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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.

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Found 6402 products of "Microbiology/Virology"

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  • Antifungal agent 11


    Antifungal agent 11 has a good antifungal effect.
    Formula:C21H19F2N7O3S2
    Color and Shape:Solid
    Molecular weight:519.55

    Ref: TM-T63627

    25mg
    1,444.00€
    50mg
    1,882.00€
    100mg
    2,375.00€
  • MTH1 activator-1

    CAS:
    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.
    Formula:C29H23F3N4O2
    Color and Shape:Solid
    Molecular weight:516.514

    Ref: TM-T204503

    10mg
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  • MI-1851

    CAS:
    MI-1851 is a potent peptidomimetic inhibitor. MI-1851could prevent proteolytic processing of the S protein from SARSCoV-2 by endogenous furin in HEK293 cells.
    Formula:C34H53N15O6
    Color and Shape:Solid
    Molecular weight:767.88

    Ref: TM-T69640

    25mg
    2,718.00€
    50mg
    3,582.00€
    100mg
    4,950.00€
  • KPC-2-IN-2


    KPC-2-IN-2 (6c) inhibits KPC-2 enzyme in Klebsiella pneumoniae (Ki 0.038 μM) and boosts cefotaxime in E. coli KPC-2.
    Formula:C12H10BN3O2S
    Color and Shape:Solid
    Molecular weight:271.1

    Ref: TM-T60470

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • PKZ18

    CAS:
    PKZ18 is an antibiotic that inhibits bacterial growth with a MIC value of 32-64 μg/mL against most Gram-positive bacteria. It suppresses the in vivo transcription and translation of glycyl-tRNA synthetase mRNA. PKZ18 selectively targets stem I specifier loops in Gram-positive bacteria, directly reducing T-box transcription readthrough of associated genes. It prevents codon-anticodon pairing necessary for tRNA binding and is less likely to induce resistance.
    Formula:C22H26N2O3S
    Purity:98.08%
    Color and Shape:Solid
    Molecular weight:398.518

    Ref: TM-T204863

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    5mg
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    10mg
    662.00€
    50mg
    1,429.00€
  • 3HKT-IN-1

    CAS:
    3HKT-IN-1 (Compound 17122279) is an inhibitor of Anopheles gambiae 3-hydroxykynurenine transaminase (3HKT) and is utilized in malaria research.
    Formula:C12H11BrN2O3
    Color and Shape:Solid
    Molecular weight:311.131

    Ref: TM-T204776

    10mg
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  • MsbA-IN-3


    MsbA-IN-3 is a potent and highly selective MsbA inhibitor (IC50: 2 nM). MsbA-IN-3 inhibits Escherichia coli activity (MIC: 35 μM).
    Formula:C24H22Cl2N2O4S
    Color and Shape:Solid
    Molecular weight:505.41

    Ref: TM-T63449

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • Tuberculosis inhibitor 4


    TB inhibitor 4, a spirothiazolidinone from mandelic acid, blocks 98% of M. tuberculosis H37Rv under 6 μg/mL.
    Formula:C23H26N2O3S
    Color and Shape:Solid
    Molecular weight:410.53

    Ref: TM-T62087

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

    CAS:
    3-Deazaguanosine (C3Guo) exhibits potent antiviral activity against SARS-CoV-2 with an EC50 of 1.14 μM and a CC50 greater than 200 μM in Vero E6 cells. It has the potential to prevent COVID-19.
    Formula:C11H14N4O5
    Color and Shape:Solid
    Molecular weight:282.25

    Ref: TM-T207642

    10mg
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  • ZK-806450

    CAS:
    ZK-806450 is a compound with antiviral properties. It exhibits high binding potential to the allosteric site of the SARS-CoV-2 3CL protease and is capable of specific and stable interaction with the GAG site of the dengue virus envelope protein.
    Formula:C31H31N5O
    Color and Shape:Solid
    Molecular weight:489.611

    Ref: TM-T206370

    10mg
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    50mg
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  • Cyclophilin inhibitor 1

    CAS:
    Cyclophilin inhibitor 1: orally available, Kd 5 nM, potent against HCV, EC50 for HCV 2a is 98 nM.
    Formula:C31H39N5O7
    Purity:98%
    Color and Shape:Solid
    Molecular weight:593.67

