Cajanin (BioDeep_00000007936)

 

Secondary id: BioDeep_00000270002, BioDeep_00000859710

human metabolite PANOMIX_OTCML-2023 Endogenous natural product


代谢物信息卡片


4H-1-Benzopyran-4-one, 3-(2,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-

化学式: C16H12O6 (300.06338519999997)
中文名称: 2,4,5-三羟基-7-甲氧基异黄酮, 2',4',5-三羟基-7-甲氧基异黄酮
谱图信息: 最多检出来源 Chinese Herbal Medicine(otcml) 12.5%

分子结构信息

SMILES: c1(cc(c2c(c1)occ(c2=O)c1c(cc(cc1)O)O)O)OC
InChI: InChI=1S/C16H12O6/c1-21-9-5-13(19)15-14(6-9)22-7-11(16(15)20)10-3-2-8(17)4-12(10)18/h2-7,17-19H,1H3

描述信息

Cajanin is a member of 7-methoxyisoflavones. It has a role as a metabolite.
Cajanin is a natural product found in Crotalaria lachnophora, Dalbergia parviflora, and other organisms with data available.
Isolated from Cajanus cajan (pigeon pea), Canavalia ensiformis (jack bean). Cajanin is found in pigeon pea, coffee and coffee products, and pulses.
Cajanin is found in coffee and coffee products. Cajanin is isolated from Cajanus cajan (pigeon pea), Canavalia ensiformis (jack bean
A natural product found in Crotalaria lachnophora.

同义名列表

14 个代谢物同义名

4H-1-Benzopyran-4-one, 3-(2,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-; 3-(2,4-DIHYDROXYPHENYL)-5-HYDROXY-7-METHOXY-4H-1-BENZOPYRAN-4-ONE; 3-(2,4-Dihydroxyphenyl)-5-hydroxy-7-methoxy-4H-chromen-4-one; 3-(2,4-Dihydroxy-phenyl)-5-hydroxy-7-methoxy-chromen-4-one; 3-(2,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-chromen-4-one; 3-(2,4-dihydroxyphenyl)-5-hydroxy-7-methoxychromen-4-one; Isoflavone, 2,,4,5-trihydroxy-7-methoxy-; 2,4,5-Trihydroxy-7-methoxyisoflavone; 5,2,4-Trihydroxy-7-methoxyisoflavone; ALFNTRJPGFNJQV-UHFFFAOYSA-N; UNII-F3QGE5M9QS; F3QGE5M9QS; Cajinin; Cajanin



数据库引用编号

20 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)

38 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

  • Ifedayo V Ogungbe, Gabrielle M Hill, Rebecca A Crouch, Bernhard Vogler, Meenakshi Nagarkoti, William A Haber, William N Setzer. Prenylated isoflavonoids from Rhynchosia edulis. Natural product communications. 2011 Nov; 6(11):1637-44. doi: . [PMID: 22224278]
  • 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]
  • Li-Wen Chen, Ming-Jen Cheng, Chien-Fang Peng, Ih-Sheng Chen. Secondary metabolites and antimycobacterial activities from the roots of Ficus nervosa. Chemistry & biodiversity. 2010 Jul; 7(7):1814-21. doi: 10.1002/cbdv.200900227. [PMID: 20658670]
  • Ss Sakat, Ar Juvekar. Comparative Study of Erythrina indica Lam. (Febaceae) Leaves Extracts for Antioxidant Activity. Journal of young pharmacists : JYP. 2010 Jan; 2(1):63-7. doi: 10.4103/0975-1483.62216. [PMID: 21331194]
  • Victor Kuete, Frédéric Nana, Bathélémy Ngameni, Armelle Tsafack Mbaveng, Félix Keumedjio, Bonaventure Tchaleu Ngadjui. Antimicrobial activity of the crude extract, fractions and compounds from stem bark of Ficus ovata (Moraceae). Journal of ethnopharmacology. 2009 Jul; 124(3):556-61. doi: 10.1016/j.jep.2009.05.003. [PMID: 19450673]
  • Rakesh Maurya, Dinesh K Yadav, Geetu Singh, Biju Bhargavan, P S Narayana Murthy, Mahendra Sahai, Man Mohan Singh. Osteogenic activity of constituents from Butea monosperma. Bioorganic & medicinal chemistry letters. 2009 Feb; 19(3):610-3. doi: 10.1016/j.bmcl.2008.12.064. [PMID: 19124244]
  • Nicole Darbour, Christine Bayet, Sylvie Rodin-Bercion, Zackariae Elkhomsi, Felix Lurel, Annie Chaboud, David Guilet. Isoflavones from Ficus nymphaefolia. Natural product research. 2007 May; 21(5):461-4. doi: 10.1080/14786410601086871. [PMID: 17487619]
  • Milena Maver, Emerson F Queiroz, Jean-Luc Wolfender, Kurt Hostettmann. Flavonoids from the stem of Eriophorum scheuchzeri. Journal of natural products. 2005 Jul; 68(7):1094-8. doi: 10.1021/np0580107. [PMID: 16038557]