A2AR-agonist-1
CAS No. 41552-95-8
A2AR-agonist-1 ( N-(2-(1H-Indol-3-yl)ethyl)adenosine )
产品货号. M26042 CAS No. 41552-95-8
A2AR-agonist-1 是一种有效的 A2AR 和 ENT1 激动剂(A2AR 和 ENT1 的 Ki 值:4.39 和 3.47)。它以腺苷 A2A 受体和腺苷转运蛋白为神经保护作用。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥1644 | 有现货 |
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| 10MG | ¥2366 | 有现货 |
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| 25MG | ¥3692 | 有现货 |
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| 50MG | ¥4920 | 有现货 |
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| 100MG | ¥6570 | 有现货 |
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| 200MG | ¥8802 | 有现货 |
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| 500MG | 获取报价 | 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 | ¥1530 | 有现货 |
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生物学信息
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产品名称A2AR-agonist-1
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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A2AR-agonist-1 是一种有效的 A2AR 和 ENT1 激动剂(A2AR 和 ENT1 的 Ki 值:4.39 和 3.47)。它以腺苷 A2A 受体和腺苷转运蛋白为神经保护作用。
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产品描述A2AR-agonist-1 is a potent A2AR and ENT1 agonist (Ki: 4.39 and 3.47 for A2AR and ENT1. It targets the Adenosine A2A Receptor and Adenosine Transporter for Neuroprotection.
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体外实验——
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体内实验——
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同义词N-(2-(1H-Indol-3-yl)ethyl)adenosine
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通路Others
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靶点Other Targets
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受体PPARγ
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研究领域——
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适应症——
化学信息
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CAS Number41552-95-8
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分子量410.434
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分子式C20H22N6O4
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 100 mg/mL (243.65 mM)
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SMILESOC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(NCCc3c[nH]c4ccccc34)ncnc12
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化学全称——
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
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CGGRGD
CGGRGD is a RGD derivative with cysteine as the n-terminal. CGGRGD was synthesized by solid phase peptide synthesis technology, and amino2-cyanobenzothiazole (2-cyanobenzothiazole) (2-cyanobenzothiazole (CBT) was added on the surface of PCL fiber for ammoniation.
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Isoangustone A
Isoangustone A has antitumor activity, it can induce G1 cycle arrest in DU145 human prostate and 4T1 murine mammary cancer cells, it inhibits cell proliferation by targeting PI3K, MKK4, and MKK7 in human melanoma.
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3-Hydroxybakuchiol
3-Hydroxybakuchiol exerts cytotoxic and anti-proliferative effects on the TA3/Ha mouse mammary adenocarcinoma cell line and induces a decrease in the mitochondrial transmembrane potential, the activation of caspase-3, the opening of the mitochondrial permeability transport pore (MPTP) and nuclear DNA fragmentation.3-Hydroxybakuchiol has antitumor activity resulting from interactions with the ETC, a system that is already deficient in cancer cells.
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