Cyproheptadine,99.86%

产品编号:Bellancom-B1622| CAS NO:129-03-3| 分子式:C21H21N| 分子量:287.40

赛庚啶是一种口服有效的5-HT2A受体拮抗剂,具有抗抑郁和抗腐烂作用。赛庚啶具有抗血小板和血栓保护活性。赛庚啶可用于研究血栓栓塞性疾病。

本网站销售的所有产品仅用于工业应用或者科学研究等非医疗目的,不可用于人类或动物的临床诊断或者治疗,非药用,非食用,

货号 包装 价格 库存与货期 购买量 操作
Bellancom-B1622
800.00 杭州 北京(现货)
Bellancom-B1622
1300.00 杭州 北京(现货)
Bellancom-B1622
2400.00 杭州 北京(现货)
Bellancom-B1622
3500.00 杭州 北京(现货)
Bellancom-B1622
5200.00 杭州 北京(现货)

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Cyproheptadine

产品介绍 Cyproheptadine 是一种有效的口服活性 5-HT2A 受体 拮抗剂,具有抗抑郁和抗血清素作用。Cyproheptadine 具有抗血小板活性。Cyproheptadine 可以用于血栓栓塞性疾病的研究。
生物活性

Cyproheptadine is a potent and orally active 5-HT2A receptor antagonist, with antidepressant and antiserotonergic effects. Cyproheptadine has antiplatelet and thromboprotective activities. Cyproheptadine can be used for the research of thromboembolic disorders.

体外研究

Cyproheptadine (0.01-100 nM; 1 minute) dose-dependently inhibits serotonin-enhanced ADP-induced mouse platelet aggregation in vitro.
Cyproheptadine (10 nM) has the ability to inhibit 15 µM serotonin-enhanced ADP-induced (1 µM) tyrosine phosphorylation in platelets in vitro.
Cyproheptadine inhibits human platelet PS exposure (Annexin V), P-selectin, and GPIIb-IIIa (PAC-1 binding) activation in vitro.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究

Cyproheptadine (1 mg/kg; i.p.; daily, for 5 days; C57BL/6 mice) exerts thromboprotective properties in vivo.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: C57BL/6 mice (8-10 weeks old)
Dosage: 1 mg/kg
Administration: Intraperitoneal injection; daily, for 5 days
Result: Prolonged occlusion times and tail bleeding times in mice.
体内研究

Cyproheptadine (1 mg/kg; i.p.; daily, for 5 days; C57BL/6 mice) exerts thromboprotective properties in vivo.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: C57BL/6 mice (8-10 weeks old)
Dosage: 1 mg/kg
Administration: Intraperitoneal injection; daily, for 5 days
Result: Prolonged occlusion times and tail bleeding times in mice.
性状Solid
溶解性数据
In Vitro: 

DMSO : 3.17 mg/mL (11.03 mM; ultrasonic and warming and adjust pH to 3 with HCl and heat to 60°C)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 3.4795 mL 17.3974 mL 34.7947 mL
5 mM 0.6959 mL 3.4795 mL 6.9589 mL
10 mM 0.3479 mL 1.7397 mL 3.4795 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month。-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
参考文献

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包装等级 I; II; III
海关编码 29143900

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129-03-3结构式

129-03-3

文献:Hatano, Manabu; Ito, Orie; Suzuki, Shinji; Ishihara, Kazuaki Journal of Organic Chemistry, 2010 , vol. 75, # 15 p. 5008 - 5016

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129-03-3

文献:Archiv der Pharmazie, , vol. 329, # 2 p. 87 - 94

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129-03-3结构式

129-03-3

文献:Tetrahedron, , vol. 44, # 19 p. 6197 - 6200

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129-03-3结构式

129-03-3

文献:Tetrahedron, , vol. 44, # 19 p. 6197 - 6200

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129-03-3结构式

129-03-3

文献:Archiv der Pharmazie, , vol. 329, # 2 p. 87 - 94

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