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Setiptiline

From Wikipedia, the free encyclopedia
Antidepressant drug

Pharmaceutical compound
Setiptiline
Clinical data
Trade namesTecipul
Other namesTeciptiline; delta(13b,4a),4a-Carba-mianserin; MO-8282; ORG-8282
AHFS/Drugs.comInternational Drug Names
Routes of
administration
Oral
ATC code
  • none
Legal status
Legal status
  • In general: ℞ (Prescription only)
Identifiers
  • 2-methyl-2,3,4,9-tetrahydro-1H-dibenzo[3,4:6,7]cyclohepta[1,2-c]pyridine
CAS Number
PubChemCID
DrugBank
ChemSpider
UNII
KEGG
ChEBI
CompTox Dashboard(EPA)
ECHA InfoCard100.055.123Edit this at Wikidata
Chemical and physical data
FormulaC19H19N
Molar mass261.368 g·mol−1
3D model (JSmol)
  • c42c(\C3=C(/c1ccccc1C2)CN(C)CC3)cccc4
  • InChI=1S/C19H19N/c1-20-11-10-18-16-8-4-2-6-14(16)12-15-7-3-5-9-17(15)19(18)13-20/h2-9H,10-13H2,1H3 checkY
  • Key:GVPIXRLYKVFFMK-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Setiptiline (brand nameTecipul), also known asteciptiline, is atetracyclic antidepressant (TeCA) that acts as anoradrenergic and specific serotonergic antidepressant (NaSSA). It was launched in 1989 for the treatment ofdepression inJapan byMochida.[1][2]

Pharmacology

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Pharmacodynamics

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See also:Pharmacology of antidepressants andTetracyclic antidepressant § Binding profiles
Setiptiline[3]
SiteKi (nM)SpeciesRef
SERTTooltip Serotonin transporter>10,000 (IC50)Rat[4]
NETTooltip Norepinephrine transporter220 (IC50)Rat[4]
DATTooltip Dopamine transporter>10,000 (IC50)Rat[4]
5-HT1ANDNDND
5-HT2ANDNDND
5-HT2CNDNDND
α1NDNDND
α224.3 (IC50)Rat[5]
H1NDNDND
mAChTooltip Muscarinic acetylcholine receptorNDNDND
Values are Ki (nM), unless otherwise noted. The smaller the value, the more strongly the drug binds to the site.

Setiptiline acts as anorepinephrine reuptake inhibitor,[4]α2-adrenergic receptorantagonist,[5] andserotonin receptor antagonist,[6] likely at the5-HT2 subtypes,[citation needed] as well as anH1 receptorinverse agonist/antihistamine.[4][additional citation(s) needed]

Chemistry

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Setiptiline has atetracyclicstructure and is a closeanalogue ofmianserin andmirtazapine, with setiptiline being delta(13b,4a),4a-carba-mianserin, and mirtazapine being 6-azamianserin.

See also

[edit]

References

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  1. ^Holenz J, Díaz JL, Buschmann H (2007)."Chemistry: Tricyclic and tetracyclic antidepressants". In Buschmann H, Torrens A, Vela JM (eds.).Antidepressants, Antipsychotics, Anxiolytics: From Chemistry and Pharmacology to Clinical Application. Vol. 1. Wiley VCH. p. 248.doi:10.1002/9783527619337.ch5.ISBN 978-3-527-31058-6.[permanent dead link]
  2. ^Swiss Pharmaceutical Society, ed. (2000).Index Nominum 2000: International Drug Directory. Medpharm Scientific Publishers. p. 942.ISBN 3-88763-075-0.
  3. ^Roth BL, Driscol J."PDSP Ki Database".Psychoactive Drug Screening Program (PDSP). University of North Carolina at Chapel Hill and the United States National Institute of Mental Health. Retrieved14 August 2017.
  4. ^abcdeNiho T, Ito C, Shibutani Y, Hashizume H, Yamaguchi K (October 1986)."[Pharmacological properties of MO-8282, a novel antidepressant]".Nihon Yakurigaku Zasshi. Folia Pharmacologica Japonica (in Japanese).88 (4):309–320.doi:10.1254/fpj.88.309.PMID 3792961.
  5. ^abMizota M, Oikawa Y, Nakayama K, Mizuguchi K, Takarada T, Kojima M, et al. (December 1986)."[Pharmacological studies of MO-8282, a new antidepressant]".Nihon Yakurigaku Zasshi. Folia Pharmacologica Japonica (in Japanese).88 (6):457–466.doi:10.1254/fpj.88.457.PMID 2881854.
  6. ^Przegaliński E, Baran L, Siwanowicz J, Rawłów A (1986). "The lack of antidepressant properties and a potent central antiserotonin activity of Org 8282".Polish Journal of Pharmacology and Pharmacy.38 (4):377–384.PMID 3774630.
SSRIsTooltip Selective serotonin reuptake inhibitors
SNRIsTooltip Serotonin–norepinephrine reuptake inhibitors
NRIsTooltip Norepinephrine reuptake inhibitors
NDRIsTooltip Norepinephrine–dopamine reuptake inhibitors
NaSSAsTooltip Noradrenergic and specific serotonergic antidepressants
SARIsTooltip Serotonin antagonist and reuptake inhibitors
SMSTooltip Serotonin modulator and stimulators
Others
TCAsTooltip Tricyclic antidepressants
TeCAsTooltip Tetracyclic antidepressants
Others
Non-selective
MAOATooltip Monoamine oxidase A-selective
MAOBTooltip Monoamine oxidase B-selective
Miscellaneous
5-HT1ARTooltip 5-HT1A receptoragonists
GABAARTooltip GABAA receptorPAMsTooltip positive allosteric modulators
Gabapentinoids
(α2δVDCCblockers)
Antidepressants
Sympatholytics
(Antiadrenergics)
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α1
Agonists
Antagonists
α2
Agonists
Antagonists
β
Agonists
Antagonists
H1
Agonists
Antagonists
H2
Agonists
Antagonists
H3
Agonists
Antagonists
H4
Agonists
Antagonists
DATTooltip Dopamine transporter
(DRIsTooltip Dopamine reuptake inhibitors)
NETTooltip Norepinephrine transporter
(NRIsTooltip Norepinephrine reuptake inhibitors)
SERTTooltip Serotonin transporter
(SRIsTooltip Serotonin reuptake inhibitors)
VMATsTooltip Vesicular monoamine transporters
Others
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
Classes
Antidepressants
(Tricyclic antidepressants(TCAs))
Antihistamines
Antipsychotics
Anticonvulsants
Anticholinergics
Others
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