Cirsilineol (BioDeep_00001867535)

PANOMIX_OTCML-2023

代谢物信息卡片

4H-1-Benzopyran-4-one, 5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-6,7-dimethoxy-

化学式: C18H16O7 (344.0895986)
中文名称: 3′-甲氧基蓟黄素, 甲基条叶蓟素
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1(OC)=CC2OC(C3C=CC(O)=C(OC)C=3)=CC(=O)C=2C(O)=C1OC
InChI: InChI=1S/C18H16O7/c1-22-13-6-9(4-5-10(13)19)12-7-11(20)16-14(25-12)8-15(23-2)18(24-3)17(16)21/h4-8,19,21H,1-3H3

描述信息

Cirsilineol is a trimethoxyflavone that is flavone substituted by methoxy groups at positions 6, 7 and 3 and hydroxy groups at positions 5 and 4 respectively. It has a role as a plant metabolite and an antineoplastic agent. It is a trimethoxyflavone and a dihydroxyflavone. It is functionally related to a flavone.
Cirsilineol is a natural product found in Thymus herba-barona, Salvia tomentosa, and other organisms with data available.
See also: Tangerine peel (part of).
A trimethoxyflavone that is flavone substituted by methoxy groups at positions 6, 7 and 3 and hydroxy groups at positions 5 and 4 respectively.

同义名列表

20 个代谢物同义名

4H-1-Benzopyran-4-one, 5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-6,7-dimethoxy-; 5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-6,7-dimethoxy-4H-1-benzopyran-4-one; 5-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)-6,7-dimethoxy-4H-chromen-4-one #; 5-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)-6,7-dimethoxy-4H-chromen-4-one; 5-hydroxy-2-(4-hydroxy-3-methoxy-phenyl)-6,7-dimethoxy-chromen-4-one; 5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-6,7-dimethoxychromen-4-one; Cirsilineol (5,4-dihydroxy-6,7,3-trimethoxyflavone); 4,5-dihydroxy-3,6,7-trimethoxy-flavone; 4,5-dihydroxy-3,6,7-trimethoxyflavone; 4,5-Dihydroxy-3,6,7-trimethoxyflavone; 5,4-Dihydroxy-6,7,3-trimethoxyflavone; Cirsilineol, analytical standard; VKOSQMWSWLZQPA-UHFFFAOYSA-N; UNII-08DZZ529FE; Cirsilineol; Cirsileneol; Fastigenin; Anisomelin; 08DZZ529FE; Eupatrin

数据库引用编号

15 个数据库交叉引用编号

ChEBI: CHEBI:3718
KEGG: C10032
PubChem: 162464
ChEMBL: CHEMBL487213
Wikipedia: Cirsilineol
LipidMAPS: LMPK12111249
MeSH: cirsilineol
ChemIDplus: 0041365326
CAS: 41365-32-6
medchemexpress: HY-119347
MetaboLights: MTBLC3718
PubChem: 12218
KNApSAcK: C00013595
3DMET: B03475
NIKKAJI: J372.166C

分类词条

Flavones and Flavonols [PK1211]

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)

60 个相关的物种来源信息

13329 - Achillea millefolium: 10.1016/0031-9422(90)85371-L
482483 - Achillea millefolium var. millefolium: 10.1016/0031-9422(90)85371-L
205360 - Ajania fastigiata:
925377 - Aloysia citrodora: 10.1021/JF990444I
516069 - Anisomeles indica: 10.1021/NP50028A034
149410 - Arnica longifolia: 10.1016/S0031-9422(00)89581-3
35608 - Artemisia annua:
262982 - Artemisia apiacea:
259893 - Artemisia argyi: 10.1007/BF00630092
1227617 - Artemisia assoana: 10.1016/S0031-9422(00)83891-1
265783 - Artemisia capillaris:
496566 - Artemisia carvifolia:
1473222 - Artemisia cina:
72342 - Artemisia fragrans:
401898 - Artemisia gmelinii:
1316680 - Artemisia halodendron: 10.1007/BF00598368
72329 - Artemisia herba-alba:
205369 - Artemisia judaica: 10.1016/S0031-9422(00)84593-8
72345 - Artemisia lucentica:
72348 - Artemisia monosperma:
1338417 - Artemisia oliveriana:
72350 - Artemisia reptans:
637484 - Artemisia rubripes: 10.1248/YAKUSHI1947.103.6_696
205374 - Artemisia rutifolia: 10.1007/BF00579497
1811969 - Artemisia vestita:
401941 - Artemisia xanthochroa: 10.1007/BF00580042
1715998 - Baccharis genistelloides: 10.1248/CPB.33.5075
1654448 - Baccharis sagittalis: 10.1248/CPB.33.5075
441183 - Blumea lacera: 10.1007/S11418-007-0180-5
124929 - Centaurea diffusa: 10.1016/S0305-1978(01)00115-6
363436 - Centaurea napifolia: 10.1023/B:CONC.0000011131.34049.E6
347528 - Centaurea pullata: 10.1007/S10600-005-0117-8
41539 - Centaurea sulphurea: 10.1007/S10600-011-9798-3
196725 - Cirsium lineare: 10.1016/0031-9422(73)80032-9
558547 - Citrus deliciosa: 10.1248/CPB.41.714
85571 - Citrus reticulata: 10.1248/CPB.41.714
99046 - Crossostephium chinense:
1770161 - Griffitharia pallescens: 10.1007/978-94-009-0975-5_12
1573925 - Heterotheca grandiflora: 10.1016/S0031-9422(00)83141-6
1241423 - Lantana montevidensis: 10.1248/BPB.25.875
29719 - Mentha spicata: 10.1016/S0031-9422(98)00672-4
39350 - Ocimum basilicum: 10.1016/S0031-9422(96)00430-X
1224218 - Ocimum kilimandscharicum: 10.1016/S0031-9422(00)00439-8
204149 - Ocimum tenuiflorum:
1721069 - Pentzia calva: 10.1016/0031-9422(90)89035-8
21880 - Salvia:
38868 - Salvia officinalis:
268920 - Salvia palaestina: 10.1016/0031-9422(95)00754-7
1132405 - Salvia tomentosa:
1391945 - Sideritis leucantha:
155258 - Sideritis pungens: 10.1016/S0031-9422(00)97932-9
680229 - Tecomella undulata: 10.1016/S0305-1978(99)00116-7
1854018 - Teucrium alyssifolium: 10.1016/0031-9422(96)00002-7
28514 - Teucrium fruticans: 10.5586/ASBP.2001.025
711380 - Teucrium marum: 10.1016/0031-9422(96)00002-7
1209879 - Teucrium orientale: 10.1007/BF00598375
1107925 - Thymus herba-barona: 10.1016/0031-9422(95)00217-U
228974 - Thymus quinquecostatus: 10.1016/0031-9422(95)00217-U
751874 - Thymus saturejoides: 10.1055/S-2007-969583
49992 - Thymus vulgaris:

