CymitQuimica logo
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"

Show 2 more subcategories

Found 5842 products of "Microbiology/Virology"

Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
products per page.
  • CymitQuimica logo
    Targetmol
    + Info

    PqsR-IN-2

    <p>PqsR-IN-2, potent PqsR inhibitor, curbs Pseudomonas aeruginosa communication, reduces pyocyanin, with low toxicity.</p>
    Formula:C18H20ClN3OS
    Color and Shape:Solid
    Molecular weight:361.89

    Ref: TM-T61353

  • HCV-IN-40
    Targetmol
    + Info

    HCV-IN-40

    CAS:
    <p>HCV-IN-39 is a potent oral drug inhibiting HCV, effective on GT1a (EC50: 0.259μM), GT1b (EC50: 0.434μM), GT1b CES1 (EC50: 0.069μM) replicons.</p>
    Formula:C21H26BrFN3O9P
    Color and Shape:Solid
    Molecular weight:594.32

    Ref: TM-T64202

  • Menoctone
    Targetmol
    + Info

    Menoctone

    CAS:
    <p>Menoctone is an orally effective antimalarial agent that inhibits blood-induced rodent malaria. It enhances the antimalarial effects of chloroquine or quinine, making it useful for malaria research.</p>
    Formula:C24H32O3
    Color and Shape:Solid
    Molecular weight:368.51

    Ref: TM-T201004

  • GSK-3036656 free base
    Targetmol
    + Info

    GSK-3036656 free base

    CAS:
    <p>GSK656 (GSK3036656) inhibits Mtb LeuRS with IC50 of 0.20 μM, promising for tuberculosis treatment.</p>
    Formula:C10H13BClNO4
    Color and Shape:Solid
    Molecular weight:257.48

    Ref: TM-T60405

  • CymitQuimica logo
    Targetmol
    + Info

    Antibacterial agent 77

    <p>Antibacterial agent 77 (compound 12) is an antibacterial agent [1].</p>
    Formula:C22H27N3OS
    Color and Shape:Solid
    Molecular weight:381.53

    Ref: TM-T61640

  • FG-2101
    Targetmol
    + Info

    FG-2101

    CAS:
    <p>FG-2101 is a selective, orally active non-hydroxamate LpxC inhibitor with an IC50 of approximately 1 nM. It demonstrates exceptional selectivity over other bacterial and human metalloproteases. FG-2101 is useful for studying infections caused by Gram-negative bacteria, including resistant strains.</p>
    Formula:C30H32N5O6P
    Color and Shape:Solid
    Molecular weight:589.579

    Ref: TM-T206566

  • Antibacterial agent 261
    Targetmol
    + Info

    Antibacterial agent 261

    CAS:
    <p>Antibacterialagent 261 (compound 43) is a potent inhibitor of the peptide deformylase (PDF) enzyme, demonstrating IC50 values of 2.5 nM against Staphylococcus aureus (S. aureus) and 10.6 nM against Escherichia coli (E. coli).</p>
    Formula:C18H24N4O3S2
    Color and Shape:Solid
    Molecular weight:408.538

    Ref: TM-T204731

  • Metallo-β-lactamase-IN-14
    Targetmol
    + Info

    Metallo-β-lactamase-IN-14

    CAS:
    <p>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].</p>
    Formula:C20H22N8O2S2
    Color and Shape:Solid
    Molecular weight:470.57

    Ref: TM-T86884

  • HT1171
    Targetmol
    + Info

    HT1171

    CAS:
    <p>HT1171 is a potent and selective inhibitor of the Mycobacterium tuberculosis proteasome. It exhibits strong antitubercular activity against Mycobacterium tuberculosis H37Rv, with a MIC90 of 2 μg/mL and MIC of 4 μg/mL. At a concentration of 100 μM, HT1171 shows an inhibition rate of 53.8% against normal human liver cells (L02). HT1171 is applicable in antituberculosis drug research.</p>
    Formula:C7H4N2O4S2
    Color and Shape:Solid
    Molecular weight:244.248

    Ref: TM-T204697

  • SARS-CoV-2 Mpro-IN-31
    Targetmol
    + Info

    SARS-CoV-2 Mpro-IN-31

    CAS:
    <p>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.</p>
    Formula:C31H34Cl2N4O7
    Color and Shape:Solid
    Molecular weight:645.53

    Ref: TM-T200958

  • BRD-4592
    Targetmol
    + Info

    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

  • SAG-524
    Targetmol
    + Info

    SAG-524

    CAS:
    <p>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].</p>
    Formula:C30H32ClN5O4S
    Color and Shape:Solid
    Molecular weight:594.12

    Ref: TM-T87352

  • CymitQuimica logo
    Targetmol
    + Info

    RdRP-IN-5

    CAS:
    <p>RdRP-IN-5 (compound 20), a potent inhibitor of the influenza virus RNA-dependent RNA polymerase (RdRP), has potential application in influenza research [1].</p>
    Formula:C23H21N3O5
    Purity:98%
    Color and Shape:Solid
    Molecular weight:419.43

    Ref: TM-T73323

  • SARS-CoV-2 Mpro-IN-32
    Targetmol
    + Info

    SARS-CoV-2 Mpro-IN-32

    CAS:
    <p>SARS-CoV-2 Mpro-IN-32 (Compound 1) is a selective inhibitor of SARS-CoV-2 MPro with an IC50 value of 230 nM. In vitro, it also inhibits the replication of various SARS-CoV-2 variants.</p>
    Formula:C34H32Cl2N4O9
    Color and Shape:Solid
    Molecular weight:711.54

    Ref: TM-T201191

  • Insecticidal agent 16
    Targetmol
    + Info

    Insecticidal agent 16

    CAS:
    <p>Insecticidal agent 16 (compound A21) exhibits insecticidal activity against Plutella xylostella, with LC50 values of 1.2 and 13.2 µg/mL respectively.</p>
    Formula:C21H13Cl2F6N5O2S
    Color and Shape:Solid
    Molecular weight:584.32

    Ref: TM-T201261

  • SARS-CoV-2 Mpro-IN-28
    Targetmol
    + Info

    SARS-CoV-2 Mpro-IN-28

    CAS:
    <p>SARS-CoV-2 Mpro-IN-28 (Compound 1K) is an inhibitor of SARS-CoV-2 Mpro, exhibiting an EC50 of 24 μM.</p>
    Formula:C14H17NO3Se
    Color and Shape:Solid
    Molecular weight:326.25

    Ref: TM-T201252

  • Fenbenicillin potassium
    Targetmol
    + Info

    Fenbenicillin potassium

    CAS:
    <p>Fenbenicillin (Phenbenicillin) potassium is a semi-synthetic penicillin with antibacterial spectrum activity.</p>
    Formula:C22H22KN2O5S
    Color and Shape:Solid
    Molecular weight:465.584

    Ref: TM-T206403

  • CymitQuimica logo
    Targetmol
    + Info

    Antifungal agent 40

    <p>Antifungal agent 40 blocks C. albicans CYP51 in pocket II, hindering lanosterol demethylase and biofilm growth.</p>
    Formula:C22H20Cl2N4Se
    Color and Shape:Solid
    Molecular weight:490.29

    Ref: TM-T63285

  • Ceftolozane TFA
    Targetmol
    + Info

    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

  • Antibacterial agent 174
    Targetmol
    + Info

    Antibacterial agent 174

    CAS:
    <p>Compound 174 (Compound 5g), an antibacterial agent, exhibits potent anti-infective properties in vivo along with appreciable pharmacokinetic profiles. This highly active substance demonstrates favorable biofilm removal capabilities, low hemolysis, and acceptable mammalian cell toxicity [1].</p>
    Formula:C25H30FN2NaO5
    Color and Shape:Solid
    Molecular weight:480.5

    Ref: TM-T85661