    Ref: TM-T10919

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  • PLP_Snyder530


    PLP_Snyder530, a potent PL pro inhibitor, halts SARS-CoV-2 by triggering protease conformation changes.
    Formula:C24H24N2O2
    Color and Shape:Solid
    Molecular weight:372.46

    Ref: TM-T61500

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • Anti-MRSA agent 6


    Anti-MRSA agent 6 (compound 3q6) is a potent anti-methicillin-resistant Staphylococcus aureus (anti-MRSA) agent with low cytoxicity for MCF-7, A549 cells [1].
    Formula:C16H11F2N3
    Color and Shape:Solid
    Molecular weight:283.28

    Ref: TM-T60546

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

    CAS:
    Trans-Clopenthixol ((E)-Clopenthixol) is an antibiotic without any sedative properties. It can be used in vitro to inhibit Pseudomonas aeruginosa and Plasmodium falciparum.
    Formula:C22H25ClN2OS
    Color and Shape:Solid
    Molecular weight:400.965

    Ref: TM-T206127

    10mg
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  • LolCDE-IN-2

    CAS:
    LolCDE-IN-2 is a potent Lol protein (LolCDE) inhibitor. LolCDE-IN-2 shows antibacterial activity with a MIC of 2 μg/ml against E. coli MG1655 [1].
    Formula:C22H17N5O
    Purity:98%
    Color and Shape:Solid
    Molecular weight:367.40

    Ref: TM-T11866

    25mg
    2,178.00€
    50mg
    2,862.00€
    100mg
    3,870.00€
  • Anti-MRSA agent 27

    CAS:
    Anti-MRSA agent 27 (compound 4a) is a potent antimicrobial agent against methicillin-resistant Staphylococcus aureus (MRSA) with a minimum inhibitory concentration (MIC) of 0.0975 μmol/L. It effectively disrupts MRSA biofilms and inhibits the production of hemolysins.
    Formula:C15H10F3N3OS
    Color and Shape:Solid
    Molecular weight:337.32

    Ref: TM-T207164

    10mg
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  • DRF-8417

    CAS:
    DRF-8417 is an oxazolidinone antibiotic, active against both Gram-positive bacteria and fastidious Gram-negative bacteria. The MIC50 and MIC90 values of DRF-8417 for Gram-positive pathogens range between 0.06-1 mg/L.
    Formula:C15H17N3O5S
    Color and Shape:Solid
    Molecular weight:351.38

    Ref: TM-T201523

    10mg
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  • A25822B

    CAS:
    A25822B is an antifungal agent.
    Formula:C28H45NO
    Purity:98%
    Color and Shape:Solid
    Molecular weight:411.66

    Ref: TM-T26473

    25mg
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  • VNI

    CAS:
    VNI is an effective inhibitor of CYP51. It suppresses sterol synthesis in Trypanosoma cruzi, exhibiting anti-Trypanosoma cruzi activity.
    Formula:C26H19Cl2N5O2
    Color and Shape:Solid
    Molecular weight:504.37

    Ref: TM-T201793

    10mg
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  • β-Glucuronidase-IN-2


    β-Glucuronidase-IN-2 is a potent inhibitor of E.
    Formula:C21H17Cl3O7
    Color and Shape:Solid
    Molecular weight:487.71

    Ref: TM-T63250

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


    PptT-IN-2 inhibits PptT enzyme crucial in tuberculosis, with 2.5 μM IC50, showing potential in TB research.
    Formula:C22H29N5O2
    Color and Shape:Solid
    Molecular weight:395.5

    Ref: TM-T61847

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

    CAS:
    KL-50, a selective toxin, effectively targets tumors deficient in the DNA repair protein O6-methylguanine-DNA-methyltransferase (MGMT), which corrects O6-alkylguanine lesions. This compound induces both DNA damage response pathways and cell cycle arrest in MGMT-deficient cells, regardless of mismatch repair (MMR) status. KL-50 shows promise in the study of brain tumors lacking MGMT.
    Formula:C7H7FN6O2
    Color and Shape:Solid
    Molecular weight:226.17

    Ref: TM-T200136

    25mg
    1,690.00€
    50mg
    2,210.00€
    100mg
    2,879.00€
  • HldA/E-IN-1

    CAS:
    HldA/E-IN-1 (compound 8) is a dual inhibitor of HldA/E, exhibiting IC50 values of 17.2 μM and 67.8 μM, respectively. This compound is utilized in research on antibacterial infections.
    Formula:C8H17FO13P2
    Color and Shape:Solid
    Molecular weight:402.16

