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Floxin; Exocin; Tarivid; Pt01; Floxal; Visren; Oflx; Oflox; Floxil; Hoe280; (+/-)-9-Fluoro-2, 3-Dihydro-3-Methyl-10-(4-Methyl-1-Piperazinyl)-7-Oxo-7H-Pyrido[1,2,3-De]-1,4-Benzoxazine-6-Carboxylic Acid; Akos Ncg1-0050; (-)-(S)-9-Fluoro-2,3-Dihydro-3-Methyl-10-(4-Methyl-1-Piperazin-Yl)-7-Oxo-7H-Pyrido(1,2,3-De)-1,4-Benzoxazine-6-Carboxylic Acid
Brief Introduction
Ofloxacin is a broad-spectrum antibacterial drug, which is effective against bacteria, mycoplasma and some anaerobic bacteria. It is mainly used for acute and chronic infections of respiratory tract, throat, tonsil and urinary tract caused by sensitive bacteria, including prostate, skin and soft tissue, intestinal tract and otorhinalogy.
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CAS:86386-73-4
Molecular Formula:C13H12F2N6O
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A.-(2,4-Difluorophenyl)-A-(1H-1,2,4,-Triazol-1-Ylmethyl)-1H-1,2 ,4-Triazole-1-Ethanol; 2-(2,4-Difluorophenyl)-1,3-Di(1H-1,2,4-Triazol-1-Yl)Propan-2-Ol; 2,4-Difluoro-Alpha,Alpha-1-Bis(1H-1,2,4-Triazol-1-Ylmethyl)Benzylalcohol; Flucanazole
Brief Introduction
The antifungal spectrum of this product is similar to that of ketoconazole, and its antibacterial activity is stronger than that of ketoconazole. The mechanism of action is to inhibit ergosterol synthetase, which is an essential component of fungal cell membrane, to block the synthesis of ergosterol, to destroy the integrity of fungal cell wall, and to inhibit its growth and reproduction. This product has strong antibacterial activity against Candida albicans, Microsporum and Microsporum, Cryptococcus neoformans, tinea epidermidis and Histoplasma capsulatum.
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CAS:122-11-2
Molecular Formula:C12H14N4O4S
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4-Amino-N-(2,6-Dimethoxy-4-Pyrimidinyl)Benzenesulfonamide; 4-Amino-N-(2,6-Dimethoxypyrimidin-4-Yl)Benzenesulfonamide; Benzenesulfonamide, 4-Amino-N-(2,6-Dimethoxy-4-Pyrimidinyl)-; Sulphadimethoxine; Sulfadimethoxin; Sulfadimethoxydiazine
Brief Introduction
Sulfonamides that block dihydrofolate synthesis by inhibiting dihydrofolate synthase. Mode of action: inhibit folate synthesis in prokaryotes. Antibacterial spectrum: resistance mechanism of Gram-positive bacteria, Gram-negative bacteria and Chlamydia: change of dihydrofolate synthase or alternative path of folate synthesis.
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CAS:1392275-56-7
Molecular Formula:C46H62N12O14P2
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Tenofovir Alafenamide Hemifumarate; GS-7340 Hemifumarate; Vemlidy; 1-Methylethyl N-((S)-(((1R)-2-(6-Amino-9H-Purin-9-yl)-1-Methylethoxy)Methyl)Phenoxyphosphinoyl)-L-Alaninate,(2E)-2-Butenedioate; Tenofovir Alafenamide Fumarate, 2:1; L-Alanine,N-((S)-(((1R)-2-(6-Amino-9H-Purin-9-yl)-1-Methylethoxy)Methyl)Phenoxyphosphinyl)-,1-Methylethyl Ester,(2E)-2-Butenedioate (2:1); TAF
Brief Introduction
Tenofovir eilanolamine fumarate can be used as solvent, catalyst for alkylation, esterification and polymerization. 99% of the products are mainly used in medicine and 70% are mainly used in electroplating industry. Nutritional drugs, combined with low protein diet, prevent and treat the damage caused by protein metabolism disorder caused by chronic renal insufficiency, and are the core drugs for chronic renal insufficiency and consumptive malnutrition.
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98.0%-102.0%
/
Pharm Grade
10kg
/
BOTTLE
CAS:147403-03-0
Molecular Formula:C25H20N4O5
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Azilva; Azilsartane; 1H-Benzimidazole-7-Carboxylic Acid,1-[[2'-(2,5-Dihydro-5-Oxo-1,2,4-Oxadiazol-3-Yl)[1,1'-Biphenyl]-4-Yl]Methyl]-2-Ethoxy; 2-Ethoxy-3-[[4-[2-(5-Oxo-2H-1,2,4-Oxadiazol-3-Yl)Phenyl]Phenyl]Methyl]Benzimidazole-4-Carboxylic Acid; 2-Ethoxy-1-[[2'-(4,5-Dihydro-5-Oxo-1,2,4-Oxadiazol-3-Yl)Biphenyl-4-Yl]Methyl]Benzimidazole-7-Carboxylic Acid
Brief Introduction
Azilsartan is an angiotensin II receptor antagonist drug under development for the treatment of hypertension. It is mostly used for the treatment of hypertension. It is also the only angiotensin II receptor antagonist (sartan) drug in late clinical stage.
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