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Levocetirizine Dihydrochloride

Catalog No. T22354   CAS 130018-87-0
Synonyms: Xyzal Dihydrochloride, (-)-Cetirizine Dihydrochloride

Levocetirizine Dihydrochloride (Xyzal Dihydrochloride) is a third-generation peripheral H1-receptor antagonist. Acting as an antihistaminic agent, it specifically targets the histamine H1-receptor. Levocetirizine Dihydrochloride is the R-enantiomer of Cetirizine, which gives it a higher affinity for the H1-receptor than the S-enantiomer. Due to this enhanced affinity, Levocetirizine Dihydrochloride is effective in treating allergic rhinitis and chronic idiopathic urticaria.

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Levocetirizine Dihydrochloride Chemical Structure
Levocetirizine Dihydrochloride, CAS 130018-87-0
Pack Size Availability Price/USD Quantity
10 mg In stock $ 43.00
25 mg In stock $ 78.00
50 mg In stock $ 133.00
100 mg In stock $ 198.00
200 mg In stock $ 297.00
500 mg In stock $ 513.00
1 g In stock $ 729.00
1 mL * 10 mM (in DMSO) In stock $ 48.00
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Purity: 99.75%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Levocetirizine Dihydrochloride (Xyzal Dihydrochloride) is a third-generation peripheral H1-receptor antagonist. Acting as an antihistaminic agent, it specifically targets the histamine H1-receptor. Levocetirizine Dihydrochloride is the R-enantiomer of Cetirizine, which gives it a higher affinity for the H1-receptor than the S-enantiomer. Due to this enhanced affinity, Levocetirizine Dihydrochloride is effective in treating allergic rhinitis and chronic idiopathic urticaria.
In vivo Levocetirizine (0.4 mg/kg; oral administration; male Sprague-Dawley rats) treatment shows that the Cmax, AUC0-t, AUC0-∞ and t1/2 are 0.34 μg/mL, 3.26 μg h/mL, 3.67 μg h/mL and 2.34 hours, respectively in Sprague-Dawley rats[1].
Synonyms Xyzal Dihydrochloride, (-)-Cetirizine Dihydrochloride
Molecular Weight 461.81
Formula C21H27Cl3N2O3
CAS No. 130018-87-0

Storage

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

Solubility Information

H2O: 90 mg/mL (194.9 mM), Sonication is recommended.

DMSO: 90 mg/mL (194.9 mM), Sonication is recommended.

TargetMolReferences and Literature

1. Lohar P, et al. Simultaneous bioanalysis and pharmacokinetic interaction study of acebrophylline, levocetirizine and pranlukast in Sprague-Dawley rats. Biomed Chromatogr. 2019 Dec;33(12):e4672.

Related compound libraries

This product is contained In the following compound libraries:
Anti-Cancer Clinical Compound Library Inhibitor Library Membrane Protein-targeted Compound Library Anti-Cancer Drug Library Anti-Cancer Approved Drug Library GPCR Compound Library Drug Repurposing Compound Library Bioactive Compounds Library Max FDA-Approved Drug Library Neuronal Signaling Compound Library

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Keywords

Levocetirizine Dihydrochloride 130018-87-0 GPCR/G Protein Immunology/Inflammation Neuroscience Histamine Receptor Cetirizine Dihydrochloride Cetirizine Levocetirizine Xyzal Dihydrochloride (-)-Cetirizine Dihydrochloride Xyzal inhibitor inhibit

 

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