JNJ 5207852 dihydrochloride
Tocris Bioscience, part of Bio-Techne | Catalog # 4020
High affinity H3 antagonist
Key Product Details
Description
High affinity H3 antagonist
Product Description
JNJ 5207852 dihydrochloride is a high affinity histamine H3 receptor neutral antagonist (pKi values are 8.9 and 9.2 in rat and human respectively). Brain penetrant and orally active. Has 3- and 100-fold higher affinity than thioperamide (Cat. No. 0644) for rat and human H3 receptors respectively. Suppresses slow-wave sleep; exhibits wake-promoting effects in rodent arousal models.Licensing Information
Sold with the permission of Ortho-McNeil-Janssen Pharmaceuticals, Inc.Product Specifications
Molecular Weight
389.40
Formula
C20H32N2O.2HCl
Storage
Desiccate at RT
Purity
≥98% (HPLC)
Chemical Name
1-[3-[4-(1-Piperidinylmethyl)phenoxy]propyl]piperidine hydrochloride
CAS Number
1782228-76-5
PubChem ID
90488903
InChI Key
RLLXSVVZCGBIJR-UHFFFAOYSA-N
SMILES
C1(CN2CCCCC2)=CC=C(OCCCN3CCCCC3)C=C1.Cl.Cl
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| water | 19.47 | 50 | |
| DMSO | 7.79 | 20 with gentle warming |
Preparing Stock Solutions
for JNJ 5207852 dihydrochloride
The following data is based on the product molecular weight 389.40
Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which all affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 0.5 mM | 5.14 mL | 25.68 mL | 51.36 mL |
| 2.5 mM | 1.03 mL | 5.14 mL | 10.27 mL |
| 5 mM | 0.51 mL | 2.57 mL | 5.14 mL |
| 25 mM | 0.10 mL | 0.51 mL | 1.03 mL |
Calculators
Molarity Calculator
Dilution Calculator
Reconstitution Calculator
Background References
References are publications that support the biological activity of the product.
- Jia Effects of histamine H3 antagonists and donep. on learning and mnemonic deficits induced by pentylenetetrazol kindling in weanling mice. Neuropharmacology 2005 PMID: 16310812
- Le Correlation between ex vivo receptor occupancy and wake-promoting activity of selective H3 receptor antagonists. J.Pharmacol.Exp.Ther. 2008 PMID: 18305012
- Barbier Acute wake-promoting actions of JNJ-5207852, a novel, diamine-based H3 antagonist. Br.J.Pharmacol. 2004 PMID: 15466448
Product Specific Notices for JNJ 5207852 dihydrochloride
For research use only
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