Hydroxyzine (pamoate)
CAT:
804-HY-B0895-01
Size:
25 mg
For Laboratory Research Only. Not for Clinical or Personal Use.
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- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No


Hydroxyzine (pamoate)
UNSPSC Description:
Hydroxyzine pamoate is a histamine receptor H1 antagonist, one of the salt forms of Hydroxyzine, soluble in dimethyl formamide and chloroform but insoluble in water and alcohol[1].Target Antigen:
Histamine ReceptorType:
Reference compoundRelated Pathways:
GPCR/G Protein;Immunology/Inflammation;Neuronal SignalingApplications:
COVID-19-immunoregulationField of Research:
Inflammation/Immunology; EndocrinologyAssay Protocol:
https://www.medchemexpress.com/Hydroxyzine-pamoate.htmlPurity:
99.85Solubility:
DMSO : 250 mg/mL (ultrasonic)Smiles:
O=C(C1=C(O)C(CC2=C3C=CC=CC3=CC(C(O)=O)=C2O)=C4C=CC=CC4=C1)O.ClC5=CC=C(C(N6CCN(CCOCCO)CC6)C7=CC=CC=C7)C=C5Molecular Weight:
763.27References & Citations:
[1]C T King, et al. Teratogenic effect of buclizine and hydroxyzine in the rat and chlorcyclizine in the mouse. Am J Obstet Gynecol. 1966 May 1;95(1):109-11.|[2]Tadiboyina Sirisha, et al. Enantioselective UFLC Determination of Hydroxyzine Enantiomers and Application to a Pharmacokinetic Study in Rabbits. J Chromatogr Sci. 2016 Nov;54(10):1806-1812.|[3]Loyd V, et al. Hydroxyzine Pamoate 5 mg/mL Oral Suspension. US Pharm. 2014;39(5):57-58.|[4]Petra Bizikova, et al. Blackwell Publishing Ltd Hydroxyzine and cetirizine pharmacokinetics and pharmacodynamics after oral and intravenous administration of hydroxyzine to healthy dogs. Vet Dermatol. 1966 May 1;95(1):109-11.|[5]J L Barbet, et al. Duration of inhibition of immediate skin test reactivity by hydroxyzine hydrochloride in dogs. J Am Vet Med Assoc. 1989 Jun 1;194(11):1565-9.Shipping Conditions:
Room TemperatureStorage Conditions:
4°C (Powder, sealed storage, away from moisture)Clinical Information:
LaunchedCAS Number:
10246-75-0
