
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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Antimalarial agent 42
<p>Compound 42 (Compound 2), an antimalarial agent, effectively inhibits Plasmodium falciparum during the asexual blood stages (IC 50 <0.5μM) and gametocytes (IC 50 is 0.14 μM).</p>Formula:C24H42N2Color and Shape:SolidMolecular weight:358.6Phosphomannose isomerase
CAS:<p>Phosphomannose isomerase, the initial enzyme in GDP-Man biosynthesis, catalytically facilitates the interconversion of fructose-6-phosphate (Fru6P) and mannose-</p>Color and Shape:SolidEFdA-TP tetraammonium
<p>EFdA-TP tetraammonium is a potent HIV-1 RT inhibitor and DNA synthesis blocker, acting as an ICT or DCT.</p>Formula:C12H27N9O12P3Color and Shape:SolidMolecular weight:601.31Antibacterial agent 142
<p>Antibacterial agent 142, an aromatic hydrazide, exhibits bacteriostatic antibacterial activity and inhibits biofilm formation [1].</p>Formula:C12H9ClFN3OColor and Shape:SolidMolecular weight:265.67RPR103611
CAS:<p>RPR103611, a betulinic acid derivative, inhibits HIV-1; IC50s: CCR5 (YU2) 80, CXCR4 (NL4-3) 0.27, dual-tropic (89.6) 0.17.</p>Formula:C46H78N2O6Color and Shape:SolidMolecular weight:755.12Tilatamig samrotecan
<p>Tilatamig samrotecan (AZD9592) is an antibody-drug conjugate (ADC) designed to deliver a topoisomerase I inhibitor (TOP1i). It targets epidermal growth factor receptor (EGFR) and c-MET and demonstrates antitumor activity. The compound induces DNA double-strand breaks, elevates pRAD50 and γH2AX expression, and inhibits the growth of non-small cell lung cancer.</p>Color and Shape:Odour SolidParvodicin C2
CAS:<p>Parvodicin C2, a glycopeptide antibiotic derived from A. parvosata and part of the parvodicin complex, serves as a component of the A40926 antibiotic complex utilized as a precursor for synthesizing dalbavancin. It exhibits activity against methicillin-sensitive and methicillin-resistant strains of S. aureus, S. epidermidis, S. saprophyticus, S. hemolyticus, and E. faecalis.</p>Formula:C83H88Cl2N8O29Color and Shape:SolidMolecular weight:1732.533-Methyl-chuangxinmycin
<p>3-Methyl-chuangxinmycin, an antibiotic, inhibits the enzyme responsible for synthesizing tryptophan tRNA (TrpRS), thereby affecting the translation process in both bacteria and mammalian cells. Additionally, it downregulates genes associated with interferon, TNF, and inflammatory responses in RDEB_L1 cells.</p>Formula:C13H13NO2SColor and Shape:SolidMolecular weight:247.31Isepamicin
CAS:<p>Isepamicin (Sch 21420) is a strong aminoglycoside antibiotic, effective on Enterobacteriaceae and staphylococci, less so on other bacteria.</p>Formula:C22H43N5O12Color and Shape:SolidMolecular weight:569.60HSGN-218
<p>HSGN-218: non-cytotoxic, gut-specific antibiotic; effective against C. difficile (MIC 0.003-0.03 μg/ml); boosts survival in mice with C. difficile.</p>Color and Shape:SolidZHAWOC25153
<p>ZHAWOC25153 (Compound 17o) is an inhibitor of the SARS-CoV-2 papain-like protease (PLpro) with an IC50 of 7 μM. It demonstrates antiviral properties and is applicable for research in the field of anti-infective studies.</p>Formula:C32H33FN2O6Color and Shape:SolidMolecular weight:560.613Orfamide A
CAS:<p>Orfamide A, a lipopeptide biosurfactant isolated from P. protegens, exhibits multifaceted bioactivity. With an LC50 of 34.5 μg/ml, it significantly increases mortality in adult green peach aphids. Additionally, at a concentration of 50 μM, Orfamide A inhibits appressoria formation in M. oryzae isolates and decreases the prevalence of sporulating blast lesions in M. oryzae-infected plants. Furthermore, it demonstrates efficacy against T. b. brucei, with an IC50 value of 6 µM.</p>Formula:C64H114N10O17Color and Shape:SolidMolecular weight:1295.678-Br-GTP
CAS:<p>8-Br-GTP, a GTP analog, inhibits FtsZ polymerization/GTPase (K i 31.8 μM), aids nucleic acid modification.</p>Formula:C10H15BrN5O14P3Color and Shape:SolidMolecular weight:602.076Antibacterial agent 138
<p>Antibacterial agent 138 effectively targets multi-drug resistant bacteria by inhibiting protein synthesis.</p>Formula:C34H52INO4SColor and Shape:SolidMolecular weight:697.75LFF 571
CAS:<p>LFF 571 is an inhibitor of protein-synthesizing GTPase (Elongation Factor).</p>Formula:C60H63N13O13S6Color and Shape:SolidMolecular weight:1366.6GSK2336805
CAS:<p>GSK-2336805, an HCV NS5A inhibitor, is effective against genotypes 1, 4, 5, and some of 6.</p>Formula:C42H52N8O8Color and Shape:SolidMolecular weight:796.91Maximin 32
<p>Maximin 32, an antimicrobial peptide originating from toad brain, exhibits activity against Staphylococcus aureus and Escherichia coli, with minimum inhibitory</p>Formula:C121H208N34O33Color and Shape:SolidMolecular weight:2667.15XT-1
CAS:<p>XT-1, an antimicrobial peptide sourced from Xenopus tropicalis skin secretions, exhibits potent activity against S.</p>Formula:C134H227N37O31Color and Shape:SolidMolecular weight:2852.47Oligomycin E
CAS:<p>Oligomycin E, a Streptomyces metabolite, has weak antifungal properties but strong Gram-positive and HeLa cell antitumor effects (IC50=14 ng/ml).</p>Formula:C45H72O13Color and Shape:SolidMolecular weight:821.058Antibacterial agent 34
CAS:<p>Antibacterial agent 35 is a compound that effectively reduces the minimum inhibitory concentration (MIC) of Ceftazidime, enhancing its antibacterial activity.</p>Formula:C13H19N5O6SColor and Shape:SolidMolecular weight:373.38

