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Mepiprazole

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Mepiprazole
Clinical data
Trade namesPsigodal
Other namesPAP; EMD-16923; H-4007
Routes of
administration
Oral
ATC code
  • none
Legal status
Legal status
  • In general: ℞ (Prescription only)
Identifiers
  • 1-(3-Chlorophenyl)-4-[2-(5-methyl-1H-pyrazol-3-yl)ethyl]piperazine
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC16H21ClN4
Molar mass304.82 g·mol−1
3D model (JSmol)
  • Cc3cc(CCN2CCN(c1cccc(Cl)c1)CC2)n[nH]3

Mepiprazole (INN,BAN) (brand namePsigodal) is ananxiolyticdrug of thephenylpiperazine group with additionalantidepressant properties[1] that is marketed inSpain.[2][3][4][5][6] It acts as a5-HT2A andα1-adrenergic receptorantagonist[7][8][9] andinhibits thereuptake and induces therelease ofserotonin,dopamine, andnorepinephrine to varying extents,[1][9] and has been described as aserotonin antagonist and reuptake inhibitor (SARI).[10]

Usages

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Controlled clinical trials of mepiprazole in patients withirritable bowel syndrome (IBS) were also carried out and suggested some benefits of the drug in relieving symptoms of IBS in some patients.[11] Similarly to other phenylpiperazines liketrazodone,nefazodone, andetoperidone, mepiprazole producesmCPP as anactive metabolite.[12]

See also

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References

[edit]
  1. ^abPlacheta P, Singer E, Kriwanek W, Hertting G (August 1976). "Mepiprazole, a new psychotropic drug: effects on uptake and retention of monoamines in rat brain synaptosomes".Psychopharmacology.48 (3):295–301.doi:10.1007/BF00496865.PMID 9660.S2CID 9194743.
  2. ^J. Elks (14 November 2014).The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 768–.ISBN 978-1-4757-2085-3.
  3. ^Swiss Pharmaceutical Society (2000).Index Nominum 2000: International Drug Directory (Book with CD-ROM). Boca Raton: Medpharm Scientific Publishers.ISBN 3-88763-075-0.
  4. ^Pöldinger W (1975). "Clinical trial of 3-methyl-5-(beta-N'-(N-m-chlorophenylpiperazino)ethyl)-pyrazole dihydrochloride (Mepiprazol) in the therapy of psychovegetative disorders".International Pharmacopsychiatry.10 (1):1–8.doi:10.1159/000468162.PMID 1095510.
  5. ^De Buck R, Van Durme R, Pelc I (May 1975). "[A controlled double-blind crossover study of the efficacy of mepiprazol (EMD 16.923) and of diazepam in the treatment of neurotic disorders]".Acta Psychiatrica Belgica (in French).75 (3):320–33.PMID 769484.
  6. ^Saldaña Hernández OH, Hernández González J (1976). "[Psychopharmological research with EMD 16-923 in patients with different degrees of anxiety]".Neurología, Neurocirugía, Psiquiatría (in Spanish).17 (1):29–33.PMID 1052713.
  7. ^Cohen ML, Fuller RW, Kurz KD (1983)."Evidence that blood pressure reduction by serotonin antagonists is related to alpha receptor blockade in spontaneously hypertensive rats".Hypertension.5 (5):676–81.doi:10.1161/01.hyp.5.5.676.PMID 6311738.
  8. ^Maj J, Sypniewska M (1980). "Central action of mepiprazole".Polish Journal of Pharmacology and Pharmacy.32 (4):475–84.PMID 7255266.
  9. ^abFuxe K, Agnati LF, Ungerstedt U (January 1976). "The effect of mepiprazole on central monoamine neurons. Evidence for increased 5-hydroxytryptamine and dopamine receptor activity".European Journal of Pharmacology.35 (1):93–108.doi:10.1016/0014-2999(76)90304-6.PMID 943291.
  10. ^Fagiolini A, Comandini A, Catena Dell'Osso M, Kasper S (December 2012)."Rediscovering trazodone for the treatment of major depressive disorder".CNS Drugs.26 (12):1033–1049.doi:10.1007/s40263-012-0010-5.PMC 3693429.PMID 23192413.
  11. ^Dotevall G, Groll E (October 1974)."Controlled clinical trial of mepiprazole in irritable bowel syndrome".The British Medical Journal.4 (5935):16–8.doi:10.1136/bmj.4.5935.16.PMC 1612118.PMID 4609545.
  12. ^Fong MH, Garattini S, Caccia S (October 1982). "1-m-Chlorophenylpiperazine is an active metabolite common to the psychotropic drugs trazodone, etoperidone and mepiprazole".The Journal of Pharmacy and Pharmacology.34 (10):674–5.doi:10.1111/j.2042-7158.1982.tb04701.x.PMID 6128394.S2CID 44968564.
5-HT1ARTooltip 5-HT1A receptoragonists
GABAARTooltip GABAA receptorPAMsTooltip positive allosteric modulators
Gabapentinoids
(α2δVDCCblockers)
Antidepressants
Sympatholytics
(Antiadrenergics)
Others
α1
Agonists
Antagonists
α2
Agonists
Antagonists
β
Agonists
Antagonists
5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
DRAsTooltip Dopamine releasing agents
NRAsTooltip Norepinephrine releasing agents
SRAsTooltip Serotonin releasing agents
Others
Phenylpiperazines
Benzylpiperazines
Naphthylpiperazines
Quinolinylpiperazines
Diphenylalkylpiperazines
Pyrimidinylpiperazines
Pyridinylpiperazines
Benzo(iso)thiazolylpiperazines
Tricyclic-linked piperazines
Others/uncategorized


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