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A propos de cet article
Formule empirique (notation de Hill) :
C11H12N4O3S
Numéro CAS:
Poids moléculaire :
280.30
UNSPSC Code:
51283913
NACRES:
NA.85
PubChem Substance ID:
EC Number:
211-480-8
Beilstein/REAXYS Number:
621130
MDL number:
Service technique
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powder
Quality Segment
storage condition
(Keep container tightly closed in a dry and well-ventilated place. Light sensitive.)
color
white to faint yellow
antibiotic activity spectrum
Gram-negative bacteria, Gram-positive bacteria, mycobacteria, parasites
mode of action
enzyme | inhibits
storage temp.
2-8°C
SMILES string
COc1cnc(NS(=O)(=O)c2ccc(N)cc2)nc1
InChI
1S/C11H12N4O3S/c1-18-9-6-13-11(14-7-9)15-19(16,17)10-4-2-8(12)3-5-10/h2-7H,12H2,1H3,(H,13,14,15)
InChI key
GPTONYMQFTZPKC-UHFFFAOYSA-N
General description
Chemical structure: sulfonamide
Application
Sulfameter is a sulfonamide antibiotic used as a leprostatic agent and to treat urinary tract infections. It has been investigated as a potential therapy for chloroquine-resistant malaria during pregnancy.
Biochem/physiol Actions
Sulfameter is a sulfonamide antibiotic. Sulfonamides block the synthesis of dihydrofolic acid by inhibiting the enzyme dihydropteroate synthase. Sulfonamides are competitive inhibitors of bacterial para-aminobenzoic acid (PABA), which is required for bacterial synthesis of folic acid. Sulfameter is a dihydrofolate reductase (DHFR) inhibitor. Sulfonamides are active against Gram positive bacteria and Gram negative bacteria. Mode of resistance is via the alteration of dihydropteroate synthase or alternative pathway for folic acid synthesis.
Other Notes
Keep container tightly closed in a dry and well-ventilated place. Light sensitive.
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Classe de stockage
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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