Mundill P H, Fries R W, Woenckhaus C, Plapp B V
J Med Chem. 1981 Apr;24(4):474-7. doi: 10.1021/jm00136a021.
2-(Adenin-9-yl)ethanesulfonic acid (1), 3-(adenin-9-yl)propanesulfonic acid (2), 9-(5-deoxy-beta-D-ribofuranosyl)-adenine-5'-sulfonic acid (3), and 9-(3-deoxy-beta-D-arabinofuranosyl)adenine-3'-sulfonic acid (4) were prepared by reaction of the corresponding chlorides by sodium sulfite (1-3) or by reaction of an epoxide with sodium hydrogen sulfite (4). They inhibited a typical nucleotide-binding enzyme, horse liver alcohol dehydrogenase, with inhibition constants in the range of 0.18-4.9 mM at pH 8, 25 degrees C.
2 -(腺嘌呤 - 9 - 基)乙烷磺酸(1)、3 -(腺嘌呤 - 9 - 基)丙烷磺酸(2)、9 -(5 - 脱氧 - β - D - 呋喃核糖基)腺嘌呤 - 5'-磺酸(3)和9 -(3 - 脱氧 - β - D - 阿拉伯呋喃糖基)腺嘌呤 - 3'-磺酸(4)通过相应的氯化物与亚硫酸钠反应(1 - 3)或通过环氧化物与亚硫酸氢钠反应(4)制备。它们抑制一种典型的核苷酸结合酶,即马肝醇脱氢酶,在pH 8、25℃时抑制常数范围为0.18 - 4.9 mM。