    Ref: TM-T200513

    25mg
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  • Laninamivir trifluoroacetate

    CAS:
    Laninamivir trifluoroacetate, a long-acting antiviral, treats and prevents Influenza A and B via nasal spray.
    Formula:C15H23F3N4O9
    Purity:98%
    Color and Shape:Solid
    Molecular weight:460.363

    Ref: TM-T25618

    25mg
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  • SARS-CoV-2-IN-99

    CAS:
    SARS-CoV-2-IN-99 (compound 58) is an inhibitor of the main protease of SARS-CoV-2.
    Formula:C20H16Br2NO4P
    Color and Shape:Solid
    Molecular weight:525.13

    Ref: TM-T200438

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

    CAS:
    Epiderstatin is isolated from Streptomyces pulveraceus subsp. epiderstagenes; inhibits mitogenic activity of epidermal growth factor.
    Formula:C15H20N2O4
    Color and Shape:Solid
    Molecular weight:292.33

    Ref: TM-T71084

    25mg
    2,448.00€
    50mg
    3,222.00€
    100mg
    4,410.00€
  • Lamivudine, (+/-)-trans-

    CAS:
    Lamivudine, a drug for HIV-1 and HBV, inhibits reverse transcriptase and resembles zalcitabine.
    Formula:C8H11N3O3S
    Purity:98%
    Color and Shape:Solid
    Molecular weight:229.26

    Ref: TM-T25609

    25mg
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  • Cefempidone

    CAS:
    Cefempidone (GR 50692) is a third-generation cephalosporin antibiotic. It exhibits antibacterial activity by inhibiting penicillin-binding proteins involved in the synthesis of bacterial cell walls.
    Formula:C22H21N7O6S2
    Molecular weight:543.58

    Ref: TM-T210004

    10mg
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  • Pks13-TE inhibitor 4

    CAS:
    Pks13-TE inhibitor 4 (compound 44) is a potent inhibitor from the thiazole series that effectively targets Pks13 to combat tuberculosis (TB) and addresses drug resistance.
    Formula:C26H25N5O6
    Molecular weight:503.51

    Ref: TM-T208278

    10mg
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  • 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
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  • 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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  • SARS-CoV-2 Mpro-IN-31

    CAS:
    SARS-CoV-2 Mpro-IN-31 (Compound 18) is an inhibitor of SARS-CoV-2 MPro with an IC50 of 11 nM. Additionally, this compound effectively inhibits the enzymatic activity of the cysteine proteases cathepsin B and cathepsin L, with IC50 values of 24 nM and 1.8 nM, respectively.
    Formula:C31H34Cl2N4O7
    Color and Shape:Solid
    Molecular weight:645.53

    Ref: TM-T200958

    25mg
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  • GRL-190-21

    CAS:

    GRL-190-21 (compound 5e), an inhibitor of SARS-Cov-2-Mpro, shows potent antiviral activity, with a K_i of 0.04 nM and an EC_50 of 0.26 μM in VeroE6 cells. It significantly reduces the infectivity, replication, and cytopathic effect of SARS-CoV-2 without notable toxicity [1].

    Formula:C24H34F3N5O4
    Color and Shape:Solid
    Molecular weight:513.55

    Ref: TM-T86525

    10mg
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  • LasR antagonist 1

    CAS:
    LasR antagonist 1 (Compound 7), with an IC50 of 0.4 μM, is an effective antagonist of LasR that modulates quorum sensing (QS) in the opportunistic pathogen Pseudomonas aeruginosa [1].
    Formula:C20H15F3N2O3
    Color and Shape:Solid
    Molecular weight:388.34

    Ref: TM-T86799

    10mg
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  • 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
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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-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
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  • Polθ-IN-5

    CAS:
    Polθ-IN-5 (Compound 139) is an inhibitor of DNA polymerase theta (Polθ) that exhibits antitumor activity.
    Formula:C23H18ClF2N7O3S
    Color and Shape:Solid
    Molecular weight:545.95

    Ref: TM-T200913

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • TBAJ-5307

    CAS:
    TBAJ-5307 is a broad-spectrum anti-non-tuberculous mycobacteria inhibitor that targets the FO-domain of the engine, preventing rotation and proton-translocation. TBAJ-5307 inhibits non-tuberculous mycobacteria in vitro and in vivo [1].
    Formula:C30H35BrN4O6
    Color and Shape:Solid
    Molecular weight:627.53

