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Protogracillin
CAS No. 54848-30-5
Protogracillin ( —— )
产品货号. M27957 CAS No. 54848-30-5
Protogracillin 是从薯蓣 (DZW) 中分离出来的一种甾体皂苷,可抑制血小板聚集 (PAG) 和血栓形成。 DZW 根茎中的类固醇皂苷具有通过抗血栓作用降低心血管疾病风险的潜力。
纯度: >98% (HPLC)
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规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥1158 | 有现货 |
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5MG | ¥2001 | 有现货 |
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10MG | ¥2981 | 有现货 |
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25MG | ¥4828 | 有现货 |
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50MG | ¥6990 | 有现货 |
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100MG | ¥9396 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Protogracillin
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Protogracillin 是从薯蓣 (DZW) 中分离出来的一种甾体皂苷,可抑制血小板聚集 (PAG) 和血栓形成。 DZW 根茎中的类固醇皂苷具有通过抗血栓作用降低心血管疾病风险的潜力。
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产品描述Protogracillin is a steroidal saponin isolated from Dioscorea zingiberensis Wright (DZW) which may inhibit platelet aggregation (PAG) and thrombosis. Steroidal saponins from DZW rhizomes have the potential to reduce the risk of cardiovascular diseases by anti-thrombotic action.(In Vitro):Paris polyphylla J.E. Smith is extensively used in traditional systems of Indian and Chinese medicines mainly for its anticancerous property. The national and international demand for P. polyphylla is constantly increasing and most of the supplies come from wild. Illegal and unscientific exploitation coupled with habitat destruction decreases the natural population of the herb, as a consequence this species comes under vulnerable category. Restoration and conservation of the natural population of this potential herb is prerequisites. METHODS AND RESULTS: This article aims to provide an overview on chemical and biological prospective of P. polyphylla. Secondary metabolites such as daucosterol, polyphyllin D, β -ecdysterone, Paris saponins I, II, V, VI, VII, H, dioscin, oligosaccharides, heptasaccharide, octasaccharide, trigofoenoside A, Protogracillin, Paris yunnanosides G-J, padelaoside B, pinnatasterone, formosanin C and 20-hydroxyecdyson saponins have been isolated from P. polyphylla. Several biological activities such as anticancerous, antitumor, cytotoxic, anthelmintic, antimicrobial, antiangiogenic, immunostimulating, contractile and hemostatic have also been reported. CONCLUSIONS: Consequently, this review will be helpful to the researcher and scientist for further research.
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体外实验——
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体内实验——
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同义词——
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通路Others
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靶点Other Targets
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受体Ca(2+) receptor
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研究领域——
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适应症——
化学信息
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CAS Number54848-30-5
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分子量1065.2
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分子式C51H84O23
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : ≥ 100 mg/mL (93.88 mM)
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SMILESO[C@H]1[C@H](OC[C@H](C)CC[C@]2(O)[C@@H](C)[C@]3([H])[C@](CC4)(C)[C@](C[C@]3([H])O2)([H])[C@@]5([H])[C@@]4([H])[C@](CC[C@H](O[C@H](O[C@H](CO)[C@H]6O)[C@H](O[C@H](O[C@H]7C)[C@H](O)[C@H](O)[C@H]7O)[C@H]6O[C@@H]([C@H](O)[C@H]8O)O[C@H](CO)[C@H]8O)C9)(C)C9=CC5)O[C@H](CO)[C@H]([C@@H]1O)O
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Sewing KF, et al. Calcium channel antagonists verapamil and gallopamil are powerful inhibitors of acid secretion in isolated and enriched guinea pig parietal cells. Pharmacology. 1983;27(1):9-14.
产品手册
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