Rotigotine

CAT:
804-HY-75502-01
Size:
5 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Rotigotine - image 1

Rotigotine

  • Description :

    Rotigotine is a potent dopamine receptor agonist with Ki values of 0.71 nM, 4-15 nM, and 83 nM for the dopamine D3 receptor and D2, D5, D4 receptors and dopamine D1 receptor. Rotigotine a partial agonist of the 5-HT1A receptor, and an antagonist of the α2B-adrenergic receptor. Rotigotine can be used for parkinson's disease (PD) research[1][2][3][4].
  • Product Name Alternative :

    N-0923; (-) -N 0437
  • UNSPSC :

    12352005
  • Hazard Statement :

    H302, H315, H319
  • Target :

    5-HT Receptor; Adrenergic Receptor; Dopamine Receptor
  • Type :

    Reference compound
  • Related Pathways :

    GPCR/G Protein; Neuronal Signaling
  • Applications :

    Neuroscience-Neuromodulation
  • Field of Research :

    Neurological Disease; Endocrinology
  • Assay Protocol :

    https://www.medchemexpress.com/rotigotine.html
  • Purity :

    99.99
  • Solubility :

    DMSO : ≥ 50 mg/mL
  • Smiles :

    CCCN(CCC1=CC=CS1)[C@H]2CCC3=C(C=CC=C3O)C2
  • Molecular Formula :

    C19H25NOS
  • Molecular Weight :

    315.47
  • Precautions :

    H302, H315, H319
  • References & Citations :

    [1]Wood M, et, al. Rotigotine is a potent agonist at dopamine D1 receptors as well as at dopamine D2 and D3 receptors. Br J Pharmacol. 2015 Feb;172 (4) :1124-35.|[2]Radad K, et, al. Neuroprotective effect of rotigotine against complex I inhibitors, MPP⁺ and rotenone, in primary mesencephalic cell culture. Folia Neuropathol. 2014;52 (2) :179-86. |[3]Bertaina-Anglade V, et, al. Antidepressant properties of rotigotine in experimental models of depression. Eur J Pharmacol. 2006 Oct 24;548 (1-3) :106-14.|[4]Scheller D, et, al. The in vitro receptor profile of rotigotine: a new agent for the treatment of Parkinson's disease. Naunyn Schmiedebergs Arch Pharmacol. 2009 Jan;379 (1) :73-86.
  • Shipping Conditions :

    Room Temperature
  • Storage Conditions :

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

    Reference compound1
  • Clinical Information :

    Launched
  • Isoform :

    5-HT1 Receptor; D1 Receptor; D2 Receptor; D3 Receptor; D4 Receptor; D5 Receptor; mLAG-3; MUC3
  • Citation 01 :

    BioRxiv. 2025 Aug 12:2025.08.08.668522.|Clin Chem. 2019 Dec;65 (12) :1522-1531. |Acta Pharmacol Sin. 2025 May 6.
  • CAS Number :

    [99755-59-6]

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