PI3K-IN-2 |
| カタログ番号GC36907 |
PI3K-IN-2 (化合物 10) は、強力な経口活性 PI3Kβ/δ (IC50=7.1/8.6 nM) 阻害剤であり、PI3Kσ および PI3Kγ (それぞれ IC50=13/190 nM) に対して優れた選択性を示します。
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 1403458-28-5
Sample solution is provided at 25 µL, 10mM.
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PI3K-IN-2 (compound 10) is a potent and orally active PI3Kβ/δ (IC50=7.1/8.6 nM) inhibitor with excellent selectivity versus PI3Kσ and PI3Kγ (IC50=13/190 nM, respectively)[1]. PI3Kα|13 nM (IC50)|PI3Kβ|7.1 nM (IC50)|PI3Kδ|190 nM (IC50)|PI3Kγ|8.6 nM (IC50)
PI3K-IN-2 (compound 10) shows PI3Kβ cell IC50 1.1 nM in phosphatase and tensin homolog (PTEN) null MDA-MB-468 cell and PI3Kδ cell IC50 14 nM in Jeko-1 B-cell[1].
PI3K-IN-2 shows profound pharmacodynamic modulation of AKT phosphorylation in PTEN-deficient PC3 prostate tumour bearing mice after oral administration and gave significant inhibition of tumour growth in the same xenograft model[1].
[1]. Barlaam B, et al. Discovery of a series of 8-(1-phenylpyrrolidin-2-yl)-6-carboxamide-2-morpholino-4H-chromen-4-one as PI3Kβ/δ inhibitors for the treatment of PTEN-deficient tumours. Bioorg Med Chem Lett. 2017 May 1;27(9):1949-1954.
Average Rating: 5 (Based on Reviews and 5 reference(s) in Google Scholar.)
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