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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AFK-108
CAS :<p>AFK-108 is a fungicide agent.</p>Formule :C21H26Cl2N2ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :393.35ACP1b
CAS :<p>ACP1b is an activator of ClpP protease.</p>Formule :C18H18ClF3N2O3S2Couleur et forme :SolidMasse moléculaire :466.93AL-9
CAS :<p>AL-9 is a GT-1b and GT-2a replication inhibitor.</p>Formule :C23H22N4O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :402.45Miloxacin
CAS :<p>Miloxacin is an antibiotic active against gram-negative bacteria.</p>Formule :C12H9NO6Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :263.20Fozivudine 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 :745.95Ametoctradin
CAS :<p>Ametoctradin is a Qo-site inhibitor of mitochondrial respiratory complex III and is used in the study of oomycete diseases.</p>Formule :C15H25N5Degré de pureté :99.65%Couleur et forme :SolidMasse moléculaire :275.39SSAA09E1
CAS :<p>SSAA09E1 blocks SARS-CoV entry, lowers ACE2-mediated HEK293T cell infection (EC50 = 6.7 μM), and inhibits cathepsin L (IC50 = 5.33 μM).</p>Formule :C7H9N3S2Couleur et forme :SolidMasse moléculaire :199.3Mtb-cyt-bd oxidase-IN-7
<p>Mtb-cyt-bd oxidase-IN-7 inhibits Cyt-bd with 4.17 μM affinity and has anti-tuberculosis properties.</p>Formule :C18H14F3NO2Couleur et forme :SolidMasse moléculaire :333.3L 870810
CAS :<p>L 870810 is a small-molecule inhibitor of HIV-1 integrase with potent antiviral activity in cell culture and good pharmacokinetic properties.</p>Formule :C20H19FN4O4SCouleur et forme :SolidMasse moléculaire :430.45(S)-Enzaplatovir
CAS :<p>(S)-Enzaplatovir, an S-enantiomer with antiviral properties, has an EC50 of 56 nM against RSV.</p>Formule :C20H19N5O3Couleur et forme :SolidMasse moléculaire :377.4HPV18-IN-1
CAS :<p>HPV18-IN-1, potent cervical cancer inhibitor, blocks E7-Rb-E2F pathway and DNA methylation.</p>Formule :C14H10N4OSCouleur et forme :SolidMasse moléculaire :282.32(+)-Dihydrocalanolide A
CAS :<p>DHCal A (NSC 678323) is an oral nonnucleoside Reverse Transcriptase inhibitor for HIV research.</p>Formule :C22H28O5Couleur et forme :SolidMasse moléculaire :372.455,10-Dideazaaminopterin
CAS :<p>5,10-Dideazaaminopterin is an antileukemic drug.</p>Formule :C21H22N6O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :438.44Tropesin
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 :505.95SP187
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 :601.53Aranotin
CAS :<p>Aranotin, from Arachniotus aureus, inhibits RNA viruses by blocking RNA polymerase.</p>Formule :C20H18N2O7S2Couleur et forme :SolidMasse moléculaire :462.5BPH-715
CAS :<p>BPH-715 inhibits the liver-stage growth of P. falciparum with an IC50 of 10 μM for P. falciparum exoerythrocytic forms in HepG2 cells.</p>Formule :C17H31NO7P2Degré de pureté :98.91%Couleur et forme :SolidMasse moléculaire :423.38Acyclovir monophosphate
CAS :<p>Acyclovir monophosphate, a strong anti-HSV agent, inhibits viral DNA polymerase, blocking DNA synthesis and chain elongation.</p>Formule :C8H12N5O6PCouleur et forme :SolidMasse moléculaire :305.18Penamecillin
CAS :<p>Penamecillin (Wy 20788) is an orally active antibacterial agent.</p>Formule :C19H22N2O6SCouleur et forme :SolidMasse moléculaire :406.45W13
CAS :<p>W13 is a potent inhibitor of MsbA and is an ATPase stimulator (EC50: 5.5 μM).</p>Formule :C30H34N4O3Couleur et forme :SolidMasse moléculaire :498.62Antimycobacterial agent-1
CAS :<p>Compound 33: antimycobacterial, MIC 1 μg/ml vs M. tuberculosis H37Ra, low toxicity (IC50 143.2 μg/ml in Vero cells).</p>Formule :C18H12N4O5SCouleur et forme :SolidMasse moléculaire :396.38HIV-1 inhibitor-50
CAS :<p>HIV-1 inhibitor-50 is a non-nucleoside reverse transcriptase inhibitor (NNRTI) that targets HIV-1 reverse transcriptase (IC50 = 50 nM).</p>Formule :C24H18FN5O2Couleur et forme :SolidMasse moléculaire :427.43GA-O-06
<p>GA-O-06: 18β-Glycyrrhetinic acid derivative with powerful antimicrobial effects on Gram-positive bacteria and anti-inflammatory properties.</p>Formule :C37H46FNO6Couleur et forme :SolidMasse moléculaire :619.76CAY10760
CAS :<p>CAY10760 inhibits RAD51-BRCA2 interaction (EC50=19 μM), reduces homologous recombination by 54%, and hinders BxPC-3/Capan-1 cancer cell proliferation.</p>Formule :C28H24ClN3O3Couleur et forme :SolidMasse moléculaire :485.96ANT431
CAS :<p>ANT431 is a novel metallo-β-lactamase inhibitor for the treatment of carbapenem-resistant enterobacteriaceae infections</p>Formule :C9H7N3O4S2Couleur et forme :SolidMasse moléculaire :285.3Metallo-β-lactamase-IN-2
CAS :<p>Metallo-β-lactamase-IN-4 (compound 40) is a potent metallo-β-lactamases (MBL) inhibitor with IC 50 values of 0.1 μM for VIM-1, 1.3 μM for NDM-1 and 5.0 μM for</p>Formule :C9H9Cl2NOSCouleur et forme :SolidMasse moléculaire :250.14JNJ-9676
CAS :<p>JNJ-9676 is an orally active inhibitor of the coronavirus membrane protein, thereby blocking viral assembly and release.coronavirus and SARS-CoV.</p>Formule :C28H21F2N5O2Degré de pureté :99.83%Couleur et forme :SoildMasse moléculaire :497.52,3-Dehydro-2-Deoxy-N-Acetylneuraminic Acid
CAS :<p>2,3-Dehydro-2-Deoxy-N-Acetylneuraminic Acid is a pan-sialidase (neuraminidase, NEU) inhibitor with inhibitory activity and against various influenza viruses.</p>Formule :C11H17NO8Couleur et forme :SolidMasse moléculaire :291.262-Keto-D-galactose
CAS :<p>2-Keto-D-galactose inhibits DNA synthesis and inhibits the proliferation of in vitro grown Ehrlich ascites tumor cells.</p>Formule :C6H10O6Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :178.14GS-9256
CAS :<p>GS-9256 is a selective inhibitor of the HCV NS3 protease, exhibiting favorable pharmacokinetic properties and antiviral activity [1].</p>Formule :C46H56ClF2N6O8PSDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :957.46Antimalarial agent 24
CAS :<p>Compound 24 (Compound 7), an in vitro antimalarial agent, demonstrates inhibitory activity against the Plasmodium falciparum W2 strain with an IC50 of 0.81 μM</p>Formule :C20H16N4O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :344.37SARS-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 :343.4Antimalarial agent 26
CAS :<p>Antimalarial agent 26, a derivative of 1,4-naphthoquinones, demonstrates antimalarial properties through oral administration.</p>Formule :C20H22N4O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :366.41Antimalarial agent 29
CAS :<p>Compound 29 (also known as Compound 16) is an antimalarial agent that demonstrates inhibition of the P.</p>Formule :C18H10ClF3N2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :346.73SARS-CoV-2-IN-19
CAS :<p>"SARS-CoV-2-IN-19: potent SARS-CoV-2 decapping enzyme inhibitor, EC50 8.8 μM, potential for HCoV outbreaks."</p>Formule :C33H38N2O6Couleur et forme :SolidMasse moléculaire :558.66S-F24
CAS :<p>S-F24 is a broad-spectrum antifungal agent that demonstrates potent inhibition of CYP3A4, with an IC50 of 0.4 μM.</p>Formule :C25H27BrF2N6OCouleur et forme :SolidMasse moléculaire :545.42PNU-176798
CAS :<p>PNU-176798 is an agent with antimicrobial.</p>Formule :C16H13FN4O3SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :360.36ST7612AA1
CAS :<p>ST7612AA1: potent, oral HDAC inhibitor; reactivates HIV-1 latency; shows antitumor effects; may study malaria.</p>Formule :C20H27N3O4SDegré de pureté :99.71%Couleur et forme :SolidMasse moléculaire :405.51(S)-Tedizolid
CAS :<p>(S)-Tedizolid is the S-enantiomer of Tedizolid. Tedizolid is a novel oxazolidinone with activity against Gram-positive pathogens.</p>Formule :C17H15FN6O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :370.34L-Eflornithine
