S80325 |
GSK2879552 |
源葉(MedMol) | 98% |
品牌 | 貨號 | 產(chǎn)品規(guī)格 | 價格(RMB) | 庫存(上海) | 北京 | 武漢 | 南京 | 數(shù)量 | 計量單位 | 加入購物車... |
---|---|---|---|---|---|---|---|---|---|---|
源葉(MedMol) | S80325-2mg | 98% | ¥360.00元 | 預計交期:2-3天 | - | - | - | EA | 加入購物車 | |
源葉(MedMol) | S80325-5mg | 98% | ¥700.00元 | 預計交期:2-3天 | - | - | - | EA | 加入購物車 | |
源葉(MedMol) | S80325-10mg | 98% | ¥1250.00元 | 預計交期:2-3天 | - | - | - | EA | 加入購物車 | |
源葉(MedMol) | S80325-25mg | 98% | ¥2520.00元 | 預計交期:2-3天 | - | - | - | EA | 加入購物車 | |
源葉(MedMol) | S80325-100mg | 98% | ¥8540.00元 | 預計交期:2-3天 | - | - | - | EA | 加入購物車 |
- 提示:詳情請下載說明書。
- 產(chǎn)品描述: GSK2879552 an orally active, selective and irreversible inhibitor of lysine specific demethylase 1 (LSD1/ KDM1A), with potential antineoplastic activity
- 靶點: Histone Demethylase;HistoneDemethylase
- 體內(nèi)研究:
GSK2879552 (1.5 mg/kg, p.o.) treatment exhibits tumor growth inhibition in SCLC xenograft bearing mice. Animal Model: NCI-H526 and NCI-H1417 xenografts. Dosage: 1.5 mg/kg. Administration: PO daily for 25-35 days. Result: There was 57% and 83% tumor growth inhibition (TGI) in NCI-H526 and NCI-H1417 tumor bearing mice respectively. NCI-H510 and NCI-H69 tumor bearing mice also demonstrated partial TGI (38% and 49% respectively) in response to GSK2879552, while no significant TGI was observed for SHP77 bearing mice.
- 參考文獻:
1. Huang M, et al. Targeting KDM1A attenuates Wnt/β-catenin signaling pathway to eliminate sorafenib-resistant stem-like cells in hepatocellular carcinoma. Cancer Lett. 2017 Apr 2;398:12-21 2. Mohammad HP, et al. A DNA Hypomethylation Signature Predicts Antitumor Activity of LSD1 Inhibitors in SCLC. Cancer Cell. 2015 Jul 13;28(1):57-69.
- 溶解性: Soluble in DMSO
- 保存條件: -20℃
- 配置溶液濃度參考:
1mg 5mg 10mg 1 mM 2.744 ml 13.718 ml 27.436 ml 5 mM 0.549 ml 2.744 ml 5.487 ml 10 mM 0.274 ml 1.372 ml 2.744 ml 50 mM 0.055 ml 0.274 ml 0.549 ml
- 注意:部分產(chǎn)品我司僅能提供部分信息,我司不保證所提供信息的權(quán)威性,僅供客戶參考交流研究之用。
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質(zhì)量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)
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