Microbiologie/Virologie
Les inhibiteurs en microbiologie et virologie sont des composés qui ciblent les microorganismes, y compris les bactéries, les virus et les champignons, perturbant leur croissance, leur réplication ou leur survie. Ces inhibiteurs sont essentiels pour étudier la pathogénie microbienne, comprendre les mécanismes de résistance et développer de nouvelles thérapies antimicrobiennes et antivirales. Les inhibiteurs de cette catégorie sont utilisés pour combattre les maladies infectieuses, explorer l'écologie microbienne et étudier les interactions hôte-pathogène. Chez CymitQuimica, nous offrons une large sélection d'inhibiteurs de haute qualité en microbiologie et virologie pour soutenir vos recherches en maladies infectieuses, microbiologie et virologie.
Sous-catégories appartenant à la catégorie "Microbiologie/Virologie"
- Antibactérien(2.966 produits)
- Antibiotique(922 produits)
- Antifection(23 produits)
- DHFR(33 produits)
- Synthèse ADN/ARN(710 produits)
- VHB(177 produits)
- Protéase du VIH(450 produits)
- HSV(91 produits)
- Intégrase(2 produits)
- Ribosome(13 produits)
Affichez 2 plus de sous-catégories
5858 produits trouvés pour "Microbiologie/Virologie"
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Protactin
CAS :<p>Protactin, a new antibiotic metabolite, is a possible precursor of the actinomycins.</p>Formule :C32H48N6O8Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :644.77Heneicomycin
CAS :Heneicomycin is a precursor antibiotic of Aurodoxin.Formule :C44H62N2O11Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :794.97Antibacterial agent 220
<p>Antibacterialagent 220 is a potent antibacterial compound that directly disrupts bacterial cell membranes. It is effective against both Gram-positive and Gram-negative bacteria, including resistant strains.</p>Formule :C37H54N8O8SMasse moléculaire :770.37853Protorubradirin
CAS :<p>Protorubradirin is an antibiotic that can be isolated from the non-pigmented Streptomyces achromogenes var. rubradiris alongside Rubradirin. It exhibits inhibitory activity against HIV reverse transcriptase. In vitro studies show that Protorubradirin also inhibits strains of Staphylococcus aureus and Streptococcus. In infected mice, subcutaneous administration of Protorubradirin demonstrates in vivo efficacy against antibiotic-resistant Staphylococcus aureus strains. However, oral administration may significantly reduce its activity compared to Rubradirin, possibly due to its C-nitroso sugar decomposing more rapidly in acidic gastric conditions.</p>Formule :C48H46N4O19Masse moléculaire :982.89AC 4437
CAS :AC 4437 is an aminoglycoside antibiotic.Formule :C14H28N6O8Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :408.41228-O-Imidazolyl-azepano-betulin
SARS-CoV-2-IN-70 (compound 6) is an effective inhibitor of SARS-CoV-2, with an IC50 value of 3.2 μM.Formule :C34H53N3O2Masse moléculaire :535.41378Mpro ligand 1
<p>Mpro ligand 1 is the target protein ligand for PROTACSARS-CoV-2 Mpro degrader-3. It is the active form of Mpro ligand 2.</p>Formule :C22H32N3NaO9SMasse moléculaire :537.1757OP-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>Formule :C142H246N46O31Masse moléculaire :3093.76BMS-955176 TFA
CAS :<p>GSK3532795: Oral HIV-1 maturation inhibitor, broad virus coverage, EC50: 15 nM, good preclinical pharmacokinetics.</p>Formule :C44H64N2O8SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :781.06MBL-IN-2
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.Formule :C9H12F3NO3SMasse moléculaire :271.049KSK-104
<p>KSK-104 exhibits potent antibacterial activity against Mycobacterium tuberculosis, with a minimum inhibitory concentration (MIC) of 0.78 μM. Its mechanism of action primarily involves the synthesis and salvage pathway of pyridoxal 5'-phosphate (PLP), as well as PLP-dependent enzymes and the oxidative stress network. KSK-104 is a promising candidate for developing novel anti-tuberculosis drugs targeted at drug-resistant strains of Mycobacterium tuberculosis.</p>Formule :C22H20N2O4Masse moléculaire :376.14231(-)-Isopinocampheol
CAS :<p>(-)-Isopinocampheol is a monoterpene and a component of several plant essential oils. It showed dual viricidal activity against herpes simplex virus 1.</p>Formule :C10H18OCouleur et forme :SolidMasse moléculaire :154.2493Antibacterial agent 182
