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5-(hydroxymethyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol | 700867-96-5

中文名称
——
中文别名
——
英文名称
5-(hydroxymethyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol
英文别名
(3aR,5R,6S,6aR)-5-(hydroxymethyl)-2,2-dimethyl-tetrahydro-2H-furo[2,3-d][1,3]dioxol-6-ol;5-(hydroxymethyl)-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-6-ol
5-(hydroxymethyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol化学式
CAS
700867-96-5
化学式
C8H14O5
mdl
——
分子量
190.196
InChiKey
JAUQZVBVVJJRKM-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):
    -0.4
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    68.2
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

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文献信息

  • [EN] PRMT5 INHIBITORS<br/>[FR] INHIBITEURS DE PRMT5
    申请人:MERCK SHARP & DOHME
    公开号:WO2020033285A1
    公开(公告)日:2020-02-13
    The present invention provides a compound of formula (I) Formula (I) and the pharmaceutically acceptable salts, esters, and prodrugs thereof, are PRMT5 inhibitors. Also provided are methods of making compounds of formula (I), pharmaceutical compositions comprising compounds of formula (I), and methods of using these compounds to treat cancer, sickle cell, and hereditary persistence of foetal hemoglobin (HPFH) mutations.
    本发明提供了一种化合物,其化学式为(I)。化学式(I)及其药用盐、酯和前药是PRMT5抑制剂。还提供了制备化合物(I)的方法,包括化合物(I)的药用组合物,以及使用这些化合物治疗癌症、镰刀细胞贫血和遗传性胎儿血红蛋白持续存在(HPFH)突变的方法。
  • [EN] SUBSTITUTED PURINE NUCLEOSIDES, PHOSPHORAMIDATE AND PHOSPHORDIAMIDATE DERIVATIVES FOR TREATMENT OF VIRAL INFECTIONS<br/>[FR] NUCLÉOSIDES DE PURINE SUBSTITUÉS, DÉRIVÉS PHOSPHORAMIDATE ET PHOSPHORDIAMIDATE DESTINÉS À TRAITER DES INFECTIONS VIRALES
    申请人:INHIBITEX INC
    公开号:WO2013070887A1
    公开(公告)日:2013-05-16
    This invention is directed to compounds of Formula (I) having the structure that are useful in the treatment of viral infections in mammals, particularly in humans, mediated, at least in part, by a virus in the Flaviviridae family of viruses.
    这项发明涉及具有结构的化合物(I)的公式,这些化合物在哺乳动物,特别是人类中,用于治疗由黄病毒科病毒介导的病毒感染。
  • [EN] METHODS AND COMPOUNDS USEFUL FOR THE PREPARATION OF SODIUM GLUCOSE CO-TRANSPORTER 2 INHIBITORS<br/>[FR] PROCÉDÉS ET COMPOSÉS UTILES POUR LA PRÉPARATION D'INHIBITEURS DE CO-TRANSPORTEUR 2 DE SODIUM-GLUCOSE
    申请人:LEXICON PHARMACEUTICALS INC
    公开号:WO2009014970A1
    公开(公告)日:2009-01-29
    Methods of synthesizing sodium glucose co-transporter 2 inhibitors, as well as compounds useful therein, are disclosed. Particular inhibitors are compounds of formula (I).
    本文公开了合成葡萄糖共运输体2抑制剂的方法,以及其中有用的化合物。特定的抑制剂是I式化合物。
  • Nucleosides with anti-hepatitis B Virus activity
    申请人:Schinazi Raymond F.
    公开号:US20090105185A1
    公开(公告)日:2009-04-23
    A method for the treatment of a host, and in particular, a human, infected with hepatitis B virus (HBV) is provided that includes administering an effective amount of a β-L-nucleotide, optionally in combination therapy with other drugs for the treatment of HBV or human immuno-deficiency virus (HIV).
    本发明提供了一种用于治疗感染乙型肝炎病毒(HBV)的宿主,特别是人类的方法,包括给予有效量的β-L-核苷酸,可选地与其他用于治疗HBV或人类免疫缺陷病毒(HIV)的药物联合治疗。
  • 2'-FLUORO-4'-SUBSTITUTED NUCLEOSIDES, THE PREPARATION AND USE
    申请人:Zhengzhou University
    公开号:EP2177527A1
    公开(公告)日:2010-04-21
    The present invention provides 2'-fluorine-4'-substituted-nucleoside analogues or their pro-drugs or 5'-phosphate esters (including the pro-drugs of the 5'-phosphate esters), preparation methods and uses thereof. The compounds have the general formula as follows: wherein: R = CH3, CH, N3, C≡CH; R' = H, F; X = F, OH, NH2; Y = H, CH3, F, OH, NH2 The compounds are used in the synthesis of drugs for the treatment of virus infection, especially for the treatment of HBV, HCV or HIV infection.
    本发明提供了2'--4'-取代-核苷类似物或其原药或5'-磷酸酯(包括5'-磷酸酯的原药)、制备方法及其用途。这些化合物的通式如下: 其中 R=CH3、CH、N3、C≡CH; R' = H、F X = F、OH、NH2; Y = H、 、F、OH、NH2 这些化合物可用于合成治疗病毒感染的药物,尤其是治疗 HBV、HCV 或 HIV 感染的药物。
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