
Carbamazepine
CAS No. 298-46-4
Carbamazepine( Carbamazepine, Tegretol, Epitol )
Catalog No. M13912 CAS No. 298-46-4
Carbamazepine, a?sodium channel?blocker, is an anticonvulsant drug.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
100MG | 33 | In Stock |
![]() ![]() |
200MG | 38 | In Stock |
![]() ![]() |
500MG | 45 | In Stock |
![]() ![]() |
1G | Get Quote | In Stock |
![]() ![]() |
Biological Information
-
Product NameCarbamazepine
-
NoteResearch use only, not for human use.
-
Brief DescriptionCarbamazepine, a?sodium channel?blocker, is an anticonvulsant drug.
-
DescriptionCarbamazepine, a?sodium channel?blocker, is an anticonvulsant drug.
-
In VitroWestern Blot Analysis Cell Line:3T3-L1 pre-adipocytes Concentration:0-500 μM Incubation Time:10 days Result:Decreased PPAR-γ and C/EPB-α protein levels.Increased ERK 1/2 phosphorylation after a 10?min exposure, and also increased p38 MAPK phosphorylation.
-
In VivoAnimal Model:70% Partial hepatectomy treated mice Dosage:250 mg/kg Administration:p.o.Result:Recoverd liver to body weight ratio.Increased the number of BrdU-positive nuclei, Increased PCNA protein.Increased mRNA levels of ccne2 and ccna2.
-
SynonymsCarbamazepine, Tegretol, Epitol
-
PathwayMembrane Transporter/Ion Channel
-
TargetSodium Channel
-
RecptorSodium Channel
-
Research AreaNeurological Disease
-
Indication——
Chemical Information
-
CAS Number298-46-4
-
Formula Weight236.27
-
Molecular FormulaC15H12N2O
-
Purity>98% (HPLC)
-
SolubilityEthanol: 18 mg/mL (76.18 mM); DMSO: 47 mg/mL (198.92 mM)
-
SMILESO=C(C1=CC2=CC=CC=C2NC3=CC=CC=C13)N
-
Chemical Namebenzo[b][1]benzazepine-11-carboxamide
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Willow M, et al. Mol Pharmacol, 1982, 22(3), 627-635.
molnova catalog



related products
-
Rilmakalim
Rilmakalim is a potassium channel opener. Rilmakalim shows antivasoconstrictor effect.
-
Huwentoxin IV
Selective NaV1.7 channel blocker. Preferentially inhibits neuronal NaV1.7, 1.2 and 1.3 (IC50 values are 26, 150 and 338 nM respectively), compared to muscle subtypes NaV1.4 and 1.5 (IC50 = >10 μM). Inhibits the channel by binding at the neurotoxin receptor site 4 in the S3-S4 linker of domain II, trapping the voltage sensor in the inward, closed configuration.
-
Tocainide
Tocainide is a blocker of the sodium channel and used for the treatment of tinnitus.