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(6S,7S,8aR)-2-phenyl-6-phenylsulfanyl-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxine-7,8-diol

中文名称
——
中文别名
——
英文名称
(6S,7S,8aR)-2-phenyl-6-phenylsulfanyl-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxine-7,8-diol
英文别名
——
(6S,7S,8aR)-2-phenyl-6-phenylsulfanyl-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxine-7,8-diol化学式
CAS
——
化学式
C19H20O5S
mdl
——
分子量
360.4
InChiKey
BDNIQCYVYFGHSI-SVJFOQKDSA-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):
    2.2
  • 重原子数:
    25
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.37
  • 拓扑面积:
    93.4
  • 氢给体数:
    2
  • 氢受体数:
    6

文献信息

  • [EN] GALACTOSIDE INHIBITORS FOR THE TREATMENT OF ALPHA-SYNUCLEINOPTHIES<br/>[FR] INHIBITEURS GALACTOSIDES POUR LE TRAITEMENT DES ALPHA-SYNUCLÉINOPATHIES
    申请人:GALECTO BIOTECH AB
    公开号:WO2015155207A1
    公开(公告)日:2015-10-15
    The present invention relates to a pharmaceutical composition for use in a method for treatment or prevention of a-synucleinopathies wherein the composition comprises a molecule for pharmacological modulation of galectin activity in a mammalian brain. The invention also concerns a method for treatment or prevention of a-synucleinopathies in a mammalian subject, the method comprising administering a therapeutically effective amount of at least one composition to the subject, wherein the composition comprises a molecule for pharmacological modulation of galectin activity in a mammalian brain.
    本发明涉及一种药物组合物,用于治疗或预防α-突触核蛋白病,其中该组合物包括一种用于在哺乳动物大脑中调节半乳糖凝集素活性的分子。该发明还涉及一种治疗或预防哺乳动物主体中α-突触核蛋白病的方法,该方法包括向主体中注射至少一种组合物的治疗有效量,其中该组合物包括一种用于在哺乳动物大脑中调节半乳糖凝集素活性的分子。
  • Novel galactoside inhibitor of galectins
    申请人:GALECTO BIOTECH AB
    公开号:US20160096861A1
    公开(公告)日:2016-04-07
    Provided is a compound of the general formula (I): The compound of formula (I) is suitable for treating pulmonary fibrosis, such as Idiopathic pulmonary fibrosis in a mammal. Also provided is a method for treatment of pulmonary fibrosis, such as Idiopathic pulmonary fibrosis in a human subject having a galectin-3 level indicative of pulmonary fibrosis or exacerbation of symptoms as well as a method for making said compound.
    提供的是通式(I)的化合物:公式(I)的化合物适用于治疗哺乳动物的肺纤维化,如特发性肺纤维化。还提供了一种治疗肺纤维化的方法,例如对于人类患有表明肺纤维化或症状加剧的半乳糖凝集素-3水平的特发性肺纤维化患者,以及制备该化合物的方法。
  • VACCINE AGAINST KLEBSIELLA PNEUMONIAE
    申请人:Vaxxilon AG
    公开号:EP3492482A1
    公开(公告)日:2019-06-05
    The present invention relates to a synthetic saccharide of general formula (I) that is related to Klebsiella pneumoniae serotype O1, O2, O2ac, and O8 O-polysaccharide and carbapenem-resistant Klebsiella pneumoniae ST258 O-polysaccharide and conjugate thereof. Said synthetic saccharide, said conjugate and pharmaceutical composition containing said synthetic saccharide or said conjugate are useful for prevention and/or treatment of diseases associated with Klebsiella pneumoniae. Furthermore, the synthetic saccharide of general formula (I) is useful as marker in immunological assays for detection of antibodies against Klebsiella pneumoniae bacteria.
    本发明涉及一种与克雷伯氏肺炎菌O1、O2、O2ac和O8 O-多糖以及碳青霉烯耐药克雷伯氏肺炎菌ST258 O-多糖相关的通式(I)的合成糖。所述合成糖、所述结合物及含有所述合成糖或所述结合物的药物组合物对于预防和/或治疗与克雷伯氏肺炎菌相关的疾病是有用的。此外,通式(I)的合成糖在免疫学检测中用作标记,以检测抗克雷伯氏肺炎菌细菌的抗体。
  • Methods, compositions and kits for treating, modulating, or preventing ocular angiogenesis or fibrosis in a subject using a galectin protein inhibitor
    申请人:TUFTS UNIVERSITY
    公开号:US20150320782A1
    公开(公告)日:2015-11-12
    Methods and kits using a pharmaceutical composition for use in inhibiting ocular angiogenesis or fibrosis are provided herein, such that composition includes a pharmaceutically suitable carrier or diluent and an amount of the inhibitor composition effective to inhibit the angiogenesis or the fibrosis by inhibiting expression and/or activity of a galectin protein or a portion thereof.
  • GALACTOSIDE INHIBITORS FOR NEW USES
    申请人:GALECTO BIOTECH AB
    公开号:US20170095496A1
    公开(公告)日:2017-04-06
    Provided is a method for treatment or prevention of α-synucleinopathies in a mammalian subject, the method comprising administering a therapeutically effective amount of at least one composition to the subject, wherein the composition comprises a molecule for pharmacological modulation of galectin activity in a mammalian brain.
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