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(2,968 products)
- Antibiotic(922 products)
- Antifection(23 products)
- DHFR(33 products)
- DNA/RNA Synthesis(711 products)
- HBV(177 products)
- HIV Protease(451 products)
- HSV(91 products)
- Integrase(2 products)
- Ribosome(13 products)
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Found 5863 products of "Microbiology/Virology"
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6-Hydroxy-DOPA
CAS:<p>6-Hydroxy-DOPA is an allosteric inhibitor of RAD52, it inhibits proliferation of BRCA-deficient cancer cells in vitro and also inhibits APE1.</p>Formula:C9H11NO5Purity:97.78% - 97.95%Color and Shape:SolidMolecular weight:213.19SARS-CoV-2-IN-13
CAS:<p>SARS-CoV-2-IN-13, a stable niclosamide analogue, enhances oral bioavailability and inhibits SARS-CoV-2 (IC50: 0.057 μM).</p>Formula:C13H8Cl2N2O4Purity:98.54%Color and Shape:SolidMolecular weight:327.12Bofutrelvir
CAS:<p>MProinhibitor 11a: SARS-CoV-2 MPro blocker, IC50=0.053μM; cuts viral yield/RNA in Vero E6 cells, EC50=0.53μM, effective 1.85-50μM.</p>Formula:C25H32N4O4Purity:99.92% - >99.99%Color and Shape:SolidMolecular weight:452.55Besifovir PM
<p>Besifovir PM (LB80331 PM) is an analogue of Besifovir, a novel orally available acyclic nucleotide phosphonate for the treatment of chronic hepatitis B</p>Formula:C11H15N5OPurity:98.48% - 99.90%Color and Shape:SoildMolecular weight:233.27Bithionol sulfoxide
CAS:<p>Bithionol sulfoxide (Bithionoloxide) is a compound with inhibitory effects against parasites, inhibiting Fasciola hepatica and Schistosoma mansoni.</p>Formula:C12H6Cl4O3SPurity:98.76%Color and Shape:Off White To Tinch Pink Crystalline PowderMolecular weight:372.05UCT943
CAS:<p>UCT943 is an inhibitor of Plasmodium falciparum PI4K (IC50 = 23 nM).</p>Formula:C22H20F3N5OPurity:99.87%Color and Shape:SolidMolecular weight:427.42Uprifosbuvir
CAS:Uprifosbuvir is an inhibitor of uridine nucleotide analog HCV NS5B polymerase.Formula:C22H29ClN3O9PPurity:99.73% - >99.99%Color and Shape:SolidMolecular weight:545.91Niridazole
CAS:<p>Niridazole (Ambilhar) is an antiparasitic compound belonging to nitroimidazoles.</p>Formula:C6H6N4O3SPurity:98.26% - 99.55%Color and Shape:Yellow Crystals From Dimethylformamide/Methanol SolidMolecular weight:214.2NITD-916
CAS:<p>NITD-916: oral Mycobacterium InhA inhibitor (IC50: 570 nM), lipophilic 4-hydroxy-2-pyridone with antituberculosis action.</p>Formula:C20H25NO2Purity:99.01% - 99.78%Color and Shape:SolidMolecular weight:311.42DDRI-18
CAS:DDRI-18 is an inhibitor that regulates the DNA damage response, has anticancer activity, and inhibits non-homologous end-joining (NHEJ) DNA repair.Formula:C26H20N6Purity:98%Color and Shape:SolidMolecular weight:416.48Mtb-IN-2
CAS:<p>Mtb-IN-2 is a Mycobacterium tuberculosis (Mtb) compound with antimicrobial activity and low toxicity for the study of tuberculosis.</p>Formula:C17H12N2O4Purity:99.27%Color and Shape:SolidMolecular weight:308.29Setrobuvir
CAS:<p>Setrobuvir (ANA-598) is an orally active non-nucleoside HCV NS5B polymerase inhibitor with inhibitory effects on de novo RNA synthesis and primer extension with</p>Formula:C25H25FN4O6S2Purity:98.92% - >99.99%Color and Shape:SolidMolecular weight:560.62MP265
CAS:<p>MP265 disrupts the MreB cytoskeleton and has antiproliferative effects.</p>Formula:C8H10Cl2N2SPurity:99.55%Color and Shape:SolidMolecular weight:237.15ABMA
CAS:<p>ABMA is a broad-spectrum inhibitor shielding cells from viruses, bacteria, and parasites, acting in late endosomes.</p>Formula:C18H24BrNOPurity:99.866%Color and Shape:SolidMolecular weight:350.29Galocitabine
