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Microbiology/Virology

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"

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Found 6397 products of "Microbiology/Virology"

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  • Ganaplacide hydrochloride

    CAS:
    Ganaplacide hydrochloride (KAF156 HCl) is an orally administered imidazopyrimidine antimalarial agent that inhibits Plasmodium PI4K activity.
    Formula:C22H24ClF2N5O
    Purity:93.97%
    Color and Shape:Soild
    Molecular weight:447.91

    Ref: TM-T62677

    1mg
    185.00€
    5mg
    467.00€
    10mg
    698.00€
    25mg
    1,324.00€
    50mg
    1,941.00€
    100mg
    2,628.00€
  • SARS-CoV-2-IN-6


    SARS-CoV-2-IN-6 is an inhibitor of SARS-CoV-2 3CLpro with the IC 50 value of 73 nM.
    Formula:C17H13ClN2O2
    Color and Shape:Solid
    Molecular weight:312.75

    Ref: TM-T60785

    25mg
    949.00€
    50mg
    1,233.00€
    100mg
    1,897.00€
  • FPI-1465

    CAS:
    FPI-1465: Dual serine-β-lactamase & PBP inhibitor; IC50 PBP2=1.0 μg/mL; Kd CTX-M-15=0.011μM, OXA-48=5.3μM.
    Formula:C11H18N4O7S
    Color and Shape:Solid
    Molecular weight:350.35

    Ref: TM-T61204

    50mg
    To inquire
    100mg
    To inquire
    25mg
    5,731.00€
  • Antibacterial agent 262

    CAS:
    Antibacterialagent 262 (compound A23) is a potent antibacterial agent that inhibits the activity of Xanthomonas oryzae pv oryzae. It also disrupts the integrity of bacterial cell membranes by preventing the formation of biofilms of Xanthomonas oryzae pv oryzae.
    Formula:C17H18F2N6O4S3
    Color and Shape:Solid
    Molecular weight:504.554

    Ref: TM-T204171

    10mg
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    50mg
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  • QPX7728 methoxy acetoxy methy ester

    CAS:
    QPX7728 methoxy acetoxy methy ester is an inhibitor of boronic acid β-lactamase.
    Formula:C14H14BFO7
    Purity:98%
    Color and Shape:Solid
    Molecular weight:324.07

    Ref: TM-T12602

    25mg
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    50mg
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    100mg
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  • HBV-IN-20


    HBV-IN-20 is a potent, orally active HBV inhibitor (EC50: 0.46 μM). HBV-IN-20 is a classical type II CpAM (core protein assembly regulator).
    Color and Shape:Solid

    Ref: TM-T64260

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • 5-Iminodaunorubicin hydrochloride

    CAS:
    5-Iminodaunorubicin HCl: quinone-modified anthracycline with antitumor properties, induces DNA breaks in cancer cells.
    Formula:C27H31ClN2O9
    Color and Shape:Solid
    Molecular weight:563.00

    Ref: TM-T72115

    25mg
    973.00€
    50mg
    1,269.00€
    100mg
    1,918.00€
  • L 702007

    CAS:
    L 702007 is an inhibitor of HIV-1 reverse transcriptase.
    Formula:C18H25N3O2
    Purity:98%
    Color and Shape:Solid
    Molecular weight:315.41

    Ref: TM-T24346

    25mg
    1,773.00€
    50mg
    2,322.00€
    100mg
    3,060.00€
  • Flutimide

    CAS:
    Flutimide: Endonuclease inhibitor, IC50 = 3μM, for research on acute respiratory diseases like influenza.
    Formula:C12H18N2O3
    Color and Shape:Solid
    Molecular weight:238.28

    Ref: TM-T70355

    5mg
    7,174.00€
  • RAD51-IN-7

    CAS:
    RAD51-IN-7 inhibits RAD51 gene, with potential for mitochondrial disorders. (From WO2021164746A1, cmpd 71)
    Formula:C25H31N5O4S2
    Color and Shape:Solid
    Molecular weight:529.67

    Ref: TM-T63728

    25mg
    1,927.00€
    50mg
    2,507.00€
    100mg
    3,168.00€
  • BMT-052

    CAS:
    BMT-052 is a potent and selective Pan-genotypic HCV NS5B Polymerase Inhibitor (EC50 = 7 nM).
    Formula:C30H17D9F4N6O5
    Purity:98%
    Color and Shape:Solid
    Molecular weight:635.61

    Ref: TM-T26871

    25mg
    2,718.00€
    50mg
    3,582.00€
    100mg
    4,950.00€
  • Antibacterial agent 75


    Antibacterial agent 75 re-sensitizes VRSA to vancomycin.
    Formula:C22H28N6O
    Color and Shape:Solid
    Molecular weight:392.5

    Ref: TM-T61799

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • NBD-10007

    CAS:
    NBD-10007 is an inhibitor of HIV-1 entry.
    Formula:C20H25ClN4O3S
    Purity:98%
    Color and Shape:Solid
    Molecular weight:436.96

