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)
Show 2 more subcategories
Found 5842 products of "Microbiology/Virology"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Chaetoviridin A
CAS:<p>Chaetoviridin A, an azaphilone isolated from Chaetomium globosum, is characterized as 6H-furo[2,3-h]isochromene-6,8(6aH)-dione with substitutions including a chloro group at position 5, a 3-hydroxy-2-methylbutanoyl group at position 9, a methyl group at position 6a, and a 3-methylpent-1-en-1yl group at position 3. It exhibits antifungal activity against plant pathogenic fungi.</p>Formula:C23H25ClO6Color and Shape:SolidMolecular weight:432.89CIM-834
<p>CIM-834 is an orally active, selective inhibitor that targets the coronavirus membrane protein (M protein), exhibiting potent inhibition of viral assembly in both SARS-CoV-2 and SARS-CoV. It binds non-covalently to the short form of the M protein (Mshort), stabilizing it and preventing its conformational change to the long form (Mlong) necessary for virion assembly, thus blocking virus particle formation. CIM-834 holds potential for research in COVID-19 and other coronavirus infections.</p>Color and Shape:Odour SolidEchinosporin
CAS:<p>Echinosporin is a biochemical.</p>Formula:C10H9NO5Color and Shape:SolidMolecular weight:223.184Cephabacin M6
CAS:<p>Cephabacin M6 is a new cephem antibiotic isolated from bacterial.</p>Formula:C47H79N13O18SPurity:98%Color and Shape:SolidMolecular weight:1146.272'-(2-Nitrobenzyl)-ATP trisodium
<p>2'-(2-Nitrobenzyl)-ATP trisodium is an rATP analogue that acts as a transcription terminator. It inhibits T7 RNA polymerase from continuing RNA chain extension.</p>Formula:C17H18N6Na3O15P3Color and Shape:SolidMolecular weight:707.97361Resolvin D4
CAS:<p>RvD4, derived from docosahexaenoic acid, reduces neutrophil infiltration and promotes phagocytosis/clearance by human cells.</p>Formula:C22H32O5Color and Shape:SolidMolecular weight:376.493MBL-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:333.25CAY10742
CAS:<p>CAY10742: Oral oxadiazole antibiotic, combats Gram-positive bacteria & MRSA, effective against resistant strains, works in mouse models. MICs = 1-4 μg/ml.</p>Formula:C22H14FN3O2Color and Shape:SolidMolecular weight:371.371Antibacterial agent 39
CAS:<p>Antibacterial agent 39 boosts Ceftazidime's efficacy by lowering its MIC.</p>Formula:C9H11N5NaO7SColor and Shape:SolidMolecular weight:356.26Aflatoxin Q1
CAS:<p>Aflatoxin Q1, a hydroxy metabolite of Aflatoxin B1, is a major detoxication product formed in human liver.</p>Formula:C17H12O7Color and Shape:SolidMolecular weight:328.27Kazinol F
CAS:<p>Kazinol F is used for skin brightening.</p>Formula:C25H32O4Color and Shape:SolidMolecular weight:396.52Mram 8
CAS:<p>Mram 8, a cyclotide isolated from Viola philippica of the Violaceae family [1], exhibits a characteristic cyclic peptide structure.</p>Formula:C132H208N36O39S6Color and Shape:SolidMolecular weight:3115.67Kirromycin
<p>Kirromycin, an antibiotic from Streptomyces, blocks protein synthesis and stunts B. brevis growth by hindering elongation factor Tu in E. coli.</p>Formula:C43H60N2O12Color and Shape:SolidMolecular weight:796.955Rubradirin
CAS:<p>Rubradirin: an antibiotic targeting methicillin-resistant staph, complex structure, inhibits peptide initiation.</p>Formula:C48H46N4O20Purity:98%Color and Shape:SolidMolecular weight:998.904SARS-CoV-2 nsp13-IN-7
<p>SARS-CoV-2 nsp13-IN-7 (Compound 6r) is an inhibitor of SARS-CoV-2 nsp13, with an IC50 of 0.28 μM. This compound disrupts the helicase function of nsp13 by binding to its 5' RNA site and ATP binding site, and it serves as a lead compound for developing antiviral drugs targeting SARS-CoV-2 nsp13.</p>Formula:C24H17ClN4O3SColor and Shape:SolidMolecular weight:476.07099Streptazolin
CAS:<p>Streptazolin is a fungal metabolite originally isolated from S.</p>Formula:C11H13NO3Color and Shape:SolidMolecular weight:207.229PF 1022A
CAS:<p>PF 1022A is an N-methylated cyclooctadepsipeptides with strong anthelmintic properties. It also acts as an ionosphere.</p>Formula:C52H76N4O12Purity:98%Color and Shape:Wei? (White) Solid Powder CrystallineMolecular weight:949.18Laccase-IN-2
<p>Laccase-IN-2 is a potent laccase inhibitor demonstrating excellent antifungal activity against Magnaporthe oryzae both in vitro and in vivo [1].</p>Color and Shape:Odour SolidRetavibart
CAS:<p>Retavibart is a fusion protein (glycoprotein F) of the human respiratory syncytial virus (RSV). It can be used for antiviral research.</p>Color and Shape:LiquidAntimicrobial agent-7
<p>Compound 12: potent antimicrobial with 2-8 μg/mL MIC, effective against Gram-positive/negative bacteria; anti-inflammatory.</p>Formula:C36H56N24Color and Shape:SolidMolecular weight:824.99
