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Details

Stereochemistry ACHIRAL
Molecular Formula C15H17NS2
Molecular Weight 275.432
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TIPEPIDINE

SMILES

CN1CCCC(C1)=C(C2=CC=CS2)C3=CC=CS3

InChI

InChIKey=JWIXXNLOKOAAQT-UHFFFAOYSA-N
InChI=1S/C15H17NS2/c1-16-8-2-5-12(11-16)15(13-6-3-9-17-13)14-7-4-10-18-14/h3-4,6-7,9-10H,2,5,8,11H2,1H3

HIDE SMILES / InChI

Molecular Formula C15H17NS2
Molecular Weight 275.432
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: http://www.journalmc.org/index.php/JMC/article/viewFile/1564/916

Tipepidine (INN) also known as tipepidine hibenzate (JAN), is a synthetic, non-opioid antitussive and expectorant of the thiambutene class. The drug was discovered in the 1950s, and was developed in Japan in 1959. It is used as the hibenzate and citrate salts. The safety of tipepidine in children and adults has already been established. It is reported that tipepidine inhibits G-protein-coupled inwardly rectifying potassium (GIRK)-channel currents. The inhibition of GIRK channels by tipepidine is expected to modulate the level of monoamines in the brain. Tipepidine can improve attention deficit/hyperactivity disorder (ADHD) symptoms by modulating monoaminergic neurotransmission through the inhibition of GIRK channels. Tipepidine also is being investigated in depression, obsessive-compulsive disorder, and attention-deficit hyperactivity disorder (ADHD). As it acts on the central nervous system, overdose can cause altered mental status and other neurological symptoms; however, there have been few reports of tipepidine intoxication, including six cases in children and no cases in adults.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
The preparation of rapidly disintegrating tablets in the mouth.
2001 Nov
The centrally acting non-narcotic antitussive tipepidine produces antidepressant-like effect in the forced swimming test in rats.
2009 Dec 14
Fixed drug eruption induced by tipepidine hibenzate.
2010 May
[Novel antidepressant-like action of drugs possessing GIRK channel blocking action in rats].
2010 May
Antidepressant-like effect of centrally acting non-narcotic antitussive caramiphen in a forced swimming test.
2010 Sep 13
Patents

Patents

Sample Use Guides

tipepidine hibenzate taken orally at 30 mg/day for 4 weeks
Route of Administration: Oral
In Vitro Use Guide
Submaximal contractions of bronchial muscle evoked by exogenous acetylcholine, ACh (1-30 microM) were inhibited by tipepidine (10-100 microM)
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:39:09 GMT 2023
Edited
by admin
on Fri Dec 15 16:39:09 GMT 2023
Record UNII
2260ZP67IT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TIPEPIDINE
INN   MI   WHO-DD  
INN  
Official Name English
TIPEPIDINE [MI]
Common Name English
AT 327
Code English
AT-327
Code English
CRJ662
Code English
CR-662
Code English
CR/662
Code English
3-(DI-2-THIENYLMETHYLENE)-1-METHYLPIPERIDINE
Systematic Name English
Tipepidine [WHO-DD]
Common Name English
tipepidine [INN]
Common Name English
Classification Tree Code System Code
WHO-ATC R05DB24
Created by admin on Fri Dec 15 16:39:09 GMT 2023 , Edited by admin on Fri Dec 15 16:39:09 GMT 2023
WHO-VATC QR05DB24
Created by admin on Fri Dec 15 16:39:09 GMT 2023 , Edited by admin on Fri Dec 15 16:39:09 GMT 2023
NCI_THESAURUS C66917
Created by admin on Fri Dec 15 16:39:09 GMT 2023 , Edited by admin on Fri Dec 15 16:39:09 GMT 2023
Code System Code Type Description
FDA UNII
2260ZP67IT
Created by admin on Fri Dec 15 16:39:09 GMT 2023 , Edited by admin on Fri Dec 15 16:39:09 GMT 2023
PRIMARY
INN
1956
Created by admin on Fri Dec 15 16:39:09 GMT 2023 , Edited by admin on Fri Dec 15 16:39:09 GMT 2023
PRIMARY
DRUG BANK
DB13474
Created by admin on Fri Dec 15 16:39:09 GMT 2023 , Edited by admin on Fri Dec 15 16:39:09 GMT 2023
PRIMARY
PUBCHEM
5484
Created by admin on Fri Dec 15 16:39:09 GMT 2023 , Edited by admin on Fri Dec 15 16:39:09 GMT 2023
PRIMARY
MERCK INDEX
m10883
Created by admin on Fri Dec 15 16:39:09 GMT 2023 , Edited by admin on Fri Dec 15 16:39:09 GMT 2023
PRIMARY Merck Index
WIKIPEDIA
Tipepidine
Created by admin on Fri Dec 15 16:39:09 GMT 2023 , Edited by admin on Fri Dec 15 16:39:09 GMT 2023
PRIMARY
EPA CompTox
DTXSID2022626
Created by admin on Fri Dec 15 16:39:09 GMT 2023 , Edited by admin on Fri Dec 15 16:39:09 GMT 2023
PRIMARY
NCI_THESAURUS
C76847
Created by admin on Fri Dec 15 16:39:09 GMT 2023 , Edited by admin on Fri Dec 15 16:39:09 GMT 2023
PRIMARY
DRUG CENTRAL
253
Created by admin on Fri Dec 15 16:39:09 GMT 2023 , Edited by admin on Fri Dec 15 16:39:09 GMT 2023
PRIMARY
MESH
C028458
Created by admin on Fri Dec 15 16:39:09 GMT 2023 , Edited by admin on Fri Dec 15 16:39:09 GMT 2023
PRIMARY
SMS_ID
100000077259
Created by admin on Fri Dec 15 16:39:09 GMT 2023 , Edited by admin on Fri Dec 15 16:39:09 GMT 2023
PRIMARY
EVMPD
SUB11102MIG
Created by admin on Fri Dec 15 16:39:09 GMT 2023 , Edited by admin on Fri Dec 15 16:39:09 GMT 2023
PRIMARY
CAS
5169-78-8
Created by admin on Fri Dec 15 16:39:09 GMT 2023 , Edited by admin on Fri Dec 15 16:39:09 GMT 2023
PRIMARY
ChEMBL
CHEMBL1899506
Created by admin on Fri Dec 15 16:39:09 GMT 2023 , Edited by admin on Fri Dec 15 16:39:09 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY