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Details

Stereochemistry ACHIRAL
Molecular Formula C19H19N
Molecular Weight 261.3609
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SETIPTILINE

SMILES

CN1CCC2=C(C1)C3=CC=CC=C3CC4=CC=CC=C24

InChI

InChIKey=GVPIXRLYKVFFMK-UHFFFAOYSA-N
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

HIDE SMILES / InChI

Molecular Formula C19H19N
Molecular Weight 261.3609
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: Description was created based on several sources, including https://www.drugbank.ca/drugs/DB09304

Setiptiline Maleate is a tetracyclic antidepressant that has been used in the treatment of depression. It has antihistamine and hypnotic–sedative effects, but almost no anticholinergic effects. It is a weak inhibitor of norepinephrine reuptake in vitro and strongly stimulates the release of central norepinephrine by blocking presynaptic α2-adrenoceptors similar to mianserin. It also acts as a 5-HT2A, 5-HT2C, and 5-HT3 receptor antagonist. Unlike most conventional antidepressants, it has no efficacy as a serotonin reuptake inhibitor. It can induce drowsiness and thirst, but it displays low toxicity. Setiptiline Maleate was launched in 1989 for the treatment of depression in Japan.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Tecipul

Approved Use

Antidepressant

Launch Date

1997
Primary
Tecipul

Approved Use

For the treatment of depression.

Launch Date

1997
Primary
Setiptiline maleate

Approved Use

Setiptiline maleate is used to treat depression or depressive state

Launch Date

1988
PubMed

PubMed

TitleDatePubMed
Effectiveness of concomitant setiptiline maleate (Tecipul) on negative symptoms of schizophrenia.
1994 Mar
Patents

Sample Use Guides

3-8 mg/day oral
Route of Administration: Oral
In Vitro Use Guide
100uM setiptiline inhibited about 60% of NMDA current in Xenopus oocytes injected with rat brain mRNA.
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:18:54 GMT 2023
Edited
by admin
on Fri Dec 15 16:18:54 GMT 2023
Record UNII
7L38105Z6E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SETIPTILINE
INN   MART.   WHO-DD  
INN  
Official Name English
setiptiline [INN]
Common Name English
Setiptiline [WHO-DD]
Common Name English
SETIPTILINE [MI]
Common Name English
ORG 8282
Code English
SETIPTILINE [MART.]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C265
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
Code System Code Type Description
CAS
57262-94-9
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
DRUG BANK
DB09304
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104895
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
MESH
C050605
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
ECHA (EC/EINECS)
260-653-4
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
SMS_ID
100000084323
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
MERCK INDEX
m11743
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
WIKIPEDIA
Setiptiline
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
EVMPD
SUB10503MIG
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
INN
5937
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
NCI_THESAURUS
C75178
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
CHEBI
135076
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
PUBCHEM
5205
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
DRUG CENTRAL
2438
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
EPA CompTox
DTXSID50205886
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
FDA UNII
7L38105Z6E
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
TARGET -> AGONIST
SHORT-ACTING
Related Record Type Details
ACTIVE MOIETY