CAS: | 72509-76-3 | ||||||
分子式: | C18H19Cl2NO4 | ||||||
分子量: | 384.25 | ||||||
熔点: | 142-145°C | ||||||
中文名称: |
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英文名称: |
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用途: | 用于治疗高血压、心胶痛、充血性心衰竭、对各种程度的高血压都有效。 |
货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | 详情 | ||||||||||||||||||||||||||||||||||||||||||||||||
F793788 | MACKLIN | 非洛地平 | 10mM in DMSO | 545元/1ml; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||
储存:-20°C | |||||||||||||||||||||||||||||||||||||||||||||||||||||
F810243 | MACKLIN | 非洛地平 | ≥98.0% | 98元/1g; 214元/5g; 739元/25g; 2026元/100g; 8998元/500g; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||
储存:2~8°C 状态:白色到黄色到黄绿色固体 | |||||||||||||||||||||||||||||||||||||||||||||||||||||
F0814 | TCI | Felodipine | >98.0%(HPLC)(N) | 890元/1G; 2990元/5G; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||
基本信息
技术规格
物性(参考值)
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相关法规
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360407 | J&K | Felodipine | 98%, 一种选择性L型Ca2+通道阻滞剂 | 201元/1g; 802元/5G; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||
基本信息
产品描述 Felodipine 是一种选择性L型Ca2+通道阻断剂,IC50为0.15 nM。 靶点(IC50 & Targe) L-type calcium channel,0.15nM 与多种其他Ca2+通道阻断剂不同, Felodipine对心脏没有副作用,因为Felodipine选择特异性作用于与心肌组织相关的血管平滑肌。 体外研究 Felodipine显著放松KCl收缩的猪冠状动脉节段,IC50为0.15 nM,通过阻断Ca2+通道,比Nifedipine(IC50 为~8 nM)效果强50倍,比Verapamil(IC50为~65 nM)效果强430倍。[1] Felodipine作用于初级人类VSMC和肺成纤维细胞,显著诱导IL-6和IL-8转录和分泌,ED50分别为 5.8 nM和5.3 nM,而Propranolol或 Furosemide 不能影响这两种IL基因表达。[2] Felodipine作用于豚鼠回肠纵平滑肌(GPILSM),阻断毒蕈碱性受体调节的(carbachol)Ca2+依赖性收缩,IC50为1.45 nM。[3] Felodipine为0.1 μM低浓度时,作用于大鼠内皮细胞,提高NOx产生, Ca2+依赖性NOS活性, 和eNOS蛋白。[4] Felodipine (10 μM) 降低p42/44分裂原活化蛋白激酶核易位和PDGF-BB刺激的Elk-1激活,导致人SMC增殖受抑制。[5] Felodipine 稍微抑制Cav3.2 T型Ca2+通道,IC50为6.8 μM。[6] 体内研究 Felodipine口服处理5/6肾脏消融大鼠,显著降低平均血压(BP)。[7] Felodipine作用于主动脉壁,通过阻断NF-κB激活, 和降低巨噬细胞显著降低收缩压(SBP), 血清胰岛素, 细胞内粘附分子-1(ICAM-1)和血管细胞黏附分子-1(VCAM-1),导致血管炎症反应受调节。[8] 动物实验 Animal Models: 5/6肾脏消融的雄性Sprague-Dawley大鼠 Formulation: 溶于DMSO,在盐水中稀释 Dosages: 1 g/kg/day Administration: 口服处理 (Only for Reference) 参考文献 [1] Johnson JD, et al. J Pharmacol Exp Ther, 1983, 226(2), 330-334. [2] R?dler S, et al. J Mol Cell Cardiol, 1995, 27(10), 2295-2302. [3] Yiu S, et al. J Med Chem, 1996, 39(23), 4576-4582. [4] Ding Y, et al. Hypertension, 1998, 32(4), 718-723. [5] Yang Z, et al. Cardiovasc Res, 2002, 53(1), 227-231. [6] Perez-Reyes E, et al. J Pharmacol Exp Ther, 2009, 328(2), 6 安全信息
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F0030000 | Felodipine | European Pharmacopoeia (EP) Reference Standard | 1277.32元/ ; | 展开 | |||||||||||||||||||||||||||||||||||||||||||||||||
产品说明 一般描述 This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia. 生化/生理作用 L-type calcium channel blocker 包装 Unit quantity: 100 mg. Subject to change. The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue. 注意 Please find SDS provided by EDQM here.. 其他说明 Sales restrictions may apply. 基本信息
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F9677 | Sigma-Aldrich | Felodipine | solid | 1237.51元/5 MG; 5271.44元/25 MG; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||
产品说明 一般描述 Felodipine is a dihydropyridine derivative. It has diuretic properties. Felodipine has high vascular selectivity. It is used to treat hypertension. Felodipine regulates chronic stable angina. 生化/生理作用 L-type calcium channel blocker 特点和优势 This compound was developed by AstraZeneca. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here. 基本信息
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1269389 | USP | Felodipine | United States Pharmacopeia (USP) Reference Standard | 3231.47元/300 MG; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||
产品说明 一般描述 This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia. 生化/生理作用 L-type calcium channel blocker 分析说明 These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind. 其他说明 Sales restrictions may apply. 基本信息
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BP777 | Felodipine | British Pharmacopoeia (BP) Reference Standard | 1916.08元/100 MG; | 展开 | |||||||||||||||||||||||||||||||||||||||||||||||||
产品说明 一般描述 This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia. For further information and support please go to the website of the issuing Pharmacopoeia. 生化/生理作用 L-type calcium channel blocker 包装 Unit quantity: 100 mg. Subject to change. The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity please visit British Pharmacopoeia 其他说明 Sales restrictions may apply. 基本信息
产品性质
安全信息
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BP758 | Felodipine impurity standard | British Pharmacopoeia (BP) Reference Standard | 2978.17元/20 MG; | 展开 | |||||||||||||||||||||||||||||||||||||||||||||||||
产品说明 一般描述 This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia. For further information and support please go to the website of the issuing Pharmacopoeia. 生化/生理作用 L-type calcium channel blocker 包装 Unit quantity: 20 mg. Subject to change. The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity please visit British Pharmacopoeia 其他说明 Sales restrictions may apply. 基本信息
产品性质
安全信息
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M06306 | Fluorochem | Felodipine | >99% | 2068元/1g; 6842元/5g; 20636元/25g; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||
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