Chemical Structure : HD202A
Catalog No.: PC-26314Not For Human Use, Lab Use Only.
HD202A is a highly potent, selective MNK1/2 inhibitor with IC50 of 6.1/8.1 nM respectively.
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HD202A is a highly potent, selective MNK1/2 inhibitor with IC50 of 6.1/8.1 nM respectively.
HD202A displays marked selectivity for MNK1/2 across a 140-kinase panel.
HD202A suppressed MNK-eIF4E signaling, downregulated perilipin 2 and stearoyl-coenzyme A desaturase 1, upregulated adipose triglyceride lipase and peroxisome proliferator-activated receptor gamma coactivator 1α, and enhanced mitochondrial fatty-acid oxidation and redox homeostasis.
HD202A markedly reduced body-weight gain, hepatic triglyceride accumulation, and serum lipids while improving glucose tolerance, insulin sensitivity, and inflammatory profiles.
| M.Wt | 456.57 | |
| Formula | C25H24N6OS | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Qiu T, et al. J Med Chem. 2026 Mar 9. doi: 10.1021/acs.jmedchem.5c03316.

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