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(3,354 products)
- Antibiotic(935 products)
- Antifection(26 products)
- DHFR(32 products)
- DNA/RNA Synthesis(798 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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4-((4-((4-Aminophenyl)sulfonyl)phenyl)amino)-4-oxobutanoic acid
CAS:4-((4-((4-Aminophenyl)sulfonyl)phenyl)amino)-4-oxobutanoic acid is a sulfonamide compound that can be used as an anti infective agent [1].Formula:C16H16N2O5SColor and Shape:SolidMolecular weight:348.37HBV-IN-4
CAS:HBV-IN-4, a phthalazinone, inhibits HBV DNA replication orally (IC50: 14 nM), encouraging genome-free capsids with strong anti-HBV effects.Formula:C24H19ClFN5O3Color and Shape:SolidMolecular weight:479.89Alamifovir
CAS:Alamifovir: HBV-specific antiviral, purine analog prodrug; active against wild-type/lamivudine-resistant HBV; inhibits DNA initiation/packaging.Formula:C19H20F6N5O5PSColor and Shape:SolidMolecular weight:575.42HIV-1 inhibitor-25
CAS:Compound R-12a is a potent HIV-1 reverse transcriptase inhibitor (IC50: 0.1061 nM), with low cytotoxicity and effective against multiple mutants.Formula:C26H19N5O2Color and Shape:SolidMolecular weight:433.46Antibacterial agent 26
CAS:Antibacterial agent 26 is an antimicrobial compound that is a potent DHFR inhibitor (S. aureus DHFR Ki of 0.020 nM).
Formula:C19H17N5O2Purity:98.86%Color and Shape:SolidMolecular weight:347.37Antimicrobial agent-8
Antimicrobial agent-8: potent against Gram+ & Gram-, 2-8 μg/mL MIC, anti-inflammatory action.Formula:C39H54N16Color and Shape:SolidMolecular weight:746.95BPH-1358 free base
CAS:BPH-1358 inhibits UPPS (IC50: 110 nM) and FPPS (IC50: 1.8 µM), effective against S. aureus (MIC ~250 ng/mL).Formula:C32H28N6O2Purity:98%Color and Shape:SolidMolecular weight:528.6gp120-IN-1
CAS:gp120-IN-1 (4e) is a potent HIV-1 inhibitor, IC50 2.2 μM, CC50 100.90 μM, and blocks HIV entry.Formula:C15H18N2O4SColor and Shape:SolidMolecular weight:322.38INSCoV-600K(1)
CAS:INSCoV-600K(1) is a potent inhibitor of Mpro (3CLpro), key in viral replication, with potential against SARS-CoV-2 (Patent WO2021219089A1).Formula:C23H22ClF2N5O2SColor and Shape:SolidMolecular weight:505.97Flomoxef sodium
CAS:Flomoxef sodium, an antibiotic belonging to the oxacephem group, exhibits excellent activity against a broad spectrum of Gram-positive bacteria.Formula:C15H17F2N6NaO7S2Purity:99.28%Color and Shape:SolidMolecular weight:518.44Caprochlorone
CAS:Caprochlorone fights orthopoxvirus, lowers influenza in mice lungs, blocks virus entry, and delays its release from cells.Formula:C19H19ClO3Color and Shape:SolidMolecular weight:330.81Anti-infective agent 5
CAS:Orally active compound 74 targets Trypanosoma cruzi with 0.10 μM IC50, reducing in vivo parasite load.Formula:C18H13N5O3Color and Shape:SolidMolecular weight:347.33HIV-1 inhibitor-57
CAS:HIV-1 Inhibitor-57 (Compound 12g) is an antiviral agent that potently inhibits both wild-type and five common NNRTI-resistant strains of HIV-1, exhibiting EC50Formula:C25H24FN5O3SColor and Shape:SolidMolecular weight:493.55BRD-8000.3
CAS:BRD-8000.3 is a narrow-spectrum antimycobacterial targeting EfpA, inhibiting lipid transport in drug-tolerant Mtb and useful in structural and functional.Formula:C19H21BrN4OPurity:99.78% - 99.78%Color and Shape:SolidMolecular weight:401.3LmCPB-IN-1
