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Loganetin/1-Epiloganetin | 392687-48-8

中文名称
——
中文别名
——
英文名称
Loganetin/1-Epiloganetin
英文别名
loganetin;methyl (4aS,6S,7R,7aS)-1,6-dihydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate
Loganetin/1-Epiloganetin化学式
CAS
392687-48-8
化学式
C11H16O5
mdl
——
分子量
228.245
InChiKey
XWOHZIIPBYAMJX-SJYPEAAASA-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):
    0.2
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.73
  • 拓扑面积:
    76
  • 氢给体数:
    2
  • 氢受体数:
    5

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    Loganetin/1-Epiloganetin盐酸 、 sodium hydroxide 作用下, 以 乙醇 为溶剂, 反应 6.0h, 生成 (1R,4aS,6S,7R,7aS)-6-Hydroxy-1-methoxy-7-methyl-1,4a,5,6,7,7a-hexahydro-cyclopenta[c]pyran-4-carboxylic acid
    参考文献:
    名称:
    10.1016/j.molstruc.2024.138608
    摘要:
    DOI:
    10.1016/j.molstruc.2024.138608
  • 作为产物:
    描述:
    loganin 以 aq. phosphate buffer 为溶剂, 以97 %的产率得到Loganetin/1-Epiloganetin
    参考文献:
    名称:
    10.1016/j.molstruc.2024.138608
    摘要:
    DOI:
    10.1016/j.molstruc.2024.138608
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文献信息

  • La dinklageine, alcaloide monoterpenique d'un type nouveau
    作者:A.L. Skaltsounis、S. Michel、F. Tillequin、M. Koch
    DOI:10.1016/s0040-4039(01)81289-2
    日期:——
    The structure of dinklageine 1, monoterpene alkaloid of a new type has been determined by spectral analysis. Its absolute stereochemistry has been established by its synthesis using loganin 2 as starting material.
    已经通过光谱分析确定了一种新型的丁克兰汀1的结构,一种单萜生物碱。它的绝对立体化学是通过使用loganin 2作为起始原料进行合成而建立的。
  • Modified iridoid glycosides as anti-implantation agents
    作者:Anju P Misra、Vijayavitthal T Mathad、Kanwal Raj、Amiya P Bhaduri、Rashmi Tiwari、Anuradha Srivastava、P.K Mehrotra
    DOI:10.1016/s0968-0896(01)00105-5
    日期:2001.11
    Structural modifications in iridoid glycosides and evaluation of their efficacy on adhering capability (in vitro) of immature hamster uterine epithelial cells to the substratum have been studied. Out of 31, eight compounds in vitro, five compounds in utero and two in vivo showed adhesion/implantation preventing activity, respectively. The results provide an indication for further exploration in the line of development of anti-adhesive agents. (C) 2001 Published by Elsevier Science Ltd.
  • Fungitoxic non-glycosidic iridoids from Alibertia macrophylla
    作者:M.Claudia M. Young、Marcia R. Braga、Sonia M.C. Dietrich、Hugo E. Gottlieb、Ligia M.V. Trevisan、Vanderlan Da S. Bolzani
    DOI:10.1016/0031-9422(92)83701-y
    日期:1992.10
    The aqueous alcohol extract of the leaves of Alibertia macrophylla afforded two epimeric pairs of iridoid aglycones and one of them showed high inhibitory activity against Aspergillus niger, Cladosporium sphaerospermum, C. cladosporioides and Colletotrichum gloesporioides. Three of the compounds are reported for the first time from natural sources. Their structures were established on the basis of spectroscopic studies, mainly through C-13 NMR analysis.
  • Compositions and methods for treatment of liver disease
    申请人:Fong Harry
    公开号:US20080319042A1
    公开(公告)日:2008-12-25
    The present invention comprises compositions and methods for the treatment of liver disease, particularly treatments for infection by HCV and/or HBV. The present invention comprises antiviral compositions comprising lamiridosin, derivatives of lamiridosin or iridoids that are effective in inhibiting one or more steps in the infection of cells by HCV or HBV. Methods for treating subjects, particularly humans, infected with HCV or HBV are provided.
  • 10.1016/j.molstruc.2024.138608
    作者:Qiu, Hong-mao、Deng, Lu-lu、Li, Jiang、Zhang, Mei、Hao, Xiao-jiang、Yuan, Chun-mao、Zhang, Peng、Mu, Shu-zhen
    DOI:10.1016/j.molstruc.2024.138608
    日期:——
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