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盐酸齐拉西酮 /Ziprasidone HCl {[allProObj[0].p_purity_real_show]}

货号:A153991 同义名: 齐拉西酮盐酸盐 / CP-88059 hydrochloride;CP-88059 Ambeed 开学季,买赠积分,赢豪礼

Ziprasidone HCl is a combined 5-HT (serotonin) and dopamine receptor antagonist which exhibits potent effects of antipsychotic activity, and is used in the treatment of schizophrenia and bipolar disorder.

Ziprasidone HCl 化学结构 CAS号:122883-93-6
Ziprasidone HCl 化学结构
CAS号:122883-93-6
Ziprasidone HCl 3D分子结构
CAS号:122883-93-6
Ziprasidone HCl 化学结构 CAS号:122883-93-6
Ziprasidone HCl 3D分子结构 CAS号:122883-93-6
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Ziprasidone HCl 纯度/质量文件 产品仅供科研

货号:A153991 标准纯度: {[allProObj[0].p_purity_real_show]}
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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

{[allProObj[0].p_purity_real_show]}
Lamotrigine +

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

5-HT (human platelets), IC50: 240 μM

{[allProObj[0].p_purity_real_show]}
Venlafaxine {[allProObj[0].p_purity_real_show]}
Fluvoxamine maleate {[allProObj[0].p_purity_real_show]}
Iloperidone {[allProObj[0].p_purity_real_show]}
Ziprasidone HCl {[allProObj[0].p_purity_real_show]}
Atomoxetine HCI +

5-HT, Ki: 77 nM

{[allProObj[0].p_purity_real_show]}
Dapoxetine HCl {[allProObj[0].p_purity_real_show]}
Trazodone {[allProObj[0].p_purity_real_show]}
Clomipramine HCl {[allProObj[0].p_purity_real_show]}
Mirtazapine {[allProObj[0].p_purity_real_show]}
Escitalopram oxalate +++

5-HT, Ki: 0.89 nM

{[allProObj[0].p_purity_real_show]}
Duloxetine {[allProObj[0].p_purity_real_show]}
Sertraline HCl ++

5-HT, Ki: 13 nM

{[allProObj[0].p_purity_real_show]}
Citalopram HBr +++

serotonin reuptake, IC50: 1.8 nM

{[allProObj[0].p_purity_real_show]}
Latrepirdine 2HCl GluR {[allProObj[0].p_purity_real_show]}
Fluoxetine HCl {[allProObj[0].p_purity_real_show]}
Paroxetine hydrochloride AChR {[allProObj[0].p_purity_real_show]}
BMY 7378 ++

5-HT1D, pIC50: 5.9

5-HT1A, pIC50: 6.4

+

5-HT2, pIC50: 5.5

{[allProObj[0].p_purity_real_show]}
Flibanserin +++

5-HT1A, Ki: 1 nM

+

5-HT2A, Ki: 49 nM

{[allProObj[0].p_purity_real_show]}
LY310762 +

5-HT1D, Ki: 249 nM

{[allProObj[0].p_purity_real_show]}
Cyclobenzaprine HCI {[allProObj[0].p_purity_real_show]}
Blonanserin +++

5-HT2, Ki: 3.98 nM

{[allProObj[0].p_purity_real_show]}
Cyproheptadine HCl ++++

5-HT2, IC50: 0.6 nM

{[allProObj[0].p_purity_real_show]}
Olanzapine {[allProObj[0].p_purity_real_show]}
Pimavanserin hemitartrate +++

5-HT2A, pIC50: 8.7

{[allProObj[0].p_purity_real_show]}
Ketanserin +++

5-HT2C (Rat), Ki: 50 nM

5-HT2C (Human), Ki: 2.5 nM

{[allProObj[0].p_purity_real_show]}
Loxapine succinate ++

5-HT2 (human), Ki: 6.8 nM

5-HT2 (bovine), Ki: 6.6 nM

{[allProObj[0].p_purity_real_show]}
Agomelatine {[allProObj[0].p_purity_real_show]}
Clozapine {[allProObj[0].p_purity_real_show]}
Amitriptyline +

