SR-57227 hydrochloride
CAS No. 77145-61-0
SR-57227 hydrochloride ( SR 57227 | SR57227 )
产品货号. M15917 CAS No. 77145-61-0
SR-57227 是一种高亲和力、选择性 5-HT3 受体激动剂,在体内具有抗惊厥作用。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥356 | 有现货 |
|
| 5MG | ¥583 | 有现货 |
|
| 10MG | ¥915 | 有现货 |
|
| 25MG | ¥1725 | 有现货 |
|
| 50MG | ¥2989 | 有现货 |
|
| 100MG | ¥4447 | 有现货 |
|
| 500MG | ¥9639 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称SR-57227 hydrochloride
-
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SR-57227 是一种高亲和力、选择性 5-HT3 受体激动剂,在体内具有抗惊厥作用。
-
产品描述SR-57227 is a high affinity, selective 5-HT3 receptor agonist, demonstrates anticonvulsant effects in vivo.Depression Discontinued.
-
体外实验SR 57227A binds to 5-HT3 receptors labelled with [3H]S-zacopride with an affinity (Ki) of 115 nM in rat cerebral cortex, 150 nM in NG 108-15 cell membranes and 103 nM in whole NG 108-15 cell.
-
体内实验SR 57227A (1-30 mg/kg; i.p.) dose-dependently reduces immobility time in the forced swimming test with an ED50 value for this effect of 14.2 mg/kg.In the forced swimming test, SR 57227A dose-dependently reduces the duration of immobility in rats after i.p. administration. (ED50=7.6 mg/kg i.p. in rats.) SR 57227A is also active in both species after oral administration. In a time-course study in mice, SR 57227A (20 mg/kg p.o.) produces a significant effect lasting 6 hours. SR 57227A (1 and 3 mg/kg i.p.) reduces the elevation of the escape failures in the learned helplessness model in rats by 50-60% on the last two days of the avoidance task, and reduces isolation-induced aggressivity in mice by 50 to 85%, an effect which is antagonised by Zacopride (1 mg/kg i.p.).
-
同义词SR 57227 | SR57227
-
通路GPCR/G Protein
-
靶点5-HT Receptor
-
受体5-HT Receptor
-
研究领域Neurological Disease
-
适应症Depression
化学信息
-
CAS Number77145-61-0
-
分子量248.151
-
分子式C10H15Cl2N3
-
纯度>98% (HPLC)
-
溶解度In Vitro:?H2O : 33.33 mg/mL (134.31 mM)
-
SMILESC1CN(CCC1N)C2=NC(=CC=C2)Cl.Cl
-
化学全称1-(6-Chloro-2-pyridinyl)-4-piperidinamine hydrochloride
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. Li B, et al. PLoS One. 2014 Apr 1;9(4):e93158.
2. Gholipour T, et al. Seizure. 2010 Jan;19(1):17-22.
3. Ortega JE, et al. Neuropharmacology. 2012 Jun;62(8):2472-9.
4. Guo W, et al. Mol Pain. 2014 Jun 9;10:35.
产品手册
关联产品
-
ATC 0175 hydrochlori...
ATC0175 是一种有效的、选择性和口服活性的黑色素浓缩激素 1 受体拮抗剂,MCH1R 和 MCH2R 的 IC50s 分别为 13.5,>10000 nM。ATC0175 在动物模型中显示出抗抑郁作用和抗焦虑作用。ATC0175 具有研究抑郁症和/或焦虑症的潜力。
-
(Iso)-Landipirdine
(Iso)-Landipirdine((Iso)-RO5025181) is a selective and potent 5-HT6R antagonist. (Iso)-Landipirdine has a significant effect on the hERG pharmacophore and can be used to study neurological disorders in the Alzheimer's disease class.
-
Ebalzotan
Ebalzotan (NAE 086) is a 5-HT1A receptor agonist that can be used to study depression.
021-51111890
购物车()
sales@molnova.cn

