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4-丙基噻唑 | 41981-60-6

中文名称
4-丙基噻唑
中文别名
——
英文名称
4-Propylthiazole
英文别名
4-propyl-1,3-thiazole
4-丙基噻唑化学式
CAS
41981-60-6
化学式
C6H9NS
mdl
——
分子量
127.21
InChiKey
XWSNBKDRTFVUMY-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

  • 沸点:
    183.7±9.0 °C(Predicted)
  • 密度:
    1.047±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.1
  • 重原子数:
    8
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    41.1
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • HETEROARYL CARBOXAMIDE COMPOUNDS AS INHIBITORS OF RIPK2
    申请人:Boehringer Ingelheim International GmbH
    公开号:US20180072717A1
    公开(公告)日:2018-03-15
    The present invention relates to compounds of formula (I): or pharmaceutically acceptable salts thereof, wherein R 1 , R 2 , X, Y, and HET are as defined herein. The invention also relates to pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, processes for preparing these compounds and intermediates useful in these processes
    本发明涉及以下式(I)的化合物: 或其药学上可接受的盐,其中R 1 ,R 2 ,X,Y和HET如本文所定义。该发明还涉及包含这些化合物的药物组合物,使用这些化合物治疗各种疾病和紊乱的方法,制备这些化合物的过程以及在这些过程中有用的中间体。
  • [EN] ARGININE METHYLTRANSFERASE INHIBITORS AND USES THEREOF<br/>[FR] INHIBITEURS D'ARGININE MÉTHYLTRANSFÉRASE ET LEURS UTILISATIONS
    申请人:EPIZYME INC
    公开号:WO2016044626A1
    公开(公告)日:2016-03-24
    Described herein are compounds of Formula (S-I), pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof. Compounds described herein are useful for inhibiting arginine methyltransferase activity. Methods of using the compounds for treating arginine methyltransferase-mediated disorders are also described.
    本文描述了式(S-I)的化合物,其药用盐以及药物组合物。本文描述的化合物对抑制精酸甲基转移酶活性有用。还描述了利用这些化合物治疗精酸甲基转移酶介导的疾病的方法。
  • MACROCYCLIC ANTAGONISTS OF THE MOTILIN RECEPTOR FOR TREATMENT OF GASTROINTESTINAL DYSMOTILITY DISORDERS
    申请人:Marsault Eric
    公开号:US20100093720A1
    公开(公告)日:2010-04-15
    The present invention provides conformationally-defined macrocyclic compounds that bind to and/or are functional modulators of the motilin receptor including subtypes, isoforms and/or variants thereof. These macrocyclic compounds, at a minimum, possess adequate pharmacological properties to be useful as therapeutics for a range of disease indications. In particular, these compounds are useful for treatment and prevention of disorders characterized by hypermotilinemia and/or gastrointestinal hypermotility, including, but not limited to, diarrhea, cancer treatment-related diarrhea, cancer-induced diarrhea, chemotherapy-induced diarrhea, radiation enteritis, radiation-induced diarrhea, stress-induced diarrhea, chronic diarrhea, AIDS-related diarrhea, C. difficile associated diarrhea, traveller's diarrhea, diarrhea induced by graph versus host disease, other types of diarrhea, dyspepsia, irritable bowel syndrome, chemotherapy-induced nausea and vomiting (emesis) and post-operative nausea and vomiting and functional gastrointestinal disorders. In addition, the compounds possess utility for the treatment of diseases and disorders characterized by poor stomach or intestinal absorption, such as short bowel syndrome, celiac disease and cachexia. The compounds also have use for the treatment of inflammatory diseases and disorders of the gastrointestinal tract, such as inflammatory bowel disease, ulcerative colitis, Crohn's disease and pancreatitis. Accordingly, methods of treating such disorders and pharmaceutical compositions including compounds of the present invention are also provided.