CAS:LmCPB-IN-1, compound 35, is a reversible inhibitor of LmCPB with strong binding (pKi 9.7).Formula:C18H30N6O2Color and Shape:SolidMolecular weight:362.47Syncytial Virus Inhibitor-1
CAS:Syncytial Virus Inhibitor-1: Potent, oral RSV fusion blocker (EC50: 0.002-0.004 μM for Long, A2, B strains).Formula:C23H26N4O3SPurity:98%Color and Shape:SolidMolecular weight:438.54Gln-AMS
CAS:Gln-AMS is an inhibitor of aminoacyl-tRNA synthetases (AARS). It specifically binds to the A-domain located within the NRPS enzymes.Formula:C15H22N8O8SPurity:98%Color and Shape:SolidMolecular weight:474.45β-L-D4A
CAS:beta-L-D4A inhibits HIV-1 reverse transcriptase, stopping DNA synthesis.Formula:C10H11N5O2Purity:99.45%Color and Shape:SolidMolecular weight:233.23Methisazone
CAS:Methisazone is an effective antiviral agent against poxviruses.Formula:C10H10N4OSPurity:98%Color and Shape:SolidMolecular weight:234.28HIV-1 integrase inhibitor 7
CAS:HIV-1 integrase inhibitor 7 is a potent HIV-1 integrase inhibitor (IC50: 33.3 nM).Formula:C30H26O16Purity:98%Color and Shape:SolidMolecular weight:642.52DHFR-IN-1
CAS:DHFR-IN-1: selective DHFR blocker, IC50 40.71 nM, antifungal, strong against Gram-positive/negative bacteria, synergizes with Levofloxacin (FIC=0.249).Formula:C22H22N6O4S2Color and Shape:SolidMolecular weight:498.58DQBS
CAS:DQBS is an HIV-1 Nef function antagonist.Formula:C22H17ClN4O4SPurity:98%Color and Shape:SolidMolecular weight:468.91Antiparasitic agent-10
CAS:Antiparasitic agent-10 (Compound 94) targets Schistosoma mansoni, shows promise for treating Schistosomiasis.Formula:C13H17N3O4S3Color and Shape:SolidMolecular weight:375.49Ribocil B
CAS:Ribocil-B is the active S-isomer of ribocil which can inhibit flavin mononucleotide (FMN,KD of 6.6 nM).Formula:C19H22N6OSPurity:98%Color and Shape:SolidMolecular weight:382.48LasR-IN-4
CAS:LasR-IN-4 is a potent inhibitor of LasR which inhibits Pseudomonas aeruginosa and its biofilm formation, pyocyanin production, and rhamnolipids production [1].Formula:C18H20N4Color and Shape:SolidMolecular weight:292.38HCV-IN-3
CAS:HCV-IN-3 is a hepatitis C virus (HCV) NS3/4a protein inhibitor (IC50: 20 μM; Kd: 29 μM).Formula:C13H11F2NOPurity:98%Color and Shape:SolidMolecular weight:235.23OX11
CAS:OX11 is a selective inhibitor of S. pneumoniae, P. aeruginosa and E. coli bacteria.Formula:C17H10Cl2N4O3S2Color and Shape:SolidMolecular weight:453.32F594-1001
CAS:F594-1001 (compound 6) serves as a potent, highly selective inhibitor of SARS-CoV-2 Mac1-ADP-ribose, displaying IC 50 values of 8.5 μM, 68 μM, and 45 μM in AS, FP, and FRET assays, respectively. It binds directly to SARS-CoV-2 Mac1 and demonstrates dose-dependent inhibition of Mac1 ADP-ribosylhydrolase activity.Formula:C23H28ClN3O4Color and Shape:SolidMolecular weight:445.94RSV/IAV-IN-2
CAS:RSV/IAV-IN-2 (compound 14c) is a potent dual RSV/IAV inhibitor with lower toxicity than Ribavirin, promising for research.Formula:C19H20N2O3SColor and Shape:SolidMolecular weight:356.44WC-9
CAS:WC-9 is a squalene synthase inhibitor. It acts by binding to TcSQS and HsSQS.Formula:C15H13NO2SPurity:98%Color and Shape:SolidMolecular weight:271.33Reverse transcriptase-IN-3
Reverse transcriptase-IN-3, a pyrimidine carboxamide, inhibits HIV-1 including mutant strains.Formula:C28H31N7O4SColor and Shape:SolidMolecular weight:561.66Dutacatib
CAS:Dutacatib is an inhibitor of SARS-CoV-2 3CLpro and cathepsin K, offering antiviral properties and potential benefits in treating cancer-induced bone disease.
