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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
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].


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产品链接:www.medchemexpress.cn/Flavopiridol.html

Purity:98%
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
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