Vítolo M J, Márquez V E, Hurtado I
J Med Chem. 1978 Jul;21(7):692-4. doi: 10.1021/jm00205a020.
The synthesis and antiallergic activity of a new heterocyclid steroidal molecule are described. Compound 1 was shown to inhibit the rat passive cutaneous anaphylaxis and its activity in this system was compared to that of disodium cromoglycate. It is orally active at a dose of 35 mg/kg (ED50) and its activity persists for up to 6 h for larger doses.
描述了一种新型杂环甾体分子的合成及其抗过敏活性。化合物1被证明能抑制大鼠被动皮肤过敏反应,并将其在该系统中的活性与色甘酸钠的活性进行了比较。它在35mg/kg(半数有效剂量)的剂量下具有口服活性,对于更大剂量,其活性可持续长达6小时。