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Antibiotic Antibiotic/Antibacterial

Cat.No.  Name Information
M3669 Micafungin Sodium Micafungin Sodium is an inhibitor of 1, 3-beta-D-glucan synthesis, it is an antifungal agent.
M5868 Penicillin G Sodium Penicillin G Sodium is a β-lactam antibiotic produced by Penicillin spp.
M4947 Streptomycin sulfate Streptomycin sulfate is an antibiotic produced by the soil actinomycete Streptomyces griseus. It acts by inhibiting the initiation and elongation processes during protein synthesis.
M4323 Physcion Physcion is an anthraquinone from roots of Rheum officinale Baill.
M2719 G-418 disulfate G-418 disulfate (Geneticin) blocks polypeptide synthesis by inhibiting the elongation step in both prokaryotic and eukaryotic cells.
M5415 Amphotericin B Amphotericin B (AmB) is an amphipathic polyene antibiotic which permeabilizes ergosterol-containing membranes.
M3594 Neomycin sulfate Neomycin sulfate belongs to a class of antibiotics known as the aminoglycosides.
M2391 Ampicillin Trihydrate Ampicillin Trihydrate is a β-lactam antibiotic, which inhibits bacterial cell-wall synthesis (peptidoglycan cross-linking) by inactivating transpeptidases on the inner surface of the bacterial cell membrane.
M3311 Metronidazole Metronidazole is a nitroimidazole antibiotic that is used specifically for anaerobic bacteria and protozoa.
M4862 Vancomycin HCl Vancomycin HCl is a hydrochloride of vancomycin that is a narrow-spectrum glycopeptide antibacterial agent.
M7845 Imipenem monohydrate Imipenem monohydrate is a broad spectrum B-lactam antibiotic. Imipenem monohydrate has the excellent activity against a broad range of gram-positive and gram-negative aerobic and anaerobic bacteria.
M7579 Tubercidin Tubercidin (7-deazaadenosine), an antibiotic obtained from Streptomyces tubercidicus, inhibits the growth of Streptococcus faecalis (8043) with an IC50 value of 0.02 μM. Tubercidin is a weak inhibitor of adenosine phosphorylase and interferes with the phosphorylation of adenosine and AMP. Tubercidin has antiviral activity.
M7574 DprE1-IN-1 DprE1-IN-1 is a potent DprE1 inhibitor, with ic50 of 10 nM, also inhibits PDE6, with IC50 of 6 uM.
M7522 5-Phenyl-2,4-pentadienoic acid 5-Phenyl-2,4-pentadienoic acid is used as Synthetic building block, anti-malarial agent.
M7516 Cefotiam hydrochloride Cefotiam hydrochloride is the hydrochloride salt form of cefotiam and has a broad spectrum of activity against both gram-positive and gram-negative microorganisms.
M7514 Cefcapene Pivoxil hydrochloride hydrate Cefcapene pivoxil hydrochloride hydrate is the pivalate ester prodrug form of cefcapene, a semi-synthetic third-generation cephalosporin with antibacterial activity.
M7513 Cefuroxime axetil Cefuroxime axetil, a prodrug of the cephalosporin cefuroxime, is a second generation oral cephalosporin antibiotic with in vitro antibacterial activity against several gram-positive and gram-negative organisms.
M7512 Chlorotetracycline Chlortetracycline is a tetracycline antibiotic and commonly used to treat conjunctivitis in cats.
M7511 Ceftizoxime Ceftizoxime is a semisynthetic cephalosporin antibiotic which can be administered intravenously or by suppository. It is highly resistant to a broad spectrum of beta-lactamases and is active against a wide range of both aerobic and anaerobic gram-positive and gram-negative organisms.
M7460 URB 602 URB602 is a selective monacylglycerol lipase (MGL) inhibitor with IC50 of 28±4 μM.
M7185 Radicicol Radicicol is a hsp90 inhibitor. Antifungal antibiotic.
M7160 Pristimerin Pristimerin is a highly reversible monacylglycerol lipase (MGL) inhibitor with an IC50 value of 93 nM.
M6903 Leptomycin B Leptomycin B (CI 940; LMB (LMB) is a protein exit nuclear transport inhibitor. Leptomycin deactivates CRM1/exportin 1 by covalent modification at cysteine residues. Leptomycin B is a potent antifungal antibiotic that blocks the eukaryotic cell cycle.
M6730 Filipin III Filipin III is a polyene antibiotic; inhibits formation of PrPSc.
M6529 BRD 7116 BRD 7116 is a inhibitor of leukemia stem cell activity.
M6349 5-Fluoroorotic acid 5-Fluoroorotic acid is a selection reagent for OMP decarboxylase mutants.
M6293 Tacrolimus monohydrate Tacrolimus monohydrate binds to FK506 binding protein (FKBP). This complex inhibits calcineurin phosphatase (PP2B). Tacrolimus monohydrate is a mTOR-independent autophagy inducer.
M6289 Erythromycin cyclocarbonate Erythromycin Cyclocarbonate, derivative of Erythromycin, inhibits protein synthesis of bacteria by binding to the 50S ribosome.
M6239 Delpazolid Delpazolid is a novel oxazolidinone antibiotic agent which can inhibit the growth of MSSA and MRSA with a MIC90 of 2 μg/mL for both of them.
M6229 Kanamycin sulfate Kanamycin sulfate is an aminoglycoside antibiotic that acts as a bacteriostatic agent by binding to the bacterial 30S ribosome.




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