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CAS:7681-54-1
Molecular Formula:C19H15ClNNaO4
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Einecs 231-670-4; Indomethacin Sodium; Na Salt; 1H-Indole-3-Acetic Acid,1-(4-Chlorobenzoyl)-5-Methoxy-2-Methyl-,Sodium Salt; Sodium Indomethacin; Sodium 1-(4-Chlorobenzoyl)-5-Methoxy-2-Methyl-1H-Indole-3-Acetate; Osmosin
Brief Introduction
Indomethacin Sodium is the sodium salt of indomethacin, a methylated indole derivative with anti-inflammatory, analgesic-antipyretic and tocolytic effects. Indomethacin is a non-selective, reversible, and competitive inhibitor of cyclooxygenases 1 and 2, thereby blocking the conversion of arachidonic acid into prostaglandin precursors. Consequently, prostaglandin synthesis is decreased, and prostaglandin-mediated activities are prevented, including pain, inflammation, fever and uterine contraction.
CAS:7681-76-7
Molecular Formula:C6H8N4O4
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Ridazole; 2-Carbamoyloxymethyl-1-Methyl-5-Nitro-1H-Imidazole; Ridzol P; Ronidazol; Ronidazole; Dugro; 2-Carbamoyloxymethyl-1-Methyl-5-Nitro-Imidazol; Ridzol
Brief Introduction
It has the effects of anti parasite (Turkey flagellate, trichomoniasis), anti fumigation bacteria and anti bacteria. It is especially effective for Treponema compactum caused by porcine dysentery. In addition, it is also a good growth promoter, which can increase weight and improve feed conversion. It has good stability and compatibility. It can be mixed with other feed additives such as bacitracin zinc, nitrofurene hydrazone, oxytetracycline, chlortetracycline, Virginia, telosin and trace elements copper and zinc without adverse effects.
CAS:79-57-2
Molecular Formula:C22H24N2O9
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Adamycin; Macocyn; Oxytetracyclin; Tetran; La200; Oxypan; Terramycin; Oxypam; (4S,4Ar,5S,5Ar,6S,12As)-4-(Dimethylamino)-1,4,4A,5,5A,6,11,12A-Octahydro-3,5,6,10,12,12A-Hexahydroxy-6-Methyl-1,11-Dioxo-2-Naphthacenecarboxamide; Terramycin Dehydrate; Geotilin; (4S,4Ar,5S,5Ar,6S,12As)-4-(Dimethylamino)-3,5,6,10,12,12A-Hexahydroxy-6-Methyl-1,11-Dioxo-1,4,4A,5,5A,6,11,12A-Octahydrotetracene-2-Carboxamide; (4S,4Ar,5S,5Ar,6S,12As)-4-Dimethylamino-1,4,4A,5,5A,6,11,12A-Octahydro-3,5,6,10,12,12A-Hexahydroxy-6-Methyl-1,11-Dioxonaphthacene-2-Carboxamide; Tarosin; 2-Naphthacenecarboxamide, 4-(Dimethylamino)-1,4,4A,5,5A,6,11,12A-Octahydro-3,5,6,10,12,12A-Hexahydroxy-6-Methyl-1,11-Dioxo-,[4S-(4α,4Aα,5Aα,6β,12Aα)]-; Oxydon; Biostat; Terramicin; 12,12A-Hexahydroxy-6-Methyl-1,11-Dioxo-10; 4-(Dimethylamino)-1,4,4A,5,5A,6,11,12A-Octahydro-3,5,6,10,12,12A-Hexahydroxy-6-Methyl-1,11-Dioxo-,2-Naphthacenecarboxamide; 5-Hydroxy-Tetracyclin; 6,10,12,12A-Hexahydroxy-6-Methyl-1,11-Dioxo-,(4S-(4-Alpha,4A-Alpha,5-Alpha,5A; 6,10,12,12A-Hexahydroxy-6-Methyl-1,11-Dioxo-,[4S-(4Alpha,4Aalpha,5Alpha,5A; 6-Beta,12A-Alpha))--Alph; Antibiotictm25
Brief Introduction
Oxytetracycline is a broad-spectrum antibiotic extracted from the culture medium of Streptomyces bifida. Oxytetracycline can inhibit both Gram-positive and Gram-negative bacteria, and can also be used as a growth promoting agent. Oxytetracycline is a fast bacteriostatic agent with broad-spectrum antimicrobial activity. It can kill some bacteria at high concentration. The mechanism of action is that the drug can specifically bind to the a position of ribosomal 30S subunit to prevent the binding of aminoacyl tRNA at this position, thus inhibiting the growth of peptide chain and affecting the protein synthesis of bacteria or other pathogenic microorganisms. Oxytetracycline has strong antibacterial activity against Staphylococcus aureus, pneumococcus, Streptococcus pyogenes, Neisseria gonorrhoeae, meningococcus, Escherichia coli, aerobacillus, Shigella, Yersinia and Listeria monocytogenes; In addition, oxytetracycline also has strong effect on Rickettsia, mycoplasma, chlamydia, actinomycetes and so on.
CAS:79660-72-3
Molecular Formula:C17H18F3N3O3
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6,8-Difluoro-1-(2-Fluoroethyl)-1,4-Dihydro-4-Oxo-7-(4-Methyl-1-Piperazinyl)-Quinoline-3-Carboxylic Acid; Megalone; 6,8-Difluoro-1-(2-Fluoro-Ethyl)-1,4-Dihydro-7-(4-Methyl-1-Piperazinyl)-4-Oxo-3-Quinolinecarboxylic Acid; Ro23-6240/000; Am-833; Megalocin; 3-Quinolinecarboxylicacid,1,4-Dihydro-6,8-Difluoro-1-(2-Fluoroethyl)-7-(4-Met; Hyl-1-Piperazinyl)-4-Oxo; 6,8-Difluoro-1-(2-Fluoroethyl)-7-(4-Methylpiperazin-1-Yl)-4-Oxoquinoline-3-Carboxylic Acid; Quinodis; 6,8-Difluoro-1-(2-Fluoroethyl)-1,4-Dihydro-7-(4-Methyl-1-Piperazinyl)-4-Oxoquinoline-3-Carboxylic Acid; Ro-23-6240; Fleroxicin
Brief Introduction
Quinolones play a bactericidal role by inhibiting bacterial DNA gyrase. There is no cross resistance with other antibiotics. It is suitable for gonococcal urethritis, acute bronchitis, acute attack of chronic bronchitis, pneumonia, cystitis, pyelonephritis, prostatitis, chronic complex urinary tract infection, typhoid, bacillary dysentery, skin and soft tissue infection and abdominal infection caused by sensitive bacteria.
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Ceftiofur Acid; Excenel; Ceftifurhcl; Ceftiofur Hcl; Ceftiofurfreeacid; Unii-83Jl932I1C; Ceftiofurum
Brief Introduction
Ceftiofur is the third generation cephalosporin for veterinary medicine developed successfully in the United States in the 1980s. It was first listed in the United States in 1988. Due to its excellent antibacterial activity and pharmacokinetic characteristics, it has been officially approved by the United States, Canada, Japan and some European countries for the treatment of respiratory diseases of beef cattle, dairy cows, horses, pigs and sheep. The appearance is off white to light yellow powder. Insoluble in water, slightly soluble in acetone and almost insoluble in ethanol.
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