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Catalog No.
Product Name
Application
Product Information
Citations
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Bacterial Inhibitor
Ribostamycin sulfate is a broad-spectrum bacterial inhibitor that targets protein synthesis by binding to the 30S and 50S ribosomal subunits. Additionally, it inhibits the chaperone activity of protein disulfide isomerase (PDI). This reagent is primarily utilized in pharmacokinetic studies and investigations of nephrotoxicity, making it valuable in the evaluation of antimicrobial efficacy and safety profiles. -
HIV Inhibitor
Salicylanilide is a known HIV inhibitor that targets HIV-1 integrase and reverse transcriptase. This compound exhibits significant antiviral potency, making it an important tool in the study of HIV biology and potential therapeutic strategies. Its multifaceted biological activities render it suitable for various research applications in the field of virology and antiviral drug development. -
Bacterial Inhibitor
Sisomicin sulfate is a broad-spectrum aminoglycoside antibiotic that targets bacterial protein synthesis. It exhibits strong antibacterial activity, particularly against Gram-positive bacteria, making it an effective choice in studies of bacterial inhibition. This compound is useful for research applications involving the characterization of bacterial resistance and the development of new antimicrobial strategies. -
Bacterial Inhibitor
Sodium 4-aminosalicylate dihydrate serves as an inhibitor of dihydrofolate reductase (DHFR) and is recognized for its antituberculous properties. This compound exhibits anti-inflammatory effects, making it a valuable tool in the study of inflammatory bowel disease (IBD). Moreover, it is characterized by its oral bioavailability, enhancing its applicability in various research settings. -
Bacterial Inhibitor
Sparfloxacin is a fluoroquinolone antibiotic that primarily targets bacterial DNA gyrase and topoisomerase IV, inhibiting bacterial DNA replication. It exhibits broad-spectrum antibacterial activity, making it effective against a variety of Gram-positive and Gram-negative pathogens. Sparfloxacin is commonly used in research applications to study bacterial resistance mechanisms and evaluate new antibacterial strategies. -
Bacterial Inhibitor
Streptomycin sulfate is an aminoglycoside antibiotic that inhibits bacterial protein synthesis by binding to the 30S ribosomal subunit. It exhibits potent antibacterial activity against a range of Gram-negative and some Gram-positive bacteria, making it useful in both clinical and research settings. This reagent is commonly employed in studies involving microbial resistance, antibiotic efficacy, and protein synthesis mechanisms. -
Bacterial Inhibitor
Sulfamethazine is an antimicrobial agent that acts as a bacterial inhibitor, demonstrating permeability across the blood-brain barrier. It is commonly utilized in veterinary medicine to treat and prevent a variety of animal diseases, including gastrointestinal and respiratory tract infections. Regulatory standards set by China and the European Commission establish a maximum residue level of 100 μg/kg for Sulfamethazine in animal products, underscoring its significance in both therapeutic and safety assessments. -
Bacterial Inhibitor
Urethane, also known as ethyl carbamate, is an ethyl ester of carbamic acid that acts as a bacterial inhibitor. It demonstrates the ability to suppress the growth of bacteria, protozoa, sea urchin eggs, and plant tissues in vitro. This compound is primarily utilized in studies examining microbial inhibition and growth regulation in various biological systems. -
Bacterial Inhibitor
Carbadox is a quinoxaline-di-N-oxide antibiotic that functions as a bacterial inhibitor. It is primarily used in veterinary medicine to control enteric infections in nursery-age pigs, enhancing feed efficiency and promoting overall health. Its antibacterial properties make it valuable for research applications focused on veterinary pharmacology and microbiology in the study of antibiotic efficacy and resistance mechanisms. -
Bacterial Inhibitor
Meclocycline Sulfosalicylate Salt is a tetracycline antibiotic that acts as a bacterial inhibitor through the inhibition of protein synthesis. It exhibits broad-spectrum antibacterial activity, making it effective against various skin infections, including acne vulgaris. This reagent is valuable for research into antibiotic resistance and the mechanisms of bacterial infection. -
Bacterial Inhibitor
Saccharin is a non-caloric artificial sweetener that primarily exhibits bacteriostatic properties. It is recognized for its ability to inhibit bacterial growth and modulate the microbiome. This compound is utilized in various research applications aimed at studying microbial dynamics and the effects of sweeteners on bacterial populations. -
Bacterial Inhibitor
Octenidine dihydrochloride is a potent bacterial inhibitor that functions as an antiseptic. Its primary mechanism involves disrupting microbial cell membranes, which results in effective antimicrobial activity against a broad spectrum of pathogens. This compound is widely utilized in medical and clinical research for its applications in wound care, skin disinfection, and maintaining sterile conditions in various settings. -
