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Sulfadiazine
Seres nomen: Sulfadiazine
Seres alias: N-2-pyrimidinyl-4-aminobenzenesulfonamide;sulfadiazine-D4;Da'anjing;sulfadiazine;2-p-aminobenzenesulfonamidepyrimidine;
Nomen anglicum: sulfadiazine
Anglicus alias: Sulfadiazine;A-306;Benzenesulfonamide, 4-amino-N-2-pyrimidinyl-;Adiazin;rp2616;PYRIMAL;sulphadiazine;Diazin;DIAZYL;DEBENAL;4-Amino-N-pyrimidin-2-yl-benzenesulfonamide;SD-Na;Trisem;
CAS No.: 68-35-9
MDL No.: MCD00006065
EINECS number: 200-685-8
RTECS No.: WP1925000
BRN Number: 6733588
PubChem Number: 24899802
Formulae hypotheticae: C 10 H 10 N 4 O 2 S
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Sulfadimethoxine Sodium
Corporalis proprietatibus Appearance】White vel off-album pulveris ad locus temperatus.Solubilitas in aqua et diluta solutiones inorganicae acidi.Stabilitas chemicae proprietatum cas registration number】1037-50-9 EINECS registration number】213-859-3【Moleculares pondus】332.31 -Reactiones communes chemicas Substitutionem reactionem proprietatum in circulos amineos et benzene annulos.【Incompatible materials】 Fortis acida, bases fortes, oxidantes fortes Poly... -
Sulfadimethoxine
Proprietates physicae Apparance Est alba vel off-alba crystallina vel crystallina pulveris in cella temperatura, fere inodora.punctum【760 mmHg（℃） 570.7 cusculum punctum】（℃） 202-206 Density】g/cm 3 1.441 Vapor pressuremmHg (℃) 4.92E-13(25) Solubilitas Insolubilis in aqua et chloroforme, in ethanolo leviter solutum, in acetone solutum, ac facile solutum in acido inorganico diluto et solutionibus alcali fortis.Chemical possessiones 【CAS registration number】122-112 E... -
Praziquantel
Praziquantel compositum organicum cum formula chemica C 19 H 24 N 2 O 2 .Est anthelmintica usus in hominibus et animalibus.Solet proprie tractare taenias et fluces.Maxime efficax est contra schistosoma japonicum, dente hepate Sinensi, et Diphyllobothrium latum.
Formulae chemicae: C 19 H 24 N 2 O 2
Pondus hypotheticum: 312.406
CAS No.: 55268-74-1
EINECS number: 259-559-6
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Sulfadiazine Sodium
Natrium sulfadiazinum est medium agens sulfonamideum antibioticum quod effectus antibacterial multos gram-positivos et gram-negativos bacteria habet.Effectus antibacterial in non-enzyme producentis Staphylococcus aureus, Streptococcus pyogenes, Streptococcus pneumoniae, Escherichia coli, Klebsiella, Salmonella, Shigella, Neisseria gonorrhoeae, Neisseria meningitidis, et Haemophilus influenzae.Activa praeterea est etiam contra Chlamydia trachomatis, Nocardia asteroides, Plasmodium, Toxoplasma in vitro.Actio antibacterial huius facti eadem est ac sulfamethoxazoli.Autem, his annis, resistentia bacterial huic producto crevit, praesertim Streptococcus, Neisseria, et Enterobacteriaceae.
