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Details

Stereochemistry ACHIRAL
Molecular Formula C12H12BrN4O2S.Na
Molecular Weight 379.208
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULFABROMOMETHAZINE SODIUM ANHYDROUS

SMILES

[Na+].CC1=NC([N-]S(=O)(=O)C2=CC=C(N)C=C2)=NC(C)=C1Br

InChI

InChIKey=BYTJZIVWFMOARV-UHFFFAOYSA-N
InChI=1S/C12H12BrN4O2S.Na/c1-7-11(13)8(2)16-12(15-7)17-20(18,19)10-5-3-9(14)4-6-10;/h3-6H,14H2,1-2H3;/q-1;+1

HIDE SMILES / InChI

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C12H13BrN4O2S
Molecular Weight 357.226
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Sulfabromomethazine is a long-acting derivative of sulfamezathine that is used in the poultry, swine and cattle industries for the treatment of coccidiosis and various bacterial infections. Single oral doses of the drug have been used to treat calf diphteria and pneumonia, metritis, foot root and septic mastitis in cattle with repeated dose 48 hors later sometimes required. Use of sulfabromomethazine during the last 3 months of pregnancy should be avoided. The compound is now rarely used.

Originator

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

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: T. gondii dihydropteroate synthase (Q2HWT3_TOXGO)
230.0 µM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Sulfabrom

Approved Use

Used in the poultry, swine and cattle industries for the treatment of coccidiosis and various bacterial infections.

Launch Date

1958
Curative
Sulfabrom

Approved Use

Used in the poultry, swine and cattle industries for the treatment of coccidiosis and various bacterial infections.

Launch Date

1958
PubMed

PubMed

TitleDatePubMed
The pharmacology of sulfabromomethazine, a new long-acting sulfonamide, in cattle.
1958 Apr
Identification of a class of sulfonamides highly active against dihydropteroate synthase form Toxoplasma gondii, Pneumocystis carinii, and Mycobacterium avium.
1996 Mar
Patents

Sample Use Guides

In Vitro Use Guide
Curator's Comment: The compounds including sulfabromomethazine (compound # 5874) were tested using a parasite growth inhibition assay to obtain dose-response curves and IC50 determinations for each compound.
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:42:20 GMT 2023
Edited
by admin
on Fri Dec 15 19:42:20 GMT 2023
Record UNII
3769OF3689
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SULFABROMOMETHAZINE SODIUM ANHYDROUS
Common Name English
SODIUM SULFABROMOMETHAZINE
Common Name English
BENZENESULFONAMIDE, 4-AMINO-N-(5-BROMO-4,6-DIMETHYL-2-PYRIMIDINYL)-, SODIUM SALT (1:1)
Common Name English
SULFABROMOMETHAZINE SODIUM SALT
Common Name English
Code System Code Type Description
FDA UNII
3769OF3689
Created by admin on Fri Dec 15 19:42:20 GMT 2023 , Edited by admin on Fri Dec 15 19:42:20 GMT 2023
PRIMARY
CAS
3691-68-7
Created by admin on Fri Dec 15 19:42:20 GMT 2023 , Edited by admin on Fri Dec 15 19:42:20 GMT 2023
PRIMARY
EPA CompTox
DTXSID90958107
Created by admin on Fri Dec 15 19:42:20 GMT 2023 , Edited by admin on Fri Dec 15 19:42:20 GMT 2023
PRIMARY
ECHA (EC/EINECS)
223-004-6
Created by admin on Fri Dec 15 19:42:20 GMT 2023 , Edited by admin on Fri Dec 15 19:42:20 GMT 2023
PRIMARY
PUBCHEM
23678871
Created by admin on Fri Dec 15 19:42:20 GMT 2023 , Edited by admin on Fri Dec 15 19:42:20 GMT 2023
PRIMARY
Related Record Type Details
SOLVATE->ANHYDROUS
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY