
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(2,959 products)
- Antibiotic(921 products)
- Antifection(23 products)
- DHFR(33 products)
- DNA/RNA Synthesis(708 products)
- HBV(176 products)
- HIV Protease(449 products)
- HSV(91 products)
- Integrase(2 products)
- Ribosome(13 products)
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Found 5843 products of "Microbiology/Virology"
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4-Ethoxyphenol
CAS:<p>Compound Fr13643, with CAS No. 622-62-8, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. Compound Fr13643 provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.</p>Formula:C8H10O2Purity:99.63%Color and Shape:Peach CrystalsMolecular weight:138.17Elebsiran
CAS:<p>Elebsiran is an antiviral agent [1] .</p>Formula:C485H658F9N158O294P39S6Color and Shape:SolidMolecular weight:14976.62A 71497
CAS:<p>A 71497 is the 3-formyl derivative of the antibiotic tosufloxacin.</p>Formula:C19H16ClF3N4O2Purity:98%Color and Shape:SolidMolecular weight:424.8LL-C 10037α
CAS:<p>LL-C 10037alpha is a gamma-aminoepoxysemiquinone isolated from Streptomyces.</p>Formula:C8H9NO4Color and Shape:SolidMolecular weight:183.16DNA gyrase B-IN-2
<p>DNA gyrase B-IN-2 (Compound E), a 2-aminobenzothiazole derivative, serves as a potent inhibitor of DNA gyrase B with substantial efficacy against ESKAPE</p>Formula:C18H18Cl2N4O4SColor and Shape:SolidMolecular weight:457.33Pristinamycin
CAS:<p>Pristinamycin, from Streptomyces pristinaespiralis, is a streptogramin antibiotic targeting Gram-positive and resistant bacteria like MRSA.</p>Formula:C73H89N11O17Color and Shape:SolidMolecular weight:1392.55β-Rubromycin
CAS:<p>β-Rubromycin is a bacterial metabolite originally isolated from Streptomyces that has diverse biological activities.1 It inhibits the growth of HMO2, KATO-III,</p>Formula:C27H20O12Color and Shape:SolidMolecular weight:536.445Neomycin C
CAS:<p>Neomycin C, less potent isomer of Neomycin complex, is part of a 2-DOS aminoglycoside.</p>Formula:C23H46N6O13Color and Shape:SolidMolecular weight:614.64GSK2818713
CAS:<p>GSK2818713 is a novel Hepatitis C NS5A replication complex inhibitor.</p>Formula:C46H56N8O8Color and Shape:SolidMolecular weight:849.002HCVcc-IN-1
<p>HCVcc-IN-1, a derivative of benzothiazole-2-thiophene S-glycoside, exhibits low toxicity and antiviral properties [1].</p>Formula:C29H25BrN2O8S3Color and Shape:SolidMolecular weight:705.62Antituberculosis agent-5
CAS:<p>Antituberculosis agent-5 is a small molecule used for high-throughput assays.</p>Formula:C13H12N2O5Purity:99.66%Color and Shape:SolidMolecular weight:276.24Antibacterial agent 127
<p>Antibacterial agent 127 (Compound 23) is a potent antibacterial agent [1] .</p>Formula:C28H37N3O5SColor and Shape:SolidMolecular weight:527.68FITC-εAhx-HHV-2 Envelope Glycoprotein G (561-578)
CAS:<p>FITC-εAhx-HHV-2 Envelope Glycoprotein G (561-578) is a fluorescein isothiocyanate (FITC)-labeled segment of the HHV-2 Envelope Glycoprotein G encompassing amino</p>Formula:C104H128N20O44SPurity:98%Color and Shape:SolidMolecular weight:2394.3Deacetylnomilin
CAS:<p>Deacetylnomilin is a useful organic compound for research related to life sciences. The catalog number is T125039 and the CAS number is 3264-90-2.</p>Formula:C26H32O8Color and Shape:SolidMolecular weight:472.534SARS-CoV-2 3CLpro-IN-19
<p>SARS-CoV-2 3CLpro-IN-19 (Compound C5a), a non-covalent, non-peptide inhibitor of the SARS-CoV-2 3CLpro enzyme, exhibits potent in vitro activity with an IC50 of</p>Formula:C24H22ClN3O2SPurity:98%Color and Shape:SolidMolecular weight:451.97Lankacidins
CAS:<p>Lankacidins is an antitumor antibiotic of the macrolide tetraenes family from Streptomyces.</p>Formula:C25H33NO7Purity:98%Color and Shape:SolidMolecular weight:459.539E07 aptamer
