U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C17H20N2O2S
Molecular Weight 316.418
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TINORIDINE

SMILES

CCOC(=O)C1=C(N)SC2=C1CCN(CC3=CC=CC=C3)C2

InChI

InChIKey=PFENFDGYVLAFBR-UHFFFAOYSA-N
InChI=1S/C17H20N2O2S/c1-2-21-17(20)15-13-8-9-19(11-14(13)22-16(15)18)10-12-6-4-3-5-7-12/h3-7H,2,8-11,18H2,1H3

HIDE SMILES / InChI

Description
Curator's Comment: description was created based on several sources, including: http://www.obatapasaja.com/2015/05/komposisi-dosis-dan-harga-nonflamin.html http://www.ncbi.nlm.nih.gov/pubmed/702946

Tinoridine is a non-steroidal anti-inflammatory and analgesic agent. This agent has been proved pharmacologically to show antiedematous and analgesic actions. The mechanism of the anti-inflammatory action of Tinoridine is attributed to its biomembrane stabilizing action particularly on the lysosomes which are related to cell or tissue damage at the time of inflammation through the release of hydrolytic enzymes. Tinoridine may produce gastrointestinal disorders (nausea, loss of appetite, diarrhea, and constipation), vertigo drowsiness, dry mouth and itching.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
Nonflamin

Approved Use

Tinoridine is indicated as anti-inflammatory agent after surgery injuries or injury in urology.
Primary
Nonflamin

Approved Use

Tinoridine is used to treat pharyngitis, laryngitis, tonsillitis.
Primary
Nonflamin

Approved Use

For analgesic purpose, Tinoridine is used to treat back pain.
Primary
Nonflamin

Approved Use

For analgesic purpose, Tinoridine is used to treat lumbago.
Primary
Nonflamin

Approved Use

Tinoridine is indicated to treat pain in chronic rheumatic diseases.
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
8.2 h
200 mg single, oral
dose: 200 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
TINORIDINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
8.2 h
200 mg single, oral
dose: 200 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
TINORIDINE plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
Doses

Doses

DosePopulationAdverse events​
100 mg 3 times / day multiple, oral
Recommended
Dose: 100 mg, 3 times / day
Route: oral
Route: multiple
Dose: 100 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Disc. AE: Nausea, Appetite lost...
AEs leading to
discontinuation/dose reduction:
Nausea
Appetite lost
Diarrhoea
Constipation
Vertigo
Drowsiness
Dry mouth
Itching
Sources:
AEs

AEs

AESignificanceDosePopulation
Appetite lost Disc. AE
100 mg 3 times / day multiple, oral
Recommended
Dose: 100 mg, 3 times / day
Route: oral
Route: multiple
Dose: 100 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Constipation Disc. AE
100 mg 3 times / day multiple, oral
Recommended
Dose: 100 mg, 3 times / day
Route: oral
Route: multiple
Dose: 100 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Diarrhoea Disc. AE
100 mg 3 times / day multiple, oral
Recommended
Dose: 100 mg, 3 times / day
Route: oral
Route: multiple
Dose: 100 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Drowsiness Disc. AE
100 mg 3 times / day multiple, oral
Recommended
Dose: 100 mg, 3 times / day
Route: oral
Route: multiple
Dose: 100 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Dry mouth Disc. AE
100 mg 3 times / day multiple, oral
Recommended
Dose: 100 mg, 3 times / day
Route: oral
Route: multiple
Dose: 100 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Itching Disc. AE
100 mg 3 times / day multiple, oral
Recommended
Dose: 100 mg, 3 times / day
Route: oral
Route: multiple
Dose: 100 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Nausea Disc. AE
100 mg 3 times / day multiple, oral
Recommended
Dose: 100 mg, 3 times / day
Route: oral
Route: multiple
Dose: 100 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Vertigo Disc. AE
100 mg 3 times / day multiple, oral
Recommended
Dose: 100 mg, 3 times / day
Route: oral
Route: multiple
Dose: 100 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
PubMed

PubMed

TitleDatePubMed
Ethyl 2-amino-6-benzyl-4,5,6,7-tetra-hydro-thieno[2,3-c]pyridine-3-carboxyl-ate.
2010-12-24
Patents

