This early phase I trial tests the safety, side effects and how well medication combinations of dasatinib, quercetin, fisetin and temozolomide work in treating patients with glioma for which the patient has received treatment in the past (previously treated) and for tumor cells that remain after attempts to treat the tumor have been made (residual disease). Dasatinib is in a class of medications called tyrosine kinase inhibitors. It works by blocking the action of an abnormal protein that signals tumor cells to multiply, which may help keep tumor cells from growing. Quercetin and fisetin are compounds found in plants. They have antioxidant and anti-inflammatory properties and help remove senescent cells, older or damaged cells that have stopped dividing but don't die off as they should and build up in tissues over time. Senescent cells may cause inflammation or damage to nearby healthy cells. Temozolomide is in a class of medications called alkylating agents. It works by damaging the cell's deoxyribonucleic acid (DNA) and may kill tumor cells and slow down or stop tumor growth. Giving medication combinations of dasatinib, quercetin, fisetin and temozolomide may be safe, tolerable and/or effective in treating patients with previously treated glioma with residual disease.

开始日期2025-11-01

申办/合作机构

Mayo Clinic

NCT05505747

/ Withdrawn临床2/3期IIT

Enhancing Recovery Through a Combined Mechanobiologic Intervention Following Meniscus Repair

Arthroscopic meniscal procedures are the most commonly performed orthopaedic procedure in the U.S. affecting 15% of Americans ages 10-65 years. Meniscus injury is also known to increase the risk of posttraumatic osteoarthritis (PTOA). The current randomized clinical trial will test a novel intervention after meniscal repair that combines an oral senolytic fisetin and real-time biofeedback program to restore joint loading and subsequent return to activity.

开始日期2025-07-01

申办/合作机构

University of Kentucky

NCT06796374

/ Not yet recruitingN/AIIT

A Comparison of Fisetin Kinetics in Young and Old Adults - FISEKIN-1

This study investigates the differences in the kinetic parameters of fisetin in two cohorts of healthy volunteers:
Cohort 1) volunteers aged 18-30 years (n = 40) Cohort 2) volunteers aged 65 years or older (n = 40)
The purpose of this study is:
1. To describe the fisetin kinetics after a single dose oral administration in older age.
2. To compare the fisetin kinetics after a single dose oral administration in old and young age.
FISEKIN-1 is designed as a four-arm study protocol. As well as two different age groups (18-30 years vs. 65 years and older), we want to compare fisetin kinetic parameters in two different fisetin formulations and dosages :
Arm 1) 100 mg fisetin (1x 1 capsule), cohort 1: young age Arm 2) 100 mg fisetin (1x 1 capsule), cohort 2: old age Arm 3) 1000 mg fisetin + 200 mg quercetin (2x 1 softgel capsule), cohort 1: young age Arm 4) 1000 mg fisetin + 200 mg quercetin (2x 1 softgel capsule), cohort 2: old age

开始日期2025-02-01

申办/合作机构

University of Greifswald

100 项与漆黄素相关的临床结果

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100 项与漆黄素相关的转化医学

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100 项与漆黄素相关的专利（医药）

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3,604

项与漆黄素相关的文献（医药）

2025-12-01·Stress biology

Transcriptional modification and the accumulation of flavonoid in the leaves of Cissus rotundifolia Lam. in respond to drought stress

作者: Gituru, Robert Wahiti ; Gichuki, Duncan Kiragu ; Hou, Yujun ; Xin, Haiping ; Zhou, Huimin ; Wang, Qingfeng ; Li, Qingyun

Abstract:

Cissus rotundifolia Lam. is an evergreen climber that mainly distributed in the tropical savannas of eastern Africa with excellent drought resistance. While the mechanism underlying drought stress response in C. rotundifolia remains unknown. In this study, we investigated the transcriptomics and flavonoid metabolomics responses of C. rotundifolia leaves under different drought conditions. We identified a total of 2401 differentially expressed genes (DEGs) in drought-treated leaves. The continuously increasing DEGs were significantly enriched in pathways related to phenylpropanoid biosynthesis, flavonoid biosynthesis, and galactose metabolism. The total flavonoids content were also found increased significantly during drought treatment in the leaves of C. rotundifolia. A total of 57 distinct flavonoids were identified using UPLC-MS/MS. Among them, nine out of ten differentially accumulated metabolites (DAMs) displayed notable accumulation profiles under drought conditions. These DAMs included two flavanols [(-)-Catechin gallate and (-)-gallocatechin gallate], two flavonols (myricetin and astragalin), four flavones (orientin, cynaroside, isoorientin, and vitexin), and one flavanone (naringenin-7-glucoside), indicating their pivotal roles in drought response. Additionally, a DEG with continuously high-expression, annotated flavone synthase (FLS) synthesises, and synthetizing myricetin under drought stress was tightly related to additional genes belonging to ABA-signaling genes, stomata movement genes, transcription factors, and protein kinases, these genes were contained Top 10 hub-genes of network constructed all DEGs. The results reflect the significance of FLS and potentially regulatory genes under drought conditions. These findings suggest that flavonoids play a pivotal role in the drought stress response of C. rotundifolia, advancing our understanding of flavonoids accumulation and the transcriptional regulation involved in this process.

2025-12-01·MOLECULAR BIOLOGY REPORTS

Fisetin mitigates cisplatin-induced peripheral neuropathy: a behavioral and immunohistochemical study

Article

作者: Çevik, Sena ; Yilmaz, Şenay Görücü ; Adıgüzel, Cansel ; Yildirim, Caner ; Bal, Ramazan

BACKGROUND:

Cisplatin (CIS), a commonly used chemotherapeutic drug, often causes peripheral neuropathy, considerably affecting patients' quality of life. The present study investigated the neuroprotective effects of fisetin, a natural flavonoid with antioxidant and anti-inflammatory features, in a rat model of cisplatin-induced peripheral neuropathy.

METHODS AND RESULTS:

Male Wistar rats were divided into six groups: sham, neuropathy (CIS, 3 mg/kg, 5 weeks), fisetin treatment (CIS + 10 mg/kg and CIS + 20 mg/kg), and drugs control groups (10 mg/kg and 20 mg/kg fisetin alone). Behavioural experiments were conducted to evaluate motor coordination and sensory function, electrophysiologically measured nerve conduction velocity (NCV). Gene expression studies were conducted for NF-kB and GPX4 to investigate oxidative stress and inflammation. Finally, confocal microscopy studies were used to evaluate the structure of the sciatic nerve. Cisplatin induced motor impairments, sensory dysfunction, mechanical allodynia, diminished nerve conduction velocity, myelin deterioration (decreased MBP), and increased neuroinflammation (elevated GFAP and NF-kB, decreased GPX4). Fisetin, specifically at a dose of 10 mg/kg, markedly enhanced motor coordination, sensory thresholds, NCV, maintained myelin integrity, reduced glial activation, and restored oxidative and inflammatory balance by elevating GPX4 levels and decreasing NF-kB expression.

CONCLUSIONS:

These results highlight fisetin's potential as a therapeutic agent for cisplatin-induced neuropathy, emphasising its role in restoring molecular, structural, and functional integrity within the peripheral nervous system.

2025-10-01·CURRENT MEDICINAL CHEMISTRY

The Role of Nutraceuticals in Chemoprevention and their Therapeutic Effects when used in Combination with Synthetic Drugs

Article

作者: Starvaggi, Josè ; Ettari, Roberta ; Zappalà, Maria ; Luca, Fabiola De ; Chio, Carla Di ; Previti, Santo

Recently, increasing attention has been directed toward nutraceuticals, natural substances extracted from plants, fruits, or cereals. These compounds are well-known for their antibacterial, anti-inflammatory, antioxidant, and antitumor properties, with the latter being the primary focus of this review. The use of nutraceuticals, both as standalone treatments and in combination with standard chemotherapy, has been extensively studied through in vitro, in vivo experiments, and clinical trials for the prevention and treatment of various types of cancer, including breast, colon, pancreatic, prostate cancers, and leukemia. Findings from these studies emphasize the benefits of nutraceuticals in improving patient compliance and mitigating the adverse effects of conventional drugs. Specifically, the combination of nutraceuticals with chemotherapy allows for reduced dosages of synthetic drugs, thereby lessening their often-severe side effects. In this review, we explore the diverse mechanisms of action underlying the antitumor activity of key nutraceuticals—including curcumin, resveratrol, tocotrienols, ursolic acid, fisetin, gambogic acid, catechins, silibinin, berberine, emodin, piperine, deguelin, garcinol, plumbagin, zerumbone, and ginger. Furthermore, we summarize the most significant outcomes from clinical trials investigating these compounds. The clinical studies addressed various aspects of treatment, such as efficacy, safety, maximum tolerated doses, potential adverse effects, and patient compliance. The majority of the findings highlight the positive impact of combining nutraceuticals with chemotherapy, demonstrating enhanced therapeutic outcomes in anticancer treatments.

项与漆黄素相关的新闻（医药）

2025-04-14

·Business Wire

BeFisetin® Announced the Global No.1 All-Natural Fisetin With SA-GRAS Status

NEW YORK--(BUSINESS WIRE)--Bonerge Lifescience, a trusted innovator in longevity ingredients, proudly announces a historic milestone: on April 2, 2025, its premium fisetin ingredient, BeFisetin®, has achieved Self-affirmed Generally Recognized as Safe (SA-GRAS) status in the United States. This landmark accomplishment positions Bonerge as the first company globally to secure GRAS certification for fisetin powder, setting a new global benchmark for safety and reliability in the next-generation anti-aging market. BeFisetin: Establishing the Gold Standard to Address Chaos in the Fisetin Market The current fisetin market is plagued by alarming quality inconsistencies. While vague claims of "Fisetin 98% HPLC" dominate as the mainstream specification, actual fisetin content in these products ranges only between 75%-85%, with significant impurities concealed under this ambiguous standard. For plant extracts derived from non-edible sources, the removal of harmful components is critical. Fisetin, extracted from inedible Anacardiaceae plants, contains large amounts of toxic lacquer, waxes, and wood debris. Eliminating these impurities is essential to producing safe, high-quality fisetin. Yet, the absence of clear, stringent quality standards has made it impossible to verify purity, allowing low-quality products to flood the market. Many suppliers exploit rudimentary testing methods to falsely label products as "98% HPLC," misleading consumers and perpetuating a cycle where inferior products overshadow genuine quality. This chaos forces brands to settle for subpar fisetin, stifling innovation in premium formulations. Establishing a gold standard for fisetin quality has been Bonerge’s mission from the start. Recognizing the challenges—extensive R&D, industry-first breakthroughs, and short-term financial sacrifices—we named our product BeFisetin as a constant reminder: "To be or not to be" hinges on our commitment to redefine excellence in fisetin. BeFisetin is not just a product—it’s a pledge to restore integrity and drive progress in the fisetin industry. What Defines the Gold Standard for Fisetin? Safety First : SA-GRAS certification ensures systemic safety evaluation, a critical gateway for market entry. Transparent Quality Metrics : BeFisetin guarantees 98% HPLC purity , 98% HPLC content , 99% total active ingredients , and <1% impurities , setting unmatched benchmarks for consistency and quality. Ongoing Clinical Validation : Bonerge has completed the first double-blind, controlled clinical trial on BeFisetin’s efficacy in skin health, with results under analysis and pending publication. A second large-scale trial on sleep and immune health, approved by ethics committees in March, is now underway. BeFisetin: The 1st All-Natural Fisetin to be Granted SA-GRAS BeFisetin® is the first all-natural fisetin to attain SA-GRAS certification. For all dietary supplement ingredients, SA-GRAS represents a critical milestone, but its significance is unparalleled in advancing fisetin as a premium raw material. This certification sets the gold standard for the industry, requiring adherence to rigorous criteria: well-defined quality specifications, scientifically validated testing protocols, GMP-compliant manufacturing environments, and comprehensive safety assessments—all of which elevate fisetin from an underregulated botanical to a clinically trusted ingredient. By establishing these benchmarks, SA-GRAS not only ensures consumer safety but also paves the way for innovation in longevity-focused formulations. “Beyond regulatory compliance, this accomplishment reflects our foundational commitment to scientific excellence and consumer safety—principles that drive every stage of our ingredient innovation,” stated Gloria, Product Manager of Bonerge. “SA-GRAS BeFisetin® provides brands with a scientifically validated ingredient that meets international regulatory requirements, enabling them to develop innovative products with assurance.” A Vision for Trusted Longevity Foundation The GRAS certification of BeFisetin® marks the beginning of Bonerge’s mission to redefine aging. By prioritizing rigorous science and consumer safety, Bonerge aims to foster transparency in the anti-aging market, and we are committed to providing scientifically grounded solutions that empower individuals to age healthily. As global interest in senotherapeutics grows, BeFisetin® stands at the forefront, offering brands a trusted, scalable ingredient to meet the rising demand for effective and safe longevity products.

