Catalog No.
Product Name
Application
Product Information
Citations
-
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. -
Stable Isotope
Loratadine-d5-1 is a deuterated analog of Loratadine, which serves as a selective inverse agonist of peripheral histamine H1 receptors. It exhibits an IC50 of greater than 32 μM and has been shown to possess anti-dengue virus (DENV) activity. Additionally, Loratadine is capable of inhibiting the immunologic release of inflammatory mediators, making it a valuable tool for research in allergy and inflammation studies. -
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. -
Insecticide
Tetramethylfluthrin is an insecticide that effectively targets Aedes albopictus, demonstrating rapid population reduction when delivered through unmanned aerial vehicle cold mist spray. This compound exhibits a strong knock-down effect and high toxicity to the target insect species. Tetramethylfluthrin is valuable for research related to dengue fever and dengue hemorrhagic fever, facilitating studies on vector control and disease transmission. -
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. -
Angucycline Antibiotic
Urdamycin A is an angucycline antibiotic derived from Streptomyces fradiae. Notably, it functions as an orange pH indicator, shifting to ultramarine blue at pH 7.7. Urdamycin A exhibits significant anticancer activity, showing IC50 values of 2.4 μg/mL in proliferation assays and 0.55 μg/mL in stem cell assays. This compound is relevant for research applications in cancer biology and antibiotic activity studies. -
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. -
Fluorescent Dye
Primulin is a fluorescent dye that exhibits strong binding affinity for albumin, making it a valuable tool in various analytical and biological studies. This compound effectively labels plant cell walls and distinguishes between live and dead spermatozoa through distinct fluorescence patterns. In neurobiology, Primulin serves as a retrograde axonal tracer, while its derivatives demonstrate inhibitory activity against HCV NS3 and interference with dengue virus NS3-mediated ATP hydrolysis. Additionally, Primulin disrupts HCV replicase assembly, highlighting its potential in virology research applications. -
Bacterial Inhibitor
Ethionamide is a second-line anti-tuberculosis agent that acts primarily by inhibiting the synthesis of mycolic acids in Mycobacterium tuberculosis. This compound demonstrates significant antibacterial activity and is effective when administered orally. Ethionamide is utilized in research applications focused on tuberculosis treatment resistance mechanisms and the development of novel therapeutics against mycobacterial infections. -
Antibiotic
Fenbendazole is an orally active benzimidazole compound that primarily targets tubulin, acting as a microtubule destabilizing agent. It exhibits a broad antiparasitic activity by disrupting microtubule equilibrium in helminths. Additionally, fenbendazole is known for its anti-proliferative effects, inducing apoptosis and causing cell-cycle arrest in various cancer models. Its antitumor properties have been demonstrated in mice xenografted with wild-type p53, making it a valuable reagent for exploring mechanisms of cancer therapy. -
Bacterial Inhibitor
Fleroxacin is a broad-spectrum fluoroquinolone antibiotic that targets bacterial DNA gyrase and topoisomerase IV, inhibiting bacterial DNA replication and transcription. This compound exhibits potent antibacterial activity against a wide range of gram-negative and some gram-positive bacteria. Fleroxacin is suitable for research applications focused on the elucidation of bacterial resistance mechanisms and the development of novel antimicrobial therapies. -
Antibiotic
Nalidixic acid is a quinolone antibiotic that primarily targets DNA gyrase and topoisomerase IV, interfering with bacterial DNA replication. It exhibits a bacteriostatic effect at lower concentrations and becomes bactericidal at higher concentrations. Nalidixic acid is effective against both gram-positive and gram-negative bacteria, making it valuable for studies involving bacterial infections and resistance mechanisms in microorganisms. -
Bacterial Inhibitor
