Catalog No.
Product Name
Application
Product Information
Citations
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Fluoroquinolone antibiotic
ABT-492 is a new fluoroquinolone against 155 aerobic and 171 anaerobic pathogens. -
nitroimidazole antibiotic medication
Metronidazole is a nitroimidazole antibiotic medication used particularly for anaerobic bacteria and protozoa. -
Antibiotic
Delamanid is a new antituberculosis drug that inhibits mycolic acid synthesis and has shown potent in vitro and in vivo activity against drug-resistant strains of Mycobacterium tuberculosis.- Seungmo Kim, .et al. , Tuberculosis, 2025, 152: 102630
- Thanh Quang Nguyen, .et al. , Antimicrob Agents Chemother, 2022, Dec 20;66(12):e0044822 PMID: 36321819
- Meikle V, .et al. , Antimicrob Agents Chemother, 2018, Nov 12. pii: AAC.01846-18 PMID: 30420480
- World Health Organization, .et al. , World Health Organization, 2018, WHO/CDS/TB/2018.24
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natural cyclic oligopeptide antibiotic
Antibiotic that inhibits bacterial protein synthesis. Inhibits mRNA-tRNA translocation by GTPase elongation factor G (EF-G), EF-TU(GTP)-catalyzed aa-tRNA delivery and the activity of initiation factor 2 (IF-2). Antitumor agent; induces cell cycle arrest and apoptosis in breast cancer cells via downregulation of FOXM1 expression. -
Glycopeptide Antibiotic
Bleomycin is a glycopeptide antibiotic produced by the bacterium Streptomyces verticillus. It acts by induction of DNA strand breaks.- Ou QX, .et al. , Bioelectrochemistry, 2017, Jun;115:47-55 PMID: 28063751
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Antibiotic
Sulfaquinoxaline sodium salt is an antibiotic which has activity against a broad spectrum of Gram-negative and Gram-positive bacteria. -
Antibiotic
Robenidine hydrochloride is an antibiotic used for the control of coccidiosis, a debilitating protozoal infection in poultry. -
Broad-spectrum antibiotic
Cefadroxil, also known as Duricef, is an antibiotic effective against pyodermic skin diseases, such as Staphylococcus aureus and Streptococcus pyogenes. -
cephalosporin antibiotic
Cefuroxime axetil is a second generation cephalosporin antibiotic with a broad spectrum activity against Gram positive and Gram negative bacteria. -
antibiotic
Cefoxitin Sodium is a semisynthetic cephamycin antibiotic resistant to beta-lactamase. It is derived from Cephamycin C and is highly resistance to β-lactamase inactivation.- Viktoria Lazar, .et al. , Nature, 2022, 610: 540-546 PMID: 36198788
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Antibiotic
Ceforanide is a semi-synthetic, broad-spectrum, beta-lactam, second-generation cephalosporin antibiotic with bactericidal activity. -
antibiotic
Penicillin G potassium is a fast-acting antibiotic; used to treat bacterial infections that affect the blood, heart, lungs, joints, and genital areas -
broad-spectrum antibiotic
Amoxicillin Trihydrate is a broad-spectrum antibiotic. It binds to and inactivates penicillin-binding protein (PBP) 1A located on the inner membrane of the bacterial cell wall. Inactivated PBP interferes with the cross-linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity. -
Antibiotics
Gamithromycin is an antimicrobial agent which can inhibit the growth of MmmSC strains B237 and Tan8 with MICs of 0.00012 and 0.00006 μg/mL, respectively. -
Antibiotic
Sulbenicillin disodium is a semisynthetic penicillin-type antibiotic. -
antibiotic
Pivmecillinam hydrochloride is active against gram-negative organisms and used as for amdinocillin. Pivmecillinam is an orally active prodrug of mecillinam, an extended-spectrum penicillin antibiotic. -
semisynthetic antibiotic
Penicillin G procaine is a semisynthetic antibiotic prepared by combining penicillin G with Procaine. -
macrolide antibiotic
Erythromycin estolate is a macrolide antibiotic, produced by Streptomyces erythreus. It is the lauryl sulfate salt of the propionic ester of erythromycin. This erythromycin salt acts primarily as a bacteriostatic agent. -
antibiotics
Midecamycin is a naturally occurring 16-membered macrolide that fits under the category of acetoxy-substituted macrolide antibiotics. In this molecule, an acetoxy group is substituted on the position 9 of the 16-member ring and on position 4 of the terminal sugar. -
antibiotic
Ceftriaxone sodium is an antibiotic, a third-generation cephalosporin. Like other third-generation cephalosporins, it has broad-spectrum activity against Gram-positive bacteria and expanded Gram-negative coverage compared to second-generation agents. -
semisynthetic antibiotic
Penicillin G benzathine anhydrous is a semisynthetic antibiotic prepared by combining the sodium salt of penicillin G with N,N'-dibenzylethylenediamine. -
broad-spectrum penicillin antibiotic
Penicillin V potassium is a broad-spectrum penicillin antibiotic used orally in the treatment of mild to moderate infections by susceptible gram-positive organisms. -
broad-spectrum antibiotic
Tobramycin Sulfate is a broad-spectrum antibiotic. It is effective against gram-negative bacteria, and especially potent against the Pseudomonas species.- Viktoria Lazar, .et al. , Nature, 2022, 610: 540-546 PMID: 36198788
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broad spectrum antibiotic
Chlorhexidine digluconate solution is a bis-biguanide family cationic broad spectrum antibiotic. Studies indicate that chlorhexidine digluconate solution functions, via destabilization of the outer bacterial membrane, which resulted in the release of periplasmic enzymes in gram negative bacteria. -
Antibiotic
Berberine hemisulfate is an alkaloid with antibiotic properties derived from the traditional Chinese herbal medicine Huanglian. It demonstrates significant antimicrobial activity and possesses anti-inflammatory, antitumor, cardiovascular protective, and neuroprotective effects. This compound is valuable for research applications exploring infections, immune response modulation, and potential therapeutic avenues for various diseases. -
Antibiotic
Ceftazidime (GR20263), an antibiotic, has a broad spectrum activity against Gram-positive and Gram-negative aerobic bacteria. Ceftazidime is also active against Enterobacteriaceae (including β-lactamase-positive strains) and is resistant to hydrolysis by most β-lactamases. -
Antibiotic
Erythromycin is a macrolide antibiotic that targets bacterial 50S ribosomal subunits, effectively inhibiting RNA-dependent protein synthesis by obstructing transpeptidation and translocation reactions. This compound demonstrates a broad spectrum of antimicrobial activity against various bacteria, making it valuable in microbiological research. Additionally, erythromycin has been shown to possess antitumor and neuroprotective properties, contributing to its usefulness in diverse areas of biomedical research. -
Antibiotic
Tetracycline is a broad-spectrum antibiotic that targets bacterial protein synthesis by binding to the 30S ribosomal subunit, inhibiting translation. It demonstrates activity against a diverse array of microorganisms, including gram-positive and gram-negative bacteria, as well as chlamydiae, mycoplasmas, and rickettsiae. This compound is widely utilized in research related to bacterial infections and antibiotic resistance mechanisms. -
Antibiotic
Acetoxycycloheximide is an antibiotic with potent antitumor properties, primarily functioning as a protein synthesis inhibitor. It effectively induces procaspase-3 activation, leading to apoptosis through the release of cytochrome c from mitochondria via the JNK signaling pathway. Additionally, acetoxycycloheximide downregulates cell surface TNF-R1 by activating the ERK and p38 MAPK pathways, thereby inhibiting TNF-α-mediated NF-κB signaling. This reagent is valuable for research related to inflammatory and immune diseases as well as cancer. -
Antibiotic
Chrysomycin A is an antibiotic derived from the Streptomyces genus. It demonstrates significant antitumor properties, alongside effective activity against Mycobacterium tuberculosis and methicillin-resistant Staphylococcus aureus (MRSA). In glioblastoma research, Chrysomycin A has been shown to inhibit cancer cell proliferation, migration, and invasion by targeting the Akt/GSK-3β/β-catenin signaling pathway, making it a valuable tool for cancer studies and antibiotic research. -
Antibiotic
Ceftiofur sodium is an antibiotic that acts as a cell wall synthesis inhibitor by targeting bacterial penicillin-binding proteins (PBPs). It exhibits bactericidal activity through the inhibition of peptidoglycan synthesis, resulting in bacterial cell lysis. Additionally, Ceftiofur sodium has anti-inflammatory properties by inhibiting the activation of NF-κB and MAPKs, which decreases the secretion of pro-inflammatory cytokines including TNF-α, IL-1β, and IL-6. This compound is applicable in research related to antibiotic resistance and inflammatory responses. -
Quinolone Antibiotic
Lomefloxacin hydrochloride is a difluoroquinolone antibiotic that primarily targets bacterial topoisomerase II, inhibiting DNA supercoiling and replication. It exhibits broad-spectrum bactericidal activity against both Gram-positive and Gram-negative bacteria and induces reactive oxygen species (ROS) production, leading to apoptosis. Additionally, Lomefloxacin hydrochloride demonstrates anticancer effects, particularly against melanoma, making it a valuable reagent for studying systemic bacterial infections and skin malignancies. -
Antibiotic
Novobiocin sodium is a potent antibiotic that primarily targets DNA gyrase, exhibiting significant inhibitory action in various bacterial strains. Additionally, it acts as an antagonist of heat shock protein 90 (Hsp90), expanding its potential applicability in therapeutic research. Novobiocin sodium is particularly valuable for studies on beta-lactam-resistant pneumococcal infections and demonstrates anti-orthopoxvirus activity, highlighting its relevance in infectious disease research. -
Antibiotic
Bifonazole is an imidazole antifungal agent that primarily targets fungal cell membranes. It exhibits broad-spectrum antibacterial and antifungal activity, making it effective against various dermatophytes and yeast infections. Bifonazole is utilized in research settings to study antifungal mechanisms and evaluate new therapeutic strategies for fungal infections. -
Antibiotic
Phenothiazine is an antibiotic that exhibits broad-spectrum biological activity, including insecticidal, fungicidal, antibacterial, and anthelmintic effects. Additionally, it is instrumental in research related to neurological diseases, offering insights into potential therapeutic mechanisms. This compound serves as a valuable tool for scientists studying microbial resistance and the treatment of parasitic infections. -
Antibiotic
Sulfacetamide sodium is a sulfonamide antibiotic targeting bacterial infections, primarily utilized in ocular research. It exhibits both antibacterial and antifungal activity, making it an important reagent for studying and treating various infections. Applications include investigation of microbial resistance and the efficacy of topical treatments against ocular pathogens. -
Antibiotic
Sulfacetamide sodium monohydrate is a sulfonamide antibiotic primarily targeting bacterial infections. It exhibits both antifungal and antibacterial activities, making it valuable for studying ocular infections. This reagent is useful in research applications that explore mechanisms of infection and treatment efficacy in ophthalmology. -
Antibiotics
Fluconazole hydrate is a triazole antifungal agent that targets fungal cell membrane synthesis by inhibiting the enzyme lanosterol 14-alpha-demethylase. It exhibits significant efficacy against a range of superficial and systemic fungal infections, making it a critical tool in the treatment and prevention of candidiasis and cryptococcosis. Fluconazole hydrate is widely utilized in clinical research to explore antifungal resistance mechanisms and assess therapeutic strategies in various fungal pathogens. -
Antibiotic
(S)-Dihydroaeruginoic acid is an antibiotic derived from Pseudomonas fluorescens, targeting various microbial pathogens. It exhibits substantial antimicrobial activity against a range of fungi, including Rhizoctonia solani, Phytophthora ultimum, Botrytis cinerea, Sclerotium rolfsii, Colletotrichum gloeosporioides, Fusarium oxysporum, and Septoria tritici, as well as against bacterial strains such as Bacillus subtilis, Erwinia herbicola, and Streptomyces albus when assessed at a concentration of 200 μg/disc. This compound is valuable for research focused on antibiotic development and the study of microbial resistance. -
Antibiotic
Verlamelin is a depsipeptide antibiotic that targets and disrupts cellular processes in fungi. It exhibits significant antifungal activity against various plant pathogens, making it a valuable tool for research into plant disease management and fungal biology. Its unique mechanism of action can be explored for insights into antibiotic resistance and the development of new antifungal therapies. -
Antifungal Antibiotic
Mucidin is an antifungal antibiotic that primarily targets the cytochrome bc1 complex within the mitochondrial respiratory chain, inhibiting electron-transfer reactions. This mechanism disrupts ATP production in fungi, leading to their growth inhibition. Mucidin is useful in research applications focused on fungal pathogenesis and mitochondrial function, providing insights into antifungal resistance and treatment strategies. -
Antibiotic
Oudemansin A is an antibiotic that targets fungal pathogens by inhibiting protein, RNA, and DNA synthesis. This compound demonstrates significant antifungal activity, making it a valuable reagent in research focused on the mechanisms of fungal infection and resistance. Its efficacy in disrupting essential cellular processes highlights its potential for exploring new therapeutic approaches in mycology. -
Antibiotic
Pulvilloric acid is an antifungal antibiotic that specifically targets fungal pathogens. Isolated from the fungus Penicillium pulvillorum, this compound exhibits significant antimicrobial activity, making it valuable in research related to antifungal drug development and microbial resistance studies. Its unique mechanism of action positions it as a critical reagent for investigating fungal infections and developing effective therapeutic strategies. -
Antibiotic
Exfoliazone is a phenoxazine antibiotic that targets fungal organisms, specifically demonstrating efficacy against Valsa ceratosperma. This compound exhibits significant antifungal activity, with an effective dose (ED50) for inhibiting mycelial growth calculated at 70 μg/mL. It serves as a valuable tool for studying fungal resistance mechanisms and exploring potential therapeutic applications in mycology research. -
Antibiotic
Pyrrolomycin E is a pyrrole antibiotic that exhibits broad-spectrum antibacterial activity. It demonstrates efficacy against both Gram-positive and Gram-negative bacteria, as well as antifungal properties against various fungal strains. This compound is valuable for research applications focused on antibiotic resistance and the development of new antimicrobial agents. -
Antitumor Antibiotic
Glidobactin F is an antitumor antibiotic known for its effectiveness against pathogenic fungi and yeast. This compound demonstrates significant anticancer activity, particularly in enhancing the survival of mice inoculated with P388 leukemia cells. Glidobactin F is valuable for research applications focused on cancer treatment and antifungal studies.