<p>SARS-CoV-2 nsp14-IN-4 (Compound 12q) is a selective inhibitor of the SARS-CoV-2 nsp14 methyltransferase with an IC50 of 19 ± 2.5 nM.</p>Purity:98%Color and Shape:Odour SolidColistin
CAS:<p>Colistin: polypeptide antibiotic for Gram-negative bacteria, including drug-resistant strains, but may cause nephrotoxicity.</p>Formula:C53H100N16O13(forE1)Color and Shape:SolidMolecular weight:1169.5NPD-2975
<p>NPD-2975 (compound 30) is an orally active antitrypanosomal agent effective against Human African Trypanosomiasis (HAT), demonstrating acceptable metabolic</p>Formula:C14H13FN4OPurity:98%Color and Shape:SolidMolecular weight:272.28Pezadeftide
CAS:<p>Pezadeftide, a potent antifungal peptide, readily penetrates fungal cells, eliciting an immediate mitochondrial response that leads to hyperpolarization of the</p>Purity:98%Color and Shape:SolidSARS-CoV-2 nsp14-IN-4
<p>SARS-CoV-2 nsp14-IN-4 (Compound 12q), a non-cytotoxic and cell-permeable inhibitor of SARS-CoV-2 nsp14 methyltransferase (IC50 = 19 nM), is employed in COVID-19</p>Formula:C31H27N7O6SPurity:98%Color and Shape:SolidMolecular weight:625.65(3R,6R)-Vaborbactam
<p>(3R,6R)-Vaborbactam ((3R,6R)-Vaborbactam (Iso-1360457-46-0)) is a cyclic boronic acid pharmacophore β-lactamase inhibitor.</p>Formula:C12H16BNO5SPurity:98.86%Color and Shape:SoildMolecular weight:297.145'-O-TBDMS-dG
CAS:<p>5’-O-TBDMS-dG is a modified nucleoside. 5’-O-DMT-2’-O-TBDMS-rI can be used in the synthesis of deoxyribonucleic acid or nucleic acid.</p>Formula:C16H27N5O4SiColor and Shape:SolidMolecular weight:381.50Antitrypanosomal agent 13
<p>Compound 4b (antitrypanosomal agent 13) is a potent antitrypanosomal with notable trypanocidal and cytotoxic activities, exhibiting GI50 values of 0.18 μM</p>Formula:C47H81N2NaO10SPurity:98%Color and Shape:SolidMolecular weight:889.21Antileishmanial agent-19
<p>Compound F27 (Antileishmanial agent-19) is an antileishmanial compound effective against L.</p>Formula:C22H18N4O3Purity:98%Color and Shape:SolidMolecular weight:386.4Cefpirome
CAS:<p>Cefpirome: fourth-gen cephalosporin, broad-spectrum, inactivates penicillin-binding proteins in bacteria.</p>Formula:C22H22N6O5S2Color and Shape:SolidMolecular weight:514.58MPI60
<p>MPI60 is a potent inhibitor of SARS-CoV-2 main protease (M^pro) exhibiting high antiviral efficacy, low cellular cytotoxicity, and considerable in vitro</p>Formula:C24H31N3O5Purity:98%Color and Shape:SolidMolecular weight:441.52Crexavibart
CAS:<p>Crexavibart (BMS-986413; C-144-LS), an IgG1 λ2 antibody, specifically targets the receptor-binding domain of the SARS-CoV-2 spike (S) glycoprotein [1].</p>Purity:98%Color and Shape:LiquidRJS308
<p>RJS308 is a PROTAC degrader of cyclosporin A (cyclosporin A) with a DC50 of 284 nM. It exhibits antiviral activity by inhibiting the replication of HIV-1 and HCV. (Pink: ligand for target protein CypA ligand-2; Black: linker; Blue: ligand for E3 ligase VHL (S,R,S)-AHPC-Me)</p>Formula:C63H75N13O11SColor and Shape:SolidMolecular weight:1222.42HBV-IN-40
<p>HBV-IN-40 (Compound 11826096), with an IC50 of 0.7 µM, serves as a potent HBV inhibitor and exhibits antiviral activity [1].</p>Formula:C29H55Cl4N11Purity:98%Color and Shape:SolidMolecular weight:699.63Pectate Lyase
CAS:<p>Pectate Lyase, an enzyme secreted by plant pathogens, is essential for pectin degradation and plays a vital role in fungal virulence.</p>Color and Shape:SolidH-Arg-OtBu dihydrochloride
CAS:<p>H-Arg-OtBu (dihydrochloride) is a membrane-targeting antimicrobial that engages the negatively charged bacterial membrane through electrostatic and hydrophobic</p>Formula:C10H24Cl2N4O2Purity:98%Color and Shape:SolidMolecular weight:303.238-Br-GTP
CAS:<p>8-Br-GTP, a GTP analog, inhibits FtsZ polymerization/GTPase (K i 31.8 μM), aids nucleic acid modification.</p>Formula:C10H15BrN5O14P3Color and Shape:SolidMolecular weight:602.076SARS-CoV-2-IN-56
