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Tiagabine hydrochloride monohydrate | 145821-57-4

中文名称
——
中文别名
——
英文名称
Tiagabine hydrochloride monohydrate
英文别名
(3R)-1-[4,4-bis(3-methylthiophen-2-yl)but-3-enyl]piperidine-3-carboxylic acid;hydrate;hydrochloride
Tiagabine hydrochloride monohydrate化学式
CAS
145821-57-4
化学式
C20H25NO2S2*ClH*H2O
mdl
——
分子量
430.032
InChiKey
KOZCGZMZXXVHCF-GGMCWBHBSA-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):
    4.64
  • 重原子数:
    27
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    98
  • 氢给体数:
    3
  • 氢受体数:
    6

反应信息

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文献信息

  • Crystalline and amorphous forms of tiagabine
    申请人:Childs L. Scott
    公开号:US20080051435A1
    公开(公告)日:2008-02-28
    The present invention provides 24 new forms of tiagabine, including 22 new crystalline forms of tiagabine and its salts, an amorphous form of tiagabine free base, and a cocrystal form of tiagabine hydrochloride with 2-furancarboxylic acid. The present invention further provides a process for preparing each of the new tiagabine forms. The present invention further provides a pharmaceutical composition containing at least one of the new tiagabine forms, and a process for the preparation thereof. The present invention further provides a method of treating a disease related to GABA uptake in a mammal, comprising the step of administering to the mammal a therapeutically effective amount of at least one of the new tiagabine forms.
    本发明提供了24种新的替加巴嗪形式,包括22种新的替加巴嗪和其盐的晶体形式,替加巴嗪游离碱的非晶形式,以及替加巴嗪盐酸盐与2-呋喃羧酸的共晶形式。本发明还提供了制备每种新替加巴嗪形式的方法。本发明还提供了含有至少一种新替加巴嗪形式的药物组合物,以及其制备方法。本发明还提供了一种治疗与哺乳动物GABA摄取相关疾病的方法,包括向哺乳动物投与至少一种新替加巴嗪形式的治疗有效量。
  • [EN] CRYSTALLINE TIAGABINE HYDROCHLORIDE MONOHYDRATE, ITS PREPARATION AND USE
    申请人:NOVO NORDISK A/S
    公开号:WO1992017473A1
    公开(公告)日:1992-10-15
    (EN) The invention provides crystalline R-isomer of N-(4,4-di(3-methylthien-2-yl)but-3-enyl-nipecotic acid hydrochloride with the generic name Tiagabine hydrochloride, process for its preparation, compositions containing the same and its therapeutic use as anti-epileptic agent.(FR) L'invention concerne la production du R-isomère cristallin d'hydrochlorure d'acide N-(4,4-di(3-méthylthien-2-yl)but-3-ényl-nipécotique portant le nom générique hydrochlorure de tiagabine, son procédé de préparation, compositions le contenant et son utilisation thérapeutique en tant qu'agent anti-épileptique.
    该发明提供了一种名为Tiagabine hydrochloride的N-(4,4-di(3-甲基噻吩-2-基)丁-3-烯基)-尼佩考酸盐的结晶R-异构体,其制备方法,含有该异构体的组合物以及其作为抗癫痫药物的治疗用途。
  • 1H-QUINAZOLINE-2,4-DIONES
    申请人:NOVARTIS AG
    公开号:US20130296332A1
    公开(公告)日:2013-11-07
    The present invention relates to 1H-Quinazoline-2,4-diones of formula (I) wherein R 1 and R 2 are as defined in the specification, their preparation, their use as pharmaceuticals, and pharmaceutical compositions containing them. Further, intermediates for the manufacture of compounds of formula (I) are and combinations comprising compounds of formula (I) are disclosed.
    本发明涉及公式(I)的1H-喹唑啉-2,4-二酮,其中R1和R2如规范所定义,它们的制备,它们作为药物的用途,以及含有它们的药物组合物。此外,还公开了制造公式(I)化合物的中间体和包含公式(I)化合物的组合物。
  • Organic Compounds
    申请人:Flor Peter Josef
    公开号:US20080242698A1
    公开(公告)日:2008-10-02
    The invention relates to novel diamines of the formula in which all variables are as defined in the specification, in free base form or in acid addition salt form, to their preparation, to their use as medicaments and to medicaments comprising them.
    本发明涉及一种新型二胺化合物,其化学式为,在该式中所有变量均如规范中定义,其为自由碱基形式或酸加成盐形式,涉及其制备方法,以及作为药物的用途和包含它们的药物。
  • Process for Preparation of Piperidine Carboxylic Acid
    申请人:Bose Prosenjit
    公开号:US20080269495A1
    公开(公告)日:2008-10-30
    A process for preparing pure tiagabine, which is a piperidine carboxylic acid compound, via pharmaceutically acceptable salts of tiagabine ester is provided. Also, L(+) tartaric acid, oxalic acid and dibenzoyl L(+) tartaric acid salts of tiagabine esters are provided. Further, process for preparing acid addition salts of tiagabine esters is provided.
    提供了一种通过苯甲酸酯的药学可接受盐制备纯的哌啶羧酸类化合物替加巴的方法。此外,还提供了替加巴酯的L(+)酒石酸盐、草酸盐和二苯乙酰基L(+)酒石酸盐。此外,还提供了制备替加巴酯酸盐的方法。
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