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Microbiologia/Virologia

Microbiologia/Virologia

Gli inibitori in microbiologia e virologia sono composti che bersagliano microrganismi, inclusi batteri, virus e funghi, interrompendo la loro crescita, replicazione o sopravvivenza. Questi inibitori sono essenziali per studiare la patogenesi microbica, comprendere i meccanismi di resistenza e sviluppare nuove terapie antimicrobiche e antivirali. Gli inibitori in questa categoria vengono utilizzati per combattere le malattie infettive, esplorare l'ecologia microbica e studiare le interazioni ospite-patogeno. Presso CymitQuimica, offriamo un'ampia selezione di inibitori di alta qualità in microbiologia e virologia per supportare la tua ricerca in malattie infettive, microbiologia e virologia.

Sottocategorie di "Microbiologia/Virologia"

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Trovati 6235 prodotti di "Microbiologia/Virologia"

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  • Logo CymitQuimica
    Targetmol
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    MtDTBS-IN-1

    MtDTBS-IN-1 is a notably potent binder (K_D = 57 nM) and inhibitor (K_i = 5 μM) of MtDTBS.
    Formula:C16H16N4O5
    Colore e forma:Solid
    Peso molecolare:344.32

    Ref: TM-T61119

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    Chitin synthase inhibitor 8

    Chitin synthase inhibitor 8 is a chitin synthase (CHS) inhibitor with broad-spectrum antifungal effects that can be used in studies related to fungal infections
    Formula:C23H23N3O5
    Colore e forma:Solid
    Peso molecolare:421.45

    Ref: TM-T62246

  • 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
    Colore e forma:Solid
    Peso molecolare:470.57

    Ref: TM-T86884

  • Pyrromycin
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    Pyrromycin

    CAS:
    Pyrromycin is a monosaccharide anthracycline which can be used to inhibit cellular RNA synthesis.
    Formula:C30H35NO11
    Colore e forma:Solid
    Peso molecolare:585.60

    Ref: TM-T68903

  • 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
    Colore e forma:Solid
    Peso molecolare:357.357

    Ref: TM-T206270

  • WM382
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    WM382

    CAS:
    WM382, a potent dual PMIX/X inhibitor, has IC50s of 1.4 nM/0.03 nM and effective against various malaria stages.
    Formula:C29H36N4O4
    Colore e forma:Solid
    Peso molecolare:504.62

    Ref: TM-T73546

  • RAD51-IN-7
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    RAD51-IN-7

    CAS:
    RAD51-IN-7 inhibits RAD51 gene, with potential for mitochondrial disorders. (From WO2021164746A1, cmpd 71)
    Formula:C25H31N5O4S2
    Colore e forma:Solid
    Peso molecolare:529.67

    Ref: TM-T63728

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    CYP2C19-IN-1

    CYP2C19-IN-1: potent CYP2C19 inhibitor, non-genotoxic, non-hepatotoxic, blocks RdRP (Ki: 6.16 μM), useful for ZIKV research.
    Formula:C26H26N2O6S
    Colore e forma:Solid
    Peso molecolare:494.56

    Ref: TM-T63337

  • Cephalosporin C
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    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>
    Formula:C16H21N3O8S
    Colore e forma:Solid
    Peso molecolare:415.418

    Ref: TM-T206388

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    KPC-2-IN-2

    KPC-2-IN-2 (6c) inhibits KPC-2 enzyme in Klebsiella pneumoniae (Ki 0.038 μM) and boosts cefotaxime in E. coli KPC-2.
    Formula:C12H10BN3O2S
    Colore e forma:Solid
    Peso molecolare:271.1

    Ref: TM-T60470

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    Colistin adjuvant-2

    Colistin adjuvant-2 is a compound that acts as a potentiation agent for colistin, effectively enhancing its activity against Gram-negative bacteria [1].
    Formula:C14H7Cl2F3N2O
    Colore e forma:Solid
    Peso molecolare:347.12

    Ref: TM-T61154

  • ZK-316
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    ZK-316

    CAS:
    ZK-316 is a potent and broad-spectrum NNRTI inhibitor with an EC50 range of 0.99 to 75.1 nM. It is applicable for HIV research.
    Formula:C27H22D6N6O3S2
    Colore e forma:Solid
    Peso molecolare:554.72

    Ref: TM-T207116

  • TAN-1057C
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    TAN-1057C

    CAS:
    TAN-1057C is a potent antibiotic with antimicrobial activity against both Gram-negative and Gram-positive bacteria, including Methicillin-resistant Staphylococcus aureus (MRSA).
    Formula:C13H25N9O3
    Colore e forma:Solid
    Peso molecolare:355.4

    Ref: TM-T201517

  • DPC 684
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    DPC 684

    CAS:
    DPC 684 is a potent and selective HIV-1 protease inhibitor with an IC90 of 5.7-40 nM and a Ki of 0.021 nM. It competitively inhibits HIV-1 protease, preventing viral polyprotein cleavage. Compared to cellular proteases, DPC 684 shows high selectivity for retroviral proteases. The compound exhibits low protein binding and offers broad-spectrum inhibition against various wild-type and mutant HIV-1 proteases, with an IC90 of 1.9-6.3 nM. DPC 684 is significant for HIV research.
    Formula:C35H48FN5O5S
    Colore e forma:Solid
    Peso molecolare:669.85

    Ref: TM-T211711

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    Chitinase-IN-4

    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.
    Formula:C21H24ClN7
    Colore e forma:Solid
    Peso molecolare:409.92

    Ref: TM-T62069

  • NBTIs-IN-5
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    NBTIs-IN-5

    CAS:
    NBTIs-IN-5 inhibits Mycobacterium abscessus DNA with IC50 1.5μM, halts growth at MIC90 0.4μM.
    Formula:C24H25F3N4O2
    Colore e forma:Solid
    Peso molecolare:458.48

    Ref: TM-T62868

  • NITD-688
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    NITD-688

    CAS:
    NITD-688 is a pan-serotype inhibitor targeting the dengue virus NS4B protein, effective through oral administration.
    Formula:C25H32N4O3S2
    Colore e forma:Solid
    Peso molecolare:500.68

    Ref: TM-T69649

  • Antifungal agent 125
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    Antifungal agent 125

    CAS:
    Antifungalagent 125 (compound 4H) is a potent succinate dehydrogenase (SDH) inhibitor with an IC50 of 3.59 μg/mL and exhibits fungicidal activity against Alternaria alternata.
    Formula:C13H10BrNO4S
    Colore e forma:Solid
    Peso molecolare:356.192

    Ref: TM-T204529

  • CDA-IN-2
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    CDA-IN-2

    CAS:
    CDA-IN-2 (Compound VS#2-3) is an inhibitor of chitin deacetylase (CDA) that exhibits antifungal properties. At a concentration of 100 μM, it inhibits P. xanthii's CDAPxCDA1 by 83.7% and PxCDA2 by 74.5%. CDA-IN-2 is applicable in research on agricultural fungal diseases, including resistance to powdery mildew and gray mold.
    Formula:C17H16N2O7
    Colore e forma:Solid
    Peso molecolare:360.318

    Ref: TM-T206594

  • LasR antagonist 1
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    LasR antagonist 1

    CAS:
    LasR antagonist 1 (Compound 7), with an IC50 of 0.4 μM, is an effective antagonist of LasR that modulates quorum sensing (QS) in the opportunistic pathogen Pseudomonas aeruginosa [1].
    Formula:C20H15F3N2O3
    Colore e forma:Solid
    Peso molecolare:388.34

    Ref: TM-T86799