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2H-[1,2,3]三唑并[4,5-f]喹喔啉 | 233-93-2

中文名称
2H-[1,2,3]三唑并[4,5-f]喹喔啉
中文别名
——
英文名称
2H-1,2,3-Triazolo[4,5-f]quinoxaline
英文别名
2H-triazolo[4,5-f]quinoxaline
2H-[1,2,3]三唑并[4,5-f]喹喔啉化学式
CAS
233-93-2
化学式
C8H5N5
mdl
MFCD18814098
分子量
171.16
InChiKey
XSJMOLCRLLDSFM-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:
    426.4±48.0 °C(Predicted)
  • 密度:
    1.571±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.3
  • 重原子数:
    13
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    67.4
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • IMIDAZOL[1,2-alpha]QUINOXALINES AND DERIVATIVES FOR THE TREATMENT OF CANCERS
    申请人:Deleuze-Masquefa Carine
    公开号:US20100249142A1
    公开(公告)日:2010-09-30
    Imidazo[1,2-a]quinoxaline compounds for the treatment of cancers as well as pharmaceutical compositions that include these compounds and their uses in therapy. The compound of general formula (I):
    咪唑并[1,2-a]喹噁啉化合物用于治疗癌症,以及包括这些化合物的药物组合物和它们在疗法中的用途。通式(I)的化合物:
  • Imidazo[1,2-a]quinoxalines and Derivatives Thereof for the Treatment of Cancer
    申请人:Universite de Montpellier
    公开号:US20180016278A1
    公开(公告)日:2018-01-18
    The invention relates to imidazo[1,2-a]quinoxaline compounds of formula (I) for the treatment of cancer, the pharmaceutical compositions comprising said chemical compounds, and the therapeutic uses thereof.
    该发明涉及公式(I)的咪唑并[1,2-a]喹喔啉化合物,用于治疗癌症,包括该化合物的药物组合物,以及其治疗用途。
  • QUINOXALINE COMPOUND
    申请人:Kaizawa Hiroyuki
    公开号:US20110319385A1
    公开(公告)日:2011-12-29
    [Problem] Provided is a compound which has a PDE9-inhibiting action and is useful as an active ingredient for an agent for treating and/or preventing storage dysfunction, voiding dysfunction, and bladder/urethral diseases, and the like. [Means for Solution] The present inventors have investigated a compound which has a PDE9-inhibiting action and is useful as an active ingredient for an agent for treating and/or preventing storage dysfunction, voiding dysfunction, and bladder/urethral diseases, and the like, and thus, have found that an imidazoquinoxaline compound or a triazoloquinoxaline compound has a PDE9-inhibiting action, thereby completing the present invention. The imidazoquinoxaline compound or the triazoloquinoxaline compound of the present invention has a PDE9-inhibiting action and can be used as an agent for preventing and/or treating storage dysfunction, voiding dysfunction, and bladder/urethral diseases, and the like.
    提供一种具有PDE9抑制作用的化合物,可用作治疗和/或预防储存功能障碍、排尿功能障碍、膀胱/尿道疾病等药剂的活性成分。现有发明人研究了一种具有PDE9抑制作用的化合物,可用作治疗和/或预防储存功能障碍、排尿功能障碍、膀胱/尿道疾病等药剂的活性成分,因此,发现咪唑喹喔啉化合物或三唑喹喔啉化合物具有PDE9抑制作用,从而完成了本发明。本发明的咪唑喹喔啉化合物或三唑喹喔啉化合物具有PDE9抑制作用,可用作预防和/或治疗储存功能障碍、排尿功能障碍、膀胱/尿道疾病等药剂。
  • [EN] PYRIMIDINES DERIVATIVES AS ADENOSINE RECEPTORS LIGANDS<br/>[FR] UTILISATION DE DERIVES DE PYRIMIDINES EN TANT QUE LIGANDS DES RECEPTEURS DE L'ADENOSINE
    申请人:UNIV LEIDEN
    公开号:WO2005033085A1
    公开(公告)日:2005-04-14
    Use of a compound of formula (I) wherein R and R' are selected from hydrogen, alkyl, alkenyl, alkynyl, or aryl; R'' and R''' are selected from hydrogen, acyl, thio-acyl, seleno-acyl, alkyl, alkenyl, alkynyl, or aryl; or a pharmaceutically acceptable salt thereof to interact with the adenosine receptors in the beneficial treatment or prevention of a (dis)order arising from the said receptors. The invention also provides pharmaceutical compositions comprising a compound according to the present invention. The invention further relates to the use of said compositions to treat and/or prevent a variety of diseases.
    使用式(I)的化合物,其中R和R'选自氢、烷基、烯基、炔基或芳基;R''和R'''选自氢、酰基、酰基、酰基、烷基、烯基、炔基或芳基;或其药学上可接受的盐与腺苷受体相互作用,有益地治疗或预防由所述受体引起的(失)调节。该发明还提供了包含根据本发明的化合物的药物组合物。该发明还涉及使用该类组合物来治疗和/或预防各种疾病。
  • 2,6,8, Trisubstituted 1-deazapurines and their different uses
    申请人:Chang Lisa Chung Wai
    公开号:US20080139608A1
    公开(公告)日:2008-06-12
    The invention provides a compound having the structure of general formula (I): or a salt thereof, wherein, R represents hydrogen (except when R′=H), halogen, (substituted) alkyl except —CH 3 , (substituted) alkenyl, (substituted) alkynyl, or (substituted) —(CH 2 ) n -aryl; R′ represents hydrogen (except when R=H), halogen, (substituted) alkyl except —CH 3 , (substituted) alkenyl, (substituted) alkynyl, or (substituted) —CH 2 ) n -aryl; R″ represents hydrogen, —(CH 2 ) n -hydroxyl, halogen, acyl, thio-acyl, seleno-acyl, (substituted) alkyl, (substituted) alkenyl, (substituted) alkynyl, or (substituted) —(CH 2 ) n -aryl; and n is a number in the range from 0 to 10. The invention further provides pharmaceutical compositions comprising said compound, and the use of said compound to treat and/or prevent a variety of diseases.
    本发明提供了具有通式(I)的化合物或其盐,其中,R代表氢(除非R′=H),卤素,(取代)烷基(除CH3),(取代)烯基,(取代)炔基或(取代)-(CH2)n-芳基;R′代表氢(除非R=H),卤素,(取代)烷基(除 ),(取代)烯基,(取代)炔基或(取代)-( )n-芳基;R″代表氢,-( )n-羟基,卤素,酰基,酰基,酰基,(取代)烷基,(取代)烯基,(取代)炔基或(取代)-( )n-芳基;n为0到10之间的数字。本发明还提供了包含上述化合物的药物组合物,以及使用该化合物治疗和/或预防各种疾病的方法。
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