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(3,355 products)
- Antibiotic(934 products)
- Antifection(26 products)
- DHFR(32 products)
- DNA/RNA Synthesis(799 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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Neuraminidase-IN-8
CAS:Neuraminidase-IN-8 (Compound 6d) is a powerful inhibitor of neuraminidase, exhibiting a low half-maximal inhibitory concentration (IC50) of 0.027 μM andFormula:C18H16FN3O3SColor and Shape:SolidMolecular weight:373.4Brassilexin
CAS:Brassilexin is a cyclobrassinin hydrolase inhibitor, a unique enzyme from the fungal pathogen Alternaria brassicicola.Formula:C9H6N2SPurity:98%Color and Shape:SolidMolecular weight:174.22DLC27-14
CAS:DLC27-14 is an HIV-1 Nef specific protein disorder catalyzer.Formula:C25H25NO4Color and Shape:SolidMolecular weight:403.47Soporidine
CAS:Soporidine, a strigolactone antagonist, blocks AtHTL, hindering SL signaling and seed germination.Formula:C27H30F3NO3Purity:98%Color and Shape:SolidMolecular weight:473.53SCY-078 phosphate
CAS:SCY-078 phosphate is a novel glucan synthesis inhibitor.Formula:C44H70N5O8PColor and Shape:SolidMolecular weight:828.04Docosylferulate
CAS:Docosylferulate is a biochemical that has been studied for its inhibition on Hep G2 cells and anti-tumor activities.Formula:C32H54O4Color and Shape:SolidMolecular weight:502.77RMI 10874
CAS:RMI 10874 is a tilorone analogue. Tilorone is an orally bioavailable antiviral agent.Formula:C21H26N2O4Purity:98%Color and Shape:SolidMolecular weight:370.44Mt KARI-IN-5
CAS:Mt KARI-IN-5 inhibits MtbKARI with Ki 4.72 μM, has MIC 1.56 μM against MtbH37Rv, and is low in cytotoxicity with IC50 >64 μg/mL in HEK.Formula:C14H10N4O5S3Color and Shape:SolidMolecular weight:410.45Influenza virus-IN-4
CAS:Influenza virus-IN-4 (compound 11e) is a potent inhibitor of influenza virus neuraminidase, acting on H5N1 (IC50: 3.4 μM), H5N2 (IC50: 0.094 μM), H5N6 (IC50: 0.Formula:C23H31FN2O4Color and Shape:SolidMolecular weight:418.5Oxocarbazate
CAS:Oxocarbazate (CID23631927) is a subnanomolar, reversible cathepsin L inhibitor, also reducing SARS-CoV and Ebola virus entry into human cells.Formula:C28H33N5O6Color and Shape:SolidMolecular weight:535.59Dermadin
CAS:Dermadin is an antibacterial and can be used in paper mill systems to inhibit the growth of Aerobacter aerogenes which is known to produce slime in such system.Formula:C9H9NO3Color and Shape:SolidMolecular weight:179.175Mt KARI-IN-4
CAS:Mt KARI-IN-4 inhibits Mtb KARI with Ki of 5.48μM, has MIC of 0.78μM against H37Rv, and IC50 >72μg/mL, low cytotoxicity.Formula:C13H8FN5O3S2Color and Shape:SolidMolecular weight:365.36HIV-1 inhibitor-35
CAS:HIV-1 inhibitor-35, potent against HIV (EC50: 80 nM LTR, 70 nM CMV), also suppresses HepG2 cells (CC50: 40 nM), may reverse HIV-1 latency.Formula:C13H12Cl3N5OSColor and Shape:SolidMolecular weight:392.69HIV-1 inhibitor-48
CAS:HIV-1 inhibitor-48 is a novel non-nucleoside reverse transcriptase inhibitor (NNRTI) and exhibits anti-HIV-1 activity .Formula:C19H16BrN5Color and Shape:SolidMolecular weight:394.27RO5464466
CAS:RO5464466 is an inhibitor of influenza A virus (H1N1) fusion.Formula:C16H26N2O3SColor and Shape:SolidMolecular weight:326.45SCH51048
CAS:SCH 51048 is a broad spectrum antifungal with oral activity.Formula:C37H42F2N8O3Color and Shape:SolidMolecular weight:684.78SW203668 (trifluoroacetate salt)
CAS:SW203668: Irreversible stearoyl-CoA desaturase blocker; IC50=54 nM; cytotoxic to CYP4F11-positive cancer cells; IC50=22-116 nM.Formula:C24H20F3N3O4SColor and Shape:SolidMolecular weight:503.49(-)-Pinocembrin
CAS:(-)-Pinocembrin: Anti-tuberculosis (IC50: 1.11 mg/mL dormant, 1.21 mg/mL active), antiproliferative (IC50: 1.88-11 mg/mL on various cell lines).Formula:C15H12O4Color and Shape:SolidMolecular weight:256.25IACS-4759
CAS:IACS-4759 is a novel potent and selective MTH1 inhibitor with excellent cell permeability and good metabolic stability in microsomes.Formula:C10H17N3O2Color and Shape:SolidMolecular weight:211.26B 669
