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首页-小分子抑制剂&激动剂-Others-Other Targets-JX-078
JX-078

Chemical Structure : JX-078

CAS No.: 3010898-81-1

JX-078 (JX078)

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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纯度 & COA & 质检文件 纯度: >98% (HPLC)

生物&药学活性

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.

物理化学性质&存储条件

分子量 373.45
分子式 C24H23NO3
外观性状 Solid
CAS No.
储存条件
固体粉末
-20°C 12 个月; 4°C 6 个月
配置液
-80°C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

7-([1,1'-biphenyl]-2-ylmethoxy)-2-amino-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid

参考文献

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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