4-[(2-Pyridylamino)sulfonyl]aniline
4-[(2-Pyridylamino)sulfonyl]aniline Brand names, 4-[(2-Pyridylamino)sulfonyl]aniline 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
4-[(2-Pyridylamino)sulfonyl]aniline 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)
4-[(2-Pyridylamino)sulfonyl]aniline Chemical_Formula
C11H11N3O2S
4-[(2-Pyridylamino)sulfonyl]aniline RX_link
No information avaliable
4-[(2-Pyridylamino)sulfonyl]aniline fda sheet
4-[(2-Pyridylamino)sulfonyl]aniline msds (material safety sheet)
4-[(2-Pyridylamino)sulfonyl]aniline Synthesis Reference
No information avaliable
4-[(2-Pyridylamino)sulfonyl]aniline Molecular Weight
249.29 g/mol
4-[(2-Pyridylamino)sulfonyl]aniline Melting Point
192 oC
4-[(2-Pyridylamino)sulfonyl]aniline H2O Solubility
268 mg/L
4-[(2-Pyridylamino)sulfonyl]aniline State
Solid
4-[(2-Pyridylamino)sulfonyl]aniline LogP
2.384
4-[(2-Pyridylamino)sulfonyl]aniline Dosage Forms
Tablet
4-[(2-Pyridylamino)sulfonyl]aniline Indication
For the treatment of dermatitis herpetiformis, benign mucous membrane pemphigoid and pyoderma gangrenosum
4-[(2-Pyridylamino)sulfonyl]aniline 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.
4-[(2-Pyridylamino)sulfonyl]aniline Absorption
approximately 60-80%
4-[(2-Pyridylamino)sulfonyl]aniline side effects and Toxicity
ORL-RAT 15800 mg/Kg
4-[(2-Pyridylamino)sulfonyl]aniline 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
4-[(2-Pyridylamino)sulfonyl]aniline Organisms Affected
Humans and other mammals
![4-[(2-Pyridylamino)sulfonyl]aniline](/images/rx/APRD00491.gif)
