Kinetin riboside
CAS No. 4338-47-0
Kinetin riboside ( N6-Furfuryladenosine | FAdo )
产品货号. M14476 CAS No. 4338-47-0
一种细胞分裂素类似物,对各种人类癌细胞系表现出有效的抗增殖活性。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 25MG | ¥243 | 有现货 |
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| 100MG | 获取报价 | 有现货 |
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| 200MG | 获取报价 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Kinetin riboside
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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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产品简述一种细胞分裂素类似物,对各种人类癌细胞系表现出有效的抗增殖活性。
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产品描述A cytokinin analog that displays potent antiproliferative activity against various human cancer cell lines; inhibits MiPaCa-2 cell proliferation with IC50 of 0.27 uM; induceds marked suppression of CCND2 transcription and rapidly suppresses cyclin D1 and D2 protein expression in primary myeloma cells and tumor lines, causing cell cycle arrest, tumor cell-selective apoptosis, and inhibition of myeloma growth in xenografted mice; also can activate PINK1 in cells independent of mitochondrial depolarization.
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体外实验Kinetin riboside displays antiproliferative and apoptogenic activity against various human cancer cell lines. Kinetin riboside is able to inhibit the proliferation in HCT-15 human colon cancer cells in a dose-dependent manner (IC50=2.5 μM). Kinetin riboside induces apoptosis in HeLa and mouse melanoma B16F-10 cells. Kinetin riboside disrupts the mitochondrial membrane potential and induces the release of cytochrome c and activation of caspase-3. Bad are up-regulated while Bcl-2 is down-regulated under kinetin riboside exposure.
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体内实验Kinetin riboside significantly suppresses tumor growth. The most effective anti-melanoma response is elicited at 40 mg/kg.
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同义词N6-Furfuryladenosine | FAdo
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通路Apoptosis
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靶点Apoptosis
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受体Apoptosis
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研究领域——
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适应症——
化学信息
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CAS Number4338-47-0
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分子量347.32598
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分子式C15H17N5O5
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纯度>98% (HPLC)
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溶解度DMSO: ≥ 29 mg/mL
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SMILESO[C@H]1[C@H](N2C=NC3=C(NCC4=CC=CO4)N=CN=C23)O[C@H](CO)[C@H]1O
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化学全称Adenosine, N-(2-furanylmethyl)-
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. Osgerby L, et al. J Med Chem. 2017 Apr 27;60(8):3518-3524.
2. Tiedemann RE, et al. J Clin Invest. 2008 May;118(5):1750-64.
3. Hertz NT, et al. Cell. 2013 Aug 15;154(4):737-47.
4. Choi BH, et al. J Biol Chem. 2010 Mar 26;285(13):9770-9.
产品手册
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