Urothion (BioDeep_00000023279)

   

human metabolite Endogenous


代谢物信息卡片


1-[4-Hydroxy-2-imino-6-(methylsulphanyl)-1H,2H-thieno[3,2-g]pteridin-7-yl]ethane-1,2-diol

化学式: C11H11N5O3S2 (325.0303296)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CSC1=C(SC2=C1N=C1C(=O)N=C(N)NC1=N2)C(O)CO
InChI: InChI=1S/C11H11N5O3S2/c1-20-7-4-10(21-6(7)3(18)2-17)14-8-5(13-4)9(19)16-11(12)15-8/h3,17-18H,2H2,1H3,(H3,12,14,15,16,19)

描述信息

Urothion is a normal molybdenum cofactor metabolite, a yellowish sulfur-containing pteridine derivative isolated from human urine. It is optically active with one chiral center (PMID: 8690716). Urothion is deficient in patients with molybdenum cofactor deficiency (PMID: 6960353) [HMDB]
Urothion is a normal molybdenum cofactor metabolite, a yellowish sulfur-containing pteridine derivative isolated from human urine. It is optically active with one chiral center (PMID: 8690716). Urothion is deficient in patients with molybdenum cofactor deficiency (PMID: 6960353).

同义名列表

7 个代谢物同义名

1-[4-Hydroxy-2-imino-6-(methylsulphanyl)-1H,2H-thieno[3,2-g]pteridin-7-yl]ethane-1,2-diol; (R)-(8CI)-2-amino-7-(1,2-dihydroxyethyl)-6-(methylthio)-thieno[3,2-g]pteridin-4(1H)-one; 2-amino-7-(1,2-dihydroxyethyl)-6-(methylsulfanyl)-1H,4H-thieno[3,2-g]pteridin-4-one; 2-amino-7-(1,2-dihydroxyethyl)-6-(methylsulfanyl)-1H-thieno[3,2-g]pteridin-4-one; 2-amino-7-(1,2-Dihydroxyethyl)-6-(methylthio)thieno(3,2-g)pteridin-4(3H)one; Urothione; Urothion



数据库引用编号

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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。

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1 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。

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文献列表

  • A Sakurai, H Horibe, N Kuboyama, Y Hashimoto, Y Okumura. Determination of the absolute configuration of urothion. Journal of biochemistry. 1995 Sep; 118(3):552-4. doi: 10.1093/oxfordjournals.jbchem.a124944. [PMID: 8690716]
  • M Volk, O Meyer, K Frunzke. Metabolic relationship between the CO dehydrogenase molybdenum cofactor and the excretion of urothione by Hydrogenophaga pseudoflava. European journal of biochemistry. 1994 Nov; 225(3):1063-71. doi: 10.1111/j.1432-1033.1994.1063b.x. [PMID: 7957196]
  • R G Boles, L R Ment, M S Meyn, A L Horwich, L E Kratz, P Rinaldo. Short-term response to dietary therapy in molybdenum cofactor deficiency. Annals of neurology. 1993 Nov; 34(5):742-4. doi: 10.1002/ana.410340520. [PMID: 7694543]
  • J L Johnson, K V Rajagopalan, S K Wadman. Human molybdenum cofactor deficiency. Advances in experimental medicine and biology. 1993; 338(?):373-8. doi: 10.1007/978-1-4615-2960-6_77. [PMID: 8304141]
  • F J Bamforth, J L Johnson, A G Davidson, L T Wong, G Lockitch, D A Applegarth. Biochemical investigation of a child with molybdenum cofactor deficiency. Clinical biochemistry. 1990 Dec; 23(6):537-42. doi: 10.1016/0009-9120(90)80046-l. [PMID: 2289312]
  • R A Roesel, F Bowyer, P R Blankenship, F A Hommes. Combined xanthine and sulphite oxidase defect due to a deficiency of molybdenum cofactor. Journal of inherited metabolic disease. 1986; 9(4):343-7. doi: 10.1007/bf01800483. [PMID: 3104671]
  • J L Johnson, K V Rajagopalan. Structural and metabolic relationship between the molybdenum cofactor and urothione. Proceedings of the National Academy of Sciences of the United States of America. 1982 Nov; 79(22):6856-60. doi: 10.1073/pnas.79.22.6856. [PMID: 6960353]