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(2.959 produits)
- Antibiotique(921 produits)
- Antifection(23 produits)
- DHFR(33 produits)
- Synthèse ADN/ARN(708 produits)
- VHB(176 produits)
- Protéase du VIH(449 produits)
- HSV(91 produits)
- Intégrase(2 produits)
- Ribosome(13 produits)
Affichez 2 plus de sous-catégories
5843 produits trouvés pour "Microbiologie/Virologie"
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CAY10784
CAS :<p>CAY10784(STAT3-IN-17) is a STAT3 inhibitor with antiproliferative and antitumor activities. CAY10784 showed antibacterial activity against Clostridium difficile</p>Formule :C11H6F3N3O3SDegré de pureté :99.74%Couleur et forme :SolidMasse moléculaire :317.24SMR000071098
CAS :<p>SMR000071098 is an inhibitor of Fe-S cluster-dependent aconitase. SMR000071098 interacts with Suf proteins to inhibit iron-sulfur (Fe-S) cluster assembly.</p>Formule :C17H12N2O2Couleur et forme :SolidMasse moléculaire :276.29TLC3407-3786
CAS :<p>MMV665916: Antimalarial quinazolinedione, effective against P. falciparum (EC50 = 0.4 µM), high selectivity (SI > 250).</p>Formule :C19H19N3O4Couleur et forme :SolidMasse moléculaire :353.37Goitrin
CAS :<p>Goitrin, from glucosinolate reactions, blocks thyroid peroxidase and iodine use, and fights H1N1.</p>Formule :C5H7NOSCouleur et forme :SolidMasse moléculaire :129.18Anti-infective agent 1
CAS :<p>Compound 3a: potent, selective antiprotozoal/antimycobacterial. IC50: P. falciparum 10.95 μM, T. brucei 0.06 μM. MIC against M. smegmatis: 8 μg/mL.</p>Formule :C16H10O2Couleur et forme :SolidMasse moléculaire :234.25ZINC04177596
CAS :<p>ZINC04177596 is a novel Nef Protein Inhibitor with anti-HIV activity.</p>Formule :C22H16N6O4Couleur et forme :SolidMasse moléculaire :428.4HIV-1 inhibitor-42
CAS :<p>HIV-1 inhibitor-42 (5b) strongly blocks HIV-1 (IC50: 0.06μM) and its RT RNA/DNA polymerases (IC50: 0.518/0.072μM).</p>Formule :C22H20N2O5SCouleur et forme :SolidMasse moléculaire :424.47SARS-CoV-2 nsp13-IN-3
CAS :<p>SARS-CoV-2 nsp13-IN-3 (Compound C3) is a small molecule inhibitor of SARS-CoV-2 non-structural protein 13 (nsp13) that acts on nsp13 ssDNA+ATPase (IC50: 32 μM).</p>Formule :C24H27N7OCouleur et forme :SolidMasse moléculaire :429.52YM-53601
CAS :<p>YM-53601 is an SQS inhibitor that inhibits adipogenic biosynthesis and lipid secretion in rodents.YM-53601 is a cholesterol-lowering agent that inhibits FDFT1.</p>Formule :C21H22ClFN2ODegré de pureté :99.65%Couleur et forme :SolidMasse moléculaire :372.86MMV688845
CAS :<p>MMV688845: NTM RNA polymerase inhibitor, kills Mycobacterium abscessus, and fights TB.</p>Formule :C24H25N3O3SCouleur et forme :SolidMasse moléculaire :435.54ORM-3819
CAS :<p>ORM-3819 is a potent and selective PDE III inhibitor. ORM-3819 promotes cardiac contractility through Ca(2+) sensitization.</p>Formule :C19H19N5O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :397.38Chitin synthase inhibitor 10
CAS :<p>Chitin Synthase Inhibitor 10: potent antifungal with 0.11 mM IC50, effective against resistant C. albicans and C. neoformans. Used in IFI research.</p>Formule :C24H23Br2N3O6Couleur et forme :SolidMasse moléculaire :609.26Anti-inflammatory agent 14
