5-(2-Fluoro-4-methoxyphenyl)-1,2-oxazole-3-carboxylic acid | 953718-97-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 5-(2-Fluoro-4-methoxyphenyl)-1,2-oxazole-3-carboxylic acid
• CAS: 953718-97-3
• 化学式: C₁₁H₈FNO₄
• mdl: MFCD09729786
• 分子量: 237.18
• InChiKey: JJOTVYNDKCWFOX-UHFFFAOYSA-N

物化性质

• 沸点：
  433.0±45.0 °C(Predicted)
• 密度：
  1.383±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.09
• 拓扑面积：
  72.6
• 氢给体数：
  1
• 氢受体数：
  6

文献信息

• [EN] PIPERIDINE CXCR7 RECEPTOR MODULATORS<br/>[FR] MODULATEURS DU RÉCEPTEUR DE CXCR7 PIPÉRIDINE
  申请人：IDORSIA PHARMACEUTICALS LTD

  公开号：WO2018019929A1

  公开（公告）日：2018-02-01

  The present invention relates to piperidine derivatives of formula (I) wherein Ar1, Ar2, RAr1, R1, R2, and R3 are as described in the description, their preparation, to pharmaceutically acceptable salts thereof, and to their use as pharmaceuticals, to pharmaceutical compositions containing one or more compounds of formula (I), and especially to their use as CXCR7 receptor modulators.

  本发明涉及式(I)的哌啶衍生物，其中Ar1、Ar2、RAr1、R1、R2和R3如描述中所述，它们的制备，其药学上可接受的盐，以及它们作为药物的用途，含有一个或多个式(I)化合物的药物组合物，特别是它们作为CXCR7受体调节剂的用途。
• Piperdine CXCR7 receptor modulators
  申请人：IDORSIA PHARMACEUTICALS LTD

  公开号：US10752620B2

  公开（公告）日：2020-08-25

  The present invention relates to piperidine derivatives of formula (I) wherein Ar1, Ar2, RAr1, R1, R2 and R3 are as described in the description, their preparation, to pharmaceutically acceptable salts thereof, and to their use as pharmaceuticals, to pharmaceutical compositions containing one or more compounds of formula (I), and especially to their use as CXCR7 receptor modulators.

  本发明涉及式 (I) 的哌啶衍生物 其中 Ar1、Ar2、RAr1、R1、R2 和 R3 如描述中所述，它们的制备，它们的药学上可接受的盐，以及它们作为药物的用途，含有一种或多种式 (I) 化合物的药物组合物，特别是它们作为 CXCR7 受体调节剂的用途。
• PIPERIDINE CXCR7 RECEPTOR MODULATORS
  申请人：Idorsia Pharmaceuticals Ltd

  公开号：EP3490986B1

  公开（公告）日：2021-11-24
• PIPERDINE CXCR7 RECEPTOR MODULATORS
  申请人：IDORSIA PHARMACEUTICALS LTD

  公开号：US20190169180A1

  公开（公告）日：2019-06-06

  The present invention relates to piperidine derivatives of formula (I) wherein Ar 1 , Ar 2 , R Ar1 , R 1 , R 2 and R 3 are as described in the description, their preparation, to pharmaceutically acceptable salts thereof, and to their use as pharmaceuticals, to pharmaceutical compositions containing one or more compounds of formula (I), and especially to their use as CXCR7 receptor modulators.