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
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
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 |
DescriptionSources: http://www.drugbank.ca/drugs/DB09304http://link.springer.com/referenceworkentry/10.1007%2F978-3-540-68706-1_1842 | http://www.rad-ar.or.jp/siori/english/kekka.cgi?n=36605Curator's Comment: Description was created based on several sources, including
https://www.drugbank.ca/drugs/DB09304
Sources: http://www.drugbank.ca/drugs/DB09304http://link.springer.com/referenceworkentry/10.1007%2F978-3-540-68706-1_1842 | http://www.rad-ar.or.jp/siori/english/kekka.cgi?n=36605
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.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: GO:0007210 Sources: https://www.ncbi.nlm.nih.gov/pubmed/3774630 |
|||
Target ID: CHEMBL2095158 Sources: http://www.ncbi.nlm.nih.gov/pubmed/2881854 |
|||
Target ID: CHEMBL2094251 Sources: http://www.genome.jp/dbget-bin/www_bget?D02034 |
|||
Target ID: CHEMBL2095200 Sources: https://www.ncbi.nlm.nih.gov/pubmed/3774630 |
|||
Target ID: CHEMBL2095158 |
|||
Target ID: CHEMBL2094251 |
|||
Target ID: CHEMBL224 |
|||
Target ID: CHEMBL225 |
|||
Target ID: CHEMBL2094132 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Tecipul Approved UseAntidepressant Launch Date1997 |
|||
Sources: http://www.drugbank.ca/drugs/DB09304 |
Primary | Tecipul Approved UseFor the treatment of depression. Launch Date1997 |
||
Primary | Setiptiline maleate Approved UseSetiptiline maleate is used to treat depression or depressive state Launch Date1988 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/7905225
3-8 mg/day oral
Route of Administration:
Oral
In Vitro Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/7787763
100uM setiptiline inhibited about 60% of NMDA current in Xenopus oocytes injected with rat brain mRNA.
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:18:54 GMT 2023
by
admin
on
Fri Dec 15 16:18:54 GMT 2023
|
Record UNII |
7L38105Z6E
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
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 | ||
---|---|---|---|---|---|
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 |