Catalog No.
Product Name
Application
Product Information
Citations
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Nonionic Surfactant
Polyoxyl 40 stearate (PEG 40 stearate) functions as a nonionic surfactant, synthesized through the esterification of stearic acid with polyethylene glycol containing approximately 40 ethoxy units. It exhibits key biological activity in the formulation of pharmaceutical preparations and nanodrug carriers, facilitating emulsification and stabilization of active compounds. Applications include its use as a matrix component in solid lipid nanoparticles for the controlled release of encapsulated antifungal drugs, as well as serving as a base material for vaginal drug delivery systems, where it can be modified with acryloyl chloride to introduce polymerizable groups. -
Glucosaminide Substrate
VLPA-GlcNAc is a chromogenic glucosaminide substrate that serves as a valuable tool for the identification of Candida species. It can be utilized in the preparation of specialized agar media, facilitating the differentiation of Candida strains based on their enzymatic activity. This reagent is essential in microbiological research and diagnostics, particularly in clinical settings where rapid identification of fungal pathogens is crucial. -
Chlorinated Phenol Active Substance
4,5-Dichloroguaiacol is a chlorinated phenol active substance known for its role in various biochemical applications. It exhibits significant antibacterial and antifungal properties, making it valuable in studies focused on microbial inhibition. This compound is commonly utilized in research involving antimicrobial assays and as a standard in environmental toxicology. -
Chlorophenolic Compound
3,4,5-Trichlorosyringol is a chlorophenolic compound that is synthesized through the chlorination of syringol in carbon disulfide (CS2). This compound exhibits anti-fungal and anti-bacterial activities, making it useful for research involving microbial growth inhibition. It is applicable in studies focused on phytopathology, environmental microbiology, and the development of antimicrobial agents. -
Detection Substrate
5-Bromo-4-chloro-3-indolyl-α-D-maltotrioside functions as a sensitive enzyme substrate with chemiluminescent properties. It facilitates the detection of various enzymatic activities, making it suitable for diagnostic assays aimed at identifying bacterial and fungal infections, as well as other diseases. Its utility in research applications enhances the reliability of assays in clinical microbiology and molecular diagnostics. -
Redox Isomer
Neopatulin is a redox isomer and a critical biogenetic precursor of the antibiotic patulin, commonly produced by various fungal species. This compound plays a significant role in studies pertaining to antibiotic synthesis and fungal metabolism. Neopatulin can be synthesized through methods such as Lewis acid-catalyzed aldol reactions or utilizing 2-formyl-1,3-dithiane in conjunction with 2-(tert-butyldimethylsiloxy)-4-[(tert-butyldimethylsiloxy)-methyl]furan, making it a valuable reagent for chemical research applications. -
Phenolic Compound
Daphneolone is a phenolic compound known for its potential antifungal properties against plant pathogenic fungi. Isolated from the roots of Daphneodora, this compound is valuable for research into natural antifungal agents and plant defense mechanisms. Its analogues may offer insights into the development of eco-friendly agricultural solutions. -
Oxylipin
8(R),11(S)-DiHODE is a fungal oxylipin that primarily targets lipid signaling pathways. It is known to play a role in modulating inflammatory responses and cell signaling processes. This compound is of particular interest in research applications related to metabolic diseases, inflammation, and fungal biology, providing insights into the biochemical pathways influenced by oxylipins. -
Penicillium Intermediate
Cyclopeptine is a key intermediate in the biosynthesis of benzodiazepine alkaloids produced by the genus Penicillium. This compound is significant for research into the metabolic pathways of fungal secondary metabolites and their potential applications in pharmacology. Cyclopeptine can also be utilized to study the structural and functional properties of benzodiazepine derivatives in various biological systems. -
Secondary Metabolite of Aspergillus flavus
5,7-Dihydroxy-4-methylphthalide is a secondary metabolite produced by Aspergillus flavus, serving as a crucial intermediate in the synthesis of Mycophenolic acid. This compound exhibits significant biological activity, contributing to the understanding of fungal metabolism and the pharmacological properties of derived compounds. Its applications encompass research into fungal biosynthesis and the exploration of potential therapeutic agents stemming from fungal secondary metabolites. -
