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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SS148
CAS:SS148 inhibits nsp14/nsp16 MTase, selective vs human MTases; promising for potent, selective coronavirus MTase inhibitors.Formula:C16H20N6O5SColor and Shape:SolidMolecular weight:408.43Antibacterial agent 126
Antibacterial agent 126 combats biofilm, disrupts membranes, and boosts ROS/RNS to prevent drug resistance.Formula:C21H24NO6PColor and Shape:SolidMolecular weight:417.39HBV-IN-14
CAS:HBV-IN-14: a pyridinopyrimidinone, potent cccDNA inhibitor for HBV study (patent WO2021190502A1, comp 5).Formula:C22H21ClN2O5Color and Shape:SolidMolecular weight:428.87BAY-707 acetate
CAS:BAY-707: potent, selective MTH1 inhibitor with excellent engagement and pharmacokinetics but no anticancer efficacy alone or combined.Formula:C17H24N4O4Color and Shape:SolidMolecular weight:348.18Cyclophilin inhibitor 3
CAS:Cyclophilin inhibitor 3 (compound 7c), a potent inhibitor of cyclophilin A (CypA), exhibited potent anti-HCV effects with an EC50 value of 4.2 μM.Formula:C34H38N4O6Color and Shape:SolidMolecular weight:598.69NEU617
CAS:NEU617 is an inhibitor of the growth of protozoan parasites, against T. brucei bloodstream proliferation.Formula:C31H26ClFN4O2Color and Shape:SolidMolecular weight:541.02Sudoterb HCl
CAS:Sudoterb has anti-tubercular activity.Formula:C29H30Cl2F3N5OPurity:98%Color and Shape:SolidMolecular weight:592.48DprE1-IN-1
CAS:DprE1-IN-1: Potent, oral DprE1 inhibitor; stable in hepatocytes, low toxicity, anti-bacilli in macrophages, -1.29 log10 CFU.Formula:C19H21N3O6S2Color and Shape:SolidMolecular weight:451.52Antifungal agent 70
CAS:Antifungal Agent 70 (Compound 13), a dihydroeugenol-imidazole, exhibits efficacy against multi-resistant Candida auris with a minimum inhibitory concentration (Formula:C23H25ClN2O4Color and Shape:SolidMolecular weight:428.91Laromustine
CAS:Laromustine (VNP40101M) is a sulfonyl hydrolysis alkylation prodrug for cancer treatment with significant anticancer activity, inhibiting thioredoxin reductase.Formula:C6H14ClN3O5S2Purity:≥98%Color and Shape:SolidMolecular weight:307.78Mycobacterial Zmp1-IN-1
Zmp1-IN-1: An inhibitor of mycobacterial Zmp1 with dose-dependent anti-tuberculosis effects.Formula:C26H27N3O7SColor and Shape:SolidMolecular weight:525.57SJ000025081
CAS:SJ000025081, a dihydropyridine, shows potent antimalarial action against P. yoelii in mice.Formula:C28H30FNO5Color and Shape:SolidMolecular weight:479.54P163-0892
CAS:P163-0892: potent, specific antifungal for Cryptococcus; moderate blood-brain barrier penetration.Formula:C19H20N2O3SColor and Shape:SolidMolecular weight:356.44Diethyl butylmalonate
CAS:Diethyl butylmalonate shows toxicity to T. pyriformis, with a log(IGC50 -1 ) of 0.557 [1].Formula:C11H20O4Color and Shape:SolidMolecular weight:216.27Vebufloxacin
CAS:Vebufloxacin (OPC-7251) shows potent antibacterial activity against gram-positive and -negative bacteria, including Staphylococcus aureus and PseudomonasFormula:C19H22FN3O3Purity:98%Color and Shape:SolidMolecular weight:359.39Dodicin
