Terazosin

CAT:
804-HY-B0371-01
Size:
10 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
Terazosin - image 1

Terazosin

  • Description :

    Terazosin is a quinazoline derivative and a competitive and orally active α1-adrenoceptor antagonist. Terazosin works by relaxing blood vessels and the opening of the bladder. Terazosin has the potential for benign prostatic hyperplasia (BPH) and high blood pressure treatment[1][2][3].
  • CAS Number :

    [63590-64-7]
  • UNSPSC :

    12352005
  • Hazard Statement :

    H302-H315-H319-H335
  • Target :

    Adrenergic Receptor
  • Type :

    Reference compound
  • Related Pathways :

    GPCR/G Protein; Neuronal Signaling
  • Applications :

    Metabolism-protein/nucleotide metabolism
  • Field of Research :

    Metabolic Disease; Endocrinology; Cardiovascular Disease
  • Assay Protocol :

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

    98.5000
  • Solubility :

    DMSO : 50 mg/mL (ultrasonic; warming; heat to 60°C)
  • Smiles :

    O=C(N1CCN(C2=NC(N)=C3C=C(OC)C(OC)=CC3=N2)CC1)C4OCCC4
  • Molecular Formula :

    C19H25N5O4
  • Molecular Weight :

    387.43
  • Precautions :

    P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362-P403+P233-P405-P501
  • References & Citations :

    [1]Michel MC, et al. Drugs for treatment of benign prostatic hyperplasia: affinity comparison at cloned alpha 1-adrenoceptor subtypes and in human prostate. J Auton Pharmacol. 1996 Feb;16 (1) :21-8.|[2]Vincent J, et al. Pharmacological tolerance to alpha 1-adrenergic receptor antagonism mediated by terazosin in humans. J Clin Invest. 1992 Nov;90 (5) :1763-8.|[3]Ju M, et al. Efficacy of combination terazosin and nifedipine therapy in postoperative treatment of distal ureteral stones after transurethral ureteroscopic lithotripsy. J Int Med Res. 2020 Apr;48 (4) :300060520904851.
  • 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 :

    Authorea. March 31, 2022.|Eur J Med Chem. 2024 Mar 5:267:116209.|Neurochem Int. 2021 Feb:143:104942.|Research Square Preprint. 2022 Jul.|Cell Prolif. 2025 Mar;58 (3) :e13764.|Cell Rep Methods. 2023 Oct 23;3 (10) :100599.|Res Sq. 2025 Mar 16.

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