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Microbiologia/Virologia

Microbiologia/Virologia

Os inibidores de microbiologia e virologia são compostos que têm como alvo microrganismos, incluindo bactérias, vírus e fungos, interrompendo seu crescimento, replicação ou sobrevivência. Esses inibidores são essenciais para estudar a patogênese microbiana, entender os mecanismos de resistência e desenvolver novas terapias antimicrobianas e antivirais. Os inibidores nessa categoria são usados para combater doenças infecciosas, explorar a ecologia microbiana e investigar as interações hospedeiro-patógeno. Na CymitQuimica, oferecemos uma ampla seleção de inibidores de alta qualidade para microbiologia e virologia para apoiar sua pesquisa em doenças infecciosas, microbiologia e virologia.

Subcategorias de "Microbiologia/Virologia"

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Foram encontrados 5842 produtos de "Microbiologia/Virologia"

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  • Chitin synthase inhibitor 9


    <p>CHS inhibitor 9: a broad-spectrum antifungal for studying fungal infections.</p>
    Fórmula:C24H25N3O6
    Cor e Forma:Solid
    Peso molecular:451.47
  • Antifungal agent 113

    CAS:
    <p>Antifungalagent 113 (compound 9a) serves as an effective antifungal and antibacterial agent. It exhibits strong inhibitory activity against both S. aureus and methicillin-resistant S. aureus.</p>
    Fórmula:C23H20O5
    Cor e Forma:Solid
    Peso molecular:376.40
  • SP-471


    <p>SP-471 is a potent inhibitor of dengue virus (DENV) protease (IC50: 18 μM) and inhibits the inter- and intramolecular protease processes of DENV.</p>
    Fórmula:C33H26BrN5
    Cor e Forma:Solid
    Peso molecular:572.5
  • K13787

    CAS:
    <p>K13787 is an acetohydroxy acid synthase (AHAS) inhibitor with antibacterial properties. It exhibits antimicrobial activity against various non-tuberculous mycobacteria (NTM) as well as clarithromycin (CLR) resistant strains.</p>
    Fórmula:C14H11F2N5O4S
    Cor e Forma:Solid
    Peso molecular:383.33
  • GC-78-HCl

    CAS:
    <p>GC-78-HCl is an orally active, non-peptidic SARS-CoV-2 Mpro inhibitor with an enzyme IC50 of 0.19 μM. It exhibits strong anti-coronavirus activity and favorable pharmacokinetic properties.</p>
    Fórmula:C25H25Cl3N4O4
    Peso molecular:551.85
  • MsbA-IN-5


    <p>MsbA-IN-5 (compound 40) is a potent and highly selective inhibitor of MsbA (IC50: 2 nM). MsbA-IN-5 can be used in Gram-negative studies.</p>
    Fórmula:C23H19Cl2N5O
    Cor e Forma:Solid
    Peso molecular:452.34
  • Antitumor agent-74


    <p>Antitumor agent-74, a quinazoline derivative, inhibits DNA, arrests cell cycle, and induces apoptosis with agent-75.</p>
    Fórmula:C26H23FN6
    Cor e Forma:Solid
    Peso molecular:438.5
  • GSK5852


    <p>GSK5852, an HCV NS5B inhibitor, has IC50 of 50 nM; potently fights HCV with EC50 of 3.0 nM for GT1a and 1.7 nM for GT1b.</p>
    Fórmula:C27H27BF2N2O6S
    Cor e Forma:Solid
    Peso molecular:556.39
  • AG-7404

    CAS:
    <p>AG-7404: strong protease inhibitor, fights poliovirus, EC50 0.080-0.674 μM, effective on V-073-resistant strains.</p>
    Fórmula:C26H29N5O7
    Cor e Forma:Solid
    Peso molecular:523.54
  • Diploicin

    CAS:
    <p>Diploicin is a dibenzofuran lactone compound with activity against Gram-positive bacteria, found in lichens (lichens).</p>
    Fórmula:C16H10Cl4O5
    Cor e Forma:Solid
    Peso molecular:424.06
  • Chitin synthase inhibitor 1


    <p>Potent, selective CHS inhibitor with 0.12 mM IC50; effective against drug-resistant fungi.</p>
    Fórmula:C22H20ClN3O3
    Cor e Forma:Solid
    Peso molecular:409.87
  • BAR-072

    CAS:
    <p>BAR-072 is a small molecule inhibitor targeting TraE with a KD value of 2.7 µM. It significantly suppresses the transfer of the antibiotic resistance-associated plasmid pKM101. BAR-072 holds promise as a candidate molecule for research in disease areas related to infection and resistance control, by inhibiting the spread of bacterial resistance genes.</p>
    Fórmula:C18H13N3O6
    Cor e Forma:Solid
    Peso molecular:367.312
  • 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>
    Fórmula:C8H17FO13P2
    Cor e Forma:Solid
    Peso molecular:402.16
  • AK-968-11563024

    CAS:
    <p>AK-968-11563024 is an inhibitor targeting marine V. vulnificus NAT [(VIBVN)NAT] with an IC50 value of 18.86 µM. In V. vulnificus, NAT (aromatic amine N-acetyltransferase) plays a role in drug metabolism, contributing to drug resistance. Thus, AK-968-11563024 can be used for research related to drug tolerance.</p>
    Fórmula:C18H13I2N9O5
    Cor e Forma:Solid
    Peso molecular:689.162
  • Antibacterial agent 78


    <p>Antibacterial agent 78 (compound 30) is an antibacterial agent with improved cytotoxicity profile[1].</p>
    Fórmula:C16H23N3S2
    Cor e Forma:Solid
    Peso molecular:321.5
  • Chitinase-IN-5


    <p>Chitinase-IN-5 (8i) blocks OfChi-h (IC50: 0.051 μM), has insecticidal qualities, useful for eco-friendly pest control.</p>
    Fórmula:C20H21ClFN7
    Cor e Forma:Solid
    Peso molecular:413.88
  • 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>
    Fórmula:C15H10Cl3NO4
    Cor e Forma:Solid
    Peso molecular:374.6
  • Antitubercular agent-15


    <p>Antitubercular agent-15 (5n): low toxicity, fights M. tuberculosis strains; MIC90 values range 0.73-18.8 μg/mL.</p>
    Fórmula:C21H29FN2
    Cor e Forma:Solid
    Peso molecular:328.47
  • AV-5080

    CAS:
    <p>AV-5080 is an orally active neuraminidase (neuraminidase) inhibitor that is utilized in the research of both Type A and Type B influenza viruses.</p>
    Fórmula:C15H25FN4O4
    Cor e Forma:Solid
    Peso molecular:344.38
  • MLEB-22043


    <p>MLEB-22043 is a synthetic siderophore-monocyclic β-lactam conjugate which enters bacteria through TonB-dependent transport proteins utilizing its siderophore component, subsequently exerting antibacterial activity via its β-lactam portion. This compound acts as a broad-spectrum antibiotic, exhibiting significant inhibitory activity against pathogens such as Klebsiella pneumoniae, Escherichia coli, Acinetobacter baumannii, and Pseudomonas aeruginosa.</p>
    Fórmula:C25H25N9O11S2
    Cor e Forma:Solid
    Peso molecular:691.65