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1357349-91-7

中文名稱 1-(1-Methylethyl)-3-(2-phenylethynyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine
英文名稱 1-(1-Methylethyl)-3-(2-phenylethynyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine
CAS 1357349-91-7
分子式 C16H15N5
分子量 277.32
MOL 文件 1357349-91-7.mol
更新日期 2024/10/25 11:12:40
1357349-91-7 結(jié)構(gòu)式 1357349-91-7 結(jié)構(gòu)式

基本信息

中文別名
化合物SPP-86
英文別名
SPP 86
SPP86 >=98% (HPLC)
1-(1-Methylethyl)-3-(2-phenylethynyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine
1H-Pyrazolo[3,4-d]pyrimidin-4-amine, 1-(1-methylethyl)-3-(2-phenylethynyl)-

物理化學(xué)性質(zhì)

沸點(diǎn)495.3±40.0 °C(Predicted)
密度1.23±0.1 g/cm3(Predicted)
儲(chǔ)存條件-20°C儲(chǔ)存
溶解度溶于二甲基亞砜
酸度系數(shù)(pKa)3.95±0.30(Predicted)
形態(tài)Solid
顏色Off-white to light yellow
1-(1-Methylethyl)-3-(2-phenylethynyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱CAS號(hào)包裝價(jià)格
2024/08/19HY-1101931-(1-Methylethyl)-3-(2-phenylethynyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine
SPP-86
1357349-91-71mg480元
2024/08/19HY-1101931-(1-Methylethyl)-3-(2-phenylethynyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine
SPP-86
1357349-91-75mg1200元
2024/08/19HY-1101931-(1-Methylethyl)-3-(2-phenylethynyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine
SPP-86
1357349-91-710mM * 1mLin DMSO1320元

常見(jiàn)問(wèn)題列表

生物活性
SPP-86 是一種選擇性的 RET 酪氨酸激酶的有效抑制劑,其 IC50 值為 8 nM。SPP-86 抑制 MCF7 細(xì)胞中 RET 誘導(dǎo)激活的 PI3K/Akt 和 MAPK 信號(hào)通路,也能抑制 RET 誘導(dǎo)的 ERα 磷酸化。
靶點(diǎn)

IC50: 8 nM (RET).

體外研究

SPP86 (0-10 μM) inhibits MAPK signaling and proliferation in RET/PTC1 expressing TPC1 but not 8505C or C643 cells.
SPP86 (0-10 μM) inhibits RET- induced phosphatidylinositide 3-kinases (PI3K)/Akt and MAPK signaling and estrogen receptorα (ERα) phosphorylation in MCF7 cells.

Western Blot Analysis

Cell Line: Thyroid cancer derived cell lines expressing the RET/PTC1 rearrangement (TPC1), BRAF V600E (8505C) or RAS G13R (C643) mutations.
Concentration: 0-10 μM.
Incubation Time: 90 min.
Result: Inhibited RET- induced ERK1/2 phosphorylation in thyroid cancer cell lines.

Western Blot Analysis

Cell Line: MCF7 cells (human breast cancer).
Concentration: 0-10 μM.
Incubation Time: 30 min.
Result: Inhibited RET- induced ERα phosphorylation and proliferation in MCF7 cells.
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