    Ref: TM-T24522

    25mg
    To inquire
    50mg
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    100mg
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  • Fipravirimat

    CAS:
    Fipravirimat is a potent inhibitor of HIV-1 with potential applications in HIV and AIDS research.
    Formula:C43H67FN2O4S
    Color and Shape:Solid
    Molecular weight:727.07

    Ref: TM-T70147

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • DC-159a

    CAS:
    DC-159a, an 8-methoxy fluoroquinolone, possesses broad-spectrum antibacterial activity, with a particular efficacy against Gram-positive pathogens. The MIC90 values for DC-159a are 0.5 μg/mL against Streptococcus anginosus group, 4 μg/mL against Clostridium difficile, and 2 μg/mL against Bacteroides fragilis.
    Formula:C21H23F2N3O40·5H2O
    Color and Shape:Solid
    Molecular weight:428.4295

    Ref: TM-T204310

    10mg
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    50mg
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  • HIV-1 protease-IN-6


    HIV-1 protease-IN-6 (17d) strongly inhibits HIV-1 protease (IC50: 21 pM, Ki: 4.7 pM) and effectively targets DRV-resistant mutants.
    Formula:C27H31FN2O6S
    Color and Shape:Solid
    Molecular weight:530.61

    Ref: TM-T63733

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • Elongation factor P-IN-1


    EFP-IN-1: potent β-lysine derivative, inhibits EFP, slows E. coli growth.
    Formula:C14H31N3O2
    Color and Shape:Solid
    Molecular weight:273.41

    Ref: TM-T60491

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • SID 26681509 quarterhydrate


    SID 26681509 is a selective inhibitor of cathepsin L (IC50: 56 nM) and blocks Plasmodium falciparum (IC50: 15.4 μM) and Leishmania major (IC50: 12.5 μM).
    Formula:C27H35N5O6S
    Color and Shape:Solid
    Molecular weight:544.16

    Ref: TM-T63831

    25mg
    1,359.00€
    50mg
    1,770.00€
    100mg
    2,657.00€
  • HCV NS5B polymerase-IN-2

    CAS:
    HCVNS5B polymerase-IN-2 (Compound 298) is an inhibitor of the Ns5b polymerase. It holds potential for research into the treatment of hepatitis C virus (HCV) infections.
    Formula:C26H24N2O4
    Color and Shape:Solid
    Molecular weight:428.48

    Ref: TM-T204671

    10mg
    To inquire
    50mg
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  • LY 215890

    CAS:
    LY 215890 is a compound that exhibits potent Gram-negative and Gram-positive antibacterial activity.
    Formula:C13H12ClN5O5S
    Purity:98%
    Color and Shape:Solid
    Molecular weight:385.78

    Ref: TM-T27898

    25mg
    2,448.00€
    50mg
    3,222.00€
    100mg
    4,410.00€
  • Purine phosphoribosyltransferase-IN-1


    Compound (S,R)-48 inhibits Pf, Pv, & Tbr PRT with Ki of 50, 20, 2 nM.
    Formula:C11H15N5Na4O10P2
    Color and Shape:Solid
    Molecular weight:531.17

    Ref: TM-T63737

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • Polθ-IN-8

    CAS:
    Polθ-IN-8 (example 77) is a DNA polymerase θ (Polθ) inhibitor with an IC50 for Polθ ATPase activity of less than 100 nM. Polθ-IN-8 is useful for researching diseases related to Polθ activity, such as cancer.
    Formula:C22H22ClN7O3S
    Color and Shape:Solid
    Molecular weight:499.97

    Ref: TM-T207723

    10mg
    To inquire
    50mg
    To inquire
  • PCTR1

    CAS:
    PCTR1, derived from DHA, hastens inflammation resolution and boosts macrophage function, reducing PGE2, PGD2, and TXB2 in mice.
    Formula:C32H47N3O9S
    Color and Shape:Solid
    Molecular weight:649.8

    Ref: TM-T37300

    10µg
    500.00€
    25µg
    1,153.00€
    50µg
    2,223.00€
    100µg
    3,898.00€
  • 6-N-Hydroxylaminopurine

    CAS:
    6-N-Hydroxylaminopurine is a base analog with mutagenic activity.
    Formula:C5H5N5O
    Molecular weight:151.13

    Ref: TM-T210412

    10mg
    To inquire
    50mg
    To inquire
  • Antifungal agent 25


    Antifungal agent 25: broad-spectrum, stable in vivo, effective against Candida albicans, including fluconazole-resistant strains.
    Color and Shape:Solid

    Ref: TM-T64235

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • MMV03

    CAS:
    MMV03 is an antimalarial compound effective against Plasmodium falciparum, with an EC50 of 0.6 μM.
    Formula:C19H14N4OS
    Color and Shape:Solid
    Molecular weight:346.406

    Ref: TM-T204698

    10mg
    To inquire
    50mg
    To inquire
  • RNase L ligand 3

    CAS:
    RNase L ligand 3 is an RNase L ligand employed in the synthesis of F3-PEG8-RiboTAC.
    Formula:C27H27N3OS
    Color and Shape:Solid
    Molecular weight:441.59

    Ref: TM-T210787

    10mg
    To inquire
    50mg
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  • Pyrromycin

    CAS:
    Pyrromycin is a monosaccharide anthracycline which can be used to inhibit cellular RNA synthesis.
    Formula:C30H35NO11
    Color and Shape:Solid
    Molecular weight:585.60

    Ref: TM-T68903

    25mg
    5,149.00€
    50mg
    6,823.00€
    100mg
    9,810.00€
  • RECTAS-2.0

    CAS:

    RECTAS-2.0 is a small molecule designed to correct RNA mis-splicing caused by the GLA c.639+919G>A mutation, intended for research in Fabry disease.

