2-Bromo-1-[1-(1-methylethyl)-1H-pyrazol-4-yl]ethanone | 1103424-91-4

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 2-Bromo-1-[1-(1-methylethyl)-1H-pyrazol-4-yl]ethanone
• 英文别名: 2-bromo-1-(1-propan-2-ylpyrazol-4-yl)ethanone
• CAS: 1103424-91-4
• 化学式: C₈H₁₁BrN₂O
• 分子量: 231.09
• InChiKey: QMPLSDOUROSVQS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  12
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  34.9
• 氢给体数：
  0
• 氢受体数：
  2

文献信息

• [EN] COLONY STIMULATING FACTOR-1 RECEPTOR (CSF-1R) INHIBITORS<br/>[FR] INHIBITEURS DU RÉCEPTEUR DE FACTEUR-1 DE STIMULATION DE COLONIES (CSF-1R)
  申请人：GENZYME CORP

  公开号：WO2017015267A1

  公开（公告）日：2017-01-26

  Compounds of the formulas I and XIII, which are useful as colony stimulating factor-1 receptor inhibitors ("CSF 1R inhibitors").

  I和XIII式化合物，可用作促细胞增殖因子-1受体抑制剂（"CSF 1R抑制剂"）。
• Colony stimulating factor-1 receptor (CSF-1R) inhibitors
  申请人：Genzyme Corporation

  公开号：US11274108B2

  公开（公告）日：2022-03-15

  Compounds of the formulas which are useful as colony stimulating factor-1 receptor inhibitors (“CSF-1R inhibitors”).

  下列式子的化合物 可用作集落刺激因子-1 受体抑制剂（"CSF-1R 抑制剂"）。
• COLONY STIMULATING FACTOR-1 RECEPTOR (CSF-1R) INHIBITORS
  申请人：Genzyme Corporation

  公开号：EP3325471A1

  公开（公告）日：2018-05-30
• [EN] NOVEL HETEROARYL DERIVATIVES AS ANTAGONISTS OF ADENOSINE A3 RECEPTOR<br/>[FR] NOUVEAUX DÉRIVÉS HÉTÉROARYLE SERVANT D'ANTAGONISTES DU RÉCEPTEUR A3 DE L'ADÉNOSINE
  申请人：ADDEX PHARMACEUTICALS SA

  公开号：WO2009010871A2

  公开（公告）日：2009-01-22

  The present invention relates to novel compounds of Formula (I), wherein X1, X2, X3, X4, Y1, Y2, Y3, Y4, M1, M2, M3, Am and Bn are defined as in Formula (I); invention compounds are antagonists of adenosine receptors - subtype 3 (A3) which are useful for the treatment or disorders modulated by A3 receptors. The invention is also directed to pharmaceutical compositions and the use of such compounds in the manufacture of medicaments, as well as to the use of such compounds for the prevention and treatment of such diseases in which A3 is involved.