Chemical Structure : BM-51
Catalog No.: PC-27980Not For Human Use, Lab Use Only.
BM-51 is a potent, specific inhibitor of cytochrome P450 enzyme CYP4Z1 with IC50 of 91.7 nM, shows high selectivity against CYP4 isozymes (>100 folds).
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BM-51 is a potent, specific inhibitor of cytochrome P450 enzyme CYP4Z1 with IC50 of 91.7 nM, shows high selectivity against CYP4 isozymes (>100 folds).
BM-51 attenuatees the tumor-initiating cells (TICs)-like traits of breast cancer cells.
BM-51 suppresses the progression and the function of PyMT-induced TICs in PyMT-CYP4Z1-KI mice and chemosensitivity of breast cancer cells.
BM-51 significantly inhibits the tumor-initiating ability of breast cancer cells and expression of stemness markers.
CYP4Z1 promotes breast cancer progression by enhancing TIC-like traits, promoting a de-differentiated and invasive phenotype, and reprogramming lipid metabolism.
| M.Wt | 285.39 | |
| Formula | C17H23N3O | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Yuan Y, et al. Exp Mol Med. 2026 Jul;58(7):2202-2222.

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