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Other Inhibitors

Other Inhibitors

This category encompasses a wide variety of inhibitors that do not fit into the standard classifications but are still critical for various biochemical and pharmacological research. These inhibitors may target unique or less-studied pathways, enzymes, and molecular interactions, providing valuable tools for specialized research areas. At CymitQuimica, we offer a diverse selection of high-quality inhibitors across multiple biological targets and research disciplines, enabling you to explore novel therapeutic avenues and deepen your understanding of complex biological processes.

Found 35846 products of "Other Inhibitors"

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  • HYL001

    CAS:
    HYL001 (compound 338) is a potent inhibitor of the TGFβ receptor 1 (ALK5), exhibiting approximately nine times the efficacy of its structurally related counterpart, galunisertib, in eliminating liver metastasis tumors generated in mice.
    Formula:C21H18N4O
    Color and Shape:Solid
    Molecular weight:342.39

    Ref: TM-T200461

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

    CAS:
    Fosfocytocin can be found in the Pseudomonas fluorescens strain PK-52 and exhibits very weak antibacterial activity.
    Formula:C12H20N4O13P2
    Color and Shape:Solid
    Molecular weight:490.254

    Ref: TM-TN10490

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  • SLC7A11-IN-2

    CAS:
    SLC7A11-IN-2 (Compound 1) is an inhibitor of SLC7A11/xCT. It disrupts the oxidative balance in HeLa cells by decreasing intracellular glutathione levels and increasing oxidative stress, thereby inducing cell death with an IC50 of 10.23 μM. Molecular dynamics simulations have demonstrated that SLC7A11-IN-2 exhibits a stronger binding affinity to SLC7A11 compared to Erastin. This compound is useful for research in the field of cervical cancer.
    Formula:C19H24N4O3
    Color and Shape:Solid
    Molecular weight:356.42

    Ref: TM-T200659

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  • S-2,3-Dicarboxyaziridine

    CAS:
    S-2,3-Dicarboxyaziridine is a metabolite that can be isolated from Streptomyces species and exhibits antibacterial activity.
    Formula:C4H5NO4
    Color and Shape:Solid
    Molecular weight:131.087

    Ref: TM-TN10341

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  • Furaquinocin A

    CAS:
    Furaquinocin A has the ability to kill HeLa S3 and B16 melanoma cells, yet it lacks antibacterial activity.
    Formula:C22H26O7
    Color and Shape:Solid
    Molecular weight:402.438

    Ref: TM-TN10058

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  • Demethylblasticidin S

    CAS:
    Demethylblasticidin S is an antifungal antibiotic produced by Streptomyces griseochromogenes.
    Formula:C16H24N8O5
    Color and Shape:Solid
    Molecular weight:408.412

    Ref: TM-TN10185

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  • 1-Deamino-1-hydroxygentamicin C2

    CAS:
    1-Deamino-1-hydroxygentamicin C2 (AntibioticSU-1) is an aminoglycoside antibiotic effective against both Gram-positive and Gram-negative bacteria.
    Formula:C20H40N4O8
    Color and Shape:Solid
    Molecular weight:464.554

    Ref: TM-TN10361

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  • Cytochalasin F

    CAS:
    Cytochalasin F reversibly inhibits cytokinesis and possesses various biological activities including the inhibition of macrophage endocytosis and exocytosis.
    Formula:C29H37NO5
    Color and Shape:Solid
    Molecular weight:479.608

    Ref: TM-TN10033

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  • Cyclophellitol

    CAS:
    Cyclophellitol is an inhibitor of β-glycosidase, with an IC50 of 0.8 μg/mL.
    Formula:C7H12O5
    Color and Shape:Solid
    Molecular weight:176.167

    Ref: TM-TN10067

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  • Oxamicetin

    CAS:
    Oxamicetin is a nucleoside antibiotic with antibacterial and antimycobacterial properties.
    Formula:C29H42N6O10
    Color and Shape:Solid
    Molecular weight:634.678

    Ref: TM-TN10095

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  • Glucoallosamidin B

    CAS:
    Glucoallosamidin B is a glycoside antibiotic identifiable in the Streptomyces species strain (Streptomycessp. SA-684). It functions as an inhibitor of chitinase activity. Experiments demonstrate that Glucoallosamidin B significantly inhibits the chitinase of Candida albicans (ATCC 10231), with an IC50 value of 0.8 μg/mL.
    Formula:C25H42N4O14
    Color and Shape:Solid
    Molecular weight:622.619

    Ref: TM-TN10337

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  • Sannamycin G

    CAS:
    Sannamycin G (Istamycin X0) is an aminoglycoside antibiotic that exhibits only weak antibacterial activity against a limited range of bacteria.
    Formula:C14H30N4O4
    Color and Shape:Solid
    Molecular weight:318.412

    Ref: TM-TN10131

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  • Neoenactin A

    CAS:
    Neoenactin A exhibits potent activity against yeasts and filamentous fungi.
    Formula:C19H36N2O5
    Color and Shape:Solid
    Molecular weight:372.5

    Ref: TM-TN10449

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  • MraY-IN-1


    MraY-IN-1 inhibits MraY (IC50: 140μM), fights E. coli K12, B. subtilis W23, P. fluorescens (MIC50: 7-46μg/ml), for antimicrobial research.
    Formula:C35H46N3O5
    Color and Shape:Solid
    Molecular weight:588.76

    Ref: TM-T64172

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • Ezomycin A2

    CAS:
    Ezomycin A2 is an antifungal antibiotic. It is primarily effective against plant pathogens such as Sclerotinia and Botrytis, showing efficacy in controlling crop diseases like sclerotinia rot, botrytis blight, and candidiasis.
    Formula:C19H26N6O12
    Color and Shape:Solid
    Molecular weight:530.443

    Ref: TM-TN10135

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  • Tabimorelin hemifumarate

    CAS:
    orally active ghrelin receptor (GHS-R1a) agonist
    Formula:C32H40N403C4H404
    Purity:98%
    Color and Shape:Solid
    Molecular weight:586.72

    Ref: TM-T23413

    10mg
    1,251.00€
  • ASP-8731

    CAS:
    ASP8731 is a selective inhibitor of BACH1 that prevents inflammation and vascular occlusion, and induces fetal hemoglobin in sickle cell disease.
    Formula:C20H21N5O4
    Color and Shape:Solid
    Molecular weight:395.41

    Ref: TM-T201687

    10mg
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    50mg
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  • