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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HBV-IN-22
CAS:HBV-IN-22 (Compound LC5f) is an HBV DNA replication inhibitor that acts on both wild-type HBV (IC50: 0.71 μM) and drug-resistant HBV (IC50: 0.84 μM).Formula:C26H29N3O2S2Color and Shape:SolidMolecular weight:479.66BI-10
CAS:BI-10, paired with fluconazole, hinders fungal growth, increases ROS, decreases MMP, and changes membrane permeability.Formula:C23H17BrN2OColor and Shape:SolidMolecular weight:417.3Cap-dependent endonuclease-IN-23
CAS:Cap-dependent endonuclease-IN-23 hinders influenza virus replication by inhibiting CEN, with potential for flu research.Formula:C26H23F2N3O7Color and Shape:SolidMolecular weight:527.47Remdesivir maleate
CAS:Remdesivir (GS-5734) is a broad-spectrum antiviral prodrug effective against SARS-CoV-2 and Ebola, used for research, not human treatment.Formula:C31H39N6O12PColor and Shape:SolidMolecular weight:718.656BMS-663749
CAS:BMS-663749 is an attachment inhibitor of human immunodeficiency virus type 1 (HIV-1).Formula:C23H25N4O9PColor and Shape:SolidMolecular weight:532.4412(S)-HpETE
CAS:12(S)-HpETE activates human blood leukocyte 5-LOE and mediates induction of c-fos and c-jun, activation of AP-1, and endothelium-dependent vasoconstriction.Formula:C20H32O4Color and Shape:SolidMolecular weight:336.47Anthrarobin
CAS:Anthrarobin is an antipsoriatic.Formula:C14H10O3Purity:98%Color and Shape:SolidMolecular weight:226.23Neoarsphenamine
CAS:Neoarsphenamine is an antisyphilitic still used for infections occasionally.Formula:C13H14As2N2NaO4SPurity:98%Color and Shape:SolidMolecular weight:467.16S 863390
CAS:S 863390 is a renin inhibitor.Formula:C37H52N6O4Purity:98%Color and Shape:SolidMolecular weight:644.85MK436
CAS:MK436 is a therapeutic agent and an antigenic animal drug that is effective in the treatment of Trypanosoma cruzonii infection.Formula:C11H14N4O3Color and Shape:SolidMolecular weight:250.25SCY-078 phosphate
CAS:SCY-078 phosphate is a novel glucan synthesis inhibitor.Formula:C44H70N5O8PColor and Shape:SolidMolecular weight:828.04Valomaciclovir
CAS:Valomaciclovir is a DNA polymerase inhibitor potentially for treatment of acute herpes zoster and EB virus infection.Formula:C15H24N6O4Color and Shape:SolidMolecular weight:352.39Antibacterial agent 96
CAS:Compound 4k is potent against drug-susceptible and resistant M. tuberculosis but toxic to HepG2 and Vero cells.Formula:C18H15Cl2NO2Color and Shape:SolidMolecular weight:348.22SARS-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:464.56Valnivudine
CAS:Valnivudine, oral BCNA antiviral, targets herpes zoster; transforms into CF-1743 in body.Formula:C27H35N3O6Purity:98%Color and Shape:SolidMolecular weight:497.58YXL-13
CAS:YXL-13 suppresses Pseudomonas aeruginosa, hampers virulence and biofilms, and reduces drug resistance with an IC50 of 3.686 μM.Formula:C13H15BrN2O4Color and Shape:SolidMolecular weight:343.17MMV676584
CAS:MMV676584 has anti-tuberculosis avtivity. MMV676584 is a novel drug candidate for eumycetoma .Formula:C12H8ClFN2OS2Color and Shape:SolidMolecular weight:314.79REV7/REV3L-IN-1
CAS:REV7/REV3L-IN-1 is a inhibitor of REV7/REV3L interaction(IC50 of 78 μM),Formula:C19H21N3O3SPurity:98%Color and Shape:SolidMolecular weight:371.45LabMol-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:316.36DprE1-IN-377790
CAS:DprE1-IN-377790 is a novel DprE1 inhibitor, killing M. tuberculosis.Formula:C13H16N4O2Color and Shape:SolidMolecular weight:260.29Grepafloxacin, (S)-
CAS:Grepafloxacin, (S)- is an oral broad-spectrum fluoroquinolone antibacterial used for the treatment of bacterial infections.Formula:C19H22FN3O3Color and Shape:SolidMolecular weight:359.39AB-182
CAS:AB-182 is an aziridine derivative with antitumor activity.Formula:C11H22N3O4PColor and Shape:SolidMolecular weight:291.28LY 215891
CAS:LY 215891 is a compound that exhibits potent Gram-negative and Gram-positive antibacterial activity.Formula:C12H10ClN5O5S2Purity:98%Color and Shape:SolidMolecular weight:403.82AHU1
CAS:AHU1 is a blocker of Shiga Toxin expression in Escherichia coli O157:H7.Formula:C14H14N2O3Color and Shape:SolidMolecular weight:258.27R78206
CAS:R 78206 is a pyridazinamine derivative that suppresses the formation of poliovirus eclipse particles.Formula:C22H29N3O3Purity:98%Color and Shape:SolidMolecular weight:383.48MBX2546
CAS:MBX2546, an influenza A inhibitor, stops HA-induced membrane fusion by binding and stabilizing HA. Resistant virus mutations occur near HA2 start.Formula:C18H21N3O5SPurity:98%Color and Shape:SolidMolecular weight:391.44Anticandidal agent-1
