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HCID 16640802作成日:2026年10月31日

1-[1-(2-チエニル)シクロヘキシル]ピペリジン·塩酸塩

1-[1-(2-チエニル)シクロヘキシル]ピペリジン·塩酸塩 · 1-[1-(2-チエニル)シクロヘキシル]ピペリジン・塩酸塩 · GK 0 · CL-421 · Thienylcyclidine · Thienylphencyclidine · 1-[1-(2-Thienyl)cyclohexyl]piperidine Hydrochloride · 1-(1-thiophen-2-ylcyclohexyl)piperidine:hydrochloride

https://huagongshe.com/ja/chemical/16640802

1-[1-(2-チエニル)シクロヘキシル]ピペリジン·塩酸塩 の分子構造式

識別子と物理属性

CAS No.1867-65-8
分子式C15H24ClNS
平均分子量285.884 g/mol
単同位体質量285.13179845 g/mol
SMILESCl.c1csc(C2(N3CCCCC3)CCCCC2)c1
InChIKeyIIPLEZRBGQCZMF-UHFFFAOYSA-N
PubChem CID16640802
EC No.631-590-3
DTXSIDDTXSID40904770
現地名1-[1-(2-チエニル)シクロヘキシル]ピペリジン·塩酸塩

化学・物理的性質

融点233-236 °C
溶解度DMF: 5 mg/mlDMF:PBS(pH 7.2)(1:1): 0.5 mg/mlDMSO: 2 mg/mlEthanol: 2 mg/mlMethanol: 1 mg/ml
外観・状態A crystalline solid

安全性と法規制

危険有害性情報コード 危険有害性情報 危険有害性クラス 区分 注意喚起語 シンボル P コード H315

用途

説明

Tenocyclidine (TCP), known more formally as N-[1-(2-thienyl)cyclohexyl] piperidine, is an analog of phencyclidine (PCP) in which the phenyl substituent is replaced with a thiophene group. TCP is a potent antagonist of the NMDA receptor-gated ion channel (Kd = 9 nM). TCP blocks NMDA-activated excitatory postsynaptic potential in brain more potently than PCP. PCP and many analogs, including TCP, block the uptake and enhance the release of dopamine both in vitro and in vivo. TCP is regulated as a Schedule I compound in the United States. This product is intended for forensic and research applications.

使用

An analog of the hallucinogen Phencyclidine (P295500).