CNDAC hydrochloride
目录号: PL04620 纯度: ≥99%
CAS No. :134665-72-8
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中文名称
CNDAC hydrochloride
中文别名
4-氨基-1-(2-氰基-2-脱氧-beta-D-呋喃阿拉伯糖基)-2(1H)-嘧啶酮单盐酸盐
英文名称
CNDAC hydrochloride
英文别名
2(1H)-Pyrimidinone,4-amino-1-(2-cyano-2-deoxy-b-D-arabinofuranosyl)-, hydrochloride (1:1);(2R,3S,4S,5R)-2-(4-amino-2-oxopyrimidin-1-yl)-4-hydroxy-5-(hydroxymethyl)oxolane-3-carbonitrile,hydrochloride;2'-cyano-2'-deoxyarabinofuranosylcytosine;2(1H)-Pyrimidinone, 4-amino-1-(2-cyano-2-deoxy-beta-D-arabinofuranosyl)-, monohydrochloride;2'-Cyano-2'deoxy-1-beta-D-arabinofuranosylcytosine;4-Amino-1-(2-cyano-2-deoxy-beta-D-arabinofuranosyl)-2(1H)-pyrimidinone monohydrochloride;4-amino-1-(2-cyano-2-deoxy-beta-D-arabinofuranosyl)pyrimidin-2(1H)-one hydrochloride;CNDAC;CNDAC hydrochloride
Cas No.
134665-72-8
分子式
C10H12N4O4.HCl
分子量
288.69
包装储存
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
产品详情
CNDAC hydrochloride 是可口服试剂 Sapacitabine (HY-16445) 的代谢物,为核苷酸类似物。CNDAC hydrochloride 诱导 DNA 损伤和凋亡 (apoptosis)。
生物活性
CNDAC hydrochloride is a metabolite of the orally active agent Sapacitabine (HY-16445), and a nucleoside analog. CNDAC hydrochloride induces DNA damage and apoptosis.
性状
Solid
体外研究(In Vitro)
CNDAC 有一个独特的作用机制: 进入 DNA 后,它诱导单链断裂 (SSBs),当细胞经历第二个 S 期时,单链断裂 (SSBs) 转化为双链断裂 (DSBs)。
缺乏 Rad51D 和 XRCC3 可使细胞对 CNDAC (0-1 μM; 24 h) 敏感。
CNDAC (0-100 μM; 3 days) 抑制 HL-60 和 THP-1 细胞的增殖。
CNDAC (0-10 μM; 3-6 days) 诱导 HL-60 和 THP-1 细胞的凋亡。
CNDAC (6 μM; 48 h) 诱导 HCT116 细胞在延迟 S 期后的 G2 期停止细胞周期。 has not independently confirmed the accuracy of these methods. They are for reference only.Cell Viability Assay
体内研究(In Vivo)
CNDAC (20mg/kg; i.p.; daily for 10 days) 显示小鼠抗肿瘤活性。 has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: CDF1 mice, P388 tumor model
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
参考文献
[1]. Liu XJ, et al. Sapacitabine, the prodrug of CNDAC, is a nucleoside analog with a unique action mechanism of inducing DNA strand breaks. Chin J Cancer. 2012 Aug;31(8):373-80.
[2]. Jagan S, et al. Bone Marrow and Peripheral Blood AML Cells Are Highly Sensitive to CNDAC, the Active Form of Sapacitabine. Adv Hematol. 2012;2012:727683.
溶解度数据
In Vitro: DMSO : 125 mg/mL (432.99 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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