Skip to main content
Food Science & Nutrition logoLink to Food Science & Nutrition
. 2026 Feb 5;14(2):e71519. doi: 10.1002/fsn3.71519

Onion (Allium cepa L.) Organosulfur Compounds: From Traditional Use to Modern Pharmacological Insights

Yuanyuan Tang 1, De Lv 2, Yijing Tao 3,
PMCID: PMC12876048  PMID: 41657530

ABSTRACT

Onion ( Allium cepa L.), as one of the earliest vegetables cultivated by humans, has a medicinal value that can be traced back to The times of ancient Egypt, Greece, and Rome. In recent years, with the development of analytical techniques and molecular biology, the unique organic sulfides (organosulfur compounds, OSCs) in onions have attracted extensive attention from the scientific community. This article conducts a detailed analysis of the chemical structural characteristics of the main organic sulfides in onions, compares the advantages and disadvantages of extraction techniques such as steam distillation, organic solvent extraction, and supercritical CO2 extraction, and elaborates on their mechanisms of action in regulating lipid metabolism, exerting antibacterial and antitumor effects, alleviating diabetes, and mitigating asthma. The article finally discusses the application prospects of onion organic sulfides in the treatment of diseases, as well as the current technical challenges, providing a reference for the determination of future research directions.

Keywords: molecular mechanism, onion, organosulfur compounds, physiological function, purification extraction and, structure–activity relationship


This review systematically examines the chemical diversity, extraction methods, and pharmacological activities of organosulfur compounds (OSCs) in onions. Key mechanisms include lipid metabolism regulation, anti‐bacterial and anti‐tumor effects, hypoglycemic activity, and anti‐asthmatic potential. The article highlights future directions for OSC‐based therapeutics amid current technical and clinical challenges.

graphic file with name FSN3-14-e71519-g005.jpg

1. Introduction

Onion ( Allium cepa L.), also known as jade onion, onion head, etc., is a plant of the genus Allium in the Liliaceae family (Yoon et al. 2024). The cultivation history of Onions can be traced back to Central Asia and the Mediterranean region around 3000 bc (Chadorshabi et al. 2022; Suleria et al. 2015). There are records about Onions in the murals of the ancient Egyptian pyramids (Kumar, Barbhai, Hasan, et al. 2022). In ancient Egypt, Greece, and Rome, Onions had already occupied an important position in folk medicine (Alzandi et al. 2022). The ancient Greek doctor Hippocrates once recommended using Onions to treat respiratory diseases, while the Roman scholar Pliny recorded 62 medicinal methods of Onions in his “Natural History” (Sharma et al. 2016). In China, the Compendium of Materia Medica records in detail the effects of Onions: “They are sweet and slightly pungent in taste, warm in nature, can unblock the five internal organs, reach all orifices, dispel cold and dampness, and ward off evil (Kumar, Barbhai, Hasan, Dhumal, et al. 2022).”

Onion, as a traditional plant that can be used both as medicine and food, has a relatively rich content of organic sulfur compounds (OSCs), which mainly exist in the vacuoles of the bulb (Muscolo et al. 2020; Qian et al. 2022). When the cell structure is damaged, allinase in the vacuole rapidly converts the odorless S‐alkane (ene)‐L‐cysteine sulfoxide into biologically active thiosulfonates, sulfides, and other compounds (Asemani et al. 2019; Kamata et al. 2016). This defense mechanism is also the chemical basis for the pungent smell and medicinal value of Onions.

Over the past two decades, the number of research papers on onion organic sulfides indexed in the PubMed database has increased nearly fivefold. The research focus has gradually shifted from the initial chemical composition analysis to the exploration of the mechanism of action and clinical application (Shang et al. 2019). At present, Japan, Germany, and the United States are in the leading position in this field. Although China's onion production accounts for nearly 40% of the global total, the development of deep processing and high value‐added products lags relatively behind. With the rising incidence of chronic diseases and the prominent issue of the side effects of chemical drugs, the development of onion organic sulfides, a natural drug resource, for the treatment of chronic diseases holds significant social and economic value (Sharma et al. 2017). The literature reviewed in this article is sourced from the Web of Science Core Collection, PubMed, and Scopus databases from 2000 to 2025, with a focus on the composition, extraction methods, and pharmacological effects of organic sulfides contained in Onions.

2. Classification and Characteristics of Organic Sulfides in Onions

The primary active constituent of onions is onion essential oil, a clear orange‐yellow volatile oil (Taghavi et al. 2022). Over 60 sulfur‐containing compounds have been identified in this oil (Kocić‐Tanackov et al. 2012). Based on their chemical structures, these compounds can be classified into three main categories (Marefati et al. 2021; Abrante‐Pascual et al. 2024; Cantrell et al. 2020). The first category comprises thiosulfinates, including propanethial‐S‐oxide, 1‐propenyl thiosulfinate, and methyl thiosulfinate. These compounds are highly reactive and serve as the primary contributors to the characteristic pungent odor of onions, as well as the foundation for numerous biological activities. The second category includes sulfides and disulfides, with representative compounds such as dipropyl disulfide, diallyl disulfide, and methyl allyl disulfide. The third category consists of cysteine derivatives, such as S‐allyl‐L‐cysteine sulfoxide (alliin), S‐methyl‐L‐cysteine sulfoxide, and cycloalliin. These derivatives are relatively stable and function as key flavor precursors in onions. Table 1 provides a systematic summary of the major OSCs in onions, including their classification, chemical names, molecular formulas, and principal biological activities and properties.

TABLE 1.

The main organic sulfides found in onions and their biological activities and properties.

