Publications by authors named "Rongqin Sun"

Background: The construction of gels from low molecular weight gelators (LMWG) has been extensively studied in the fields of bio-nanotechnology and other fields. However, the understanding gaps still prevent the prediction of LMWG from the full design of those gel systems. Gels with multicomponent become even more complicated because of the multiple interference effects coexist in the composite gel systems.

View Article and Find Full Text PDF

Self-assembly peptide-based hydrogels are well known and popular in biomedical applications due to the fact that they are readily controllable and have biocompatibility properties. A dipeptide is the shortest self-assembling motif of peptides. Due to its small size and simple synthesis method, dipeptide can provide a simple and easy-to-use method to study the mechanism of peptides' self-assembly.

View Article and Find Full Text PDF

Self-assembling peptides can be used to design new materials for medical and biological applications. Here we synthesized and characterized two novel cyclic γ-peptides (γ-CPs) with hydrophobic inner surfaces. The NMR and FT-IR studies confirmed that the CPs could self-assemble into parallel stacking structures via intermolecular H-bonds and π-π interactions.

View Article and Find Full Text PDF

A series of new quinoline derivatives was designed, synthesized and evaluated for their antiproliferative activity. The results demonstrated that compounds 11p, 11s, 11v, 11x and 11y exhibited potent antiproliferative activity with IC value of lower than 10 μM against seven human tumor cell lines, and N-(3-methoxyphenyl)-7- (3-phenylpropoxy)quinolin-4-amine 11x was found to be the most potent antiproliferative agent against HCT-116, RKO, A2780 and Hela cell lines with an IC value of 2.56, 3.

View Article and Find Full Text PDF
Article Synopsis
  • A novel series of harmine derivatives, specifically N2-benzylated β-carbolines, were synthesized and evaluated for their anticancer properties, with compound 3c showing the most promising results.
  • Compound 3c demonstrated strong anticancer activity against various cancer cell lines (gastric carcinoma, melanoma, colorectal cancer) while exhibiting low toxicity to normal cells, effectively inducing cell apoptosis.
  • The mechanism of action for compound 3c involved the inhibition of the PI3K/AKT signaling pathway and increased production of reactive oxygen species (ROS), which together led to significant tumor growth suppression in a nude mice model.
View Article and Find Full Text PDF