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. |
M4356 | β-Mangostin | Beta-mangostin (β -mangostin) is a compound of oxyxanthone present in Cratoxylum arborescens, which has antibacterial and antimalarial activities. The MIC value of beta-mangostin against M. tuberculosis was 6.25 μg/mL. Beta-mangostin showed anti-malarial activity in vitro with IC50 value of 3.00 μg/mL against P. falciparum. Beta-mangostin has strong anticancer activity against various cancers, such as hepatocellular carcinoma and leukemia. |
M4342 | Isoshaftoside | Isoschaftosid is a C-glycosylated flavonoid extracted from the root exudate of Desmodium uncinatum, which can inhibit the growth of s. Hermonthica embryo. |
M4294 | Magnoflorine-iodide | (+) -magnoflorine iodide (Magnoflorine iodide) is an apomorphine alkaloid from Acoruscalamus that reduces the formation of c. albicans biofilms. (+) -magnoflorine iodide has antifungal activity, antioxidant and antidiabetic effects. |
M4293 | Magnoflorine-chloride | Magnoflorine chloride (chloride), an apomorphine alkaloid extracted from Acoruscalamus, reduces the formation of c. albicans biofilms. Magnoflorine chloride has anti-fungal activity, antioxidant, and anti-diabetic effects. |
M4171 | 1-Deacetylnimbolinin-B | 1-Deacetylnimbolinin B is a natural product from Melia toosendan Sieb. |
M4116 | Kalopanaxsaponin H | Kalopanaxsaponin H is a triterpenoid glycoside with antibacterial activity. |
M4056 | Grosvenorine | Grosvenorine is the main flavonoid in momordica Grosvenorine. Grosvenorine has good antibacterial and antioxidant activity. |
M4007 | Isoliquiritin | Isoliquiritin is isolated from licorice root and inhibits angiogenesis and duct formation. Isoliquiritin also has antidepressant and antifungal activity. |
M3992 | Avibactam | Avibactam is a non-β-lactam β-lactamase inhibitor with a spectrum of activity that includes β-lactamase enzymes of classes A, C, and selected D examples. |
M3986 | Bruceantin | Bruceantin was first isolated from Brucea antidysenterica, a tree used in Ethiopia for the treatment of cancer. |
M3911 | Hederacoside C | Hederacoside C (HDC) is one of the active ingredients in Hedera helix leaf extract (Ivy Ex.) |
M3779 | Sancycline | Sancycline is a rare semi-synthetic tetracycline prepared by hydrogenolysis of the chloro and benzylic hydroxy moieties of declomycin. |
M3733 | Pneumocandin B0 | Pneumocandin B0 (L-688786) is a key intermediate in the synthesis of the antifungal agent, Cancidas, has led to the identification of several materials with potential for improved performance. |
M3712 | Mafenide acetate | Mafenide is a sulfonamide-type medication that works by reducing the bacterial population present in the avascular tissues of burns and permits spontaneous healing of deep partial-thickness burns. |
M3705 | Thiacetazone | Thiacetazone (TAC) is an anti-tubercular inhibitor that was formerly used in conjunction with isoniazid, but removed from the antitubercular chemotherapeutic arsenal due to toxic side effects. |
M3695 | Tulathromycin A | Tulathromycin A inhibits protein synthesis by targeting bacterial ribosomes (IC50=0.26 µM). It has immunomodulatory effect. |
M3681 | LFF571 | LFF571 is a novel semisynthetic thiopeptide antibiotic with potent activity against a variety of Gram-positive pathogens, including Clostridium difficile. |
M3644 | Demeclocycline hydrochloride | Demeclocycline hydrochloride is a tetracycline antibiotic, an antibiotic in the treatment of Lyme disease, acne and bronchitis. |
M3609 | Oxacillin sodium monohydrate | Oxacillin sodium monohydrate is an antibacterial agent and is a narrow spectrum beta-lactam antibiotic of the penicillin class. |
M3602 | Sulbactam sodium | Sulbactam sodium (Unasyn) is an irreversible β-lactamase inhibitor. |
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