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

Dinesh Kumar Patel. Health Benefits, Therapeutic Applications, and Recent Advances of Cirsilineol in the Medicine: Potential Bioactive Natural Flavonoids of Genus Artemisia. Endocrine, metabolic & immune disorders drug targets. 2022 Nov; ?(?):. doi: 10.2174/1871530323666221122123456. [PMID: 36415094]
Meimei Ai, Shusheng Lin, Meixia Zhang, Tieli Wu, Nan Yang, Yu Li, Li Li. Cirsilineol attenuates LPS-induced inflammation in both in vivo and in vitro models via inhibiting TLR-4/NFkB/IKK signaling pathway. Journal of biochemical and molecular toxicology. 2021 Aug; 35(8):e22799. doi: 10.1002/jbt.22799. [PMID: 33949057]
Mahmoud A Al-Qudah, Hasan I Tashtoush, Ethar F Khlaifat, Sahar O Ibrahim, Ayman M Saleh, Hala I Al-Jaber, Musa H Abu Zarga, Sultan T Abu Orabi. Chemical constituents of the aerial parts of Salvia judaica Boiss. from Jordan. Natural product research. 2020 Oct; 34(20):2981-2985. doi: 10.1080/14786419.2019.1597349. [PMID: 31161797]
Akram Taleghani, Seyed Ahmad Emami, Zahra Tayarani-Najaran. Artemisia: a promising plant for the treatment of cancer. Bioorganic & medicinal chemistry. 2020 01; 28(1):115180. doi: 10.1016/j.bmc.2019.115180. [PMID: 31784199]
Zsuzsanna Hajdú, Judit Hohmann, Peter Forgo, Imre Máthé, Judit Molnár, István Zupkó. Antiproliferative activity of Artemisia asiatica extract and its constituents on human tumor cell lines. Planta medica. 2014 Dec; 80(18):1692-7. doi: 10.1055/s-0034-1383146. [PMID: 25295671]
Kaan Polatoğlu, Omer Cem Karakoç, Fatih Demirci, Ayhan Gökçe, Nezhun Gören. Chemistry and biological activities of Tanacetum chiliophyllum var. oligocephalum extracts. Journal of AOAC International. 2013 Nov; 96(6):1222-7. doi: 10.5740/jaoacint.sgepolatoglu. [PMID: 24645497]
Hyun Ah Jung, Jin Ju Park, Md Nurul Islam, Seung Eun Jin, Byung-Sun Min, Je-Hyun Lee, Hee Sook Sohn, Jae Sue Choi. Inhibitory activity of coumarins from Artemisia capillaris against advanced glycation endproduct formation. Archives of pharmacal research. 2012 Jun; 35(6):1021-35. doi: 10.1007/s12272-012-0610-0. [PMID: 22870812]
Shuangqing Wu, Qun Sun, Chunjun Chu, Jian Zhang. [Chemical constituents of Eupatorium lindleyanum]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2012 Apr; 37(7):937-40. doi: . [PMID: 22792793]
Hala I Al-Jaber, Khadeja K Abrouni, Mahmuod A Al-Qudah, Musa H Abu Zarga. New terpenes from Salvia palaestina Benth. and Salvia syriaca L. growing wild in Jordan. Journal of Asian natural products research. 2012; 14(7):618-25. doi: 10.1080/10286020.2012.682151. [PMID: 22574636]
Gjoshe Stefkov, Svetlana Kulevanova, Biljana Miova, Suzana Dinevska-Kjovkarovska, Per Mølgaard, Anna K Jäger, Knud Josefsen. Effects of Teucrium polium spp. capitatum flavonoids on the lipid and carbohydrate metabolism in rats. Pharmaceutical biology. 2011 Sep; 49(9):885-92. doi: 10.3109/13880209.2011.552187. [PMID: 21619454]
Philippe Rasoanaivo, Colin W Wright, Merlin L Willcox, Ben Gilbert. Whole plant extracts versus single compounds for the treatment of malaria: synergy and positive interactions. Malaria journal. 2011 Mar; 10 Suppl 1(?):S4. doi: 10.1186/1475-2875-10-s1-s4. [PMID: 21411015]
