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N6-(2-Phenylethyl)adenosine (Synonyms: N6-Phenethyladenosine; N6-Phenylethyladenosine) 纯度: 99.86%
N6-(2-Phenylethyl)adenosine (N6-Phenethyladenosine) 是一种腺苷衍生物,是有效的腺苷受体 (AR) 激动剂,对大鼠 A1AR,人 A1AR 和人 A3AR 的 Ki 值分别为 11.8 nM,30.1 nM,0.63 nM。
N6-(2-Phenylethyl)adenosine Chemical Structure
CAS No. : 20125-39-7
规格 | 价格 | 是否有货 | 数量 |
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10 mM * 1 mL in DMSO | ¥660 | In-stock | |
10 mg | ¥600 | In-stock | |
50 mg | ¥2200 | In-stock | |
100 mg | ¥3900 | In-stock | |
200 mg | ¥6900 | In-stock | |
500 mg | 询价 | ||
1 g | 询价 |
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N6-(2-Phenylethyl)adenosine 相关产品
•相关化合物库:
- Natural Product Like Compound Library
- Bioactive Compound Library Plus
- GPCR/G Protein Compound Library
- Immunology/Inflammation Compound Library
- Anti-Cancer Compound Library
- Small Molecule Immuno-Oncology Compound Library
- Nucleotide Compound Library
- Neurotransmitter Receptor Compound Library
生物活性 |
N6-(2-Phenylethyl)adenosine (N6-Phenethyladenosine), an adenosine derivative, is a potent adenosine receptors (AR) agonist with Ki values of 11.8 nM, 30.1 nM, 0.63 nM for rat A1AR, human A1AR and hA3AR, respectively[1]. |
IC50 & Target |
Ki: 11.8 nM (rA1AR), 30.1 nM (hA1AR) and 0.63 nM (hA3AR)[1] |
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体外研究 (In Vitro) |
N6-(2-Phenylethyl)adenosine (N6-Phenethyladenosine) inhibits rA2AR (IC50=560 nM), hA2AR (IC50=2250 nM) in CHO cells[1]. 上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only. |
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分子量 |
371.39 |
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Formula |
C18H21N5O4 |
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CAS 号 |
20125-39-7 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:
DMSO : 100 mg/mL (269.26 mM; Need ultrasonic) H2O : < 0.1 mg/mL (insoluble) 配制储备液
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请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo:
请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
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参考文献 |
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