Xanthoxylin (BioDeep_00000230839)

 

Secondary id: BioDeep_00000003896, BioDeep_00000863679

human metabolite PANOMIX_OTCML-2023 Endogenous


代谢物信息卡片


2 inverted exclamation mark -Hydroxy-4 inverted exclamation mark ,6 inverted exclamation mark -dimethoxyacetophenone

化学式: C10H12O4 (196.0735552)
中文名称: 2-羟基-4,6-二甲氧基苯乙酮, 花椒油素, 花椒素, 4',6-二甲基-2-羟基苯乙酮
谱图信息: 最多检出来源 Chinese Herbal Medicine(otcml) 16.67%

分子结构信息

SMILES: c1(cc(cc(c1C(=O)C)O)OC)OC
InChI: InChI=1S/C10H12O4/c1-6(11)10-8(12)4-7(13-2)5-9(10)14-3/h4-5,12H,1-3H3

描述信息

obtained from Zanthoxylum piperitum (Japanese pepper tree) and Sapium sebiferum (Chinese tallowtree). Xanthoxylin is found in many foods, some of which are herbs and spices, german camomile, fats and oils, and pomegranate.
Xanthoxylin is a carboxylic ester. It is functionally related to a phloroglucinol.
Xanthoxylin is a natural product found in Euphorbia portulacoides, Pulicaria incisa, and other organisms with data available.
Xanthoxylin is found in fats and oils. Xanthoxylin is obtained from Zanthoxylum piperitum (Japanese pepper tree) and Sapium sebiferum (Chinese tallowtree
Xanthoxylin (Xanthoxyline) is isolated from Zanthoxylum simulans. Xanthoxylin (Xanthoxyline) has antifungal and antispasmodic activities[1][2].
Xanthoxylin (Xanthoxyline) is isolated from Zanthoxylum simulans. Xanthoxylin (Xanthoxyline) has antifungal and antispasmodic activities[1][2].

同义名列表

52 个代谢物同义名

2 inverted exclamation mark -Hydroxy-4 inverted exclamation mark ,6 inverted exclamation mark -dimethoxyacetophenone; Ethanone, 1-(2-hydroxy-4,6-dimethoxyphenyl)-; Acetophenone, 2-hydroxy-4,6-dimethoxy- (8CI); 1-(2-Hydroxy-4,6-dimethoxyphenyl)ethan-1-one; 1-(2-Hydroxy-4,6-dimethoxyphenyl)ethanone #; Ethanone,1-(2-hydroxy-4,6-dimethoxyphenyl)-; 1-(2-hydroxy-4,6-dimethoxyphenyl)-ethanone; 1-(2-hydroxy-4,6-dimethoxy-phenyl)ethanone; (2-hydroxy-4,6-dimethoxy-phenyl)-ethanone; 2-Hydroxy-4,6-dimethoxyacetophenone, 97\\%; 1-(2-Hydroxy-4,6-dimethoxyphenyl)ethanone; 1-(2-Hydroxy-4,6-dimethylphenyl)-ethanone; 1-Acetyl-2-hydroxy-4,6-dimethoxybenzene; Acetophenone, 2-hydroxy-4,6-dimethoxy-; 2-Hydroxyl-4,6-dimethoxy-acetophenone; Phloroacetophenone 2,4-dimethyl ether; 2-Hydroxy-4,6-dimethoxy-Acetophenone; 2-Hydroxy-4, 6-dimethoxyacetophenone; 4, 6-Dimethoxy-2-hydroxyacetophenone; 4,6-dimethoxy-2-hydroxyacetophenone; 4,6-Dimethoxy-2-hydroxyacetophenone; 2-hydroxy-4,6-dimethoxyacetophenone; 2,4-DIMETHOXY-6-HYDROXYACETOPHENONE; 2-Hydroxy-4,6-dimethoxyacetophenone; 2-hyroxy-4,6-dimethoxyacetophenone; 2,4-Di-O-methylphloroacetophenone; PHLOROACETOPHENONE DIMETHYL ETHER; Phloracetophenone dimethyl ether; 2-Acetyl-3,5-dimethoxyphenol; Acetophenone,6-dimethoxy-; Brevifolin (Zanthoxylum); XANTHOXYLINE [WHO-DD]; Acetophenone der.; XANTHOXYLIN [MI]; Spectrum2_000463; Spectrum5_000237; Spectrum4_001499; Brevifolin (VAN); 6-Methoxypaeonol; Spectrum3_000181; UNII-Z8RSY5TZPA; DivK1c_006809; KBio3_001201; Xanthoxyline; KBio1_001753; KBio2_003625; KBio2_001057; KBio2_006193; Xanthoxylin; brevifolin; Z8RSY5TZPA; AI3-26010



数据库引用编号

17 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)

