
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(3,421 products)
- Antibiotic(945 products)
- Antifection(27 products)
- DHFR(30 products)
- DNA/RNA Synthesis(808 products)
- HBV(186 products)
- HIV Protease(507 products)
- HSV(99 products)
- Integrase(2 products)
- Ribosome(6 products)
Show 2 more subcategories
Found 6441 products of "Microbiology/Virology"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Primordazine NC-6364997
CAS:Primordazine NC-6364997 is a negative control for Primordazine A and Primordazine B.Formula:C22H23N5OSColor and Shape:SolidMolecular weight:405.52Sesquicillin A
CAS:Sesquicillin A: insecticidal antibiotic from white plantain; stops A. salina growth; MIC 6.25 µg/mL.Formula:C29H42O5Color and Shape:SolidMolecular weight:470.64Benastatin C
CAS:Benastatin C, from Streptomyces, inhibits GST (IC50=24 μg/ml) & porcine pancreatic lipase (IC50=10 μg/ml), boosts mouse spleen lymphocyte blastogenesis.Formula:C29H28O5Color and Shape:SolidMolecular weight:456.53Antibacterial agent 270
Antibacterialagent 270 (Compound 3e) is an antibacterial agent that targets bacterial membrane components such as phosphatidylglycerol (PG), cardiolipin (CL), and bacterial DNA. It disrupts the bacterial membrane structure and binds to DNA, interfering with genetic information transfer. Antibacterialagent 270 holds potential for research into infections caused by methicillin-resistant Staphylococcus aureus (MRSA).Color and Shape:Odour SolidSARS-CoV-2-IN-25
SARS-CoV-2-IN-25 (CP026): Strong inhibitor of spike-driven entry with IC50 at 1.6 μM, affects enveloped viruses, liposomes.Formula:C58H48O8P2Color and Shape:SolidMolecular weight:934.94Bacillosporin C
CAS:Bacillosporin C, an oxaphenalenone dimer with antibiotic properties, inhibits acetylcholinesterase; derived from mangrove fungus T. bacillosporus.Formula:C26H18O10Color and Shape:SolidMolecular weight:490.42Bassianin
CAS:Bassianin, a fungal metabolite identified in Beauveria, demonstrates inhibition of Mg2+-, Ca2+-, and Na+/K+-ATPase activities in equine erythrocyte ghosts, with inhibition rates of 81%, 58%, and 23%, respectively, at a concentration of 200 µg/ml. Additionally, bassianin exhibits cytotoxic properties against Sf9 and Sf21 insect cells, with 50% cytotoxic concentration (CC50) values of 4.91 µM and 12.12 µM, respectively.Formula:C23H25NO5Color and Shape:SolidMolecular weight:395.5Targeting the bacterial sliding clamp peptide 46 TFA
Targeting thebacterialsliding clamp peptide 46 TFA is a short peptide that specifically targets the bacterial sliding clamp (SC) and inhibits SC-dependent DNA synthesis.Color and Shape:Odour Solid2'-Deoxy-2'-fluoro-l-uridine
CAS:2'-Deoxy-2'-fluoro-1-uridine: an L-nucleoside, inhibits RNA viruses by blocking viral RNA polymerase.Formula:C9H11FN2O5Color and Shape:SolidMolecular weight:246.192,4-Dichlorobenzenesulfonyl chloride
CAS:2,4-Dichlorobenzenesulfonyl chloride aids in creating cancer/bacteria-fighting nicotinyl arylsulfonylhydrazides.Formula:C6H3Cl3O2SColor and Shape:White PowderMolecular weight:245.51Cacaoidin
Cacaoidin, a glycosylated lantibiotic extracted from Streptomyces cacaoi, exhibits strong antibacterial effects against Gram-positive pathogens, notablyFormula:C107H162N24O32S2Color and Shape:SolidMolecular weight:2360.7HIV-1 inhibitor-80
HIV-1inhibitor-80 (compound M44) is an HIV-1 inhibitor with an EC50 of 5-148 nM. It demonstrates excellent metabolic stability and low cytotoxicity in human plasma and liver microsomes.Formula:C26H19N7OColor and Shape:SolidMolecular weight:445.475Antituberculosis agent-15
Antituberculosis agent-15 (Compound 18c) is a selective antimycobacterial agent with a minimum inhibitory concentration (MIC) of 0.45 μM against Mycobacterium tuberculosis H37Rv (ATCC 27294) and 0.28 μM against its wild-type strain H37Rv-LP (ATCC 25618). It exhibits potent intracellular inhibitory activity in macrophage infection models, with an IC50 of 0.16 μM. Antituberculosis agent-15 is applicable for tuberculosis research.Color and Shape:Odour Solid2'-Deoxytubercidin 5'-triphosphate sodium
2'-Deoxytubercidin 5'-triphosphate (C7dATP) sodium is a deoxyadenosine triphosphate (dATP) analog designed to reduce electrophoretic mobility anomalies caused by compression at G or A residues, thereby enhancing the quality of DNA sequencing data.Formula:C11H13N4Na4O12P3Molecular weight:577.93336AZD-CO-Ph-PEG4-Ph-CO-AZD
CAS:AZD-CO-Ph-PEG4-Ph-CO-AZD is a bis-β-lactam linker, commonly employed in the synthesis of antibody-siRNA conjugates.Formula:C26H28N2O8Color and Shape:SolidMolecular weight:496.516Z-Antiepilepsirine
CAS:Z-Antiepilepsirine, an amide alkaloid from Piper capense L.f, has antiplasmodial properties with an IC50 of 27 µM against Plasmodium falciparum W2.Formula:C15H17NO3Color and Shape:SolidMolecular weight:259.3Leucanicidin
CAS:Leucanicidin: a macrolide from S. halstedii, toxic to L. separata larvae at 20 ppm; LD50: 0.23-0.42 µg/ml for some worms.Formula:C42H70O13Color and Shape:SolidMolecular weight:783.009AR-201
AR-201 is a human IgG1 monoclonal antibody that targets the F glycoprotein F0. It exhibits activity against the respiratory syncytial virus (RSV) and can be utilized in studies related to lower respiratory tract infections (LRTI). The recommended isotype control is HumanIgG1kappa, Isotype Control.Color and Shape:Odour LiquidProtein kinase G inhibitor-1
CAS:Protein kinase G inhibitor-1 is a potent Protein kinase G inhibitor, IC50= 0.9 uM.Formula:C14H18N2O2SPurity:98.64%Color and Shape:SoildMolecular weight:278.37Ref: TM-T67755
1mg71.00€1mL*10mM (DMSO)161.00€5mg170.00€10mg250.00€25mg371.00€50mg525.00€100mg705.00€200mg954.00€Thiocoraline
CAS:Thiocoraline: depsipeptide, DNA intercalator, antibacterial, anticancer, targets Gram-positive, inhibits polymerases, cytotoxic to cancer cells.
Formula:C48H56N10O12S6Color and Shape:SolidMolecular weight:1157.39Tenofovir-C3-O-C12-trimethylsilylacetylene ammonium
CAS:Tenofovir-C3-O-C12 has a longer half-life, potent anti-HIV effects, and better pharmacokinetics than tenofovir.Formula:C29H55N6O5PSiColor and Shape:SolidMolecular weight:626.855Antituberculosis agent-9
Antituberculosis agent-9 (Compound 5a), an orally administered compound, demonstrates potent antitubercular activity, exhibiting a minimum inhibitoryFormula:C25H29ClN4OColor and Shape:SolidMolecular weight:436.98MurA-IN-5
MurA-IN-5 (compound 4c) demonstrates a minimum inhibitory concentration (MIC) of 1.95 μg/mL against Escherichia coli and exhibits significant potency as a MurA inhibitor with an IC50 of 3.77 μg/mL. It also shows antibiofilm activity against various microorganisms, indicating its potential in combating biofilm-related infections.Formula:C33H28N6O2Color and Shape:SolidMolecular weight:540.614NDM-1 inhibitor-8
NDM-1 inhibitor-8 (Compound 18b) is a covalent inhibitor of New Delhi metallo-β-lactamase-1 (NDM-1), with an IC50 of 7.03 μM. It effectively inhibits resistant bacterial strains and demonstrates synergistic antibacterial effects when used in combination with Meropenem. In mouse models, NDM-1 inhibitor-8 exhibits anti-infective activity.Formula:C28H23Cl2N3O4SSeColor and Shape:SolidMolecular weight:647.43CK 683A
CAS:CK 683A is a bio-active chemical.Formula:C32H57N9O5SColor and Shape:SolidMolecular weight:679.922-Bromoaldisine
CAS:2-Bromoaldisine, a pyrrole alkaloid isolated from Stylissa carter, is known to inhibit HIV-1 infection and suppress the Raf/MEK/MAPK pathway.Formula:C8H7BrN2O2Color and Shape:SolidMolecular weight:243.06Chartreusin sodium
CAS:Chartreusin sodium is a biochemical.Formula:C32H31NaO14Color and Shape:SolidMolecular weight:662.57Peniterphenyl A
CAS:Peniterphenyl A from deep-sea Penicillium blocks HSV-1/2 entry by targeting glycoprotein D, hindering adsorption and fusion.Formula:C19H14O6Color and Shape:SolidMolecular weight:338.31Antibiotic LB 10517
CAS:Antibiotic LB 10517 is a catechol-substituted cephalosporin with a broad spectrum of antibacterial.Formula:C27H25N9NaO9S2Purity:98%Color and Shape:SolidMolecular weight:706.66BO 1236
CAS:BO-1236 is an antipseudomonal cephalosporin.Formula:C26H28N6O9S2Purity:98%Color and Shape:SolidMolecular weight:632.66Pomolic acid 3-acetate
CAS:Pomolic Acid 3-Acetate, an antitubercular compound, exhibits a minimum inhibitory concentration (MIC) of 32 μM against Mycobacterium tuberculosis H37Rv [1].Formula:C32H50O5Color and Shape:SolidMolecular weight:514.74c(R3W4V)
c(R3W4V) is an antimicrobial peptide with a stable transmembrane structure. It exhibits inhibitory concentrations (IC50) of 0.27 μM for E. coli, 0.46 μM for S. aureus, and 0.05 μM for B. subtilis.Color and Shape:Odour SolidSannamycin B
CAS:Sannamycin B is a bioactive chemical.Formula:C15H32N4O4Color and Shape:SolidMolecular weight:332.44Emoquine-1
Emoquine-1 is a potent orally active antimalarial agent effective against various drug-resistant Plasmodium strains, including artemisinin-resistant dormant parasites. It demonstrates efficacy against proliferative malignant Plasmodium with an IC50 value ranging from 20 to 55 nM. Emoquine-1 holds potential for treating Plasmodium strains resistant to artemisinin combination therapy (ACT), with the capability to eradicate persistent parasites.Formula:C30H28ClN3O6Color and Shape:SolidMolecular weight:562.013Angolamycin
CAS:Angolamycin is a macrolide antibiotic (antibiotic) effective against Gram-positive bacteria.Formula:C46H77NO17Color and Shape:SolidMolecular weight:916.1RSV-IN-11
