M and B 693
M and B 693 Brand names, M and B 693 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
M and B 693 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)
M and B 693 Chemical_Formula
C11H11N3O2S
M and B 693 RX_link
No information avaliable
M and B 693 fda sheet
M and B 693 msds (material safety sheet)
M and B 693 Synthesis Reference
No information avaliable
M and B 693 Molecular Weight
249.29 g/mol
M and B 693 Melting Point
192 oC
M and B 693 H2O Solubility
268 mg/L
M and B 693 State
Solid
M and B 693 LogP
2.384
M and B 693 Dosage Forms
Tablet
M and B 693 Indication
For the treatment of dermatitis herpetiformis, benign mucous membrane pemphigoid and pyoderma gangrenosum
M and B 693 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.
M and B 693 Absorption
approximately 60-80%
M and B 693 side effects and Toxicity
ORL-RAT 15800 mg/Kg
M and B 693 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
M and B 693 Organisms Affected
Humans and other mammals
