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(2.957 produits)
- Antibiotique(920 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
5842 produits trouvés pour "Microbiologie/Virologie"
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NK007
CAS :<p>NK007 is a novel anti-SARS-CoV-2 agent with an EC 50 value of 30 nM.</p>Formule :C28H33NO9Couleur et forme :SolidMasse moléculaire :527.56SARS-CoV-2-IN-66
CAS :<p>SARS-CoV-2-IN-66 (1), a derivative of vitamin K, functions as an inhibitor of SARS-CoV-2, exhibiting an effective concentration (EC50) of 70.8 μM in VeroE6/</p>Formule :C28H30O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :398.54HBV-IN-17
CAS :<p>HBV-IN-17 (compound 8) is a potent regulator of HBV capsid assembly (EC50: 511 nM).</p>Formule :C17H15F6N5O2Couleur et forme :SolidMasse moléculaire :435.32Bio-AMS
CAS :<p>Bio-AMS is a potent inhibitor of bacterial biotin protein ligase, exhibiting selective activity against Mycobacterium tuberculosis (Mtb) and disrupting fatty</p>Formule :C20H29N9O7S2Couleur et forme :SolidMasse moléculaire :571.63SARS-CoV-2-IN-43
CAS :<p>Compound 8h, also known as SARS-CoV-2-IN-43, is a powerful inhibitor effective in obstructing the replication of SARS-CoV-2, exhibiting significant antiviral</p>Formule :C16H12O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :252.26Besifovir Dipivoxil maleate
CAS :<p>Besifovir Dipivoxil maleate, an oral HBV prodrug (LB80380), suppresses HBV DNA in naive and lamivudine-resistant CHB cases.</p>Formule :C22H34N5O8PDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :527.51(E)-LHF-535
CAS :<p>(E)-LHF-535, an E-isomer antiviral, EC50 <1 μM vs Lassa/Machupo/Junin, 1-10 μM vs VSVg.</p>Formule :C27H28N2O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :412.52WQ 2743
CAS :<p>WQ 2743 is a potent agent of antimicrobial.</p>Formule :C19H15BrF3N5O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :498.25Lagociclovir valactate
CAS :<p>Lagociclovir valactate is a prodrug of Lagociclovir . Lagociclovir valactate is an orally active anti- HBV agent [1] .</p>Formule :C18H25FN6O6Couleur et forme :SolidMasse moléculaire :440.43DMP 323
CAS :<p>DMP 323 is a potent inhibitor of HIV-1 protease.</p>Formule :C35H38N2O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :566.69Antitrypanosomal agent 14
CAS :Antitrypanosomal agent 14 (Compound 1), a potent T.Formule :C14H23N3OSDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :281.42AZ-27
CAS :<p>AZ-27 is a respiratory syncytial virus inhibitor which differentially inhibits different polymerase activities at the promoter.</p>Formule :C36H35N5O4SCouleur et forme :SolidMasse moléculaire :633.76Valnemulin
CAS :<p>Valnemulin, a broad-spectrum pleuromutilin antibiotic, targets peptidyl transferase within the 50S ribosomal subunit, effectively used in veterinary medicine to address swine diseases such as B. hyodysenteriae and M. hyopneumoniae.</p>Formule :C31H52N2O5SCouleur et forme :SolidMasse moléculaire :564.83SARS-CoV-2/MERS Mpro-IN-2
<p>SARS-CoV-2/MERS Mpro-IN-2 is a potent inhibitor of the main proteases of SARS-CoV-2 and MERS, demonstrating IC50 values of 0.21 and 0.07 µM, respectively.</p>Formule :C28H30Cl2N4O6Couleur et forme :SolidMasse moléculaire :589.47Antibacterial agent 135
CAS :<p>Antibacterial Agent 135 (example 7) effectively inhibits various bacteria, including P.</p>Formule :C11H15N5O6SCouleur et forme :SolidMasse moléculaire :345.33G4/HDAC-IN-1
<p>G4/HDAC-IN-1, a G4/HDAC dual inhibitor, IC50 1.1 µM, blocks TNBC growth, useful in cancer research.</p>Formule :C36H49ClFN7O4Couleur et forme :SolidMasse moléculaire :698.27Acorafloxacin HCl
CAS :<p>Acorafloxacin: broad-spectrum fluoroquinolone antibacterial for acute skin infections and pneumonia.</p>Formule :C21H24ClF2N3O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :455.888-Azahypoxanthine
CAS :<p>8-Azahypoxanthine (NSC-22709) inhibits hypoxanthine-guanine-xanthine phosphoribosyltransferase and has antimalarial properties.</p>Formule :C4H3N5ODegré de pureté :99.66%Couleur et forme :Light Yellow To Light Beige Fine CrystallineMasse moléculaire :137.1WRN inhibitor 1
CAS :<p>WRN Inhibitor 1 (example 7) is an inhibitor of the Werner Syndrome ATP-dependent helicase enzyme (WRN), selectively targeting its helicase domain.</p>Formule :C16H13FN2O4SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :348.35U 89360E
CAS :<p>U 89360E is a peptidic inhibitor.</p>Formule :C28H52N8O6Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :596.76Balapiravir hydrochloride
CAS :<p>Balapiravir HCl, an NS5B inhibitor, is used potentially for the treatment of HCV infection.</p>Formule :C21H31ClN6O8Couleur et forme :SolidMasse moléculaire :530.96T145
CAS :<p>T145 halts key bacteria growth at sub μg/ml, deters resistance, and may enhance drug lifespan.</p>Formule :C18H16N2O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :340.33Ulonivirine
CAS :<p>Ulonivirine is an orally active non-nucleoside reverse transcriptase inhibitor that exhibits high antiviral activity and can be used to study HIV-1 infection.</p>Formule :C18H8ClF6N5O3Couleur et forme :SolidMasse moléculaire :491.73L-697661
CAS :<p>L-697661, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formule :C16H15Cl2N3O2Couleur et forme :SolidMasse moléculaire :352.22Glycolithocholic acid 3-sulfate disodium
CAS :<p>Glycolithocholic acid 3-sulfate (disodium) demonstrates inhibitory effects on in vitro HIV-1 replication and has potential applications in HIV infection and</p>Formule :C26H41NNa2O7SCouleur et forme :SolidMasse moléculaire :557.65Aminoacyl tRNA synthetase-IN-1
CAS :<p>Aminoacyl tRNA synthetase-IN-1 is an inhibitor of bacterial aminoacyl tRNA synthetase (aaRS).</p>Formule :C16H25N7O7SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :459.48Levofuraltadone
CAS :<p>Levofuraltadone is an antiprotozoal and antibacterial agent.</p>Formule :C13H16N4O6Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :324.29Propiolactone
CAS :<p>Propiolactone (β-propiolactone; 2-Oxetanone), a chemosterilant, effectively inactivates viruses, rendering them non-infectious.</p>Formule :C3H4O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :72.06Myrrhterpenoid O
CAS :<p>Unfortunately, you did not provide the description of the chemical compound that needs to be rewritten.</p>Formule :C16H20O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :260.33DHX9-IN-4
CAS :<p>DHX9-IN-4 is an ATP-dependent RNA helicase DHX9 inhibitor used in cancer research.</p>Formule :C21H22ClN5O4S2Degré de pureté :98.12%Couleur et forme :SolidMasse moléculaire :508.01Du011
