Aboul-Fadl T, El Shorbagi A N
Faculty of Pharmacy, University of Assiut, Egypt.
Arch Pharm (Weinheim). 1997 Nov;330(11):327-32. doi: 10.1002/ardp.19973301103.
3,5-Disubstituted tetrahydro-2H-1,3,5-thiadiazine-2-thione (THTT) derivatives; 4a-g were prepared and found to be a promising prodrug approach for peptide drugs. The pH profile for their degradation in aqueous buffer solutions was determined using HPLC technique and accounted for, in terms of specific base-catalyzed reactions. All of the compounds however, showed high acid-stability. Enzymatic (human serum) hydrolysis of the different derivatives offered an advantageous range of t1/2's, the property that permits controlling onset and duration of actions of drugs.
3,5-二取代四氢-2H-1,3,5-噻二嗪-2-硫酮(THTT)衍生物;4a - g已制备完成,并被发现是一种很有前景的肽类药物前药方法。使用高效液相色谱技术测定了它们在水性缓冲溶液中的降解pH曲线,并根据特定的碱催化反应进行了解释。然而,所有化合物均表现出高酸稳定性。不同衍生物的酶促(人血清)水解提供了一系列有利的半衰期,这一特性可用于控制药物作用的起效时间和持续时间。