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Anticonvulsant evaluation of aminoalkanol derivatives of 2- and 4-methylxanthone.
- Source :
-
Bioorganic & medicinal chemistry [Bioorg Med Chem] 2013 Mar 01; Vol. 21 (5), pp. 1190-8. Date of Electronic Publication: 2013 Jan 09. - Publication Year :
- 2013
-
Abstract
- A series of 17 new aminoalkanol derivatives of 6-methoxy- or 7-chloro-2-methylxanthone as well as 6-methoxy-4-methylxanthone was synthesized and evaluated for anticonvulsant activity. All compounds were verified in mice after intraperitoneal (ip) administration in maximal electroshock (MES) and subcutaneous pentetrazole (scMet) induced seizures as well as neurotoxicity assessment. Eleven of the tested substances showed protection against electrically evoked seizures in the majority of the tested mice at the dose of 100 mg/kg. Additionally, one was effective at the dose of 30 mg/kg. Five substances were active at the dose of 300 mg/kg or at the dose of 100 mg/kg in the minority of the tested mice. The most promising compound revealed ED(50) value of 47.57 mg/kg in MES (mice, ip, 1h after administration) and at the same time its TD(50) was evaluated as above 400 mg/kg. Those values gave PI (calculated as TD(50)/ED(50)) of more than 8.41. Three other synthesized xanthone derivatives also proved to act as anticonvulsants and showed ED(50) values in MES test (mice, ip) ranged 80-110 mg/kg. Results were quite encouraging and suggested that in the group of xanthone derivatives new potential anticonvulsants might be found.<br /> (Copyright © 2013 Elsevier Ltd. All rights reserved.)
- Subjects :
- Animals
Anticonvulsants therapeutic use
Anticonvulsants toxicity
Calcium Channels chemistry
Calcium Channels metabolism
Electroshock
Injections, Intraperitoneal
Mice
Neurons drug effects
Pentylenetetrazole therapeutic use
Pentylenetetrazole toxicity
Seizures drug therapy
Seizures prevention & control
Structure-Activity Relationship
Xanthones therapeutic use
Xanthones toxicity
Anticonvulsants chemistry
Xanthones chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1464-3391
- Volume :
- 21
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 23375095
- Full Text :
- https://doi.org/10.1016/j.bmc.2012.12.051