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3-isobutyl-5-isopropyl-1H-[1,2,4]triazole | 99066-16-7

中文名称
——
中文别名
——
英文名称
3-isobutyl-5-isopropyl-1H-[1,2,4]triazole
英文别名
3-Isobutyl-5-isopropyl-1H-[1,2,4]triazol;3-Isobutyl-5-isopropyl-1H-1,2,4-triazole;5-(2-methylpropyl)-3-propan-2-yl-1H-1,2,4-triazole
3-isobutyl-5-isopropyl-1<i>H</i>-[1,2,4]triazole化学式
CAS
99066-16-7
化学式
C9H17N3
mdl
——
分子量
167.254
InChiKey
YNYBGYJEMRELEH-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):
    2.8
  • 重原子数:
    12
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.78
  • 拓扑面积:
    41.6
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

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文献信息

  • PYRIDINE DERIVATIVE SUBSTITUTED BY HETEROARYL RING, AND ANTIFUNGAL AGENT COMPRISING THE SAME
    申请人:Matsukura Masayuki
    公开号:US20100099718A1
    公开(公告)日:2010-04-22
    The present invention provides an antifungal agent that has excellent antifungal action, and is also excellent in terms of its properties, safety, and metabolic stability. The present invention discloses a compound represented by the following formula I or a salt thereof, and an antifungal agent comprising the compound or the salt: wherein R 1 represents a hydrogen atom, a halogen atom, an amino group, a C 1-6 alkyl group, a C 1-6 alkoxy group, or a C 1-6 -alkoxy-C 1-6 -alkyl group; R 2 represents a hydrogen atom or an amino group; X, Y, Z, and W independently represent a nitrogen atom, an oxygen atom, a sulfur atom, or —CH—, provided that at least two among X, Y, and W are nitrogen atoms; the ring A represents a 5- or 6-membered heteroaryl ring or a benzene ring; Q represents a methylene group, an oxygen atom, —CH 2 O—, —OCH 2 —, —NH—, —NHCH 2 —, or —CH 2 NH—; and R 3 represents a C 1-6 alkyl group, a C 3-8 cycloalkyl group, a C 6-10 aryl group, or a 5- or 6-membered heteroaryl group, each of which may have one or two substituents.
    本发明提供了一种具有优异的抗真菌作用的抗真菌剂,同时在其性质、安全性和代谢稳定性方面也具有优异的性能。本发明揭示了以下式I或其盐所表示的化合物以及包含该化合物或其盐的抗真菌剂:其中,R1表示氢原子、卤素原子、基、C1-6烷基、C1-6烷氧基或C1-6烷氧基-C1-6烷基;R2表示氢原子或基;X、Y、Z和W独立地表示氮原子、氧原子、原子或-CH-,但至少有两个是氮原子;环A表示5-或6-成员杂芳环或苯环;Q表示亚甲基、氧原子、-CH2O-、-OCH2-、-NH-、-NHCH2-或-CH2NH-;R3表示C1-6烷基、C3-8环烷基、C6-10芳基或5-或6-成员杂芳基,每个基团都可以有一个或两个取代基。
  • Polycyclic pyridone derivative having integrase inhibitory activity
    申请人:Shionogi & Co., Ltd.
    公开号:US10011613B2
    公开(公告)日:2018-07-03
    The present invention relates to a novel compound having an antiviral effect, more specifically, a pyridone derivative having HIV integrase inhibitory activity, and a medicament containing the same, in particular, an anti-HIV agent. The compound of the present invention has integrase inhibitory activity and/or cell proliferation inhibitory activity against viruses, in particular, HIV and drug-resistant strains thereof. Thus, the compound is useful in preventing or treating various diseases, viral infections (for example, AIDS), and the like in which integrase participates.
    本发明涉及一种具有抗病毒作用的新型化合物,更具体地说,是一种具有艾滋病病毒整合酶抑制活性的吡啶酮衍生物,以及含有该化合物的药物,特别是抗艾滋病病毒药物。本发明的化合物对病毒,特别是艾滋病毒及其耐药菌株具有整合酶抑制活性和/或细胞增殖抑制活性。因此,本发明化合物可用于预防或治疗整合酶参与的各种疾病、病毒感染(如艾滋病)等。
  • POLYCYCLIC PYRIDONE DERIVATIVE HAVING INTEGRASE INHIBITORY ACTIVITY
    申请人:Shionogi & Co., Ltd.
    公开号:US20170226128A1
    公开(公告)日:2017-08-10
    The present invention relates to a novel compound having an antiviral effect, more specifically, a pyridone derivative having HIV integrase inhibitory activity, and a medicament containing the same, in particular, an anti-HIV agent. The compound of the present invention has integrase inhibitory activity and/or cell proliferation inhibitory activity against viruses, in particular, HIV and drug-resistant strains thereof. Thus, the compound is useful in preventing or treating various diseases, viral infections (for example, AIDS), and the like in which integrase participates.
  • US8183264B2
    申请人:——
    公开号:US8183264B2
    公开(公告)日:2012-05-22
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