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JNJ 10191584

Chemical Structure : JNJ 10191584

CAS No.: 73903-17-0

JNJ 10191584 (JNJ-10191584, VUF6002)

Catalog No.: PC-20926Not For Human Use, Lab Use Only.

JNJ 10191584 (VUF6002) is a potent, highly selective, orally active histamine H(4) receptor antagonist with binding Ki of 26 nM, 540-fold selectivity to H4 receptor over H3 receptor.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

JNJ 10191584 (VUF6002) is a potent, highly selective, orally active histamine H(4) receptor antagonist with binding Ki of 26 nM, 540-fold selectivity to H4 receptor over H3 receptor.
JNJ 10191584 (VUF6002) shows inhibitory effects to chemotaxis of eosinophils and mast cells with IC50 values of 530 nM and 138 nM, respectively.
JNJ 10191584 (10-100 mg/kg p.o., b.i.d.) caused a dose-dependent reduction in macroscopic damage, inhibition of the TNBS-provoked elevation of both colonic myeloperoxidase and tumour necrosis factor-alpha (TNF-alpha), and a reduction in the histologically assessed increase in mucosal and submucosal thickness and neutrophil infiltration.

Physicochemical Properties

M.Wt 278.74
Formula C13H15ClN4O
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

(5-chloro-1H-benzo[d]imidazol-2-yl)(4-methylpiperazin-1-yl)methanone

References

1. Varga C, et al. Eur J Pharmacol. 2005 Oct 17;522(1-3):130-8.

2. Venable JD, et al. J Med Chem. 2005 Dec 29;48(26):8289-98.

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