Varenicline Tartrate
CAS No. 375815-87-5
Varenicline Tartrate ( CP 526,555-18 )
产品货号. M14295 CAS No. 375815-87-5
Varenicline Tartrate 是一种烟碱 AChR 部分激动剂,用于治疗尼古丁成瘾。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥275 | 有现货 |
|
| 10MG | ¥392 | 有现货 |
|
| 25MG | ¥693 | 有现货 |
|
| 50MG | ¥1144 | 有现货 |
|
| 100MG | ¥1791 | 有现货 |
|
| 500MG | ¥4302 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Varenicline Tartrate
-
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
-
产品简述Varenicline Tartrate 是一种烟碱 AChR 部分激动剂,用于治疗尼古丁成瘾。
-
产品描述Varenicline Tartrate is a nicotinic AChR partial agonist, used to treat nicotine addiction.
-
体外实验Cell Viability AssayCell 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 AnalysisCell Line:HUVECConcentration: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 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.
-
体内实验——
-
同义词CP 526,555-18
-
通路Endocrinology/Hormones
-
靶点AChR
-
受体mAChR
-
研究领域Neurological Disease
-
适应症——
化学信息
-
CAS Number375815-87-5
-
分子量361.35
-
分子式C13H13N3·C4H6O6
-
纯度>98% (HPLC)
-
溶解度Water: 72 mg/mL (199.25 mM); DMSO: 1 mg/mL (2.76 mM)
-
SMILESC1[C@@H]2CNC[C@H]1C3=CC4=NC=CN=C4C=C23.[C@@H]([C@H](C(=O)O)O)(C(=O)O)O
-
化学全称(6R,10S)-7,8,9,10-tetrahydro-6H-6,10-methanoazepino[4,5-g]quinoxaline (2R,3R)-2,3-dihydroxysuccinate
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1.Rollema H, et al. Neuropharmacology, 2007, 52(3), 985-994.
产品手册
关联产品
-
Piperidolate hydroch...
盐酸哌啶醇酯是一种抗毒蕈碱药,可抑制乙酰胆碱引起的异常活性。抑制乙酰胆碱引起的肠痉挛(大鼠和狗)。
-
Rhapontigenin
Rhapontigenin 是一种基于机制的细胞色素 P450 1A1 选择性灭活剂 (IC50: 400 nM),细胞色素 P450 1A1 是一种芳基烃羟化酶,可激活作为致癌物的多环芳烃。
-
α-Conotoxin AuIB
Selective antagonist of α3β4 nicotinic acetylcholine receptors. Displays > 100-fold selectivity over other receptor subunit combinations including α2β2, α2β4, α3β2, α4β2, α4β4 and α1β1γδ.
021-51111890
购物车()
sales@molnova.cn