Anticancer Agent
Antitumor Agent-160 is a derivative of the antifungal compound phenalenone, serving as an anticancer agent. It exhibits significant antitumor activity, making it a valuable tool in cancer research. Its potential applications include the study of cancer cell proliferation and the evaluation of therapeutic strategies in oncological research. -
Phenolic Compound
3,4,5-Trichloroguaiacol is a phenolic compound primarily targeted for its antibacterial and antifungal properties. It is often utilized in studies examining environmental contaminants, particularly in the context of effluents from bleached kraft pulp mills. This compound serves as an important research tool in understanding the biochemical pathways influenced by chlorinated phenols and their impacts on microbial activity. -
Lanostane-type Triterpenoid Compound
Inonotusane A is a lanostane-type triterpenoid compound isolated from the sclerotia of Inonotus obliquus. This compound exhibits notable biological activity, including potential anticancer properties and immunomodulatory effects. It serves as a valuable reagent for research focused on natural products, herbal medicine, and the therapeutic potential of fungal metabolites in various biological systems. -
Terpenoid
Monardin C is a natural terpenoid known for its ability to modulate various biological pathways. It exhibits significant antibacterial and antifungal activities, making it a valuable compound in microbiological research. Monardin C's unique properties render it useful for studies focused on the therapeutic potential of terpenoids in infectious diseases and alternative medicine approaches. -
Sesquiterpene
10(14)-Cadinene-4,5-diol is a natural sesquiterpene that modulates various biochemical pathways through its interaction with biological targets. Exhibiting antibacterial and antifungal properties, this compound demonstrates significant activity against a range of microbial strains. Its application in research includes the study of plant secondary metabolites and their potential therapeutic uses in combating infections. -
Drug Derivative
Roseofungin is a drug derivative that primarily targets fungal infections by inhibiting fungal cell wall synthesis. Its key biological activity includes antifungal effects against a variety of pathogenic fungi. This compound is valuable in research applications focusing on antifungal drug development and the study of resistance mechanisms in fungal pathogens. -
Sesquiterpene
Phaeocaulisin F is a natural sesquiterpene known for its potential effects on various biological pathways. This compound exhibits significant antibacterial and antifungal activities, making it valuable in research focused on infectious diseases and microbial resistance. Its unique structure and biological properties enable exploration in diverse fields, including pharmacology and natural product chemistry. -
Active Compound
Nikkomycin J is an active compound that functions as an inhibitor of chitin synthase, targeting fungal cell wall biosynthesis. Its primary biological activity includes antifungal effects, making it particularly valuable in research related to fungal infections and the development of antifungal therapies. Nikkomycin J is utilized in studies focused on fungal pathogenesis and drug resistance mechanisms. -
Chlorinated Phenol
Tetrachloroguaiacol is a chlorinated phenol primarily formed during the chlorine bleaching of wood pulp. It exhibits significant antibacterial and antifungal activities, making it relevant for studies in environmental science and biochemistry. This compound serves as a valuable reagent in research focused on the effects of chlorinated compounds on biological systems and their potential environmental impact. -
α,β-unsaturated Fatty Acid
2-Decenoic acid is an α,β-unsaturated fatty acid known to inhibit plant pollen germination and pollen tube elongation. This compound exhibits significant biological activity, making it a valuable tool for research in plant reproductive biology. Additionally, its antimicrobial properties suggest potential applications in developing antifungal and antibacterial agents. -
Antimicrobial Agent
1,2-Hexanediol serves as a broad-spectrum antimicrobial agent with significant antibacterial and antifungal properties. It exhibits bactericidal activity against both Gram-positive and Gram-negative bacteria, while also effectively inhibiting various fungal organisms. The compound disrupts the cytoplasmic membrane potential of bacteria, making it an essential tool in research focused on bacterial and fungal infections, as well as applications in cosmetic preservation. -
Fungicide
Nuarimol is a fungicide that primarily targets fungal pathogens to protect crops in agricultural applications. This compound functions as a phenobarbital-type inducer of hepatic drug-metabolizing enzymes, leading to transient, significant hepatic regenerative proliferation and accompanying hepatomegaly through reversible hepatocellular injury. Research indicates its potential utility in studies exploring liver regeneration and metabolic enzyme regulation. -
Pesticide
Thiuram disulfide is a sulfenamide compound primarily utilized as a pesticide. It functions through its inhibitory effects on various pathogens, showcasing significant antifungal and antibacterial activities. This compound is widely applied in agricultural research for evaluating pesticide efficacy and developing novel pest control strategies. Its absorbance is assessed at 435 nm, facilitating quantitative analysis in laboratory settings. -
Bactericidal Preservative
Copper naphthenate is an organocopper compound functioning primarily as a bactericidal preservative. It exhibits significant antifungal properties, effectively inhibiting the growth of decay fungi and molds, as well as targeting wood-boring insects and termites. Additionally, it has been shown to eliminate free-living stages of Ichthyophthirius multifiliis, making it valuable for both industrial and ecological applications. Research involving copper naphthenate can provide insights into its cytotoxic effects and potential environmental impacts. -
Isomer
(E/Z)-Diniconazole is an isomer of the well-studied fungicide Diniconazole, primarily targeting plant fungal pathogens. Its biological activity includes the inhibition of specific fungal processes, making it valuable for research focused on the control of plant fungal diseases. Additionally, it plays a role in studies regarding plant growth regulation, offering insights into its effects on agricultural practices and crop management. -
Drug Isomer
rel-Hydroxy Itraconazole is a relative stereoisomer of Hydroxy Itraconazole, which serves as the primary active metabolite of the antifungal agent Itraconazole. This compound exhibits significant antifungal activity and is crucial in studying the pharmacological effects of its parent drug. It is primarily utilized in research applications focused on antifungal mechanisms and drug metabolism. -
Azasterol
Fluoro azasterol is an azasterol derivative that functions as a potent inhibitor of parasitic and fungal growth. This compound exhibits significant biological activity against various pathogens, making it a valuable tool for research in the fields of parasitology and mycology. Its applications include studying the mechanisms of anti-parasitic and antifungal action, as well as exploring potential therapeutic uses in infectious disease models. -
Active Component of Radix
Phytolaccagenin is a triterpenoid saponin that is the active component of Radix Phytolaccae. This compound exhibits significant antifungal and anti-inflammatory activities, making it a valuable reagent for research in pharmacology and toxicology. Its lower toxicity profile enhances its potential as a candidate for therapeutic applications and further biological studies. -
Fungicide
8-Hydroxyquinoline is a lipophilic metal chelator primarily utilized as a fungicide. It demonstrates antimicrobial activity with a minimum inhibitory concentration (MIC) range of 27.56-55.11 μM against clinical isolates of Neisseria gonorrhoeae. The compound is capable of binding copper, facilitating its transport into cells, and has been observed to induce an increase in micronucleated polychromatic erythrocytes, with additional effects on hair depigmentation in murine models. This reagent is valuable for research in metal ion interactions and fungal pathology. -
Antifungal Agent
α-Terpinene is a monoterpene with notable antifungal activity, primarily derived from the essential oils of various aromatic plants, including Mentha piperita. It demonstrates efficacy against Trypanosoma evansi, indicating potential applications in trypanosomosis treatment. In addition to its antifungal properties, α-Terpinene exhibits significant antioxidant activity, making it a valuable reagent for further research in microbiology and pharmacology. -
Fungi Metabolite
