N-(3-Oxodecanoyl)-L-homoserine lactone

CHF 64.00
In stock
CDX-O0059-M01010 mgCHF 64.00
CDX-O0059-M100100 mgCHF 293.00
More Information
Product Details
Synonyms 3-oxo-C10-HSL; 3OC10-HSL; 3-​oxo-​N-​[(3S)​-​Tetrahydro-​2-​oxo-​3-​furanyl]​-decanamide
Product Type Chemical
Properties
Formula

C14H23NO4

MW 269.3
CAS 147795-40-2
Source/Host Chemicals Synthetic.
Purity Chemicals ≥97% (HPLC)
Appearance White solid.
Solubility Soluble in chloroform.
Identity Determined by NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key KYGIKEQVUKTKRR-LBPRGKRZSA-N
Smiles [H][C@@]1(CCOC1=O)NC(=O)CC(=O)CCCCCCC
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice Keep cool and dry.
Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at -20°C.
Documents
MSDS Download PDF
Product Specification Sheet
Datasheet Download PDF

N-(3-Oxodecanoyl)-DL-homoserine lactone is a small diffusible signaling molecule and is a member of N-acyl-homoserine lactone family. N-acylhomoserine lactones (AHL) are involved in quorum sensing, controlling gene expression, and cellular metabolism. The diverse applications of this kind of molecule include regulation of virulence in general, infection prevention, and formation of biofilms. It was used as an autoinducer of quorum signaling by Pseudomonas putida, Yersinia enterocolitica and other Gram-negative bacteria.

Product References

(1) D.L. Milton, et al.; J. Bacteriol. 179, 3004 (1997) | (2) P.S. Shaw, et al.; PNAS 94, 6036 (1997) | (3) S.R. Chhabra, et al.; J. Med. Chem. 46, 97 (2003) | (4) C. Nantasenamat, et al.; J. Biol. Sys. 16, 279 (2008) | (5) B.K. Khajanchi, et al.; Infect. Immun. 79, 2646 (2011) | (6) M.E.A. Churchill, et al.; Meth. Mol.Biol. 692, 159 (2011) | (7) X. Bai, et al.; Plant Physiol. 158, 725 (2012) | (8) C.H. Tan, et al.; ISME J. 8, 1186 (2014)

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