CAS :<p>Anti-inflammatory agent 14 (compound 28) has a MIC 50 of 2 μM for Mtb H37Rv. Anti-inflammatory agent 14 is also an anti-inflammatory agent [1].</p>Formule :C16H16N2O2SCouleur et forme :SolidMasse moléculaire :300.38SARS-CoV-2 nsp13-IN-6
CAS :<p>nsp13-IN-6 inhibits SARS-CoV-2 nsp13, targeting ssDNA+ATPase (IC50: 27 μM) and ssDNA-ATPase (IC50: 33 μM) for COVID-19 research.</p>Formule :C21H19N5O3SCouleur et forme :SolidMasse moléculaire :421.47Antibacterial agent 126
<p>Antibacterial agent 126 combats biofilm, disrupts membranes, and boosts ROS/RNS to prevent drug resistance.</p>Formule :C21H24NO6PCouleur et forme :SolidMasse moléculaire :417.39HBV-IN-14
CAS :<p>HBV-IN-14: a pyridinopyrimidinone, potent cccDNA inhibitor for HBV study (patent WO2021190502A1, comp 5).</p>Formule :C22H21ClN2O5Couleur et forme :SolidMasse moléculaire :428.87FPI-1602
CAS :<p>FPI-1602 is a β-lactamase inhibitor with strong antimicrobial activity against Pseudomonas aeruginosa, Escherichia coli, and Enterobacter species [1].</p>Formule :C11H17N5O7SCouleur et forme :SolidMasse moléculaire :363.35KAR425
CAS :<p>KAR425 is a bipyrrole tambjamines. KAR425 has antimalarial activity against multidrug-resistant P. yoelii in mice.</p>Formule :C19H27N3Couleur et forme :SolidMasse moléculaire :297.44Bederocin
CAS :<p>Bederocin (REP8839), a METS inhibitor, has strong activity against S. aureus, S. pyogenes, and Gram-positive bacteria.</p>Formule :C20H21BrFN3OSDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :450.37PC58538
CAS :<p>PC58538 is an inhibitor of FtsZ protein, a important role in the division machinery of bacterial cells.</p>Formule :C24H25NO3Couleur et forme :SolidMasse moléculaire :375.46TBI-166
CAS :<p>TBI-166, an oral riminophenazine, treats tuberculosis with fewer side effects than Clofazimine.</p>Formule :C32H30F3N5O3Couleur et forme :SolidMasse moléculaire :589.61SARS-CoV-2 3CLpro-IN-1
CAS :<p>SARS-CoV-2 3CLpro-IN-1 is a potent inhibitor of the key enzyme 3CL pro in coronaviruses, promising for antiviral drug R&D.</p>Formule :C27H30ClN3O3SCouleur et forme :SolidMasse moléculaire :512.06HCV-IN-35
CAS :<p>HCV-IN-35 is a potent inhibitor of HCV and shows potential for infectious disease research.</p>Formule :C30H36ClN5Couleur et forme :SolidMasse moléculaire :502.09RO5464466
CAS :<p>RO5464466 is an inhibitor of influenza A virus (H1N1) fusion.</p>Formule :C16H26N2O3SCouleur et forme :SolidMasse moléculaire :326.454-Piperidinecarboxamide
CAS :<p>4-Piperidinecarboxamide is a mycobacterial aspartyl-tRNA synthetase (AspS) inhibitor and a potential anti-tuberculosis (TB) agent [1].</p>Formule :C16H15Cl2N3O2SCouleur et forme :SolidMasse moléculaire :384.28Tropesin
CAS :<p>Tropesin is a non-steroidal anti-inflammatory agent (NSAIA) that has inhibitory effects on the growth of Xylaria green.</p>Formule :C28H24ClNO6Couleur et forme :SolidMasse moléculaire :505.95Ceftobiprole medocaril sodium
CAS :<p>Ceftobiprole medocaril sodium (BAL5788) is a prodrug of broad-spectrum cephalosporin active against MRSA, VRSA, and resistant streptococci.</p>Formule :C26H25N8NaO11S2Couleur et forme :SolidMasse moléculaire :712.64Exeporfinium chloride
CAS :<p>Exeporfinium chloride(XF-73) is an antimicrobial agent that can weaken bacterial cell walls.</p>Formule :C44H50Cl2N6O2Couleur et forme :SolidMasse moléculaire :765.81UIAA-II-232
CAS :<p>UIAA-II-232 (compound 19b) is a potent inhibitor of DNA gyrase catalytic (IC 50= 3.5 μM).</p>Formule :C20H24FN5O3Couleur et forme :SolidMasse moléculaire :401.43Elsamitrucin
CAS :<p>Elsamitrucin, a heterocyclic antibiotic, disrupts DNA replication by intercalating into G-C sequences and inhibiting topoisomerases.</p>Formule :C33H35NO13Couleur et forme :SolidMasse moléculaire :653.63MMV008138
CAS :<p>MMV008138 inhibits the growth of P. falciparum Dd2 strain (IC50 of 250 nM).</p>Formule :C18H14Cl2N2O2Couleur et forme :SolidMasse moléculaire :361.22Aranotin
CAS :<p>Aranotin, from Arachniotus aureus, inhibits RNA viruses by blocking RNA polymerase.</p>Formule :C20H18N2O7S2Couleur et forme :SolidMasse moléculaire :462.5Metallo-β-lactamase-IN-6
CAS :<p>Metallo-β-lactamase-IN-6 is a highly effective inhibitor of VIM-Type metallo-β-lactamase, demonstrating IC 50 values of 0.56 μM, 29.50 μM, and 5.78 μM for VIM-2</p>Formule :C10H9N3O2Couleur et forme :SolidMasse moléculaire :203.2BMY-27709
CAS :<p>BMY-27709 inhibits influenza growth (IC50: 3-8 μM, A/WSN/33), targets H1/H2 subtypes via hemagglutinin, ineffective against H3/B Lee/40.</p>Formule :C17H24ClN3O2Degré de pureté :98.37% - 98.55%Couleur et forme :SolidMasse moléculaire :337.84Vapendavir diphosphate
CAS :<p>Vapendavir diphosphate binds enterovirus capsids, inhibiting EV71 replication effectively (EC50: 0.5-1.4 μM).</p>Formule :C21H32N4O11P2Degré de pureté :98.75% - 98.75%Couleur et forme :SolidMasse moléculaire :578.45DVR-01
CAS :<p>DVR-01 is an HBV capsid inhibitor and can be used in studies about the treatment of Hepatitis B virus (HBV) infection and related conditions.</p>Formule :C20H23ClN2O3SDegré de pureté :99.95%Couleur et forme :SolidMasse moléculaire :406.93Bofumustine
CAS :<p>Bofumustine is a chloroethyl nitrosourea with anti tumor properties.</p>Formule :C18H21ClN4O9Couleur et forme :SolidMasse moléculaire :472.83FR900098 (sodium salt)
CAS :<p>FR900098, a fosmidomycin derivative, has potent antimalarial effects, targeting DOXP reductoisomerase and eradicating P. vinckei in mice at >10 mg/kg.</p>Formule :C5H12NNaO5PCouleur et forme :SolidMasse moléculaire :220.117MurA-IN-2
CAS :<p>MurA-IN-2: potent MurA inhibitor, IC50 of 39μM, chloroacetamide with aliphatic amine; has antibacterial properties.</p>Formule :C12H20ClNOCouleur et forme :SolidMasse moléculaire :229.75BMVC
CAS :<p>BMVC is a potent G-quadruplex (G4) stabilizer and a selective telomerase inhibitor (IC50: ~0.2 μM) with anticancer activities.</p>Formule :C28H25I2N3Couleur et forme :SolidMasse moléculaire :657.33HadAB-IN-1
CAS :<p>HadAB-IN-1: potent TB research chemical; IC50 = 0.03μM; inhibits HadAB, affecting Mtb mycolic acid synthesis.</p>Formule :C19H17BrClN3O3SCouleur et forme :SolidMasse moléculaire :482.78Antibacterial agent 74
CAS :<p>Antibacterial agent 74 (compound 36) has anti-Salmonella activity [1].</p>Formule :C16H20N2O3Couleur et forme :SolidMasse moléculaire :288.3441F5
CAS :<p>41F5: Anti-fungal with MIC50 0.4-0.8 μM and IC50 0.87 μM against Histoplasma; 62x more selective for yeast vs host cells.</p>Formule :C21H22N2OSCouleur et forme :SolidMasse moléculaire :350.48Antibacterial agent 67
CAS :<p>Antibacterial agent 67 blocks succinate dehydrogenase more effectively than haloperidol, with IC50 of 0.03 μM vs 4.40 μM.</p>Formule :C24H15F6N5OCouleur et forme :SolidMasse moléculaire :503.4Quinuronium Sulfate
CAS :<p>Quinuronium sulfate treats Babesia in calves; doesn't stop carrier state; may lead to hepatic fat degeneration, not GSH depletion.</p>Formule :C22H23N4O5SCouleur et forme :SolidMasse moléculaire :455.51Diamthazole hydrochloride
CAS :<p>Diamthazole (Dimazole) hydrochloride, an antifungal agent, is utilized in infection research.</p>Formule :C15H24ClN3OSCouleur et forme :SolidMasse moléculaire :329.89Influenza virus-IN-4
CAS :<p>Influenza virus-IN-4 (compound 11e) is a potent inhibitor of influenza virus neuraminidase, acting on H5N1 (IC50: 3.4 μM), H5N2 (IC50: 0.094 μM), H5N6 (IC50: 0.</p>Formule :C23H31FN2O4Couleur et forme :SolidMasse moléculaire :418.5Dealanylalahopcin
CAS :<p>Dealanylalahopcin is a procollagen prolyl-4-hydroxylase inhibitor.</p>Formule :C6H10N2O5Couleur et forme :SolidMasse moléculaire :190.15RSV/IAV-IN-3
CAS :<p>RSV/IAV-IN-3 is a dual inhibitor of RSV (EC50: 2.92μM) and IAV (EC50:1.90μM), blocking virus replication post-entry.</p>Formule :C19H19BrN2O3SCouleur et forme :SolidMasse moléculaire :435.332-Hydroxydocosanoic acid
CAS :<p>2-Hydroxydocosanoic acid exhibits antioxidant, cholinesterase inhibitory, and antimicrobial properties [1].</p>Formule :C22H44O3Couleur et forme :SolidMasse moléculaire :356.58Antitubercular agent-17
CAS :<p>Compound 8a: Antitubercular with MIC of 2 μg/ml for H37Rv, Spec 192, 210; 128 μg/ml for Spec 800. Selective effects.</p>Formule :C14H12BrN5OCouleur et forme :SolidMasse moléculaire :346.18CRS400393
CAS :<p>CRS400393: Anti-tuberculosis drug, MIC - M. abs.: 0.03μg/mL, M. avium: 2μg/mL, M. intracellulare: ≤0.12 μg/mL, M. tuberculosis: ≤0.12 μg/mL.</p>Formule :C18H20Cl2N2OSDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :383.34Aztreonam lysine
CAS :<p>Aztreonam lysine is an inhaled anti-pseudomonal treatment for people who have pulmonary Pseudomonas aeruginosa infection with cystic fibrosis (CF).</p>Formule :C19H31N7O10S2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :581.62Salazopyridazine
CAS :<p>Salazopyridazine is an antibacterial agent that inhibits ulcerative colitis. salazopyridazine can be used in the study of rheumatic diseases.</p>Formule :C18H15N5O6SCouleur et forme :SolidMasse moléculaire :429.41VEC-5
CAS :<p>VEC-5: an HIV-1 inhibitor, outperforms RN18 by better binding with Vif in studies.</p>Formule :C29H21NO4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :447.48P516-0475
CAS :<p>P516-0475, a novel inducer, enhances Streptococcus quorum sensing by blocking PepO, stabilizing SHP pheromones.</p>Formule :C15H17N5O3Couleur et forme :SolidMasse moléculaire :315.33PC170942 Sodium
CAS :<p>PC170942 Sodium is a water-soluble bacterial cytokinesis inhibitor that acts by inhibiting FtsZ.</p>Formule :C24H24ClNO2SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :425.97Antileishmanial agent-8
CAS :<p>Compound 18: Antileishmanial, IC50=5.64 μM for L. donovani, low toxicity in L-6 cells, IC50=73.9 μM.</p>Formule :C18H16O4Couleur et forme :SolidMasse moléculaire :296.32SARS-CoV-2 Mpro-IN-6
CAS :<p>SARS-CoV-2 Mpro-IN-6: irreversible Mpro inhibitor, IC50 0.18 μM, selective; doesn't block cathepsins B/F/K/L or caspase 3.</p>Formule :C18H18Cl3N3O2SCouleur et forme :SolidMasse moléculaire :446.78Antitubercular agent 34
CAS :<p>Compound 42g: potent antitubercular, MIC 90 of 1.25 µg/mL, resists liver metabolism.</p>Formule :C19H14N4O2SCouleur et forme :SolidMasse moléculaire :362.41pUL89 Endonuclease-IN-1
CAS :<p>Compound 13d: potent pUL89 endonuclease inhibitor, IC50 0.88 μM, anti-HCMV activity.</p>Formule :C10H8N2O4SCouleur et forme :SolidMasse moléculaire :252.25Diamthazole
CAS :<p>Diamthazole (Dimazole) is an antifungal agent that can be used in the infection research[1].</p>Formule :C15H23N3OSCouleur et forme :SolidMasse moléculaire :293.43Antibacterial agent 97
CAS :<p>Antibacterial agent 97 is potent; MIC: 16 μg/mL for E. coli and S. aureus.</p>Formule :C19H23N5SCouleur et forme :SolidMasse moléculaire :353.48Ingavirin
CAS :<p>Ingavirin, a novel inhibitor of the influenza virus reproduction, inhubits the formation of the virus specific hemagglutinin.</p>Formule :C10H15N3O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :225.24SARS-CoV-2 3CLpro-IN-6
CAS :<p>SARS-CoV-2 3CLpro-IN-6: reversible inhibitor for COVID-19 3CL protease, IC50 4.9 μM, useful in research.</p>Formule :C22H15NO7Couleur et forme :SolidMasse moléculaire :405.36ThrRS-IN-1
CAS :<p>ThrRS-IN-1 inhibits Salmonella ThrRS with IC50 1.4μM, Kd 1.36μM, targets tRNA/L-threonine sites, has strong antibacterial effects.</p>Formule :C16H18Cl2N4O3Couleur et forme :SolidMasse moléculaire :385.25HIV-1 inhibitor-30
CAS :<p>HIV-1 inhibitor-30 (10i) targets RT enzyme, EC50=40nM, IC50=80nM. Effective against seven NNRTI-resistant HIV-1 strains.</p>Formule :C19H20ClN3O2Couleur et forme :SolidMasse moléculaire :357.83FLDP-5
CAS :<p>FLDP-5: BBB-penetrant curcuminoid, induces ROS, DNA damage, S phase arrest, suppresses tumors in LN-18 cells.</p>Formule :C21H21NO5Couleur et forme :SolidMasse moléculaire :367.4Antifungal agent 2
CAS :<p>Antifungal agent 2 suppresses growth of Cryptococcus, Candida, Aspergillus at ≥0.5 μg/mL.</p>Formule :C19H11Br2F3N4O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :544.12AB-506
CAS :<p>AB-506: Oral HBV replication blocker, targets core protein, hinders pgRNA encapsidation, for CHB study.</p>Formule :C21H18ClF2N5O3Couleur et forme :SolidMasse moléculaire :461.85SARS-CoV-2-IN-20
CAS :<p>SARS-CoV-2-IN-20 inhibits virus effectively with 6.5 μM EC50, promising for disease research.</p>Formule :C24H30N2O2Couleur et forme :SolidMasse moléculaire :378.51Phosphoglycolohydroxamic acid
CAS :<p>Phosphoglycolohydroxamic acid inhibits aldolase/triose-phosphate isomerase; used in antibacterial/antifungal research.</p>Formule :C2H6NO6PCouleur et forme :SolidMasse moléculaire :171.05Antifungal agent 22
CAS :<p>Orally active antifungal D16 (IC50: 0.5 μg/mL) passes blood-brain barrier, stable, low toxicity, targets C. neoformansH99 cells.</p>Formule :C21H26Cl3NOSCouleur et forme :SolidMasse moléculaire :446.86NB-598 hydrochloride
CAS :<p>NB-598 hydrochloride is a competitive squalene epoxidase (SE) inhibitor.</p>Formule :C27H32ClNOS2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :486.13RD3-0028
CAS :<p>RD3-0028 is a potent and selective RSV replication inhibitor(EC50 of 4.5 μM).</p>Formule :C8H8S2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :168.28RSV-IN-4
CAS :<p>RSV-IN-4 is a dual inhibitor for RSV and IAV with an EC50 of 11.76 μM.</p>Formule :C18H18N2O2SCouleur et forme :SolidMasse moléculaire :326.41BMH-22
CAS :<p>BMH-22 is an RNA polymerase I inhibitor that acts by causing nucleolar stress and showing potent anticancer activity across many tumor types.</p>Formule :C16H17N3Couleur et forme :SolidMasse moléculaire :251.33Edelfosine
CAS :<p>inhibits phosphatidylinositol phospholipase C</p>Formule :C27H58NO6PDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :523.73FadD32 Inhibitor-1
CAS :<p>FadD32 inhibitor -1 has anti-tuberculosis activity and is an effective FadD32 inhibitor.</p>Formule :C24H20ClN3ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :401.89Metallo-β-lactamase-IN-4
CAS :<p>Metallo-β-lactamase-IN-4 (compound 40) is a potent inhibitor of metallo-β-lactamases (MBL) with IC 50 values of 0.5 μM, 2.1 μM, and 3.3 μM for VIM-1, NDM-1 and</p>Formule :C10H14N4O3S2Couleur et forme :SolidMasse moléculaire :302.37SARS-CoV-2-IN-18
CAS :<p>SARS-CoV-2-IN-18 (Compound 26) is a potent inhibitor of SARS-CoV-2 3C-like protease (IC50 = 45 nM) [1].</p>Formule :C20H14N2O3Couleur et forme :SolidMasse moléculaire :330.34Besifloxacin
CAS :<p>Besifloxacin is the fourth generation of fluoroquinolones, which can be used to treat bacterial conjunctivitis</p>Formule :C19H21ClFN3O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :393.84Dihydropteroate synthase-IN-1
CAS :<p>"Dihydropteroate synthase-IN-1 (5g) inhibits DHPS and cytochrome P450, useful as radiographic diagnostic material."</p>Formule :C19H23N5O4S2Couleur et forme :SolidMasse moléculaire :449.55Antiviral agent 18
CAS :<p>Compound 5, an antiviral agent, effectively targets murine norovirus, with potential in infectious disease and oncology research.</p>Formule :C11H13ClN4O4Couleur et forme :SolidMasse moléculaire :300.7SDH-IN-5
CAS :<p>SDH-IN-5 (compound 7d), a potent inhibitor of succinate dehydrogenase (SDH) with an IC50 of 3.293 μM, additionally demonstrates antifungal efficacy, exhibiting</p>Formule :C16H19F2N3O2Couleur et forme :SolidMasse moléculaire :323.34Antitubercular agent-28
CAS :<p>Antitubercular agent-28 targets resistant Mycobacterium tuberculosis; MIC: 4.5 μM, IC50: 1.5 μM, IC90: 2.5 μM; low cytotoxicity.</p>Formule :C17H14N4O2Couleur et forme :SolidMasse moléculaire :306.32DprE1-IN-4
CAS :<p>DprE1-IN-4: Potent DprE1 inhibitor (IC50: 0.90 μg/mL), good pharmacokinetics, kills TB bacteria in mice.</p>Formule :C20H21N3O5SCouleur et forme :SolidMasse moléculaire :415.46Chlorhexidine-d8 HCl
