Esculeoside A (BioDeep_00000231894)

   

natural product


代谢物信息卡片


Esculeoside A

化学式: C58H95NO29 (1269.598946)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC(=O)OC1CC(COC2OC(CO)C(O)C(O)C2O)CNC12OC1CC3C4CCC5CC(OC6OC(CO)C(OC7OC(CO)C(O)C(O)C7OC7OC(CO)C(O)C(OC8OCC(O)C(O)C8O)C7O)C(O)C6O)CCC5(C)C4CCC3(C)C1C2C
InChI: InChI=1S/C58H95NO29/c1-21-36-30(88-58(21)35(79-22(2)64)11-23(14-59-58)19-77-51-45(74)41(70)38(67)31(15-60)81-51)13-28-26-6-5-24-12-25(7-9-56(24,3)27(26)8-10-57(28,36)4)80-53-47(76)43(72)48(34(18-63)84-53)85-55-50(87-54-46(75)42(71)39(68)32(16-61)82-54)49(40(69)33(17-62)83-55)86-52-44(73)37(66)29(65)20-78-52/h21,23-55,59-63,65-76H,5-20H2,1-4H3/t21-,23-,24-,25-,26+,27-,28-,29+,30-,31+,32+,33+,34+,35-,36-,37-,38+,39+,40+,41-,42-,43+,44+,45+,46+,47+,48-,49-,50+,51+,52-,53+,54-,55-,56-,57-,58-/m0/s1

描述信息

A steroid saponin that is spirosolane-3,23,27-triol in which the hydroxy group at position 23 is acetylated and the hydroxy groups at positions 3 and 27 are glycosylated by lycotetraosyl and a beta-D-glucopyranosyl moieties respectively. Isolated from the fruits of Lycopersicon esculentum, it exhibits cytotoxic activity.

同义名列表

1 个代谢物同义名

Esculeoside A



数据库引用编号

8 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

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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)

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

  • Nasser A Alsabaani, Kawther Amawi, Samy M Eleawa, Wisam Nabeel Ibrahim, Walid Aldhaban, Ahmad Mohammad Alaraj, Badr Alkhalaf, Waqas Sami, Hisham Alshaikhli, Mahmoud A Alkhateeb. Nrf-2-dependent antioxidant and anti-inflammatory effects underlie the protective effect of esculeoside A against retinal damage in streptozotocin-induced diabetic rats. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2024 Apr; 173(?):116461. doi: 10.1016/j.biopha.2024.116461. [PMID: 38503237]
  • Prashant D Sonawane, Sachin A Gharat, Adam Jozwiak, Ranjit Barbole, Sarah Heinicke, Efrat Almekias-Siegl, Sagit Meir, Ilana Rogachev, Sarah E O' Connor, Ashok P Giri, Asaph Aharoni. A BAHD-type acyltransferase concludes the biosynthetic pathway of non-bitter glycoalkaloids in ripe tomato fruit. Nature communications. 2023 07; 14(1):4540. doi: 10.1038/s41467-023-40092-5. [PMID: 37500644]
  • Jian-Rong Zhou, Yurina Kanda, Anna Tanaka, Hideyuki Manabe, Toshihiro Nohara, Kazumi Yokomizo. Anti-hyaluronidase Activity in Vitro and Amelioration of Mouse Experimental Dermatitis by Tomato Saponin, Esculeoside A. Journal of agricultural and food chemistry. 2016 Jan; 64(2):403-8. doi: 10.1021/acs.jafc.5b05320. [PMID: 26716906]
  • Hideyuki Manabe, Ayumi Takemoto, Hiromichi Maehara, Mizuho Ohno, Yoshihiro Murakami, Shigeru Itoh, Toshihiro Nohara. Efficient improved extraction of tomato saponin using shock waves. Chemical & pharmaceutical bulletin. 2011; 59(11):1406-8. doi: 10.1248/cpb.59.1406. [PMID: 22041080]
  • Toshihiro Nohara, Masateru Ono, Tsuyoshi Ikeda, Yukio Fujiwara, Mona El-Aasr. The tomato saponin, esculeoside A. Journal of natural products. 2010 Oct; 73(10):1734-41. doi: 10.1021/np100311t. [PMID: 20853874]