Benocyclidine
(Synonyms: N-[1-(2-苯并[B]噻嗯-2-基)环己基)]哌啶马来酸) 目录号 : GC16782An Analytical Reference Standard
Cas No.:112726-66-6
Sample solution is provided at 25 µL, 10mM.
Quality Control & SDS
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- Purity: >98.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
Benocyclidine is an inhibitor of dopamine reuptake [1, 2].
Dopamine plays important roles in the brain and body. In the brain, dopamine functions as a neurotransmitter involved in reward-motivated behavior, motor control and controlling the release of various hormones. Dysfunctions of the dopamine system have been associated several important diseases including Parkinson's disease, attention deficit hyperactivity disorder, schizophrenia, and addiction [3]. Dopamine also functions in blood vessels, kidneys, pancreas, the digestive system, the immune system, and the blood vessels.
Benocyclidine (BTCP) was a derivative of phencyclidine (PCP) with a benzothiophenyl group instead of a phenyl ring. BTCP potently inhibited dopamine (DA) uptake with the IC50 of 7-8 nM. BTCP showed low affinity for the PCP receptor with the IC50 of 6 μM [1, 2]. In the striatum, BTCP binding was dose-dependently inhibited by unlabeled BTCP and nomifensine with the ID50 of 6.34 mg/kg and 11.06 mg/kg, respectively. BTCP bound to the dopamine uptake complex in the mouse brain in vivo [4].
References:
[1] Vignon J, Pinet V, Cerruti C, et al. [3H] N-[1-(2-Benzo (b) thiophenyl) cycohexyl] piperidine ([3H] BTCP): a new phencyclidine analog selective for the dopamine uptake complex[J]. European journal of pharmacology, 1988, 148(3): 427-436.
[2] Chaudieu I, Vignon J, Chicheportiche M, et al. Role of the aromatic group in the inhibition of phencyclidine binding and dopamine uptake by PCP analogs[J]. Pharmacology Biochemistry and Behavior, 1989, 32(3): 699-705.
[3] Seeman P. Brain dopamine receptors[J]. Pharmacological Reviews, 1980, 32(3): 229-313.
[4] Maurice T, Vignon J, Kamenka J M, et al. In vivo labelling of the mouse dopamine uptake complex with the phencyclidine derivative [3 H] BTCP[J]. Neuroscience letters, 1989, 101(2): 234-238.
Cas No. | 112726-66-6 | SDF | |
别名 | N-[1-(2-苯并[B]噻嗯-2-基)环己基)]哌啶马来酸 | ||
化学名 | 1-(1-(benzo[b]thiophen-2-yl)cyclohexyl)piperidine | ||
Canonical SMILES | C1CCC(CC1)(C2=CC3=CC=CC=C3S2)N4CCCCC4 | ||
分子式 | C19H25NS | 分子量 | 299.47 |
溶解度 | DMF: 5 mg/ml,Ethanol: 2 mg/ml | 储存条件 | Store at -20°C |
General tips | 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 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。 为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。 |
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制备储备液 | |||
1 mg | 5 mg | 10 mg | |
1 mM | 3.3392 mL | 16.6962 mL | 33.3923 mL |
5 mM | 0.6678 mL | 3.3392 mL | 6.6785 mL |
10 mM | 0.3339 mL | 1.6696 mL | 3.3392 mL |
第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量) | ||||||||||
给药剂量 | mg/kg | 动物平均体重 | g | 每只动物给药体积 | ul | 动物数量 | 只 | |||
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% DMSO % % Tween 80 % saline | ||||||||||
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工作液浓度: mg/ml;
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1. 首先保证母液是澄清的;
2.
一定要按照顺序依次将溶剂加入,进行下一步操作之前必须保证上一步操作得到的是澄清的溶液,可采用涡旋、超声或水浴加热等物理方法助溶。
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