5-HT2, Ki: 235 nM

SERT {[allProObj[0].p_purity_real_show]}
PRX-08066 maleate +++

5-HT2B, IC50: 3.4 nM

{[allProObj[0].p_purity_real_show]}
RS-127445 ++++

5-HT2B, pIC50: 10.4

5-HT2B, pKi: 9.5

{[allProObj[0].p_purity_real_show]}
Sarpogrelate HCl ++++

5-HT2C, Kd: 1.1 nM

5-HT2A, Kd: 2.1 nM

{[allProObj[0].p_purity_real_show]}
Tropisetron {[allProObj[0].p_purity_real_show]}
Palonosetron {[allProObj[0].p_purity_real_show]}
Ramosetron HCl ++++

5-HT3 receptor, Ki: 0.091 nM

{[allProObj[0].p_purity_real_show]}
Ondansetron {[allProObj[0].p_purity_real_show]}
Granisetron {[allProObj[0].p_purity_real_show]}
Alosetron HCl {[allProObj[0].p_purity_real_show]}
Ondansetron hydrochloride dihydrate {[allProObj[0].p_purity_real_show]}
VUF10166 ++++

5-HT3AB, Ki: 22 nM

5-HT3A, Ki: 0.04 nM

{[allProObj[0].p_purity_real_show]}
Azasetron hydrochloride ++++

5-HT3, IC50: 0.33 nM

{[allProObj[0].p_purity_real_show]}
Asenapine maleate +++

5-HT1A, pKi: 8.6

5-HT1B, pKi: 8.4

++++

5-HT2C, pKi: 10.46

5-HT2A, pKi: 9.75

+++

5-HT5A, pKi: 8.84

++++

5-HT6, pKi: 9.6

++++

5-HT7, pKi: 9.94

{[allProObj[0].p_purity_real_show]}
Risperidone ++

5-HT1D, Ki: 84.6 nM

5-HT1B, Ki: 14.9 nM

++++

5-HT2C, Ki: 12 nM

5-HT2A, Ki: 61.9 nM

+

5-HT5A, Ki: 206 nM

++

5-HT7, Ki: 6.6 nM

{[allProObj[0].p_purity_real_show]}
SB 271046 HCl +++

5-HT6, pKi: 8.92

{[allProObj[0].p_purity_real_show]}
Intepirdine ++++

5-HT6, pKi: 9.63

{[allProObj[0].p_purity_real_show]}
SB-269970 HCl ++

5-HT7, pKi: 8.3

{[allProObj[0].p_purity_real_show]}
BRL 15572 ++

5-HT1D, pKi: 6

5-HT1B, pKi: 6.1

++

5-HT2A, pKi: 6.6

5-HT2B, pKi: 6.2

+

5-HT6, pKi: 5.9

+

5-HT7, pKi: 6.3

{[allProObj[0].p_purity_real_show]}
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。
产品名称 D1 receptor D2 receptor D3 receptor D4 receptor D5 receptor DAT Dopamine receptor 其他靶点 纯度
Penfluridol +

Dopamine receptor, Ki: 1.6 μM

{[allProObj[0].p_purity_real_show]}
Ansofaxine HCl ++

Dopamine receptor, IC50: 491 nM

{[allProObj[0].p_purity_real_show]}
Tetrahydroberberine,THB +

D2 receptor, pKi: 6.08

{[allProObj[0].p_purity_real_show]}
Prochlorperazine Maleate {[allProObj[0].p_purity_real_show]}
Olanzapine {[allProObj[0].p_purity_real_show]}
Trifluoperazine ++++

Dopamine D2 receptor, IC50: 1.1 nM

{[allProObj[0].p_purity_real_show]}
Ropinirole hydrochloride ++

D2 receptor, Ki: 29 nM

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Lurasidone ++++

D2 receptor, Ki: 1 nM

{[allProObj[0].p_purity_real_show]}
Levosulpiride {[allProObj[0].p_purity_real_show]}
Pridopidine {[allProObj[0].p_purity_real_show]}
Metoclopramide {[allProObj[0].p_purity_real_show]}
Molindone HCl {[allProObj[0].p_purity_real_show]}
Sulpiride {[allProObj[0].p_purity_real_show]}
Perospirone ++++

D2 receptor, Ki: 1.4 nM

{[allProObj[0].p_purity_real_show]}
Perospirone HCl ++++

D2 receptor, Ki: 1.4 nM

{[allProObj[0].p_purity_real_show]}
Phenothiazine {[allProObj[0].p_purity_real_show]}
Pimozide +

