| 價格 | ¥41.90 | ¥473.90 | ¥1544.90 |
| 包裝 | 1g | 25g | 100g |
| 最小起訂量 | 1g |
| 發(fā)貨地 | 上海 |
| 更新日期 | 2026-06-10 |
| 中文名稱:鹽酸去甲烏藥堿 | 英文名稱:Higenamine hydrochloride |
| CAS:11041-94-4 | 品牌: 阿拉丁 |
| 產(chǎn)地: 上海 | 保存條件: 避光,-20°C儲存,充氬 |
| 純度規(guī)格: ≥99% | 產(chǎn)品類別: 小分子和化合物庫 |
| 分子式: C16H18ClNO3 | 分子量: 307.77 |
| 運輸條件: 超低溫運輸 | 產(chǎn)品規(guī)格: 100g、1g、25g |
| 貨號: H413084 | 是否進口: 否 |
中文名:鹽酸去甲烏藥堿
英文名:Higenamine hydrochloride
純度:≥99%
貨號:H413084
Cas號:11041-94-4
存儲溫度:避光,-20°C儲存,充氬
運輸條件:超低溫運輸
產(chǎn)品介紹:
Information
Higenamine (Norcoclaurine, (+-)-Demethylcoclaurine), also known as Norcoclaurine HCl, is a non-selectiveβ2 adrenoceptoragonist which is a chemical compound naturally occurring in a number of plants.
Targets
β2-adrenoceptor ; α1-adrenoceptor
In vitro
Higenamine is a potential β2-adrenoceptor agonist. As a potent cardiotonic and vasodilator, It is also an α1 antagonist and a weak α2 agonist. Higenamine decreases the intracellular dopamine content dose-dependently and shows 55.2% inhibition of dopamine content in PC12 cells at a concentration of 2OM with 24h incubation. The IC50 value of higenamine for inhibiting dopamine biosynthesis in PC12 cells is 18.2 μM. Dopamine content is lowered and reaches minimal level at 12—24h after exposure to higenamine.
In vivo
Higenamine can produce relaxation in tracheal muscle. Higenamine has anti-thrombotic effects in both mouse acute thrombosis model and rat arterio-venous shunt (AV-shunt) models. The oral administration of higenamine (50 or 100 mg/kg) increases the recovery rates from the acute thrombotic challenge in mice and lowers the weight of thrombus formed inside the AV-shunt tube in rats.
Cell Research(from reference)
Cell lines:PC12 cells?
Concentrations:5-20 μM?
Incubation Time:12-48 h?
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| 成立日期 | 2009-03-16 (18年) | 注冊資本 | 14130.676萬人民幣 |
| 員工人數(shù) | 500人以上 | 年營業(yè)額 | ¥ 1億以上 |
| 主營行業(yè) | 生物化工,化學(xué)試劑 | 經(jīng)營模式 | 工廠,試劑 |
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