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

Details

Stereochemistry ACHIRAL
Molecular Formula C10H11N3O2S2
Molecular Weight 269.343
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULFASOMIZOLE

SMILES

CC1=NSC(NS(=O)(=O)C2=CC=C(N)C=C2)=C1

InChI

InChIKey=JVYKJZPZFIUYAB-UHFFFAOYSA-N
InChI=1S/C10H11N3O2S2/c1-7-6-10(16-12-7)13-17(14,15)9-4-2-8(11)3-5-9/h2-6,13H,11H2,1H3

HIDE SMILES / InChI

Molecular Formula C10H11N3O2S2
Molecular Weight 269.343
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Sulfasomizole is a sulfanilamide derivative patented by Chemie Grunenthal G. m. b. H. as an antibiotic with broad-spectrum activity. Sulfasomizole is active against a wide range of gram-positive and gram-negative organisms. Sulfasomizole is well absorbed and distributed in the body, and is readily excreted in the urine.

Approval Year

PubMed

PubMed

TitleDatePubMed
[THE TREATMENT OF RECURRENT BRONCHOPULMONARY INFECTIONS AND PROTRACTED PURULENT BRONCHORRHEA WITH SULFASOMIZOLE].
1964 Oct 25
Patents

Patents

Sample Use Guides

1g
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:35:21 GMT 2023
Edited
by admin
on Fri Dec 15 15:35:21 GMT 2023
Record UNII
U3227B174V
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SULFASOMIZOLE
INN   MI   USAN  
INN   USAN  
Official Name English
NSC-139593
Code English
SULFASOMIZOLE [MI]
Common Name English
sulfasomizole [INN]
Common Name English
SULFASOMIZOLE [USAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29739
Created by admin on Fri Dec 15 15:35:21 GMT 2023 , Edited by admin on Fri Dec 15 15:35:21 GMT 2023
Code System Code Type Description
FDA UNII
U3227B174V
Created by admin on Fri Dec 15 15:35:21 GMT 2023 , Edited by admin on Fri Dec 15 15:35:21 GMT 2023
PRIMARY
NCI_THESAURUS
C76980
Created by admin on Fri Dec 15 15:35:21 GMT 2023 , Edited by admin on Fri Dec 15 15:35:21 GMT 2023
PRIMARY
ECHA (EC/EINECS)
211-167-6
Created by admin on Fri Dec 15 15:35:21 GMT 2023 , Edited by admin on Fri Dec 15 15:35:21 GMT 2023
PRIMARY
DRUG CENTRAL
3835
Created by admin on Fri Dec 15 15:35:21 GMT 2023 , Edited by admin on Fri Dec 15 15:35:21 GMT 2023
PRIMARY
ChEMBL
CHEMBL2107088
Created by admin on Fri Dec 15 15:35:21 GMT 2023 , Edited by admin on Fri Dec 15 15:35:21 GMT 2023
PRIMARY
MERCK INDEX
m943
Created by admin on Fri Dec 15 15:35:21 GMT 2023 , Edited by admin on Fri Dec 15 15:35:21 GMT 2023
PRIMARY Merck Index
EVMPD
SUB10728MIG
Created by admin on Fri Dec 15 15:35:21 GMT 2023 , Edited by admin on Fri Dec 15 15:35:21 GMT 2023
PRIMARY
INN
961
Created by admin on Fri Dec 15 15:35:21 GMT 2023 , Edited by admin on Fri Dec 15 15:35:21 GMT 2023
PRIMARY
PUBCHEM
69433
Created by admin on Fri Dec 15 15:35:21 GMT 2023 , Edited by admin on Fri Dec 15 15:35:21 GMT 2023
PRIMARY
EPA CompTox
DTXSID20212547
Created by admin on Fri Dec 15 15:35:21 GMT 2023 , Edited by admin on Fri Dec 15 15:35:21 GMT 2023
PRIMARY
NSC
139593
Created by admin on Fri Dec 15 15:35:21 GMT 2023 , Edited by admin on Fri Dec 15 15:35:21 GMT 2023
PRIMARY
CAS
632-00-8
Created by admin on Fri Dec 15 15:35:21 GMT 2023 , Edited by admin on Fri Dec 15 15:35:21 GMT 2023
PRIMARY
SMS_ID
100000083298
Created by admin on Fri Dec 15 15:35:21 GMT 2023 , Edited by admin on Fri Dec 15 15:35:21 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY