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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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  • HBV-IN-48
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    HBV-IN-48

    CAS:
    <p>HBV-IN-48, an HBV inhibitor, exhibits potent antiviral activity against HBV in HepDE19 cells, demonstrated by its EC 50 value of 0.005 μM. Additionally, it effectively reduces serum HBV DNA levels in mouse models of HBV infection.</p>
    Formula:C22H15F4N3O3
    Color and Shape:Solid
    Molecular weight:445.37

    Ref: TM-T200299

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    Mt KARI-IN-1

    <p>Mt KARI-IN-1 inhibits Mtb KARI with a 3.06 μM Ki, targeting tuberculosis.</p>
    Formula:C14H11N5O4S2
    Color and Shape:Solid
    Molecular weight:377.4

    Ref: TM-T61569

  • Mycobacterium Tuberculosis-IN-6
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    Mycobacterium Tuberculosis-IN-6

    CAS:
    <p>Mycobacterium Tuberculosis-IN-6 (compound b1) is an inhibitor of the enoyl reductase InhA from Mycobacterium tuberculosis, with an IC50 value of 7.74 μM. It is useful in antibacterial research.</p>
    Formula:C19H20FNO
    Color and Shape:Solid
    Molecular weight:297.367

    Ref: TM-T204419

  • Antimicrobial agent-38
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    Antimicrobial agent-38

    CAS:
    <p>Antimicrobial agent-38 (compound 10) effectively inhibits methicillin-resistant Staphylococcus aureus (S. aureus) strain ATCC 700699 and non-resistant strain ATCC 29213, with minimum inhibitory concentrations (MIC) of 32 mg/L and 64 mg/L, respectively.</p>
    Formula:C14H11N3O4S
    Color and Shape:Solid
    Molecular weight:317.32

    Ref: TM-T204599

  • GTSE1-IN-1
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    GTSE1-IN-1

    CAS:
    <p>GTSE1-IN-1 (compound Y18), an orally active GTSE1 inhibitor, exhibits notable anticancer properties. It effectively represses the proliferation of cancer cells by downregulating GTSE1 transcription and expression, which leads to DNA damage and promotes persistent cell cycle arrest and cellular senescence. Moreover, GTSE1-IN-1 substantially reduces the adhesion, migration, and invasion of colorectal cancer HCT116 cells and non-small cell lung cancer A549 cells in vitro.</p>
    Formula:C21H24FN7
    Color and Shape:Solid
    Molecular weight:393.46

    Ref: TM-T200127

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    Neuraminidase-IN-4

    <p>Neuraminidase-IN-4 inhibits neuraminidase (EC50: 1.59 μM) and has strong anti-H5N1 activity.</p>
    Formula:C21H20N2O6S
    Color and Shape:Solid
    Molecular weight:428.46

    Ref: TM-T62345

  • Methyl 3-oxodecanoate
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    Methyl 3-oxodecanoate

    CAS:
    <p>Methyl 3-oxodecanoate exhibits virulence factor activity against human pathogens and shows effects on Synechococcus elongatus (a species of fluorescent algae) as well as on culture supernatant. Additionally, Methyl 3-oxodecanoate inhibits DNA synthesis by suppressing protein synthesis at the translation initiation level.</p>
    Formula:C11H20O3
    Color and Shape:Solid
    Molecular weight:200.275

    Ref: TM-T206384

  • MPro N3
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    MPro N3

    CAS:
    <p>Mpro inhibitor blocks MHV-A29, HCoV-229E, FOPV (IC50: 2.7–8.8 μM), and SARS-CoV-2 (IC50: 16.8 μM) in plaque assays.</p>
    Formula:C35H48N6O8
    Color and Shape:Solid
    Molecular weight:680.79

    Ref: TM-T38175

  • Secutrelvir
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    Secutrelvir

    CAS:
    <p>Secutrelvir inhibits the 3CL protease (3CL protease), thereby exhibiting antiviral activity by preventing the replication of SARS-CoV-2.</p>
    Formula:C23H16Cl2F3N5O2
    Color and Shape:Solid
    Molecular weight:522.307

    Ref: TM-T206356

  • Flutimide
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    Flutimide

    CAS:
    <p>Flutimide: Endonuclease inhibitor, IC50 = 3μM, for research on acute respiratory diseases like influenza.</p>
    Formula:C12H18N2O3
    Color and Shape:Solid
    Molecular weight:238.28