Bacterial Inhibitor
Ceftezole is a broad-spectrum cephem antibiotic that effectively targets both gram-positive and gram-negative bacteria. Its primary mechanism involves inhibiting bacterial cell wall synthesis, making it valuable in combating various bacterial infections. Additionally, Ceftezole acts as an alpha-glucosidase inhibitor, demonstrating potential in in vivo anti-diabetic applications. It is suitable for use in microbiological research and studies related to diabetes management. -
Bacterial Inhibitor
Ceftezole sodium is a broad-spectrum cephem antibiotic primarily targeting various gram-positive and gram-negative bacteria. Its mechanism of action involves inhibiting bacterial cell wall synthesis, leading to cell lysis and death. Additionally, ceftezole sodium demonstrates alpha-glucosidase inhibition, contributing to its in vivo anti-diabetic effects. This compound is relevant for research in microbial resistance and diabetes therapeutic development. -
Bacterial Inhibitor
Sultamicillin tosylate is a broad-spectrum beta-lactamase inhibitor with potent antibacterial activity. This compound targets bacterial cell wall synthesis, making it effective against a variety of Gram-positive and Gram-negative bacteria. It is commonly used in microbiological research to study bacterial resistance mechanisms and to evaluate the efficacy of other antimicrobial agents. -
Bacterial Inhibitor
Sultamicillin is a broad-spectrum beta-lactam antibiotic that functions primarily by inhibiting bacterial cell wall synthesis. It exhibits significant antibacterial activity against a variety of gram-positive and gram-negative bacteria. This compound is utilized in research applications focused on investigating bacterial resistance mechanisms and evaluating the efficacy of antibiotic treatments. -
Bacterial Inhibitor
Clindamycin hydrochloride monohydrate is a bacterial inhibitor primarily targeting protein synthesis by binding to the 50S ribosomal subunit. This compound effectively suppresses the expression of virulence factors in Staphylococcus aureus, even at sub-inhibitory concentrations. Clindamycin hydrochloride monohydrate notably decreases the production of key toxins, including Panton-Valentine leucocidin (PVL), toxic-shock-staphylococcal toxin (TSST-1), and alpha-haemolysin (Hla), making it a valuable tool in microbiological research and the study of antibiotic resistance mechanisms. -
Bacterial Inhibitor
Cefoperazone sodium salt is a semisynthetic cephalosporin antibiotic that targets bacterial cell wall synthesis. It exhibits a broad spectrum of antibacterial activity against both Gram-positive and Gram-negative bacteria. This compound is widely utilized in microbiological research and clinical applications to study bacterial resistance and the efficacy of antibacterial therapies. -
Bacterial Inhibitor
Cefotiam hexetil hydrochloride is a prodrug of cefotiam, functioning primarily as a bacterial inhibitor. While it is designed for oral administration, this third-generation cephalosporin itself does not exhibit antibacterial activity until metabolized to cefotiam in the body. It is used in research applications to study antibiotic effects and efficacy in targeting gram-negative and gram-positive bacterial infections. -
Bacterial Inhibitor
Ceftizoxime sodium is a third-generation cephalosporin antibiotic that functions as a bacterial inhibitor by binding to penicillin-binding proteins (PBPs). This action prevents bacterial cell wall synthesis, leading to cell lysis and death. It exhibits effectiveness against both Gram-negative and Gram-positive bacteria, making it valuable for research applications related to antibiotic resistance and bacterial infections. -
Bacterial Inhibitor
Saccharin sodium hydrate functions as a bacterial inhibitor, exhibiting bacteriostatic properties. This compound modulates the microbiome and serves as a non-caloric artificial sweetener. It is applicable in research exploring bacterial growth inhibition and the effects of sweeteners on microbial populations. -
Bacterial Inhibitor
(2S,5R,6R)-Ticarcillin disodium is a semisynthetic antibiotic that targets bacterial cell wall synthesis, exhibiting bactericidal activity. This compound serves as the (2S,5R,6R)-enantiomer of Ticarcillin, demonstrating efficacy against a broad range of Gram-negative bacteria. It is widely utilized in microbiological research for testing susceptibility and evaluating the mechanisms of antibiotic resistance. -
Bacterial Inhibitor
Cetylpyridinium chloride monohydrate is a cationic quaternary ammonium compound that serves as a bacterial inhibitor. It exhibits significant antimicrobial activity, making it effective in preventing plaque formation and reducing gingivitis. This compound is commonly utilized in oral care products, such as mouthwashes and toothpastes, as well as in throat and nasal sprays for its antiseptic properties. -
Bacterial Inhibitor
Bacampicillin hydrochloride is a prodrug of ampicillin that acts as a bacterial inhibitor by disrupting cell wall synthesis in susceptible bacteria. It exhibits enhanced oral bioavailability compared to its parent compound, making it a valuable tool in studying bacterial infections and antibiotic resistance. This reagent is applicable in microbiological research and can facilitate investigations into the efficacy of penicillin derivatives in various laboratory settings. -
