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佐替平

佐替平用途

佐替平是一种抗精神病药物,是5-HT2A、5-HT2C、组胺H1、α1-肾上腺素能受体和多巴胺D2受体的有效拮抗剂,Kds分别为2.6 nM、3.2 nM、3.3 nM、7.3 nM和8 nM。佐替平在体内具有抗抑郁和抗焦虑作用[1][2]。

佐替平名称

[ CAS 号 ]:
26615-21-4

[ 中文名 ]:
佐替平

[ 英文名 ]:
Zotepine

[中文别名 ]:

[英文别名 ]:

佐替平生物活性

[ 描述 ]:

佐替平是一种抗精神病药物,是5-HT2A、5-HT2C、组胺H1、α1-肾上腺素能受体和多巴胺D2受体的有效拮抗剂,Kds分别为2.6 nM、3.2 nM、3.3 nM、7.3 nM和8 nM。佐替平在体内具有抗抑郁和抗焦虑作用[1][2]。

[ 相关类别 ]:

信号通路 >> 免疫及炎症 >> 组胺受体
信号通路 >> G 蛋白偶联受体/G 蛋白 >> 肾上腺素能受体
信号通路 >> G 蛋白偶联受体/G 蛋白 >> 多巴胺受体
信号通路 >> 神经信号通路 >> 多巴胺受体
研究领域 >> 神经疾病
信号通路 >> G 蛋白偶联受体/G 蛋白 >> 5-HT受体
信号通路 >> 神经信号通路 >> 5-HT受体
信号通路 >> G 蛋白偶联受体/G 蛋白 >> 组胺受体

[体外研究]

佐替平显示出多种拮抗谱,与α1-肾上腺素能、α2-肾上腺素能、多巴胺D2、组胺H1、毒蕈碱、5-HT1A、5-HT1D、5-HT2A和5-HT2C受体具有强亲和力,Kds分别为7.3、180、8、3.3、330、280、80、2.6、3.2nm[1]。

[体内研究]

佐替平(1-3 mg/kg;单次腹腔注射)剂量依赖性地增加去甲肾上腺素、多巴胺、GABA和谷氨酸的释放,而不影响大鼠内侧前额叶皮质的5-HT水平[2]。动物模型:雄性Sprague-Dawley大鼠(250-300 g)[1]剂量:1,3 mg/kg给药:单次腹腔注射结果:增加去甲肾上腺素、多巴胺、GABA和谷氨酸的释放,而不影响内侧前额叶皮质的5-HT水平。VTA、DRN、LC和MTN的神经元放电频率呈剂量依赖性增加。

[参考文献]

[1]. Richelson E, et, al. Binding of antipsychotic drugs to human brain receptors focus on newer generation compounds. Life Sci. 2000 Nov 24;68(1):29-39.

[2]. Yamamura S, et, al. Effects of zotepine on extracellular levels of monoamine, GABA and glutamate in rat prefrontal cortex. Br J Pharmacol. 2009 Jun;157(4):656-65.

佐替平物理化学性质

[ 密度 ]:
1.3±0.1 g/cm3

[ 沸点 ]:
478.4±45.0 °C at 760 mmHg

[ 熔点 ]:
90-91 °C

[ 分子式 ]:
C18H18ClNOS

[ 分子量 ]:
331.86

[ 闪点 ]:
243.2±28.7 °C

[ 精确质量 ]:
331.079773

[ PSA ]:
37.77000

[ LogP ]:
6.57

[ 蒸汽压 ]:
0.0±1.2 mmHg at 25°C

[ 折射率 ]:
1.656

[ 储存条件 ]:
室温

佐替平MSDS

佐替平毒性和生态

CHEMICAL IDENTIFICATION

RTECS NUMBER :
HQ2541700
CHEMICAL NAME :
Dibenzo(b,f)thiepin, 2-chloro-11-(2-(dimethylamino)ethoxy)-
CAS REGISTRY NUMBER :
26615-21-4
BEILSTEIN REFERENCE NO. :
1435710
LAST UPDATED :
199612
DATA ITEMS CITED :
15
MOLECULAR FORMULA :
C18-H18-Cl-N-O-S
MOLECULAR WEIGHT :
331.88
WISWESSER LINE NOTATION :
T C676 BSJ FG IO2N1&1

