Department of Pharmacology and Developmental Therapeutics Program, Cancer Center, Yale University School of Medicine, 333 Cedar Street, New Haven, CT 06520-8066, United States.
Bioorg Med Chem Lett. 2012 Oct 1;22(19):6242-7. doi: 10.1016/j.bmcl.2012.08.008. Epub 2012 Aug 10.
The efficacy of agents that alkylate the O-6 position of guanine is inhibited by O(6)-alkylguanine-DNA alkyltransferase (AGT) which removes these lesions from the tumor DNA. To increase differential toxicity, inhibitors must selectively deplete AGT in tumors, while sparing normal tissues where this protein serves a protective function. A newly synthesized prodrug of the AGT inhibitor O(6)-benzylguanine (O(6)-BG) with an α,α-dimethyl-4-nitrobenzyloxycarbonyl moiety masking the essential 2-amino group has demonstrated the feasibility of targeting hypoxic regions that are unique to solid tumors, for drug delivery. However, these modifications resulted in greatly decreased solubility. Recently, new potent global AGT inhibitors with improved formulatability such as O(6)-[(3-aminomethyl)benzylguanine (1) have been developed. However, acetylamino (N-(3-(((2-amino-9H-purin-6-yl)oxy)methyl)benzyl)acetamide) (2) exhibits a pronounced decrease in activity. Thus, 1 would be inactivated by N-acetylation and probably N-glucuronidation. To combat potential conjugational inactivation while retaining favorable solubility, we synthesized 6-((3-((dimethylamino)methyl)benzyl)oxy)-9H-purin-2-amine (3) in which the 3-aminomethyl moiety is protected by methylation; and to impart tumor selectivity we synthesized 2-(4-nitrophenyl)propan-2-yl(6-((3-((dimethylamino)methyl)benzyl)oxy)-9H-purin-2-yl)carbamate (7), a hypoxia targeted prodrug of 3 utilizing an α,α-dimethyl-4-nitrobenzyloxycarbonyl moiety. Consistent with this design, 7 demonstrates both hypoxia selective conversion by EMT6 cells of 7 to 3 and hypoxic sensitization of AGT containing DU145 cells to the cytotoxic actions of laromustine, while exhibiting improved solubility.
O(6)- 烷基鸟嘌呤-DNA 烷基转移酶 (AGT) 可将鸟嘌呤 O-6 位上的烷基移除,从而抑制具有烷化 O-6 位鸟嘌呤作用的试剂的疗效。为了提高差异毒性,抑制剂必须选择性地耗尽肿瘤中的 AGT,同时保护正常组织,因为该蛋白在正常组织中具有保护功能。新合成的 AGT 抑制剂 O(6)- 苯甲基鸟嘌呤 (O(6)-BG) 的前药,具有 α,α- 二甲基-4-硝基苯甲酰氧基羰基部分掩蔽必需的 2-氨基,已证明可以针对实体瘤特有的缺氧区域进行药物输送。然而,这些修饰导致溶解度大大降低。最近,已经开发出具有更好可成型性的新型有效全球 AGT 抑制剂,例如 O(6)-[(3- 氨甲基)苯甲基]鸟嘌呤(1)。然而,乙酰氨基(N-(3-(((2-氨基-9H-嘌呤-6-基)氧基)甲基)苯甲基)乙酰胺)(2)表现出活性明显降低。因此,1 可能会被 N-乙酰化和可能的 N-葡糖醛酸化失活。为了防止潜在的共轭失活,同时保持有利的溶解度,我们合成了 6-((3-((二甲氨基)甲基)苯甲基)氧基)-9H-嘌呤-2-胺(3),其中 3-氨甲基部分被甲基化保护;为了赋予肿瘤选择性,我们合成了 2-(4-硝基苯基)丙-2-基(6-((3-((二甲氨基)甲基)苯甲基)氧基)-9H-嘌呤-2-基)氨基甲酸酯(7),这是 3 的缺氧靶向前药,利用 α,α- 二甲基-4-硝基苯甲酰氧基羰基部分。与该设计一致,7 证明 EMT6 细胞对 7 向 3 的缺氧选择性转化以及含有 AGT 的 DU145 细胞对拉罗莫司汀的细胞毒性作用的缺氧敏感性增强,同时表现出改善的溶解度。