Formula:C23H31N7OColor and Shape:SolidMolecular weight:421.54Antibacterial agent 101
CAS:Antibacterial agent 101 exhibited antibacterial and antifungal effects (MIC=4-32 μg/mL).Formula:C28H29BrN2OColor and Shape:SolidMolecular weight:489.45Succinate dehydrogenase-IN-1
CAS:Succinate dehydrogenase-IN-1 (Compound 34) acts as an inhibitor of succinate dehydrogenase (SDH), exhibiting an IC50 value of 0.94 μM and a KD of 22.4 μM. This compound also demonstrates antifungal activity, with EC50 values against Rhizoctonia solani, Sclerotinia sclerotiorum, Monilinia fructicola, and Botrytis cinerea measured at 0.04 μM, 1.13 μM, 1.61 μM, and 1.21 μM, respectively.Formula:C20H13F6N3OColor and Shape:SolidMolecular weight:425.33Phen-DC3
CAS:Phen-DC3 is a G-quadruplex (G4) specific ligand which can inhibit FANCJ and DinG helicases (IC50s of 65±6 and 50±10 nM, respectively).Formula:C34H26N6O2Purity:98%Color and Shape:SolidMolecular weight:550.61Antifungal agent 2
CAS:Antifungal agent 2 suppresses growth of Cryptococcus, Candida, Aspergillus at ≥0.5 μg/mL.Formula:C19H11Br2F3N4O2Purity:98%Color and Shape:SolidMolecular weight:544.12Ingavirin
CAS:Ingavirin, a novel inhibitor of the influenza virus reproduction, inhubits the formation of the virus specific hemagglutinin.Formula:C10H15N3O3Purity:98%Color and Shape:SolidMolecular weight:225.24Aztreonam lysine
CAS:Aztreonam lysine is an inhaled anti-pseudomonal treatment for people who have pulmonary Pseudomonas aeruginosa infection with cystic fibrosis (CF).Formula:C19H31N7O10S2Purity:98%Color and Shape:SolidMolecular weight:581.62Cefroxadine
CAS:Cefroxadine: an oral cephalosporin antibiotic, broad-spectrum, bactericidal, effective for acute uncomplicated cystitis.Formula:C16H19N3O5SPurity:98%Color and Shape:SolidMolecular weight:365.4Lipoxamycin
CAS:Lipoxamycin is an inhibitor of serine palmitoyl-transferase.Formula:C19H36N2O5Purity:98%Color and Shape:SolidMolecular weight:372.52',5-Difluoro-2'-deoxycytidine
CAS:2',5-Difluoro-2'-deoxycytidine has potent anti-HCV activity and toxicity to rRNA.Formula:C9H11F2N3O4Purity:98%Color and Shape:SolidMolecular weight:263.2Antitumor agent-84
Antitumor agent-84 stabilizes G-quadruplex DNA, exhibits potent anti-tumor effects.Formula:C24H31N7Color and Shape:SolidMolecular weight:417.55InhA-IN-4
CAS:InhA-IN-4 (TU14) is a Mycobacterium tuberculosis InhA (enoyl ACP reductase) inhibitor for the study of Mycobacterium tuberculosis infection.Formula:C14H12BrN3O2SPurity:>99.99%Color and Shape:SolidMolecular weight:366.23Ormetoprim
CAS:Ormetoprim (Ro 5-9754), an antibiotic approved for use in the United States, is used to prevent the spread of disease in freshwater aquaculture.Formula:C14H18N4O2Purity:99.92%Color and Shape:SolidMolecular weight:274.32Ref: TM-T20702
5mg48.00€10mg70.00€25mg104.00€50mg153.00€100mg216.00€500mg540.00€1mL*10mM (DMSO)84.00€RSV/IAV-IN-3
CAS:RSV/IAV-IN-3 is a dual inhibitor of RSV (EC50: 2.92μM) and IAV (EC50:1.90μM), blocking virus replication post-entry.Formula:C19H19BrN2O3SColor and Shape:SolidMolecular weight:435.3341F5
CAS:41F5: Anti-fungal with MIC50 0.4-0.8 μM and IC50 0.87 μM against Histoplasma; 62x more selective for yeast vs host cells.Formula:C21H22N2OSColor and Shape:SolidMolecular weight:350.48MMV008138
CAS:MMV008138 inhibits the growth of P. falciparum Dd2 strain (IC50 of 250 nM).Formula:C18H14Cl2N2O2Color and Shape:SolidMolecular weight:361.22Elsamitrucin
CAS:Elsamitrucin, a heterocyclic antibiotic, disrupts DNA replication by intercalating into G-C sequences and inhibiting topoisomerases.
Formula:C33H35NO13Color and Shape:SolidMolecular weight:653.63Lagociclovir
CAS:Lagociclovir (MIV-210), a nucleoside analogue antiviral, treats HBV by inhibiting its replication in liver cancer cells.Formula:C10H12FN5O3Purity:99.18% - 99.74%Color and Shape:SolidMolecular weight:269.23Sakyomicin A
CAS:Sakyomicin A is an inhibitor of reverse transcriptase.Formula:C25H26O10Color and Shape:SolidMolecular weight:486.47