Antibiotic, ArlS Kinase Inhibitor
Oritavancin diphosphate is a glycopeptide antibiotic that targets bacterial cell wall synthesis and inhibits ArlS kinase activity, thus disrupting signal transduction pathways. It exhibits potent bactericidal activity against gram-positive organisms, including Bacillus anthracis, with a minimum inhibitory concentration (MIC) of 0.015 µg/mL for the Ames strain. Oritavancin diphosphate is effective in various research applications related to antibiotic resistance and cell wall biochemistry, making it a valuable tool for microbiological studies. -
Bacterial Inhibitor
Benzalkonium chloride (51% in water) is a widely utilized bacterial inhibitor that acts by disrupting microbial cell membranes. This potent antimicrobial agent is commonly deployed in various applications, including as a preservative in ophthalmic formulations, such as eye drops. Its effectiveness against a broad spectrum of bacteria makes it an essential reagent for research and development in microbiology and pharmaceutical studies. -
Bacterial Inhibitor
Isoniazid is a prodrug that targets the bacterial enzyme catalase-peroxidase (KatG) for activation, leading to its bactericidal effects against rapidly dividing mycobacteria. This compound exhibits significant anti-tuberculostatic activity and is widely used in research focused on tuberculosis and other mycobacterial infections. Its mechanism of action makes it a valuable reagent for investigating bacterial resistance and developing novel therapeutic strategies. -
Bacterial Inhibitor
Ethambutol is an antimycobacterial agent that targets arabinosyltransferase, inhibiting cell wall synthesis in bacteria. This compound is primarily utilized in research related to mycobacterial infections and has applications in developing animal models for conditions such as hyperuricemia and optic neuropathy. Ethambutol's ability to interrupt bacterial growth makes it valuable for studying microbial pathogenesis and treatment strategies. -
Bacterial Inhibitor
Puromycin is an aminoglycoside antibiotic that functions as a protein synthesis inhibitor through its action on bacterial ribosomes. By mimicking aminoacyl-tRNA, puromycin interferes with the elongation step of translation, leading to the premature termination of peptide chains. This compound is widely utilized in molecular biology studies, particularly in selection and maintenance of genetically modified cells, as well as in cancer research to elucidate apoptosis pathways. -
HIV Inhibitor
Oxindole, also known as Indolin-2-one, functions as an HIV inhibitor. This compound is of significant interest in the development of kinase inhibitors, with 2-indolinone derivatives serving as promising lead compounds in various therapeutic applications. Its selective biological activity makes it a valuable reagent for research focused on HIV treatment and other related pathways in viral infections. -
Bacterial Inhibitor
3,5,4'-Tribromosalicylanilide is a bacterial inhibitor that exhibits potent antituberculosis activity. This compound effectively inhibits the growth of Mycobacterium tuberculosis and Mycobacterium abscessus, demonstrating its potential in combating mycobacterial infections. Additionally, it influences gene expression, suggesting its utility in research focused on antibiotic resistance and microbial gene regulation. -
HIV-1 Inhibitor
Thiamine disulfide is an oxidized dimer of vitamin B1 that serves as a potent inhibitor of HIV-1. Its primary mechanism involves the suppression of HIV-1 transactivator (Tat) activity, which is crucial for viral replication and pathogenesis. This compound is valuable in research applications focused on HIV-1-related studies and the development of antiviral strategies. -
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. -
Bacterial Inhibitor
Benzoyleneurea is a bacterial inhibitor that demonstrates significant anti-bacterial activity. This compound serves as a valuable scaffold for the development of novel protein geranylgeranyltransferase-I (PGGTase-I) inhibitors, making it a useful tool in antibiotic research and drug discovery aimed at combating bacterial infections. -
Bacterial Inhibitor
Tenuazonic acid is a mycotoxin belonging to the tetramic acids family, functioning primarily as an inhibitor of bacterial protein biosynthesis by promoting the suppression of new protein release on ribosomes. It exhibits acute toxicity, with oral LD50 values ranging between 81-186 mg/kg in rodents. Tenuazonic acid also acts as a photosystem II inhibitor by preventing electron transport beyond the primary quinone receptor (QA) through its interaction with the D1 protein. Furthermore, this compound has demonstrated antiviral activity against various viruses, including measles and respiratory viruses, and exhibits potential inhibitory effects on skin cancer. -
Lanosterol Synthase Inhibitor
Lanopylin A2 is a potent inhibitor of lanosterol synthase (EC 5.4.99.7), demonstrating an IC50 of 18 μM. Its primary mechanism targets the biosynthetic pathway of sterols, making it a valuable tool for studying cholesterol biosynthesis and related metabolic processes. Lanopylin A2 is particularly useful in research involving fungal biochemistry and the development of antifungal therapies.
