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- 结果与结论在NO释放的前提下激活血管内皮细胞上嘌呤受体新亚型可介导血管收缩反应,该受体可同时被P1受体激动剂腺苷、CPA、CPCA和P2受体激动剂ATP、ADP、UTP、2-MeSATP所激活;Results and Conclusion The endothelium-dependent vascular contraction induced by the novel purinoceptor subtypes was dependent on the presence of nitric oxide released from endothelium. The pharmacological characteristics of the receptor could be summarized as follows; 1) it can be activated by the P1 receptor agonist adenosine, CPA, CPCA and the P2 receptor agonists ATP, ADP, UTP, 2-MeSATP;
- P1受体的内源性配体主要是腺苷(ADO),P2受体的内源性配体主要有ATP、二磷酸腺苷(ADP)、三磷酸尿苷(UTP)和二磷酸尿苷(UDP)等。P receptors are divided into two major classes termed adenosine or P1 receptors, at which adenosine is the principal natural ligand, and P2 receptors, at which ATP, ADP, UTP and UDP are the principal natural ligands.
- 受体2AT2
- 受体Arecep-tor A
- P2卡P2 card
- P2.5PM2.5
- VIP受体VIP receptor
- APJ受体APJ receptor
- AVS-P2AVS-P2
- P2受体P2 receptors
- CSa受体C5a receptor
- Fc受体1CD89
- P2技术P2 technology
- 脑M受体muscarinic acetylcholine receptor
- P2-支配图P3 -dominated graph
- EP受体EP receptor
- P2-PackingP2-packing
- ATI受体receptor ATI
- KDR受体KDR receptor
- M2受体M2 - receptor