128811-37-0Relevant articles and documents
Discovery of an 8-aza-5-thiaProstaglandin E1 analog as a highly selective EP4 receptor agonist
Kambe, Tohru,Maruyama, Toru,Naganawa, Atsushi,Asada, Masaki,Seki, Akiteru,Maruyama, Takayuki,Nakai, Hisao,Toda, Masaaki
, p. 1494 - 1508 (2012/01/13)
For the purpose of discovering an orally available EP4 subtype-selective agonist, a series of 8-aza prostaglandin E1 (PGE1) analogs were synthesized and evaluated for their affinity for PGE2 receptor subtypes. Additionally
Total syntheses of N-boc-protected 3′-deoxy-4′-azathymidine and 4′-azauridine
Rassu, Gloria,Pinna, Luigi,Spanu, Pietro,Ulgheri, Fausta,Casiraghi, Giovanni
, p. 4019 - 4022 (2007/10/02)
Novel modified nucleosides 4, 11, ent-11, and 17, wherein the furanose ring oxygen is replaced by nitrogen, have been synthesized by reacting azasugars 3, 10, ent-10, and 15 with silylated uracil or thymine bases.