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L-161982

Cat. No. M6876

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L-161982 Structure
Synonym:

L161982

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1mg USD 120 4-7 Days
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Quality Control & Documentation
Biological Activity

L-161982 is a EP4 receptor antagonist that is selective over all other members of the prostanoid receptor family (Ki values are 0.024, 0.71, 1.90, 5.10, 5.63, 6.74, 19 and 23 μM for human EP4, TP, EP3, DP, FP, IP, EP1 and EP2 receptors respectively).

L-161982 completely blocks PGE2-induced ERK phosphorylation and cell proliferation of HCA-7 cells. L-161982 induces apoptosis, cell cycle arrest, and inhibits prostaglandin E2-induced proliferation in oral squamous carcinoma Tca8113 cells.

L-161982 suppresses PGE2-induced bone formation in rats and prevents the nociceptive response induced by misoprostol in formalin-injected mice. L-161982 (5 mg/kg; i.p.; once per day for 2 weeks) reduces arthritis lesions and lesion progression in CIA mice.

Chemical Information
Molecular Weight 654.72
Formula C32H29F3N4O4S2
CAS Number 147776-06-5
Solubility (25°C) DMSO 90 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Huang, et al. Nature. Tankyrase inhibition stabilizes axin and antagonizes wnt signalling.

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Keywords: L-161982, L161982 supplier, Prostaglandin Receptor, inhibitors, activators

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