CAS NO: | 288591-93-5 |
生物活性 | Leu-AMS (compound 6), a leucine analogue, is a potent inhibitor ofleucyl-tRNA synthetase(LRS) with anIC50of 22.34 nM, which inhibits the catalytic activity of LRS but did not affect the leucine-inducedmTORC1activation. Leu-AMS shows cytotoxicity incancercells and normal cells, and inhibits the growth of bacteria[1]. | ||||||||||||||||
IC50& Target | IC50: 22.34 nM (LRS)[1] | ||||||||||||||||
体外研究 (In Vitro) | Leu-AMS is proved to be a potent inhibitor of Leucyl-tRNA Synthetase (LRS) with an IC50value of 22.34 nM. Leu-AMS is highly cytotoxic in both cancer cells and normal cells. Leu-AMS does not affect S6 kinase (S6K) phosphorylation at all. Leu-AMS inhibits the catalytic activity of LRS but does not affect the leucine-induced mTORC1 activation[1]. | ||||||||||||||||
分子量 | 459.48 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C16H25N7O7S | ||||||||||||||||
CAS 号 | 288591-93-5 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : ≥ 49.17 mg/mL(107.01 mM) *"≥" means soluble, but saturation unknown. 配制储备液
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