NG-52
CAS No. 212779-48-1
NG-52 ( Compound 52 )
产品货号. M13385 CAS No. 212779-48-1
NG 52 (Compound 52 ) 是一种有效的、细胞可渗透的、可逆的、选择性的、ATP 相容的细胞周期调节激酶抑制剂。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥681 | 有现货 |
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| 5MG | ¥1121 | 有现货 |
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| 10MG | ¥2052 | 有现货 |
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| 25MG | ¥3432 | 有现货 |
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| 50MG | ¥4920 | 有现货 |
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| 100MG | ¥6741 | 有现货 |
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| 500MG | ¥13410 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥1226 | 有现货 |
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生物学信息
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产品名称NG-52
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述NG 52 (Compound 52 ) 是一种有效的、细胞可渗透的、可逆的、选择性的、ATP 相容的细胞周期调节激酶抑制剂。
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产品描述NG 52 (Compound 52 ) is a potent, cell-permeable, reversible, selective, and ATP-compatible inhibitor of the cell cycle-regulating kinase, Cdc28p (IC50 = 7 μM).
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体外实验Cell Proliferation Assay Cell Line:Glioma U87 and U251 cells Concentration:0 μM, 12.5 μM, 25 μM, 50 μM Incubation Time:6 days Result:Potently inhibited the proliferation of primary glioma cells.Western Blot Analysis Cell Line:Glioma U87 and U251 cells Concentration:0 μM, 12.5 μM, 25 μM, 50 μM Incubation Time:12 hours or 24 hours Result:Potently inhibited the proliferation of primary glioma cells.
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体内实验Animal Model:Female nu/nu mice (5-week-old) injected with glioma cells Dosage:50 mg/kg, 100 mg/kg, 150 mg/kg Administration:Oral administration; daily; for 13 daysResult:Dose-dependently suppressed the growth of glioma xenograft.
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同义词Compound 52
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通路Angiogenesis
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靶点CDK
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受体Cdc28p
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研究领域Cancer
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适应症——
化学信息
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CAS Number212779-48-1
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分子量346.81
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分子式C16H19ClN6O
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纯度>98% (HPLC)
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溶解度DMSO: > 100mM
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SMILESCC(C)N1C2=NC(NCCO)=NC(NC3=CC=CC(Cl)=C3)=C2N=C1
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化学全称2-((6-((3-chlorophenyl)amino)-9-isopropyl-9H-purin-2-yl)amino)ethan-1-ol
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.ray NS, et al. Science. 1998 Jul 24;281(5376):533-8.
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