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(3,334 products)
- Antibiotic(937 products)
- Antifection(26 products)
- DHFR(32 products)
- DNA/RNA Synthesis(796 products)
- HBV(189 products)
- HIV Protease(507 products)
- HSV(96 products)
- Integrase(2 products)
- Ribosome(11 products)
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Found 6383 products of "Microbiology/Virology"
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(5S,8R)-HBV-IN-10
CAS:'(5S,8R)-HBV-IN-10 is an EC50 0.1-1 μM HBsAg inhibitor, isomer of compound 6 from patent WO2021204258A1.Formula:C23H24FN7OColor and Shape:SolidMolecular weight:433.48Caprochlorone
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:347.33Influenza virus-IN-5
CAS:Influenza virus-IN-5 (Compound 5f) is an influenza virus hemagglutinin (HA) inhibitor that acts on the A/H3N2 virus (EC50: 1 nM).Formula:C21H26ClN3O2SColor and Shape:SolidMolecular weight:419.97Urease-IN-7
CAS:Urease-IN-7 (Compound 5k) acts as a competitive inhibitor of the enzyme urease, exhibiting an IC50 value of 3.33 μM and a K_i of 3.62 μM.Formula:C16H10BrFN4SColor and Shape:SolidMolecular weight:389.24FR-182024
CAS:FR-182024 is a novel cephem derivative, it has potent anti-Helicobacter pylori activity.Formula:C18H16N4O4S3Color and Shape:SolidMolecular weight:448.54cp028
CAS:cp028 inhibits pre-mRNA splicing in vitro.Formula:C23H17FN2O4Color and Shape:SolidMolecular weight:404.39Debneyol
CAS:Debneyol exhibits more potent fungicidal activity than validamycin.Formula:C15H26O2Color and Shape:SolidMolecular weight:238.37Antituberculosis agent-2
CAS:Compound 8d: treats MDR and sensitive tuberculosis, low toxicity, good oral bioavailability, stable in humans/mice; MIC: 0.454-1.757 μg/mL.Formula:C19H17NO4Color and Shape:SolidMolecular weight:323.34Edelfosine
CAS:inhibits phosphatidylinositol phospholipase CFormula:C27H58NO6PPurity:98%Color and Shape:SolidMolecular weight:523.73Chlorhexidine-d8 HCl
CAS:Chlorhexidine-d8: internal standard for GC/LC-MS, antimicrobial, inhibits MRSA/MSSA/MRSP/MSSP, affects E. faecium/C. albicans, destabilizes cell walls.Formula:C22H24D8Cl4N10Color and Shape:SolidMolecular weight:586.4168Deaminase inhibitor-1
CAS:Deaminase inhibitor-1 is an APOBEC3G DNA Deaminase inhibitor with an IC 50 value of 18.9 μM [1].Formula:C11H12BrN3OSColor and Shape:SolidMolecular weight:314.2MMV666810
CAS:MMV666810 is a potent 2-aminopyrazine, effective against asexual parasites at 5.94 nM and 3.3x more selective for late-stage gametocytes.Formula:C23H21F3N4O2Color and Shape:SolidMolecular weight:442.43Influenza virus-IN-1
CAS:Influenza virus-IN-1, a potent anti-influenza A compound, has CC50 >200 μM, EC50 2.46 μM, and inhibits PAN endonuclease (EC50 312.36 nM).Formula:C16H17NO5Color and Shape:SolidMolecular weight:303.31HSV-1/HSV-2-IN-1
CAS:HSV-1/HSV-2-IN-1 inhibits HSV-1, HSV-2, and cowpox virus with EC50 values of 7.6, 7.6, 4, and 12 μM, respectively.Formula:C18H14F4N4OSColor and Shape:SolidMolecular weight:410.39Dutacatib
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:421.54HCV-IN-36
