Risperidone-d4
CAT:
804-HY-110232-01
Size:
500 µg
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


Risperidone-d4
UNSPSC Description:
Risperidone-d4 is the deuterium labeled Risperidone. Risperidone is a serotonin 5-HT2 receptor blocker, P-Glycoprotein inhibitor and potent dopamine D2 receptor antagonist, with Kis of 4.8, 5.9 nM for 5-HT2A and dopamine D2 receptor, respectively.Target Antigen:
5-HT Receptor; Dopamine Receptor; P-glycoproteinType:
Isotope-Labeled CompoundsRelated Pathways:
GPCR/G Protein;Membrane Transporter/Ion Channel;Neuronal SignalingField of Research:
Neurological DiseasePurity:
99.40Solubility:
DMSO : 10 mg/mL (ultrasonic;warming)Smiles:
FC1=CC=C(C(C2CCN(C([2H])([2H])C([2H])([2H])C3=C(C)N=C(CCCC4)N4C3=O)CC2)=NO5)C5=C1Molecular Weight:
414.51References & Citations:
[1]Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. |[2]Nyberg S, et al. 5-HT2 and D2 dopamine receptor occupancy in the living human brain. A PET study with risperidone. Psychopharmacology (Berl). 1993;110(3):265-72.;Zhu HJ, et al. Risperidone and paliperidone inhibit p-glycoprotein activity in vitro. Neuropsychopharmacology. 2007 Apr;32(4):757-64.;Chen ML, et al. Risperidone modulates the cytokine and chemokine release of dendritic cells and induces TNF-α-directed cell apoptosis in neutrophils. Int Immunopharmacol. 2012 Jan;12(1):197-204.;Bardgett ME, et al. Adult rats treated with risperidone during development are hyperactive. Exp Clin Psychopharmacol. 2013 Jun;21(3):259-67.Shipping Conditions:
Blue IceStorage Conditions:
-20°C, 3 years (Powder)Clinical Information:
No Development ReportedCAS Number:
1020719-76-9