Sulfacetamide drug data and news

Sulfacetamide 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 Sulfacetamide
Brand Names/Synonyms A-500; Acetocid; Acetosulfamin; Acetosulfamine; Ak-Sulf; Albamine; Albucid; Alesten; Bleph-10; Bleph-10 Liquifilm; Cetamide; Formosulfacetamide; Gyne-Sulf; I-Sulfacet; Isopto Cetamide; Isopto-Cetamide; Klaron; N'-Acetylsulfanilamide; N-Acetylsulfanilamide; N-Acetylsulfanilamine; N-Sulfanilylacetamide; N-Sulphanilylacetamide; Oclucid; Ocusulf-10; Op-Sulfa 30; Ophthacet; Ophthel-S; P-Aminobenzenesulfonacetamide; P-Aminobenzenesulfonoacetamide; Region; Sebizon; Sodium Sulamyd; Sodium Sulfacetamide; Steramide; Steri-Units Sulfacetamide; Sulamyd; Sulf-10; Sulf-15; Sulfacel-15; Sulfacet; Sulfacetamide; Sulfacetamide Sodium; Sulfacetamide Sodium Anhydrous; Sulfacetamide Sodium Usp; Sulfacetimide; Sulfacyl; Sulfair; Sulfair 10; Sulfair 15; Sulfair Forte; Sulfair-15; Sulfamide; Sulfanilacetamide; Sulfanilazetamid; Sulfex; Sulphacetamide; Sulphacetamide Sodium; Sulphasil; Sulten-10; Sultrin; Triple Sulfa; Trysul; Urosulfon; Urosulfone; Vagilia
Indication For the treatment of bacterial vaginitis, keratitis, acute conjunctivitis, blepharitis
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Description Not Available
Pharmacology Sulfacetamide 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 Sulfacetamide is a competitive inhibitor of bacterial para-aminobenzoic acid (PABA), an essential component for bacterial growth (according to the Woods-Fildes theory). The inhibited reaction is necessary in these organisms for the synthesis of folic acid.
Sulfacetamide News
(When available)

Medicis Announces FDA Approval of SOLODYN -- minocycline HCl, USP ...  May 8, 2006
...prescription brands RESTYLANE(R), DYNACIN(R) (minocycline HCl), LOPROX(R) (ciclopirox), OMNICEF(R) (cefdinir), PLEXION(R) (sodium sulfacetamide/sulfur), SOLODYN ... - PharmaLive.com (press release),

Dosage Forms DROPS; LIQUID; OINTMENT
Drug_Category Anti-Infectives Agents, Local; Anti-Infectives Agents, Urinary; Anti-bacterial Agents; ATC:S01AB04
Absorption Not Available
Interactions Interactions for Sulfacetamide:

Sulfacetamide preparations are incompatible with silver preparations.

Toxicity Oral LD50 Mouse : 16500 mg/kg. Side effects include moderate to severe erythema (redness) and moderate edema (raised kin), nausea, vomiting, headache, dizziness, tiredness. Higher exposure causes unconsciousness.
Organisms Affected Enteric bacteria and other eubacteria
Chemical IUPAC Name N-acetyl-4-amino-benzenesulfonamide
Chemical Formula C8H10N2O3S
Molecular Weight 214.243 g/mol
Smiles String CC(=O)NS(=O)(=O)C1=CC=C(C=C1)N
Melting Point 183 °C
Water Solubility 1.25E+004 mg/L
State Solid
LogP/Hphobicity 0.201
Isoelectric Point Not Available
Biotransformation Not Available
Half Life 7-12.8 hours
Protein Binding [%] Not Available
RxList Link RXlist
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Drug Reference http://www.pdrhealth.com/drug_info/rxdrugprofiles/drugs/ava1674.shtml
http://www.drugs.com/cons/Sulfacetamide.html
http://www.rxlist.com/cgi/generic3/plexion.htm
Drug Type Approved Drug
Accession No APRD00452
CAS Registry Number 144-80-9
KEGG Compound ID Not Available
PubChem ID SID:152109
PharmGKB ID PA451536
SwissProt ID Not Available
GenBank ID Not Available
Drug ID Number [DIN] 838934

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