Patents

Sample Use Guides

1-2 capsules 3 times a day
Route of Administration: Oral
In Vitro Use Guide
Curator's Comment: Tinoridine, at concentrations from 5 microM up to 100 microM, produced a concentration-dependent inhibition on the simultaneous increases in lipid peroxide formation and renin release induced by 50 microM ascorbic acid in the renin granule fraction. http://www.ncbi.nlm.nih.gov/pubmed/3906080
30 uM of Tinoridine HCl hydrochloride inhibited the Phospholipase C-induced lysosomal enzyme release from rat liver lysosomes.
Name Type Language
NSC-158555
Preferred Name English
TINORIDINE
INN   MI   WHO-DD  
INN  
Official Name English
tinoridine [INN]
Common Name English
Y-3642
Code English
Tinoridine [WHO-DD]
Common Name English
Y 3642
Code English
TINORIDINE [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C257
Created by admin on Mon Mar 31 18:07:49 GMT 2025 , Edited by admin on Mon Mar 31 18:07:49 GMT 2025
Code System Code Type Description
MERCK INDEX
m1263
Created by admin on Mon Mar 31 18:07:49 GMT 2025 , Edited by admin on Mon Mar 31 18:07:49 GMT 2025
PRIMARY Merck Index
EVMPD
SUB11077MIG
Created by admin on Mon Mar 31 18:07:49 GMT 2025 , Edited by admin on Mon Mar 31 18:07:49 GMT 2025
PRIMARY
SMS_ID
100000077227
Created by admin on Mon Mar 31 18:07:49 GMT 2025 , Edited by admin on Mon Mar 31 18:07:49 GMT 2025
PRIMARY
DRUG CENTRAL
2672
Created by admin on Mon Mar 31 18:07:49 GMT 2025 , Edited by admin on Mon Mar 31 18:07:49 GMT 2025
PRIMARY
NSC
158555
Created by admin on Mon Mar 31 18:07:49 GMT 2025 , Edited by admin on Mon Mar 31 18:07:49 GMT 2025
PRIMARY
FDA UNII
C9Z9ICZ7YR
Created by admin on Mon Mar 31 18:07:49 GMT 2025 , Edited by admin on Mon Mar 31 18:07:49 GMT 2025
PRIMARY
NCI_THESAURUS
C76821
Created by admin on Mon Mar 31 18:07:49 GMT 2025 , Edited by admin on Mon Mar 31 18:07:49 GMT 2025
PRIMARY
CAS
24237-54-5
Created by admin on Mon Mar 31 18:07:49 GMT 2025 , Edited by admin on Mon Mar 31 18:07:49 GMT 2025
PRIMARY
INN
3079
Created by admin on Mon Mar 31 18:07:49 GMT 2025 , Edited by admin on Mon Mar 31 18:07:49 GMT 2025
PRIMARY
ChEMBL
CHEMBL592943
Created by admin on Mon Mar 31 18:07:49 GMT 2025 , Edited by admin on Mon Mar 31 18:07:49 GMT 2025
PRIMARY
DRUG BANK
DB13001
Created by admin on Mon Mar 31 18:07:49 GMT 2025 , Edited by admin on Mon Mar 31 18:07:49 GMT 2025
PRIMARY
MESH
C100290
Created by admin on Mon Mar 31 18:07:49 GMT 2025 , Edited by admin on Mon Mar 31 18:07:49 GMT 2025
PRIMARY
PUBCHEM
5480
Created by admin on Mon Mar 31 18:07:49 GMT 2025 , Edited by admin on Mon Mar 31 18:07:49 GMT 2025
PRIMARY
ECHA (EC/EINECS)
246-102-0
Created by admin on Mon Mar 31 18:07:49 GMT 2025 , Edited by admin on Mon Mar 31 18:07:49 GMT 2025
PRIMARY
EPA CompTox
DTXSID9023677
Created by admin on Mon Mar 31 18:07:49 GMT 2025 , Edited by admin on Mon Mar 31 18:07:49 GMT 2025
PRIMARY