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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 6352 products of "Microbiology/Virology"

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  • GRL-190-21
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    GRL-190-21

    CAS:
    <p>GRL-190-21 (compound 5e), an inhibitor of SARS-Cov-2-Mpro, shows potent antiviral activity, with a K_i of 0.04 nM and an EC_50 of 0.26 μM in VeroE6 cells. It significantly reduces the infectivity, replication, and cytopathic effect of SARS-CoV-2 without notable toxicity [1].</p>
    Formula:C24H34F3N5O4
    Color and Shape:Solid
    Molecular weight:513.55

    Ref: TM-T86525

  • WRN inhibitor 7
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    WRN inhibitor 7

    CAS:
    <p>WRN inhibitor 7 (Compound h6), a potent inhibitor of Werner syndrome helicase, demonstrates effective suppression of WRN's helicase and ATPase activities with IC50 values of 9.8 μM and 15.8 μM, respectively. This compound is utilized in the study of microsatellite instable (MSI) cancers [1].</p>
    Formula:C27H23N3O6
    Color and Shape:Solid
    Molecular weight:485.49

    Ref: TM-T87635

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    Antiviral agent 15

    Compound 15f, a Clofazimine derivative, inhibits rabies (EC50: 1.45 μM) and SARS-CoV-2 (EC50: 14.6 μM).
    Formula:C27H24FN5O
    Color and Shape:Solid
    Molecular weight:453.51

    Ref: TM-T62780

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    HIV-1 inhibitor-14

    HIV-1 inhibitor-14: potent, broad HIV-1 RT inhibitor. IC50=0.14μM. Effective against wild-type and resistant strains, EC50=5.79-28.3nM.
    Formula:C29H32N6O4S
    Color and Shape:Solid
    Molecular weight:560.67

    Ref: TM-T63963

  • Metallo-β-lactamase-IN-14
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    Metallo-β-lactamase-IN-14

    CAS:
    Metallo-β-lactamase-IN-14 (Compound 17e) serves as an inhibitor of Metallo-β-Lactamase, displaying inhibitory activity against VIM-1 and VIM-2. This compound also exhibits antibacterial effects on Gram-negative (GN) bacteria and P. aeruginosa [1].
    Formula:C20H22N8O2S2
    Color and Shape:Solid
    Molecular weight:470.57

    Ref: TM-T86884

  • SARS-CoV-2 Mpro-IN-31
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    SARS-CoV-2 Mpro-IN-31

    CAS:
    SARS-CoV-2 Mpro-IN-31 (Compound 18) is an inhibitor of SARS-CoV-2 MPro with an IC50 of 11 nM. Additionally, this compound effectively inhibits the enzymatic activity of the cysteine proteases cathepsin B and cathepsin L, with IC50 values of 24 nM and 1.8 nM, respectively.
    Formula:C31H34Cl2N4O7
    Color and Shape:Solid
    Molecular weight:645.53

    Ref: TM-T200958

  • SAG-524
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    SAG-524

    CAS:
    SAG-524 is a powerful oral small molecule that inhibits HBV viral replication. In HepG2.2.15 cells, SAG-524 reduced HBV-DNA and HbsAg levels in the supernatant with IC₅₀ values of 0.92 nM and 1.4 nM, respectively [1].
    Formula:C30H32ClN5O4S
    Color and Shape:Solid
    Molecular weight:594.12

    Ref: TM-T87352

  • LpxA-IN-1
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    LpxA-IN-1

    CAS:
    <p>LpxA-IN-1, a novel UDP-N-acetylglucosamine acyltransferase (LpxA) inhibitor exhibiting potent activity (IC 50 2 nM), effectively targets Pseudomonas aeruginosa</p>
    Formula:C21H11D7F3N5O3
    Color and Shape:Solid
    Molecular weight:452.44

    Ref: TM-T62624

  • CMX990
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    CMX990

    CAS:
    CMX990, a SARS-CoV-2 3CL protease inhibitor, exhibits EC90 values of 9.6 nM in human bronchial epithelial cells (HBECs) and 101 nM in HeLa-ACE2 cells. It also demonstrates good ADME and pharmacokinetic properties [1].
    Formula:C22H32F3N3O6
    Color and Shape:Solid
    Molecular weight:491.50

    Ref: TM-T86068

  • Ipronidazole
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    Ipronidazole

