阿扎环醇
有效期 | 2年 |
描述 | 是一种中枢神经系统抑制剂,可用于减少精神病引起的幻觉的相关研究。 |
EC | EINECS 204-092-5 |
MDL | MFCD00066980 |
InChIKey | ZMISODWVFHHWNR-UHFFFAOYSA-N |
InChI | InChI=1S/C18H21NO/c20-18(15-7-3-1-4-8-15,16-9-5-2-6-10-16)17-11-13-19-14-12-17/h1-10,17,19-20H,11-14H2 |
PubChem CID | 15723 |
别名 | MER-17;MDL-4829;二苯基哌啶甲醇;α,α-二苯基-4-哌啶甲醇 |
英文名称 | Azacyclonol |
CAS | 115-46-8 |
分子式 | C18H21NO |
分子量 | 267.37 |
储存条件 | -20℃ |
纯度 | ≥98% |
外观(性状) | White to light beige crystalline Powder |
单位 | 瓶 |
生物活性 | Azacyclonol (γ-pipradol), a metabolite of Terfenadine, is a central depressant agent. Azacyclonol is a ganglion-blocking agent. Azacyclonol can be used to diminish psychoses-induced hallucinations[1-3]. |
In Vitro | Azacyclonol is formed from Terfenadine in rat liver[2]. |
In Vivo | Azacyclonol causes depressed activity in mice and rats[3].Azacyclonol antagonizes increased coordination activity in mice induced by pipradrol, amphetamine, morphine and cocaine and prolongs Hexobarbital hypnosis[3]. |
SMILES | OC(C1=CC=CC=C1)(C2CCNCC2)C3=CC=CC=C3 |
靶点 | Others |
数据来源文献 | [1]. Brown DA, et, al. The effects of some centrally acting drugs on ganglionic transmission in the cat. [2]. Jurima-Romet M, et, al. Induction of CYP3A and associated terfenadine N-dealkylation in rat hepatocytes cocultured with 3T3 cells. Cell Biol Toxicol. 1995 Dec;11(6):313-27. [3]. BRAUN DL, et, al. The pharmacologic activity of alpha-(4-piperidyl)-benzhydrol hydrochloride (azacyclonol hydrochloride); an ataractive agent. J Pharmacol Exp Ther. 1956 Oct;118(2):153-61. |
规格 | 500mg 1g |