1) anticholinergic potency
抗胆碱效能
2) anticholinergic
[英][,ænti,kəuli'nə:dʒik] [美][,ænti,kolə'nɝdʒɪk]
抗胆碱能
1.
The progress in devising synthesis of anticholinergic drugs is reviewed in the aspects of interdiction group,link group and cation group with 32 references.
综述了近年来抗胆碱能药物设计合成在阻断基团设计、连接基团设计、阳离子头设计方面的研究进展
2.
Therefore, looking for good activity,high selectivity,the role of strong,low toxicity and a new indication for a new anticholinergic drags has become the one of the hot spots for drug synthetic workers.
抗胆碱能药物是一类重要的外周神经系统药物,它能阻滞胆碱受体,使递质乙酰胆碱不能与受体结合。
3) anticholinergic
[英][,ænti,kəuli'nə:dʒik] [美][,ænti,kolə'nɝdʒɪk]
抗胆碱能的
4) anticholinergic drugs
抗胆碱能药物
1.
In order to investigate the molecular recognition mechanism of molecularly imprinted polymer (MIP) and relative influence factors, a series of MIPs were prepared with three structural analog anticholinergic drugs as templates.
以3种结构类似的抗胆碱能药物盐酸新托品(1116)、盐酸苯环壬酯(8021)和盐酸戊乙奎醚(8018)为模板分子合成分子烙印聚合物,采用固相萃取-高效液相色谱法(SPE-HPLC)考察各MIP对乙腈溶液中结构类似的药物1116、8021、8018及盐酸卡马特灵(1113)、氯苯那敏(CPA)和樟柳碱(AT3)的固相吸附行为,探讨MIP特异性识别的影响因素及机理。
2.
The specific solid phase extraction of MIPs was investigated for anticholinergic drugs:neotropine,penequinine,bencynonatine and anisodine,chlorphenamine with different hydrogen-band groups.
方法以抗胆碱能药物盐酸新托品为模板分子、甲基丙烯酸为功能单体、三羟甲基丙烷三甲基丙烯酸酯为交联剂在乙腈中合成MIP,采用固相萃取-高效液相色谱方法考察MIP对乙腈溶液中的模板分子和结构类似物盐酸苯环壬酯、盐酸戊乙奎醚及结构有一定差异的化合物樟柳碱和氯苯那敏的固相吸附行为。
5) cholinergic antagonists
胆碱能拮抗剂
6) Cholinergic Anti-Inflammatory Pathway
胆碱能抗炎通路
1.
Study on Electro-acupuncture at "Zusanli" Points Against Septic Shock of Rats Through Activating the Cholinergic Anti-inflammatory Pathway;
电针足三里激活胆碱能抗炎通路抗大鼠感染性休克
2.
It is recently found that the efferent vague nerve inhibits pro-inflammatory cytokine release and protects against IRI and termed this vagal function "the cholinergic anti-inflammatory pathway".
胆碱能抗炎通路是新发现的一条与神经免疫机制相关的抗炎通路,通过分泌乙酰胆碱,抑制炎症因子释放,为防治心肌缺血再灌注损伤提供新的治疗策略。
3.
Objective To investigate the changes of the cholinergic anti-inflammatory pathway in patients with severe acute pancreatitis(SAP) and the impact of Chai Qin Cheng Qi Decoction (CQCQD) on the pathway.
目的:探讨重症急性胰腺炎(SAP)胆碱能抗炎通路的变化及柴芩承气汤(CQCQD)对其的影响。
补充资料:节后抗胆碱药
分子式:
CAS号:
性质:又称节后抗胆碱药,M胆碱受体阻断药。代表药是阿托品,能阻断节后胆碱能神经支配效应器上的M胆碱受体,从而对抗乙酰胆碱和拟胆碱药的毒蕈碱样作用,引起平滑肌松弛、腺体分泌抑制、心率加速、瞳孔扩大等。临床应用广泛,主要用于内脏平滑肌绞痛。常见副作用是口干、乏汗、心悸、视力模糊等。青光眼和前列腺肥大者禁用。合成解痉药包括季铵类(如溴丙胺太林)和叔胺类(如贝那替嗪)两大类,主要用于溃疡病。
CAS号:
性质:又称节后抗胆碱药,M胆碱受体阻断药。代表药是阿托品,能阻断节后胆碱能神经支配效应器上的M胆碱受体,从而对抗乙酰胆碱和拟胆碱药的毒蕈碱样作用,引起平滑肌松弛、腺体分泌抑制、心率加速、瞳孔扩大等。临床应用广泛,主要用于内脏平滑肌绞痛。常见副作用是口干、乏汗、心悸、视力模糊等。青光眼和前列腺肥大者禁用。合成解痉药包括季铵类(如溴丙胺太林)和叔胺类(如贝那替嗪)两大类,主要用于溃疡病。
说明:补充资料仅用于学习参考,请勿用于其它任何用途。
参考词条