Sulfanilamide, N1-2-pyridyl- en es it fr

Sulfanilamide, N1-2-pyridyl- Brand names, Sulfanilamide, N1-2-pyridyl- Analogs

Sulfanilamide, N1-2-pyridyl- 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)

Sulfanilamide, N1-2-pyridyl- Chemical_Formula

C11H11N3O2S

Sulfanilamide, N1-2-pyridyl- RX_link

No information avaliable

Sulfanilamide, N1-2-pyridyl- fda sheet

Sulfanilamide, N1-2-pyridyl- msds (material safety sheet)

Sulfanilamide,_N1-2-pyridyl- MSDS

Sulfanilamide, N1-2-pyridyl- Synthesis Reference

No information avaliable

Sulfanilamide, N1-2-pyridyl- Molecular Weight

249.29 g/mol

Sulfanilamide, N1-2-pyridyl- Melting Point

192 oC

Sulfanilamide, N1-2-pyridyl- H2O Solubility

268 mg/L

Sulfanilamide, N1-2-pyridyl- State

Solid

Sulfanilamide, N1-2-pyridyl- LogP

2.384

Sulfanilamide, N1-2-pyridyl- Dosage Forms

Tablet

Sulfanilamide, N1-2-pyridyl- Indication

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

Sulfanilamide, N1-2-pyridyl- 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.

Sulfanilamide, N1-2-pyridyl- Absorption

approximately 60-80%

Sulfanilamide, N1-2-pyridyl- side effects and Toxicity

ORL-RAT 15800 mg/Kg

Sulfanilamide, N1-2-pyridyl- Patient Information

PATIENT INFORMATION

Follow the links

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

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

Sulfanilamide, N1-2-pyridyl- Organisms Affected

Humans and other mammals