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Microbiology/Virology

Microbiology/Virology

Microbiology and virology inhibitors are compounds that target microorganisms, including bacteria, viruses, and fungi, disrupting their growth, replication, or survival. These inhibitors are essential for studying microbial pathogenesis, understanding resistance mechanisms, and developing new antimicrobial and antiviral therapies. Inhibitors in this category are used to combat infectious diseases, explore microbial ecology, and investigate host-pathogen interactions. At CymitQuimica, we provide a broad selection of high-quality microbiology and virology inhibitors to support your research in infectious diseases, microbiology, and virology.

Subcategories of "Microbiology/Virology"

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Found 5842 products of "Microbiology/Virology"

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  • Antimalarial agent 42


    <p>Compound 42 (Compound 2), an antimalarial agent, effectively inhibits Plasmodium falciparum during the asexual blood stages (IC 50 &lt;0.5μM) and gametocytes (IC 50 is 0.14 μM).</p>
    Formula:C24H42N2
    Color and Shape:Solid
    Molecular weight:358.6
  • Phosphomannose isomerase

    CAS:
    <p>Phosphomannose isomerase, the initial enzyme in GDP-Man biosynthesis, catalytically facilitates the interconversion of fructose-6-phosphate (Fru6P) and mannose-</p>
    Color and Shape:Solid
  • EFdA-TP tetraammonium


    <p>EFdA-TP tetraammonium is a potent HIV-1 RT inhibitor and DNA synthesis blocker, acting as an ICT or DCT.</p>
    Formula:C12H27N9O12P3
    Color and Shape:Solid
    Molecular weight:601.31
  • Antibacterial agent 142


    <p>Antibacterial agent 142, an aromatic hydrazide, exhibits bacteriostatic antibacterial activity and inhibits biofilm formation [1].</p>
    Formula:C12H9ClFN3O
    Color and Shape:Solid
    Molecular weight:265.67
  • RPR103611

    CAS:
    <p>RPR103611, a betulinic acid derivative, inhibits HIV-1; IC50s: CCR5 (YU2) 80, CXCR4 (NL4-3) 0.27, dual-tropic (89.6) 0.17.</p>
    Formula:C46H78N2O6
    Color and Shape:Solid
    Molecular weight:755.12
  • Tilatamig samrotecan


    <p>Tilatamig samrotecan (AZD9592) is an antibody-drug conjugate (ADC) designed to deliver a topoisomerase I inhibitor (TOP1i). It targets epidermal growth factor receptor (EGFR) and c-MET and demonstrates antitumor activity. The compound induces DNA double-strand breaks, elevates pRAD50 and γH2AX expression, and inhibits the growth of non-small cell lung cancer.</p>
    Color and Shape:Odour Solid
  • Parvodicin C2

    CAS:
    <p>Parvodicin C2, a glycopeptide antibiotic derived from A. parvosata and part of the parvodicin complex, serves as a component of the A40926 antibiotic complex utilized as a precursor for synthesizing dalbavancin. It exhibits activity against methicillin-sensitive and methicillin-resistant strains of S. aureus, S. epidermidis, S. saprophyticus, S. hemolyticus, and E. faecalis.</p>
    Formula:C83H88Cl2N8O29
    Color and Shape:Solid
    Molecular weight:1732.53
  • 3-Methyl-chuangxinmycin


    <p>3-Methyl-chuangxinmycin, an antibiotic, inhibits the enzyme responsible for synthesizing tryptophan tRNA (TrpRS), thereby affecting the translation process in both bacteria and mammalian cells. Additionally, it downregulates genes associated with interferon, TNF, and inflammatory responses in RDEB_L1 cells.</p>
    Formula:C13H13NO2S
    Color and Shape:Solid
    Molecular weight:247.31
  • Isepamicin

    CAS:
    <p>Isepamicin (Sch 21420) is a strong aminoglycoside antibiotic, effective on Enterobacteriaceae and staphylococci, less so on other bacteria.</p>
    Formula:C22H43N5O12
    Color and Shape:Solid
    Molecular weight:569.60
  • HSGN-218


    <p>HSGN-218: non-cytotoxic, gut-specific antibiotic; effective against C. difficile (MIC 0.003-0.03 μg/ml); boosts survival in mice with C. difficile.</p>
    Color and Shape:Solid
  • ZHAWOC25153


    <p>ZHAWOC25153 (Compound 17o) is an inhibitor of the SARS-CoV-2 papain-like protease (PLpro) with an IC50 of 7 μM. It demonstrates antiviral properties and is applicable for research in the field of anti-infective studies.</p>
    Formula:C32H33FN2O6
    Color and Shape:Solid
    Molecular weight:560.613
  • Orfamide A

    CAS:
    <p>Orfamide A, a lipopeptide biosurfactant isolated from P. protegens, exhibits multifaceted bioactivity. With an LC50 of 34.5 μg/ml, it significantly increases mortality in adult green peach aphids. Additionally, at a concentration of 50 μM, Orfamide A inhibits appressoria formation in M. oryzae isolates and decreases the prevalence of sporulating blast lesions in M. oryzae-infected plants. Furthermore, it demonstrates efficacy against T. b. brucei, with an IC50 value of 6 µM.</p>
    Formula:C64H114N10O17
    Color and Shape:Solid
    Molecular weight:1295.67
  • 8-Br-GTP

    CAS:
    <p>8-Br-GTP, a GTP analog, inhibits FtsZ polymerization/GTPase (K i 31.8 μM), aids nucleic acid modification.</p>
    Formula:C10H15BrN5O14P3
    Color and Shape:Solid
    Molecular weight:602.076
  • Antibacterial agent 138


    <p>Antibacterial agent 138 effectively targets multi-drug resistant bacteria by inhibiting protein synthesis.</p>
    Formula:C34H52INO4S
    Color and Shape:Solid
    Molecular weight:697.75
  • LFF 571

    CAS:
    <p>LFF 571 is an inhibitor of protein-synthesizing GTPase (Elongation Factor).</p>
    Formula:C60H63N13O13S6
    Color and Shape:Solid
    Molecular weight:1366.6
  • GSK2336805

    CAS:
    <p>GSK-2336805, an HCV NS5A inhibitor, is effective against genotypes 1, 4, 5, and some of 6.</p>
    Formula:C42H52N8O8
    Color and Shape:Solid
    Molecular weight:796.91
  • Maximin 32


    <p>Maximin 32, an antimicrobial peptide originating from toad brain, exhibits activity against Staphylococcus aureus and Escherichia coli, with minimum inhibitory</p>
    Formula:C121H208N34O33
    Color and Shape:Solid
    Molecular weight:2667.15
  • XT-1

    CAS:
    <p>XT-1, an antimicrobial peptide sourced from Xenopus tropicalis skin secretions, exhibits potent activity against S.</p>
    Formula:C134H227N37O31
    Color and Shape:Solid
    Molecular weight:2852.47
  • Oligomycin E

    CAS:
    <p>Oligomycin E, a Streptomyces metabolite, has weak antifungal properties but strong Gram-positive and HeLa cell antitumor effects (IC50=14 ng/ml).</p>
    Formula:C45H72O13
    Color and Shape:Solid
    Molecular weight:821.058
  • Antibacterial agent 34

    CAS:
    <p>Antibacterial agent 35 is a compound that effectively reduces the minimum inhibitory concentration (MIC) of Ceftazidime, enhancing its antibacterial activity.</p>
    Formula:C13H19N5O6S
    Color and Shape:Solid
    Molecular weight:373.38