Timapiprant
CAS No. 851723-84-7
Timapiprant( OC000459 | OC-000459 | OC 000459 | Timapiprant )
Catalog No. M17616 CAS No. 851723-84-7
OC000459 is a potent and selective D prostanoid receptor 2 (DP2) antagonist (IC50: 13 nM).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 34 | In Stock |
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| 5MG | 55 | In Stock |
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| 10MG | 91 | In Stock |
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| 25MG | 151 | In Stock |
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| 50MG | 237 | In Stock |
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| 100MG | 356 | In Stock |
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| 200MG | 533 | In Stock |
|
| 500MG | 852 | In Stock |
|
| 1G | Get Quote | In Stock |
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Biological Information
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Product NameTimapiprant
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NoteResearch use only, not for human use.
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Brief DescriptionOC000459 is a potent and selective D prostanoid receptor 2 (DP2) antagonist (IC50: 13 nM).
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DescriptionTimapiprant, also known as OC000459, is a potent, selective and orally active CRTH2 antagonist. OC000459 reduces nasal and ocular symptoms in allergic subjects exposed to grass pollen, a randomised, placebo-controlled, double-blind trial. OC000459 inhibits mast cell-dependent activation of T helper 2 lymphocytes and eosinophils. OC000459 treatment inhibited LAR and post-allergen increase in sputum eosinophils. OC000459 appears to inhibit allergic inflammation in asthma.(In Vitro):Timapiprant (OC000459) (0.0001 μM-10 μM; 5 hours) inhibits chemotaxis (IC50=0.028 μM) of human Th2 lymphocytes and cytokine production (IC50=0.019 μM) by human Th2 lymphocytes.Timapiprant (OC000459) (1 μM) inhibits the activation of Th2 cells and eosinophils in response to supernatants from IgE/anti-IgE-activated human mast cells.Timapiprant (OC000459) (1 nM–1000 nM; 16 hours) inhibits the anti-apoptotic effect of PGD2 on Th2 cells with an IC50 of 0.035 uM.(In Vivo):Timapiprant (OC000459) (gavage; 2 mg/kg, 10 mg/kg) inhibits blood eosinophilia induced by 13,14-dihydro-15-keto-PGD2 (DK-PGD2) in Rat (ED50=0.04 mg/kg).Timapiprant (OC000459) (gavage; 0.01 mg/kg, 0.1 mg/kg, 1.0 mg/kg) inhibits airway eosinophilia in response to an aerosol of DK-PGD2 in guinea pigs (ED50=0.01 mg/kg).
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In VitroTimapiprant (OC000459) (0.0001 μM-10 μM; 5 hours) inhibits chemotaxis (IC50=0.028 μM) of human Th2 lymphocytes and cytokine production (IC50=0.019 μM) by human Th2 lymphocytes.Timapiprant (OC000459) (1 μM) inhibits the activation of Th2 cells and eosinophils in response to supernatants from IgE/anti-IgE-activated human mast cells.Timapiprant (OC000459) (1 nM–1000 nM; 16 hours) inhibits the anti-apoptotic effect of PGD2 on Th2 cells with an IC50 of 0.035 uM. Apoptosis Analysis Cell Line:Th2 Cells Concentration:0.0001 μM-10 μM Incubation Time:16 hours Result:Inhibited the antiapoptotic effect of PGD2.
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In VivoTimapiprant (OC000459) (gavage; 2 mg/kg, 10 mg/kg) inhibits blood eosinophilia induced by 13,14-dihydro-15-keto-PGD2 (DK-PGD2) in Rat (ED50=0.04 mg/kg).Timapiprant (OC000459) (gavage; 0.01 mg/kg, 0.1 mg/kg, 1.0 mg/kg) inhibits airway eosinophilia in response to an aerosol of DK-PGD2 in guinea pigs (ED50=0.01 mg/kg).
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SynonymsOC000459 | OC-000459 | OC 000459 | Timapiprant
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PathwayNeuroscience
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TargetNorepinephrine
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RecptorDP2
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Research AreaInflammation/Immunology
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Indication——
Chemical Information
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CAS Number851723-84-7
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Formula Weight348.37
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Molecular FormulaC21H17FN2O2
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Purity>98% (HPLC)
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SolubilityDMSO : 4 mg/mL 11.48 mM; H2O : < 0.1 mg/mL
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SMILESCc1c(Cc2nc3ccccc3cc2)c2c(ccc(F)c2)n1CC(=O)O
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Chemical Name2-(5-fluoro-2-methyl-3-(quinolin-2-ylmethyl)-1H-indol-1-yl)acetic acid
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Pettipher R, et al. J Pharmacol Exp Ther, 2012, 340(2), 473-482.
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