Tulopafant 是血小板激活因子 (PAF) 拮抗剂。 Flavopiridol产品描述:Flavopiridol is a broad inhibitor of CDK, competing with ATP to inhibit CDKs including CDK1, CDK2, CDK4 and CDK6 with IC50 of around 40 nM.IC50 & Target: IC50: 40 nM (CDK)In Vitro: Flavopiridol (2 μM) robustly induces a distinct pattern of ER stress in CLL cells that contributes to cell death through IRE1-mediated activation of ASK1 and possibly downstream caspases[1]. Flavopiridol results in potent upregulation of a number of PRGs in treatments lasting 4-24 h. Flavopiridol has and immediate and long-term effect on the expression of several PRGs. In serum starved cells re-stimulated with serum, flavopiridol also inhibits the expression of these genes, but subsequently, JUNB, GADD45B and EGR1 are upregulated in the presence of flavopiridol[2]. 公司介绍:MedChemExpress(MCE)专注于各种抑制剂、激动剂、API及化合物库,总部位于美国新泽西,分别在瑞典和上海设有欧洲区子公司和亚洲区总代理,营销网点遍及全球20多个国家地区。MCE经过多年努力已成为全球生物活性小分子领域的一流供应商, 产品涵盖癌症、神经科学、抗感染、表观遗传学等20个热门研究领域,PI3K、MAPK等近千个细分靶点,超过4000个活性小分子化合物现货,以及GPCR、API、离子通道等超过20种不同类型的化合物库,同时提供从毫克到千克的专业定制合成服务。 MCE 对每批产品都进行严格的LCMS和NMR检验,其产品已被全球近万名客户广泛使用并发表大量文章、专利; MCE 定期增加各领域热门抑制剂、激动剂,不断扩增已有化合物库,以满足最新的科研需求; 数千种产品在上海有充足备货,24-48小时内送达客户; 大量产品提供免费试用装;已为全球多个知名企业、院校构建各种定制型化合物库。 产品链接:www.medchemexpress.cn/Flavopiridol.html ![]() MWt:425.5023 Formula:C25H19N3O2S SMILES:O=C(C(C=C1)=C2N1C(C3=CC=CN=C3)SC2)NC4=CC=CC(C(C5=CC=CC=C5)=O)=C4 Pathway:Others; Mechanisms:Others; Research Area:Cardiovascular Disease 电话: 021-58955995 网址: www.MedChemExpress.cn 地址: 上海市浦东新区蔡伦路720号2号楼3层 |
Tulopafant前沿研究进展
发布日期:2017-11-13 浏览次数:1
核心提示:Tulopafant 是血小板激活因子 (bPAF/b) 拮抗剂。BRa href=https://www.medchemexpress.cn/Flavopiridol.htmlFlavopiridol/a产品
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