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15-deoxy-Δ12,14-Prostaglandin D2

15-deoxy-Δ12,14-Prostaglandin D2 (15-Deoxy-Δ12,14-PGD2), a metabolite of PGD2 (HY-101988), is an agonist of prostaglandin receptor 2 (DP2) . 15-deoxy-Δ12,14-Prostaglandin D2 binds to DP2 (Ki=50 nM) and induces eosinophil activation (EC50=8 nM) . 15-deoxy-Δ12,14-Prostaglandin D2 also stimulates the recruitment of steroid receptor coactivator-1 (SRC-1) to peroxisome proliferator-activated receptor γ (PPARγ), inducing PPARγ-mediated transcription. 15-deoxy-Δ12,14-Prostaglandin D2 (15-Deoxy-Δ12,14-PGD2) is cytotoxic to L1210 murine leukemia cells (IC50=0.3 μg/ml) and inhibits ADP-induced platelet aggregation (IC50=320 ng/mL) .

Product Specifications

CAS Number

[85235-11-6]

Product Name Alternative

15-Deoxy-Δ12,14-PGD2

UNSPSC

12352211

Hazard Statement

H225, H319, H336

Target

Endogenous Metabolite; PPAR; Prostaglandin Receptor; Src

Type

Reference compound

Related Pathways

Cell Cycle/DNA Damage; GPCR/G Protein; Metabolic Enzyme/Protease; Protein Tyrosine Kinase/RTK; Vitamin D Related/Nuclear Receptor

Applications

Neuroscience-Neuromodulation

Field of Research

Cardiovascular Disease

Assay Protocol

https://www.medchemexpress.com/15-deoxy-12-14-prostaglandin-d2.html

Concentration

2.99 mM * 1 mL in Methyl acetate

Purity

98.0

Smiles

O=C1/C([C@H]([C@H](C1)O)C/C=C\CCCC(O)=O)=C/C=C/CCCCC

Molecular Formula

C20H30O4

Molecular Weight

334.45

Precautions

H225, H319, H336

References & Citations

[1]Bundy, et al. Synthesis and platelet aggregation inhibiting activity of prostaglandin D analogues. J. Med. Chem. 26 (6), 790-799 (1983) .

Shipping Conditions

Blue Ice

Storage Conditions

Solution, -20°C, 2 years

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Curated Selection

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