CAS: 31008-19-2; Rel-5-((1S,3Ar,4R,6Ar)-4-(3,4-Dimethoxyphenyl)Tetrahydro-1H,3H-Furo[3,4-C]Furan-1-yl)Benzo[d][1,3]Dioxole
该化合物是一种自然形成的化合物,被归类为氟氯素甘油,主要来自各种植物来源,特别是包括某些竹类的五花香* forgesia* , 其特点是其芬特林结构,它有助于其抗氧化特性.该化合物具有潜在的健康惠益,包括防炎和抗微生物活动.从溶解性来看,芳香素一般在极地溶剂中溶解,许多氟化素都是典型的.其分子结构包括附于氟化素骨骨的糖味,影响其生物活动和溶液.对远地的研究表明其在食品保存和自然健康补充方面的潜在用途,尽管需要进一步研究以充分阐明其行动和治疗潜力的机制.
- 英文名称Rel-5-((1S,3Ar,4R,6Ar)-4-(3,4-Dimethoxyphenyl)Tetrahydro-1H,3H-Furo[3,4-C]Furan-1-yl)Benzo[d][1,3]Dioxole
- 中文名称辛夷脂素
- IUPAC名称5-((1S,3aR,4R,6aR)-4-(3,4-dimethoxyphenyl)tetrahydro-1H,3H-furo[3,4-c]furan-1-yl)benzo[d][1,3]dioxole
- 其它别名(+/-)-Fargesin; Rel-5-[(1R,3As,4S,6As)-4-(3,4-Dimethoxyphenyl)Tetrahydro-1H,3H-Furo[3,4-C]Furan-1-Yl]-1,3-Benzodioxole; Fargesin; 5-[(3S,3Ar,6R,6Ar)-6-(3,4-Dimethoxyphenyl)-1,3,3A,4,6,6A-Hexahydrofuro[3,4-C]Furan-3
- CAS编号31008-19-2
- MFCD编号:MFCD07781423
- FDA UNII编号:GR9853GI71
- 分子式:C21H22O6分子量:370.4
- 产品CID: 1297712
- 产品分类生物化工 → 植物提取物
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diazomethane Pluviatilol methyl iodide 4-methanesulfonyloxy-3-methoxybenzaldehyde合成工艺路线路线简述
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主要参考文献
1: Sultana B, Yaqoob S, Zafar Z, Bhatti HN. Escalation of liver malfunctioning: A step toward Herbal Awareness. J Ethnopharmacol. 2018 Jan 6;216:104-119. doi: 10.1016/j.jep.2018.01.002. [Epub ahead of print] Review. pii: E952. doi: 10.3390/ijms18050952.
3: Pham TH, Kim MS, Le MQ, Song YS, Bak Y, Ryu HW, Oh SR, Yoon DY. Fargesin exerts anti-inflammatory effects in THP-1 monocytes by suppressing PKC-dependent AP-1 and NF-ĸB signaling. Phytomedicine. 2017 Jan 15;24:96-103. doi: 10.1016/j.phymed.2016.11.014. Epub 2016 Nov 21. doi: 10.1016/j.jpba.2016.09.035. Epub 2016 Sep 26. doi: 10.1139/cjpp-2015-0615. Epub 2016 Apr 19. doi: 10.1002/jssc.201501167. Epub 2016 Mar 1. doi: 10.3390/molecules200815273. doi: 10.1016/j.fitote.2015.05.016. Epub 2015 May 27. doi: 10.1080/10286020.2014.967228. Epub 2014 Oct 30. Chinese. doi: 10.1016/j.jpba.2014.01.028. Epub 2014 Jan 30. doi: 10.1007/s10637-013-9969-0. Epub 2013 May 15. doi: 10.1002/anie.201300571. Epub 2013 Mar 20. doi: 10.1007/s11418-012-0685-4. Epub 2012 Jul 12. doi: 10.1002/biof.1022. Epub 2012 Jun 2. doi: 10.1155/2012/593403. Epub 2012 Feb 16.
19: Guo T, Deng YX, Xie H, Yao CY, Cai CC, Pan SL, Wang YL. Antinociceptive and anti-inflammatory activities of ethyl acetate fraction from Zanthoxylum armatum in mice. Fitoterapia. 2011 Apr;82(3):347-51. doi: 10.1016/j.fitote.2010.11.004. Epub 2010 Nov 6. doi: 10.1002/bmc.1538. Epub 2010 Nov 5.
合成参考文献
参考文献:10.1016/0031-9422(95)00464-i
摘要:Vidigal MCS, Cavalheiro AJ, Kato MJ, Yoshida M. Lignans from kernels of Virola michelii Heckel. Phytochemistry. 1995 Nov;40(4):1259–61. doi: 10.1016/0031-9422(95)00464-i.
参考文献:10.1016/0031-9422(95)00578-1
摘要:Yu-Liang Ma, Qiuli Huang, Gui-Qiu Han. A neolignan and lignans from Magnolia biondii. Phytochemistry. 1996 Jan;41(1):287–8. doi: 10.1016/0031-9422(95)00578-1.
参考文献:10.1016/0031-9422(88)80760-x
摘要:Koul SK, Taneja SC, Agarwal VK, Dhar KL. Minor amides of Piper species. Phytochemistry. 1988 Jan;27(11):3523–7. doi: 10.1016/0031-9422(88)80760-x.
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