2. Signaling Pathways
  3. Anti-infection
  4. Fungal

Fungal

Fungal

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An antifungal agent is a drug that selectively eliminates fungal pathogens from a host with minimal toxicity to the host.

Classes: 1. Polyene Antifungal Drugs: Amphotericin, nystatin, and pimaricin interact with sterols in the cell membrane (ergosterol in fungi, cholesterol in humans) to form channels through which small molecules leak from the inside of the fungal cell to the outside. 2. Azole Antifungal Drugs: Fluconazole, itraconazole, and ketoconazole inhibit cytochrome P450-dependent enzymes (particularly C14-demethylase) involved in the biosynthesis of ergosterol, which is required for fungal cell membrane structure and function. 3. Allylamine and Morpholine Antifungal Drugs: lylamines (naftifine, terbinafine) inhibit ergosterol biosynthesis at the level of squalene epoxidase. The morpholine drug, amorolfine, inhibits the same pathway at a later step. 4. Antimetabolite Antifungal Drugs: 5-Fluorocytosine acts as an inhibitor of both DNA and RNA synthesis via the intracytoplasmic conversion of 5-fluorocytosine to 5-fluorouracil.

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-B0888
    Sulfacetamide sodium monohydrate
    		Inhibitor 99.76%
    Sulfacetamide (Sulphacetamide) sodium monohydrate is a sulfonamide antibiotic that can be used for the study of ocular infections. Sulfacetamide sodium monohydrate has antifungal and antibacterial activities.
    Sulfacetamide sodium monohydrate
  • HY-181784
    Ac-CoA-IN-1
    		Inhibitor
    Ac-CoA-IN-1 is an acyl-AMP phosphate analog and weak inhibitor of Candida albicans acetyl-CoA synthetase 2, with no activity against Cryptococcus neoformans acetyl-CoA synthetase 1. Ac-CoA-IN-1 crystallizes with Cryptococcus neoformans ACS1 enzyme to yield structural insight for inhibitor design. Ac-CoA-IN-1 can be used for the research of fungal infections.
    Ac-CoA-IN-1
  • HY-B0847S
    Propiconazole-d7
    		Inhibitor
    Propiconazole-d7 is the deuterium labeled Propiconazole. Propiconazole is a broad-spectrum triazole fungicide that inhibits the conversion of lanosterol to ergosterol, leading to fungal cell membrane disruption. Propiconazole inhibits S. cerevisiae, but not rat liver, microsomal cytochrome P450 (IC50s=0.04 and >200 μM, respectively). Propiconazole inhibits the growth of T. deformans and R. stolonifer (ED50s=0.073 and 4.6 μg/mL, respectively). Propiconazole increases production of reactive oxygen species (ROS).
    Propiconazole-d<sub>7</sub>
  • HY-178799
    SDH-IN-37
    		Inhibitor
    SDH-IN-37 (Compound A37) is a potent SDH inhibitor, with an IC50 value of 0.0263 μM. SDH-IN-37 is also an antifungal agent. SDH-IN-37 demonstrates antifungal activities against Rhizoctonia solani, S. sclerotiorum and F. graminearum, with EC50 values of 0.0144, 0.882 and 1.99 μg/mL, respectively.
    SDH-IN-37
  • HY-W043791
    4-Dodecyl-2,6-dimethylmorpholine
    		Inhibitor
    4-Dodecyl-2,6-dimethylmorpholine is a morpholine fungicide and plant-growth regulator. 4-Dodecyl-2,6-dimethylmorpholine targets phytopathogenic fungi including Oomycetes, Ascomycetes and Basidiomycetes. 4-Dodecyl-2,6-dimethylmorpholine acts synergistically with acylalanine fungicides to enhance antifungal efficacy and regulate plant growth. 4-Dodecyl-2,6-dimethylmorpholine can be applied to the study of plant fungal diseases and phytopathogenic fungal infections.
    4-Dodecyl-2,6-dimethylmorpholine
  • HY-N10014
    Bulnesol
    		Inhibitor
    Bulnesol is a sesquiterpenoid that can be isolated from Salvia dorystaechas. Bulnesol inhibits the activity of Fusarium moniliforme with an EC50 value of 0.6 mg/mL. Bulnesol can be used for the research of fungal infection.
    Bulnesol
  • HY-138439
    Mandestrobin
    		Inhibitor
    Mandestrobin is a fungicide that exerts fungal killing activity by inhibiting mitochondrial respiratory chain complex III. Mandestrobin exhibits differential fungicidal activity between its enantiomers, and the R-enantiomer possesses stronger activity than the S-enantiomer. Mandestrobin is used in studies related to fungal infections and the agricultural field.