Nitrofurazone is a nitro-aromatic antibacterial compound primarily targeting bacterial DNA and RNA synthesis. It exhibits broad-spectrum activity against both Gram-positive and Gram-negative bacteria, making it suitable for a variety of microbiological research applications. Nitrofurazone is often utilized in studies assessing antimicrobial resistance and the efficacy of antibiotic treatments. -
Antibiotic
Secnidazole is an orally active azole antibiotic that primarily targets bacterial quorum sensing (QS) mechanisms. By inhibiting acylhomoserine lactones, Secnidazole attenuates the virulence of Pseudomonas aeruginosa and exhibits antimicrobial activity against a range of anaerobic Gram-negative and Gram-positive bacteria. This reagent is valuable for research applications related to diseases such as amoebiasis, giardiasis, and bacterial vaginitis, facilitating studies on their pathogenesis and treatment. -
Sulfonamide Antibiotic
Sulfadiazine is a sulfonamide antibiotic that inhibits bacterial folic acid synthesis by competitively antagonizing para-aminobenzoic acid (PABA). It exhibits antimalarial properties and is primarily utilized in research involving toxoplasmosis. Sulfadiazine's mechanism of action makes it a valuable tool for studying sulfamethoxazole efficacy and the interplay of antibiotics in parasitic infections. -
Antibiotic
Sulfameter, a sulfonamide antibiotic, exhibits broad-spectrum activity against both Gram-positive and Gram-negative bacteria. Its long-acting formulation makes it suitable for research applications targeting bacterial infections, particularly in respiratory and urinary tracts. This compound serves as a valuable tool in the study of antibiotic efficacy and resistance mechanisms in various pathogens. -
Sulfathiazole Antibiotic
Sulfamethizole is a sulfathiazole antibiotic that inhibits the synthesis of folic acid and thymine, thereby affecting bacterial growth. It demonstrates antibacterial activity against Escherichia coli in urinary tract infections, though it is ineffective against sulII gene-positive strains. This compound is valuable for research into the mechanisms of urinary tract infections and the bioluminescence of Photobacterium phosphoreum. -
Sulfonamide Antibiotic
Sulfamethoxazole is a sulfonamide antibiotic that exerts its antibacterial effect by inhibiting bacterial folate metabolism. It achieves this by competitively interfering with 4-Aminobenzoic acid (PABA) at the active site of dihydropteroate synthetase and dihydropteroate reductase. This compound is primarily utilized in the research of urinary tract infections (UTIs), prostatitis, and bronchitis, making it a valuable tool for studying antibiotic resistance and bacterial infections. -
Antibiotic
Sulfanilamide is a potent sulfonamide antibiotic that primarily targets bacterial growth by inhibiting dihydropteroate synthase. This compound demonstrates significant biological activity against various pathogens, including inhibition of the lymphogranuloma venereum virus. Additionally, sulfanilamide acts as a carbonic anhydrase inhibitor, making it useful in a range of biochemical research applications, particularly in studies involving antibiotic resistance and enzyme dynamics. -
Antibacterial Antibiotic
Tebipenem pivoxil is an orally active antibacterial antibiotic that targets penicillin-binding proteins (PBPs) to inhibit bacterial cell wall synthesis. Its efficacy against a range of pathogenic bacteria makes it a valuable tool for research applications in microbiology and pharmacology, particularly in studying antibiotic resistance mechanisms and developing new therapeutic strategies. -
Bacterial Inhibitor
Teicoplanin is a glycopeptide antibiotic primarily targeting Gram-positive bacteria, demonstrating potent activity against methicillin-resistant Staphylococcus aureus (MRSA) and Enterococcus aureus. In addition to its antibacterial properties, teicoplanin exhibits antiviral effects against HIV-1, SARS-CoV-1, and SARS-CoV-2. This versatile compound is utilized in research related to bacterial resistance and viral infections, making it a valuable tool for studying antimicrobial efficacy and therapeutic interventions. -
Bacterial Inhibitor
Tobramycin is a broad-spectrum aminoglycoside antibiotic that primarily targets bacterial protein synthesis by binding to the 30S ribosomal subunit. It exhibits significant antibacterial activity against a variety of Gram-negative and some Gram-positive bacteria. Tobramycin is particularly effective in research applications focused on infections caused by Pseudomonas aeruginosa, including studies related to pneumonia. Its efficacy makes it a valuable reagent in microbial pathogenesis and antibiotic resistance research. -
