Chemical Structure : Lysosome inhibitor LLAD
Catalog No.: PC-25859Not For Human Use, Lab Use Only.
LLAD is a long-term lysosome-targeting anticancer drug, inhibits SLC38A9 in lysosomes and alkalinizes lysosomes, induces apoptosis through long-term lysosomal damage in vivo and in vitro.
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LLAD is a long-term lysosome-targeting anticancer drug, inhibits SLC38A9 in lysosomes and alkalinizes lysosomes, induces apoptosis through long-term lysosomal damage in vivo and in vitro.
LLAD exhibited a potent binding ability with SLC38A9 with SPR KD of 1.29 uM.
LLAD shows anti-proliferation activity with IC50 of 26.66 uM in A549 cells and 2.478 uM in HL-60 cells.
directly inhibit the activity of SLC38A9, inhibits mTOR signaling pathway and phosphorylation of mTOR and the substrates S6 kinase (S6K).
LLAD induces lysosomal damage (lysosomal stress response, LSR) by long-term retention.
LLAD (2.5 mg/kg) exhibited excellent long-term anticancer effect in HeLa xenograft mouse model.
| M.Wt | 401.47 | |
| Formula | C22H23N7O | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Zhao S, et al. Acta Pharm Sin B. 2025 Nov;15(11):5867-5879.

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