    Mandestrobin
  • HY-40284A
    3-Piperidinopropiophenone hydrochloride
    		Inhibitor
    3-Piperidinopropiophenone (hydrochloride) (Compound 2) is a mono Mannich base derived from acetophenone and has antifungal activity.
    3-Piperidinopropiophenone hydrochloride
  • HY-N7135R
    Tropolone (Standard)
    		Inhibitor
    Tropolone is a seven-membered non-benzenoid aromatic compound, which is the precursor of many Azulene derivatives. Tropolone is a potent mushroom tyrosinase inhibitor with an IC50 value of 0.4 μM. Its inhibitory effect can be achieved by dialysis or excess CU2+ Reversa. Tropolone exhibits broad anti-viral and anti-fungal activity and is synergistic upon co-treatment with nucleos(t)ide analog drugs. Tropolone is a promising candidate for research in osteosarcoma.
    Tropolone (Standard)
  • HY-123779
    RWJ-49815
    		Inhibitor
    RWJ-49815 is a histidine kinase inhibitor. RWJ-49815 inhibits the autokinase activity of purified GST-Sln1 and the autophosphorylation of KinA in vitro. RWJ-49815 acts as a fungal growth inhibitor. RWJ-49815 serves as a bactericide against Gram-positive pathogenic bacteria. RWJ-49815 is applicable to research related to fungal infections and Gram-positive bacterial infections.
    RWJ-49815
  • HY-N12164
    Linearmycin B
    		Inhibitor
    Linearmycin B is an antibacterial and antifungal agent. Linearmycin B shows activity against Bacillus subtilis (Bs), Staphylococcus aureus (Sa). Candida albicans (Ca), and Saccharomyces cerevisiae (Sc), with MIC values of 0.097, 1.5, 0.0008, and 0.0002 μg/mL, respectively.
    Linearmycin B
  • HY-W748786
    Fenpyrazamine
    		Inhibitor
    Fenpyrazamine is an antifungal agent. Fenpyrazamine possesses antifungal, preventative, systemic, and lesion-inhibiting activities, as well as a long-lasting effect. Fenpyrazamine targets 3-keto reductase in the ergosterol biosynthesis pathway. Fenpyrazamine is effective against gray mold, stem rot, and brown rot.
    Fenpyrazamine
  • HY-181404
    PA36-2
    		Inhibitor
    PA36-2 is an Mdr1 inhibitor and azole resistance reversal agent, with a IC50 of 1.0 μg/mL and a Kd of 4.209 μM against Candida albicans Mdr1. By effectively inhibiting the activity of the Mdr1 efflux pump, PA36-2 prevents the pumping of substrates out of cells, enhances the intracellular accumulation of azole antibiotics, and exerts a synergistic effect with antifungal agents such as Fluconazole (FLC) (HY-B0101). PA36-2 can be used in the research of azole-resistant candidiasis.
    PA36-2
  • HY-N14998
    Damavaricin D
    		Inhibitor
    Damavaricin D has anti-Gram-positive bacteria, anti-Gram-negative bacteria and anti-fungal effects.
    Damavaricin D
  • HY-U00249R
    Saperconazole (Standard)
    		Inhibitor
    Saperconazole (R66905) is a broad-spectrum antifungal triazole and has potent activity against Aspergillus with an MIC90 of 0.19 mg/L.
    Saperconazole (Standard)
  • HY-N14252
    Melithiazole N
    		Inhibitor
    Melithiazol N is an antibiotic. Melithiazole N is a β-methoxyacrylate (MOA) inhibitor with strong anti-agent activity.
    Melithiazole N
  • HY-158980
    Antifungal agent 103
    		Inhibitor
    Antifungal agent 103 (compound 7y) is a potent antifungal agent. Antifungal agent 103 inhibits R. solani with an EC50 of 0.47 μg/mL.
    Antifungal agent 103
  • HY-N12180
    Hodgkinsine B
    		Inhibitor
    Hodgkinsine B is an opioid receptor agonist and NMDA receptor antagonist, which has analgesic and anti-injurial effects. In addition, Hodgkinsine B has antiviral, antibacterial and antifungal activities.
    Hodgkinsine B
  • HY-124522
    (E)-Metominostrobin
    		Inhibitor
    (E)-Metominostrobin is a strobilurin fungicide that can be used for pest control during strawberry cultivation.
    (E)-Metominostrobin
  • HY-N14102
    Chlorflavonin
    		Inhibitor
    Chlorflavonin has the activities of anti-aspergillus, yeast, botrytis, and other fungal. Among these fungi, anti-Aspergillus fumigatus activity is particularly strong, the minimum inhibitory concentration up to 0.08 μg/mL.
    Chlorflavonin
Cat. No. Product Name / Synonyms Application Reactivity