Antibacterial Agent
Mafenide hydrochloride is a sulfonamide-type antimicrobial agent that targets bacterial infections. It exhibits antibacterial activity against a range of Gram-positive and Gram-negative bacteria, including Pseudomonas aeruginosa, primarily through the inhibition of nucleotide synthesis. Mafenide hydrochloride is commonly utilized in the treatment of burn wounds, making it a valuable reagent in research focused on wound healing and infection control. -
Cephalosporin Antibiotic
Cephalexin is a semisynthetic cephalosporin antibiotic known for its broad-spectrum activity against numerous gram-positive and gram-negative bacteria. It functions primarily by inhibiting penicillin-binding proteins (PBPs), which are essential for bacterial cell wall synthesis. This compound is widely utilized in research related to bacterial infections, including pneumonia, streptococcal throat infections, and bacterial endocarditis. Its oral bioavailability and efficacy make it a valuable tool in microbiological studies. -
Antibiotic
Amoxicillin is a beta-lactam antibiotic that targets bacterial cell wall synthesis. It exerts its antimicrobial activity by inhibiting the peptidoglycan biosynthesis necessary for cell wall formation, leading to impaired cell growth and division. Amoxicillin is widely used in various research applications to study bacterial infections and resistance mechanisms. -
Bacterial Inhibitor
Ampicillin sodium is a broad-spectrum beta-lactam antibiotic that targets bacterial cell wall synthesis. It is effective against a wide range of gram-positive and gram-negative bacteria, making it a valuable reagent for microbiological research. Ampicillin sodium is commonly used in cell culture and for selecting genetically modified organisms, as well as in the study of bacterial resistance mechanisms. Its ability to inhibit bacterial growth supports investigations into antibiotic efficacy and microbial interactions. -
Aminoglycoside Antibiotic
Amikacin hydrate is an aminoglycoside antibiotic that serves as a semisynthetic analog of kanamycin. It exhibits bactericidal activity by binding to the 30S and 50S ribosomal subunits in bacteria, ultimately inhibiting protein synthesis. This reagent is particularly effective against a wide range of Gram-negative bacteria, including strains resistant to gentamicin and tobramycin, as well as infections caused by susceptible Nocardia and nontuberculous mycobacteria. Amikacin hydrate is commonly utilized in research focused on combating antibiotic-resistant infections and studying mechanisms of antibiotic action. -
Antibiotic
Bacitracin Zinc is a complex of Bacitracin and zinc ions, functioning primarily as an antibiotic with bactericidal activity. This polypeptide antibiotic is effective in causing damage to bacterial DNA and deoxyribose, making it a valuable agent in combating microbial infections. Additionally, Bacitracin Zinc has been shown to enhance gut microbiota composition in broiler and beef cattle, contributing to improved overall health and growth performance in livestock research applications. -
Bacterial Inhibitor
Cefoperazone is a semisynthetic cephalosporin that functions as a bacterial inhibitor by interfering with cell wall synthesis. It exhibits a broad spectrum of antibacterial activity against both Gram-positive and Gram-negative bacteria. This reagent is commonly employed in microbiological research to study bacterial infections and assess the efficacy of antimicrobial agents. -
Antibiotic
Carbenicillin disodium is a broad-spectrum semi-synthetic penicillin antibiotic targeting gram-negative bacteria. It exerts its antibacterial activity by inhibiting cell wall synthesis, making it effective in various microbiological applications. Due to its low toxicity, it is also suitable for use in plant tissue research. -
Antibiotic
Dimetridazole is a nitroimidazole antibiotic that primarily targets protein synthesis in various bacteria, including Campylobacter jejuni. It exhibits genotoxic properties, making it a valuable tool in research related to protozoal and bacterial infections. Its ability to disrupt microbial growth provides insights into pathogenic mechanisms and supports the development of therapeutic strategies. -