    Formula:C18H17ClN4O4
    Color and Shape:Solid
    Molecular weight:388.805

    Ref: TM-T206725

    10mg
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    50mg
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  • Clavicoronic acid

    CAS:
    Clavicoronic acid, a β-lactamase inhibitor, boosts penicillin antibiotics against resistant bacteria.
    Formula:C15H18O4
    Color and Shape:Solid
    Molecular weight:262.3

    Ref: TM-T70774

    25mg
    2,583.00€
    50mg
    3,402.00€
    100mg
    4,680.00€
  • (±)-Tuaimenal A

    CAS:
    (±)-Tuaimenal A ((+)-1) is a secondary metabolite and a derivative of Sesamol. It exhibits potent inhibitory activity against SARS-CoV-2 3CLpro, with an IC50 of 33.3 μM. (±)-Tuaimenal A is applicable in research related to SARS-CoV-2 infection.
    Formula:C23H30O4
    Color and Shape:Solid
    Molecular weight:370.48

    Ref: TM-T211190

    10mg
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    50mg
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  • D-CS319

    CAS:
    D-CS319 is a potent inhibitor of metal-𝛽-lactamases (MBLs), exhibiting IC50 values of 2.0 μM for IMP-1 and 3.0 μM for IMP-78. RPX 7546 possesses antibacterial activity.
    Formula:C7H11NO2S3
    Color and Shape:Solid
    Molecular weight:237.36

    Ref: TM-T212067

    10mg
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    50mg
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  • MtDTBS-IN-1


    MtDTBS-IN-1 is a notably potent binder (K_D = 57 nM) and inhibitor (K_i = 5 μM) of MtDTBS.
    Formula:C16H16N4O5
    Color and Shape:Solid
    Molecular weight:344.32

    Ref: TM-T61119

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • β-Glucuronidase-IN-3

    CAS:
    β-Glucuronidase-IN-3 (Compound 49) is a covalent allosteric inhibitor targeting β-glucuronidase. It exhibits potent inhibitory activity against Escherichia coli β-glucuronidase (EcGUS) with an IC50 of 12.9 nM. The compound exerts its inhibitory effect through reversible covalent modification of cysteine residues (Cys28, Cys443, and Cys197) on EcGUS. It is applicable in research on gut microbiota-related diseases, particularly in reducing the toxic side effects of Irinotecan and non-steroidal anti-inflammatory drugs (NSAIDs).
    Formula:C10H7N3OSe
    Color and Shape:Solid
    Molecular weight:264.14

    Ref: TM-T206953

    10mg
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    50mg
    To inquire
  • Antimalarial agent 9


    Antimalarial 9, a quinoline-imidazole derivative, effectively targets CQ-susceptible (IC50-0.14 μM) and MDR strains (IC50-0.41 μM) with low toxicity.
    Formula:C28H32BrN3O2
    Color and Shape:Solid
    Molecular weight:522.48

    Ref: TM-T63655

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • SARS-CoV-2-IN-23


    SARS-CoV-2-IN-23 (compound GRL-0617) is an inhibitor of SARS-COV-2 papain-like protease (PLpro) (IC 50 = 2.3 μM) [1].
    Formula:C21H22N2O
    Color and Shape:Solid
    Molecular weight:318.41

    Ref: TM-T60841

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • Antimalarial agent 48

    CAS:
    Antimalarial agent 48 (Compound 15a) is a triazine compound with antimalarial activity, showing effectiveness against Plasmodium falciparum K1 and Plasmodium falciparum FCR3 with IC50 values of 280 and 290 nM, respectively. It holds promise for research in the field of anti-infective treatments.
    Formula:C19H14F3N11
    Color and Shape:Solid
    Molecular weight:453.383

    Ref: TM-T205719

    10mg
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    50mg
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  • 3′-Amino-2′,3′-dideoxy-CTP

    CAS:
    3′-Amino-2′,3′-dideoxy-CTP is an analog of nucleoside triphosphates. It selectively inhibits DNA polymerase β.
    Formula:C9H17N4O12P3
    Color and Shape:Solid
    Molecular weight:466.17

    Ref: TM-TSW-01126

    10mg
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    50mg
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  • Mer-NF5003F

