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

Details

Stereochemistry ACHIRAL
Molecular Formula C12H14N4O3S
Molecular Weight 294.33
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULFAMETOMIDINE

SMILES

COC1=CC(NS(=O)(=O)C2=CC=C(N)C=C2)=NC(C)=N1

InChI

InChIKey=QKLSCPPJEVXONT-UHFFFAOYSA-N
InChI=1S/C12H14N4O3S/c1-8-14-11(7-12(15-8)19-2)16-20(17,18)10-5-3-9(13)4-6-10/h3-7H,13H2,1-2H3,(H,14,15,16)

HIDE SMILES / InChI

Description
Curator's Comment: description was created based on several sources, including http://datagovtw.com/fda.php?id=%E5%85%A7%E8%A1%9B%E8%97%A5%E8%A3%BD%E5%AD%97%E7%AC%AC016294%E8%99%9F

Sulfametomidine (or sulfamethomidine) is a sulfonamide antibacterial with a broad spectrum of activity; it’s an inhibitor of dihydrofolate reductase.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
METHOFADIN INJECTION

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Acetylation phenotype status in a Bangladeshi population and its comparison with that of other Asian population data.
2004 Sep
Comparative therapeutic effect of toltrazuril, sulphadimidine and amprolium on Eimeria bovis and Eimeria zuernii given at different times following infection in buffalo calves (Bubalus bubalis).
2008 Apr 17
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: http://datagovtw.com/fda.php?id=%E5%85%A7%E8%A1%9B%E8%97%A5%E8%A3%BD%E5%AD%97%E7%AC%AC016294%E8%99%9F
initially 2 mg. subsequently 24 hour intervals in an average total dose of 6.3 mg.
Route of Administration: Other
In Vitro Use Guide
Unknown
Name Type Language
SULFAMETOMIDINE
INN   JAN   WHO-DD  
INN  
Official Name English
SULFAMETHOMIDINE [MI]
Common Name English
Sulfametomidine [WHO-DD]
Common Name English
sulfametomidine [INN]
Common Name English
SULFAMETOMIDINE [JAN]
Common Name English
Classification Tree Code System Code
WHO-ATC J01ED03
Created by admin on Sat Dec 16 16:13:51 UTC 2023 , Edited by admin on Sat Dec 16 16:13:51 UTC 2023
NCI_THESAURUS C29739
Created by admin on Sat Dec 16 16:13:51 UTC 2023 , Edited by admin on Sat Dec 16 16:13:51 UTC 2023
Code System Code Type Description
INN
1126
Created by admin on Sat Dec 16 16:13:51 UTC 2023 , Edited by admin on Sat Dec 16 16:13:51 UTC 2023
PRIMARY
CAS
3772-76-7
Created by admin on Sat Dec 16 16:13:51 UTC 2023 , Edited by admin on Sat Dec 16 16:13:51 UTC 2023
PRIMARY
FDA UNII
940ZL3AHKB
Created by admin on Sat Dec 16 16:13:51 UTC 2023 , Edited by admin on Sat Dec 16 16:13:51 UTC 2023
PRIMARY
EVMPD
SUB10713MIG
Created by admin on Sat Dec 16 16:13:51 UTC 2023 , Edited by admin on Sat Dec 16 16:13:51 UTC 2023
PRIMARY
NCI_THESAURUS
C72851
Created by admin on Sat Dec 16 16:13:51 UTC 2023 , Edited by admin on Sat Dec 16 16:13:51 UTC 2023
PRIMARY
WIKIPEDIA
SULFAMETOMIDINE
Created by admin on Sat Dec 16 16:13:51 UTC 2023 , Edited by admin on Sat Dec 16 16:13:51 UTC 2023
PRIMARY
ECHA (EC/EINECS)
223-219-5
Created by admin on Sat Dec 16 16:13:51 UTC 2023 , Edited by admin on Sat Dec 16 16:13:51 UTC 2023
PRIMARY
EPA CompTox
DTXSID0023616
Created by admin on Sat Dec 16 16:13:51 UTC 2023 , Edited by admin on Sat Dec 16 16:13:51 UTC 2023
PRIMARY
MERCK INDEX
m10319
Created by admin on Sat Dec 16 16:13:51 UTC 2023 , Edited by admin on Sat Dec 16 16:13:51 UTC 2023
PRIMARY Merck Index
SMS_ID
100000083271
Created by admin on Sat Dec 16 16:13:51 UTC 2023 , Edited by admin on Sat Dec 16 16:13:51 UTC 2023
PRIMARY
PUBCHEM
19596
Created by admin on Sat Dec 16 16:13:51 UTC 2023 , Edited by admin on Sat Dec 16 16:13:51 UTC 2023
PRIMARY
ChEMBL
CHEMBL485940
Created by admin on Sat Dec 16 16:13:51 UTC 2023 , Edited by admin on Sat Dec 16 16:13:51 UTC 2023
PRIMARY
DRUG BANK
DB13485
Created by admin on Sat Dec 16 16:13:51 UTC 2023 , Edited by admin on Sat Dec 16 16:13:51 UTC 2023
PRIMARY
DRUG CENTRAL
2513
Created by admin on Sat Dec 16 16:13:51 UTC 2023 , Edited by admin on Sat Dec 16 16:13:51 UTC 2023
PRIMARY