上市批准

2025-01-09

·Business Wire

Bonerge Announces the New 108 Person Clinical Trial: Exploring Skin and Organ Anti-Aging Innovations

NEW YORK--( BUSINESS WIRE )--Bonerge announced the initiation of its clinical trial, focusing on Fisetin, Urolithin A, and Ergothioneine. Involving 108 participants, this trial aims to evaluate their combined effects on skin health and organ rejuvenation when taking orally, providing more reliable options for the market. Senolytics Research: Advancing the Science of Anti-Aging In recent years, Senolytics research has advanced rapidly, with institutions like the Mayo Clinic and Wake Forest University at the forefront. Despite fruitful research, identifying optimal applications to translate Senolytics into market solutions remains crucial. In October 2024, the Mayo Clinic published groundbreaking findings in Nature Aging, identifying 67 plasma proteins, with IL-23R emerging as a promising anti-aging biomarker 1 . The study explored various promising Senolytics, including Fisetin, demonstrating a positive response in reducing senescence-related proteins and indicating potential for organ rejuvenation via senescent cell clearance 2 . The concept of organ rejuvenation offering deeper insights into its systemic effects and guiding anti-aging strategies. Senolytics show strong potential for organ rejuvenation applications and promise broader future prospects. Bonerge’s Clinical Trial: Exploring Skin as the Key to Rejuvenation The skin, the largest organ of the human body, is the most visible indicator of aging and a key target for anti-aging. Bonerge has launched a clinical trial focused on skin anti-aging, involving 108 participants. The trial evaluates skin anti-aging effects by assessing factors like skin heme, skin inflammation, transepidermal water loss, wrinkles, skin elasticity, skin firmness, melanin levels, and skin tone. Spanning 56 days, it aligns with two skin regeneration cycles, providing a detailed analysis of these key skin health indicators. Three ingredients tested in the trail: Fisetin: Among natural ingredients, fisetin has the strongest activity in clearing senescent cells. Its core mechanism promotes apoptosis of senescent cells and reduces SASP (Senescence-Associated Secretory Phenotype) secretion, alleviating chronic inflammation and combating inflammaging 3 , contributing to organ rejuvenation. Urolithin A: A rising star in nutritional supplements, Urolithin A has shown significant anti-photoaging effects. Photoaging, primarily caused by UVA (ultraviolet A) radiation, accelerates skin aging. Urolithin A helps protect skin by reducing the senescent phenotype of skin fibroblasts triggered by UVA, lowering intracellular ROS (reactive oxygen species), and activating antioxidant enzymes. These actions collectively support skin health and combat the harmful effects of photoaging 4 . Ergothioneine : Currently recognized as the only antioxidant that targets mitochondria, it reduces oxidative damage within mitochondria, supporting energy production and potentially preventing cellular aging 5 . Key Focus: Exploring Individual Ingredients and Combined Synergies In this clinical trial, while examining the skin anti-aging effects of individual ingredients, the combination of the three ingredients have also been tested to explore the synergistic effects on skin health and anti-aging. Path Ahead: Trial Progress and Future Expectations The clinical trial is progressing as planned and is expected to conclude in March 2025. Bonerge is hopeful that this study will provide valuable evidence for the anti-aging market, paving the way for the application of Senolytics in skin health and broader anti-aging treatments. References [1] Chase M. Carver, et al. IL-23R is a senescence-linked circulating and tissue biomarker of aging. Nature Aging, Dec 2024. [2] Researchers discover an aging and inflammation biomarker - Mayo Clinic News Network [3] Matthew J. et al. Fisetin is a senotherapeutic that extends health and lifespan. EBioMedicine 36 (2018). [4] Wenjie Liu , et al. Urolithin A protects human dermal fibroblasts from UVA-induced photoaging through NRF2 activation and mitophagy. J Photochem Photobiol B. 2022 Jul. [5] Brown, Lisa, et al. L-Ergothioneine and Its Protective Role in Cellular Health. Journal of Clinical Nutrition, vol 56.

