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N-(3-Oxododecanoyl)-L-homoserine lactone - 97%, high purity , CAS No.168982-69-2

  • ≥97%
Item Number
N478346
Grouped product items
SKUSizeAvailabilityPrice Qty
N478346-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$69.90
N478346-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$249.90
N478346-100mg
100mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$389.90
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Amino acids and their derivatives Serine

Basic Description

Synonyms(S)-3-Oxo-N-(2-oxotetrahydrofuran-3-yl)dodecanamide | DB08324 | 3-oxo-C12-HSL | N-(3-oxododecanoyl)-L-homoserine lactone L-enantiomer | PAI-1 | 3-oxo-N-[(3S)-2-oxooxolan-3-yl]dodecanamide | N-(3-oxododecanoyl) homoserine lactone | AKOS015899709 | LMFA0803
Specifications & Purity≥97%
Biochemical and Physiological MechanismsN-(3-oxododecanoyl)homoserine-L-lactone (3-oxo-C12-HSL) is among a group of homoserine lactones that includes:N-octanoyl-homoserine lactone (N-C8-HSL),N-(3-oxodecanoyl) homoserine-L-lactone (3-oxo-C10 HSL),N-(3-Oxotetradecanoyl)-L-homoserine
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
Product Description

Description

N-(3-Oxododecanoyl)-L-homoserine lactone (3-Oxo-C12-HSL), a member of a family of acyl homoserine lactones, may be used to determine its mechanisms and specificity of action as a signaling molecule involved in the regulation of bacterial quorum sensing.

Associated Targets

EIF2S1 Tchem Eukaryotic translation initiation factor 2 subunit 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CHUK Tchem Inhibitor of nuclear factor kappa-B kinase subunit alpha 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

RELA Tchem Transcription factor p65 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

MAPK12 Tchem Mitogen-activated protein kinase 12 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

MAPK14 Tchem Mitogen-activated protein kinase 14 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name 3-oxo-N-[(3S)-2-oxooxolan-3-yl]dodecanamide
INCHI InChI=1S/C16H27NO4/c1-2-3-4-5-6-7-8-9-13(18)12-15(19)17-14-10-11-21-16(14)20/h14H,2-12H2,1H3,(H,17,19)/t14-/m0/s1
InChi Key PHSRRHGYXQCRPU-AWEZNQCLSA-N
Canonical SMILES CCCCCCCCCC(=O)CC(=O)NC1CCOC1=O
Isomeric SMILES CCCCCCCCCC(=O)CC(=O)N[C@H]1CCOC1=O
PubChem CID 3246941
Molecular Weight 297.39

Certificates

Certificate of Analysis(COA)

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6 results found

Lot NumberCertificate TypeDateItem
A2429132Certificate of AnalysisJan 19, 2024 N478346
A2429133Certificate of AnalysisJan 19, 2024 N478346
A2429134Certificate of AnalysisJan 19, 2024 N478346
A2429135Certificate of AnalysisJan 19, 2024 N478346
A2429136Certificate of AnalysisJan 19, 2024 N478346
A2429139Certificate of AnalysisJan 19, 2024 N478346

Safety and Hazards(GHS)

Pictogram(s) GHS07
Signal Warning
Hazard Statements

H302:Harmful if swallowed

Precautionary Statements

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P270:Do not eat, drink or smoke when using this product.

P330:Rinse mouth.

P301+P317:IF SWALLOWED: Get medical help.

Related Documents

 SDS

 Specification Sheet

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  2. N-(3-Oxodecanoyl)-L-homoserine lactone
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  3. N-(3-Oxotetradecanoyl)-L-homoserine lactone
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  4. N-3-oxo-octanoyl-L-Homoserine lactone
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References

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55. Omar González,Randy Ortíz-Castro,César Díaz-Pérez,Alma L Díaz-Pérez,Viridiana Magaña-Dueñas,José López-Bucio,Jesús Campos-García.  (2016-12-03)  Non-ribosomal Peptide Synthases from Pseudomonas aeruginosa Play a Role in Cyclodipeptide Biosynthesis, Quorum-Sensing Regulation, and Root Development in a Plant Host..  Microbial ecology,  73  ((3)): (616-629).  [PMID:27900439]
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