Itaconic acid is a versatile fungal metabolite with significant roles in macrophage metabolism. Its primary biological activities include anti-inflammatory, antimicrobial, and immunomodulatory effects, making it valuable for immunological research. Itaconic acid mediates crosstalk between macrophages and peritoneal tumors, highlighting its potential in studies related to cancer and immune responses. This compound can also serve as a precursor in the synthesis of various polymers, chemicals, and fuels. -
Mycotoxin
Patulin is a mycotoxin synthesized by various fungal species, including Aspergillus, Penicillium, and Byssochlamys. It is known to induce chromosome breakage and mutations, exhibiting teratogenic and cytotoxic effects. Patulin triggers autophagy-dependent apoptosis via the lysosomal-mitochondrial axis, leading to DNA damage. This compound is relevant for research into the mechanisms of mycotoxin toxicity and apoptosis. -
CCR5 Receptor Antagonist
Fuscin is a fungal metabolite that acts as a CCR5 receptor antagonist, exhibiting notable anti-HIV activity. Additionally, it has been identified as an inhibitor of respiration and oxidative phosphorylation, as well as a disruptor of mitochondrial SH-dependent transport-linked functions. This compound serves as a valuable tool in research related to HIV infection and mitochondrial function. -
RXRα Activator
2,4-Di-tert-butylphenol (2,4-DTBP) is a potent RXRα activator and a ligand for human estrogen receptors, exhibiting significant anti-inflammatory and antioxidant properties. This compound has the capacity to induce apoptosis in tumor cells and can activate various RXRα-associated pathways, including LXRα/RXRα and PPARγ/RXRα. Additionally, 2,4-DTBP demonstrates antiviral and antifungal activities while also showing potential to mitigate Aβ-induced neurotoxicity. It serves as a valuable intermediate for synthesizing antioxidants, UV stabilizers, and is utilized in pharmaceutical and fragrance manufacturing. -
Secondary Metabolite
3-Phenylphenol is a secondary metabolite that targets specific gene expression in microbial systems. It has been shown to induce the hbp gene cluster in Pseudomonas sp. strain P1B16, enhancing metabolic pathways of interest. Additionally, 3-Phenylphenol interacts with the Sge1 transcription factor in Fusarium oxysporum f. sp. cubense, disrupting virulence regulation and offering insights into plant pathogen interactions. This compound is valuable for research focused on banana fusarium wilt and other related fungal pathogenic studies. -
Valine-derived Analogue
Isobutyl heptanoate is a valine-derived analogue that exhibits potential biological activity. This compound can be isolated from the volatile metabolites of Aspergillus clavatus NRRL1. Its role in biochemical studies may extend to investigating metabolic pathways and structural biology related to amino acid derivatives. Researchers can utilize isobutyl heptanoate in applications involving metabolic profiling and the exploration of fungal metabolite functionality. -
Bactericide
Poly diallyldimethylammonium chloride is a cationic antimicrobial polymer that acts as a bactericide through its quaternary ammonium side chains. It demonstrates significant microbicidal activity against a range of microorganisms, including bacteria and fungi. This reagent is suited for research applications involving bacterial and fungal infections, such as those caused by E. coli, S. aureus, and C. albicans, making it a valuable tool in the study of antimicrobial resistance and infection control. -
Fungicide
Cyflufenamid is an oxime amide fungicide that targets fungal growth by inhibiting the formation of haustoria, colonies, and spores of Blumeria graminis f. sp. tritici, as well as preventing germ tube elongation in Monilinia fructicola. This compound is valuable for research applications focused on controlling powdery mildew and brown rot, facilitating the study of fungal infection mechanisms and the development of sustainable agricultural practices. -
Fungicide
Methfuroxam is a potent fungicide that effectively targets and inhibits key pathogenic fungi, including Colletotrichum salmonicolor, Rhizopus lignosus, and Ganoderma species, which are detrimental to rubber trees and oil palms. Its high level of antifungal activity makes it a valuable tool for research applications aimed at studying plant-pathogen interactions and developing disease management strategies in agriculture. -
Fungicide
