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Mianserin

Catalog No. DB06148 Name DrugBank
CAS Number 24219-97-4 Website http://www.ualberta.ca/
M. F. C18H20N2 Telephone (780) 492-3111
M. W. 264.3648 Fax (780) 492-1071
Purity Email david.wishart@ualberta.ca
Storage Chembase ID: 4416

SYNONYMS

IUPAC name
5-methyl-2,5-diazatetracyclo[13.4.0.0^{2,7}.0^{8,13}]nonadeca-1(15),8(13),9,11,16,18-hexaene
IUPAC Traditional name
5-methyl-2,5-diazatetracyclo[13.4.0.0^{2,7}.0^{8,13}]nonadeca-1(15),8(13),9,11,16,18-hexaene
Brand Name
Norval
Bolvidon
Tolvan
Synonyms
Mianserine [inn-french]
Mianserina [inn-spanish]
Mianserine
Mianseryna [polish]
Mianserinum [inn-latin]

DATABASE IDS

CAS Number 24219-97-4
PubChem CID 4184
PubChem SID 46508096

PROPERTIES

DETAILS

Description (English)
Item Information
Drug Groups approved
Description A tetracyclic compound with antidepressant effects. Mianserin was previously available internationally, however in most markets it has been phased out in favor of Mirtazapine.
Indication For the treatment of depression.
Pharmacology Mianserin is a tetracyclic antidepressant that has antihistaminic and hypnosedative, but almost no anticholinergic, effect. It is a weak inhibitor of norepinephrine reuptake and strongly stimulates the release of norepinephrine. Interactions with serotonin receptors in the central nervous system have also been found. Its effect is usually noticeable after one to three weeks. Mianserin may cause drowsiness and hematological problems.
Toxicity Oral rat LD50: 780mg/kg
Affected Organisms
Humans and other mammals
Biotransformation Hepatic.
Absorption Absorbed following oral administration.
Half Life 10-17 hours
Protein Binding 90%
References
Koyama E, Chiba K, Tani M, Ishizaki T: Identification of human cytochrome P450 isoforms involved in the stereoselective metabolism of mianserin enantiomers. J Pharmacol Exp Ther. 1996 Jul;278(1):21-30. [Pubmed]
de Boer TH, Nefkens F, van Helvoirt A, van Delft AM: Differences in modulation of noradrenergic and serotonergic transmission by the alpha-2 adrenoceptor antagonists, mirtazapine, mianserin and idazoxan. J Pharmacol Exp Ther. 1996 May;277(2):852-60. [Pubmed]
Kelder J, Funke C, De Boer T, Delbressine L, Leysen D, Nickolson V: A comparison of the physicochemical and biological properties of mirtazapine and mianserin. J Pharm Pharmacol. 1997 Apr;49(4):403-11. [Pubmed]
External Links
Wikipedia

REFERENCES

  • Koyama E, Chiba K, Tani M, Ishizaki T: Identification of human cytochrome P450 isoforms involved in the stereoselective metabolism of mianserin enantiomers. J Pharmacol Exp Ther. 1996 Jul;278(1):21-30. Pubmed
  • de Boer TH, Nefkens F, van Helvoirt A, van Delft AM: Differences in modulation of noradrenergic and serotonergic transmission by the alpha-2 adrenoceptor antagonists, mirtazapine, mianserin and idazoxan. J Pharmacol Exp Ther. 1996 May;277(2):852-60. Pubmed
  • Kelder J, Funke C, De Boer T, Delbressine L, Leysen D, Nickolson V: A comparison of the physicochemical and biological properties of mirtazapine and mianserin. J Pharm Pharmacol. 1997 Apr;49(4):403-11. Pubmed