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(3aR,5aS,9bS)-3a,4,5,5a,6,7-hexahydro-3a-hydroxy-5a,9-dimethyl-3-methylenenaphtho[1,2-b]furan-2,8(3H,9bH)-dione | 144860-23-1

中文名称
——
中文别名
——
英文名称
(3aR,5aS,9bS)-3a,4,5,5a,6,7-hexahydro-3a-hydroxy-5a,9-dimethyl-3-methylenenaphtho[1,2-b]furan-2,8(3H,9bH)-dione
英文别名
(3aR,5aS,9bS)-3a-hydroxy-5a,9-dimethyl-3-methylidene-5,6,7,9b-tetrahydro-4H-benzo[g][1]benzofuran-2,8-dione
(3aR,5aS,9bS)-3a,4,5,5a,6,7-hexahydro-3a-hydroxy-5a,9-dimethyl-3-methylenenaphtho[1,2-b]furan-2,8(3H,9bH)-dione化学式
CAS
144860-23-1
化学式
C15H18O4
mdl
——
分子量
262.306
InChiKey
JJQNORUJCLAZCD-NWANDNLSSA-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):
    0.7
  • 重原子数:
    19
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    63.6
  • 氢给体数:
    1
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    7-hydroxyfrullanolide 在 sodium chromate(VI) 、 sodium acetate乙酸酐溶剂黄146 作用下, 以 为溶剂, 反应 24.0h, 以24 mg的产率得到(3aR,5aS,9bS)-3a,4,5,5a,6,7-hexahydro-3a-hydroxy-5a,9-dimethyl-3-methylenenaphtho[1,2-b]furan-2,8(3H,9bH)-dione
    参考文献:
    名称:
    7-Hydroxyeudesmanolides from Sphaeranthus indicus
    摘要:
    Two new eudesmanolides, along with one known eudesmanolide and two sesquiterpenoids, cryptomeridiol and 4-epicryptomeridiol, have been isolated from Sphaeranthus indicus. The structures of the new compounds have been established by spectral methods, and in one case by chemical correlation.
    DOI:
    10.1016/0031-9422(92)83492-h
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文献信息

  • [EN] 7-HYDROXYFRULLANOLIDE AND ITS ANALOGS FOR PREVENTION, CONTROL AND TREATMENT OF METABOLIC DISORDERS<br/>[FR] 7-HYDROXYFRULLANOLIDE ET SES ANALOGUES POUR LA PRÉVENTION, LA MAÎTRISE ET LE TRAITEMENT DE TROUBLES DU MÉTABOLISME.
    申请人:LAILA NUTRACEUTICALS
    公开号:WO2012014216A1
    公开(公告)日:2012-02-02
    The invention discloses biologically active ingredient(s) selected from 7- hydroxyfrullanolide, its analogs, the extract(s) and fraction(s) standardized to 7- hydroxyfrullanolide or its analogs or both or mixtures thereof or their composition(s) for the prevention, control and treatment of one or more obesity, overweight, metabolic syndrome, diabetes and other metabolic disorders or for producing lean body mass in a warm blooded animal in need thereof.
    本发明揭示了从7- 羟基富尔醛内酯、其类似物、提取物和分离物中选择的生物活性成分,这些成分经标准化处理得到7- 羟基富尔醛内酯或其类似物或两者或二者的混合物,或它们的组合物,用于预防、控制和治疗一种或多种肥胖、超重、代谢综合征、糖尿病和其他代谢紊乱,或用于在需要的温血动物中产生瘦体重。
  • 7-HYRDROXYFRULLANOLIDE ITS ANALOGS FOR PREVENTION CONTROL AND TREATMENT OF METABOLIC DISORDERS
    申请人:LAILA NUTRACEUTICALS
    公开号:US20130136809A1
    公开(公告)日:2013-05-30
    The invention discloses biologically active ingredient(s) selected from 7-hydroxyfrullanolide, its analogs, the ex-tract(s) and fraction(s) standardized to 7-hydroxyfrullanolide or its analogs or both or mixtures thereof or their composition(s) for the prevention, control and treatment of one or more obesity, overweight, metabolic syndrome, diabetes and other metabolic disorders or for producing lean body mass in a warm blooded animal in need thereof.
  • CARRIER SYSTEM FOR PREPARING HERBACEOUS EXTRACTS
    申请人:SISAF LIMITED
    公开号:US20220174952A1
    公开(公告)日:2022-06-09
    A method for stabilizing a bioactive herbaceous extract in a composition comprising silicon particles, the method comprising bringing the bioactive herbaceous extract into contact with the silicon particles, in the presence of at least one non-reducing disaccharide. Also related compositions and methods.
  • Rojatkar, Supada R.; Sawaikar, Dilip D.; Nagasampagi, Bhimsen A., Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1994, vol. 33, p. 1203 - 1204
    作者:Rojatkar, Supada R.、Sawaikar, Dilip D.、Nagasampagi, Bhimsen A.
    DOI:——
    日期:——
  • 7-Hydroxyeudesmanolides from Sphaeranthus indicus
    作者:Supada R. Rojatkar、Bhimsen A. Nagasampagi
    DOI:10.1016/0031-9422(92)83492-h
    日期:1992.9
    Two new eudesmanolides, along with one known eudesmanolide and two sesquiterpenoids, cryptomeridiol and 4-epicryptomeridiol, have been isolated from Sphaeranthus indicus. The structures of the new compounds have been established by spectral methods, and in one case by chemical correlation.
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