Poltavchenko G M, Katkov V F, Pavlov V N, Travkin O V
Biull Eksp Biol Med. 1990 Feb;109(2):165-7.
Several N6-adenosine analogs were synthesized and their A1-purine receptor binding affinities were determined. Our results demonstrate that N6-allyl- and N6-aminopropanol-adenosine increase affinities to A1-purine receptor in guinea pig ileum.
合成了几种N6-腺苷类似物,并测定了它们对A1嘌呤受体的结合亲和力。我们的结果表明,N6-烯丙基腺苷和N6-氨基丙醇腺苷可增加豚鼠回肠对A1嘌呤受体的亲和力。