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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 5832 produtos de "Microbiologia/Virologia"

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  • Vecantoxatug

    CAS:
    <p>Vecantoxatug is a humanized monoclonal antibody designed to target Clostridium tetani toxin (TeNT, a neurotoxin). It specifically binds to the tetanus toxin, preventing the toxin from interacting with cell receptors and thus exhibits antitoxin activity. Vecantoxatug holds potential for tetanus research.</p>
    Cor e Forma:Liquid
  • T3SS-IN-2


    <p>T3SS-IN-2 (Compound 2h) serves as an inhibitor of the type three secretion system (T3SS), with applications in bacterial infection research [1].</p>
    Fórmula:C16H25N3O3
    Cor e Forma:Solid
    Peso molecular:307.39
  • AI 3-16787

    CAS:
    <p>AI 3-16787 is an HIV-1 integrase inhibitor exhibiting inhibitory activity against strand transfer in the presence of Mn²⁺.</p>
    Fórmula:C21H24O4
    Pureza:99.01%
    Cor e Forma:Solid
    Peso molecular:340.41
  • Enzyme-IN-2


    <p>Enzyme-IN-2 (compound 15) serves as a potent urease inhibitor, exhibiting anti-ureolytic activity with a K i of 2.36 µM and an IC 50 of 0.75 µM [1].</p>
    Fórmula:C9H11O7P
    Cor e Forma:Solid
    Peso molecular:262.15
  • Succinate dehydrogenase-IN-9


    <p>Succinate dehydrogenase-IN-9 (Compound Iik) is an inhibitor of succinate dehydrogenase with an IC50 of 3.6 μM. It demonstrates strong inhibitory activity against various fungi, such as S. sclerotiorum, with an EC50 of 1.14 μg/mL. Additionally, Succinate dehydrogenase-IN-9 enhances nitrate reductase activity, promoting plant growth.</p>
    Fórmula:C24H29F2N3O5
    Cor e Forma:Solid
    Peso molecular:477.20753
  • Micrococcin P1

    CAS:
    <p>Micrococcin P1 is a macrocyclic peptide antibiotic and is a potent hepatitis C virus (HCV) inhibitor(EC50 range of 0.1-0.5 μM)</p>
    Fórmula:C48H49N13O9S6
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:1144.36
  • 3'-Hydroxyxanthyletin


    <p>3'-Hydroxyxanthyletin is a useful organic compound for research related to life sciences and the catalog number is T125640.</p>
    Fórmula:C14H12O4
    Cor e Forma:Solid
    Peso molecular:244.246
  • Antibacterial agent 57

    CAS:
    <p>Antibacterial agent 57 (example 25) is a antibacterial agent.</p>
    Fórmula:C11H13N4NaO8S
    Cor e Forma:Solid
    Peso molecular:384.30
  • Esculentin 1A

    CAS:
    <p>Esculentin 1A, a potent antimicrobial peptide (AMP) derived from frog skin, demonstrates significant in vitro activity against Pseudomonas [1].</p>
    Fórmula:C212H369N59O60S3
    Cor e Forma:Solid
    Peso molecular:4800.75
  • Polybia-MP1

    CAS:
    <p>Polybia-MP1 is an antimicrobial mastoparan peptide [1] .</p>
    Fórmula:C78H132N20O19
    Cor e Forma:Solid
    Peso molecular:1654.01
  • SARS-CoV-2-IN-93


    <p>SARS-CoV-2-IN-93 (compound 24) acts as an inhibitor of both SARS-CoV-2 and HCoV-OC43. It is utilized in antiviral research.</p>
    Cor e Forma:Odour Solid
  • Gilvocarcin V

    CAS:
    <p>Gilvocarcin V, a metabolite from Actinomycete DO-38, exhibits potent antibacterial, antifungal, and antiviral activity.</p>
    Fórmula:C27H26O6
    Cor e Forma:Solid
    Peso molecular:446.499
  • UX4O


    <p>UX4O is an allosteric inhibitor of UDP-glucose dehydrogenase (UGDH). The human UGDH (hUGDH) is a hexamer that catalyzes the oxidation of UDP-glucose to UDP-glucuronic acid. It exists in an active (E) state and an inactive (EΩ) state, which requires binding with the allosteric inhibitor UDP-xylose (UDP-Xyl) to stabilize the inactive form. UX4O may also serve as a physiologically relevant inhibitor of bacterial allosteric UGDH that does not produce UDP-Xyl.</p>
    Fórmula:C14H22N2O17P2
    Cor e Forma:Solid
    Peso molecular:552.28
  • Amcipatricin L-aspartate

    CAS:
    <p>Amcipatricin diaspartate (SPA-S-753), a semi-synthetic polyene antibiotic, exhibits potent broad-spectrum antifungal activity [1].</p>
    Fórmula:C75H117N7O27
    Cor e Forma:Solid
    Peso molecular:1548.76
  • Tetromycin C1

    CAS:
    <p>Tetromycin C1 is a useful organic compound for research related to life sciences. The catalog number is T125395 and the CAS number is 205433-82-5.</p>
    Fórmula:C50H64O14
    Cor e Forma:Solid
    Peso molecular:889.048
  • [(Cys(Bzl)84,Glu(OBzl)85)]CD4 (81-92)

    CAS:
    <p>[(Cys(Bzl)84, Glu(OBzl)85)]CD4 (81-92) is a selective HIV-1 inhibitor that blocks the interaction between HIV-1 and CD4 molecules, thereby inhibiting viral infection and cell fusion. At a concentration of 25 μM, it can completely prevent fusion formation [1].</p>
    Fórmula:C76H108N14O26S
    Cor e Forma:Solid
    Peso molecular:1665.81
  • CSP1

    CAS:
    <p>CSP1: potent ComD1 receptor agonist, IC50 of 10.3 nM, important in S. pneumoniae transformation, and has antibacterial properties.</p>
    Fórmula:C103H168N30O24S
    Cor e Forma:Solid
    Peso molecular:2242.72
  • PP102


    <p>PP102, an antimicrobial peptide, exhibits activity against gram-positive bacteria, including B.</p>
    Fórmula:C173H285N53O58S3
    Cor e Forma:Solid
    Peso molecular:4131.63
  • Dabcyl-KTSAVLQSGFRKME-Edans TFA


    <p>Fluorogenic peptide Dabcyl-KTSAVLQSGFRKME-Edans TFA measures protease activity, may aid in COVID-19 research.</p>
    Fórmula:C97H142F3N25O26S2
    Cor e Forma:Solid
    Peso molecular:2195.44
  • Quorum sensing-IN-7


    <p>Quorum sensing-IN-7 (compound HSL 4) is an effective quorum sensing (QS) inhibitor. It interacts with the binding sites Leu 72 and Gln 95 of CviR. As an antimicrobial agent, Quorum sensing-IN-7 effectively inhibits the production of homoserine lactones (HSLs) and biofilms in C. violaceum at concentrations ranging from 0.25-1 mg/mL.</p>
    Cor e Forma:Odour Solid