Pyrametostrobin is a strobilurin fungicide that targets mitochondrial respiration in fungi. It exhibits broad-spectrum biological activity against various fungal pathogens, including cucumber powdery mildew, blight, rust, and downy mildew. This compound is widely utilized in agricultural research to investigate fungal resistance and the efficacy of fungicides in crop protection. -
Fungicide
Dodemorph is a fungicide that targets ergosterol biosynthesis, disrupting fungal cell membrane integrity. It exhibits effective antifungal activity, making it suitable for studies addressing fungal mildew, particularly in rose cultivation. This reagent can be employed in various research applications focused on plant pathology and disease management in horticultural settings. -
Fungicide
Coumoxystrobin is a methoxyacrylate strobilurin fungicide that targets fungal pathogens. It exhibits potent inhibitory activity against the mycelial growth of Magnaporthe oryzae, enhancing cell membrane permeability and reducing respiration rates. Additionally, Coumoxystrobin demonstrates protective effects in detached barley leaves against Magnaporthe oryzae and impairs ATP activity in Chlorella vulgaris, leading to algal mortality. This reagent is valuable for research on rice blast disease and other related fungal studies. -
Fungicide
4-Dodecyl-2,6-dimethylmorpholine is a morpholine-based fungicide that primarily targets phytopathogenic fungi, including Oomycetes, Ascomycetes, and Basidiomycetes. This compound exhibits antifungal activity and functions as a plant growth regulator, enhancing the efficacy of acylalanine fungicides when used in combination. It is suitable for research applications focused on plant fungal diseases and the mechanisms underlying phytopathogenic fungal infections. -
Fungicide
(E)-Metominostrobin is a strobilurin fungicide that acts by inhibiting mitochondrial respiration in fungal cells. It demonstrates potent activity against a variety of phytopathogenic fungi, making it effective for use in agricultural applications, particularly in strawberry cultivation. This compound aids in protecting crops from fungal diseases, thereby enhancing yield and crop quality. -
Fungicide
Metconazole is a 14α-demethylation inhibitor (DMI) fungicide that targets fungal ergosterol biosynthesis. This compound effectively inhibits mycelial growth and conidial germ tube elongation, demonstrating significant antifungal activity. Additionally, Metconazole has been shown to reduce antioxidant enzyme activities and is particularly effective in decreasing the incidence of Fusarium crown rot in wheat, making it valuable for agricultural research and crop protection studies. -
Phytopathogenic Fungi Inhibitoir
Antifungal agent 157 is a heterocyclic pyridazine compound that targets phytopathogenic fungi. It demonstrates effective inhibitory activity against various fungal strains responsible for plant diseases. This agent is valuable for research focused on controlling fungal infestations in agricultural settings, aiding in the development of strategies for plant disease management. -
Phytopathogenic Fungal Inhibtor
Antifungal agent 156 is a heterocyclic pyridazine compound that acts as a phytopathogenic fungal inhibitor. It exhibits significant antifungal activity, making it suitable for research involving phytopathogenic fungal infections. This reagent can be utilized to explore mechanisms of fungal pathogenesis and to develop new strategies for fungal disease management in agricultural settings. - Propiosyringone is a natural compound resulting from the degradation of Eucalyptus globulus wood by wood-decaying fungi. It serves as a signaling molecule in various biological systems and plays a role in plant-microbe interactions. Research applications include studies on plant immunity, microbial symbiosis, and the effects of fungal metabolites on plant growth and development.
- Bisdionin F is a compound that enhances the antibacterial function of macrophages by inhibiting arginase activity induced by Candida albicans. This action effectively restores nitric oxide production, thereby reinforcing the macrophages' innate immune response. Bisdionin F is relevant for research focused on innate immunity, macrophage activation, and fungal infections.
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Antifungal Inhibitor
Hunnemanine is a protoberberine-type isoquinoline alkaloid that acts as a potent antifungal inhibitor. At a concentration of 1000 ppm, it effectively prevents the spore germination of various phytopathogenic fungi, including Alternaria brassicae, Helminthosporium pennisetti, and Fusarium lini. This compound is valuable for research on the infection mechanisms of phytopathogenic fungi and the development of related control strategies.
