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Catalog No.
Product Name
Application
Product Information
Citations
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Influenza Virus Inhibitor
Oseltamivir is an orally active neuraminidase inhibitor targeting the influenza virus. It demonstrably inhibits various strains of influenza, including A/H3N2, A/H1N2, A/H1N1, and B, with mean IC50 values of 0.67 nM, 0.9 nM, 1.34 nM, and 13 nM, respectively. This compound is essential for studying antiviral strategies and evaluating the efficacy of flu treatments in laboratory settings. -
Parasite Inhibitor
Albendazole sulfoxide, the principal active metabolite of Albendazole, acts as a potent inhibitor of parasite growth. It demonstrates significant anti-parasitic activity against Echinococcus multilocularis metacestodes, making it valuable in the study of parasitic infections and potential therapeutic interventions. This compound is utilized in research focused on parasitology and drug efficacy against helminthic diseases. -
Parasite Inhibitor
Oxfendazole is a sulfoxide derivative of fenbendazole that targets parasitic organisms through inhibition of energy metabolism. Its primary biological activity is the effective combat against a broad spectrum of parasites. This compound is utilized in research focused on parasitology and can also be studied for its potential effects in tumor promotion investigations. -
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. -
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. -
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. -
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. -
HBV Inhibitor
Catalpol, an iridoid glycoside derived from Rehmannia glutinosa, primarily targets hepatitis B virus (HBV) inhibition. It exhibits a broad range of biological activities including neuroprotection, hypoglycemic effects, anti-inflammatory properties, and antioxidant effects. Additionally, Catalpol demonstrates potential in anti-cancer and anti-spasmodic applications, making it valuable for various research contexts focusing on viral infections and related therapeutic interventions. -
Bacterial Inhibitor
3,3'-Di-O-methylellagic acid is a bacterial inhibitor derived from Euphorbia adenochlora. It selectively inhibits the development of acid-fastness in mycobacteria without affecting their growth rates. Additionally, this compound exhibits hepatoprotective properties, likely attributed to its antioxidative effects, making it valuable for research in microbial resistance and liver health. -
SARS-CoV-2 PLpro Inhibitor
Aloin B (Isobarbaloin) is an orally active inhibitor of the SARS-CoV-2 papain-like protease (PLpro), with reported IC50 values of 16.08 μM for hydrolytic activity and 17.51 μM for deubiquitinase activity. This compound demonstrates biological activity in anti-inflammatory pathways and tumor promotion inhibition, making it valuable for research in cancer biology and COVID-19. Additionally, Aloin B is metabolized by intestinal flora to produce aloe-emodin-9-anthrone, which may contribute to its laxative effects. -
Parasite Inhibitor
β-Hederin is a saponin derived from Hedera helix L. (Araliaceae) that demonstrates significant antileishmanial activity. It exhibits IC50 values of 1.5 μM against L. mexicana promastigotes, 68 nM against L. mexicana amastigotes, and 4.57 μM in THP-1 cells. This compound may be utilized in research applications targeting leishmaniasis, providing insights into potential therapeutic strategies against parasitic infections. -
Cholinesterase (ChE) Inhibitor
Corydaline is an isoquinoline alkaloid that functions as a cholinesterase (ChE) inhibitor with an IC50 of 226 μM. In addition to its cholinergic activity, Corydaline acts as a μ-opioid receptor agonist (Ki of 1.23 μM) and demonstrates significant antiviral effects by inhibiting enterovirus 71 (EV71) replication, with an IC50 of 25.23 μM. This compound also exhibits anti-angiogenic, anti-allergic, gastric-emptying, and antinociceptive properties, making it a valuable reagent for various biological research applications. -
HIV Inhibitor
Gomisin G is a lignan derived from Schisandra chinensis that acts as an anti-HIV agent with an EC50 of 0.006 μg/mL. It exhibits anti-liver cancer and anti-inflammatory properties while utilizing an AKT-cyclin D1 dependent mechanism to target triple-negative breast cancer cells by inhibiting phosphorylation rather than promoting apoptosis. Additionally, Gomisin G leads to G1 phase cell cycle arrest and inhibition of AKT phosphorylation. This compound is suitable for research applications focusing on HIV and various cancer types, including breast and liver cancers. -
HIV Protease Inhibitor
Ganoderic acid B is a triterpene derived from the medicinal mushroom Ganoderma lucidum, functioning as an inhibitor of HIV protease. This compound exhibits moderate inhibitory activity against HIV-1 protease, with an IC50 value of 170 μM, making it a potential candidate for research into antiviral therapies. Additionally, ganoderic acid B has demonstrated the ability to inhibit Epstein-Barr virus (EBV) antigen activation and may serve as a telomerase inhibitor, highlighting its broad potential in virology and cancer research applications. -
Bacterial Inhibitor
Methyl Paraben is a bacterial inhibitor primarily used as a preservative in various applications due to its stability and non-volatility. It has been shown to enhance histamine release and modulate cellular immune responses, in addition to blocking sodium channels. Its properties make it valuable for studies exploring microbial inhibition and the mechanisms of ischemia-reperfusion injury. -
Bacterial Inhibitor
Enrofloxacin is a potent bacterial inhibitor belonging to the fluoroquinolone class. It exhibits an MIC90 value of 0.312 μg/mL against Mycoplasma bovis, demonstrating its effectiveness in combating bacterial infections. This compound is widely utilized in research applications focused on antibiotic resistance, microbiology, and the study of bacterial pathogens. -
Bacterial Inhibitor
Florfenicol is a broad-spectrum antibacterial agent that exerts its effects primarily through inhibition of bacterial protein synthesis. This orally active compound demonstrates additional properties, including anti-inflammatory, pro-apoptotic, and immunomodulatory functions. Florfenicol is commonly utilized in research focused on bacterial infections and the modulation of immune responses. -
Bacterial Inhibitor
Furaltadone hydrochloride is an orally active antibacterial agent targeting bacterial infections. It exhibits in vitro inhibitory effects on Staphylococcus and can be utilized in the study of intestinal Salmonella infections. Additionally, Furaltadone demonstrates potential inhibitory effects on allergic reactions, making it a valuable tool for research in microbiology and immunology. -
Bacterial Inhibitor
Penicillin G sodium salt is a β-lactam antibiotic that inhibits bacterial cell wall synthesis by targeting penicillin-binding proteins. It demonstrates broad-spectrum antibacterial activity against various Gram-positive and some Gram-negative organisms. This reagent is commonly used in microbiological studies to evaluate susceptibility patterns and in the development of antibiotic resistance models. -
Bacterial Inhibitor
Piperacillin sodium is a semisynthetic β-lactam antibiotic that targets penicillin-binding proteins, exhibiting potent bactericidal activity against a broad range of Gram-negative bacteria and select Gram-positive strains. This compound is widely utilized in pharmaceutical research to study bacterial infections and antibiotic resistance. Piperacillin sodium is frequently employed in combination with the β-lactamase inhibitor Tazobactam to enhance its efficacy against resistant bacterial strains. -
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. -
Parasite Inhibitor
Morantel tartrate is an effective anthelmintic agent targeting gastrointestinal parasites. It is primarily utilized in veterinary medicine to control subclinical gastrointestinal parasitism in cattle on pasture. Following administration, morantel tartrate can be detected in ruminal, abomasal, ileal fluids, and feces for up to 98 days, indicating its prolonged activity. This compound is instrumental in research related to parasitic infections and antiparasitic drug development. -
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.
