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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PSI-7409 tetrasodium
CAS:PSI-7409 tetrasodium, a sofosbuvir metabolite, inhibits GT 1b, 2a, 3a, 4a NS5B polymerases with IC50s of 1.6, 2.8, 0.7, 2.6 μM.Formula:C10H16FN2Na4O14P3Purity:98%Color and Shape:SolidMolecular weight:592.117BMVC2
CAS:BMVC2 (o-BMVC), a carbazole derivative of BMVC, is a G-quadruplex (G4) stabilizer.Formula:C28H25I2N3Color and Shape:SolidMolecular weight:657.332,3-Dehydro-2-Deoxy-N-Acetylneuraminic Acid
CAS:2,3-Dehydro-2-Deoxy-N-Acetylneuraminic Acid is a pan-sialidase (neuraminidase, NEU) inhibitor with inhibitory activity and against various influenza viruses.Formula:C11H17NO8Color and Shape:SolidMolecular weight:291.26Cefmenoxime
CAS:Cefmenoxime: IV/IM cephalosporin antibiotic, resists beta-lactamase, targets Enterobacteriaceae, gram-positive/negative bacteria.Formula:C16H17N9O5S3Purity:98%Color and Shape:Almost White Or Almost Yellow Crystalline PowderMolecular weight:511.558(R)-Gyramide A hydrochloride
CAS:(R)-Gyramide A HCl inhibits DNA gyrase in bacteria (IC50: 875 μM), with MIC 10-80 μM against P. aeruginosa & E. coli, sparing topoisomerase IV.Formula:C21H28ClFN2O3SColor and Shape:SolidMolecular weight:442.97Epsiprantel
CAS:Epsiprantel is an orally active antiparasitic drug that inhibits various tapeworms, including Echinococcus granulosus (granular echinococcus), in dogs.Formula:C20H26N2O2Purity:98.09%Color and Shape:SolidMolecular weight:326.43PXYC1
CAS:PXYC1 binds Mtb RpsA-CTD (Kd 0.81 μM) & RpsA-CTD Δ438A (Kd 0.31 μM), hindering trans-translation.Formula:C9H10N4O3SColor and Shape:SolidMolecular weight:254.27AFK-108
CAS:AFK-108 is a fungicide agent.Formula:C21H26Cl2N2OPurity:98%Color and Shape:SolidMolecular weight:393.35Antibacterial agent 48
CAS:Antibacterial agent 48 is an antimicrobial agent that reduces the MIC of the antimicrobial agent Ceftazidime.Formula:C13H18N5NaO7SColor and Shape:SolidMolecular weight:411.36FabH-IN-1
CAS:FabH-IN-1, a broad-spectrum antibiotic and antioxidant, inhibits bacterial FabH enzyme.Formula:C17H16N2OSColor and Shape:SolidMolecular weight:296.39Urease-IN-8
CAS:Urease-IN-8 (Compound 5e) functions as a competitive inhibitor of urease, with an IC50 value of 3.51 μM and a Ki of 3.11 μM.Formula:C23H18N4OSColor and Shape:SolidMolecular weight:398.482-Keto-D-galactose
CAS:2-Keto-D-galactose inhibits DNA synthesis and inhibits the proliferation of in vitro grown Ehrlich ascites tumor cells.Formula:C6H10O6Purity:98%Color and Shape:SolidMolecular weight:178.14AN7973
CAS:AN7973 inhibits Cryptosporidium, blocks parasites, orally active, safe, stable, good PK.Formula:C19H17BClN3O3Color and Shape:SolidMolecular weight:381.62TKB245
CAS:TKB245为SARS-CoV-2 Mpro的高效抑制剂，能有效抑制VeroE6细胞内SARS-CoV-2的复制。Formula:C30H35F4N5O5SPurity:98%Color and Shape:SolidMolecular weight:653.69Cap-dependent endonuclease-IN-19
CAS:Cap-dependent endonuclease-IN-19, a spirocyclic pyridinone, strongly inhibits influenza A virus RNA polymerase.Formula:C28H31N3O4Color and Shape:SolidMolecular weight:473.56NVP018
CAS:NVP018 (BC 556) inhibits HBV, HCV, HIV-1 replication, barely affects drug transporters, and resists HCV/HIV-1 resistance development.Formula:C45H62FN5O11Color and Shape:SolidMolecular weight:868Vibunazole
CAS:Vibunazole is an antifungal agent.Formula:C15H20ClN3O2Color and Shape:SolidMolecular weight:309.79NS2B/NS3-IN-3 hydrochloride
CAS:NS2B/NS3-IN-3 hydrochloride is a Flavivirus NS2B-NS3 protease inhibitor [1].Formula:C19H22ClN3O2Purity:98%Color and Shape:SolidMolecular weight:359.85Piperic acid
CAS:Piperic acid is a powerful antioxidant and has potent antibacterial propertiesFormula:C12H10O4Color and Shape:SolidMolecular weight:218.21YKAs3003
CAS:YKAs3003 inhibits KAS III with MICs 128-256 μg/mL against multiple bacteria.Formula:C13H17NO2Purity:98%Color and Shape:SolidMolecular weight:219.28PXYD4
CAS:PXYD4 antagonizes RpsA, key in Mtb translocation, binding RpsA-CTD (Kd 3.24 μM) & RpsA-CTD Δ438A (Kd 1.64 μM).Formula:C25H21NO5Color and Shape:SolidMolecular weight:415.44Antileishmanial agent-14
CAS:Antileishmanial agent-14, a sulfuretin analog, exhibits potential activity against Leishmania donovani promastigotes (IC 50 = 4.1 μM) and inhibits infection byFormula:C23H26ClNO5Purity:98%Color and Shape:SolidMolecular weight:431.91JMI-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:336.39Antitubercular agent-33
