Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Cyanodothiepin

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Cyanodothiepin
Clinical data
Other namesBTS-56424
ATC code
  • None
Identifiers
  • 11-(3-(dimethylamino)propylidene)-6,11-dihydrodibenzo[b,e]thiepine-2-carbonitrile
CAS Number
PubChemCID
ChemSpider
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC20H20N2S
Molar mass320.45 g·mol−1
3D model (JSmol)
  • CN(C)CC/C=C1C2=C(C=CC(C#N)=C2)SCC3=C/1C=CC=C3
  • InChI=1S/C20H20N2S/c1-22(2)11-5-8-18-17-7-4-3-6-16(17)14-23-20-10-9-15(13-21)12-19(18)20/h3-4,6-10,12H,5,11,14H2,1-2H3/b18-8+
  • Key:FSIRGTNPQFDCCD-QGMBQPNBSA-N

Cyanodothiepin (developmental code nameBTS-56424) is atricyclic antidepressant (TCA) acting as apotent and highlyselective (overnorepinephrine anddopamine uptake)inhibitor of thereuptake ofserotonin that was never marketed.[1][2][3] It also has moderateaffinity for themuscarinic acetylcholine receptors and weak/negligible affinity for theα1-adrenergic,5-HT2A,D1, andD2 receptors;[1][2][3] theH1 receptor has not been assayed,[3] but cyanodothiepin is lesssedating than the related drugcianopramine, suggesting that itsantihistamine activity is not as pronounced as other TCAs.[1][3] Cyanodothiepin isactive in theforced swimming test (FST), implying that it may possessantidepressant properties in humans. However, it is only weakly active compared to cianopramine andimipramine inmonoamine depletion-based tests of antidepressant potential.[1]

See also

[edit]

References

[edit]
  1. ^abcdLuscombe GP, Buckett WR (1993). "Pharmacology of Cyanodothiepin (BTS 56 424), a Selective 5-Hydroxytryptamine Reuptake Inhibitor".Drug Development Research.29 (3):235–248.doi:10.1002/ddr.430290311.S2CID 84257024.
  2. ^abJucker E (2000).Progress in Drug Research. Birkhäuser. pp. 79–80.ISBN 978-3-7643-6113-6. Retrieved2011-11-25.
  3. ^abcdOlivier B, van Wijngaarden I, Soudijn W (1997).Serotonin Receptors and their Ligands. Elsevier. p. 332.ISBN 978-0-444-82041-9. Retrieved2011-11-25.
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
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
mAChRsTooltip Muscarinic acetylcholine receptors
Agonists
Antagonists
Precursors
(andprodrugs)
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
Stub icon

Thisdrug article relating to thenervous system is astub. You can help Wikipedia byexpanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Cyanodothiepin&oldid=1222274738"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp