Allicin

The compound is not present in garlic unless tissue damage occurs,[1] and is formed by the action of the enzyme alliinase on alliin.

[7] The racemic form can also be generated by oxidation of diallyl disulfide:[8][9] Alliinase is irreversibly deactivated below pH 3; as such, allicin is generally not produced in the body from the consumption of fresh or powdered garlic.

The enzyme alliinase, which contains pyridoxal phosphate (PLP), cleaves alliin, generating allylsulfenic acid (CH2=CHCH2SOH), pyruvate, and ammonium ions.

[13] A Cochrane review found there to be insufficient clinical evidence regarding the effects of allicin in preventing or treating common cold.

These compounds are hydrophobic, easily pass from the intestines to the bloodstream, and are reduced to thiamine by cysteine or glutathione.

Structural formula of R-allicin
Structural formula of R-allicin
Ball and stick model of R-allicin
Ball and stick model of R-allicin