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(2.949 produits)
- Antibiotique(918 produits)
- Antifection(23 produits)
- DHFR(32 produits)
- Synthèse ADN/ARN(706 produits)
- VHB(176 produits)
- Protéase du VIH(447 produits)
- HSV(91 produits)
- Intégrase(2 produits)
- Ribosome(13 produits)
Affichez 2 plus de sous-catégories
5832 produits trouvés pour "Microbiologie/Virologie"
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CRS-3123
CAS :<p>CRS-3123, a methionyl-tRNA synthetase inhibitor, is used potentially for the treatment of enteric infections.</p>Formule :C19H19Br2N3O2SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :513.25Antiviral agent 67
CAS :<p>Antiviralagent 67 (compound PC6) is an inhibitor of DENVNS5 (RNA-dependent RNA polymerase) with a Ki value of 1.12 nM.</p>Formule :C19H19N3OCouleur et forme :SolidMasse moléculaire :305.374Antibacterial agent 99
CAS :<p>Compound 7b (Antibacterial agent 99) is an effective agent with antibacterial, antifungal properties and no haemolytic activity.</p>Formule :C27H27BrN2Couleur et forme :SolidMasse moléculaire :459.42Asukamycin
CAS :<p>Asukamycin, from S. nodosus asukaensis, is a polyketide antibiotic inhibiting tumor cells by activating caspases 8 and 3.</p>Formule :C31H34N2O7Couleur et forme :SolidMasse moléculaire :546.61FGI-106
CAS :<p>FGI-106 combats Ebola, Rift Valley, Dengue Fever, HCV, and HIV-1; EC50s range from 100-900 nM.</p>Formule :C28H38N6Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :458.64HIV-IN-3
<p>HIV-IN-3 (Compound 22a) is a potent inhibitor of HIV (IC50: 1.5 μM). HIV-IN-3 has potential for the study of HIV-related diseases.</p>Formule :C21H32ClN7O3Couleur et forme :SolidMasse moléculaire :465.98Flutimide
CAS :<p>Flutimide: Endonuclease inhibitor, IC50 = 3μM, for research on acute respiratory diseases like influenza.</p>Formule :C12H18N2O3Couleur et forme :SolidMasse moléculaire :238.28(S)-ZG197
<p>(S)-ZG197 is a compound that acts as a highly selective activator of the Staphylococcus aureus Caseinolytic Protease P (Sa ClpP), demonstrating efficacy at a</p>Formule :C28H35F3N4O3Couleur et forme :SolidMasse moléculaire :532.6SARS-CoV-2-IN-6
<p>SARS-CoV-2-IN-6 is an inhibitor of SARS-CoV-2 3CLpro with the IC 50 value of 73 nM.</p>Formule :C17H13ClN2O2Couleur et forme :SolidMasse moléculaire :312.75DIDS
CAS :<p>DIDS inhibits anion exchangers reversibly then irreversibly and blocks RAD51.</p>Formule :C16H10N2O6S4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :454.52Methyl 3-oxodecanoate
CAS :<p>Methyl 3-oxodecanoate exhibits virulence factor activity against human pathogens and shows effects on Synechococcus elongatus (a species of fluorescent algae) as well as on culture supernatant. Additionally, Methyl 3-oxodecanoate inhibits DNA synthesis by suppressing protein synthesis at the translation initiation level.</p>Formule :C11H20O3Couleur et forme :SolidMasse moléculaire :200.275CYP2C19-IN-1
<p>CYP2C19-IN-1: potent CYP2C19 inhibitor, non-genotoxic, non-hepatotoxic, blocks RdRP (Ki: 6.16 μM), useful for ZIKV research.</p>Formule :C26H26N2O6SCouleur et forme :SolidMasse moléculaire :494.56epi-D-Captopril
CAS :<p>epi-D-Captopril (epi-D-SQ 14225) is a stereoisomer of Captopril and functions as an inhibitor of metallo-beta-lactamases (MBLs). The IC50 values of epi-D-Captopril for NDM-1, IMP-1, and VIM-2 are 64 μM, 173 μM, and 5.5 μM, respectively. This compound holds potential for research in MBLs-related antibiotic-resistant infections.</p>Formule :C9H15NO3SCouleur et forme :SolidMasse moléculaire :217.285Mt KARI-IN-1
<p>Mt KARI-IN-1 inhibits Mtb KARI with a 3.06 μM Ki, targeting tuberculosis.</p>Formule :C14H11N5O4S2Couleur et forme :SolidMasse moléculaire :377.4C-467929
CAS :<p>C-467929 is an inhibitor of the Nsp15 endoribonuclease, exhibiting an IC50 value of 8 μM. This compound binds to the SARS-CoVNsp15 protein and is applicable for infection research.</p>Formule :C29H20N4O10Couleur et forme :SolidMasse moléculaire :584.494'-Ethynyl-2'-deoxyadenosine
