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(2.968 produits)
- Antibiotique(922 produits)
- Antifection(23 produits)
- DHFR(33 produits)
- Synthèse ADN/ARN(711 produits)
- VHB(177 produits)
- Protéase du VIH(451 produits)
- HSV(91 produits)
- Intégrase(2 produits)
- Ribosome(13 produits)
Affichez 2 plus de sous-catégories
5863 produits trouvés pour "Microbiologie/Virologie"
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MptpB-IN-1
CAS :<p>MptpB-IN-1: orally active, potent MptpB inhibitor; reduces drug-resistant tuberculosis.</p>Formule :C17H11Cl2NO4Couleur et forme :SolidMasse moléculaire :364.18Sudoterb HCl
CAS :<p>Sudoterb has anti-tubercular activity.</p>Formule :C29H30Cl2F3N5ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :592.48Tropesin
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 :505.954-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 :384.28HCV-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 :502.09PC58538
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 :375.46HBV-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 :428.87Antibacterial 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 :417.39MMV688845
CAS :<p>MMV688845: NTM RNA polymerase inhibitor, kills Mycobacterium abscessus, and fights TB.</p>Formule :C24H25N3O3SCouleur et forme :SolidMasse moléculaire :435.54TLC3407-3786
CAS :<p>MMV665916: Antimalarial quinazolinedione, effective against P. falciparum (EC50 = 0.4 µM), high selectivity (SI > 250).</p>Formule :C19H19N3O4Couleur et forme :SolidMasse moléculaire :353.37GRL-1720
CAS :<p>GRL-1720 is a SARS-CoV-2 Protease inhibitor (IC50 = 320 nM). GRL-1720 contains an indoline which targets the SARS-CoV-2 main protease (Mpro)</p>Formule :C14H11ClN2O2Couleur et forme :SolidMasse moléculaire :274.7HBV-IN-29
CAS :<p>HBV-IN-29 (ex8), a flavone derivative, inhibits cccDNA in HBV research.</p>Formule :C22H19ClO6Couleur et forme :SolidMasse moléculaire :414.84Antitrypanosomal agent 7
CAS :<p>Compound 18c, an antitrypanosomal, is twice as potent as Nifurtimox against T. brucei (IC50: 0.71 μM), with favorable ADME and AT-DNA binding affinity.</p>Formule :C23H29N5O2Couleur et forme :SolidMasse moléculaire :407.51Antitrypanosomal agent 9
CAS :<p>Agent 9 inhibits T. b. brucei (IC50: 1.15 μM), used in HAT research.</p>Formule :C22H27NO3Couleur et forme :SolidMasse moléculaire :353.45Pyrrofolic acid
CAS :<p>Pyrrofolic acid shows high anti-folate biological activity for S. faecalis.</p>Formule :C23H21N7O7Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :507.46Thiamphenicol glycinate hydrochloride
CAS :<p>Thiamphenicol glycinate hydrochloride is a broad-spectrum antibacterial agent utilized in research on respiratory tract infections.</p>Formule :C14H19Cl3N2O6SCouleur et forme :SolidMasse moléculaire :449.73Caspofungin
CAS :<p>Caspofungin is a cyclic lipopeptide echinocandin and beta-(1,3)-D-glucan synthase inhibitor that is used to treat internal or systemic mycoses.</p>Formule :C52H88N10O15Couleur et forme :SolidMasse moléculaire :1093.31HBV-IN-10
CAS :<p>HBV-IN-10, an isomer of compound 6, inhibits HBsAg with EC50 between 0.1-1 μM (Patent WO2021204258A1).</p>Formule :C23H24FN7OCouleur et forme :SolidMasse moléculaire :433.48HIV-1 inhibitor-53
CAS :<p>HIV-1 Inhibitor-53 targets HIV-1 protease (IC50: 1.93 nM) and reverse transcriptase (IC50: 2.35 μM), aiding AIDS research.</p>Formule :C30H34N2O8SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :582.66Antibacterial agent 65
CAS :<p>Antibacterial agent 65 is a potential antimicrobial agent and antioxidant agent.</p>Formule :C17H16O3Couleur et forme :SolidMasse moléculaire :268.31HIV-1 protease-IN-5
