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4-methyl-2-{4-[(methylsulfonyl)oxy]phenyl}-1,3-thiazole-5-carboxylic acid | 929693-90-3

中文名称
——
中文别名
——
英文名称
4-methyl-2-{4-[(methylsulfonyl)oxy]phenyl}-1,3-thiazole-5-carboxylic acid
英文别名
4-Methyl-2-(4-methylsulfonyloxyphenyl)-1,3-thiazole-5-carboxylic acid
4-methyl-2-{4-[(methylsulfonyl)oxy]phenyl}-1,3-thiazole-5-carboxylic acid化学式
CAS
929693-90-3
化学式
C12H11NO5S2
mdl
——
分子量
313.355
InChiKey
OYEVNLTVIOAOSM-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 熔点:
    145 °C(Solvent: Pentane)
  • 沸点:
    558.4±60.0 °C(predicted)
  • 密度:
    1.483±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    20
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    130
  • 氢给体数:
    1
  • 氢受体数:
    7

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    4-methyl-2-{4-[(methylsulfonyl)oxy]phenyl}-1,3-thiazole-5-carboxylic acid 在 lithium hydroxide 、 1-羟基苯并三唑盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺三乙胺 作用下, 以 四氢呋喃N,N-二甲基甲酰胺 为溶剂, 反应 24.0h, 生成 2-{4-[({2-[4-(Methanesulfonyloxy)phenyl]-4-methyl-1,3-thiazol-5-yl}formamido)methyl]phenoxy}-2-methylpropanoic acid
    参考文献:
    名称:
    Substituted 2-[(4-Aminomethyl)phenoxy]-2-methylpropionic Acid PPARα Agonists. 1. Discovery of a Novel Series of Potent HDLc Raising Agents
    摘要:
    The peroxisome proliferator activated receptors PPAR alpha, PPAR gamma, and PPAR delta are ligand-activated transcription factors that play a key role in lipid homeostasis. The fibrates raise circulating levels of high-density lipoprotein cholesterol and lower levels of triglycerides in part through their activity as PPAR alpha agonists; however, the low potency and restricted selectivity of the fibrates may limit their efficacy, and it would be desirable to develop more potent and selective PPAR alpha agonists. Modification of the selective PPAR delta agonist 1 (GW501516) so as to incorporate the 2-aryl-2-methylpropionic acid group of the fibrates led to a marked shift in potency and selectivity toward PPAR alpha agonism. Optimization of the series gave 25a, which shows EC50 = 4 nM on PPAR alpha and at least 500-fold selectivity versus PPAR delta and PPAR gamma. Compound 25a (GW590735) has been progressed to clinical trials for the treatment of diseases of lipid imbalance.
    DOI:
    10.1021/jm058056x
  • 作为产物:
    参考文献:
    名称:
    Substituted 2-[(4-Aminomethyl)phenoxy]-2-methylpropionic Acid PPARα Agonists. 1. Discovery of a Novel Series of Potent HDLc Raising Agents
    摘要:
    The peroxisome proliferator activated receptors PPAR alpha, PPAR gamma, and PPAR delta are ligand-activated transcription factors that play a key role in lipid homeostasis. The fibrates raise circulating levels of high-density lipoprotein cholesterol and lower levels of triglycerides in part through their activity as PPAR alpha agonists; however, the low potency and restricted selectivity of the fibrates may limit their efficacy, and it would be desirable to develop more potent and selective PPAR alpha agonists. Modification of the selective PPAR delta agonist 1 (GW501516) so as to incorporate the 2-aryl-2-methylpropionic acid group of the fibrates led to a marked shift in potency and selectivity toward PPAR alpha agonism. Optimization of the series gave 25a, which shows EC50 = 4 nM on PPAR alpha and at least 500-fold selectivity versus PPAR delta and PPAR gamma. Compound 25a (GW590735) has been progressed to clinical trials for the treatment of diseases of lipid imbalance.
    DOI:
    10.1021/jm058056x
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