聯(lián)系電話
參考價(jià): | 面議 |
- IPA1033 產(chǎn)品型號(hào)
- 品牌
- 生產(chǎn)商 廠商性質(zhì)
- 上海市 所在地
訪問次數(shù):414更新時(shí)間:2023-03-15 09:42:09
- 聯(lián)系人:
- 曹女士
- 電話:
- 400-6111-883
- 手機(jī):
- 售后:
- 4006-111-883
- 傳真:
- 86-21-34615995
- 地址:
- 上海市浦東新區(qū)天雄路166弄1號(hào)3樓
- 網(wǎng)址:
- www.yeasen.com
掃一掃訪問手機(jī)商鋪
OSU-03012,≥99%
【英文同義名】:AR-12, OSU 03012, OSU03012, N/AAR-12.
【中文同義名】:
訂購(gòu)信息:(*,常備現(xiàn)貨)
品 牌 | 產(chǎn)品名稱 | 產(chǎn)品貨號(hào) | 規(guī) 格 | 目錄價(jià)(元) |
Gene Operation | OSU-03012 | IPA1033-0005MG | 5 mg | ¥569.00 |
IPA1033-0025MG | 25 mg | ¥1769.00 | ||
IPA1033-0050MG | 50 mg | ¥3389.00 | ||
IPA1033-0100MG | 100 mg | ¥5989.00 |
產(chǎn)品描述
是一種可口服的,PDK-1抑制劑,IC50為5μM,并且比OSU-02067要高出2倍的效能[1]。體外研究證明能抑制Huh7, Hep3B和HepG2等細(xì)胞系的生長(zhǎng)。還能夠通過抑制PDK/AKT信號(hào)通路,誘導(dǎo)非小細(xì)胞肺癌和乳腺癌細(xì)胞的凋亡[2,3,4]。另外,體內(nèi)研究顯示,具有良好的耐受性并在九周后抑制了55%的HMS-97神經(jīng)鞘瘤移植瘤的生長(zhǎng)。因此,被認(rèn)為是一種潛在VS和惡性神經(jīng)鞘瘤的化學(xué)治療藥物 [5]。
靶點(diǎn)
Targets | PDK-1 |
IC50 | 5μM[1] |
化學(xué)特性
Cas No.: 742112-33-0 | M. Wt.: 460.45 |
Formula: C26H19F3N4O | Purity: ≥99% |
Synonym: AR-12, OSU 03012, OSU03012, N/AAR-12. | |
Chemical Name: 2-amino-N-(4-(5-(phenanthren-2-yl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)phenyl)acetamide | |
Appearance: White to off-white solid | |
Solubility: Soluble in DMSO (11 mg/ml) | |
Storage:Store powder at -20 ºC for the stability of three years. |
結(jié)構(gòu)式
Reference
[1]Zhu J, et al. From the Cyclooxygenase-2 Inhibitor Celecoxib to a Novel Class of 3-Phosphoinositide-Dependent Protein Kinase-1 Inhibitors.Cancer Res, 64(12), 4309-4318(2004).
[2] Gao M, et al. , a novel celecoxib derivative, induces reactive oxygen species-related autophagy in hepatocellular carcinoma. Cancer Res. 68(22):9348-57(2008).
[3] Wang YC, et al. Targeting endoplasmic reticulum stress and Akt with and gefitinib or erlotinib to overcome resistance to epidermal growth factor receptor inhibitors. Cancer Res. 68(8):2820-30(2008).
[4] Kucab JE, et al. Celecoxib analogues disrupt Akt signaling, which is commonly activated in primary breast tumours. Breast Cancer Res. 7(5):R796-807(2005).
[5] Lee TX, et al. Growth inhibitory and anti-tumour activities of , a novel PDK-1 inhibitor, on vestibular schwannoma and malignant schwannoma cells. Eur J Cancer. 45(9):1709-20.