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(3,421 products)
- Antibiotic(945 products)
- Antifection(27 products)
- DHFR(30 products)
- DNA/RNA Synthesis(808 products)
- HBV(186 products)
- HIV Protease(508 products)
- HSV(99 products)
- Integrase(2 products)
- Ribosome(6 products)
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Found 6441 products of "Microbiology/Virology"
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Antileishmanial agent-20
Antileishmanial agent-20 exhibits selectivity against the Leishmania parasite, with IC50 values of 2.8 μM for L.Formula:C15H16N4O3Purity:98%Color and Shape:SolidMolecular weight:300.31SARS-CoV-2-IN-64
SARS-CoV-2-IN-64 (compound 9), derived from chenodeoxycholic acid, serves as a potent inhibitor of the SARS-CoV-2 spike glycoprotein [1].Purity:98%Color and Shape:Odour SolidMajoranaquinone
CAS:Majoranaquinone demonstrates potent antibacterial activity against four Staphylococcus strains, one Moraxella strain, and one Enterococcus strain.
Formula:C14H10O4Purity:98%Color and Shape:SolidMolecular weight:242.23HA-IN-1
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 decreaseFormula:C42H35NO6Purity:98%Color and Shape:SolidMolecular weight:649.73Citrullinated LL-37 3cit
Citrullinated LL-37 3cit is a host defense peptide with potent immunomodulatory and antimicrobial properties, demonstrating direct antiviral activity againstFormula:C205H337N57O56Purity:98%Color and Shape:SolidMolecular weight:4496.22Z-L(D-Val)G-CHN2
Z-L(D-Val)G-CHN2, an isoform of Z-LVG-CHN2, serves as a cell-permeable and irreversible inhibitor of cysteine proteinase.Formula:C22H31N5O5Purity:98%Color and Shape:SolidMolecular weight:445.51Antimalarial agent 31
Compound 31 (compound 7k) is an orally active inhibitor of Plasmodium falciparum aspartic protease, plasmepsin X (PMX), with antimalarial properties [1].Formula:C36H47N3O4Purity:98%Color and Shape:SolidMolecular weight:585.78Antitrypanosomal agent 17
Compound 17 (Compd 7a) exhibits potent antiamastigote activity, demonstrated by its IC50 value of 0.03 μM against the T. congolense strain IL3000 [1].Purity:98%Color and Shape:Odour SolidSARS-CoV-2-IN-42
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 hostFormula:C20H20O7Purity:98%Color and Shape:SolidMolecular weight:372.37SARS-CoV-2-IN-67
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/Purity:98%Color and Shape:Odour SolidGRL-1720 TFA
GRL-1720 TFA is a potent SARS-CoV-2 Mpro inhibitor, demonstrating anti-SARS-CoV-2 activity with an EC50 of 15 μM [1].Purity:98%Color and Shape:Odour SolidAurein 2.6
CAS:Aurein 2.6, an antibiotic antimicrobial peptide, exhibits activity against various Gram-positive bacteria with minimum inhibitory concentrations (MIC) of 25, 25Formula:C77H133N19O19Purity:98%Color and Shape:SolidMolecular weight:1629Aurein 5.2
CAS:Aurein 5.2 is an antibiotic antimicrobial peptide [1].Formula:C110H194N28O32SPurity:98%Color and Shape:SolidMolecular weight:2452.95Dermcidin-1L (human)
CAS:Dermcidin-1L (human), an antibiotic peptide secreted by sweat glands, exhibits antimicrobial activity and is utilized in the research of inflammatory skinFormula:C210H359N57O71Purity:98%Color and Shape:SolidMolecular weight:4818.44Cysteine protease inhibitor-3
Cysteine protease inhibitor-3 (Compound 15), a cysteine protease inhibitor, exhibits anti-plasmodial activity, effectively inhibiting Pf3D7 (IC50 = 0.74 μM),Formula:C26H22ClF2N3OPurity:98%Color and Shape:SolidMolecular weight:465.92HAT-IN-8
HAT-IN-8 (Compound 38), a blood-brain barrier-permeable inhibitor of Trypanosoma brucei with an EC50 of 0.18 μM, is utilized in the study of Human AfricanFormula:C14H15F2N3O2SPurity:98%Color and Shape:SolidMolecular weight:327.35SARS-CoV-2-IN-56
SARS-CoV-2-IN-56 (Compound 63) is a SARS-CoV-2 inhibitor with antiviral activity, demonstrating inhibition of the virus in Vero E6 cells with an IC50 of 0.7 μMFormula:C70H72N12O19S3Purity:98%Color and Shape:SolidMolecular weight:1481.58Antitrypanosomal agent 12
