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Cyamemazine 98%

货号:A411163 Ambeed 开学季,买赠积分,赢豪礼

Cyamemazine 是一种含有吩噻嗪发色团的抗精神病药,常用作抗焦虑药。Cyamemazine 是一种强效的 5-HT3(Ki = 12 nM)、5-HT2A(Ki = 1.5 nM)和 5-HT2C(Ki = 75 nM)受体拮抗剂。

HazMat Fee +

There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Cyamemazine 化学结构 CAS号:3546-03-0
Cyamemazine 化学结构
CAS号:3546-03-0
Cyamemazine 3D分子结构
CAS号:3546-03-0
Cyamemazine 化学结构 CAS号:3546-03-0
Cyamemazine 3D分子结构 CAS号:3546-03-0
规格 价格 会员价 库存 数量
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Cyamemazine 纯度/质量文件 产品仅供科研

货号:A411163 标准纯度: 98%
批次查询: 批次纯度:

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产品名称 5-HT 5-HT1 5-HT2 5-HT3 5-HT5 5-HT6 5-HT7 其他靶点 纯度
Desvenlafaxine ++

5-HT, Ki: 40.2 nM

98%
Lamotrigine +

5-HT (rat brain synaptosomes), IC50: 474 μM

5-HT (human platelets), IC50: 240 μM

99%+
Venlafaxine 99%+
Fluvoxamine maleate 99%
Iloperidone 99%+
Ziprasidone HCl 98+%
Atomoxetine HCI +

5-HT, Ki: 77 nM

98%
Dapoxetine HCl 99%+
Trazodone 98+%
Clomipramine HCl 99%+
Mirtazapine 99+%
Escitalopram oxalate +++

5-HT, Ki: 0.89 nM

99%+
Duloxetine 98+%
Sertraline HCl ++

5-HT, Ki: 13 nM

99%+
Citalopram HBr +++

serotonin reuptake, IC50: 1.8 nM

99%+
Latrepirdine 2HCl GluR 99%+
Fluoxetine hydrochloride 98%
Paroxetine hydrochloride AChR 99%+
BMY 7378 ++

5-HT1D, pIC50: 5.9

5-HT1A, pIC50: 6.4

+

5-HT2, pIC50: 5.5

97%
Flibanserin +++

5-HT1A, Ki: 1 nM

+

5-HT2A, Ki: 49 nM

98%
LY310762 +

5-HT1D, Ki: 249 nM

99%+
Cyclobenzaprine HCI 99%
Blonanserin +++

5-HT2, Ki: 3.98 nM

99%+
Cyproheptadine HCl ++++

5-HT2, IC50: 0.6 nM

99+%
Olanzapine 99+%
Pimavanserin hemitartrate +++

5-HT2A, pIC50: 8.7

99%
Ketanserin +++

5-HT2C (Human), Ki: 2.5 nM

5-HT2C (Rat), Ki: 50 nM

99%+
Loxapine succinate ++

5-HT2 (bovine), Ki: 6.6 nM

5-HT2 (human), Ki: 6.8 nM

99%
Agomelatine 99%+
Clozapine 99%+
Amitriptyline +

5-HT2, Ki: 235 nM

SERT 98%
PRX-08066 maleate +++

5-HT2B, IC50: 3.4 nM

98+%
RS-127445 ++++

5-HT2B, pKi: 9.5

5-HT2B, pIC50: 10.4

99%+
Sarpogrelate HCl ++++

5-HT2A, Kd: 2.1 nM

5-HT2C, Kd: 1.1 nM

98%
Tropisetron 99%
Palonosetron 98+%
Ramosetron HCl ++++

5-HT3 receptor, Ki: 0.091 nM

99%+
Ondansetron 99%
Granisetron 98%
Alosetron HCl 98%
Ondansetron hydrochloride dihydrate 99%+
VUF10166 ++++

5-HT3AB, Ki: 22 nM

5-HT3A, Ki: 0.04 nM

99%+
Azasetron hydrochloride ++++

5-HT3, IC50: 0.33 nM

98%
Asenapine maleate +++

5-HT1B, pKi: 8.4

5-HT1A, pKi: 8.6

++++

5-HT2A, pKi: 9.75

5-HT2C, pKi: 10.46

+++

5-HT5A, pKi: 8.84

++++

5-HT6, pKi: 9.6

++++

5-HT7, pKi: 9.94

99%+
Risperidone ++

5-HT1B, Ki: 14.9 nM

5-HT1D, Ki: 84.6 nM

++++

5-HT2A, Ki: 61.9 nM

5-HT2C, Ki: 12 nM

+

5-HT5A, Ki: 206 nM

++

5-HT7, Ki: 6.6 nM

99%+
SB 271046 HCl +++

5-HT6, pKi: 8.92

99%+
Intepirdine ++++

5-HT6, pKi: 9.63

99%+
SB-269970 HCl ++

5-HT7, pKi: 8.3

98+%
BRL 15572 ++

5-HT1B, pKi: 6.1

5-HT1D, pKi: 6

++

5-HT2A, pKi: 6.6

5-HT2B, pKi: 6.2

+

5-HT6, pKi: 5.9

+

5-HT7, pKi: 6.3

98%
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Cyamemazine 生物活性

描述 Cyamemazine, a neuroleptic containing the phenothiazine chromophore, is often utilized for its anxiolytic properties. It is a potent antagonist at 5-HT3 (Ki of 12 nM), 5-HT2A (Ki = 1.5 nM), and 5-HT2C (Ki = 75 nM) receptors, demonstrating antipsychotic activity[1][2].
体内研究

Cyamemazine acts as an antagonist at the 5-HT3, 5-HT2C, and 5-HT2A receptors, affecting 5-HT3-dependent contractions in isolated guinea pig ileum, 5-HT2C-dependent phospholipase C activation in rat brain membranes, and 5-HT2A-dependent contractions in isolated rat aorta rings and guinea pig trachea. Its antagonism of 5-HT3 and 5-HT2C receptors partially explains its therapeutic action in anxiety disorders. Acute, low doses of Cyamemazine reduce extracellular dopamine and its metabolites in the rat striatum[1].

体外研究

Cyamemazine shows high affinity for dopamine receptors, aligning with its antipsychotic effects. It also displays antagonist activity at muscarinic receptors, with affinities for M1 (Ki = 13 nM), M2 (Ki = 42 nM), M3 (Ki = 321 nM), M4 (Ki = 12 nM), and M5 (Ki = 35 nM) receptors[1].

Cyamemazine 参考文献

[1]Bourin M, et al. Preclinical and clinical pharmacology of cyamemazine: anxiolytic effects and prevention of alcohol and benzodiazepine withdrawal syndrome. CNS Drug Rev. 2004 Fall;10(3):219-29.

[2]Vendrell-Criado V, et al. Photobehavior of the antipsychotic drug cyamemazine in a supramolecular gel protective environment. J Photochem Photobiol B. 2020 Jan;202:111686.

Cyamemazine 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.09mL

0.62mL

0.31mL

15.46mL

3.09mL

1.55mL

30.92mL

6.18mL

3.09mL

Cyamemazine 技术信息

CAS号3546-03-0
分子式C19H21N3S
分子量 323.455
别名
运输蓝冰
存储条件

粉末 Sealed in dry,2-8°C

液体 -20°C:3-6个月-80°C:12个月

溶解度

DMSO: 105 mg/mL(324.62 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方
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