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
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 GMT 2023 , Edited by admin on Sat Dec 16 16:13:51 GMT 2023
NCI_THESAURUS C29739
Created by admin on Sat Dec 16 16:13:51 GMT 2023 , Edited by admin on Sat Dec 16 16:13:51 GMT 2023
Code System Code Type Description
INN
1126
Created by admin on Sat Dec 16 16:13:51 GMT 2023 , Edited by admin on Sat Dec 16 16:13:51 GMT 2023
PRIMARY
CAS
3772-76-7
Created by admin on Sat Dec 16 16:13:51 GMT 2023 , Edited by admin on Sat Dec 16 16:13:51 GMT 2023
PRIMARY
FDA UNII
940ZL3AHKB
Created by admin on Sat Dec 16 16:13:51 GMT 2023 , Edited by admin on Sat Dec 16 16:13:51 GMT 2023
PRIMARY
EVMPD
SUB10713MIG
Created by admin on Sat Dec 16 16:13:51 GMT 2023 , Edited by admin on Sat Dec 16 16:13:51 GMT 2023
PRIMARY
NCI_THESAURUS
C72851
Created by admin on Sat Dec 16 16:13:51 GMT 2023 , Edited by admin on Sat Dec 16 16:13:51 GMT 2023
PRIMARY
WIKIPEDIA
SULFAMETOMIDINE
Created by admin on Sat Dec 16 16:13:51 GMT 2023 , Edited by admin on Sat Dec 16 16:13:51 GMT 2023
PRIMARY
ECHA (EC/EINECS)
223-219-5
Created by admin on Sat Dec 16 16:13:51 GMT 2023 , Edited by admin on Sat Dec 16 16:13:51 GMT 2023
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EPA CompTox
DTXSID0023616
Created by admin on Sat Dec 16 16:13:51 GMT 2023 , Edited by admin on Sat Dec 16 16:13:51 GMT 2023
PRIMARY
MERCK INDEX
m10319
Created by admin on Sat Dec 16 16:13:51 GMT 2023 , Edited by admin on Sat Dec 16 16:13:51 GMT 2023
PRIMARY Merck Index
SMS_ID
100000083271
Created by admin on Sat Dec 16 16:13:51 GMT 2023 , Edited by admin on Sat Dec 16 16:13:51 GMT 2023
PRIMARY
PUBCHEM
19596
Created by admin on Sat Dec 16 16:13:51 GMT 2023 , Edited by admin on Sat Dec 16 16:13:51 GMT 2023
PRIMARY
ChEMBL
CHEMBL485940
Created by admin on Sat Dec 16 16:13:51 GMT 2023 , Edited by admin on Sat Dec 16 16:13:51 GMT 2023
PRIMARY
DRUG BANK
DB13485
Created by admin on Sat Dec 16 16:13:51 GMT 2023 , Edited by admin on Sat Dec 16 16:13:51 GMT 2023
PRIMARY
DRUG CENTRAL
2513
Created by admin on Sat Dec 16 16:13:51 GMT 2023 , Edited by admin on Sat Dec 16 16:13:51 GMT 2023
PRIMARY