    Ref: TM-T87495

    10mg
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  • NNRT-IN-5

    CAS:
    NNRT-IN-5 (compound 10d) is an orally available non-nucleoside reverse transcriptase (Reverse Transcriptase) inhibitor.
    Formula:C27H22N8
    Color and Shape:Solid
    Molecular weight:458.52

    Ref: TM-T201040

    25mg
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  • SARS-CoV-IN-6

    CAS:
    SARS-CoV-IN-6 (Compound 17) acts as an inhibitor of SARS-CoV-1 and SARS-CoV-2 RdRp, demonstrating an IC50 value of 7.8 μM against SARS-CoV-2 RdRp. This compound reduces the cytopathic effects of single-round infectious particles (SRIP) infected with SARS-CoV-1 and SARS-CoV-2 replicons and inhibits the expression of SARS-CoVN proteins. The EC50 values for SRIP based on SARS-CoV-1 and SARS-CoV-2 replicons are 0.12 µM and 1.47 µM, respectively.
    Formula:C25H29N5O3
    Color and Shape:Solid
    Molecular weight:447.53

    Ref: TM-T200730

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • (E)-Cefodizime

    CAS:
    (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.
    Formula:C20H20N6O7S4
    Color and Shape:Solid
    Molecular weight:584.669

    Ref: TM-T206930

    10mg
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  • Eravacycline

    CAS:
    Eravacycline (TP-434) is a potent and broad-spectrum antibacterial agent.
    Formula:C27H31FN4O8
    Purity:97.46%
    Color and Shape:Solid
    Molecular weight:558.56

    Ref: TM-T11227

    25mg
    3,258.00€
    50mg
    4,303.00€
    100mg
    6,030.00€
  • SARS-CoV-2 Mpro-IN-44

    CAS:
    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.
    Formula:C29H19Cl2FN8O4S
    Color and Shape:Solid
    Molecular weight:665.48

    Ref: TM-T207266

    10mg
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  • Omaciclovir

    CAS:
    Omaciclovir (ABT-091) is a herpesvirus herpesvirus replication inhibitor with antiviral activity that is used in the study of herpesvirus infections.
    Formula:C10H15N5O3
    Purity:99.46% - 99.46%
    Color and Shape:Solid
    Molecular weight:253.26

    Ref: TM-T28234

    1mL*10mM (DMSO)
    33.00€
    1mg
    139.00€
  • Saroaspidin B

    CAS:
    Saroaspidin B is a dimeric form of a biphenyl triphenol, characterized as an antibiotic compound.
    Formula:C25H32O8
    Color and Shape:Solid
    Molecular weight:460.52

    Ref: TM-T89874

    10mg
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  • APE1-IN-3

    CAS:
    APE1-IN-3 (Compound 1), an APE1 inhibitor, is utilized in cancer research.
    Formula:C17H16O4
    Color and Shape:Solid
    Molecular weight:284.31

    Ref: TM-T89919

    10mg
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    50mg
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  • 2-Acetyl-2-decarboxamidotetracycline

    CAS:

    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.

    Formula:C23H25NO8
    Color and Shape:Solid
    Molecular weight:443.45

    Ref: TM-T200223

    25mg
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  • Etofamide

    CAS:
    Etofamide, an antimicrobial agent, exhibits an IC50 of 5.96 mg/L against amoebae.
    Formula:C19H20Cl2N2O5
    Color and Shape:Solid
    Molecular weight:427.28

    Ref: TM-T200359

    25mg
    1,564.00€
    50mg
    2,034.00€
    100mg
    2,517.00€
  • Saptomycin E

    CAS:
    Saptomycin E is an antitumor antibiotic.
    Formula:C33H35NO9
    Color and Shape:Solid
    Molecular weight:589.63

    Ref: TM-T200377

    25mg
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  • 2-Bromo-2'-methoxyacetophenone

    CAS:
    2-Bromo-2'-methoxyacetophenone acts as an irreversible inhibitor of MurA, effectively inhibiting MurA in E. coli with an IC50 of 0.38 μM. This compound helps inhibit bacterial cell wall synthesis, making it useful in antimicrobial research.
    Formula:C9H9BrO2
    Molecular weight:229.07

