3-O-METHYLOROBOL (BioDeep_00000396365)

Main id: BioDeep_00000267688

 

PANOMIX_OTCML-2023


代谢物信息卡片


5,7-dihydroxy-3-(4-hydroxy-3-methoxyphenyl)chromen-4-one

化学式: C16H12O6 (300.06338519999997)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1(O)=CC2OC=C(C3C=CC(O)=C(OC)C=3)C(=O)C=2C(O)=C1
InChI: InChI=1S/C16H12O6/c1-21-13-4-8(2-3-11(13)18)10-7-22-14-6-9(17)5-12(19)15(14)16(10)20/h2-7,17-19H,1H3

描述信息

3-O-methylorobol is a hydroxyisoflavone that is orobol in which the hydroxy group at position 3 has been replaced by a methoxy group. It has been isolated from Crotalaria lachnophora. It has a role as a plant metabolite. It is a methoxyisoflavone and a hydroxyisoflavone. It is functionally related to an orobol.
3-O-Methylorobol is a natural product found in Dalbergia sissoo, Crotalaria lachnophora, and other organisms with data available.
A hydroxyisoflavone that is orobol in which the hydroxy group at position 3 has been replaced by a methoxy group. It has been isolated from Crotalaria lachnophora.

同义名列表

5 个代谢物同义名

5,7-dihydroxy-3-(4-hydroxy-3-methoxyphenyl)chromen-4-one; 5,7,4-trihydroxy-3-methoxyisoflavone; Orobol-3-methyl ether; 3-O-METHYLOROBOL; 3-O-Methylorobol



数据库引用编号

8 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)

16 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

  • Ran Wen, Haining Lv, Yong Jiang, Pengfei Tu. Anti-inflammatory isoflavones and isoflavanones from the roots of Pongamia pinnata (L.) Pierre. Bioorganic & medicinal chemistry letters. 2018 04; 28(6):1050-1055. doi: 10.1016/j.bmcl.2018.02.026. [PMID: 29482940]
  • Yang Hee Jo, Seon Beom Kim, Qing Liu, Jin Woo Lee, Bang Yeon Hwang, Mi Kyeong Lee. Benzylated and prenylated flavonoids from the root barks of Cudrania tricuspidata with pancreatic lipase inhibitory activity. Bioorganic & medicinal chemistry letters. 2015 Sep; 25(17):3455-7. doi: 10.1016/j.bmcl.2015.07.017. [PMID: 26227773]
  • Maurice Ducret Awouafack, Peter Spiteller, Marc Lamshöft, Souvik Kusari, Bojidarka Ivanova, Pierre Tane, Michael Spiteller. Antimicrobial isopropenyl-dihydrofuranoisoflavones from Crotalaria lachnophora. Journal of natural products. 2011 Feb; 74(2):272-8. doi: 10.1021/np1005218. [PMID: 21265557]
  • Mi Kyeong Lee, Na Ry Ha, Hyekyung Yang, Sang Hyun Sung, Young Choong Kim. Stimulatory constituents of Eclipta prostrata on mouse osteoblast differentiation. Phytotherapy research : PTR. 2009 Jan; 23(1):129-31. doi: 10.1002/ptr.2560. [PMID: 18683850]
  • Hisashi Matsuda, Kazutoshi Yoshida, Katsutoshi Miyagawa, Yasunobu Asao, Saya Takayama, Souichi Nakashima, Fengming Xu, Masayuki Yoshikawa. Rotenoids and flavonoids with anti-invasion of HT1080, anti-proliferation of U937, and differentiation-inducing activity in HL-60 from Erycibe expansa. Bioorganic & medicinal chemistry. 2007 Feb; 15(3):1539-46. doi: 10.1016/j.bmc.2006.09.024. [PMID: 17158054]
  • Hisashi Matsuda, Toshio Morikawa, Fengming Xu, Kiyofumi Ninomiya, Masayuki Yoshikawa. New isoflavones and pterocarpane with hepatoprotective activity from the stems of Erycibe expansa. Planta medica. 2004 Dec; 70(12):1201-9. doi: 10.1055/s-2004-835852. [PMID: 15643558]
  • Toshio Fukai, Makiko Yonekawa, Ai-Jun Hou, Taro Nomura, Han-Dong Sun, Jun Uno. Antifungal agents from the roots of Cudrania cochinchinensis against Candida, Cryptococcus, and Aspergillus species. Journal of natural products. 2003 Aug; 66(8):1118-20. doi: 10.1021/np030024u. [PMID: 12932139]