Dopamine D1 receptor, Ki: 6600 nM

+++

Dopamine D2 receptor, Ki: 3.0 nM

++++

Dopamine D3 receptor, Ki: 0.83 nM

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Rotundine ++

D1 receptor, IC50: 166 nM

+

D2 receptor, IC50: 1.47 μM

+

D3 receptor, IC50: 3.25 μM

{[allProObj[0].p_purity_real_show]}
Domperidone {[allProObj[0].p_purity_real_show]}
ONC206 {[allProObj[0].p_purity_real_show]}
Pimethixene maleate ++

Dopamine D1 Receptor, pKi: 6.37

+++

Dopamine D2 Receptor, pKi: 8.19

++

Dopamine D4.4 Receptor, pKi: 7.54

{[allProObj[0].p_purity_real_show]}
Loxapine succinate ++

D2 receptor (Human), Ki: 62 nM

D1 receptor (human), Ki: 26 nM

++

D2 receptor (human), Ki: 24 nM

D2 receptor (bovine), Ki: 26 nM

+++

D4 receptor (human), Ki: 7.5 nM

{[allProObj[0].p_purity_real_show]}
Chlorprothixene +++

D1 receptor, Ki: 18 nM

+++

D2 receptor, Ki: 2.96 nM

+++

D3 receptor, Ki: 4.56 nM

+++

D5 receptor, Ki: 9 nM

{[allProObj[0].p_purity_real_show]}
SCH-23390 HCl ++++

D1 dopamine receptor, Ki: 0.2 nM

++++

D5 dopamine receptor, Ki: 0.3 nM

{[allProObj[0].p_purity_real_show]}
MPP+ iodide {[allProObj[0].p_purity_real_show]}
σ1 Receptor antagonist-1 +

DAT, pKi: 5.8

{[allProObj[0].p_purity_real_show]}
Benztropine mesylate ++

DAT, IC50: 118 nM

{[allProObj[0].p_purity_real_show]}
Azaperone {[allProObj[0].p_purity_real_show]}
Ziprasidone HCl {[allProObj[0].p_purity_real_show]}
Paliperidone {[allProObj[0].p_purity_real_show]}
Alizapride HCl {[allProObj[0].p_purity_real_show]}
Amisulpride {[allProObj[0].p_purity_real_show]}
Quetiapine hemifumarate Adrenergic Receptor {[allProObj[0].p_purity_real_show]}
Clozapine N-oxide {[allProObj[0].p_purity_real_show]}
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。

Ziprasidone HCl 生物活性

靶点
  • 5-HT

  • Dopamine receptor

描述 Ziprasidone hydrochloride is a combined 5-HT (serotonin) and dopamine receptor antagonist which exhibits potent effects of antipsychotic activity, and is used in the treatment of schizophrenia and bipolar disorder.

Ziprasidone HCl 临床研究

NCT号 适应症或疾病 临床期 招募状态 预计完成时间 地点
NCT01185743 Schizophrenia ... 展开 >> Diabetes 收起 << Phase 4 Completed - Austria ... 展开 >> Medical University of Vienna Vienna, Austria, 1090 收起 <<
NCT00288366 Schizophrenia ... 展开 >> Schizoaffective Disorder Bipolar Disorder 收起 << Not Applicable Completed - United States, Tennessee ... 展开 >> Psychiatric Hospital at Vanderbilt Nashville, Tennessee, United States, 37212 收起 <<
NCT01598324 - Terminated(Clinical trial from... 展开 >> which subjects were recruited closed to enrollment) 收起 << - United States, Massachusetts ... 展开 >> McLean Hospital - McLean Imaging Center Belmont, Massachusetts, United States, 02478 收起 <<

Ziprasidone HCl 参考文献

[1]Su Z, Chen J, et al. Block of hERG channel by ziprasidone: biophysical properties and molecular determinants. Biochem Pharmacol. 2006 Jan 12;71(3):278-86.

[2]Schmidt AW, Lebel LA, et al. Ziprasidone: a novel antipsychotic agent with a unique human receptor binding profile. Eur J Pharmacol. 2001 Aug 17;425(3):197-201.

Ziprasidone HCl 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.23mL

0.45mL

0.22mL

11.13mL

2.23mL

1.11mL

22.25mL

4.45mL

2.23mL

Ziprasidone HCl 技术信息

CAS号122883-93-6
分子式C21H22Cl2N4OS
分子量 449.397
别名 齐拉西酮盐酸盐 ;CP-88059 hydrochloride;CP-88059;Ziprasidone hydrochloride
运输蓝冰
存储条件

粉末 Inert atmosphere,Store in freezer, under -20°C

液体 -20°C:3-6个月-80°C:12个月

溶解度
动物实验配方
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