬組成物。
  40. 前記抗がん剤がMEKを標的とする治療法または治療剤である、請求項37に記載の医薬組成物。
  41. 効量の、請求項1〜35のうちのいずれか1項に記載の化合物を含んでなる、がんを治療することに用いるための医薬組成物
  42. 前記がんが複数の内分泌新生物2(multiple endocrine neoplasm 2)と関連している、請求項41に記載の医薬組成物
  43. 前記がんが異常なRetキナーゼ活性と関連している、請求項41に記載の医薬組成物
  44. 前記がんが異常なAXLキナーゼ活性と関連している、請求項41に記載の医薬組成物
  45. 前記がんが抗がん剤に耐性を示す、請求項44に記載の医薬組成物
  46. 前記抗がん剤がEGFRを標的とする治療法または治療剤である、請求項45に記載の医薬組成物
  47. 前記EGFRを標的とする治療法または治療剤がエルロチニブまたはゲフィチニブである、請求項46に記載の医薬組成物
  48. 前記がんが、家族性甲状腺髄様がん、甲状腺髄様癌、褐色細胞腫、原発性副甲状腺機能亢進症、腸管神経節神経腫症(intestinal ganglioneuromatosis)、副甲状腺過形成、粘膜神経腫、黒色腫、結腸直腸がん、乳頭様甲状腺がん、乳がん、肝細胞癌、肺がん、膵がん、慢性骨髄性白血病、グリア芽腫、骨肉腫、赤血球性もしくは巨核球性白血病、子宮がん、結腸がん、前立腺がん、甲状腺がん、卵巣がん、肝臓がん、腎細胞癌、急性骨髄性白血病、胃がん、非小細胞肺がん、または消化管間質腫瘍である、請求項41に記載の医薬組成物
  49. 治療有効量の抗がん剤をさらに含んでなる、請求項41に記載の医薬組成物
  50. 前記抗がん剤がEGFRを標的とする治療法または治療剤である、請求項49に記載の医薬組成物
  51. 前記EGFRを標的とする治療法または治療剤がエルロチニブまたはゲフィチニブである、請求項50に記載の医薬組成物
  52. 前記抗がん剤がMEKを標的とする治療法または治療剤である、請求項49に記載の医薬組成物
  53. Retキナーゼ、Rafキナーゼ、Srcキナーゼ、およびS6Kキナーゼの活性を低減させる方法であって、Retキナーゼ、Rafキナーゼ、Srcキナーゼ、およびS6Kキナーゼを、有効量の、請求項1〜35のうちのいずれか1項に記載の化合物と接触させることを含む、上記方法。
  54. AXLキナーゼの活性を低減させる方法であって、AXLキナーゼを、有効量の、請求項1〜35のうちのいずれか1項に記載の化合物と接触させることを含む、上記方法。
  55. 化合物が、以下:
    からなる群から選択される、請求項41〜52のいずれか1項に記載の医薬組成物
  56. 化合物が以下:
    からなる群から選択される、請求項41〜52のいずれか1項に記載の医薬組成物
JP2014528675A 2011-09-02 2012-08-31 置換ピラゾロ[3,4−d]ピリミジンおよびその用途 Active JP6342805B2 (ja)

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US201161530847P 2011-09-02 2011-09-02
US61/530,847 2011-09-02
US201261606296P 2012-03-02 2012-03-02
US61/606,296 2012-03-02
PCT/US2012/053542 WO2013077921A2 (en) 2011-09-02 2012-08-31 Substituted pyrazolo[3,4-d]pyrimidines and uses thereof

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JP2014525464A JP2014525464A (ja) 2014-09-29
JP2014525464A5 true JP2014525464A5 (ja) 2015-10-29
JP6342805B2 JP6342805B2 (ja) 2018-06-13

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US (2) US9321772B2 (ja)
EP (1) EP2751112B1 (ja)
JP (1) JP6342805B2 (ja)
AU (1) AU2012341028C1 (ja)
CA (1) CA2846496C (ja)
MX (1) MX370814B (ja)
WO (1) WO2013077921A2 (ja)

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