Category Compound name Chemical formula Primary biological activity and properties Reference(s)
Thiosulfinates Propanethial‐S‐oxide CH3CH2CH = S = O The primary direct source of onion's pungent odor and lachrymatory (tear‐inducing) effect; possesses activities such as antibacterial and antiplatelet aggregation Taghavi et al. (2022), Kocić‐Tanackov et al. (2012), Cantrell et al. (2020)
1‐Propenyl thiosulfinate CH2 = CHCH2‐S (O)‐S‐CH3 Highly chemically reactive, serving as the core material basis for many biological activities; can be converted into various sulfides in the body Kocić‐Tanackov et al. (2012), Marefati et al. (2021)
Methyl thiosulfinate CH3‐S (O)‐S‐CH3 Chemically reactive, exhibits significant antibacterial and anticancer activity Kocić‐Tanackov et al. (2012), Cantrell et al. (2020)
Sulfides and Disulfides Dipropyl disulfide (CH3CH2 CH2)2S2 or C6H14S2 The most abundant sulfur‐containing compound in onions, accounting for 80%–93% of total sulfur content; possesses physiological activities such as antioxidant, anticancer, and lipid‐lowering effects Kocić‐Tanackov et al. (2012), Cantrell et al. (2020)
Diallyl disulfide (CH2 = CHCH2)2S2 or C6 H10S2 Low content (< 1%), but contributes to the main aroma of onions; possesses potent antibacterial, anticancer, and blood glucose‐lowering activities Kocić‐Tanackov et al. (2012), Cantrell et al. (2020), Shala et al. (2023)
Methyl allyl disulfide CH3‐S‐S‐CH2CH = CH2 or C4H8S2 Exhibits various biological activities including anticancer and antibacterial effects; is an important flavor component in onion essential oil Kocić‐Tanackov et al. (2012), Cantrell et al. (2020)
Cysteine derivatives S‐Allyl‐L‐cysteine sulfoxide (Alliin) C6H11NO3S A precursor to thiosulfinates (e.g., 1‐Propenyl thiosulfinate); converted by the enzyme alliinase when onions are cut; possesses activities like hypoglycemic and antioxidant effects. Kocić‐Tanackov et al. (2012), Subramanian et al. (2020), Yang et al. (2018)
S‐Methyl‐L‐cysteine sulfoxide C4H9NO2S Similarly, a precursor to flavor compounds like methyl thiosulfinate; also exhibits hypoglycemic and antioxidant properties Kocić‐Tanackov et al. (2012), Castro et al. (2021)
Cycloalliin C6H11NO3S A natural sulfur‐containing amino acid in onions, stable and nonpungent; possesses physiological activities such as hypoglycemic and cholesterol‐lowering effects Yanagita et al. (2003), Ichikawa et al. (2006)

3. The Extraction Method of Organic Sulfides in Onions

Most organic sulfides are present in onion essential oil. Traditional methods for the extraction of onion oil include atmospheric steam distillation, solvent extraction, and supercritical CO2 extraction. Figure 1 illustrates a comparison of the essential principles, equipment, and process flows of three primary methods for extracting organic sulfide from onions.

FIGURE 1.

FIGURE 1

Comparison of three organic sulfide extraction methods. This illustration presents three methods for the extraction of onion essential oil. (a) Steam distillation method: Involves crushing fresh or dried onions, then conducting steam distillation under atmospheric or reduced pressure, followed by oil–water separation to obtain onion essential oil. (b) Organic solvent extraction method: Starts with crushing raw onions, then uses solvent immersion for extraction. After that, solvent evaporation and recovery are carried out, and the resulting crude extract requires further purification. (c) Supercritical CO2 extraction method: Begins by crushing fresh or dried onions, then performs supercritical CO2 fluid extraction. Subsequently, pressure reduction in a separation vessel is done to obtain high‐quality onion essential oil.

3.1. Steam Distillation Extraction Method

This is the most commonly used method for extracting the volatile oil (onion essential oil) from Onions (Wang et al. 2018). This method utilizes Dalton's law of partial pressure to separate components that are insoluble in water. Usually, fresh or dried scallions are crushed before distillation, and then steam is introduced under normal or reduced pressure to distill the onion essential oil at a temperature lower than its boiling point. This is mainly to obtain the more volatile essential oil in Onions. This method is simple to operate and requires less investment, but its disadvantages are that the distillation time is long, the oil yield is low, and the temperature during the steam distillation process is high, which causes some heat‐sensitive substances to change. This is extremely unfavorable for studying the effective components in the extract, especially certain biologically active components in the volatile oil. Therefore, the flavor of the extracted onion essential oil is somewhat different from that of raw scallions (Takahashi and Shibamoto 2008).

3.2. Organic Solvent Extraction Method

Solvent extraction method has the characteristics of simple equipment, low investment and wide extraction range (Ciardi et al. 2021). The principle of solvent extraction: By taking advantage of the differences in solubility and polarity of different substances in solvents, they become less likely to dissolve each other, thereby achieving the purpose of separation and purification (Trigueros et al. 2024). Based on the principle of like dissolves like, solvents of different polarities were selected to extract the effective components from Onions. However, due to the similar polarities of the effective components and the poor selectivity of organic solvents, the leaching method cannot only obtain nonpolar lipid components but also extract a large amount of polar substances. Single leaching cannot obtain high‐purity target products. Generally, further separation and purification are required. Meanwhile, organic solvents can easily destroy proteins, hormones, and enzymes in raw materials, causing denaturation and inactivation of bioactive substances, etc. (Srivastava and Balakrishnan 2022).

3.3. Supercritical CO2 Extraction Method

Supercritical CO2 extraction can be operated at relatively low temperatures, thus resulting in less decomposition loss of heat‐sensitive compounds. It can obtain high‐quality extracts without leaving any residual solvents. However, the equipment used is complex, the investment is large, and the operating conditions are harsh. Sometimes, the extraction effect is not very ideal (Tolcha et al. 2020). Using CO2 as a supercritical fluid, the essential oil from Onions is extracted. Then, the CO2 fluid carrying the essential oil undergoes a phase transformation from a supercritical state or liquid to a gas state to release the essential oil it carries. This method can simultaneously obtain volatile and nonvolatile onion essential oils (Putnik et al. 2019).

4. Biological Functions of Organic Sulfides in Onions

OSCs derived from onions have a wide range of biological properties, which involve lipid metabolism regulation, antibacterial effects, antitumor properties, hypoglycemic activity, and anti‐asthmatic potential. The following subsections provide an in‐depth account of the pharmacological actions and fundamental mechanisms of organic sulfides in onions.

4.1. Onion‐Derived Compounds in Regulation of Lipid Metabolism

Hyperlipidemia is a metabolic disorder characterized by elevated levels of lipids in the blood and represents one of the primary risk factors for cardiovascular diseases. The principal clinical consequence of hyperlipidemia is atherosclerosis, which results from the accumulation of lipids within vascular walls.

