Obtusifolin (BioDeep_00000285929)

Main id: BioDeep_00000000482

 

PANOMIX_OTCML-2023


代谢物信息卡片


2,8-DIHYDROXY-1-METHOXY-3-METHYL-9,10-DIHYDROANTHRACENE-9,10-DIONE

化学式: C16H12O5 (284.0684702)
中文名称: 决明蒽醌
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC1=CC2=C(C(=C1O)OC)C(=O)C3=C(C2=O)C=CC=C3O
InChI: InChI=1S/C16H12O5/c1-7-6-9-12(16(21-2)13(7)18)15(20)11-8(14(9)19)4-3-5-10(11)17/h3-6,17-18H,1-2H3

描述信息

Obtusifolin is a dihydroxyanthraquinone.
Obtusifolin is a natural product found in Senna obtusifolia and Senna tora with data available.
Obtusifolin, isolated from the seeds of Cassia obtusifolia, regulates the gene expression and production of MUC5AC mucin in airway epithelial cells via inhibiting NF-kB pathway[1]. Obtusifolin suppresses phthalate esters-induced breast cancer bone metastasis by targeting parathyroid hormone-related protein[2].
Obtusifolin, isolated from the seeds of Cassia obtusifolia, regulates the gene expression and production of MUC5AC mucin in airway epithelial cells via inhibiting NF-kB pathway[1]. Obtusifolin suppresses phthalate esters-induced breast cancer bone metastasis by targeting parathyroid hormone-related protein[2].

同义名列表

11 个代谢物同义名

2,8-DIHYDROXY-1-METHOXY-3-METHYL-9,10-DIHYDROANTHRACENE-9,10-DIONE; 9,10-Anthracenedione, 2,8-dihydroxy-1-methoxy-3-methyl-; 2,8-dihydroxy-1-methoxy-3-methylanthracene-9,10-dione; 2,8-Dihydroxy-1-methoxy-3-methyl-9,10-anthracenedione; Anthraquinone, 2,8-dihydroxy-1-methoxy-3-methyl-; 2,8-Dihydroxy-1-methoxy-3-methylanthraquinone; Obtusifolin (anthraquinone); Obtusifolin; 2,8-dihydroxy-1-methoxy-3-methyl-anthracene-9,10-dione; 2,8-dihydroxy-1-methoxy-3-methyl-9,10-anthraquinone; 477-85-0



数据库引用编号

11 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)

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

  • Zhu Huang, Qiao Sun, Wenwen Hao, Junyu Zhao. Pharmacokinetics and tissue distribution study of obtusifolin in rats by liquid chromatography-tandem mass spectrometry. Biomedical chromatography : BMC. 2021 Mar; 35(3):e5009. doi: 10.1002/bmc.5009. [PMID: 33119923]
  • Xu Pang, Li-Ming Wang, You-Cai Zhang, Li-Ping Kang, He-Shui Yu, Guan-Wei Fan, Li-Feng Han. New anthraquinone and eurotinone analogue from the seeds of Senna obtusifolia and their inhibitory effects on human organic anion transporters 1 and 3. Natural product research. 2019 Dec; 33(23):3409-3416. doi: 10.1080/14786419.2018.1480621. [PMID: 29863900]
  • Ki Sun Kwon, Ju Hee Lee, Kyung Su So, Byung Kyu Park, Hyun Lim, Jae Sue Choi, Hyun Pyo Kim. Aurantio-obtusin, an anthraquinone from cassiae semen, ameliorates lung inflammatory responses. Phytotherapy research : PTR. 2018 Aug; 32(8):1537-1545. doi: 10.1002/ptr.6082. [PMID: 29675883]
  • Xue Wang, Lifeng Han, Gentao Li, Wei Peng, Xiumei Gao, Curtis D Klaassen, Guanwei Fan, Youcai Zhang. From the Cover: Identification of Natural Products as Inhibitors of Human Organic Anion Transporters (OAT1 and OAT3) and Their Protective Effect on Mercury-Induced Toxicity. Toxicological sciences : an official journal of the Society of Toxicology. 2018 02; 161(2):321-334. doi: 10.1093/toxsci/kfx216. [PMID: 29045746]
  • Si-Yi Zhuang, Miao-Li Wu, Peng-Jv Wei, Zhi-Ping Cao, Peng Xiao, Chu-Hua Li. Changes in Plasma Lipid Levels and Antioxidant Activities in Rats after Supplementation of Obtusifolin. Planta medica. 2016 Apr; 82(6):539-43. doi: 10.1055/s-0042-102458. [PMID: 27002399]
  • Yu Tang, Zhiying Zhong. Obtusifolin treatment improves hyperlipidemia and hyperglycemia: possible mechanism involving oxidative stress. Cell biochemistry and biophysics. 2014 Dec; 70(3):1751-7. doi: 10.1007/s12013-014-0124-0. [PMID: 25015065]
  • Lijia Xu, Chi-On Chan, Ching-Ching Lau, Zhiling Yu, Daniel K W Mok, Sibao Chen. Simultaneous determination of eight anthraquinones in Semen Cassiae by HPLC-DAD. Phytochemical analysis : PCA. 2012 Mar; 23(2):110-6. doi: 10.1002/pca.1331. [PMID: 21618311]
  • Zhi-Xiong Zhang, Yong-Feng Liang. [Study on chemical constituents from the root of Hemerocallis citrina]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2011 Sep; 34(9):1371-3. doi: . [PMID: 22260003]
  • Dong Hyun Kim, Sook Kyung Hyun, Byung Hoon Yoon, Ji-Hyung Seo, Kyung-Tae Lee, Jae Hoon Cheong, Seo Yun Jung, Changbae Jin, Jae Sue Choi, Jong Hoon Ryu. Gluco-obtusifolin and its aglycon, obtusifolin, attenuate scopolamine-induced memory impairment. Journal of pharmacological sciences. 2009 Oct; 111(2):110-6. doi: 10.1254/jphs.08286fp. [PMID: 19834282]
  • H S Yun-Choi, J H Kim, M Takido. Potential inhibitors of platelet aggregation from plant sources, V. Anthraquinones from seeds of Cassia obtusifolia and related compounds. Journal of natural products. 1990 May; 53(3):630-3. doi: 10.1021/np50069a014. [PMID: 2213033]