Lesopitron
CAS No. 132449-46-8
Lesopitron ( —— )
产品货号. M34092 CAS No. 132449-46-8
Lesopitron is an anxiolytic with pre- and postsynaptic 5-HT1A agonist activity and is more effective than 5-HT1A agonists in rat social interaction and marmoset anxiety models. lesopitron counteracts benzodiazepine withdrawal-induced anxiety in rodents with low acute toxicity and does not potentiate the effects of alcohol or barbiturates.
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥1848 | 有现货 |
|
| 5MG | ¥2907 | 有现货 |
|
| 10MG | ¥4280 | 有现货 |
|
| 25MG | ¥6717 | 有现货 |
|
| 50MG | ¥9228 | 有现货 |
|
| 100MG | ¥12164 | 有现货 |
|
| 500MG | ¥24404 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Lesopitron
-
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Lesopitron is an anxiolytic with pre- and postsynaptic 5-HT1A agonist activity and is more effective than 5-HT1A agonists in rat social interaction and marmoset anxiety models. lesopitron counteracts benzodiazepine withdrawal-induced anxiety in rodents with low acute toxicity and does not potentiate the effects of alcohol or barbiturates.
-
产品描述Lesopitron is an anxiolytic with pre- and postsynaptic 5-HT1A agonist activity and is more effective than 5-HT1A agonists in rat social interaction and marmoset anxiety models. lesopitron counteracts benzodiazepine withdrawal-induced anxiety in rodents with low acute toxicity and does not potentiate the effects of alcohol or barbiturates.
-
体外实验——
-
体内实验——
-
同义词——
-
通路GPCR/G Protein
-
靶点5-HT Receptor
-
受体5-HT Receptor
-
研究领域——
-
适应症——
化学信息
-
CAS Number132449-46-8
-
分子量320.82
-
分子式C15H21ClN6
-
纯度>98% (HPLC)
-
溶解度——
-
SMILESC(CCCN1C=C(Cl)C=N1)N2CCN(CC2)C=3N=CC=CN3
-
化学全称——
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
产品手册
关联产品
-
Iloperidone hydrochl...
一种非典型抗精神病药,对血清素 5HT2A (Ki = 5.6 nM)、多巴胺 D2 (Ki = 6.3 nM) 和 D3 (Ki = 7.1 nM) 以及去甲肾上腺素 α1 受体 (Ki = 0.36 nM) 具有高亲和力。
-
(Rac)-Norcisapride
Norcisapride is a 5-hydroxytryptamine receptor 3 (5-HT3) and (5-hydroxytryptamine receptor 4 (5-HT4) dual agonist used for the treatment of gastrointestinal disorders, orofacial disorders, and otorhinolaryngologic disorders.
-
Clovoxamine
Clovoxamine (DU23811) (Compound 35) 对血清素转运蛋白 (SERT) 具有结合亲和力 (Ki: 61 nM)。Clovoxamine 是一种 5-HT 和去甲肾上腺素再摄取 (NE) 再摄取抑制剂。Clovoxamine 是一种抗抑郁化合物。
021-51111890
购物车()
sales@molnova.cn

