K3007
N-(β-Ketocaproyl)-L-homoserine lactone
≥98%, detection, for peptide synthesis
Sinónimos:
N-(3-Oxohexanoyl)-L-homoserine lactone
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Fórmula empírica (notación de Hill):
C10H15NO4
Número CAS:
Peso molecular:
213.23
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.22
MDL number:
Servicio técnico
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Permítanos ayudarleNombre del producto
N-(β-Ketocaproyl)-L-homoserine lactone, ≥98%
Quality Level
assay
≥98%
form
powder
color
white
application(s)
detection
peptide synthesis
storage temp.
−20°C
SMILES string
CCCC(=O)CC(=O)N[C@H]1CCOC1=O
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
General description
N-(β-Ketocaproyl)-L-homoserine lactone (3-oxo-C6-HSL) is one of the quorum signaling molecules for V. fischeri. 3-oxo-C6-HSL is produced by LuxI autoinducer synthase catalyzed reaction between S-adenosylmethionine and acylated-acyl carrier proteins (Acyl-ACPs). It can be used in analyzing the expression of the orthogonal specialized reporter genes.
Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Ling Yan et al.
Journal of microbiological methods, 68(1), 40-45 (2006-08-19)
The autoinducer N-(3-oxo-hexanoyl)-L-homoserine lactone (3-oxo-C6-HSL) plays a significant role in the quorum-sensing system of the marine bacterium Vibrio fischeri. Upon forming a transcriptional activation complex with LuxR, 3-oxo-C6-HSL induces transcription of the luxICDABEG operon, leading to the increased production of
Lorenzo Pasotti et al.
Biotechnology journal, 6(7), 784-795 (2011-06-18)
Building biological devices to perform computational and signal processing tasks is one of the main research issues in synthetic biology. Herein, two modular biological systems that could mimic multiplexing and demultiplexing logic functions are proposed and discussed. These devices, called
Xiaofei Qin et al.
Biomolecules, 8(3) (2018-09-06)
New approaches to deal with drug-resistant pathogenic bacteria are urgent. We studied the antibacterial effect of chitosans against an Escherichia coli quorum sensing biosensor reporter strain and selected a non-toxic chitosan to evaluate its quorum sensing (QS) inhibition activity and