JOURNAL 2334
Records of Natural Products
Year: 2022 Issue: 6 November-December
p.622 - 632
Viewed 2422 times.
-
Xuebo Zeng
-
Shengyan Qian
-
Yongzhong Lu
-
Yongjie Li
-
Lizhuang Chen
-
Yixin Qian
-
Zhangjiang He
-
Jichuan Kang
GRAPHICAL ABSTRACT

ABSTRACT
AA chemical investigation of secondary metabolites from the saprobic fungus Tubeufia rubra led to isolation of a novel nitrogen-containing glyceride, Rubracin A (1), and a novel eight-membered cyclic ether carboxylate methyl ester, Rubracin H (2). Together with six known compounds (3-8). The chemical structure of these new compounds were elucidated by 1D and 2D NMR and HR-ESI-MS techniques. Although, there are no observed cytotoxic effects of compound 1 against MCF-7/Dox, A549/Dox, and K562/Dox cells at oncentrations below 25 μg/mL, usage of compound 1 and doxorubicin revealed the MDR reversal via decreased IC50 values than that of sole doxorubicin application in the cell lines. A preliminary Western Blot assay indicated that the MDR reversal of compound 1 was due to suppression of P-glycoprotein (P-gp) expression.
KEYWORDS- Rubracin A
- Tubeufia rubra PF02-2
- cytotoxic activity
- MDR reversal