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(2.949 produits)
- Antibiotique(919 produits)
- Antifection(23 produits)
- DHFR(32 produits)
- Synthèse ADN/ARN(707 produits)
- VHB(176 produits)
- Protéase du VIH(447 produits)
- HSV(91 produits)
- Intégrase(2 produits)
- Ribosome(13 produits)
Affichez 2 plus de sous-catégories
5832 produits trouvés pour "Microbiologie/Virologie"
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3-Cyanovinylcarbazole phosphoramidite
CAS :<p>3-Cyanovinylcarbazole phosphoramidite: an antiviral, hinders viral DNA synthesis, modifies ribonucleotides.</p>Formule :C50H53N4O6PCouleur et forme :SolidMasse moléculaire :836.95Zika virus-IN-1
CAS :<p>Zika virus-IN-1 is an inhibitor of Zika virus (EC50: 1.56 μM).</p>Formule :C30H37N3O3SiCouleur et forme :SolidMasse moléculaire :515.72Caerulomycin A
CAS :<p>Caerulomycin A (Caerulomycin) (Cerulomycin; Caerulomycin) is an antifungal compound.</p>Formule :C12H11N3O2Degré de pureté :99.28%Couleur et forme :SolidMasse moléculaire :229.23R 87366
CAS :<p>R 87366 is used as a water-soluble HIV protease inhibitor.</p>Formule :C32H39N7O6Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :617.7HBV-IN-13
CAS :<p>HBV-IN-12 is a potent inhibitor of hepatitis B surface antigen (HBsAg).</p>Formule :C22H25NO7Couleur et forme :SolidMasse moléculaire :415.44BILR-355
CAS :<p>BILR-355 is a reverse transcriptase inhibitor.</p>Formule :C25H23N5O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :441.48Valtorcitabine dihydrochloride
CAS :<p>Valtorcitabine dihydrochloride, a DNA polymerase inhibitor, is used potentially for the treatment of HBV infection.</p>Formule :C14H24Cl2N4O5Couleur et forme :SolidMasse moléculaire :399.27Vinclozolin M2
CAS :<p>Vinclozolin M2, an active metabolite of vinclozolin, is generated through successive esterase activity and decarboxylation in C. elegans, as well as decarboxylation in human liver microsomes. It functions as an antagonist to the mineralocorticoid (IC50= 1,400 nM) and androgen receptors (IC50= 0.17 nM), demonstrated in reporter assays with MCF-7 cells. This compound is exclusively sold for research and analytical purposes, tailored for controlled laboratory use, and is not available in bulk sizes.</p>Formule :C11H11Cl2NO2Couleur et forme :SolidMasse moléculaire :260.1Chitin 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 :511.96NSC 288387
CAS :<p>NSC 288387, a pan-flavivirus MTase inhibitor, binds to the SAM-binding pocket and effectively inhibits Zika virus (ZIKV) with an IC50 of 0.2 μM, also preventing</p>Formule :C19H16N4O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :348.36SA09-Cu
CAS :<p>SA09-Cu is a potent, noncompetitive inhibitor of NDM-1, with an IC50 of 9.6 nM.</p>Formule :C8H16CuN2O2S4Couleur et forme :SolidMasse moléculaire :364.03Cap-dependent endonuclease-IN-13
CAS :<p>Cap-dependent endonuclease-IN-13 is a potent inhibitor of cap-dependent endonuclease (CEN) and shows research potential against influenza virus infection (</p>Formule :C25H20F2N4O4SCouleur et forme :SolidMasse moléculaire :510.51Palinavir
CAS :<p>Palinavir is an antiviral, it inhibits HIV-1 protease.</p>Formule :C41H52N6O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :708.892-Dodecanol
CAS :<p>2-Dodecanol suppresses both hyphal development and SIR2 gene expression in Candida albicans [1].</p>Formule :C12H26OCouleur et forme :SolidMasse moléculaire :186.33Pinokalant
CAS :<p>Pinokalant (LOE-908) is a novel non-selective cation channel inhibitor.Pinokalant significantly reduces cortical infarct volume in in vivo experiments, improves</p>Formule :C41H48N2O9Degré de pureté :98.04%Couleur et forme :SolidMasse moléculaire :712.83Pyrethrin II
CAS :<p>Pyrethrin II, an active insecticidal component of pyrethrins, is a biogenic insecticide derived from Chrysanthemum cinerariifolium [1].</p>Formule :C22H28O5Couleur et forme :SolidMasse moléculaire :372.45Antifungal agent 48
CAS :<p>Antifungal agent 48 (Example 308), active against Cryptococcus neoformans, exhibits a minimum inhibitory concentration (MIC) value of 11 μM [1].</p>Formule :C13H10O4SCouleur et forme :SolidMasse moléculaire :262.28Roseoflavin
CAS :<p>Roseoflavin, a chemical analog of FMN and riboflavin that has antimicrobial activity, can directly bind to FMN riboswitch aptamers and downregulate the</p>Formule :C18H23N5O6Degré de pureté :99.81% - 99.89%Couleur et forme :SolidMasse moléculaire :405.41BAY-Y 3118
CAS :<p>BAY-Y 3118, a new chlorofluoroquinolone, has antimicrobial activity.</p>Formule :C20H21ClFN3O3Couleur et forme :SolidMasse moléculaire :405.85Tuberculosis inhibitor 8
CAS :<p>Tuberculosis inhibitor 8 (compound 3b), a 3-methoxy-2-phenylimidazo[1,2-b]pyridazine derivative, exhibits potent activity against both Mycobacterium</p>Formule :C21H19FN4OCouleur et forme :SolidMasse moléculaire :362.4Antiparasitic 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 :351.37AG 85
CAS :<p>AG 85 is a major secretion protein of Mycobacterium tuberculosis.</p>Formule :C27H22N4O3SCouleur et forme :SolidMasse moléculaire :482.55Antibacterial agent 91
<p>Antibacterial 91: Inhibits aaRS, IC50 2.10μM vs. S. enterica ThrRS, has antibacterial properties. [1]</p>Formule :C33H31BrClN5O4Couleur et forme :SolidMasse moléculaire :676.99Koshidacin B
