Risperidone-d4
For Laboratory Research Only. Not for Clinical or Personal Use.
- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No


Risperidone-d4
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.Product Name Alternative :
R 64 766-d4UNSPSC :
12352005Hazard Statement :
H301Target :
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 Formula :
C23H23D4FN4O2Molecular Weight :
414.51Precautions :
H301References & 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)Scientific Category :
Isotope-Labeled CompoundsClinical Information :
No Development ReportedIsoform :
5-HT2 Receptor; D2 ReceptorCAS Number :
[1020719-76-9]