    Ref: TM-T201807

    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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  • AYK004-C1

    CAS:
    AYK004-C1 is a TLR agonist used in the formulation of immunological adjuvants.
    Formula:C35H58F3N7O3
    Molecular weight:681.88

    Ref: TM-T201419

    10mg
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    50mg
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  • HIV-1 inhibitor-82

    CAS:
    HIV-1inhibitor-82 (Compound L14) is a small molecule inhibitor of HIV-1 entry with oral bioavailability, exhibiting an IC50 value of 0.39 μM. It holds potential for research in combating HIV-1 infection.
    Formula:C37H37ClN2O6S2
    Color and Shape:Solid
    Molecular weight:705.28

    Ref: TM-T207341

    10mg
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    50mg
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  • Tetrahydrouridine dihydrate


    THU dihydrate, a potent CDA inhibitor, outperforms cytidine by blocking the enzyme's active site.
    Formula:C9H20N2O8
    Color and Shape:Solid
    Molecular weight:284.26

    Ref: TM-T60553

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • Doxazosin impurity 12

    CAS:

    Doxazosin impurity 12 acts as an inhibitor of CTX-M β-lactamase (Beta-lactamase) with a Ki value of 0.7 mM against CTX-M.

    Formula:C10H6O5S
    Color and Shape:Solid
    Molecular weight:238.217

    Ref: TM-T204282

    10mg
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    50mg
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  • PCNA-IN-1

    CAS:
    PCNA-IN-1 (Compound 11) is an inhibitor of the PCNA/PIP-box interaction, with an IC50 greater than 50 μM. It is applicable in cancer research.
    Formula:C19H18I3NO3
    Color and Shape:Solid
    Molecular weight:689.065

    Ref: TM-T204170

    10mg
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    50mg
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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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  • H2S scavenger 1 (triflate)


    H2S scavenger 1 triflate (Compound 7b) serves as a selective H2S depleting agent, particularly against glutathione. This compound impedes the formation of bacterial biofilms and enhances the sensitivity of Staphylococcus aureus to gentamicin or photosensitizers by depleting H2S.
    Formula:C13H16F3N5O6S
    Molecular weight:427.36

    Ref: TM-T201478

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  • Anti-ToCV agent 1


    Anti-ToCV agent 1 can be used as a potential anti-ToCV drug.
    Formula:C22H19FN2O5S
    Color and Shape:Solid
    Molecular weight:442.46

    Ref: TM-T62575

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

    CAS:
    Kikumycin A, an antibiotic produced by Streptomyces, exhibits antimicrobial activity against both Gram-positive and Gram-negative bacteria. Additionally, it demonstrates antitrichomonal activity with a minimum inhibitory concentration (MIC) of 25 μg/mL against Trichomonas foetus.
    Formula:C13H17N7O2
    Color and Shape:Solid
    Molecular weight:303.32

    Ref: TM-T200235

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  • 4-Chloropyridine

    CAS:
    4-Chloropyridine acts as an inhibitor of Nicotinamide N-methyltransferase (NNMT). Serving as a substrate for NNMT, this compound enhances the electrophilicity at the C4 position through methylation of the pyridine nitrogen. This modification facilitates an aromatic nucleophilic substitution reaction with the non-catalytic cysteine (C159) in NNMT, ultimately leading to suicidal activity inhibition of the enzyme. 4-Chloropyridine is a promising candidate for the development of activity-based probes targeting NNMT functions.
    Formula:C5H4ClN
    Color and Shape:Solid
    Molecular weight:113.55

    Ref: TM-T201645

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  • Antibacterial agent 281

    CAS:
    Antibacterialagent 281 (Compound 95,186) effectively inhibits the growth of GAS by binding to the ligand-binding pocket of SPs0871, competing with the ligand. It exhibits concentration-dependent growth inhibition against Streptococcus pyogenes (S. pyogenes).
    Formula:C23H24N6O
    Color and Shape:Solid
    Molecular weight:400.48

    Ref: TM-T211109

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  • Gougerotin

    CAS:
    Gougerotin is an inhibitor of protein synthesis.
    Formula:C16H25N7O8
    Color and Shape:Solid
    Molecular weight:443.41