CAS :<p>Koshidacin B, a cyclic tetrapeptide, inhibits malaria strains FCR3/K1 (IC50: 0.89/0.83 μM), showing promise for antiplasmodial research.</p>Formule :C28H40N4O7Couleur et forme :SolidMasse moléculaire :544.64RSV L-protein-IN-2
CAS :<p>RSV L-protein-IN-2 (Compound A), a noncompetitive inhibitor of the RSV polymerase (IC50: 4.5 μM), exhibits antiviral activity against long RSV strains (EC50: 1.</p>Formule :C32H36N4O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :556.65NEU-730
CAS :<p>NEU-730, a novel inhibitor of TbrPDEB1, shows modest inhibition of T. brucei proliferation.</p>Formule :C25H29NO5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :423.5BMS-433771 dihydrochloride hydrate
CAS :<p>BMS-433771 dihydrochloride hydrate is a potent oral RSV inhibitor, affects groups A & B, with a 20 nM EC50, used in respiratory disease research.</p>Formule :C21H27Cl2N5O3Couleur et forme :SolidMasse moléculaire :468.38Ro 31-8588
CAS :<p>Talviraline (HBY 097) inhibits HIV-1 replication and reduces cell death in various cells and immune cells.</p>Formule :C33H56N4O5Couleur et forme :SolidMasse moléculaire :588.82HBV-IN-8
CAS :<p>HBV-IN-6 is a potent inhibitor of HBV (EC50: 287.9 nM).</p>Formule :C21H25ClFN5O5S2Couleur et forme :SolidMasse moléculaire :546.04Micronomicin
CAS :<p>Micronomicin (Gentamicin C2b) is an antibiotic exhibiting antibacterial and bactericidal capacity.</p>Formule :C20H41N5O7Degré de pureté :97.05% - 99.79%Couleur et forme :SolidMasse moléculaire :463.57Anti-MRSA agent 8
CAS :<p>Anti-MRSA Agent 8 (Compound 7g), a derivative of DAPG, exhibits potent antibacterial properties by interacting with bacterial cell membranes and is useful for</p>Formule :C20H30O5Couleur et forme :SolidMasse moléculaire :350.45HOE961
CAS :<p>HOE961, a diacetate ester prodrug of S2242, is an oral anti-orthopoxvirus agent effective against cowpox.</p>Formule :C13H17N5O5Couleur et forme :SolidMasse moléculaire :323.3Antibacterial agent 154
CAS :<p>Antibacterial Agent 154 (Compound 7), a Fluoroquinolone derivative, exhibits broad-spectrum efficacy against both Gram-positive and Gram-negative bacteria when</p>Formule :C25H28ClFN4O5Couleur et forme :SolidMasse moléculaire :518.97BDM91270
CAS :<p>BDM91270 (compound 29) serves as an inhibitor of the E.</p>Formule :C17H21Cl3N4O2Couleur et forme :SolidMasse moléculaire :419.73HIV-1 integrase inhibitor 3
CAS :<p>HIV-1 integrase inhibitor 3 is an HIV-1 integrase strand transfer (INST) inhibitor (IC50: 2.7 nM).</p>Formule :C21H22F2N4O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :432.42PYR01
CAS :<p>PYR01 is a potent nonnucleoside reverse transcriptase inhibitor of HIV-1 and concurrently acts as a targeted activator to eliminate cells expressing HIV-1 [1].</p>Formule :C21H13F7N4O3Couleur et forme :SolidMasse moléculaire :502.34Antituberculosis agent-1
CAS :<p>Antituberculosis Agent-1 (Compound 8a) is an effective antituberculosis agent, demonstrating a minimum inhibitory concentration (MIC) of 3.84 μg/mL against</p>Formule :C21H21NO4Couleur et forme :SolidMasse moléculaire :351.4Fenpropidin
CAS :<p>Fenpropidin (Ro-12-3049), a fungicide, is a specific inhibitor of sterol 14-reductase and biosynthesis.</p>Formule :C19H31NDegré de pureté :98.58% - 99.54%Couleur et forme :SolidMasse moléculaire :273.46Beclabuvir HCl
CAS :<p>Beclabuvir (BMS-791325) is an HCV inhibitor targeting NS5B polymerase with sub-28 nM potency for genotypes 1, 3, 4, 5.</p>Formule :C36H46ClN5O5SCouleur et forme :SolidMasse moléculaire :696.3Berkeleylactone E
CAS :<p>Berkeleylactone E, a macrolide antibiotic [1], exhibits antimicrobial properties.</p>Formule :C20H32O7Couleur et forme :SolidMasse moléculaire :384.469H3B-968
CAS :<p>H3B-968 is a potent inhibitor of Werner syndrome protein (WRN) with an IC50 of approximately 10 nM, effectively targeting its helicase, ATPase, and exonuclease</p>Formule :C22H18F6N4O4SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :548.46L 687908
CAS :<p>L 687908 is a potent inhibitor of hydroxyethylene-containing HIV protease.</p>Formule :C40H51N5O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :681.86A 77003
CAS :<p>A 77003 is a HIV-1 protease inhibitor. A77003 impairs HIV-1 protease-mediated Gag processing.</p>Formule :C44H58N8O6Couleur et forme :SolidMasse moléculaire :794.98Levofuraltadone
CAS :<p>Levofuraltadone is an antiprotozoal and antibacterial agent.</p>Formule :C13H16N4O6Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :324.291R-cis-Permethrin
CAS :<p>1R-cis-Permethrin, an insecticide and neurotoxin, acts on neuron membranes by extending the activation of sodium channels [1].</p>Formule :C21H20Cl2O3Couleur et forme :SolidMasse moléculaire :391.29NSC309401
CAS :<p>NSC309401 is an E. coli dihydrofolate reductase inhibitor, displaying potency with an IC50 value of 189 nM and a dissociation constant (KD) of 14.57 nM [1].</p>Formule :C17H16N6Couleur et forme :SolidMasse moléculaire :304.35N-(3-Oxobutanoyl)-L-homoserine lactone
CAS :<p>N-(3-Oxobutanoyl)-L-homoserine lactone (3-oxo-C4-HSL) serves as an autoregulator for carbapenem antibiotic biosynthesis in Erwinia carotovora ATCC 39048 and induces the expression of rhiI in R. leguminosarum [1].</p>Formule :C8H11NO4Couleur et forme :SolidMasse moléculaire :185.18SARS-CoV-2-IN-59
