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- Naloxone is a specific opioid receptor antagonist,which is used on treating a lot of diseases of endogenous opioid peptides. 纳洛酮是阿片受体特异拮抗剂,用于治疗与内源性阿片类物质释放有关的多种疾病。
- opioid receptor antagonists 阿片受体拮抗剂
- Human Interleukin 1 receptor antagonist, IL... 人白介素1受体拮抗剂(IL1Ra)试剂盒;
- Amiodarone also acts as a thyroid hormone receptor antagonist. 胺碘酮也可作为甲状腺激素受体拮抗剂。
- One SNP was identified in kappa opioid receptor gene (GenBank: AY130756). 阿片受体基因在杜洛克猪种中表现较大的变异性,在大白猪种中变异相对较小。
- Objective:To synthesize a new H1 receptor antagonist olopatadine. 目的:合成新型H1受体阻滞剂奥洛他定。
- Spectroscopic Analysis on 5-HT3 Receptor Antagonist Dolasetron Mesylate[J]. 引用该论文 陈晓红;张倩芝;张卫红;陈建.
- In the normal brain and the body of some organs, the existence of endogenous opioid peptides and opioid receptor. 在正常人的脑内和体内一些器官,存在着内源性阿片肽和阿片受体。
- Antinociceptive Effect of Morphine, but Not? Opioid Receptor Number, Is Attenuated in the Spinal Cord of Diabetic Rats Chen S-R, et al. 是吗啡的抗伤害作用,而非阿片受体的数目在糖尿病性大鼠的脊髓中降低。
- Today many pharmaceutical companies are competing to develop capsaicin receptor antagonists. 今日,许多制药公司正争相发展辣椒素受体的拮抗剂。
- Till now, Mu opioid receptor's DNA and genomic DNA of human, mouse and pig were cloned in many laboratories in the world. Mu阿片受体cDNA由我国学者于雷最先成功克隆,到目前为止,世界上已有多个试验室克隆到人、鼠和猪的Mu阿片受体的cDNA和基因组DNA。
- Endorphins, a known substances produced in brains is an opioid receptor agonist which the brain produce in the presence of pain stimulus. 如果你一连几天、一天几次进行实验:诱发某人身感疼痛,再用吗啡为他止疼,到最后一天,悄悄用盐水取代吗啡,你会发现,此时盐水也能止痛。
- In this paper, recent advances in the Study on chemokines and chemokine receptor antagonists were reviewed. 本文对趋化因子及其受体拮抗剂的研究进展进行综述。
- Conclusion: PPL has a dose-dependent analgesic effect and its analgesic effect might be mediated by central opioid receptor. 结论:灯笼草具有镇痛作用,其镇痛作用可能涉及中枢阿片受体。
- The effects of MEL could be blocked by cyprohetadine(CPD), one orthe 5-HT receptor antagonists. MEL的效应能被5-HT的拮抗剂噻庚啶(CPD)所阻断。
- Under normal circumstances, the role of endogenous opioid peptides in the opioid receptor, regulating a person's mood and behavior. 在正常情况下,内源性阿片肽作用于阿片受体,调节着人的情绪和行为。
- The ionotropic glutamate receptor antagonists D-AP5 and CNQX could not fully block the action of ACM. 离子型谷氨酸受体拮抗剂D-AP5和CNQX不能完全阻断条件培养基的作用。
- However,endothelin receptor antagonists could block those physiological action meditated by endothelin. 而内皮素受体拮抗剂却可阻断内皮素相应受体的生理学作用。
- Our results suggest that the delta opioid receptor can modulate EAAC1function by direct protein-protein interaction and that activation of DOR releases theinhibitory interaction. 与EAAC1功能实验一致的是DPDPE激活DOR会减弱他们之间的相互作用。 我们的结果提示delta阿片受体可以通过蛋白-蛋白间的相互作用来调节EAAC1的功能,而DOR的激活可以释放这种相互作用导致的抑制作用。
- OBJECTIVE:To evaluate the clinical application of leukotriene receptor antagonists. 目的:评价白三烯受体拮抗剂的临床应用概况。