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黄芩素,491-67-8,分析标准品,≥98%
品牌 | 厂商性质 | 产地 | 货期 |
---|---|---|---|
阿拉丁 | 总代理 | 中国 | 现货 |
性能特点
Baicalein is a cell-permeable flavone, originally isolated from the roots of Scutellaria baicale
货号 | 规格 | CAS号 | 价格 | 操作 |
---|---|---|---|---|
B107323-20mg | 20mg | 491-67-8 | ¥86.90 | 询底价 |
中文名:黄芩素
英文名:Baicalein
中文别名:三羟黄酮
英文别名:SpecPlus_000758|Spectrum5_001418|W-202870|baicalein|BAICALEIN [WHO-DD]|MFCD00017459|SDCCGMLS-0066744.P001|NCGC00025282-01|NCGC00025282-02|NCGC00025282-03|BAICALEIN [INCI]|Baicalein, 98%|HMS3412F14|HMS3655P18|MLS002473007|NCGC00017236-03|NSC661431|NSC-6614
纯度:分析标准品,≥98%
货号:B107323
Cas号:491-67-8
存储温度:2-8°C储存
产品介绍:
Baicalein is a cell-permeable flavone, originally isolated from the roots of Scutellaria baicalensis, that inhibits cellular Ca2+ uptake, calcium mobilization, and adjuvant-induced arthritis. Baicalein has been shown to inhibit platelet 5-LO (5-lipoxygenase) (IC50=9.5 mM) and 12-LO (12-lipoxygenases) (IC50=0.12 mM) and reverse transcriptase. Baicalein reduces leukotriene biosynthesis and inhibits the release of lysosomal enzymes. Baicalein is a potent anti-inflammatory and anti-tumor agent, and it blocks PREP (prolyl oligopeptidase). Baicalein induces the S-phase arrest and apoptosis in proliferation of human lung squamous carcinoma CH27 cells. The declining expression of cdk1, cdk2, cyclin D2 and cyclin A by Baicalein resulted in the G1 and G2 cell cycle arrest in C6 rat glioma cells. Baicalein has anti-thrombotic, antiproliferative and anti-mitogenic effects. Baicalein inhibits protein tyrosine kinase in leukemia (CEM) cells and PMA-stimulated PKC (protein kinase C). Baicalein is an inhibitor of 15-LO and CYP2C9.An inhibitor of Ca2+ uptake, 5-LO, and 12-LO
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注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途