CAS :<p>SARS-CoV-2-IN-59 (compound E07), an imidazoline derivative, is a non-peptide small molecule that inhibits SARS-CoV-2 by targeting its main protease (Mpro).</p>Formule :C10H9N3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :171.2Antifungal agent 24
CAS :<p>Antifungal agent 24 (Compound 6) is an antifungal agent that inhibits Candida albicans (MIC: 0.03 μg/ml).</p>Formule :C24H18F2N4OCouleur et forme :SolidMasse moléculaire :416.42Sulfisoxazole acetyl
CAS :<p>Sulfisoxazole acetyl (Gantrisin) is an agent with antibacterial activity.</p>Formule :C13H15N3O4SDegré de pureté :99.85%Couleur et forme :SolidMasse moléculaire :309.34CDD-1845
CAS :<p>CDD-1845, a non-covalent, non-peptide inhibitor, exhibits potent inhibition of SARS-CoV-2 M^pro with a K_i value of 3 nM.</p>Formule :C34H31N5O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :541.64MPI8
CAS :<p>MPI8 is a SARS-CoV-2 Protease inhibitor (IC50 = 105 nM).</p>Formule :C32H48N4O7Couleur et forme :SolidMasse moléculaire :600.75Votoplam
CAS :<p>Votoplam functions as a gene splicing modulator, employed in the inhibition of Huntington's disease [1].</p>Formule :C21H25N9ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :419.48Dup-721
CAS :<p>DuP-721: broad-spectrum, oral antibiotic targeting various bacteria, including M. tuberculosis.</p>Formule :C14H16N2O4Degré de pureté :99.84%Couleur et forme :SolidMasse moléculaire :276.29HCV-IN-44
CAS :<p>HCV-IN-44 (compound 28) is an inhibitor of the HCV NS5B protein, efficacious in suppressing HCV virus replication and useful for researching HCV infection [1].</p>Formule :C24H26FN3O5SCouleur et forme :SolidMasse moléculaire :487.54HIV-IN-8
CAS :<p>HIV-IN-8 (Compound 9) acts as an HIV inhibitor, suppressing HIV replication with an effective concentration (EC50) of 13 μg/mL [1].</p>Formule :C36H30O16Couleur et forme :SolidMasse moléculaire :718.61Oxynitidine
CAS :<p>Oxynitidine, an HBV inhibitor (ID50 = 30.8 µg/mL), effectively suppresses HBV DNA replication and may be utilized in viral infection research [1].</p>Formule :C21H17NO5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :363.36LtaS-IN-1
CAS :<p>LtaS-IN-1 inhibits LTA synthesis in MDR E. faecium; alters cell walls; MIC: 0.5-64 μg/mL for 28 Enterococcus strains.</p>Formule :C24H17N3O5Degré de pureté :93.44%Couleur et forme :SolidMasse moléculaire :427.41I-A09
CAS :<p>I-A09 is a noncompetitive mPTPB inhibitor.</p>Formule :C29H25N5O6Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :539.54BMS-561390
CAS :<p>BMS-561390, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formule :C14H12ClF3N2OCouleur et forme :SolidMasse moléculaire :316.71DQn-1
CAS :<p>DQn-1, a potent antifolate, demonstrates efficacy against Mycobacterium tuberculosis (Mtb) with an MIC 90 of 0.03 µM.</p>Formule :C16H14ClN5O2Couleur et forme :SolidMasse moléculaire :343.77Zika virus-IN-2
CAS :<p>Zika virus-IN-2 (Compd 3) is a Zika virus inhibitor (EC 50= 7.4 μM).</p>Formule :C24H23N3O3Couleur et forme :SolidMasse moléculaire :401.46RNA polymerase II-IN-1
CAS :<p>RNA polymerase II-IN-1 (19iv), an amatoxin, inhibits Pol II at 36.66 nM IC50, is more toxic to cancer cells, less to normal cells than α-Amanitin.</p>Formule :C38H53N11O12SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :887.96Deacylketoconazole
CAS :<p>Deacylketoconazole (Deacyl ketoconazole) is a Ketoconazole derivative and is also an antifungal agent.</p>Formule :C24H26Cl2N4O3Degré de pureté :98.35%Couleur et forme :SolidMasse moléculaire :489.394-Hydroxy-2-methylbenzenesulfonic acid ammonium
CAS :<p>4-Hydroxy-2-methylbenzene ammonium: Policresulen impurity, inhibits NS2B/NS3 protease (IC50: 0.48 μg/mL), hinders DENV2 in BHK-21 cells (IC50: 4.99 μg/mL).</p>Formule :C7H11NO4SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :205.23Antibiofilm agent-1
CAS :<p>Antibiofilm Agent-1, as detailed in WO2017011725A1 (compound 17) [1], serves as an antibacterial agent effective against Gram-positive pathogens.</p>Formule :C11H5Br2Cl2NO2Couleur et forme :SolidMasse moléculaire :413.88Antibacterial compound 1
CAS :<p>Antibacterial compound 1 is an antibacterial compound.</p>Formule :C14H16FN3O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :309.29MAC13772
CAS :<p>MAC13772 is a potent inhibitor of the enzyme BioA with an IC50 of 250 nM thereby inhibiting biotin biosynthesis. MAC13772 exhibits antibacterial activity.</p>Formule :C8H9N3O3SDegré de pureté :98.7%Couleur et forme :SolidMasse moléculaire :227.24DB-766
CAS :<p>DB-766: Chagas' treatment candidate with potent, selective trypanocidal action. IC50: 60 nM (bloodstream), 25 nM (intracellular). Promising new lead.</p>Formule :C34H34N6O3Couleur et forme :SolidMasse moléculaire :574.67Isotianil
CAS :<p>Isotianil is a plant defense inducer that activates typical plant defense responses without direct antimicrobial effects, serving as a plant protection agent</p>Formule :C11H5Cl2N3OSCouleur et forme :SolidMasse moléculaire :298.15Propamidine
CAS :<p>Propamidine acts as a covalent inhibitor of TMPRSS2 and exhibits antibacterial properties. [1]</p>Formule :C17H20N4O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :312.37Ipflufenoquin
CAS :<p>Ipflufenoquin, an insecticide, effectively combats primary apple scab infections. Its application is optimal between the stages of half an inch of green and fruit set [1].</p>Formule :C19H16F3NO2Couleur et forme :SolidMasse moléculaire :347.33Flurofamide
