光明正大 发表于 2025-3-25 04:04:37
http://reply.papertrans.cn/43/4230/422919/422919_21.pngTOXIC 发表于 2025-3-25 08:59:47
mide, identified as HENECA (Fig. 17-1), which was shown to possess high affinity at A. adenosine receptors combined with a good A. versus A. selectivityTable 17-1 shows the ability of HENECA to inhibit the binding of radioligands to A. and A. receptors compared with that of NECA , 2-[[4-(2carb座右铭 发表于 2025-3-25 12:28:48
http://reply.papertrans.cn/43/4230/422919/422919_23.png去掉 发表于 2025-3-25 16:43:07
mide, identified as HENECA (Fig. 17-1), which was shown to possess high affinity at A. adenosine receptors combined with a good A. versus A. selectivityTable 17-1 shows the ability of HENECA to inhibit the binding of radioligands to A. and A. receptors compared with that of NECA , 2-[[4-(2carb令人心醉 发表于 2025-3-25 21:44:35
August Flammervel of the plasma membrane. The pioneering studies in the early 1970s by Rall, Daly, Schwabe, and Fain clearly established that adenosine and its analogs could modulate both cyclic AMP levels in intact cells and adenylate cyclase activity in broken cell preparations. Systematic studies by Londos andexhilaration 发表于 2025-3-26 03:19:44
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http://reply.papertrans.cn/43/4230/422919/422919_28.pnganachronistic 发表于 2025-3-26 15:54:53
Johanna Mierendorff,Thomas Olkr myocytes. Since its discovery, a number of factors and endogenous substances such as the ATP/ADP ratio, certain nucleotide diphosphates, Mg++, lactate, pH, protein kinase C, adenosine and bradykinin have been shown to modulate the gating properties of this channel in the heart.. Since K. channel a恭维 发表于 2025-3-26 18:34:57
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