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| 货号 | 产品名 | CAS号 | 信息 |
|---|---|---|---|
| CSN12882 | Toltrazuril | 69004-03-1 | Toltrazuril is an antiprotozoal agent used in Coccidia parasites infection. |
| CSN12911 | 5,7-Dichloro-2-methylquinolin-8-ol | 72-80-0 | Chlorquinaldol is a halogenated hydroxyquinoline mainly applied topically in infected skin conditions and in vaginal infections. |
| CSN12925 | Imipenem monohydrate | 74431-23-5 | Imipenem Monohydrate is a broad-spectrum, semi-synthetic β-lactam carbapenem antibiotic derived from thienamycin. |
| CSN12926 | Sodium (6R,7R)-7-((Z)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetamido)-3-(((2-methyl-5,6-dioxo-1,2,5,6-tetrahydro-1,2,4-triazin-3-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | 958633-51-7 | Ceftriaxone Sodium is the third-generation cephalosporin useful for the treatment of a number of bacterial infections. |
| CSN12940 | 1-((2R,3R,4R,5R)-3-Fluoro-4-hydroxy-5-(hydroxymethyl)-3-methyltetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione | 863329-66-2 | PSI-6206, the deaminated derivative of PSI-6130, is a selective inhibitor of HCV NS5B polymerase and the EC50 for inhibition of HCV replicon is > 100 μM. |
| CSN12957 | Silmitasertib | 1009820-21-6 | CX-4945 is a potent and selective ATP-competitive small molecule protein kinase CK2 inhibitor with a Ki and an IC50 of 0.38 and 1 nM for recombinant human CK2α, respectively. |
| CSN12959 | 4,4'-Sulfonyldianiline | 80-08-0 | Dapsone is a sulfone with anti-inflammatory immunosuppressive properties as well as antibacterial and antibiotic properties. |
| CSN12979 | 9-Fluoro-3-methyl-10-(4-methylpiperazin-1-yl)-7-oxo-3,7-dihydro-2H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid | 82419-36-1 | Ofloxacin, a fluoroquinolone compound, can inhibit bacterial DNA gyrase. |
| CSN12993 | Diniconazol | 83657-24-3 | Diniconazole is a broad-spectrum triazole fungicide working by inhibiting ergosterol biosynthesis via inhibition of the cytochrome P450-dependent 14α-demethylation of lanosterol. |
| CSN13000 | Isopropyl ((S)-((((R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)(phenoxy)phosphoryl)-L-alaninate | 379270-37-8 | GS-7340 is the prodrug of tenofovir which inhibits reverse transcriptase and is used to treat HIV and hepatitis B. |
| CSN13003 | Itraconazole | 84625-61-6 | Itraconazole is a relatively potent inhibitor of CYP3A4 with IC50 of 6.1 nM, used as a triazole antifungal agent. |
| CSN13053 | Fluconazole | 86386-73-4 | Fluconazole, an inhibitor of CYP2C19, CYP2C9 and CYP3A4, is a triazole antifungal drug used in the treatment and prevention of superficial and systemic fungal infections. |
| CSN13068 | 4-Chloro-3,5-dimethylphenol | 88-04-0 | Chloroxylenol is an antiseptic and disinfectant which is used for skin disinfection and cleaning surgical instruments. |
| CSN13071 | 4-Oxo-4-(((3R,5aS,6R,8aS,9R,10R,12R,12aR)-3,6,9-trimethyldecahydro-3H-3,12-epoxy[1,2]dioxepino[4,3-i]isochromen-10-yl)oxy)butanoic acid | 88495-63-0 | Artesunate is a part of the artemisinin group of agents with an IC50 of < 5 μM for small cell lung carcinoma cell line H69. It is a potential inhibitor of STAT-3 and EXP1 and exhibits selective cytotoxicity of cancer cells over normal cells in vitro. |
| CSN13081 | 1-Cyclopropyl-7-(4-ethylpiperazin-1-yl)-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid | 93106-60-6 | Enrofloxacin is a fluoroquinolone antibiotic used as a veterinary antibacterial agent. |
| CSN13089 | (4S,4aS,5aS,6S,12aS)-7-Chloro-4-(dimethylamino)-3,6,10,12,12a-pentahydroxy-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydrotetracene-2-carboxamide hydrochloride | 64-73-3 | Demeclocycline HCl is a tetracycline antibiotic used for the treatment of bacterial infections, such as Lyme disease, acne, and bronchitis. |
| CSN13145 | (2S,5R,6R)-6-((R)-2-Amino-2-(4-hydroxyphenyl)acetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid | 26787-78-0 | Amoxicillin is an antibiotic used for the treatment of a number of bacterial infections. |
| CSN13184 | Fusidate Sodium | 751-94-0 | Fusidic Acid Sodium is an antibiotic working by inhibition of protein synthesis in prokaryotes through inhibiting the ribosome-dependent activity of G factor and translocation of peptidyl-tRNA. |
| CSN13486 | Tetramisole HCl | 5086-74-8 | Tetramisole HCl is an inhibitor of alkaline phosphatases, is used to treat parasitic worm infections. |
| CSN13497 | (4R,12aS)-N-(2,4-Difluorobenzyl)-7-hydroxy-4-methyl-6,8-dioxo-3,4,6,8,12,12a-hexahydro-2H-pyrido[1',2':4,5]pyrazino[2,1-b][1,3]oxazine-9-carboxamide | 1051375-16-6 | Dolutegravir is an integrase inhibitor (IC50= 2.7 nM), modest activity against raltegravir-resistant signature mutants Y143R, Q148K, N155H, and G140S/Q148H. |
| CSN13578 | Fosamprenavir Calcium Salt | 226700-81-8 | Fosamprenavir Calcium the prodrug of amprenavir which is an HIV protease inhibitor with antiviral property. |
| CSN13585 | Tedizolid | 856866-72-3 | Tedizolid is an oxazolidinone-class antibiotic used to treat for acute bacterial skin and skin structure infections, working by inhibition of protein synthesis by binding to the 50S ribosomal subunit of the bacteria. |
| CSN13704 | Dasabuvir | 1132935-63-7 | ABT-333 is an inhibitor of the RNA-dependent RNA polymerase with IC50 range from 2.2 nM to 10.7 nM. |
| CSN13065 | Salicylanilide | 87-17-2 | Salicylanilides can inhibit HIV-1 integrase or reverse transcriptase with potent antiviral activity. |
| CSN13600 | Gatifloxacin mesylate | 316819-28-0 | Gatifloxacin is an antibiotic of the fourth-generation fluoroquinolone family, it inhibits the bacterial enzymes DNA gyrase and topoisomerase IV. |
| CSN12894 | Cercosporamide | 131436-22-1 | Cercosporamide is a potent and selective Mnk inhibitor, and an orally bioavailable antifungal agent, suppresses phosphorylation of eIF4E and exhibits antileukemic effects. |
| CSN12996 | (2R,3S,4R,5R,8R,10R,11R,12S,13S,14R)-11-(((2S,3R,4S,6R)-4-(Dimethylamino)-3-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-2-ethyl-3,4,10-trihydroxy-13-(((2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyltetrahydro-2H-pyran-2-yl)oxy)-3,5,6,8,10,12,14-heptamethyl-1-oxa-6-azacyclopentadecan-15-one | 83905-01-5 | Azithromycin is an antibiotic for inhibition of parasite growth with IC50 of 8.4 μM. |
| CSN12898 | (3R,5aS,6R,8aS,9R,10S,12R,12aR)-10-Methoxy-3,6,9-trimethyldecahydro-3H-3,12-epoxy[1,2]dioxepino[4,3-i]isochromene | 71963-77-4 | Artemether is an antimalarial for the treatment of resistant strains of falciparum malaria. |
| CSN13200 | Tetrahydroxysqualene | 1043629-23-7 | Tetrahydroxysqualene is a natural product isolated and purified from the barks of Toxicodendron vernicifluum exhibiting antimycobacterial activity with an MIC of 10.0 mg/mL, while showing only modest cytotoxicity. |
| CSN13079 | 9-Nitrocamptothecin | 91421-42-0 | Rubitecan is an oral topoisomerase inhibitor. |
