Brimonidine

CAT:
804-HY-B0659-01
Size:
5 mg

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
Brimonidine - image 1

Brimonidine

  • Description :

    Brimonidine (UK 14304) is a full α2-adrenergic receptor (α2-AR) agonist.
  • CAS Number :

    [59803-98-4]
  • Product Name Alternative :

    UK 14304; AGN190342
  • UNSPSC :

    12352005
  • Hazard Statement :

    H301
  • Target :

    Adrenergic Receptor
  • Type :

    Reference compound
  • Related Pathways :

    GPCR/G Protein; Neuronal Signaling
  • Field of Research :

    Endocrinology; Cancer; Cardiovascular Disease
  • Assay Protocol :

    https://www.medchemexpress.com/uk-14,304.html
  • Purity :

    99.98
  • Solubility :

    DMSO : 50 mg/mL (ultrasonic)
  • Smiles :

    BrC1=C2N=CC=NC2=CC=C1NC3=NCCN3
  • Molecular Formula :

    C11H10BrN5
  • Molecular Weight :

    292.13
  • Precautions :

    H301
  • References & Citations :

    [1]Andorn, A.C., M.A. Carlson, and R.C. Gilkeson, Specific [3H]UK 14,304 binding in human cortex occurs at multiple high affinity states with alpha 2-adrenergic selectivity and differing affinities for GTP. Life Sci, 1988. 43 (22) : p. 1805-12.|[2]Cambridge, D., UK-14,304, a potent and selective alpha2-agonist for the characterisation of alpha-adrenoceptor subtypes. Eur J Pharmacol, 1981. 72 (4) : p. 413-5.|[3]Chopin, P., F.C. Colpaert, and M. Marien, Effects of alpha-2 adrenoceptor agonists and antagonists on circling behavior in rats with unilateral 6-hydroxydopamine lesions of the nigrostriatal pathway. J Pharmacol Exp Ther, 1999. 288 (2) : p. 798-804.
  • Shipping Conditions :

    Room Temperature
  • Storage Conditions :

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

    Reference compound1
  • Clinical Information :

    Launched
  • Isoform :

    α adrenergic receptor
  • Citation 01 :

    Anal Chem. 2025 Jun 3;97 (21) :11099-11109.|Nat Biomed Eng. 2025 Apr 30.|Cell Rep. 2019 Dec 3;29 (10) :2929-2935.e4|Int J Pharm. 2022 Feb 5:613:121361.|J Ocul Pharmacol Ther. 2023 Sep;39 (7) :456-462.|J Ocul Pharmacol Ther. 2025 Sep 18.

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