CAS :<p>4'-E-dA is a potent nucleoside RT inhibitor for drug-resistant HIV (EC50: 98 nM in MT-4 cells).</p>Formule :C12H13N5O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :275.26L 689065
CAS :<p>L 689065 is a 5-lipoxygenase inhibitor.</p>Formule :C35H33ClN2O3SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :597.17DNA polymerase-IN-6
CAS :<p>DNA polymerase-IN-6 (Compound 27) exhibits inhibitory activity against DNA polymerase, with EC50 values of 0.33 µM for HCMV, 1.9 µM for HSV-1, 0.76 µM for HSV-2, and 0.066 µM for EBV.</p>Formule :C26H28ClFN8O4Couleur et forme :SolidMasse moléculaire :571.003ACHN-975 TFA
CAS :<p>ACHN-975 TFA is a selective LpxC inhibitor with a subnanomolar inhibitory. It is against a wide range of gram-negative bacterias with low MIC values (≤1 μg/mL).</p>Formule :C22H24F3N3O6Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :483.4377WRN inhibitor 13
CAS :<p>WRN inhibitor 13 is an inhibitor of the WRN helicase with a pIC50 value ranging from 6 to 7.</p>Formule :C16H20N2O5SCouleur et forme :SolidMasse moléculaire :352.405Chitinase-IN-4
<p>Chitinase-IN-4 (compound 8f) is a potent and selective inhibitor of OfChi-h with an IC50 value of 0.1 μM and good insecticidal activity.</p>Formule :C21H24ClN7Couleur et forme :SolidMasse moléculaire :409.928-Hydroxyerythromycin A
CAS :<p>8-Hydroxyerythromycin A is a semi-synthetic antibiotic with antibacterial activity.</p>Formule :C37H67NO14Couleur et forme :SolidMasse moléculaire :749.926BMT-052
CAS :<p>BMT-052 is a potent and selective Pan-genotypic HCV NS5B Polymerase Inhibitor (EC50 = 7 nM).</p>Formule :C30H17D9F4N6O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :635.61Antibacterial agent 75
<p>Antibacterial agent 75 re-sensitizes VRSA to vancomycin.</p>Formule :C22H28N6OCouleur et forme :SolidMasse moléculaire :392.5Metesind Glucuronate
CAS :<p>Metesind Glucuronate is an antineoplastic. It also is a specific thymidylate synthase inhibitor.</p>Formule :C29H34N4O10SCouleur et forme :SolidMasse moléculaire :630.67WQ3810
CAS :<p>WQ3810 is an orally active fluoroquinolone, has potent antibacterial activities.</p>Formule :C22H22F3N5O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :461.44Kinamycin B
CAS :<p>Kinamycin B is an antibacterial agent with anticancer activity.</p>Formule :C20H16N2O8Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :412.35Antibacterial agent 79
<p>Antibacterial agent 79 is an antibacterial agent.</p>Formule :C18H27N3O2S3Couleur et forme :SolidMasse moléculaire :413.628-Deazafolic acid
CAS :<p>8-Deazafolic acid inhibits folate-dependent bacteria S. faecium & L. casei, and fights lymphoid leukemia L1210 in mice.</p>Formule :C20H20N6O6Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :440.41YKL-04-085
CAS :<p>YKL-04-085 inhibits viral translation effectively, with strong antiviral action at much lower doses than those affecting host-cell growth.</p>Formule :C30H29N5O2Couleur et forme :SolidMasse moléculaire :491.6NBTIs-IN-4
<p>NBTIs-IN-4, a broad-spectrum Gram-positive antibacterial, inhibits DNA rotamases/topoisomerase IV, with low resistance.</p>Formule :C22H24FN5O5SCouleur et forme :SolidMasse moléculaire :489.52NSC 641396
CAS :<p>NSC 641396 is a ribonucleotide reductase (RNR) inhibitor with an IC50 value of 1.2 μM. Additionally, it acts as an inhibitor of protein arginine N-methyltransferase 9 (PRMT9) and exhibits antitumor properties.</p>Formule :C18H13NO3Couleur et forme :SolidMasse moléculaire :291.301MsbA-IN-1
<p>MsbA-IN-1: Potent MsbA inhibitor (IC50: 4 nM), anti-E. coli (MIC: 79 μM), penetrates Gram-negative bacteria.</p>Formule :C23H18Cl2FNO3Couleur et forme :SolidMasse moléculaire :446.3Antifungal agent 40
<p>Antifungal agent 40 blocks C. albicans CYP51 in pocket II, hindering lanosterol demethylase and biofilm growth.</p>Formule :C22H20Cl2N4SeCouleur et forme :SolidMasse moléculaire :490.29Chitin synthase inhibitor 11
<p>Potent CHS inhibitor with an IC50 of 0.10 mM; exhibits broad-spectrum antifungal properties.</p>Formule :C24H24N4O8Couleur et forme :SolidMasse moléculaire :496.47PRRSV-IN-1