临床研究

2024-12-31

·Business Wire

BeFisetin® is Gaining the First Fisetin Ingredient SA-GRAS Certification

NEW YORK--( BUSINESS WIRE )--In 2024, Bonerge's premium fisetin branded ingredient, BeFisetin®, initiated the SA-GRAS (Self-Affirmed Generally Recognized As Safe) certification process, with completion expected in February 2025. This certification underscores Bonerge's unwavering commitment to product safety, quality control and serves as a key milestone in its expansion into the global fisetin market. Fisetin: The Anti-aging Potential of Natural Polyphenols Fisetin is a natural polyphenol widely present in various fruits and vegetables such as strawberries, apples, and persimmons. In recent years, the scientific community's enthusiasm for exploring fisetin has been continuously rising. Numerous research findings have revealed that fisetin has unique biological properties in reducing inflammatory factors, strengthening cell health, and delaying aging [1-3], and its related applications have also attracted extensive and in-depth attention. Biochemical studies have shown that fisetin can exert its effects through multiple mechanisms. It can effectively reduce senescent cells in the brain, skin, and various organs, regulate inflammatory factors, and scavenge free radicals [4]. This makes fisetin an attractive dietary supplement, showing broad application prospects in healthy aging and long-term health management. BeFisetin®: Marketing Strategy and Innovation As a company dedicated to the development and research of high-quality ingredients, Bonerge recognizes the growing global demand for safe and effective dietary supplements. It is Bonerge’s principle to leverage cutting-edge science to transform advanced research into practical health solutions. Bonerge is continuously improving the purity and bioavailability of BeFisetin®, while integrating sustainable production practice, demonstrating a strong commitment to environmental responsibility. Focusing on the great potential of fisetin, Bonerge has engaged in in-depth strategic collaborations with multiple research institutions and universities to strengthen the scientific validation and credibility of BeFisetin®, continuously enhancing its trust and reputation through rigorous scientific verification. This ensures consumers have access to transparent, reliable health solutions. SA-GRAS Certification: An Extended Standard in Safety and Trust SA-GRAS certification, a critical extension of the FDA's GRAS framework, allows companies to confirm the safety of their products through rigorous self-assessment. This process involves establishing stringent product standards, conducting comprehensive toxicity and safety evaluations, and systematically assessing raw materials, manufacturing processes, and product stability. Companies need to work with independent professional organizations to prepare detailed safety assessment reports, which are reviewed by an expert panel. The rigorous certification process drives Bonerge to further optimize its product quality systems and elevated BeFisetin®'s competitiveness in the global market. For Bonerge, SA-GRAS certification is not merely a regulatory milestone but a testament to its relentless pursuit of product excellence and its commitment to consumer safety. Looking Ahead: Responsibility and Opportunity The expansion of aging population is a global challenge, driving increasing demand for health-focused anti-aging solutions. Bonerge is committed to leveraging BeFisetin®'s superior quality to advance scientific research, foster innovation, and provide consumers with safer and trustworthy products. To be or not to be, that is the question! BeFisetin®: A scientific breakthrough as the world’s first SA-GRAS-certified fisetin ingredient, setting a new industry standard. References [1] Yoon S, Lee H, Kim J, et al. A natural flavonoid, fisetin, alleviates neuroinflammation and memory impairment in D-galactose-treated mice[J]. Frontiers in Pharmacology, 2023, 14: 1134733. [2] Li X, Zhang H, Guo Y, et al. Fisetin promotes osteoblastogenesis and inhibits adipogenesis in bone marrow stromal cells through the activation of the Wnt/β-catenin pathway[J]. International Journal of Molecular Sciences, 2019, 20(23): 5957. [3] Yousefzadeh MJ, Zhu Y, McGowan SJ, et al. Fisetin is a senotherapeutic that extends health and lifespan[J]. EBioMedicine, 2018, 36: 18-28. [4] Takaya K, Kawaguchi M, Mizutani K, et al. Fisetin, a potential skin rejuvenation drug that eliminates senescent cells in the dermis[J]. Biogerontology, 2023, 24(5): 409-421.

