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GSK2879552

    
≥98%

GSK2879552

源葉(MedMol)
S80325 一鍵復制產品信息
1401966-69-5
C23H28N2O2
364.4806
4-((4-((((1R,2S)-2-phenylcyclopropyl)amino)methyl)piperidin-1-yl)methyl)benzoic acid; GSK2879552; GSK-2879552;
貨號 規格 價格 上海 北京 武漢 南京 購買數量
S80325-2mg
≥98% ¥360.00 貨期:2-3天 - - -
S80325-5mg
≥98% ¥700.00 貨期:2-3天 - - -
S80325-10mg
≥98% ¥1250.00 貨期:2-3天 - - -
S80325-25mg
≥98% ¥2520.00 貨期:2-3天 - - -
S80325-100mg
≥98% ¥8540.00 貨期:2-3天 - - -
產品介紹 參考文獻 質檢證書(COA) 摩爾濃度計算器 相關產品

產品介紹

GSK2879552 an orally active, selective and irreversible inhibitor of lysine specific demethylase 1 (LSD1/ KDM1A), with potential antineoplastic activity

產品描述: 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: 部分產品我司僅能提供部分信息,我司不保證所提供信息的權威性,僅供客戶參考交流研究之用。

參考文獻

質檢證書(COA)

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請輸入貨號和一個與之匹配的批號。
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批號:JS298415 貨號:S20001-25g
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摩爾濃度計算器

質量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)

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