OC000459

"目录号: HY-15342

GPCR/G Protein-

OC000459是D型前列腺素受体2(DP2)拮抗剂,IC50为13 nM。

Prostaglandin Receptor

相关产品

Prostaglandin E1-Grapiprant-NS-304-TG6-10-1-Terutroban-Latanoprost-PF-04418948-Dinoprost tromethamine salt-Iloprost-ONO-AE3-208-Bimatoprost-Laropiprant-Setipiprant-AH 6809-CJ-42794-

生物活性

Description

OC000459 is a potent and selective D prostanoid receptor 2 (DP2) antagonist with IC50 of 13 nM.IC50 Value: 13 nM( Ki for hrCRTH2); 3 nM( Ki for Rat rCRTH2);13 nM(Ki for human native CRTH2)Target: D prostanoid receptor 2CRTH2 (chemoattractant receptor expressed on T-helper (Th) type 2 cells) is a G-protein-coupled receptor expressed by Th2 lymphocytes and eosinophils that mediates prostaglandin (PG)D(2)-driven chemotaxis[1]. CRTH2 mediates activation of Th2 cells, eosinophils and basophils in response to prostaglandin D(2). The CRTH2 antagonist OC000459 has been demonstrated to reduce airway inflammation and improve lung function in moderate persistent asthma[2].in vitro: OC000459 is an indole-acetic acid derivative that potently displaces [3H]PGD2from human recombinant DP2 (Ki = 0.013 μM), rat recombinant DP2 (Ki = 0.003 μM), and human native DP2 (Th2 cell membranes; Ki = 0.004 μM) but does not interfere with the ligand binding properties or functional activities of other prostanoid receptors (prostaglandin E1-4 receptors, D prostanoid receptor 1, thromboxane receptor, prostacyclin receptor, and prostaglandin F receptor). OC000459 inhibited chemotaxis (IC50 = 0.028 μM) of human Th2 lymphocytes and cytokine production (IC50 = 0.019 μM) by human Th2 lymphocytes. OC000459 competitively antagonized eosinophil shape change responses induced by PGD2 in both isolated human leukocytes (pKB = 7.9) and human whole blood (pKB = 7.5) but did not inhibit responses to eotaxin, 5-oxo-eicosatetraenoic acid, or complement component C5a. OC000459 also inhibited the activation of Th2 cells and eosinophils in response to supernatants from IgE/anti-IgE-activated human mast cells. OC000459 had no significant inhibitory activity on a battery of 69 receptors and 19 enzymes including cyclooxygenase 1 (COX1) and COX2[3] .in vivo: OC000459 was found to be orally bioavailable in rats and effective in inhibiting blood eosinophilia induced by 13,14-dihydro-15-keto-PGD2 (DK-PGD2) in this species (ED50 = 0.04 mg/kg p.o.) and airway eosinophilia in response to an aerosol of DK-PGD2 in guinea pigs (ED50 = 0.01 mg/kg p.o.) [3].Clinical trial: N/A.

Clinical Trial

NCT01056575

Oxagen Ltd

Healthy Volunteers

February 2010

Phase 1

NCT01056783

Oxagen Ltd

Eosinophilic Esophagitis

August 2010

Phase 2

NCT02560610

Atopix Therapeutics, Ltd.

Severe Eosinophilic Asthma

September 2016

Phase 2

NCT01448902

Oxagen Ltd

Allergic Rhinitis

March 2007

Phase 2

NCT02341521

Atopix Therapeutics, Ltd.-Simbec Research

Asthma

March 2015

Phase 1

NCT02002208

Atopix Therapeutics, Ltd.

Atopic Dermatitis

October 2013

Phase 2

NCT01057927

Oxagen Ltd

Asthma

January 2007

Phase 2

NCT01056692

Oxagen Ltd-Medicines Evaluation Unit, Manchester, UK-King's College Hospital NHS Trust

Bronchial Asthma

February 2006

Phase 2

NCT00890877

Oxagen Ltd

Mild to Moderate Persistent Asthma

April 2009

Phase 2

NCT00697281

Oxagen Ltd

Allergic Rhinitis

May 2008

Phase 2

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References

[1].Singh D, Cadden P, Hunter M, Inhibition of the asthmatic allergen challenge response by the CRTH2 antagonist OC000459. Eur Respir J. 2013 Jan;41(1):46-52.

[2].Horak F, Zieglmayer P, Zieglmayer R, The CRTH2 antagonist OC000459 reduces nasal and ocular symptoms in allergic subjects exposed to grass pollen, a randomised, placebo-controlled, double-blind trial. Allergy. 2012 Dec;67(12):1572-9.

[3].Pettipher R, Vinall SL, Xue L, Pharmacologic profile of OC000459, a potent, selective, and orally active D prostanoid receptor 2 antagonist that inhibits mast cell-dependent activation of T helper 2 lymphocytes and eosinophils. J Pharmacol Exp Ther. 2012

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