RSV-IN-11 (compound 10b) exhibits antiviral activity against RSV, with an IC50 value of 4 μM. It is applicable for research on respiratory infections.Formula:C25H18Cl2N2O5Molecular weight:496.0592810-Norparvulenone
CAS:10-Norparvulenone, a fungal metabolite from Microsphaeropsis, inhibits viral sialidase and boosts survival in flu-infected MDCK cells at 1 μg/ml.Formula:C12H14O5Color and Shape:SolidMolecular weight:238.24Tte UvrD Helicase
Tte UvrD Helicase is a thermostable UvrD helicase initially isolated from Thermoanaerobacter tengcongensis. This enzyme can unwind DNA duplexes that have 3' or 5' single-stranded DNA tails, as well as DNA substrates with blunt ends.Luminamicin
CAS:Luminamicin is active against anaerobic bacteria, especially Clostridium sp.; isolated from actinomycete strain OMR-59.Formula:C32H38O12Color and Shape:SolidMolecular weight:614.644Potassium clavulanate cellulose
Potassium clavulanate cellulose is a mixture of potassium clavulanate and cellulose, is an inhibitor of beta-lactamase.Formula:C8H9NO5K·(C6H10O5)nPurity:98%Color and Shape:SolidYJ196
Compound YJ196 (Compound 59) serves as an inhibitor of New Delhi Metallo-β-lactamase-1 (NDM-1) [1].Color and Shape:Odour SolidTetrachloroveratrole
CAS:Tetrachloroveratrole forms from chloroguaiacols' degradation, byproducts of wood pulp bleaching in paper production.Formula:C8H6Cl4O2Color and Shape:SolidMolecular weight:275.93Carbendazim mixture with flusilazole
CAS:Carbendazim mixture with flusilazole is a bioactive chemical.Formula:C25H24F2N6O2SiColor and Shape:SolidMolecular weight:506.58(−)-Voacangarine
CAS:(–)-Voacangarine, an indole alkaloid isolated from V. africana, exhibits cytotoxicity towards various cell lines including HepG2, A375, MDA-MB-231, SH-SY5Y, and CT26 with IC50 values of 20 µg/ml. Additionally, it demonstrates cytostatic effects on wild-type S. cerevisiae and is cytotoxic to Δrad3-e5 and Δrad6-1 mutant strains of S. cerevisiae, which have defects in DNA strand break repair and the mutagenic repair pathway, respectively.Formula:C22H28N2O4Color and Shape:SolidMolecular weight:384.47A-315675
CAS:A-315675 is a neuramidase inhibitor with anti-infuenza activity.Formula:C17H30N2O4Color and Shape:SolidMolecular weight:326.43Antifungal agent 117
Antifungalagent 117 is a bipyrrole carboxamide derivative with antifungal activity, exhibiting an EC50 value of 11.58 mg/L against Sclerotinia sclerotiorum. This compound induces cell death by increasing cell membrane permeability, causing an imbalance in osmotic pressure between the interior and exterior of the cell. It also promotes oxidative damage to the cell membrane by inducing the accumulation of reactive oxygen species (ROS), leading to the leakage of cellular contents. RNA sequencing analysis has demonstrated that Antifungalagent 117 disrupts cell membrane structure by downregulating catalase genes and upregulating neutral ceramidase genes, accelerating ceramide metabolism and hastening cell death. The compound holds significant potential for application in plant protection and the control of fungal infections.Color and Shape:Odour SolidFITC-LC-TAT (47-57) acetate
FITC-LC-TAT (47-57) acetate is an FITC-labeled TAT peptide known as a cell-penetrating peptide (CPP). It enhances the yield and solubility of heterologous proteins.Color and Shape:Odour SolidGuignardone K
CAS:Guignardone K, a meroterpene compound extracted from solid cultures of the endophytic fungus Guignardia sp., exhibits antifungal activity [1].Formula:C17H24O6Color and Shape:SolidMolecular weight:324.37Neuraminidase-IN-16
Neuraminidase-IN-16 (43b) inhibits H5N1, H5N8, H1N1, H3N2, H5N1-H274Y, H1N1-H274Y neuraminidases; IC50: 0.031-10.08 μM.Formula:C26H35FN2O4Color and Shape:SolidMolecular weight:458.57

