2. Disease Areas
  3. Infection
  4. Fungal Infection
  5. Yeast Infection

Yeast Infection

Yeast infection, commonly known as candidiasis, is a prevalent vulvovaginal condition primarily caused by the fungus Candida albicans, a type of unicellular eukaryotic microorganism belonging to the fungal kingdom. These yeasts are heterotrophic, relying on organic matter for nutrition, and reproduce via budding or fission. While capable of existing in both aerobic and anaerobic environments, they exhibit efficient growth under oxygen-rich conditions through oxidative metabolism, but shift to ethanol production under anaerobic conditions. Although many women experience symptomatic infections, Candida can also colonize the vagina asymptomatically. The infection arises due to an overgrowth of yeast, often triggered by disruptions in the normal vaginal microbiota, immune status, or hormonal changes, leading to symptoms such as itching, irritation, and abnormal discharge.

References:

Yeast Infection (18):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-113143
    Galactose 1-phosphate 2255-14-3
    Galactose 1-phosphate acts as a competitive substrate inhibitor of galactose-1-phosphate uridylyltransferase (GALT). Galactose 1-phosphate is a competitive inhibitor of Phosphoglucomutase, yet the rate at which this enzyme converts Galactose 1-phosphate to Galactose-6-phosphate is 400 times slower than the rate of converting Glucose-1-phosphate. Galactose 1-phosphate can be used in studies related to Saccharomyces cerevisiae infection and type I galactosemia.
    Galactose 1-phosphate
  • HY-113143A
    Galactose 1-phosphate Potassium salt 19046-60-7 99.0%
    Galactose 1-phosphate Potassium salt acts as a competitive substrate inhibitor of galactose-1-phosphate uridylyltransferase (GALT). Galactose 1-phosphate Potassium salt is a competitive inhibitor of Phosphoglucomutase, yet the rate at which this enzyme converts Galactose 1-phosphate to Galactose-6-phosphate is 400 times slower than the rate of converting Glucose-1-phosphate. Galactose 1-phosphate Potassium salt can be used in studies related to Saccharomyces cerevisiae infection and type I galactosemia.
    Galactose 1-phosphate Potassium salt
  • HY-N7814
    2-Hydroxypalmitic acid 764-67-0 99.42%
    2-Hydroxypalmitic acid is an intermediate in the phytosphingosine metabolic pathway. 2-Hydroxypalmitic acid is exclusively incorporated into sphingolipids and not used for other lipids. 2-Hydroxypalmitic acid promotes the production of odd-carbon phosphatidylcholine species. 2-Hydroxypalmitic acid is applicable to studies of Saccharomyces cerevisiae infection.
    2-Hydroxypalmitic acid
  • HY-P2992
    Inorganic pyrophosphatase, Saccharomyces cerevisiae 9024-82-2
    Inorganic pyrophosphatase is a ubiquitous enzyme that converts pyrophosphate (PPi) to phosphate and, in this way, controls numerous biosynthetic reactions that produce PPi as a byproduct. Inorganic pyrophosphatase, Saccharomyces cerevisiae is an Inorganic pyrophosphatase isolated from Saccharomyces cerevisiae.
    Inorganic pyrophosphatase, Saccharomyces cerevisiae
  • HY-W005297
    4,6-Dimethoxysalicylaldehyde 708-76-9 99.96%
    4,6-dimethoxysalicylaldehyde is an antifungal agent. 4,6-dimethoxysalicylaldehyde has considerable activity against C. albicans and slight activity against S. cerevisiae.
    4,6-Dimethoxysalicylaldehyde
  • HY-N18360
    Tunicamycin X 66081-38-7
    Tunicamycin X (Tunicamycin 17:1) is a nucleoside Antibiotic. Tunicamycin X is isolated from Streptomyces xinghaiensis SCSIO S15077. Tunicamycin X acts as a growth inhibitor against bacteria and fungi. Tunicamycin X inhibits the growth of Bacillus thuringiensis strains. Tunicamycin X inhibits the growth of Candida albicans strains.
    Tunicamycin X
  • HY-N18269
    3-O-α-L-Arabinopyranosyl hederagenin 28-O-α-L-rhamnopyranosyl ester 639515-41-6
    3-O-α-L-Arabinopyranosyl hederagenin 28-O-α-L-rhamnopyranosyl ester is an anti-fungal triterpene saponin. 3-O-α-L-Arabinopyranosyl hederagenin 28-O-α-L-rhamnopyranosyl ester can be isolated from the aerial parts of Clematis tangutica. 3-O-α-L-Arabinopyranosyl hederagenin 28-O-α-L-rhamnopyranosyl ester exhibits antifungal activity against fungal strains (P. avellaneum, C. glabrata, S. cerevisiae, T. beigelii), with the strongest activity against S. cerevisiae.
