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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MmpL3-IN-1
CAS :<p>MmpL3-IN-1 (compound 32) inhibits MmpL3 with <0.016 μg/mL MIC against M. tuberculosis, aiding drug-resistant TB research.</p>Formule :C20H21F2N3OCouleur et forme :SolidMasse moléculaire :357.4NIC
CAS :<p>NIC is an inhibitor of host invasion. It is also an inhibitor of VEGF binding to immobilized heparin.</p>Formule :C15H16ClN3O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :321.76Neoarsphenamine
CAS :<p>Neoarsphenamine is an antisyphilitic still used for infections occasionally.</p>Formule :C13H14As2N2NaO4SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :467.16S 863390
CAS :<p>S 863390 is a renin inhibitor.</p>Formule :C37H52N6O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :644.854-((4-((4-Aminophenyl)sulfonyl)phenyl)amino)-4-oxobutanoic acid
CAS :<p>4-((4-((4-Aminophenyl)sulfonyl)phenyl)amino)-4-oxobutanoic acid is a sulfonamide compound that can be used as an anti infective agent [1].</p>Formule :C16H16N2O5SCouleur et forme :SolidMasse moléculaire :348.37SPR39
<p>SPR39 inhibits SARS-CoV-2 protease (Ki: 0.252µM), with lesser effect on hCatL/B, and has antiviral, cytotoxic properties.</p>Formule :C24H31N3O5Couleur et forme :SolidMasse moléculaire :441.52Urease-IN-4
<p>Urease-IN-4 inhibits urease (IC50: 1.64 µM), targets P. vulgaris (IC50: 15.27 µg/mL), and is low in cytotoxicity.</p>Formule :C16H20N2O3SCouleur et forme :SolidMasse moléculaire :320.41C562-1101
CAS :<p>C562-1101 is a novel potent botulinum neurotoxin serotype E (BoNT/E) inhibitor.</p>Formule :C22H27N3O5SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :445.53SEC inhibitor KL-2
CAS :<p>KL-2: potent SEC inhibitor, selectively disrupts AFF4-CCNT1, dose-dependent, Ki: 1.50 μM.</p>Formule :C17H13ClFNO3Degré de pureté :99.86%Couleur et forme :SolidMasse moléculaire :333.74Acyclovir alaninate
CAS :<p>Acyclovir alanine is a pro-drug of Acyclovir. Acyclovir works by decreasing the production of DNA of the virus and it shows very low cytotoxicity.</p>Formule :C11H16N6O4Couleur et forme :SolidMasse moléculaire :296.28L-708906
CAS :<p>L-708906 is the Human Immunodeficiency Virus Type 1 inhibitor.</p>Formule :C24H20O6Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :404.41BPH-651
CAS :<p>BPH-651 is a CrtM inhibitor.</p>Formule :C19H21NOCouleur et forme :SolidMasse moléculaire :279.38Antibacterial agent 96
CAS :<p>Compound 4k is potent against drug-susceptible and resistant M. tuberculosis but toxic to HepG2 and Vero cells.</p>Formule :C18H15Cl2NO2Couleur et forme :SolidMasse moléculaire :348.22Lascufloxacin HCl
CAS :<p>Lascufloxacin (KRP-AM-1977) is a strong antibiotic, most effective against gram-positive bacteria, with limited cross-resistance.</p>Formule :C21H25ClF3N3O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :475.89Antifungal agent 31
CAS :<p>Orally active triazole, antifungal 31 with pyrrolizinone structure, combats Candida, reduces mortality and renal infection in mice.</p>Formule :C25H22F2N6O3Couleur et forme :SolidMasse moléculaire :492.48TXA6101
CAS :<p>TXA6101: FtsZ inhibitor, blocks bacterial division, MIC 1 μg/mL against MRSA, effective on TXA707-resistant mutants. Potential anti-Gram-negative agent.</p>Formule :C18H10BrF5N2O3Couleur et forme :SolidMasse moléculaire :477.18DENV-IN-4
CAS :<p>DENV-IN-4: Effective DENV inhibitor (EC50=4.79 μM), low toxicity (CC50>100 μM), and strong selectivity (SI>20.9); suppresses DENV2 and RdRp.</p>Formule :C28H32N4O4SiCouleur et forme :SolidMasse moléculaire :516.66Antitubercular agent-39
