芹菜苷
外觀
芹菜苷 | |
---|---|
IUPAC名 4′,5-Dihydroxy-7-[3-C-(hydroxymethyl)-β-D-erythrofuranosyl-(1→2)-β-D-glucopyranosyloxy]flavone | |
系統名 7[(2S,3R,4S,5S,6R)-2[(2S,3R,4R)-3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one | |
別名 | Apioside Apigenin-7-apioglucoside Apigenin-7-O-apioglucoside |
識別 | |
CAS號 | 26544-34-3 |
PubChem | 5280746 |
ChemSpider | 4444321 |
SMILES |
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ChEBI | 15932 |
KEGG | C04858 |
性質 | |
化學式 | C26H28O14 |
摩爾質量 | 564.49 g·mol−1 |
危險性 | |
GHS危險性符號 | |
GHS提示詞 | 警告 |
H-術語 | H315, H319, H335 |
P-術語 | P261, P264, P271, P280, P302+352, P304+340, P305+351+338, P312, P321, P332+313, P337+313, P362, P403+233, P405 |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
芹菜苷(英語:Apiin)是一種天然黃酮類化合物,是芹菜素的二糖苷,可以在歐芹[1]和芹菜[2]等耐寒植物以及香蕉葉中發現。[3]
芹菜苷在製備金或銀球形膠體過程中被用作還原劑和穩定劑。[4]
參考資料
[編輯]- ^ H. Meyer; A. Bolarinwa; G. Wolfram; J. Linseisen. Bioavailability of Apigenin from Apiin-Rich Parsley in Humans. Ann Nutr Metab. 2006, 50 (3): 167–172. PMID 16407641. S2CID 8223136. doi:10.1159/000090736.
- ^ S. R. Gupta. A study of apiin from the parsley seeds and plant. Proceedings of the Indian Academy of Sciences, Section A. 1952, 35 (5). S2CID 91953908. doi:10.1007/BF03172503.
- ^ Sayadi, Khali; Akbarzadeh, Fatemeh; Pourmardan, Vahid; Saravani-Aval, Mehdi; Sayadi, Jalis; Chauhan, Narendra Pal Singh; Sargazi, Ghasem. Methods of green synthesis of Au NCs with emphasis on their morphology: A mini-review. Heliyon (Cell Press). 2021, 7 (6): e07250. Bibcode:2021Heliy...707250S. ISSN 2405-8440. PMC 8220187 . PMID 34189304. doi:10.1016/j.heliyon.2021.e07250 .
- ^ Kasthuri, J.; Veerapandian, S.; Rajendiran, N. Biological synthesis of silver and gold nanoparticles using apiin as reducing agent. Colloids and Surfaces B: Biointerfaces. 2009-01-01, 68 (1). ISSN 0927-7765. doi:10.1016/j.colsurfb.2008.09.021.
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