    CAS:
    Mer-NF5003F (Stachybotrydial; F 1839M) is a sesquiterpene isolated from Stachybotrys, effective in inhibiting avian myeloblastosis virus (AMV) protease with an IC50 of 7.8 μM. It also inhibits sialyltransferases ST6N, ST3O, and ST3N with IC50 values of 0.61, 6.7, and 10 μg/mL, respectively, and fucosyltransferase with an IC50 of 11.3 μg/mL. Additionally, Mer-NF5003F exhibits in vitro activity against herpes simplex virus HSV-1 (IC50=4.32 μg/mL) and multi-drug-resistant Plasmodium falciparum K1 strain (IC50=0.85 μg/mL).
    Formula:C23H30O5
    Molecular weight:386.48

    Ref: TM-T208688

    10mg
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    50mg
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  • (S)-ZG197


    (S)-ZG197 is a compound that acts as a highly selective activator of the Staphylococcus aureus Caseinolytic Protease P (Sa ClpP), demonstrating efficacy at a
    Formula:C28H35F3N4O3
    Color and Shape:Solid
    Molecular weight:532.6

    Ref: TM-T73315

    25mg
    2,313.00€
    50mg
    3,042.00€
    100mg
    4,140.00€
  • N6-Benzoyl-2'-deoxyadenosine monohydrate

    CAS:
    N6-Benzoyl-2'-deoxyadenosine monohydrate is a nucleoside analogue that helps diagnose bacterial infections by binding to double-stranded DNA and altering its structure, which can subsequently be detected using electrophoresis.
    Formula:C17H19N5O5
    Color and Shape:Solid
    Molecular weight:373.363

    Ref: TM-T206583

    10mg
    To inquire
    50mg
    To inquire
  • Antibacterial agent 76


    Antibacterial agent 76 (compound 9) is a potent antibacterial agent.
    Formula:C23H27N3O2S
    Color and Shape:Solid
    Molecular weight:409.54

    Ref: TM-T62063

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • Amicoumacin A

    CAS:
    Amicoumacin A has antibacterial activity. It also strongly suppresses inflammatory and ulcer activity.
    Formula:C20H29N3O7
    Purity:98%
    Color and Shape:Solid
    Molecular weight:423.46

    Ref: TM-T23725

    25mg
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    50mg
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    100mg
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  • Antibacterial agent 81

    CAS:
    Antibacterial agent 81 blocks DNA transcription, targets S. aureus (MIC 12.5μM) & M. smegmatis (MIC 7.8μM). Used in infection research.
    Formula:C33H28N2O8
    Color and Shape:Solid
    Molecular weight:580.58

    Ref: TM-T64100

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • FtsZ-IN-4


    FtsZ-IN-4 is an oral FtsZ inhibitor with strong antibacterial effects and good drug traits, low toxicity (CC50 >20μg/mL).
    Formula:C21H16ClF2NO2
    Color and Shape:Solid
    Molecular weight:387.81

    Ref: TM-T61737

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • Antimalarial agent 3


    Antimalarial agent 3 has a potent IC50 of 0.035 μM against Plasmodium and high selectivity for mammalian cells.
    Formula:C15H16BrN3O2
    Color and Shape:Solid
    Molecular weight:350.21

    Ref: TM-T61200

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • ZHSI-1

    CAS:
    ZHSI-1 is an EV71 (Enterovirus 71) inhibitor that blocks EV71/CVA16 replication and virus-induced pyroptosis linked to viral pathogenesis. It effectively prevents EV71 infection in neonatal and young mice in animal models and can be used to study viral infections such as hand, foot, and mouth disease (HFMD) [1].
    Formula:C17H19N5
    Color and Shape:Solid
    Molecular weight:293.37

    Ref: TM-T87665

    10mg
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    50mg
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  • MsbA-IN-4


    MsbA-IN-4 (Compound 32) is a highly selective and potent inhibitor of MsbA (IC50: 3 nM).MsbA-IN-4 inhibits Escherichia coli (MIC: 12 μM).
    Formula:C23H18Cl2FN5O
    Color and Shape:Solid
    Molecular weight:470.33

    Ref: TM-T63033

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • BMIM-TFSI

    CAS:
    BMIM-TFSI (compound8) is an HIV-1 integrase inhibitor that effectively suppresses both the 3'-processing (3'-P) and strand transfer (ST) steps of the integration process. It is applicable in HIV-1 research.
    Formula:C10H15F6N3O4S2
    Color and Shape:Solid
    Molecular weight:419.364

    Ref: TM-T204101

    10mg
    To inquire
    50mg
    To inquire
  • GT-055


    GT-055 (LCB18-055) is a novel inhibitor of broad-spectrum β-lactamase.
    Formula:C13H20F3N5O8S
    Color and Shape:Solid
    Molecular weight:463.39

    Ref: TM-T62930

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • SARS-CoV-2 Mpro-IN-28

    CAS:
    SARS-CoV-2 Mpro-IN-28 (Compound 1K) is an inhibitor of SARS-CoV-2 Mpro, exhibiting an EC50 of 24 μM.
    Formula:C14H17NO3Se
    Color and Shape:Solid
    Molecular weight:326.25

