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(2,957 products)
- Antibiotic(920 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 5842 products of "Microbiology/Virology"
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Psoracorylifol C
<p>Psoracorylifol C is a useful organic compound for research related to life sciences and the catalog number is T124015.</p>Formula:C18H24O3Color and Shape:SolidMolecular weight:288.387apo-Enterobactin
CAS:<p>apo-Enterobactin is a derivative of Enterobactin, which is a bacterial iron carrier that facilitates iron absorption.</p>Formula:C30H29N3O16Color and Shape:SolidMolecular weight:687.56NEU3-IN-1
<p>NEU3-IN-2 (compound 963), a derivative of 2-deoxy-2,3-didehydro-N-acetylneuraminic acid (DANA) and a C9 biphenylcarbamate, functions as an inhibitor of NEU3, a human neuraminidase with four isozymes. This compound exhibits inhibitory activity with a Ki of 0.12 μM and an IC50 of 0.31 μM. It serves as a crucial tool in the exploration of NEU3 isozyme functionality. Additionally, its analogs, featuring an amide and a triazole linker, show selectivity towards NEU1 and NEU4 isozymes, respectively.</p>Formula:C24H26N2O9Color and Shape:SolidMolecular weight:486.47CI-39
CAS:<p>CI-39, an NNRTI with EC50 of 3.40 µM, inhibits HIV-1 reverse transcriptase and RNase H, with CC50 >30 µM.</p>Formula:C19H18N2O4Color and Shape:SolidMolecular weight:338.36L 685818
CAS:<p>L 685818 is the C18-hydroxy, C21-ethyl of FK-506 analog.</p>Formula:C43H69NO13Color and Shape:SolidMolecular weight:808.019SARS-CoV-2 Mpro-IN-26
<p>SARS-CoV-2 Mpro-IN-26 (compound 13) is a covalent inhibitor targeting SARS-CoV-2 Mpro.</p>Color and Shape:Odour SolidJanthitrem G
CAS:<p>Janthitrem G is a type of naphthopyran. Janthitrem G is obtained from Penicillium janthinellum. Tremorgenic mycotoxi.</p>Formula:C39H51NO6Color and Shape:SolidMolecular weight:629.838HIV-IN-2
CAS:<p>HIV-IN-2 (Compound 100) is a potent inhibitor of HIV, showing potential for research into HIV infection [1].</p>Formula:C34H27ClF7N9O3SColor and Shape:SolidMolecular weight:810.14Paldimycin B
CAS:<p>Paldimycin B is a semi-synthetic antibiotic.</p>Formula:C43H62N4O23S3Purity:98%Color and Shape:SolidMolecular weight:1099.15Dendryphiellin D
CAS:<p>Dendryphiellin D from Septoria rudbeckiae fungus inhibits NO production.</p>Formula:C21H28O5Color and Shape:SolidMolecular weight:360.44Antibacterial agent 54
CAS:<p>Antibacterial agent 54 (example 20) is a antibacterial agent.</p>Formula:C9H11N4NaO5S2Color and Shape:SolidMolecular weight:342.33Ilicicolin F
CAS:<p>Ilicicolin F is a useful organic compound for research related to life sciences. The catalog number is T125283 and the CAS number is 22738-98-3.</p>Formula:C25H31ClO6Color and Shape:SolidMolecular weight:462.97NL3
CAS:<p>NL3 is an inhibitor of bacterial cystathionine gamma-lyase, exhibiting IC50 values of 0.7 μM for [bCSE] and 3.4 μM for [hCSE]. It is applicable in research focused on antibacterial activity and overcoming bacterial resistance.</p>Formula:C21H14ClN3O2SColor and Shape:SolidMolecular weight:407.87Amphocil
CAS:<p>Amphocil is used to treat patients with invasive fungal infection.</p>Formula:C74H119NO21SColor and Shape:SolidMolecular weight:1390.81ML338
CAS:<p>ML338 is a potent inhibitor of dormant M. tuberculosis with IC90 of 1 μM and IC99 of 4 μM, aiding in tuberculosis research.</p>Formula:C17H12ClN5OSColor and Shape:SolidMolecular weight:369.83Landomycin A
CAS:<p>Landomycin A is a prominent angucycline hexasaccharide antibiotic from Streptomyces sp.</p>Formula:C55H74O22Purity:98%Color and Shape:SolidMolecular weight:1087.175Linearolactone