68 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

  • Carmen Rossini, Lucía Almeida, Daniela Arredondo, Karina Antúnez, Estela Santos, Alejandra Rodríguez Haralambides, Ciro Invernizzi. When a Tritrophic Interaction Goes Wrong to the Third Level: Xanthoxylin From Trees Causes the Honeybee Larval Mortality in Colonies Affected by the River Disease. Journal of chemical ecology. 2021 Sep; 47(8-9):777-787. doi: 10.1007/s10886-021-01296-5. [PMID: 34287796]
  • Chun-Ling Zhu. [Chemical constituents of n-BuOH extract from Phyllanthus matsumurae]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2014 Apr; 37(4):608-10. doi: . [PMID: 25345134]
  • Congzhou Wang, Jianhua Wang, Linhong Deng. Evaluating interaction forces between BSA and rabbit anti-BSA in sulphathiazole sodium, tylosin and levofloxacin solution by AFM. Nanoscale research letters. 2011 Nov; 6(1):579. doi: 10.1186/1556-276x-6-579. [PMID: 22053876]
  • Wenjuan Feng, Yang Fa Ou, Yalun Su, Jin Li, Tengfei Ji. [Chemical constituents of Ammopiptanthus mongolicus]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2011 Apr; 36(8):1040-2. doi: . [PMID: 21809581]
  • Ying Tian, Limin Sun, Xiqiao Liu, Junxing Dong. [Phenols from Euphorbia humifusa]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2010 Mar; 35(5):613-5. doi: 10.4268/cjcmm20100516. [PMID: 20506823]
  • Joo Hyuk Yim, Ok-Hwan Lee, Ung-Kyu Choi, Young-Chan Kim. Antinociceptive and anti-inflammatory effects of ethanolic extracts of Glycine max (L.) Merr and Rhynchosia nulubilis seeds. International journal of molecular sciences. 2009 Nov; 10(11):4742-4753. doi: 10.3390/ijms10114742. [PMID: 20087462]
  • Hua Du, Ye Wang, Xiaojiang Hao, Chun Li, Youliang Peng, Jihua Wang, Hao Liu, Ligang Zhou. Antimicrobial phenolic compounds from Anabasis aphylla L. Natural product communications. 2009 Mar; 4(3):385-8. doi: . [PMID: 19413118]
  • Xiao-lan Wang, Kai-bei Yu, Shu-lin Peng. [Chemical constituents of aerial part of Acalypha australis]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2008 Jun; 33(12):1415-7. doi: . [PMID: 18837345]
  • Xiao-Feng Niu, Lang-Chong He, Te Fan, Yan Li. [Protecting effect of brevifolin and 8,9-single-epoxy brevifolin of Phyllanthus simplex on rat liver injury]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2006 Sep; 31(18):1529-32. doi: . [PMID: 17144473]
  • Xin-Hong Shi, Xiao-Li Du, Ling-Yi Kong. [Studies on chemical constituents in roots of Euphorbia soongarica]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2006 Sep; 31(18):1503-6. doi: . [PMID: 17144466]
  • Henrik Toft Simonsen, Anne Adsersen, Paul Bremner, Michael Heinrich, Ulla Wagner Smitt, Jerzy W Jaroszewski. Antifungal constituents of Melicope borbonica. Phytotherapy research : PTR. 2004 Jul; 18(7):542-5. doi: 10.1002/ptr.1482. [PMID: 15305313]
  • César A N Catalán, Carola S de Heluani, Claudia Kotowicz, Thomas E Gedris, Werner Herz. A linear sesterterpene, two squalene derivatives and two peptide derivatives from Croton hieronymi. Phytochemistry. 2003 Sep; 64(2):625-9. doi: 10.1016/s0031-9422(03)00202-4. [PMID: 12943786]
  • Hongpeng Luo, Lirong Chen, Zhengquan Li, Zhensheng Ding, Xiaojie Xu. Frontal immunoaffinity chromatography with mass spectrometric detection: a method for finding active compounds from traditional Chinese herbs. Analytical chemistry. 2003 Aug; 75(16):3994-8. doi: 10.1021/ac034190i. [PMID: 14632110]
  • Wellington de A Gonzaga, Andréia D Weber, Sandro R Giacomelli, Ionara I Dalcol, Solange C S Hoelzel, Ademir F Morel. Antibacterial alkaloids from Zanthoxylum rhoifolium. Planta medica. 2003 Apr; 69(4):371-4. doi: 10.1055/s-2003-38882. [PMID: 12709908]
  • I Fecka, A Kowalczyk, W Cisowski. Phenolic acids and depsides from some species of the Erodium genera. Zeitschrift fur Naturforschung. C, Journal of biosciences. 2001 Nov; 56(11-12):943-50. doi: 10.1515/znc-2001-11-1205. [PMID: 11837680]
  • C Tringali, C Spatafora, V Calì, M S Simmonds. Antifeedant constituents from Fagara macrophylla. Fitoterapia. 2001 Jun; 72(5):538-43. doi: 10.1016/s0367-326x(01)00265-9. [PMID: 11429249]
  • V Cechinel Filho, E O Lima, V M Morais, S T Gomes, O G Miguel, R A Yunes. Fungicide and fungiostatic effects of xanthoxyline. Journal of ethnopharmacology. 1996 Sep; 53(3):171-3. doi: 10.1016/0378-8741(96)01436-5. [PMID: 8887025]