ST 27:2;O5 (BioDeep_00000636734)

 

Secondary id: BioDeep_00000011220


代谢物信息卡片


3alpha,7alpha,12alpha-trihydroxy-5alpha-23E-cholesten-26-oic acid

化学式: C27H44O5 (448.3189)
中文名称:
谱图信息: 最多检出来源 Homo sapiens(bile_acids) 7.4%

分子结构信息

SMILES: C12=CC([C@]3([H])C[C@@H](O)CC[C@]3(C)[C@@]1([H])CC[C@@]1(C)[C@@]2(O)CC[C@@]1([C@H](C)[C@H](O)CCC(O)(C)C)[H])=O
InChI: InChI=1S/C27H44O5/c1-15(6-5-7-16(2)25(31)32)19-8-9-20-24-21(14-23(30)27(19,20)4)26(3)11-10-18(28)12-17(26)13-22(24)29/h5,7,15-24,28-30H,6,8-14H2,1-4H3,(H,31,32)/b7-5+/t15-,16?,17+,18-,19-,20+,21+,22-,23+,24+,26+,27-/m1/s1

描述信息

D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones

同义名列表

30 个代谢物同义名

(3beta,5beta,22R)-3,14,22,25-Tetrahydroxycholest-7-en-6-one; (22R)-3beta,14,22,25-tetrahydroxy-5beta-cholest-7-en-6-one; 2-Deoxy-alpha-ecdysone; 2-deoxyecdysone; ST 27:2;O5; 7alpha,12alpha,24,25-Tetrahydroxycholest-4-en-3-one; 7alpha,12alpha-dihydroxy-3-oxo-5beta-cholestan-(25R)26-oic acid; 7alpha,12alpha-dihydroxy-3-oxo-5beta-cholestanoic acid; 3beta,7beta, 25-trihydroxycholest-5-en-26-oic acid; 7beta,25-dihydroxy-cholestenoic acid; 3beta,7beta, 24-trihydroxycholest-5-en-25R-26-oic acid; 7beta,24-dihydroxy-cholestenoic acid; 3alpha,7alpha,12alpha-Trihydroxy-5beta-24Z-cholesten-26-oic acid; 3alpha,7alpha,12alpha-trihydroxy-5alpha-23E-cholesten-26-oic acid; 3alpha,7alpha-Dihydroxy-12-oxo-5alpha-cholestan-26-oic acid; 3alpha,7alpha,12alpha-Trihydroxy-5beta-cholest-23-en-26-oic acid; 3alpha,7alpha,12alpha-Trihydroxy-5beta-24E-cholesten-26-oic acid; 3alpha,12alpha-Dihydroxy-7-oxo-5beta-cholestan-26-oic acid; 7alpha,12alpha-Dihydroxy-3-oxo-5alpha-cholestan-26-oic acid; 7alpha,12alpha-Dihydroxy-3-oxo-5beta-cholestan-26-oic acid; 7beta,12alpha-Dihydroxy-3-oxo-5beta-cholestan-26-oic acid; 3beta,14alpha,23S,25-tetrahydroxy-5beta-cholest-7-en-6-one; 2,22-dideoxy-23-hydroxyecdysone; 3beta,14alpha,20R,25-tetrahydroxy-5beta-cholest-7-en-6-one; 2,22-Dideoxy-20-hydroxyecdysone; 2,22-bisdeoxyecdysone; 3beta,14alpha,20,25-tetrahydroxy-5alpha-cholest-7-en-6-one; (22R)-2beta,3beta,14,22-tetrahydroxy-5beta-cholest-7-en-6-one; 25-deoxyecdysone; 2-Deoxyecdysone



数据库引用编号

52 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)

10 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

  • Donald L Mykles. Ecdysteroid metabolism in crustaceans. The Journal of steroid biochemistry and molecular biology. 2011 Nov; 127(3-5):196-203. doi: 10.1016/j.jsbmb.2010.09.001. [PMID: 20837145]
  • Larisa Zibareva, Valentina I Yeriomina, Nyamjav Munkhjargal, Jean-Pierre Girault, Laurence Dinan, Rene Lafont. The phytoecdysteroid profiles of 7 species of Silene (Caryophyllaceae). Archives of insect biochemistry and physiology. 2009 Dec; 72(4):234-48. doi: 10.1002/arch.20331. [PMID: 19750548]
  • Ahmed Bakrim, Emilie Guittard, Annick Maria, Jacques Davy De Virville, René Lafont, Najat Takvorian. Phytoecdysteroid C2-hydroxylase is microsomal in spinach, Spinacia oleracea L. Archives of insect biochemistry and physiology. 2009 Dec; 72(4):210-9. doi: 10.1002/arch.20330. [PMID: 19750551]
  • Raimana Ho, Jean-Pierre Girault, Pierre-Yves Cousteau, Jean-Pierre Bianchini, Phila Raharivelomanana, René Lafont. Isolation of a new class of ecdysteroid conjugates (glucosyl-ferulates) using a combination of liquid chromatographic methods. Journal of chromatographic science. 2008 Feb; 46(2):102-10. doi: 10.1093/chromsci/46.2.102. [PMID: 18366867]
  • Dean A Cuebas, Christopher Phillips, Werner Schmitz, Ernst Conzelmann, Dmitry K Novikov. The role of alpha-methylacyl-CoA racemase in bile acid synthesis. The Biochemical journal. 2002 May; 363(Pt 3):801-7. doi: 10.1042/0264-6021:3630801. [PMID: 11964182]
  • Y Meng, P Whiting, L Zibareva, G Bertho, J P Girault, R Lafont, L Dinan. Identification and quantitative analysis of the phytoecdysteroids in Silene species (Caryophyllaceae) by high-performance liquid chromatography. Novel ecdysteroids from S. pseudotites. Journal of chromatography. A. 2001 Nov; 935(1-2):309-19. doi: 10.1016/s0021-9673(01)00893-7. [PMID: 11762783]
  • M Une, A Inoue, T Kurosawa, M Tohma, T Hoshita. Identification of (24E)-3 alpha,7 alpha-dihydroxy-5 beta-cholest-24-enoic acid and (24R,25S)-3 alpha,7 alpha,24-trihydroxy-5 beta-cholestanoic acid as intermediates in the conversion of 3 alpha,7 alpha-dihydroxy-5 beta-cholestanoic acid to chenodeoxycholic acid in rat liver homogenates. Journal of lipid research. 1994 Apr; 35(4):620-4. doi: 10.1016/s0022-2275(20)41175-7. [PMID: 8006516]