Antibacterialagent 182 (compound 8c) is an antibacterial agent that exhibits activity against various Gram-positive bacteria, particularly displaying efficacy against vancomycin-resistant Enterococcus faecium (MIC ≤0.125 μg/mL). At sub-MIC levels, Antibacterialagent 182 can inhibit biofilm formation by Staphylococcus aureus and Pseudomonas aeruginosa.Formule :C14H5Br4F3N2OSMasse moléculaire :621.68082Antibacterial agent 226
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.Formule :C24H26F3N3O2Masse moléculaire :445.19771SARS-CoV-2 Mpro-IN-7
<p>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 (</p>Formule :C33H34Br2N3O5PDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :743.42Niddamycin
CAS :Niddamycin is a new macrolide antibiotic.Formule :C40H65NO14Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :783.953Acryl42-10
<p>Acryl42-10 serves as a covalent inhibitor for the SARS-CoV-2 Nsp14 N7-Methyltransferase, exhibiting an inhibition concentration (IC50) of 7 μM [1].</p>Formule :C20H24ClN3O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :405.88Cangorinine E-1
CAS :<p>Cangorinine E-1 (compound 11), a dihydroagarofuran sesquiterpenoid derivative, exhibits weak inhibitory effects on herpes simplex virus type II (HSV) [1].</p>Formule :C43H49NO18Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :867.85PBP10
CAS :<p>FPR2 antagonist; blocks NADPH oxidase, no FPR1 effect; hinders cell movement; antiviral against influenza.</p>Formule :C84H126N24O15Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :1712.1Fumigaclavine A
CAS :<p>Fumigaclavine A, a clavine alkaloid mycotoxin produced by Aspergillus fumigatus, can be isolated from mold-contaminated silage [1].</p>Formule :C18H22N2O2Couleur et forme :SolidMasse moléculaire :298.38BMAP-28
CAS :<p>BMAP-28, an antibiotic peptide, induces cell death by triggering the mitochondrial permeability transition pore and serves as a research tool in the study of</p>Formule :C145H250N44O29Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :3073.81D-4-77
<p>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.</p>Formule :C23H34BrN3O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :512.44Dendryphiellin D
CAS :<p>Dendryphiellin D from Septoria rudbeckiae fungus inhibits NO production.</p>Formule :C21H28O5Couleur et forme :SolidMasse moléculaire :360.44Antibacterial agent 54
CAS :<p>Antibacterial agent 54 (example 20) is a antibacterial agent.</p>Formule :C9H11N4NaO5S2Couleur et forme :SolidMasse moléculaire :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>Formule :C25H31ClO6Couleur et forme :SolidMasse moléculaire :462.97Calpain inhibitor V
CAS :<p>Calpain Inhibitor V (Mu-Val-HPh-FMK) is a cell-permeable, irreversible calpain inhibitor with demonstrated anti-chlamydial activity [1].</p>Formule :C21H30FN3O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :407.48Amphocil
CAS :<p>Amphocil is used to treat patients with invasive fungal infection.</p>Formule :C74H119NO21SCouleur et forme :SolidMasse moléculaire :1390.81Plutavimab
CAS :<p>Plutavimab is a humanized IgG1-κ monoclonal antibody targeting the receptor binding domain (RBD) of the SARS-CoV-2 spike (S) glycoprotein [1] [2].</p>Degré de pureté :98%Couleur et forme :Liquid7-51A
<p>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 as</p>Degré de pureté :98%Couleur et forme :Odour SolidGSK2336805
CAS :<p>GSK-2336805, an HCV NS5A inhibitor, is effective against genotypes 1, 4, 5, and some of 6.</p>Formule :C42H52N8O8Couleur et forme :SolidMasse moléculaire :796.91LF11
CAS :<p>LF11 displays antimicrobial activity.</p>Formule :C69H112N26O14Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :1529.79LFF 571
CAS :<p>LFF 571 is an inhibitor of protein-synthesizing GTPase (Elongation Factor).</p>Formule :C60H63N13O13S6Couleur et forme :SolidMasse moléculaire :1366.6Moloney murine leukemia virus RT
<p>Moloney murine leukemia virus reverse transcriptase (MMLV RT) is a monomeric replicative polymerase intrinsic to the retrovirus life cycle [1].</p>Degré de pureté :98%Couleur et forme :Odour SolidUrease
CAS :<p>Urease, made by various bacteria, aids pathogen virulence and is key to Helicobacter pylori's stomach colonization.</p>Couleur et forme :Solid(±)-Emodin bianthrone
CAS :<p>(±)-Emodin bianthrone (compound 10), a naturally occurring substance, demonstrates antimalarial, antitubercular, and antifungal properties [1].</p>Formule :C30H22O8Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :510.49Antibacterial agent 41
