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JNJ 10191584 maleate

Catalog No. T22879   CAS 869497-75-6
Synonyms: JNJ 10191584 maleate salt, VUF6002 maleate

JNJ 10191584 maleate (VUF6002 maleate) is an orally active and selective antagonist of H4 receptor (Ki = 26 nM). JNJ 10191584 maleate inhibits chemotaxis of eosinophils and mast cells (IC50 = 530 nM and 138 nM).

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JNJ 10191584 maleate Chemical Structure
JNJ 10191584 maleate, CAS 869497-75-6
Pack Size Availability Price/USD Quantity
1 mg In stock $ 84.00
2 mg In stock $ 126.00
5 mg In stock $ 183.00
10 mg In stock $ 226.00
25 mg In stock $ 497.00
50 mg In stock $ 723.00
100 mg In stock $ 987.00
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Purity: 99.82%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description JNJ 10191584 maleate (VUF6002 maleate) is an orally active and selective antagonist of H4 receptor (Ki = 26 nM). JNJ 10191584 maleate inhibits chemotaxis of eosinophils and mast cells (IC50 = 530 nM and 138 nM).
In vitro JNJ 10191584 maleate shows 540-fold selectivity to H4 receptor(Ki = 14.1 μM)[2].
In vivo In spared nerve injury mice, JNJ 10191584 maleate (10 μg/μL; intra locus coeruleus administration) abolishes VUF-induced anti-allodynic effect and prevents the anti-allodynic effect of VUF 8430. JNJ 10191584 maleate (6 μg/mouse; intrathecal administration) prevents VUF 8430-induced anti-allodynic effect[2].
Synonyms JNJ 10191584 maleate salt, VUF6002 maleate
Molecular Weight 394.81
Formula C17H19ClN4O5
CAS No. 869497-75-6

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 18mg/mL (45.6mM)

TargetMolReferences and Literature

1. Sanna MD, et al. Histamine H4 receptor stimulation in the locus coeruleus attenuates neuropathic pain by promoting the coeruleospinal noradrenergic inhibitory pathway. Eur J Pharmacol. 2020 Feb 5;868:172859. 2. Venable JD, et al. Preparation and biological evaluation of indole, benzimidazole, and thienopyrrole piperazine carboxamides: potent human histamine h(4) antagonists. J Med Chem. 2005 Dec 29;48(26):8289-98.

Related compound libraries

This product is contained In the following compound libraries:
Inhibitor Library Membrane Protein-targeted Compound Library GPCR Compound Library Neuronal Signaling Compound Library Bioactive Compounds Library Max Bioactive Compound Library ReFRAME Related Library Neurotransmitter Receptor Compound Library

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Keywords

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