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(2,968 products)
- Antibiotic(922 products)
- Antifection(23 products)
- DHFR(33 products)
- DNA/RNA Synthesis(711 products)
- HBV(177 products)
- HIV Protease(451 products)
- HSV(91 products)
- Integrase(2 products)
- Ribosome(13 products)
Show 2 more subcategories
Found 5863 products of "Microbiology/Virology"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Murabutide
CAS:<p>Murabutide, a safe synthetic immunomodulator, diminishes the expression of CD4 and CCR5 receptors and promotes the secretion of high levels of beta-chemokines,</p>Formula:C23H40N4O11Color and Shape:SolidMolecular weight:548.58Urease Inhibitor 07
CAS:Urease Inhibitor 07 is an isosubstituted metalloproteinase inhibitor with potential activity against Mycobacterium tuberculosis strain H37Rv.Formula:C7H5N3OSPurity:99.65%Color and Shape:SolidMolecular weight:179.2Du011
CAS:<p>Du011 is a biogenesis inhibitor of the E.</p>Formula:C20H15F2NO4SColor and Shape:SolidMolecular weight:403.4GSK3839919A
CAS:<p>GSK3839919A is a potent allosteric inhibitor of HIV-1 integrase [1].</p>Formula:C36H46ClN3O3Color and Shape:SolidMolecular weight:604.22Micronomicin
CAS:<p>Micronomicin (Gentamicin C2b) is an antibiotic exhibiting antibacterial and bactericidal capacity.</p>Formula:C20H41N5O7Purity:97.05% - 99.79%Color and Shape:SolidMolecular weight:463.57VT-1598
CAS:<p>VT-1598 is a novel, selective, orally active fungal CYP51 inhibitor. VT-1598 exhibits antifungal effects against Candida albicans.</p>Formula:C31H20F4N6O2Color and Shape:SolidMolecular weight:584.52DHFR-IN-10
CAS:<p>DHFR-IN-10 (compound 4c) is a potent inhibitor of dihydrofolate reductase (DHFR), displaying an inhibition concentration half-maximum (IC50) of 4.21 μM against</p>Formula:C20H14BrN3S3Color and Shape:SolidMolecular weight:472.44Antibacterial compound 2
CAS:<p>Antibacterial compound 2 is a potent antimicrobial agent effective against many human veterinary pathogens, inhibiting multi-drug resistant staphylococci,</p>Formula:C22H30FN5O6Purity:90.4%Color and Shape:SolidMolecular weight:479.5LtaS-IN-1
CAS:LtaS-IN-1 inhibits LTA synthesis in MDR E. faecium; alters cell walls; MIC: 0.5-64 μg/mL for 28 Enterococcus strains.Formula:C24H17N3O5Purity:93.44%Color and Shape:SolidMolecular weight:427.41Variculanol
CAS:<p>Variculanol, a compound with antimicrobial, anticancer, and anti-HCV NS3/4A protease properties, is derived from the marine fungus Aspergillus versicolor [1].</p>Formula:C25H40O2Color and Shape:SolidMolecular weight:372.58Tuberculosis inhibitor 6
CAS:<p>Tuberculosis inhibitor 6 (compound 2c), a 3-methoxy-2-phenylimidazo[1,2-b]pyridazine derivative, is highly active against Mycobacterium tuberculosis (MIC 90 of</p>Formula:C21H19N3O2SColor and Shape:SolidMolecular weight:377.46DQn-1
CAS:<p>DQn-1, a potent antifolate, demonstrates efficacy against Mycobacterium tuberculosis (Mtb) with an MIC 90 of 0.03 µM.</p>Formula:C16H14ClN5O2Color and Shape:SolidMolecular weight:343.77Fosalvudine tidoxil
CAS:<p>Fosalvudine tidoxil, a nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formula:C35H64FN2O8PSPurity:98%Color and Shape:SolidMolecular weight:722.93Antibacterial agent 94
CAS:<p>Compound 5b, an antibacterial, effectively targets MRSA and disrupts bacterial membranes and PG synthesis.</p>Formula:C21H21FO4Color and Shape:SolidMolecular weight:356.39Antibiofilm agent-1
CAS:<p>Antibiofilm Agent-1, as detailed in WO2017011725A1 (compound 17) [1], serves as an antibacterial agent effective against Gram-positive pathogens.</p>Formula:C11H5Br2Cl2NO2Color and Shape:SolidMolecular weight:413.88TH-Z145
CAS:<p>TH-Z145 is a potent FPPS inhibitor for the study of myeloma and lung cancer.</p>Formula:C16H28O7P2Purity:98.29%Color and Shape:SolidMolecular weight:394.34AU1235
CAS:<p>AU1235 is a Mycobacterium tuberculosis inhibitor.</p>Formula:C17H19F3N2OPurity:99.54% - 99.87%Color and Shape:SolidMolecular weight:324.34Antifungal agent 26
