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4-(2-(phenylamino)thiazol-4-yl)benzene-1,3-diol | 924173-79-5

中文名称
——
中文别名
——
英文名称
4-(2-(phenylamino)thiazol-4-yl)benzene-1,3-diol
英文别名
4-(2-anilino-1,3-thiazol-4-yl)benzene-1,3-diol
4-(2-(phenylamino)thiazol-4-yl)benzene-1,3-diol化学式
CAS
924173-79-5
化学式
C15H12N2O2S
mdl
——
分子量
284.338
InChiKey
FXVHSVUUZUOZDG-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):
    3.8
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    93.6
  • 氢给体数:
    3
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    2-溴-2,4-二羟基苯乙酮苯基硫脲乙醇 为溶剂, 反应 0.01h, 以95%的产率得到4-(2-(phenylamino)thiazol-4-yl)benzene-1,3-diol
    参考文献:
    名称:
    A library of novel allosteric inhibitors against fructose 1,6-bisphosphatase
    摘要:
    The identification of a proper lead compound for fructose 1,6-bisphosphatase (FBPase) is a critical step in the process of developing novel therapeutics against type-2 diabetes. Herein, we have successfully generated a library of allosteric inhibitors against FBPase as potential anti-diabetic drugs, of which, the lead compound 1b was identified through utilizing a virtual high-throughput screening (vHTS) system, which we have developed. The thiazole-based core structure was synthesized via the condensation of alpha-bromoketones with thioureas and substituents on the two aryl rings were varied. 4c was found to inhibit pig kidney FBPase approximately fivefold better than 1b. In addition, we have also identified 10b, a tight binding fragment, which can be use for fragment-based drug design purposes. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2009.04.030
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文献信息

  • Cosmetic Or Dermatological Preparations With A Content Of One Or More Thiazole Derivates
    申请人:Kolbe Ludger
    公开号:US20130039870A1
    公开(公告)日:2013-02-14
    Cosmetic or dermatological preparations having an effective content of one or more thiazoles of the general formula
  • US8920785B2
    申请人:——
    公开号:US8920785B2
    公开(公告)日:2014-12-30
  • [DE] KOSMETISCHE ODER DERMATOLOGISCHE ZUBEREITUNGEN MIT EINEM GEHALT AN EINEM ODER MEHREREN THIAZOLDERIVATEN<br/>[EN] COSMETIC OR DERMATOLOGICAL PREPARATIONS WITH A CONTENT OF ONE OR MORE THIAZOLE DERIVATIVES<br/>[FR] PRÉPARATIONS COSMÉTIQUES OU DERMATOLOGIQUES CONTENANT UN OU PLUSIEURS DÉRIVÉS DE THIAZOL
    申请人:BEIERSDORF AG
    公开号:WO2011117034A2
    公开(公告)日:2011-09-29
    Kosmetische oder dermatologische Zubereitungen mit einem wirksamen Gehalt an einem oder mehreren Thiazolen der allgemeinen Formel
  • A library of novel allosteric inhibitors against fructose 1,6-bisphosphatase
    作者:Sabrina Heng、Kimberly R. Gryncel、Evan R. Kantrowitz
    DOI:10.1016/j.bmc.2009.04.030
    日期:2009.6
    The identification of a proper lead compound for fructose 1,6-bisphosphatase (FBPase) is a critical step in the process of developing novel therapeutics against type-2 diabetes. Herein, we have successfully generated a library of allosteric inhibitors against FBPase as potential anti-diabetic drugs, of which, the lead compound 1b was identified through utilizing a virtual high-throughput screening (vHTS) system, which we have developed. The thiazole-based core structure was synthesized via the condensation of alpha-bromoketones with thioureas and substituents on the two aryl rings were varied. 4c was found to inhibit pig kidney FBPase approximately fivefold better than 1b. In addition, we have also identified 10b, a tight binding fragment, which can be use for fragment-based drug design purposes. (C) 2009 Elsevier Ltd. All rights reserved.
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