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JNJ-41443532

Catalog No.GC70720

JNJ-41443532 (antagonista CCR2 5) es un inhibiselectivo de hCCR2 activo por vía oral con buena afinde Unión (IC50=37 nM) y potente antagonismo funcional (quimiotaxis IC50=30 nM).

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JNJ-41443532 Chemical Structure

Cas No.: 1228650-83-6

Tamaño Precio Disponibilidad Cantidad
1 mg
116,00 $
Disponible

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents
JNJ-41443532 (CCR2 antagonist 5) is a selective, orally active hCCR2 inhibitor with good binding affinity (IC50=37 nM) and potent functional antagonism (chemotaxis IC50=30 nM). JNJ-41443532 displays a Ki of 9.6 µM for mCCR2 binding. JNJ-41443532 can be used in the research of inflammatory disease.

JNJ-41443532 (compound 8d) dose-dependently inhibits the influx of leukocytes, monocytes/macrophages and T-lymphocytes into the peritoneal cavity with an ED50 of 3 mg/kg p.o. bid in a thioglycollate-induced peritonitis (TG) model[1].
JNJ-41443532 has good CV safety profile. It does not induce dose-dependent or notable effects on most cardiohemodynamic, functional respiratory and electrophysiological parameters up to 10 mg/kg (i.v.) with plasma level at 70 µM in an anesthetized dog[1].
JNJ-41443532 has amendable oral bioavailability in dogs and primates. Pharmacokinetic parameters (p.o.)[1]:

SpeciesDose
(mg/kg)
Cmax
(ng/mL)
AUClast
(h*ng/mL)
Oral bioavailability
(%)
dogs6.71617588770.2
non-human primates7.2740306125.4
mice107420419
rats1010041615.3

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Average Rating: 5 ★★★★★ (Based on Reviews and 30 reference(s) in Google Scholar.)

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