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5-Pyrimidinecarboxamide,2-[[4-(2-hydroxyethyl)phenyl]amino]-4-[(phenylmethyl)amino]-,monohydrochloride | 643089-97-8

中文名称
——
中文别名
——
英文名称
5-Pyrimidinecarboxamide,2-[[4-(2-hydroxyethyl)phenyl]amino]-4-[(phenylmethyl)amino]-,monohydrochloride
英文别名
4-benzylamino-2-{[4-(2-hydroxyethyl)phenyl]amino}pyrimidine-5-carboxamide hydrochloride
5-Pyrimidinecarboxamide,2-[[4-(2-hydroxyethyl)phenyl]amino]-4-[(phenylmethyl)amino]-,monohydrochloride化学式
CAS
643089-97-8
化学式
C20H21N5O2*ClH
mdl
——
分子量
399.88
InChiKey
IHWQSBDIKHGTFQ-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

计算性质

  • 辛醇/水分配系数(LogP):
    2.89
  • 重原子数:
    28.0
  • 可旋转键数:
    8.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    113.16
  • 氢给体数:
    4.0
  • 氢受体数:
    6.0

反应信息

  • 作为产物:
    描述:
    4-(benzylamino)-2-chloropyrimidine-5-carboxamide4-氨基苯乙醇N-甲基吡咯烷酮 为溶剂, 反应 0.5h, 以327 mg的产率得到5-Pyrimidinecarboxamide,2-[[4-(2-hydroxyethyl)phenyl]amino]-4-[(phenylmethyl)amino]-,monohydrochloride
    参考文献:
    名称:
    Identification of 4-benzylamino-2-[(4-morpholin-4-ylphenyl)amino]pyrimidine-5-carboxamide derivatives as potent and orally bioavailable STAT6 inhibitors
    摘要:
    Signal transducers and activators of transcription 6 (STAT6) is a key regulator of the type 2 helper T (Th2) cell immune response and a potential therapeutic target for allergic diseases such as asthma and atopic diseases. To search for potent and orally bioavailable STAT6 inhibitors, we synthesized a series of 4-benzylaminopyrimidine-5- carboxamide derivatives and evaluated their STAT6 inhibitory activities. Among these compounds, 2-[(4-morpholin-4-ylphenyl)amino]-4-[(2,3,6- trifluorobenzyl)amino]pyrimidine-5-carboxamide (25y, YM-341619, AS1617612) showed potent STAT6 inhibition with an IC(50) of 0.70 nM, and also inhibited Th2 differentiation in mouse spleen T cells induced by interleukin (IL)-4 with an IC(50) of 0.28 nM without affecting type 1 helper T (Th1) cell differentiation induced by IL-12. In addition, compound 25y showed an oral bioavailability of 25% in mouse. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2008.05.031
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