D-Ribofuranose (BioDeep_00001868469)

Main id: BioDeep_00000004143

 

PANOMIX_OTCML-2023


代谢物信息卡片


D-Ribofuranose

化学式: C5H10O5 (150.052821)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C(C1C(C(C(O1)O)O)O)O
InChI: InChI=1S/C5H10O5/c6-1-2-3(7)4(8)5(9)10-2/h2-9H,1H2/t2-,3-,4-,5?/m1/s1

描述信息

A ribofuranose having D-configuration.
D-Ribose(mixture of isomers) is an energy enhancer, and acts as a sugar moiety of ATP, and widely used as a metabolic therapy supplement for chronic fatigue syndrome or cardiac energy metabolism. D-Ribose(mixture of isomers) is active in protein glycation, induces NF-κB inflammation in a RAGE-dependent manner[1].
D-Ribose(mixture of isomers) is an energy enhancer, and acts as a sugar moiety of ATP, and widely used as a metabolic therapy supplement for chronic fatigue syndrome or cardiac energy metabolism. D-Ribose(mixture of isomers) is active in protein glycation, induces NF-κB inflammation in a RAGE-dependent manner[1].
D-Ribose(mixture of isomers) is an energy enhancer, and acts as a sugar moiety of ATP, and widely used as a metabolic therapy supplement for chronic fatigue syndrome or cardiac energy metabolism. D-Ribose(mixture of isomers) is active in protein glycation, induces NF-κB inflammation in a RAGE-dependent manner[1].

同义名列表

2 个代谢物同义名

D-Ribofuranose; D-Ribose(mixture of isomers)



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(3)

BioCyc(6)

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)

2 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

  • Biswas Gopa, Jagatkumar Bhatt, Kovur G Hemavathi. A comparative clinical study of hypolipidemic efficacy of Amla (Emblica officinalis) with 3-hydroxy-3-methylglutaryl-coenzyme-A reductase inhibitor simvastatin. Indian journal of pharmacology. 2012 Mar; 44(2):238-42. doi: 10.4103/0253-7613.93857. [PMID: 22529483]
  • Hong Zhu, Yunbo Li. NAD(P)H: quinone oxidoreductase 1 and its potential protective role in cardiovascular diseases and related conditions. Cardiovascular toxicology. 2012 Mar; 12(1):39-45. doi: 10.1007/s12012-011-9136-9. [PMID: 21818552]
  • J Vasantha, P Soundararajan, N Vanitharani, G Kannan, P Thennarasu, G Neenu, C Umamaheswara Reddy. Safety and efficacy of nicotinamide in the management of hyperphosphatemia in patients on hemodialysis. Indian journal of nephrology. 2011 Oct; 21(4):245-9. doi: 10.4103/0971-4065.83735. [PMID: 22022084]
  • Elena Synesiou, Lynnette D Fairbanks, H Anne Simmonds, Ewa M Slominska, Ryszard T Smolenski, Elizabeth A Carrey. 4-Pyridone-3-carboxamide-1-β-D-ribonucleoside triphosphate (4PyTP), a novel NAD metabolite accumulating in erythrocytes of uremic children: a biomarker for a toxic NAD analogue in other tissues?. Toxins. 2011 06; 3(6):520-37. doi: 10.3390/toxins3060520. [PMID: 22069723]
  • Huawen Lin, Alan L Kwan, Susan K Dutcher. Synthesizing and salvaging NAD: lessons learned from Chlamydomonas reinhardtii. PLoS genetics. 2010 Sep; 6(9):e1001105. doi: 10.1371/journal.pgen.1001105. [PMID: 20838591]
  • Riko Katahira, Hiroshi Ashihara. Profiles of the biosynthesis and metabolism of pyridine nucleotides in potatoes (Solanum tuberosum L.). Planta. 2009 Dec; 231(1):35-45. doi: 10.1007/s00425-009-1023-2. [PMID: 19820966]
  • Kentaro Ohyama, Hidefumi Shinohara, Mari Ogawa-Ohnishi, Yoshikatsu Matsubayashi. A glycopeptide regulating stem cell fate in Arabidopsis thaliana. Nature chemical biology. 2009 Aug; 5(8):578-80. doi: 10.1038/nchembio.182. [PMID: 19525968]
  • P Vyskocilová, P Hornik, D Friedecký, P Frycák, K Lemr, T Adam. Synthesis and mass spectrometric fragmentation characteristics of imidazole ribosides-analogs of intermediates of purine de novo synthetic pathway. Nucleosides, nucleotides & nucleic acids. 2006; 25(9-11):1237-40. doi: 10.1080/15257770600894691. [PMID: 17065098]
  • William L Nyhan. Disorders of purine and pyrimidine metabolism. Molecular genetics and metabolism. 2005 Sep; 86(1-2):25-33. doi: 10.1016/j.ymgme.2005.07.027. [PMID: 16176880]
  • Xiaojun Wang, Rose Wang, Thomas A Nemcek, Ning Cao, Jeffrey Y Pan, Ernst U Frevert. A self-contained 48-well fatty acid oxidation assay. Assay and drug development technologies. 2004 Feb; 2(1):63-9. doi: 10.1089/154065804322966324. [PMID: 15090211]
  • Christian Andersen, Elke Maier, Gabrielle Kemmer, Julia Blass, Anna-Karina Hilpert, Roland Benz, Joachim Reidl. Porin OmpP2 of Haemophilus influenzae shows specificity for nicotinamide-derived nucleotide substrates. The Journal of biological chemistry. 2003 Jul; 278(27):24269-76. doi: 10.1074/jbc.m213087200. [PMID: 12695515]
  • J Schmidt-Brauns, M Herbert, G Kemmer, A Kraiss, S Schlör, J Reidl. Is a NAD pyrophosphatase activity necessary for Haemophilus influenzae type b multiplication in the blood stream?. International journal of medical microbiology : IJMM. 2001 Aug; 291(3):219-25. doi: 10.1078/1438-4221-00122. [PMID: 11554562]