Current Bioactive Compounds - Volume 22, Issue 3, 2026
Volume 22, Issue 3, 2026
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Pre-clinical Outcomes of Plant-based Male Oral Contraceptive: A Critical Review
More LessThis current review provides a thorough examination of the potential of plant-based chemicals as effective male contraceptive treatments by synthesizing results from several pre-clinical investigations. The established literature highlights the urgent requirement for male contraceptive strategies that are safe, effective, and reversible, considering the drawbacks and difficulties of current options. The need for male contraceptive research and the inherent drawbacks of available solutions are also covered in this review. It clarifies the possible benefits of plant-based contraceptives by emphasizing their natural source, expected safety profile, and low side effect rate. In this review, 49 plants evaluated for male oral contraceptive action are discussed. PubMed, Cochrane library, Embase, ScienceDirect, and Google Scholar databases are used for the literature search. This review explores the complex pathways, including hormone regulation, spermatogenesis suppression, sperm motility interference, and sperm maturation disruption, by which plant-based chemicals may have contraceptive effects. Pre-clinical investigations have examined a wide range of plant-derived substances, including flavonoids, anthraquinones, glycosides, alkaloids, phenolics, diterpenes, triterpenes, tannins, saponins, steroids, and phytosterols, among other phytochemical families. Every phytochemical is thoroughly examined, including its botanical origins, phytoconstituents, native name, and unique effects on male fertility. Results from research conducted on animals are methodically summarised in this study, including information on the effectiveness, dose, delivery methods, and reversibility of contraceptive effects. Furthermore, the discussion includes findings from in vitro research, emphasizing the possible influence on sperm parameters (sperm production, deformation, count, viability, and motility), reproductive hormones (testosterone level), thickness and diameter of seminiferous tubules (ST) as well as spermatocytes and secondary spermatocytes, Sertoli cells (SCs), and Leydig cell (LCs). According to the assessment, male contraceptives made of plants have a lot of potential as a future weapon in the arsenal of contraceptives. Pre-clinical research has shown the safety, effectiveness, and reversibility of several plant-derived drugs, which offers a solid basis for more investigation and advancement. However, there are still a lot of obstacles to overcome, like standardizing plant extracts, guaranteeing uniform effectiveness, and carrying out thorough safety evaluations. This review emphasizes the significance of undertaking well-designed clinical studies to validate pre-clinical findings, creating standardized formulations for consistent outcomes, and resolving regulatory issues as well as ethical considerations for human use to progress this subject.
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An Extensive Evaluation of Recent Developments in B. orellana's Phytochemistry and Pharmacology
More LessAuthors: Wasim Akhtar, Himanchal Sharma, Rustam Ekbbal and Anuj Kumar SharmaBixa orellana, known as annatto, has gained significant attention due to its diverse phytochemical composition and wide range of pharmacological activities. This review provides a comprehensive evaluation of the latest advancements in the phytochemistry and pharmacology of B. orellana. The plant is rich in a variety of bioactive compounds, including carotenoids, flavonoids, and tocotrienols, which contribute to its therapeutic potential. Recent studies have highlighted the antioxidative, antimicrobial, anti-inflammatory, and anticancer properties of these compounds, supporting the traditional use of B. orellana in various ethno-medicinal practices. Furthermore, the underlying mechanisms of action of these bioactive constituents are discussed, with an emphasis on their interaction with molecular targets that regulate oxidative stress, inflammation, and cell proliferation. The pharmacokinetics, safety profile, and potential side effects of B. orellana extracts are also reviewed, underscoring the need for further research to establish standardized dosages and formulations. Additionally, the application of advanced extraction techniques and novel delivery systems to enhance the bioavailability and efficacy of B. orellana-derived compounds is explored. This review aims to consolidate the current knowledge on B. orellana, providing insights into its potential as a source of natural therapeutics and laying the groundwork for future research and development in this field. By synthesizing the findings from recent studies, this paper contributes to a deeper understanding of B. orellana’s pharmacological potential, ultimately supporting its integration into modern healthcare practices.
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Ethnopharmacological Insights on Plumeria obtusa L.: A Comprehensive Review of its Phytochemistry and Pharmacological Properties
More LessAuthors: Sapna Salar, Mhaveer Singh, Dinesh Kumar Yadav, Vijay Kumar, Rustam Ekbbal and Santosh KumarThis extensive review paper explores the ethnopharmacological viewpoints of Plumeria obtusa L., commonly referred to as “Frangipani”, clarifying its complex phytochemistry and range of pharmacological characteristics. Plumeria obtusa has a long history of ethnobotanical uses and is widely used in traditional medicinal practices across many countries. Through a methodical investigation of its phytochemical components, the review reveals a diverse range of bioactive substances, such as phenolic compounds, alkaloids, flavonoids, and terpenoids. The plant's potential for medicinal use is greatly enhanced by these ingredients. There is a thorough discussion of Plumeria obtusa’s pharmacological characteristics, including its anti-inflammatory, antibacterial, antioxidant, and anticancer effects. Using information gathered from both current and historic studies, the article offers a comprehensive overview of the plant's many therapeutic uses. It also provides insights into the significance of using scientific research to validate traditional applications, opening the door for Plumeria obtusa incorporation into contemporary healthcare procedures. This paper focuses on Plumeria obtusa ethnomedical usage, describing its traditional use in the treatment of a range of ailments. The study points out information gaps and suggests future studies to explore its therapeutic and multi-mechanistic approaches. It also suggests possible directions for clinical investigations. To sum up, this study provides a comprehensive overview of Plumeria obtusa L. by combining ethnopharmacological ideas, phytochemical data, and pharmacological discoveries. This plant presents itself as a good option for new medicinal uses when conventional wisdom and scientific investigation are combined.