CAS:<p>Galocitabine (Neofrutulon), a thymidylate synthase inhibitor, is used potentially for the treatment of cancer.</p>Formula:C19H22FN3O8Purity:99.89%Color and Shape:SolidMolecular weight:439.39COH1
CAS:<p>COH1 is a ribonucleotide reductase (RR) inhibitor utilized in research pertaining to cancer, mitochondrial diseases, and neurodegenerative disorders [1].</p>Formula:C11H10N2O3SPurity:98%Color and Shape:SolidMolecular weight:250.27Antimalarial agent 10
CAS:<p>Compound 17b, an amino alcohol-quinoline, targets Pf3D7 (IC50: 14.9 nM) and PfW2 (IC50: 11 nM) with selectivity index >770.</p>Formula:C23H22F6N2O2Color and Shape:SolidMolecular weight:472.42SARS-CoV-2/MERS Mpro-IN-2
<p>SARS-CoV-2/MERS Mpro-IN-2 is a potent inhibitor of the main proteases of SARS-CoV-2 and MERS, demonstrating IC50 values of 0.21 and 0.07 µM, respectively.</p>Formula:C28H30Cl2N4O6Color and Shape:SolidMolecular weight:589.47Zika virus-IN-1
CAS:<p>Zika virus-IN-1 is an inhibitor of Zika virus (EC50: 1.56 μM).</p>Formula:C30H37N3O3SiColor and Shape:SolidMolecular weight:515.72CDD-1733
CAS:<p>CDD-1733 is a potent, non-covalent, and non-peptide inhibitor of the SARS-CoV-2 main protease (Mpro) with an inhibition constant (K i) of 12 nM.</p>Formula:C34H32F3N5O2Purity:98%Color and Shape:SolidMolecular weight:599.65DGKα-IN-8
CAS:<p>DGKα-IN-8 (Example 51) is a potent diacylglycerol kinase alpha (DGKα) inhibitor, exhibiting an IC50 of 22.491 nM and an EC50 of 0.256 nM.</p>Formula:C23H19ClF3N5OColor and Shape:SolidMolecular weight:473.88WRN inhibitor 2
CAS:<p>WRN Inhibitor 2 (example 118), a potent inhibitor of the WRN (Werner Syndrome ATP-dependent helicase enzyme), exhibits a pIC50 value of 7.0 or greater [1].</p>Formula:C15H11F3N2O5S2Purity:98%Color and Shape:SolidMolecular weight:420.38SARS-CoV-2 Mpro-IN-12
CAS:<p>SARS-CoV-2 Mpro-IN-12 (compound D026) serves as an inhibitor of the main protease (Mpro) of SARS-CoV-2, exhibiting antiviral properties [1].</p>Formula:C20H17NO3Purity:98%Color and Shape:SolidMolecular weight:319.35Acorafloxacin HCl
CAS:<p>Acorafloxacin: broad-spectrum fluoroquinolone antibacterial for acute skin infections and pneumonia.</p>Formula:C21H24ClF2N3O4Purity:98%Color and Shape:SolidMolecular weight:455.88SARS-CoV-2 3CLpro-IN-5
CAS:<p>SARS-CoV-2 3CLpro-IN-5 is a covalent inhibitor targeting the 3C-like protease (3CLpro), exhibiting potent inhibitory activity with an IC50 of 3.8 nM and</p>Formula:C22H26ClF2N5O4Purity:98%Color and Shape:SolidMolecular weight:497.92L-742001 Hydrochloride
CAS:<p>L-742001 Hydrochloride is an RNA polymerase inhibitor.</p>Formula:C23H25Cl2NO4Color and Shape:SolidMolecular weight:450.36A 74704
CAS:A 74704 is a pseudo C2-symmetric inhibitor of HIV-1 protease and its diester analog.Formula:C43H52N4O7Purity:98%Color and Shape:SolidMolecular weight:736.9Laxifloran
CAS:<p>Laxifloran possesses antibacterial and antifungal properties.</p>Formula:C17H18O5Color and Shape:SolidMolecular weight:302.32L-696229
CAS:<p>L-696229: specific HIV-1 RT inhibitor, blocks viral spread in various cells.</p>Formula:C17H18N2O2Purity:98%Color and Shape:SolidMolecular weight:282.34AZD-7295
CAS:<p>AZD-7295 (A-689) is an NS5A inhibitor that may be used to treat HCV infection.</p>Formula:C32H35F3N4O5SColor and Shape:SolidMolecular weight:644.7AB-836
CAS:<p>AB-836, an orally active hepatitis B virus (HBV) capsid inhibitor, hampers viral replication by engaging with the HBV core protein.</p>Formula:C20H15F3N4O2Color and Shape:SolidMolecular weight:400.35TAS-114
CAS:<p>TAS-114 is a dUTPase and DPD inhibitor that modulates catabolic pathways to improve systemic availability of 5-FU.</p>Formula:C21H29N3O6SPurity:99.76%Color and Shape:SolidMolecular weight:451.54D1N52