CAS :<p>Antibacterial agent 41 (example 3) is a antibacterial agent.</p>Formule :C9H9F3N4NaO6SCouleur et forme :SolidMasse moléculaire :381.24Wulfenioidin F
<p>Wulfenioidin F, a diterpenoid isolated from the whole plant of Orthosiphon wulfenioides, exhibits anti-Zika virus (ZIKV) activity with an EC50 of 8.07 μM and</p>Formule :C21H28O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :328.45HBV-IN-36
<p>HBV-IN-36 (also known as compound 42) is a hepatitis B virus (HBV) inhibitor with an IC50 of 2 μM, exhibiting anti-HBV activity characterized by an EC50 of 0.58</p>Formule :C21H18ClFN4O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :412.84MptpB-IN-2
<p>MptpB-IN-2 (compound 20), a selective inhibitor for mycobacterium tuberculosis protein tyrosine phosphatase B (MptpB), exhibits half maximal inhibitory</p>Formule :C23H20F3NO3S2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :479.54SARS-CoV-2-IN-65
<p>SARS-CoV-2-IN-65 (compound 2f (81)) is a potent, orally active reversible inhibitor of SARS-CoV-2 entry, primarily obstructing the RBD:ACE2 interaction and</p>Degré de pureté :98%Couleur et forme :Odour Solid10-Hydroxyaloin A
CAS :<p>Hydroxyaloin A (10-10-Hydroxyaloin A) is a potent inhibitor of SARS-CoV-2, demonstrating significant efficacy in binding to the active site of the SARS-CoV-2</p>Formule :C21H22O10Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :434.39Tuvirumab
CAS :<p>Tuvirumab, a human IgG1 monoclonal antibody, targets HBsAg with high affinity (K=3.6 nM) for chronic hepatitis B research.</p>Couleur et forme :LiquidCefotiam dihydrochloride hydrate
<p>Cefotiam dihydrochloride hydrate: parenteral cephalosporin antibiotic with broad-spectrum Gram-positive and Gram-negative activity.</p>Formule :C18H25Cl2N9O4S3·xH2OCouleur et forme :SolidMasse moléculaire :C18H25Cl2N9O4S3.xH2ORNA binder 1
<p>RNA binder 1 (Compound 4b) is an RNA-binding agent capable of crossing the blood-brain barrier. It selectively binds to the G-quadruplex structure of the G4C2 repeat sequence RNA of the C9orf72 gene. This compound significantly reduces levels of the toxic polypeptides poly(GA) and poly(GP) in cells derived from amyotrophic lateral sclerosis (ALS) patients, while it has no significant impact on the antisense polypeptide poly(PR), demonstrating selectivity for sense RNA. RNA binder 1 is useful for studying ALS and frontotemporal dementia (FTD).</p>Formule :C22H20N10S2Couleur et forme :SolidMasse moléculaire :488.13138LF 11 acetate
<p>LF 11 acetate exhibits antibacterial activities and can be used for the development of endotoxin-neutralizing and antibacterial agents.</p>Formule :C71H116N26O16Degré de pureté :98.85%Couleur et forme :SolidMasse moléculaire :1589.85AI 3-16787
CAS :<p>AI 3-16787 is an HIV-1 integrase inhibitor exhibiting inhibitory activity against strand transfer in the presence of Mn²⁺.</p>Formule :C21H24O4Degré de pureté :99.01%Couleur et forme :SolidMasse moléculaire :340.41Lentinellic acid
CAS :<p>Lentinellic acid, derived from Lentinellus species (Basidiomycetes), is an antimicrobial and cytotoxic sesquiterpenoid and biologically active protoilludane.</p>Formule :C18H20O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :316.35Vecantoxatug
CAS :<p>Vecantoxatug is a humanized monoclonal antibody designed to target Clostridium tetani toxin (TeNT, a neurotoxin). It specifically binds to the tetanus toxin, preventing the toxin from interacting with cell receptors and thus exhibits antitoxin activity. Vecantoxatug holds potential for tetanus research.</p>Couleur et forme :LiquidBAY38-7690
CAS :<p>BAY38-7690, a hepatitis B virus inhibitor, may have potential for future therapeutic regimens to combat chronic HBV infection.</p>Formule :C19H16ClF2N3O2Couleur et forme :SolidMasse moléculaire :391.8Antibacterial agent 233
<p>Antibacterialagent 233 (Compound 7c) demonstrates inhibitory activity against Helicobacter pylori, with a minimum inhibitory concentration (MIC) ranging from 0.4 to 1.6 μg/mL. It inhibits jack bean urease with an IC50 of 0.27 μg/mL, alters the permeability of the H. pylori cell membrane, and leads to the leakage of cellular contents. Antibacterialagent 233 shows metabolic stability in both whole blood and artificial gastric fluid. Additionally, it exhibits antitumor activity against U2OS in mice.</p>Couleur et forme :Odour Solid
