CAS: 14259-46-2; (S)-5-Hydroxy-2-(4-Hydroxyphenyl)-7-(((2S,3R,4S,5S,6R)-3,4,5-Trihydroxy-6-((((2R,3R,4R,5R,6S)-3,4,5-Trihydroxy-6-Methyltetrahydro-2H-Pyran-2-yl)Oxy)Methyl)Tetrahydro-2H-Pyran-2-yl)Oxy)Chroman-4-One
该化合物是一种自然形成的氟氯素胶片,具有强效抗氧化性特性. 它的化学结构允许清扫自由基和防范氧化性压力. 柑橘水果中已经发现了这一化合物,并证明它具有防止细胞损伤,炎症和其他与活性氧物种相关的病理过程的潜力.
- 英文名称(S)-5-Hydroxy-2-(4-Hydroxyphenyl)-7-(((2S,3R,4S,5S,6R)-3,4,5-Trihydroxy-6-((((2R,3R,4R,5R,6S)-3,4,5-Trihydroxy-6-Methyltetrahydro-2H-Pyran-2-yl)Oxy)Methyl)Tetrahydro-2H-Pyran-2-yl)Oxy)Chroman-4-One
- 中文名称芸香柚皮苷
- IUPAC名称(S)-5-hydroxy-2-(4-hydroxyphenyl)-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)chroman-4-one
- 其它别名芸香柚皮苷
- CAS编号14259-46-2
- MFCD编号:MFCD00017316
- EINECS号:238-138-0
- FDA UNII编号:06M5EAT0YC
- 分子式:C27H32O14
- 分子量:580.53
- 产品CID: 651098
- 产品分类有机原料→分子砌块→手性化合物→手性砌块
相似化合物
60-81-1 7061-54-3 58001-41-5物理性质
MSDS等安全信息
合成工艺路线路线简述
- 480-41-1 = 14259-46-2 + 5180-65-4 + 529-41-9 + 81202-36-0 + 1160434-47-8 + 529-55-5
反应条件:1.1 Solvents: Water; 5 D,25 °C
标题:Biotransformation Of Naringin And Naringenin By Cultured Eucalyptus Perriniana Cells
作者:Shimoda,Kei; Et Al
参考文献:Phytochemistry (Elsevier) 日期:2010 卷标:71(2-3) 页码:201-205]
10236-47-2 = 14259-46-2 + 5180-65-4 + 529-41-9 + 81202-36-0 + 1160434-47-8 + 529-55-5
反应条件:1.1 Solvents: Water; 5 D,25 °C2.1 Solvents: Water; 5 D,25 °C
标题:Biotransformation Of Naringin And Naringenin By Cultured Eucalyptus Perriniana Cells
作者:Shimoda,Kei; Et Al
参考文献:Phytochemistry (Elsevier) 日期:2010 卷标:71(2-3) 页码:201-205
专利信息
专利号:CN-119331888-A
优先权日:2024-10-10
标题:Polygonatum cyrtonema PcF3H gene and application thereof in promotion of synthesis of dihydroflavonoid compounds and catalysis of naringenin hydroxylation
专利号:CN-114226746-A
优先权日:2021-12-17
标 题 :Method for green synthesis of gold nanoparticles by using orange peel extract under assistance of ultrasonic waves
专利号:US-2025255893-A1
优先权日:2021-10-25
标题 :Isopropyl-d-glucopyranoside derivative, and preparation method therefor and use thereof
发明人：CHEN LINYI; WANG YI; LIAO WEN-LING; LEE YU-TANG; LU TING-HSUAN; HUANG YU-WEN; LI CHIA-WEI; WANG CHEN; CHEN FANG-YI; CHIAO CHUAN-CHIN
权利人:UNIV NAT TSING HUA
摘要:A chemical compound including Isopropyl-D-glucopyranoside derivatives and its chemical synthesis to prepare the chemical compound. The Isopropyl-D-glucopyranoside derivatives is used for promoting regeneration of injured brain neurons and retinal neurons.
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主要参考文献
1: Li Y, Du Y, Yang J, Xiu Z, Yang N, Zhang J, Gao Y, Li B, Shi H. Narirutin produces antidepressant-like effects in a chronic unpredictable mild stress mouse model. Neuroreport. 2018 Jul 18. doi: 10.1097/WNR.0000000000001102. [Epub ahead of print] doi: 10.1016/j.ijbiomac.2017.05.110. Epub 2017 May 19. doi: 10.1016/j.jchromb.2015.10.005. Epub 2015 Oct 22. doi: 10.1016/j.fct.2013.01.060. Epub 2013 Feb 13. doi: 10.1016/j.fct.2012.07.007. Epub 2012 Jul 17. Epub 2004 Oct 26.
合成参考文献
参考文献:10.1021/np50001a002
摘要:Edwards JM, Raffauf RF, Le Quesne PW. Antineoplastic activity and cytotoxicity of flavones, isoflavones, and flavanones. J Nat Prod. 1979 Jan;42(1):85–91. doi: 10.1021/np50001a002.
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