CAS:<p>Pradimicin A derivative 26 exhibits antifungal, antiviral, and antiparasitic properties by attaching to d-mannose (Man)-rich glycans in pathogenic organisms [1</p>Formula:C40H45N3O18Color and Shape:SolidMolecular weight:855.79PTC725
CAS:<p>PTC725 is a selective HCV 1b replicons inhibitor. It has been shown to target the nonstructural protein 4B.</p>Formula:C23H18F4N6O2SPurity:98%Color and Shape:SolidMolecular weight:518.49MC-VC-PAB-Cyclohexanediamine-Thailanstatin A
CAS:<p>MC-VC-PAB-Cyclohexanediamine-Thailanstatin A is a spliceostatin analog and a drug-linker conjugate for antibody-drug conjugates (ADC), comprising the cytotoxic</p>Formula:C63H91N9O16Purity:98%Color and Shape:SolidMolecular weight:1230.45WRN inhibitor 4
CAS:<p>WRN Inhibitor 4 (Example 107), a cyclic vinyl sulfone-based compound, serves as an inhibitor of the Werner Syndrome ATP-dependent helicase enzyme (WRN).</p>Formula:C16H14N2O5SColor and Shape:SolidMolecular weight:346.36WRN inhibitor 3
CAS:<p>WRN Inhibitor 3 (example 110), a cyclic vinyl sulfone-based compound, serves as an inhibitor of the Werner Syndrome ATP-dependent helicase enzyme (WRN).</p>Formula:C20H20N2O5SColor and Shape:SolidMolecular weight:400.45HIV-1 inhibitor-3
CAS:<p>HIV-1 inhibitor-3 is an HIV infection inhibitor.</p>Formula:C9H10F2N2O5Purity:98%Color and Shape:SolidMolecular weight:264.18Icofungipen
CAS:Icofungipen is an oral antifungals with active against Candida species.Formula:C7H11NO2Purity:98%Color and Shape:SolidMolecular weight:141.17SARS-CoV-2 3CLpro-IN-2
CAS:<p>SARS-CoV-2 3CLpro-IN-2 is a potent inhibitor of the 3CL protease pair and has shown research potential for SARS-CoV-2 disease.</p>Formula:C21H18F5N5O4Color and Shape:SolidMolecular weight:499.39Hinokinin
CAS:<p>Hinokinin (Cubebinolide), a bioactive lignan, exhibits a broad spectrum of pharmacological activities.</p>Formula:C20H18O6Color and Shape:SolidMolecular weight:354.35Mtb-IN-4
CAS:<p>Mtb-IN-4 (compound 17h) is a non-toxic isoxazole that exhibits anti-Mycobacterium tuberculosis (Mtb) activity, with an IC50 value of 0.70 μM.</p>Formula:C24H18N2O4SColor and Shape:SolidMolecular weight:430.48Daldinone A
CAS:<p>Daldinone A (Compound 4), isolated from Nigrospora oryzae, exhibits antibacterial properties, specifically demonstrating antimicrobial potential against P. aeruginosa [1].</p>Formula:C20H16O5Color and Shape:SolidMolecular weight:336.34Nilofabicin
CAS:<p>Nilofabicin (CG-400549) is a potent inhibitor of enoyl-(acyl-carrier-protein) reductase fall(FabI) and can be used in studies about the treatment of complicated</p>Formula:C19H20N2O2SPurity:98.66%Color and Shape:SolidMolecular weight:340.44NCI-B16
CAS:<p>NCI-B16 is a small-molecule RNA binder that inhibits HCV (hepatitis C virus) replication [1].</p>Formula:C27H26N8O4Color and Shape:SolidMolecular weight:526.55Capravirine
CAS:<p>Capravirine, a non-nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formula:C20H20Cl2N4O2SPurity:98%Color and Shape:SolidMolecular weight:451.37Bio-AMS
CAS:<p>Bio-AMS is a potent inhibitor of bacterial biotin protein ligase, exhibiting selective activity against Mycobacterium tuberculosis (Mtb) and disrupting fatty</p>Formula:C20H29N9O7S2Color and Shape:SolidMolecular weight:571.63(E)-LHF-535
CAS:<p>(E)-LHF-535, an E-isomer antiviral, EC50 <1 μM vs Lassa/Machupo/Junin, 1-10 μM vs VSVg.</p>Formula:C27H28N2O2Purity:98%Color and Shape:SolidMolecular weight:412.52UNC2170 maleate
CAS:<p>53BP1-binding protein 1 (53BP1) engages with dimethylated lysine 20 on histone 4 (H4K20me2) through its tandem tudor domains within a homodimer configuration, crucial for the DNA damage response. UNC2170, a micromolar 53BP1 ligand, selectively interacts with this site, demonstrating at least 17-fold preference for 53BP1 over similar proteins. This interaction occurs in a pocket formed by the 53BP1's tudor domains. Moreover, UNC2170 acts as an antagonist to 53BP1 in cellular lysates, effectively inhibiting class switch recombination, a process dependent on the functional 53BP1 tudor domain, thus confirming its cellular activity.</p>Formula:C14H21BrN2OC4H4O4Color and Shape:SolidMolecular weight:429.31WQ 2743
