Struga Marta, Kossakowski Jerzy, Kedzierska Ewa, Fidecka Sylwia, Stefańska Joanna
Department of Medical Chemistry, The Medical University, 3 Oczki Str., 02-007 Warsaw, Poland.
Chem Pharm Bull (Tokyo). 2007 May;55(5):796-9. doi: 10.1248/cpb.55.796.
A series of nineteen new thiourea and urea derivatives of 10-isopropyl-8-methyl-4-azatricyclo[5.2.2.0(2,6)]undec-8-ene-3,5-dione, 1-isopropyl-7-methyl-4-azatricyclo[5.2.2.0(2,6)]undec-8-ene-3,5-dione and 1,7,8,9,10-pentamethyl-4-azatricyclo[5.2.1.0(2,6)]dec-8-ene-3,5-dione have been prepared and studied by (1)H-NMR. The compound k1a (1-(1,7,8,9,10-pentamethyl-3,5-dioxo-4-aza-tricyclo[5.2.1.0(2,6)]dec-8-en-4-yl)-3-phenyl-urea) was tested for pharmacological activity on animal central nervous system (CNS). The activities of synthesized compounds were evaluated for their cytotoxicity and anti-HIV-1 activity in MT-4 cells. Antimicrobial activity of the newly obtained derivatives was tested against some Gram-positive and Gram-negative bacteria and fungi of the Candida species.
已制备了一系列19种新的硫脲和脲衍生物,它们分别是10-异丙基-8-甲基-4-氮杂三环[5.2.2.0(2,6)]十一碳-8-烯-3,5-二酮、1-异丙基-7-甲基-4-氮杂三环[5.2.2.0(2,6)]十一碳-8-烯-3,5-二酮和1,7,8,9,10-五甲基-4-氮杂三环[5.2.1.0(2,6)]癸-8-烯-3,5-二酮的衍生物,并通过¹H-NMR进行了研究。化合物k1a(1-(1,7,8,9,10-五甲基-3,5-二氧代-4-氮杂三环[5.2.1.0(2,6)]癸-8-烯-4-基)-3-苯基脲)在动物中枢神经系统(CNS)上进行了药理活性测试。对合成化合物在MT-4细胞中的细胞毒性和抗HIV-1活性进行了评估。对新得到的衍生物针对一些革兰氏阳性和革兰氏阴性细菌以及念珠菌属真菌进行了抗菌活性测试。