2β,3β,16α-trihydroxyolean-12(13)-en-23,28-dioic acid | 84161-89-7

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 异戊烯醇脂质
• 英文名称: 2β,3β,16α-trihydroxyolean-12(13)-en-23,28-dioic acid
• 英文别名: 2β,3β,16α-trihydroxyolean-12-ene-23,28-dioic acid；2β,3β,16α-trihydroxyolean-12-en-23,28-dioic acid；acide zanhique；zanhic acid；(2S,3R,4S,4aR,6aR,6bS,8R,8aR,12aS,14aR,14bR)-2,3,8-trihydroxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylic acid
• CAS: 84161-89-7
• 化学式: C₃₀H₄₆O₇
• 分子量: 518.691
• InChiKey: PLERLWUIYWAWRU-XTQHQJBBSA-N

物化性质

• 沸点：
  668.7±55.0 °C(Predicted)
• 密度：
  1.28±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5.2
• 重原子数：
  37
• 可旋转键数：
  2
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.87
• 拓扑面积：
  135
• 氢给体数：
  5
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  2β,3β,16α-trihydroxyolean-12(13)-en-23,28-dioic acid 在 吡啶 作用下， 反应 96.0h， 生成 triacetate du methylester de l'acide zanhique
  参考文献：
  名称：

  Dimbi, Makoso Zeza; Warin, Roger; Delaude, Clement, Bulletin des Societes Chimiques Belges, 1987, vol. 96, # 3, p. 207 - 218

  摘要：

  DOI：
• 作为产物：
  描述：

  3β-O-(4-deoxy-β-D-hex-4-enopyranosyluronic acid), 2β,16α-dihydroxy-olean-12-en-23,18-dioic acid 在 高氯酸 作用下， 以 水 为溶剂， 反应 2.5h， 生成 2β,3β,16α-trihydroxyolean-12(13)-en-23,28-dioic acid
  参考文献：
  名称：

  Dimbi, Makoso Zeza; Warin, Roger; Delaude, Clement, Bulletin des Societes Chimiques Belges, 1987, vol. 96, # 3, p. 207 - 218

  摘要：

  DOI：

文献信息

• Artefact formation during acid hydrolysis of saponins from Medicago spp.
  作者：Aldo Tava、Elisa Biazzi、Mariella Mella、Paolo Quadrelli、Pinarosa Avato

  DOI：10.1016/j.phytochem.2017.02.018

  日期：2017.6

  sapogenol artefact identified as 3β,22β,24-trihydroxyolean-18(19)-en and named soyasapogenol H. From a zanhic acid saponin two major artefact compounds identified as 2β,3β,16α-trihydroxyolean-13(18)-en-23,28-dioic acid and 2β,3β,16α-trihydroxyolean-28,13β-olide-23-oic acid were obtained, together with some zanhic acid. Other compounds, detected in very small amount in the reaction mixture, were also tentatively

  紫花苜蓿皂苷酸水解过程中获得的人工制品化合物。（豆科），已通过 GC-FID 进行监测和评估。它们的鉴定已通过 GC-MS 和 1H 和 13C NMR 进行。考虑了在三萜五环苷元上具有不同取代基的皂苷，并在 10 小时的时程反应中检测和量化了它们的水解产物。从大豆皂甙 B、C、D 和 F 中获得众所周知的大豆皂甙 B、C、D 和 F，以及先前未描述的皂甙人工制品，鉴定为 3β,22β,24-trihydroxyolean-18(19)-en 并命名为 soyasapogenol H。来自 zanhic acid saponin鉴定为 2β,3β,16α-trihydroxyolean-13(18)-en-23,28-dioic acid 和 2β,3β,16α-trihydroxyolean-28,13β-olide-23-oic acid 的两种主要人工合成化合物被一起获得用一些山楂酸
• ACCELERATOR FOR INITIAL INSULIN SECRETION
  申请人：Use-Techno Corporation

  公开号：EP1674089A1

  公开（公告）日：2006-06-28

  The present invention provides an early insulin secretion stimulator consisting of a triterpene represented by the following general formula (1) and/or a triterpene represented by the following general formula (2). [where R1 represents COOH, etc., R11 and R12 represent CH2OH, etc., X1 represents hydrogen or OH and X11, X12, X21 and X22 represent OH, etc.]

  本发明提供了一种早期胰岛素分泌刺激剂，由以下通式（1）代表的三萜和/或以下通式（2）代表的三萜组成。 [其中 R1 代表 COOH 等，R11 和 R12 代表 CH2OH 等，X1 代表氢或 OH，X11、X12、X21 和 X22 代表 OH 等。］
• Cytotoxic 16-β-[(d-xylopyranosyl)oxy]oxohexadecanyl triterpene glycosides from a Malagasy plant, Physena sessiliflora
  作者：Masaki Inoue、Kazuhiro Ohtani、Ryoji Kasai、Mayu Okukubo、Marta Andriantsiferana、Kazuo Yamasaki、Tohru Koike

  DOI：10.1016/j.phytochem.2009.06.002

  日期：2009.6

  Brine shrimp lethality assay-guided separation of the MeOH extract of leaves of Physena sessiliflora, which is endemic to Madagascar, afforded eight triterpene glycosides Physenoside S1-4 and 16-beta-[(D-Xylopyranosyl)oxy]oxohexadecanyl homologues, Physenoside S5-8. Structural elucidation of these compounds was based on both spectroscopic analyses and chemical properties. Physenoside S7 and S8 have significant cytotoxic activities in the brine shrimp lethality assay. (C) 2009 Elsevier Ltd. All rights reserved.
• Insulin secretion potentiator
  申请人：Matsuyama Futoshi

  公开号：US20050143464A1

  公开（公告）日：2005-06-30

  The present invention provides early insulin secretion stimulators consisting of triterpenes represented by the following general formula (1) and/or triterpenes represented by the following general formula (2). [where R 1 represents COOH, etc., R 11 and R 12 represent CH 2 OH, etc., X 1 represents hydrogen or OH and X 11 , X 12 , X 21 and X 22 represent OH, etc.]
• [EN] GLUCONEOGENESIS INHIBITING AGENT<br/>[FR] AGENTS D'INHIBITION DE LA GLUCONEOGENESE
  申请人：USE TECHNO CORP

  公开号：WO2006054370A1

  公开（公告）日：2006-05-26

  [EN] The present invention provides a gluconeogenesis inhibiting agent containing as an active ingredient corosolic acid, an analogous compound of corosolic acid, or a pharmaceutically acceptable salt thereof.
  [FR] La présente invention concerne un agent d'inhibition de la gluconéogenèse, contenant en tant qu'ingrédient actif de l'acide corosolique, un analogue de l'acide corosolique ou l'un de leurs sels pharmaceutiquement acceptables.