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前列腺素H1和H2。便捷的生化合成与分离。进一步的生物学和光谱学表征。

Prostaglandins H1 and H2. Convenient biochemical synthesis and isolation. Further biological and spectroscopic characterization.

作者信息

Gorman R R, Sun F F, Miller O V, Johnson R A

出版信息

Prostaglandins. 1977 Jun;13(6):1043-53. doi: 10.1016/0090-6980(77)90132-0.

Abstract

An easy biochemical preparation of the prostaglandin endoperoxides, PGH1 and PGH2, is described. Both of the endoperoxides are potent contractors of isolated gerbil colon smooth muscle. Contracture with PGH2 is about equal to that caused by the standard, PGE1, while contracture with PGH1 is about half of that caused by PGE1. PGH1 was found to inhibit platelet aggregation induced by PGH2 and is about 1/10 as potent a stimulator of cAMP accumulation as is PGE1. The mass spectra of the methyl esters of both PGH1 and PGH2 were obtained, as were the infrared spectra of the two compounds. The nuclear magnetic resonance spectrum of PGH2 is characterized by signals at 4.58 delta and 4.47 delta for the C-9 and C-11 protons, respectively.

摘要

本文描述了前列腺素内过氧化物PGH1和PGH2的一种简便生化制备方法。这两种内过氧化物都是分离的沙鼠结肠平滑肌的强力收缩剂。PGH2引起的挛缩与标准品PGE1引起的挛缩大致相当,而PGH1引起的挛缩约为PGE1引起的挛缩的一半。发现PGH1可抑制PGH2诱导的血小板聚集,其作为环磷酸腺苷(cAMP)积累刺激剂的效力约为PGE1的1/10。获得了PGH1和PGH2甲酯的质谱以及这两种化合物的红外光谱。PGH2的核磁共振谱的特征在于,C-9质子和C-11质子的信号分别位于4.58δ和4.47δ处。

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