Naluzotan hydrochloride
CAS No. 740873-82-9
Naluzotan hydrochloride ( —— )
产品货号. M36203 CAS No. 740873-82-9
Naluzotan hydrochloride (PRX 00023 hydrochloride) is a hERG K+ channel blocker with an IC50 value of 3800 nM and is commonly used in the study of anxiety and depression.Naluzotan hydrochloride is also a novel, potent, and selective 5-HT1A agonist, with an IC50 value of about 20 nM and a Ki value of about 5.1 Naluzotan hydrochloride is also a novel, potent and selective 5-HT1A agonist with an IC50 of approximately 20 nM and a Ki of approximately 5.1 nM.
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥3772 | 有现货 |
|
| 10MG | ¥5377 | 有现货 |
|
| 25MG | ¥8072 | 有现货 |
|
| 50MG | ¥10881 | 有现货 |
|
| 100MG | ¥14220 | 有现货 |
|
| 500MG | ¥28530 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Naluzotan 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Naluzotan hydrochloride (PRX 00023 hydrochloride) is a hERG K+ channel blocker with an IC50 value of 3800 nM and is commonly used in the study of anxiety and depression.Naluzotan hydrochloride is also a novel, potent, and selective 5-HT1A agonist, with an IC50 value of about 20 nM and a Ki value of about 5.1 Naluzotan hydrochloride is also a novel, potent and selective 5-HT1A agonist with an IC50 of approximately 20 nM and a Ki of approximately 5.1 nM.
-
产品描述Naluzotan hydrochloride (PRX 00023 hydrochloride) is a hERG K+ channel blocker with an IC50 value of 3800 nM and is commonly used in the study of anxiety and depression.Naluzotan hydrochloride is also a novel, potent, and selective 5-HT1A agonist, with an IC50 value of about 20 nM and a Ki value of about 5.1 Naluzotan hydrochloride is also a novel, potent and selective 5-HT1A agonist with an IC50 of approximately 20 nM and a Ki of approximately 5.1 nM.
-
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 | EGFR
-
研究领域——
-
适应症——
化学信息
-
CAS Number740873-82-9
-
分子量487.1
-
分子式C23H39ClN4O3S
-
纯度>98% (HPLC)
-
溶解度——
-
SMILESCl.O=C(NC1=CC=CC(=C1)N2CCN(CC2)CCCCNS(=O)(=O)CC3CCCCC3)C
-
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
-
Oxatomide
Oxatomide 是一种有效的具有口服活性的双重 H1 组胺受体 (H1-histamine receptor) 和 P2X7 受体拮抗剂,具有抗组胺和抗过敏活性。Oxatomide 几乎完全阻断人 P2X7 受体中 ATP 诱导的电流 (IC50 为 0.95 μM)。Oxatomide 可抑制 ATP 诱导的 Ca2+ 内流,IC50 值为 0.43 μM,并且还抑制 5-羟色胺 (serotonin)。
-
Tedatioxetine hydrob...
Tedatioxetine (Lu AA24530) hydrobromide 是一种倾向于 5-羟色胺、去甲肾上腺素的三重再摄取抑制剂,且是 5-HT2A,5-HT2C,5-HT3 和 α1A 肾上腺素能受体拮抗剂。
-
rac Desmethyl Citalo...
Desmethylcitalopram (DCIT) 是 Citalopram (HY-121203) 的活性代谢物。Desmethylcitalopram 具有抗抑郁作用。Desmethylcitalopram 还抑制细胞色素 P450-2D6、-2C19,IC50s 分别为 39.5 和 53.5 μM。
021-51111890
购物车()
sales@molnova.cn

