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Pixatimod(亦称PG-545)是一种合成糖类改良的肝素硫酸仿生物及Toll样受体9(TLR9)的激动剂,具有潜在的免疫增强、抗肿瘤和抗病毒作用。Pixatimod (PG545) 强效地通过破坏刺突蛋白-ACE2相互作用抑制SARS-CoV-2。此外,Pixatimod阻断多种促癌过程,包括细胞增殖、侵袭、转移、血管生成和上皮-间充质转化。这些作用在多种不同的小鼠癌症模型中展现出强大的效力,包括约30种异种移植模型和20种同种移植模型。Pixatimod已与多种批准的抗癌化合物联合测试,展示了其临床潜力,包括与gemcitabine、paclitaxel、sorafenib、铂类化合物及抗PD-1抗体合用。
Pixatimod(亦称PG-545)是一种合成糖类改良的肝素硫酸仿生物及Toll样受体9(TLR9)的激动剂,具有潜在的免疫增强、抗肿瘤和抗病毒作用。Pixatimod (PG545) 强效地通过破坏刺突蛋白-ACE2相互作用抑制SARS-CoV-2。此外,Pixatimod阻断多种促癌过程,包括细胞增殖、侵袭、转移、血管生成和上皮-间充质转化。这些作用在多种不同的小鼠癌症模型中展现出强大的效力,包括约30种异种移植模型和20种同种移植模型。Pixatimod已与多种批准的抗癌化合物联合测试,展示了其临床潜力,包括与gemcitabine、paclitaxel、sorafenib、铂类化合物及抗PD-1抗体合用。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | 询价 | 期货 | |
50 mg | 询价 | 期货 |
产品描述 | Pixatimod (also known as PG-545) is a synthetic carbohydrate-modified heparan sulfate mimetic and a Toll-like receptor 9 (TLR9) agonist. It exhibits potential immunostimulatory, antitumor, and antiviral effects. Pixatimod effectively inhibits SARS-CoV-2 by disrupting the spike protein-ACE2 interaction. Additionally, it blocks various cancer-promoting processes such as cell proliferation, invasion, metastasis, angiogenesis, and epithelial-mesenchymal transition. These effects have demonstrated significant efficacy in numerous mouse cancer models, including about 30 xenograft models and 20 syngeneic models. Pixatimod has been tested in combination with several approved anticancer compounds, showing clinical potential when used with gemcitabine, paclitaxel, sorafenib, platinum compounds, and anti-PD-1 antibodies. |
别名 | CHEMBL2059499, 99N289ZQ8L |
分子量 | 2363.82 |
分子式 | C51H75Na13O60S13 |
CAS No. | 1144492-69-2 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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