Natural Anticancer Molecules and Their Therapeutic Potential DOI Open Access
Junmin Zhang, Elaine Lai‐Han Leung

International Journal of Molecular Sciences, Journal Year: 2023, Volume and Issue: 24(22), P. 16066 - 16066

Published: Nov. 8, 2023

Cancer poses a significant global public health challenge [...]

Language: Английский

Insight into the molecular interaction between the anticancer drug, enzalutamide and human alpha-2-macroglobulin: Biochemical and biophysical approach DOI
Mohammad Khalid Zia, Tooba Siddiqui,

Sana Ansari

et al.

Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy, Journal Year: 2024, Volume and Issue: 311, P. 123957 - 123957

Published: Jan. 26, 2024

Language: Английский

Citations

6

Optimizing Enantiomeric Resolution of Chiral Triazoles in Supercritical Fluid Chromatography DOI Open Access
Codruţa Frîncul, Alina Ghinet, Dalila Belei

et al.

Chirality, Journal Year: 2025, Volume and Issue: 37(2)

Published: Jan. 23, 2025

Chirality plays a crucial role in the pharmacological activity of triazoles, key scaffold antifungal agents and various therapeutic applications. This study focuses on optimizing enantiomeric resolution chiral triazoles using supercritical fluid chromatography (SFC) 10 different columns, either immobilized or coated, chlorinated nonchlorinated, cellulose amylose-based stationary phases (CSPs). Four novel two marketed ones (tebuconazole hexaconazole) were separated to determine optimal conditions. The best was achieved CSPs across tested compounds. Optical rotation X-ray crystallography employed absolute configurations purified enantiomers.

Language: Английский

Citations

0

Long-term bioreactor cultivation affects dioscin content and the ratio of 25(S)- and 25(R)-protodioscin isomers in the suspension cell culture of Dioscorea deltoidea Wall DOI
М. В. Титова, Elena Popova,

Igor M. Ivanov

et al.

Journal of Biotechnology, Journal Year: 2025, Volume and Issue: unknown

Published: March 1, 2025

Language: Английский

Citations

0

From extract to chiral analyses of the natural products DOI
Imran Ali, Mohd Mustaqeem, Ersin Demır

et al.

Elsevier eBooks, Journal Year: 2025, Volume and Issue: unknown, P. 75 - 122

Published: Jan. 1, 2025

Language: Английский

Citations

0

Myrsinane-Type Diterpenes: A Comprehensive Review on Structural Diversity, Chemistry and Biological Activities DOI Open Access
Eduarda Mendes, Cátia Ramalhete, Noélia Duarte

et al.

International Journal of Molecular Sciences, Journal Year: 2023, Volume and Issue: 25(1), P. 147 - 147

Published: Dec. 21, 2023

species are important sources of polycyclic and macrocyclic diterpenes, which have been the focus natural-product-based drug research due to their relevant biological properties, including anticancer, multidrug resistance reversal, antiviral, anti-inflammatory activities. Premyrsinane, cyclomyrsinane, myrsinane diterpenes generally collectively designated as myrsinane-type diterpenes. These compounds derived from lathyrane structure characterized by having highly oxygenated rearranged systems. This review aims describe summarize distribution diversity 220 isolated in last four decades about 20

Language: Английский

Citations

9

Scutellarein inhibits lung cancer growth by inducing cell apoptosis and inhibiting glutamine metabolic pathway DOI
Di Zhang,

Yinwen Wang,

Peng Yu

et al.

Journal of Ethnopharmacology, Journal Year: 2024, Volume and Issue: 337, P. 118999 - 118999

Published: Oct. 28, 2024

Language: Английский

Citations

1

Evaluation of Antitumor Activity of Xanthones Conjugated with Amino Acids DOI Open Access
Flávia Barbosa, Joana Araújo, Virgínia M. F. Gonçalves

et al.

International Journal of Molecular Sciences, Journal Year: 2024, Volume and Issue: 25(4), P. 2121 - 2121

Published: Feb. 9, 2024

Cancer is a complex disease characterized by several alterations, which confer, to the cells, capacity proliferate uncontrollably and resist cellular death. Multiresistance conventional chemotherapy drugs often cause of treatment failure; thus, search for natural products or their derivatives with therapeutic action essential. Chiral xanthones (CDXs) have shown potential inhibitory activity against growth some human tumor cell lines. This work reports screening library CDXs, through viability assays, in different cancer lines: A375-C5, MCF-7, NCI-H460, HCT-15. CDXs’ effect was analyzed based on parameters it also verified if these compounds were substrates glycoprotein-P (Pgp), one main mechanisms resistance therapy. Pgp expression evaluated all lines, but no observed, except Also, when humanized yeast expressing gene MDR1 used, conclusions could be drawn about CDXs as substrates. The selected did not induce significant differences metabolic analyzed. These results show that present promising antitumor activity, other should triggered compounds.

Language: Английский

Citations

0

Determination of the Absolute Configuration of Secondary Alcohols in a Compound Mixture via the Application of Competing Enantioselective Acylation Coupled with LC/MS Analysis DOI Creative Commons

Bum Soo Lee,

Hoon Kim, Jiwon Baek

et al.

Pharmaceutics, Journal Year: 2024, Volume and Issue: 16(3), P. 364 - 364

Published: March 5, 2024

The determination of natural product stereochemistry plays a significant role in drug discovery and development. Understanding the products is essential for predicting optimizing their interactions with biological targets, which, turn, influences therapeutic efficacy, safety, overall impact on living organisms. Here, we present first application competitive enantioselective acylation (CEA) reactions conjunction LC/MS analysis determining absolute configuration secondary alcohols which were purified as mixture. This approach utilizes enantiomeric pair HBTM (homobenzotetramisole) catalysts, demonstrating sufficient kinetic resolution alcohols. rapid reaction kinetics quantitatively estimated characterization technique transformations. Our study has expanded CEA coupled to mixtures. Utilizing analysis, offers sensitive simple method determination. Additionally, cost/time-effective since only small quantities substrates short time are required characterizing compared other conventional methods.

Language: Английский

Citations

0

Stereoselective Signal Amplification for Multiplex Detection of Tyrosinamide DOI
Xinying Zhang,

Xiaoqian Zhou,

Ziheng Hu

et al.

Published: Jan. 1, 2024

Download This Paper Open PDF in Browser Add to My Library Share: Permalink Using these links will ensure access this page indefinitely Copy URL DOI

Language: Английский

Citations

0

Stereoselective Signal Amplification for Multiplex Detection of Tyrosinamide DOI
Xinying Zhang,

Xiaoqian Zhou,

Ziheng Hu

et al.

Published: Jan. 1, 2024

The recognition and separation of stereoselective molecules with similar chemical properties structures are great biological significance. Developing a highly effective chiral platform is crucial for further research on molecules. Herein, aptamer-modified gold nanoclusters functionalized electrochemical device that exhibits an ideal enantioselective reported. Its current restriction amplification strategy enables signal electrode. It found introducing aptamers into the would result in nice tyrosinamide recognition. This work has liner range ranging from 1 nM to 10 μM. Furthermore, ratio peak change was 4. study might provide useful designing sensitive devices materials restricting their currents.

Language: Английский

Citations

0