CAS :<p>Du011 is a biogenesis inhibitor of the E.</p>Formule :C20H15F2NO4SCouleur et forme :SolidMasse moléculaire :403.49-Deazaguanine
CAS :<p>9-Deazaguanine is a nucleoside analogue exhibiting inhibitory activity against bovine purine nucleoside phosphorylase (PNP).</p>Formule :C6H6N4ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :150.14LS-BF1
CAS :<p>LS-BF1: Stable, low-toxic antimicrobial peptide targeting ESKAPE pathogens via cell membrane disruption, effective in mouse infection model.</p>Formule :C107H166N28O15Couleur et forme :SolidMasse moléculaire :2084.64Pexiganan acetate
CAS :<p>Pexiganan acetate (MSI 78), a 22-residue peptide analogue of magainin 2, disrupts bacterial membranes or walls, leading to antibacterial activity.</p>Formule :C122H210N32O22·xC2H4O2Degré de pureté :99.88%Couleur et forme :SolidMasse moléculaire :2477.22 (free base)FWM-4
CAS :<p>FWM-4 is a potent inhibitor of SARS-COV-2 NSP13 decapping enzyme.</p>Formule :C24H18N4O4Couleur et forme :SolidMasse moléculaire :426.42Variculanol
CAS :<p>Variculanol, a compound with antimicrobial, anticancer, and anti-HCV NS3/4A protease properties, is derived from the marine fungus Aspergillus versicolor [1].</p>Formule :C25H40O2Couleur et forme :SolidMasse moléculaire :372.58Mirincamycin HCl
CAS :<p>Mirincamycin HCl is a close analog of the drug clindamycin used for the treatment of Plasmodium falciparum blood stages.</p>Formule :C19H36Cl2N2O5SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :475.47AZD-7295
CAS :<p>AZD-7295 (A-689) is an NS5A inhibitor that may be used to treat HCV infection.</p>Formule :C32H35F3N4O5SCouleur et forme :SolidMasse moléculaire :644.7A 33853
CAS :<p>A 33853 is an antibiotic isolated from culture broth of Streptomyces sp.</p>Formule :C20H13N3O6Couleur et forme :SolidMasse moléculaire :391.33KNI-272
CAS :<p>Kynostatin-272 is a HIV protease inhibitor. KNI-272 blocked the maturation of viral particles.</p>Formule :C33H41N5O6S2Couleur et forme :SolidMasse moléculaire :667.84UNC-2170
CAS :<p>UNC-2170 (UNC2170 Maleate) is the methyl-lysine binding protein, 53BP1 ligand.</p>Formule :C14H21BrN2ODegré de pureté :97.44%Couleur et forme :SolidMasse moléculaire :313.232-Dodecanol
CAS :<p>2-Dodecanol suppresses both hyphal development and SIR2 gene expression in Candida albicans [1].</p>Formule :C12H26OCouleur et forme :SolidMasse moléculaire :186.33Chitin synthase inhibitor 14
CAS :<p>Chitin Synthase Inhibitor 14 (compound 4n), a potent chitin synthase (CHS) inhibitor, exhibits antifungal activity and is effective against drug-resistant</p>Formule :C25H26ClN5O5Couleur et forme :SolidMasse moléculaire :511.96Berlopentin
CAS :<p>Berlopentin is splenopentin analog used to treat HIV-positive patients. It also has immunostimulatory properties.</p>Formule :C35H55N9O11Couleur et forme :SolidMasse moléculaire :777.86OfChi-h-IN-2
CAS :<p>OfChi-h-IN-2 (compound TQ19) is a potent inhibitor of OfChi-h, exhibiting a K i of 0.33 μM, and significantly impairs the growth and development of Ostrinia</p>Formule :C25H28ClN5O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :481.98SIMR3030
CAS :<p>SIMR3030, a potent inhibitor of SARS-CoV-2 PLpro, possesses an IC50 of 0.0399 µg/mL and demonstrates antiviral activity by diminishing the expression of SARS-</p>Formule :C27H29N3O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :427.545,6,7,8-Tetrahydro-8-deazahomofolic acid
CAS :<p>5,6,7,8-Tetrahydro-8-deazahomofolic acid is a potential thymidylate synthase (TS) inhibitor and other folate related enzymes inhibitor.</p>Formule :C21H26N6O6Couleur et forme :SolidMasse moléculaire :458.47COH1
CAS :<p>COH1 is a ribonucleotide reductase (RR) inhibitor utilized in research pertaining to cancer, mitochondrial diseases, and neurodegenerative disorders [1].</p>Formule :C11H10N2O3SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :250.27SARS-CoV-2-IN-1
CAS :<p>SARS-CoV-2-IN-1 is a potent inhibitor of Mpro(SARS-CoV-2 Mpro, SARS-CoV Mpro and MERS-CoV Mpro with IC50s of 0.67, 0.90 and 0.58 μM, respectively).</p>Formule :C31H39N5O7Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :593.67CDD-1733
CAS :<p>CDD-1733 is a potent, non-covalent, and non-peptide inhibitor of the SARS-CoV-2 main protease (Mpro) with an inhibition constant (K i) of 12 nM.</p>Formule :C34H32F3N5O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :599.65WRN inhibitor 2
CAS :<p>WRN Inhibitor 2 (example 118), a potent inhibitor of the WRN (Werner Syndrome ATP-dependent helicase enzyme), exhibits a pIC50 value of 7.0 or greater [1].</p>Formule :C15H11F3N2O5S2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :420.38Sulfachloropyridazine sodium
CAS :<p>Sulfachloropyridazine (sodium) is a sulfonamide antibiotic that impedes bacterial proliferation [1].</p>Formule :C10H8ClN4NaO2SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :306.7Antiparasitic agent-8
CAS :<p>Antiparasitic agent-8 (Compound 9) exhibits potent antiparasitic activity against Hymenolepis nana, while demonstrating low levels of cytotoxicity [1].</p>Formule :C17H22FN3O4Couleur et forme :SolidMasse moléculaire :351.37Antituberculosis agent-6
CAS :<p>Antituberculosis agent-6: potent against M. tuberculosis (MIC 3.49 μM), antifungal (MIC 62.5 μM), high GI absorption.</p>Formule :C27H20F2N2O3Couleur et forme :SolidMasse moléculaire :458.46Urease Inhibitor 07
CAS :<p>Urease Inhibitor 07 is an isosubstituted metalloproteinase inhibitor with potential activity against Mycobacterium tuberculosis strain H37Rv.</p>Formule :C7H5N3OSDegré de pureté :99.65%Couleur et forme :SolidMasse moléculaire :179.2Ziresovir
CAS :<p>Ziresovir (RO-0529) is a respiratory syncytial virus fusion protein (RSV F) inhibitor that inhibits RSV and can be used to study syncytial virus sense.</p>Formule :C22H25N5O3SDegré de pureté :95.51% - >99.99%Couleur et forme :SolidMasse moléculaire :439.53TCMDC-135051
CAS :<p>TCMDC-135051: Selective PfCLK3 inhibitor, low toxicity, halts parasite growth & transmission; EC50=320 nM.</p>Formule :C29H33N3O3Degré de pureté :99.05%Couleur et forme :SolidMasse moléculaire :471.59Linvencorvir
CAS :<p>Linvencorvir is a hepatitis B virus (HBV) core protein variant modifier used to treat chronic HBV infection.</p>Formule :C29H35FN6O5SDegré de pureté :99.9% - 99.9%Couleur et forme :SolidMasse moléculaire :598.69Filibuvir
CAS :<p>Filibuvir (PF-00868554) inhibits HCV polymerase genotypes 1a/1b, EC50s 59 nM.</p>Formule :C29H37N5O3Degré de pureté :99.28% - >99.99%Couleur et forme :SolidMasse moléculaire :503.64CWHM-1552
CAS :<p>CWHM-1552 is an effective Plasmodium falciparum inhibitor. For the 3D7 and Dd2 strains, the IC50s are 51 nM and 53 nM.</p>Formule :C22H27F2N3ODegré de pureté :99.56%Couleur et forme :SolidMasse moléculaire :387.47Nesbuvir
CAS :<p>Nesbuvir: HCV NS5B polymerase inhibitor, IC50 9 nM against HCV 1b replicon in liver cancer cells.</p>Formule :C22H23FN2O5SDegré de pureté :99.99%Couleur et forme :SolidMasse moléculaire :446.49DHX9-IN-2
CAS :<p>DHX9-IN-2 is an inhibitor targeting ATP-dependent RNA de-helicase A (DHX9) with anticancer and antitumor activity for cancer research.</p>Formule :C18H16ClN3O3S2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :421.922,4′-Dichloroacetanilide
CAS :<p>2,4′-Dichloroacetanilide (2-chloro-N-(4-chlorophenyl)acetamide) has antifungal activity and inhibits T. asteroides with a MIC value of 6.25 μg/mL.</p>Formule :C8H7Cl2NODegré de pureté :99.36%Couleur et forme :SolidMasse moléculaire :204.05A7132
CAS :<p>A7132 is an antibacterial agent and possesses broad and potent antibacterial activity.</p>Formule :C19H16F2N4O3Degré de pureté :95.49%Couleur et forme :SolidMasse moléculaire :386.35Valomaciclovir stearate
CAS :<p>S-Allylmercapturic Acid (N-Acetyl-S-allyl-L-cysteine) is a metabolite of S-allyl-L-cysteine present in black garlic, with potential anti-gout effects.</p>Formule :C33H58N6O5Degré de pureté :99.18% - >99.99%Couleur et forme :SolidMasse moléculaire :618.85Dehydroemetine
CAS :<p>Dehydroemetine, a synthetic emetine, treats amoebic infections and leishmaniasis, and resists metronidazole amoebiosis.</p>Formule :C29H38N2O4Degré de pureté :98.68% - 99.68%Couleur et forme :SolidMasse moléculaire :478.62Thymectacin
CAS :<p>Thymectacin (NB 1011) is a selective thymidine synthase (TS) inhibitor with anticancer activity for the study of colon cancer and solid tumors.</p>Formule :C21H25BrN3O9PDegré de pureté :97.05% - 99.49%Couleur et forme :SolidMasse moléculaire :574.32SMN-C3
CAS :<p>SMN-C3 (MV8T2MCK57) is an orally active modulator of SMN2 splicing, and has the potential to treat spinal muscular atrophy (SMA).</p>Formule :C24H28N6ODegré de pureté :99.01% - 99.05%Couleur et forme :SolidMasse moléculaire :416.52Salicyl-AMS
CAS :<p>Salicyl-AMS is an inhibitor of mycobacterium auxin biosynthesis that inhibits the growth of mycobacterium in the presence of iron deficiency in vitro.</p>Formule :C17H18N6O8SDegré de pureté :98.19%Couleur et forme :SolidMasse moléculaire :466.43ZY-19489
CAS :<p>ZY-19489: Antimalarial, potential single-dose cure, FDA orphan drug status.</p>Formule :C24H32FN9Degré de pureté :>99.99%Couleur et forme :SoildMasse moléculaire :465.57GSK3186899
CAS :<p>GSK3186899 is an inhibitor of Cdc2-related kinase 12 with an EC50 of 1.4 μM for L. donovani.</p>Formule :C19H28F3N7O3SDegré de pureté :98.35% - 99.61%Couleur et forme :SolidMasse moléculaire :491.53LNA-Adenosine
CAS :<p>LNA-Adenosine (LNA-A) is a nucleoside analogue that acts as a ligand for adenosine A3 receptors.</p>Formule :C11H13N5O4Degré de pureté :99.15%Couleur et forme :SolidMasse moléculaire :279.25Leritrelvir