    Ref: TM-T201252

    25mg
    To inquire
    50mg
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    100mg
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  • Insecticidal agent 16

    CAS:
    Insecticidal agent 16 (compound A21) exhibits insecticidal activity against Plutella xylostella, with LC50 values of 1.2 and 13.2 µg/mL respectively.
    Formula:C21H13Cl2F6N5O2S
    Color and Shape:Solid
    Molecular weight:584.32

    Ref: TM-T201261

    25mg
    1,458.00€
    50mg
    1,839.00€
    100mg
    2,322.00€
  • SARS-CoV-2 Mpro-IN-32

    CAS:
    SARS-CoV-2 Mpro-IN-32 (Compound 1) is a selective inhibitor of SARS-CoV-2 MPro with an IC50 value of 230 nM. In vitro, it also inhibits the replication of various SARS-CoV-2 variants.
    Formula:C34H32Cl2N4O9
    Color and Shape:Solid
    Molecular weight:711.54

    Ref: TM-T201191

    25mg
    To inquire
    50mg
    To inquire
    100mg
    To inquire
  • GC-78-HCl

    CAS:
    GC-78-HCl is an orally active, non-peptidic SARS-CoV-2 Mpro inhibitor with an enzyme IC50 of 0.19 μM. It exhibits strong anti-coronavirus activity and favorable pharmacokinetic properties.
    Formula:C25H25Cl3N4O4
    Molecular weight:551.85

    Ref: TM-T208240

    10mg
    To inquire
    50mg
    To inquire
  • NS2B/NS3-IN-2


    Potent dengue inhibitor NS2B/NS3-IN-2 (IC50: 6 nM, Ki: 0.66 μM) boosts cell viability, non-toxic.
    Formula:C24H21N3O5S
    Color and Shape:Solid
    Molecular weight:463.51

    Ref: TM-T62932

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • Menoctone

    CAS:
    Menoctone is an orally effective antimalarial agent that inhibits blood-induced rodent malaria. It enhances the antimalarial effects of chloroquine or quinine, making it useful for malaria research.
    Formula:C24H32O3
    Color and Shape:Solid
    Molecular weight:368.51

    Ref: TM-T201004

    25mg
    To inquire
    50mg
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    100mg
    To inquire
  • Cefclidin

    CAS:
    Cefclidin (Cefclidine) is a cephalosporin compound.
    Formula:C21H26N8O6S2
    Color and Shape:Solid
    Molecular weight:550.611

    Ref: TM-T206507

    10mg
    To inquire
    50mg
    To inquire
  • CYP51-IN-14

    CAS:
    CYP51-IN-14 (compound 1n), a derivative of Fluconazole, functions as an effective antifungal agent. This compound inhibits Microsporum gypseum and Candida albicans with a minimum inhibitory concentration (MIC80) of 1 μg/mL.
    Formula:C21H20Cl2F2N4O
    Molecular weight:453.31

    Ref: TM-T201651

    10mg
    To inquire
    50mg
    To inquire
  • CYP2C19-IN-1


    CYP2C19-IN-1: potent CYP2C19 inhibitor, non-genotoxic, non-hepatotoxic, blocks RdRP (Ki: 6.16 μM), useful for ZIKV research.
    Formula:C26H26N2O6S
    Color and Shape:Solid
    Molecular weight:494.56

    Ref: TM-T63337

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • PRRSV-IN-1

    CAS:
    PRRSV-IN-1 (Compound 4s) acts as an inhibitor of the nsp4 protease of PRRSV. It has an EC50 value of 0.45 μM against PRRSV, binds to the nsp4 protease with a Kd of 29.24 pM, and exhibits an IC50 value of 80.36 pM for nsp4 protease inhibition. PRRSV-IN-1 is applicable in antiviral infection research.
    Formula:C19H18BrNO3
    Color and Shape:Solid
    Molecular weight:388.255

    Ref: TM-T206242

    10mg
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  • Lapyrium chloride

    CAS:
    Lapyrium chloride (Emcol E 607) is a broad-spectrum antibacterial agent that serves as a preservative and disinfectant.
    Formula:C21H35ClN2O3
    Molecular weight:398.97

    Ref: TM-T208654

    10mg
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  • Cap-dependent endonuclease-IN-2


    Cap-dependent endonuclease-IN-2 strongly blocks influenza A virus RNA polymerase; it's a CEN inhibitor.
    Formula:C30H24FN3O7S
    Color and Shape:Solid
    Molecular weight:589.59

    Ref: TM-T64177

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • Methyl 3-oxodecanoate

    CAS:
    Methyl 3-oxodecanoate exhibits virulence factor activity against human pathogens and shows effects on Synechococcus elongatus (a species of fluorescent algae) as well as on culture supernatant. Additionally, Methyl 3-oxodecanoate inhibits DNA synthesis by suppressing protein synthesis at the translation initiation level.
    Formula:C11H20O3
    Color and Shape:Solid
    Molecular weight:200.275

    Ref: TM-T206384

    10mg
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  • BAR-072

    CAS:
    BAR-072 is a small molecule inhibitor targeting TraE with a KD value of 2.7 µM. It significantly suppresses the transfer of the antibiotic resistance-associated plasmid pKM101. BAR-072 holds promise as a candidate molecule for research in disease areas related to infection and resistance control, by inhibiting the spread of bacterial resistance genes.
    Formula:C18H13N3O6
    Color and Shape:Solid
    Molecular weight:367.312

    Ref: TM-T206165

    10mg
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    50mg
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  • ZIKV-IN-5


    ZIKV-IN-5 is an acid-stable, low cytotoxic anti-ZIKV agent with an EC50 value of 0.71 μM. ZIKV-IN-5 showed effective inhibition of ZIKV NS5 MTase activity.
    Formula:C36H45NO4Si
    Color and Shape:Solid
    Molecular weight:583.83

    Ref: TM-T64123

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • C-467929

    CAS:
    C-467929 is an inhibitor of the Nsp15 endoribonuclease, exhibiting an IC50 value of 8 μM. This compound binds to the SARS-CoVNsp15 protein and is applicable for infection research.
    Formula:C29H20N4O10
    Color and Shape:Solid
    Molecular weight:584.49

    Ref: TM-T204797

    10mg
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  • GSK-2878175

    CAS:
    GSK-2878175, a NS5B inhibitor, is used potentially for the treatment of HCV infection.
    Formula:C27H23BClFN2O6S
    Purity:98%
    Color and Shape:Solid
    Molecular weight:568.81

    Ref: TM-T27470

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • Hyalodendrin

    CAS:
    Hyalodendrin ((+)-Hyalodendrin) acts as a fungal growth inhibitor, specifically targeting wood decay fungi. It exhibits low phytotoxicity and possesses an acute toxicity (LD50) level of 75 mg/kg in mice.
    Formula:C14H16N2O3S2
    Color and Shape:Solid
    Molecular weight:324.42

    Ref: TM-T88147

    10mg
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    50mg
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  • VV261

    CAS:
    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.
    Formula:C28H34FN3O11
    Color and Shape:Solid
    Molecular weight:607.58

    Ref: TM-T207125

    10mg
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  • Ep vinyl quinidine

    CAS:
    3-Epiquinine is a Quinidine stereoisomer, used in malaria, antiarrhythmic, inhibits P450db, and blocks K+ channels, IC50: 19.9 μM.
    Formula:C20H24N2O2
    Color and Shape:Solid
    Molecular weight:324.42

    Ref: TM-T60893

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • Isopyrazam

    CAS:
    Isopyrazam, a plant protection product, exhibits potent antifungal activity. When applied to crops, it effectively inhibits the growth of various plant pathogenic fungi, significantly enhancing both the yield and quality of the crops. This compound demonstrates exceptional disease resistance capabilities in agricultural applications.
    Formula:C20H23F2N3O
    Color and Shape:Solid
    Molecular weight:359.41

    Ref: TM-T201235

    25mg
    1,564.00€
    50mg
    2,053.00€
    100mg
    2,535.00€
  • MK-8876

    CAS:
    MK-8876 is an Inhibitor of HCV NS5B Site D.
    Formula:C32H24F2N4O5S
    Purity:98%
    Color and Shape:Solid
    Molecular weight:614.62

    Ref: TM-T28061

    25mg
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    100mg
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  • Antibacterial agent 261

    CAS:
    Antibacterialagent 261 (compound 43) is a potent inhibitor of the peptide deformylase (PDF) enzyme, demonstrating IC50 values of 2.5 nM against Staphylococcus aureus (S. aureus) and 10.6 nM against Escherichia coli (E. coli).
    Formula:C18H24N4O3S2
    Color and Shape:Solid
    Molecular weight:408.538

    Ref: TM-T204731

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  • HT1171

    CAS:
    HT1171 is a potent and selective inhibitor of the Mycobacterium tuberculosis proteasome. It exhibits strong antitubercular activity against Mycobacterium tuberculosis H37Rv, with a MIC90 of 2 μg/mL and MIC of 4 μg/mL. At a concentration of 100 μM, HT1171 shows an inhibition rate of 53.8% against normal human liver cells (L02). HT1171 is applicable in antituberculosis drug research.
    Formula:C7H4N2O4S2
    Color and Shape:Solid
    Molecular weight:244.248

    Ref: TM-T204697

    10mg
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    50mg
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  • PROTAC eDHFR Degrader-2

    CAS:
    PROTACeDHFR Degrader-2 (compound 7b) is an effective degrader targeting Escherichia coli dihydrofolate reductase (eDHFR), capable of reliably degrading eDHFR-tagged proteins.
    Formula:C34H40N8O9
    Molecular weight:704.73

    Ref: TM-T208225

    10mg
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    50mg
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  • Noracronycine

    CAS:
    Noracronycine is an alkaloid originally isolated from G. pentaphylla, known for its antimalarial activity. It is effective against P. yoelii at a concentration of 10 μg/mL.
    Formula:C19H17NO3
    Molecular weight:307.34