CAS :<p>L-Eflornithine: irreversible ODC inhibitor, KD 1.3±0.3 μM, Kinact 0.15±0.03 min-1, enantiomer of Eflornithine.</p>Formule :C6H12F2N2O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :182.17(R,R)-BAY-Y 3118
CAS :<p>(R,R)-BAY-Y 3118, the R-enantiomer of BAY-Y 3118, exhibits weak bactericidal activity.</p>Formule :C20H21ClFN3O3Couleur et forme :SolidMasse moléculaire :405.85DHDPS-IN-1
CAS :<p>DHDPS-IN-1 (compound 8), a DHDPS inhibitor with 39 μM IC50, has potential in antibacterial and herbicidal applications.</p>Formule :C13H11NO5SCouleur et forme :SolidMasse moléculaire :293.3Lalistat 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 :298.36MDRTB-IN-1
CAS :<p>MDRTB-IN-1 (5aα) is an antibiotic which is against Mycobacterium tuberculosis H37Rv(MIC90 :10.5 μM).</p>Formule :C15H18N2O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :274.32PC190723
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 :355.75RO-9187
CAS :<p>RO-9187 is an effective HCV virus replication inhibitor(IC50: 171 nM).</p>Formule :C9H12N6O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :284.23Bentysrepinine
CAS :<p>Bentysrepinine, a novel anti-HBV agent, inhibits DNA-HBV and cccDNA activities for the treatment of hepatitis B virus (HBV)-infected hepatitis.</p>Formule :C29H35N3O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :489.61NVP018
CAS :<p>NVP018 (BC 556) inhibits HBV, HCV, HIV-1 replication, barely affects drug transporters, and resists HCV/HIV-1 resistance development.</p>Formule :C45H62FN5O11Couleur et forme :SolidMasse moléculaire :868Cap-dependent endonuclease-IN-19
CAS :<p>Cap-dependent endonuclease-IN-19, a spirocyclic pyridinone, strongly inhibits influenza A virus RNA polymerase.</p>Formule :C28H31N3O4Couleur et forme :SolidMasse moléculaire :473.56RSV-IN-6
CAS :<p>RSV-IN-6, or Compound 53, inhibits RSV by targeting M2-1; EC50: 4.4 μM (RSV-A), 1.3 μM (RSV-B).</p>Formule :C19H19N3S3Couleur et forme :SolidMasse moléculaire :385.57FabH-IN-1
CAS :<p>FabH-IN-1, a broad-spectrum antibiotic and antioxidant, inhibits bacterial FabH enzyme.</p>Formule :C17H16N2OSCouleur et forme :SolidMasse moléculaire :296.39Olanexidine Hydrochloride semihydrate
CAS :<p>Olanexidine is a monobiguanide compound with the activity of bactericidal.</p>Formule :C17H31Cl4N5ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :463.27GW8510
CAS :<p>GW8510 is a CDK2 and RRM2 inhibitor that affects DNA synthesis and antiproliferation in tumor cells. In mammalian aging models, GW851 prolongs lifespan.</p>Formule :C21H15N5O3S2Degré de pureté :99.32%Couleur et forme :SolidMasse moléculaire :449.51Antifungal agent 74
CAS :<p>Antifungal agent 74 (compound 3c), is a potent substance that exhibits excellent fungicidal activity against C.</p>Formule :C4HCl3N4SCouleur et forme :SolidMasse moléculaire :243.5BMVC2
CAS :<p>BMVC2 (o-BMVC), a carbazole derivative of BMVC, is a G-quadruplex (G4) stabilizer.</p>Formule :C28H25I2N3Couleur et forme :SolidMasse moléculaire :657.33PSI-7409 tetrasodium
CAS :<p>PSI-7409 tetrasodium, a sofosbuvir metabolite, inhibits GT 1b, 2a, 3a, 4a NS5B polymerases with IC50s of 1.6, 2.8, 0.7, 2.6 μM.</p>Formule :C10H16FN2Na4O14P3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :592.117Nucleoside-Analog-2
CAS :<p>Nucleoside-Analog-2 is a 4'-Azidocytidine analogue, used to against Hepatitis C virus (HCV) replication.</p>Formule :C9H11N5O6Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :285.21VP-4509
CAS :<p>VP-4509: Anti-MRSA, MIC 49.3 μM; combats Pseudomonas aeruginosa.</p>Formule :C14H16N2O5SCouleur et forme :SolidMasse moléculaire :324.35RNPA1000
CAS :<p>RNPA1000 is an attractive antimicrobial development candidate and RnpA inhibitor.</p>Formule :C23H18BrN3O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :464.31Antiparasitic agent-9
CAS :<p>Antiparasitic agent-9 (compound 47) - orally active with high efficacy against human parasites.</p>Formule :C18H20N6O2SCouleur et forme :SolidMasse moléculaire :384.46SARS-CoV-IN-2
CAS :<p>SARS-CoV-IN-2 is an effective SARS-CoV replication inhibitor</p>Formule :C24H26ClFeN3ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :463.78Taribavirin hydrochloride
CAS :<p>Taribavirin HCl: oral drug targeting HCV in liver, spares red blood cells, aims to reduce anemia risk.</p>Formule :C8H14ClN5O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :279.68D-Xylofuranose, 1,2,3,5-tetraacetate
CAS :<p>1,2,3,5-Tetra-O-acetyl-D-xylofuranose is a starting material for the synthesis of nucleosides.</p>Formule :C13H18O9Couleur et forme :SolidMasse moléculaire :318.28Rovafovir Etalafenamide
CAS :<p>Rovafovir Etalafenamide is a prodrug of anti-HIV nucleoside phosphonate.</p>Formule :C21H24FN6O6PDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :506.42Trovirdine hydrochloride
CAS :<p>Trovirdine hydrochloride is a reverse transcriptase inhibitor.</p>Formule :C13H14BrClN4SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :373.7Exeporfinium chloride
CAS :<p>Exeporfinium chloride(XF-73) is an antimicrobial agent that can weaken bacterial cell walls.</p>Formule :C44H50Cl2N6O2Couleur et forme :SolidMasse moléculaire :765.81FPI-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 :363.35Influenza virus-IN-5
CAS :<p>Influenza virus-IN-5 (Compound 5f) is an influenza virus hemagglutinin (HA) inhibitor that acts on the A/H3N2 virus (EC50: 1 nM).</p>Formule :C21H26ClN3O2SCouleur et forme :SolidMasse moléculaire :419.97Urease-IN-7
CAS :<p>Urease-IN-7 (Compound 5k) acts as a competitive inhibitor of the enzyme urease, exhibiting an IC50 value of 3.33 μM and a K_i of 3.62 μM.</p>Formule :C16H10BrFN4SCouleur et forme :SolidMasse moléculaire :389.24HIV-1 inhibitor-33
CAS :<p>HIV-1 inhibitor-33, potent against HIV-1 (EC50: 8.6 nM), low toxicity to MT-4 cells (CC50: 18 μM), useful for AIDS research.</p>Formule :C25H28N6OCouleur et forme :SolidMasse moléculaire :428.53Buclosamide
CAS :<p>Buclosamide is a topical antimycotic agent that can be used in dermatomycoses [1].</p>Formule :C11H14ClNO2Couleur et forme :SolidMasse moléculaire :227.69INSCoV-614(1B)
CAS :<p>INSCoV-614(1B), a potent Mpro inhibitor, may help fight SARS-CoV-2, per patent WO2021219089A1.</p>Formule :C23H21ClF3N5O3Couleur et forme :SolidMasse moléculaire :507.89Pirlindole free base
CAS :<p>Pirlindole is a reversible inhibitor of monoamine oxidase A (RIMA). It is structurally and pharmacologically related to metralindole.</p>Formule :C15H18N2Couleur et forme :SolidMasse moléculaire :226.32SPR39
<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 :441.52Metallo-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 :332.34Antifungal agent 35
CAS :<p>Antifungal agent 35 is an effective antifungal agent that potentiates the antifungal activity of fluconazole against C. albicans.</p>Formule :C26H27BrN4O4Couleur et forme :SolidMasse moléculaire :539.42BA-53038B
CAS :<p>BA-53038B is an HBV core protein allosteric modulator (CpAM), binding to the HAP pocket and modulating HBV capsid assembly in a distinct manner (EC50: 3.32 μM).</p>Formule :C14H16ClNOCouleur et forme :SolidMasse moléculaire :249.74Closthioamide
CAS :<p>Closthioamide is a potent inhibitor of bacterial DNA gyrase and highly active against MRSA, Ec, VRE, and Mv (MICs: 0.58 μM, 9.00 μM, 0.58 μM and 72.03 μM).</p>Formule :C29H38N6O2S6Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :695.04Succinate dehydrogenase-IN-1
CAS :<p>Succinate dehydrogenase-IN-1 (Compound 34) acts as an inhibitor of succinate dehydrogenase (SDH), exhibiting an IC50 value of 0.94 μM and a KD of 22.4 μM. This compound also demonstrates antifungal activity, with EC50 values against Rhizoctonia solani, Sclerotinia sclerotiorum, Monilinia fructicola, and Botrytis cinerea measured at 0.04 μM, 1.13 μM, 1.61 μM, and 1.21 μM, respectively.</p>Formule :C20H13F6N3OCouleur et forme :SolidMasse moléculaire :425.33cp028
CAS :<p>cp028 inhibits pre-mRNA splicing in vitro.</p>Formule :C23H17FN2O4Couleur et forme :SolidMasse moléculaire :404.39Debneyol
CAS :<p>Debneyol exhibits more potent fungicidal activity than validamycin.</p>Formule :C15H26O2Couleur et forme :SolidMasse moléculaire :238.37InhA-IN-4
CAS :<p>InhA-IN-4 (TU14) is a Mycobacterium tuberculosis InhA (enoyl ACP reductase) inhibitor for the study of Mycobacterium tuberculosis infection.</p>Formule :C14H12BrN3O2SDegré de pureté :>99.99%Couleur et forme :SolidMasse moléculaire :366.23Antituberculosis 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 :323.34AB-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 :461.85Lupulon
CAS :<p>Lupulon has a role as an apoptosis inducer, antimicrobial agent, angiogenesis inhibitor, and antineoplastic agent.</p>Formule :C26H38O4Couleur et forme :SolidMasse moléculaire :414.58Phosphoglycolohydroxamic acid
CAS :<p>Phosphoglycolohydroxamic acid inhibits aldolase/triose-phosphate isomerase; used in antibacterial/antifungal research.</p>Formule :C2H6NO6PCouleur et forme :SolidMasse moléculaire :171.05Aliconazole
CAS :<p>Aliconazole is an imidazole derivative with antifungal activity for the study of skin infections.</p>Formule :C18H13Cl3N2Degré de pureté :99.21% - 99.79%Couleur et forme :SolidMasse moléculaire :363.67Lipoxamycin hemisulfate
CAS :<p>Lipoxamycin hemisulfate (Lipoxamycin) is an inhibitor of serine palmitoyltransferase (IC50 = 21 nM) with antifungal activity.</p>Formule :C38H74N4O14SDegré de pureté :99.14% - 99.93%Couleur et forme :SolidMasse moléculaire :843.08Quinfamide
CAS :<p>Quinfamide is a compound with the potential to treat tropical parasitic infections such as Amoebiasis and Helminthiasis.</p>Formule :C16H13Cl2NO4Degré de pureté :99.92%Couleur et forme :SolidMasse moléculaire :354.18Edelfosine
CAS :<p>inhibits phosphatidylinositol phospholipase C</p>Formule :C27H58NO6PDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :523.73Tuberculosis inhibitor 3
CAS :<p>Tuberculosis inhibitor 3 is a highly potent and oral anti-tuberculosis drug against both drug-sensitive and drug-resistant Mycobacterium , H37RV & MDR-TB.</p>Formule :C21H22F6N4O3SDegré de pureté :98.8%Couleur et forme :SolidMasse moléculaire :524.483CPLro-IN-2
CAS :<p>3CPLro-IN-2: Potent oral SARS-CoV-2 3CLpro inhibitor, IC50: 1.55 μM, Ki: 6.09 μM, targets vital COVID-19 protein.</p>Formule :C32H24BrNO2Couleur et forme :SolidMasse moléculaire :534.44Nitrobenzofuroxan
CAS :<p>Nitrobenzofuroxan, is a HIV-1 and IDO1 inhibitor.</p>Formule :C6H3N3O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :181.11R78206
CAS :<p>R 78206 is a pyridazinamine derivative that suppresses the formation of poliovirus eclipse particles.</p>Formule :C22H29N3O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :383.48GSK5750
CAS :GSK5750 is the ribonuclease H activity inhibitor.Formule :C16H12N4O2SCouleur et forme :SolidMasse moléculaire :324.36Cefcanel daloxate
CAS :<p>Cefcanel daloxate is a pro-drug of KY-087.</p>Formule :C27H27N5O9S3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :661.73Acaterin
CAS :Acaterin, an inhibitor of acyl-CoA: cholesterol acyltransferase (ACAT), inhibits synthesis of cholesteryl ester in macrophage J774.Formule :C13H22O3Couleur et forme :SolidMasse moléculaire :226.31Benthiavalicarb isopropyl
CAS :<p>Benthiavalicarb isopropyl is a fungicide, specifically targeting downy mildew and blight.</p>Formule :C18H24FN3O3SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :381.465-Et-ddU
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