Kreutzberger A, Tantawy A
Arzneimittelforschung. 1983;33(4):512-4.
With reference to the role that (2-adamantyl), urea, and thiourea moieties play in antiviral drugs, these structural elements have been included in the present investigations aimed at the development of the N-substituted N'-(2-adamantyl)-thioureas 3a-d through the reaction of 2-aminoadamantane (1) with the isothiocyanates 2a-d. In an analogous manner, the interaction of 1 with the isocyanates 2e-f has led to the N-substituted N'-(2-adamantyl)ureas 3e-f. Within structure type 3 there occur representatives exhibiting antiviral, antimycotic, and herbicidal activity.
关于(2-金刚烷基)、脲和硫脲部分在抗病毒药物中所起的作用,这些结构单元已被纳入目前的研究中,旨在通过2-氨基金刚烷(1)与异硫氰酸酯2a-d反应来开发N-取代的N'-(2-金刚烷基)硫脲3a-d。以类似的方式,1与异氰酸酯2e-f的相互作用产生了N-取代的N'-(2-金刚烷基)脲3e-f。在3型结构中存在具有抗病毒、抗真菌和除草活性的代表物。