CAS:<p>Linearolactone, isolated from Salvia polystachya, inhibits Entamoeba histolytica and Giardia lamblia.</p>Formula:C20H20O5Purity:98%Color and Shape:SolidMolecular weight:340.37Antibacterial agent 34
CAS:<p>Antibacterial agent 35 is a compound that effectively reduces the minimum inhibitory concentration (MIC) of Ceftazidime, enhancing its antibacterial activity.</p>Formula:C13H19N5O6SColor and Shape:SolidMolecular weight:373.38Polymyxin D2
CAS:<p>Polymyxin D2 is a cationic lipopeptide antibiotic against many species of Gram-negative bacteria.</p>Formula:C49H91N15O15Purity:98%Color and Shape:SolidMolecular weight:1130.34Oxadixyl
CAS:<p>Oxadixyl is used as a fungicide.</p>Formula:C14H18N2O4Purity:98%Color and Shape:SolidMolecular weight:278.30Leucinostatin K
CAS:<p>Leucinostatin K is a new peptide antibiotic from Paecilomyces lilacinus.</p>Formula:C62H111N11O14Purity:98%Color and Shape:SolidMolecular weight:1234.633Antibiotic SF 2132
CAS:<p>Antibiotic SF 2132 is a bioactive chemical.</p>Formula:C30H52N12O10Purity:98%Color and Shape:SolidMolecular weight:740.82Trimethacarb
CAS:<p>Trimetharba is a kind of insecticide.</p>Formula:C11H15NO2Purity:98%Color and Shape:SolidMolecular weight:193.24Rifamexil
CAS:<p>Rifamexil is a rifamycin (antibiotic produced naturally by the bacterium Amycolatopsis rifamycinica) derivative.</p>Formula:C42H55N3O11SPurity:98%Color and Shape:SolidMolecular weight:809.97Surgumycin
CAS:<p>Surgumycin is a carbonyl-conjugated pentaenic antibiotic.</p>Formula:C36H60O11Color and Shape:SolidMolecular weight:668.865Nocardicin A
CAS:<p>Nocardicin A, a moderate antibiotic agent, shows inhibitory for a wild spectrum of gram-negative bacteria.</p>Formula:C23H24N4O9Purity:98%Color and Shape:SolidMolecular weight:500.46Tebipenem pivoxil hydrochloride
CAS:<p>Tebipenem pivoxil HCl: oral antibiotic that targets PBPs to block bacterial cell wall synthesis.</p>Formula:C22H32ClN3O6S2Color and Shape:SolidMolecular weight:534.09RSV-IN-2
CAS:<p>RSV-IN-2, a dual inhibitor for wild-type/mutant RSV fusion proteins, has EC50 of 0.27 nM (wild-type) and 0.70 nM (D486N mutant).</p>Formula:C27H31ClN6O4Color and Shape:SolidMolecular weight:539.03ML188 enantiomer
CAS:<p>16-(S)-ML188 is a inhibitor of HKU4-CoV 3CLpro, showing effective enzyme inhibition and antiviral activity.</p>Formula:C26H31N3O3Color and Shape:SolidMolecular weight:433.54Thermopterin
CAS:<p>Thermopterin is isolated from Methanoculleus thermophilic.</p>Formula:C33H44N7O21PPurity:98%Color and Shape:SolidMolecular weight:905.717Antibacterial 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:445.19771Tuvirumab
CAS:<p>Tuvirumab, a human IgG1 monoclonal antibody, targets HBsAg with high affinity (K=3.6 nM) for chronic hepatitis B research.</p>Color and Shape:LiquidCefotiam dihydrochloride hydrate
<p>Cefotiam dihydrochloride hydrate: parenteral cephalosporin antibiotic with broad-spectrum Gram-positive and Gram-negative activity.</p>Formula:C18H25Cl2N9O4S3·xH2OColor and Shape:SolidMolecular weight:C18H25Cl2N9O4S3.xH2Oc-Fos-IN-1
<p>c-Fos-IN-1 (Compound P16) acts as a c-Jun inhibitor, effectively reducing the mRNA and protein levels of c-Fos. It also inhibits the phosphorylation activity of ERK and the transcriptional activity of AP-1. This compound demonstrates anticancer properties through the inhibition of the ERK/c-Fos/Jun pathway. c-Fos-IN-1 curbs the proliferation and migration of gastric cancer cells, with an IC50 of 2.31 μM for MGC-803 cells, causing cell cycle arrest at the G2/M phase and inducing apoptosis in cancer cells. Additionally, c-Fos-IN-1 hampers the growth of gastric cancer tumors.</p>Formula:C28H35NO3Color and Shape:SolidMolecular weight:433.582β-Lactamase-IN-9
<p>β-Lactamase-IN-9 (compound 2) is an inhibitor of β-lactamase, capable of restoring the sensitivity of pathogens to β-lactam antibiotics.</p>Formula:C21H17N2NaO9SMolecular weight:496.05525Antifungal agent 58
CAS:<p>Compound A21 is a potent anti-Candida drug effective against Fluconazole-resistant strains, surpassing Miconazole, with MIC 0.06-8 μg/mL.</p>Formula:C18H15F3N2SeColor and Shape:SolidMolecular weight:395.28Galbinic Acid
CAS:<p>Galbinic acid, a lichen-derived depsidone from U. undulata, inhibits B. cereus, B. subtilis, S. aureus, and E. coli, with varying MICs.</p>Formula:C20H14O11Color and Shape:SolidMolecular weight:430.32Cecropin A TFA
<p>Cecropin A TFA: a 37-residue peptide from Hyalaphora cecropia, with antibacterial, anti-inflammatory, and anticancer properties.</p>Formula:C186H314N53O48F3Color and Shape:SolidMolecular weight:4117.8MRV03-037
CAS:<p>MRV03-037 inhibits ClbP, blocking colibactin's genotoxic impact on cells, and stops gut bacterial genotoxin production.</p>Formula:C9H19BN2O4Color and Shape:SolidMolecular weight:230.07PD 116779
CAS:<p>PD 116779 is a new antitumor antibiotic in the class os benz[a]anthraquinone.</p>Formula:C19H14O6Color and Shape:SolidMolecular weight:338.315Kalimantacin A
CAS:<p>Kalimantacin A: a potent antibiotic effective against MRSA and other staphylococci.</p>Formula:C30H48N2O7Color and Shape:SolidMolecular weight:548.715'-O-DMT-N4-Ac-2'-F-dC
CAS:<p>5’-O-DMT-N4-Ac-2’-F-dC is a modified nucleoside and can be used to synthesize DNA or RNA.</p>Formula:C32H32FN3O7Color and Shape:SolidMolecular weight:589.61δ-hemolysin TFA
<p>Delta-hemolysin (Delta-lysin) TFA is a peptide composed of 26 amino acids, produced by staphylococci as a hemolytic peptide. It may slightly disrupt cell membranes or lead to cell lysis and serves as a model for studying peptide-membrane interactions. Its activity against bacteria is relatively weak.</p>Formula:C137H225N33O40S·xC2HF3O2PLpro-IN-2
<p>PLpro-IN-2 (Compound 16) is an inhibitor of the SARS-CoV-2 papain-like protease (PLpro), with an IC50 value of 0.25 μM.</p>Formula:C30H38N4O3SMolecular weight:534.26646MBL-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:271.049OP-145
CAS:<p>OP-145 is a derivative of the antimicrobial peptide LL-37, known for its antibacterial properties against multiple MRSA strains. This compound is applicable in studies on chronic suppurative otitis media.</p>Formula:C142H246N46O31Molecular weight:3093.76Antifungal agent 96
<p>Antifungalagent 96 (Compound WZ-2) is an antifungal agent with excellent blood-brain barrier permeability and brain penetration. It inhibits the growth of C. neoformans H99 and C. albicans 0304103, with MIC values of 0.016 and 32 μg/mL, respectively.</p>Formula:C11H8N2O3SMolecular weight:248.02556Gramicidin A TFA
<p>Gramicidin A (TFA) is a peptide component of Gramicidin, an antibiotic mixture originally isolated from B. brevis. It is a highly hydrophobic channel-forming ion carrier that creates monovalent cation-permeable channels in artificial membranes. Additionally, Gramicidin A (TFA) induces the degradation of hypoxia-inducible factor 1α (HIF-1α).</p>Formula:C99H140N20O17·xC2HF3O2Mtb-IN-7
Mtb-IN-7 (compound R7) is a MAO-A/MAO-B inhibitor with an IC50 greater than 40 μM. It exhibits antibacterial activity against Mycobacterium tuberculosis H37Rv, with a MIC of 2.01 μM.Formula:C16H22FN3O5SMolecular weight:387.12642Laccase-IN-5
<p>Laccase-IN-5 (Compound 2b) is an inhibitor of laccase with an IC50 of 0.82 μM. It enhances cell membrane permeability, restricts mycelial growth, disrupts cell walls, and induces oxidative stress responses. Laccase-IN-5 exhibits antifungal activity against various plant pathogenic fungi and oomycetes, effectively inhibiting B. dothidea with an EC50 of 0.96 mg/L.</p>Formula:C16H17FN2OColor and Shape:SolidMolecular weight:272.317
