Natural Products Journal, The - Online First
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Mechanistic Overview on Therapeutic Potential of Phenols Targeting the Breast Cancer: Molecular Insights and Future Road to Drug Design
Available online: 04 February 2025More LessBreast cancer is the most common malignancy globally. It is associated with genetic and lifestyle risk factors. Many chemotherapeutic agents are currently available for breast cancer. Despite their moderate efficacy in breast cancer therapy, many of these chemotherapeutic agents are associated with adverse effects. A few patients also have the possibility of developing resistance to these drugs over time. The resistance to these chemotherapeutic agents illustrates the necessity to seek novel therapeutic strategies. Phenols are a class of plant-derived compounds that have an aromatic ring with at least one hydroxyl group. They are well known for their antioxidant, anti-inflammatory, and anti-proliferative effects. A diet rich in fruits and vegetables has a high content of polyphenols. Various in vitro and in vivo studies in the past two decades have demonstrated the therapeutic potential of phenol in breast cancer. Each of these polyphenol compounds has promising potential to modulate breast cancer in various stages, including proliferation, angiogenesis, invasion, and metastasis. This review focuses on the various in vitro and in vivo studies done in both phenolic compounds and phenolic extracts and the efficacy of phenols in modulating breast carcinogenesis by various mechanisms. The potential of phenols to inhibit various oncogenes and tumor-associated proteins is also discussed. The ability of polyphenols to sensitize hormone-resistant and chemoresistant breast cancer cell lines to various chemotherapeutic agents has also been highlighted.
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Potential Plant-based Remedies for Gouty Arthritis: A Comprehensive Review on Counterweighing the Inflammatory Pathways
Authors: Rupama Thakuria, Purbajit Chetia and Abu Saif MustaqueAvailable online: 24 January 2025More LessThe complex etiology of Gouty Arthritis (GA) makes it a multidimensional illness for which there are now no effective therapeutic therapies that can stop its development entirely. This review examines how effectively different plants and their constituents reduce blood uric acid levels and lessen the predisposition to gout. Research has looked at the possible roles of oxidative stress markers, inflammatory pathways, important transport and signaling proteins, and the health benefits of different plants and their components in the development of GA. Plant remedies have been used for a long time to treat human and animal ailments. Most people in developing countries use traditional plant-based medicine for basic care due to its affordability, availability, and cultural acceptability. This review aims to gather comprehensive information on plants and their compounds that exhibit anti-gout activities, focusing on in vitro and in vivo investigations. The scientific database was searched by using different keywords, and papers published between March 2008 and December 2023 were considered. The inclusion criteria were publications on inflammatory mediators, free radicals, oxidative stress, or proteins in gout etiology or evolution, along with plant-based remedies. Finally, 27 publications based on inclusion and exclusion criteria reported the active compounds and analyzed parameters and outcomes of research carried out with these medicinal plants. This paper extensively explores the potential mechanism of employing medicinal herbs for the management of gout. However, more investigation is needed to fully comprehend the role that various biomarkers play in the development of GA, as well as to investigate the possible functions of different plants and the substances found in them.
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Medicinal Benefits of Frankincense: Future Approach to Effective Drug Design
Available online: 21 January 2025More LessFrankincense is obtained from the tree, which belongs to the Bowellia family. Frankincense is found in China, India, Middle-East Asia, the Arabian Peninsula, and different parts of Africa. Incisions are given on the tree trunk to obtain the gum, which hardens to form frankincense. It has been used as a traditional medicine to treat diarrhea, infection, tuberculosis, asthma, arthritis, cancer, wounds, gingivitis, psoriasis, and other inflammatory conditions. Frankincense gum is used for its aromatic properties and fragrance. Frankincense contains essential oils, gum resins, alcohol, and water-soluble resins. The chemical compounds present in the natural product and their yield depend on various factors such as geographical location, the surface area of the wood, climatic conditions in which it is grown, the age of the tree, and the methods of collection. Among the active compounds, unique pentacyclic triterpene acids such as boswellic acid (BA) are present. The phytochemicals include β-boswellic acid, acetyl-β-boswellic acid (ABA), 11-keto-β-boswellic acid (KBA), and 3-acetyl-11-keto-β-boswellic acid (AKBA) form the major components. BA possesses anti-inflammatory action due to its control of cytokine production. The active compounds in frankincense act on 5-lipooxygenase and cyclooxygenase, thereby producing an anti-inflammatory effect. We discuss the role of frankincense on the integumentary, nervous, cardiovascular, respiratory, digestive, endocrine, musculoskeletal, and immune systems with special emphasis on the molecular basis of action and signaling pathways. Recent approaches in therapeutics by designing new nanoformulations of frankincense may be beneficial for better drug delivery to the desired site, help in controlled release, increase solubility and bioavailability, and reduce toxicity.
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Qualitative and Structural Insights into Levantilides C/D via LC-MS
Authors: Wei Zhao, Jian Zhou, Nan-Nan Chen, Jingming Zhou, Hong Jiang and Bin WuAvailable online: 20 January 2025More LessIn this study, we utilized high-performance liquid chromatography coupled with quadrupole-time of flight mass spectrometry (HPLC-Q-TOF/MS/MS), combined with electrospray ionization in the positive mode (ESI+), to establish a comprehensive framework for chromatographic separation and mass spectrometric detection.
The primary focus was on performing collision-induced dissociation (CID) experiments on levantilide D, a newly identified macrolide, and its well-established analog, levantilide C, in order to elucidate their mass spectral fragmentation patterns.
The results revealed that the cleavage patterns of levantilides were successfully characterized when ionized in the positive mode. These fragmentation profiles provide valuable insights for the rapid and accurate structural identification and quantitative analysis of levantilides when they often occur in trace amounts.
Furthermore, this methodology offers crucial technical references for environmental pollutant monitoring and pharmacokinetic investigations for levantilide-related compounds.
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Recent Advances in the Microbial Oxidation and Ring Rearrangement of Terpenoidal Compounds by Aspergillus niger
Authors: Mohammad Yasin Mohammad and M. Iqbal ChoudharyAvailable online: 24 December 2024More LessIn this review, recent advances in the microbial oxidation and ring rearrangement of various terpenoidal compounds by Aspergillus niger are reviewed. Studies on hydroxylation, acid and keto formations, Baeyer-Villiger oxidation, and ring rearrangements are also explored. Moreover, various terpenoidal compound substrates and their metabolites used for fungal biotransformations are compiled. This review attempts to cover the latest developments in the scientific literature from 2018 to 2023.
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Antimicrobial Macrolide Levantilide D from Rare Marine Micromonospora sp.
Authors: Wei Zhao, Jian Zhou, Honglei Jiang, Yichao Ge, Jingming Zhou, Meilu Zhao, Ru Lin, Hong Jiang and Bin WuAvailable online: 10 October 2024More LessIntroductionOne new levantilide D (2) with a 20-membered macrolide, along with one known levantilide C (1), was isolated from a rare marine actinomycetes Micromonospora sp. (FIMYZ52).
MethodThe structural elucidation of the compounds was based on integrated analyses involving 1D and 2D NMR spectroscopy and HR-ESI-MS.
ResultThe relative and absolute configurations of compounds 1 and 2 were ascertained by integrating multispectral ROESY and NOESY information from analogs in conjunction with theoretical TDDFT-ECD calculations. Levantilide D (2) exhibited antibacterial activity against Staphylococcus aureus.
ConclusionA plausible biosynthetic pathway of the macrolide compounds (1-2) was proposed.
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Metabolites of Culinary-medicinal Mushroom Hericium erinaceus Showed Anti-neuroinflammatory Activity in BV2 Cells and Anti-H2O2-induced Oxidative Stress Activity in SH-SY5Y Cells
Authors: Jing Wei, Chao Lin, Zhen-Xin Wang, Yi-Lin Zhang, Shi-Xi Li, Xuan-Sheng Hu, He-Ping Hui, Zhe Wang, Yi-Qi Zhao, Xue-Jun Wang and Jianzhao Qi
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