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(3,355 products)
- Antibiotic(934 products)
- Antifection(26 products)
- DHFR(32 products)
- DNA/RNA Synthesis(799 products)
- HBV(186 products)
- HIV Protease(497 products)
- HSV(98 products)
- Integrase(2 products)
- Ribosome(11 products)
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Found 6336 products of "Microbiology/Virology"
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RNA binder 1
RNA binder 1 (Compound 4b) is an RNA-binding agent capable of crossing the blood-brain barrier. It selectively binds to the G-quadruplex structure of the G4C2 repeat sequence RNA of the C9orf72 gene. This compound significantly reduces levels of the toxic polypeptides poly(GA) and poly(GP) in cells derived from amyotrophic lateral sclerosis (ALS) patients, while it has no significant impact on the antisense polypeptide poly(PR), demonstrating selectivity for sense RNA. RNA binder 1 is useful for studying ALS and frontotemporal dementia (FTD).Formula:C22H20N10S2Color and Shape:SolidMolecular weight:488.13138Adeninobananin
CAS:Adeninobananin, a negative control tool, exhibits no inhibitory activity against the SARS Coronavirus helicase.Formula:C19H19ClN6O9Color and Shape:SolidMolecular weight:510.84N-(3-hydroxy-7-cis tetradecenoyl)-L-Homoserine lactone
CAS:N-(3-hydroxy-7-cis-tetradecenoyl)-L-homoserine lactone, an AHL for bacterial quorum sensing, does not affect cytokines in LPS-stimulated macrophages.Formula:C18H31NO4Color and Shape:SolidMolecular weight:325.444"-(2-(p-Chlorophenyl)acetoxyl)spiramycin
4"-(2-(p-Chlorophenyl)acetoxyl)spiramycin (Compound 2d) is a broad-spectrum anti-coronavirus agent that targets the frameshifting element (FSE). It inhibits HCoV-OC43 and HCoV-229E with EC50 values of 0.85 μM and 1.45 μM, respectively. This compound exhibits a dual-target mechanism by acting on both viral FSE RNA and host DIS3L2.Formula:C51H79ClN2O15Color and Shape:SolidMolecular weight:995.63Vecantoxatug
CAS: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.Color and Shape:LiquidGuaiacylglycerol-β-guaiacyl Ether
CAS:Guaiacylglycerol-beta-guaiacyl Ether is degraded by microorganisms and is commonly used as a substrate to mimic microbial degradation of cell walls of lignin-living plants.Formula:C17H20O6Purity:99.08%Color and Shape:SolidMolecular weight:320.34BRP
BRP, a peptide related to BRINP2, exhibits anti-obesity activity through the activation of FOS. It triggers FOS activation in the central nervous system, and its effect is independent of leptin, GLP-1 receptor, and melanocortin 4 receptor.Color and Shape:Odour SolidGallinamide A TFA
CAS:Gallinamide A TFA is a peptide that exhibits linear deposition and serves as a potent inhibitor of cathepsin L (CatL) with an IC50 of 17.6 pM. It inhibits SARS-CoV-2 infection by targeting CatL (EC50: 28 nM) and also inhibits Plasmodium falciparum with an IC50 of 50 nM [1] [2].Formula:C33H53F3N4O9Color and Shape:SolidMolecular weight:706.79Farobin A
CAS:Farobin A, a natural compound, exhibits antibacterial, antioxidant, and anti-inflammatory properties. It is effective against Streptococcus mutans ATCC 25175 and Streptococcus sobrinus ATCC 33478. Additionally, Farobin A demonstrates anti-inflammatory activity by targeting cytokine IL-6 and TNF-α [1].Formula:C27H30O14Color and Shape:SolidMolecular weight:578.52Pyrrocidine A
CAS:Pyrrocidine A, an antibiotic known for its antibacterial properties, can be isolated from LL-Cyan426.Formula:C31H37NO4Color and Shape:SolidMolecular weight:487.63Tetrahydrobostrycin