Ye Yin, Fang-Yuan Gong, Xing-Xin Wu, Yang Sun, Yi-Hua Li, Ting Chen, Qiang Xu. Anti-inflammatory and immunosuppressive effect of flavones isolated from Artemisia vestita. Journal of ethnopharmacology. 2008 Oct; 120(1):1-6. doi: 10.1016/j.jep.2008.07.029. [PMID: 18721870]
Takahiko Isobe, Matsumi Doe, Yoshiki Morimoto, Kumiko Nagata, Ayumi Ohsaki. The anti-Helicobacter pylori flavones in a Brazilian plant, Hyptis fasciculata, and the activity of methoxyflavones. Biological & pharmaceutical bulletin. 2006 May; 29(5):1039-41. doi: 10.1248/bpb.29.1039. [PMID: 16651742]
Ipseeta Mohanty, Dharamvir Singh Arya, Suresh Kumar Gupta. Effect of Curcuma longa and Ocimum sanctum on myocardial apoptosis in experimentally induced myocardial ischemic-reperfusion injury. BMC complementary and alternative medicine. 2006 Feb; 6(?):3. doi: 10.1186/1472-6882-6-3. [PMID: 16504000]
Sam Medhat Salah, Anna Katharina Jäger. Two flavonoids from Artemisia herba-alba Asso with in vitro GABAA-benzodiazepine receptor activity. Journal of ethnopharmacology. 2005 May; 99(1):145-6. doi: 10.1016/j.jep.2005.01.031. [PMID: 15848034]
Chun-nian He, Chun-lan Wang, Shun-xing Guo, Jun-shan Yang, Pei-gen Xiao. [Study on chemical constituents in herbs of Anoectochilus roxburghii II]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2005 May; 30(10):761-3. doi: ". [PMID: 16075715]
Sheng Lin, Qi-Wei Zhang, Ning-Ning Zhang, Yong-Xin Zhang. [Determination of flavonoids in buds of Herba Artemisiae Scopariae by HPLC]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2005 Apr; 30(8):591-4. doi: . [PMID: 16011282]
Jun Watanabe, Hiroshi Shinmoto, Tojiro Tsushida. Coumarin and flavone derivatives from estragon and thyme as inhibitors of chemical mediator release from RBL-2H3 Cells. Bioscience, biotechnology, and biochemistry. 2005 Jan; 69(1):1-6. doi: 10.1271/bbb.69.1. [PMID: 15665459]
Tsuneatsu Nagao, Fumiko Abe, Junei Kinjo, Hikaru Okabe. Antiproliferative constituents in plants 10. Flavones from the leaves of Lantana montevidensis Briq. and consideration of structure-activity relationship. Biological & pharmaceutical bulletin. 2002 Jul; 25(7):875-9. doi: 10.1248/bpb.25.875. [PMID: 12132661]
Qi-wei Zhang, Yong-xi Zhang, Ying Zhang, Yong-qing Xiao, Zhi-min Wang. [Studies on chemical constituents in buds of Artemisia scoparia]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2002 Mar; 27(3):202-4. doi: . [PMID: 12774401]
Qi-wei Zhang, Yong-xin Zhang, Ying Zhang, Guo-gang Liang. [Determination of cirsilineol in Herba Artemisiae scopariae collected in autumn by HPLC]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2002 Jan; 27(1):23-5. doi: ". [PMID: 12774348]
H J Heo, H Y Cho, B Hong, H K Kim, E K Kim, B G Kim, D H Shin. Protective effect of 4',5-dihydroxy-3',6,7-trimethoxyflavone from Artemisia asiatica against Abeta-induced oxidative stress in PC12 cells. Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis. 2001 Sep; 8(3):194-201. doi: 10.3109/13506120109007362. [PMID: 11676296]
P Valentão, P B Andrade, F Areias, F Ferreres, R M Seabra. Analysis of vervain flavonoids by HPLC/Diode array detector method. Its application to quality control. Journal of agricultural and food chemistry. 1999 Nov; 47(11):4579-82. doi: 10.1021/jf990444i. [PMID: 10552853]