Tetradecylphosphonic acid [4671-75-4]

Commande minimum 2

Référence HY-132238-100mg

Conditionnement : 100mg

Marque : MedChemExpress


Description

Tetradecylphosphonic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

Cellular Effect
Cell Line Type Value Description References
PC-3 IC50
9674 nM
Compound: 16c
Inhibition of LPA-induced calcium transients in PC-3 cells
Inhibition of LPA-induced calcium transients in PC-3 cells
[PMID: 16033271]
RH7777 IC50
3100 nM
Compound: 16c
Inhibition of LPA-induced calcium transients in RH7777 rat hepatoma cells expressing LPA3 receptor
Inhibition of LPA-induced calcium transients in RH7777 rat hepatoma cells expressing LPA3 receptor
[PMID: 16033271]
RH7777 IC50
5500 nM
Compound: 16c
Inhibition of LPA-induced calcium transients in RH7777 rat hepatoma cells expressing LPA2 receptor
Inhibition of LPA-induced calcium transients in RH7777 rat hepatoma cells expressing LPA2 receptor
[PMID: 16033271]
RH7777 IC50
~ 10000 nM
Compound: 16c
Inhibition of LPA-induced calcium transients in RH7777 rat hepatoma cells expressing LPA1 receptor
Inhibition of LPA-induced calcium transients in RH7777 rat hepatoma cells expressing LPA1 receptor
[PMID: 16033271]
In Vitro

Tetradecyl phosphonate is a pan-antagonist of lysophosphatidic acid 1 (LPA1), LPA2, and LPA3 receptors. The IC50 value for inhibition of LPA-induced calcium mobilization was 10 μM, 5.5 μM, and 3.1 μM, respectively. At a concentration of 10 μM, tetradecyl phosphonate activates a peroxisome proliferator-activated receptor γ reporter construct 4-fold when compared with the controls and partially inhibits autotaxin with an IC50 value of approximately 3 μM. Lysophosphatidic acid (LPA) , also known as autotaxin (ATX ), is a lipid signaling molecule formed by the hydrolysis of lysophosphatidyl choline by lysophospholipase D. LPA signals through four different G protein-coupled receptors, named as LPA1/EDG-2, LPA2/EDG-4, LPA3/EDG-7, and LPA4/GPR23 . It has been reported that LPA was involved in activating peroxisome proliferator-activated receptor γ (PPARγ) .

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Pureté et documentation