目录:MedChemExpress LLC>>生化试剂>> TA-02 | MCE
CAS | 1784751-19-4 | 纯度 | 99.57% |
---|---|---|---|
分子量 | 333.33 | 分子式 | C₂₀H₁₃F₂N₃ |
供货周期 | 现货 | 规格 | 1 mg |
货号 | HY-100115 | 应用领域 | 医疗卫生,化工,生物产业,制药/生物制药 |
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CAS No. : 1784751-19-4
产品活性:TA-02, an analog of SB 203580 (HY-10256), is a p38 MAPK inhibitor with an IC50 of 20 nM. TA-02 especially inhibits TGFBR-2. TA-02 exhibits similar cardiogenic properties as SB 203580 and SB 202190 (HY-10295).
研究领域:MAPK/ERK Pathway | Autophagy
作用靶点:p38 MAPK | Autophagy
In Vitro: TA-02 (5 μM) inhibits the phosphorylation of proteins downstream of p38α MAPK such asMAPKAPK2 and HSP27 during cardiogenesis. TA-02 at 5 μM concentration induces cardiogenesis, but also increases ATF-2 phosphorylation and MEF2C õexpression in contrast to what would be expected with a mechanism dependent on p38α MAPK inhibition.
TA-02 induces T/Brachyury whereas SB203580 addition increased MESP1 and T/Brachyury transcripts.
TA-02 significantly induces high NKX2-5 expression when applied between days 0-8.
TA-02 is found to inhibit multiple targets with similar potency to p38α MAPK, such as p38α, p38β, JNK3, JNK2, CIT, CK1ε, DMPK2, JNK1, DDR1 CK1δ, MEK5, and ERBB2.
TA-02 and SB203580 reduce the nuclear TCF/LEF-1 driven transcription of luciferase similar to DKK-1.
TA-02 (5 nM-5 μM) inhibits p38 and increases the anti-inflammation effects of BDNF on inflammation in vitro.
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