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  • 黄芪皂苷 IV|T2973

黄芪皂苷 IV|T2973

Astragaloside IV
84687-43-4
230 5mg 起订
393 10mg 起订
658 25mg 起订
上海 更新日期:2024-12-02

TargetMol中国(陶术生物)

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产品详情:

中文名称:
黄芪皂苷 IV
英文名称:
Astragaloside IV
CAS号:
84687-43-4
品牌:
TargetMol
产地:
美国
保存条件:
Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
纯度规格:
99.84%
产品类别:
抑制剂
货号:
T2973

Product Introduction

Bioactivity

名称Astragaloside IV
描述Astragaloside IV (AS-IV), an active component isolated from Astragalus membranaceus, suppresses the activation of ERK1/2 and JNK, and downregulates matrix metalloproteases (MMP)-2, (MMP)-9 in MDA-MB-231 breast cancer cells. Astragaloside IV is a bioactive saponin first isolated from the dried plant roots of the genus Astragalus, which is used in traditional Chinese medicine.1 It dose-dependently inhibits human adenovirus type 3 (HAdV-3) in A549 cells (IC50 = 23 μM; LC50 = 865 μM).It inhibits replication of HAdV-3 and decreases HAdV-3-induced apoptosis. It has diverse protective effects for the cardiovascular, immune, digestive, and nervous systems. In particular, it reduces myocardial infarct size in dogs when administered prior to coronary ligation and reduces reperfusion arrhythmias in isolated rat hearts.
细胞实验CCK-8 assay is adopted to determine cell viability. cultured NSCLC cells are seeded into 96-well plates at the density of 4×104 (cells/well). Then 10 μL?well CCK8 solution is added and incubated in dark at 37°C for another 2 h. The absorbance is determined with the wavelength of 490 nm.
激酶实验MDA-MB-231 cells treated as indicated or tumor tissues are harvested and lysed in Mg2+ lysis buffer containing 50 mM Tris (pH 7.5), 10 mM MgCl2, 0.5 M NaCl, and protease inhibitor cocktail. Equal amounts of lysates are incubated with PAK-PBD beads at 4°C for 1 h. PAK-PBD beads are pelleted by centrifugation and washed with ish buffer containing 25 mM Tris (pH 7.5), 30 mM MgCl2, 40 mM NaCl. Active Rac1 is detected by western blotting.
动物实验Transient cerebral ischemia and reperfusion is prepared by BCCAO. Mice are randomly divided into the Sham, Model, Astragaloside IV (10 mg/kg) and Astragaloside IV (20 mg/kg) treatment groups. The Astragaloside IV treatment groups are intragastrically administered 7 days before the surgery and terminated on the day of sacrifice. On the day of the surgery, Astragaloside IV is administrated 2 h prior to ischemia. The Sham-operated and Model groups are treated with distilled water. After the mice are anesthetized with an intraperitoneal injection of chloral hydrate (350 mg/kg), the bilateral common carotid arteries are exposed and carefully separated with a small ventral neck incision and occluded twice (20 min each) with ligated surgical silk as described previously with minor modifications. There is a 10 min reperfusion period between the two occlusion periods (ischemia 20 min ? reperfusion 10 min ? ischemia 20 min). Sham-operated mice are subjected to the same surgical operation without the surgical silk ligation. Mouse body temperature is maintained at 37±0.5°C during the surgery with heating equipment until recovery from the anesthesia.
体外活性Astragaloside IV对MDA-MB-231乳腺癌细胞的活性和侵袭性产生抑制作用,能够压抑丝裂原活化蛋白激酶(MAPK)家族成员ERK1/2和JNK的激活,并下调金属蛋白酶(MMP)-2和-9的表达。在NSCLC细胞生长抑制方面,Astragaloside IV(10、20、40 ng/mL)显示出明显的作用,而低浓度Astragaloside IV(1、2.5、5 ng/mL)对细胞活性无明显细胞毒性。此外,Astragaloside IV与化疗化合物顺铂联合治疗显著提高了NSCLC细胞对化疗化合物的敏感性。在分子水平上,Astragaloside IV与顺铂联合使用显著抑制了B7-H3的mRNA和蛋白水平的表达。
体内活性在小鼠模型中,高剂量的Astragaloside IV组在48小时存活率上显示出显著增加[60%(9/15)对比13.3%(2/15), P<0.05],血清ALT和AST水平显著降低(P<0.01),肝脏组织病理学指数及肝细胞凋亡程度显著降低(P<0.01),以及肝匀浆中MDA含量显著减少(P<0.01),SOD活性显著增加。Astragaloside IV(10, 20 mg/kg, p.o.)显著地预防了短暂脑缺血及再灌注所诱导的认知缺陷。与模型组相比,Astragaloside IV(10 mg/kg)和Astragaloside IV(20 mg/kg)能显著降低这些细胞因子的水平。Astragaloside IV明显抑制了TLR4及其下游蛋白的水平,表明MyD88依赖性和非依赖性途径在Astragaloside IV的抗炎作用中发挥了重要作用。此外,Astragaloside IV减少了NLRP3和活化的caspase-1的表达,同时也降低了Iba1蛋白的表达。
存储条件Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
溶解度DMSO : 50 mg/mL (63.7 mM), Sonication is recommended.
关键字JNK | Extracellular signal regulated kinases | Inhibitor | MMP | inhibit | Astragaloside IV | ERK | Matrix metalloproteinases
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黄芪皂苷 IV|||黄芪甲苷IV|||AST-IV|||AS-IV|TargetMol

公司简介

上海陶术生物科技有限公司为美国Target Molecule Corp. ( Target Mol ) 在上海建立的全资子公司。我们与美国波士顿、德国慕尼黑的同事一起,为北美、欧洲和亚洲从事药物研发和生物学研究的科学家提供优质的产品和专业的服务。公司下设筛选事业部,化学事业部,生物事业部和新材料部。 从虚拟筛选到实体化合物分子供应;从商业化产品销售到个性化定制合成;从对明确靶点的分子筛选到对明确分子的多靶点筛选,从高通量筛选到化学结构优化,我们都可以满足您的科研用品及技术服务的需求。 经过在中国市场五年的精心耕耘,我们已成为筛选化合物领域优秀的供应商,为超过五百家学校和各类企业提供了品质卓越的小分子化合物和药物筛

成立日期 (12年)
注册资本 566.2651万人民币
员工人数 100-500人
年营业额 ¥ 1亿以上
经营模式 贸易,试剂,定制,服务
主营行业 化学试剂,生物活性小分子

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