    Ref: TM-T69919

    25mg
    2,448.00€
    50mg
    3,222.00€
    100mg
    4,410.00€
  • HC2210

    CAS:
    HC2210 exhibits antibacterial effects against Mycobacterium abscessus (Mab) with an EC50 of 0.72 µM. It modulates the expression of Mab genes associated with oxidative stress and lipid metabolism. HC2210 is applicable for studies on Mab infections.
    Formula:C17H18N4O9
    Color and Shape:Solid
    Molecular weight:422.35

    Ref: TM-T210948

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  • DPC 684

    CAS:
    DPC 684 is a potent and selective HIV-1 protease inhibitor with an IC90 of 5.7-40 nM and a Ki of 0.021 nM. It competitively inhibits HIV-1 protease, preventing viral polyprotein cleavage. Compared to cellular proteases, DPC 684 shows high selectivity for retroviral proteases. The compound exhibits low protein binding and offers broad-spectrum inhibition against various wild-type and mutant HIV-1 proteases, with an IC90 of 1.9-6.3 nM. DPC 684 is significant for HIV research.
    Formula:C35H48FN5O5S
    Color and Shape:Solid
    Molecular weight:669.85

    Ref: TM-T211711

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  • Pyriofenone

    CAS:
    Pyriofenone (IKF-309) is an aryl phenyl ketone fungicide predominantly used to control powdery mildew on crops such as cereals, rice, fruit trees, and vegetables. It exhibits moderate efficacy against rice blast disease. Pyriofenone functions through prevention, residue activity, treatment, rainfastness, translaminar action, and fumigation.
    Formula:C18H20ClNO5
    Color and Shape:Solid
    Molecular weight:365.81

    Ref: TM-T211342

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  • L-Tyrosyl-L-glutamic acid

    CAS:
    L-Tyrosyl-L-glutamic acid acts as an inhibitor of the amino acid permease GAP1.
    Formula:C14H18N2O6
    Color and Shape:Solid
    Molecular weight:310.3

    Ref: TM-T201575

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  • 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€
  • FIZ1 degrader 1

    CAS:
    FIZ1 degrader 1 (compound 1) is an IMiD-based molecular glue degrader targeting FIZ1.
    Formula:C16H15N3O4
    Color and Shape:Solid
    Molecular weight:313.31

    Ref: TM-T201843

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  • 6-N-Hydroxylaminopurine

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

    Ref: TM-T210412

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  • GTSE1-IN-1

    CAS:
    GTSE1-IN-1 (compound Y18), an orally active GTSE1 inhibitor, exhibits notable anticancer properties. It effectively represses the proliferation of cancer cells by downregulating GTSE1 transcription and expression, which leads to DNA damage and promotes persistent cell cycle arrest and cellular senescence. Moreover, GTSE1-IN-1 substantially reduces the adhesion, migration, and invasion of colorectal cancer HCT116 cells and non-small cell lung cancer A549 cells in vitro.
    Formula:C21H24FN7
    Color and Shape:Solid
    Molecular weight:393.46

    Ref: TM-T200127

    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

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  • 17,17-Ethylendioxyandrost-5-en-3β-ol

    CAS:
    17,17-Ethylendioxyandrost-5-en-3β-ol, with an EC 50 of 629 μM, acts as an inhibitor of HSV-1. This compound is applicable in research studies focusing on viral infections.
    Formula:C21H32O3
    Color and Shape:Solid
    Molecular weight:332.48

    Ref: TM-T200287

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • CCC-0975

    CAS:
    CCC-0975 is an inhibitor of hepatitis B virus (HBV) with an EC50 of 10 μM. It interferes with the conversion of relaxed circular DNA (rcDNA) to covalently closed circular DNA (cccDNA) and reduces cccDNA and its precursor deproteinized rcDNA (DP-rcDNA), without promoting their degradation inside cells. CCC-0975 holds potential for chronic hepatitis B research.
    Formula:C21H17ClF3N3O3S
    Color and Shape:Solid
    Molecular weight:483.89

    Ref: TM-T210630

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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€
  • 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

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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

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  • HIV-1-IN-86

    CAS:
    HIV-1-IN-86 (compound 6m) is an HIV-1 inhibitor with an EC50 of 0.77 μM, exhibiting antiviral activity.
    Formula:C20H17N3O7S
    Color and Shape:Solid
    Molecular weight:443.43

    Ref: TM-T212486

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  • (-)-15-Deoxyspergualin

    CAS:
    (-)-15-Deoxyspergualin is a potent antitumor agent that demonstrates significant inhibition against mouse leukemia L-1210.
    Formula:C17H37N7O3
    Color and Shape:Solid
    Molecular weight:387.52

    Ref: TM-T72325

    25mg
    2,448.00€
    50mg
    3,222.00€
    100mg
    4,410.00€
  • Ibafloxacine

    CAS:
    Ibafloxacine (R835) is a fluoroquinolone antibiotic that is used exclusively in veterinary applications and shows zero good bacteriostatic effect against
    Formula:C15H14FNO3
    Purity:97.67%
    Color and Shape:Solid
    Molecular weight:275.27

    Ref: TM-T12649

    1mg
    354.00€
    5mg
    848.00€
  • MB076

    CAS:
    MB076 is an innovative heterocyclic triazole designed with enhanced plasma stability. It effectively inhibits seven distinct Class C Acinetobacter-derived cephalosporinases (ADCs) β-lactamase variants with K i values less than 1 μM. Additionally, MB076 demonstrates a synergistic effect when combined with various cephalosporins to restore pBCSK(−) susceptibility [1].
    Formula:C9H12BN7O5S2
    Color and Shape:Solid
    Molecular weight:373.18

    Ref: TM-T86864

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  • HBV-IN-48

    CAS:
    HBV-IN-48, an HBV inhibitor, exhibits potent antiviral activity against HBV in HepDE19 cells, demonstrated by its EC 50 value of 0.005 μM. Additionally, it effectively reduces serum HBV DNA levels in mouse models of HBV infection.
    Formula:C22H15F4N3O3
    Color and Shape:Solid
    Molecular weight:445.37

    Ref: TM-T200299

    25mg
    1,468.00€
    50mg
    1,990.00€
    100mg
    2,457.00€
  • DXR-IN-3

    CAS:
    DXR-IN-3 is an anti-Toxoplasma DXR inhibitor. It exhibits in vitro activity against the TgDXR enzyme, with an IC50 value of 0.62 μM and a Ki value of 0.19 μM. Furthermore, DXR-IN-3 can inhibit the proliferation of Toxoplasma, displaying an IC50 value of 5.46 μM.
    Formula:C10H12Cl2NO5PS
    Color and Shape:Solid
    Molecular weight:360.15

    Ref: TM-T200712

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

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  • Triazophos

    CAS:
    Triazophos is a non-systemic pesticide that acts as an acetylcholinesterase (AChE) inhibitor, forming a covalent and irreversible bond with the acetylcholine binding site. This action blocks the hydrolysis of acetylcholine, leading to increased excitability. It is effective against a wide range of soil insects and mites, including aphids, thrips, midges, beetles, lepidopteran larvae, mole crickets, and red spiders. Triazophos is suitable for use on various crops such as ornamental plants, cotton, rice, corn, soybeans, oil palm, olives, and coffee.
    Formula:C12H16N3O3PS
    Color and Shape:Solid
    Molecular weight:313.31

    Ref: TM-T201053

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • Enantiomer of Sofosbuvir


    Inactive enantiomer of Sofosbuvir, used for chronic hepatitis C; lacks reported biological activity.
    Formula:C22H29FN3O9P
    Purity:98%
    Color and Shape:Solid
    Molecular weight:529.45

    Ref: TM-T11195

    25mg
    1,494.00€
    50mg
    2,043.00€
    100mg
    2,512.00€
  • 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€
  • GSK_WRN4

    CAS:
    GSK_WRN4 is a WRN helicase inhibitor with anti-cancer activity, inhibiting MSI tumor cell growth by inducing DNA double-strand breaks, useful in cancer research
    Formula:C16H20N2O4S
    Purity:99.95%
    Color and Shape:Solid
    Molecular weight:336.41

    Ref: TM-T200332

    1mg
    858.00€
    5mg
    1,603.00€
    10mg
    2,142.00€
    25mg
    3,213.00€
    50mg
    4,311.00€
  • Anti-infective agent 10

    CAS:
    Anti-infective agent 10 (Compound Example 30) is an ns5b polymerase inhibitor that functions as an anti-HCV agent.
    Formula:C26H25N3O7S
    Color and Shape:Solid
    Molecular weight:523.56