CAS:<p>WQ 2743 is a potent agent of antimicrobial.</p>Formula:C19H15BrF3N5O3Purity:98%Color and Shape:SolidMolecular weight:498.25Valnemulin
CAS:<p>Valnemulin, a broad-spectrum pleuromutilin antibiotic, targets peptidyl transferase within the 50S ribosomal subunit, effectively used in veterinary medicine to address swine diseases such as B. hyodysenteriae and M. hyopneumoniae.</p>Formula:C31H52N2O5SColor and Shape:SolidMolecular weight:564.83Antibacterial agent 135
CAS:<p>Antibacterial Agent 135 (example 7) effectively inhibits various bacteria, including P.</p>Formula:C11H15N5O6SColor and Shape:SolidMolecular weight:345.33Ganfeborole HCl
CAS:<p>Ganfeborole HCl (GSK3036656 HCl) is a compound with anti-tuberculosis activity and is an inhibitor of Mycobacterium tuberculosis (Mtb) leucyl-tRNA synthetase.</p>Formula:C10H14BCl2NO4Purity:99.88%Color and Shape:SolidMolecular weight:293.94Methyl 3,4-dimethoxycinnamate
CAS:<p>Methyl 3,4-dimethoxycinnamate impedes uredospore germination and concurrently inhibits global DNA methylation in Hep3B cells [1] [2].</p>Formula:C12H14O4Color and Shape:SolidMolecular weight:222.24Bavtavirine
CAS:<p>Bavtavirine is a non-nucleoside reverse HIV-1 transcriptase inhibitor (NNRTIs),inhibits HIV replication by preventing the transcription of viral RNA into DNA.</p>Formula:C26H20N6Purity:97.2%Color and Shape:SolidMolecular weight:416.484'-Acetyl-chrysomycin B
CAS:<p>4'-Acetyl-chrysomycin B, a 4'-acetylated analog of chrysomycin B, exhibits anti-Gram-positive bacterial and antimicrobial activities [1].</p>Formula:C29H30O10Color and Shape:SolidMolecular weight:538.54ZINC475239213
CAS:<p>ZINC475239213 acts as an inhibitor targeting the SARS-CoV-2 Nsp14 N7-Methyltransferase with an IC50 value of 20 μM [1].</p>Formula:C21H15N5O2Purity:98%Color and Shape:SolidMolecular weight:369.38NS5A-IN-3
CAS:<p>NS5A-IN-3 is a potent NS5A inhibitor with high efficacy against HCV 1b, good activity on 3a, and strong metabolic stability; superior to daclatasvir.</p>Formula:C44H44N6O8Purity:98%Color and Shape:SolidMolecular weight:784.86GlcNAcstatin
CAS:<p>GlcNAcstatin, a selective glucoimidazole-based inhibitor of bacterial O-GlcNAcase, exhibits a K_i value of 4.6 pM and demonstrates a specificity that is 100,000</p>Formula:C20H27N3O4Color and Shape:SolidMolecular weight:373.45UCB7362
CAS:<p>UCB7362 (GLXC-26743) is an orally available and potent plasmepsin X (PMX) inhibitor with anti-malarial activity.UCB7362 inhibits parasite reproduction.</p>Formula:C25H26ClN5O3Purity:97.67%Color and Shape:SolidMolecular weight:479.96SARS-CoV-2 3CLpro-IN-5
CAS:<p>SARS-CoV-2 3CLpro-IN-5 is a covalent inhibitor targeting the 3C-like protease (3CLpro), exhibiting potent inhibitory activity with an IC50 of 3.8 nM and</p>Formula:C22H26ClF2N5O4Purity:98%Color and Shape:SolidMolecular weight:497.92Antileishmanial agent-16
CAS:<p>Antileishmanial agent-16 (compound 14c), an anti-Leishmania agent, exhibits potent activity against Leishmania major promastigotes (IC50 = 0.59 µM) and</p>Formula:C27H37N5O4Purity:98%Color and Shape:SolidMolecular weight:495.61MsbA-IN-6
CAS:<p>MsbA-IN-6: potent antibiotic, hinders MsbA in gram-negative bacteria, kills E. coli, effective on drug-resistant strains.</p>Formula:C24H20Cl2N4OPurity:98%Color and Shape:SolidMolecular weight:451.35(S)-Mosnodenvir
CAS:<p>(S)-Mosnodenvir, a pan-serotype dengue antiviral agent, exhibits picomolar to low nanomolar in vitro activity with a high barrier to resistance and is</p>Formula:C26H22ClF3N2O6SPurity:98%Color and Shape:SolidMolecular weight:582.98Tuberculosis inhibitor 8
CAS:<p>Tuberculosis inhibitor 8 (compound 3b), a 3-methoxy-2-phenylimidazo[1,2-b]pyridazine derivative, exhibits potent activity against both Mycobacterium</p>Formula:C21H19FN4OColor and Shape:SolidMolecular weight:362.4
