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2-cyclohexyl-4-methyl-1,3-thiazole-5-carboxylic acid | 472805-56-4

中文名称
——
中文别名
——
英文名称
2-cyclohexyl-4-methyl-1,3-thiazole-5-carboxylic acid
英文别名
——
2-cyclohexyl-4-methyl-1,3-thiazole-5-carboxylic acid化学式
CAS
472805-56-4
化学式
C11H15NO2S
mdl
MFCD10007074
分子量
225.312
InChiKey
JIDVCEPMJHOXPB-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):
    3.4
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.636
  • 拓扑面积:
    78.4
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

点击查看最新优质反应信息

文献信息

  • COMPOSITIONS AND METHODS OF TARGETING MUTANT K-RAS
    申请人:Nantbio, Inc.
    公开号:US20180201610A1
    公开(公告)日:2018-07-19
    Compounds and compositions are presented that inhibit K-Ras, and especially mutant K-Ras. Certain compounds preferentially or even selectively inhibit specific forms of mutant K-Ras, and particularly the G12D mutant form.
    提供了抑制K-Ras的化合物和组合物,特别是突变型K-Ras。某些化合物优先甚至选择性地抑制特定形式的突变型K-Ras,特别是G12D突变形式。
  • [EN] NEW AMINO-PYRIMIDONYL-PIPERIDINYL DERIVATIVES, A PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM<br/>[FR] NOUVEAUX DÉRIVÉS D'AMINO-PYRIMIDONYL-PIPÉRIDINYL, LEUR PROCÉDÉ DE PRÉPARATION ET COMPOSITIONS PHARMACEUTIQUES LES CONTENANT
    申请人:SERVIER LAB
    公开号:WO2020079205A1
    公开(公告)日:2020-04-23
    Compounds of formula (I) wherein R1, R2, R3, R4, R5, n and Q are as defined in the description. Medicaments.
    式(I)中R1、R2、R3、R4、R5、n和Q的化合物如描述中所定义。药物。
  • Expanding Synthesizable Space of Disubstituted 1,2,4-Oxadiazoles
    作者:Andrey Tolmachev、Andrey V. Bogolubsky、Sergey E. Pipko、Alexander V. Grishchenko、Dmytro V. Ushakov、Anton V. Zhemera、Oleksandr O. Viniychuk、Anzhelika I. Konovets、Olga A. Zaporozhets、Pavel K. Mykhailiuk、Yurii S. Moroz
    DOI:10.1021/acscombsci.6b00103
    日期:2016.10.10
    One-pot synthesis of 3,5-disubstituted 1,2,4-oxadiazoles from carboxylic acids and nitriles was optimized to parallel chemistry. The method was validated on a 141 member library; the desired products were recovered with a high success rate and in moderate yields. Practical application of the approach was demonstrated in the synthesis of bioactive compound pifexole and agonists of free fatty acid receptor
    优化了从羧酸和腈的一锅法合成3,5-二取代的1,2,4-恶二唑的平行化学反应。该方法已在141个成员库中得到验证;以高成功率和中等收率回收了所需的产品。该方法在生物活性化合物非索和游离脂肪酸受体1激动剂的合成中得到了实际应用。在此基础上,列举了4 948 100种可合成的药物样3,5-二取代1,2,4-恶二唑类化合物。方法和可用的经过验证的试剂。
  • Difluoroalkene derivative, pest control agent containing the same, and intermediate therefor
    申请人:——
    公开号:US20040248872A1
    公开(公告)日:2004-12-09
    A difluoroalkene derivative which is sufficiently effective in controlling various pests even when used in a small dose and is highly safe for crops, natural enemies to the pests, and animals; and an intermediate for the derivative. The difluoroalkene derivative is represented by the general formula: [I] wherein L 1 and L 2 are the same or different and each represents oxygen or sulfur; n is an integer of 2 to 8; and Q represents a 5- to 12-membered heterocyclic group having any desired heteroatom selected among nitrogen, oxygen, and sulfur. 1
    一种二烯衍生物,即使使用小剂量也足以有效控制各种害虫,并且对作物,害虫的天敌和动物非常安全;以及该衍生物的中间体。该二烯衍生物由通式表示:[I]其中L1和L2相同或不同,每个代表氧或;n为2至8的整数;Q表示任何所需杂原子在氮、氧和之间选择的5-至12成员杂环基团。
  • Compositions and methods of targeting mutant K-ras
    申请人:NANTBIO, INC.
    公开号:US10344026B2
    公开(公告)日:2019-07-09
    Compounds and compositions are presented that inhibit K-Ras, and especially mutant K-Ras. Certain compounds preferentially or even selectively inhibit specific forms of mutant K-Ras, and particularly the G12D mutant form.
    本文介绍了抑制 K-Ras,特别是突变型 K-Ras 的化合物和组合物。某些化合物优先或甚至选择性地抑制特定形式的突变 K-Ras,特别是 G12D 突变形式。
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