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2-(4-ethylthiobenzyl)phenyl β-D-glucopyranoside

中文名称
——
中文别名
——
英文名称
2-(4-ethylthiobenzyl)phenyl β-D-glucopyranoside
英文别名
2-(4-ethylthiobenzyl)phenyl beta-D-glucopyranoside;(2S,3R,4S,5S,6R)-2-[2-[(4-ethylsulfanylphenyl)methyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol
2-(4-ethylthiobenzyl)phenyl β-D-glucopyranoside化学式
CAS
——
化学式
C21H26O6S
mdl
——
分子量
406.5
InChiKey
VJUOHAYKLFTDRL-YMQHIKHWSA-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):
    2.5
  • 重原子数:
    28
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    125
  • 氢给体数:
    4
  • 氢受体数:
    7

反应信息

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文献信息

  • Glucopyranosyloxybenzylbenzene derivatives and medicinal compositions containing the same
    申请人:——
    公开号:US20040018998A1
    公开(公告)日:2004-01-29
    The present invention relates to glucopyranosyloxybenzylbenzene derivatives represented by the general formula: 1 wherein P represents a group forming a prodrug; and R represents a lower alkyl group, a lower alkoxy group, a lower alkylthio group, a lower alkoxy-substituted (lower alkyl) group, a lower alkoxy-substituted (lower alkoxy) group or a lower alkoxy-substituted (lower alkylthio) group, which have an improved oral absorption and can exert an excellent inhibitory activity in human SGLT2 in vivo and which are useful as agents for the prevention or treatment of a disease associated with hyperglycemia such as diabetes, diabetic complications or obesity, and pharmaceutical compositions comprising the same.
    本发明涉及由通式表示的葡萄糖吡喃基氧基苯基苄基苯基衍生物:其中P代表形成前药的基团;R代表下位烷基基团、下位烷氧基基团、下位烷基硫基团、下位烷氧基取代的(下位烷基)基团、下位烷氧基取代的(下位烷氧基)基团或下位烷氧基取代的(下位烷基硫)基团,这些衍生物具有改善的口服吸收能力,在人体SGLT2中可以发挥出色的抑制活性,对于预防或治疗与高血糖相关的疾病,如糖尿病、糖尿病并发症或肥胖症等,以及包含这些衍生物的药物组合物,具有应用价值。
  • Glucopyranosyloxybenzylbenzene derivatives, medicinal compositions containing the same and intermediates for the preparation of the derivatives
    申请人:Fujikura Hideki
    公开号:US20050080022A1
    公开(公告)日:2005-04-14
    The present invention relates to glucopyranosyloxybenzylbenzene derivatives represented by the general formula: wherein R 1 represents a hydrogen atom or a hydroxy(lower alkyl) group; and R 2 represents a lower alkyl group, a lower alkoxy group, a lower alkylthio group, a hydroxy(lower alkyl) group, a hydroxy(lower alkoxy) group, a hydroxy(lower alkylthio) group etc., and salts thereof, which have an excellent inhibitory activity in human SGLT2 and are useful as agents for the prevention or treatment of diabetes, obesity etc., and intermediates thereof.
    本发明涉及一种由通式表示的葡萄糖吡喃基氧基苄基苯衍生物:其中R1表示氢原子或羟基(较低烷基)基团;R2表示较低烷基基团、较低烷氧基团、较低烷基硫基团、羟基(较低烷基)基团、羟基(较低烷氧基)基团、羟基(较低烷基硫基)基团等,以及其盐。该化合物在人类SGLT2中具有优异的抑制活性,可用作预防或治疗糖尿病、肥胖等的药物,以及其中间体。
  • Glucopyranosyloxy benzylbenzene derivatives, medicinal compositions containing the same and intermediates for the preparation of the derivatives
    申请人:——
    公开号:US20040053855A1
    公开(公告)日:2004-03-18
    The present invention relates to glucopyranosyloxybenzylbenzene derivatives represented by the general formula: 1 wherein R 1 represents a hydrogen atom or a hydroxy(lower alkyl) group; and R 2 represents a lower alkyl group, a lower alkoxy group, a lower alkylthio group, a hydroxy(lower alkyl) group, a hydroxy(lower alkoxy) group, a hydroxy(lower alkylthio) group etc., and salts thereof, which have an excellent inhibitory activity in human SGLT2 and are useful as agents for the prevention or treatment of diabetes, obesity etc., and intermediates thereof.
    本发明涉及一种由通式1所表示的葡萄糖吡喃基氧基苯基苯基衍生物,其中R1代表氢原子或羟基(较低烷基)基团;R2代表较低烷基基团、较低烷氧基基团、较低烷基硫基基团、羟基(较低烷基)基团、羟基(较低烷氧基)基团、羟基(较低烷基硫基)基团等,以及其盐,具有出色的人类SGLT2抑制活性,并可用作糖尿病、肥胖等的预防或治疗药物及其中间体。
  • PROGRESSION INHIBITOR FOR DISEASE ATTRIBUTED TO ABNORMAL ACCUMULATION OF LIVER FAT
    申请人:Kissei Pharmaceutical Co., Ltd.
    公开号:EP1782828A1
    公开(公告)日:2007-05-09
    The present invention provides pharmaceutical compositions useful as agents for the inhibition of progression of diseases associated with abnormal accumulation ofliverlipids. In particular, the pharmaceutical compositions of the present invention which comprise as an active ingredient a sodium/glucose co-transporter 2 inhibitor are highly suitable as an agent for the inhibition of progression of not only common fatty liver but also non-alcholic fatty liver disease (NAFL), non-alcholic steatohepatitis (NASH), hypernutritive fatty liver, diabetic fatty liver, alcholic fatty liver disease toxic fatty liver or the like.
    本发明提供的药物组合物可作为抑制与肝脂异常积聚有关的疾病进展的药物。特别是,本发明的药物组合物包含钠/葡萄糖共转运体 2 抑制剂作为活性成分,非常适合作为不仅是普通脂肪肝,而且是非胆汁性脂肪肝(NAFL)、非胆汁性脂肪性肝炎(NASH)、高营养脂肪肝、糖尿病脂肪肝、胆汁性脂肪肝中毒性脂肪肝或类似疾病的进展抑制剂。
  • GLUCOPYRANOSYLOXYBENZYLBENZENE DERIVATIVES AND MEDICINAL COMPOSITIONS CONTAINING THE SAME
    申请人:Kissei Pharmaceutical Co., Ltd.
    公开号:EP1329456B1
    公开(公告)日:2006-08-09
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