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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 5863 produtos de "Microbiologia/Virologia"

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  • Fipravirimat

    CAS:
    <p>Fipravirimat is a potent inhibitor of HIV-1 with potential applications in HIV and AIDS research.</p>
    Fórmula:C43H67FN2O4S
    Cor e Forma:Solid
    Peso molecular:727.07
  • MtMetAP1-IN-1


    <p>MtMetAP1-IN-1 is an inhibitor of methionine aminopeptidase 1 ( MetAP1 ). MtMetAP1-IN-1 shows antimycobacterial activity.</p>
    Fórmula:C15H10BrN5O2S
    Cor e Forma:Solid
    Peso molecular:404.24
  • Diclosulam

    CAS:
    <p>Diclosulam (XDE 564) is an herbicide with a Ki value of less than 32 nM. It exhibits a MIC of 6.25 and 12.5 μM, and a MIC50 of 1.40 and 3.01 μM against the CBS10913 and CBS12373 strains, respectively.</p>
    Fórmula:C13H10Cl2FN5O3S
    Cor e Forma:Solid
    Peso molecular:406.22
  • T-2513 hydrochloride

    CAS:
    <p>T-2513 hydrochloride: selective topoisomerase I inhibitor, binds DNA complex, halts DNA/RNA synthesis, causes cell death.</p>
    Fórmula:C25H28ClN3O5
    Cor e Forma:Solid
    Peso molecular:485.96
  • Ac-Atovaquone

    CAS:
    <p>Ac-Atovaquone, an ester-acetylated derivative of atovaquone, acts as a potent inhibitor of cytochrome bc1 (cytochrome bc1). This compound shows potential for use in malaria research.</p>
    Fórmula:C24H21ClO4
    Cor e Forma:Solid
    Peso molecular:408.87
  • RAD51-IN-6

    CAS:
    <p>RAD51-IN-6, a potent RAD51 gene inhibitor, may help research mitochondrial disorders. (WO2021164746A1, cmpd 23)</p>
    Fórmula:C27H40N3O5PS
    Cor e Forma:Solid
    Peso molecular:549.66
  • DC-159a

    CAS:
    <p>DC-159a, an 8-methoxy fluoroquinolone, possesses broad-spectrum antibacterial activity, with a particular efficacy against Gram-positive pathogens. The MIC90 values for DC-159a are 0.5 μg/mL against Streptococcus anginosus group, 4 μg/mL against Clostridium difficile, and 2 μg/mL against Bacteroides fragilis.</p>
    Fórmula:C21H23F2N3O40·5H2O
    Cor e Forma:Solid
    Peso molecular:428.4295
  • Squalamine lactate

    CAS:
    <p>Squalamine lactate is an aminosterol compound discovered in the tissues of the dogfish shark, with antimicrobial activity.</p>
    Fórmula:C37H71N3O8S
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:718.04
  • Antitubercular agent-29


    <p>Compound 6xa inhibits drug-resistant tuberculosis with MICs 0.03 μg/mL for DS-Mtb and 0.03-0.06 for DR-Mtb, SI&gt;40 for Vero cells.</p>
    Fórmula:C20H12ClN3O5
    Cor e Forma:Solid
    Peso molecular:409.78
  • EBOV-GP-IN-1


    <p>EBOV-GP-IN-1 (Compound 28) is a potent inhibitor of Ebola entry, acting on the Ebola virus envelope glycoprotein (EBOV-GP) (IC50: 0.05 μM).</p>
    Fórmula:C25H40ClN3O2
    Cor e Forma:Solid
    Peso molecular:450.06
  • HIV-1 inhibitor-61

    CAS:
    <p>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].</p>
    Fórmula:C24H24F2N2O2S
    Cor e Forma:Solid
    Peso molecular:442.52
  • 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>
    Fórmula:C19H19NO6
    Cor e Forma:Solid
    Peso molecular:357.357
  • WM382

    CAS:
    <p>WM382, a potent dual PMIX/X inhibitor, has IC50s of 1.4 nM/0.03 nM and effective against various malaria stages.</p>
    Fórmula:C29H36N4O4
    Cor e Forma:Solid
    Peso molecular:504.62
  • Cephalosporin C

    CAS:
    <p>Cephalosporin C exhibits relatively weak resistance to Gram-positive and Gram-negative bacteria. It is stable against penicillinase, but can be decomposed by cephalosporinase. When hydrolyzed to remove its side chain, it yields 7-amino-cefenoic acid (7-ACA), which is an essential raw material for the production of semisynthetic cephalosporins.</p>
    Fórmula:C16H21N3O8S
    Cor e Forma:Solid
    Peso molecular:415.418
  • HCV-IN-38


    <p>Potent oral HCV inhibitor HCV-IN-38 has 15 nM EC50, 431 SI, high efficacy, and low toxicity.</p>
    Fórmula:C22H24ClF3N4O4
    Cor e Forma:Solid
    Peso molecular:500.9
  • WQ3810 TFA


    <p>WQ3810 TFA is an orally available fluoroquinolone with antimicrobial activity against Mycobacterium tuberculosis and inhibits the DNA rotamase activity of</p>
    Fórmula:C24H23F6N5O5
    Pureza:99.52%
    Cor e Forma:Soild
    Peso molecular:575.46
  • Urease-IN-2


    <p>Urease-IN-2 is a non-competitive inhibitor of urease (IC50: 0.94 μM, Ki: 1.6 μM) that non-competitively inhibits Jack bean urease (JBU).</p>
    Fórmula:C26H25N5O5S3
    Cor e Forma:Solid
    Peso molecular:583.7
  • Anti-Trypanosoma cruzi agent-2


    <p>Compd 3b: anti-trypanosomal, IC50 0.51 μM (NINOA), 3.06 μM (INC-5), also combats T. gondii.</p>
    Fórmula:C17H10ClNO5
    Cor e Forma:Solid
    Peso molecular:343.72
  • 20S Proteasome-IN-4

    CAS:
    <p>20S Proteasome-IN-4: brain-penetrant, parasite-specific, oral, inhibits T.b. brucei proteasome (IC50: 6.3nM), for HAT research.</p>
    Fórmula:C20H18ClF2N3O3
    Cor e Forma:Solid
    Peso molecular:421.83
  • UNC0638 hydrate

    CAS:
    UNC0638 hydrate selectively inhibits G9a and GLP histone methyltransferases with IC50 values of 15 nM and 19 nM, respectively. It is effective in inhibiting invasion and migration of TNBC cells in vitro. Additionally, UNC0638 hydrate acts as an inhibitor of EHMT1/2 and induces the expression of fetal hemoglobin (HbF) in cultures of human erythroid progenitor cells. Furthermore, it exhibits antiviral activity against FMDV (foot-and-mouth disease virus) and VSV (vesicular stomatitis virus), demonstrating remarkable potency and selectivity across various epigenetic and non-epigenetic targets.
    Fórmula:C30H49N5O3
    Cor e Forma:Solid
    Peso molecular:527.74