Bacterial Inhibitor
Erdosteine functions as a bacterial inhibitor by inhibiting lipopolysaccharide (LPS)-induced activation of NF-κB. This compound exhibits muco-modulatory, anti-bacterial, anti-inflammatory, and antioxidant properties. Erdosteine is primarily utilized in research applications focused on respiratory disorders and inflammation, supporting the study of therapeutic interventions in these areas. -
Bacterial Inhibitor
Erianin is a bacterial inhibitor that exhibits potent anticancer properties by inhibiting indoleamine 2,3-dioxygenase (IDO). This activity contributes to its ability to suppress tumor angiogenesis, making it a valuable compound in cancer research. Erianin's dual role as an antipyretic and analgesic further broadens its potential applications in therapeutic studies. -
HIV Inhibitor
Sennoside A is an anthraquinone glycoside derived from the senna plant (Cassia angustifolia) that exhibits inhibitory activity against HIV-1. This compound demonstrates an IC50 value of 3.8 μM in preventing HIV-1 replication and effectively inhibits HIV-1 reverse transcriptase-related DNA polymerase and ribonuclease H, with IC50 values of 1.9 μM and 5.3 μM, respectively. Sennoside A serves as a valuable tool in antiviral research, particularly in studies of HIV-1 replication mechanisms and potential therapeutic interventions. -
Bacterial Inhibitor
Allicin (diallyl thiosulfinate) is a potent bacterial inhibitor derived from garlic extracts, primarily responsible for the antimicrobial properties of garlic. It demonstrates significant antimicrobial activity against a wide range of microorganisms, including antibiotic-resistant strains, making it a valuable reagent for research in microbiology and pharmacology. Allicin is commonly utilized in studies investigating natural antibacterial compounds and their mechanisms of action. -
Antibacterial Drug
p-Anisic acid, also known as 4-Methoxybenzoic acid, acts primarily as a tyrosinase inhibitor. It exhibits multiple biological activities, including antioxidant, anti-anxiety, anti-inflammatory, anti-tumor, and anti-diabetic effects. This compound is also utilized as a preservative in cosmetic formulations, making it relevant for research in medicinal chemistry and cosmetic science. -
Antibiotic
Ertapenem is a broad-spectrum β-lactam antibiotic, characterized by its long-acting properties and efficacy against a wide range of anaerobic bacteria. With a minimum inhibitory concentration (MIC) of 0.12 μg/mL, it demonstrates significant anti-anaerobic activity. Ertapenem is utilized in research focused on severe bacterial infections affecting various human systems, including the skin, lungs, gastrointestinal tract, pelvis, and urinary tract. -
Antitumor Antibiotic
Quinocarcin is a potent antitumor antibiotic that primarily targets and inhibits DNA, RNA, and protein synthesis in Bacillus subtilis. This compound demonstrates significant cytotoxic activity against various cancer cell lines, making it a valuable tool in cancer research. Its unique mechanism of action supports its applications in studying tumorigenesis and the development of novel therapeutic strategies. -
Bacterial Inhibitor
Evoxine, also known as Haplophytin B, is a bacterial inhibitor that selectively targets CO2-induced immunosuppression. It demonstrates significant antimicrobial activity, particularly against common pathogens such as Escherichia coli, Bacillus subtilis, and Staphylococcus aureus, as evidenced by its performance in minimum inhibitory concentration (MIC) assays. Evoxine also inhibits the expression of pro-inflammatory cytokines such as interleukin-6 and chemokine CCL2 in human THP-1 macrophages, indicating its potential utility in therapeutic applications and crude drug preparations, particularly in the context of traditional medicine in West Africa. -
Antibiotic
Tetracycline hydrochloride is a broad-spectrum antibiotic targeting bacterial protein synthesis. It demonstrates antibacterial activity against a wide array of microorganisms, including gram-positive and gram-negative bacteria, as well as chlamydiae, mycoplasmas, and rickettsiae. This reagent is suitable for research applications involving bacterial infections and studies related to antibiotic resistance mechanisms. -
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.
