Chemical Structure : ALT-007
Catalog No.: PC-23850Not For Human Use, Lab Use Only.
ALT-007 is a potent, selective and orally bioavailable inhibitor of serine palmitoyltransferase (SPT) with enzyme IC50 of 0.54 nM.
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ALT-007 is a potent, selective and orally bioavailable inhibitor of serine palmitoyltransferase (SPT) with enzyme IC50 of 0.54 nM.
ALT-007 potently inhibited both SPT enzyme (IC50 =1.2 nM) and HCC4006 cell growth (IP = 3.9 nM).
ALT-007 displayed potent growth inhibitory activity against both HCC4006 and PL-21 cells on the same level with Myriocin.
ALT-007 is an orally bioavailable SPT inhibitor with in vivo antitumor efficacy, which provides a useful tool for assessing the pharmaceutical potential of SPT inhibitors especially against cancer.
M.Wt | 533.51 | |
Formula | C25H26F3N5O5 | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Poisson J, et al. ACS Pharmacol Transl Sci. 2024 Dec 29;8(1):203-215.
2. Kojima T, et al. Bioorg Med Chem. 2018 May 15;26(9):2452-2465.
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