Li et al. (2021) investigated the lipid‐lowering effects of onion extract in hyperlipidemic rats and demonstrated that onion extract exerts an auxiliary hypolipidemic effect in Sprague–Dawley (SD) rats. Han et al. (2002) conducted an in vitro study using human hepatocytes to examine the influence of sulfur‐containing compounds in onions on lipid metabolism, particularly focusing on apolipoprotein B100 secretion. Their findings indicate that S‐propyl cysteine significantly reduces apolipoprotein B100 secretion, thereby inhibiting lipoprotein synthesis and secretion. (Yanagita et al. 2003) explored the impact of cycloalliin on lipid metabolism in SD rats and reported that cycloalliin derivatives modulate hepatic lipid synthesis and secretion, leading to reduced cholesterol levels. Castro et al. (2021) confirmed that S‐methylcysteine sulfoxide, a bioactive compound in onions, exhibits both hypoglycemic and hypolipidemic effects in alloxan‐induced diabetic mice. Furthermore, Ichikawa et al. (2006) demonstrated that sulfur‐containing amino acids—specifically S‐methylcysteine sulfoxide and S‐allylcysteine sulfoxide—can mitigate cholesterol elevation induced by high‐fat and heat‐sensitive diets.

Overall, these findings show that sulfur‐containing flavor precursors in onions, such as S‐methylcysteine sulfoxide, which are enzymatically converted into volatile thiosulfinates responsible for onion flavor and biological activity, have significant lipid‐lowering properties, as shown in Figure 2.

FIGURE 2.

FIGURE 2

Lipid‐lowering properties of organic sulfides in onions. This image depicts the lipid‐lowering properties of onion‐derived compounds. S‐propyl cysteine significantly reduces apolipoprotein B100 secretion; cycloalliin derivatives modulate hepatic lipid synthesis and secretion, contributing to lower cholesterol levels; and S‐methylcysteine sulfoxide and S‐allylcysteine sulfoxide demonstrate potential in cholesterol reduction.

4.2. Anti‐Bacterial Properties of Onion Sulfur Compound

Allicin compounds in fresh onion juice have a moderate bactericidal effect (Kong et al. 2024). Allicin and disulfide compounds can react with compounds similar to certain amino acids (e.g., cysteine) preventing them from binding to proteins. This reaction can inhibit bacterial reproduction (Hai et al. 2025). When Kim et al. (2018) conducted a study on the antibacterial activity of Onions, they found that sulfur‐containing compounds could effectively inhibit both Gram‐positive and Gram‐negative bacteria. At the same time, they believed that the sulfur substances in Onions also had a selective inhibitory effect on bacteria in the digestive tract. Lazarević et al. (2011) conducted a comparative study on 12 Allium species, including Onions, and found that sulfur compounds in Onions had the strongest antibacterial activity.

Onions' antibacterial properties have been suggested to be due to sulfides reacting with cysteine that have a sulfur group (‐SH) on microorganisms' cell walls, preventing them from forming corresponding proteins and inhibiting their growth and reproduction (Mawouma et al. 2023; Guillamón et al. 2021). Figure 3 demonstrates this process.

FIGURE 3.

FIGURE 3

Anti‐bacterial properties of sulfides in onions. Image illustrates the interaction between sulfides in onions and thiol groups (‐SH) present on microbial cell walls. This interaction disrupts the formation of essential proteins, thereby inhibiting microbial growth and reproduction.

4.3. Anti‐Tumor Properties of Onion OSCs

According to scientific investigations, the antitumor effects of organic sulfides are primarily attributed to their ability to inhibit carcinogen activation, enhance intracellular detoxification enzyme systems, repair DNA damage, and modulate tumor cell gene expression to induce apoptosis (Adico et al. 2024; Liang et al. 2024). These compounds also exert anticancer activity by arresting the cell cycle, suppressing tumor metastasis, and inhibiting angiogenesis.

Viry et al. (2011) demonstrated that allyl sulfides found in onions act as preventive agents against breast cancer and exhibit significant inhibitory effects on gastric, esophageal, and colorectal cancers. The mechanism involves inhibition of carcinogen activation, thereby interfering with DNA damage repair and promoting apoptosis induction in breast cancer. Shala et al. (2023) and Sak (2014) further reported that diallyl disulfide, contained in onions, effectively induces cell cycle arrest, suppresses tumor metastasis, and inhibits angiogenesis—particularly in gastric and esophageal cancers. S‐allylcysteine was shown to reduce N‐nitroso compounds derived from pickled foods, thereby lowering the risk of brain cancer (Velmurugan et al. 2005). Furthermore, Ghinet et al. (2016) and Nakajima et al. (2007) indicated that S‐methylcysteine may interfere with carcinogenic processes associated with colon and kidney cancers. Figure 4 illustrates antitumor properties of OSCs derived from onions, particularly Allyl sulfides, Diallyl disulfide, S‐allylcysteine, and S‐methylcysteine.

FIGURE 4.

FIGURE 4

Antitumor properties of sulfides in onions. Image describes the anti tumor mechanisms of major organosulfur compounds produced from onions. The graphic depicts the therapeutic properties of allyl sulfides, diallyl disulfide, S‐allylcysteine, and S‐methylcysteine through multiple pathways, which includes carcinogenesis inhibition, apoptosis induction, cell cycle arrest, metastasis and angiogenesis suppression, and detoxification.

4.4. Onion Compounds in Diabetes Alleviation

Sheela et al. isolated S‐allylcysteine sulfoxide from onions in 1992 and reported that it has hypoglycemic properties (Subramanian et al. 2020). Onions' diabetes‐relieving impact is mainly associated with their extracts' ability to considerably improve indicators such as glucose, urea, creatinine, and bilirubin in the blood (Egbuna et al. 2021; Calis et al. 2020). Investigations have demonstrated that the sulfoxide amino acids identified in onions could interact with NADPH, inhibiting the reduction process of insulin, lowering blood glucose levels, and producing a hypoglycemic impact (Kim et al. 2024). Yang et al. (2018) confirmed, in an experiment on the hypoglycemic effects of garlic oil and onion oil in tetraoxan‐induced diabetic mice, that organic sulfides obtained from onion oil, such as S‐allylcysteine sulfoxide and S‐methylcysteine sulfoxide, are closely associated with diabetic condition improvement. In addition, animal studies have demonstrated that oral administration of sulfur‐containing compounds derived from onions can enhance insulin secretion, modulate hepatic activities of hexokinase and glucose‐6‐phosphatase, and significantly reduce blood glucose levels in alloxan‐induced diabetic rats (Sajitha et al. 2016; Ikechukwu and Ifeanyi 2016). Figure 5 illustrates hypolipidemic effects of onion sulfur compounds.