| CSN13316 | 6,8-Diprenylgenistein | 51225-28-6 | 6,8-Diprenylgenistein is a natural product isolated and purified from the roots of Lupinus mutabilis with antimicrobial activity against Gram-negative and Gram-positive bacteria. |
| CSN13095 | Pterodondiol | 60132-35-6 | Pterodondiol has moderate activity against bacteria including Staphylococcus aureus, Pseudomonas aeruginosa, Bacillus subtilis, Mycobacteium phlei and Bacillus circulans. |
| CSN13048 | Ciprofloxacin | 85721-33-1 | Ciprofloxacin is a fluoroquinolone antibiotic, shows broad and potent antibacterial activity, with MIC90 of 0.024-6 μM. |
| CSN13063 | PSI-6130 | 817204-33-4 | PSI-6130 is a potent and selective inhibitor of HCV NS5B polymerase. |
| CSN13187 | R-1479 | 478182-28-4 | R-1479 is a specific inhibitor of HCV replication in the HCV subgenomic replicon system (IC50=1.28 μM). |
| CSN13659 | Pivmecillinam HCl | 32887-03-9 | Pivmecillinam HCl is a pivaloyloxymethyl ester of amdinocillin with improved bioavailability mainly used to treat urinary tract infections. |
| CSN13681 | Fosfluconazole | 194798-83-9 | Fosfluconazole is a prodrug of Fluconazole that is widely used as an antifungal agent. |
| CSN13696 | Radezolid | 869884-78-6 | Radezolid is an oxazolidinone antibiotic agent. |
| CSN12875 | 1-Docosanol | 661-19-8 | 1-Docosanol is an inhibitor of lipid-enveloped viruses which can inhibit replication of herpes simplex virus and respiratory syncytial virus. |
| CSN12927 | Ornidazole (Levo-) | 166734-83-4 | Levo-ornidazole is the levo-isomer of ornidazole. |
| CSN13462 | Bicyclol | 118159-48-1 | Bicyclol is an anti-hepatitis drug. |
| CSN12955 | (S)-6-(3-Chloro-2-fluorobenzyl)-1-(1-hydroxy-3-methylbutan-2-yl)-7-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid | 697761-98-1 | Elvitegravir is a quinolinemonocarboxylic-acid HIV-1 integrase strand transfer inhibitor used to treat HIV infection. It is also a cytochrome P450 2C9 inducer. |
| CSN12977 | 2-Amino-9-(((1,3-dihydroxypropan-2-yl)oxy)methyl)-1H-purin-6(9H)-one | 82410-32-0 | Ganciclovir is a potent inhibitor of viruses of the herpes family, working as a competitive inhibitor of deoxyguanosine triphosphate (dGTP) incorporation into DNA and preferentially inhibits viral DNA polymerases more than cellular DNA polymerases. |
| CSN12990 | Methyl ((S)-1-((S)-2-(5-(4'-(2-((S)-1-((methoxycarbonyl)-L-valyl)pyrrolidin-2-yl)-1H-imidazol-5-yl)-[1,1'-biphenyl]-4-yl)-1H-imidazol-2-yl)pyrrolidin-1-yl)-3-methyl-1-oxobutan-2-yl)carbamate | 1009119-64-5 | Daclatasvir is a first-in-class, highly-selective oral HCV NS5A inhibitor. |
| CSN13623 | Flumorph | 211867-47-9 | Flumorph is a carboxylic acid amide (CAA) fungicide. |
| CSN13108 | Meropenem | 96036-03-2 | Meropenem is a carbapenem antibiotic, which displaying a broad spectrum of antibacterial activity. |
| CSN13640 | Anacardic Acid | 16611-84-0 | Anacardic acid is a potent inhibitor of p300 and p300/CBP-associated factor histone acetyltranferases, which also has antibacterial activity, antimicrobial activity,prostaglandin synthase inhibition, and tyrosinase and lipoxygenase inhibition. |
| CSN12909 | Retapamulin | 224452-66-8 | Retapamulin is the first agent in the new pleuromutilin class of antibacterials, used as a topical antibiotic. |
| CSN12913 | Sulfacetamide Sodium | 6209-17-2 | Sulfacetamide Sodium Monohydrate is a synthetic sulfanylacetamide, working by inhibiting bacterial folic acid synthesis through competing with para amino benzoic acid. |
