A primary metabolite of L-deoxyalliin
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Parent Compound(s)
14014L-Deoxyalliin
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N-Acetyl-S-allyl-L-cysteine

Item No. 17592

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
N-acetyl-S-2-propen-1-yl-L-cysteine
CAS Number
23127-41-5
Molecular Formula
C8H13NO3S
Formula Weight
203.3
Purity
≥98%
Formulation (Request formulation change)
A crystalline solid
Solubility(Learn about Variance in Solubility)
DMF: 50 mg/mlDMSO: 50 mg/mlEthanol: 50 mg/mlPBS (pH 7.2): 30 mg/ml
SMILES
C=CCSC[C@H](NC(C)=O)C(O)=O
InChi Code
InChI=1S/C8H13NO3S/c1-3-4-13-5-7(8(11)12)9-6(2)10/h3,7H,1,4-5H2,2H3,(H,9,10)(H,11,12)/t7-/m0/s1
InChi Key
LKRAEHUDIUJBSF-ZETCQYMHSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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Certificates of Analysis & Batch Specific Data

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    1 mg

    $36

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    5 mg

    $128

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    10 mg

    $203

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    Product Description

    N-Acetyl-S-allyl-L-cysteine is a principal metabolite of L-deoxyalliin in humans, mice, rats, and dogs.1,2,3 It is readily detected in plasma and urine. The conversion of L-deoxyalliin to N-acetyl-S-allyl-L-cysteine appears to be mediated by a family of flavin-containing monooxygenases.2,4

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. de Rooij, B.M., Boogaard, P.J., Rijksen, D.A., et al. Urinary excretion of N-acetyl-S-allyl-L-cysteine upon garlic consumption by human volunteers. Arch. Toxicol. 70(10), 635-639 (1996).

    2. Krause, R.J., Glocke, S.C., and Elfarra, A.A. Sulfoxides as urinary metabolites of S-allyl-L-cysteine in rats: Evidence for the involvement of flavin-containing monooxygenases. Drug Metab. Dispos. 30(10), 1137-1142 (2002).

    3. Amano, H., Kazamori, D., Itoh, K., et al. Metabolism, excretion, and pharmacokinetics of S-allyl-l-cysteine in rats and dogs. Drug Metab. Dispos. 43(5), 749-755 (2015).

    4. Krause, R.J., Lash, L.H., and Elfarra, A.A. Human kidney flavin-containing monooxygenases and their potential roles in cysteine S-conjugate metabolism and nephrotoxicity. J. Pharmacol. Exp. Ther. 304(1), 185-191 (2003).