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在色谱分析、有机合成和交叉偶联反应领域已被 0 篇同行评审文献引用。
VT02956 is a LATS inhibitor ( IC 50 : 0.76 nM for LATS1, 0.52 nM for LATS2). VT02956 targets the Hippo pathway. VT02956 inhibits ESR1 expression and growth of ER+ breast cancer cell lines and patient-derived tumor organoids.
IC50& Target:IC50: 0.76 nM for LATS1, 0.52 nM for LATS2
In Vitro:VT02956 (2 μM, 0-30 min) reduces YAP/TAZ phosphorylation in HEK293A cells and 4T1 cells. VT02956 (2 μM, 2 days) reduces ERα and its target genes TFF1 and GREB1 in breast tumor organoids BTO-02. VT02956 (2 μM, 4 days) inhibits the proliferation o
Biological Activity:VT02956 is a LATS inhibitor ( IC 50 : 0.76u2009nM for LATS1, 0.52u2009nM for LATS2). VT02956 targets the Hippo pathway. VT02956 inhibits ESR1 expression and growth of ER+ breast cancer cell lines and patient-derived tumor organoids.