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5-异丙基-4-甲基-4H-[1,2,4]三唑-3-硫醇 | 588680-36-8

中文名称
5-异丙基-4-甲基-4H-[1,2,4]三唑-3-硫醇
中文别名
4-甲基-5-丙-2-基-2H-1,2,4-三唑-3-硫酮;5-异丙基-4-甲基-2H-1,2,4-三唑-3-硫酮;5-异丙基-4-甲基-4H-1,2,4-噻唑-3-硫醇
英文名称
4-methyl-5-isopropyl-4H-[1,2,4]triazole-3-thiol
英文别名
5-isopropyl-4-methyl-4H-1,2,4-triazole-3-thiol;4-methyl-3-propan-2-yl-1H-1,2,4-triazole-5-thione
5-异丙基-4-甲基-4H-[1,2,4]三唑-3-硫醇化学式
CAS
588680-36-8
化学式
C6H11N3S
mdl
MFCD03423410
分子量
157.239
InChiKey
GYHLFQXWXOVOKL-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):
    1
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.666
  • 拓扑面积:
    59.7
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2933990090

反应信息

  • 作为反应物:
    描述:
    3-(3-Chloropropyl)-7-(5-methyl-isoxazol-3-yl)-2,3,4,5-tetrahydro-1H-3-benzazepine5-异丙基-4-甲基-4H-[1,2,4]三唑-3-硫醇 在 sodium iodide potassium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 24.0h, 生成 5-Methyl-3-[3-[3-[(4-methyl-5-propan-2-yl-1,2,4-triazol-3-yl)sulfanyl]propyl]-1,2,4,5-tetrahydro-3-benzazepin-7-yl]-1,2-oxazole
    参考文献:
    名称:
    1,2,4-Triazol-3-yl-thiopropyl-tetrahydrobenzazepines:  A Series of Potent and Selective Dopamine D3 Receptor Antagonists
    摘要:
    The discovery of new highly potent and selective dopamine D-3 receptor antagonists has recently permitted characterization of the role of the dopamine D-3 receptor in a wide range, of preclinical animal models. A novel series of 1,2,4-triazol-3-yl-thiopropyl-tetrahydrobenzazepines demonstrating a high level of D3 affinity and selectivity with an excellent pharmacokinetic profile is reported here. In particular, the pyrazolyl derivative 35 showed good oral bioavailability and brain penetration associated with high potency and selectivity in vitro. In vivo characterization of 35 confirmed that this compound blocks the expression of nicotine- and cocaine-conditioned place preference in the rat, prevents nicotine-triggered reinstatement of nicotine- seeking behavior in the rat, reduces oral operant alcohol self- administration in the mouse, increases extracellular levels of acetylcholine in the rat medial prefrontal cortex, and potentiates the amplitude of the relative cerebral blood volume response to d-amphetamine in a regionally specific manner in the rat brain.
    DOI:
    10.1021/jm0705612
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文献信息

  • [EN] 4-PIPERAZINYL-PYRIMIDINE COMPOUNDS SUITABLE FOR TREATING DISORDERS THAT RESPOND TO MODULATION OF THE DOPAMINE D3 RECEPTOR<br/>[FR] COMPOSÉS DE 4-PIPÉRAZINYLPYRIMIDINE CONVENANT POUR TRAITER DES TROUBLES QUI RÉPONDENT À UNE MODULATION DU RÉCEPTEUR D3 DE LA DOPAMINE
    申请人:ABBOTT GMBH & CO KG
    公开号:WO2006015842A1
    公开(公告)日:2006-02-16
    The present invention relates to novel 4-piperazinylpyrimidine compounds. The compounds possess valuable therapeutic properties and are suitable, in particular, for treating diseases that respond to modulation of the dopamine D3 receptor. The 4­ piperzinylpyrimidine compounds have the general formula (I), wherein Ar, X, A, R1 and R1a are as defined in the claims.
    本发明涉及新颖的4-哌嗪嘧啶化合物。这些化合物具有有价值的治疗特性,特别适用于治疗对多巴胺D3受体调节产生反应的疾病。4-哌嗪嘧啶化合物具有通式(I),其中Ar、X、A、R1和R1a如权利要求中所定义。
  • [EN] PYRIDO[4,3-B]INDOLE AND PYRIDO[3,4-B]INDOLE DERIVATIVES AND METHODS OF USE<br/>[FR] DÉRIVÉS DE PYRIDO[4,3-B]INDOLE ET DE PYRIDO[3,4-B]INDOLE ET PROCÉDÉS D'UTILISATION
    申请人:MEDIVATION TECHNOLOGIES INC
    公开号:WO2011103430A1
    公开(公告)日:2011-08-25
    This disclosure is directed to tetracyclic pyrido[4,3-b]indole and pyrido[3,4-b]indoles. Pharmaceutical compositions comprising the compounds are also provided, as are methods of using the compounds in a variety of therapeutic applications, including the treatment of a cognitive disorder, psychotic disorder, neurotransmitter-mediated disorder and/or a neuronal disorder.
    本公开涉及四环吡啶并[4,3-b]吲哚吡啶[3,4-b]吲哚。还提供了包含这些化合物的药物组合物,以及使用这些化合物进行各种治疗应用的方法,包括治疗认知障碍、精神病性障碍、神经递质介导的障碍和/或神经元障碍。
  • Tetracyclic compounds
    申请人:HUNG David T.
    公开号:US20090239854A1
    公开(公告)日:2009-09-24
    This disclosure relates to new tetracyclic compounds that may be used to modulate a histamine receptor in an individual. The compounds in one embodiment are tetracyclic [4,3-b]indoles. Pharmaceutical compositions comprising the compounds are also provided, as are methods of using the compounds in a variety of therapeutic applications, including the treatment of a cognitive disorder, psychotic disorder, neurotransmitter-mediated disorder and/or a neuronal disorder.
    本公开涉及新的四环化合物,可用于调节个体中的组胺受体。在一种实施例中,该化合物为四环[4,3-b]吲哚。还提供了包含该化合物的药物组合物,以及使用该化合物进行各种治疗应用的方法,包括治疗认知障碍、精神障碍、神经递质介导的障碍和/或神经元障碍。
  • Aminotriazole compounds useful as inhibitors of protein kinases
    申请人:Arnost J. Michael
    公开号:US20080096901A1
    公开(公告)日:2008-04-24
    The present invention relates to inhibitors of protein kinases. The invention also provides pharmaceutical compositions comprising the compounds of the invention, processes for preparing the compounds and methods of using the compositions in the treatment of various disorders.
    本发明涉及蛋白激酶抑制剂。本发明还提供了包含本发明化合物的药物组合物,制备该化合物的过程以及使用该组合物治疗各种疾病的方法。
  • 4-Piperazinyl-Pyrimidine Compounds Suitable for Treating Disorders that Respond to Modulation of the Dopamine D3 Receptor
    申请人:Haupt Andreas
    公开号:US20090264437A1
    公开(公告)日:2009-10-22
    The present invention relates to novel 4-piperazinylpyrimidine compounds. The compounds possess valuable therapeutic properties and are suitable, in particular, for treating diseases that respond to modulation of the dopamine D 3 receptor. The 4-piperzinylpyrimidine compounds have the general formula I wherein Ar, X, A, R 1 and R 1a are as defined in the claims.
    本发明涉及新型4-哌嗪嘧啶化合物。这些化合物具有有价值的治疗性质,特别适用于治疗对多巴胺D3受体调节有反应的疾病。4-哌嗪嘧啶化合物具有一般式I,其中Ar、X、A、R1和R1a如权利要求中所定义。
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