    Ref: TM-T207374

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  • Antimalarial agent 44


    Antimalarial agent 44 (Compound 3) is an antiparasitic agent effective against malaria. It exhibits good permeability in MDCK-MDR1 cell monolayers and has a high clearance rate in mouse liver microsomes.
    Formula:C37H37N5O7
    Color and Shape:Solid
    Molecular weight:663.72

    Ref: TM-T201453

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  • MLEB-22043


    MLEB-22043 is a synthetic siderophore-monocyclic β-lactam conjugate which enters bacteria through TonB-dependent transport proteins utilizing its siderophore component, subsequently exerting antibacterial activity via its β-lactam portion. This compound acts as a broad-spectrum antibiotic, exhibiting significant inhibitory activity against pathogens such as Klebsiella pneumoniae, Escherichia coli, Acinetobacter baumannii, and Pseudomonas aeruginosa.
    Formula:C25H25N9O11S2
    Color and Shape:Solid
    Molecular weight:691.65

    Ref: TM-T201750

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  • 2,5-Di-tert-butyl-1,4-benzoquinone

    CAS:
    2,5-Di-tert-butyl-1,4-benzoquinone is a potent antibacterial agent found primarily in marine Streptomyces sp. VITVSK1, effective against emerging antibiotic resistance. Additionally, it serves as a powerful inhibitor of RNA polymerase.
    Formula:C14H20O2
    Color and Shape:Solid
    Molecular weight:220.31

    Ref: TM-T201504

    10mg
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  • SARS-CoV-2 Mpro-IN-34


    SARS-CoV-2 Mpro-IN-34 (Compound 26) acts as an inhibitor of SARS-CoV-2 Mpro with an IC50 of 6 nM. It also inhibits OC43 Mpro, demonstrating an IC50 of 33 nM. Furthermore, this compound exhibits antiviral activity in Vero E6 cells infected with SARS-CoV-2, with an EC50 of 0.103 μM.
    Formula:C30H37Cl2N5O3
    Color and Shape:Solid
    Molecular weight:586.55

    Ref: TM-T201527

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  • Cefamandole lithium

    CAS:
    Cefamandole (lithium), a second-generation broad-spectrum cephalosporin antibiotic, exhibits antimicrobial activity. Upon metabolism in the body, it releases free NMTT, which can lead to hypoprothrombinemia.
    Formula:C18H17LiN6O5S2
    Color and Shape:Solid
    Molecular weight:468.44

    Ref: TM-T201722

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  • Cilastatin ammonium salt

    CAS:
    Cilastatin ammonium salt is an antibiotic that is particularly effective against Gram-positive cocci, with a half-life of 3-4 hours.
    Formula:C16H29N3O5S
    Color and Shape:Solid
    Molecular weight:375.48

    Ref: TM-T201424

    10mg
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  • Antibacterial agent 66


    Compound 6q, a trifluoromethylpyridine oxadiazole, targets Xanthomonas oryzae with EC50 of 7.2 μg/mL.
    Formula:C17H10ClF6N3O2S
    Color and Shape:Solid
    Molecular weight:469.79

    Ref: TM-T63027

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • (Rac)-Plevitrexed

    CAS:
    (Rac)-Plevitrexed is a racemate of Plevitrexed. Plevitrexed is an orally active and potent inhibitor of thymidylate synthase (TS).
    Formula:C26H25FN8O4
    Purity:98%
    Color and Shape:Solid
    Molecular weight:532.53

    Ref: TM-T12674

    25mg
    2,988.00€
    50mg
    3,943.00€
    100mg
    5,490.00€
  • PFK-IN-1

    CAS:
    PFK-IN-1 (compound 1) is an inhibitor of 6-phosphofructo-1-kinase (PFK), demonstrating IC50 values of 0.41 and 0.23 μM against T. brucei and T. cruzi PFK, respectively, and an ED50 of 15.18 μg/mL for T. brucei. The compound has a half-life of 9.7 minutes in rat liver microsomes and 408 minutes in mouse liver microsomes.
    Formula:C18H15Cl2N3O4S
    Color and Shape:Solid
    Molecular weight:440.3

    Ref: TM-T204311

    10mg
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  • Saussureamine C

    CAS:
    Saussureamine C is an inhibitor of H274Y and N294S mutants.
    Formula:C19H26N2O5
    Color and Shape:Solid
    Molecular weight:362.42

    Ref: TM-T70565

    25mg
    2,178.00€
    50mg
    2,862.00€
    100mg
    3,870.00€