FIGURE 5.

FIGURE 5

Hypoglycemic effects of onion sulfur compounds. This schematic diagram illustrates the hypoglycemic mechanisms of the primary sulfur‐containing compounds in onions, including S‐allylcysteine sulfoxide, sulfoxide amino acids and S‐methylcysteine sulfoxide. The central focus of the illustration highlights how these bioactive constituents exert hypoglycemic effects through modulation of NADPH levels, insulin secretion, and outcomes observed in diabetic rat models.

4.5. Anti‐Asthmatic Effects of Onion‐Derived Sulfur Compounds

Onions consist of chemical components including thiosulfinates, α‐thioacyl disulfides, and thiosulfonates, which contribute to their anti‐asthmatic effects (Memarzia et al. 2019; Dorsch et al. 1987; Zhao et al. 2021). These sulfur‐containing compounds perform by regulating fundamental biochemical processes involved in inflammation. They significantly impact the metabolism of arachidonic acid, especially the cyclooxygenase (COX) and lipoxygenase (LOX) pathways. Interference with these pathways has important physiologic consequences, particularly a reduction in eicosanoid metabolism. This reduction subsequently helps prevent bronchial constriction (Sharma et al. 2012). Figure 6 demonstrates the mechanisms underlying onion's anti‐asthmatic effectiveness, including molecular structures, biological processes, and therapeutic effects.

FIGURE 6.

FIGURE 6

Anti‐asthmatic effects of onion‐derived sulfur compounds. Figure shows onion contain sulfhydryl compounds including thiosulfites, α‐thioacyl disulfides, and thiosulfonates, which significantly influence arachidonic acid metabolism by modulating the cyclooxygenase (COX) and lipoxygenase (LOX) pathways. These components interfere with eicosanoid production, leading to a reduction in eicosanoid metabolism. As a result, they have anti‐inflammatory and asthma‐relieving benefits.

Among them, saturated thiosulfinates exhibit lower biological activity than their unsaturated analogs. Conjugated thiosulfinates, particularly α, β‐unsaturated and aromatic derivatives, exhibit the greatest anti‐asthmatic properties (Li et al. 2023, 2017). According to Kianian and Dorsch, the organic sulfur compounds in onions perform an essential part in anti‐asthmatic activity (Kianian et al. 2021; Al‐Sanea et al. 2023; Dorsch et al. 1988). Thiosulfonates, formed during the degradation or mechanical disruption of onion tissues, are capable of effectively suppressing the arachidonic acid metabolic pathway, resulting in both anti‐inflammatory and anti‐asthmatic effects (Yamasaki et al. 2021; Kumar et al. 2015).

In conclusion, Table 2 presents a comprehensive Summary of Key Pharmacological Studies on Onion OSCs, which includes extraction methods, experimental models, doses, key findings, and corresponding references, thereby facilitating a rapid understanding and comparison of onion‐derived sulfur compounds.

TABLE 2.

Summary of key pharmacological studies on onion organosulfur compounds.

Extract/Compound Extraction method Experimental model Dose/Concentration Key findings References.
Onion extract (polyphenol‐rich) Ethanol extraction SD rats (hyperlipidemic) 200 mg/kg/day, 4 weeks Reduced serum TC, TG, LDL‐C; increased HDL‐C; improved lipid profile Li et al. (2021)
S‐propyl cysteine Not specified (commercial standard) HepG2 cells 50–200 μM Reduced apoB100 secretion and TG synthesis; inhibited lipoprotein assembly Han et al. (2002)
Cycloalliin Not specified (isolated compound) SD rats 100 mg/kg/day, 4 weeks Reduced serum TG; modulated hepatic lipid synthesis and secretion Yanagita et al. (2003)
S‐methylcysteine sulfoxide Not specified (isolated compound) Alloxan‐induced diabetic mice 50 mg/kg/day, 21 days Hypoglycemic and hypolipidemic effects; improved duodenal morphology Castro et al. (2021)
Onion essential oil Steam distillation Salmonella Typhimurium (in vitro) 0.5–2.0 mg/mL Exhibited dose‐dependent antibacterial activity; synergistic effect with ultrasound Kong et al. (2024)
Purple onion fermented extract Fermentation + solvent extraction Chickens (in vivo challenge) 10 mL/kg feed, 7 days Reduced toxin‐carrying bacteria; improved gut health and immunity Hai et al. (2025)
Allyl sulfides (onion‐derived) Not specified (commercial) MCF‐7 breast cancer cells 10–50 μM Inhibited cell proliferation; induced apoptosis; suppressed carcinogen activation Viry et al. (2011)
Diallyl disulfide Not specified (synthetic) Gastric/esophageal cancer cells 20–100 μM Induced cell cycle arrest; inhibited metastasis and angiogenesis Shala et al. (2023); Sak (2014)
S‐allylcysteine sulfoxide Isolated from onion bulbs Alloxan‐induced diabetic rats 50 mg/kg/day, 28 days Enhanced insulin secretion; improved glucose tolerance; regulated hepatic enzymes Yang et al. (2018)
Onion oil fraction Solvent fractionation Lead acetate‐exposed rats 100 mg/kg/day, 30 days Attenuated oxidative stress and lipid peroxidation; comparable to vitamin E Sajitha et al. (2016)
Thiosulfinates‐rich extract Subcritical water extraction RAW264.7 cells (LPS‐induced inflammation) 10–100 μg/mL Inhibited COX‐2 and LOX pathways; reduced eicosanoid production; anti‐inflammatory Trigueros et al. (2024)
Onion‐derived nanoparticles Aqueous extraction + ultracentrifugation RAW264.7 cells (LPS‐stimulated) 10–50 μg/mL Suppressed NO production; anti‐inflammatory effect independent of endocytosis Yamasaki et al. (2021)

5. Conclusion

Onions are widely distributed and have a high production in China. They could be used as both medicine and dietary supplements. Numerous studies have reported the health advantages of organic sulfur compounds found in onions. The academic community has done much research on onion organic sulfur compounds, which exhibit important biological properties. According to the literature, onions and their extracts exhibit an enormous variety of pharmacological effects, including lipid‐lowering, antibacterial, antitumor, antidiabetic, and anti‐asthmatic properties. These numerous biological properties indicate that onion‐based medications might possess potential applications for the treatment of a variety of diseases, especially atherosclerosis, diabetes, tumors, and asthma. However, how to apply the medicinal components of these drugs in clinical practice still requires in‐depth research.

