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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Mycobacterium Tuberculosis-IN-8
<p>Mycobacterium Tuberculosis-IN-8 (Compound 6g) is a selective inhibitor of Mycobacterium tuberculosis (MTB), with a MIC value of 6.25 µg/mL against MTB H37Rv. It demonstrates potent antitubercular activity by inhibiting mycolic acid biosynthesis, which is crucial for maintaining bacterial cell wall integrity. Mycobacterium Tuberculosis-IN-8 holds potential for research in antitubercular agents.</p>Formula:C36H23Cl3N4Color and Shape:SolidMolecular weight:616.09883Leu-Val
CAS:<p>Leu-Val (L-leucyl-L-valine) is a novel potent dipeptide with antibacterial and antimalarial activity.</p>Formula:C11H22N2O3Purity:97.72%Color and Shape:SolidMolecular weight:230.3DG1
<p>DG1 (Compound 8Nc), a Thymidylate Synthase (TS) inhibitor, impedes angiogenesis and alters metabolic reprogramming in NSCLC cells, while effectively suppressing</p>Formula:C19H17N5O5SColor and Shape:SolidMolecular weight:427.43pCDPK1/TgCDPK1-IN-3
CAS:<p>CpCDPK1/TgCDPK1-IN-3 inhibits Cp/TgCDPK1; IC50: 0.003/0.0036 µM. It's used to research Toxoplasma, Cryptosporidium diseases.</p>Formula:C17H18N6Purity:99.63%Color and Shape:SoildMolecular weight:306.36Insecticidal agent 24
<p>Insecticidal agent 24 is an orally active pyridinyl spiroindoline lead compound. It demonstrates antimalarial activity with Pf NF54IC50 of 0.08 μM. Insecticidal agent 24 also inhibits hERG activity with an IC50 of 6.5 μM. In a humanized immunodeficient NSG mouse model of malaria infection, it effectively reduces parasitemia.</p>Formula:C26H29N3O2Color and Shape:SolidMolecular weight:415.22598Ledipasvir D-tartrate
CAS:<p>Ledipasvir D-tartrate (GS-5885 D-tartrate) is an HCV NS5A inhibitor that suppresses viral overphosphorylation and replication</p>Formula:C53H60F2N8O12Purity:99.83%Color and Shape:SolidMolecular weight:1039.09Amicoumacin A FA
<p>Amicoumacin A FA has antimicrobial activity, inhibiting S. purpureus and S. aureus, and can be used in the study of microbial infections.</p>Formula:C21H31N3O9Purity:98.74% - 99.34%Color and Shape:SolidMolecular weight:469.49TNM001
<p>TNM001 is an anti-RSV fully humanized monoclonal antibody for the study of lower respiratory tract disease due to RSV infection.</p>Purity:99% (SDS-PAGE); 99.6% (SEC-HPLC) - 99% (SDS-PAGE); 99.6% (SEC-HPLC)Color and Shape:Odour LiquidRSM01
<p>RSM01 is a fully human IgG1 monoclonal antibody that targets a site in the pre-F region of RSV with a YTE half-life prolongation mutation.</p>Purity:97.5% (SDS-PAGE); 99.5% (SEC-HPLC) - 97.5% (SDS-PAGE); 99.5% (SEC-HPLC)Color and Shape:Odour LiquidS2H97
<p>S2H97 is a neutralizing antibody that broadly protects against viruses such as neococcal pneumonia and SARS under clade B of coronavirus B.</p>Purity:98.8% (SDS-PAGE); 98.5% (SEC-HPLC) - 98.8% (SDS-PAGE); 98.5% (SEC-HPLC)Color and Shape:Odour LiquidCW-2
<p>CW-2 is a PARP1 PROTAC degrader known for its potent antiproliferative effects against MDA-MB-231 cells (IC50 = 0.72 μM) and cisplatin-resistant cells (A549/CDDP: IC50 = 3.52 μM). It exhibits synergistic antitumor activity and enhanced membrane permeability. CW-2 exerts its antitumor effects by inducing DNA damage, disrupting DNA repair, and triggering mitochondrial-dependent apoptosis (apoptosis).</p>Formula:C43H42Cl2FN11O10PtColor and Shape:SolidMolecular weight:1156.21251c-Met-IN-15
CAS:<p>c-Met-IN-15 exhibits antibacterial activity.</p>Formula:C15H10FN3O3Purity:99.58%Color and Shape:SolidMolecular weight:299.26Golotimod hydrochloride
CAS:<p>Golotimod hydrochloride (SCV 07 hydrochloride) is an immunomodulatory peptide with antibacterial activity.</p>Formula:C16H20ClN3O5Purity:99.64% - 99.86%Color and Shape:SolidMolecular weight:369.8ML-60218
CAS:<p>ML-60218 inhibits RNA pol III in yeast/humans with IC50s of 32/27 μM; disrupts and prevents viroplasms.</p>Formula:C19H15Cl2N3O2S2Purity:98.1%Color and Shape:SolidMolecular weight:452.38SARS-CoV-2-IN-101
<p>SARS-CoV-2-IN-101 (compound 10O) is an effective orally active inhibitor of SARS-CoV-2 with an EC50 value of 0.64 µM against HCoV-229E. This compound exhibits cytotoxicity and can reduce the expression levels of HCoV-229E N protein and RNA. Additionally, SARS-CoV-2-IN-101 has broad-spectrum antiviral activity against coronaviruses.</p>Formula:C22H23N5O3Color and Shape:SolidMolecular weight:405.45SARS-CoV-2 3CLpro-IN-27
<p>SARS-CoV-2 3CLpro-IN-27 (Compound 9H) is an inhibitor of SARS-CoV-2 3CLpro, demonstrating an IC50 of 21 nM. It also exhibits robust anti-replicase activity against SARS-CoV-2, with an EC50 of 5 nM.</p>Formula:C29H27F4N5O4Color and Shape:SolidMolecular weight:585.55SARS-CoV-2 3CLpro-IN-26
<p>SARS-CoV-2 3CLpro-IN-26 (Compound (S,R)-4y) is a conformational inhibitor of SARS-CoV-2 3CLpro with an IC50 of 0.43 μM. It demonstrates good cellular permeability, being able to effectively cross the cell membrane following co-incubation with Vero-E6 cells.</p>Formula:C24H18Cl3N3O3Color and Shape:SolidMolecular weight:502.78ATV03
<p>ATV03 is an antiviral agent exhibiting potent activity against both type A and type B influenza viruses. It inhibits the type A (H3N2) and type B influenza viruses with EC50 values of 0.78 nM and 2.02 nM, respectively. The mechanism of action of ATV03 involves the inhibition of the polymerase acidic protein (PA) and RNA-dependent RNA polymerase (RdRp), as well as the disruption of nucleoprotein, thereby exerting its antiviral effects against influenza.</p>Formula:C24H20FN3O5Color and Shape:SolidMolecular weight:449.43SARS-CoV-2 Mpro-IN-27
<p>SARS-CoV-2 Mpro-IN-27 (Compound 4h) is an effective inhibitor of SARS-CoV-2 Mpro.</p>Formula:C22H16N4OColor and Shape:SolidMolecular weight:352.39sPLA2 inhibitor 2
<p>sPLA2 inhibitor 2 (compound 6a) is an sPLA2 inhibitor with an IC50 value of 0.0475 μM, making it valuable for diabetes research.</p>Formula:C20H18N6O4S2Color and Shape:SolidMolecular weight:470.52