100 项与漆黄素相关的药物交易

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外链

KEGG	Wiki	ATC	Drug Bank
-	-	-	DB07795

研发状态

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适应症	最高研发状态	国家/地区	公司	日期
普通可变性免疫缺陷	临床2期	美国	Mayo Clinic	2023-04-12
系统性硬化相关的间质性肺病	临床2期	美国	Mayo Clinic	2023-04-12
腕管综合征	临床2期	美国	Mayo Clinic	2022-10-09
新冠肺炎后遗症	临床2期	美国	Mayo Clinic	2020-08-03
Crouzon综合征伴黑棘皮症	临床2期	美国	Mayo Clinic	2018-02-06
炎症	临床2期	美国	Mayo Clinic	2018-02-06
IDH1突变胶质瘤	临床1期	美国	Mayo Clinic	2025-11-01
肌萎缩侧索硬化	临床前	中国	哈尔滨医科大学附属第一医院（哈尔滨医科大学第一临床医学院、黑龙江省血液肿瘤研究所、黑龙江省干细胞库、黑龙江省肝脾外科中心）	2025-06-28
肾纤维化	临床前	中国	四川大学华西医院（四川省国际医院）	2023-03-01
黑色素瘤	临床前	美国	University of Wisconsin Madison	2013-04-15

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研究	分期	人群特征	评价人数	分组	结果	评价	发布日期


AACR2025	N/A	胰腺导管腺癌 CD44 \| CD24 \| CD133 ... 更多	-	Fisetin	醖遞製廠遞願夢餘齋齋(艱遞齋艱糧餘膚製衊選) = 遞觸網網觸願顧蓋簾網積蓋獵繭憲構鬱憲鹽鹹 (網願艱獵顧襯簾鑰壓膚 )	-	2025-04-27
				Fisetin (Untreated)	醖遞製廠遞願夢餘齋齋(艱遞齋艱糧餘膚製衊選) = 製壓夢獵顧網構網襯糧積蓋獵繭憲構鬱憲鹽鹹 (網願艱獵顧襯簾鑰壓膚 )
NCT04210986 (CTgov)	临床1/2期	膝关节炎	75	Fisetin (Fisetin)	獵獵觸獵憲鹽蓋網夢鏇 = 鬱築願鏇積遞壓壓鏇遞構蓋構網願廠積積襯繭 (顧鑰壓範鏇鬱範齋艱艱, 構憲淵齋衊選艱選淵獵 ~ 膚簾淵蓋蓋鹽製積襯簾) 更多	-	2024-09-19
				Placebo oral capsule (Placebo)	獵獵觸獵憲鹽蓋網夢鏇 = 壓糧獵顧醖顧積選蓋夢構蓋構網願廠積積襯繭 (顧鑰壓範鏇鬱範齋艱艱, 膚觸簾製廠鏇壓鏇顧艱 ~ 餘齋夢蓋獵鹹遞願構廠) 更多
NCT04771611 (COVFIS-HOME, CTgov)	临床2期	新型冠状病毒感染	55	Fisetin (Treatment Group)	餘鏇鑰廠選構衊夢選壓 = 觸鬱壓夢製網膚繭醖鹽鏇夢襯夢鹹壓觸蓋夢築 (繭衊廠廠膚窪醖淵網鏇, 簾觸鏇鹽遞選製簾製鹹 ~ 繭積鏇選糧願餘範壓範) 更多	-	2023-08-01
				Placebo (Placebo)	餘鏇鑰廠選構衊夢選壓 = 蓋選鬱壓襯網積獵願構鏇夢襯夢鹹壓觸蓋夢築 (繭衊廠廠膚窪醖淵網鏇, 簾窪衊鬱憲夢獵觸構夢 ~ 製獵齋鹹選襯窪憲築選) 更多