[CAS NO. 851723-84-7]  OC000459

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PRODUCTS SPECIFICATIONS [851723-84-7]

Catalog
SLK-S2822
Brand
Selleck
CAS
851723-84-7

DESCRIPTION [851723-84-7]

Overview

MDLMFCD18633254
Molecular Weight348.37
Molecular FormulaC21H17FN2O2
SMILES-

For research use only.

Storage

3 years,-20°C,powder
1 years,-80°C,in solvent

Shipping

Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

1 mg5 mg10 mg
1 mM2.8705 mL14.3526 mL28.7051 mL
5 mM0.5741 mL2.8705 mL5.7410 mL
10 mM0.2871 mL1.4353 mL2.8705 mL
50 mM---

Description

OC000459 is a potent and selective antagonist with of 13 nM. Phase 2.

Targets

DP2 [1]
13 nM

In vitro

OC000459 inhibits the binding of [H]PGD2 to membranes from CHO cells transfected with human DP2 with K of 13 nM. OC000459 also displaces [H]PGD2 from membranes from human Th2 lymphocytes with K of 4 nM. OC000459 antagonizes PGD2-mediated calcium mobilization in a concentration-dependent manner with IC50 of 28 nM in intact CHO cells expressing DP2. OC000459 inhibits chemotaxis of human Th2 cells in response to PGD2 (10 nM) with IC50 of 28 nM. OC000459 (< 3 μM) antagonizes the effect of PGD2 competitively in both the isolated leukocyte preparation and heparinized human whole blood. OC000459 inhibits eosinophil shape change responses to DK-PGD2 with IC50 of 11 nM. OC000459 (1 μM) inhibits the activation of Th2 cells and eosinophils in response to mast cell supernatants.

In vivo

OC000459 administrated at doses of 2 mg/kg p.o. in the Sprague-Dawley rats shows plasma half-life of 2.9 hours, time that maximal plasma concentration is achieved of 1.3 hours, maximal plasma concentration achieved is 1.54 μg/mL. OC000459 orally administrated 0.5 hour before injection of DK-PGD2 leads to a dose-dependent reduction in blood eosinophilia with ED50 of 0.04 mg/kg in rats. OC000459 orally administrated 0.5 hour before injection of DK-PGD2 also leads to a dose-dependent inhibition eosinophil accumulation ED50 of 0.01 mg/kg in rats. OC000459 (200 mg twice daily for 28 days) administrated in patients with moderate persistent asthma shows improvement in quality of life as analysed for both the Full Analysis (FA) population and the Per Protocol (PP) population. In those patients, OC000459 improves the night-time symptom scores, reduces the geometric mean sputum eosinophil count and respiratory infections. OC000459 (200 mg twice daily) treatment inhibits the later asthmatic responses and the post allergen increase in sputum eosinophils in steroid naive asthmatic patients.