CAS :<p>Chlorhexidine-d8: internal standard for GC/LC-MS, antimicrobial, inhibits MRSA/MSSA/MRSP/MSSP, affects E. faecium/C. albicans, destabilizes cell walls.</p>Formule :C22H24D8Cl4N10Couleur et forme :SolidMasse moléculaire :586.4168Benzoxonium chloride
CAS :<p>Benzoxonium chloride used in Thio-Ben for cutaneous leishmaniasis treatment with cryotherapy.</p>Formule :C23H42ClNO2Couleur et forme :SolidMasse moléculaire :400.04Antimalarial agent 16
CAS :<p>Antimalarial agent 16 is a parasite inhibitor that exhibits antimalarial effects and inhibits the growth of Plasmodium falciparum with an IC50 value of 2.0 nM.</p>Formule :C30H32N2O6Couleur et forme :SolidMasse moléculaire :516.58Laburnetin
CAS :<p>Laburnetin: an isoflavone antibacterial, combats fungi/S. vesicarium, boosts MRSA methicillin susceptibility, used in pest control.</p>Formule :C20H18O6Couleur et forme :SolidMasse moléculaire :354.35OYYF-175
CAS :<p>OYYF-175: potent antimicrobial antifolate; targets multi-drug resistant Gram-Negative bacteria; DHFR inhibitor with 2.36 nM IC50 against E. coli.</p>Formule :C17H14FN5Couleur et forme :SolidMasse moléculaire :307.33CBR-3465
CAS :<p>CBR-3465 is an inhibitor of mycobacterium tuberculosis (Mtb) type II NADH dehydrogenase. The MIC of CBR-3465 against Mtb is 0.16 μM [1].</p>Formule :C16H18FN3O2SCouleur et forme :SolidMasse moléculaire :335.4F594-1001
CAS :<p>F594-1001 (compound 6) serves as a potent, highly selective inhibitor of SARS-CoV-2 Mac1-ADP-ribose, displaying IC 50 values of 8.5 μM, 68 μM, and 45 μM in AS, FP, and FRET assays, respectively. It binds directly to SARS-CoV-2 Mac1 and demonstrates dose-dependent inhibition of Mac1 ADP-ribosylhydrolase activity.</p>Formule :C23H28ClN3O4Couleur et forme :SolidMasse moléculaire :445.94Phen-DC3
CAS :<p>Phen-DC3 is a G-quadruplex (G4) specific ligand which can inhibit FANCJ and DinG helicases (IC50s of 65±6 and 50±10 nM, respectively).</p>Formule :C34H26N6O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :550.61Afabicin
CAS :<p>Afabicin is an antibiotic targeting Staphylococcus aureus. treat acute bacterial skin and skin structure infections.the prodrug of Debio1452.</p>Formule :C23H24N3O7PDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :485.43cis-ccc_R08
CAS :<p>cis-ccc_R08 infection . cis-ccc_R08 is a cccDNA (covalently closed circular DNA) inhibitor .</p>Formule :C22H19ClO6Couleur et forme :SolidMasse moléculaire :414.84RHI002-Me
CAS :<p>RHI002-Me is a methylated derivative of RHI002, a selective inhibitor of human RNaseH2.</p>Formule :C18H19N3O2S2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :373.49Antibacterial agent 72
CAS :<p>Antibacterial agent 72 has an antibacterial effect by selectively acting on bacterial membranes.</p>Formule :C19H21BrN4SCouleur et forme :SolidMasse moléculaire :417.37HIV-1 inhibitor-49
<p>HIV-1 inhibitor-49, an oral HEPT analog, has strong pharmacokinetics, potent reverse transcriptase inhibition (IC50=30nM), and is safe in mice.</p>Formule :C21H18F2N2O3SCouleur et forme :SolidMasse moléculaire :416.44