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Insights of Natural Isoquinoline Alkaloids in the Management of Trachoma
More LessAuthors: Manish Kaushik, Aditi Kaushik, Surya Prakash Gautam and Deewakar BaralThe neglected tropical disease (NTD), trachoma comprises the infection of eye produced by a pathogenic bacteria known as Chlamydia trachomatis, a sexually transmitted bacterium that leads to ocular infection which ultimately leads to ocular destruction or complete blindness. Around 80-85 million individuals worldwide are infected wherein 60-90 percent of the said infection is detected only in youngsters in several places. Trachoma considerably prevails in rural areas where sanitation and healthcare are the major issues and these are the world’s low-income countries. The epidemiology of the said disease is complex and related to the environmental conditions. This review article focused on the pathophysiology of trachoma and the use of phytochemicals from herbal sources. Herbal remedies are the best way to manage any disease as they are comparatively safer and have fewer side effects. Although there are various conventional treatments including the use of antibiotics like erythromycin, sulphonamides, and azithromycin for the management of said diseases. They have various adverse effects including, abdominal pain, vomiting, and over usage can even lead to permanent blindness. Thus, to avoid these adverse effects the scientific community focused on herbal therapeutics and their secondary metabolites that have a major role in the designing and development of safer therapeutics. This review focused on the isoquinoline alkaloids obtained from medicinal plants that can be used in the development of the newer pharmacophore for the management of trachoma.
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Biologically Active Components of Seven Saussurea Species and their Osteogenic and Hematopoietic Activity in Experimental Osteomyelitis
More LessBackground/IntroductionPlant extracts containing polysaccharides, flavonoids, and chelated calcium compounds are effective for the complex therapy of osteomyelitis. In this study, the content of target components in the extracts of seven Saussurea DC species was studied, and their osteogenic and hematopoietic activities in model osteomyelitis were investigated.
MethodsThe content of chelidonic acid by high-performance liquid chromatography, flavonoids by spectrophotometric method, polysaccharides by gravimetric method, and calcium by automatic analyzer in extracts was determined. Biological experiments were carried out on rats using the model of experimental osteomyelitis.
Results and DiscussionThe largest amount of calcium (3-4 mmol/l) in S. controversa, S. salicifolia, and S. frolowii, chelidonic acid (122 mg/g) in S. controversa, and flavonoids (63-74 mg/g) and polysaccharides (218-251 mg/g) in S. frolowii and S. parviflora extracts was found. In the model osteomyelitis, the studied extracts stimulated bone marrow hematopoiesis, and the total number of bone marrow cells increased after treatment with S. controversa extract by 50% and with S. parviflora and S. daurica extracts by 28% compared to the control. After treatment with Saussurea extracts, the intensity of inflammation in the bone tissue decreased, and regenerative processes intensified. Moreover, the area of mature bone tissue increased by 72% after treatment with S. controversa and S. parviflora extracts, indicating the successful completion of the bone regeneration process.
ConclusionPlants of the genus Saussurea (S. controversa DC, S. parviflora (Poir.) DC, S. frolovii Ledeb., S. daurica Adams., and S. salicifolia (L.) DC) showed osteogenic and hematopoietic efficacy in the osteomyelitis model of rats. Extracts and biologically active components of these plants can expand the arsenal of sources for the complex therapy of osteomyelitis.
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Computational Study on Antheraea assamensis Helfer Metabolites: Targeting FGFR, EGFR, mTOR, and VEGFR1 for Cancer Therapy
More LessBackground/IntroductionCancer, a disease with substantial worldwide health consequences, is driven by the uncontrolled division and spread of cells. A combination of genetics, environmental factors, and personal lifestyle choices influences its development. Cancer remains a significant global health challenge, driving the need for new therapeutic compounds. Antheraea assamensis Helfer, an edible insect, contains bioactive compounds that may provide a natural approach to reducing cancer progression through dietary intake. Rich in proteins, fatty acids, and bioactive compounds, this insect shows promise in its anti-inflammatory and antioxidant properties.
AimCancer, characterized by uncontrolled cell growth, poses global health challenges, while natural bioactive compounds offer a cost-effective and less toxic alternative by targeting cancer pathways. This current study aims to identify potential bioactive compounds from silk warm pupa and screen their bioactivity against various cancers through in-silico approaches.
