Chemical Structure : GSK-F1
CAS No.: 1402345-92-9
Catalog No.: PC-26709Not For Human Use, Lab Use Only.
GSK-F1 is a potent, selective phosphatidylinositol 4-kinase type IIIα (PI4KA) inhibitor with pIC50 of 8.0, also directly binds to NSUN2 and promote its proteasomal degradation.
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|---|---|---|---|
| 5 mg | $158 | In stock | |
| 10 mg | $248 | In stock | |
| 25 mg | $428 | In stock | |
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GSK-F1 is a potent, selective phosphatidylinositol 4-kinase type IIIα (PI4KA) inhibitor with pIC50 of 8.0, also directly binds to NSUN2 and promote its proteasomal degradation.
GSK-F1shows selectivity over PI4KB, PI3KA, PI3KB, PI3KG and PI3KD.
GSK-F1 activates the downstream TP53/RAD51 signaling axis and increasing NPC cell cytotoxicity and radiosensitivity.
| M.Wt | 603.52 | |
| Formula | C27H18F5N5O4S | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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| Chemical Name/SMILES |
5-(2-Amino-4-oxo-3-(2-(trifluoromethyl)phenyl)-3,4-dihydroquinazolin-6-yl)-N-(2,4-difluorophenyl)-2-methoxypyridine-3-sulfonamide |
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1. Bojjireddy N, et al. J Biol Chem. 2014 Feb 28;289(9):6120-32.
2. Lemei Zheng, et al. Int J Biol Sci. 2026 Mar 30;22(8):4043-4058.

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