CAS :<p>Antitubercular agent-39 (Compound P1) is a potent agent effective against both drug-resistant strains and drug-susceptible clinical isolates of tuberculosis,</p>Formule :C26H30N4O2Couleur et forme :SolidMasse moléculaire :430.54SARS-CoV-2 Mpro-IN-1
CAS :<p>SARS-CoV-2 Mpro-IN-1 (compound 16b-3) is a potent, selective and irreversible SARS-CoV-2 main protease (Mpro) inhibitor (IC 50 = 116 nM) [1].</p>Formule :C15H11FN2O2SCouleur et forme :SolidMasse moléculaire :302.32Antibacterial agent 111
CAS :<p>Compound 3: potent against B. cereus & K. pneumonia; MICs: 3.90 & 0.49 μg/mL; targets tyrosyl-tRNA synthetase.</p>Formule :C18H12N6SCouleur et forme :SolidMasse moléculaire :344.39L 738372
CAS :<p>L 738372 is a non-nucleoside inhibitor of HIV-1 reverse transcriptase.</p>Formule :C18H15N3OCouleur et forme :SolidMasse moléculaire :289.33Cap-dependent endonuclease-IN-23
CAS :<p>Cap-dependent endonuclease-IN-23 hinders influenza virus replication by inhibiting CEN, with potential for flu research.</p>Formule :C26H23F2N3O7Couleur et forme :SolidMasse moléculaire :527.47Homocarbonyltopsentin
CAS :<p>Homocarbonyltopsentin: Small molecule, binds TSL2 pentaloops, enhances SMN2 E7 splicing, EC50 16 μM.</p>Formule :C21H14N4O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :370.36Antibacterial agent 124
CAS :<p>Antibacterial agent 124 inhibits Sa ProRS with an IC50 of 0.18 μM.</p>Formule :C16H17ClFN3O2Couleur et forme :SolidMasse moléculaire :337.78Phelorphan
CAS :<p>Phelorphan is an inhibitor of enkephalinase.</p>Formule :C20H22N2O4SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :386.46HIV-1 inhibitor-47
CAS :<p>HIV-1 Inhibitor-47 blocks Vif-APOBEC3G interaction, has 14.33 μM IC50, and may yield antianxiety and antipsychotic derivatives.</p>Formule :C12H14N6Couleur et forme :SolidMasse moléculaire :242.28Rosaramicin
CAS :<p>Rosaramicin, a lipid-soluble basic macrolide, is an antibacterial substance similar to erythromycin but with a better activity against Gram-negative bacteria.</p>Formule :C31H51NO9Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :581.74L-erythro-Chloramphenicol
CAS :<p>L-erythro-Chloramphenicol functions as a potent inhibitor of electron transport.</p>Formule :C11H12Cl2N2O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :323.13HBV-IN-25
CAS :<p>HBV-IN-25: oral HBV cccDNA reducer, anti-HBeAg, anti-HBV (IC50: 0.58/1.15 μM), soluble (>452 μg/mL), non-toxic.</p>Formule :C18H14ClNO4Couleur et forme :SolidMasse moléculaire :343.76Antimalarial agent 18
<p>Potent antimalarial, lipophilic, inhibits P. falciparum (IC50=50nM) & A. baumanii (IC50=390nM), blocks non-mevalonate pathway.</p>Formule :C23H44NO9PCouleur et forme :SolidMasse moléculaire :509.57Anti-infective agent 4
CAS :<p>Oral Trypanosoma cruzi inhibitor (IC50: 0.016 μM), Anti-infective agent 4 reduces in vivo parasite load.</p>Formule :C19H12F3N5O4Couleur et forme :SolidMasse moléculaire :431.32CAY10704
CAS :<p>CAY10704: Potent HCV inhibitor, EC50=17 nM, low cytotoxicity, good in mice, liver-targeted, not hepatotoxic, weak against dengue.</p>Formule :C18H20Cl2N2Couleur et forme :SolidMasse moléculaire :335.27Antimicrobial agent-5
<p>Antimicrobial agent-5: potent, selective for Gram-negative/positive bacteria, blocks LPS-CD14/TLR4, anti-inflammatory.</p>Formule :C32H48N16Couleur et forme :SolidMasse moléculaire :656.83Abimtrelvir
CAS :<p>Abimtrelvir exhibited antiviral activity.</p>Formule :C24H17ClF3N7O2Couleur et forme :SolidMasse moléculaire :527.89Globosuxanthone A
