Schottenol (BioDeep_00000007003)

 

Secondary id: BioDeep_00000637164

human metabolite PANOMIX_OTCML-2023 Endogenous


代谢物信息卡片


(2S,5S,7S,14R,15R)-14-[(2R,5S)-5-ethyl-6-methylheptan-2-yl]-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-9-en-5-ol

化学式: C29H50O (414.386145)
中文名称:
谱图信息: 最多检出来源 Chinese Herbal Medicine(otcml) 1.59%

分子结构信息

SMILES: CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C
InChI: InChI=1S/C29H50O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h11,19-23,25-27,30H,7-10,12-18H2,1-6H3/t20-,21+,22+,23+,25-,26?,27?,28+,29-/m1/s1

描述信息

Schottenol is found in cucumber. Schottenol is a constituent of cucumber leaves (Cucumis sativus).

同义名列表

15 个代谢物同义名

(2S,5S,7S,14R,15R)-14-[(2R,5S)-5-ethyl-6-methylheptan-2-yl]-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-9-en-5-ol; 24-Ethyl-5alpha -cholest-7-en-3beta -ol; (3beta ,5alpha )-Stigmast-7-en-3-ol; 16,17,25,26-tetrahydro-Elasterol; 16,17,25,26-Tetrahydroelasterol; 5alpha -Stigmast-7-en-3beta -ol; 5alpha -Stigma-7-en-3beta -ol; 22,23-dihydro-a-Spinasterol; 22-Dihydrochondrillasterol; 24alpha -Ethyllathosterol; stigmast-7-en-3β-ol; 7-Stigmasten-3beta -ol; delta(7)-Stigmastenol; 22-Dihydrospinasterol; Schottenol



数据库引用编号

15 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(0)

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

23 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：

  • PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。



文献列表

  • Farid Khallouki, Mohamed Ksila, Imen Ghzaiel, Soukaina Essadek, Mounia Tahri Joutey, Samah Maaloul, Wafa Zennouhi, Laila Benbacer, Mohamed Bourhia, Lhoussain Hajji, Amira Zarrouk, Leila Rezig, Sandrine Rup-Jacques, Raoudha Abdellaoui, Taoufik Ghrairi, Olfa Masmoudi-Kouki, Boubker Nasser, Pierre Andreoletti, Mustapha-Cherkaoui-Malki, Mohammad Samadi, Anne Vejux, Gérard Lizard. Chemical and Biochemical Features of Spinasterol and Schottenol. Advances in experimental medicine and biology. 2024; 1440(?):45-55. doi: 10.1007/978-3-031-43883-7_3. [PMID: 38036874]
  • Maqsood Ahmed, Allah Rakha Sajid, Ansar Javeed, Muhammad Aslam, Taswar Ahsan, Dilbar Hussain, Abdul Mateen, Xiuwei Li, Peiwen Qin, Mingshan Ji. Antioxidant, antifungal, and aphicidal activity of the triterpenoids spinasterol and 22,23-dihydrospinasterol from leaves of Citrullus colocynthis L. Scientific reports. 2022 03; 12(1):4910. doi: 10.1038/s41598-022-08999-z. [PMID: 35318417]
  • Maqsood Ahmed, Peiwen Qin, Mingshan Ji, Ran An, Hongxia Guo, Jamil Shafi. Spinasterol, 22,23-Dihydrospinasterol and Fernenol from Citrullus Colocynthis L. with Aphicidal Activity against Cabbage Aphid Brevicoryne Brassicae L. Molecules (Basel, Switzerland). 2020 May; 25(9):. doi: 10.3390/molecules25092184. [PMID: 32392823]
  • Garcia Gonzalez Jessica, Garcia Lorenzana Mario, Zamilpa Alejandro, Almanza Perez Julio Cesar, Jasso Villagomez E Ivan, Roman Ramos Ruben, Alarcon-Aguilar Francisco Javier. CHEMICAL CHARACTERIZATION OF A HYPOGLYCEMIC EXTRACT FROM CUCURBITA FICIFOLIA BOUCHE THAT INDUCES LIVER GLYCOGEN ACCUMULATION IN DIABETIC MICE. African journal of traditional, complementary, and alternative medicines : AJTCAM. 2017; 14(3):218-230. doi: 10.21010/ajtcam.v14i3.24. [PMID: 28480434]
  • Linda H Münger, Sabrina Jutzi, Anna-Maija Lampi, Laura Nyström. Comparison of Enzymatic Hydrolysis and Acid Hydrolysis of Sterol Glycosides from Foods Rich in Δ(7)-Sterols. Lipids. 2015 Aug; 50(8):735-48. doi: 10.1007/s11745-015-4002-3. [PMID: 25757602]
  • Asmaa Badreddine, El Mostafa Karym, Amira Zarrouk, Thomas Nury, Youssef El Kharrassi, Boubker Nasser, Mustapha Cherkaoui Malki, Gérard Lizard, Mohammad Samadi. An expeditious synthesis of spinasterol and schottenol, two phytosterols present in argan oil and in cactus pear seed oil, and evaluation of their biological activities on cells of the central nervous system. Steroids. 2015 Jul; 99(Pt B):119-24. doi: 10.1016/j.steroids.2015.01.005. [PMID: 25595450]
  • Youssef El Kharrassi, Mohammad Samadi, Tatiana Lopez, Thomas Nury, Riad El Kebbaj, Pierre Andreoletti, Hammam I El Hajj, Joseph Vamecq, Khadija Moustaid, Norbert Latruffe, M'Hammed Saïd El Kebbaj, David Masson, Gérard Lizard, Boubker Nasser, Mustapha Cherkaoui-Malki. Biological activities of Schottenol and Spinasterol, two natural phytosterols present in argan oil and in cactus pear seed oil, on murine miroglial BV2 cells. Biochemical and biophysical research communications. 2014 Apr; 446(3):798-804. doi: 10.1016/j.bbrc.2014.02.074. [PMID: 24582563]
  • W S Chang, Y H Chang, F J Lu, H C Chiang. Inhibitory effects of phenolics on xanthine oxidase. Anticancer research. 1994 Mar; 14(2A):501-6. doi: . [PMID: 8017853]
  • Z Chao, J Liu. [Chemical constituents of the pericarp of Trichosanthes rosthornii Harms]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 1991 Feb; 16(2):97-9, 127. doi: ". [PMID: 1872972]
  • K Yasukawa, S Yamanouchi, M Takido. [Studies on the constituents in the water extracts of crude drugs. III. On the roots of Stellaria dichotoma L. var. lanceolata Bge. (author's transl)]. Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan. 1981 Jan; 101(1):64-6. doi: 10.1248/yakushi1947.101.1_64. [PMID: 7252785]