N(sup 1)-2-Pyridylsulfanilamide
N(sup 1)-2-Pyridylsulfanilamide Brand names, N(sup 1)-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
N(sup 1)-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)
N(sup 1)-2-Pyridylsulfanilamide Chemical_Formula
C11H11N3O2S
N(sup 1)-2-Pyridylsulfanilamide RX_link
No information avaliable
N(sup 1)-2-Pyridylsulfanilamide fda sheet
N(sup 1)-2-Pyridylsulfanilamide msds (material safety sheet)
N(sup 1)-2-Pyridylsulfanilamide Synthesis Reference
No information avaliable
N(sup 1)-2-Pyridylsulfanilamide Molecular Weight
249.29 g/mol
N(sup 1)-2-Pyridylsulfanilamide Melting Point
192 oC
N(sup 1)-2-Pyridylsulfanilamide H2O Solubility
268 mg/L
N(sup 1)-2-Pyridylsulfanilamide State
Solid
N(sup 1)-2-Pyridylsulfanilamide LogP
2.384
N(sup 1)-2-Pyridylsulfanilamide Dosage Forms
Tablet
N(sup 1)-2-Pyridylsulfanilamide Indication
For the treatment of dermatitis herpetiformis, benign mucous membrane pemphigoid and pyoderma gangrenosum
N(sup 1)-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.
N(sup 1)-2-Pyridylsulfanilamide Absorption
approximately 60-80%
N(sup 1)-2-Pyridylsulfanilamide side effects and Toxicity
ORL-RAT 15800 mg/Kg
N(sup 1)-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
N(sup 1)-2-Pyridylsulfanilamide Organisms Affected
Humans and other mammals
