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Merck
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文件

91255

Sigma-Aldrich

杨梅甙

≥99.0% (HPLC)

别名:

, , Myricitroside

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About This Item

经验公式（希尔记法）:
C21H20O12
CAS号:
17912-87-7
分子量:
464.38
EC號碼:
241-856-7
MDL號碼:
MFCD00016930
分類程式碼代碼:
12352201
PubChem物質ID:
329770016
NACRES:
NA.25

化驗

≥99.0% (HPLC)

形狀

powder

技術

HPLC: suitable

顏色

light yellow

儲存溫度

2-8°C

SMILES 字串

C[C@@H]1O[C@@H](OC2=C(Oc3cc(O)cc(O)c3C2=O)c4cc(O)c(O)c(O)c4)[C@H](O)[C@H](O)[C@H]1O

InChI

1S/C21H20O12/c1-6-14(26)17(29)18(30)21(31-6)33-20-16(28)13-9(23)4-8(22)5-12(13)32-19(20)7-2-10(24)15(27)11(25)3-7/h2-6,14,17-18,21-27,29-30H,1H3/t6-,14-,17+,18+,21-/m0/s1

InChI 密鑰

DCYOADKBABEMIQ-OWMUPTOHSA-N

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相关类别

生化／生理作用

代谢产物杨梅苷，即杨梅素的 3-O-鼠李糖苷，发现于植物中，如毛杨梅（杨梅科）的树皮、风杨梅的叶子和金鱼草。它是某些叶虫的摄食刺激剂 ；并显示对 DPPH 具有较强的抗氧化活性。杨梅苷可能有利于管理炎症条件 ，并可以是一种非常有用的、能帮助镇痛药物研发的分子。杨梅苷是一种一氧化氮（NO）和蛋白激酶 C（PKC）抑制剂，具有中枢神经系统活性，包括抗焦虑作用。

包裝

无底玻璃瓶。内含物装在插入式熔锥内。

其他說明

为了全面了解我们针对客户研究提供的各种单糖产品，建议您访问我们的碳水化合物分类页面。

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

分析证书(COA)

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Feeding stimulation of flavonoids for various leaf beetles (Coleoptera: Chrysomelidae).
Matsuda, K.
Appl. Entomol. Zool, 13, 228-230 (1978)
Lalith Jayasinghe et al.
Natural product research, 26(8), 717-721 (2011-09-20)
Chemical investigation of the leaves of Elaeocarpus serratus yielded myricitrin (1), mearnsetin 3-O-β-D-glucopyranoside (2), mearnsitrin (3), tamarixetin 3-O-α-L-rhamnopyranoside (4) and the fruits of Filicium decipiens yielded three flavonol glycosides, kaempferol 3-O-rutinoside (5), kaempferol 3-O-robinobioside (6) and trifolin (7). Compound 1
Simone Quintyne-Walcott et al.
Journal of natural products, 70(8), 1374-1376 (2007-08-07)
A new cyclic nonapeptide, crotogossamide (1), was isolated from the latex of Croton gossypifolius. Its structure was elucidated by use of 1D and 2D NMR and MS and by hydrolysis followed by GC-MS analysis as cyclo(-Gly(1)-Ala(2)-Ser(3)-Gly(4)-Leu(5)-Asn(6)-Gly(7)-Ile(8)-Phe(9)-). This is the first
Wei Chen et al.
Food chemistry, 141(2), 927-933 (2013-06-26)
Peroxynitrite, a potent oxidising and nitrating species, has been implicated in the pathogenesis of neurodegenerative diseases. This study was undertaken to investigate the protective effect of myricitrin on peroxynitrite-mediated toxicity and the underlying mechanism. Our results showed that the presence
Flavia Carla Meotti et al.
The Journal of pharmacology and experimental therapeutics, 316(2), 789-796 (2005-11-02)
The present study investigated the antinociceptive effects of the flavonoid myricitrin in chemical behavioral models of pain in mice and rats. Myricitrin given by i.p. or p.o. routes produced dose-related antinociception when assessed on acetic acid-induced visceral pain in mice.
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