チロホスチンAG 879
- ¥24500 - ¥46000
- 化學(xué)名: チロホスチンAG 879
- 英語名: TYRPHOSTIN AG 879
- 別名:チロホスチンAG 879
- CAS番號(hào): 148741-30-4
- 分子式: C18H24N2OS
- 分子量: 316.46
- EINECS:
- MDL Number:MFCD00236450
2物価
選択條件:
ブランド
- 富士フイルム和光純薬株式會(huì)社(wako)
- Sigma-Aldrich Japan
パッケージ
- 5mg
- 10mg
- 生産者富士フイルム和光純薬株式會(huì)社(wako)
- 製品番號(hào)W01TOC2617
- 製品説明
- 英語製品説明AG 879
- 包裝単位10mg
- 価格¥46000
- 更新しました2021-03-23
- 購(gòu)入
- 生産者Sigma-Aldrich Japan
- 製品番號(hào)T2067
- 製品説明チロホスチンAG 879 99% (HPLC)
- 英語製品説明Tyrphostin AG 879 99% (HPLC)
- 包裝単位5mg
- 価格¥24500
- 更新しました2023-06-01
- 購(gòu)入
生産者 | 製品番號(hào) | 製品説明 | 包裝単位 | 価格 | 更新時(shí)間 | 購(gòu)入 |
---|---|---|---|---|---|---|
富士フイルム和光純薬株式會(huì)社(wako) | W01TOC2617 | AG 879 |
10mg | ¥46000 | 2021-03-23 | 購(gòu)入 |
Sigma-Aldrich Japan | T2067 | チロホスチンAG 879 99% (HPLC) Tyrphostin AG 879 99% (HPLC) |
5mg | ¥24500 | 2023-06-01 | 購(gòu)入 |
プロパティ
沸點(diǎn) :432.7±55.0 °C(Predicted)
比重(密度) :1.127±0.06 g/cm3(Predicted)
貯蔵溫度 :Keep in dark place,Sealed in dry,Store in freezer, under -20°C
溶解性 :DMSO: at 26 mg/mlsoluble
酸解離定數(shù)(Pka) :9.63±0.70(Predicted)
外見 :Orange-yellow solid
色 :Yellow
安定性: :Stable for 1 year as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 3 months.
比重(密度) :1.127±0.06 g/cm3(Predicted)
貯蔵溫度 :Keep in dark place,Sealed in dry,Store in freezer, under -20°C
溶解性 :DMSO: at 26 mg/mlsoluble
酸解離定數(shù)(Pka) :9.63±0.70(Predicted)
外見 :Orange-yellow solid
色 :Yellow
安定性: :Stable for 1 year as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 3 months.
安全情報(bào)
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注意喚起語: | Warning | ||||||||||||||||||||||||||||||||||||||||||
危険有害性情報(bào): |
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注意書き: |
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説明
Protein tyrosine kinase (PTK) inhibitors are potential antiproliferative agents for diseases caused by the hyperactivity of PTKs. Tyrphostins are a class of antiproliferative compounds which selectively inhibit PTKs of key growth factors. AG-879 is a tyrphostin compound that inhibits nerve growth factor (NGF)-dependent TrkA tyrosine phosphorylation in PC-12 cells (IC50 = ~40 μM), HER2-ErbB2 kinase in several breast and ovarian cancer cell lines (IC50 = ~0.5 μM), and the VEGF receptor FLK1 (IC50 = ~1 μM). Additionally, AG-879 inhibits the activation of ETK with an IC50 value of ~5 nM, which blocks tyrosine phosphorylation of PAK1, suppressing Ras transformation of NIH 3T3 fibroblasts. AG-879 has also been shown to suppress IL-6-induced tyrosine phosphorylation of STAT3 (IC50 = 15 μM) in schwannoma cells.関連商品価格
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