| 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. Neomycin is suitable for resistance screening in common prokaryotic cells. For resistance screening in eukaryotic cells using the neo gene (neomycin resistance gene) as a marker, G418 (M2719) is recommended. |
| 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. Vancomycin hydrochloride acts by inhibiting the second stage of cell wall synthesis of susceptible bacteria. Vancomycin also alters the permeability of the cell membrane and selectively inhibits ribonucleic acid synthesis. |
| M2652 | Doxycycline monohydrate | Doxycycline monohydrate is a tetracycline antibiotic that commonly used to treat a variety of infections and MMP inhibitor. |
| M2404 | Apramycin Sulfate | Apramycin is an aminoglycoside antibiotic, which binds to the deep groove of the RNA. |
| M2387 | Aminothiazole | Aminothiazole can be used as a thyroid inhibitor and it has antibacterial activity. |
| M2269 | Tigecycline | Tigecycline (GAR-936) is a broad-spectrum glycylcycline antibiotic. The mean inhibitory concentration (MIC) of Tigecycline for E. coli (MG1655 strain) is approximately 125 ng/mL. |
| M2259 | Biapenem | Biapenem is a new parenteral carbapenem antibacterial agent with a broad spectrum of in vitro antibacterial activity. |
| M2254 | Gatifloxacin | Gatifloxacin is an antibiotic of the fourth-generation fluoroquinolone family. |
| M2168 | Aztreonam | Aztreonam is a synthetic monocyclic beta-lactam antibiotic. |
| M2009 | Teicoplanin | Teicoplanin is a long-acting glycopeptide antibiotic derived from actinomycetes that inhibits cell wall synthesis and interferes with the process of synthesizing new portions of peptidoglycan, and has a good inhibitory effect on gram-positive pathogens (including staphylococcal biofilms). |
| M1958 | Natamycin | Natamycin is an antifungal polyene macrolide that binds specifically to ergosterol and blocks fungal growth. |
| M1939 | Sulfadimethoxine | Sulfadimethoxine (trade name Di-Methox, Albon) is a sulfonamide antibiotic. |
| M1938 | Daptomycin | Daptomycin is the first member of a new class of bactericidal antibiotics, the cyclic lipopeptides. |
| M1870 | Marbofloxacin | Marbofloxacin is a potent antibiotic of the 3rd generation fluoroquinolone group which inhibiting bacterial DNA replication. |
| M1587 | Hydroxy Itraconazole | Itraconazole metabolite Hydroxy Itraconazole is an active metabolite of Itraconazole (ITZ), which is a triazole antifungal agent. |
| M1546 | Amphotericin B Solubilized | Amphotericin B Solubilized is a powdery form composed of amphotericin sodium deoxycholate and a buffer. This special design enables amphotericin B can be completely dissolved in aqueous solution. |
| M59404 | Mandelic acid | Mandelic acid ((±)-Mandelic acid), an alpha-hydroxycarboxylic acid, has been widely used as an intermediate of pharmaceutical and fine chemicals. |
| M59403 | MP265 | MP265 (4-Chlorobenzyl carbamimidothioate hydrochloride) is a structural analogue of A22 but is less toxic. |
| M59235 | PXYC1 | PXYC1 is a ribosomal protein S1 (RpsA) antagonist with Kd values of 0.81 and 0.31 μM for RpsA-CTD and RpsA-CTD Δ438A, respectively. |
| M59198 | Pulcherriminic acid | Pulcherriminic acid is a cyclic dipeptide antimicrobial agent with high affinity for Fe3+. Pulcherriminic acid chelates iron ions through a non-enzymatic reaction to form the extracellular red pigment pulcherrimin, which competes for iron nutrition and thus achieves an antibacterial effect. |
| M59142 | DATPT | DATPT is a 12WLVSKF17 peptide-mimetic molecule, with anti-inflammatory and antibacterial activities. DATPT blocks the SNX9-p47phox interaction in the endosome and suppresses reactive oxygen species and inflammatory cytokine production. |
| M58694 | Puromycin-d3 | Puromycin-d3 is the deuterium labeled Puromycin. Puromycin dihydrochloride is the dihydrochloride salt of puromycin. Puromycin is an aminoglycoside antibiotic that inhibits protein synthesis. |
| M58693 | BSH-IN-1 | BSH-IN-1 is a potent and covalent inhibitor of gut bacterial recombinant bile salt hydrolases (BSHs) with IC50s of 108 nM and 427 nM for B. longum BSH (Gram positive) and B. theta BSH (Gram negative), respectively. |
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