New asterosaponin, acanthaglycoside G (), along with three previously known steroidal oligoglycosides (), were isolated from the ethanolic extract of the starfish , collected off the coast of Vietnam. The structure of was mainly elucidated by extensive NMR and ESIMS techniques as sodium 6--{-D-fucopyranosyl-(1→2)--D-quinovopyranosyl-(1→4)-[-D-quinovopyranosyl-(1→2)]--D-quinovopyranosyl-(1→3)--D-quinovopyranosyl}-6-hydroxy-5-pregn-9(11)-en-20-one-3-yl sulfate. Compounds and showed slight cytotoxic activities against cancer RPMI-7951, HT-29, and MDA-MB-231 cell lines, but effectively inhibited in non-toxic concentrations colony formation of HT-29 and MDA-MB-231 cells and cell migration of MDA-MB-231 cells. Compounds and were inactive or less active, respectively.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1080/14786419.2019.1585845 | DOI Listing |
Anticancer Agents Med Chem
January 2025
Department of Pharmaceutics, College of Pharmacy, Jazan University, Saudi Arabia.
Nitrogen-based organic heterocyclic compounds are an important source of therapeutic agents. About 75% of drugs approved by the FDA and currently available in the market are N-heterocyclic organic compounds. The N-heterocyclic organic compounds like pyridine, indole, triazoles, triazine, imidazoles, benzimidazoles, quinazolines, pyrazoles, quinolines, pyrimidines, porphyrin, etc.
View Article and Find Full Text PDFMolecules
December 2024
Institute of Chemistry, Faculty of Science and Technology, Jan Dlugosz University in Czestochowa, Armii Krajowej 13/15, 42-200 Czestochowa, Poland.
This study investigates the structural, vibrational, and biological properties of novel palladium(II) and platinum(II) complexes with 5-chloro-7-azaindole-3-carbaldehyde (5ClL) and 4-chloro-7-azaindole-3-carbaldehyde (4ClL) ligands. Infrared and Raman spectroscopy, combined with DFT (ωB97X-D) calculations, provided valuable information about metal-ligand interactions, the or conformation of the aldehyde group in the ligands, and the presence of isomers in the metal complexes obtained in the solid state. tests were used to evaluate the antiproliferative activity of the novel complexes against several cancer cell lines, including ovarian cancer (A2780), cisplatin-resistant ovarian cancer (A2780cis), colon cancer (HT-29), and triple-negative breast cancer (MDA-MB-231), as well as normal mouse fibroblasts (BALB/3T3).
View Article and Find Full Text PDFLife (Basel)
November 2024
Department of Plant Physiology, Faculty of Biology, Sofia University "St. Kliment Ohridski", 8 Dragan Tsankov Blvd., 1164 Sofia, Bulgaria.
Despite significant efforts, cancer remains the second leading cause of mortality worldwide. The medicinal plant L. represents a valuable source of biologically active compounds with pharmacological activities including antioxidant, anti-inflammatory, antimicrobial, and antiviral.
View Article and Find Full Text PDFSci Rep
November 2024
Medicinal and Natural Products Chemistry Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
A new series of 2-amino-1,4-naphthoquinone-benzamides 5a-n was designed based on previously reported potent cytotoxic agents. These compounds were synthesized from the reaction of 1,4-naphthoquinone, 4-aminobenzoic acid, and appropriate amine derivatives in good yields. Cytotoxic activities of the target compounds 5a-n were evaluated against three cancer cell lines MDA-MB-231, SUIT-2, and HT-29 by MTT assay and the obtained in vitro data.
View Article and Find Full Text PDFMolecules
August 2024
LABCiS, UR 22722, Faculté de Pharmacie, Univ. Limoges, F-87000 Limoges, France.
The endolichenic fungus sp. was isolated from the lichen harvested in France. sp.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!