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- muscarinic agonist 毒蕈碱性激动剂
- Blocks agonist or antagonist activity at adenosine, adrenergic, dopaminergic, muscarinic, opioid and P2Y receptors. 阻碍腺苷酸、肾上腺素、毒蕈碱、类鸦片活性肽和P2Y的受体的拮抗剂或对抗剂活性。
- Inverse agonist is a new type of classification. 摘要反向激动剂指一种新分类概念。
- Rat muscarinic acetylcholine receptor... 大鼠毒蕈碱型乙酰胆碱受体(M-AChR)ELISA Kit;
- When bending the elbow the biceps are the agonist. 曲肘时,肱二头肌会收缩。
- In conclusion, GSH may act as an agonist for NMDA receptor. 综合以上结果可知,GSH 可能是 NMDA 受体的致活剂。
- A muscle that counteracts the action of another muscle, the agonist. 拮抗肌,对抗肌抵消肌肉作用的另一块肌肉,收缩肌
- Physiology A muscle that counteracts the action of another muscle, the agonist. 拮抗肌,对抗肌:抵消肌肉作用的另一块肌肉,收缩肌
- AT_ 2 agonist group (n=8) was treated with AT_ 2 agonist (CGP42112A) (i.p). AT2 激动剂组(8 只), 腹腔注射AT2激动剂(CGP42112A);
- The M receptor agonist pilocarpine was similar to the effects of ACh. M受体激动剂毛果芸香碱能产生与ACh相似的效应。
- Specific binding is found in tissues where muscarinic receptors are demonstrable pharmacologically. 在药理学方法证明有毒蕈碱样受体的组织中发现了特异的结合作用。
- The modulatory effect of Ach on the IATP may be achieved by activating muscarinic receptor (M receptor). 乙酰胆碱对I(下标ATP)的调制作用是通过毒蕈碱样乙酰胆碱受体(M受体)激活实现的。
- A noncompetitive antagonist prevents the agonist from producing any effect at a given receptor site. 非竞争性拮抗剂可阻止激动剂在特定受体部位产生任何效应。
- AIM To examine whether the endo-thelial-target for acetylcholine is different from muscarinic receptors. 目的研究内皮细胞乙酰胆碱靶标与M受体药理学特征的差异。
- M5 muscarinic receptor may be a useful pharmacological target for the treatment of heroin addiction. M5毒蕈碱受体可作为改变海洛因行为学效应的有效药理学靶点之一.
- Recent investigation suggested that inverse agonist has potential clinical application. 反向激动剂有良好的临床应用前景。
- Aim To clone the muscarinic receptors M1, M3 and M5 sequences of astrocyte cells,and compare the gene and protein sequences with those of neurons. 目的克隆胶质细胞M1、M3、M5受体亚型基因序列,比较胶质细胞和神经细胞M1、M3、M5受体亚型基因序列、蛋白质序列的差异。
- This is most effective if a specific receptor blocking agent is available to counter the effects of a given agonist. 在这方面最有效的是利用特效的受体阻滞药对抗特定激剂的作用。
- Pirenzenpine is a relatively selective M1 subtype muscarinic receptor antagonist and used to treat digestive system ulcer. 哌仑西平是一种M1受体选择性的抗胆碱药,临床上用于治疗消化性溃疡。
- Different form antagonist that blocks the effect of agonist, inverse agonist produces opposite effect to that of agonist. 与阻断激动剂效应的拮抗剂不同,反向激动剂产生的效应与激动剂相反。