CAS :<p>HIV-1 protease-IN-5 is an HIV-1 protease inhibitor (IC50: 1.64 nM). HIV-1 protease-IN-5 exhibits significant effects on wild-type and DRV-resistant HIV-1.</p>Formule :C27H29F3N2O7SCouleur et forme :SolidMasse moléculaire :582.59Diethofencarb
CAS :<p>Diethofencarb: a fungicide effective against Botrytis cinerea and resistant Botryis strains.</p>Formule :C14H21NO4Couleur et forme :SolidMasse moléculaire :267.32Antitubercular agent-32
CAS :<p>Antitubercular agent-32, a Benzothiazinone, inhibits DprE1 in tuberculosis, stable and water-soluble, IC50: 3.9 μM.</p>Formule :C22H28N4O5S2Couleur et forme :SolidMasse moléculaire :492.61Brecanavir
CAS :<p>Brecanavir is a tyrosyl-based arylsulfonamide, high affinity, protease inhibitor (PI) for the treatment of human immunodeficiency virus type 1.</p>Formule :C33H41N3O10S2Couleur et forme :SolidMasse moléculaire :703.82ML372
CAS :<p>ML372 is a potent and selective SMN Modulator (EC50 = 12 nM, 325% increase inSMN2) with good potency, pharmacokinetics, tolerance, and CNS penetration.</p>Formule :C18H20N2O4SCouleur et forme :SolidMasse moléculaire :360.43Antibacterial agent 114
CAS :<p>Compound 1: Potent antibacterial, MIC 625-1250μM for P.aeruginosa to S.aureus.</p>Formule :C19H14N4OCouleur et forme :SolidMasse moléculaire :314.34HIV-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 :429.52Chitin 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 :609.26SARS-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 :421.47TBI-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 :512.06Bunamidine hydrochloride
CAS :<p>Bunamidine hydrochloride is a veterinary anthelmintic that acts against Echinococcus granulosus and Tapeworm.</p>Formule :C25H39ClN2OCouleur et forme :SolidMasse moléculaire :419.05SARS-CoV-2 3CLpro-IN-3
CAS :SARS-CoV-2 3CLpro-IN-3 is a SARS CoV-2 3CLpro inhibitor that exhibits antiviral, antibacterial, and antifungal effects.Formule :C23H21BrN6O2SCouleur et forme :SolidMasse moléculaire :525.42Antifungal agent 30
CAS :<p>Potent antifungal, works against Candida albicans (MIC: 0.03 μg/mL) & Aspergillus fumigatus (MIC: 0.5 μg/mL) via CYP51 interactions.</p>Formule :C18H14Cl2F2N2SeCouleur et forme :SolidMasse moléculaire :446.18Anthrarobin
CAS :<p>Anthrarobin is an antipsoriatic.</p>Formule :C14H10O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :226.23FR900098 (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 :229.75HadAB-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 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 :503.4SARS-CoV-2-IN-16
CAS :<p>SARS-CoV-2-IN-16 strongly inhibits NPro, with EC50 of 3.69 μM and Kd of 7.82 μM, suggesting effective binding and antiviral properties.</p>Formule :C17H20N2O2Couleur et forme :SolidMasse moléculaire :284.35Antibacterial agent 121
CAS :<p>Antibacterial agent 121 exhibits anti-TB and anti-inflammatory properties.</p>Formule :C18H22N2O3SCouleur et forme :SolidMasse moléculaire :346.44Antibacterial 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 :353.48Antitubercular agent-26
CAS :<p>Compound 32: oral antitubercular, acts on M. tuberculosis, IC50 ~0.50μM, stable, low cardiotoxicity, non-genotoxic.</p>Formule :C22H23N5O3S2Couleur et forme :SolidMasse moléculaire :469.58Antitubercular agent-14
CAS :<p>Antitubercular agent-14 (Compound 1) shows antitubercular activity. The MIC value of Antitubercular agent-14 against M. tuberculosis is 0.3 μg/mL [1].</p>Formule :C20H27ClN2Couleur et forme :SolidMasse moléculaire :330.89Anticandidal agent-1
CAS :<p>Compound C2 is a broad-spectrum anticandidal, blocking biofilm and filament growth with MIC50 of 13.51μg/mL (C. glabrata) and 8.65μg/mL (C. albicans).</p>Formule :C19H22O5Couleur et forme :SolidMasse moléculaire :330.38Berteroin
CAS :<p>Berteroin, found in cruciferous veggies like rucola and mustard, may act as an antioxidant, reducing inflammation and androgen receptors in cancer.</p>Formule :C7H13NS2Couleur et forme :SolidMasse moléculaire :175.31ATD-3169
CAS :<p>ATD-3169 is a ROS generator with antibacterial activity.</p>Formule :C15H14O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :242.27A3N19
CAS :<p>A3N19 is a potent inhibitor of HIV-1 non-nucleoside reverse transcriptase and is able to act on HIV-1 IIIB (EC50: 3.28 nM).</p>Formule :C31H31N9O2SCouleur et forme :SolidMasse moléculaire :593.7PXYC13
CAS :<p>PXYC13 inhibits Mtb RpsA essential for trans-translation with Kd of 7.61 μM; less effective on RpsA-CTD Δ438A (Kd 8.50 μM).</p>Formule :C15H15N5O2SCouleur et forme :SolidMasse moléculaire :329.38RyRs activator 1
CAS :<p>RyRs activator 1 triggers ranibulin receptors; 100% larvicidal at 0.5 mg/L, 90% at 0.01 mg/L.</p>Formule :C21H14ClF3N6O4Couleur et forme :SolidMasse moléculaire :506.82Crisnatol mesylate
CAS :<p>Crisnatol, a potent and selective DNA intercalator, has potential anticancer activity.</p>Formule :C24H27NO5SCouleur et forme :SolidMasse moléculaire :441.54Marasmic acid
CAS :<p>Marasmic acid is a bioactive antifungal.</p>Formule :C15H18O4Couleur et forme :SolidMasse moléculaire :262.3EV-A71-IN-1
CAS :<p>EV-A71-IN-1: potent EV-A71 capsid inhibitor, EC50 0.27 μM, disrupts VP1/hSCARB2 interaction, broad-spectrum antiviral, non-toxic to human cells.</p>Formule :C21H15N5SCouleur et forme :SolidMasse moléculaire :369.44Werner syndrome RecQ helicase-IN-3
CAS :<p>Potent WRN inhibitor, Werner syndrome RecQ helicase-IN-3, is orally active with 0.06 µM IC50; exhibits antiproliferative and anticancer effects.</p>Formule :C31H30ClF3N8O5Couleur et forme :SolidMasse moléculaire :687.07Sitamaquine tosylate
CAS :<p>Sitamaquine: antileishmanial, targets L. donovani species, EC50 = 9.5-19.8 μM, inhibits mitochondrial complex II, induces apoptosis in promastigotes.</p>Formule :C28H41N3O4SCouleur et forme :SolidMasse moléculaire :515.71Antimalarial agent 11
CAS :<p>Antimalarial compound 1: Spirocyclic chromane, EC50 - D6: 1.48 μM, ARC08-022: 1.81 μM.</p>Formule :C25H25F2NO3Couleur et forme :SolidMasse moléculaire :425.47SARS-CoV-2 3CLpro-IN-7
CAS :<p>SARS-CoV-2 3CLpro-IN-7 is a reversible covalent inhibitor of the SARS-CoV-2 3CL protease, exhibiting an inhibitory concentration (IC50) value of 1.4 µM.</p>Formule :C24H17ClN2O6Couleur et forme :SolidMasse moléculaire :464.85DHQZ 36
CAS :<p>DHQZ 36: retrograde trafficking inhibitor, anti-parasite, stops Leishmania amazonensis (EC50: 13.63 μM).</p>Formule :C21H18F2N2OSDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :384.44Mt KARI-IN-2
CAS :<p>Mt KARI-IN-2, an inhibitor for Mtb KARI (Ki: 2.02 μM) and Mtb H37Rv (MIC: 0.78 μM), has low cytotoxicity (HEK IC50: >86 μg/mL).</p>Formule :C14H11N5O4S2Couleur et forme :SolidMasse moléculaire :377.4Halofantrine, (-)-
CAS :<p>Halofantrine, (-)- is an antimalarial agent.</p>Formule :C26H30Cl2F3NOCouleur et forme :SolidMasse moléculaire :500.42Cap-dependent endonuclease-IN-21
CAS :<p>Cap-dependent endonuclease-IN-21 inhibits CEN and flu virus replication, potential against influenza A. (From patent WO2021233302A1, compound 8B/8A)</p>Formule :C26H23F2N3O7Couleur et forme :SolidMasse moléculaire :527.47Antibacterial agent 105
CAS :<p>Compound 17, a phenanthrolinic quinolone, fights M. tuberculosis (MIC 90: 2.64 μM) and various bacteria (MIC 90: 0.70-44.70 μM).</p>Formule :C14H9N3O5Couleur et forme :SolidMasse moléculaire :299.24PqsR/LasR-IN-3
CAS :<p>PqsR/LasR-IN-3 (Compound 7a) inhibits hERG with the IC 50 of 109.01 μM which is also a PqsR and LasR systems inhibitor in P. aeruginosa [1].</p>Formule :C14H17NO5SCouleur et forme :SolidMasse moléculaire :311.35Antitrypanosomal agent 11
<p>Antitrypanosomal Agent 11 is a chemical compound effective against Trypanosoma cruzi, exhibiting an inhibition concentration (IC 50) of 0.23 μM.</p>Formule :C16H10F6N6OCouleur et forme :SolidMasse moléculaire :416.28Purfalcamine
CAS :<p>Purfalcamine, a selective PfCDPK1 inhibitor effective against malaria, has IC50 of 17 nM and EC50 of 230 nM; halts parasites at schizont stage.</p>Formule :C29H33FN8OCouleur et forme :SolidMasse moléculaire :528.62HIV-IN-5
CAS :<p>HIV-IN-5 (5r) inhibits HIV-1 with 0.16 μM IC50, targeting NNIBP as a NNRTI.</p>Formule :C30H24N2O8SCouleur et forme :SolidMasse moléculaire :572.59Metallo-β-lactamase-IN-9
CAS :<p>Metallo-β-lactamase-IN-9 (Compound 23) serves as a broad-spectrum inhibitor of metallo-beta-lactamases (MBL), exhibiting inhibition constants (IC50) of 35 nM</p>Formule :C13H12N6O3SCouleur et forme :SolidMasse moléculaire :332.34RmlA-IN-1
CAS :<p>RmlA-IN-1 inhibits RmlA enzyme with 0.073 μM IC50, affecting l-Rhamnose synthesis and bacterial wall permeability.</p>Formule :C18H18N4O4SCouleur et forme :SolidMasse moléculaire :386.42Antifungal agent 32
CAS :<p>Antifungal 32 (1a) strongly inhibits Candida albicans growth, filamentation, biofilm, and adhesion.</p>Formule :C25H28N2OCouleur et forme :SolidMasse moléculaire :372.5HCV-IN-33
CAS :<p>HCV-IN-33 (Compound (S)-3i) is an inhibitor of HCV entry.</p>Formule :C31H36ClN5Couleur et forme :SolidMasse moléculaire :514.1B 669
CAS :<p>B 669 has antibacterial activity.</p>Formule :C30H28N4Couleur et forme :SolidMasse moléculaire :444.57IACS-4759
CAS :<p>IACS-4759 is a novel potent and selective MTH1 inhibitor with excellent cell permeability and good metabolic stability in microsomes.</p>Formule :C10H17N3O2Couleur et forme :SolidMasse moléculaire :211.26Norstictic acid
CAS :<p>Norstictic acid: a potent, selective transcription regulator with anticancer, antioxidant, and antimicrobial properties.</p>Formule :C18H12O9Couleur et forme :SolidMasse moléculaire :372.28Antimicrobial agent-6
<p>Antimicrobial agent-6: MIC 4-8 μg/mL for gram+ & gram- bacteria, anti-inflammatory.</p>Formule :C40H64N16Couleur et forme :SolidMasse moléculaire :769.04Mtb-cyt-bd oxidase-IN-4
<p>Mtb-cyt-bd oxidase inhibitor; IC50=0.25μM; MIC=8μM against Mycobacterium tuberculosis; for TB research.</p>Formule :C25H32FNOCouleur et forme :SolidMasse moléculaire :381.53Efavirenz, (R)-
CAS :<p>Efavirenz, (R)- is an antiviral agent and a nonnucleoside HIV-1 reverse transcriptase inhibitor.</p>Formule :C14H9ClF3NO2Couleur et forme :SolidMasse moléculaire :315.67Antistaphylococcal agent 1
CAS :<p>Antistaphylococcal agent 1 is an antistaphylococcal therapeutic agent.</p>Formule :C22H16N6O2Couleur et forme :SolidMasse moléculaire :396.4Enisamium iodide
CAS :<p>Enisamium iodide is used as an antiviral agent.</p>Formule :C14H15IN2OCouleur et forme :SolidMasse moléculaire :354.19Antiviral agent 19
CAS :<p>Antiviral agent 19 (Compound 3) is a selective inhibitor of Zika virus (EC50: 1.3 μM) with low cytotoxicity.</p>Formule :C29H35NO5Couleur et forme :SolidMasse moléculaire :477.59Antibacterial agent 64
CAS :<p>Potent antibacterial, YycG inhibitor with 6.1 µM IC50. Synergistic with ampicillin against biofilm bacteria.</p>Formule :C29H20ClN3O6S2Couleur et forme :SolidMasse moléculaire :606.07Mt KARI-IN-5
