Org-12962

CAT:
804-HY-118152-01
Size:
5 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Org-12962 - image 1

Org-12962

  • Description :

    Org-12962 is a potent, selective and orally active 5-HT2C receptor agonist with a pEC50 value of 7.01. Org-12962 also exhibits high effacy for the 5-HT2A and 5-HT2B receptor with pEC50s of 6.38 and 6.28, respectively[1][3].Org-12962 displays antiaversive effects in a rat model of panic-like anxiety[2].
  • CAS Number :

    [132834-56-1]
  • Product Name Alternative :

    SR-202
  • UNSPSC :

    12352005
  • Hazard Statement :

    H301, H311, H331
  • Target :

    5-HT Receptor
  • Type :

    Reference compound
  • Related Pathways :

    GPCR/G Protein; Neuronal Signaling
  • Applications :

    Neuroscience-Neuromodulation
  • Field of Research :

    Neurological Disease
  • Assay Protocol :

    https://www.medchemexpress.com/org-12962.html
  • Purity :

    99.93
  • Solubility :

    DMSO : 250 mg/mL (ultrasonic)
  • Smiles :

    FC(F)(F)C1=C(N=C(C=C1)N2CCNCC2)Cl
  • Molecular Formula :

    C10H11ClF3N3
  • Molecular Weight :

    265.66
  • Precautions :

    H301, H311, H331
  • References & Citations :

    [1]Porter RH, et al. Functional characterization of agonists at recombinant human 5-HT2A, 5-HT2B and 5-HT2C receptors in CHO-K1 cells.Br J Pharmacol. 1999 Sep;128 (1) :13-20.|[2]Jenck F, et al. Antiaversive effects of 5HT2C receptor agonists and fluoxetine in a model of panic-like anxiety in rats.Eur Neuropsychopharmacol. 1998 Aug;8 (3) :161-8.|[3]Faassen F, et al. Caco-2 permeability, P-glycoprotein transport ratios and brain penetration of heterocyclic drugs.Int J Pharm. 2003 Sep 16;263 (1-2) :113-22.
  • Shipping Conditions :

    Room Temperature
  • Storage Conditions :

    -20°C, 3 years; 4°C, 2 years (Powder)
  • Scientific Category :

    Reference compound1
  • Clinical Information :

    No Development Reported
  • Isoform :

    5-HT2 Receptor; α-1 microglobulin

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