00017
刺槐素
≥97.0% (HPLC)
别名:
4′-甲基芹菜素, 5,7-二羟基-4′-甲氧基黄酮, 佛手黄酮醇, 芹菜素 4′-甲基醚, 蒙花苷
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关于此项目
经验公式（希尔记法）:
C16H12O5
化学文摘社编号:
分子量:
284.26
PubChem Substance ID:
eCl@ss:
32150233
UNSPSC Code:
12352200
NACRES:
NA.47
EC Number:
207-552-3
MDL number:
Beilstein/REAXYS Number:
277879
InChI key
DANYIYRPLHHOCZ-UHFFFAOYSA-N
InChI
1S/C16H12O5/c1-20-11-4-2-9(3-5-11)14-8-13(19)16-12(18)6-10(17)7-15(16)21-14/h2-8,17-18H,1H3
assay
≥97.0% (HPLC)
form
powder or crystals
mp
260-265 °C (lit.)
application(s)
metabolomics
vitamins, nutraceuticals, and natural products
storage temp.
2-8°C
Quality Level
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General description
刺槐黄素属于维管植物中天然存在的类黄酮类植物色素，最早报道提取自Robinia pseuducacia叶，已被用作中药雪莲啊我想让有效成分。
Biochem/physiol Actions
具有抗过氧化和抗炎属性的黄酮类化合物。用于中药。
具有抗过氧化和抗炎属性的黄酮类化合物。用于中药。它通过诱导细胞凋亡，将细胞周期阻滞于 G1 期而成为公认的抗增殖药物。
刺槐黄素具有抗过氧化、抗炎和抗疟原虫等特性，公认可以阻止Hep G2 细胞的增殖，进而导致细胞凋亡及随后的抗癌效果。它具有抗心律失常的特性，可用于房颤的治疗。
Packaging
无底玻璃瓶。内含物装在插入的融合锥内。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Acacetin, a natural flavone, selectively inhibits human atrial repolarization potassium currents and prevents atrial fibrillation in dogs
Li GR, et al.,
Circulation, 117(19), 2449-2457 (2008)
Acacetin inhibits the proliferation of Hep G2 by blocking cell cycle progression and inducing apoptosis
Hsu YL, et al.,
Biochemical Pharmacology, 67(5), 823-829 (2004)
V Zimkhitha Sotenjwa et al.
Fitoterapia, 147, 104740-104740 (2020-10-12)
Artemisia afra (African wormwood) is a popular medicinal plant of southern Africa and is an excellent candidate for commercialisation. This current study was aimed at exploring the phytochemistry and chemical variation of non-volatile compounds within wild populations of A. afra
Hui-Jun Wu et al.
PloS one, 8(3), e57864-e57864 (2013-03-26)
The natural flavone acacetin has been demonstrated to inhibit transient outward potassium current (Ito) in human atrial myocytes. However, the molecular determinants of acacetin for blocking Ito are unknown. The present study was designed to investigate the properties and molecular
Jidan Liu et al.
Carbohydrate research, 357, 41-46 (2012-06-27)
Apigenin-7-O-β-D-glycosides 1-8 and acacetin-7-O-β-D-glycosides 9-16 were semisynthesized from 4'-O-benzyl apigenin 17 and acacetin 18 by glycosidation and deprotection with the corresponding α-acetylglycosyl bromide, respectively. Compounds 17 and 18 were prepared by iodination followed by base-induced elimination, 4'-O-benzylation, or 4'-O-methylation and
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