N-(Ketocaproyl)-L-homoserine Lactone - ≥98%, high purity , CAS No.143537-62-6

  • ≥98%
Item Number
N137466
Grouped product items
SKUSizeAvailabilityPrice Qty
N137466-2mg
2mg
Available within 8-12 weeks(?)
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$27.90
N137466-10mg
10mg
Available within 4-8 weeks(?)
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$106.90
N137466-50mg
50mg
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$382.90
N137466-250mg
250mg
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$1,722.90

Basic Description

SynonymsN-(beta-Ketocaproyl)-L-homoserine lactone; N-(3-Oxohexanoyl)-L-homoserine lactone; N-(beta-Ketocaproyl)-DL-homoserine lactone
Specifications & Purity≥98%
Storage TempStore at -20°C,Argon charged
Shipped InIce chest + Ice pads
Product Description

N-(β-ketocaproyl)-L-Homoserine lactone is a component of quorum regulatory sensing which is a regulatory system used by bacteria for controlling gene expression in response to increasing cell density. This regulatory process manifests itself with a variety of phenotypes including biofilm formation and virulence factor production. Coordinated gene expression is achieved by the production, release, and detection of small diffusible signal molecules called autoinducers. The N-acylated homoserine lactones (AHLs) comprise one such class of autoinducers, each of which generally consists of a fatty acid coupled with homoserine lactone (HSL). Regulation of bacterial quorum sensing signaling systems to inhibit pathogenesis represents a new approach to antimicrobial therapy in the treatment of infectious diseases. AHLs vary in acyl group length (C4-C18), in the substitution of C3 (hydrogen, hydroxyl, or oxo group), and in the presence or absence of one or more carbon-carbon double bonds in the fatty acid chain. These differences confer signal specificity through the affinity of transcriptional regulators of the LuxR family. In one of the most-studied quorum-sensing systems in gram-negative bacteria, the LuxI AHL synthase catalyzes the production of N-(β-ketocaproyl)-L-homoserine lactone utilizing S-adenosylmethionine and hexanoyl-acyl carrier protein as reaction substrates in the marine bioluminescence bacterium V. fischeri. At increased populations of the bacteria, localized higher concentrations of 3-O-C6-HSL, an endogenous ligand to transcriptional factor LuxR, leads to increased production of both the AHL synthase and proteins responsible for bioluminescence. Numerous other species of bacteria also employ N-(β-ketocaproyl)-L-homoserine lactone in cell-to-cell communication.
A component of quorum regulatory sensing.

Associated Targets(non-human)

Agrobacterium tumefaciens (620 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
luxR Transcriptional activator protein luxR (400 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
traR Transcriptional activator protein traR (147 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
lasR Transcriptional activator protein lasR (432 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Names and Identifiers

IUPAC Name 3-oxo-N-[(3S)-2-oxooxolan-3-yl]hexanamide
INCHI InChI=1S/C10H15NO4/c1-2-3-7(12)6-9(13)11-8-4-5-15-10(8)14/h8H,2-6H2,1H3,(H,11,13)/t8-/m0/s1
InChi Key YRYOXRMDHALAFL-QMMMGPOBSA-N
Canonical SMILES CCCC(=O)CC(=O)NC1CCOC1=O
Isomeric SMILES CCCC(=O)CC(=O)N[C@H]1CCOC1=O
WGK Germany 3
PubChem CID 688505
Molecular Weight 213.23

Certificates

Certificate of Analysis(COA)

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5 results found

Lot NumberCertificate TypeDateItem
H2317081Certificate of AnalysisOct 11, 2022 N137466
L2207881Certificate of AnalysisOct 11, 2022 N137466
L2207882Certificate of AnalysisOct 11, 2022 N137466
L2207883Certificate of AnalysisOct 11, 2022 N137466
G2102233Certificate of AnalysisAug 24, 2022 N137466

Chemical and Physical Properties

SolubilitySoluble in ethanol, DMSO (~30 mg/ml), DMF (~30 mg/ml), methanol, and chloroform.
SensitivityLight & Moisture Sensitive.

Safety and Hazards(GHS)

WGK Germany 3

Related Documents

Solution Calculators