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Merck

17794

Sigma-Aldrich

异鼠李素

≥95.0% (HPLC)

别名:

3′-甲基槲皮素, 3′-甲氧基-3,4′,5,7-四羟基黄酮, 3,4′,5,7-四羟基3′-甲氧基黄酮, 异戊烯醇, 槲皮素3′-甲醚

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About This Item

经验公式(希尔记法):
C16H12O7
CAS号:
分子量:
316.26
Beilstein:
44723
EC號碼:
MDL號碼:
分類程式碼代碼:
12352205
PubChem物質ID:
NACRES:
NA.47

品質等級

化驗

≥95.0% (HPLC)

應用

metabolomics
vitamins, nutraceuticals, and natural products

SMILES 字串

COc1cc(ccc1O)C2=C(O)C(=O)c3c(O)cc(O)cc3O2

InChI

1S/C16H12O7/c1-22-11-4-7(2-3-9(11)18)16-15(21)14(20)13-10(19)5-8(17)6-12(13)23-16/h2-6,17-19,21H,1H3

InChI 密鑰

IZQSVPBOUDKVDZ-UHFFFAOYSA-N

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一般說明

异鼠李素是一种 O-甲基化黄酮醇,存在于水果、植物和草药中。它是槲皮素的代谢物。

應用

异鼠李素(IRN)可用于:
  • 作为神经保护剂,以研究东莨菪碱所致小鼠皮质-海马学习和记忆障碍的影响
  • 作为四极杆飞行时间串联质谱法(QTOF MS)的参考标准,以分析并量化蜂蜜提取物中的酚类化合物
  • 作为参考标准品,通过反相高效液相色谱法及二极管阵列检测和电喷雾质谱法(RP-HPLC-DAD-ESI-TQ-MS/MS)测定蒿属酚的含量

生化/生理作用

异鼠李素具有抗氧化、抗炎症、抗肿瘤、抗菌和抗病毒的作用。作为一种潜在的神经保护剂,可抑制糖尿病(DM)患者海马结构的神经退行性变。低水平的异鼠李素可以作为一种抗糖尿病药物,促进骨骼肌细胞对葡萄糖的摄取并在高血糖情况下维持血糖稳态。它调节了核因子 kB(NF-κB)、磷脂酰肌醇 3-激酶(PI3K)/蛋白激酶(AKT)、丝裂原活化蛋白激酶(MAPK)等细胞信号通路。异鼠李素对动脉粥样硬化和心血管疾病具有保护和治疗作用。
异鼠李素通过干扰脂肪干细胞的分化来抑制脂肪形成,其机制为稳定 β-连环蛋白和上调 Wnt 信号通路。

包裝

无底玻璃瓶。内含物在插入的融合锥体内。

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

個人防護裝備

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Rongsheng E Wang et al.
Journal of medicinal chemistry, 52(7), 1912-1921 (2009-03-20)
Inhibitors of heat-induced heat shock protein 70 (HSP70) expression have the potential to enhance the therapeutic effectiveness of heat-induced radiosensitization of tumors. Among known small molecule inhibitors, quercetin has the advantage of being easily modified for structure-activity studies. Herein, we
Lutz Franke et al.
Journal of medicinal chemistry, 50(11), 2640-2646 (2007-04-28)
A natural product collection and natural-product-derived combinatorial libraries were virtually screened for potential inhibitors of human 5-lipoxygenase (5-LO) activity. We followed a sequential ligand-based approach in two steps. First, similarity searching with a topological pharmacophore descriptor (CATS 2D method) was
Gang Gong et al.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 128, 110301-110301 (2020-06-06)
Isorhamnetin is one of the most important active ingredients in the fruits of Hippophae rhamnoides L. and the leaves of Ginkgo biloba L., which possesses extensive pharmacological activities. At present, there have been numerous investigations on isorhamnetin, which has the
Ismail O Ishola et al.
Brain research, 1712, 188-196 (2019-02-18)
Isorhamnetin (IRN), a 3'-O-methylated metabolite of quercetin has antioxidant, anti-inflammatory and neuroprotective properties. In this study, we investigated the learning and memory enhancing effects of IRN on spatial and non-spatial learning and memory deficits induced by scopolamine (3 mg/kg, i.p; muscarinic
Mohamed Moalin et al.
Molecules (Basel, Switzerland), 16(11), 9636-9650 (2011-11-23)
The polyphenol quercetin (Q) that has a high antioxidant capacity is a lead compound in the design of antioxidants. We investigated the possibility of modifying quercetin while retaining its antioxidant capacity as much as possible. To this end, the antioxidant

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