CAS :<p>Mt KARI-IN-5 inhibits MtbKARI with Ki 4.72 μM, has MIC 1.56 μM against MtbH37Rv, and is low in cytotoxicity with IC50 >64 μg/mL in HEK.</p>Formule :C14H10N4O5S3Couleur et forme :SolidMasse moléculaire :410.45RMI 10874
CAS :<p>RMI 10874 is a tilorone analogue. Tilorone is an orally bioavailable antiviral agent.</p>Formule :C21H26N2O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :370.44DprE1-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 :415.46cis-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 :414.84Neuraminidase-IN-8
CAS :<p>Neuraminidase-IN-8 (Compound 6d) is a powerful inhibitor of neuraminidase, exhibiting a low half-maximal inhibitory concentration (IC50) of 0.027 μM and</p>Formule :C18H16FN3O3SCouleur et forme :SolidMasse moléculaire :373.4Neuraminidase-IN-3
CAS :<p>Neuraminidase-IN-3 inhibits flu NA: H1N1 IC50=0.73nM, H5N1=0.26nM, H5N8=0.63nM.</p>Formule :C27H32N2O4SCouleur et forme :SolidMasse moléculaire :480.62Antiviral agent 10
CAS :<p>Antiviral agent 10 effectively inhibits the respiratory syncytial virus (RSV) [1], serving as a potent anti-viral compound.</p>Formule :C22H24N2O5Couleur et forme :SolidMasse moléculaire :396.443-Chlorogentisyl alcohol
CAS :<p>3-Chlorogentisyl alcohol: E. coli β-glucuronidase inhibitor (IC50=0.74µM, Ki=0.58µM), antiproliferative, for anti-cancer/inflammatory research.</p>Formule :C7H7ClO3Couleur et forme :SolidMasse moléculaire :174.58Influenza A virus-IN-4
CAS :<p>Influenza A virus-IN-4 (23b), a potent neuraminidase inhibitor derived from Oseltamivir, effectively targets influenza viruses.</p>Formule :C19H28N4O4Couleur et forme :SolidMasse moléculaire :376.45Silthiofam
CAS :<p>Silthiofam effectively combats Ggt, a wheat take-all fungus, now widely used for control in China.</p>Formule :C13H21NOSSiDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :267.46FtsZ-IN-2
CAS :<p>FtsZ-IN-2, a bacterial FtsZ inhibitor, hampers GTPase; has anti-MRSA/MSSA effects with 2 μg/ml MIC.</p>Formule :C30H35N5SCouleur et forme :SolidMasse moléculaire :497.7SJ-3366
CAS :<p>SJ3366 is a unique and highly potent nonnucleoside reverse transcriptase human immunodeficiency virus type 1 and HIV-2 inhibitor.</p>Formule :C21H24N2O3Couleur et forme :SolidMasse moléculaire :352.43Phenosulfazole
CAS :<p>Phenosulfazole is a potent antiviral agent which has the potential for the research of poliomyelitis virus [1].</p>Formule :C9H8N2O3S2Couleur et forme :SolidMasse moléculaire :256.3NEU617
CAS :<p>NEU617 is an inhibitor of the growth of protozoan parasites, against T. brucei bloodstream proliferation.</p>Formule :C31H26ClFN4O2Couleur et forme :SolidMasse moléculaire :541.02Cylindrospermopsin
CAS :<p>Cylindrospermopsin: a toxic cyanobacterial uracil derivative, disrupts protein/glutathione synthesis in hepatocytes, and is genotoxic.</p>Formule :C15H21N5O7SCouleur et forme :SolidMasse moléculaire :415.42SARS-CoV-2-IN-36
<p>SARS-CoV-2-IN-36: strong Mpro inhibitor, IC50=2.37μM, Kd=1.19μM, fights UC-1074/RG2674/NVDBB-2220 variants.</p>Formule :C17H21N5O3Couleur et forme :SolidMasse moléculaire :343.38MMT5-14
CAS :<p>MMT5-14: potent SARS-CoV-2 inhibitor, improves antiviral activity (2-7x), boosts prodrug in plasma/lungs (200-300x), raises NTP in lungs (5x).</p>Formule :C39H55N6O8PCouleur et forme :SolidMasse moléculaire :766.86HCV-IN-34
CAS :<p>HCV-IN-35, an oral HCV blocker, has an EC50 of 0.010 μM and a CC50 of 7.5 μM, indicating strong antiviral effects.</p>Formule :C31H36ClN5Couleur et forme :SolidMasse moléculaire :514.1HIV-1 protease-IN-2
CAS :<p>HIV-1 protease-IN-2: strong HIV-1 protease blocker, IC50 2.53 nM, fights DRV-sensitive/resistant HIV-1.</p>Formule :C27H34N4O7SCouleur et forme :SolidMasse moléculaire :558.65
