Carbamazepine

CAT:
804-HY-B0246-01
Size:
100 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
Carbamazepine - image 1

Carbamazepine

  • Description :

    Carbamazepine is an orally active pressure-sensitive sodium ion channel blocker with an IC50 of 131 μM. Carbamazepine blocks voltage gated Na+, Ca2+, and K+ channels, and is also a HDAC inhibitor (IC50: 2 μM) . Carbamazepine is an anticonvulsant and can be used for research of epilepsy and neuropathic pain[1][2][3].
  • Product Name Alternative :

    CBZ; NSC 169864
  • UNSPSC :

    12352005
  • Hazard Statement :

    H302, H317, H336, H360
  • Target :

    Autophagy; Calcium Channel; HDAC; Mitophagy; Potassium Channel; Sodium Channel
  • Type :

    Reference compound
  • Related Pathways :

    Autophagy; Cell Cycle/DNA Damage; Epigenetics; Membrane Transporter/Ion Channel; Neuronal Signaling
  • Applications :

    Cancer-programmed cell death
  • Field of Research :

    Neurological Disease; Cancer
  • Assay Protocol :

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

    99.95
  • Solubility :

    DMSO : 50 mg/mL (ultrasonic) |H2O : < 0.1 mg/mL (ultrasonic)
  • Smiles :

    O=C(N1C2=CC=CC=C2C=CC3=CC=CC=C31)N
  • Molecular Formula :

    C15H12N2O
  • Molecular Weight :

    236.27
  • Precautions :

    H302, H317, H336, H360
  • References & Citations :

    [1]Willow, M. and W.A. Catterall, Inhibition of binding of [3H]batrachotoxinin A 20-alpha-benzoate to sodium channels by the anticonvulsant drugs diphenylhydantoin and carbamazepine. Mol Pharmacol, 1982. 22 (3) : p. 627-35.|[2]Okada, M., et al., Biphasic effects of carbamazepine on the dopaminergic system in rat striatum and hippocampus. Epilepsy Res, 1997. 28 (2) : p. 143-53.|[3]Beutler AS, et al. Carbamazepine is an inhibitor of histone deacetylases. Life Sci. 2005 May 13;76 (26) :3107-15.|[4]Turpin E, et al. Carbamazepine directly inhibits adipocyte differentiation through activation of the ERK 1/2 pathway. Br J Pharmacol. 2013 Jan;168 (1) :139-50.|[5]Wang CH, et al. Carbamazepine attenuates inducible nitric oxide synthase expression through Akt inhibition in activated microglial cells. Pharm Biol. 2014 Nov;52 (11) :1451-9. |[6]Kawaguchi T, et al. Carbamazepine promotes liver regeneration and survival in mice. J Hepatol. 2013 Dec;59 (6) :1239-45.|[7]Kara NZ, et al. Chronic oral carbamazepine treatment elicits mood-stabilising effects in mice. Acta Neuropsychiatr. 2014 Feb;26 (1) :29-34.
  • Shipping Conditions :

    Room Temperature
  • Storage Conditions :

    Store at room temperature 3 years
  • Scientific Category :

    Reference compound1
  • Clinical Information :

    Launched
  • CAS Number :

    [298-46-4]