Golmakaniyoon Sima, Askari Vahid Reza, Abnous Khalil, Zarghi Afshin, Ghodsi Razieh
Biotechnology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Department of Medicinal Chemistry, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.
Iran J Pharm Res. 2019 Winter;18(1):16-29.
Quinones such as 1,4-naphthoquinones are abundant in nature and naphthoquinone based natural products are known to possess anticancer activity. This pharmacophore is known to convey anticancer activity to some drugs such as streptonigrin, mitomycin A, . We synthesized and characterized different classes of naphthoquinone derivatives including bis naphthoquinone, 2-arylaminonaphthoquinone, benzoxantene-6,11-dione and benzoacridine-5,6-dione derivatives instead of the expected 2-hydroxy-3-(substituted phenyl(aryl amino)methyl)naphthalene-1,4-dione derivatives from the reaction of 2-hydroxy1,4-naphthoquinone (lawson) with different benzaldehydes and aryl amines. Benzoacridine-5,6-dione derivatives and related imines showed potent anti-breast cancer activity in MCF-7 cancer cells. The results revealed that five compounds benzoacridinedione derivatives ( and ) and imines (, and ) by the IC range of 5.4-47.99 μM are the most potent anti-breast cancer structures.
醌类化合物如1,4-萘醌在自然界中广泛存在,基于萘醌的天然产物具有抗癌活性。已知这种药效基团能赋予某些药物如链黑菌素、丝裂霉素A等抗癌活性。我们合成并表征了不同类别的萘醌衍生物,包括双萘醌、2-芳基氨基萘醌、苯并氧杂蒽-6,11-二酮和苯并吖啶-5,6-二酮衍生物,而不是2-羟基-3-(取代苯基(芳基氨基)甲基)萘-1,4-二酮衍生物,后者是由2-羟基-1,4-萘醌(劳森)与不同的苯甲醛和芳基胺反应生成的。苯并吖啶-5,6-二酮衍生物及相关亚胺在MCF-7癌细胞中显示出强大的抗乳腺癌活性。结果表明,五种苯并吖啶二酮衍生物( 和 )和亚胺(, 和 )的IC范围为5.4 - 47.99 μM,是最有效的抗乳腺癌结构。