CAS:<p>D1N52 is a potent inhibitor of the SARS-CoV-2 3CL protease, demonstrating an inhibitory concentration half-maximal (IC50) value of 0.53 μM [1].</p>Formula:C20H13F4N5O3Purity:98%Color and Shape:SolidMolecular weight:447.34Antileishmanial agent-16
CAS:<p>Antileishmanial agent-16 (compound 14c), an anti-Leishmania agent, exhibits potent activity against Leishmania major promastigotes (IC50 = 0.59 µM) and</p>Formula:C27H37N5O4Purity:98%Color and Shape:SolidMolecular weight:495.618-Azahypoxanthine
CAS:<p>8-Azahypoxanthine (NSC-22709) inhibits hypoxanthine-guanine-xanthine phosphoribosyltransferase and has antimalarial properties.</p>Formula:C4H3N5OPurity:99.66%Color and Shape:Light Yellow To Light Beige Fine CrystallineMolecular weight:137.1Alteconazole
CAS:Alteconazole is an antifungal drug.Formula:C17H12Cl3N3OPurity:98%Color and Shape:SolidMolecular weight:380.66L 680833
CAS:<p>L 680833 is an orally active monocyclic beta-lactam human polymorphonuclear leukocyte elastase inhibitor.</p>Formula:C27H34N2O5Color and Shape:SolidMolecular weight:466.57Oxamniquine
CAS:<p>Oxamniquine is an effective compound for the treatment of schistosomiasis.</p>Formula:C14H21N3O3Purity:98%Color and Shape:Pale Yellow Crystals From Isopropanol SolidMolecular weight:279.33Dup-721
CAS:<p>DuP-721: broad-spectrum, oral antibiotic targeting various bacteria, including M. tuberculosis.</p>Formula:C14H16N2O4Purity:99.84%Color and Shape:SolidMolecular weight:276.29DprE1-IN-9
CAS:<p>DprE1-IN-9 (compound B18) is an efficient reversible inhibitor of DprE1, interacting with the enzyme's receptor cavity.</p>Formula:C22H25F3N4O2Color and Shape:SolidMolecular weight:434.45DHFR-IN-10
CAS:<p>DHFR-IN-10 (compound 4c) is a potent inhibitor of dihydrofolate reductase (DHFR), displaying an inhibition concentration half-maximum (IC50) of 4.21 μM against</p>Formula:C20H14BrN3S3Color and Shape:SolidMolecular weight:472.44Droxinavir HCl
CAS:<p>Droxinavir HCl is an antiviral agent and HIV protease inhibitor.</p>Formula:C29H52ClN5O4Purity:98%Color and Shape:SolidMolecular weight:570.22Pencitabine
CAS:<p>Pen is an oral cancer drug that blocks DNA synthesis by inhibiting key enzymes and integrating into DNA.</p>Formula:C15H20F3N3O6Color and Shape:SolidMolecular weight:395.33BMS-561390
CAS:<p>BMS-561390, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formula:C14H12ClF3N2OColor and Shape:SolidMolecular weight:316.71β-Lactamase-IN-8
CAS:<p>β-Lactamase-IN-8 (compound 20) is a potent and oral bioavailable broad-spectrum cyclic boronate β-lactamase inhibitor that can be used for researching</p>Formula:C10H14BNO4SColor and Shape:SolidMolecular weight:255.1MsbA-IN-6
CAS:<p>MsbA-IN-6: potent antibiotic, hinders MsbA in gram-negative bacteria, kills E. coli, effective on drug-resistant strains.</p>Formula:C24H20Cl2N4OPurity:98%Color and Shape:SolidMolecular weight:451.35AZ-27
CAS:<p>AZ-27 is a respiratory syncytial virus inhibitor which differentially inhibits different polymerase activities at the promoter.</p>Formula:C36H35N5O4SColor and Shape:SolidMolecular weight:633.76GS-6620
CAS:<p>GS-6620 is a HCV nonstructural protein 5B (NS5B) inhibitor.</p>Formula:C29H37N6O9PColor and Shape:SolidMolecular weight:644.61APX2039
CAS:<p>APX2039 is an orally active fungal Gwt1 enzyme inhibitor and a prodrug of the novel Gwt2096 inhibitor APX1.APX2039 exhibits potent anti-Kryptococcal activity</p>Formula:C20H15FN4O2Purity:98.72% - 99.07%Color and Shape:SolidMolecular weight:362.36CDD-1845
CAS:<p>CDD-1845, a non-covalent, non-peptide inhibitor, exhibits potent inhibition of SARS-CoV-2 M^pro with a K_i value of 3 nM.</p>Formula:C34H31N5O2Purity:98%Color and Shape:SolidMolecular weight:541.64