ObjectiveCurrently, available cancer medications are often associated with a range of side effects. Plant-derived compounds present a promising alternative for cancer treatment, offering the potential for fewer side effects. This research aims to identify the most effective bioactive lead molecule for future drug development in the fight against various types of cancer.
MethodsTo evaluate the therapeutic potential of metabolites from Antheraea assamensis Helfer, various in-silico techniques were used. Molecular docking analysis were conducted to assess the binding affinity and stability of the compounds with cancer-related targets such as EGFR, FGFR, VEGFR1, and mTOR, revealing their inhibitory potential. ADMET analysis predicted the pharmacokinetic properties, including absorption, toxicity, and drug-likeness. In contrast, QSAR analysis forecasted the biological activity of the compounds, helping to quantify their effectiveness in triggering specific biological responses.
Results and DiscussionThe molecular docking studies showed promising results, with several bioactive compounds from Antheraea assamensis Helfer exhibiting strong binding affinities to EGFR, FGFR, VEGFR1, and mTOR, suggesting significant inhibitory potential against these cancer-related targets. ADMET analysis further supported these findings by indicating favorable pharmacokinetic properties, such as good absorption, low toxicity, and minimal risk of side effects. QSAR analysis predicted high biological activity for the compounds, reinforcing their potential as effective anticancer agents.
ConclusionThe study identifies Antheraea assamensis Helfer as a significant source of bioactive agents like 2-(Dimethylamino) ethyl (9Z,12Z)-octadeca-9,12-dienoate, Echinulin, and Phorbol 12-tiglate 13-decanoate, with promising anticancer activity. In-silico analysis indicates these compounds could inhibit key cancer-related targets like EGFR, FGFR, VEGFR1, and mTOR. Further in-vitro and experimental studies are needed to validate their therapeutic efficacy and safety.
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Polyphenolics Profile of Casimiroa edulis Llave. and Evaluation of its Hepatoprotective Potential
More LessAuthors: Marwa Gamal, Samir Othman, Manal M. Sabry, Mohammed A. Hussein and Heba A. El GizawyBackground/IntroductionParacetamol overdose can lead to severe liver damage due to the formation of toxic metabolites. Casimiroa edulis, rich in polyphenols and flavonoids, and silymarin, a known liver protectant, may help mitigate this damage.
ObjectiveThis study aims to characterize the main phytoconstituents of Casimiroa edulis leaves and evaluate their hepatoprotective activity.
MethodsLeaves of Casimiroa edulis were extracted with methanol. The total flavonoid and phenolic contents in the methanol extract were identified using HPLC. The hepatoprotective effects were assessed in 30 mice divided into five groups, treated with paracetamol to induce liver damage, and administered Casimiroa edulis extract or silymarin at different doses. Blood and liver samples were collected to measure biochemical markers, oxidative stress indicators, inflammatory markers, and gene expression. Histopathological examination of liver tissues was also performed.
Results and DiscussionHPLC analysis revealed a rich polyphenolic profile, with gallic acid (1905.83 µg/g) and daidzein (7039.18 µg/g) as predominant compounds. Paracetamol administration significantly increased TC, TG, liver enzyme levels (ALT, AST, LDH, ALP), MDA, IL-6, TNF-α, and CYP2E1, while decreasing HDL-c, SOD, GSH, and CAT levels, as well as BcL-2 and P53 gene expression, indicating hepatotoxicity. Treatment with Casimiroa edulis extract and silymarin significantly mitigated these adverse effects, improving plasma lipid profiles, liver enzyme levels, oxidative stress biomarkers, inflammatory mediators, and gene expression. In addition, Casimiroa edulis extract and silymarin significantly improve liver histopathological scores in paracetamol-treated mice. Despite severe congestion and necrosis, the liver maintained its typical structure with central veins and hepatocyte cords, highlighting the potential therapeutic benefits of these treatments.
ConclusionCasimiroa edulis extract and silymarin demonstrate significant hepatoprotective effects against paracetamol-induced liver damage. Their rich polyphenolic and flavonoid content effectively mitigates oxidative stress and inflammation, improving biochemical markers and preserving liver structure. These findings highlight their potential as therapeutic agents for liver health.
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Volumes & issues
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Volume 22 (2026)
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Volume 21 (2025)
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Volume 20 (2024)
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Volume 19 (2023)
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Volume 18 (2022)
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Volume 17 (2021)
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Volume 16 (2020)
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Volume 15 (2019)
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Volume 14 (2018)
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Volume 13 (2017)
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Volume 12 (2016)
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Volume 11 (2015)
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Volume 10 (2014)
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Volume 9 (2013)
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Volume 8 (2012)
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Volume 7 (2011)
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Volume 6 (2010)
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Volume 5 (2009)
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Volume 4 (2008)
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Volume 3 (2007)
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Volume 2 (2006)
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Volume 1 (2005)
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Podophyllotoxin: Current Perspectives
Authors: Ying Qian Liu, Liu Yang and Xuan Tian
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