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Details

Stereochemistry RACEMIC
Molecular Formula C19H24NS2
Molecular Weight 330.531
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 1

SHOW SMILES / InChI
Structure of TIQUIZIUM

SMILES

[H][C@]12CCCC[N@+]1(C)CC(CC2)=C(C3=CC=CS3)C4=CC=CS4

InChI

InChIKey=ZGSDGGRVFIYKKE-OXQOHEQNSA-N
InChI=1S/C19H24NS2/c1-20-11-3-2-6-16(20)10-9-15(14-20)19(17-7-4-12-21-17)18-8-5-13-22-18/h4-5,7-8,12-13,16H,2-3,6,9-11,14H2,1H3/q+1/t16-,20-/m1/s1

HIDE SMILES / InChI

Molecular Formula C19H24NS2
Molecular Weight 330.531
Charge 1
Count
Stereochemistry EPIMERIC
Additional Stereochemistry No
Defined Stereocenters 1 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Tiquizium is an antispasmodic agent used to treat disorders of the gastrointestinal, biliary, and urinary systems. Tiquizium is available commercially in Japan for the treatment of gastrointestinal disease. Tiquizium shows anti-muscarinic action to improve convulsion and hypermobility of intestinal smooth muscle. It is usually used to treat convulsion and hypermobility in gastritis, gastric ulcer, duodenal ulcer, enteritis, irritable bowel syndrome, gallbladder disease, biliary tract disease and urolithiasis.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Thiaton

Approved Use

Thiaton is usually used to treat convulsion and hypermobility in gastritis, gastric ulcer, duodenal ulcer, enteritis, irritable bowel syndrome, gallbladder disease, biliary tract disease and urolithiasis.
Primary
Thiaton

Approved Use

Thiaton is usually used to treat convulsion and hypermobility in gastritis, gastric ulcer, duodenal ulcer, enteritis, irritable bowel syndrome, gallbladder disease, biliary tract disease and urolithiasis.
Primary
Thiaton

Approved Use

Thiaton is usually used to treat convulsion and hypermobility in gastritis, gastric ulcer, duodenal ulcer, enteritis, irritable bowel syndrome, gallbladder disease, biliary tract disease and urolithiasis.
Primary
Thiaton

Approved Use

Thiaton is usually used to treat convulsion and hypermobility in gastritis, gastric ulcer, duodenal ulcer, enteritis, irritable bowel syndrome, gallbladder disease, biliary tract disease and urolithiasis.
Primary
Thiaton

Approved Use

Thiaton is usually used to treat convulsion and hypermobility in gastritis, gastric ulcer, duodenal ulcer, enteritis, irritable bowel syndrome, gallbladder disease, biliary tract disease and urolithiasis.
PubMed

PubMed

TitleDatePubMed
Pharmacological profile of ramosetron, a novel therapeutic agent for IBS.
2007 Feb
Inhibitory effects of ramosetron, a potent and selective 5-HT3-receptor antagonist, on conditioned fear stress-induced abnormal defecation and normal defecation in rats: comparative studies with antidiarrheal and spasmolytic agents.
2008 Feb
Effects of serotonin 5-HT3 receptor antagonists on stress-induced colonic hyperalgesia and diarrhoea in rats: a comparative study with opioid receptor agonists, a muscarinic receptor antagonist and a synthetic polymer.
2008 May
Development of a list of potentially inappropriate drugs for the korean elderly using the delphi method.
2010 Dec
Patents

Sample Use Guides

In general, for adults, take 5 to 10 mg of the active ingredient at a time, three times a day. The dosage may be adjusted according to the age and symptoms. This preparation contains 10 mg of the active ingredient in a capsule.
Route of Administration: Oral
In Vitro Use Guide
Tiquizium (1 x 10(-6) - 1x10(-5)g/ml) increased transmural stimulation (TM contraction) and/or resting tone (1 x 10(-5)g/ml) in isolated guinea pig urinary bladder.
Substance Class Chemical
Created
by admin
on Sat Dec 16 01:46:21 GMT 2023
Edited
by admin
on Sat Dec 16 01:46:21 GMT 2023
Record UNII
340Q44041A
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TIQUIZIUM
WHO-DD  
Common Name English
2H-QUINOLIZINIUM, 3-(DI-2-THIENYLMETHYLENE)OCTAHYDRO-5-METHYL-, TRANS-
Systematic Name English
TIQUIZIUM CATION
Common Name English
Tiquizium [WHO-DD]
Common Name English
TIQUIZIUM ION
Common Name English
Code System Code Type Description
CAS
149755-23-7
Created by admin on Sat Dec 16 01:46:22 GMT 2023 , Edited by admin on Sat Dec 16 01:46:22 GMT 2023
PRIMARY
DRUG CENTRAL
2678
Created by admin on Sat Dec 16 01:46:22 GMT 2023 , Edited by admin on Sat Dec 16 01:46:22 GMT 2023
PRIMARY
FDA UNII
340Q44041A
Created by admin on Sat Dec 16 01:46:22 GMT 2023 , Edited by admin on Sat Dec 16 01:46:22 GMT 2023
PRIMARY
EVMPD
SUB04884MIG
Created by admin on Sat Dec 16 01:46:22 GMT 2023 , Edited by admin on Sat Dec 16 01:46:22 GMT 2023
PRIMARY
EPA CompTox
DTXSID2048292
Created by admin on Sat Dec 16 01:46:22 GMT 2023 , Edited by admin on Sat Dec 16 01:46:22 GMT 2023
PRIMARY
SMS_ID
100000084630
Created by admin on Sat Dec 16 01:46:22 GMT 2023 , Edited by admin on Sat Dec 16 01:46:22 GMT 2023
PRIMARY
PUBCHEM
72160
Created by admin on Sat Dec 16 01:46:22 GMT 2023 , Edited by admin on Sat Dec 16 01:46:22 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY