 
                Chemical Structure : GH501
Catalog No.: PC-24401Not For Human Use, Lab Use Only.
GH501 is a small molecule inhibitor of Skp1-Skp2 interaction, may bind Skp1 and disrupts the physical interaction between Skp1 and S-phase kinase-associated protein 2 (Skp2) within the Skp1-Cullin1-F-box protein ubiquitin ligase complexes (SCF).
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	GH501 is a small molecule inhibitor of Skp1-Skp2 interaction, may bind Skp1 and disrupts the physical interaction between Skp1 and S-phase kinase-associated protein 2 (Skp2) within the Skp1-Cullin1-F-box protein ubiquitin ligase complexes (SCF).
	GH501 affects multiple oncogenic signals in mCRPC cells, affects multiple oncogenic signals implicated in mCRPC progression, including p21, p27, β-catenin, cyclin D1, enhancer of zeste homolog 2 (EZH2), c-Myc, and survivin.
	GH501 monotherapy inhibits the in vivo growth of mCRPC in multiple xenograft models.
| M.Wt | 605.79 | |
| Formula | C39H44FN3O2 | |
| Appearance | Solid | |
| Storage | 
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| Solubility | 10 mM in DMSO | |
1. Li X, et al. Br J Cancer. 2025 Apr 19. doi: 10.1038/s41416-025-02993-8.

 
                 
                 
                 
                 
                 
                 
                 
                 
            
            
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