    Ref: TM-TN11123

    10mg
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    50mg
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  • Antifungal agent 125

    CAS:
    Antifungalagent 125 (compound 4H) is a potent succinate dehydrogenase (SDH) inhibitor with an IC50 of 3.59 μg/mL and exhibits fungicidal activity against Alternaria alternata.
    Formula:C13H10BrNO4S
    Color and Shape:Solid
    Molecular weight:356.192

    Ref: TM-T204529

    10mg
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    50mg
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  • Antibacterial agent 68


    Antibacterial agent 68 targets drug-resistant E. coli at 0.007 mM with low cytotoxicity.
    Formula:C26H25BrN4O7
    Color and Shape:Solid
    Molecular weight:585.4

    Ref: TM-T64135

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • RAD51-IN-6

    CAS:
    RAD51-IN-6, a potent RAD51 gene inhibitor, may help research mitochondrial disorders. (WO2021164746A1, cmpd 23)
    Formula:C27H40N3O5PS
    Color and Shape:Solid
    Molecular weight:549.66

    Ref: TM-T63883

    25mg
    1,927.00€
    50mg
    2,507.00€
    100mg
    3,168.00€
  • MT0703

    CAS:
    MT0703 is a cephalosporin antibiotic featuring an aminothiazolylglycyl moiety with a 1,5-dihydroxy-4-pyridinone-2-carbonyl group, displaying potent activity against Pseudomonas species.
    Formula:C26H25N7O9S3
    Color and Shape:Solid
    Molecular weight:675.71

    Ref: TM-T200616

    25mg
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    50mg
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    100mg
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  • Antifungal agent 42


    Antifungal 42 blocks biofilm formation and inhibits C.albicans' CYP51.
    Formula:C22H20Cl2N4Se2
    Color and Shape:Solid
    Molecular weight:569.25

    Ref: TM-T64029

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • MDL-860

    CAS:

    MDL-860 is a broad-spectrum antiviral compound targeting small RNA viruses and exhibits low cytotoxicity to human cells. MDL-860 is useful for research into viral infections.

    Formula:C13H6Cl2N2O3
    Color and Shape:Solid
    Molecular weight:309.104

    Ref: TM-T204603

    10mg
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  • Piperacillin hydrate

    CAS:
    Piperacillin hydrate is a semisynthetic broad-spectrum β-lactam antibiotic. It exhibits potent bactericidal activity against Gram-negative bacteria and some Gram-positive bacteria by targeting penicillin-binding proteins. Piperacillin hydrate is frequently combined with the β-lactamase inhibitor Tazobactam for enhanced efficacy.
    Formula:C23H29N5O8S
    Color and Shape:Solid
    Molecular weight:535.57

    Ref: TM-T204418

    10mg
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    50mg
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  • (R)-CSN5i-3

    CAS:
    (R)-CSN5i-3 is CSN5i-3 of the R configuration.
    Formula:C28H29F2N5O2
    Purity:99.76% - 99.97%
    Color and Shape:Solid
    Molecular weight:505.56

    Ref: TM-T12620

    1mg
    148.00€
    5mg
    334.00€
    10mg
    465.00€
    25mg
    800.00€
  • CDA-IN-2

    CAS:
    CDA-IN-2 (Compound VS#2-3) is an inhibitor of chitin deacetylase (CDA) that exhibits antifungal properties. At a concentration of 100 μM, it inhibits P. xanthii's CDAPxCDA1 by 83.7% and PxCDA2 by 74.5%. CDA-IN-2 is applicable in research on agricultural fungal diseases, including resistance to powdery mildew and gray mold.
    Formula:C17H16N2O7
    Color and Shape:Solid
    Molecular weight:360.318

    Ref: TM-T206594

    10mg
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    50mg
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  • Antitubercular agent-16


    Compound 5q is a potent antitubercular with low MIC90 values (0.40-23.51 μg/mL) against M. tuberculosis strains, showing minimal cytotoxicity.
    Formula:C21H27N3S
    Color and Shape:Solid
    Molecular weight:353.52

    Ref: TM-T61252

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • LpxC-IN-10

    CAS:
    LpxC-IN-10 is a selective LpxC inhibitor with an MIC of 0.5 μg/mL against E. coli and K. pneumoniae and is capable of being used to study bacterial infections.
    Formula:C30H31N5O3
    Color and Shape:Solid
    Molecular weight:509.6

    Ref: TM-T63512

    25mg
    2,043.00€
    50mg
    2,682.00€
  • Cetefloxacin

    CAS:
    Cetefloxacin (E 4868) is a broad-spectrum antibacterial antibiotic with a minimum inhibitory concentration (MIC) ranging from 0.007 to 8 µg/ml. In mice, cetefloxacin demonstrates favorable pharmacokinetic properties and provides protection against Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Streptococcus pneumoniae.
    Formula:C20H16F3N3O3
    Molecular weight:403.35

    Ref: TM-T208886

    10mg
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  • 3'-NH-Tr-2',3'-DMF-ddA-5'-CE-Phosphoramidite

