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(2,949 products)
- Antibiotic(919 products)
- Antifection(23 products)
- DHFR(32 products)
- DNA/RNA Synthesis(707 products)
- HBV(176 products)
- HIV Protease(447 products)
- HSV(91 products)
- Integrase(2 products)
- Ribosome(13 products)
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Found 5832 products of "Microbiology/Virology"
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Aurein 1.2
CAS:<p>Aurein 1.2, an amphibian-derived peptide, exhibits both antibiotic and anticancer properties [1].</p>Formula:C71H114N16O18Purity:98%Color and Shape:SolidMolecular weight:1479.76T7 RNA polymerase
CAS:<p>T7 RNA polymerase, expressed by Escherichia coli from the T7 bacteriophage RNA polymerase gene, is a highly specific enzyme utilized for in vitro transcription</p>Purity:98%Color and Shape:SolidHA-IN-1
<p>HA-IN-1 (compound 5g), a high-affinity Hemagglutinin (HA) ligand, targets the trypsin cleavage site of HA to inhibit HA-mediated membrane fusion and decrease</p>Formula:C42H35NO6Purity:98%Color and Shape:SolidMolecular weight:649.73Citrullinated 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:4496.22Z-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:445.51Antimalarial 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:585.78Antitrypanosomal 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 SolidSARS-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:372.37SARS-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 SolidSARS-CoV-2-IN-54
<p>SARS-CoV-2-IN-54 (Compound 2), a SARS-CoV-2 inhibitor, exhibits antiviral activity by impeding the virus in Vero E6 cells with an inhibitory concentration (IC50</p>Formula:C63H59N11O16S3Purity:98%Color and Shape:SolidMolecular weight:1322.4β-Herpesvirus protease-IN-1
<p>β-Herpesvirus protease-IN-1 (compound 19) serves as an inhibitor of β-herpesvirus protease, exhibiting IC50 values of 2.5 μM for HCMVPro and 0.33 μM for HHV6Pro</p>Purity:98%Color and Shape:Odour SolidSARS-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:323.39RdRP-IN-6
<p>RdRP-IN-6 (compound 27) is an inhibitor of RNA-dependent RNA polymerase (RdRp), exhibiting an IC90 value of 14.1 μM.</p>Formula:C41H67N8O7PSi2Purity:98%Color and Shape:SolidMolecular weight:871.16Lugdunin
CAS:<p>Lugdunin is an antibiotic peptide that disrupts membrane potential in bacteria, demonstrating activity against Gram-positive species including S.</p>Formula:C40H62N8O6SPurity:98%Color and Shape:SolidMolecular weight:783.04Antitrypanosomal agent 16
<p>Antitrypanosomal agent 16 functions as a potent trypanocide, exhibiting an inhibitory concentration 50 (IC50) of 0.04μM against the T.</p>Purity:98%Color and Shape:Odour SolidSARS-CoV-2-IN-50
<p>SARS-CoV-2-IN-50 (Compound X77C) is a potent inhibitor of the SARS-CoV-2 main protease (M^pro), exhibiting high affinity for the enzyme's catalytic site [1].</p>Formula:C26H28FN5O4Purity:98%Color and Shape:SolidMolecular weight:493.53Antileishmanial agent-21
<p>Antileishmanial agent-21 (compound 4e) functions as an inhibitor of Leishmania pteridine reductase 1 (Lm-PTR1), employing an anti-folate mechanism.</p>Formula:C21H16N2O3Purity:98%Color and Shape:SolidMolecular weight:344.36SARS-CoV-2-IN-53
<p>ARS-CoV-2-IN-53 (Compd 5d) exhibits an inhibitory effect on SARS-CoV-2 replication, with an effective concentration (EC50) value of 14.3 μM, and demonstrates</p>Formula:C23H18F2N2O4SPurity:98%Color and Shape:SolidMolecular weight:456.46Anticancer agent 140
<p>Compound 140 (Compd 3) exhibits potential anticancer and antiparasitic activities [1].</p>Formula:C20H26N2OPurity:98%Color and Shape:SolidMolecular weight:310.43Simaravibart
<p>Simaravibart (MAD-0004J08), an IgG1κ monoclonal antibody, specifically targets the receptor-binding domain of the SARS-CoV-2 spike (S) glycoprotein [1].</p>Purity:98%Color and Shape:Odour Liquid
