Chalcomoracin (BioDeep_00000022132)

   

human metabolite Endogenous natural product


代谢物信息卡片


2-{6-[2,4-dihydroxy-3-(3-methylbut-2-en-1-yl)benzoyl]-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl}-5-(6-hydroxy-1-benzofuran-2-yl)benzene-1,3-diol

化学式: C39H36O9 (648.2359206)
中文名称:
谱图信息: 最多检出来源 Mentha canadensis(plant) 37.5%

分子结构信息

SMILES: CC(C)=CCC1=C(O)C(=CC=C1O)C(=O)C1C(CC(C)=CC1C1=C(O)C=C(C=C1O)C1=CC2=C(O1)C=C(O)C=C2)C1=C(O)C=C(O)C=C1
InChI: InChI=1S/C39H36O9/c1-19(2)4-8-26-30(42)11-10-27(38(26)46)39(47)36-28(25-9-7-23(40)17-31(25)43)12-20(3)13-29(36)37-32(44)14-22(15-33(37)45)34-16-21-5-6-24(41)18-35(21)48-34/h4-7,9-11,13-18,28-29,36,40-46H,8,12H2,1-3H3

描述信息

Chalcomoracin is found in fruits. Phytoalexin from diseased white mulberry (Morus alba

同义名列表

2 个代谢物同义名

2-{6-[2,4-dihydroxy-3-(3-methylbut-2-en-1-yl)benzoyl]-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl}-5-(6-hydroxy-1-benzofuran-2-yl)benzene-1,3-diol; CHALCOMORACIN



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)

39 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

  • Yang Liu, Xue Zhou, Dan Zhou, Yongxing Jian, Jingfu Jia, Fahuan Ge. Isolation of Chalcomoracin as a Potential α-Glycosidase Inhibitor from Mulberry Leaves and Its Binding Mechanism. Molecules (Basel, Switzerland). 2022 Sep; 27(18):. doi: 10.3390/molecules27185742. [PMID: 36144478]
  • Meng Wang, Li-Xin Gao, Jue Wang, Jing-Ya Li, Mei-Hua Yu, Jia Li, Ai-Jun Hou. Diels-Alder adducts with PTP1B inhibition from Morus notabilis. Phytochemistry. 2015 Jan; 109(?):140-6. doi: 10.1016/j.phytochem.2014.10.015. [PMID: 25457492]
  • Xiao-Yu Tao, De-Wu Zhang, Ri-Dao Chen, Yun-Ze Yin, Jian-Hua Zou, Dan Xie, Lin Yang, Chun-Mei Wang, Jun-Gui Dai. [Chemical constituents from cell cultures of Morus alba]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2012 Dec; 37(24):3738-42. doi: ". [PMID: 23627170]
  • Yu Jin Kim, Mi-Jin Sohn, Won-Gon Kim. Chalcomoracin and moracin C, new inhibitors of Staphylococcus aureus enoyl-acyl carrier protein reductase from Morus alba. Biological & pharmaceutical bulletin. 2012; 35(5):791-5. doi: 10.1248/bpb.35.791. [PMID: 22687419]
  • Xi-Da Gu, Ming-Yao Sun, Lin Zhang, Hong-Wei Fu, Lei Cui, Run-Ze Chen, Da-Wei Zhang, Jing-Kui Tian. UV-B induced changes in the secondary metabolites of Morus alba L. leaves. Molecules (Basel, Switzerland). 2010 Apr; 15(5):2980-93. doi: 10.3390/molecules15052980. [PMID: 20657460]
  • Yan Yang, Hong-Qing Wang, Ruo-Yun Chen. [Flavonoids from the leaves of Morus alba L]. Yao xue xue bao = Acta pharmaceutica Sinica. 2010 Jan; 45(1):77-81. doi: . [PMID: 21351454]
  • Qing-Jian Zhang, Yan-Bo Tang, Ruo-Yun Chen, De-Quan Yu. Three new cytotoxic Diels-Alder-type adducts from Morus australis. Chemistry & biodiversity. 2007 Jul; 4(7):1533-40. doi: 10.1002/cbdv.200790133. [PMID: 17638335]