    CAS:
    3'-NH-Tr-2',3'-DMF-ddA-5'-CE-Phosphoramidite serves as a precursor of adenosine nucleotide monomers used in the solid-phase synthesis of oligonucleotides, particularly for modifying oligonucleotides such as terminally modified DNA strands. It features Trityl (Tr), Cyanoethyl (CE), and Dimethylformamidine (DMF) protective groups, classifying it as a ddNTP adenosine nucleoside suitable for applications like oligonucleotide solid-phase synthesis, probe design, and chain termination sequencing.
    Formula:C41H50N9O3P
    Color and Shape:Solid
    Molecular weight:747.87

    Ref: TM-TSW-01106

    10mg
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    50mg
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  • Antibacterial agent 118


    Antibacterial agent 118, potent against various mycobacteria, has MIC values ranging from 10.2 to 163.0 μM. Useful in TB research.
    Formula:C19H21N5O2S
    Color and Shape:Solid
    Molecular weight:383.47

    Ref: TM-T61665

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • Faldaprevir sodium

    CAS:
    Faldaprevir sodium: HCV treatment, inhibits NS3/NS4A protease, P-glycoprotein, CYP3A4, UGT1A1.
    Formula:C40H48BrN6NaO9S
    Color and Shape:Solid
    Molecular weight:891.81

    Ref: TM-T71215

    25mg
    2,718.00€
    50mg
    3,582.00€
    100mg
    4,950.00€
  • Antifungal agent 27


    Antifungal agent 27 shows moderate action against MRSA, weak against C. albicans, with MICs of 8 μg/mL and 32 μg/mL, respectively.
    Formula:C18H23N5OS
    Color and Shape:Solid
    Molecular weight:357.47

    Ref: TM-T61308

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • OPC-167832

    CAS:
    OPC-167832: oral dprE1 inhibitor, IC50 0.258 μM, anti-tuberculosis, for Mycobacterium tuberculosis research.
    Formula:C21H20ClF3N2O4
    Color and Shape:Solid
    Molecular weight:456.84

    Ref: TM-T37880

    25mg
    1,054.00€
    50mg
    1,378.00€
    100mg
    2,197.00€
  • HBV-IN-18


    HBV-IN-18 (Compound 3) is an HBV capsid assembly modulator (CpAM) (EC50: 2790 nM).
    Formula:C17H15F6N5O2
    Color and Shape:Solid
    Molecular weight:435.32

    Ref: TM-T62467

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • HIV-1 inhibitor-14


    HIV-1 inhibitor-14: potent, broad HIV-1 RT inhibitor. IC50=0.14μM. Effective against wild-type and resistant strains, EC50=5.79-28.3nM.
    Formula:C29H32N6O4S
    Color and Shape:Solid
    Molecular weight:560.67

    Ref: TM-T63963

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • NIP-22c

    CAS:
    NIP-22c, a novel inhibitor of coronavirus 3CL pro, exhibits antiviral activity [1]. The compound's EC50 values are 4.6 μM for Verona, 1.1 μM for Calu3, 0.1 μM for Caco2, and 0.6 μM for HBTEC-ALI.
    Formula:C32H39N5O6
    Color and Shape:Solid
    Molecular weight:589.68

    Ref: TM-T87007

    25mg
    2,088.00€
    50mg
    3,042.00€
    100mg
    3,690.00€
  • RMG8-8


    RMG8-8 shows the excellent efficacy against C. neoformans (1.56 μg/mL).
    Formula:C41H78N8O5
    Color and Shape:Solid
    Molecular weight:763.11

    Ref: TM-T73480

    25mg
    2,178.00€
    50mg
    2,862.00€
    100mg
    3,870.00€
  • GSK 932121

    CAS:
    GSK 932121: potent antimalarial, targets P. falciparum by inhibiting cytochrome bc1 in the electron transport chain.
    Formula:C20H15ClF3NO4
    Purity:98%
    Color and Shape:Solid
    Molecular weight:425.79

    Ref: TM-T27444

    25mg
    1,908.00€
    50mg
    2,502.00€
    100mg
    3,330.00€
  • Cap-dependent endonuclease-IN-6

    CAS:
    Cap-dependent endonuclease-IN-6 (compound 13) is a Cap-dependent endonuclease (CEN) inhibitor that inhibits influenza virus.
    Formula:C23H21N3O3S
    Color and Shape:Solid
    Molecular weight:419.5

    Ref: TM-T62208

    25mg
    1,927.00€
    50mg
    2,507.00€
    100mg
    3,168.00€
  • AK-968-11563024

    CAS:
    AK-968-11563024 is an inhibitor targeting marine V. vulnificus NAT [(VIBVN)NAT] with an IC50 value of 18.86 µM. In V. vulnificus, NAT (aromatic amine N-acetyltransferase) plays a role in drug metabolism, contributing to drug resistance. Thus, AK-968-11563024 can be used for research related to drug tolerance.
    Formula:C18H13I2N9O5
    Color and Shape:Solid
    Molecular weight:689.162

    Ref: TM-T204280

    10mg
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    50mg
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