Kamernitzky A V, Levina I S, Kulikova L E, Ignatov V N, Korkhov V V, Nikitina G V, Terekhina A I
J Steroid Biochem. 1982 Jan;16(1):61-7. doi: 10.1016/0022-4731(82)90144-3.
A new class of modified progesterones with an additional ring in the 16 alpha , 17 alpha-position (pregna-D'-pentaranes) are described. Compounds containing 4- and 6-membered D'-ring (D'4- and D'6-pentaranes) were synthesized by the cycloaddition of acetylene or 1,3-butadiene, respectively, to the conjugated 16-double bond of 16-dehydro-20-keto steroids. The D'3-pentarane was prepared by the addition of diazomethane to the steroidal olefin followed by decomposition of the intermediate 16 alpha , 17 alpha-pyrazoline. The D'5-pentarane was obtained by conventional contraction of cyclohexane D'-ring of the corresponding D'6-pentarane. Progestational and contraceptive activity has been investigated for these compounds. They were found to exhibit a high progestational activity in the McPhail assay and also to be active in the pregnancy maintenance test in ovariectomized rabbits. Some of the D'-pentaranes displayed a remarkable contraceptive effect in combination with mestranol.
描述了一类新型的修饰孕酮,其在16α,17α位带有一个额外的环(孕甾-D'-戊环烷)。分别通过乙炔或1,3-丁二烯与16-脱氢-20-酮甾体的共轭16-双键进行环加成反应,合成了含有4-和6-元D'-环(D'4-和D'6-戊环烷)的化合物。通过将重氮甲烷加成到甾体烯烃上,然后分解中间体16α,17α-吡唑啉来制备D'3-戊环烷。通过相应的D'6-戊环烷的环己烷D'-环的常规缩环反应获得D'5-戊环烷。已经对这些化合物的孕激素活性和避孕活性进行了研究。发现它们在麦克费尔试验中表现出高孕激素活性,并且在去卵巢兔的妊娠维持试验中也具有活性。一些D'-戊环烷与炔雌醇联合使用时显示出显著的避孕效果。