Sulfanilamidopyrimidine
Sulfanilamidopyrimidine Brand names, Sulfanilamidopyrimidine Analogs
- Adiazin
- Adiazine
- Coco-Diazine
- Cocodiazine
- Codiazine
- Cremodiazine
- Cremotres
- Debenal
- Deltazina
- Diazin
- Diazolone
- Diazovit
- Diazyl
- Eskadiazine
- Honey Diazine
- Lantrisul
- Lipo-Diazine
- Lipo-Levazine
- Liquadiazine
- Metha-Meridiazine
- Microsulfon
- Neazine
- Neotrizine
- Palatrize
- Pecta-Diazine, Suspension
- Piridisir
- Pirimal
- Pyrimal
- Quadetts
- Quadramoid
- SDA
- Sanodiazine
- Sildaflo
- Silvadene
- Spofadrizine
- Ssd
- Sterazine
- Sulfa-Triple #2
- Sulfacombin
- Sulfadiazene
- Sulfadiazin
- Sulfaloid
- Sulfanilamidopyrimidine
- Sulfapirimidin
- Sulfapyrimidin
- Sulfapyrimidine
- Sulfatryl
- Sulfazin
- Sulfazine
- Sulfolex
- Sulfonamides Duplex
- Sulfonsol
- Sulfose
- Sulphadiazine
- Terfonyl
- Theradiazine
- Thermazene
- Tri-Sulfameth
- Trifonamide
- Triple Sulfa
- Triple Sulfas
- Triple Sulfoid
- Trisem
- Trisulfapyrimidine, Oral Suspension
- Truozine
Sulfanilamidopyrimidine Brand Names Mixture
- No information avaliable
Sulfanilamidopyrimidine Chemical_Formula
C10H10N4O2S
Sulfanilamidopyrimidine RX_link
http://www.rxlist.com/cgi/generic3/silversulf.htm
Sulfanilamidopyrimidine fda sheet
Sulfanilamidopyrimidine msds (material safety sheet)
Sulfanilamidopyrimidine Synthesis Reference
No information avaliable
Sulfanilamidopyrimidine Molecular Weight
250.278 g/mol
Sulfanilamidopyrimidine Melting Point
No information avaliable
Sulfanilamidopyrimidine H2O Solubility
No information avaliable
Sulfanilamidopyrimidine State
Solid
Sulfanilamidopyrimidine LogP
1.883
Sulfanilamidopyrimidine Dosage Forms
Cream
Sulfanilamidopyrimidine Indication
For the treatment of rheumatic fever and meningococcal meningitis
Sulfanilamidopyrimidine Pharmacology
Sulfadiazine 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.
Sulfanilamidopyrimidine Absorption
No information avaliable
Sulfanilamidopyrimidine side effects and Toxicity
No information avaliable
Sulfanilamidopyrimidine Patient Information
No information avaliable
Sulfanilamidopyrimidine Organisms Affected
Enteric bacteria and other eubacteria
