GLPBio

Carbamazepine

Catalog No.: GC17340Purity:>99.50%
Carbamazepine is an anticonvulsant and antiepileptic, which can decrease the release of high-frequency rhythmic action potentials.

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Carbamazepine
Cas No.: 298-46-4
10mM (in 1mL DMSO)In Stock
$23.00
1
100mgIn Stock
$21.00
1
500mgIn Stock
$31.00
1

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Description

Carbamazepine is an anticonvulsant and antiepileptic, which can decrease the release of high-frequency rhythmic action potentials [1]. Carbamazepine binds to the inactivated Na+ channel and slows the renewal of inactivation, thereby inhibiting the generation of action potentials and reducing synaptic transmission [2]. Carbamazepine has been broadly used to modify the activities of second messengers like cAMP and cGMP, and to modulate different neurotransmitter systems[3].

In vitro, Carbamazepine significantly inhibited Vero cell proliferation for 24 hours, with an IC50 value of 406.2μM[4]. Carbamazepine treatment (40μM) for 7 days significantly enhanced adipocyte differentiation in 3T3-L1 cells and promoted fat production [5]. Treatment with 100μM carbamazepine for 24 hours resulted in changes in the morphology of red blood cells, including shrinkage and deformation of the cell membrane[6].

In vivo, Carbamazepine treatment via oral administration at a dose of 7.5g/kg daily for three consecutive weeks reduced the immobility time of C57BL/6 mice in the forced swimming test (FST)[7]. A single oral dose of 250mg/kg of Carbamazepine significantly promoted liver regeneration in mice after partial hepatectomy within 14 days, and increased the survival rate of the mice[8].

References:
[1] Tolou-Ghamari Z, Zare M, Habibabadi J M, et al. A quick review of carbamazepine pharmacokinetics in epilepsy from 1953 to 2012[J]. Journal of research in medical sciences: the official journal of Isfahan University of Medical Sciences, 2013, 18(Suppl 1): S81.
[2] Gambeta E, Chichorro J G, Zamponi G W. Trigeminal neuralgia: An overview from pathophysiology to pharmacological treatments[J]. Molecular pain, 2020, 16: 1744806920901890.
[3] Matalon S, Schechtman S, Goldzweig G, et al. The teratogenic effect of carbamazepine: a meta-analysis of 1255 exposures[J]. Reproductive toxicology, 2002, 16(1): 9-17.
[4] Martín J M P, Freire P F, Labrador V, et al. Carbamazepine induces mitotic arrest in mammalian Vero cells[J]. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 2008, 637(1-2): 124-133.
[5] Im D U, Kim S C, Chau G C, et al. Carbamazepine enhances adipogenesis by inhibiting Wnt/β-catenin expression[J]. Cells, 2019, 8(11): 1460.
[6] Ficarra S, Misiti F, Russo A, et al. Antiepileptic carbamazepine drug treatment induces alteration of membrane in red blood cells: possible positive effects on metabolism and oxidative stress[J]. Biochimie, 2013, 95(4): 833-841.
[7] Kara N Z, Karpel O, Toker L, et al. Chronic oral carbamazepine treatment elicits mood-stabilising effects in mice[J]. Acta Neuropsychiatrica, 2014, 26(1): 29-34.
[8] Kawaguchi T, Kodama T, Hikita H, et al. Carbamazepine promotes liver regeneration and survival in mice[J]. Journal of Hepatology, 2013, 59(6): 1239-1245.

Protocol

Cell experiment [1]:

Cell lines

3T3-L1 cells

Preparation Method

3T3-L1 cells were grown in DMEM medium with 10% (v/v) fetal bovine serum (FBS), at 37°C in 5% CO2/atmosphere. Cells were seeded at a density of 1×105 cells/ml in the 6-well plates and allowed to adhere in a 5% CO2 incubator at 37°C for 2 days. The cells were treated with different concentrations of Carbamazepine (0, 5, 10, 20, 30, and 40μM) for 7 days. The lipid accumulation in cells was evaluated.

Reaction Conditions

0, 5, 10, 20, 30, and 40μM; 7 days

Applications

Carbamazepine treatment significantly enhanced lipid accumulation within 3T3-L1 cells in a dose-dependent manner.
Animal experiment [2]:

Animal models

C57BL6/J mice

Preparation Method

C57BL6/J mice (6-week-old) were housed singly in a standard environment with food and water ad libitum. The mice were anesthetized with inhaled isoflurane and subjected to sham operation or 70% partial hepatectomy (PHx). The mice were orally administered 250mg/kg of Carbamazepine or an equivalent volume of DMSO 2h before PHx surgery. Collect mouse liver tissues for analysis after 14 days.

Dosage form

250mg/kg for once; p.o.

Applications

Carbamazepine treatment significantly promoted liver regeneration in mice after PHx.

References:
[1] Im D U, Kim S C, Chau G C, et al. Carbamazepine enhances adipogenesis by inhibiting Wnt/β-catenin expression[J]. Cells, 2019, 8(11): 1460.
[2] Kawaguchi T, Kodama T, Hikita H, et al. Carbamazepine promotes liver regeneration and survival in mice[J]. Journal of Hepatology, 2013, 59(6): 1239-1245.

Product Documents

Purity:>99.50%Appearance:A solid

Chemical Properties

CAS No.
298-46-4
Chemical Name
benzo[b][1]benzazepine-11-carboxamide
SMILES
C1=CC=C2C(=C1)C=CC3=CC=CC=C3N2C(=O)N
Molecular Formula
C15H12N2O
Molecular Weight
236.27
Solubility
≥ 10.85mg/mL in DMSO
Storage
Store at -20°C
General tips
Select a suitable solvent according to the product solubility data. Once prepared, aliquot the stock solution to avoid repeated freeze-thaw cycles.
Use stock solutions within 6 months when stored at -80°C or within 1 month when stored at -20°C.
To improve solubility, warm the tube to 37°C and sonicate it for an appropriate period.
Shipping Condition
Evaluation samples are shipped with blue ice. Other available sizes are shipped at room temperature or with blue ice upon request.

CalculatorsMolarity / Dilution / Molecular Weight / Unit Conversion / In Vivo Formulation / Solubility

g/mol

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