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MedChemExpressModel Filgotinib maleate - 1802998-75-9

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Filgotinib maleate (GLPG0634 maleate) is a selective, orally available JAK1 inhibitor with anti-inflammatory and antiviral activities. Filgotinib maleate can effectively inhibit the activities of JAK1, JAK2, JAK3 and TYK2 with IC50 values ​​of 10 nM, 28 nM, 810 nM and 116 nM, respectively. Filgotinib maleate also inhibits HIV-1 driven gene transcription and reduces proliferation of HIV-1 infected cells. Filgotinib maleate can be used in the study of rheumatoid arthritis and inflammatory bowel disease[1][2][3].
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Filgotinib maleate

MCE China:Filgotinib maleate

Brand:MedChemExpress (MCE)

Cat. No.HY-18300A

CAS:1802998-75-9

Synonyms:GLPG0634 maleate

Purity:99.88%

Storage:4°C, sealed storage, away from moisture *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

Shipping:Room temperature in continental US; may vary elsewhere.

Description:Filgotinib maleate (GLPG0634 maleate) is a selective, orally available JAK1 inhibitor with anti-inflammatory and antiviral activities. Filgotinib maleate can effectively inhibit the activities of JAK1, JAK2, JAK3 and TYK2 with IC50 values ​​of 10 nM, 28 nM, 810 nM and 116 nM, respectively. Filgotinib maleate also inhibits HIV-1 driven gene transcription and reduces proliferation of HIV-1 infected cells. Filgotinib maleate can be used in the study of rheumatoid arthritis and inflammatory bowel disease.

In Vitro:Filgotinib maleate (0.1, 1 and 10 μM) inhibits the differentiation of Th2 cells and Th1 cells in a dose-dependent manner[1].

In Vivo:Filgotinib maleate (0.1, 0.3, 1, 3, 10 and 30 mg/kg, i.g.; once daily for 15 days) produces dose-dependent bone damage protection and prevents the development of inflammation in a rat model of collagen-induced arthritis[1]. Pharmacokinetic analysis of GLPG0634 in mice[1] Route Dose (mg/kg) C0 or C0 (ng/mL) Tmax (h) T1/2 (h) Cl (L•h/kg) Vss (L/kg) F (%) i.v. 1 637 / 2.5 2.9 6 / p.o. 5 920 0.5 1.7 / / 100 Pharmacokinetic analysis of GLPG0634 in rats[1] Route Dose (mg/kg) C0 or C0 (ng/mL) Tmax (h) T1/2 (h) Cl (L•h/kg) Vss (L/kg) F (%) i.v. 1 1407 / 1.6 1.4 1.8 / p.o. 5 310 2.2 3.9 / / 45

IC50 & Target:JAK1 10 nM (IC50) JAK2 28 nM (IC50) JAK3 810 nM (IC50) Tyk2 116 nM (IC50)

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References:

[1]. Van Rompaey L, et, al. Preclinical characterization of GLPG0634, a selective inhibitor of JAK1, for the treatment of inflammatory diseases. J Immunol. 2013 Oct 1;191(7):3568-77.  [Content Brief]

[2]. Labetoulle R, et al. Filgotinib for the treatment of Crohn's disease. Expert Opin Investig Drugs. 2018 Mar;27(3):295-300.  [Content Brief]

[3]. Yeh, et al. "Filgotinib suppresses HIV-1–driven gene transcription by inhibiting HIV-1 splicing and T cell activation." The Journal of Clinical Investigation 130.9 (2020): 4969-4984.  [Content Brief]

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