    本发明提供了与胃动素受体及其亚型、异构体和/或变体结合和/或是功能调节剂的构象定义明确的大环化合物。这些大环化合物至少具有足够的药理特性,可用作治疗一系列疾病指示的治疗药物。特别是,这些化合物对于治疗和预防以高胃动素血症和/或胃肠道高蠕动性为特征的疾病非常有用,包括但不限于腹泻、癌症治疗相关腹泻、癌症诱导腹泻、化疗诱导腹泻、放射性肠炎、放射性腹泻、压力诱导腹泻、慢性腹泻、艾滋病相关腹泻、C. difficile相关腹泻、旅行者腹泻、移植物宿主病引起的腹泻、其他类型的腹泻、消化不良、肠易激综合征、化疗诱导的恶心和呕吐(呕吐)以及术后恶心和呕吐和功能性胃肠道疾病。此外,这些化合物对于治疗以胃或肠道吸收不良为特征的疾病和疾病也具有用途,例如短肠综合征、乳糜泻和虚弱。这些化合物还可用于治疗胃肠道炎症性疾病和疾病,如炎症性肠病、溃疡性结肠炎、克罗恩病和胰腺炎。因此,本发明还提供了治疗此类疾病的方法和包括本发明化合物的药物组合物。
  • Macrocyclic Ghrelin Receptor Antagonists and Inverse Agonists and Methods of Using the Same
    申请人:Hoveyda Hamid R.
    公开号:US20110105389A1
    公开(公告)日:2011-05-05
    The present invention provides novel conformationally-defined macrocyclic compounds that have been demonstrated to be selective modulators of the ghrelin receptor (GRLN, growth hormone secretagogue receptor, GHS-R1a and subtypes, isoforms and/or variants thereof). Methods of synthesizing the novel compounds are also described herein. These compounds are useful as antagonists or inverse agonists of the ghrelin receptor and as medicaments for treatment and prevention of a range of medical conditions including, but not limited to, metabolic and/or endocrine disorders, obesity and obesity-associated disorders, appetite or eating disorders, addictive disorders, cardiovascular disorders, gastrointestinal disorders, genetic disorders, hyperproliferative disorders, central nervous system disorders and inflammatory disorders.
    本发明提供了新型构象定义的大环化合物,已被证明是生长激素分泌素受体(GRLN,生长激素分泌素受体,GHS-R1a及其亚型、异构体和/或变种)的选择性调节剂。本文还描述了合成这些新型化合物的方法。这些化合物可用作生长激素分泌素受体的拮抗剂或逆向激动剂,以及用于治疗和预防一系列医学疾病,包括但不限于代谢和/或内分泌紊乱、肥胖和与肥胖相关的疾病、食欲或进食紊乱、成瘾紊乱、心血管疾病、胃肠道疾病、遗传疾病、过度增殖性疾病、中枢神经系统疾病和炎症性疾病。
  • Macrocyclic Modulators of the Ghrelin Receptor
    申请人:Marsault Eric
    公开号:US20090221689A1
    公开(公告)日:2009-09-03
    The present invention provides novel conformationally-defined macrocyclic compounds that have been demonstrated to be selective modulators of the ghrelin receptor (growth hormone secretagogue receptor, GHS-R1a and subtypes, isoforms and variants thereof). Methods of synthesizing the novel compounds are also described herein. These compounds are useful as agonists of the ghrelin receptor and as medicaments for treatment and prevention of a range of medical conditions including, but not limited to, metabolic and/or endocrine disorders, gastrointestinal disorders, cardiovascular disorders, obesity and obesity-associated disorders, central nervous system disorders, genetic disorders, hyperproliferative disorders and inflammatory disorders.
    本发明提供了新型构象定义的大环化合物,已被证明是生长激素释放肽受体(GHS-R1a及其亚型,同工型和变异体)的选择性调节剂。本文还描述了合成新型化合物的方法。这些化合物可用作生长激素释放肽受体的激动剂,并作为治疗和预防一系列医疗状况的药物,包括但不限于代谢和/或内分泌紊乱,胃肠道疾病,心血管疾病,肥胖和肥胖相关疾病,中枢神经系统疾病,遗传性疾病,高增殖性疾病和炎症性疾病。
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