Allicin 180mg capsules
Allicin has been used in trials studying the treatment of Follicular Lymphoma.
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Safety monitoring data
Yellow Card reports
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Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.
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1 branded products available
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Guidelines from the National Institute for Health and Care Excellence
NICE clinical guidance(1)
Source: National Institute for Health and Care Excellence (NICE). Contains public sector information licensed under the Open Government Licence v3.0.
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Supply & safety information
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Codes for healthcare professionals and prescribing systems
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NHS UK identifiers
SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0.
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 28 · 1956–2026
Showing the 50 most relevant studies, sorted by most relevant.
B. Salehi, P. Zucca, I. Orhan, et al.
Trends in Food Science & Technology, 2019
M. Nakamoto, Kayo Kunimura, J. Suzuki, et al.
Experimental and Therapeutic Medicine, 2019
Xiaobei Si
2019
Backgrounds: Allicin (allyl 2-propene-1-thiosulfinate or diallyl thiosulfinate), a garlic compound, had been proved to be one of the active ingredients of anti-Hp effects. In recent years, a series of clinical trials further explored the anti-Hp effect of allicin as a complementary therapy were published with variable results. Aim: This study aims to systemic review the allicin as a Complementary medicine of Triple/Quadruple Therapy for Hp infection and further assess such efficacy based on previous randomized controlled trials. We also aim to assess the quality of current evidences of allicin as complementary therapy of Hp infection. Methods: Electronic databases, including Medline, Embase, Web of Science, Cochrane Central Register of Controlled Trial, Wanfang Database, and VIP Database, will be searched using the keywords of “allicin”, “Helicobacter pylori”, “randomized clinical trials” and their synonyms. A funnel plot may be adopted to evaluate the publication bias. The meta-analysis may be performed using fixed effect model for low heterogeneity and randomized effect model for high heterogeneity. Publication bias will be evaluated by Egger’s test, and funnel plot as well if enough (n>10) studies are included. What’s more, Trial Sequential Analysis (TSA) will be performed to evaluate whether the required information size has been met in order to make a determination of treatment benefit, harm or futility. The results of the meta-analysis will also be evaluated using the GRADE method and whether degradation is considered in terms of risk of bias, inconsistency, indirectness, accuracy, and publication bias, divided into “high quality”, “moderate quality”, “low quality”, and “very low quality”. Conclusions: Our review will provide an evidence of moderate quality that allicin as a complementary medicine for Helicobacter pylori.
Abstract licence: CC BY 4.0
Roman Leontiev, Nils Hohaus, C. Jacob, et al.
Scientific Reports, 2018
L. Lawson, Scott Hunsaker
Nutrients, 2018
Elena Catanzaro, Donatella Canistro, Valentina Pellicioni, et al.
Pharmacological Research, 2022
M. Nadeem, I. Kazmi, I. Ullah, et al.
Antioxidants, 2021
Yupei Deng, Chi-Tang Ho, Yaqi Lan, et al.
Journal of agricultural and food chemistry, 2023
Serge Ankri, David Mirelman
Microbes and Infection, 1999
Jan Borlinghaus, Frank Albrecht, Martin Gruhlke, et al.
Molecules, 2014
Allicin (diallylthiosulfinate) is a defence molecule from garlic (Allium sativum L.) with a broad range of biological activities. Allicin is produced upon tissue damage from the non-proteinogenic amino acid alliin (S-allylcysteine sulfoxide) in a reaction that is catalyzed by the enzyme alliinase. Current understanding of the allicin biosynthetic pathway will be presented in this review. Being a thiosulfinate, allicin is a reactive sulfur species (RSS) and undergoes a redox-reaction with thiol groups in glutathione and proteins that is thought to be essential for its biological activity. Allicin is physiologically active in microbial, plant and mammalian cells. In a dose-dependent manner allicin can inhibit the proliferation of both bacteria and fungi or kill cells outright, including antibiotic-resistant strains like methicillin-resistant Staphylococcus aureus (MRSA). Furthermore, in mammalian cell lines, including cancer cells, allicin induces cell-death and inhibits cell proliferation. In plants allicin inhibits seed germination and attenuates root-development. The majority of allicin’s effects are believed to be mediated via redox-dependent mechanisms. In sub-lethal concentrations, allicin has a variety of health-promoting properties, for example cholesterol- and blood pressure-lowering effects that are advantageous for the cardio-vascular system. Clearly, allicin has wide-ranging and interesting applications in medicine and (green) agriculture, hence the detailed discussion of its enormous potential in this review. Taken together, allicin is a fascinating biologically active compound whose properties are a direct consequence of the molecule’s chemistry.
Abstract licence: CC BY 3.0
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Pharmacology and chemical data from DrugBank
Key facts
Drug status
Investigational
Major interactions
None known
Half-life
Not available
Mechanism
Not available
Food interactions
None known
Human targets
None mapped
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Known interactions with other medicines. Always consult a healthcare professional.
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Chemical identifiers
CAS, UNII, InChI Key and database cross-references
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Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Linked compound data from DrugBank Open Data (CC BY-NC 4.0)
Allicin
DrugBank citations
If you use DrugBank data in your research, please cite:
- DrugBank 6.02024Recommended citationKnox C., Wilson M., Klinger C.M., et alDrugBank 6.0: the DrugBank Knowledgebase for 2024Nucleic Acids Res. 2024 Jan 552(D1):D1265-D1275
- DrugBank 5.02018Wishart D.S., Feunang Y.D., Guo A.C., et alDrugBank 5.0: a major update to the DrugBank database for 2018Nucleic Acids Res. 2017 Nov 846(D1):D1074-D1082
- DrugBank 4.02014Law V., Knox C., Djoumbou Y., et alDrugBank 4.0: shedding new light on drug metabolismNucleic Acids Res. 2014 Jan 142(1):D1091-7
- DrugBank 3.02011Knox C., Law V., Jewison T., et alDrugBank 3.0: a comprehensive resource for 'omics' research on drugsNucleic Acids Res. 2011 Jan39(Database issue):D1035-41
- DrugBank 2.02008Wishart D.S., Knox C., Guo A.C., et alDrugBank: a knowledgebase for drugs, drug actions and drug targets.Nucleic Acids Research2008 Jan36(Database issue):D901-6
- DrugBank 1.02006Wishart D.S., Knox C., Guo A.C., et alDrugBank: a comprehensive resource for in silico drug discovery and exploration.Nucleic Acids Research2006 Jan 134(Database issue):D668-72