N1-2-Pyridylsulfanilamide
N1-2-Pyridylsulfanilamide Brand names, N1-2-Pyridylsulfanilamide Analogs
- 2-Sulfanilamidopyridin
- 2-Sulfanilamidopyridine
- 2-Sulfanilylaminopyridine
- 2-Sulfapyridine
- 4-(2-Pyridinylsulfonyl)aniline
- 4-[(2-Pyridylamino)sulfonyl]aniline
- Adiplon
- Coccoclase
- Dagenan
- Eporal
- Eubasin
- Eubasinum
- Haptocil
- M and B 693
- N(sup 1)-2-Pyridylsulfanilamide
- N(sup1)-Pyridylsulfanilamide
- N-2-Pyridylsulfanilamide
- N1-2-Pyridylsulfanilamide
- Piridazol
- Plurazol
- Pyriamid
- Pyridazol
- Relbapiridina
- Ronin
- Septipulmon
- Streptosilpyridine
- Sulfanilamide, N(sup 1)-2-pyridyl-
- Sulfanilamide, N1-2-pyridyl-
- Sulfapyridine (USP)
- Sulfidin
- Sulfidine
- Sulphapyridine
- Thioseptal
- Trianon
N1-2-Pyridylsulfanilamide 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)
N1-2-Pyridylsulfanilamide Chemical_Formula
C11H11N3O2S
N1-2-Pyridylsulfanilamide RX_link
No information avaliable
N1-2-Pyridylsulfanilamide fda sheet
N1-2-Pyridylsulfanilamide msds (material safety sheet)
N1-2-Pyridylsulfanilamide Synthesis Reference
No information avaliable
N1-2-Pyridylsulfanilamide Molecular Weight
249.29 g/mol
N1-2-Pyridylsulfanilamide Melting Point
192 oC
N1-2-Pyridylsulfanilamide H2O Solubility
268 mg/L
N1-2-Pyridylsulfanilamide State
Solid
N1-2-Pyridylsulfanilamide LogP
2.384
N1-2-Pyridylsulfanilamide Dosage Forms
Tablet
N1-2-Pyridylsulfanilamide Indication
For the treatment of dermatitis herpetiformis, benign mucous membrane pemphigoid and pyoderma gangrenosum
N1-2-Pyridylsulfanilamide 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.
N1-2-Pyridylsulfanilamide Absorption
approximately 60-80%
N1-2-Pyridylsulfanilamide side effects and Toxicity
ORL-RAT 15800 mg/Kg
N1-2-Pyridylsulfanilamide Patient Information
PATIENT INFORMATION
Follow the links
http://www.nlm.nih.gov/medlineplus/druginfo/uspdi/202536.html
http://www.drugs.com/cons/Sulfapyridine.html
Follow the links
http://www.nlm.nih.gov/medlineplus/druginfo/uspdi/202536.html
http://www.drugs.com/cons/Sulfapyridine.html
N1-2-Pyridylsulfanilamide Organisms Affected
Humans and other mammals
