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Details

Stereochemistry ACHIRAL
Molecular Formula C12H14N4O2S
Molecular Weight 278.33
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULFISOMIDINE

SMILES

CC1=CC(NS(=O)(=O)C2=CC=C(N)C=C2)=NC(C)=N1

InChI

InChIKey=YZMCKZRAOLZXAZ-UHFFFAOYSA-N
InChI=1S/C12H14N4O2S/c1-8-7-12(15-9(2)14-8)16-19(17,18)11-5-3-10(13)4-6-11/h3-7H,13H2,1-2H3,(H,14,15,16)

HIDE SMILES / InChI

Molecular Formula C12H14N4O2S
Molecular Weight 278.33
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Sulfisomidine (INN), also known as sulphasomidine (BAN until 2003), is a sulfonamide antibacterial. It’s used in the treatment, control, prevention, and improvement of the following conditions and symptoms: Lower urinary tract infections; Meningococcal meningitis; Streptococcal pharyngitis; Gum infection; Bacillary dysentery.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Unknown

Approved Use

Unknown
Curative
Unknown

Approved Use

Unknown
Curative
Unknown

Approved Use

Unknown
Curative
Unknown

Approved Use

Unknown
Curative
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
[Drugs and breastfeeding].
2002 Apr-Jun
In-vitro antifungal activities of sulfa drugs against clinical isolates of Aspergillus and Cryptococcus species.
2007
Patents

Sample Use Guides

2 g twice daily
Route of Administration: Oral
In Vitro Use Guide
The monotherapy of S suis infections with sulfonamides (SULFISOMIDINE was one of them) should not be encouraged because the MIC50 of all sulfonamides investigated was greater than 32 micrograms/ml. The MIC50 of the sulfonamides against B bronchiseptica ranged from 0.5 to 8 micrograms/ml, against P multocida from 2 to 32 micrograms/ml, and against H pleuropneumoniae from 8 to 64 micrograms/ml.
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:17:59 UTC 2023
Edited
by admin
on Fri Dec 15 15:17:59 UTC 2023
Record UNII
W03L3ODK6E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SULFISOMIDINE
EP   INN   JAN   MART.   MI   WHO-DD  
INN  
Official Name English
Sulfisomidine [WHO-DD]
Common Name English
SULFISOMIDINE [MART.]
Common Name English
sulfisomidine [INN]
Common Name English
N1-(2,6-DIMETHYL-4-PYRIMIDINYL)SULFANILAMIDE
Systematic Name English
SULFISOMIDINE [EP IMPURITY]
Common Name English
N(SUP 1)-(2,6-DIMETHYL-4-PYRIMIDINYL)SULFANILAMIDE
Systematic Name English
SULPHASOMIDINE
Common Name English
SULFISOMIDINE [MI]
Common Name English
SULFISOMIDINE [JAN]
Common Name English
SULFAISODIMIDINE
Common Name English
Classification Tree Code System Code
WHO-ATC J01EB01
Created by admin on Fri Dec 15 15:17:59 UTC 2023 , Edited by admin on Fri Dec 15 15:17:59 UTC 2023
NCI_THESAURUS C29739
Created by admin on Fri Dec 15 15:17:59 UTC 2023 , Edited by admin on Fri Dec 15 15:17:59 UTC 2023
Code System Code Type Description
DRUG BANK
DB13283
Created by admin on Fri Dec 15 15:17:59 UTC 2023 , Edited by admin on Fri Dec 15 15:17:59 UTC 2023
PRIMARY
PUBCHEM
5343
Created by admin on Fri Dec 15 15:17:59 UTC 2023 , Edited by admin on Fri Dec 15 15:17:59 UTC 2023
PRIMARY
FDA UNII
W03L3ODK6E
Created by admin on Fri Dec 15 15:17:59 UTC 2023 , Edited by admin on Fri Dec 15 15:17:59 UTC 2023
PRIMARY
EVMPD
SUB10739MIG
Created by admin on Fri Dec 15 15:17:59 UTC 2023 , Edited by admin on Fri Dec 15 15:17:59 UTC 2023
PRIMARY
RXCUI
10206
Created by admin on Fri Dec 15 15:17:59 UTC 2023 , Edited by admin on Fri Dec 15 15:17:59 UTC 2023
PRIMARY RxNorm
DRUG CENTRAL
2526
Created by admin on Fri Dec 15 15:17:59 UTC 2023 , Edited by admin on Fri Dec 15 15:17:59 UTC 2023
PRIMARY
NCI_THESAURUS
C152463
Created by admin on Fri Dec 15 15:17:59 UTC 2023 , Edited by admin on Fri Dec 15 15:17:59 UTC 2023
PRIMARY
EPA CompTox
DTXSID1046390
Created by admin on Fri Dec 15 15:17:59 UTC 2023 , Edited by admin on Fri Dec 15 15:17:59 UTC 2023
PRIMARY
MESH
D013443
Created by admin on Fri Dec 15 15:17:59 UTC 2023 , Edited by admin on Fri Dec 15 15:17:59 UTC 2023
PRIMARY
ECHA (EC/EINECS)
208-204-3
Created by admin on Fri Dec 15 15:17:59 UTC 2023 , Edited by admin on Fri Dec 15 15:17:59 UTC 2023
PRIMARY
INN
99
Created by admin on Fri Dec 15 15:17:59 UTC 2023 , Edited by admin on Fri Dec 15 15:17:59 UTC 2023
PRIMARY
CHEBI
32166
Created by admin on Fri Dec 15 15:17:59 UTC 2023 , Edited by admin on Fri Dec 15 15:17:59 UTC 2023
PRIMARY
MERCK INDEX
m10351
Created by admin on Fri Dec 15 15:17:59 UTC 2023 , Edited by admin on Fri Dec 15 15:17:59 UTC 2023
PRIMARY Merck Index
SMS_ID
100000085219
Created by admin on Fri Dec 15 15:17:59 UTC 2023 , Edited by admin on Fri Dec 15 15:17:59 UTC 2023
PRIMARY
WIKIPEDIA
Sulfisomidine
Created by admin on Fri Dec 15 15:17:59 UTC 2023 , Edited by admin on Fri Dec 15 15:17:59 UTC 2023
PRIMARY
CAS
515-64-0
Created by admin on Fri Dec 15 15:17:59 UTC 2023 , Edited by admin on Fri Dec 15 15:17:59 UTC 2023
PRIMARY
ChEMBL
CHEMBL485696
Created by admin on Fri Dec 15 15:17:59 UTC 2023 , Edited by admin on Fri Dec 15 15:17:59 UTC 2023
PRIMARY
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