CAS:Antitubercular agent-33 is a 2-aminothiazole derivative with potent anti-tubercular activity against Mycobacterium tuberculosis ( Mtb ) [1].Formula:C15H10N4O3SColor and Shape:SolidMolecular weight:326.33Antimalarial agent 19
CAS:Compound 6e, an antimalarial, targets P. falciparum K1 (EC50 0.3 µM) and P. berghei (EC50 15.3 µM); has high solubility and stability.Formula:C22H33Cl2N5SPurity:98%Color and Shape:SolidMolecular weight:470.5SARS-CoV-2 nsp14-IN-3
CAS:SARS-CoV-2 nsp14-IN-3 (4975) is a potent inhibitor targeting the N7-Methyltransferase activity of SARS-CoV-2 nonstructural protein 14 (Nsp14), with an IC50Formula:C17H17N3O3SPurity:98%Color and Shape:SolidMolecular weight:343.4MMV687807
CAS:MMV687807: potent anthelmintic, IC50 0.15 μM, CC50 1.69 μM against T. gondii.Formula:C15H8ClF6NO2Color and Shape:SolidMolecular weight:383.67Antimalarial agent 26
CAS:Antimalarial agent 26, a derivative of 1,4-naphthoquinones, demonstrates antimalarial properties through oral administration.Formula:C20H22N4O3Purity:98%Color and Shape:SolidMolecular weight:366.41B 746
CAS:B 746 is an antibacterial for leprosy, Mycobacterium avium, and drug-resistant tuberculosis.Formula:C26H20Cl2N4Color and Shape:SolidMolecular weight:459.37CTP Synthetase-IN-1
CAS:CTP Synthetase-IN-1 is a cytidine 5'-triphosphate synthetase (CTPS) inhibitor with antitumor activity for the study of arthritis and rheumatoid arthritis.Formula:C20H19F3N6O3S2Purity:98.11% - 99.18%Color and Shape:SolidMolecular weight:512.53Ref: TM-T72505
1mg65.00€5mg141.00€10mg230.00€25mg477.00€50mg803.00€100mg1,378.00€1mL*10mM (DMSO)158.00€Antiparasitic 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:333.34BAY-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:288.34Furalaxyl
CAS:Furalaxyl is an fungicide of acyl amino chiral.Formula:C17H19NO4Color and Shape:SolidMolecular weight:301.34ASN03576800
CAS:ASN03576800 is an inhibitor of the VP40 matrix protein.Formula:C11H11NO6SPurity:99.76%Color and Shape:SolidMolecular weight:285.27Antimalarial agent 29
CAS:Compound 29 (also known as Compound 16) is an antimalarial agent that demonstrates inhibition of the P.Formula:C18H10ClF3N2Purity:98%Color and Shape:SolidMolecular weight:346.73Ametoctradin
CAS:Ametoctradin is a Qo-site inhibitor of mitochondrial respiratory complex III and is used in the study of oomycete diseases.Formula:C15H25N5Purity:99.65%Color and Shape:SolidMolecular weight:275.39Mycobactin-IN-2
CAS:Mycobactin-IN-2 inhibits mycobactin production by targeting salicyl-AMP ligase (MbtA), a crucial enzyme in its pathway.Formula:C15H13BrN2OColor and Shape:SolidMolecular weight:317.18(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:405.85L-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:182.17SARS-CoV-2 Mpro-IN-9
CAS:SARS-CoV-2 Mpro-IN-9 (compound c7), a nonpeptidic, noncovalent inhibitor of SARS-CoV-2 main protease (Mpro), exhibits potent inhibitory action (IC50 = 0.085 μMFormula:C20H14N2O4Purity:99.74% - 99.89%Color and Shape:SolidMolecular weight:346.34SDH-IN-5
CAS:SDH-IN-5 (compound 7d), a potent inhibitor of succinate dehydrogenase (SDH) with an IC50 of 3.293 μM, additionally demonstrates antifungal efficacy, exhibitingFormula:C16H19F2N3O2Color and Shape:SolidMolecular weight:323.34BMH-22
CAS:BMH-22 is an RNA polymerase I inhibitor that acts by causing nucleolar stress and showing potent anticancer activity across many tumor types.Formula:C16H17N3Color and Shape:SolidMolecular weight:251.33BPH-1218
CAS:BPH-1218 is a SQS inhibitor.Formula:C15H30N2O6P2Purity:98%Color and Shape:SolidMolecular weight:396.36(S)-Tedizolid
CAS:(S)-Tedizolid is the S-enantiomer of Tedizolid. Tedizolid is a novel oxazolidinone with activity against Gram-positive pathogens.Formula:C17H15FN6O3Purity:98%Color and Shape:SolidMolecular weight:370.34Sotirimod
CAS:Sotirimod（R850） is a novel immunomodulator with antitumor and antiviral activity for the study of actinic keratoses.Formula:C14H17N5Purity:95.87%Color and Shape:SolidMolecular weight:255.32KDU731
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:396.4A110
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:366.8CID 5951923
CAS:CID 5951923 is an inhibitor of KLF5 transcription factor with an IC50 of 603 nM.Formula:C16H18N2O7SPurity:99.95%Color and Shape:SolidMolecular weight:382.39HIV-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:550.63ST7612AA1
CAS:ST7612AA1: potent, oral HDAC inhibitor; reactivates HIV-1 latency; shows antitumor effects; may study malaria.Formula:C20H27N3O4SPurity:99.71%Color and Shape:SolidMolecular weight:405.51