CAS:Dodicin is a potent disinfectant exhibiting broad-spectrum antimicrobial activity [1].Formula:C18H39N3O2Color and Shape:SolidMolecular weight:329.52Efavirenz, (R)-
CAS:Efavirenz, (R)- is an antiviral agent and a nonnucleoside HIV-1 reverse transcriptase inhibitor.Formula:C14H9ClF3NO2Color and Shape:SolidMolecular weight:315.67ERCC1-XPF-IN-1
CAS:ERCC1-XPF-IN-1: potent ERCC1-XPF inhibitor (IC50: 0.49 μM), hampers CPD removal, boosts UV toxicity, hinders DNA repair.Formula:C28H32ClN5O2Color and Shape:SolidMolecular weight:506.04GAK inhibitor 2
CAS:GAK inhibitor 2, IC50: 0.024μM, strongly blocks GAK; potent against dengue virus, EC50: 1.049μM.Formula:C20H23N3O3SColor and Shape:SolidMolecular weight:385.48Antimicrobial agent-4
CAS:Antimicrobial agent-4 (6a) has potent activity against pathogens; binds target enzyme with 10.0 kcal/mol affinity.Formula:C22H16ClN5O2SColor and Shape:SolidMolecular weight:449.91Antiviral agent 9
Antiviral agent 9: EC50 0.006 nM vs HIV-1, 300x more selective than TAF.Formula:C38H50N7O8PColor and Shape:SolidMolecular weight:763.82As-358 hydrochloride
CAS:As-358 (hydrochloride) shows well in vivo safety as well as inhibits Ebola virus and Marburg virus with IC 50 values of 9.1 μM and 18.1 μM [1].Formula:C18H32ClNO2Color and Shape:SolidMolecular weight:329.91Antimicrobial agent-1
CAS:Antimicrobial Agent-1 (compound 6C) shows strong activity (MIC = 2 μg/mL) against TolC mutant E.Formula:C22H21N3O2SColor and Shape:SolidMolecular weight:391.49As-358
CAS:As-358 has inhibitory effects against Ebola virus (IC50 = 47.5 μM) and Marburg virus (IC50 = 3.7 μM) [1].Formula:C18H31NO2Color and Shape:SolidMolecular weight:293.4413(S)-HpOTrE
CAS:13(S)-HpOTrE, a fatty acid from soy LO-2 action on α-linolenic acid, forms in soybeans (9:1 ratio). It generates plant defense signals against pests.Formula:C18H30O4Color and Shape:SolidMolecular weight:310.43HIV-1 inhibitor-39
CAS:HIV-1 inhibitor-39: blocks HIV-1, anti-RT (IC50=15.75 μM), toxic to MT-4 cells (CC50=112.9 μM).Formula:C20H17ClN4O4S4Color and Shape:SolidMolecular weight:541.09β-Lactamase-IN-7
CAS:β-Lactamase-IN-7 (compound 14) effectively inhibit Klebsiella pneumoniae that is a potent inhibitor of VIM-Type metallo-β-lactamase with Ki values of 1.26 μMFormula:C16H15N3S2Color and Shape:SolidMolecular weight:313.44Antimicrobial agent-8
Antimicrobial agent-8: potent against Gram+ & Gram-, 2-8 μg/mL MIC, anti-inflammatory action.Formula:C39H54N16Color and Shape:SolidMolecular weight:746.95Sch 25393
CAS:Sch 25393 is an antibacterial agent in vitro.Formula:C12H14F3NO4SPurity:98%Color and Shape:SolidMolecular weight:325.3Antistaphylococcal agent 2
CAS:Antistaphylococcal agent 2 is an anti-staphylococcal therapeutic agent.Formula:C23H21N5O5Color and Shape:SolidMolecular weight:447.44BiPNQ
CAS:BiPNQ is a Trypanosoma cruzi inhibitor. Trypanosoma cruzi is the etiological agent of Chagas disease (American trypanosomiasis).Formula:C16H12N6OColor and Shape:SolidMolecular weight:304.31Mpro/PLpro-IN-1
CAS:Compound 29 inhibits SARS-CoV-2 Mpro (IC50:1.72μM) & PLpro (IC50:0.67μM) proteases effectively.Formula:C25H27ClN4O3Color and Shape:SolidMolecular weight:466.96Buclosamide
CAS:Buclosamide is a topical antimycotic agent that can be used in dermatomycoses [1].Formula:C11H14ClNO2Color and Shape:SolidMolecular weight:227.693'-Deoxyuridine-5'-triphosphate
CAS:3'-dUTP, a nucleotide analogue, competitively inhibits RNA polymerases I & II, with a Ki of 2.0 µM.Formula:C9H15N2O14P3Color and Shape:SolidMolecular weight:468.14VIM-2-IN-1
CAS:VIM-2-IN-1 (compound 1dj) is a β-lactamase inhibitor with antibacterial activity. IC50: 48 μM) and New Delhi Metal (NDM-1) (IC50: 231 μM).Formula:C12H13IN4O4SColor and Shape:SolidMolecular weight:436.23HIV-1 inhibitor-33
CAS:HIV-1 inhibitor-33, potent against HIV-1 (EC50: 8.6 nM), low toxicity to MT-4 cells (CC50: 18 μM), useful for AIDS research.Formula:C25H28N6OColor and Shape:SolidMolecular weight:428.53Influenza 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:419.97FabG1-IN-1
CAS:FabG1-IN-1 (Compound 29) is a potent inhibitor of MabA (FabG1) (IC50: 38 μM).Formula:C14H8Cl2INO3Color and Shape:SolidMolecular weight:436.03Urease-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:389.24DC07090 Dihydrochloride
CAS:DC07090 Dihydrochloride is a potent inhibitor of human enterovirus 71 3C protease.
Formula:C18H16Cl2N4OColor and Shape:SolidMolecular weight:375.25Purfalcamine
CAS:Purfalcamine, a selective PfCDPK1 inhibitor effective against malaria, has IC50 of 17 nM and EC50 of 230 nM; halts parasites at schizont stage.Formula:C29H33FN8OColor and Shape:SolidMolecular weight:528.62Antitrypanosomal agent 11
Antitrypanosomal Agent 11 is a chemical compound effective against Trypanosoma cruzi, exhibiting an inhibition concentration (IC 50) of 0.23 μM.Formula:C16H10F6N6OColor and Shape:SolidMolecular weight:416.28Cap-dependent endonuclease-IN-21
CAS:Cap-dependent endonuclease-IN-21 inhibits CEN and flu virus replication, potential against influenza A. (From patent WO2021233302A1, compound 8B/8A)Formula:C26H23F2N3O7Color and Shape:SolidMolecular weight:527.47Halofantrine, (-)-
CAS:Halofantrine, (-)- is an antimalarial agent.Formula:C26H30Cl2F3NOColor and Shape:SolidMolecular weight:500.42Metallo-β-lactamase-IN-6
CAS:Metallo-β-lactamase-IN-6 is a highly effective inhibitor of VIM-Type metallo-β-lactamase, demonstrating IC 50 values of 0.56 μM, 29.50 μM, and 5.78 μM for VIM-2Formula:C10H9N3O2Color and Shape:SolidMolecular weight:203.2Antimalarial agent 16
CAS:Antimalarial agent 16 is a parasite inhibitor that exhibits antimalarial effects and inhibits the growth of Plasmodium falciparum with an IC50 value of 2.0 nM.Formula:C30H32N2O6Color and Shape:SolidMolecular weight:516.58F8-S43-S3
CAS:F8-S43-S3 is a SARS-CoV-2 main protease inhibitor (IC 50 = 9.69 μM) [1].Formula:C12H10N4O3SColor and Shape:SolidMolecular weight:290.3Chlorhexidine-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:586.4168Antitubercular agent-18
CAS:Antitubercular agent-18 (9a) MIC: 2 μg/ml for H37Rv, Spec 192, 210; 128 μg/ml for Spec 800. Selective antimycobacterial.Formula:C14H12BrN5OColor and Shape:SolidMolecular weight:346.18C16-K-cBB1
C16-K-cBB1: potent, selective MRSA killer; MIC 1µg/mL, low hemolysis, works in 120 min at 12.5µg/mL.Formula:C33H58ClN5O5SColor and Shape:SolidMolecular weight:672.36
