SRSMC, UMR 7565 Nancy Université, CNRS, Equipe Groupe d'Etude des Vecteurs Supramoléculaires du Médicament, Faculté de Pharmacie, 5 rue Albert Lebrun, 54001 Nancy Cedex, France.
Bioorg Med Chem. 2010 Jan 1;18(1):36-45. doi: 10.1016/j.bmc.2009.11.016. Epub 2009 Nov 12.
Nine anionic water-soluble calix[4]arene species, incorporating sulfonate, carboxylate or phosphonate groups, six of them incorporating two 2,2'-bithiazole subunits in alternate position at the lower rim, have been synthesised and evaluated as anti-HIV agents on various HIV strains and cells of the lymphocytic lineage (HIV-1 III B/MT4, HIV-1 LAI/CEM-SS, HIV-1 Bal/PBMC), using AZT as reference compound. A toxicity was detected for a minority of compounds on PBMC whereas for the others no cellular toxicity was measured at concentrations up to 100 microM. Most of the compounds have an antiviral activity in a 10-50 microM range, and one of them, sulfonylated, displays its activity, whatever the tropism of the virus, at a micromolar concentration.
已合成了 9 种阴离子水溶性杯[4]芳烃,其中包含磺酸酯、羧酸酯或膦酸酯基团,其中 6 种在较低的边缘处以交替位置包含两个 2,2'-联噻唑亚基,将它们作为抗 HIV 药物进行评估,针对各种 HIV 株和淋巴细胞系的细胞(HIV-1 III B/MT4、HIV-1 LAI/CEM-SS、HIV-1 Bal/PBMC),以 AZT 作为参考化合物。在 PBMC 中检测到少数化合物具有毒性,而对于其他化合物,在高达 100 μM 的浓度下未测量到细胞毒性。大多数化合物在 10-50 μM 的范围内具有抗病毒活性,其中一种磺化化合物,无论病毒的趋向如何,在微摩尔浓度下都表现出其活性。