CAS :Globosuxanthone A: a dihydroxanthenone with anticancer and antifungal properties (MIC: F. graminearum 4, F. solani 8, B. cinerea 16 μg/mL).Formule :C15H12O7Couleur et forme :SolidMasse moléculaire :304.25BPH-1086
CAS :<p>BPH-1086 inhibits IspH, which with RPS1 binds mRNA or integrates into bacterial ribosomes.</p>Formule :C4H8O7P2Couleur et forme :SolidMasse moléculaire :230.05Hexamide
CAS :<p>Hexamide is a protein inhibitor.</p>Formule :C13H17NOCouleur et forme :SolidMasse moléculaire :203.28Antiviral 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 :396.44Polyketide synthase 13-IN-2
CAS :<p>Comp 42 is a potent PKS13 inhibitor in M. tuberculosis with MIC of 0.25 μg/mL.</p>Formule :C22H21NO5Couleur et forme :SolidMasse moléculaire :379.41Antifungal agent 70
CAS :<p>Antifungal Agent 70 (Compound 13), a dihydroeugenol-imidazole, exhibits efficacy against multi-resistant Candida auris with a minimum inhibitory concentration (</p>Formule :C23H25ClN2O4Couleur et forme :SolidMasse moléculaire :428.91Quinuronium 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 :455.51RMI 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 :370.44FR-182024
CAS :<p>FR-182024 is a novel cephem derivative, it has potent anti-Helicobacter pylori activity.</p>Formule :C18H16N4O4S3Couleur et forme :SolidMasse moléculaire :448.54Mt 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 :410.45Antituberculosis agent-2
CAS :<p>Compound 8d: treats MDR and sensitive tuberculosis, low toxicity, good oral bioavailability, stable in humans/mice; MIC: 0.454-1.757 μg/mL.</p>Formule :C19H17NO4Couleur et forme :SolidMasse moléculaire :323.34SP187
CAS :<p>SP187 (MON-DNJ) is a host-targeted iminosugar. It has anti-filovirus infection activity.SP187 is used for therapeutic use against influenza and dengue viruses.</p>Formule :C16H33NO5Degré de pureté :99.18%Couleur et forme :SolidMasse moléculaire :319.44BPH-1358
CAS :<p>BPH-1358 (NSC-50460) inhibits FPPS and UPPS (IC50: 1.8 μM, 110 nM), active against S. aureus (MIC ~250 ng/mL).</p>Formule :C32H30Cl2N6O2Degré de pureté :99.74%Couleur et forme :SolidMasse moléculaire :601.53AB-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 :461.85Phosphoglycolohydroxamic acid
CAS :<p>Phosphoglycolohydroxamic acid inhibits aldolase/triose-phosphate isomerase; used in antibacterial/antifungal research.</p>Formule :C2H6NO6PCouleur et forme :SolidMasse moléculaire :171.05HIV-1 inhibitor-35
CAS :<p>HIV-1 inhibitor-35, potent against HIV (EC50: 80 nM LTR, 70 nM CMV), also suppresses HepG2 cells (CC50: 40 nM), may reverse HIV-1 latency.</p>Formule :C13H12Cl3N5OSCouleur et forme :SolidMasse moléculaire :392.69Antiparasitic agent-2
CAS :<p>Compound 8a: potent against L. infantum (IC50=7.28μM) & T. cruzi (IC50=2.30μM); mildly toxic to HepG2 (CC50=26.79μM).</p>Formule :C20H17N3O3Couleur et forme :SolidMasse moléculaire :347.37HIV-1 inhibitor-48
CAS :<p>HIV-1 inhibitor-48 is a novel non-nucleoside reverse transcriptase inhibitor (NNRTI) and exhibits anti-HIV-1 activity .</p>Formule :C19H16BrN5Couleur et forme :SolidMasse moléculaire :394.27Mtb-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 :381.53Stampidine
CAS :<p>Stampidine prevents HIV-1, effective against resistant strains at subnanomolar levels.</p>Formule :C20H23BrN3O8PDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :544.29Derquantel
CAS :<p>nicotinic acetylcholine receptor antagonist</p>Formule :C28H37N3O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :479.61FLDP-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 :367.4Tromantadine
CAS :<p>Tromantadine is an amantadine derivative with antiherpetic activity (inhibits HSV-1 and HSV-2 replication).</p>Formule :C16H28N2O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :280.41Purfalcamine
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 :528.62NS2B/NS3-IN-3 hydrochloride
CAS :<p>NS2B/NS3-IN-3 hydrochloride is a Flavivirus NS2B-NS3 protease inhibitor [1].</p>Formule :C19H22ClN3O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :359.85Antileishmanial agent-14
CAS :<p>Antileishmanial agent-14, a sulfuretin analog, exhibits potential activity against Leishmania donovani promastigotes (IC 50 = 4.1 μM) and inhibits infection by</p>Formule :C23H26ClNO5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :431.91SARS-CoV-2 nsp14-IN-3
CAS :<p>SARS-CoV-2 nsp14-IN-3 (4975) is a potent inhibitor targeting the N7-Methyltransferase activity of SARS-CoV-2 nonstructural protein 14 (Nsp14), with an IC50</p>Formule :C17H17N3O3SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :343.4SARS-CoV-2-IN-41
CAS :<p>SARS-CoV-2-IN-41 (compound 2) is a potent inhibitor of SARS-CoV-2 3CL protease, exhibiting an IC50 of 0.022 µM and demonstrating antiviral efficacy [1].</p>Formule :C22H30F3N5O4S2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :549.63BK 218
CAS :<p>BK 218: New cephalosporin, treats S. pneumoniae, H. influenzae, M. catarrhalis; less effective on penicillin-resistant strains; oral/IV use.</p>Formule :C15H14ClN7NaO5S2Couleur et forme :SolidMasse moléculaire :494.88HIV-1 inhibitor-37
CAS :<p>HIV-1 inhibitor-37, a potent HIV-1 suppressant, shows promise as a novel latent reactivator.</p>Formule :C14H11Cl3N4OCouleur et forme :SolidMasse moléculaire :357.62Antitrypanosomal 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 :416.28Cap-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 :527.47Halofantrine, (-)-
CAS :<p>Halofantrine, (-)- is an antimalarial agent.</p>Formule :C26H30Cl2F3NOCouleur et forme :SolidMasse moléculaire :500.42Metallo-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 :203.2Antimalarial 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 :516.58F8-S43-S3
CAS :<p>F8-S43-S3 is a SARS-CoV-2 main protease inhibitor (IC 50 = 9.69 μM) [1].</p>Formule :C12H10N4O3SCouleur et forme :SolidMasse moléculaire :290.3Antitubercular agent-18
CAS :<p>Antitubercular agent-18 (9a) MIC: 2 μg/ml for H37Rv, Spec 192, 210; 128 μg/ml for Spec 800. Selective antimycobacterial.</p>Formule :C14H12BrN5OCouleur et forme :SolidMasse moléculaire :346.18SARS-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 :378.51Crisnatol mesylate
CAS :<p>Crisnatol, a potent and selective DNA intercalator, has potential anticancer activity.</p>Formule :C24H27NO5SCouleur et forme :SolidMasse moléculaire :441.54SARS-CoV-2-IN-31
CAS :<p>SARS-CoV-2-IN-31: COVID-19 inhibitor, IC50: 28.84-38.36 μM, useful in cancer studies.</p>Formule :C29H28N4O2Couleur et forme :SolidMasse moléculaire :464.56LabMol-301
CAS :<p>LabMol-301 blocks NS5 RdRp/NS2B-NS3pro (IC50: 0.8/7.4µM), protects cells from ZIKV death.</p>Formule :C18H16N6Couleur et forme :SolidMasse moléculaire :316.36Furalaxyl
CAS :<p>Furalaxyl is an fungicide of acyl amino chiral.</p>Formule :C17H19NO4Couleur et forme :SolidMasse moléculaire :301.34HIV-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 :357.83MMV687807
CAS :<p>MMV687807: potent anthelmintic, IC50 0.15 μM, CC50 1.69 μM against T. gondii.</p>Formule :C15H8ClF6NO2Couleur et forme :SolidMasse moléculaire :383.67Amiprilose
CAS :<p>Amiprilose is an Immunopotentiator.</p>Formule :C14H27NO6Degré de pureté :99.82% - >99.99%Couleur et forme :SolidMasse moléculaire :305.37Lalistat 1
CAS :<p>Lalistat 1 inhibits LAL (IC50=68 nM) and H. influenzae IgA1 protease; useful in Niemann-Pick C research.</p>Formule :C12H18N4O3SDegré de pureté :99.87%Couleur et forme :SolidMasse moléculaire :298.36P516-0475
CAS :<p>P516-0475, a novel inducer, enhances Streptococcus quorum sensing by blocking PepO, stabilizing SHP pheromones.</p>Formule :C15H17N5O3Couleur et forme :SolidMasse moléculaire :315.33Rufloxacin hydrochloride
CAS :<p>Rufloxacin HCl (MF-934 HCl): a fluoroquinolone that inhibits topoisomerase and B-cell differentiation.</p>Formule :C17H19ClFN3O3SDegré de pureté :99.80%Couleur et forme :SolidMasse moléculaire :399.867β-Lactamase-IN-1
CAS :β-Lactamase-IN-1 (4-(1,3-dihydroxypropan-2-yl)-6-methoxypyrido[2,3-b]pyrazin-3-one) is a β-Lactamase inhibitor and targets the infection of NeisseriaFormule :C11H13N3O4Degré de pureté :99.89%Couleur et forme :SolidMasse moléculaire :251.24PC190723
CAS :<p>PC190723 is an inhibitor of the bacterial cytosolic protein FtsZ with antimicrobial activity against Staphylococcus spp.</p>Formule :C14H8ClF2N3O2SDegré de pureté :97.64%Couleur et forme :SolidMasse moléculaire :355.75VEC-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 :447.48Salazopyridazine
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 :429.41Diamthazole hydrochloride
CAS :<p>Diamthazole (Dimazole) hydrochloride, an antifungal agent, is utilized in infection research.</p>Formule :C15H24ClN3OSCouleur et forme :SolidMasse moléculaire :329.89FR900098 (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 :220.117F-17
CAS :<p>F-17 inhibits biofilm, elastase, pyocyanin, and motility, binds to LasR/PqsR, and is non-cytotoxic.</p>Formule :C17H15BrO4Couleur et forme :SolidMasse moléculaire :363.2Laromustine
CAS :<p>Laromustine (VNP40101M) is a sulfonyl hydrolysis alkylation prodrug for cancer treatment with significant anticancer activity, inhibiting thioredoxin reductase.</p>Formule :C6H14ClN3O5S2Degré de pureté :≥98%Couleur et forme :SolidMasse moléculaire :307.78MK436
CAS :<p>MK436 is a therapeutic agent and an antigenic animal drug that is effective in the treatment of Trypanosoma cruzonii infection.</p>Formule :C11H14N4O3Couleur et forme :SolidMasse moléculaire :250.25Tromantadine hydrochloride
CAS :<p>Tromantadine hydrochloride is an amantadine derivative with antiherpetic activity (inhibits HSV-1 and HSV-2 replication).</p>Formule :C16H29ClN2O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :316.87Antimalarial agent 20
CAS :<p>Antimalarial agent 20, exhibiting potent efficacy with an IC50 value of 0.6 nM against the P.</p>Formule :C31H38N4O3Couleur et forme :SolidMasse moléculaire :514.66SARS-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 :421.47Fozivudine tidoxil
CAS :<p>Fozivudine tidoxil, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formule :C35H64N5O8PSCouleur et forme :SolidMasse moléculaire :745.95HIV-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 :582.59Antibacterial agent 65
CAS :<p>Antibacterial agent 65 is a potential antimicrobial agent and antioxidant agent.</p>Formule :C17H16O3Couleur et forme :SolidMasse moléculaire :268.3110-Formyl-5,8-dideazafolic acid
CAS :<p>10-Formyl-5,8-dideazafolic acid is a thymidylate synthase inhibitor.</p>Formule :C22H21N5O7Degré de pureté :96.04%Couleur et forme :SolidMasse moléculaire :467.43HIV-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 :582.66HBV-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 :433.48