In addition, the current technical challenges involve the inherent pungency of onion‐derived organic sulfur compounds, which restricts their application in highly processed food and pharmaceutical formulations. This limitation underscores the necessity for effective flavor‐masking techniques or structural modification approaches. Future research is expected to uncover additional crucial therapeutic properties by exploring onion organic sulfur compounds in depth, giving onion organic sulfur compounds extensive development and utilization value, as well as the potential to contribute good economic, social, and environmental benefits.

Author Contributions

Yijing Tao: writing – original draft, writing – review and editing. De Lv: writing – original draft, writing – review and editing. Yuanyuan Tang: investigation, funding acquisition, validation, visualization, project administration.

Funding

This study was supported by Changshu Health Commission Science and Technology Program of 2022 (CSWSQ202203) and Changshu Science and Technology Program of 2023 (CY202301).

Ethics Statement

The authors have nothing to report.

Conflicts of Interest

The authors declare no conflicts of interest.

Acknowledgments

We gratefully acknowledge the support provided by the Pharmacy Department of Chengdu University of Traditional Chinese Medicine during the preparation of this article. Figures are supported by Figdraw.

Tang, Y. , Lv D., and Tao Y.. 2026. “Onion (Allium cepa L.) Organosulfur Compounds: From Traditional Use to Modern Pharmacological Insights.” Food Science & Nutrition 14, no. 2: e71519. 10.1002/fsn3.71519.

Data Availability Statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.

