價(jià)格 | ¥5580.81 |
包裝 | 1 MG |
最小起訂量 | 1MG |
發(fā)貨地 | 上海 |
更新日期 | 2023-10-27 |
中文名稱:GW1929 Calbiochem | CAS:196808-24-9 |
品牌: Sigma | 純度規(guī)格: A potent, tyrosine-based peroxisome proliferator-activated receptor γ (PPARγ) agonist (EC?? = 13 nM for murine receptor and 6.2 nM for human receptor in cell-based transactivation assays). |
產(chǎn)品編號 | 370695 |
品牌 | Sigma |
顏色 | yellow |
運(yùn)輸 | ambient |
測定 | ≥97% (NMR) |
警告 | Toxicity: Standard Handling (A) |
形式 | crystalline solid |
分子量 | 495.57 |
溶解性 | DMSO: 100?mg/mL |
儲存溫度 | ?20°C |
質(zhì)量水平 | 100 |
儲存條件 | OK to freeze protect from light |
別名
GW1929 - CAS 196808-24-9 - Calbiochem,PPAR Agonist V, PPARγ Agonist IV
一般描述
A potent, tyrosine-based peroxisome proliferator-activated receptor γ (PPARγ) agonist (EC50 = 13 nM for murine PPARγ and 6.2 nM for human PPARγ in cell-based transactivation assays). A potent, tyrosine-based peroxisome proliferator-activated receptor γ (PPARγ) agonist (EC50 = 13 nM for murine receptor and 6.2 nM for human receptor in cell-based transactivation assays).
生化/生理作用
Cell permeable: no
EC50 = 13 nM as peroxisome proliferator-activated receptor γ (PPARγ) agonist for murine receptor and 6.2 nM for human receptor in cell-based transactivation assays
Primary Target
Peroxisome proliferator-activated receptor γ (PPARγ) agonist
Product does not compete with ATP.
Reversible: no
重懸
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
其他說明
Han, S., et al. 2004. Clin. Cancer Res.10, 1911.
Willson, T.M., et al. 2000. J. Med. Chem.43, 527.
Brown, K.K., et al. 1999. Diabetes48, 1415.
成立日期 | 2005-12-27 (20年) | 注冊資本 | 600.0萬美元 |
員工人數(shù) | 100-500人 | 年?duì)I業(yè)額 | ¥ 1億以上 |
主營行業(yè) | 分析化學(xué),材料化學(xué),生物化工,化學(xué)試劑,催化劑 | 經(jīng)營模式 | 貿(mào)易,試劑,定制,服務(wù) |
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