CAS :<p>Flurofamide is an effective bacterial urease inhibitor and has potential in the treatment of infected urinary calculi.</p>Formule :C7H9FN3O2PDegré de pureté :96.01% - 98%Couleur et forme :SolidMasse moléculaire :217.146-Chloro-7-deazapurine-β-D-riboside
CAS :<p>6-Chloro-7-deazapurine-β-D-riboside shows antifungal activity.</p>Formule :C11H12ClN3O4Degré de pureté :98.26%Couleur et forme :SolidMasse moléculaire :285.68ZINC475239213
CAS :<p>ZINC475239213 acts as an inhibitor targeting the SARS-CoV-2 Nsp14 N7-Methyltransferase with an IC50 value of 20 μM [1].</p>Formule :C21H15N5O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :369.38FX-06
CAS :<p>FX-06 (Fibrin-derived peptide Bβ15-42) is a peptide derived from the fibrin Bbeta chain.</p>Formule :C133H216N44O38Couleur et forme :SolidMasse moléculaire :3039.417-Deaza-2',3'-dideoxyguanosine
CAS :<p>7-Deaza-2',3'-dideoxyguanosine (7-Deaza-ddG) is a 2′,3′-dideoxynucleoside 5′-triphosphate that inhibits HIV-1 reverse transcriptase with a Ki of 25 nM [1].</p>Formule :C11H14N4O3Couleur et forme :SolidMasse moléculaire :250.25GSK3532795
CAS :<p>GSK3532795: potent oral HIV-1 maturation inhibitor; EC50: 1.9-13 nM for various strains.</p>Formule :C42H62N2O4SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :691.02Besifovir 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 :527.51RSV L-protein-IN-5
CAS :<p>RSV L-protein-IN-5 (Compound E) serves as a potent inhibitor of the Respiratory Syncytial Virus (RSV), with an EC50 value of 0.1 μM.</p>Formule :C31H36N6O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :556.66COH1
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 :250.27Zevotrelvir
CAS :<p>Zevotrelvir (Compound 52) serves as an inhibitor of coronavirus, demonstrating IC50 values below 0.1 μM for 229E hCoV protease and below 0.1 mM for SARS-CoV-3C-</p>Formule :C28H26F3N5O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :537.53Antiviral agent 43
CAS :<p>Antiviral agent 43 (compound 16) serves as a potent, orally active inhibitor of influenza A virus entry, demonstrating efficacy by inhibiting the replication of the influenza A strains VH04-H5N1 and PR8-H1N1 with EC50 values of 240 nM and 72 nM, respectively [1].</p>Formule :C17H22ClF3N2OCouleur et forme :SolidMasse moléculaire :362.82DDD85646
CAS :<p>DDD85646 is an inhibitor of T. brucei N-myristoyltransferase with a Ki of 1.44 nM, an IC50 of 2 nM and an EC50 of 2 nM. The IC50 of hNMT is 4 nM.</p>Formule :C21H24Cl2N6O2SDegré de pureté :97.8% - 99.76%Couleur et forme :SolidMasse moléculaire :495.43Loflucarban
CAS :<p>Loflucarban (Fluonilid) is an antimycotic compoud.</p>Formule :C13H9Cl2FN2SDegré de pureté :98.08% - 98.15%Couleur et forme :SolidMasse moléculaire :315.19SIMR3030
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 :427.54BRL44385
CAS :<p>BRL44385 is an effective and selective inhibitor of the replication of HSV-1 and HSV2, Epstein-Barr virus (EBV), and varicella-zoster virus (VZV).</p>Formule :C8H11N5O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :225.2PC786
CAS :<p>PC786 is a potent and selective non-nucleoside RSV L-protein polymerase inhibitor for inhalation therapy of RSV infections,antiviral activity against RSV.</p>Formule :C41H38FN5O4SDegré de pureté :99.26% - 99.26%Couleur et forme :SolidMasse moléculaire :715.84TH-Z145
CAS :<p>TH-Z145 is a potent FPPS inhibitor for the study of myeloma and lung cancer.</p>Formule :C16H28O7P2Degré de pureté :98.29%Couleur et forme :SolidMasse moléculaire :394.34MoTPS1-IN-1
CAS :<p>MoTPS1-IN-1 is a potent MoTPS1 inhibitor with antifungal anti-inflammatory activity that acts through interaction with Glu396 study ulcerative colitis.</p>Formule :C23H27F3N2O4Degré de pureté :99.28%Couleur et forme :SoildMasse moléculaire :452.47LY 173013
CAS :<p>LY 173013 is a bicyclic pyrazolidinone, it has antibacterial properties.</p>Formule :C15H16N6O7SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :424.39Antitrypanosomal agent 14
CAS :<p>Antitrypanosomal agent 14 (Compound 1), a potent T.</p>Formule :C14H23N3OSDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :281.42YH-53
CAS :<p>YH-53: potent inhibitor for SARS-CoV-1 (Ki=6.3 nM) & SARS-CoV-2 3CLpro (Ki=34.7 nM); hinders SARS-CoV-2 replication; aids COVID-19 research.</p>Formule :C30H33N5O5SCouleur et forme :SolidMasse moléculaire :575.68SARS-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 :252.26CGP 20376
CAS :<p>CGP 20376: Benzothiazole anthelmintic, modulates eosinophil burst, antifibrillatory, dose-dependent effects.</p>Formule :C16H20N2O3S3Degré de pureté :95.11%Couleur et forme :SolidMasse moléculaire :384.54Verazine
CAS :<p>(-)-Verazine is an antifungal agent isolated from the dried roots and rhizome of Veratrum maackii Regel, which induces DNA damage in the cerebellum and cerebral</p>Formule :C27H43NOCouleur et forme :SolidMasse moléculaire :397.64BLI-489 Hydrate
CAS :<p>BLI-489 hydrate is a penicillin β-lactamase inhibitor that acts on classes A and C and some class D β-lactamases.</p>Formule :C13H10N3NaO4SCouleur et forme :SolidMasse moléculaire :327.29NVS-SM2
CAS :<p>NVS-SM2 boosts SMN2 splicing, enhances exon 7 inclusion, and raises SMN protein levels orally.</p>Formule :C23H30N6OCouleur et forme :SolidMasse moléculaire :406.52Dihydroaltenuene B
CAS :<p>Dihydroaltenuene B inhibits mushroom tyrosinase (IC50: 38.33µM) and binds His244, Met280, Gly281 via hydrogen bonds.</p>Formule :C15H18O6Couleur et forme :SolidMasse moléculaire :294.3Bio-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 :571.63G4/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 :698.27HBV-IN-41
CAS :<p>HBV-IN-41 (compound 45) is a potent, orally active inhibitor of Hepatitis B Virus (HBV), exhibiting an EC50 value of 0.027μM [1].</p>Formule :C18H19ClFN5O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :407.83Japonilure
CAS :<p>Japonilure is an agent of insecticide and pheromone.</p>Formule :C14H24O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :224.34SARS-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 :589.47UNC2170 maleate
CAS :<p>53BP1-binding protein 1 (53BP1) engages with dimethylated lysine 20 on histone 4 (H4K20me2) through its tandem tudor domains within a homodimer configuration, crucial for the DNA damage response. UNC2170, a micromolar 53BP1 ligand, selectively interacts with this site, demonstrating at least 17-fold preference for 53BP1 over similar proteins. This interaction occurs in a pocket formed by the 53BP1's tudor domains. Moreover, UNC2170 acts as an antagonist to 53BP1 in cellular lysates, effectively inhibiting class switch recombination, a process dependent on the functional 53BP1 tudor domain, thus confirming its cellular activity.</p>Formule :C14H21BrN2OC4H4O4Couleur et forme :SolidMasse moléculaire :429.31EBOV-IN-1
CAS :<p>EBOV-IN-1 is an adamantane dipeptide piperazine inhibitor of Ebola virus (EBOV) that inhibits EBOV infection and suppresses pseudotypic EBOV infection.</p>Formule :C34H43N3O5Degré de pureté :98.62% - 98.92%Couleur et forme :SolidMasse moléculaire :573.72β-Gal-NONOate
CAS :<p>Beta-gal-nonoate, a β-galactosidase dependent nitric oxide (NO) donor, releases NO upon activation by β-galactosidase. It exhibits bactericidal activity, thus serving as an effective bactericide [1].</p>Formule :C10H19N3O7Couleur et forme :SolidMasse moléculaire :293.27Sulfachloropyridazine 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 :306.7Antimicrobial photosensitizer-1
CAS :<p>Photosensitizer-1 shows promise in treating infections, effective against S. aureus in mouse wounds.</p>Formule :C19H19BF2I3N3Couleur et forme :SolidMasse moléculaire :718.9Δ2-trans Eicosenoic Acid
CAS :<p>Δ2-transEicosenoic acid, an α,β-unsaturated fatty acid, emerges as a by-product during the synthesis of Δ2-ciseicosenoic acid, which along with its salts, shows promise in diabetes treatment and lipid metabolism enhancement. Additionally, the compound 2-octadecenoic acid is recognized for its ability to enhance liver function and reduce blood sugar levels in streptozocin-induced diabetic rats.</p>Formule :C20H38O2Couleur et forme :SolidMasse moléculaire :310.5Brevicompanine B
CAS :<p>Brevicompanine B: fungal metabolite, regulates plant growth/circadian rhythm, inhibits Arabidopsis roots, affects gene transcription, anti-P. falciparum.</p>Formule :C22H29N3O2Couleur et forme :SolidMasse moléculaire :367.48N-Acetylpurinomycin
CAS :<p>N-Acetylpurinomycin is a selective agonist of CB2 receptor.</p>Formule :C24H31N7O6Couleur et forme :SolidMasse moléculaire :513.55AB-836
CAS :<p>AB-836, an orally active hepatitis B virus (HBV) capsid inhibitor, hampers viral replication by engaging with the HBV core protein.</p>Formule :C20H15F3N4O2Couleur et forme :SolidMasse moléculaire :400.35Cochliodone A
CAS :<p>Cochliodone A, a bioactive compound isolated from the deep-sea fungus Chaetomium sp., exhibits both antibacterial and anticancer properties.</p>Formule :C34H38O12Couleur et forme :SolidMasse moléculaire :638.66GS-6620
CAS :<p>GS-6620 is a HCV nonstructural protein 5B (NS5B) inhibitor.</p>Formule :C29H37N6O9PCouleur et forme :SolidMasse moléculaire :644.61A 33853
CAS :<p>A 33853 is an antibiotic isolated from culture broth of Streptomyces sp.</p>Formule :C20H13N3O6Couleur et forme :SolidMasse moléculaire :391.33Laxifloran
CAS :<p>Laxifloran possesses antibacterial and antifungal properties.</p>Formule :C17H18O5Couleur et forme :SolidMasse moléculaire :302.32TAS-114
CAS :<p>TAS-114 is a dUTPase and DPD inhibitor that modulates catabolic pathways to improve systemic availability of 5-FU.</p>Formule :C21H29N3O6SDegré de pureté :99.76%Couleur et forme :SolidMasse moléculaire :451.54Laninamivir Octanoate Monohydrate
CAS :<p>Laninamivir Octanoate Monohydrate is a neuraminidase inhibitor.</p>Formule :C21H38N4O9Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :490.55Clazuril
CAS :<p>Clazuril, a phenylacetonitrile derivative, treats coccidiosis in poultry by killing Eimeria species.</p>Formule :C17H10Cl2N4O2Couleur et forme :SolidMasse moléculaire :373.19(1R,4S)-Yimitasvir diphosphate
CAS :<p>Yimitasvir diphosphate, also known as Emitasvir, is an orally-administered inhibitor of the hepatitis C virus (HCV) nonstructural protein 5A (NS5A).</p>Formule :C49H64N8O14P2Couleur et forme :SolidMasse moléculaire :1051.03Icofungipen
CAS :<p>Icofungipen is an oral antifungals with active against Candida species.</p>Formule :C7H11NO2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :141.17MF 5137
CAS :<p>MF 5137 is an effective antimicrobial agent.</p>Formule :C23H23N3O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :389.45Azaconazole
CAS :<p>Azaconazole, an agricultural fungicide, is used for controlling powdery mildew on crops and bean rust.</p>Formule :C12H11Cl2N3O2Couleur et forme :SolidMasse moléculaire :300.14BMY-43748
CAS :<p>BMY-43748 is an antibacterial compound with great in vitro and in vivo antibacterial activity.</p>Formule :C20H17F3N4O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :418.37Fervenulin
CAS :<p>Fervenulin, from Streptomyces sp. CMU-MH021, halts egg hatch (MIC: 30 μg/mL) and kills J2 larvae (MIC: 120 μg/mL) of M. incognita.</p>Formule :C7H7N5O2Degré de pureté :99.75%Couleur et forme :SolidMasse moléculaire :193.16Valnemulin
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 :564.83ZIKV-IN-1
CAS :<p>ZIKV-IN-1 blocks Zika virus effectively (EC50: 2.8 μM, EC90: 6.8 μM), targets the RdRp domain, and is low-toxic.</p>Formule :C21H18BrF2N3O3Couleur et forme :SolidMasse moléculaire :478.29Antibacterial agent 135
CAS :<p>Antibacterial Agent 135 (example 7) effectively inhibits various bacteria, including P.</p>Formule :C11H15N5O6SCouleur et forme :SolidMasse moléculaire :345.33HIV-1 inhibitor-3
CAS :<p>HIV-1 inhibitor-3 is an HIV infection inhibitor.</p>Formule :C9H10F2N2O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :264.18Tirfipiravir
CAS :<p>Tirapiravir is an antiviral nucleoside analog that exhibits activity against both the novel coronavirus and influenza virus [1].</p>Formule :C14H17N3O8Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :355.3Zoxamide
CAS :<p>Zoxamide (RH-7281) is an oomycete-specific fungicide that impedes nuclear division in Phytophthora capsici germlings and disrupts the microtubule cytoskeleton [</p>Formule :C14H16Cl3NO2Couleur et forme :SolidMasse moléculaire :336.64Du011
CAS :<p>Du011 is a biogenesis inhibitor of the E.</p>Formule :C20H15F2NO4SCouleur et forme :SolidMasse moléculaire :403.4ZINC03129319
CAS :<p>ZINC03129319 is an inhibitor of dengue virus (DENV) NS2B-NS3 protease.</p>Formule :C24H14N2O6S2Degré de pureté :90%Couleur et forme :SolidMasse moléculaire :490.51ddUTP
CAS :<p>ddUTP (2′,3′-Dideoxyuridine-5′-triphosphate) serves as a selective inhibitor of HIV and AMV reverse transcriptases with Ki values of 0.05 µM for HIV and 1 µM</p>Formule :C9H15N2O13P3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :448.111AB131
CAS :<p>AB131, an inhibitor of MSMEG 6649 and Rv2172c (KD values of 0.16 and 0.02 μM, respectively), enhances the antimycobacterial efficacy of the antitubercular agent</p>Formule :C21H19NO6SCouleur et forme :SolidMasse moléculaire :413.44Urease 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 :179.2SARS-CoV-2 Mpro-IN-12
CAS :<p>SARS-CoV-2 Mpro-IN-12 (compound D026) serves as an inhibitor of the main protease (Mpro) of SARS-CoV-2, exhibiting antiviral properties [1].</p>Formule :C20H17NO3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :319.35JNJ4796
CAS :<p>JNJ4796 is an oral fusion inhibitor that neutralizes influenza A group 1 by blocking HA-mediated fusion, mimicking bnAbs.</p>Formule :C28H27N9O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :537.57Inz-5
CAS :<p>Inz-5 is a fungal-selective inhibitor of mitochondrial cytochrome bc1. Inz-5 impairs fungal virulence. It also prevents the evolution of drug resistance.</p>Formule :C18H14F4N6Couleur et forme :SolidMasse moléculaire :390.34Galidesivir dihydrochloride
CAS :<p>Galidesivir inhibits RdRP; has broad antiviral effects on various RNA viruses; effective against Ebola, Marburg in animals.</p>Formule :C11H17Cl2N5O3Couleur et forme :SolidMasse moléculaire :338.19Droxinavir HCl
CAS :<p>Droxinavir HCl is an antiviral agent and HIV protease inhibitor.</p>Formule :C29H52ClN5O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :570.228-NH2-ATP tetrasodium
CAS :<p>8-NH2-ATP tetrasodium, an inactive ATP variant, originates from 8-NH2-Ado tetrasodium, which triggers the apoptosis-associated cleavage of poly (ADP-ribose) polymerase [1] [2].</p>Formule :C10H13N6Na4O13P3Couleur et forme :SolidMasse moléculaire :610.12L 694746
CAS :<p>L 694746 is an inhibitor of HIV-1 protease.</p>Formule :C35H42N2O8Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :618.72Anti-MRSA agent 5
CAS :<p>Potent anti-MRSA compound, MIC50: 0.38 μg/mL, minimal hERG activity (IC50: 40 μM), low toxicity, and resistance unlikely.</p>Formule :C25H22N4O4Couleur et forme :SolidMasse moléculaire :442.47KY386
CAS :<p>KY386 is a potent and selective DHX33 helicase inhibitor with an IC50 value of 19 nM.</p>Formule :C21H19N5O2SCouleur et forme :SolidMasse moléculaire :405.47(-)-Neplanocin A
CAS :<p>S-Adenosylhomocysteine (SAH) hydrolase is responsible for the reversible hydrolysis of SAH into adenosine and homocysteine. Inhibition of this enzyme leads to the accumulation of SAH within cells, thereby increasing the SAH to S-adenosylmethionine (SAM) ratio and subsequently inhibiting SAM-dependent methyltransferases. (−)-Neplanocin A, a potent and irreversible inhibitor of SAH hydrolase (Ki= 8.39 nM), exhibits significant antitumor activity against mouse leukemia L1210 cells and holds broad-spectrum antiviral properties. Its efficacy notably surpasses that of the reversible inhibitor 3-deazaneplanocin, especially in combating vesicular stomatitis, evidencing a higher potency with ID50 values of 0.07 μg/ml for Neplanocin A versus 0.3 μg/ml for 3-deazaneplanocin.</p>Formule :C11H13N5O3Couleur et forme :SolidMasse moléculaire :263.3Fosalvudine tidoxil
CAS :<p>Fosalvudine tidoxil, a nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formule :C35H64FN2O8PSDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :722.93FAICAR
CAS :<p>FAICAR (5-Formamidoimidazole-4-carboxamide ribotide), a purine nucleotide, plays a crucial role in metabolic processes.</p>Formule :C10H15N4O9PCouleur et forme :SolidMasse moléculaire :366.22Targeting the bacterial sliding clamp peptide 46
CAS :<p>Peptide 46 is a short peptide that inhibits SC-dependent DNA synthesis by targeting the bacterial sliding clamp (SC).</p>Formule :C47H64N8O11Couleur et forme :SolidMasse moléculaire :917.06AZD-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 :644.7SARS-CoV-2/MERS Mpro-IN-1
<p>SARS-CoV-2/MERS Mpro-IN-1 is a potent inhibitor of the main proteases in SARS-CoV-2 and MERS, exhibiting IC50 values of 0.10 and 0.06 µM, respectively.</p>Formule :C30H36N4O7Couleur et forme :SolidMasse moléculaire :564.63Antibacterial agent 92
<p>Antibacterial agent 92 inhibits Salmonella's aaRS; IC50 of 0.58 μM for Se ThrRS. Exhibits antibacterial effects.</p>Formule :C30H28Cl2F3N5O4Couleur et forme :SolidMasse moléculaire :650.48HCV-IN-43
CAS :<p>HCV-IN-43 (compound 2), an HCV NS5B protein inhibitor, efficiently inhibits HCV virus replication and is utilized in the study of HCV infection [1].</p>Formule :C26H26FN3O5SCouleur et forme :SolidMasse moléculaire :511.57Aranciamycin
CAS :<p>Aranciamycin (Compound 1), an anthracycline antibiotic, exhibits collagenase inhibitory activity (IC50 3.7*10^-7 M) and can inhibit DNA synthesis in tumor cells</p>Formule :C27H28O12Couleur et forme :SolidMasse moléculaire :544.5LS-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 :2084.64Quorum Sensing-IN-2
CAS :<p>Quorum Sensing-IN-2 (compound 23e) is a quorum sensing inhibitor that curtails bacterial pathogenicity without impeding growth.</p>Formule :C19H13F2NO3Couleur et forme :SolidMasse moléculaire :341.31Tuberculosis inhibitor 12
CAS :<p>Tuberculosis Inhibitor 12, an oxadiazole derivative, effectively inhibits Mycobacterium tuberculosis, demonstrating inhibition rates of 82% and 78% at a</p>Formule :C15H9FN4O3SCouleur et forme :SolidMasse moléculaire :344.32WRN inhibitor 3
CAS :<p>WRN Inhibitor 3 (example 110), a cyclic vinyl sulfone-based compound, serves as an inhibitor of the Werner Syndrome ATP-dependent helicase enzyme (WRN).</p>Formule :C20H20N2O5SCouleur et forme :SolidMasse moléculaire :400.45APX001
CAS :<p>APX001 is a prodrug of APX-001A. APX001 is the first-in-class inhibitor of the fungal protein Gwt1.</p>Formule :C22H21N4O6PDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :468.4Antibacterial agent 158
CAS :<p>Compound 158 (6c), a Micrococcin analogue, serves as an antibacterial agent effective against impetigo and Clostridium difficile infection (CDI) [1].</p>Formule :C54H61N15O8S6Couleur et forme :SolidMasse moléculaire :1240.55Tuberculosis inhibitor 7
CAS :<p>Tuberculosis inhibitor 7 (compound 2d), a 3-methoxy-2-phenylimidazo[1,2-b]pyridazine derivative, exhibits potent activity against Mycobacterium tuberculosis and</p>Formule :C21H18FN3O2SCouleur et forme :SolidMasse moléculaire :395.45Antituberculosis 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 :458.46Ibuzatrelvir
CAS :<p>Ibuzatrelvir (PF-07817883) is an antiviral compound designed to inhibit the SARS-CoV-2 3CL protease, and is utilized in the treatment of COVID-19 [1].</p>Formule :C21H30F3N5O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :489.49Glycolithocholic 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 :557.65Ulonivirine
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 :491.73WRNA10
CAS :<p>WRNA10 is a potent binding agent for HIV-1TAR RNA (IC50: 10 μM, CC50: 40 μM).</p>Formule :C25H32N4O4Couleur et forme :SolidMasse moléculaire :452.55DMP 323
CAS :<p>DMP 323 is a potent inhibitor of HIV-1 protease.</p>Formule :C35H38N2O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :566.69AU1235
CAS :<p>AU1235 is a Mycobacterium tuberculosis inhibitor.</p>Formule :C17H19F3N2ODegré de pureté :99.54% - 99.87%Couleur et forme :SolidMasse moléculaire :324.34UNC-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 :313.23WRN inhibitor 4
CAS :<p>WRN Inhibitor 4 (Example 107), a cyclic vinyl sulfone-based compound, serves as an inhibitor of the Werner Syndrome ATP-dependent helicase enzyme (WRN).</p>Formule :C16H14N2O5SCouleur et forme :SolidMasse moléculaire :346.36Arbemnifosbuvir
CAS :<p>Arbemnifosbuvir, a drug interfering with the nidovirus DdRp-associated nucleotidyltransferase (NiRAN) domain of non-structural protein 12 (nsp12), is utilized</p>Formule :C24H33FN7O7PDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :581.53(+)-Thienamycin
CAS :<p>(+)-Thienamycin, a powerful broad-spectrum antibacterial and β-lactamase inhibitor, is isolated from Streptomyces cattleya [1].</p>Formule :C11H16N2O4SCouleur et forme :SolidMasse moléculaire :272.32AZ-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 :633.76Antifungal agent 66
