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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MBL-IN-2
<p>MBL-IN-2 ((2R, 2R')-5αC) is a Metallo-β-lactamase (MBL) inhibitor that effectively inhibits New Delhi Metallo-β-lactamase-1 (NDM-1) with an IC50 of 0.3 μM. MBL-IN-2 ((2R, 2R')-5αC) can be used in research on resistance to β-lactam antibiotics.</p>Formula:C9H12F3NO3SMolecular weight:271.049MCG-02
<p>MCG-02 is an inhibitor of cruzain (CRZ) and cathepsin L-like protease (CATL), capable of inhibiting CRZ in Trypanosoma cruzi and CATL in Trypanosoma brucei, with IC50 values of 0.2 μM and 0.02 μM, respectively.</p>Formula:C13H13N3O2SColor and Shape:SolidMolecular weight:275.33ACHE-IN-38
CAS:<p>ACHE-IN-38, an Acetylcholinesterase inhibitor, can be used to synthesize compounds with anti-inflammatory activity.</p>Formula:C17H23NO3Purity:99.52%Color and Shape:SolidMolecular weight:289.37SARS-CoV-2 3CLpro-IN-17
<p>Compound 3h, also known as SARS-CoV-2 3CLpro-IN-17, is a selective inhibitor of the SARS-CoV-2 3CL protease, demonstrating an IC50 of 0.322 μM [1].</p>Formula:C16H9N3OS2Purity:98%Color and Shape:SolidMolecular weight:323.39Methylclonazepam
CAS:<p>Methylclonazepam is a benzodiazepine with anxiolytic properties. It inhibits the uptake of 5-hydroxytryptamine by Schistosoma mansoni, and its derivatives exhibit anti-Schistosoma mansoni activity.</p>Formula:C16H12ClN3O3Color and Shape:SolidMolecular weight:329.74Tibezonium iodide
CAS:<p>Tibezonium iodide, an oropharyngeal disinfectant, possesses antibacterial properties that aid in preventing mouth infections [1].</p>Formula:C28H32IN3S2Color and Shape:SolidMolecular weight:601.61Antimalarial agent 46
CAS:<p>Antimalarial agent 46 (Compound 42a) is a compound with antimalarial activity, effective in inhibiting P. falciparum lines.</p>Formula:C21H17Cl3N4OColor and Shape:SolidMolecular weight:447.75Chalcomycin
CAS:<p>Chalcomycin is a macrolide antibiotic effective against Gram-positive Staphylococcus aureus and Streptococcus pyogenes. It protects mice from infections caused by various Staphylococcus and Streptococcus strains and exhibits no significant toxicity (LD50>2500 mg/kg).</p>Formula:C35H56O14Molecular weight:700.36701CHEMBL1380345
CAS:<p>CHEMBL1380345 fights S. aureus, B. cereus, E. coli; pMICs: 3.64, 3.56, 3.70.</p>Formula:C16H20N2O4S2Purity:98.18%Color and Shape:SolidMolecular weight:368.47DOTA-ubiquicidin (29-41)
<p>DOTA-ubiquicidin (29-41) is a derivative of an antimicrobial peptide fragment employed for synthesizing [68Ga]Ga-DOTA-Ubiquicidin29-41, which is subsequently utilized in PET/CT imaging of infection processes. Additionally, DOTA-ubiquicidin (29-41) is applicable in the synthesis and research of radiopharmaceuticals known as radionuclide conjugates (RDC).</p>Formula:C84H147N35O25SMolecular weight:2078.10281SARS-CoV-2 Mpro-IN-17
SARS-CoV-2 Mpro-IN-17 (compound S5-28) is an orally active, non-covalent inhibitor of SARS-CoV-2 Mpro, with an EC50 value of 1.35 μM. It is applicable for research related to COVID-19.Formula:C20H19BrClN3O2Molecular weight:447.03492L-Ent-oxPt(IV)
<p>L-Ent-oxPt IV (L-EOP) is an oxaliplatin-based ferric carrier-platinum conjugate. It selectively targets Escherichia coli and exhibits antibacterial activity through DNA damage.</p>Formula:C54H65N9O27PtMolecular weight:1466.36378AS-0017445
<p>AS-0017445 is an inhibitor targeting the main protease of the coronavirus and the virus causing Middle East Respiratory Syndrome (MERS). It functions by inhibiting viral protein processing within host cells, thereby preventing viral replication.</p>Color and Shape:Odour SolidInfluenza HA (307-319)
CAS:<p>Influenza Hemagglutinin is an HLA-DRB 0101-restricted epitope from influenza hemagglutinin (307-319).</p>Formula:C69H118N18O19Purity:98%Color and Shape:SolidMolecular weight:1503.78Amoxicillin, L-
CAS:<p>Amoxicillin, L- is an antibiotic. It is also useful for the treatment of a number of bacterial infections.</p>Formula:C16H19N3O5SColor and Shape:SolidMolecular weight:365.40KSK-104
<p>KSK-104 exhibits potent antibacterial activity against Mycobacterium tuberculosis, with a minimum inhibitory concentration (MIC) of 0.78 μM. Its mechanism of action primarily involves the synthesis and salvage pathway of pyridoxal 5'-phosphate (PLP), as well as PLP-dependent enzymes and the oxidative stress network. KSK-104 is a promising candidate for developing novel anti-tuberculosis drugs targeted at drug-resistant strains of Mycobacterium tuberculosis.</p>Formula:C22H20N2O4Molecular weight:376.14231Antibacterial agent 185
<p>Antibacterialagent 185 (compound IP-01) is a potent antibacterial agent. It inhibits the polymerization and bundling of filamentous temperature-sensitive mutant Z (FtsZ) by enhancing GTP hydrolysis. Antibacterialagent 185 is effective against Streptococcus pneumoniae and displays a narrow spectrum of activity.</p>Formula:C18H17BrN2O3SMolecular weight:420.01433Ys-II
CAS:<p>Compound 1 (Ys-II) is a spirostanol glycoside extracted from the stem of Yucca elephantipes, exhibiting antifungal properties by inhibiting Candida albicans and</p>Formula:C45H76O19Color and Shape:SolidMolecular weight:921.07Antibacterial agent 226
<p>Antibacterialagent 226 (Compound 7f) is an antibacterial agent effective against Staphylococcus aureus strains, including methicillin-resistant S. aureus, with a MIC of 2 μg/mL. It exhibits cytotoxicity towards HEK293 cells with an IC50 of 1.9 μM.</p>Formula:C24H26F3N3O2Molecular weight:445.19771