CAS:Tetrahydrobostrycin is a secondary metabolite produced by Aspergillus sp., demonstrating mild inhibitory effects against Staphylococcus aureus and Escherichia coli, with inhibition zones measuring 15 mm and 9.2 mm respectively (100 mg/disc).Formula:C16H20O8Color and Shape:SolidMolecular weight:340.33Salivaricin B
CAS:Salivaricin B is a broad-spectrum bacteriocin produced by Lactobacillus M7, capable of inhibiting the growth of Listeria monocytogenes, Bacillus cereus, Brochothrix thermosphacta, Enterococcus faecalis, and various Lactobacilli.Formula:C120H182N34O36S4Color and Shape:SolidMolecular weight:2805.2Adustin
CAS:Adustin is an antifungal antibiotic characterized as a polypeptide that inhibits translation. It effectively suppresses translation in a cell-free rabbit reticulocyte lysate system, exhibiting an IC50 of 0.34 μM.Formula:C11H8O3Color and Shape:SolidMolecular weight:188.179Vasoactive intestinal contractor
CAS:Vasoactive intestinal contractor, a novel member of the endothelin family, stimulates a rapid increase in intracellular Ca2+ concentration in fura-2-overexpressed Swiss 3T3 cells [1.Formula:C116H161N27O32S4Color and Shape:SolidMolecular weight:2573.94Macropin
CAS:Macropin (MAC-1 peptide) is an antimicrobial peptide found in the venom of the solitary bee Macropis fulvipes. It exhibits antibacterial properties against both Gram-positive and Gram-negative bacteria, demonstrates inhibitory effects on fungi, and possesses moderate hemolytic activity on human red blood cells. Macropin is utilized in research for anti-infective therapies.Formula:C68H121N17O13SColor and Shape:SolidMolecular weight:1416.86HYNIC-UBI29-41
CAS:HYNIC-UBI29-41 is composed of the bifunctional chelator HYNIC and the antimicrobial peptide UBI 29-41. It retains the antimicrobial properties of UBI 29-41, showing strong affinity for both Gram-positive and Gram-negative bacteria. When labeled with the radioactive element Technetium (99mTc), HYNIC-UBI29-41 can be used as an imaging agent for detecting bacterial infections in mouse models.Formula:C74H126N34O19SColor and Shape:SolidMolecular weight:1828.07Benz[g]isoquinoline-5,10-dione
CAS:Benz[g]isoquinoline-5,10-dione, an active component isolated from the ethanol extract of the aerial parts of Mitracarpus scaber, has been demonstrated through agar diffusion tests to exhibit significant in vitro inhibitory activity against AIDS-related pathogens. Additionally, it possesses notable antibacterial and antifungal properties.Formula:C13H7NO2Color and Shape:SolidMolecular weight:209.2SARS-CoV-2 Mpro-IN-43
SARS-CoV-2 Mpro-IN-43 (Compound 1) is an inhibitor of the coronavirus main protease (Mpro) with an IC50 of 72 μM. It exerts its antiviral effects by interacting non-covalently with the key residues at the Mpro active site. This compound exhibits moderate to low cytotoxicity with CC50 values of 13.24, 41.02, and 42.26 µM in HaCaT, HEK293T, and HepG2 cells, respectively. SARS-CoV-2 Mpro-IN-43 is applicable for SARS-CoV-2 research.Formula:C32H41F3N2O4S2Color and Shape:SolidMolecular weight:638.24598Anhydrotetracycline hydrochloride
CAS:Anhydrotetracycline (hydrochloride) is a potent competitive inhibitor of broad-spectrum tetracycline destructase enzymes.Formula:C22H23ClN2O7Purity:98% - 98.90%Color and Shape:SolidMolecular weight:462.88RJPXD33
RJPXD33 is an inhibitor of LpxD and LpxA, with IC50 values of 3.5 μM and 19 μM, respectively. Additionally, RJPXD33 can inhibit LpxD and LpxA in E. coli, with Kd values of 6 μM and 20 μM.Formula:C71H107N15O18SColor and Shape:SolidMolecular weight:1490.76
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