Varenicline
CAS No. 866823-63-4
Varenicline ( —— )
产品货号. M19196 CAS No. 866823-63-4
Varenicline 是一种选择性 α4β2 烟碱乙酰胆碱受体部分激动剂。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥591 | 有现货 |
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| 10MG | ¥941 | 有现货 |
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| 25MG | ¥1544 | 有现货 |
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| 50MG | ¥2688 | 有现货 |
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| 100MG | ¥3852 | 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 | ¥562 | 有现货 |
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生物学信息
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产品名称Varenicline
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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Varenicline 是一种选择性 α4β2 烟碱乙酰胆碱受体部分激动剂。
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产品描述Varenicline is a Selective α4β2 nicotinic acetylcholine receptor partial agonist.(In Vitro):Varenicline (1 μM, 24 h ) inhibits LPS-Induced cytokine secretions (IL-1β, IL-6, and TNF α) and cell proliferation rate in RAW 264.7 macrophages.Varenicline (250 nM) evokes action potentials (Aps) in the absence of ACh stimulation in Human adrenal chromaffin cells isolated from male and female organ donors.Varenicline (100 μM, 4 h) promotes migration of HUVECs by lowering the protein expression of VE-cadherin.(In Vivo):Varenicline (Subcutaneous injection, 0.01-1 mg/kg, 3 days) given 10 min prior to nicotine (0.5 mg/kg, s.c.) inhibits nicotine conditioned place preference (CPP).Varenicline (Subcutaneous injection, 2.5 mg/kg, 3 days) results in a place aversion which is dependent on α5 nAChRs but not β2 nAChRs.Varenicline (Subcutaneous injection, 0.1 and 0.5 mg/kg, 3 days) reverses nicotine withdrawal signs such as hyperalgesia and somatic signs and withdrawal-induced aversion in a dose-related manner.
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体外实验Cell Viability Assay Cell Line:HUVEC Concentration:100, 200, 300, 500 μM Incubation Time:24 h Result:Did not affect cell viability at 100 and 200 μM (96.8 ± 0.1% and 93.9 ± 1.8%, respectively). Decreased cell viability to 85.7 ± 7.5% and 57.8 ± 7.7% for 300 and 500 μM, respectively.Western Blot Analysis Cell Line:HUVEC Concentration:100 μM Incubation Time:1, 5, 10, 15 ,30 ,60 min, 24 h Result:Significantly activated ERK1/2 and p38 signaling with peak activity at 10–15 min and 10–30 min after treatment, respectively, lowered expression of VE-cadherin at 24 h. MLA (100 nM) significantly reversed the Varenicline-induced effects.Cell Migration Assay Cell Line:HUVEC Concentration:100, 200, 300, 500 μM Incubation Time:4 h Result:Significantly increased the number of migrating cells by 2.4-fold compared with vehicle treatment. MLA (100 nM) completely blocked Varenicline-stimulated migration.
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体内实验——
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同义词——
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通路Endocrinology/Hormones
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靶点AChR
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受体α4β2 nAChR
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研究领域Neurological Disease
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适应症——
化学信息
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CAS Number866823-63-4
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分子量284.18
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分子式C13H15Cl2N3
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 62.5 mg/mL (219.93 mM)
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SMILESCl.Cl.c1c4c(cc2nccnc12)C3CC4CNC3
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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
产品手册
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