6,7-dehydroroyleanone (BioDeep_00000257312)

   


代谢物信息卡片


6,7-dehydroroyleanone

化学式: C20H26O3 (314.1881846)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1CC([C@H]2[C@](C1)(C1=C(C=C2)C(=O)C(=C(C1=O)O)C(C)C)C)(C)C
InChI: InChI=1S/C20H26O3/c1-11(2)14-16(21)12-7-8-13-19(3,4)9-6-10-20(13,5)15(12)18(23)17(14)22/h7-8,11,13,21H,6,9-10H2,1-5H3/t13-,20-/m0/s1

描述信息

同义名列表

1 个代谢物同义名

6,7-dehydroroyleanone



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)

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

  • Mustafa Abdullah Yilmaz, Abdulselam Ertas, Ismail Yener, Ozge Tokul Olmez, Mehmet Firat, Hamdi Temel, Mehmet Ozturk, Ufuk Kolak. Development and Validation of a Novel LC-MS/MS Method for the Quantitation of 19 Fingerprint Phytochemicals in Salvia Species: A Chemometric Approach. Journal of chromatographic science. 2022 Oct; 60(8):770-785. doi: 10.1093/chromsci/bmab125. [PMID: 34725681]
  • Vanessa Pietrowski Baldin, Regiane Bertin de Lima Scodro, Mariana Aparecida Lopes-Ortiz, Aryadne Larissa de Almeida, Zilda Cristiani Gazim, Letícia Ferarrese, Viviane Dos Santos Faiões, Eduardo Caio Torres-Santos, Claudia Terencio Agostinho Pires, Katiany Rizzieri Caleffi-Ferracioli, Vera Lucia Dias Siqueira, Diógenes Aparício Garcia Cortez, Rosilene Fressatti Cardoso. Anti-Mycobacterium tuberculosis activity of essential oil and 6,7-dehydroroyleanone isolated from leaves of Tetradenia riparia (Hochst.) Codd (Lamiaceae). Phytomedicine : international journal of phytotherapy and phytopharmacology. 2018 Aug; 47(?):34-39. doi: 10.1016/j.phymed.2018.04.043. [PMID: 30166106]
  • Catarina Garcia, Catarina Oliveira Silva, Carlos M Monteiro, Marisa Nicolai, Ana Viana, Joana M Andrade, Isabel Barasoain, Tijana Stankovic, José Quintana, Inmaculada Hernández, Ignacio González, Francisco Estévez, Ana M Díaz-Lanza, Catarina P Reis, Carlos Am Afonso, Milica Pesic, Patrícia Rijo. Anticancer properties of the abietane diterpene 6,7-dehydroroyleanone obtained by optimized extraction. Future medicinal chemistry. 2018 05; 10(10):1177-1189. doi: 10.4155/fmc-2017-0239. [PMID: 29749759]
  • Izabel Galhardo Demarchi, Mateus Vailant Thomazella, Mariana de Souza Terron, Lilian Lopes, Zilda Cristiani Gazim, Diógenes Aparício Garcia Cortez, Lucélia Donatti, Sandra Mara Alessi Aristides, Thaís Gomes Verzignassi Silveira, Maria Valdrinez Campana Lonardoni. Antileishmanial activity of essential oil and 6,7-dehydroroyleanone isolated from Tetradenia riparia. Experimental parasitology. 2015 Oct; 157(?):128-37. doi: 10.1016/j.exppara.2015.06.014. [PMID: 26116864]
  • Shiyou Li, Ping Wang, Guangrui Deng, Wei Yuan, Zushang Su. Cytotoxic compounds from invasive giant salvinia (Salvinia molesta) against human tumor cells. Bioorganic & medicinal chemistry letters. 2013 Dec; 23(24):6682-7. doi: 10.1016/j.bmcl.2013.10.040. [PMID: 24210499]
  • Chih-Chun Wen, Yueh-Hsiung Kuo, Jia-Tsrong Jan, Po-Huang Liang, Sheng-Yang Wang, Hong-Gi Liu, Ching-Kuo Lee, Shang-Tzen Chang, Chih-Jung Kuo, Shoei-Sheng Lee, Chia-Chung Hou, Pei-Wen Hsiao, Shih-Chang Chien, Lie-Fen Shyur, Ning-Sun Yang. Specific plant terpenoids and lignoids possess potent antiviral activities against severe acute respiratory syndrome coronavirus. Journal of medicinal chemistry. 2007 Aug; 50(17):4087-95. doi: 10.1021/jm070295s. [PMID: 17663539]
  • Ayhan Ulubelen, Hüsniye Birman, Sevil Oksüz, Gülaçti Topçu, Ufuk Kolak, Asli Barla, Wolfgang Voelter. Cardioactive diterpenes from the roots of Salvia eriophora. Planta medica. 2002 Sep; 68(9):818-21. doi: 10.1055/s-2002-34408. [PMID: 12357394]