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JNJ 10191584 maleate

JNJ 10191584 maleate
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Purity:99.82%
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JNJ 10191584 maleate

Catalog No. T22879Cas No. 869497-75-6
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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Pack SizePriceAvailabilityQuantity
1 mg$49In Stock
2 mg$75In Stock
5 mg$109In Stock
10 mg$135In Stock
25 mg$298In Stock
50 mg$433In Stock
100 mgInquiryIn Stock
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Product Introduction

Bioactivity
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].
AliasJNJ 10191584 maleate salt, VUF6002 maleate
Chemical Properties
Molecular Weight394.81
FormulaC17H19ClN4O5
Cas No.869497-75-6
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 18 mg/mL (45.6 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.5329 mL12.6643 mL25.3286 mL126.6432 mL
5 mM0.5066 mL2.5329 mL5.0657 mL25.3286 mL
10 mM0.2533 mL1.2664 mL2.5329 mL12.6643 mL
20 mM0.1266 mL0.6332 mL1.2664 mL6.3322 mL

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Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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