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

Details

Stereochemistry ACHIRAL
Molecular Formula C15H13NO2S
Molecular Weight 271.334
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of METIAZINIC ACID

SMILES

CN1C2=CC=CC=C2SC3=CC=C(CC(O)=O)C=C13

InChI

InChIKey=LMINNBXUMGNKMM-UHFFFAOYSA-N
InChI=1S/C15H13NO2S/c1-16-11-4-2-3-5-13(11)19-14-7-6-10(8-12(14)16)9-15(17)18/h2-8H,9H2,1H3,(H,17,18)

HIDE SMILES / InChI

Molecular Formula C15H13NO2S
Molecular Weight 271.334
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Sources: DOI: 10.1177/030006057200100106

Metiazinic acid is a non-steroidal agent and has been found in rheumatoid arthritis, ankylosing spondylitis, psoriatic arthritis and osteoarthrosis to possess anti-inflammatory activity

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Sources: DOI: 10.1177/030006057200100106
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
[Methiazinic acid (Soripal) in the treatment of inflammatory and degenerative diseases of the knee joint].
1974-04
[Toxicologic study of methiazinic acid (16091 R.P)].
1969-08
[General pharmacological properties of methiazinic acid (16091 RP)].
1969-08

Sample Use Guides

In Vivo Use Guide
Sources: DOI: 10.1177/030006057200100106
1.5 g per day for a week
Route of Administration: Oral
In Vitro Use Guide
50 uM to protect bacteriophage T2 from inactivation by the model peroxy radical CCl3O2
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:55:57 GMT 2025
Edited
by admin
on Mon Mar 31 17:55:57 GMT 2025
Record UNII
12I0HHE2ZY
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
METIAZINIC ACID
INN   JAN   MART.   MI   WHO-DD  
INN  
Official Name English
RP 16091
Preferred Name English
METIAZINIC ACID [MART.]
Common Name English
METIAZINIC ACID [MI]
Common Name English
metiazinic acid [INN]
Common Name English
10-METHYL-2-PHENOTHIAZINYL ACETIC ACID
Systematic Name English
Metiazinic acid [WHO-DD]
Common Name English
RP-16091
Code English
METIAZINIC ACID [JAN]
Common Name English
Code System Code Type Description
PUBCHEM
4164
Created by admin on Mon Mar 31 17:55:57 GMT 2025 , Edited by admin on Mon Mar 31 17:55:57 GMT 2025
PRIMARY
NCI_THESAURUS
C166452
Created by admin on Mon Mar 31 17:55:57 GMT 2025 , Edited by admin on Mon Mar 31 17:55:57 GMT 2025
PRIMARY
MERCK INDEX
m7485
Created by admin on Mon Mar 31 17:55:57 GMT 2025 , Edited by admin on Mon Mar 31 17:55:57 GMT 2025
PRIMARY Merck Index
ECHA (EC/EINECS)
237-795-0
Created by admin on Mon Mar 31 17:55:57 GMT 2025 , Edited by admin on Mon Mar 31 17:55:57 GMT 2025
PRIMARY
EPA CompTox
DTXSID7023308
Created by admin on Mon Mar 31 17:55:57 GMT 2025 , Edited by admin on Mon Mar 31 17:55:57 GMT 2025
PRIMARY
CHEBI
31838
Created by admin on Mon Mar 31 17:55:57 GMT 2025 , Edited by admin on Mon Mar 31 17:55:57 GMT 2025
PRIMARY
CAS
13993-65-2
Created by admin on Mon Mar 31 17:55:57 GMT 2025 , Edited by admin on Mon Mar 31 17:55:57 GMT 2025
PRIMARY
SMS_ID
100000080911
Created by admin on Mon Mar 31 17:55:57 GMT 2025 , Edited by admin on Mon Mar 31 17:55:57 GMT 2025
PRIMARY
ChEMBL
CHEMBL2105269
Created by admin on Mon Mar 31 17:55:57 GMT 2025 , Edited by admin on Mon Mar 31 17:55:57 GMT 2025
PRIMARY
DRUG CENTRAL
1776
Created by admin on Mon Mar 31 17:55:57 GMT 2025 , Edited by admin on Mon Mar 31 17:55:57 GMT 2025
PRIMARY
FDA UNII
12I0HHE2ZY
Created by admin on Mon Mar 31 17:55:57 GMT 2025 , Edited by admin on Mon Mar 31 17:55:57 GMT 2025
PRIMARY
EVMPD
SUB08883MIG
Created by admin on Mon Mar 31 17:55:57 GMT 2025 , Edited by admin on Mon Mar 31 17:55:57 GMT 2025
PRIMARY
INN
2519
Created by admin on Mon Mar 31 17:55:57 GMT 2025 , Edited by admin on Mon Mar 31 17:55:57 GMT 2025
PRIMARY
MESH
C100259
Created by admin on Mon Mar 31 17:55:57 GMT 2025 , Edited by admin on Mon Mar 31 17:55:57 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY