Microbiology/Virology
Microbiology and virology inhibitors are compounds that target microorganisms, including bacteria, viruses, and fungi, disrupting their growth, replication, or survival. These inhibitors are essential for studying microbial pathogenesis, understanding resistance mechanisms, and developing new antimicrobial and antiviral therapies. Inhibitors in this category are used to combat infectious diseases, explore microbial ecology, and investigate host-pathogen interactions. At CymitQuimica, we provide a broad selection of high-quality microbiology and virology inhibitors to support your research in infectious diseases, microbiology, and virology.
Subcategories of "Microbiology/Virology"
- Antibacterial(2,949 products)
- Antibiotic(919 products)
- Antifection(23 products)
- DHFR(32 products)
- DNA/RNA Synthesis(707 products)
- HBV(176 products)
- HIV Protease(447 products)
- HSV(91 products)
- Integrase(2 products)
- Ribosome(13 products)
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Found 5832 products of "Microbiology/Virology"
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Tuberculosis inhibitor 6
CAS:<p>Tuberculosis inhibitor 6 (compound 2c), a 3-methoxy-2-phenylimidazo[1,2-b]pyridazine derivative, is highly active against Mycobacterium tuberculosis (MIC 90 of</p>Formula:C21H19N3O2SColor and Shape:SolidMolecular weight:377.46BAY-Y 3118
CAS:<p>BAY-Y 3118, a new chlorofluoroquinolone, has antimicrobial activity.</p>Formula:C20H21ClFN3O3Color and Shape:SolidMolecular weight:405.85Urease Inhibitor 07
CAS:<p>Urease Inhibitor 07 is an isosubstituted metalloproteinase inhibitor with potential activity against Mycobacterium tuberculosis strain H37Rv.</p>Formula:C7H5N3OSPurity:99.65%Color and Shape:SolidMolecular weight:179.2RyRs activator 2
CAS:<p>RyRs activator 2: potent ranibulin receptor stimulant, 30% larvicidal activity, equals chlorfenvinphos, outperforms cyanobenzamide.</p>Formula:C23H18Cl2F3N5O2Color and Shape:SolidMolecular weight:524.32Antibiofilm 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>Formula:C11H5Br2Cl2NO2Color and Shape:SolidMolecular weight:413.88IpOHA
CAS:<p>IpOHA is a potent inhibitor of plant KARI and functions as an antimycobacterial agent, demonstrating a K_i value of 97.7 nM against Mycobacterium tuberculosis (</p>Formula:C5H9NO4Color and Shape:SolidMolecular weight:147.13WRN 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>Formula:C20H20N2O5SColor and Shape:SolidMolecular weight:400.45I-A09
CAS:<p>I-A09 is a noncompetitive mPTPB inhibitor.</p>Formula:C29H25N5O6Purity:98%Color and Shape:SolidMolecular weight:539.54β-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>Formula:C10H19N3O7Color and Shape:SolidMolecular weight:293.27FR194738 free base
CAS:<p>FR194738 free base inhibits squalene epoxidase activity in HepG2 cell homogenates with an IC50 of 9.8 nM. </p>Formula:C27H37NO2SPurity:99.13%Color and Shape:SolidMolecular weight:439.65(E)-LHF-535
CAS:<p>(E)-LHF-535, an E-isomer antiviral, EC50 <1 μM vs Lassa/Machupo/Junin, 1-10 μM vs VSVg.</p>Formula:C27H28N2O2Purity:98%Color and Shape:SolidMolecular weight:412.52Mirincamycin HCl
CAS:<p>Mirincamycin HCl is a close analog of the drug clindamycin used for the treatment of Plasmodium falciparum blood stages.</p>Formula:C19H36Cl2N2O5SPurity:98%Color and Shape:SolidMolecular weight:475.47APX001
CAS:<p>APX001 is a prodrug of APX-001A. APX001 is the first-in-class inhibitor of the fungal protein Gwt1.</p>Formula:C22H21N4O6PPurity:98%Color and Shape:SolidMolecular weight:468.4IR415
CAS:<p>IR415 selectively interacts with Hepatitis B virus X protein (HBx, Kd = 2 nM) and blocks HBV-mediated RNAi suppression, reverses the inhibitory effect of HBx</p>Formula:C13H14F2N4SPurity:99.85%Color and Shape:SolidMolecular weight:296.34DDD85646
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>Formula:C21H24Cl2N6O2SPurity:97.8% - 99.76%Color and Shape:SolidMolecular weight:495.43Tobevibart
CAS:<p>Tobevibart, an IgG1-lambda humanized monoclonal antibody targeting the hepatitis B virus (HBV) surface envelope protein, exhibits antiviral activity [1].</p>Purity:98%Color and Shape:LiquidEDI048
CAS:<p>EDI048, also known as compound 1.16, is an orally active inhibitor of Cryptosporidium PI4K, utilized in the study of cryptosporidiosis [1].</p>Formula:C25H21ClN4O4Purity:98%Color and Shape:SolidMolecular weight:476.918-Azahypoxanthine
CAS:<p>8-Azahypoxanthine (NSC-22709) inhibits hypoxanthine-guanine-xanthine phosphoribosyltransferase and has antimalarial properties.</p>Formula:C4H3N5OPurity:99.66%Color and Shape:Light Yellow To Light Beige Fine CrystallineMolecular weight:137.1DU-34569 Maleate
CAS:<p>DU-34569 Maleate, an antiviral agent, acts against influenza A, parainfluenza Sendai, coxsackie A21, and rhinovirus.</p>Formula:C18H27NO4Purity:98%Color and Shape:SolidMolecular weight:321.41Droxinavir HCl
CAS:<p>Droxinavir HCl is an antiviral agent and HIV protease inhibitor.</p>Formula:C29H52ClN5O4Purity:98%Color and Shape:SolidMolecular weight:570.22Cap-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>Formula:C25H20F2N4O4SColor and Shape:SolidMolecular weight:510.51Pencitabine
CAS:<p>Pen is an oral cancer drug that blocks DNA synthesis by inhibiting key enzymes and integrating into DNA.</p>Formula:C15H20F3N3O6Color and Shape:SolidMolecular weight:395.33Acorafloxacin HCl
CAS:<p>Acorafloxacin: broad-spectrum fluoroquinolone antibacterial for acute skin infections and pneumonia.</p>Formula:C21H24ClF2N3O4Purity:98%Color and Shape:SolidMolecular weight:455.88WRN 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>Formula:C16H14N2O5SColor and Shape:SolidMolecular weight:346.36RNA 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>Formula:C38H53N11O12SPurity:98%Color and Shape:SolidMolecular weight:887.96WRN inhibitor 1
CAS:<p>WRN Inhibitor 1 (example 7) is an inhibitor of the Werner Syndrome ATP-dependent helicase enzyme (WRN), selectively targeting its helicase domain.</p>Formula:C16H13FN2O4SPurity:98%Color and Shape:SolidMolecular weight:348.35Fervenulin
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>Formula:C7H7N5O2Purity:99.75%Color and Shape:SolidMolecular weight:193.164-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>Formula:C7H11NO4SPurity:98%Color and Shape:SolidMolecular weight:205.23SHR5133
CAS:<p>SHR5133 is a potent, orally active regulator of HBV capsid assembly that reduces HBV DNA (EC50: 26.6 nM).</p>Formula:C19H18F4N6O2Color and Shape:SolidMolecular weight:438.38AU1235
CAS:<p>AU1235 is a Mycobacterium tuberculosis inhibitor.</p>Formula:C17H19F3N2OPurity:99.54% - 99.87%Color and Shape:SolidMolecular weight:324.346-Chloro-7-deazapurine-β-D-riboside
CAS:<p>6-Chloro-7-deazapurine-β-D-riboside shows antifungal activity.</p>Formula:C11H12ClN3O4Purity:98.26%Color and Shape:SolidMolecular weight:285.68Vinclozolin 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>Formula:C11H11Cl2NO2Color and Shape:SolidMolecular weight:260.1Propamidine
CAS:<p>Propamidine acts as a covalent inhibitor of TMPRSS2 and exhibits antibacterial properties. [1]</p>Formula:C17H20N4O2Purity:98%Color and Shape:SolidMolecular weight:312.37Antiviral 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>Formula:C17H22ClF3N2OColor and Shape:SolidMolecular weight:362.82MC-VC-PAB-Cyclohexanediamine-Thailanstatin A
CAS:<p>MC-VC-PAB-Cyclohexanediamine-Thailanstatin A is a spliceostatin analog and a drug-linker conjugate for antibody-drug conjugates (ADC), comprising the cytotoxic</p>Formula:C63H91N9O16Purity:98%Color and Shape:SolidMolecular weight:1230.45Ravidasvir HCl
CAS:<p>Ravidasvir, also known as PPI-668 and ASC16, is a second-generation, orally active, potent and selective HCV NS5A protein inhibitor.</p>Formula:C42H52Cl2N8O6Color and Shape:SolidMolecular weight:835.828Dihydroaltenuene B
CAS:<p>Dihydroaltenuene B inhibits mushroom tyrosinase (IC50: 38.33µM) and binds His244, Met280, Gly281 via hydrogen bonds.</p>Formula:C15H18O6Color and Shape:SolidMolecular weight: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>Formula:C20H29N9O7S2Color and Shape:SolidMolecular weight:571.63SPR38
<p>SPR38: SARS-CoV-2 protease inhibitor with Ki 0.260 μM; also blocks hCatL (Ki 1.92 μM) and hCatB (Ki 11.1 μM).</p>Formula:C24H33N3O5Color and Shape:SolidMolecular weight:443.54ELQ-596
CAS:<p>ELQ-596, a quinolone derivative, exhibits antimicrobial activity against several protozoan parasites, including the intraerythrocytic parasites Plasmodium and Babesia. ELQ-596 attenuates babesiosis in immunosuppressed mice [1].</p>Formula:C24H17ClF3NO3Color and Shape:SolidMolecular weight:459.84MF 5137
CAS:<p>MF 5137 is an effective antimicrobial agent.</p>Formula:C23H23N3O3Purity:98%Color and Shape:SolidMolecular weight:389.45AB-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>Formula:C20H15F3N4O2Color and Shape:SolidMolecular weight:400.35SLU-10482
CAS:<p>SLU-10482, an antiparasitic agent, effectively reduces C.</p>Formula:C18H16F4N6OColor and Shape:SolidMolecular weight:408.35Antibacterial compound 2
CAS:<p>Antibacterial compound 2 is a potent antimicrobial agent effective against many human veterinary pathogens, inhibiting multi-drug resistant staphylococci,</p>Formula:C22H30FN5O6Purity:90.4%Color and Shape:SolidMolecular weight:479.5Du011
CAS:<p>Du011 is a biogenesis inhibitor of the E.</p>Formula:C20H15F2NO4SColor and Shape:SolidMolecular weight:403.4Antituberculosis 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>Formula:C21H21NO4Color and Shape:SolidMolecular weight:351.4Aranciamycin
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>Formula:C27H28O12Color and Shape:SolidMolecular weight:544.5Quorum Sensing-IN-2
CAS:<p>Quorum Sensing-IN-2 (compound 23e) is a quorum sensing inhibitor that curtails bacterial pathogenicity without impeding growth.</p>Formula:C19H13F2NO3Color and Shape:SolidMolecular weight:341.31FWM-4
CAS:<p>FWM-4 is a potent inhibitor of SARS-COV-2 NSP13 decapping enzyme.</p>Formula:C24H18N4O4Color and Shape:SolidMolecular weight:426.42Fenpropidin
CAS:<p>Fenpropidin (Ro-12-3049), a fungicide, is a specific inhibitor of sterol 14-reductase and biosynthesis.</p>Formula:C19H31NPurity:98.58% - 99.54%Color and Shape:SolidMolecular weight:273.46Balapiravir hydrochloride
CAS:<p>Balapiravir HCl, an NS5B inhibitor, is used potentially for the treatment of HCV infection.</p>Formula:C21H31ClN6O8Color and Shape:SolidMolecular weight:530.965,6,7,8-Tetrahydro-8-deazahomofolic acid
CAS:<p>5,6,7,8-Tetrahydro-8-deazahomofolic acid is a potential thymidylate synthase (TS) inhibitor and other folate related enzymes inhibitor.</p>Formula:C21H26N6O6Color and Shape:SolidMolecular weight:458.47DQn-1
CAS:<p>DQn-1, a potent antifolate, demonstrates efficacy against Mycobacterium tuberculosis (Mtb) with an MIC 90 of 0.03 µM.</p>Formula:C16H14ClN5O2Color and Shape:SolidMolecular weight:343.77Antibacterial agent 91
<p>Antibacterial 91: Inhibits aaRS, IC50 2.10μM vs. S. enterica ThrRS, has antibacterial properties. [1]</p>Formula:C33H31BrClN5O4Color and Shape:SolidMolecular weight:676.99Antifungal agent 50
CAS:<p>Antifungal agent 50 exhibits minimum inhibitory concentrations (MICs) ranging from less than 0.063 to 1 μg/mL [1].</p>Formula:C25H20ClN5O2SColor and Shape:SolidMolecular weight:489.98XZ426
CAS:<p>XZ426 is a potent integrase strand transfer inhibitor with anti- HIV activity .</p>Formula:C22H24F2N4O4Color and Shape:SolidMolecular weight:446.45N-(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>Formula:C8H11NO4Color and Shape:SolidMolecular weight:185.18NSC309401
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>Formula:C17H16N6Color and Shape:SolidMolecular weight:304.35D1N8
CAS:<p>D1N8 is a potent inhibitor of the SARS-CoV-2 3CL protease, displaying an IC50 value of 0.44 μM and a CC50 value of greater than 20 μM.</p>Formula:C19H14ClN5O3Purity:98%Color and Shape:SolidMolecular weight:395.8hDHODH-IN-1
CAS:<p>hDHODH-IN-1 is an inhibitor of human dihydroorotate dehydrogenase (hDHODH) with an anti-inflammatory effect.</p>Formula:C17H14N2O2Purity:99.97%Color and Shape:SolidMolecular weight:278.31Koshidacin 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>Formula:C28H40N4O7Color and Shape:SolidMolecular weight:544.64Capravirine
CAS:<p>Capravirine, a non-nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formula:C20H20Cl2N4O2SPurity:98%Color and Shape:SolidMolecular weight:451.37Propiolactone
CAS:<p>Propiolactone (β-propiolactone; 2-Oxetanone), a chemosterilant, effectively inactivates viruses, rendering them non-infectious.</p>Formula:C3H4O2Purity:98%Color and Shape:SolidMolecular weight:72.06L 687908
CAS:<p>L 687908 is a potent inhibitor of hydroxyethylene-containing HIV protease.</p>Formula:C40H51N5O5Purity:98%Color and Shape:SolidMolecular weight:681.86Phylloflavan
CAS:<p>Phylloflavan, an antileishmanial compound, exhibits an intracellular half maximal effective concentration (EC50) of 3.2 nM in RAW 264.7 cells and inhibits the</p>Formula:C26H26O10Purity:98%Color and Shape:SolidMolecular weight:498.48Variculanol
CAS:<p>Variculanol, a compound with antimicrobial, anticancer, and anti-HCV NS3/4A protease properties, is derived from the marine fungus Aspergillus versicolor [1].</p>Formula:C25H40O2Color and Shape:SolidMolecular weight:372.58AS-2077715
CAS:<p>AS-2077715, an antifungal agent, exhibits inhibitory activity against Trichophyton species and is derived from the fermentation broth of Capnodium sp. 339855. It is utilized in the study of fungal infections [1].</p>Formula:C25H41NO7Color and Shape:SolidMolecular weight:467.6Despropylene gatifloxacin
CAS:<p>Despropylene gatifloxacin, a metabolite of AM-1155, exhibits potent antibacterial activity and has favorable pharmacokinetics [1].</p>Formula:C16H18FN3O4Color and Shape:SolidMolecular weight:335.33SARS-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>Formula:C16H12O3Purity:98%Color and Shape:SolidMolecular weight:252.26Antileishmanial 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>Formula:C27H37N5O5Purity:98%Color and Shape:SolidMolecular weight:511.61Antimalarial agent 10
CAS:<p>Compound 17b, an amino alcohol-quinoline, targets Pf3D7 (IC50: 14.9 nM) and PfW2 (IC50: 11 nM) with selectivity index >770.</p>Formula:C23H22F6N2O2Color and Shape:SolidMolecular weight:472.42Berlopentin
CAS:<p>Berlopentin is splenopentin analog used to treat HIV-positive patients. It also has immunostimulatory properties.</p>Formula:C35H55N9O11Color and Shape:SolidMolecular weight:777.86RSV L-protein-IN-4
CAS:<p>RSV L-protein-IN-4 (Compound C) is a noncompetitive inhibitor of the RSV polymerase with an IC50 of 0.88 μM.</p>Formula:C32H35N5O6Purity:98%Color and Shape:SolidMolecular weight:585.65Loflucarban
CAS:<p>Loflucarban (Fluonilid) is an antimycotic compoud.</p>Formula:C13H9Cl2FN2SPurity:98.08% - 98.15%Color and Shape:SolidMolecular weight:315.19SARS-CoV-2-IN-69
CAS:<p>SARS-CoV-2-IN-69 (Compound 7E) is a potent, non-covalent inhibitor of the SARS-CoV-2 main protease (M^pro) with an EC50 of 7.4 μM and also inhibits the papain-</p>Formula:C15H11NO3SPurity:98%Color and Shape:SolidMolecular weight:285.32LtaS-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>Formula:C24H17N3O5Purity:93.44%Color and Shape:SolidMolecular weight:427.41Debrisoquin
CAS:<p>Debrisoquin (Isocaramidine) is a TMPRSS2 inhibitor that prevents SARS-CoV-2 from entering human lung cells through TMPRSS2-dependent pathways, exhibiting an</p>Formula:C10H13N3Purity:98%Color and Shape:SolidMolecular weight:175.23Mansonone F
CAS:<p>Mansonone F is a topoisomerase II inhibitor with cytotoxic and topo inhibitory potencies.</p>Formula:C15H12O3Color and Shape:SolidMolecular weight:240.25(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>Formula:C26H22ClF3N2O6SPurity:98%Color and Shape:SolidMolecular weight:582.98DAM-IN-1
CAS:<p>DMA-IN-1 is a DNA adenine methyltransferase (DAM) inhibitor with an IC50 value of 48 μM.</p>Formula:C16H17NO4Purity:98%Color and Shape:SolidMolecular weight:287.31SDH-IN-3
CAS:<p>SDH-IN-3 is a succinate dehydrogenase (SDH) inhibitor, demonstrating potent antifungal activity with an inhibition concentration (IC50) of 7.2 μg/mL and an</p>Formula:C15H11F2N3OSPurity:98%Color and Shape:SolidMolecular weight:319.33XSJ2-46
CAS:<p>XSJ2-46, a 5'-amino NI analog, is an antiviral agent possessing anti-Zika virus properties and demonstrates reasonable inhibition of RNA-dependent RNA</p>Formula:C25H24ClF3N6O3Purity:98%Color and Shape:SolidMolecular weight:548.95RSV L-protein-IN-3
CAS:<p>RSV L-protein-IN-3 is an inhibitor of the wild-type RSV polymerase, exhibiting an IC50 of 10.4 μM and an EC50 of 2.1 μM (against RSV), and possesses lower</p>Formula:C31H34N4O4Purity:98%Color and Shape:SolidMolecular weight:526.63CDD-1733
CAS:<p>CDD-1733 is a potent, non-covalent, and non-peptide inhibitor of the SARS-CoV-2 main protease (Mpro) with an inhibition constant (K i) of 12 nM.</p>Formula:C34H32F3N5O2Purity:98%Color and Shape:SolidMolecular weight:599.65WRN inhibitor 2
CAS:<p>WRN Inhibitor 2 (example 118), a potent inhibitor of the WRN (Werner Syndrome ATP-dependent helicase enzyme), exhibits a pIC50 value of 7.0 or greater [1].</p>Formula:C15H11F3N2O5S2Purity:98%Color and Shape:SolidMolecular weight:420.383,4'-Dihydroxyflavone
CAS:<p>3,4'-Dihydroxyflavone (3,4'-DHF) is an oral active flavonoid. 3,4'-Dihydroxyflavone (3,4'-DHF) shows antiviral activity against Influenza A virus.</p>Formula:C15H10O4Purity:98.33%Color and Shape:SolidMolecular weight:254.24Palinavir
CAS:<p>Palinavir is an antiviral, it inhibits HIV-1 protease.</p>Formula:C41H52N6O5Purity:98%Color and Shape:SolidMolecular weight:708.89UNC-2170
CAS:<p>UNC-2170 (UNC2170 Maleate) is the methyl-lysine binding protein, 53BP1 ligand.</p>Formula:C14H21BrN2OPurity:97.44%Color and Shape:SolidMolecular weight:313.23U 89360E
CAS:<p>U 89360E is a peptidic inhibitor.</p>Formula:C28H52N8O6Purity:98%Color and Shape:SolidMolecular weight:596.7612R-LOX-IN-1
CAS:<p>12R-LOX-IN-1 (Compound 4a), with an IC50 of 28.25 µM, is an inhibitor of 12R-LOX.</p>Formula:C15H11NO2Color and Shape:SolidMolecular weight:237.25FAICAR
CAS:<p>FAICAR (5-Formamidoimidazole-4-carboxamide ribotide), a purine nucleotide, plays a crucial role in metabolic processes.</p>Formula:C10H15N4O9PColor and Shape:SolidMolecular weight:366.22NEU-730
CAS:<p>NEU-730, a novel inhibitor of TbrPDEB1, shows modest inhibition of T. brucei proliferation.</p>Formula:C25H29NO5Purity:98%Color and Shape:SolidMolecular weight:423.5Cladosporin
CAS:<p>Cladosporin, from Cladosporium cladosporioid fungus, halts dermatophyte growth on agar at 75 μg/mL.</p>Formula:C16H20O5Color and Shape:SolidMolecular weight:292.33Micronomicin
CAS:<p>Micronomicin (Gentamicin C2b) is an antibiotic exhibiting antibacterial and bactericidal capacity.</p>Formula:C20H41N5O7Purity:97.05% - 99.79%Color and Shape:SolidMolecular weight:463.57Nilofabicin
CAS:<p>Nilofabicin (CG-400549) is a potent inhibitor of enoyl-(acyl-carrier-protein) reductase fall(FabI) and can be used in studies about the treatment of complicated</p>Formula:C19H20N2O2SPurity:98.66%Color and Shape:SolidMolecular weight:340.44Anti-Trypanosoma cruzi agent-3
CAS:<p>Anti-Trypanosoma cruzi agent-3 is an antiprotozoal agent.</p>Formula:C29H29N3O6SColor and Shape:SolidMolecular weight:547.62Antiviral agent 35
CAS:<p>Antiviral agent 35 (compound 4d) serves as a potent orally active inhibitor of the influenza virus, targeting early stages of viral replication.</p>Formula:C23H18N2O4SPurity:98%Color and Shape:SolidMolecular weight:418.47NS5A-IN-2
CAS:<p>NS5A-IN-2, a potent inhibitor, is highly effective against HCV 1b and shows increased activity for GT 3a with good metabolic stability.</p>Formula:C46H45N7O7Purity:98%Color and Shape:SolidMolecular weight:807.89CcpA-IN-1
CAS:<p>CcpA-IN-1 is a Staphylococcus aureus antibiotic exhibiting significant bactericidal activity (MICs=460 nM) [1].</p>Formula:C77H82F12N8OP3RuPurity:98%Color and Shape:SolidMolecular weight:1557.5Dup-721
CAS:<p>DuP-721: broad-spectrum, oral antibiotic targeting various bacteria, including M. tuberculosis.</p>Formula:C14H16N2O4Purity:99.84%Color and Shape:SolidMolecular weight:276.29AB131
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>Formula:C21H19NO6SColor and Shape:SolidMolecular weight:413.44Roseoflavin
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>Formula:C18H23N5O6Purity:99.81% - 99.89%Color and Shape:SolidMolecular weight:405.41Emzadirib
CAS:<p>Emzadirib (RAD51-IN-2) is a potent RAD51 inhibitor with potential anticancer activity for the study of DNA damage repair.</p>Formula:C27H40N4O6S2Purity:99.79% - 99.9%Color and Shape:SolidMolecular weight:580.76NSC309401 dihydrochloride
CAS:<p>NSC309401 is an E. coli dihydrofolate reductase inhibitor with an IC50 value of 189 nM and a dissociation constant (Kd) of 14.57 nM [1].</p>Formula:C17H18Cl2N6Color and Shape:SolidMolecular weight:377.27Prochloraz manganese
CAS:<p>Prochloraz manganese, an antifungal agent utilized in the agricultural sectors [1], serves to protect crops by inhibiting fungal growth.</p>Formula:C60H64Cl14MnN12O8Color and Shape:SolidMolecular weight:1632.51Ibuzatrelvir
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>Formula:C21H30F3N5O5Purity:98%Color and Shape:SolidMolecular weight:489.49Rosoxacin
CAS:<p>Rosoxacin (Acrosoxacin) shows antibacterial activities against a broad spectrum of Gram-negative bacteria including Neisseria gonorrhoeae (MIC90 = 0.03mg/ml).</p>Formula:C17H14N2O3Purity:99.1%Color and Shape:SolidMolecular weight:294.3RSV 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>Formula:C31H36N6O4Purity:98%Color and Shape:SolidMolecular weight:556.66Oxynitidine
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>Formula:C21H17NO5Purity:98%Color and Shape:SolidMolecular weight:363.36Berkeleylactone E
CAS:<p>Berkeleylactone E, a macrolide antibiotic [1], exhibits antimicrobial properties.</p>Formula:C20H32O7Color and Shape:SolidMolecular weight:384.469DprE1-IN-9
CAS:<p>DprE1-IN-9 (compound B18) is an efficient reversible inhibitor of DprE1, interacting with the enzyme's receptor cavity.</p>Formula:C22H25F3N4O2Color and Shape:SolidMolecular weight:434.45Elastase LasB-IN-1
CAS:<p>Elastase LasB-IN-1 (Compound 4b), a potent and selective inhibitor of elastase LasB, exhibits antibacterial activity and has been determined to possess an IC50</p>Formula:C13H17F3NO4PColor and Shape:SolidMolecular weight:339.25HCoV-OC43-IN-1
CAS:<p>HCoV-OC43-IN-1 (Compound IV-16) serves as an inhibitor of the coronavirus HCoV-OC43, exhibiting antiviral efficacy with an EC50 of 90 nM.</p>Formula:C23H22F6N4O2Purity:98%Color and Shape:SolidMolecular weight:500.44SARS-CoV-2 3CLpro-IN-15
CAS:<p>SARS-CoV-2 3CLpro-IN-15 (compound a), a beta-nitrostyrene derivative, acts as an inhibitor of the SARS-CoV-2 3CL protease (3CLpro), effectively inhibiting viral</p>Formula:C8H6N2O4Purity:98%Color and Shape:SolidMolecular weight:194.14NSC 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>Formula:C19H16N4O3Purity:98%Color and Shape:SolidMolecular weight:348.36RSV 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>Formula:C32H36N4O5Purity:98%Color and Shape:SolidMolecular weight:556.65ZINC475239213
CAS:<p>ZINC475239213 acts as an inhibitor targeting the SARS-CoV-2 Nsp14 N7-Methyltransferase with an IC50 value of 20 μM [1].</p>Formula:C21H15N5O2Purity:98%Color and Shape:SolidMolecular weight:369.38MoTPS1-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>Formula:C23H27F3N2O4Purity:99.28%Color and Shape:SoildMolecular weight:452.47Influenza 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>Formula:C27H26ClNO7Purity:98%Color and Shape:SolidMolecular weight:511.95Votoplam
CAS:<p>Votoplam functions as a gene splicing modulator, employed in the inhibition of Huntington's disease [1].</p>Formula:C21H25N9OPurity:98%Color and Shape:SolidMolecular weight:419.48(-)-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>Formula:C11H13N5O3Color and Shape:SolidMolecular weight:263.3Brevicompanine B
CAS:<p>Brevicompanine B: fungal metabolite, regulates plant growth/circadian rhythm, inhibits Arabidopsis roots, affects gene transcription, anti-P. falciparum.</p>Formula:C22H29N3O2Color and Shape:SolidMolecular weight:367.48Chitin 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>Formula:C25H26ClN5O5Color and Shape:SolidMolecular weight:511.96Antimicrobial photosensitizer-1
CAS:<p>Photosensitizer-1 shows promise in treating infections, effective against S. aureus in mouse wounds.</p>Formula:C19H19BF2I3N3Color and Shape:SolidMolecular weight:718.9A 33853
CAS:<p>A 33853 is an antibiotic isolated from culture broth of Streptomyces sp.</p>Formula:C20H13N3O6Color and Shape:SolidMolecular weight:391.33BVDU 5′-Triphosphate
CAS:<p>BVDU 5′-Triphosphate is an antiviral agent labeled with 5′-Triphosphate that specifically targets viral DNA polymerase.</p>Formula:C11H16BrN2O14P3Purity:98%Color and Shape:SolidMolecular weight:573.08Arbemnifosbuvir
CAS:<p>Arbemnifosbuvir, a drug interfering with the nidovirus DdRp-associated nucleotidyltransferase (NiRAN) domain of non-structural protein 12 (nsp12), is utilized</p>Formula:C24H33FN7O7PPurity:98%Color and Shape:SolidMolecular weight:581.53SARS-CoV-2-IN-1
CAS:<p>SARS-CoV-2-IN-1 is a potent inhibitor of Mpro(SARS-CoV-2 Mpro, SARS-CoV Mpro and MERS-CoV Mpro with IC50s of 0.67, 0.90 and 0.58 μM, respectively).</p>Formula:C31H39N5O7Purity:98%Color and Shape:SolidMolecular weight:593.67BMS-561390
CAS:<p>BMS-561390, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formula:C14H12ClF3N2OColor and Shape:SolidMolecular weight:316.71Ganfeborole HCl
CAS:<p>Ganfeborole HCl (GSK3036656 HCl) is a compound with anti-tuberculosis activity and is an inhibitor of Mycobacterium tuberculosis (Mtb) leucyl-tRNA synthetase.</p>Formula:C10H14BCl2NO4Purity:99.88%Color and Shape:SolidMolecular weight:293.94APX2039
CAS:<p>APX2039 is an orally active fungal Gwt1 enzyme inhibitor and a prodrug of the novel Gwt2096 inhibitor APX1.APX2039 exhibits potent anti-Kryptococcal activity</p>Formula:C20H15FN4O2Purity:98.72% - 99.07%Color and Shape:SolidMolecular weight:362.36Methyl 2-amino-5-bromobenzoate
CAS:<p>Methyl 2-amino-5-bromobenzoate (Methyl 5-Bromoanthranilate) is an HCV NS5b RNA polymerase inhibitor with antimicrobial activity.</p>Formula:C8H8BrNO2Purity:98.05%Color and Shape:SolidMolecular weight:230.06EHNA hydrochloride
CAS:<p>EHNA hydrochloride is a PDE2 and ADA inhibitor with anticancer activity, increasing intracellular adenosine concentration in a treatment time-dependent manner.</p>Formula:C14H24ClN5OPurity:98%Color and Shape:SolidMolecular weight:313.83DHX9-IN-6
CAS:<p>DHX9-IN-6 is a highly effective ATP-dependent RNA helicase A (DHX9) inhibitor, used in cancer research.</p>Formula:C23H18ClFN4O4S2Purity:99.71%Color and Shape:SolidMolecular weight:533Zevotrelvir
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>Formula:C28H26F3N5O3Purity:98%Color and Shape:SolidMolecular weight:537.53Antibacterial 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>Formula:C51H50N16O10S6Purity:98%Color and Shape:SolidMolecular weight:1239.43L-697661
CAS:<p>L-697661, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formula:C16H15Cl2N3O2Color and Shape:SolidMolecular weight:352.22Diazoketone methotrexate
CAS:<p>Diazoketone methotrexate is an analog of methotrexate with potential antitumor activity.</p>Formula:C21H22N10O4Color and Shape:SolidMolecular weight:478.46Indinavir, threo-
CAS:<p>Indinavir, threo- is a protease inhibitor utilized as a component of highly active antiretroviral treatment to HIV/AIDS.</p>Formula:C36H47N5O4Purity:98%Color and Shape:SolidMolecular weight:613.79Alteconazole
CAS:<p>Alteconazole is an antifungal drug.</p>Formula:C17H12Cl3N3OPurity:98%Color and Shape:SolidMolecular weight:380.66LY 173013
CAS:<p>LY 173013 is a bicyclic pyrazolidinone, it has antibacterial properties.</p>Formula:C15H16N6O7SPurity:98%Color and Shape:SolidMolecular weight:424.39Antibacterial compound 1
CAS:<p>Antibacterial compound 1 is an antibacterial compound.</p>Formula:C14H16FN3O4Purity:98%Color and Shape:SolidMolecular weight:309.29Deacylketoconazole
CAS:<p>Deacylketoconazole (Deacyl ketoconazole) is a Ketoconazole derivative and is also an antifungal agent.</p>Formula:C24H26Cl2N4O3Purity:98.35%Color and Shape:SolidMolecular weight:489.39Antibiofilm agent-9
CAS:<p>Antibiofilm agent-9 (Compound 4), a derivative of pyrrolnitrin, exhibits antimicrobial activity. It inhibits Bacillus anthracis with a Minimum Inhibitory Concentration (MIC) of 0.031 μg/mL. The compound demonstrates significant antibiofilm activity, achieving an inhibition rate of 84% after 24 hours at a concentration of 8.0 μg/mL. Additionally, Antibiofilm agent-9 shows favorable pharmacokinetic properties in mouse models.</p>Formula:C11H5BrCl2FNO2Color and Shape:SolidMolecular weight:352.97AG 85
CAS:<p>AG 85 is a major secretion protein of Mycobacterium tuberculosis.</p>Formula:C27H22N4O3SColor and Shape:SolidMolecular weight:482.55LNA-Adenosine
CAS:<p>LNA-Adenosine (LNA-A) is a nucleoside analogue that acts as a ligand for adenosine A3 receptors.</p>Formula:C11H13N5O4Purity:99.15%Color and Shape:SolidMolecular weight:279.252,4′-Dichloroacetanilide
CAS:<p>2,4′-Dichloroacetanilide (2-chloro-N-(4-chlorophenyl)acetamide) has antifungal activity and inhibits T. asteroides with a MIC value of 6.25 μg/mL.</p>Formula:C8H7Cl2NOPurity:99.36%Color and Shape:SolidMolecular weight:204.05Linvencorvir
CAS:<p>Linvencorvir is a hepatitis B virus (HBV) core protein variant modifier used to treat chronic HBV infection.</p>Formula:C29H35FN6O5SPurity:99.9% - 99.9%Color and Shape:SolidMolecular weight:598.69CWHM-1552
CAS:<p>CWHM-1552 is an effective Plasmodium falciparum inhibitor. For the 3D7 and Dd2 strains, the IC50s are 51 nM and 53 nM.</p>Formula:C22H27F2N3OPurity:99.56%Color and Shape:SolidMolecular weight:387.47Salicyl-AMS
CAS:<p>Salicyl-AMS is an inhibitor of mycobacterium auxin biosynthesis that inhibits the growth of mycobacterium in the presence of iron deficiency in vitro.</p>Formula:C17H18N6O8SPurity:98.19%Color and Shape:SolidMolecular weight:466.43Dehydroemetine
CAS:<p>Dehydroemetine, a synthetic emetine, treats amoebic infections and leishmaniasis, and resists metronidazole amoebiosis.</p>Formula:C29H38N2O4Purity:98.68% - 99.68%Color and Shape:SolidMolecular weight:478.62Leritrelvir
CAS:<p>Dermatan sulphate sodium (Chondroitin sulfate B sodium salt) is a linear sulfated polysaccharide, a glycosaminoglycan component of important proteoglycans.</p>Formula:C31H44F3N5O6Purity:97.42%Color and Shape:SolidMolecular weight:639.71Thymectacin
CAS:<p>Thymectacin (NB 1011) is a selective thymidine synthase (TS) inhibitor with anticancer activity for the study of colon cancer and solid tumors.</p>Formula:C21H25BrN3O9PPurity:97.05% - 99.49%Color and Shape:SolidMolecular weight:574.32A7132
CAS:<p>A7132 is an antibacterial agent and possesses broad and potent antibacterial activity.</p>Formula:C19H16F2N4O3Purity:95.49%Color and Shape:SolidMolecular weight:386.35MMV688533
CAS:<p>MMV688533 has antimalarial activity.</p>Formula:C24H15F6N5O2Purity:99.12%Color and Shape:SoildMolecular weight:519.4ZY-19489
CAS:<p>ZY-19489: Antimalarial, potential single-dose cure, FDA orphan drug status.</p>Formula:C24H32FN9Purity:>99.99%Color and Shape:SoildMolecular weight:465.57Nesbuvir
CAS:<p>Nesbuvir: HCV NS5B polymerase inhibitor, IC50 9 nM against HCV 1b replicon in liver cancer cells.</p>Formula:C22H23FN2O5SPurity:99.99%Color and Shape:SolidMolecular weight:446.49Tenofovir amibufenamide
CAS:<p>Tenofovir amibufenamide (HS-10234) 是一种 Tenofovir 前药，是一种具有口服活性的抗病毒化合物。Tenofovir amibufenamide 对乙型肝炎病毒 (HBV)具有抑制作用，可用于慢性乙型肝炎 (CHB) 研究。</p>Formula:C22H31N6O5PPurity:99.19% - 99.87%Color and Shape:SolidMolecular weight:490.49TCMDC-135051
CAS:<p>TCMDC-135051: Selective PfCLK3 inhibitor, low toxicity, halts parasite growth & transmission; EC50=320 nM.</p>Formula:C29H33N3O3Purity:99.05%Color and Shape:SolidMolecular weight:471.59Valomaciclovir stearate
CAS:<p>S-Allylmercapturic Acid (N-Acetyl-S-allyl-L-cysteine) is a metabolite of S-allyl-L-cysteine present in black garlic, with potential anti-gout effects.</p>Formula:C33H58N6O5Purity:99.18% - >99.99%Color and Shape:SolidMolecular weight:618.85SMN-C3
CAS:<p>SMN-C3 (MV8T2MCK57) is an orally active modulator of SMN2 splicing, and has the potential to treat spinal muscular atrophy (SMA).</p>Formula:C24H28N6OPurity:99.01% - 99.05%Color and Shape:SolidMolecular weight:416.52Contezolid
CAS:<p>Contezolid (MRX-I) is an antibiotic with bactericidal activity and can be used to study tuberculosis.</p>Formula:C18H15F3N4O4Purity:99.41%Color and Shape:SolidMolecular weight:408.33Ziresovir
CAS:<p>Ziresovir (RO-0529) is a respiratory syncytial virus fusion protein (RSV F) inhibitor that inhibits RSV and can be used to study syncytial virus sense.</p>Formula:C22H25N5O3SPurity:95.51% - >99.99%Color and Shape:SolidMolecular weight:439.53Filibuvir
CAS:<p>Filibuvir (PF-00868554) inhibits HCV polymerase genotypes 1a/1b, EC50s 59 nM.</p>Formula:C29H37N5O3Purity:99.28% - >99.99%Color and Shape:SolidMolecular weight:503.64DHX9-IN-2
CAS:<p>DHX9-IN-2 is an inhibitor targeting ATP-dependent RNA de-helicase A (DHX9) with anticancer and antitumor activity for cancer research.</p>Formula:C18H16ClN3O3S2Purity:98%Color and Shape:SolidMolecular weight:421.92GSK3186899
CAS:<p>GSK3186899 is an inhibitor of Cdc2-related kinase 12 with an EC50 of 1.4 μM for L. donovani.</p>Formula:C19H28F3N7O3SPurity:98.35% - 99.61%Color and Shape:SolidMolecular weight:491.53Lomibuvir
CAS:<p>Lomibuvir (VCH-222, VX-222) is an allosteric inhibitor of HCV NS5B with Kd 17 nM, blocks RNA elongation, EC50 5.2 nM for 1b/Con1.</p>Formula:C25H35NO4SPurity:99.83%Color and Shape:SolidMolecular weight:445.61Sorivudine
CAS:<p>Sorivudine (BV-araU) is an antiviral blocking DNA synthesis in viruses like varicella, HSV-1, and Epstein-Barr.</p>Formula:C11H13BrN2O6Purity:99.74%Color and Shape:SolidMolecular weight:349.13CeMMEC1
CAS:<p>CeMMEC1 is an inhibitor of BRD4, and also has a great affinity for TAF1(IC50=0.9 μM).</p>Formula:C19H16N2O4Purity:98.9% - 99.92%Color and Shape:SolidMolecular weight:336.34Carumonam Sodium
CAS:<p>Carumonam Sodium is a monobactam, penicillin-binding protein inhibitor. It is used as antibacterials.</p>Formula:C12H12N6Na2O10S2Purity:98%Color and Shape:SolidMolecular weight:510.37SARS-CoV-2 3CLpro-IN-28
CAS:<p>SARS-CoV-2 3CLpro-IN-28 (Compound 19) is an inhibitor of SARS-CoV-2 3CLpro, exhibiting an IC50 value of 0.018 μM.</p>Formula:C27H18Cl2N4O4Color and Shape:SolidMolecular weight:533.362(E)-Cefodizime
CAS:<p>(E)-Cefodizime ((E)-THR-221) is an antibiotic that selectively binds to penicillin-binding proteins (PBPs), inhibiting bacterial cell wall synthesis, which results in its antibacterial activity. It holds potential for research into various bacterial infections, including the prevention of preoperative infections.</p>Formula:C20H20N6O7S4Color and Shape:SolidMolecular weight:584.6691,5-Dideoxy-1,5-imino-D-mannitol
CAS:<p>1,5-Dideoxy-1,5-imino-D-mannitol is an antibiotic with antibacterial properties.</p>Formula:C6H13NO4Color and Shape:SolidMolecular weight:163.172VV261
CAS:<p>VV261 is an orally active inhibitor of the Influenza Virus. It exhibits activity against the Severe Fever with Thrombocytopenia Syndrome Virus (SFTSV) and the Lymphocytic Choriomeningitis Virus (LCMV), with EC50 values of 0.89 and 0.15, respectively.</p>Formula:C28H34FN3O11Color and Shape:SolidMolecular weight:607.58SARS-CoV-2-IN-8
<p>SARS-CoV-2-IN-8 is a major protease inhibitor of SARS-CoV-2 (IC50: 0.75 μM).</p>Formula:C35H38N6O3Color and Shape:SolidMolecular weight:590.71CYP2C19-IN-1
<p>CYP2C19-IN-1: potent CYP2C19 inhibitor, non-genotoxic, non-hepatotoxic, blocks RdRP (Ki: 6.16 μM), useful for ZIKV research.</p>Formula:C26H26N2O6SColor and Shape:SolidMolecular weight:494.56SARS-CoV-2-IN-80
CAS:<p>SARS-CoV-2-IN-80 (compound 13), identified as a potent inhibitor of SARS-CoV-2 3CLpro, exhibits an IC50 value of 0.964 µM [1].</p>Formula:C16H10O2SColor and Shape:SolidMolecular weight:266.3112(S)-HETE
CAS:<p>Enpatoran hydrochloride (M5049 hydrochloride) is a TLR7/8 inhibitor with antiviral activity that is used in the study of autoimmune diseases.</p>Formula:C20H32O3Color and Shape:SolidMolecular weight:320.47N'-(2-Fluorophenyl)pyrazine-2-carbohydrazide
<p>N'-(2-Fluorophenyl)pyrazine-2-carbohydrazide is a Ole1p desaturase inhibitor as well as antifungal agent [1].</p>Formula:C11H9FN4OColor and Shape:SolidMolecular weight:232.21SARS-CoV-2 Mpro-IN-44
CAS:<p>SARS-CoV-2 Mpro-IN-44 (Compound 25) is a broad-spectrum inhibitor of the main protease (Mpro) for coronaviruses. It exhibits inhibitory activity against several high-risk coronaviruses, including SARS-CoV-2 and PEDV, with an IC50 of less than 0.6 μM. The broad inhibition of coronaviruses by SARS-CoV-2 Mpro-IN-44 is achieved through enhanced interaction with conserved sites of Mpro. This compound is a potential candidate for the development of antiviral drugs against coronaviruses.</p>Formula:C29H19Cl2FN8O4SColor and Shape:SolidMolecular weight:665.48Omaciclovir
CAS:<p>Omaciclovir (ABT-091) is a herpesvirus herpesvirus replication inhibitor with antiviral activity that is used in the study of herpesvirus infections.</p>Formula:C10H15N5O3Purity:99.46% - 99.46%Color and Shape:SolidMolecular weight:253.26MTH1 activator-1
CAS:<p>MTH1 activator-1 is an MTH1 activator that enhances endogenous MTH1 activity and significantly reduces 8-oxo-dG levels in cellular DNA. It is useful for investigating the upregulation of oxidative damage repair in nucleotide pools and examining biological effects, as well as for studies aiming to delay or prevent tumorigenesis.</p>Formula:C29H23F3N4O2Color and Shape:SolidMolecular weight:516.514Ibafloxacine
CAS:<p>Ibafloxacine (R835) is a fluoroquinolone antibiotic that is used exclusively in veterinary applications and shows zero good bacteriostatic effect against</p>Formula:C15H14FNO3Purity:97.67%Color and Shape:SolidMolecular weight:275.27Saroaspidin B
CAS:<p>Saroaspidin B is a dimeric form of a biphenyl triphenol, characterized as an antibiotic compound.</p>Formula:C25H32O8Color and Shape:SolidMolecular weight:460.52Neuraminidase-IN-4
<p>Neuraminidase-IN-4 inhibits neuraminidase (EC50: 1.59 μM) and has strong anti-H5N1 activity.</p>Formula:C21H20N2O6SColor and Shape:SolidMolecular weight:428.46Secutrelvir
CAS:<p>Secutrelvir inhibits the 3CL protease (3CL protease), thereby exhibiting antiviral activity by preventing the replication of SARS-CoV-2.</p>Formula:C23H16Cl2F3N5O2Color and Shape:SolidMolecular weight:522.307Cap-dependent endonuclease-IN-25
CAS:<p>Cap-dependent endonuclease-IN-25 is a potent inhibitor of CEN, useful in studying Orthomyxoviridae viruses. (See WO2020075080A1, compound 4.)</p>Formula:C25H25N3O3Color and Shape:SolidMolecular weight:415.48APE1-IN-3
CAS:<p>APE1-IN-3 (Compound 1), an APE1 inhibitor, is utilized in cancer research.</p>Formula:C17H16O4Color and Shape:SolidMolecular weight:284.31epi-D-Captopril
CAS:<p>epi-D-Captopril (epi-D-SQ 14225) is a stereoisomer of Captopril and functions as an inhibitor of metallo-beta-lactamases (MBLs). The IC50 values of epi-D-Captopril for NDM-1, IMP-1, and VIM-2 are 64 μM, 173 μM, and 5.5 μM, respectively. This compound holds potential for research in MBLs-related antibiotic-resistant infections.</p>Formula:C9H15NO3SColor and Shape:SolidMolecular weight:217.285MCB-3681
CAS:<p>MCB-3681, active against gram-positive bacterium, is the antibacterial Oxaquin's active substance.</p>Formula:C31H32F2N4O8Color and Shape:SolidMolecular weight:626.62-Acetyl-2-decarboxamidotetracycline
CAS:<p>2-Acetyl-2-decarboxamidotetracycline is a tetracycline-class antibiotic. It exhibits a UV absorption spectrum similar to that of tetracycline or 5-oxytetracycline at concentrations above 300 mμ, characteristic of the BCD ring system.</p>Formula:C23H25NO8Color and Shape:SolidMolecular weight:443.45Mt KARI-IN-1
<p>Mt KARI-IN-1 inhibits Mtb KARI with a 3.06 μM Ki, targeting tuberculosis.</p>Formula:C14H11N5O4S2Color and Shape:SolidMolecular weight:377.47-Hydroxytropolone
CAS:<p>7-Hydroxytropolone (3-Hydroxytropolone) is an antibiotic that exhibits activity against Gram-positive and Gram-negative bacteria, as well as yeasts and fungi. It also functions as an inhibitor of 2''-O-adenylate transferase.</p>Formula:C7H6O3Color and Shape:SolidMolecular weight:138.12Zorubicin
CAS:<p>Zorubicin, a Daunorubicin derivative, targets topoisomerase II, inhibits DNA polymerase, and researches acute leukemia, sarcomas.</p>Formula:C34H35N3O10Color and Shape:SolidMolecular weight:645.66SARS-CoV-2 3CLpro-IN-32
CAS:<p>SARS-CoV-2 3CLpro-IN-32 (compound B16) is a potent inhibitor of the SARS-CoV-2 3CLpro enzyme, with an IC50 of 0.109 μM. It also demonstrates antiviral activity against the coronavirus HCoV-OC43, with an EC50 of 1.99 μM.</p>Formula:C30H37N3O4S3Color and Shape:SolidMolecular weight:599.83Chitin synthase inhibitor 7
<p>Compound 9c, a chitin synthase inhibitor, has an IC50 of 0.37 nM and is useful for studying fungal infections.</p>Formula:C24H25N3O5Color and Shape:SolidMolecular weight:435.47RAD51-IN-5
CAS:<p>RAD51-IN-5 blocks RAD51; may aid mitochondrial disorder research. (WO2021164746A1, cmpd 3)</p>Formula:C26H38N4O5S2Color and Shape:SolidMolecular weight:550.73Colistin adjuvant-2
<p>Colistin adjuvant-2 is a compound that acts as a potentiation agent for colistin, effectively enhancing its activity against Gram-negative bacteria [1].</p>Formula:C14H7Cl2F3N2OColor and Shape:SolidMolecular weight:347.12Antibacterial agent 169
CAS:<p>Antibacterial agent 169 (Compound 28), a pyrrolamide-type GyrB/ParE inhibitor, exhibits antibacterial properties by inhibiting Gyrase and Topo IV in Staphylococcus aureus. It has IC 50 values of 49 nmol/L and 1.513 μmol/L, respectively [1].</p>Formula:C19H25Cl2N5O3Color and Shape:SolidMolecular weight:442.34HBV-IN-18
<p>HBV-IN-18 (Compound 3) is an HBV capsid assembly modulator (CpAM) (EC50: 2790 nM).</p>Formula:C17H15F6N5O2Color and Shape:SolidMolecular weight:435.32