References

  1. Abrante‐Pascual, S. , Nieva‐Echevarría B., and Goicoechea‐Oses E.. 2024. “Vegetable Oils and Their Use for Frying: A Review of Their Compositional Differences and Degradation.” Food 13, no. 24: 4186. 10.3390/foods13244186. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Adico, M. D. , Bayala B., Zoure A. A., et al. 2024. “In Vitro Activities and Mechanisms of Action of Anti‐Cancer Molecules From African Medicinal Plants: A Systematic Review.” American Journal of Cancer Research 14, no. 3: 1376–1401. 10.62347/AUHB5811. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Al‐Sanea, M. M. , Abdel‐Maksoud M. S., El‐Behairy M. F., et al. 2023. “Anti‐Inflammatory Effect of 3‐Fluorophenyl Pyrimidinylimidazo[2,1‐b]Thiazole Derivatives as p38α Inhibitors.” Bioorganic Chemistry 139: 106716. 10.1016/j.bioorg.2023.106716. [DOI] [PubMed] [Google Scholar]
  4. Alzandi, A. A. , Naguib D. M., and Abas A. M.. 2022. “Onion Extract Encapsulated on Nano Chitosan: A Promising Anticancer Agent.” Journal of Gastrointestinal Cancer 53: 211–216. 10.1007/s12029-020-00561-2. [DOI] [PubMed] [Google Scholar]
  5. Asemani, Y. , Zamani N., Bayat M., and Amirghofran Z.. 2019. “Allium Vegetables for Possible Future of Cancer Treatment.” Phytotherapy Research 33: 3019–3039. 10.1002/ptr.6490. [DOI] [PubMed] [Google Scholar]
  6. Calis, Z. , Mogulkoc R., and Baltaci A. K.. 2020. “The Roles of Flavonols/Flavonoids in Neurodegeneration and Neuroinflammation.” Mini Reviews in Medicinal Chemistry 20, no. 15: 1475–1488. 10.2174/1389557519666190617150051. [DOI] [PubMed] [Google Scholar]
  7. Cantrell, M. S. , Seale J. T., Arispe S. A., and McDougal O. M.. 2020. “Determination of Organosulfides From Onion Oil.” Food 9, no. 7: 884. 10.3390/foods9070884. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Castro, V. M. D. , Medeiros K. C. P., Lemos L. I. C., et al. 2021. “S‐Methyl Cysteine Sulfoxide Ameliorates Duodenal Morphological Alterations in Streptozotocin‐Induced Diabetic Rats.” Tissue and Cell 69: 101483. 10.1016/j.tice.2020.101483. [DOI] [PubMed] [Google Scholar]
  9. Chadorshabi, S. , Hallaj‐Nezhadi S., and Ghasempour Z.. 2022. “Red Onion Skin Active Ingredients, Extraction and Biological Properties for Functional Food Applications.” Food Chemistry 386: 132737. 10.1016/j.foodchem.2022.132737. [DOI] [PubMed] [Google Scholar]
  10. Ciardi, M. , Ianni F., Sardella R., et al. 2021. “Effective and Selective Extraction of Quercetin From Onion ( Allium cepa L.) Skin Waste Using Water Dilutions of Acid‐Based Deep Eutectic Solvents.” Materials 14, no. 21: 6465. 10.3390/ma14216465. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Dorsch, W. , Ettl M., Hein G., et al. 1987. “Antiasthmatic Effects of Onions. Inhibition of Platelet‐Activating Factor‐Induced Bronchial Obstruction by Onion Oils.” International Archives of Allergy and Applied Immunology 82, no. 3: 535–536. [PubMed] [Google Scholar]
  12. Dorsch, W. , Wagner H., Bayer T., et al. 1988. “Anti‐Asthmatic Effects of Onions. Alk(En)ylsulfinothioic Acid Alk(En)yl‐Esters Inhibit Histamine Release, Leukotriene and Thromboxane Biosynthesis In Vitro and Counteract PAF and Allergen‐Induced Bronchial Obstruction In Vivo.” Biochemical Pharmacology 37, no. 23: 4479–4486. 10.1016/0006-2952(88)90663-6. [DOI] [PubMed] [Google Scholar]
  13. Egbuna, C. , Awuchi C. G., Kushwaha G., et al. 2021. “Bioactive Compounds Effective Against Type 2 Diabetes Mellitus: A Systematic Review.” Current Topics in Medicinal Chemistry 21, no. 12: 1067–1095. 10.2174/1568026621666210509161059. [DOI] [PubMed] [Google Scholar]
  14. Ghinet, A. , Moise I. M., Rigo B., et al. 2016. “Studies on Phenothiazines: New Microtubule‐Interacting Compounds With Phenothiazine A‐Ring as Potent Antineoplastic Agents.” Bioorganic & Medicinal Chemistry 24, no. 10: 2307–2317. 10.1016/j.bmc.2016.04.001. [DOI] [PubMed] [Google Scholar]
  15. Guillamón, E. , Andreo‐Martínez P., Mut‐Salud N., Fonollá J., and Baños A.. 2021. “Beneficial Effects of Organosulfur Compounds From Allium cepa on Gut Health: A Systematic Review.” Foods 10, no. 8: 1680. 10.3390/foods10081680. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Hai, P. V. , Hoa N. X., and Phuong H. T. A.. 2025. “Fermented Purple Onion (Allium cepa L.) and Chive (Allium schoenoprasum) Bulb Extracts as Antibiotic Alternatives Against Toxin‐Carrying Bacteria: In Vitro and Pathogenicity Assessment in Chickens.” Open Veterinary Journal 15, no. 6: 2355–2364. 10.5455/OVJ.2025.v15.i6.8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Han, S. Y. , Hu Y., Anno T., and Yanagita T.. 2002. “S‐Propyl Cysteine Reduces the Secretion of Apolipoprotein B100 and Triacylglycerol by HepG2 Cells.” Nutrition 18, no. 6: 505–509. 10.1016/s0899-9007(02)00749-9. [DOI] [PubMed] [Google Scholar]
  18. Ichikawa, M. , Mizuno I., Yoshida J., et al. 2006. “Pharmacokinetics of Cycloalliin, an Organosulfur Compound Found in Garlic and Onion, in Rats.” Journal of Agricultural and Food Chemistry 54, no. 26: 9811–9819. 10.1021/jf062252a. [DOI] [PubMed] [Google Scholar]
  19. Ikechukwu, O. J. , and Ifeanyi O. S.. 2016. “The Antidiabetic Effects of the Bioactive Flavonoid (Kaempferol‐3‐O‐β‐D‐6{P‐ Coumaroyl} Glucopyranoside) Isolated From Allium cepa .” Recent Patents on Anti‐Infective Drug Discovery 11, no. 1: 44–52. 10.2174/1574891x11666151105130233. [DOI] [PubMed] [Google Scholar]
  20. Kamata, Y. , Aoyagi M., Sawada Y., et al. 2016. “Changes in Trans‐S‐1‐Propenyl‐l‐Cysteine Sulfoxide and Related Sulfur‐Containing Amino Acids During Onion Storage.” Journal of Agricultural and Food Chemistry 64, no. 47: 9063–9071. 10.1021/acs.jafc.6b04073. [DOI] [PubMed] [Google Scholar]
  21. Kianian, F. , Marefati N., Boskabady M., Ghasemi S. Z., and Boskabady M. H.. 2021. “Pharmacological Properties of Allium cepa, Preclinical and Clinical Evidences; A Review.” Iranian Journal of Pharmaceutical Research 20, no. 2: 107–134. 10.22037/ijpr.2020.112781.13946. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Kim, J. S. , Liu L., Kant S., et al. 2024. “Anaerobic Respiration of Host‐Derived Methionine Sulfoxide Protects Intracellular Salmonella From the Phagocyte NADPH Oxidase.” Cell Host & Microbe 32, no. 3: 411–424.e10. 10.1016/j.chom.2024.01.004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Kim, S. , Kim D. B., Jin W., et al. 2018. “Comparative Studies of Bioactive Organosulphur Compounds and Antioxidant Activities in Garlic (Allium sativum L.), elephant Garlic (Allium ampeloprasum L.) and Onion (Allium cepa L.).” Natural Product Research 32, no. 10: 1193–1197. 10.1080/14786419.2017.1323211. [DOI] [PubMed] [Google Scholar]
  24. Kocić‐Tanackov, S. , Dimić G., Lević J., et al. 2012. “Effects of Onion ( Allium cepa L.) and Garlic ( Allium sativum L.) Essential Oils on the Aspergillus Versicolor Growth and Sterigmatocystin Production.” Journal of Food Science 77, no. 5: M278–M284. 10.1111/j.1750-3841.2012.02662.x. [DOI] [PubMed] [Google Scholar]
  25. Kong, Y. , Cai X., Li Y., et al. 2024. “Synergistic Bactericidal Effect and Mechanism of Ultrasound Combined With Lauroyl Arginate Ethyl Against Salmonella typhimurium and Its Application in the Preservation of Onions.” International Journal of Food Microbiology 413: 110611. 10.1016/j.ijfoodmicro.2024.110611. [DOI] [PubMed] [Google Scholar]
  26. Kumar, M. , Barbhai M. D., Hasan M., et al. 2022. “Onion (Allium cepa L.) Peel: A Review on the Extraction of Bioactive Compounds, Its Antioxidant Potential, and Its Application as a Functional Food Ingredient.” Journal of Food Science 87: 4289–4311. 10.1111/1750-3841.16297. [DOI] [PubMed] [Google Scholar]
  27. Kumar, M. , Barbhai M. D., Hasan M., et al. 2022. “Onion (Allium cepa L.) Peels: A Review on Bioactive Compounds and Biomedical Activities.” Biomedicine & Pharmacotherapy 146: 112498. 10.1016/j.biopha.2021.112498. [DOI] [PubMed] [Google Scholar]
  28. Kumar, V. P. , Prashanth K. V. H., and Venkatesh Y. P.. 2015. “Structural Analyses and Immunomodulatory Properties of Fructo‐Oligosaccharides From Onion ( Allium cepa ).” Carbohydrate Polymers 117: 115–122. 10.1016/j.carbpol.2014.09.039. [DOI] [PubMed] [Google Scholar]
  29. Lazarević, J. S. , Ethorđević A. S., Zlatković B. K., Radulović N. S., and Palić R. M.. 2011. “Chemical Composition and Antioxidant and Antimicrobial Activities of Essential Oil of Allium sphaerocephalon L. Subsp. sphaerocephalon (Liliaceae) Inflorescences.” Journal of the Science of Food and Agriculture 91, no. 2: 322–329. 10.1002/jsfa.4189. [DOI] [PubMed] [Google Scholar]
  30. Li, B. , Cai S., Yang Y. A., et al. 2017. “Novel Unsaturated Glycyrrhetic Acids Derivatives: Design, Synthesis and Anti‐Inflammatory Activity.” European Journal of Medicinal Chemistry 139: 337–348. 10.1016/j.ejmech.2017.08.002. [DOI] [PubMed] [Google Scholar]
  31. Li, S. , Xu D., Jia J., et al. 2023. “Structure and Anti‐Inflammatory Activity of Neo‐Clerodane Diterpenoids From Scutellaria barbata .” Phytochemistry 213: 113771. 10.1016/j.phytochem.2023.113771. [DOI] [PubMed] [Google Scholar]
  32. Li, W. , Yang C., Mei X., et al. 2021. “Effect of the Polyphenol‐Rich Extract From Allium cepa on Hyperlipidemic Sprague‐Dawley Rats.” Journal of Food Biochemistry 45, no. 1: e13565. 10.1111/jfbc.13565. [DOI] [PubMed] [Google Scholar]
  33. Liang, J. , Ling J., Zhang X., Ouyang X. K., Omer A. M., and Yang G.. 2024. “pH/Glutathione Dual‐Responsive Copper Sulfide‐Coated Organic Mesoporous Silica for Synergistic Chemo‐Photothermal Therapy.” Journal of Colloid and Interface Science 657: 1–14. 10.1016/j.jcis.2023.11.146. [DOI] [PubMed] [Google Scholar]
  34. Marefati, N. , Ghorani V., Shakeri F., et al. 2021. “A Review of Anti‐Inflammatory, Antioxidant, and Immunomodulatory Effects of Allium cepa and Its Main Constituents.” Pharmaceutical Biology 59, no. 1: 287–302. 10.1080/13880209.2021.1874028. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Mawouma, S. , Doudou Walko F., Mbyeya J., Hamidou Yaya S., Awoudamkine E., and Funtong C. M. M.. 2023. “Effect of Allium Spices (Garlic and Onion) on the Bioaccessibility of Iron From Moringa oleifera Leaves.” Food Science & Nutrition 12, no. 3: 2115–2121. 10.1002/fsn3.3913. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Memarzia, A. , Amin F., Saadat S., Jalali M., Ghasemi Z., and Boskabady M. H.. 2019. “The Contribution of Beta‐2 Adrenergic, Muscarinic and Histamine (H1) Receptors, Calcium and Potassium Channels and Cyclooxygenase Pathway in the Relaxant Effect of Allium cepa L. on the Tracheal Smooth Muscle.” Journal of Ethnopharmacology 241: 112012. 10.1016/j.jep.2019.112012. [DOI] [PubMed] [Google Scholar]
  37. Muscolo, A. , Papalia T., Settineri G., Mallamaci C., and Panuccio M. R.. 2020. “Sulfur Bentonite‐Organic‐Based Fertilizers as Tool for Improving Bio‐Compounds With Antioxidant Activities in Red Onion.” Journal of the Science of Food and Agriculture 100: 785–793. 10.1002/jsfa.10086. [DOI] [PubMed] [Google Scholar]
  38. Nakajima, S. , Shikano N., Kotani T., et al. 2007. “Pharmacokinetics of 3‐[125I]Iodo‐Alpha‐Methyl‐L‐Tyrosine, a Tumor Imaging Agent, After Probenecid Loading in Mice Implanted With Colon Cancer DLD‐1 Cells.” Nuclear Medicine and Biology 34, no. 8: 1003–1008. 10.1016/j.nucmedbio.2007.06.017. [DOI] [PubMed] [Google Scholar]
  39. Putnik, P. , Gabrić D., Roohinejad S., et al. 2019. “An Overview of Organosulfur Compounds From Allium spp.: From Processing and Preservation to Evaluation of Their Bioavailability, Antimicrobial, and Anti‐Inflammatory Properties.” Food Chemistry 276: 680–691. 10.1016/j.foodchem.2018.10.068. [DOI] [PubMed] [Google Scholar]
  40. Qian, Y. L. , Hua G. K. H., Scott J. C., Dung J. K. S., and Qian M. C.. 2022. “Evaluation of Sulfur‐Based Biostimulants for the Germination of Sclerotium cepivorum Sclerotia and Their Interaction With Soil.” Journal of Agricultural and Food Chemistry 70, no. 48: 15038–15045. 10.1021/acs.jafc.2c05862. [DOI] [PubMed] [Google Scholar]
  41. Sajitha, G. R. , Augusti K. T., and Jose R.. 2016. “Prophylactic Effects of Garlic Oil and Onion Oil Fractions as Compared to Vitamin E on Rats Orally Fed With Lead Acetate Solution.” Indian Journal of Clinical Biochemistry 31, no. 3: 260–269. 10.1007/s12291-015-0526-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Sak, K. 2014. “Site‐Specific Anticancer Effects of Dietary Flavonoid Quercetin.” Nutrition and Cancer 66, no. 2: 177–193. 10.1080/01635581.2014.864418. [DOI] [PubMed] [Google Scholar]
