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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VT-1598
CAS:<p>VT-1598 is a novel, selective, orally active fungal CYP51 inhibitor. VT-1598 exhibits antifungal effects against Candida albicans.</p>Formula:C31H20F4N6O2Color and Shape:SolidMolecular weight:584.52IpOHA
CAS:<p>IpOHA is a potent inhibitor of plant KARI and functions as an antimycobacterial agent, demonstrating a K_i value of 97.7 nM against Mycobacterium tuberculosis (</p>Formula:C5H9NO4Color and Shape:SolidMolecular weight:147.13Dihydroaltenuene B
CAS:<p>Dihydroaltenuene B inhibits mushroom tyrosinase (IC50: 38.33µM) and binds His244, Met280, Gly281 via hydrogen bonds.</p>Formula:C15H18O6Color and Shape:SolidMolecular weight:294.3SARS-CoV-2 3CLpro-IN-2
CAS:<p>SARS-CoV-2 3CLpro-IN-2 is a potent inhibitor of the 3CL protease pair and has shown research potential for SARS-CoV-2 disease.</p>Formula:C21H18F5N5O4Color and Shape:SolidMolecular weight:499.39BMS-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:316.71U 89360E
CAS:<p>U 89360E is a peptidic inhibitor.</p>Formula:C28H52N8O6Purity:98%Color and Shape:SolidMolecular weight:596.76Murabutide
CAS:<p>Murabutide, a safe synthetic immunomodulator, diminishes the expression of CD4 and CCR5 receptors and promotes the secretion of high levels of beta-chemokines,</p>Formula:C23H40N4O11Color and Shape:SolidMolecular weight:548.58Japonilure
CAS:<p>Japonilure is an agent of insecticide and pheromone.</p>Formula:C14H24O2Purity:98%Color and Shape:SolidMolecular weight:224.34WRN 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:420.38MPI8
CAS:<p>MPI8 is a SARS-CoV-2 Protease inhibitor (IC50 = 105 nM).</p>Formula:C32H48N4O7Color and Shape:SolidMolecular weight:600.75Quorum Sensing-IN-2
CAS:<p>Quorum Sensing-IN-2 (compound 23e) is a quorum sensing inhibitor that curtails bacterial pathogenicity without impeding growth.</p>Formula:C19H13F2NO3Color and Shape:SolidMolecular weight:341.31GS-6620
CAS:<p>GS-6620 is a HCV nonstructural protein 5B (NS5B) inhibitor.</p>Formula:C29H37N6O9PColor and Shape:SolidMolecular weight:644.61OfChi-h-IN-2
CAS:<p>OfChi-h-IN-2 (compound TQ19) is a potent inhibitor of OfChi-h, exhibiting a K i of 0.33 μM, and significantly impairs the growth and development of Ostrinia</p>Formula:C25H28ClN5O3Purity:98%Color and Shape:SolidMolecular weight:481.98Aranciamycin
CAS:<p>Aranciamycin (Compound 1), an anthracycline antibiotic, exhibits collagenase inhibitory activity (IC50 3.7*10^-7 M) and can inhibit DNA synthesis in tumor cells</p>Formula:C27H28O12Color and Shape:SolidMolecular weight:544.5OM173-αA
CAS:<p>OM173-αA is a quinone bacterial metabolite that inhibits the growth of the bacteria M.</p>Formula:C17H16O6Color and Shape:SolidMolecular weight:316.31SARS-CoV-2/MERS Mpro-IN-1
<p>SARS-CoV-2/MERS Mpro-IN-1 is a potent inhibitor of the main proteases in SARS-CoV-2 and MERS, exhibiting IC50 values of 0.10 and 0.06 µM, respectively.</p>Formula:C30H36N4O7Color and Shape:SolidMolecular weight:564.63MurA-IN-4
CAS:<p>MurA-IN-4 exhibits antibacterial properties as a MurA inhibitor, impeding the synthesis of bacterial cell walls [1].</p>Formula:C8H12ClNO3Color and Shape:SolidMolecular weight:205.64β-Lactamase-IN-2