CAS:HCV-IN-36: oral HCV inhibitor, EC50 0.016 μM, CC50 8.78 μM, potent antiviral.Formula:C30H36ClN5Color and Shape:SolidMolecular weight:502.09Derquantel
CAS:nicotinic acetylcholine receptor antagonistFormula:C28H37N3O4Purity:98%Color and Shape:SolidMolecular weight:479.61FLDP-5
CAS:FLDP-5: BBB-penetrant curcuminoid, induces ROS, DNA damage, S phase arrest, suppresses tumors in LN-18 cells.Formula:C21H21NO5Color and Shape:SolidMolecular weight:367.4KFU-127
KFU-127: broad-spectrum antimicrobial; targets bacterial/fungal biofilms; toxic to eukaryotic cells.Formula:C34H43BrN2O3Color and Shape:SolidMolecular weight:607.62Ipconazole [ISO]
CAS:Ipconazole, a cyclopentanol with 1,2,4-triazolylmethyl, 4-chlorobenzyl & isopropyl groups, is a fungicide that targets seed diseases.Formula:C18H24ClN3OColor and Shape:SolidMolecular weight:333.86HIV-1 inhibitor-22
CAS:HIV-1 inhibitor-22 effectively blocks HIV-1 RT (IC50=3.63 μM) with low cytotoxicity (CC50 > 227 μM).Formula:C30H26N6O3SColor and Shape:SolidMolecular weight:550.63Sulfasymazine
CAS:Sulfasymazine is a sulfonamide drug.Formula:C13H17N5O2SPurity:98%Color and Shape:SolidMolecular weight:307.37Bay 41-4109 (less active enantiomer)
CAS:Bay 41-4109 less active enantiomer shows less activity than Bay 41-4109. BAY 41-4109 is a potent HBV inhibitor (IC50: 53 nM).Formula:C18H13ClF3N3O2Purity:98%Color and Shape:SolidMolecular weight:395.76FGF22-IN-1
CAS:FGF22-IN-1 is a CD4 N-terminal immunoglobulin variable region-like structural domain (CD4 D1) inhibitor that suppresses the immune response.Formula:C14H11N3OSPurity:99.18%Color and Shape:SolidMolecular weight:269.322',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:263.2A110
CAS:A110 is a potent and selective IMPDHs inhibitor. It binds to the NAD(+) cofactor site and forms a ternary complex with IMP.Formula:C19H15ClN4O2Purity:98%Color and Shape:SolidMolecular weight:366.8KDU731
CAS:KDU731: oral drug for Cryptosporidium-induced diarrhea, safe PI4K inhibitor (IC50: 25 nM), effective in vitro/in vivo.Formula:C22H16N6O2Purity:98%Color and Shape:SolidMolecular weight:396.4Zelpolib
CAS:Zelpolib is a specific inhibitor of DNA polymerase δ (Pol δ), inhibiting DNA replication. antiproliferative.Formula:C22H21N3O5S2Purity:98.79%Color and Shape:SolidMolecular weight:471.55InhA-IN-3
CAS:InhA-IN-3 (TU13) is a Mycobacterium tuberculosis InhA (enoyl ACP reductase) inhibitor for the study of Mycobacterium tuberculosis infection.Formula:C14H12ClN3O2SPurity:99.48%Color and Shape:SolidMolecular weight:321.78Amiprilose
CAS:Amiprilose is an Immunopotentiator.Formula:C14H27NO6Purity:99.82% - >99.99%Color and Shape:SolidMolecular weight:305.37BPH-1218
CAS:BPH-1218 is a SQS inhibitor.Formula:C15H30N2O6P2Purity:98%Color and Shape:SolidMolecular weight:396.36L-Eflornithine
CAS:L-Eflornithine: irreversible ODC inhibitor, KD 1.3±0.3 μM, Kinact 0.15±0.03 min-1, enantiomer of Eflornithine.Formula:C6H12F2N2O2Purity:98%Color and Shape:SolidMolecular weight:182.17(R,R)-BAY-Y 3118
CAS:(R,R)-BAY-Y 3118, the R-enantiomer of BAY-Y 3118, exhibits weak bactericidal activity.Formula:C20H21ClFN3O3Color and Shape:SolidMolecular weight:405.85DHDPS-IN-1
