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5-isopropyl-1H-1,2,3-triazole-4-carboxylic acid | 862112-06-9

中文名称
——
中文别名
——
英文名称
5-isopropyl-1H-1,2,3-triazole-4-carboxylic acid
英文别名
4-isopropyl-1H-1,2,3-triazole-5-carboxylic acid;5-propan-2-yl-2H-triazole-4-carboxylic acid
5-isopropyl-1H-1,2,3-triazole-4-carboxylic acid化学式
CAS
862112-06-9
化学式
C6H9N3O2
mdl
——
分子量
155.156
InChiKey
WSKQPJMEHUFYME-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):
    0.6
  • 重原子数:
    11
  • 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:
    78.9
  • 氢给体数:
    2
  • 氢受体数:
    4

文献信息

  • COMPOUNDS AND METHODS FOR TREATING CANCER
    申请人:ANTIDOTE IP HOLDINGS, LLC
    公开号:US20200299282A1
    公开(公告)日:2020-09-24
    Substituted cinnamamide compounds and analogs, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds to treat, prevent or ameliorate cancer are provided.
    提供了替代肉桂酰胺化合物和类似物、制备这类化合物的方法、包含这类化合物的药物组合物和药物、以及使用这类化合物治疗、预防或改善癌症的方法。
  • 6-Membered aryl and heteroaryl derivatives for treating viruses
    申请人:Botyanszki Janos
    公开号:US20070032488A1
    公开(公告)日:2007-02-08
    Disclosed are compounds, compositions and methods for treating Flaviviridae family virus infections.
    公开了用于治疗黄病毒科病毒感染的化合物、组合物和方法。
  • USE OF SOLUBLE EPOXIDE HYDROLASE INHIBITORS IN THE TREATMENT OF SMOOTH MUSCLE DISORDERS
    申请人:Webb Hsu Heather K.
    公开号:US20090270452A1
    公开(公告)日:2009-10-29
    Disclosed herein are compounds, compositions, and methods for enhancing smooth muscle function in a subject by administration of soluble epoxide hydrolase inhibitors and for treating subjects with smooth muscle disorders including erectile dysfunction, overactive bladder, uterine contractions and irritable bowel syndrome.
    本文揭示了一种通过给予可溶性环氧化物解酶抑制剂来增强受试者平滑肌功能的化合物、组合物和方法,并用于治疗患有平滑肌障碍的受试者,包括勃起功能障碍、膀胱过度活跃、子宫收缩和肠易激综合征。
  • SOLUBLE EPOXIDE HYDROLASE INHIBITORS
    申请人:Gless D. Richard
    公开号:US20080076770A1
    公开(公告)日:2008-03-27
    Disclosed are urea and thiourea compounds and compositions that inhibit soluble epoxide hydrolase (sEH), methods for preparing the compounds and compositions, and methods for treating patients with such compounds and compositions. The compounds, compositions, and methods are useful for treating a variety of sEH mediated diseases, including hypertensive, cardiovascular, inflammatory, and diabetes related diseases.
    揭示了抑制可溶性环氧解酶(sEH)的尿素硫脲化合物及组合物,制备这些化合物和组合物的方法,以及使用这些化合物和组合物治疗患者的方法。这些化合物、组合物和方法可用于治疗多种由sEH介导的疾病,包括高血压、心血管、炎症和糖尿病相关疾病。
  • CEPHEM COMPOUND HAVING PYRIDINIUM GROUP
    申请人:Nishitani Yasuhiro
    公开号:US20140114060A1
    公开(公告)日:2014-04-24
    The present invention provides a novel compound which has a broad antibacterial spectrum and particularly exhibits a high antibacterial activity on β-lactamase-producing gram-negative bacteria. Specifically provided are: a compound represented by formula (I) wherein the meaning of each symbol is as defined in the description, an amino-group-protected form of a type of the compound which has the amino group on a ring in a position-7 side chain, or a pharmaceutically acceptable salt of the compound or the amino-group-protected form; and a pharmaceutical composition containing the compound, the amino-group-protected form or the pharmaceutically acceptable salt.
    本发明提供了一种新型化合物,具有广泛的抗菌谱,特别对产β-内酰胺酶的革兰氏阴性细菌表现出高抗菌活性。具体提供的是:一种由式(I)表示的化合物,其中每个符号的含义如描述中定义的那样,一种在环上具有基团的化合物的保护形式,该化合物在位置-7侧链上具有基团,或者化合物或基团保护形式的药用可接受盐;以及含有该化合物、基团保护形式或药用可接受盐的药物组合物。
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