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Synthetic Anti Infective Drugs

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CAS:165800-03-3
Molecular Formula:C16H20FN3O4
N-{[(5S)-3-[3-Fluoro-4-(Morpholin-4-Yl)Phenyl]-2-Oxo-1,3-Oxazolidin-5-Yl]Methyl}Acetamide; (S)-N-((3-(3-Fluoro-4-Morpholinophenyl)-2-Oxooxazolidin-5-Yl)Methyl)Acetamide; Linezolid (S)-N-[[3-(3-Fluoro-4-Morpholinylphenyl)-2-Oxo-5-Oxazolidinyl]Methyl]Acetamide
Brief Introduction
This product is a fully synthetic oxazolidinone antibiotic, which is a kind of oxazolidinone antibiotic. It is an antipyretic and analgesic drug.
CAS:186826-86-8
Molecular Formula:C21H25ClFN3O4
Avelox; (1'S,6'S)-1-Cyclopropyl-7-(2,8-Diazabicyclo[4.3.0]Non-8-Yl)-6-Fluoro-8-Methoxy-4-Oxo-(1,4-Dihydroquinoline)-3-Carboxylic Acid Hydrochloride Salt; 1-Cyclopropyl-6-Fluoro-1,4-Dihydro-8-Methoxy-7-[(4As,7As)-Octahydro-6H-Pyrrolo-[3,4-B]Pyridin-6-Yl]-4-Oxo-3-Quinolinecarboxylic Acid Hydrochloride; 1-Cyclopropyl-6-Fluoro-8-Methoxy-7-[(4As,7As)-Octahydropyrrolo[3,4-B]Pyridin-6-Yl]-4-Oxo-1,4-Dihydroquinoline-3-Carboxylic Acid Hydrochloride; Moxifloxacin (Hydrochloride); Moxifloxacinehcl; Bay-12-8039; Actira; Moxifloxacinehydrochloride; Proflox; 1-Cyclopropyl-7-(S,S)-2,8-Diazabicyclo(4.3.0)-Non-8-Yl-6-Fluoro-8-Methoxy-1,4-Dihydro-4-Oxo-3-Quinoline Carboxylic Acid Hydrochloride; Moxifloxacin Hcl; Moxifloxacin; Avalox
Brief Introduction
Moxifloxacin hydrochloride is a fluoroquinolone antibiotic developed by Bayer medicine of Germany. Its mechanism of action and antibacterial spectrum in vitro are similar to other fluoroquinolones, but its antibacterial activity against Gram-positive bacteria and anaerobic bacteria is similar to that of travafloxacin, which is superior to some old varieties. Compared with other fluoroquinolones, there were few or slow resistant Gram-positive bacteria. Cross resistant bacteria with other fluoroquinolones were found in Gram-negative bacteria and Enterococcus. Moxifloxacin hydrochloride can be used in the treatment of social acquired pneumonia, acute attack of chronic bronchitis and acute sinusitis caused by Staphylococcus aureus, influenza bacillus, pneumococcus, Moraxella mucositis, and pneumonia.
CAS:2022-85-7
Molecular Formula:C4H4FN3O
5-Fluorocytosine; 4-Amino-5-Fluoro-2(1H)-Pyrimidinone,5-Fluorocytosine,Flucytosine; 4-Amino-5-Fluoro-1,2-Dihydropyrimidin-2-One; 4-Amino-5-Fluoro-2(1H)-Pyrimidinone,Flucytosine; 4-Amino-5-Fluoro-2-Pyrimidone; Fluocytosine; Ancotil; 5-Fluorocytosin; Fluorcytosine; 6-Amino-5-Fluoro-1H-Pyrimidin-2-One; Flucytosin; 5-Fluorocystosine; 4-Amino-5-Fluoro-2-Hydroxypyrimidine; 4-Amino-5-Fluoro-2(1H)-Pyrimidinone; Ancobon; Fluorocytosine
Brief Introduction
5-fluorocytosine (5-FC), also known as 5-fluorocytosine, 5-fluorocytidine, anjezhi, and anlapen, is a white or quasi white crystalline powder. The inhibitory effect of 5-fluorocytosine on fungi is due to its entering into the cells of sensitive fungi, and under the action of cytosine deaminase, 5-fluorouracil, an anti metabolite, is formed. The latter is converted to 5-fluorouracil-2-deoxyriboside, which inhibits thymidine synthase, blocks the conversion of 5-fluorouracil-2-deoxyriboside to thymidine, and affects DNA synthesis. It has a good inhibitory effect on Candida, Cryptococcus and hyphomycetes, and also has an effect on some Aspergillus, as well as mycospores and bottle fungi which cause skin fungal diseases.
CAS:3697-42-5
Molecular Formula:C22H32Cl4N10
Chlorhexidine Dihydrochloride; Chlorhexidine HCl; CHH; Chlorhexidine (Dihydrochloride)
Brief Introduction
Chlorhexidine (chlorhexidine) is a chemically synthesized broad-spectrum antibacterial and bactericidal drug. It has a strong inhibitory and killing effect on Gram-negative and positive bacteria. It is a strong antiseptic disinfectant widely used at home and abroad. Usage: suitable for burn, scald, wound disinfection, skin disinfection, medical equipment disinfection, sterile room disinfection, etc. Features: rapid and lasting effect; It is hardly absorbed by the body, so it has no toxic and side effects, and does not produce drug resistance after long-term use.
CAS:5508-58-7
Molecular Formula:C20H30O5
Andrographis; Rhizoma Sparganii; Andrographolid; Andrographis Paniculata(Burm.f) Nees; Andro; Andrographalide; Ent-(3β,12E,14R)-3,14,19-Trihydroxy-8(17),12-Labdadien-16,15-Olide; Andrographolide/Andrographis Paniculata P.E.; 5-Alpha,6-Alpha,8A-Alpha))-T; 2(3H)-Furanone,3-(2-(Decahydro-6-Hydroxy-5-(Hydroxymethyl)-5,8A-Dimethyl-2-Met; 3-(2-(Decahydro-6-Hydroxy-5-(Hydroxymethyl)-5,8A-Dimethyl-2-Methylene- 1-Naphthalenyl)Ethylidene)Dihydro-4-Hydroxy-, (1R-(1-Alpha(E(S*)),4A-Beta,5- Alpha,6-Alpha,8A-Alpha))-2(3H)-Furanone; (3E,4S)-3-[2-[(1R,4As,5R,6R,8As)-1,2,3,4,4A,5,6,7,8,8A-Decahydro-6-Hydroxy-5-(Hydroxymethyl)-5,8A-Dimethyl-2-Methylenenaphthalene-1-Yl]Ethylidene]Dihydro-4-Hydroxy-2(3H)-Furanone; (S)-3-[(E)-2-[[(1R,4Aα)-Decahydro-6β-Hydroxy-5β-Hydroxymethyl-5,8Aβ-Dimethyl-2-Methylenenaphthalen]-1β-Yl]Ethylidene]Dihydro-4-Hydroxy-2(3H)-Furanone
Brief Introduction
Andrographolide is a labdane diterpenoid that has been isolated from the stem and leaves of Andrographis paniculata. Andrographolide is an extremely bitter substance. Andrographolide has been studied for its effects on cell signaling, immunomodulation, and stroke. Study has shown that andrographlide may bind to a spectrum of protein targets including NF-κB and actin by covalent modification.
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