
Amlodipine Besylate
CAS No. 111470-99-6
Amlodipine Besylate ( Amlodipine besylate | Cardiorex | Cordarene )
产品货号. M10421 CAS No. 111470-99-6
苯磺酸氨氯地平是一种长效钙通道阻滞剂。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
500MG | ¥267 | 有现货 |
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1G | ¥405 | 有现货 |
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生物学信息
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产品名称Amlodipine Besylate
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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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产品简述苯磺酸氨氯地平是一种长效钙通道阻滞剂。
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产品描述Amlodipine Besylate is a long-acting calcium channel blocker.(In Vitro):Amlodipine besylate (20-40 μM; 48 h) reduces BrdU incorporation to 68.6% and 26.3% at concentrations of 20 and 30 μM in A431 cells, respectively.Amlodipine besylate (30 μM; pretreated for 1 h) significantly attenuates the uridine 5′-triphosphate (UTP)-induced increases of [Ca2+]i in A431 cells.Amlodipine besylate (30 μM) inhibits the store-operated Ca2+influx evoked by Thapsigargin in Fluo-3-loaded cells.(In Vivo):Amlodipine besylate (5 mg/kg/day; s.c. for 2 weeks) significantly decreases systolic blood pressure (SBP) in VSMC ATP2B1 KO mice.Amlodipine besylate (10 mg/kg; i.p. once daily for 20 days) causes a significant retardation of tumor growth and prolongs the survival of A431 tumor-bearing mice.
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体外实验Amlodipine besylate (20-40 μM; 48 h) reduces BrdU incorporation to 68.6% and 26.3% at concentrations of 20 and 30 μM in A431 cells, respectively.Amlodipine besylate (30 μM; pretreated for 1 h) significantly attenuates the uridine 5′-triphosphate (UTP)-induced increases of [Ca2+]i in A431 cells.Amlodipine besylate (30 μM) inhibits the store-operated Ca2+influx evoked by Thapsigargin in Fluo-3-loaded cells.
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体内实验Amlodipine besylate (5 mg/kg/day; s.c. for 2 weeks) significantly decreases systolic blood pressure (SBP) in VSMC ATP2B1 KO mice.Amlodipine besylate (10 mg/kg; i.p. once daily for 20 days) causes a significant retardation of tumor growth and prolongs the survival of A431 tumor-bearing mice. Animal Model:ATP2B1loxP/loxP mice Dosage:5 mg/kg/day Administration: Subcutaneously implanted osmotic pump for 2 weeks Result:Significantly decreased the blood pressure.
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同义词Amlodipine besylate | Cardiorex | Cordarene
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通路GPCR/G Protein
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靶点Calcium Channel
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受体Calcium Channel
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研究领域Cardiovascular Disease
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适应症——
化学信息
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CAS Number111470-99-6
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分子量567.05
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分子式C26H31ClN2O8S
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纯度>98% (HPLC)
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溶解度Ethanol: 14 mg/mL (24.68 mM); DMSO: 113 mg/mL (199.27 mM)
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SMILESO=C(C1=C(COCCN)NC(C)=C(C(OC)=O)C1C2=CC=CC=C2Cl)OCC.O=S(C3=CC=CC=C3)(O)=O
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化学全称3,5-Pyridinedicarboxylic acid, 2-((2-aminoethoxy)methyl)-4-(2-chlorophenyl)-1,4-dihydro-6-methyl-, 3-ethyl 5-methyl ester, (+-)-, monobenzenesulfonate
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
1. Lee YJ, et al. J Neurochem, 2011, 119(6), 1262-1270.
产品手册




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