A C2 N-acyl homoserine lactone
Technical Support & Resources

Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.

Visit our FAQ

Contact Us

Toll Free Phone (USA and Canada Only): (888) 526-5351
Direct Phone: (734) 975-3888

Request Technical Support

Technical Support Request

To streamline the process attach the appropriate questionnaire to your inquiry.

Download IHC QuestionnaireDownload WB Questionnaire

View Our Privacy Statement for details on how we use and protect your data. In addition, this site is protected by hCaptcha and its Privacy Policy and Terms of Service apply.

Product Categories

Research Area

Acetyl-L-Homoserine lactone

Item No. 23241

Technical Information
Formal Name
N-[(3S)-tetrahydro-2-oxo-3-furanyl]-acetamide
CAS Number
51524-71-1
Synonyms
  • Acetyl-L-HSL
  • C2-HSL
Molecular Formula
C6H9NO3
Formula Weight
Purity
≥98%
A crystalline solid
DMF: SolubleDMSO: Soluble
SMILES
O=C1OCC[C@@H]1NC(C)=O
InChi Code
InChI=1S/C6H9NO3/c1-4(8)7-5-2-3-10-6(5)9/h5H,2-3H2,1H3,(H,7,8)/t5-/m0/s1
InChi Key
XGSXMDQVYYCSDA-YFKPBYRVSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
Recommended Products

Certificates of Analysis & Batch Specific Data

Provide batch numbers separated by commas to download or request available product inserts, QC sheets, certificates of analysis, data packs, and GC-MS data.

    Add

    Add

    Add

    Product Description

    Acetyl-L-homoserine lactone belongs to the family of N-acylated homoserine lactones (HSLs) and has an acyl chain length of two carbons.1 HSLs perform a role in quorum sensing; however, unlike other HSLs, acetyl-L-homoserine lactone does not elicit a response in bacteria. In an assay of carbapenem antibiotic biosynthesis, acetyl-L-homoserine lactone does not induce a response in E. carotovora.2 In a fluorescence assay using E. coli containing a reporter plasmid of GFP expression in response to exogenous HSLs, acetyl-L-homoserine does not elicit GFP production.3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. González, J.E., and Keshavan, N.D. Messing with bacterial quorum sensing. Microbiol. Mol. Biol. Rev. 70(4), 859-875 (2006).

    2. Chhabra, S.R., Stead, P., Bainton, N.J., et alAutoregulation of carbapenem biosynthesis in Erwinia carotovora by analogues of N-(3-oxohexanoyl)-L-homoserine lactone. J. Antibiot. (Tokyo) 46(3), 441-454 (1993).

    3. Syrpas, M., Ruysbergh, E., Blommaert, L., et alHaloperoxidase mediated quorum quenching by Nitzschia cf pellucida: Study of the metabolization of N-acyl homoserine lactones by a benthic diatom. Mar. Drugs 12(1), 352-367 (2014).

    Product Citations

    Pundir, P., Liu, R., Vasavda, C., et alA connective tissue mast-cell-specific receptor detects bacterial quorum-sensing molecules and mediates antibacterial immunity. Cell Host Microbe 26, 114-122 (2019).