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Results for "

basidiomycete

" in MedChemExpress (MCE) Product Catalog:

16

Inhibitors & Agonists

10

Natural
Products

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-148054
    Antifungal agent 36

    		Fungal Infection
    Antifungal agent 36 is a potent anti-fungal agent. Antifungal agent 36 shows anti-fungal activity for Basidiomycetes .
    Antifungal agent 36
  • HY-A0278
    Hexaconazole

    (-)-Hexaconazol

    		 Fungal Reactive Oxygen Species SOD Infection Endocrinology
    Hexaconazole is a demethylation enzyme inhibitor and a synthetic fungicide that targets many fungi, especially ascomycetes and basidiomycetes, and it can enhance the activity of SOD and peroxidase. Hexaconazole causes endocrine disorders in zebrafish larvae .
    Hexaconazole
  • HY-121387
    Furmecyclox

    		Fungal Infection
    Furmecyclox is an effective fungicide. Furmecyclox shows great effects against basidiomycetes .
    Furmecyclox
  • HY-124408
    Mepronil

    		Fungal Infection
    Mepronil, a compound belonging to the carboxyamine group of fungicides, has a particularly strong bactericidal effect on basidiomycete fungi. Mepronil acts as a single point inhibitor of the succinate ubiquinone reductase or succinate dehydrogenase complex. Mepronil can be used in the study of cross resistance and biological infection .
    Mepronil
  • HY-125652
    Macrosphelide A

    		Antibiotic Infection
    Macrosphelide A is a macrolide antibiotic. Macrosphelide A inhibits growth of some ascomycetes, basidiomycetes, oomycetes and all four Gram-positive bacteria tested, including the medically important Staphylococcus aureus with a MIC of ≤500 μg/mL .
    Macrosphelide A
  • HY-124408R
    Mepronil (Standard)

    		Fungal Infection
    Mepronil (Standard) is the analytical standard of Mepronil. This product is intended for research and analytical applications. Mepronil, a compound belonging to the carboxyamine group of fungicides, has a particularly strong bactericidal effect on basidiomycete fungi. Mepronil acts as a single point inhibitor of the succinate ubiquinone reductase or succinate dehydrogenase complex. Mepronil can be used in the study of cross resistance and biological infection .
    Mepronil (Standard)
  • HY-N8409
    FD-838

    		Others Others
    FD-838 is a Alkaloids product that can be isolated from the mycelia of the basidiomycete Hericium erinaceum. .
    FD-838
  • HY-N8403
    Vibralactone B

    		Others Others
    Vibralactone B is a Sesquiterpenoids product that can be isolated from From the cultures of the Basidiomycete Boreostereum vibrans. .
    Vibralactone B
  • HY-N3104
    Paxiphylline E

    Daphnilongeranine A N-oxide

    		 Others Others
    Paxiphylline E (Daphnilongeranine A N-oxide) is a Alkaloids product that can be isolated from the mycelia of the basidiomycete Hericium erinaceum. .
    Paxiphylline E
  • HY-N8942
    (S)-17-Hydroxy-18,20-ene-neogrifolin

    		Others Others
    (S)-17-Hydroxy-18,20-ene-neogrifolin is a natural product that can be isolated from the Basidiomycete Albatrellus Caeruleoporus .
    (S)-17-Hydroxy-18,20-ene-neogrifolin
  • HY-N9533
    16R-Hydroxy-3-oxolanosta7,9(11),24-trien-21-oic acid

    		Others Others
    16R-Hydroxy-3-oxolanosta7,9(11),24-trien-21-oic acid is a lanostanoid that can be found in the Sri Lankan basidiomycete Ganoderma applanatum .
    16R-Hydroxy-3-oxolanosta7,9(11),24-trien-21-oic acid
  • HY-N8523
    Vibralactone D

    		Others Metabolic Disease
    Vibralactone D (Compound 1) is a metabolite isolated and cultured from natural basidiomycetes Boreostereum vibrans. Vibralactone D shows weak inhibitory activity against isoenzymes of 11b-hydroxysteroid dehydrogenase (HSD) (IC50 85.7 μM).
    Vibralactone D
  • HY-126224
    Driselase, Basidiomycetes sp

    		Others Others
    Driselase, Basidiomycetes sp, a complex mixt. of wall-digesting enzymes, is a specific commercial fungal protoplasting enzyme preparation. Driselase is by far the most potent of the enzymes tested for polysaccharide digestion and greatly increases both tensile and indentation compliances, yet it does not induce wall creep, even after 6 h of digestion .
    Driselase, Basidiomycetes sp
  • HY-N12776
    Illudalic acid

    		Phosphatase Cancer
    Illudalic acid is a potent and selective Leukocyte antigen-related (LAR) phosphatase inhibitor with an IC50 value of 1.30 µM. Illudalic acid inhibits LAR phosphatase through covalent ligation to the catalytic cysteine residue .
    Illudalic acid
  • HY-N9768
    (10E,12E)-9-Oxo-10,12-octadecadienoic acid

    9-oxo-ODA

    		 Fungal PPAR Infection
    (10E,12E)-9-Oxo-10,12-octadecadienoic acid (9-oxo-ODA) is a PPARα agonist that can be isolated from the basidiomycete Gomphus floccosus. (10E,12E)-9-Oxo-10,12-octadecadienoic acid enhances fatty acid oxidation through PPARα activation, thereby inhibiting triglyceride accumulation. (10E,12E)-9-Oxo-10,12-octadecadienoic acid also has antifungal (Fungal) activity .
    (10E,12E)-9-Oxo-10,12-octadecadienoic acid
  • HY-126637
    Marasmic acid

    		Bacterial Fungal Infection
    Marasmic acid is a sesquiterpenoid with unsaturated dialdehyde functionality, first isolated from the Basidiomycete Marasmus conigenus. Marasmic acid has antibacterial, antifungal, cytotoxic and mutagenic activities, and its broad-spectrum activity is related to the α,β-unsaturated aldehyde group. However, its detailed biological mechanism of action has not been clarified. Previous studies have suggested that marasmic acid may exert its effects by reacting with endogenous nucleophiles or forming pyrrole derivatives. This study found that marasmic acid interferes with the membrane sensor histidine kinase MoSln1p of M. oryzae, superactivates the HOG pathway and causes cell death, indicating that its mechanism of action is different from other unsaturated dialdehyde sesquiterpenoids.
    Marasmic acid

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