Sulfisoxazole drug data and news

Sulfisoxazole drug data, resources, and news articles (when available). Onconews.org provides news on cancer research. This section, which includes profiles on medicines that may or not be cancer-related is in beta form. If things run smoothly we will be releasing a new format late in the summer of 2006.

Generic name Sulfisoxazole
Brand Names/Synonyms Accuzole; Alphazole; Amidoxal; Astrazolo; Azo Gantrisin; Azosulfizin; Bactesulf; Barazae; Chemouag; Cosoxazole; Dorsulfan; Dorsulfan Warthausen; Entusil; Entusul; G-Sox; Ganda; Gantrisin; Gantrisine; Gantrisona; Gantrosan; Isoxamin; J-Sul; Koro-Sulf; NU 445; Neazolin; Neoxazol; Norilgan-S; Novazolo; Novosaxazole; Pancid; Renosulfan; Resoxol; Roxosul; Roxosul Tablets; Roxoxol; SI; Saxosozine; Sk-Soxazole; Sodizole; Sosol; Soxamide; Soxazole; Soxisol; Soxitabs; Soxo; Soxomide; Stansin; Sulbio; Sulfadimethylisoxazole; Sulfafurazol; Sulfafurazole; Sulfagan; Sulfagen; Sulfaisoxazole; Sulfalar; Sulfapolar; Sulfasan; Sulfasol; Sulfasoxazole; Sulfazin; Sulfisin; Sulfisonazole; Sulfisoxasole; Sulfisoxazol; Sulfisoxazole; Sulfisoxazole Dialamine; Sulfisoxazole Diolamine; Sulfizin; Sulfizol; Sulfizole; Sulfofurazole; Sulfoxol; Suloxsol; Sulphadimethylisoxazole; Sulphafuraz; Sulphafurazol; Sulphafurazole; Sulphafurazolum; Sulphaisoxazole; Sulphisoxazol; Sulphofurazole; Sulsoxin; Thiasin; Tl-Azole; U.S.-67; Unisulf; Urisoxin; Uritrisin; Urogan; V-Sul; Vagilia
Indication Treatment of severe, repeated, or long-lasting urinary tract infections;Bacterial meningitis;Middle ear infections;Toxoplasmosis;Malaria;Other bacterial infections
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Description Not Available
Pharmacology Sulfisoxazole is a sulfonamide antibiotic. The sulfonamides are synthetic bacteriostatic antibiotics with a wide spectrum against most gram-positive and many gram-negative organisms. However, many strains of an individual species may be resistant. Sulfonamides inhibit multiplication of bacteria by acting as competitive inhibitors of p-aminobenzoic acid in the folic acid metabolism cycle. Bacterial sensitivity is the same for the various sulfonamides, and resistance to one sulfonamide indicates resistance to all. Most sulfonamides are readily absorbed orally. However, parenteral administration is difficult, since the soluble sulfonamide salts are highly alkaline and irritating to the tissues. The sulfonamides are widely distributed throughout all tissues. High levels are achieved in pleural, peritoneal, synovial, and ocular fluids. Although these drugs are no longer used to treat meningitis, CSF levels are high in meningeal infections. Their antibacterial action is inhibited by pus.
Mechanism Of Action Sulfisoxazole is a competitive inhibitor of the enzyme dihydropteroate synthetase. It inhibits bacterial synthesis of of dihydrofolic acid by preventing the condensation of the pteridine with para-aminobenzoic acid (PABA), a substrate of the enzyme dihydropteroate synthetase. The inhibited reaction is necessary in these organisms for the synthesis of folic acid.
Sulfisoxazole News
(When available)

Study: Antibiotic ban reduces incidence of drug resistance  Apr 18, 2006
About 55 per cent of the samples also exhibited resistance to sulfisoxazole, 46 per cent to ampicillin, roxithromycin (38 per cent), tetracycline (seven per ... - FoodProductionDaily-USA,

Dosage Forms TABLET; Oral Suspension; Eye Drops
Drug_Category Anti-Infectives; Sulfonamides;
Absorption Not Available
Interactions [an error occurred while processing this directive]
Toxicity LD50=6800 mg/kg (Orally in mice)
Organisms Affected Not Available
Chemical IUPAC Name 4-amino-N-(3,4-dimethyloxazol-5-yl)-benzenesulfonamide
Chemical Formula C11H13N3O3S
Molecular Weight 267.305 g/mol
Smiles String CC1=C(ON=C1C)NS(=O)(=O)C2=CC=C(C=C2)N
Melting Point 194 °C
Water Solubility 0.13 mg/ml (25 oC)
State Solid
LogP/Hphobicity 2.569
Isoelectric Point 5
Biotransformation Not Available
Half Life Not Available
Protein Binding [%] Not Available
RxList Link Not Available>RXlist
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Drug Reference http://www.drugs.com/cons/Sulfisoxazole.html
Drug Type Approved Drug
Accession No APRD00595
CAS Registry Number 127-69-5
KEGG Compound ID C07318
PubChem ID SID:9526
PharmGKB ID PA451552
SwissProt ID Not Available
GenBank ID Not Available
Drug ID Number [DIN] 363774

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