CAS :<p>Dermatan sulphate sodium (Chondroitin sulfate B sodium salt) is a linear sulfated polysaccharide, a glycosaminoglycan component of important proteoglycans.</p>Formule :C31H44F3N5O6Degré de pureté :97.42%Couleur et forme :SolidMasse moléculaire :639.71Tenofovir amibufenamide
CAS :<p>Tenofovir amibufenamide (HS-10234) 是一种 Tenofovir 前药，是一种具有口服活性的抗病毒化合物。Tenofovir amibufenamide 对乙型肝炎病毒 (HBV)具有抑制作用，可用于慢性乙型肝炎 (CHB) 研究。</p>Formule :C22H31N6O5PDegré de pureté :99.19% - 99.87%Couleur et forme :SolidMasse moléculaire :490.49MMV688533
CAS :<p>MMV688533 has antimalarial activity.</p>Formule :C24H15F6N5O2Degré de pureté :99.12%Couleur et forme :SoildMasse moléculaire :519.4Contezolid
CAS :<p>Contezolid (MRX-I) is an antibiotic with bactericidal activity and can be used to study tuberculosis.</p>Formule :C18H15F3N4O4Degré de pureté :99.41%Couleur et forme :SolidMasse moléculaire :408.33CeMMEC1
CAS :<p>CeMMEC1 is an inhibitor of BRD4, and also has a great affinity for TAF1(IC50=0.9 μM).</p>Formule :C19H16N2O4Degré de pureté :98.9% - 99.92%Couleur et forme :SolidMasse moléculaire :336.34Sorivudine
CAS :<p>Sorivudine (BV-araU) is an antiviral blocking DNA synthesis in viruses like varicella, HSV-1, and Epstein-Barr.</p>Formule :C11H13BrN2O6Degré de pureté :99.74%Couleur et forme :SolidMasse moléculaire :349.13Lomibuvir
CAS :<p>Lomibuvir (VCH-222, VX-222) is an allosteric inhibitor of HCV NS5B with Kd 17 nM, blocks RNA elongation, EC50 5.2 nM for 1b/Con1.</p>Formule :C25H35NO4SDegré de pureté :99.83%Couleur et forme :SolidMasse moléculaire :445.61GC373
CAS :<p>GC373, an effective inhibitor of the SARS-CoV-2 M pro, impedes virus replication, exhibiting an inhibition concentration (IC 50) of 0.4 μM. This compound is valuable for use in anti-COVID-19 research.</p>Formule :C21H29N3O5Couleur et forme :SolidMasse moléculaire :403.47BRD-K98645985
CAS :<p>BRD-K98645985: BAF inhibitor, binds ARID1A, reverses HIV-1 latency, EC50 ~2.37μM, alters nucleosome placement.</p>Formule :C33H43N5O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :573.73SARS-CoV-2 nsp14-IN-2
<p>SARS-CoV-2 nsp14-IN-2: Strong Nsp14 methyltransferase inhibitor (IC50: 0.09 μM), potential for COVID-19 research.</p>Formule :C21H21N5O5SCouleur et forme :SolidMasse moléculaire :455.49ZINC000104379474
<p>ZINC000104379474 is a compound that targets SARS-CoV-2 endoribonuclease.</p>Formule :C27H33N3O10Couleur et forme :SolidMasse moléculaire :559.57Antitumor agent-74
<p>Antitumor agent-74, a quinazoline derivative, inhibits DNA, arrests cell cycle, and induces apoptosis with agent-75.</p>Formule :C26H23FN6Couleur et forme :SolidMasse moléculaire :438.5HBV-IN-19 TFA
CAS :<p>HBV-IN19 TFA suppresses HBsAg, hampers HBV infection, and aids in HBV research.</p>Formule :C26H31F3N2O8Couleur et forme :SolidMasse moléculaire :556.53Enzyme-IN-3 disodium
CAS :<p>Enzyme-IN-3 disodium (compound 7) is a selective inhibitor of Mycobacterium tuberculosis shikimate kinase with an IC50 of 1.6 μM. Additionally, Enzyme-IN-3 disodium exhibits antibacterial properties.</p>Formule :C20H13N3Na2O8S2Couleur et forme :SolidMasse moléculaire :533.442SP-471
<p>SP-471 is a potent inhibitor of dengue virus (DENV) protease (IC50: 18 μM) and inhibits the inter- and intramolecular protease processes of DENV.</p>Formule :C33H26BrN5Couleur et forme :SolidMasse moléculaire :572.5Fabimycin
