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首页-小分子抑制剂&激动剂-PI3K/Akt/mTOR Pathway-PI3K-PF-06843195
PF-06843195

Chemical Structure : PF-06843195

CAS No.: 2067281-51-8

PF-06843195 (PF06843195)

货号: PC-49021Not For Human Use, Lab Use Only.

PF-06843195 is a potent, selective PI3Kα inhibitor with Ki value of <0.018 nM, IC50 of 18 nM (RAT1 PI3Kα), with cellular isoform selectivity of 20-fold over PI3Kβ and 9-fold over PI3Kδ.

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

PF-06843195 is a potent, selective PI3Kα inhibitor with Ki value of <0.018 nM, IC50 of 18 nM (RAT1 PI3Kα), with cellular isoform selectivity of 20-fold over PI3Kβ and 9-fold over PI3Kδ.
PF-06843195 also demonstrated high selectivity over mTOR.
PF-06843195 is a potent inhibitor of both PI3Kα (Ki< 0.018 nM) and PI3Kδ (Ki< 0.28 nM), but found to be 9-fold selective for PI3Kα over PI3Kδ in cell assays.
PF-06843195 is selective over two other members of the class I catalytic PI3K kinase group, PI3Kβ and PI3Kγ, >100- and >10 000-fold, respectively, in biochemical assays and 20-fold selective over PI3Kβ in cell assays.

物理化学性质&存储条件

分子量 498.467
分子式 C20H25F3N8O4
外观性状 Solid
CAS No.
储存条件
固体粉末
-20°C 12 个月; 4°C 6 个月
配置液
-80°C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

2,2-difluoroethyl (3S)-3-{[2'-amino-5-fluoro-2-(morpholin-4-yl)-4,5'-bipyrimidin-6-yl]amino}-3-(hydroxymethyl)pyrrolidine-1-carboxylate

参考文献

1. Cheng H, et al. J Med Chem. 2021 Jan 14;64(1):644-661.

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