PeerJ Special Issue: Organic Chemistry for Health

PeerJ are delighted to announce the publication of “Organic Chemistry for Health“, a cross-journal Special Issue published by PeerJ Organic Chemistry and PeerJ Life and Environment, led by Editorial Board Members Pedro SilvaEder J. Lenardao and Christof Jäger.

Download the Special Issue PDF here

 

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GC-MS analysis of phytochemical compounds of Opuntia megarrhiza (Cactaceae), an endangered plant of Mexico

Madeleyne Cupido, Arturo De-Nova, María L Guerrero-González, Francisco Javier Pérez-Vázquez, Karen Beatriz Méndez-Rodríguez, Pablo Delgado-Sánchez​​​

Prevailing phytochemical compounds of Opuntia megarrhiza (10.7717/peerj-ochem.5/fig-3)

 

Opuntia megarrhiza is an endemic plant used in Mexican traditional medicine for the treatment of bones fractures in humans and domestic animals. This study from Cupido and colleagues aimed to identify and characterize the phytochemical compounds present in wild individuals of O. megarrhiza using Gas Chromatography Coupled to Mass Spectrometry – one of the most prevalent techniques for the detection and characterization of the structure of phytochemical compound. The authors used chloroform and methanol extracts from cladodes, which were analyzed by gas chromatography-electron impact-mass spectrometry. They obtained 53 phytochemical compounds, 19 of which have been previously identified as having some biological activity. Most of these compounds are alkanes, alkenes, aromatic hydrocarbons, fatty acids, and ketones. The researchers detected some fragmentation patterns that are described for the first time for this species. The variety of metabolites presents in O. megarrhiza justifies the medicinal use of this plant in traditional medicine and highlight it as a source of phytochemical compounds with potential in medicine and biotechnology.

 

Abubidentin A, New Oleanane-type Triterpene Ester from Abutilon bidentatum and its antioxidant, cholinesterase and antimicrobial activities

Gadah A. Al-Hamoud​, Nawal M. Al-Musayeib​, Musarat Amina, Sabrin R.M. Ibrahim​​​

This article, from Al-Hamoud et al.,  describes a phytochemical and biological investigation of aerial parts of Abutilon bidentatum (Hochst.) of Saudi origin. Petroleum ether fraction of ethanolic extract A. bidentatum was fractionated on a silica gel column and further purified with different chromatographic procedures for the isolation of chemical compounds. The chemical structures of all the pure isolated compounds were elucidated by the interpretation of their spectral data using IR, UV, 1H, 13C NMR, and MS spectroscopy and chemical methods (alkaline hydrolysis), and comparison with data reported in the literature.

A new oleanane-type triterpene ester, namely abubidentin A (3) (α, 3β, 30-trihydroxy-29-carboxy-olean-9(11), 12-diene-3-dotriacontanoate), along with two known compounds: 2-hydroxydocosanoic acid (1) and stigmasta-22-ene-3-β-ol (2) were isolated from the aerial parts of A. bidentatum. The abubidentinA displayed antioxidant, cholinesterase inhibitory and antimicrobial activities. AbubidentinA possessed strong antioxidant activity against DPPH and ABTS+ radical scavenging assays. This new triterpene exhibited high inhibition against acetylcholinesterase (IC50 38.13 ± 0.07 µgmL−1) and butyrylcholinesterase (IC50 32.68 ± 0.37 µgmL−1). Abubidentin A displayed promising antimicrobial activity against Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus (125–150 µgmL−1), which ultimately suggest that A. bidentatum can contribute as a source of new biologically active compounds, especially antioxidants and antimicrobial agents.

 

Analysis of the role and mechanism of EGCG in septic cardiomyopathy based on network pharmacology

Ji Wu, Zhenhua Wang, Shanling Xu, Yang Fu, Yi Gao, Zuxiang Wu, Yun Yu, Yougen Yuan, Lin Zhou, Ping Li​​​​

Schematic diagram of EGCG in the treatment of septic cardiomyopathy (10.7717/peerj.12994/fig-9)

 

Septic cardiomyopathy (SC) is a common complication of sepsis that leads to an increase in mortality. The pathogenesis of septic cardiomyopathy is unclear, and there is currently no effective treatment. EGCG (epigallocatechin gallate) is a polyphenol that has anti-inflammatory, antiapoptotic, and antioxidative stress effects. However, the role of EGCG in septic cardiomyopathy is unknown. In this study, Wu et al. used network pharmacology to predict the potential targets and molecular mechanisms of EGCG in the treatment of septic cardiomyopathy in a mouse model. The authors found that EGCG may be a potentially effective drug to improve septic cardiomyopathy. They show the potential mechanism by which EGCG improves myocardial injury in septic cardiomyopathy is through anti-inflammatory and anti-apoptotic effects. The anti-inflammatory and anti-apoptotic effects of EGCG occur not only through direct binding to six target proteins (IL-6,TNF-α, Caspase3, MAPK3, AKT1, and VEGFA) but also by reducing their expression.

 

Investigating effect of mutation on structure and function of G6PD enzyme: A comparative Molecular Dynamics Simulation study

Sadaf Rani, Fouzia Perveen Malik, Jamshed Anwar, Rehan Zafar Paracha​​​

 

Modelled structure of G6PD enzyme ( 10.7717/peerj.12984/fig-1)

Several natural mutants of the human G6PD enzyme exist and have been reported. Because the enzymatic activities of many mutants are different from that of the wildtype, the genetic polymorphism of G6PD plays an important role in the synthesis of nucleic acids via ribulose-5-phosphate and formation of reduced NADP in response to oxidative stress. G6PD mutations leading to its deficiency result in the neonatal jaundice and acute hemolytic anemia in human. Rani et al. demonstrate molecular dynamics simulations of the wildtype G6PD and its three mutants to monitor the effect of mutations on dynamics and stability of the protein. They revealed that a decrease in the stability of mutants is key factor for loss of their activity. The results demonstrated that mutations in the G6PD sequence resulted in altered structural stability and hence functional changes in enzymes. Our study also provides an insight in identifying the key inhibitory site in G6PD and its mutants which can be exploited to use them as a target for developing new inhibitors in rational drug design.

 

 

Combining biomedical knowledge graphs and text to improve predictions for drug-target interactions and drug-indications

Mona Alshahrani, Abdullah Almansour, Asma Alkhaldi, Maha A Thafar, Mahmut Uludag, Magbubah Essack, Robert Hoehndorf​​​

Knowledge graph used to repurpose the drugs (10.7717/peerj.13061/fig-1)

Biomedical knowledge is represented in structured databases and published in biomedical literature, and different computational approaches have been developed to exploit each type of information in predictive models. However, the information in structured databases and literature is often complementary. Alshahrani and collagues developed a machine learning method that combines information from literature and databases to predict drug targets and indications. To effectively utilize information in published literature, the authors integrate knowledge graphs and published literature using named entity recognition and normalization before applying a machine learning model that utilizes the combination of graph and literature. They then use supervised machine learning to show the effects of combining features from biomedical knowledge and published literature on the prediction of drug targets and drug indications. It is then demonstrated that this approach – using datasets for drug-target interactions and drug indications – is scalable to large graphs and can be used to improve the ranking of targets and indications by exploiting features from either structure or unstructured information alone.

 

 

 

 

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