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(2,957 products)
- Antibiotic(920 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 5842 products of "Microbiology/Virology"
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FtsZ-IN-6
<p>FtsZ-IN-6: strong FtsZ polymerization promoter, GTPase inhibitor, kills bacteria, low resistance and toxicity.</p>Formula:C28H22BrN3O2Color and Shape:SolidMolecular weight:512.4DIZ-3
CAS:<p>DIZ-3: Selective G4 ligand, stabilizes structure, inhibits ALT cancer cell growth by inducing cell cycle arrest and apoptosis.</p>Formula:C46H44F2N8Color and Shape:SolidMolecular weight:746.89Thrazarine
CAS:<p>Thrazarine is a new antitumor antibiotic agent produced by Streptomyces coerulescens MH802-fF5.</p>Formula:C7H11N3O5Purity:98%Color and Shape:SolidMolecular weight:217.18Plectasin
<p>Plectasin, a peptide antibiotic derived from saprophytic fungi, can effectively kill Streptococcus pneumoniae in vitro. Additionally, it alleviates experimental peritonitis and pneumonia caused by Streptococcus pneumoniae in mice.</p>Formula:C189H267N53O56S7Color and Shape:SolidMolecular weight:4401.92Psoracorylifol C
<p>Psoracorylifol C is a useful organic compound for research related to life sciences and the catalog number is T124015.</p>Formula:C18H24O3Color and Shape:SolidMolecular weight:288.387Cecropin A (1-7)-Melittin A (2-9)
CAS:<p>Cecropin A-Melittin peptide combats Gram+ & Gram- bacteria, has antimalarial effects, no hemolysis like bee venom.</p>Formula:C89H152N22O15Color and Shape:SolidMolecular weight:1770.3(+)-Macrosphelide A
CAS:<p>(+)-Macrosphelide A, from Microsphaeropsis, thwarts HL-60 cell adhesion and SKOV3 cancer growth, fights Gram-positive bacteria, not Gram-negatives or fungi.</p>Formula:C16H22O8Color and Shape:SolidMolecular weight:342.344CI-39
CAS:<p>CI-39, an NNRTI with EC50 of 3.40 µM, inhibits HIV-1 reverse transcriptase and RNase H, with CC50 >30 µM.</p>Formula:C19H18N2O4Color and Shape:SolidMolecular weight:338.36HIV-IN-2
CAS:<p>HIV-IN-2 (Compound 100) is a potent inhibitor of HIV, showing potential for research into HIV infection [1].</p>Formula:C34H27ClF7N9O3SColor and Shape:SolidMolecular weight:810.14Spm viii
CAS:<p>Spm viii is a derivative of the nucleoside antibiotic spicamycin that has antitumor activity.</p>Formula:C26H43N7O7Purity:98%Color and Shape:SolidMolecular weight:565.66Neuraminidase-IN-22
<p>Neuraminidase-IN-22 (compound 3e) serves as a potent, selective, and orally active inhibitor of neuraminidase, exhibiting a low IC 50 value of 0.03 µM. This compound demonstrates cytotoxic effects and possesses activity against the influenza A virus.</p>Formula:C17H13FN2O2Color and Shape:SolidMolecular weight:296.3Fenpicoxamid
CAS:<p>Fenpicoxamid is a biochemcial.</p>Formula:C31H38N2O11Color and Shape:SolidMolecular weight:614.64CKP-25
<p>CKP-25 is an inhibitor that disrupts the interaction between Spike RBD and ACE2, preventing virus entry into host cells, thus reducing viral replication and infection. It inhibits SARS-CoV-2 with an IC50 of 3.5 μM in Vero E6 cells.</p>Formula:C19H16N2OColor and Shape:SolidMolecular weight:288.343Herbicidin A
CAS:<p>Herbicidin A is an adenosine nucleoside antibiotic isolated from Streptomyces scopuliridis M40. Herbicidin A is also a herbicide against dicotyledonous plants.</p>Formula:C23H29N5O11Color and Shape:SolidMolecular weight:551.5Tuberculosis inhibitor 11
<p>Compound 14, also known as Tuberculosis Inhibitor 11, enhances the antimycobacterial efficacy of antitubercular agent [1].</p>Color and Shape:Odour SolidAltromycin B
CAS:<p>Altromycin B is a new pluramycin-like antibiotic.</p>Formula:C47H59NO18Purity:98%Color and Shape:SolidMolecular weight:925.978FR-295389
CAS:<p>FR-295389 is a cephalosporin. FR-295389 shows effective antibacterial activity against metallo-beta-lactamase (MBL)-producers in vitro.</p>Formula:C25H35N13O11S3Purity:98%Color and Shape:SolidMolecular weight:789.82SARS-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 SolidMtb-IN-11
<p>Mtb-IN-11 (Compound 1e) is an inhibitor of Mycobacterium tuberculosis salicylate synthase (MbtI) with an IC50 of 11.2 μM. It exhibits strong in vitro antitubercular activity, with an MIC99 of 32 μM against Mycobacterium bovis BCG. Mtb-IN-11 is applicable for tuberculosis research.</p>Formula:C16H15NO4Color and Shape:SolidMolecular weight:285.295Antimicrobial agent-12
<p>Antimicrobial agent-12 serves as a powerful antibacterial compound that also exhibits inhibitory activity against SARS-CoV-2 [1].</p>Formula:C69H61Cl2F3N10O25Color and Shape:SolidMolecular weight:1558.18Cyclo(Arg-Pro) TFA
<p>Cyclo(Arg-Pro) TFA, also known as Cyclo(Pro-Arg) TFA, serves as an inhibitor of chitinase. This compound impedes the cell separation of Saccharomyces cerevisiae without affecting its growth. Additionally, Cyclo(Arg-Pro) TFA inhibits the morphological transition of Candida albicans from a yeast form to a filamentous form.</p>Formula:C13H20F3N5O4Color and Shape:SolidMolecular weight:367.32Angustifoline hydrochloride
CAS:<p>Angustifoline HCl, from Lupinus angustifolius, has antimicrobial effects on S. aureus, B. subtilis, E. coli, P. aeruginosa, B. thuringiensis.</p>Formula:C14H23ClN2OColor and Shape:SolidMolecular weight:270.8Mycobactin P
CAS:<p>Mycobactin P is one of iron(III) chelating compounds produced by most species of Mycobacteria which act as growth factors.</p>Formula:C47H75N5O10Color and Shape:SolidMolecular weight:870.142Bikaverin
CAS:<p>Bikaverin: A red fungal pigment with antibiotic effects on protozoa/fungi and antitumor properties.</p>Formula:C20H14O8Purity:98%Color and Shape:SolidMolecular weight:382.32Antifungal agent 18
CAS:<p>Antifungal agent 18 is a novel antifungal agent for the treatment of fungal infection.</p>Formula:C19H23Cl3N2OColor and Shape:SolidMolecular weight:401.76ML338
CAS:<p>ML338 is a potent inhibitor of dormant M. tuberculosis with IC90 of 1 μM and IC99 of 4 μM, aiding in tuberculosis research.</p>Formula:C17H12ClN5OSColor and Shape:SolidMolecular weight:369.83SDH-IN-2
CAS:<p>SDH-IN-2: Strong SDH blocker (IC50 0.55 μg/mL), antifungal; EC50 3.82-9.81 μg/mL against plant fungi.</p>Formula:C10H6F3NOPurity:99.82%Color and Shape:SolidMolecular weight:213.16MBL-IN-1
<p>MBL-IN-1 (compound 41), a β-Lactamase inhibitor, exhibits an IC50 range of 0.10 to 25.85 µM and is utilized in the study of bacterial infections [1].</p>Formula:C15H13FN3O3PColor and Shape:SolidMolecular weight:333.25CSP1
CAS:<p>CSP1: potent ComD1 receptor agonist, IC50 of 10.3 nM, important in S. pneumoniae transformation, and has antibacterial properties.</p>Formula:C103H168N30O24SColor and Shape:SolidMolecular weight:2242.72JE-2178
CAS:<p>JE-2178 is compound with high bioavailability .</p>Formula:C35H51N5O6SColor and Shape:SolidMolecular weight:669.87Nystatin A1
CAS:<p>Nystatin A1, a polyene macrolide (antibiotic), is isolated from the Streptomyces noursei bacterium. It functions by binding with ergosterol on fungal cell membranes, enhancing membrane permeability, and consequently causing leakage of cellular contents, which inhibits fungal growth and reproduction.</p>Formula:C47H75NO17Color and Shape:SolidMolecular weight:926.09Antibacterial agent 142
<p>Antibacterial agent 142, an aromatic hydrazide, exhibits bacteriostatic antibacterial activity and inhibits biofilm formation [1].</p>Formula:C12H9ClFN3OColor and Shape:SolidMolecular weight:265.67Thiophene-2
CAS:<p>TP2 inhibits Pks13, halting mycolic acid production and killing mycobacteria, with a 1 μM MIC against Mycobacterium tuberculosis.</p>Formula:C18H14F5NO3SColor and Shape:SolidMolecular weight:419.37Antibacterial agent 34
CAS:<p>Antibacterial agent 35 is a compound that effectively reduces the minimum inhibitory concentration (MIC) of Ceftazidime, enhancing its antibacterial activity.</p>Formula:C13H19N5O6SColor and Shape:SolidMolecular weight:373.38Funalenone
CAS:<p>Funalenone, from A. niger, inhibits HIV-1 integrase, HIV replication, and MMP-1, also curbing S. aureus growth. Less toxic to human cells.</p>Formula:C15H12O6Color and Shape:SolidMolecular weight:288.255Pks13-IN-1
<p>Pks13-IN-1 (Compound 44) is an orally active inhibitor of Mycobacterium tuberculosis polyketide synthase 13 (Pks13). It inhibits the M. tuberculosis H37Rv strain with a minimum inhibitory concentration (MIC) of 0.07 μM. In mouse models, Pks13-IN-1 demonstrates antibacterial activity.</p>Formula:C20H17BrN4O2Color and Shape:SolidMolecular weight:425.279Antimalarial agent 23
<p>Antimalarial 23: a benzimidazole with IC50s 0.08 μM (PfNF54), 0.10 μM (PfK1), inhibits β-hematin but not hemozoin formation.</p>Formula:C24H23ClF3N5OColor and Shape:SolidMolecular weight:489.92SARS-CoV-2 Mpro-IN-7
<p>SARS-CoV-2 Mpro-IN-7 (compound 6g) effectively inhibits SARS-CoV-2 main protease (Mpro) with an IC50 value of 8.8 μM and exhibits a cytotoxic concentration (</p>Formula:C33H34Br2N3O5PPurity:98%Color and Shape:SolidMolecular weight:743.42Kapurimycin A2
CAS:<p>Kapurimycin A2 is an antitumor antibiotics.</p>Formula:C26H24O9Purity:98%Color and Shape:SolidMolecular weight:480.46LAB 149202F
CAS:<p>LAB 149202F is a bioactive chemical.</p>Formula:C16H18N2O4Color and Shape:SolidMolecular weight:302.33Bulevirtide
CAS:<p>Bulevirtide (Myrcludex B) inhibits HBV/HDV entry into hepatocytes, treating chronic hepatitis D.</p>Formula:C248H355N65O72Purity:98%Color and Shape:SolidMolecular weight:5398.86LB80317
CAS:<p>LB-80317, a DNA polymerase inhibitor, is used potentially for the potential treatment of hepatitis B virus infection.</p>Formula:C10H14N5O5PColor and Shape:SolidMolecular weight:315.22Lenapenem
CAS:<p>Lenapenem is a broad-spectrum, carbapenem antibiotic with bactericidal activity by weakens the bacterial cell wall and leads to lytic cell death.</p>Formula:C18H29N3O5SColor and Shape:SolidMolecular weight:399.51Bismuth Subcitrate Potassium
CAS:<p>Bismuth Subcitrate is an antibiotic used to treat stomach ulcers associated with Helicobacter pylori, a bacterial infection.</p>Formula:C12H8BiK5O14Purity:99.00% - 99.00%Color and Shape:SolidMolecular weight:780.66Laidlomycin phenylcarbamate
CAS:<p>Laidlomycin phenylcarbamate is a semi-synthetic polyether antibiotic.</p>Formula:C44H67NO13Color and Shape:SolidMolecular weight:818.014Termicin
<p>Termicin, an antimicrobial peptide derived from Pseudacanthotermes spiniger, exhibits activity against gram-positive bacteria, filamentous fungi, and yeasts [1</p>Color and Shape:Odour SolidTemporin F
CAS:<p>Temporin F exhibits antimicrobial activity against Legionella pneumophila [1].</p>Formula:C68H117N15O14Color and Shape:SolidMolecular weight:1368.75UCM53
CAS:<p>UCM53 has a wide range of applications in life science related research.</p>Formula:C24H15ClO7Color and Shape:SolidMolecular weight:450.83Rivabazumab pegol
CAS:<p>Rivabazumab pegol, a pegylated Fab antibody targeting the PcrV protein, is utilized in phase II studies for chronic Pseudomonas aeruginosa infections [1].</p>Color and Shape:LiquidAVX 13616
CAS:<p>AVX 13616: potent antibacterial vs. drug-resistant Staph, similar to mupirocin with single-use efficiency. MIC: 2-4 ug/ml. Targets various staph, MRSA.</p>Formula:C50H73Cl2N7O7Purity:98%Color and Shape:SolidMolecular weight:955.08
