Chemical Structure : JX-078
货号: PC-25184Not For Human Use, Lab Use Only.
JX-078 is a potent, selective inhibitor of L-type amino acid transporters LAT1 (SLC7A5), inhibits [3H]-L-leucine uptake into HT-29 cells with IC50 of 121 nM, >10-fold selective over in LAT2.
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JX-078 is a potent, selective inhibitor of L-type amino acid transporters LAT1 (SLC7A5), inhibits [3H]-L-leucine uptake into HT-29 cells with IC50 of 121 nM, >10-fold selective over in LAT2.
JX-078 induces differential metabolomic changes in human PBMCs upon incubation in blood.
JX-078 induces significantly different metabolomic changes in LAT1-expressing cells.
JX-078 exerts antiproliferative effects in cancer cells independent of LAT1.
分子量 | 373.45 | |
分子式 | C24H23NO3 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
1. Yan R, et al. Cell Discov. 2021 Mar 23;7(1):16.
2. Morozova V, et al. Biomed Pharmacother. 2025 Jul 31;190:118402.
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