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目錄:MedChemExpress LLC>>生化試劑>> TA-02 | MCE

TA-02 | MCE
  • TA-02 | MCE
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CAS 1784751-19-4 純度 99.57%
分子量 333.33 分子式 C??H??F?N?
供貨周期 現(xiàn)貨 規(guī)格 1 mg
貨號 HY-100115 應(yīng)用領(lǐng)域 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥
TA-02 | MCETA-02, an analog of SB 203580 (HY-10256), is a <b>p38 MAPK</b> inhibitor with an <b>IC<sub>50</sub></b> of 20 nM. TA-02 especially inhibits TGFBR-2. TA-02 exhibits similar cardiogenic properties as SB 203580 and SB 202190 (HY-10295)<sup>[1]</sup>.

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TA-02

CAS No. : 1784751-19-4

產(chǎn)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).

研究領(lǐng)域:MAPK/ERK Pathway  |  Autophagy

作用靶點(diǎn):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 ?expression 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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