
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"
- Antibacterial(2,957 products)
- Antibiotic(920 products)
- Antifection(23 products)
- DHFR(33 products)
- DNA/RNA Synthesis(708 products)
- HBV(176 products)
- HIV Protease(449 products)
- HSV(91 products)
- Integrase(2 products)
- Ribosome(13 products)
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Found 5842 products of "Microbiology/Virology"
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NR-NO2
<p>NR-NO2 is a prospective therapeutic agent with targeted delivery and image-guided capability for use in antitumor studies, also demonstrating antibacterial</p>Color and Shape:Odour SolidYl 704 A1
CAS:<p>Yl 704 A1 is a primary component of macrolide antibiotic YL-704 from Streptomyces platensis subsp. malvinus.</p>Formula:C43H71NO15Purity:98%Color and Shape:SolidMolecular weight:842.033TAT peptide
<p>TAT peptide, a CPP, delivers molecules into cells by traversing membrane barriers using aa49-57 of TAT protein.</p>Formula:C65H124N34O15Purity:98%Color and Shape:SolidMolecular weight:1621.91Antimicrobial agent-39
<p>Antimicrobial agent-39 (Compound 8i) is an antibiotic that targets the 50S ribosomal subunit, inhibiting bacterial protein synthesis. It disrupts bacterial cell membranes, causing leakage of cellular contents and demonstrating broad-spectrum antibacterial activity. Additionally, Antimicrobial agent-39 targets organic cation transporters (OCT) and accumulates in infected kidneys, improving pyelonephritis in mouse models.</p>Formula:C36H46BrN3O4SColor and Shape:SolidMolecular weight:696.74Proteasome-IN-6
<p>Proteasome-IN-6 (Compound J-80) inhibits the β5 catalytic subunit of the Trypanosoma brucei 20S proteasome, effectively blocking T. b. brucei, T. b. gambiense, and T. b. rhodesiense with EC50 values of 157 nM, 220 nM, and 156 nM, respectively. Additionally, Proteasome-IN-6 has demonstrated antitrypanosomal activity in a mouse model.</p>Formula:C35H45F3N4O6Color and Shape:SolidMolecular weight:674.75Desferriferribactin
CAS:<p>Desferriferribactin is a biogenetic precursor of pyoverdin.</p>Formula:C46H73N13O16Color and Shape:SolidMolecular weight:1064.165Allosamidin
CAS:<p>Allosamidin, a chitinase inhibitor and typical secondary metabolite of Streptomyces, may be used as a pesticide and anti-asthmatic agent.</p>Formula:C25H42N4O14Color and Shape:SolidMolecular weight:622.625HIV p17 Gag (77-85)
CAS:<p>Targeting HIV Gag p17 (77-85) with intracellular Ab cDNA disrupts viral replication pre/post-integration.</p>Formula:C44H72N10O15Purity:98%Color and Shape:SolidMolecular weight:981.1Erythromycin A enol ether
CAS:<p>Erythromycin A enol ether is a degradation product of Erythromycin A which is a macrolide antibiotic.</p>Formula:C37H65NO12Purity:99.94%Color and Shape:SolidMolecular weight:715.91Gemifloxacin
CAS:<p>Gemifloxacin is a fluoronaphthyridone with strong antibacterial effect.</p>Formula:C18H20FN5O4Purity:98%Color and Shape:SolidMolecular weight:389.38NNRT-IN-6
<p>NNRT-IN-6 (Compound 13a) is a non-nucleoside reverse transcriptase inhibitor (NNRT) used to inhibit HIV-1 reverse transcriptase (HIV-1RT), with an IC50 of 0.41 μM. It effectively suppresses both wild-type HIV-1 and mutants L100I, K103N, Y181C, Y188L, E138K, F227L/V106A, and RES056, with an EC50 range of 6.2-250 nM.</p>Formula:C32H31N9O3SColor and Shape:SolidMolecular weight:621.71Propionylmaridomycin
CAS:<p>Propionylmaridomycin is a macrolide antibiotic.</p>Formula:C46H75NO17Purity:98%Color and Shape:SolidMolecular weight:914.096Lychnopholide
CAS:<p>Lychnopholide is isolated from Vanillosmopsis erythropappa.</p>Formula:C20H22O6Color and Shape:SolidMolecular weight:358.39Fumonisin B3
CAS:<p>Fumonisin B3 is a mycotoxin derived from fusarium fungi, a member of fumonisins.</p>Formula:C34H59NO14Purity:98%Color and Shape:SolidMolecular weight:705.83PR-39
CAS:<p>Antibacterial peptide. Stimulates angiogenesis and inhibits inflammatory responses by selectively blocking proteasome degradation of IκBα.</p>Formula:C229H346N70O40Purity:98%Color and Shape:SolidMolecular weight:4719.7Antibacterial agent 233
<p>Antibacterialagent 233 (Compound 7c) demonstrates inhibitory activity against Helicobacter pylori, with a minimum inhibitory concentration (MIC) ranging from 0.4 to 1.6 μg/mL. It inhibits jack bean urease with an IC50 of 0.27 μg/mL, alters the permeability of the H. pylori cell membrane, and leads to the leakage of cellular contents. Antibacterialagent 233 shows metabolic stability in both whole blood and artificial gastric fluid. Additionally, it exhibits antitumor activity against U2OS in mice.</p>Color and Shape:Odour SolidIsatropolone A
CAS:<p>Isatropolone A from Streptomyces Gö66 has a 1,5-diketone; it's potent against Leishmania with IC50 of 0.5μM.</p>Formula:C24H24O9Color and Shape:SolidMolecular weight:456.44γ-Glutamyl Transferase-IN-1
<p>Gamma-Glutamyl Transferase-IN-1 (compound 4de), a β-carboline 1-hydrazide inhibitor, exhibits antifungal and antibacterial properties by targeting</p>Color and Shape:Odour SolidNeuraminidase-IN-16
<p>Neuraminidase-IN-16 (43b) inhibits H5N1, H5N8, H1N1, H3N2, H5N1-H274Y, H1N1-H274Y neuraminidases; IC50: 0.031-10.08 μM.</p>Formula:C26H35FN2O4Color and Shape:SolidMolecular weight:458.57Antituberculosis agent-7
CAS:<p>Antituberculosis agent-7: active against P. mirabilis (MIC 31.25μM), A. niger (MIC 62.5μM), and M. tuberculosis (MIC 3.41μM).</p>Formula:C26H19F4NO3Color and Shape:SolidMolecular weight:469.43

