p-aminophenyl α-D-mannoside (BioDeep_00000671810)

   


代谢物信息卡片


4-Aminophenyl alpha-D-mannopyranoside

化学式: C12H17NO6 (271.1055822)
中文名称: 4-氨基苯基 α-D-吡喃甘露糖苷
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1=CC(=CC=C1N)OC2C(C(C(C(O2)CO)O)O)O
InChI: InChI=1S/C12H17NO6/c13-6-1-3-7(4-2-6)18-12-11(17)10(16)9(15)8(5-14)19-12/h1-4,8-12,14-17H,5,13H2/t8-,9-,10+,11+,12+/m1/s1

描述信息

同义名列表

2 个代谢物同义名

4-Aminophenyl alpha-D-mannopyranoside; p-aminophenyl α-D-mannoside



数据库引用编号

4 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

  • Chaoyang Lai, Cong Li, Xiang Luo, Mengyang Liu, Xinrong Liu, Ling Hu, Le Kang, Qiujun Qiu, Yihui Deng, Yanzhi Song. Use of Dual-Ligand Modification in Kupffer Cell-Targeted Liposomes To Examine the Contribution of Kupffer Cells to Accelerated Blood Clearance Phenomenon. Molecular pharmaceutics. 2018 07; 15(7):2548-2558. doi: 10.1021/acs.molpharmaceut.8b00042. [PMID: 29768009]
  • Indu Singh, Rajan Swami, Manish Kumar Jeengar, Wahid Khan, Ramakrishna Sistla. p-Aminophenyl-α-D-mannopyranoside engineered lipidic nanoparticles for effective delivery of docetaxel to brain. Chemistry and physics of lipids. 2015 May; 188(?):1-9. doi: 10.1016/j.chemphyslip.2015.03.003. [PMID: 25819559]
  • Shin-Yi Yang, Ying-Jung Chen, Pei-Hsiu Kao, Long-Sen Chang. Bovine serum albumin with glycated carboxyl groups shows membrane-perturbing activities. Archives of biochemistry and biophysics. 2014 Dec; 564(?):43-51. doi: 10.1016/j.abb.2014.10.001. [PMID: 25449061]
  • Xue Ying, He Wen, Hong-Juan Yao, Yan Zhang, Wei Tian, Liang Zhang, Rui-Jun Ju, Xiao-Xing Wang, Yang Yu, Wan-Liang Lu. Pharmacokinetics and tissue distribution of dual-targeting daunorubicin liposomes in mice. Pharmacology. 2011; 87(1-2):105-14. doi: 10.1159/000323222. [PMID: 21282968]
  • Ciara Kelly, Caroline Jefferies, Sally-Ann Cryan. Targeted liposomal drug delivery to monocytes and macrophages. Journal of drug delivery. 2011; 2011(?):727241. doi: 10.1155/2011/727241. [PMID: 21512579]
  • Sofie Tanghe, A Van Soom, L Duchateau, A De Kruif. Inhibition of bovine sperm-oocyte fusion by the p-aminophenyl derivative of D-mannose. Molecular reproduction and development. 2004 Feb; 67(2):224-32. doi: 10.1002/mrd.10387. [PMID: 14694439]
  • M Triggiani, F Granata, A Oriente, V De Marino, M Gentile, C Calabrese, C Palumbo, G Marone. Secretory phospholipases A2 induce beta-glucuronidase release and IL-6 production from human lung macrophages. Journal of immunology (Baltimore, Md. : 1950). 2000 May; 164(9):4908-15. doi: 10.4049/jimmunol.164.9.4908. [PMID: 10779801]
  • K Shimura, K Kasai. Capillary affinophoresis of pea lectin with polyliganded affinophores: a model study of divalent-polyvalent interactions. Electrophoresis. 1998 Mar; 19(3):397-402. doi: 10.1002/elps.1150190306. [PMID: 9551791]
  • K Shimura, K Kasai. Determination of the affinity constants of pea lectin for neutral sugars by capillary affinophoresis with a monoligand affinophore. Journal of biochemistry. 1996 Dec; 120(6):1146-52. doi: 10.1093/oxfordjournals.jbchem.a021534. [PMID: 9010763]
  • G Molema, R W Jansen, R Pauwels, E de Clercq, D K Meijer. Targeting of antiviral drugs to T4-lymphocytes. Anti-HIV activity of neoglycoprotein-AZTMP conjugates in vitro. Biochemical pharmacology. 1990 Dec; 40(12):2603-10. doi: 10.1016/0006-2952(90)90577-8. [PMID: 1979734]
  • K Shimura, K Kasai. Affinophoresis of pea lectin and fava bean lectin with an anionic affinophore, bearing rho-aminophenyl-alpha-D-mannoside as an affinity ligand. Journal of chromatography. 1987 Jul; 400(?):353-9. doi: 10.1016/s0021-9673(01)81630-7. [PMID: 3667759]