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
306 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 29,1600,1979
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
97 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 29,1600,1979
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
1290 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 29,1600,1979
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
36800 ug/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 29,1600,1979
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
108 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 29,1600,1979
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
36200 ug/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 29,1600,1979
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
84900 ug/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 29,1600,1979
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
43300 ug/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 29,1600,1979
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Mammal - dog
DOSE/DURATION :
>1 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 29,1600,1979
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Mammal - dog
DOSE/DURATION :
26600 ug/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 29,1600,1979
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rabbit
DOSE/DURATION :
250 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 29,1600,1979
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - rabbit
DOSE/DURATION :
23800 ug/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 29,1600,1979 ** OTHER MULTIPLE DOSE TOXICITY DATA **
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
7280 mg/kg/1Y-C
TOXIC EFFECTS :
Endocrine - effect on menstrual cycle Skin and Appendages - breast Related to Chronic Data - changes in uterine weight
REFERENCE :
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 29,1600,1979 ** REPRODUCTIVE DATA **
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
DOSE :
176 mg/kg
SEX/DURATION :
female 7-17 day(s) after conception
TOXIC EFFECTS :
Reproductive - Effects on Embryo or Fetus - fetotoxicity (except death, e.g., stunted fetus)
REFERENCE :
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 29,1600,1979
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
DOSE :
44 mg/kg
SEX/DURATION :
female 7-17 day(s) after conception
TOXIC EFFECTS :
Reproductive - Effects on Newborn - live birth index (measured after birth)
REFERENCE :
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 29,1600,1979

佐替平安全信息

[ 符号 ]:

GHS07, GHS09

[ 信号词 ]:
Warning

[ 危害声明 ]:
H302-H400

[ 警示性声明 ]:
P273

[ 危害码 (欧洲) ]:
T+

[ 风险声明 (欧洲) ]:
25-50/53

[ 安全声明 (欧洲) ]:
45-60-61

[ 危险品运输编码 ]:
UN 2811 6.1 / PGIII

佐替平文献

Safety evaluation of zotepine for the treatment of schizophrenia.

Expert Opin. Drug Saf. 9(4) , 659-66, (2010)

Atypical antipsychotics have become the first-line treatment for patients suffering from schizophrenia in the industrialized world. Given the frequent necessity of a life-long enduring antipsychotic t...

Zotepine for schizophrenia.

Cochrane Database Syst. Rev. (4) , CD001948, (2006)

Zotepine is a relatively new antipsychotic often used for the treatment of people with schizophrenia. It is claimed to be particularly effective for negative symptoms.To determine the effects of zotep...

Differences in the effect of second-generation antipsychotics on prolactinaemia: six weeks open-label trial in female in-patients.

Neuro Endocrinol. Lett. 28(6) , 881-8, (2007)

The main objective was to evaluate the effect of five second-generation antipsychotics (amisulpride, quetiapine, olanzapine, risperidone, and zotepine) on prolactinaemia during 6 week therapy in 433 f...


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公司名:上海化源世纪贸易有限公司

区域:上海市普陀区

价格:

联系人:徐经理

产品详情:Zotepine


公司名:上海源溪生物科技有限公司

区域:上海市浦东新区

价格:
¥需询单/1g

联系人:赖经理

产品详情:Zotepine


公司名:上海脉铂医药科技有限公司

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价格:
¥8369.0/50mg ¥2069.0/10mg ¥需询单/1g ¥需询单/1g

联系人:李先生

产品详情:Zotepine


公司名:上海阿拉丁生化科技股份有限公司

区域:上海市浦东新区

价格:
¥164.9/10mg ¥3266.9/1g ¥1371.9/250mg ¥459.9/50mg

联系人:阿拉丁

产品详情:Zotepine


公司名:上海创赛科技有限公司

区域:上海市嘉定区

价格:
¥8212.4/50mg ¥2038.4/10mg

联系人:夏言

产品详情:Zotepine


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相关化合物

【佐替平】化源网提供佐替平CAS号26615-21-4,佐替平MSDS及其说明、性质、英文名、生产厂家、作用/用途、分子量、密度、沸点、熔点、结构式等。CAS号查询佐替平上化源网,专业又轻松。>>电脑版:佐替平

标题:佐替平_MSDS_用途_密度_佐替平CAS号【26615-21-4】_化源网 地址:https://www.chemsrc.com/amp/cas/26615-21-4_28410.html