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Fevipiprant (Synonyms: NVP-QAW039, QAW039)

Katalog-Nr.GC19153 Copy One-Click Copy Product Info

Fevipiprant (QAW039, NVP-QAW039) ist ein oral aktiver, selektiver, reversibler Prostaglandin-D2-(DP2)-Rezeptorantagonist mit einem Kd-Wert von 1,14 nM.

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Fevipiprant Chemische Struktur

Cas No.: 872365-14-5

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1mg
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5mg
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10mg
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25mg
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50mg
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100mg
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Sample solution is provided at 25 µL, 10mM.



Description of Fevipiprant

Fevipiprant(QAW039) is a selective, potent, reversible competitive CRTh2 antagonist with an in vitro dissociation constant KD value of 1.1nM at the CRTh2 receptor and an IC50 value of 0.44 nM for inhibition of PGD2-induced eosinophil shape change in human whole blood.IC50:0.44 nM(PGD2-induced eosinophil shape change)Kd value:1.1nM(CRTh2 receptor)[1]In vitro: CRTh2-mediated shape change in eosinophils was used to profile QAW039 in whole blood and represents a physiologically relevant environment. The comparable IC50 values for QAW039 in the whole blood and isolated shape-change assays are consistent with its lower plasma-protein binding and its relatively slow dissociation kinetics that drive its increased potency .QAW039 is highly potent in whole-blood systems, with the IC50 value obtained consistent with the affinity values calculated from radioligand experiments. In a further disease-relevant cellular context, the potency of QAW039 in the isolated Th2 cell cytokine inhibition assay is consistent with its CRTh2 receptor affinity, and, as with eosinophil assay readouts, this represents an improved potency compared with QAV680[2].

References:
[1]. Erpenbeck, V. J. et al. Pharmacokinetics, Safety, and Tolerability of Fevipiprant (QAW039), a Novel CRTh2 Receptor Antagonist: Results From 2 Randomized, Phase 1, Placebo-Controlled Studies in Healthy Volunteers. Clinical pharmacology in drug development 5, 306-313, doi:10.1002/cpdd.244 (2016).
[2]. Sykes, D. A. et al.Fevipiprant (QAW039), a Slowly Dissociating CRTh2 Antagonist with the Potential for Improved Clinical Efficacy. Molecular pharmacology 89, 593-605, doi:10.1124/mol.115.101832 (2016).

Chemical Properties of Fevipiprant

Cas No. 872365-14-5 SDF
Überlieferungen NVP-QAW039, QAW039
Canonical SMILES O=C(O)CC1=C(C)N(CC2=CC=C(S(=O)(C)=O)C=C2C(F)(F)F)C3=NC=CC=C31
Formula C19H17F3N2O4S M.Wt 426.41
Löslichkeit DMSO : ≥ 32 mg/mL (75.05 mM) Storage Store at -20°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of Fevipiprant

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1 mg 5 mg 10 mg
1 mM 2.3452 mL 11.7258 mL 23.4516 mL
5 mM 469 μL 2.3452 mL 4.6903 mL
10 mM 234.5 μL 1.1726 mL 2.3452 mL
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Average Rating: 5 ★★★★★ (Based on Reviews and 28 reference(s) in Google Scholar.)

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