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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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  • CymitQuimica logo
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    RdRP-IN-4

    <p>RdRP-IN-4, an oral arylbenzohydrazide, inhibits influenza A/B by targeting PB1 of RdRP, with EC50s of 53 nM (H1N1) and 20 nM (Flu B), and aids infected mice.</p>
    Formula:C17H17Br2N3O2
    Color and Shape:Solid
    Molecular weight:455.14

    Ref: TM-T62812

  • BRD-4592
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    BRD-4592

    CAS:
    <p>BRD-4592 is an allosteric inhibitor targeting tryptophan synthase (TrpAB) of Mycobacterium tuberculosis. It binds at the α-β subunit interface of TrpAB, with an IC50 of 70.9 nM for the α subunit and 22.6 nM for the β subunit.</p>
    Formula:C17H15FN2O
    Color and Shape:Solid
    Molecular weight:282.312

    Ref: TM-T206428

  • MIV-150
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    MIV-150

    CAS:
    <p>MIV-150 is a nonnucleoside inhibitor of reverse transcriptase (NNRT). MIV-150 also blocking HIV-1 and HIV-2 infections (EC50&lt;1 nM against HIV-1/HIV-2MN).</p>
    Formula:C19H17FN4O3
    Purity:98%
    Color and Shape:Solid
    Molecular weight:368.36

    Ref: TM-T16081

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    Pol I-IN-1

    <p>Pol I-IN-1 is a powerful inhibitor of RNA polymerase I (Pol I), specifically targeting the large catalytic subunit RPA194, demonstrating an inhibition</p>
    Formula:C23H22N4O2
    Color and Shape:Solid
    Molecular weight:386.45

    Ref: TM-T61720

  • 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

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    MraY-IN-3

    <p>MraY-IN-3 (12a) is a potent inhibitor of the bacterial translocase MraY (IC50: 140 μM). 46 μg/ml).</p>
    Formula:C35H45N3O5
    Color and Shape:Solid
    Molecular weight:587.75

    Ref: TM-T64160

  • DIDS
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    DIDS

    CAS:
    <p>DIDS inhibits anion exchangers reversibly then irreversibly and blocks RAD51.</p>
    Formula:C16H10N2O6S4
    Purity:98%
    Color and Shape:Solid
    Molecular weight:454.52

    Ref: TM-T20694

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    TCMDC-136230

    <p>TCMDC-136230 is a novel inhibitor of Plasmodium calcium kinetics with minimal inhibition of haemoglobin crystallisation.</p>
    Formula:C24H34N4O2S
    Color and Shape:Solid
    Molecular weight:442.62

    Ref: TM-T62588

  • CDA-IN-1
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    CDA-IN-1

    CAS:
    <p>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.</p>
    Formula:C15H14N2O6
    Color and Shape:Solid
    Molecular weight:318.281

    Ref: TM-T206164

  • NEU-1017
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    NEU-1017

    CAS:
    <p>NEU-1017 serves as a broad-spectrum antiparasitic compound, effectively inhibiting T. brucei, L. major, and P. falciparum with EC50 values of 210 nM, 240 nM, and 3 nM, respectively.</p>
    Formula:C33H31ClFN5O3S
    Color and Shape:Solid
    Molecular weight:632.147

    Ref: TM-T205599

  • Ceftolozane TFA
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    Ceftolozane TFA

    CAS:
    <p>Ceftolozane TFA is a cephalosporin class antibiotic (antibiotic) designed to inhibit Gram-negative bacterial infections. Additionally, it can be utilized in the synthesis of novel antibiotics (antibiotic) that are more efficacious and safer.</p>
    Formula:C25H31F3N12O10S2
    Color and Shape:Solid
    Molecular weight:780.71

    Ref: TM-T201544

  • DRF-8417
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    DRF-8417

    CAS:
    <p>DRF-8417 is an oxazolidinone antibiotic, active against both Gram-positive bacteria and fastidious Gram-negative bacteria. The MIC50 and MIC90 values of DRF-8417 for Gram-positive pathogens range between 0.06-1 mg/L.</p>
    Formula:C15H17N3O5S
    Color and Shape:Solid
    Molecular weight:351.38

    Ref: TM-T201523

  • HldA/E-IN-1
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    HldA/E-IN-1

    CAS:
    <p>HldA/E-IN-1 (compound 8) is a dual inhibitor of HldA/E, exhibiting IC50 values of 17.2 μM and 67.8 μM, respectively. This compound is utilized in research on antibacterial infections.</p>
    Formula:C8H17FO13P2
    Color and Shape:Solid
    Molecular weight:402.16

    Ref: TM-T200513

  • SLU-10906
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    SLU-10906

    CAS:
    <p>SLU-10906 (Compound 63) is an orally active inhibitor of Cryptosporidium. It demonstrates activity against the parasite in cell-based infection models with an EC50 of 0.19 μM and exhibits no cytotoxicity. SLU-10906 is a promising candidate for research in cryptosporidiosis.</p>
    Formula:C22H21BFN5O2
    Color and Shape:Solid
    Molecular weight:417.244

    Ref: TM-T205063

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    HIV-1 inhibitor-18

    <p>HIV-1 inhibitor-18 blocks HIV-1 capsid, effective on NL4-3 strain (EC50: 5.14 μM), slightly toxic (MT-4CC50&gt;9.51).</p>
    Formula:C27H31N3O6S
    Color and Shape:Solid
    Molecular weight:525.62

    Ref: TM-T63687

  • NFC nitro probe 1
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    NFC nitro probe 1

    CAS:
    <p>NFC nitro probe 1 (compound 18) is a chemical probe designed for the detection of Mtb, exhibiting high potency against both R-Mtb and NR-Mtb.</p>
    Formula:C19H19NO6
    Color and Shape:Solid
    Molecular weight:357.357

    Ref: TM-T206270

  • BPR3P0128
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    BPR3P0128

    CAS:
    <p>BPR3P0128, a non-nucleoside RNA-dependent RNA polymerase (RdRp) inhibitor, is effective orally and can inhibit various SARS-CoV-2 variants. It exhibits EC 50 values of 0.62 µM for SARS-CoV-2 and 0.14 µM for HCoV-229E, demonstrating potent anti-pancoronavirus activity at submicromolar concentrations. Additionally, BPR3P0128 displays synergistic antiviral effects when used in combination with Remdesivir [1].</p>
    Formula:C22H18BrN3O2
    Color and Shape:Solid
    Molecular weight:436.30

    Ref: TM-T85904

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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

  • Erythromycin B
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    Erythromycin B

    CAS:
    <p>Erythromycin B exhibits antimalarial activity by effectively inhibiting the asexual growth of Plasmodium falciparum.</p>
    Formula:C37H67NO12
    Color and Shape:Solid
    Molecular weight:717.93

    Ref: TM-T201497

  • Metesind Glucuronate
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    Metesind Glucuronate

    CAS:
    <p>Metesind Glucuronate is an antineoplastic. It also is a specific thymidylate synthase inhibitor.</p>
    Formula:C29H34N4O10S
    Color and Shape:Solid
    Molecular weight:630.67

    Ref: TM-T24454