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Details

Stereochemistry ACHIRAL
Molecular Formula C14H12N2O2S
Molecular Weight 272.322
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ZOLIMIDINE

SMILES

CS(=O)(=O)C1=CC=C(C=C1)C2=CN3C=CC=CC3=N2

InChI

InChIKey=VSLIUWLPFRVCDL-UHFFFAOYSA-N
InChI=1S/C14H12N2O2S/c1-19(17,18)12-7-5-11(6-8-12)13-10-16-9-3-2-4-14(16)15-13/h2-10H,1H3

HIDE SMILES / InChI

Molecular Formula C14H12N2O2S
Molecular Weight 272.322
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Zolimidine, a derivate of imidazopyridine, has a gastroprotective effect. It is used in the treatment of peptic ulcer and gastro-oesophageal reflux disease.

CNS Activity

Curator's Comment: Zolimidine is brain penetrant in animals. No human data available.

Originator

Curator's Comment: reference retrieved from http://www.drugfuture.com/chemdata/zolimidine.html

Approval Year

PubMed

PubMed

TitleDatePubMed
6-Benzyl-3,4-dimeth-oxy-10-methyl-pyrido[2',1':2,3]imidazo[4,5-c]isoquinolin-5(6H)-one.
2009 Sep 12
Ethyl 8-(4-nitro-phen-yl)imidazo[1,2-a]pyridine-7-carboxyl-ate.
2010 Nov 24
Patents

Patents

Sample Use Guides

1200 mg/day
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:33:14 GMT 2023
Edited
by admin
on Sat Dec 16 16:33:14 GMT 2023
Record UNII
YCF001N8QB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ZOLIMIDINE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
ZOLIRIDINE
Common Name English
SOLIMIDIN
Brand Name English
Zolimidine [WHO-DD]
Common Name English
zolimidine [INN]
Common Name English
ZOLIMIDINE [MI]
Common Name English
ZOLIMIDINE [MART.]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29701
Created by admin on Sat Dec 16 16:33:14 GMT 2023 , Edited by admin on Sat Dec 16 16:33:14 GMT 2023
WHO-VATC QA02BX10
Created by admin on Sat Dec 16 16:33:14 GMT 2023 , Edited by admin on Sat Dec 16 16:33:14 GMT 2023
WHO-ATC A02BX10
Created by admin on Sat Dec 16 16:33:14 GMT 2023 , Edited by admin on Sat Dec 16 16:33:14 GMT 2023
Code System Code Type Description
SMS_ID
100000078815
Created by admin on Sat Dec 16 16:33:14 GMT 2023 , Edited by admin on Sat Dec 16 16:33:14 GMT 2023
PRIMARY
DRUG CENTRAL
3661
Created by admin on Sat Dec 16 16:33:14 GMT 2023 , Edited by admin on Sat Dec 16 16:33:14 GMT 2023
PRIMARY
EPA CompTox
DTXSID9057630
Created by admin on Sat Dec 16 16:33:14 GMT 2023 , Edited by admin on Sat Dec 16 16:33:14 GMT 2023
PRIMARY
MESH
C073260
Created by admin on Sat Dec 16 16:33:14 GMT 2023 , Edited by admin on Sat Dec 16 16:33:14 GMT 2023
PRIMARY
FDA UNII
YCF001N8QB
Created by admin on Sat Dec 16 16:33:14 GMT 2023 , Edited by admin on Sat Dec 16 16:33:14 GMT 2023
PRIMARY
CAS
1222-57-7
Created by admin on Sat Dec 16 16:33:14 GMT 2023 , Edited by admin on Sat Dec 16 16:33:14 GMT 2023
PRIMARY
EVMPD
SUB00179MIG
Created by admin on Sat Dec 16 16:33:14 GMT 2023 , Edited by admin on Sat Dec 16 16:33:14 GMT 2023
PRIMARY
ChEMBL
CHEMBL2105534
Created by admin on Sat Dec 16 16:33:14 GMT 2023 , Edited by admin on Sat Dec 16 16:33:14 GMT 2023
PRIMARY
WIKIPEDIA
ZOLIMIDINE
Created by admin on Sat Dec 16 16:33:14 GMT 2023 , Edited by admin on Sat Dec 16 16:33:14 GMT 2023
PRIMARY
DRUG BANK
DB13593
Created by admin on Sat Dec 16 16:33:14 GMT 2023 , Edited by admin on Sat Dec 16 16:33:14 GMT 2023
PRIMARY
PUBCHEM
14652
Created by admin on Sat Dec 16 16:33:14 GMT 2023 , Edited by admin on Sat Dec 16 16:33:14 GMT 2023
PRIMARY
INN
3089
Created by admin on Sat Dec 16 16:33:14 GMT 2023 , Edited by admin on Sat Dec 16 16:33:14 GMT 2023
PRIMARY
ECHA (EC/EINECS)
214-947-4
Created by admin on Sat Dec 16 16:33:14 GMT 2023 , Edited by admin on Sat Dec 16 16:33:14 GMT 2023
PRIMARY
MERCK INDEX
m11659
Created by admin on Sat Dec 16 16:33:14 GMT 2023 , Edited by admin on Sat Dec 16 16:33:14 GMT 2023
PRIMARY Merck Index
NCI_THESAURUS
C66705
Created by admin on Sat Dec 16 16:33:14 GMT 2023 , Edited by admin on Sat Dec 16 16:33:14 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY