Chemical Structure : TNG917
货号: PC-26996Not For Human Use, Lab Use Only.
TNG917 is a potent, selective, histone substrate-competitive, orally active dual inhibitor of EHMT1/2, shows high selectivity over other methyltransferases.
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TNG917 is a potent, selective, histone substrate-competitive, orally active dual inhibitor of EHMT1/2, shows high selectivity over other methyltransferases.
TNG917 relieved H3K9-mediated repression, restored interferon-stimulated gene expression, and triggered secretion of T-cell chemoattractant cytokines, including CXCL10, in cancer cells.
TNG917 monotherapy led to marked tumor growth inhibition, while combination with anti-PD1 therapy produced complete, durable regressions and established protective immune memory in both syngeneic and humanized mouse models.
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| 外观性状 | Solid | |
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| Solubility |
10 mM in DMSO |
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1. Lu AZ, et al. Cancer Res. 2026 Jun 10. doi: 10.1158/0008-5472.CAN-25-4720.
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