N-butyryl-L-Homoserine lactone-d

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N-butyryl-L-Homoserine lactone-d₅

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Cat No: 10007899

Biochemicals - Isotopically Labeled Standards

N-butyryl-L-Homoserine lactone-d5 is intended for use as an internal standard for the quantification of N-butyryl-L-homoserine lactone (Item No. 10007898) by GC- or LC-MS. N-butyryl-L-Homoserine lactone is a quorum-sensing signaling molecule produced ...

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Territorial Availability: Available through Bertin Technologies only in France

Synonyms:

N-[(3S)-tetrahydro-2-oxo-3-furanyl]-butanamide-3,3,4,4,4-d5

Correlated keywords:

GC/MS deuteriums isotopes internal standards deuterateds LC/MS GC-MS LC-MS mass spectrometry bacterial quorums sensing signaling molecules regulatory regulates systems genes expressions cells density infections transcriptional regulators LuxIR proteins synthesis N-acylhomoserine lactones AHL cellular metabolism regulation virulence slime biofilms transduction activation signalling 67605-85-0 Pseudomonas

Product Overview:
N-butyryl-L-Homoserine lactone-d5 is intended for use as an internal standard for the quantification of N-butyryl-L-homoserine lactone (Item No. 10007898) by GC- or LC-MS. N-butyryl-L-Homoserine lactone is a quorum-sensing signaling molecule produced by P. aeruginosa.{58759} It induces expression of the virulence genes lasB and rhlA in P. aeruginosa when used at a concentration of 10 µM.{16309} N-butyryl-L-Homoserine lactone (50 µM) induces rhamnolipid accumulation in P. aeruginosa growth media.{58760}

Size	500 µg
Shipping	dry ice
CAS Number	2701379-46-4
Molecular Formula	C₈H₈D₅NO₃
SMILES	CCCC(=O)N[C@H]1CCOC1=O
Molecular Weight	176,2
Formulation	A crystalline solid
Purity	≥99% deuterated forms (d1-d5)
Custom Code	3822.19
UNSPSC code	12352100

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Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

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