    Ref: TM-T70355

  • Plevitrexed
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    Plevitrexed

    CAS:
    <p>Plevitrexed, an oral TS inhibitor (Ki: 0.44 nM), targets α-folate receptor &amp; reduced folate carrier, treats gastric cancer.</p>
    Formula:C26H25FN8O4
    Purity:98%
    Color and Shape:Solid
    Molecular weight:532.53

    Ref: TM-T12635L

  • LpxH-IN-2
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    LpxH-IN-2

    CAS:
    <p>LpxH-IN-2 (compound 014), a potent inhibitor of LpxH, exhibits antibacterial activity against E. coli.</p>
    Formula:C27H33ClF2N6O4S
    Color and Shape:Solid
    Molecular weight:611.10

    Ref: TM-T89832

  • Penethamate hydriodide
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    Penethamate hydriodide

    CAS:
    <p>Penethamate hydriodide is a diethylaminoethyl ester prodrug of penicillin, utilized via intramuscular injection to treat mastitis in cattle.</p>
    Formula:C22H32IN3O4S
    Color and Shape:Solid
    Molecular weight:561.477

    Ref: TM-T206114

  • FGI-106
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    FGI-106

    CAS:
    <p>FGI-106 combats Ebola, Rift Valley, Dengue Fever, HCV, and HIV-1; EC50s range from 100-900 nM.</p>
    Formula:C28H38N6
    Purity:98%
    Color and Shape:Solid
    Molecular weight:458.64

    Ref: TM-T11281

  • Isazofos
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    Isazofos

    CAS:
    <p>Isazofos is a broad-spectrum organophosphate insecticide and nematicide effective in controlling a variety of lawn pests, such as nematodes (Radopholus similis). It also demonstrates efficacy in managing rice gall midge.</p>
    Formula:C9H17ClN3O3PS
    Color and Shape:Solid
    Molecular weight:313.74

    Ref: TM-T201803

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    FNC-TP trisodium

    <p>FNC-TP trisodium, active intracellular FNC form, inhibits NRTI, fights HIV, HBV, and HCV.</p>
    Formula:C9H11FN6Na3O13P3
    Color and Shape:Solid
    Molecular weight:592.11

    Ref: TM-T64188

  • Succinate dehydrogenase-IN-8
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    Succinate dehydrogenase-IN-8

    CAS:
    <p>Succinate dehydrogenase-IN-8 (compound i19) is a potent inhibitor of succinate dehydrogenase (SDH). This indanoyl amino acid derivative demonstrates strong antifungal activity in vitro against Rhizoctonia solani (EC50 = 0.1843 mg/L), Botrytis cinerea (EC50 = 0.4829 mg/L), and Sclerotinia sclerotiorum (EC50 = 0.1349 mg/L).</p>
    Formula:C22H19Cl2F2N5O2
    Color and Shape:Solid
    Molecular weight:494.32

    Ref: TM-T207398

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    Encephalitic alphavirus-IN-1

    <p>Alphavirus-IN-1 blocks VEEV (EC50: 0.24 μM) &amp; EEEV (EC50: 0.16 μM), non-toxic, stable in mice plasma.</p>
    Formula:C27H25FN6O2
    Color and Shape:Solid
    Molecular weight:484.52

    Ref: TM-T63218

  • Anti-MRSA agent 19
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    Anti-MRSA agent 19

    CAS:
    <p>Anti-MRSA agent 19 (Compound 1) is an antibiotic that exhibits activity against Staphylococcus aureus. It is active against 40 clinical isolates from the CDC, representing diverse bacterial species with various resistance factors, including resistance to vancomycin, aminoglycoside/tetracycline, and oxazolidinone (median MIC=4 μg/mL).</p>
    Formula:C15H10Cl3NO4
    Color and Shape:Solid
    Molecular weight:374.6

    Ref: TM-T201507

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    Chitinase-IN-4

    <p>Chitinase-IN-4 (compound 8f) is a potent and selective inhibitor of OfChi-h with an IC50 value of 0.1 μM and good insecticidal activity.</p>
    Formula:C21H24ClN7
    Color and Shape:Solid
    Molecular weight:409.92

    Ref: TM-T62069