Poststerone (BioDeep_00000007001)

 

Secondary id: BioDeep_00001470988

PANOMIX_OTCML-2023 natural product


代谢物信息卡片


(2S,3R,5R,9R,10R,13R,14S,17S)-17-ethanoyl-2,3,14-trihydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one

化学式: C21H30O5 (362.209313)
中文名称:
谱图信息: 最多检出来源 Viridiplantae(plant) 12.9%

分子结构信息

SMILES: C1[C@@]2(C)[C@]([H])(C(=O)C=C3[C@]2([H])CC[C@]2(C)[C@@]([H])(C(=O)C)CC[C@@]32O)C[C@@H](O)[C@H]1O
InChI: InChI=1S/C21H30O5/c1-11(22)12-5-7-21(26)14-8-16(23)15-9-17(24)18(25)10-19(15,2)13(14)4-6-20(12,21)3/h8,12-13,15,17-18,24-26H,4-7,9-10H2,1-3H3/t12-,13+,15+,17-,18+,19-,20-,21-/m1/s1

描述信息

D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones
Origin: Plant, Pregnanes

同义名列表

8 个代谢物同义名

Poststerone; (2S,3R,5R,9R,10R,13R,14S,17S)-17-ethanoyl-2,3,14-trihydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one; (2S,3R,5R,9R,10R,13R,14S,17S)-17-acetyl-2,3,14-trihydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one; ZINC04081397; 10162-99-9; C08837; 2beta,3beta,14-trihydroxy-5beta-pregn-7-ene-6,20-dione; ST 21:3;O5



数据库引用编号

23 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

  • Christine Balducci, Laurence Dinan, Louis Guibout, Anne-Sophie Foucault, Christel Carbonne, Jean-Denis Durand, Cédric Caradeuc, Gildas Bertho, Jean-Pierre Girault, René Lafont. The complex metabolism of poststerone in male rats. The Journal of steroid biochemistry and molecular biology. 2021 09; 212(?):105897. doi: 10.1016/j.jsbmb.2021.105897. [PMID: 33862260]
  • S Kumpun, J-P Girault, L Dinan, C Blais, A Maria, C Dauphin-Villemant, B Yingyongnarongkul, A Suksamrarn, R Lafont. The metabolism of 20-hydroxyecdysone in mice: relevance to pharmacological effects and gene switch applications of ecdysteroids. The Journal of steroid biochemistry and molecular biology. 2011 Aug; 126(1-2):1-9. doi: 10.1016/j.jsbmb.2011.03.016. [PMID: 21439380]
  • Sophie Crouzet, Annick Maria, Laurence Dinan, René Lafont, Jean-Pierre Girault. Ecdysteroids from Cyanotis longifolia Benth. (Commelinaceae). Archives of insect biochemistry and physiology. 2009 Dec; 72(4):194-209. doi: 10.1002/arch.20329. [PMID: 19760659]
  • Juraj Harmatha, Karel Vokác, Eva Kmonícková, Zdenek Zídek. Lack of interference of common phytoecdysteroids with production of nitric oxide by immune-activated mammalian macrophages. Steroids. 2008 Apr; 73(4):466-71. doi: 10.1016/j.steroids.2007.12.014. [PMID: 18243265]
  • Cheng-Yu Tan, Jin-Hui Wang, Xian Li. Phytoecdysteroid constituents from Cyanotis arachnoidea. Journal of Asian natural products research. 2003 Dec; 5(4):237-40. doi: 10.1080/1028602031000105830. [PMID: 14604231]
  • M Báthori, R Lafont, J P Girault, I Máthé. [Structural diversity of ecdysteroids of Lychnis flos-cuculi]. Acta pharmaceutica Hungarica. 2001 Aug; 71(2):157-67. doi: . [PMID: 11862663]