CAS:B 669 has antibacterial activity.Formula:C30H28N4Color and Shape:SolidMolecular weight:444.57Sch 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:447.44VIM-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:436.23FabG1-IN-1
CAS:FabG1-IN-1 (Compound 29) is a potent inhibitor of MabA (FabG1) (IC50: 38 μM).Formula:C14H8Cl2INO3Color and Shape:SolidMolecular weight:436.03DC07090 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:528.62Antibacterial agent 19
CAS:Antibacterial agent 19 targets K. pneumoniae and multi-resistant S. aureus with MICs: 0.022 and 0.045 mg/mL.Formula:C16H16F2N2O4Color and Shape:SolidMolecular weight:338.31Antibacterial agent 95
CAS:Antibacterial 95, a quinoline-derived antituberculotic, shows 0.3 μM MIC against Mycobacterium tuberculosis H37Rv and inhibits its growth in macrophages.Formula:C19H16ClNO3Color and Shape:SolidMolecular weight:341.79PqsR/LasR-IN-3
CAS:PqsR/LasR-IN-3 (Compound 7a) inhibits hERG with the IC 50 of 109.01 μM which is also a PqsR and LasR systems inhibitor in P. aeruginosa [1].Formula:C14H17NO5SColor and Shape:SolidMolecular weight:311.35Ametantrone Acetate
CAS:Ametantrone Acetate is a topoisomerase II inhibitor of anthrapyrazole family, which can lead to DNA covalent crosslinking.Formula:C24H32N4O6Color and Shape:SolidMolecular weight:472.542Antibacterial agent 105
CAS:Compound 17, a phenanthrolinic quinolone, fights M. tuberculosis (MIC 90: 2.64 μM) and various bacteria (MIC 90: 0.70-44.70 μM).Formula:C14H9N3O5Color and Shape:SolidMolecular weight:299.24Cap-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:500.42Antifungal agent 68
CAS:Antifungal agent 68 (compound 10) effectively combats fungal infections caused by Candida and Cryptococcus gattii through the inhibition of ergosterolFormula:C23H27ClN2O3Color and Shape:SolidMolecular weight:414.93Metallo-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:290.3Antitubercular 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:346.18Antitrypanosomal agent 10
Antitrypanosomal agent 10, an antitrypanosomal compound, effectively inhibits Trypanosoma cruzi with an IC50 of 0.28 μM.Formula:C17H9F6N5OColor and Shape:SolidMolecular weight:413.28Mtb-cyt-bd oxidase-IN-6
CAS:Mtb-cyt-bd oxidase-IN-6, a potent inhibitor of Mycobacterium tuberculosis (Mtb) cytochrome bd (cyt-bd) oxidase (MtbCyt-bd Oxidase), exhibits an inhibitoryFormula:C20H27NOColor and Shape:SolidMolecular weight:297.43Floxacrine
CAS:Floxacrine is drug candidate for chemoprophylaxis of malaria.Formula:C20H13ClF3NO3Purity:98%Color and Shape:SolidMolecular weight:407.77DMJ-I-228
CAS:DMJ-I-228 is a specific inhibitor of HIV-1 entry through interaction with the Env spike by virtue of the incorporation of a guandinium group.Formula:C19H19ClFN5O4Color and Shape:SolidMolecular weight:435.84Isobellidifolin
CAS:Isobellidifolin, a xanthone compound, serves as a free radical scavenger and antioxidant. It exhibits a potent antifungal effect.Formula:C14H10O6Color and Shape:SolidMolecular weight:274.23Crisnatol mesylate
CAS:Crisnatol, a potent and selective DNA intercalator, has potential anticancer activity.Formula:C24H27NO5SColor and Shape:SolidMolecular weight:441.54HBV-IN-16
CAS:HBV-IN-16, a quinoline derivative, inhibits HBV cccDNA, key for viral replication (from patent WO2019121357A1).Formula:C22H20ClNO4Color and Shape:SolidMolecular weight:397.85Urease-IN-5
Urease-IN-5: urease inhibitor, IC50 1.473 µM, low cytotoxicity, IC50 17.78 µg/mL on P. vulgaris.Formula:C16H20N2O3SColor and Shape:SolidMolecular weight:320.41Brobactam Sodium Salt
CAS:Brobactam Sodium Salt is a β-lactamase inhibitor.Formula:C8H9BrNNaO3SColor and Shape:SolidMolecular weight:302.12SARS-CoV-2-IN-31
CAS:SARS-CoV-2-IN-31: COVID-19 inhibitor, IC50: 28.84-38.36 μM, useful in cancer studies.Formula:C29H28N4O2Color and Shape:SolidMolecular weight:464.56LabMol-301
CAS:LabMol-301 blocks NS5 RdRp/NS2B-NS3pro (IC50: 0.8/7.4µM), protects cells from ZIKV death.Formula:C18H16N6Color and Shape:SolidMolecular weight:316.36Antitubercular agent-26
CAS:Compound 32: oral antitubercular, acts on M. tuberculosis, IC50 ~0.50μM, stable, low cardiotoxicity, non-genotoxic.Formula:C22H23N5O3S2Color and Shape:SolidMolecular weight:469.58
