Unknown

Dataset Information

0

Synthesis, characterization and activity evaluation of matrinic acid derivatives as potential antiproliferative agents.


ABSTRACT: A series of new matrinic acid derivatives 5a-e was synthesized. The chemical structures of the synthesized compounds were confirmed by ¹H-NMR, ¹³C-NMR, and electrospray ionization mass spectroscopy. The anti-tumor activities were also investigated in vitro by evaluating the effect of synthesized compounds on the proliferation of A375, A549, HeLa, and HepG2 cells. Compound 5e was found to be the most potent against A375 and HeLa cells, with IC?? values of 37 and 75.5 ?g/mL, respectively. Compounds 5b, 5c, 5g, and 5h also exhibited antiproliferative activities against A549 cells, with IC?? values within the 36.2-47 ?g/mL range. For HepG2 cells, 5e and 5i, with IC?? values of 78.9 and 61 ?g/mL, respectively, showed higher antiproliferative activity than taxol.

SUBMITTER: Chao F 

PROVIDER: S-EPMC6269743 | biostudies-literature | 2013 May

REPOSITORIES: biostudies-literature

altmetric image

Publications

Synthesis, characterization and activity evaluation of matrinic acid derivatives as potential antiproliferative agents.

Chao Fan F   Wang Dong-En DE   Liu Rui R   Tu Qin Q   Liu Jian-Jun JJ   Wang Jinyi J  

Molecules (Basel, Switzerland) 20130510 5


A series of new matrinic acid derivatives 5a-e was synthesized. The chemical structures of the synthesized compounds were confirmed by ¹H-NMR, ¹³C-NMR, and electrospray ionization mass spectroscopy. The anti-tumor activities were also investigated in vitro by evaluating the effect of synthesized compounds on the proliferation of A375, A549, HeLa, and HepG2 cells. Compound 5e was found to be the most potent against A375 and HeLa cells, with IC₅₀ values of 37 and 75.5 μg/mL, respectively. Compound  ...[more]

Similar Datasets

| S-EPMC7428852 | biostudies-literature
| S-EPMC9501232 | biostudies-literature
| S-EPMC7728372 | biostudies-literature
| S-EPMC6630221 | biostudies-literature
| S-EPMC6470795 | biostudies-literature
| S-EPMC6269912 | biostudies-literature
| S-EPMC6429172 | biostudies-literature
| S-EPMC8693647 | biostudies-literature
| S-EPMC6412232 | biostudies-literature
| S-EPMC4834670 | biostudies-literature