IBMX

CAT:
804-HY-12318-01
Size:
10 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
IBMX - image 1

IBMX

  • Description :

    IBMX is a broad-spectrum phosphodiesterase (PDE) inhibitor, with IC50s of 6.5, 26.3 and 31.7 μM for PDE3, PDE4 and PDE5, respectively.
  • Product Name Alternative :

    3-Isobutyl-1-methylxanthine; Isobutylmethylxanthine
  • UNSPSC :

    12352005
  • Hazard Statement :

    H302, H315, H319, H335
  • Target :

    Phosphodiesterase (PDE)
  • Type :

    Reference compound
  • Related Pathways :

    Metabolic Enzyme/Protease
  • Applications :

    COVID-19-immunoregulation
  • Field of Research :

    Inflammation/Immunology
  • Assay Protocol :

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

    99.99
  • Solubility :

    DMSO : 125 mg/mL (ultrasonic) |Ethanol : ≥ 7.14 mg/mL
  • Smiles :

    O=C(N1C)N(CC(C)C)C2=C(N=CN2)C1=O
  • Molecular Formula :

    C10H14N4O2
  • Molecular Weight :

    222.25
  • Precautions :

    H302, H315, H319, H335
  • References & Citations :

    [1]Wu BN, et al. KMUP-1, a xanthine derivative, induces relaxation of guinea-pig isolated trachea: the role of the epithelium, cyclic nucleotides and K+ channels. Br J Pharmacol. 2004 Aug;142 (7) :1105-14|[2]Wei Y, et al. Angiotensin II type 2 receptor regulates ROMK-like K+ channel activity in the renal cortical collecting duct during high dietary K+ adaptation. Am J Physiol Renal Physiol. 2014 Oct 1;307 (7) :F833-43|[3]Hosseini A, et al. Differential metabolic effects of novel cilostamide analogs, methyl carbostiryl derivatives, on mouse and hyperglycemic rat. Iran J Basic Med Sci. 2012 Jul;15 (4) :916-25.|[4]Crosswhite P, et al. Inhibition of phosphodiesterase-1 attenuates cold-induced pulmonary hypertension. Hypertension. 2013 Mar;61 (3) :585-92.
  • 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 :

    PDE3; PDE4
  • CAS Number :

    [28822-58-4]

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