CAS :<p>Antifungal agent 66 (compound 10) exhibits broad-spectrum antifungal activity against seven phytopathogenic fungal mycelia and significant inhibitory effects on</p>Formule :C19H25ClO6Couleur et forme :SolidMasse moléculaire :384.85NNRTIs-IN-1
CAS :<p>NNRTIs-IN-1 is a potent non-nucleoside reverse transcriptase inhibitor (NNRTI) with notable anti-resistance efficacy, effectively inhibiting both the wild-type</p>Formule :C28H22N6O3Couleur et forme :SolidMasse moléculaire :490.51HBV-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 :435.3217(R)-Resolvin D4
CAS :<p>17(R)-Resolvin D4 (17(R)-RvD4) is an epimer of RvD4, generated through the aspirin-induced modification process.</p>Formule :C22H32O5Couleur et forme :SolidMasse moléculaire :376.5Influenza virus-IN-6
CAS :<p>Influenza virus-IN-6 (Compound 35) serves as a potent inhibitor targeting the N-terminal domain of the polymerase acidic protein (PA N ) endonuclease subunit of</p>Formule :C27H26ClNO7Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :511.95Antibacterial compound 2
CAS :<p>Antibacterial compound 2 is a potent antimicrobial agent effective against many human veterinary pathogens, inhibiting multi-drug resistant staphylococci,</p>Formule :C22H30FN5O6Degré de pureté :90.4%Couleur et forme :SolidMasse moléculaire :479.5Anti-Trypanosoma cruzi agent-3
CAS :<p>Anti-Trypanosoma cruzi agent-3 is an antiprotozoal agent.</p>Formule :C29H29N3O6SCouleur et forme :SolidMasse moléculaire :547.62Antileishmanial agent-17
CAS :<p>Antileishmanial agent-17, a coumarin hybrid, exhibits potent antileishmanial activity (IC50 <0.78 μM) while proving non-toxic to normal VERO cells.</p>Formule :C27H37N5O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :511.61SARS-CoV-2-IN-44
CAS :<p>SARS-CoV-2-IN-44, an inhibitor of SARS-CoV-2, effectively suppresses viral replication with an EC50 value of 0.6μM and exhibits negligible cytotoxicity in Calu-</p>Formule :C18H16O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :312.32Antibacterial agent 159
CAS :<p>Compound 6d (Antibacterial agent 159) is an antibiotic effective against impetigo and Clostridium difficile infection (CDI), with no observed recurrence for CDI</p>Formule :C51H50N16O10S6Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :1239.43DHFR-IN-10
CAS :<p>DHFR-IN-10 (compound 4c) is a potent inhibitor of dihydrofolate reductase (DHFR), displaying an inhibition concentration half-maximum (IC50) of 4.21 μM against</p>Formule :C20H14BrN3S3Couleur et forme :SolidMasse moléculaire :472.44KNI-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 :667.84Cladosporin
CAS :<p>Cladosporin, from Cladosporium cladosporioid fungus, halts dermatophyte growth on agar at 75 μg/mL.</p>Formule :C16H20O5Couleur et forme :SolidMasse moléculaire :292.33BVDU 5′-Triphosphate
CAS :<p>BVDU 5′-Triphosphate is an antiviral agent labeled with 5′-Triphosphate that specifically targets viral DNA polymerase.</p>Formule :C11H16BrN2O14P3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :573.08Ianthelliformisamine B TFA
CAS :<p>Ianthelliformisamine B TFA, an antibiotic enhancer, is used to against resistant Gram-negative bacteria.</p>Formule :C21H27Br2F6N3O6Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :691.25Despropylene gatifloxacin
CAS :<p>Despropylene gatifloxacin, a metabolite of AM-1155, exhibits potent antibacterial activity and has favorable pharmacokinetics [1].</p>Formule :C16H18FN3O4Couleur et forme :SolidMasse moléculaire :335.33OfChi-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 :481.98OM173-αA
CAS :<p>OM173-αA is a quinone bacterial metabolite that inhibits the growth of the bacteria M.</p>Formule :C17H16O6Couleur et forme :SolidMasse moléculaire :316.31Antibiofilm agent-2
CAS :<p>Antibiofilm Agent-2 (Compound 4T) serves as a potent biofilm inhibitor, exhibiting an IC50 of 3.6 μM, and impairs the quorum sensing system along with iron</p>Formule :C17H21NO5Couleur et forme :SolidMasse moléculaire :319.35MurA-IN-4
CAS :<p>MurA-IN-4 exhibits antibacterial properties as a MurA inhibitor, impeding the synthesis of bacterial cell walls [1].</p>Formule :C8H12ClNO3Couleur et forme :SolidMasse moléculaire :205.64Y18501
CAS :<p>Y18501, an oxysterol-binding protein (OSBPI) inhibitor structurally akin to Oxathiapiprolin, demonstrates potent inhibition against Phytophthora spp.</p>Formule :C27H26F2N6O2SCouleur et forme :SolidMasse moléculaire :536.6FR194738 free base
CAS :<p>FR194738 free base inhibits squalene epoxidase activity in HepG2 cell homogenates with an IC50 of 9.8 nM. </p>Formule :C27H37NO2SDegré de pureté :99.13%Couleur et forme :SolidMasse moléculaire :439.65Capravirine
CAS :<p>Capravirine, a non-nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formule :C20H20Cl2N4O2SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :451.37Cyclic HPMPC
CAS :<p>Cyclic HPMPC: Potent antiviral, raises O2 in mice with lethal vaccinia, lowers guinea pig CMV replication.</p>Formule :C8H12N3O5PCouleur et forme :SolidMasse moléculaire :261.17(S)-Mosnodenvir
CAS :<p>(S)-Mosnodenvir, a pan-serotype dengue antiviral agent, exhibits picomolar to low nanomolar in vitro activity with a high barrier to resistance and is</p>Formule :C26H22ClF3N2O6SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :582.98SLU-10482
CAS :<p>SLU-10482, an antiparasitic agent, effectively reduces C.</p>Formule :C18H16F4N6OCouleur et forme :SolidMasse moléculaire :408.35
