
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(3,364 products)
- Antibiotic(937 products)
- Antifection(27 products)
- DHFR(30 products)
- DNA/RNA Synthesis(800 products)
- HBV(182 products)
- HIV Protease(496 products)
- HSV(99 products)
- Integrase(2 products)
- Ribosome(10 products)
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Found 6326 products of "Microbiology/Virology"
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DMJ-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:435.84Antitrypanosomal agent 8
CAS:Antitrypanosomal agent 8 (compound 3b) showed a strong antitrypanosomal effect against Trypanosoma brucei (IC50: 0.79 μM). The IC50 value was 80.95 μM.Formula:C23H19N5O2SColor and Shape:SolidMolecular weight:429.49Globosuxanthone A
CAS:Globosuxanthone A: a dihydroxanthenone with anticancer and antifungal properties (MIC: F. graminearum 4, F. solani 8, B. cinerea 16 μg/mL).Formula:C15H12O7Color and Shape:SolidMolecular weight:304.25TMC310911
CAS:TMC310911 is an oral HIV-1 protease inhibitor with an EC50 of 2.2-14.2 nM, effective against various HIV-1 strains.Formula:C38H53N5O7S2Purity:98%Color and Shape:SolidMolecular weight:755.99BPH-1086
CAS:BPH-1086 inhibits IspH, which with RPS1 binds mRNA or integrates into bacterial ribosomes.Formula:C4H8O7P2Color and Shape:SolidMolecular weight:230.05REV7/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:371.45DprE1-IN-377790
CAS:DprE1-IN-377790 is a novel DprE1 inhibitor, killing M. tuberculosis.Formula:C13H16N4O2Color and Shape:SolidMolecular weight:260.29VP-4556
CAS:VP-4556 is a potent anti-MRSA compound with >95% inhibition at 8 μg/mL MIC.Formula:C12H12N2O4SColor and Shape:SolidMolecular weight:280.3Grepafloxacin, (S)-
CAS:Grepafloxacin, (S)- is an oral broad-spectrum fluoroquinolone antibacterial used for the treatment of bacterial infections.Formula:C19H22FN3O3Color and Shape:SolidMolecular weight:359.39Sch 25393
CAS:Sch 25393 is an antibacterial agent in vitro.Formula:C12H14F3NO4SPurity:98%Color and Shape:SolidMolecular weight:325.3Vibunazole
CAS:Vibunazole is an antifungal agent.Formula:C15H20ClN3O2Color and Shape:SolidMolecular weight:309.79Isobellidifolin
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:274.23Antitubercular agent-20
CAS:Antitubercular agent-20 is an orally active antitubercular agent. agent-20 showed low cytotoxicity and good tolerability in BALB/c mice.Formula:C25H22F6N4O3SColor and Shape:SolidMolecular weight:572.52A 80987
CAS:A 80987 is an inhibitor of HIV-1 protease.Formula:C37H43N5O6Color and Shape:SolidMolecular weight:653.77INF55
CAS:INF55 inhibits NorA efflux pump.Formula:C14H10N2O2Purity:98%Color and Shape:SolidMolecular weight:238.24AV-1101
CAS:AV-1101, a cytokine production inhibitor, is used potentially for the treatment of HIV infection.Formula:C19H20N2O4Purity:98%Color and Shape:SolidMolecular weight:340.37HCV-086
CAS:HCV-086, a RNA-directed RNA polymerase (NS5B) inhibitor, is used for the treatment of HCV infection.Formula:C20H21FN2O5SPurity:98%Color and Shape:SolidMolecular weight:420.45ANT431
CAS:ANT431 is a novel metallo-β-lactamase inhibitor for the treatment of carbapenem-resistant enterobacteriaceae infectionsFormula:C9H7N3O4S2Color and Shape:SolidMolecular weight:285.3Antitrypanosomal agent 4
CAS:Compound 19: potent, blood-brain penetrant antitrypanosomal; IC50: T. cruzi 1.2 μM, T.b. brucei 70 nM.Formula:C18H14ClN3O5SColor and Shape:SolidMolecular weight:419.84Ofurace
CAS:Ofurace is a fungicide.Formula:C14H16ClNO3Purity:98%Color and Shape:SolidMolecular weight:281.73Antitubercular agent 34
CAS:Compound 42g: potent antitubercular, MIC 90 of 1.25 µg/mL, resists liver metabolism.Formula:C19H14N4O2SColor and Shape:SolidMolecular weight:362.41Chitin synthase inhibitor 2
CAS:Chitin synthase inhibitor 2 (2b) has an IC50 of 0.09 mM, K i 0.12 mM, shows in vitro antimicrobial activity and boosts fluconazole/polyoxin B.Formula:C20H19N3O3Color and Shape:SolidMolecular weight:349.38A 30641
CAS:A 30641, an epidithioketopiperazine, has in vitro activity against Gram-positive bacteria and fungi.Formula:C12H9ClN2O5S2Purity:98%Color and Shape:SolidMolecular weight:360.79AB-182
CAS:AB-182 is an aziridine derivative with antitumor activity.Formula:C11H22N3O4PColor and Shape:SolidMolecular weight:291.28Pamaqueside
CAS:Pamaqueside is an anti-atherosclerotic agent.Formula:C39H62O14Purity:98%Color and Shape:SolidMolecular weight:754.9LY 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:258.27BP13944
CAS:BP13944 is used as a potential dengue virus NS2B/NS3 protease inhibitor.Formula:C20H44BrNO2Color and Shape:SolidMolecular weight:410.47CAY10760
CAS:CAY10760 inhibits RAD51-BRCA2 interaction (EC50=19 μM), reduces homologous recombination by 54%, and hinders BxPC-3/Capan-1 cancer cell proliferation.Formula:C28H24ClN3O3Color and Shape:SolidMolecular weight:485.96Dutacatib
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:421.54DNAC-1
CAS:DNAC-1 is against Gram-positive and Gram-negative pathogens potentiator of β-lactam activity.Formula:C11H9BrN2S2Purity:98%Color and Shape:SolidMolecular weight:313.24Piposulfan
CAS:Piposulfan, a water-insoluble alkylating agent, is used as an antineoplastic and anti-tumor agent.Formula:C12H22N2O8S2Color and Shape:SolidMolecular weight:386.44Antibacterial agent 117
CAS:Triazole-derived Antibacterial 117 inhibits R. prowazekii MetAP1 with a 15 μM IC50 and rickettsial growth.Formula:C9H9ClN4SColor and Shape:SolidMolecular weight:240.71Navuridine
CAS:Navuridine (AZdU) is an oral active inhibitor of HIV reverse transcriptase with a relatively short half-life.Formula:C9H11N5O4Purity:99.83%Color and Shape:SolidMolecular weight:253.22Nifuroxime
CAS:Nifuroxime, an anti-infective agent, is utilized in researching fungal infections.Formula:C5H4N2O4Color and Shape:SolidMolecular weight:156.1DPC-681
CAS:DPC-681 is a potent and selective HIV protease inhibitor (IC90s: 4 to 40 nM for wild-type HIV-1).Formula:C35H48FN5O5SColor and Shape:SolidMolecular weight:669.85Crisnatol mesylate
CAS:Crisnatol, a potent and selective DNA intercalator, has potential anticancer activity.Formula:C24H27NO5SColor and Shape:SolidMolecular weight:441.54Vapendavir
CAS:Vapendavir binds enterovirus capsids; effective against EV71 with EC50 of 0.5-1.4 μM.Formula:C21H26N4O3Purity:98%Color and Shape:SolidMolecular weight:382.46Adafosbuvir PM
CAS:Adafosbuvir PM (AL-335 PM) is a small molecule NS5B inhibitor that can be used to study chronic hepatitis C.Formula:C10H13FN2O6Purity:98.39%Color and Shape:SolidMolecular weight:276.22R78206
CAS:R 78206 is a pyridazinamine derivative that suppresses the formation of poliovirus eclipse particles.Formula:C22H29N3O3Purity:98%Color and Shape:SolidMolecular weight:383.48Chitin synthase inhibitor 13
CAS:Chitin Synthase Inhibitor 13 (compound 12g), a non-competitive antagonist of chitin synthase, demonstrates broad-spectrum antifungal activity and has anFormula:C21H19N5O5SColor and Shape:SolidMolecular weight:453.47HIV-1 inhibitor-19
CAS:HIV-1 inhibitor-19 is a potent NNRTI targeting L100I, K103N, V106A/F227L mutants; EC50s: 7.3, 9.2, 21.0 nM respectively.Formula:C24H22BClN2O5SColor and Shape:SolidMolecular weight:496.77Stampidine
CAS:Stampidine prevents HIV-1, effective against resistant strains at subnanomolar levels.Formula:C20H23BrN3O8PPurity:98%Color and Shape:SolidMolecular weight:544.29Lexithromycin
CAS:Lexithromycin is an erythromycin A derivative. It has antibacterial activity.Formula:C38H70N2O13Purity:98%Color and Shape:SolidMolecular weight:762.97HCV-IN-34
CAS:HCV-IN-35, an oral HCV blocker, has an EC50 of 0.010 μM and a CC50 of 7.5 μM, indicating strong antiviral effects.Formula:C31H36ClN5Color and Shape:SolidMolecular weight:514.1MMT5-14
CAS:MMT5-14: potent SARS-CoV-2 inhibitor, improves antiviral activity (2-7x), boosts prodrug in plasma/lungs (200-300x), raises NTP in lungs (5x).Formula:C39H55N6O8PColor and Shape:SolidMolecular weight:766.86HIV-1 inhibitor-15
CAS:HIV-1 inhibitor-15 (compound 9d): Potent, broad-spectrum, EC50=1.7-9 nM for various strains, good solubility/safety, oral use.Formula:C24H20N6Color and Shape:SolidMolecular weight:392.46SARS-CoV-2-IN-36
SARS-CoV-2-IN-36: strong Mpro inhibitor, IC50=2.37μM, Kd=1.19μM, fights UC-1074/RG2674/NVDBB-2220 variants.Formula:C17H21N5O3Color and Shape:SolidMolecular weight:343.38HBV-IN-19
CAS:HBV-IN19 suppresses HBV, cutting HBsAg output, useful for chronic HBV study.Formula:C24H30N2O6Color and Shape:SolidMolecular weight:442.5Cylindrospermopsin
CAS:Cylindrospermopsin: a toxic cyanobacterial uracil derivative, disrupts protein/glutathione synthesis in hepatocytes, and is genotoxic.Formula:C15H21N5O7SColor and Shape:SolidMolecular weight:415.42

