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148-72-1

中文名称 硝酸毛果芸香碱
英文名称 Pilocarpine nitrate
CAS 148-72-1
EINECS 编号 205-723-7
分子式 C11H17N3O5
MDL 编号 MFCD00078497
分子量 271.27
MOL 文件 148-72-1.mol
更新日期 2024/04/15 13:30:30
148-72-1 结构式 148-72-1 结构式

基本信息

中文别名
硝酸毛果芸香碱
硝酸匹鲁卡品
硝酸匹鲁卡品(硝酸毛果芸香碱)
(3S,4R)-3-乙基二氢-4-[(1-甲基-1H-咪唑-5-基)甲基]-2(3H)-呋喃酮硝酸盐
英文别名
3-ETHYLDIHYDRO-4-[(1-METHYL-1H-IMIDAZOL-5-YL)-METHYL]-2-(3H)-FURANONE NITRATE
PILOCARPINE NITRATE
PILOCARPINE NITRATE SALT
3-ethyldihydro-4-[(1-methyl-1h-imidazol-5-yl)methyl]-2(3h)-furanon(3s-cis)
p.v.carpineliquifilm
pilocarpine,mononitrate
Pilocarpinenitrateusp
pilocarpinesubnitrate
pilofrin
PILOCARPINE NITRATE, PH EUR
2(3H)-Furanone, 3-ethyldihydro-4-(1-methyl-1H-imidazol-5-yl)methyl-, (3S,4R)-, mononitrate
PILOCARPINENITRATE,CRYSTAL,USP
Pilagan
Pilocarpinnitrat
(3S)-3-Ethyl-4-[(3-methylimidazol-4-yl)methyl]oxolan-2-one nitrate
(3S,4R)-3-Ethyldihydro-4-((1-methyl-1H-imidazol-5-yl)methyl)-2(3H)-furanone mononitrate
Pilocarpini nitras

物理化学性质

熔点173,5-174°C
比旋光度D +77 to +83° (c = 10)
折射率81 ° (C=2, H2O)
储存条件2-8°C
溶解度H2O: 0.1 g/mL, clear, very faintly yellow
形态粉末
颜色白色
旋光性 (optical activity)[α]25/D +83°, c = 10 in H2O(lit.)
Merck7424
BRN4171406
EPA化学物质信息Pilocarpine nitrate (148-72-1)

安全数据

危险性符号(GHS)
GHS03,GHS06
警示词危险
危险性描述H272-H302-H330
危险品标志Xn,T+
危险类别码R22-R26/28
安全说明S1-S25-S45
危险品运输编号3087
WGK Germany3
RTECS号TK1455000
危险等级6.1(b)
包装类别III
海关编码2939800000
毒性LD50 oral in rat: 911mg/kg

制备方法

方法1

可由植物毛果芸香提取毛果芸香碱后,再用硝酸处理而制得。

常见问题列表

简介

硝酸毛果芸香碱呈无色结晶或白色结晶性粉末;无臭;遇光易变质。其可用于青光眼、虹膜炎的治疗。

禁忌症

1.对本药过敏者。

2.支气管哮喘患者。

3.急性虹膜炎、虹膜睫状体炎等不应缩瞳的眼病患者。

生物活性
Pilocarpine nitrate 是一种选择性的 M3 型毒蕈碱乙酰胆碱受体 (M3 muscarinic receptor) 激动剂。
靶点

M3 muscarinic receptor

体外研究

To evaluate the cytotoxicity of Pilocarpine, the morphology and viability of human corneal stromal (HCS) cells are examined by light microscopy and MTT assay, respectively. Morphological observations show that HCS cells exposed to Pilocarpine at a concentration from 0.625 to 20 g/L exhibit dose- and time-dependent proliferation retardation and morphological abnormality such as cellular shrinkage, cytoplasmic vacuolation, detachment from culture matrix, and eventually death, while no obvious difference is observed between those exposed to Pilocarpine below the concentration of 0.625 g/L and controls. Results of MTT assay reveal that the cell viability of HCS cells decrease with time and concentration after exposing to Pilocarpine above the concentration of 0.625 g/L (P<0.01 or 0.05), while that of HCS cells treated with Pilocarpine below the concentration of 0.625 g/L show no significant difference to controls. The partial muscarinic agonist, Pilocarpine, evokes concentration-dependent relaxation with an EC 50 of 2.4 mM in isolated segments of rat tail artery that were constricted with Penylephrine (10 to 200 nM).

体内研究

The Pilocarpine-induced saliva secretion of the control rats (CN) and exercised (EX) rats is examined. A significantly greater amount of saliva is induced by Pilocarpine in the EX rats than in the CN rats (P<0.01). Conversely, the Na + concentration in the saliva of the EX rats is significantly lower than that of the CN rats (P<0.05).

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