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Supplier NameMedChemExpress (MCE)
Contactsales
Tel609-228-6898
Mobile609-228-6898
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Emailsales@medchemexpress.com; tech@medchemexpress.com
Websitehttps://www.medchemexpress.com/
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Product NameAllicin
SynonymsAlliin
Allicin
ALLICIN
alliosan
Allitrid
Allisatin
ARICINE(P)

Synonyms

Alliin
Allicin
ALLICIN
alliosan
Allitrid
Allisatin
ARICINE(P)
ALLICIN(SH)
Dianyctrsnlgide
DIALLYLTHIOSULPHINATE
S-Allyl acrylo-1-sulphinothioate
S-prop-2-en-1-yl prop-2-ene-1-sulfinothioate
2-propene-1-sulfinothioicacid,s-2-propenylester
CAS539-86-6
EINECS208-727-7
Chemical FormulaC6H10OS2
Molecular Weight162.27
inchiInChI=1/C6H10OS2/c1-3-5-8-9(7)6-4-2/h3-4H,1-2,5-6H2
Package10 mM * 1 mL;5 mg;10 mg;25 mg;50 mg;100 mg;500 mg
PriceGet quote
DescriptionsAllicin

Allicin

MedChemExpress (MCE)

HY-N0315

539-86-6

Diallyl thiosulfinate

97.74%

4°C, sealed storage, away from moisture and light *In solvent : -80°C, 6 months

Descriptions

Allicin

Allicin

MedChemExpress (MCE)

HY-N0315

539-86-6

Diallyl thiosulfinate

97.74%

4°C, sealed storage, away from moisture and light *In solvent : -80°C, 6 months
-20°C, 1 month (sealed storage, away from moisture and light)

Room temperature in continental US
may vary elsewhere.

Allicin (diallyl thiosulfinate) is isolated from garlic including Diallyl monosulfide, Diallyl disulfide, Diallyl trisulfide, Diallyl tetrasulfide, and Methyl allyl disulphide etc. They accounts for 98% of the extract. Allicin (diallyl thiosulfinate) has highly potent antimicrobial activity, and inhibits growth of a variety of microorganisms, among them antibiotic-resistant strains.

Allicin exhibits comparable MICs (32-64 μg/mL) toward methicillin-resistant S. aureus ATCC 43300, the type strain S. aureus DSM 20231, E. coli DSM 30083, A. baumannii DSM 30007, and C. albicans DSM 1386[1].

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[1]. Rahman, et al. Allicin and Other Functional Active Components in Garlic: Health Benefits and Bioavailability[J]. International Journal of Food Properties, 2007, 10(2):245-268.

[2]. Müller A, et al. Allicin Induces Thiol Stress in Bacteria through S-Allylmercapto Modification of ProteinCysteines. J Biol Chem. 2016 May 27
291(22):11477-90.
[Content Brief]

Supplier Websitehttps://www.medchemexpress.com/allicin.html
Last Update2025-05-21 16:50:25
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