Ozanimod (RPC1063)

Ozanimod (RPC1063)

Catalog Number:
L002371395APE
Mfr. No.:
APE-B6038
Price:
$292
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      • Overview
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          Background

          Ozanimod (RPC1063) is a high orallybioavailable agonist of the sphingosine-1-phosphate receptor subtypes 1 (S1P1) and 5 (S1P5). S1P receptors belong to the family of G-protein-coupled receptor which contains five subtypes, denoting S1P1-5. S1P receptors are involved in coronary artery caliber,endothelial integrity, cardiac function, and lymphocyte recirculation [1].In vitro: Ozanimod(RPC1063) was a specific agonist for S1P1 and S1P5 receptors. The EC50values were 160 ± 60 pM and 410 ± 160 pM for S1P1 receptors in the inhibition of cAMP generation and[35S]-GTPγS binding. The 83% Emax value of ozanimod against S1P5 receptor was 11 ± 4.3 nM. RPC1063 dose-dependently decreased S1P1 receptor re-expression on the cell surface and resulted in near complete and sustained loss of cell surface receptor expression at concentrations above 10 nM in S1P1 receptor-HEK293T cells after 1 h incubation [1]. In vivo: The t1/2 of ozanimod was 4.7 h and 5.1 h in mice and rats after p.o. administration, respectively. About 81–82% decrease in circulating T lymphocyte was observed after dosing administration for 6 h, with a maximal blood concentration of 45 nM and 159 nM in rats and mice respectively. Oral gavage of ozanimod dose-dependently reduced the disease score of mice in both doses (0.2 or 0.6 mg/kg/day) [1]. Clinical trial: In the double-blind, placebo-controlled phase 2 trial in adult patients with moderate-to-severe ulcerative colitis, when treated with 1 mg ozanimod for 8 weeks, clinical response occurred in 57% of the patients while 0.5 mg ozanimod caused a 54% response. At week 32, the rate of clinical remission was 21% and 26% at the dose of 1 mg and 0.5 mg. The side effects were mainly anemia and headache [2].

          Scott F L, Clemons B, Brooks J, et al. Ozanimod (RPC1063) is a potent sphingosine‐1‐phosphate receptor‐1 (S1P1) and receptor‐5 (S1P5) agonist with autoimmune disease‐modifying activity[J]. British Journal of Pharmacology, 2016.
          Sandborn WJ, Feagan BG1, et al. Ozanimod Induction and Maintenance Treatment for Ulcerative Colitis. N Engl J Med. 2016, 374(18):1754-1762.

      • Properties
        • Categories
          agonist of the sphingosine-1-phosphate receptor subtypes 1 and 5
          Alternative Name
          (S)-5-(3-(1-((2-hydroxyethyl)amino)-2,3-dihydro-1H-inden-4-yl)-1,2,4-oxadiazol-5-yl)-2-isopropoxybenzonitrile
          CAS Number
          1306760-87-1
          Molecular Formula
          C23H24N4O3
          Molecular Weight
          404.46
          Appearance
          A solid
          Purity
          99.85%
          Solubility
          ≥40.4 mg/mL in DMSO; insoluble in H2O; ≥2.25 mg/mL in EtOH with ultrasonic
          Storage
          Store at -20°C
          SMILES
          CC(OC1=C(C#N)C=C(C2=NC(C3=CC=CC4=C3CC[[email protected]]4([H])NCCO)=NO2)C=C1)C

          * For Research Use Only

      • Reference
        • 1. Patrick Grailhe, Asma Boutarfa-Madec, et al. "A label‐free impedance assay in endothelial cells differentiates the activation and desensitization properties of clinical S1P1 agonists." FEBS Open Bio. 2020 Oct;10(10):2010-2020. PMID:32810927

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