    3-O-α-L-Arabinopyranosyl hederagenin 28-O-α-L-rhamnopyranosyl ester
  • HY-P10304D
    Cyclo(Pro-dArg) acetate 98.12%
    Cyclo(Pro-dArg) acetate is a chitinase inhibitor. Cyclo(Pro-dArg) acetate inhibits the cell separation of Saccharomyces cerevisiae but does not affect its growth. Cyclo(Pro-dArg) acetate inhibits the transition of Candida albicans from yeast to filamentous morphology.
    Cyclo(Pro-dArg) acetate
  • HY-N17734
    2-Deethoxy-2-hydroxyphantomolin 821799-76-2
    2-Deethoxy-2-hydroxyphantomolin, Germacranolide, is an Antifungal and Antibacterial agent. 2-Deethoxy-2-hydroxyphantomolin can be isolated from Elephantopus tomentosus Linn and E. mollis. 2-Deethoxy-2-hydroxyphantomolin is moderately active against Candida albicans (14 mm clearing zone) and slightly active against Escherichia coli (12 mm), Pseudomonas aeruginosa (12 mm), Bacillus subtilis (14 mm), and Trichophyton mentagrophytes (13 mm).
    2-Deethoxy-2-hydroxyphantomolin
  • HY-117650
    (R)-RG7834 2072057-18-0
    (R)-RG7834 is an inactive enantiomer (“R” configuration) of RG7834 (HY-117650A).
    (R)-RG7834
  • HY-P11465
    Histone H3 (73-83) 738626-01-2
    Histone H3 (73-83) is a histone H3 fragment. Histone H3 (73-83) can be obtained from incomplete tryptic digestion of underivatized wild-type histone H3. Histone H3 (73-83) can be used in the research of yeast infection.
    Histone H3 (73-83)
  • HY-176964
    N-Choloylphenylalanine 19651-46-8
    N-Choloylphenylalanine (Compound 6273) (PheCA) is a VPR-induced growth arrest inhibitor. N-Choloylphenylalanine alleviates VPR-induced growth arrest. N-Choloylphenylalanine can be used in yeast and HIV-1 infection research.
    N-Choloylphenylalanine
  • HY-W142457
    Dihydromyrcenol 18479-58-8
    Dihydromyrcenol is an orally active flavor ingredient and Antifungal agent. Dihydromyrcenol acts as a toxicant. Dihydromyrcenol induces phototoxicity-related growth inhibition in Bakers' Yeast. In pregnant rats, Dihydromyrcenol causes threshold maternal toxicity by reducing feed consumption and body weight gain, and also induces threshold developmental toxicity by decreasing fetal body weight, inhibiting ossification of metatarsal bones in the hind paws, increasing the number of extra thoracic vertebrae ribs, and altering vertebral counts.
    Dihydromyrcenol
  • HY-N19846
    Pithecolobine 22368-82-7
    Pithecolobine is a saponin-like alkaloid found in the bark, seeds, and leaves of Samanea saman. Pithecolobine can inhibit the growth of Gram-positive bacteria, Gram-negative bacteria, and pathogenic yeasts. Pithecolobine scavenges DPPH radicals. Pithecolobine can be used for the research of infections caused by pathogenic bacteria and yeasts.
    Pithecolobine
  • HY-182488
    Pulvinamide 31673-63-9
    Pulvinamide is a tetronic acid pigment, a pulvinic acid derivative, an Antibacterial agent and Antifungal agent. Pulvinamide can be isolated from lichens. Pulvinamide weakly inhibits the growth of Bacillus subtilis (ATCC 6633) with an MIC of 50 μg/mL. Pulvinamide weakly inhibits the growth of Candida albicans (ATCC 10231) and Saccharomyces cerevisiae (ATCC 9763), with MIC values of 200 μg/mL and 100 μg/mL, respectively.
    Pulvinamide
  • HY-108874A
    Candicidin (≥50%) 1403-17-4
    Candicidin (≥50%) (Levorin (≥50%)) is an Antifungal antibiotic. Candicidin (≥50%) exhibits potent antifungal activity against yeasts and yeast-like fungi, such as Candida albicans and Saccharomyces cerevisiae. Low concentrations of Candicidin (≥50%) do not adversely affect pea seed germination.
    Candicidin (≥50%)
  • HY-W278073
    RNA splicing modulator 6 430443-35-9
    RNA splicing modulator 6 (Compound c7) is a RNA splicing modulator. RNA splicing modulator 6 induces changes in pre-mRNA splicing. RNA splicing modulator 6 causes accumulation of unspliced RNA in the Hs-Hsh155 strain. RNA splicing modulator 6 reduces proliferation of chronic myeloid leukemia cells harboring the cancer-associated SRSF2P95H mutation.
    RNA splicing modulator 6
  • HY-N14690
    Piperazinomycin 83858-82-6
    Piperazinomycin is an antifungal and antibacterial antibiotic. Piperazinomycin is isolated from the culture broth of Streptoverticillium olivoreticuli subsp. neoenacticus. Piperazinomycin inhibits the growth of fungi, yeasts and some Mycobacterium species. Piperazinomycin exhibits inhibitory activity against Trichophyton species.
    Piperazinomycin