29331-92-8
29331-92-8 structure
- Name: Licarbazepine
- Chemical Name: Licarbazepine
- CAS Number: 29331-92-8
- Molecular Formula: C15H14N2O2
- Molecular Weight: 254.28400
- Catalog: analytical chemistry Analytical reagent Ion chromatography reagent
- Create Date: 2018-12-21 09:52:36
- Modify Date: 2026-07-04 20:25:18
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Licarbazepine (BIA 2-005; GP 47779) is a voltage-gated sodium channel blocker with anticonvulsant and mood-stabilizing effects[1].
| Name | Licarbazepine |
|---|---|
| Synonyms |
5-hydroxy-5,6-dihydrobenzo[b]benzazine-11-cboxamide
10-Hydroxy-10,11-dihydrocbamazine 1.0 mg/ml in Acetonitrile GP 47779-d3 10,11-Dihydro-10-hydroxy-5H-dibenz(Z)[b,f]azin-5-cboxamide 10,11-Dihydro-10-hydroxy-5H-dibenz[b,f]azine-5-cboxamide Licarbazepine,10,11-Dihydro-10-hydroxy-5H-dibenz(Z)[b,f]azepin-5-carboxamide 10-hydroxy-10,11-dihydro-5H-dibenzo[b,f]azine-5-cboxaMide 10-Hydroxy-10,11-dihydrocbamezine-d3 Licbazine 10,11-hydroxy-10,11 Dihydrocbamezer 10,11-Dihydro-10-hydroxy-5H-dibenz[b,f]azepine-5-carboxamide,Licarbazepine icbazine 10,11-Dihydro-10-hydroxycbamazine in methanol 10-Hydroxy-10,11-dihydrocbamazi 10,11-Dihydro-10-hydroxycbamazine 100 μg/mL in Acetonitrile (±)-10-Hydroxy-10,11-dihydro-5H-dibenz[b,f]azine-5-cbox Dihydrohydroxy cbamazine-D4 10,11-Dihydro-10-hydroxy-Cbamazin 10,11-Dihydro-10-Hydroxycbamazine solution 1H-Benzimidazole,2-(6-methoxyethyl) Oxcbazine Hydroxy Impurity LICBAZINE SEE 10,11-Dihydro-10-hydroxycarbamazepine Licbazine (10,11-Dihydro-10-hydroxycbamazine), Active oxcbazine metabolite (±)-10-Hydroxy-10,11-dihydro-5H-dibenz[b,f]azine-5-cboxaMide BIA -d3 10,11-dihydro-10-Hydroxy CbamazineQ: What is 10,11-dihydro-10-Hydroxy Cbamazine Q: What is the CAS Number of 10,11-dihydro-10-Hydroxy Cbamazine Q: What is the storage condition of 10,11-dihydro-10-Hydroxy Cbamazine Q: What e the applications of 10,11-dihydro-10-Hydroxy Cbamazine 5H-Dibenz[b,f]azine-5-cboxaMide,10,11-dihydro-10-hydroxy 5-Cbamoyl-10,11-dihydro-5H-dibenzo[b,f]azine-10-ol 10,11-Dihydro-10-hydroxy cbamazine D7 10,11-Dihydro-10-hydroxy 10,11-Dihydro-10-hydroxy Carbamazepine 10-Hydroxy-10,11-dihydrocbamezine Hydroxycbamazine (±) -10,11-Dihydro-10-hydroxy-5H-dibenzo[b,f]azine-5-cboxamide 6-hydroxy-5,6-dihydrobenzo[b]benzazine-11-cboxamide 10,11-Dihydro-10-hydroxy-5H-dibenz[b,f]azine-5-cboxamide-d3 Licbazine Racemate 10,11-Dihydro-10-hydroxycbazine-d3 |
| Description | Licarbazepine (BIA 2-005; GP 47779) is a voltage-gated sodium channel blocker with anticonvulsant and mood-stabilizing effects[1]. |
|---|---|
| Related Catalog | |
| Target |
Sodium Channel[1] |
| In Vivo | Eslicarbazepine acetate (ESL) is an oral pro-drug that is rapidly and extensively metabolized by the liver via a hydrolytic first-pass metabolism into S-Licarbazepine, the biologically active drug. The plasma level of the prodrug remains below quantification[1]. ESL is a potent antiepileptic agent with a spectrum of action essentially limited to partial-onset and generalized tonic-clonic seizures. Its main mechanism of action is by blocking the voltage-gated sodium channel. ESL works by blocking the voltage-gated sodium channel, which play an essential role in the generation and propagation of the epileptic discharge. ESL is well absorbed after oral administration with a bio-availability about 16% higher than that observed after an equivalent dose of Oxcarbazepine (OXC)[1]. |
| References |
| Density | 1.336g/cm3 |
|---|---|
| Boiling Point | 431.3ºC at 760mmHg |
| Melting Point | 186-189ºC |
| Molecular Formula | C15H14N2O2 |
| Molecular Weight | 254.28400 |
| Flash Point | 214.6ºC |
| Exact Mass | 254.10600 |
| PSA | 66.56000 |
| LogP | 3.25820 |
| Vapour Pressure | 3.33E-08mmHg at 25°C |
| Index of Refraction | 1.677 |
| Storage condition | Store at RT |
| Symbol |
GHS02, GHS07 |
|---|---|
| Signal Word | Danger |
| Hazard Statements | H225-H302 + H332-H319 |
| Precautionary Statements | P210-P305 + P351 + P338 |
| Hazard Codes | N,Xn,F |
| Risk Phrases | 51/53-36-20/21/22-11 |
| Safety Phrases | 61-36/37-26-16 |
| RIDADR | UN 3077 9 / PGIII |
| HS Code | 2933990090 |
|
~90%
29331-92-8 |
| Literature: KANDULA, Mahesh Patent: WO2013/167985 A1, 2013 ; Location in patent: Paragraph 00102; 00103 ; |
|
~91%
29331-92-8 |
| Literature: Portela and Ca., S.A. Patent: EP1477480 A1, 2004 ; Location in patent: Page 6, 7 ; |
|
~91%
29331-92-8 |
| Literature: RANBAXY LABORATORIES LIMITED; HIRPARA, Ketan; KHANDURI, Chandra, Has; SHARMA, Mukesh, Kumar Patent: WO2013/8194 A2, 2013 ; Location in patent: Page/Page column 12; 13 ; |
|
~68%
29331-92-8 |
| Literature: Panunzio, Mauro; Campana, Eileen; Breviglieri, Gabriele Patent: US2008/221320 A1, 2008 ; Location in patent: Page/Page column 2 ; |
|
~%
29331-92-8 |
| Literature: Tian, Maoqun; Abdelrahman, Aliaa; Weinhausen, Stephanie; Hinz, Sonja; Weyer, Stefanie; Dosa, Stefan; El-Tayeb, Ali; Mueller, Christa E. Bioorganic and Medicinal Chemistry, 2014 , vol. 22, # 3 p. 1077 - 1088 |
|
~%
29331-92-8 |
| Literature: Kittelman, Matthias; Lattmann, Rene; Ghisalba, Preste Bioscience, Biotechnology, and Biochemistry, 1993 , vol. 57, # 9 p. 1589 - 1590 |
| Precursor 6 | |
|---|---|
| DownStream 3 | |
| HS Code | 2933990090 |
|---|---|
| Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |