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(3,386 products)
- Antibiotic(941 products)
- Antifection(27 products)
- DHFR(30 products)
- DNA/RNA Synthesis(803 products)
- HBV(185 products)
- HIV Protease(506 products)
- HSV(99 products)
- Integrase(2 products)
- Ribosome(6 products)
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Found 6395 products of "Microbiology/Virology"
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ART899
CAS:ART899, a derivative of ART558, is a potent and specific conformational inhibitor of DNA polymerase θ (Polθ). It specifically inhibits the MMEJ activity of Polθ with an IC50 of 180 nM. Additionally, ART899 selectively enhances the radiosensitivity of tumor cells and possesses a strong independent antitumor effect on cancer cells.Formula:C19H16ClF4N3O4Color and Shape:SolidMolecular weight:464.81Flutianil
CAS:Flutianil is a chemical compound from the group of thiazolidines .Formula:C19H14F4N2OS2Color and Shape:SolidMolecular weight:426.45Scirpusin A
CAS:Scirpusin A is a hydroxystilbene dimer from the rhizome of Scirpus fluviatilis and Xinjiang wine grape.Formula:C28H22O7Color and Shape:SolidMolecular weight:470.47HPV16-E711-20 epitope
CAS:HPV16-E711-20: HLA-A*0201-restricted CTL epitope, binds strongly to HLA-A2.Formula:C53H83N11O19SPurity:98%Color and Shape:SolidMolecular weight:1210.35LtaS-IN-2
LtaS-IN-2 (compound 13), a derivative of LtaS-IN-1 [1], is an LTA synthesis inhibitor with antibacterial properties against S.Color and Shape:Odour SolidAmoxycillin arginine salt
CAS:Amoxycillin arginine salt is a bioactive chemical.Formula:C22H33N7O7SColor and Shape:SolidMolecular weight:539.61Carviolin
CAS:Carviolin is a natural product found in Penicillium purpureum. Carviolin has antifungal, antibacterial or phytotoxic activity. Cost-effective and quality-assured.Formula:C16H12O6Color and Shape:SolidMolecular weight:300.26CTP Synthetase-IN-1 Ammonium salt
CTP Synthetase-IN-1 Ammonium salt is a CTPS inhibitor with potential antibacterial, anti-inflammatory, and antitumor activity for the study of SARS-CoV-2 viral infectionsFormula:C20H22F3N7O3S2Purity:99.97%Color and Shape:SolidMolecular weight:529.56Emestrin
CAS:Emestrin, a mycotoxin with antimicrobial and immunomodulatory properties, combats various pathogens and can induce tissue necrosis.Formula:C27H22N2O10S2Color and Shape:SolidMolecular weight:598.6Emicoron
CAS:Importazole is an inhibitor of the transport receptor importin-β. It specifically inhibits importin-β likely by altering its interaction with RanGTP.Formula:C52H58N6O4Purity:98%Color and Shape:SolidMolecular weight:831.05SARS-CoV-2-IN-30
SARS-CoV-2-IN-30: two-armed diphosphate benzene, antiviral IC50 0.6/6.9μM, disrupts membranes EC50 6.9μM.Formula:C60H52O8P2Color and Shape:SolidMolecular weight:963TXY541
CAS:TXY541 is an orally active antibacterial agent that is converted into PC190723 under physiological conditions. It demonstrates strong antibacterial activity against Staphylococcus aureus and exhibits low cytotoxicity towards mammalian cells.Formula:C21H19ClF2N4O3SColor and Shape:SolidMolecular weight:480.92MDP1
MDP1, a Melittin-based peptide, disrupts and kills various bacteria, including MDR strains of S. aureus, E. coli, and P. aeruginosa, by damaging membranes.Formula:C111H202N34O28Color and Shape:SolidMolecular weight:2461SARS-CoV-2 nsp13-IN-7
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.Formula:C24H17ClN4O3SColor and Shape:SolidMolecular weight:476.07099CCOE-5
CCOE-5 is a chalcone derivative with antimalarial activity, exhibiting an IC50 of 1.4 μg/mL against P. falciparum (3D7) and an IC50 of less than 5 μg/mL against P. falciparum (INDO). CCOE-5 shows potential for research in the anti-infective domain.Formula:C34H31NO6Color and Shape:SolidMolecular weight:549.61Sofosbuvir impurity K
CAS:Sofosbuvir impurity K is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.Formula:C22H29ClN3O9PPurity:98%Color and Shape:SolidMolecular weight:545.91HIV-1 inhibitor-81
HIV-1inhibitor-81 (Compound 14g) is an HIV-1 protease inhibitor with a Ki of 1.6 nM. This compound exhibits antiviral activity against HIV-1, with an EC50 value of 250 nM.Formula:C32H44N2O8SColor and Shape:SolidMolecular weight:616.77Fosfomycin
CAS:Fosfomycin is an antibiotic that is produced by Streptomyces fradiae.Formula:C3H7O4PPurity:98%Color and Shape:SolidMolecular weight:138.069-AMN
9-AMN is an inhibitor of the SARS-CoV-2 papain-like protease (SARS-CoV-2 PLpro), effectively reducing its deubiquitinating (DUB) activity and protease activity, with IC50 values of 4.55 µM and 4.15 µM, respectively. Additionally, 9-AMN suppresses the replication of the SARS-CoV variants Delta and Omicron in Calu-3 cells, with IC50 values of 1.04 µM and 2.35 µM, respectively.Formula:C23H28N4O7Color and Shape:SolidMolecular weight:472.49Antiparasitic agent-24
Antiparasitic agent-24 (Compound 14a) is an antiparasitic compound with EC50 values of 0.005 μM for L. maj, 0.069 μM for L. don, 0.82 μM for T. brucei, and 4.1 μM for T. cruzi.Formula:C23H22ClN7O2SColor and Shape:SolidMolecular weight:495.98
