- ￥375 - 3900
- MedChemExpress(MCE)
- 美国
- HY-101854
- 2025年12月05日
企业认证
相关产品推荐更多 >
万千商家帮你免费找货
0 人在求购买到急需产品
- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 英文名：
N6-Phenethyladenosine; N6-Phenylethyladenosine
- 库存：
货期：1-2天
- 供应商：
MedChemExpress LLC
- CAS号：
20125-39-7
- 规格：
10 mM * 1 mL/5 mg/10 mg/50 mg/100 mg
| 规格： | 10 mM * 1 mL | 产品价格： | ￥660.0 |
|---|---|---|---|
| 规格： | 5 mg | 产品价格： | ￥375.0 |
| 规格： | 10 mg | 产品价格： | ￥600.0 |
| 规格： | 50 mg | 产品价格： | ￥2200.0 |
| 规格： | 100 mg | 产品价格： | ￥3900.0 |
MCE 的所有产品仅用作科学研究或药证申报，我们不为任何个人用途提供产品和服务。
N6-(2-Phenylethyl)adenosine
CAS No. : 20125-39-7
MCE 国际站：N6-(2-Phenylethyl)adenosine
产品活性：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。
研究领域：GPCR/G Protein
作用靶点：Adenosine Receptor
In Vitro: N6-(2-Phenylethyl)adenosine (N6-Phenethyladenosine) inhibits rA2AR (IC50=560 nM), hA2AR (IC50=2250 nM) in CHO cells.
相关产品：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 | Heterocyclic Compound Library | Membrane Protein-targeted Compound Library | Membrane Receptor-targeted Compound Library | 5'-N-Ethylcarboxamidoadenosine | Theophylline | ZM241385 | CGS 21680 Hydrochloride | SCH 58261 | Etrumadenant | Istradefylline | Inosine | BAY 60-6583 | DPCPX | Ciforadenant | Imaradenant | Namodenoson | Piclidenoson | Regadenoson | MRS 1754 | PSB-603 | SCH442416 | Adenosine 5'-monophosphate monohydrate | Preladenant | MRS-1191 | Theobromine | MRS-1706 | Inupadenant | Ticlopidine hydrochloride | Acefylline | Aminophylline | Nitrobenzylthioinosine | Derenofylline | GR79236
热门产品线：重组蛋白 | 化合物库 | 天然产物 | 荧光染料 | PROTAC | 同位素标记物
Trending products：Recombinant Proteins | Bioactive Screening Libraries | Natural Products | Dye Reagents | PROTAC | Isotope-Labeled Compounds
风险提示：丁香通仅作为第三方平台，为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全，合理判断，谨慎选购商品，商家和用户对交易行为负责。对于医疗器械类产品，请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验Characterization of P1 (Adenosine) Purinoceptors
subtype. J. Med. Chem. 39:4142‐4148. Müller, C.E. and Jacobson, K.A. 2011. Recent developments in adenosine receptor ligands. and their potential as novel drugs. Biochim
Overview of Receptor Allosterism
of the binding of the agonist, [3 H] N6 ‐cyclohexyladenosine ([3 H]CHA) by the modulator PD 81,723 at the A1 adenosine receptor in rat brain membranes. Data taken from Bruns and Fergus (). (C ) Simulations based on a model of concomitant orthosteric
N6 ‐Isobutyryl‐5′‐O ‐(4,4′‐dimethoxytrityl)‐3′‐O ‐[(N,N ‐diisopropylamino)(2‐cyanoethyloxy)]phosphinyl‐2′‐O ‐(tert ‐butyldimethylsilyl)adenosine (ChemGenes) 5′‐O ‐(4,4′
技术资料暂无技术资料 索取技术资料
