3,4-Difluoro-2-(4-bromo-2-methyl-phenylamino)-N-(2-thienylmethoxy)-benzamide

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 3,4-Difluoro-2-(4-bromo-2-methyl-phenylamino)-N-(2-thienylmethoxy)-benzamide
• 英文别名: 3,4-Difluoro-2-(4-bromo-2-methyl-phenylamino)-N-(thien-2-ylmethoxy)-benzamide；2-(4-bromo-2-methylanilino)-3,4-difluoro-N-(thiophen-2-ylmethoxy)benzamide
• 化学式: C₁₉H₁₅BrF₂N₂O₂S
• 分子量: 453.307
• InChiKey: ULZOCHGQJGYENN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.8
• 重原子数：
  27
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.11
• 拓扑面积：
  78.6
• 氢给体数：
  2
• 氢受体数：
  6

文献信息

• 4-bromo or 4-iodo phenylamino benzhydroxamic acid derivatives and their use as MEK inhibitors
  申请人：——

  公开号：US20030078428A1

  公开（公告）日：2003-04-24

  Phenylamino benzhydroxamic acid derivatives of formula (I) where R 1 , R 2 , R 3 , R 4 , R 5 , and R 6 are hydrogen or substituent groups such as alkyl, and where R 7 is hydrogen or an organic radical, are potent inhibitors of MEK and, as such, are effective in treating cancer and other proliferative diseases such as psoriasis and restenosis.

  苯胺基苯基羟羟肟酸衍生物的化学式（I），其中R1、R2、R3、R4、R5和R6为氢或取代基，如烷基，R7为氢或有机基团，是MEK的有效抑制剂，因此在治疗癌症和其他增殖性疾病（如牛皮癣和再狭窄）方面具有良好效果。
• Combination chemotherapy
  申请人：——

  公开号：US20040171632A1

  公开（公告）日：2004-09-02

  Mitotic inhibitors such as paclitaxel have improved antitumor activity when used in combination with a selective MEK inhibitor, especially a phenyl amine compound of Formula I and II: 1

  有丝分裂抑制剂如紫杉醇在与选择性MEK抑制剂结合使用时，特别是Formula I和II的苯胺化合物，已提高抗肿瘤活性。
• [EN] 4-BROMO OR 4-IODO PHENYLAMINO BENZHYDROXAMIC ACID DERIVATIVES AND THEIR USE AS MEK INHIBITORS<br/>[FR] DERIVES D'ACIDE BENZHYDROXAMIQUE PHENYLAMINO 4-BROMO OU 4-IODO ET UTILISATION DE CES DERNIERS EN TANT QU'INHIBITEURS DE MEK
  申请人：WARNER-LAMBERT COMPANY

  公开号：WO1999001426A1

  公开（公告）日：1999-01-14

  (EN) Phenylamino benzhydroxamic acid derivatives of formula (I) where R1, R2, R3, R4, R5, and R6 are hydrogen or substituent groups such as alkyl, and where R7 is hydrogen or an organic radical, are potent inhibitors of MEK and, as such, are effective in treating cancer and other proliferative diseases such as psoriasis and restenosis.(FR) On décrit des dérivés d'acide benzhydroxamique phénylamino de formule (I). Dans la formule R1, R2, R3, R4, R5 et R6 représentent hydrogène ou des groupes substituants tels que alkyle; R7 représentant hydrogène ou un radical organique. Ces dérivés sont de puissants inhibiteurs de MEK et en tant que tels ils sont efficaces dans le traitement du cancer et d'autres maladies proliférantes telles que le psoriasis et la resténose.

  Phenylamino benzhydroxamic acid derivatives of formula (I) where R1, R2, R3, R4, R5, and R6 are hydrogen or substituent groups such as alkyl, and where R7 is hydrogen or an organic radical, are potent inhibitors of MEK and, as such, are effective in treating cancer and other proliferative diseases such as psoriasis and restenosis. 翻译：公式（I）中的苯氨基苯甲酰羟肟酸衍生物，其中R1、R2、R3、R4、R5和R6是氢或取代基，例如烷基，而R7是氢或有机基团，是MEK的强效抑制剂，因此在治疗癌症和其他增生性疾病，如银屑病和再狭窄方面非常有效。
• Treatment of asthma with MEK inhibitors
  申请人：——

  公开号：US20040141924A1

  公开（公告）日：2004-07-22

  This invention provides a method of preventing or treating asthma by administering to a patient in need of treatment an effective amount of a selective MEK inhibitor, especially a phenyl amine of Formula I and II: 1

  本发明提供了一种通过向需要治疗的患者施用有效量的选择性MEK抑制剂，特别是公式I和II的苯胺，来预防或治疗哮喘的方法。
• Method of treating or inhibiting neutrophil chemotaxis by administering a mek inhibitor
  申请人：WARNER-LAMBERT COMPANY

  公开号：EP1262176A1

  公开（公告）日：2002-12-04

  The present invention provides a method of treating or preventing neutrophil chemotaxis. Specifically, the present invention provides a method of treating or preventing neutrophil migration by administering to a patient a MEK inhibitor.

  本发明提供了一种治疗或预防中性粒细胞趋化的方法。具体而言，本发明提供了一种通过向患者施用MEK抑制剂治疗或预防中性粒细胞迁移的方法。