4-<(Phenylsulfinyl)methyl>benzoic acid | 110046-28-1

• 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: 4-<(Phenylsulfinyl)methyl>benzoic acid
• 英文别名: 4-(Benzenesulfinylmethyl)benzoic acid
• CAS: 110046-28-1
• 化学式: C₁₄H₁₂O₃S
• mdl: MFCD13225090
• 分子量: 260.313
• InChiKey: OQGJNAPHCFYVFE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  18
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.071
• 拓扑面积：
  73.6
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  4-[(苯基硫代)甲基]苯甲酸 在 间氯过氧苯甲酸 作用下， 以 氯仿 为溶剂， 反应 24.0h， 以92%的产率得到4-<(Phenylsulfinyl)methyl>benzoic acid
  参考文献：
  名称：

  一些新的硫化物，亚砜和砜的合成和光谱研究。2个

  摘要：

  DOI：

  10.1021/je00050a033

文献信息

• Novel Glucagon Antagonists/Inverse Agonists
  申请人：Madsen Peter

  公开号：US20070015757A1

  公开（公告）日：2007-01-18

  Novel compounds that act to antagonize the action of the glucagon peptide hormone on the glucagon receptor. More particularly, it relates to glucagon antagonists or inverse agonists.

  这是关于新型化合物，可拮抗胰高血糖素肽激素在胰高血糖素受体上的作用。更具体地说，它涉及胰高血糖素拮抗剂或反向激动剂。
• [EN] NOVEL GLUCAGON ANTAGONISTS/INVERSE AGONISTS<br/>[FR] NOUVEAUX ANTAGONISTES/AGONISTES INVERSES DU GLUCAGON
  申请人：NOVO NORDISK AS

  公开号：WO2005058845A2

  公开（公告）日：2005-06-30

  Novel compounds that act to antagonize the action of the glucagon peptide hormone on the glucagon receptor. More particularly, it relates to glucagon antagonists or inverse agonists. (I) wherein A is (II), (III) or (IV), Y is a valence bond, >C=O, =CR1-, -(CR1R2)m-, -NR1-,=N-, E is: C1-10-alkyl or C2-10-alkenyl; C3-10-cycloalkyl, C3-10-cycloalkenyl, C7-10-bicycloalkyl, C3-10-cycloakyl-C1-6-alkyl, C3-10-cycloalkenyl-C1-6-alkyl or C7-10-bicycloalkyl-C1-6-alkyl, wherein the rings may optionally be substituted with one or more substituents selected from halogen, C1-6-alkyl, C2-6-alkenyl, C1-6-alkoxy, C1-6-thioalkyl, -CF3, -OCF3, -SCF3, -OCHF2 and -SCHF2; aryl, aryloxy, arylthio, heteroaryl, aryl-C1-6-alkyl, aryloxy-C1-6-alkyl, arylthio-C1-6-alkyl, heteroaryl-C1-6-alkyl, diaryl-C1-6-alkyl or (C1-6 -alkyl)(aryl)-C1-7-alkyl, wherein the non-aromatic and aromatic rings may optinally be substituted with one or more substituents selected from halogen, C1-6-alkyl, C2-6-alkenyl, C1-6 -alkoxy, C1-6-thioalkyl, -CF3, -OCF3, -SCF3, -OCHF2, SCHF2, C3-10-cycloalkyl and C3-10-cycloalkenyl, or with two substituents on adjacent positions which are combined to form a bridge C1-6-alkylene, C2-6-alkenylene or -O-C1-6-alkylene-O-; (V) represents a phenyl, C3-8-cycloalkyl, or a 4-, 5-, 6- or 7-membered heterocycle, D is aryl or heteroaryl.
• Synthesis and spectral studies of some new sulfides, sulfoxides, and sulfones. 2
  作者：Ahmed A. Kassem、Ali A. El-Bardan、El Sayed M. E. Mansour

  DOI：10.1021/je00050a033

  日期：1987.10