    CAS:
    Ipronidazole (RO-71554) is an orally effective antiprotozoal agent used to prevent and ameliorate histomoniasis in turkeys, commonly referred to as blackhead disease.
    Formula:C7H11N3O2
    Color and Shape:Solid
    Molecular weight:169.18

    Ref: TM-T200810

  • SARS-CoV-2-IN-99
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    SARS-CoV-2-IN-99

    CAS:
    SARS-CoV-2-IN-99 (compound 58) is an inhibitor of the main protease of SARS-CoV-2.
    Formula:C20H16Br2NO4P
    Color and Shape:Solid
    Molecular weight:525.13

    Ref: TM-T200438

  • HIV-1 inhibitor-61
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    HIV-1 inhibitor-61

    CAS:
    HIV-1 Inhibitor-61 (2c) serves as a potent inhibitor of HIV-1 reverse transcriptase, exhibiting an EC50 value of 0.07 nM in NL4-3 wt MT-4 cells [1].
    Formula:C24H24F2N2O2S
    Color and Shape:Solid
    Molecular weight:442.52

    Ref: TM-T86580

  • BI-2540
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    BI-2540

    CAS:
    BI-2540 is a HIV non-nucleoside reverse transcriptase ( NNRT ) inhibitor .
    Formula:C24H15ClF5NO5
    Color and Shape:Solid
    Molecular weight:527.83

    Ref: TM-T73435

  • DL-2-Aminopimelic Acid
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    DL-2-Aminopimelic Acid

    CAS:
    DL-2-Aminopimelic Acid acts as a weak agonist for glutamate receptors and also reduces the sensitivity of leech glutamate receptors to glutamate.
    Formula:C7H13NO4
    Color and Shape:Solid
    Molecular weight:175.18

    Ref: TM-T201414

  • Teslexivir hydrochloride
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    Teslexivir hydrochloride

    CAS:
    Teslexivir (BTA074) HCl inhibits HPV 6/11 by blocking E1-E2 protein interaction, vital for DNA replication. Used in condyloma research.
    Formula:C35H37BrClN3O4
    Color and Shape:Solid
    Molecular weight:679.04

    Ref: TM-T72241

  • Antimicrobial agent-29
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    Antimicrobial agent-29

    CAS:
    Antimicrobial Agent-29 (Compound C35) influences the interaction between human hemoglobin and the Staphylococcus aureus IsdB hemophore. This compound facilitates the identification of IsdB:Hb PPI inhibitors [1].
    Formula:C19H14N4O4S
    Color and Shape:Solid
    Molecular weight:394.4

    Ref: TM-T85694

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    HIV-1 inhibitor-41

    HIV-1 inhibitor-41 (B23): Oral non-nucleoside reverse transcriptase blocker, EC50 of 50 nM (E138K), 20.8 nM (WT), low hERG/CYP impact, non-toxic.
    Formula:C16H15F2N3OS
    Color and Shape:Solid
    Molecular weight:335.37

    Ref: TM-T61031

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    Antibacterial agent 76

    Antibacterial agent 76 (compound 9) is a potent antibacterial agent.
    Formula:C23H27N3O2S
    Color and Shape:Solid
    Molecular weight:409.54

    Ref: TM-T62063

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    SP-471

    SP-471 is a potent inhibitor of dengue virus (DENV) protease (IC50: 18 μM) and inhibits the inter- and intramolecular protease processes of DENV.
    Formula:C33H26BrN5
    Color and Shape:Solid
    Molecular weight:572.5

    Ref: TM-T64044

  • CDA-IN-1
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    CDA-IN-1

    CAS:
    CDA-IN-1 (Compound vs#2-1) is an inhibitor of chitin deacetylase (CDA) that exhibits antifungal activity. By inhibiting fungal CDA activity, it activates plant immune responses and leads to the accumulation of reactive oxygen species (ROS), hindering fungal growth. At a concentration of 100 μM, CDA-IN-1 achieves inhibition rates of 86.9% on P. xanthii's PxCDA1 and 74.5% on PxCDA2. CDA-IN-1 is applicable in research on fungal plant diseases, such as cucumber powdery mildew and tomato gray mold.
    Formula:C15H14N2O6
    Color and Shape:Solid
    Molecular weight:318.281

    Ref: TM-T206164