CAS:<p>β-Lactamase-IN-2 is an inhibitor of β-Lactamase with anti-microbial and anti-bacterial effects.</p>Formula:C11H9FO3Purity:99.52%Color and Shape:SolidMolecular weight:208.19CDD-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:599.65Ravidasvir HCl
CAS:<p>Ravidasvir, also known as PPI-668 and ASC16, is a second-generation, orally active, potent and selective HCV NS5A protein inhibitor.</p>Formula:C42H52Cl2N8O6Color and Shape:SolidMolecular weight:835.828SPR38
<p>SPR38: SARS-CoV-2 protease inhibitor with Ki 0.260 μM; also blocks hCatL (Ki 1.92 μM) and hCatB (Ki 11.1 μM).</p>Formula:C24H33N3O5Color and Shape:SolidMolecular weight:443.54XSJ2-46
CAS:<p>XSJ2-46, a 5'-amino NI analog, is an antiviral agent possessing anti-Zika virus properties and demonstrates reasonable inhibition of RNA-dependent RNA</p>Formula:C25H24ClF3N6O3Purity:98%Color and Shape:SolidMolecular weight:548.95Glycolithocholic acid 3-sulfate disodium
CAS:<p>Glycolithocholic acid 3-sulfate (disodium) demonstrates inhibitory effects on in vitro HIV-1 replication and has potential applications in HIV infection and</p>Formula:C26H41NNa2O7SColor and Shape:SolidMolecular weight:557.65FIKK9.1-IN-1
CAS:<p>FIKK9.1-IN-1 (Compound 1), an antimalarial agent (IC50: 2.68 μg/mL), serves as a FIKK9.1 inhibitor by interacting with the ATP-binding residues within FIKK9.1,</p>Formula:C22H22N2SePurity:98%Color and Shape:SolidMolecular weight:393.38HIV-1 inhibitor-3
CAS:<p>HIV-1 inhibitor-3 is an HIV infection inhibitor.</p>Formula:C9H10F2N2O5Purity:98%Color and Shape:SolidMolecular weight:264.18D1N52
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:447.34Tuberculosis inhibitor 12
CAS:<p>Tuberculosis Inhibitor 12, an oxadiazole derivative, effectively inhibits Mycobacterium tuberculosis, demonstrating inhibition rates of 82% and 78% at a</p>Formula:C15H9FN4O3SColor and Shape:SolidMolecular weight:344.32SARS-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:319.35Tuberculosis inhibitor 6
CAS:<p>Tuberculosis inhibitor 6 (compound 2c), a 3-methoxy-2-phenylimidazo[1,2-b]pyridazine derivative, is highly active against Mycobacterium tuberculosis (MIC 90 of</p>Formula:C21H19N3O2SColor and Shape:SolidMolecular weight:377.46Flurofamide
CAS:<p>Flurofamide is an effective bacterial urease inhibitor and has potential in the treatment of infected urinary calculi.</p>Formula:C7H9FN3O2PPurity:96.01% - 98%Color and Shape:SolidMolecular weight:217.14XZ426
CAS:<p>XZ426 is a potent integrase strand transfer inhibitor with anti- HIV activity .</p>Formula:C22H24F2N4O4Color and Shape:SolidMolecular weight:446.45Antileishmanial agent-17
CAS:<p>Antileishmanial agent-17, a coumarin hybrid, exhibits potent antileishmanial activity (IC50 <0.78 μM) while proving non-toxic to normal VERO cells.</p>Formula:C27H37N5O5Purity:98%Color and Shape:SolidMolecular weight:511.61AZ-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:633.76DDD85646
CAS:<p>DDD85646 is an inhibitor of T. brucei N-myristoyltransferase with a Ki of 1.44 nM, an IC50 of 2 nM and an EC50 of 2 nM. The IC50 of hNMT is 4 nM.</p>Formula:C21H24Cl2N6O2SPurity:97.8% - 99.76%Color and Shape:SolidMolecular weight:495.43UCB7362