  43. Shala, A. L. , Arduino I., Salihu M. B., and Denora N.. 2023. “Quercetin and Its Nano‐Formulations for Brain Tumor Therapy‐Current Developments and Future Perspectives for Paediatric Studies.” Pharmaceutics 15, no. 3: 963. 10.3390/pharmaceutics15030963. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Shang, A. , Cao S. Y., Xu X. Y., et al. 2019. “Bioactive Compounds and Biological Functions of Garlic (Allium sativum L.).” Foods 8, no. 7: 246. 10.3390/foods8070246. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Sharma, K. , Mahato N., Cho M. H., and Lee Y. R.. 2017. “Converting Citrus Wastes Into Value‐Added Products: Economic and Environmentally Friendly Approaches.” Nutrition 34: 29–46. 10.1016/j.nut.2016.09.006. [DOI] [PubMed] [Google Scholar]
  46. Sharma, K. , Mahato N., Nile S. H., Lee E. T., and Lee Y. R.. 2016. “Economical and Environmentally‐Friendly Approaches for Usage of Onion (Allium cepa L.) Waste.” Food & Function 7: 3354–3369. 10.1039/c6fo00251j. [DOI] [PubMed] [Google Scholar]
  47. Sharma, P. , Ryu M. H., Basu S., et al. 2012. “Epithelium‐Dependent Modulation of Responsiveness of Airways From Caveolin‐1 Knockout Mice Is Mediated Through Cyclooxygenase‐2 and 5‐Lipoxygenase.” British Journal of Pharmacology 167, no. 3: 548–560. 10.1111/j.1476-5381.2012.02014.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Srivastava, V. , and Balakrishnan M.. 2022. “Phytochemicals From Fruit and Vegetable Waste Generated in Hotels: Optimization of Recovery Procedure and Potential for Value‐Addition.” Waste Management 144: 401–410. 10.1016/j.wasman.2022.04.019. [DOI] [PubMed] [Google Scholar]
  49. Subramanian, M. S. , Nandagopal M. S. G., Amin Nordin S., Thilakavathy K., and Joseph N.. 2020. “Prevailing Knowledge on the Bioavailability and Biological Activities of Sulphur Compounds From Alliums: A Potential Drug Candidate.” Molecules 25, no. 18: 4111. 10.3390/molecules25184111. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Suleria, H. A. , Butt M. S., Anjum F. M., Saeed F., and Khalid N.. 2015. “Onion: Nature Protection Against Physiological Threats.” Critical Reviews in Food Science and Nutrition 55: 50–66. 10.1080/10408398.2011.646364. [DOI] [PubMed] [Google Scholar]
  51. Taghavi, E. , Abdul Salam A. S., Anarjan N., Nillian E., and Lani M. N.. 2022. “Onion Essential Oil‐In‐Water Emulsion as a Food Flavoring Agent: Effect of Environmental Stress on Physical Properties and Antibacterial Activity.” International Journal of Food Science 2022: 1363590. 10.1155/2022/1363590. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Takahashi, M. , and Shibamoto T.. 2008. “Chemical Compositions and Antioxidant/Anti‐Inflammatory Activities of Steam Distillate From Freeze‐Dried Onion ( Allium cepa L.) Sprout.” Journal of Agricultural and Food Chemistry 56, no. 22: 10462–10467. 10.1021/jf801220b. [DOI] [PubMed] [Google Scholar]
  53. Tolcha, T. , Gemechu T., Al‐Hamimi S., Megersa N., and Turner C.. 2020. “High Density Supercritical Carbon Dioxide for the Extraction of Pesticide Residues in Onion With Multivariate Response Surface Methodology.” Molecules 25, no. 4: 1012. 10.3390/molecules25041012. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Trigueros, E. , Benito‐Román Ó., Oliveira A. P., et al. 2024. “Onion (Allium cepa L.) Skin Waste Valorization: Unveiling the Phenolic Profile and Biological Potential for the Creation of Bioactive Agents Through Subcritical Water Extraction.” Antioxidants 13, no. 2: 205. 10.3390/antiox13020205. [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. Velmurugan, B. , Mani A., and Nagini S.. 2005. “Combination of S‐Allylcysteine and Lycopene Induces Apoptosis by Modulating Bcl‐2, Bax, Bim and Caspases During Experimental Gastric Carcinogenesis.” European Journal of Cancer Prevention 14, no. 4: 387–393. 10.1097/00008469-200508000-00012. [DOI] [PubMed] [Google Scholar]
  56. Viry, E. , Anwar A., Kirsch G., Jacob C., Diederich M., and Bagrel D.. 2011. “Antiproliferative Effect of Natural Tetrasulfides in Human Breast Cancer Cells Is Mediated Through the Inhibition of the Cell Division Cycle 25 Phosphatases.” International Journal of Oncology 38, no. 4: 1103–1111. 10.3892/ijo.2011.913. [DOI] [PubMed] [Google Scholar]
  57. Wang, Z. D. , Li L. H., Xia H., et al. 2018. “Optimisation of Steam Distillation Extraction Oil From Onion by Response Surface Methodology and Its Chemical Composition.” Natural Product Research 32, no. 1: 112–115. 10.1080/14786419.2017.1327863. [DOI] [PubMed] [Google Scholar]
  58. Yamasaki, M. , Yamasaki Y., Furusho R., et al. 2021. “Onion ( Allium cepa L.)‐derived Nanoparticles Inhibited LPS‐Induced Nitrate Production, However, Their Intracellular Incorporation by Endocytosis Was Not Involved in This Effect on RAW264 Cells.” Molecules 26, no. 9: 2763. 10.3390/molecules26092763. [DOI] [PMC free article] [PubMed] [Google Scholar]
  59. Yanagita, T. , Han S. Y., Wang Y. M., Tsuruta Y., and Anno T.. 2003. “Cycloalliin, a Cyclic Sulfur Imino Acid, Reduces Serum Triacylglycerol in Rats.” Nutrition 19, no. 2: 140–143. 10.1016/s0899-9007(02)00857-2. [DOI] [PubMed] [Google Scholar]
  60. Yang, C. , Li L., Yang L., Lǚ H., Wang S., and Sun G.. 2018. “Anti‐Obesity and Hypolipidemic Effects of Garlic Oil and Onion Oil in Rats Fed a High‐Fat Diet.” Nutrition & Metabolism 15: 43. 10.1186/s12986-018-0275-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  61. Yoon, H. J. , Won J. P., Lee H. G., and Seo H. G.. 2024. “Green Onion‐Derived Exosome‐Like Nanoparticles Prevent Ferroptotic Cell Death Triggered by Glutamate: Implication for GPX4 Expression.” Nutrients 16: 3257. 10.3390/nu16193257. [DOI] [PMC free article] [PubMed] [Google Scholar]
  62. Zhao, X. X. , Lin F. J., Li H., et al. 2021. “Recent Advances in Bioactive Compounds, Health Functions, and Safety Concerns of Onion ( Allium cepa L.).” Frontiers in Nutrition 8: 669805. 10.3389/fnut.2021.669805. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.


Articles from Food Science & Nutrition are provided here courtesy of Wiley

RESOURCES