Derrone (BioDeep_00000269633)

   

PANOMIX_OTCML-2023 natural product


代谢物信息卡片


3- (4-Hydroxyphenyl) -5-hydroxy-8,8-dimethyl-4H,8H-benzo [ 1,2-b:3,4-b ] dipyran-4-one

化学式: C20H16O5 (336.0997686)
中文名称: DERRONE
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: c(c14)(OC=C(C4=O)c(c3)ccc(O)c3)c(C=2)c(OC(C2)(C)C)cc1O
InChI: InChI=1S/C20H16O5/c1-20(2)8-7-13-16(25-20)9-15(22)17-18(23)14(10-24-19(13)17)11-3-5-12(21)6-4-11/h3-10,21-22H,1-2H3

描述信息

Derrone is a natural product found in Erythrina senegalensis, Ficus nymphaeifolia, and other organisms with data available.

同义名列表

5 个代谢物同义名

5-Hydroxy-3-(4-hydroxyphenyl)-8,8-dimethyl-4H,8H-pyrano[2,3-f]chromen-4-one; 5-hydroxy-3-(4-hydroxyphenyl)-8,8-dimethyl-pyrano[2,3-h]chromen-4-one; 5-hydroxy-3-(4-hydroxyphenyl)-8,8-dimethylpyrano[2,3-h]chromen-4-one; Derrone; 3- (4-Hydroxyphenyl) -5-hydroxy-8,8-dimethyl-4H,8H-benzo [ 1,2-b:3,4-b ] dipyran-4-one



数据库引用编号

12 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)

31 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

  • Myung-Ji Kang, Soo-Yeon Kim, Eun-Bin Kwon, Yang Hee Jo, Mi Kyeong Lee, Hyun-Sun Lee, Dong-Oh Moon, Mun-Ock Kim. Derrone induces autophagic cell death through induction of ROS and ERK in A549 cells. PloS one. 2019; 14(6):e0218659. doi: 10.1371/journal.pone.0218659. [PMID: 31216334]
  • Yi Kuang, Yan Lin, Kai Li, Wei Song, Shuai Ji, Xue Qiao, Qingying Zhang, Min Ye. Screening of hepatoprotective compounds from licorice against carbon tetrachloride and acetaminophen induced HepG2 cells injury. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2017 Oct; 34(?):59-66. doi: 10.1016/j.phymed.2017.08.005. [PMID: 28899510]
  • Binh Thi Dieu Trinh, Anna K Jäger, Dan Staerk. High-Resolution Inhibition Profiling Combined with HPLC-HRMS-SPE-NMR for Identification of PTP1B Inhibitors from Vietnamese Plants. Molecules (Basel, Switzerland). 2017 Jul; 22(7):. doi: 10.3390/molecules22071228. [PMID: 28726759]
  • Kai Li, Shuai Ji, Wei Song, Yi Kuang, Yan Lin, Shunan Tang, Zexu Cui, Xue Qiao, Siwang Yu, Min Ye. Glycybridins A-K, Bioactive Phenolic Compounds from Glycyrrhiza glabra. Journal of natural products. 2017 02; 80(2):334-346. doi: 10.1021/acs.jnatprod.6b00783. [PMID: 28140583]
  • Yun-Ze Yin, Rui-Shan Wang, Ri-Dao Chen, Li-Rui Qiao, Lin Yang, Chun-Mei Wang, Jun-Gui Dai. [Chemical constituents from cell suspension cultures of Cudrania tricuspidata]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2012 Dec; 37(24):3734-7. doi: . [PMID: 23627169]
  • Hayet Edziri, Maha Mastouri, Mohamed Ali Mahjoub, Zine Mighri, Aouni Mahjoub, Luc Verschaeve. Antibacterial, antifungal and cytotoxic activities of two flavonoids from Retama raetam flowers. Molecules (Basel, Switzerland). 2012 Jun; 17(6):7284-93. doi: 10.3390/molecules17067284. [PMID: 22695233]
  • Witabouna Mamidou Kone, Kakou-Ngazoa E Solange, Mireille Dosso. Assessing sub-Saharan Erythrina for efficacy: traditional uses, biological activities and phytochemistry. Pakistan journal of biological sciences : PJBS. 2011 May; 14(10):560-71. doi: 10.3923/pjbs.2011.560.571. [PMID: 22097091]
  • Myung Sun Lee, Chung Hee Kim, Duc Manh Hoang, Bo Yeon Kim, Cheon Bae Sohn, Mee Ree Kim, Jong Seog Ahn. Genistein-derivatives from Tetracera scandens stimulate glucose-uptake in L6 myotubes. Biological & pharmaceutical bulletin. 2009 Mar; 32(3):504-8. doi: 10.1248/bpb.32.504. [PMID: 19252305]
  • Jisuk Lee, Won Keun Oh, Jong Seog Ahn, Yong Hae Kim, J Tanyi Mbafor, Jean Wandji, Z Tanee Fomum. Prenylisoflavonoids from Erythrina senegalensis as novel HIV-1 protease inhibitors. Planta medica. 2009 Feb; 75(3):268-70. doi: 10.1055/s-0028-1088395. [PMID: 19097000]
  • Sergey A Fedoreyev, Victor P Bulgakov, Olga V Grishchenko, Marina V Veselova, Olga E Krivoschekova, Nadezda I Kulesh, Vladimir A Denisenko, Galina K Tchernoded, Yury N Zhuravlev. Isoflavonoid composition of a callus culture of the relict tree Maackia amurensis Rupr. et Maxim. Journal of agricultural and food chemistry. 2008 Aug; 56(16):7023-31. doi: 10.1021/jf801227q. [PMID: 18671403]
  • Adiaratou Togola, Ingvild Austarheim, Annette Theïs, Drissa Diallo, Berit Smestad Paulsen. Ethnopharmacological uses of Erythrina senegalensis: a comparison of three areas in Mali, and a link between traditional knowledge and modern biological science. Journal of ethnobiology and ethnomedicine. 2008 Mar; 4(?):6. doi: 10.1186/1746-4269-4-6. [PMID: 18321374]
  • 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]
  • 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]
  • Paul Erasto, Gomotsang Bojase-Moleta, Runner R T Majinda. Antimicrobial and antioxidant flavonoids from the root wood of Bolusanthus speciosus. Phytochemistry. 2004 Apr; 65(7):875-80. doi: 10.1016/j.phytochem.2004.02.011. [PMID: 15081287]