Spongothymidine (BioDeep_00000399621)

Main id: BioDeep_00000003091

 

natural product Volatile Flavor Compounds


代谢物信息卡片


Thymine-beta-D-arabinofuranoside

化学式: C10H14N2O6 (258.0851824)
中文名称: 阿糖胸苷
谱图信息: 最多检出来源 Homo sapiens(natural_products) 96.43%

分子结构信息

SMILES: CC1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O
InChI: InChI=1S/C10H14N2O6/c1-4-2-12(10(17)11-8(4)16)9-7(15)6(14)5(3-13)18-9/h2,5-7,9,13-15H,3H2,1H3,(H,11,16,17)/t5-,6-,7+,9-/m1/s1

描述信息

D000890 - Anti-Infective Agents > D000998 - Antiviral Agents

同义名列表

3 个代谢物同义名

Thymine-beta-D-arabinofuranoside; Spongothymidine; Spongothymidine



数据库引用编号

9 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)

0 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

  • R Sienaert, G Andrei, R Snoeck, E De Clercq, C McGuigan, J Balzarini. Inactivity of the bicyclic pyrimidine nucleoside analogues against simian varicella virus (SVV) does not correlate with their substrate activity for SVV-encoded thymidine kinase. Biochemical and biophysical research communications. 2004 Mar; 315(4):877-83. doi: 10.1016/j.bbrc.2004.01.136. [PMID: 14985094]
  • Donald F Smee, Robert W Sidwell. Anti-cowpox virus activities of certain adenosine analogs, arabinofuranosyl nucleosides, and 2'-fluoro-arabinofuranosyl nucleosides. Nucleosides, nucleotides & nucleic acids. 2004; 23(1-2):375-83. doi: 10.1081/ncn-120028334. [PMID: 15043161]
  • Xinyu Zheng, Mathias Lundberg, Anna Karlsson, Magnus Johansson. Lipid-mediated protein delivery of suicide nucleoside kinases. Cancer research. 2003 Oct; 63(20):6909-13. doi: . [PMID: 14583490]
  • G A Gentry, N Lawrence, W Lushbaugh. Isolation and differentiation of herpes simplex virus and Trichomonas vaginalis in cell culture. Journal of clinical microbiology. 1985 Aug; 22(2):199-204. doi: 10.1128/jcm.22.2.199-204.1985. [PMID: 2993349]
  • J Reefschläger, G Herrmann, D Bärwolff, B Schwarz, D Cech, P Langen. Antiherpes activity of (E)-5-(2-bromovinyl)- and 5-vinyl-1-beta-D-arabinofuranosyluracil and some other 5-substituted uracil arabinosyl nucleosides in two different cell lines. Antiviral research. 1983 Sep; 3(3):175-87. doi: 10.1016/0166-3542(83)90024-4. [PMID: 6316849]
  • H Machida, S Sakata, M Morozumi, T Kiyanagi, A Kuninaka, H Yoshino. Comparison of the in vitro and in vivo anti-herpes activities of 1-beta-D-arabinofuranosylthymine and its 5'-monophosphate. Antiviral research. 1982 Sep; 2(4):217-26. doi: 10.1016/0166-3542(82)90044-4. [PMID: 6293376]
  • E De Clercq, J Descamps, P De Somer, P J Barr, A S Jones, R T Walker. (E)-5-(2-Bromovinyl)-2'-deoxyuridine: a potent and selective anti-herpes agent. Proceedings of the National Academy of Sciences of the United States of America. 1979 Jun; 76(6):2947-51. doi: 10.1073/pnas.76.6.2947. [PMID: 223163]
  • D Falke, H Moser, D Link, W E Müller. The effects of alpha- and beta-D-arabinosyladenosine and beta-D-arabinosylthymine on the synthesis of HSV types 1- and 2-infected cells. Advances in ophthalmology = Fortschritte der Augenheilkunde = Progres en ophtalmologie. 1979; 38(?):197-203. doi: NULL. [PMID: 230716]