Antitrypanosomal agent 12, a C20-phenylthiourea, exhibits trypanocidal and cytotoxic activities, demonstrating antitrypanosomal activity with GI50 values of 0.Formula:C49H77N2NaO10SPurity:98%Color and Shape:SolidMolecular weight:909.2SARS-CoV-2-IN-55
SARS-CoV-2-IN-55 (compound 65) is an inhibitor of SARS-CoV-2 exhibiting low cytotoxicity, characterized by an IC50 of 0.3 μM, effectuated through directFormula:C138H136N22O32S6Purity:98%Color and Shape:SolidMolecular weight:2807.07Clovibactin
CAS:Clovibactin, a novel antibiotic, effectively eradicates drug-resistant bacterial pathogens and demonstrates no discernible resistance.Formula:C43H70N10O11Purity:98%Color and Shape:SolidMolecular weight:903.08Antiparasitic agent-17
Antiparasitic Agent-17 (compound 5u), an orally active antiparasitic, demonstrates inhibition against both Chloroquine-sensitive (Pf3D7) and Chloroquine-Formula:C32H30N2O4Purity:98%Color and Shape:SolidMolecular weight:506.59Defensin HNP-3 human
CAS:Defensin HNP-3 human, a cytotoxic antibiotic peptide referred to as "defensin," exhibits inhibitory effects on Staphylococcus aureus, Pseudomonas aeruginosa,Formula:C151H222N44O40S6Purity:98%Color and Shape:SolidMolecular weight:3486.04SARS-CoV-2-IN-60
SARS-CoV-2-IN-60 (compound 5a) is a specific, irreversible inhibitor of SARS-CoV-2 nsp16-nsp10 methyltransferase, competing with S-adenosylmethionine (SAM) andFormula:C13H7Cl2F3N2OPurity:98%Color and Shape:SolidMolecular weight:335.11SARS-CoV-2 3CLpro-IN-18
SARS-CoV-2 3CLpro-IN-18 (Compound 3C) is a covalent inhibitor of SARS-CoV-2 3CLpro with an IC50 of 0.478 μM.Formula:C17H13ClN2OSPurity:98%Color and Shape:SolidMolecular weight:328.82(±)-Emodin bianthrone
CAS:(±)-Emodin bianthrone (compound 10), a naturally occurring substance, demonstrates antimalarial, antitubercular, and antifungal properties [1].Formula:C30H22O8Purity:98%Color and Shape:SolidMolecular weight:510.49Moloney murine leukemia virus RT
Moloney murine leukemia virus reverse transcriptase (MMLV RT) is a monomeric replicative polymerase intrinsic to the retrovirus life cycle [1].Purity:98%Color and Shape:Odour Solid7-51A
7-51A is an effective inhibitor of the PB2 subunit of the influenza RNA-dependent RNA polymerase (RdRP), with a dissociation constant (K_D) of 1.64 nM asPurity:98%Color and Shape:Odour SolidPlutavimab
CAS:Plutavimab is a humanized IgG1-κ monoclonal antibody targeting the receptor binding domain (RBD) of the SARS-CoV-2 spike (S) glycoprotein [1] [2].Purity:98%Color and Shape:LiquidCalpain inhibitor V
CAS:Calpain Inhibitor V (Mu-Val-HPh-FMK) is a cell-permeable, irreversible calpain inhibitor with demonstrated anti-chlamydial activity [1].Formula:C21H30FN3O4Purity:98%Color and Shape:SolidMolecular weight:407.48D-4-77
D-4-77 is a potent inhibitor of SARS-CoV-2 Mpro, exhibiting an IC 50 of 0.95 μM, and possesses antiviral activity with an EC 50 of 0.49 μM.Formula:C23H34BrN3O5Purity:98%Color and Shape:SolidMolecular weight:512.44BMAP-28
CAS:BMAP-28, an antibiotic peptide, induces cell death by triggering the mitochondrial permeability transition pore and serves as a research tool in the study ofFormula:C145H250N44O29Purity:98%Color and Shape:SolidMolecular weight:3073.81Cangorinine E-1
CAS:Cangorinine E-1 (compound 11), a dihydroagarofuran sesquiterpenoid derivative, exhibits weak inhibitory effects on herpes simplex virus type II (HSV) [1].Formula:C43H49NO18Purity:98%Color and Shape:SolidMolecular weight:867.85Acryl42-10
Acryl42-10 serves as a covalent inhibitor for the SARS-CoV-2 Nsp14 N7-Methyltransferase, exhibiting an inhibition concentration (IC50) of 7 μM [1].Formula:C20H24ClN3O4Purity:98%Color and Shape:SolidMolecular weight:405.88SARS-CoV-2 Mpro-IN-7
SARS-CoV-2 Mpro-IN-7 (compound 6g) effectively inhibits SARS-CoV-2 main protease (Mpro) with an IC50 value of 8.8 μM and exhibits a cytotoxic concentration (Formula:C33H34Br2N3O5PPurity:98%Color and Shape:SolidMolecular weight:743.42Xenopsin precursor fragment
