Synthesis and HPLC-ECD Study of Cytostatic Condensed O,N-Heterocycles Obtained from 3-Aminoflavanones
作者:Ádám Szappanos、Attila Mándi、Katalin Gulácsi、Erika Lisztes、Balázs István Tóth、Tamás Bíró、Anita Kónya-Ábrahám、Attila Kiss-Szikszai、Attila Bényei、Sándor Antus、Tibor Kurtán
DOI:10.3390/biom10101462
日期:——
Racemic chiral O,N-heterocycles containing 2-arylchroman or 2-aryl-2H-chromene subunit condensed with morpholine, thiazole, or pyrrole moieties at the C-3-C-4 bond were synthesized with various substitution patterns of the aryl group by the cyclization of cis- or trans-3-aminoflavanone analogues. The 3-aminoflavanone precursors were obtained in a Neber rearrangement of oxime tosylates of flavanones
合成了具有在C-3-C-4键上与吗啉,噻唑或吡咯部分缩合的2-芳基苯并二氢吡喃或2-芳基-2 H-亚甲基亚基的外消旋手性O,N-杂环通过将顺式或反式-3-氨基黄酮类似物环化。3-氨基黄烷酮前体是在黄烷酮的肟甲苯磺酸盐的Neber重排中获得的,这提供了反式非对映异构体作为主要产物,并能够分离顺式和反式非对映异构体。该顺-和反式-氨基黄酮被用于制备5-芳基-铬诺[4,3-b] [ 1,4 ]恶嗪的三种非对映异构体。评估了稠合的杂环和前体的抗增殖活性,针对A2780和WM35癌细胞系。对于3-(N-氯乙酰氨基)-flavan-4-ol衍生物,显示与无环酸神经酰胺酶抑制剂的结构相似性,针对A2780,WM35和HaCat细胞系,测量了0.15μM,3.50μM和6.06μM的IC 50值,并证实了其凋亡机制。噻唑和吡咯缩合的2 H的低微摩尔IC 50值低至2.14μM-色烯衍生物。使用手性固定相通