CAS:DHDPS-IN-1 (compound 8), a DHDPS inhibitor with 39 μM IC50, has potential in antibacterial and herbicidal applications.Formula:C13H11NO5SColor and Shape:SolidMolecular weight:293.3Lagociclovir
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:269.23Diazaborine
CAS:Diazaborine disrupts large ribosome formation by inhibiting rRNA maturation and AAA-ATPase Drg1, leading to rapid protein redistribution.Formula:C14H13BN2O3SPurity:98%Color and Shape:SolidMolecular weight:300.14(±)-Hydnocarpin
CAS:(±)-Hydnocarpin, a flavonolignan, demonstrates inhibitory activity against S.Formula:C25H20O9Color and Shape:SolidMolecular weight:464.42ASN03576800
CAS:ASN03576800 is an inhibitor of the VP40 matrix protein.Formula:C11H11NO6SPurity:99.76%Color and Shape:SolidMolecular weight:285.27BAY-707
CAS:BAY-707: tolerable in mice, no anticancer efficacy; potent, selective MTH1 inhibitor, IC50 = 2.3 nM; good PK profile.Formula:C15H20N4O2Purity:98%Color and Shape:SolidMolecular weight:288.34Antiparasitic agent-6
CAS:Compound 5b: antiparasitic against L. infantum (IC50 = 3.89 μM), cytotoxic to HepG2 cells (CC50 = 13.64 μM).
Formula:C19H15N3O3Color and Shape:SolidMolecular weight:333.34Jobosic acid
CAS:Jobosic acid is a saturated fatty acid and a selective inhibitor of SARS-CoV-2. It inhibits the Mpro and the interaction between spike-RBD/ACE-2 with IC50 values of 7.5 μg/mL and 3 μg/mL, respectively. Jobosic acid also exhibits viral entry inhibition against the omicron variant of SARS-CoV-2.Formula:C16H32O2Color and Shape:SolidMolecular weight:256.42BMH-23
CAS:BMH-23 is an RNA polymerase I inhibitor that acts by causing nucleolar stress and showing potent anticancer activity across many tumor types.Formula:C15H15N3Purity:98%Color and Shape:SolidMolecular weight:237.3JMI-346
CAS:JMI-346: Anti-malarial, inhibits P. falciparum (CQS, CQR), IC50: 13 μM (3D7), 33 μM (RKL-9), targets PfFP-2 protease.Formula:C19H20N4O2Color and Shape:SolidMolecular weight:336.39Piperic acid
CAS:Piperic acid is a powerful antioxidant and has potent antibacterial propertiesFormula:C12H10O4Color and Shape:SolidMolecular weight:218.21Vibunazole
CAS:Vibunazole is an antifungal agent.Formula:C15H20ClN3O2Color and Shape:SolidMolecular weight:309.79Aliconazole
CAS:Aliconazole is an imidazole derivative with antifungal activity for the study of skin infections.Formula:C18H13Cl3N2Purity:99.21% - 99.79%Color and Shape:SolidMolecular weight:363.67Antimicrobial agent-14
CAS:Antimicrobial agent-14, a benzyl thiophene sulfonamide, has a 200 μM MIC against Campylobacter coli ATCC33559.Formula:C9H8ClNO3S2Purity:99.02%Color and Shape:SolidMolecular weight:277.75Germination-IN-2
CAS:Germination-IN-2 (compound 15) is a potent germination inhibitor (IC50: 1.3 μM) with anti-germination effects (germination rate = 3%).Formula:C30H45NO3Color and Shape:SolidMolecular weight:467.68Pyribencarb
CAS:Pyribencarb, a benzylcarbamate-type fungicide, exhibits broad-spectrum activity against various plant pathogenic fungi.Formula:C18H20ClN3O3Purity:99.75%Color and Shape:SolidMolecular weight:361.82
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