CAS:Xenopsin precursor fragment, an antimicrobial peptide, exhibits both antibacterial/antifungal activity at concentrations ranging from 10 to 500 μg/mL and anti-Formula:C123H211N33O32Purity:98%Color and Shape:SolidMolecular weight:2664.19Z795161988
Z795161988 functions as an inhibitor targeting the SARS-CoV-2 Nsp14 N7-Methyltransferase, exhibiting an inhibitory concentration (IC50) of 2.2 μM [1].Formula:C16H12BrN3O4Purity:98%Color and Shape:SolidMolecular weight:390.19Antimalarial agent 33
Antimalarial agent 33 (compound 5g) exhibits antiplasmodial activity targeting both erythrocytic and hepatic stages of Plasmodium, with an effectivePurity:98%Color and Shape:Odour SolidUNC9512
UNC9512 is a potent antagonist of the methyl-lysine reader protein 53BP1, which can be utilized to investigate the function of 53BP1 in DNA repair, gene editingFormula:C31H34N6O3Purity:98%Color and Shape:SolidMolecular weight:538.64SARS-CoV-2-IN-49
SARS-CoV-2-IN-49 acts as an irreversible covalent inhibitor targeting the main protease of SARS-CoV-2 [1].Formula:C29H34FN5O4Purity:98%Color and Shape:SolidMolecular weight:535.61rCRAMP (rat) acetate
rCRAMP (rat) acetate, a cathelin-related antimicrobial peptide, exhibits antibacterial activity in rat brain peptide/protein extracts.Purity:97.01%Color and Shape:Liquid(Rac)-Golgicide A
CAS:(Rac)-Golgicide A ((Rac)-GCA) is a racemate of Golgicide A. It is used in the manufacture of Golgicide A.Formula:C17H14F2N2Color and Shape:SolidMolecular weight:284.3(E)-hexadec-11-en-1-ol
CAS:(E)-hexadec-11-en-1-ol is a pheromone of the spotted stem borer Chilo partellus and is a long-chain fatty acid found in the volatile oil of Daphne genkwa.Formula:C16H32OPurity:99.19%Color and Shape:SolidMolecular weight:240.42Cilastatin sodium
CAS:Cilastatin is a renal dehydropeptidase-I and leukotriene D4 dipeptidase inhibitor.Formula:C16H26N2NaO5SColor and Shape:A White Colour PowderMolecular weight:381.44Kasugamycin hydrochloride (Standard)
CAS:Kasugamycin hydrochloride (Standard) is the standard substance of Kasugamycin hydrochloride, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Kasugamycin hydrochloride (Kasumin) is an aminoglycoside antibiotic that was originally isolated in 1965, from Streptomyces kasugaensis, a Streptomyces strain found near the Kasuga shrine in Nara, Japan. Kasugamycin hydrochloride was discovered by Hamao Umezawa, who also discovered kanamycin and bleomycin, as a drug which could prevent growth of a fungus causing rice blast disease.Formula:C14H26ClN3O9Color and Shape:SolidMolecular weight:415.83Captan
CAS:Captan (Aacaptan) is a phthalimide fungicide that disrupts oocyte development.
Formula:C9H8Cl3NO2SPurity:99.93%Color and Shape:White To Cream Powder Poses A Threat To The Environment In Case Of Release Immediate Steps Should Be Taken To Limit ItsMolecular weight:300.59RNase L-IN-1
RNase L-IN-1 is an RNase L inhibitor with potential anticancer activity and inhibits viral replication.Formula:C27H35FN6O3SPurity:98.55%Color and Shape:SolidMolecular weight:542.67Kanamycin
CAS:Kanamycin (Kanamycin A) is an aminoglycoside antibiotic with antibacterial activity, used in research on tuberculosis and pneumonia.Formula:C18H36N4O11Purity:98.22% - 99.92%Color and Shape:SoildMolecular weight:484.50Sulfamethazine-D4
CAS:Deuterium-labeled Sulfamethazine, an antimicrobial for treating animal diseases.Formula:C12H14N4O2SPurity:98%Color and Shape:SolidMolecular weight:282.36Fludioxonil (Standard)
CAS:Fludioxonil (Standard) is the standard substance of Fludioxonil, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Fludioxonil (CGA 173506), a phenylpyrrole fungicide, inhibits the growth of B. cinerea from strawberry and blackberry crops.Formula:C12H6F2N2O2Molecular weight:248.18Eckol
CAS:Eckol inhibits ultraviolet B-induced cell damage by a decrease in oxidative stress in human keratinocytes.Formula:C18H12O9Purity:98%Color and Shape:SolidMolecular weight:372.28