CAS :<p>Fabimycin, a FabI inhibitor, combats drug-resistant gram-negative bacterial infections effectively.</p>Formule :C23H25ClN4O3Couleur et forme :SolidMasse moléculaire :440.92MsbA-IN-5
<p>MsbA-IN-5 (compound 40) is a potent and highly selective inhibitor of MsbA (IC50: 2 nM). MsbA-IN-5 can be used in Gram-negative studies.</p>Formule :C23H19Cl2N5OCouleur et forme :SolidMasse moléculaire :452.34AG-7404
CAS :<p>AG-7404: strong protease inhibitor, fights poliovirus, EC50 0.080-0.674 μM, effective on V-073-resistant strains.</p>Formule :C26H29N5O7Couleur et forme :SolidMasse moléculaire :523.54Palmitanilide
CAS :<p>Palmitanilide (Palmitic acid anilide) is an antimicrobial agent effective against Gram-positive bacteria. It can electrostatically bind to components of the cell wall of Gram-positive bacteria (such as Bacillus cereus), altering the membrane structure and affecting normal cellular functions. Palmitanilide shows potential for research into infections caused by Gram-positive bacteria.</p>Formule :C22H37NOCouleur et forme :SolidMasse moléculaire :331.535BAY-364
CAS :<p>BAY-364 (BAY-299N) functions as an inhibitor targeting the second bromine domain in TAF1, demonstrating inhibitory effects on TAF1 in Kasumi-1 cells, CD34+</p>Formule :C23H19N3O4Couleur et forme :SolidMasse moléculaire :401.41HCV-IN-40
CAS :<p>HCV-IN-39 is a potent oral drug inhibiting HCV, effective on GT1a (EC50: 0.259μM), GT1b (EC50: 0.434μM), GT1b CES1 (EC50: 0.069μM) replicons.</p>Formule :C21H26BrFN3O9PCouleur et forme :SolidMasse moléculaire :594.32Chitin synthase inhibitor 8
<p>Chitin synthase inhibitor 8 is a chitin synthase (CHS) inhibitor with broad-spectrum antifungal effects that can be used in studies related to fungal infections</p>Formule :C23H23N3O5Couleur et forme :SolidMasse moléculaire :421.45Antitubercular agent-15
<p>Antitubercular agent-15 (5n): low toxicity, fights M. tuberculosis strains; MIC90 values range 0.73-18.8 μg/mL.</p>Formule :C21H29FN2Couleur et forme :SolidMasse moléculaire :328.47DNDI-8219
CAS :<p>DNDI-8219 is an antitubercular agent. It has potent antileishmanial effects.</p>Formule :C13H10F3N3O5Couleur et forme :SolidMasse moléculaire :345.23GSK-3036656 free base
CAS :<p>GSK656 (GSK3036656) inhibits Mtb LeuRS with IC50 of 0.20 μM, promising for tuberculosis treatment.</p>Formule :C10H13BClNO4Couleur et forme :SolidMasse moléculaire :257.48Antibacterial agent 77
<p>Antibacterial agent 77 (compound 12) is an antibacterial agent [1].</p>Formule :C22H27N3OSCouleur et forme :SolidMasse moléculaire :381.53FG-2101
CAS :<p>FG-2101 is a selective, orally active non-hydroxamate LpxC inhibitor with an IC50 of approximately 1 nM. It demonstrates exceptional selectivity over other bacterial and human metalloproteases. FG-2101 is useful for studying infections caused by Gram-negative bacteria, including resistant strains.</p>Formule :C30H32N5O6PCouleur et forme :SolidMasse moléculaire :589.579Antibacterial agent 261
CAS :<p>Antibacterialagent 261 (compound 43) is a potent inhibitor of the peptide deformylase (PDF) enzyme, demonstrating IC50 values of 2.5 nM against Staphylococcus aureus (S. aureus) and 10.6 nM against Escherichia coli (E. coli).</p>Formule :C18H24N4O3S2Couleur et forme :SolidMasse moléculaire :408.538
