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JNJ-5207852

CAT: 0013-GTR19167632-01Size: 5 mgDry Ice: NoHazardous: No
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CAT#:0013-GTR19167632-01Size:5 mg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
JNJ-5207852 is a potent and selective non-imidazole histamine H3 receptor antagonist, demonstrating high affinity for both rat and human receptors. It is a valuable research tool for investigating H3 receptor function in neurological disorders, with utility in both in vitro binding assays and in vivo models of cognition and sleep-wake regulation.
CAS Number
398473-34-2
Product Name Alternative
H3 receptor, HistamineReceptor, Histamine Receptor, Inhibitor, JNJ5207852, JNJ-5207852, JNJ 5207852, inhibit, low, sleep, REM, toxicity
Field of Research
Immunology & Inflammation, Neuroscience, Pharmacology & Drug Discovery
Purity
97.19% (May vary between batches)
Solubility
DMSO:77.5 mg/mL (244.88 mM) ;10% DMSO+40% PEG300+5% Tween 80+45% Saline:2 mg/mL (6.32 mM)
Smiles
C (COC1=CC=C (CN2CCCCC2) C=C1) CN1CCCCC1
Molecular Formula
C20H32N2O
Molecular Weight
316.48
Storage Conditions
-20°C
Notes
For research use only.

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526662JNJ-5207852
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A21480-200JNJ-5207852 200mg
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A21480-50JNJ-5207852 50mg
A21480-25JNJ-5207852 25mg
A21480-10JNJ-5207852 10mg
A21480-5JNJ-5207852 5mg
A21480-100JNJ-5207852 100mg

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