<p>SARS-CoV-2-IN-56 (Compound 63) is a SARS-CoV-2 inhibitor with antiviral activity, demonstrating inhibition of the virus in Vero E6 cells with an IC50 of 0.7 μM</p>Formula:C70H72N12O19S3Purity:98%Color and Shape:SolidMolecular weight:1481.58HAT-IN-8
<p>HAT-IN-8 (Compound 38), a blood-brain barrier-permeable inhibitor of Trypanosoma brucei with an EC50 of 0.18 μM, is utilized in the study of Human African</p>Formula:C14H15F2N3O2SPurity:98%Color and Shape:SolidMolecular weight:327.35Cysteine protease inhibitor-3
<p>Cysteine protease inhibitor-3 (Compound 15), a cysteine protease inhibitor, exhibits anti-plasmodial activity, effectively inhibiting Pf3D7 (IC50 = 0.74 μM),</p>Formula:C26H22ClF2N3OPurity:98%Color and Shape:SolidMolecular weight:465.92Dermcidin-1L (human)
CAS:<p>Dermcidin-1L (human), an antibiotic peptide secreted by sweat glands, exhibits antimicrobial activity and is utilized in the research of inflammatory skin</p>Formula:C210H359N57O71Purity:98%Color and Shape:SolidMolecular weight:4818.44Aurein 5.2
CAS:<p>Aurein 5.2 is an antibiotic antimicrobial peptide [1].</p>Formula:C110H194N28O32SPurity:98%Color and Shape:SolidMolecular weight:2452.95Aurein 2.6
CAS:<p>Aurein 2.6, an antibiotic antimicrobial peptide, exhibits activity against various Gram-positive bacteria with minimum inhibitory concentrations (MIC) of 25, 25</p>Formula:C77H133N19O19Purity:98%Color and Shape:SolidMolecular weight:1629GRL-1720 TFA
<p>GRL-1720 TFA is a potent SARS-CoV-2 Mpro inhibitor, demonstrating anti-SARS-CoV-2 activity with an EC50 of 15 μM [1].</p>Purity:98%Color and Shape:Odour SolidSARS-CoV-2-IN-67
<p>SARS-CoV-2-IN-67 (Compound 16), a derivative of vitamin K, exhibits anti-SARS-CoV-2 properties, with an effective concentration (EC50) of 64.8 μM in VeroE6/</p>Purity:98%Color and Shape:Odour SolidAntituberculosis agent-7
CAS:<p>Antituberculosis agent-7: active against P. mirabilis (MIC 31.25μM), A. niger (MIC 62.5μM), and M. tuberculosis (MIC 3.41μM).</p>Formula:C26H19F4NO3Color and Shape:SolidMolecular weight:469.43SARS-CoV-2-IN-42
<p>SARS-CoV-2-IN-42 (Compound 8q) effectively inhibits SARS-CoV-2 replication with an EC50 value of 0.4 μM and demonstrates no significant toxicity to the host</p>Formula:C20H20O7Purity:98%Color and Shape:SolidMolecular weight:372.37Antitrypanosomal agent 17
<p>Compound 17 (Compd 7a) exhibits potent antiamastigote activity, demonstrated by its IC50 value of 0.03 μM against the T. congolense strain IL3000 [1].</p>Purity:98%Color and Shape:Odour SolidCefuzonam
CAS:<p>Cefazolin is a novel cephalosporin with anti-inflammatory activity and may be used in studies of respiratory tract infections and hepatobiliary infections.</p>Formula:C16H15N7O5S4Purity:97.79% - 99.60%Color and Shape:SolidMolecular weight:513.59Antimalarial agent 31
<p>Compound 31 (compound 7k) is an orally active inhibitor of Plasmodium falciparum aspartic protease, plasmepsin X (PMX), with antimalarial properties [1].</p>Formula:C36H47N3O4Purity:98%Color and Shape:SolidMolecular weight:585.781-O-Methylemodin
CAS:<p>1-O-Methylemodin, a natural product isolated from Zopfiella longicaudata, exhibits antifungal activity [1].</p>Formula:C16H12O5Color and Shape:SolidMolecular weight:284.26SARS-CoV-2 Mpro-IN-38
<p>SARS-CoV-2 Mpro-IN-38 (2-5a) is an inhibitor of SARS-CoV‑2 Mpro with an IC50 value of 0.0435 μM.</p>Color and Shape:Odour SolidZ-L(D-Val)G-CHN2
<p>Z-L(D-Val)G-CHN2, an isoform of Z-LVG-CHN2, serves as a cell-permeable and irreversible inhibitor of cysteine proteinase.</p>Formula:C22H31N5O5Purity:98%Color and Shape:SolidMolecular weight:445.51Citrullinated LL-37 3cit
<p>Citrullinated LL-37 3cit is a host defense peptide with potent immunomodulatory and antimicrobial properties, demonstrating direct antiviral activity against</p>Formula:C205H337N57O56Purity:98%Color and Shape:SolidMolecular weight:4496.22