CAS:<p>UCB7362 (GLXC-26743) is an orally available and potent plasmepsin X (PMX) inhibitor with anti-malarial activity.UCB7362 inhibits parasite reproduction.</p>Formula:C25H26ClN5O3Purity:97.67%Color and Shape:SolidMolecular weight:479.96Antimalarial agent 15
CAS:<p>Antimalarial agent 15 halts Plasmodium falciparum growth with a 20 nM IC50.</p>Formula:C29H30N2O6Color and Shape:SolidMolecular weight:502.56CDD-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:541.64NIK-250
CAS:<p>NIK-250 is a P-glycoprotein inhibitor. NIK250 could reverse multidrug resistance in human glioma cells.</p>Formula:C26H25N3O4S2Color and Shape:SolidMolecular weight:507.62Antituberculosis agent-1
CAS:<p>Antituberculosis Agent-1 (Compound 8a) is an effective antituberculosis agent, demonstrating a minimum inhibitory concentration (MIC) of 3.84 μg/mL against</p>Formula:C21H21NO4Color and Shape:SolidMolecular weight:351.4Cap-dependent endonuclease-IN-13
CAS:<p>Cap-dependent endonuclease-IN-13 is a potent inhibitor of cap-dependent endonuclease (CEN) and shows research potential against influenza virus infection (</p>Formula:C25H20F2N4O4SColor and Shape:SolidMolecular weight:510.51DAM-IN-1
CAS:<p>DMA-IN-1 is a DNA adenine methyltransferase (DAM) inhibitor with an IC50 value of 48 μM.</p>Formula:C16H17NO4Purity:98%Color and Shape:SolidMolecular weight:287.31Antiviral agent 35
CAS:<p>Antiviral agent 35 (compound 4d) serves as a potent orally active inhibitor of the influenza virus, targeting early stages of viral replication.</p>Formula:C23H18N2O4SPurity:98%Color and Shape:SolidMolecular weight:418.47EHNA hydrochloride
CAS:<p>EHNA hydrochloride is a PDE2 and ADA inhibitor with anticancer activity, increasing intracellular adenosine concentration in a treatment time-dependent manner.</p>Formula:C14H24ClN5OPurity:98%Color and Shape:SolidMolecular weight:313.83Galidesivir dihydrochloride
CAS:<p>Galidesivir inhibits RdRP; has broad antiviral effects on various RNA viruses; effective against Ebola, Marburg in animals.</p>Formula:C11H17Cl2N5O3Color and Shape:SolidMolecular weight:338.19Votoplam
CAS:<p>Votoplam functions as a gene splicing modulator, employed in the inhibition of Huntington's disease [1].</p>Formula:C21H25N9OPurity:98%Color and Shape:SolidMolecular weight:419.48Tuberculosis inhibitor 8
CAS:<p>Tuberculosis inhibitor 8 (compound 3b), a 3-methoxy-2-phenylimidazo[1,2-b]pyridazine derivative, exhibits potent activity against both Mycobacterium</p>Formula:C21H19FN4OColor and Shape:SolidMolecular weight:362.4Propamidine
CAS:<p>Propamidine acts as a covalent inhibitor of TMPRSS2 and exhibits antibacterial properties. [1]</p>Formula:C17H20N4O2Purity:98%Color and Shape:SolidMolecular weight:312.375,6,7,8-Tetrahydro-8-deazahomofolic acid
CAS:<p>5,6,7,8-Tetrahydro-8-deazahomofolic acid is a potential thymidylate synthase (TS) inhibitor and other folate related enzymes inhibitor.</p>Formula:C21H26N6O6Color and Shape:SolidMolecular weight:458.47RSV L-protein-IN-2
CAS:<p>RSV L-protein-IN-2 (Compound A), a noncompetitive inhibitor of the RSV polymerase (IC50: 4.5 μM), exhibits antiviral activity against long RSV strains (EC50: 1.</p>Formula:C32H36N4O5Purity:98%Color and Shape:SolidMolecular weight:556.65WQ 2743
CAS:<p>WQ 2743 is a potent agent of antimicrobial.</p>Formula:C19H15BrF3N5O3Purity:98%Color and Shape:SolidMolecular weight:498.25