CAS:Compound C2 is a broad-spectrum anticandidal, blocking biofilm and filament growth with MIC50 of 13.51μg/mL (C. glabrata) and 8.65μg/mL (C. albicans).Formula:C19H22O5Color and Shape:SolidMolecular weight:330.38Antitubercular agent-14
CAS:Antitubercular agent-14 (Compound 1) shows antitubercular activity. The MIC value of Antitubercular agent-14 against M. tuberculosis is 0.3 μg/mL [1].Formula:C20H27ClN2Color and Shape:SolidMolecular weight:330.89IMB-26
CAS:IMB-26 is an HCV inhibitor (EC50: 2.1 μM) and has shown potent anti-HCV effects.Formula:C20H23BrN2O6Color and Shape:SolidMolecular weight:467.31Acrisorcin
CAS:Acrisorcin is a topical anti-infective typically used as a fungicide.Formula:C25H28N2O2Purity:98%Color and Shape:SolidMolecular weight:388.5InhA-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:321.78Chlorozotocin
CAS:Chlorozotocin is a nitrosourea. It is used for cancer therapy.Formula:C9H16ClN3O7Color and Shape:SolidMolecular weight:313.694,4'-Dicyanostilbene
CAS:4,4'-Dicyanostilbene: potent anti-Dd2 malaria, EC50=27nM; effective vs. MRSA.Formula:C16H10N2Color and Shape:SolidMolecular weight:230.26Ceftobiprole medocaril sodium
CAS:Ceftobiprole medocaril sodium (BAL5788) is a prodrug of broad-spectrum cephalosporin active against MRSA, VRSA, and resistant streptococci.Formula:C26H25N8NaO11S2Color and Shape:SolidMolecular weight:712.64Rovafovir Etalafenamide
CAS:Rovafovir Etalafenamide is a prodrug of anti-HIV nucleoside phosphonate.Formula:C21H24FN6O6PPurity:98%Color and Shape:SolidMolecular weight:506.42D-Xylofuranose, 1,2,3,5-tetraacetate
CAS:1,2,3,5-Tetra-O-acetyl-D-xylofuranose is a starting material for the synthesis of nucleosides.Formula:C13H18O9Color and Shape:SolidMolecular weight:318.28Taribavirin hydrochloride
CAS:Taribavirin HCl: oral drug targeting HCV in liver, spares red blood cells, aims to reduce anemia risk.Formula:C8H14ClN5O4Purity:98%Color and Shape:SolidMolecular weight:279.685'-Hydroxy-staurosporine
CAS:5'-Hydroxy-staurosporine is an AMPK inhibitor with selective toxicity toward human colon tumor cells.Formula:C28H26N4O4Color and Shape:SolidMolecular weight:482.53Antitubercular agent-37
CAS:Antitubercular Agent-37 exhibits antimycobacterial properties and functions as an antibacterial agent with an MIC (minimum inhibitory concentration) value of 0.Formula:C22H22N8O2Color and Shape:SolidMolecular weight:430.46TDRL-551
CAS:TDRL-551 is a novel and potent replication protein A (RPA) inhibitor (IC50=18 µM) with potential anticancer activity.TDRL-551 inhibits RPA-DNA interaction andFormula:C25H23ClIN3O4Purity:98.09%Color and Shape:SolidMolecular weight:591.83Ref: TM-T28935
1mg87.00€5mg202.00€10mg298.00€25mg630.00€50mg1,008.00€100mg1,644.00€200mg2,213.00€1mL*10mM (DMSO)224.00€Neuraminidase-IN-3
CAS:Neuraminidase-IN-3 inhibits flu NA: H1N1 IC50=0.73nM, H5N1=0.26nM, H5N8=0.63nM.Formula:C27H32N2O4SColor and Shape:SolidMolecular weight:480.62Covidcil-19
CAS:Covidcil-19 targets SARS-CoV-2 FSE with 11 nM affinity, cuts frameshifting, and lowers infectivity sharply.Formula:C16H14N4O2Color and Shape:SolidMolecular weight:294.31Antifungal agent 31
CAS:Orally active triazole, antifungal 31 with pyrrolizinone structure, combats Candida, reduces mortality and renal infection in mice.Formula:C25H22F2N6O3Color and Shape:SolidMolecular weight:492.48Antimalarial agent 20
CAS:Antimalarial agent 20, exhibiting potent efficacy with an IC50 value of 0.6 nM against the P.Formula:C31H38N4O3Color and Shape:SolidMolecular weight:514.66Lufotrelvir
CAS:Lufotrelvir (PF-07304814), a prodrug of PF-00835231, is a potent SARS-CoV-2 3CL protease inhibitor with antiviral properties, Ki 174nM.Formula:C24H33N4O9PPurity:99.43% - >99.99%Color and Shape:SolidMolecular weight:552.51Neuraminidase-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:373.4DLC27-14
CAS:DLC27-14 is an HIV-1 Nef specific protein disorder catalyzer.Formula:C25H25NO4Color and Shape:SolidMolecular weight:403.47CB 3731
CAS:CB 3731 is used in fluorine-19 nuclear magnetic resonance studies of binary and ternary complexes of thymidylate synthase.Formula:C23H24FN5O6Color and Shape:SolidMolecular weight:485.46Antimicrobial agent-5
Antimicrobial agent-5: potent, selective for Gram-negative/positive bacteria, blocks LPS-CD14/TLR4, anti-inflammatory.Formula:C32H48N16Color and Shape:SolidMolecular weight:656.83CM03
CAS:CM03 is a cell-selective G-quadruplex ligand with anti-cancer activity, stabilizing G4 genes, useful in pancreatic cancer research.Formula:C34H44N6O6Purity:98.65%Color and Shape:SolidMolecular weight:632.75
