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2-Sulfanilamidopyridine en es it fr

2-Sulfanilamidopyridine Brand names, 2-Sulfanilamidopyridine Analogs

2-Sulfanilamidopyridine Brand Names Mixture

  • Foot Rot Boluses (Ethylenediamine Dihydroiodide + Sulfapyridine)
  • Neutral Sulfa 50 (Sulfamethazine + Sulfapyridine + Sulfathiazole)
  • Neutral Sulfa 7 (Sulfamethazine + Sulfapyridine + Sulfathiazole)
  • Trisulfa G Liq (Sulfamethazine + Sulfapyridine + Sulfathiazole)

2-Sulfanilamidopyridine Chemical_Formula

C11H11N3O2S

2-Sulfanilamidopyridine RX_link

No information avaliable

2-Sulfanilamidopyridine fda sheet

2-Sulfanilamidopyridine msds (material safety sheet)

2-Sulfanilamidopyridine MSDS

2-Sulfanilamidopyridine Synthesis Reference

No information avaliable

2-Sulfanilamidopyridine Molecular Weight

249.29 g/mol

2-Sulfanilamidopyridine Melting Point

192 oC

2-Sulfanilamidopyridine H2O Solubility

268 mg/L

2-Sulfanilamidopyridine State

Solid

2-Sulfanilamidopyridine LogP

2.384

2-Sulfanilamidopyridine Dosage Forms

Tablet

2-Sulfanilamidopyridine Indication

For the treatment of dermatitis herpetiformis, benign mucous membrane pemphigoid and pyoderma gangrenosum

2-Sulfanilamidopyridine Pharmacology

Sulfapyridine 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.

2-Sulfanilamidopyridine Absorption

approximately 60-80%

2-Sulfanilamidopyridine side effects and Toxicity

ORL-RAT 15800 mg/Kg

2-Sulfanilamidopyridine Patient Information

PATIENT INFORMATION

Follow the links

http://www.nlm.nih.gov/medlineplus/druginfo/uspdi/202536.html

http://www.drugs.com/cons/Sulfapyridine.html

2-Sulfanilamidopyridine Organisms Affected

Humans and other mammals