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N-3-oxo-dodecanoyl-L-Homoserine lactone (Synonyms: 3-oxo-C12-HSL)

Katalog-Nr.GC17279

N-3-oxo-dodecanoyl-L-Homoserine lactone (3-oxo-C12-HSL), as a quorum-sensing (QS) molecule produced by Gram-negative bacteria in the gastrointestinal tract, is a major inducer of oxidative stress indicated by a high level of intracellular reactive oxygen species (ROS).

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N-3-oxo-dodecanoyl-L-Homoserine lactone Chemische Struktur

Cas No.: 168982-69-2

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Sample solution is provided at 25 µL, 10mM.

Description of N-3-oxo-dodecanoyl-L-Homoserine lactone

N-3-oxo-dodecanoyl-L-Homoserine lactone (3-oxo-C12-HSL), as a quorum-sensing (QS) molecule produced by Gram-negative bacteria in the gastrointestinal tract, is a major inducer of oxidative stress indicated by a high level of intracellular reactive oxygen species (ROS)[1].

In vitro, 100μM 3-oxo-C12 HSL elevates intracellular free calcium in platelet, and 3-oxo-C12 HSL induces intracellular calcium-dependent ROS generation[2]In vitro, 3-oxo-12-HSL also significantly inhibited LPS (lipopolysaccharides) induced IL-6 release at 10 μM, while 100 μM reduced IL-6 release by almost 75%[3]In vitro, treatment of fibroblasts with 50 μM 3O-C12-HSL for 1 or 3 h (in contrast to 10 μM and the control) resulted in a rapid fragmentation of mitochondrial network, as evidenced by decreased mitochondrial length and area and an elevated number of small mitochondria[4]. In addition, 50 μM 3O-C12-HSL increases the cell area and protrusive activity of macrophages[5].

In vivo, Passively sensitized mice that had been treated with 3-oxo-12-HSL (3 mg/kg) 1 h prior to antigen exposure showed a significant (60%) decrease in PCA (passive cutaneous anaphylaxis) response[3].

References:
[1] Tao S, et al. Caspase-1-dependent mechanism mediating the harmful impacts of the quorum-sensing molecule N-(3-oxo-dodecanoyl)-l-homoserine lactone on the intestinal cells. J Cell Physiol. 2019 Apr;234(4):3621-3633.
[2] Yadav VK, et al. Pseudomonas aeruginosa quorum sensing molecule N-3-oxo-dodecanoyl-l-homoserine lactone activates human platelets through intracellular calcium-mediated ROS generation. Int J Med Microbiol. 2018 Oct;308(7):858-864.
[3] Khambati I, et al. The bacterial quorum-sensing molecule, N-3-oxo-dodecanoyl-L-homoserine lactone, inhibits mediator release and chemotaxis of murine mast cells. Inflamm Res. 2017 Mar;66(3):259-268.
[4] Josephson H, et al. Pseudomonas aeruginosa N-3-Oxo-Dodecanoyl-Homoserine Lactone Impacts Mitochondrial Networks Morphology, Energetics, and Proteome in Host Cells. Front Microbiol. 2020 May 25;11:1069.
[5]Holm A, et al. Pseudomonas aeruginosa N-3-oxo-dodecanoyl-homoserine Lactone Elicits Changes in Cell Volume, Morphology, and AQP9 Characteristics in Macrophages. Front Cell Infect Microbiol. 2016 Mar 24;6:32. 

Protocol of N-3-oxo-dodecanoyl-L-Homoserine lactone

Cell experiment [1]:

Cell lines

Platelet cells

Preparation method

Platelet cells were incubated with 5 μM Fluo-4 AM for 45–50 min at 37 °C in the dark. After 60 s of baseline, 3-oxo-C12 HSL (100 μM), or DMSO as vehicle control were added in a different set of samples, and after 300 s 1 mM of CaCl2 was added, and fluorescence intensity was recorded up to 600 s.

Reaction Conditions

100 μM;300 s

Applications

3-oxo-C12 HSL induces intracellular calcium in a dose-dependent manner, and the maximum rise was obtained at 100 μM

Animal experiment [2]:

Animal models

8 week-old C57BL/6 mice or in 6 week-old athymic nude mice

Preparation method

For C12 (N-3-oxo-dodecanoyl-L-Homoserine lactone) toxicity studies, DMSO or C12 (25 mg/kg/day) was administered intraperitoneally each day in 8 week-old C57BL/6 mice or in 6 week-old athymic nude mice. For wild-type A549 tumors, animals were treated with C12 for 6 times/week. For Bcl-2 over-expressing A549 cells tumors, DMSO or C12 was administered with C12 each day. For A549-control-shRNA and A549-PON2-shRNA tumors, DMSO or C12 was administered twice every three days. At the end of the experiments, tumors were excised for apoptosis evaluation.

Dosage form

25 mg/kg/day; i.p.

Applications

C12 inhibits lung tumor growth and induces tumor cell apoptosis in vivo. C12 inhibits LLC tumor growth and induces tumor cell apoptosis in vivo in a dose-dependent fashion. C12 induces tumor apoptotic cell death independent of anti-apoptotic Bcl-2 proteins. PON3 (lactonase paraoxonase) expression recovers C12 cytotoxicity in PON2-deficient tumor cells.

References:

[1] Yadav VK, et al. Mechanism underlying N-(3-oxo-dodecanoyl)-L-homoserine lactone mediated intracellular calcium mobilization in human platelets. Blood Cells Mol Dis. 2019 Nov;79:102340.

[2] Zhao G, et al. N-(3-oxo-acyl) homoserine lactone inhibits tumor growth independent of Bcl-2 proteins. Oncotarget. 2016 Feb 2;7(5):5924-42.

Chemical Properties of N-3-oxo-dodecanoyl-L-Homoserine lactone

Cas No. 168982-69-2 SDF
Überlieferungen 3-oxo-C12-HSL
Chemical Name 3-oxo-N-[(3S)-tetrahydro-2-oxo-3-furanyl]-dodecanamide
Canonical SMILES CCCCCCCCCC(=O)CC(=O)N[C@H]1CCOC1=O
Formula C16H27NO4 M.Wt 297.4
Löslichkeit ≤20mg/ml in DMSO;20mg/ml in dimethyl formamide Storage Store at -20°C, protect from light
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of N-3-oxo-dodecanoyl-L-Homoserine lactone

Prepare stock solution
1 mg 5 mg 10 mg
1 mM 3.3625 mL 16.8124 mL 33.6247 mL
5 mM 672.5 μL 3.3625 mL 6.7249 mL
10 mM 336.2 μL 1.6812 mL 3.3625 mL
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