CAS :<p>PRRSV-IN-1 (Compound 4s) acts as an inhibitor of the nsp4 protease of PRRSV. It has an EC50 value of 0.45 μM against PRRSV, binds to the nsp4 protease with a Kd of 29.24 pM, and exhibits an IC50 value of 80.36 pM for nsp4 protease inhibition. PRRSV-IN-1 is applicable in antiviral infection research.</p>Formule :C19H18BrNO3Couleur et forme :SolidMasse moléculaire :388.255Antitubercular agent-22
<p>Antitubercular agent-22 combats Candida albicans (MIC: 2.34 μg/ml) and M. tuberculosis (MIC: 2 μg/ml).</p>Formule :C24H28FN5O8Couleur et forme :SolidMasse moléculaire :533.51Fosmanogepix
CAS :<p>Fosmanogepix (APX001) is a broad-spectrum oral antifungal that targets Gwt1 enzyme, transforming into active APX001A in the body.</p>Formule :C22H21N4O6PDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :468.40FtsZ-IN-4
<p>FtsZ-IN-4 is an oral FtsZ inhibitor with strong antibacterial effects and good drug traits, low toxicity (CC50 >20μg/mL).</p>Formule :C21H16ClF2NO2Couleur et forme :SolidMasse moléculaire :387.81Ceftolozane TFA
CAS :<p>Ceftolozane TFA is a cephalosporin class antibiotic (antibiotic) designed to inhibit Gram-negative bacterial infections. Additionally, it can be utilized in the synthesis of novel antibiotics (antibiotic) that are more efficacious and safer.</p>Formule :C25H31F3N12O10S2Couleur et forme :SolidMasse moléculaire :780.71DRF-8417
CAS :<p>DRF-8417 is an oxazolidinone antibiotic, active against both Gram-positive bacteria and fastidious Gram-negative bacteria. The MIC50 and MIC90 values of DRF-8417 for Gram-positive pathogens range between 0.06-1 mg/L.</p>Formule :C15H17N3O5SCouleur et forme :SolidMasse moléculaire :351.38DNA crosslinker 6
CAS :<p>DNA crosslinker 6 (compound 1) is an anti-mitotic agent known for its strong binding affinity to AT-DNA and inhibition of AT-hook 1 binding to DNA (IC50=0.03 µM). Additionally, it exhibits anti-protozoal activity, effectively inhibiting T. brucei with an EC50 of 0.83 µM.</p>Formule :C19H21N7OCouleur et forme :SolidMasse moléculaire :363.42Antifungal agent 28
<p>Antifungal 28 disrupts Candida, hits fluconazole-resistant strains, and inhibits biofilms.</p>Formule :C22H29N5OSCouleur et forme :SolidMasse moléculaire :411.56VNI
CAS :<p>VNI is an effective inhibitor of CYP51. It suppresses sterol synthesis in Trypanosoma cruzi, exhibiting anti-Trypanosoma cruzi activity.</p>Formule :C26H19Cl2N5O2Couleur et forme :SolidMasse moléculaire :504.37WR-27653
CAS :<p>WR-27653 (RC-12), a derivative of Catechol, demonstrates significant activity against hypnozoites in the Plasmodium cynomolgi-Rhesus monkey (Macaca mulatta) model, which is considered the gold standard. Additionally, WR-27653 exhibits antimalarial properties.</p>Formule :C20H36BrN3O2Couleur et forme :SolidMasse moléculaire :430.423NBD-10007
CAS :<p>NBD-10007 is an inhibitor of HIV-1 entry.</p>Formule :C20H25ClN4O3SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :436.96Erythromycin B
CAS :<p>Erythromycin B exhibits antimalarial activity by effectively inhibiting the asexual growth of Plasmodium falciparum.</p>Formule :C37H67NO12Couleur et forme :SolidMasse moléculaire :717.93Carbonic anhydrase inhibitor 28
<p>Carbonic anhydrase inhibitor28 (Compound 11) serves as an inhibitor for the Pseudomonas aeruginosa carbonic anhydrase. It exhibits antibacterial activity, with minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) values of 0.5 and 1 μg/mL, respectively, against P. aeruginosa. Carbonic anhydrase inhibitor28 is utilized in research focused on anti-infection applications.</p>Formule :C24H24FN5O7SCouleur et forme :SolidMasse moléculaire :545.54L 702007
CAS :<p>L 702007 is an inhibitor of HIV-1 reverse transcriptase.</p>Formule :C18H25N3O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :315.41SARS-CoV-2-IN-106
CAS :<p>SARS-CoV-2-IN-106 (compound 19) is a SARS-CoV-2 papain-like protease inhibitor, displaying IC50 values of 0.44 μM for papain-like proteases and 0.18 μM for viral replication.</p>Formule :C31H38FN5O2Couleur et forme :SolidMasse moléculaire :531.66
