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. |
M4862 | Vancomycin HCl | Vancomycin HCl is a hydrochloride of vancomycin that is a narrow-spectrum glycopeptide antibacterial agent. |
M2652 | Doxycycline monohydrate | Doxycycline monohydrate is a tetracycline antibiotic that commonly used to treat a variety of infections and MMP inhibitor. |
M9186 | Bedaquiline | Bedaquiline (TMC207) is a diarylquinoline antibiotic that targets ATP synthase, can be used for the research of Mycobacterium tuberculosis infections. |
M9163 | Blasticidin S hydrochloride | Blasticidin S HCl is a potent inhibitor of protein synthesis in both prokaryotic and eukaryotic cells. Blasticidin S hydrochloride is a nucleoside antibiotic isolated from Streptomyces griseochromogenes. |
M9030 | Cefquinome sulfate | Cefquinome sulfate is a broad-spectrum fourth-generation cephalosporin antibiotic. |
M8982 | Azaserine | Azaserine is an inhibitor of the rate limiting step of the hexosamine biosynthethic pathway (HBP) and an irreversible inhibitor of GGT1 (gamma-Glutamyltranspeptidase). |
M8883 | Ceforanide | Ceforanide is a new cephalosporin with antibacterial activity and has a longer elimination half-life than any currently available cephalosporin. |
M8842 | Valinomycin | Valinomycin is a K+-selective ionophoric cyclodepsipeptide; potassium ionophore which uncouples oxidative phosphorylation, induces apoptosis in murine thymocytes, inhibits NGF-induced neuronal differentiation and antagonizes ET-induced vasoconstriction. |
M8824 | Taurolidine | Taurolidine is a broad spectrum antibiotic with antineoplastic activity, which induces apoptosis and decreases tumor cell proliferation. |
M8276 | Pleuromutilin | Pleuromutilin is an antibiotic natural product that inhibits bacterial protein synthesis by binding to bacterial ribosomes in the peptidyl transferase center and inhibiting peptide bond formation. |
M8037 | Sutezolid | Sutezolid (PNU-100480), an orally active oxazolidinone antimicrobial agent, acts by inhibiting bacterial protein synthesis. Sutezolid has potent activity against mycobacteria, and is used for the research of drug-resistant tuberculosis. |
M7963 | Nalidixic acid sodium salt | Nalidixic acid sodium salt is an inhibitor of bacterial DNA polymerase (DNA gyrase) and avian myeloblastoma virus reverse transcriptase. Nalidixic acid sodium salt is a quinolone antibiotic, it is effective against both gram-positive and gram-negative bacteria. Nalidixic acid acts in a bacteriostatic manner in lower concentrations and is bactericidal in higher concentrations. |
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 broad-spectrum antibiotic tetracycline with a 7-chloro substitution. It inhibits growth of both Gram-negative and Gram-positive bacteria by inhibiting protein synthesis. |
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. |
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