Gomisin G (BioDeep_00000000569)

Main id: BioDeep_00000230410

 

natural product PANOMIX_OTCML-2023


代谢物信息卡片


[(9S,10S,11S)-10-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-yl] benzoate

化学式: C30H32O9 (536.2046222)
中文名称: 戈米辛G, 戈米辛 G
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(C1(C)O)OC(=O)C5=CC=CC=C5)OCO4)OC)OC)OC)OC
InChI: InChI=1S/C30H32O9/c1-16-12-18-13-20(33-3)24(34-4)26(35-5)22(18)23-19(14-21-25(27(23)36-6)38-15-37-21)28(30(16,2)32)39-29(31)17-10-8-7-9-11-17/h7-11,13-14,16,28,32H,12,15H2,1-6H3/t16-,28-,30-/m0/s1

描述信息

Gomisin G is a natural product found in Kadsura heteroclita, Schisandra henryi, and other organisms with data available.
See also: Schisandra chinensis fruit (part of).
Gomisin G is an ethanolic extract of the stems of Kadsura interior; exhibits potent anti-HIV activity with EC50 and therapeutic index (TI) values of 0.006 microgram/mL and 300, respectively.
Gomisin G is an ethanolic extract of the stems of Kadsura interior; exhibits potent anti-HIV activity with EC50 and therapeutic index (TI) values of 0.006 microgram/mL and 300, respectively.

同义名列表

10 个代谢物同义名

Gomisin G; [(9S,10S,11S)-10-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-yl] benzoate; Benzo[3,4]cycloocta[1,2:4,5]benzo[1,2-d][1,3]dioxole-7,8-diol, 5,6,7,8-tetrahydro-1,2,3,13-tetramethoxy-6,7-dimethyl-, 8-benzoate, (6S,7S,8S)-; Benzo(3,4)cycloocta(1,2-f)(1,3)benzodioxole-7,8-diol, 5,6,7,8-tetrahydro-1,2,3,13-tetramethoxy-6,7-dimethyl-, 8-benzoate, (6S,7S,8S,13aS)-; (hydroxy-tetramethoxy-dimethyl-[?]yl) benzoate; UNII-6B4CV8T31X; (-)-Gomisin G; 6B4CV8T31X; FT-0701664; GOMISING



数据库引用编号

11 个数据库交叉引用编号

分类词条

相关代谢途径

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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。

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文献列表

  • Kuo-Hsiung Lee. Discovery and development of natural product-derived chemotherapeutic agents based on a medicinal chemistry approach. Journal of natural products. 2010 Mar; 73(3):500-16. doi: 10.1021/np900821e. [PMID: 20187635]
  • Yuan-Bin Cheng, Meng-Ting Chang, Yi-Wen Lo, Ching-Jen Ho, Yuh-Chi Kuo, Ching-Te Chien, Shun-Ying Chen, Shorong-Shii Liou, Yao-Haur Kuo, Ya-Ching Shen. Oxygenated lignans from the fruits of Schisandra arisanensis. Journal of natural products. 2009 Sep; 72(9):1663-8. doi: 10.1021/np9003678. [PMID: 19673515]
  • Kuo-Hsiung Lee. Current developments in the discovery and design of new drug candidates from plant natural product leads. Journal of natural products. 2004 Feb; 67(2):273-83. doi: 10.1021/np030373o. [PMID: 14987069]
  • Dao-Feng Chen, Shun-Xiang Zhang, Mutsuo Kozuka, Quan-Zhong Sun, Ju Feng, Qiang Wang, Teruo Mukainaka, Yoshitaka Nobukuni, Harukuni Tokuda, Hoyoku Nishino, Hui-Kang Wang, Susan L Morris-Natschke, Kuo-Hsiung Lee. Interiotherins C and D, two new lignans from Kadsura interior and antitumor-promoting effects of related neolignans on Epstein-Barr virus activation. Journal of natural products. 2002 Sep; 65(9):1242-5. doi: 10.1021/np0105127. [PMID: 12350139]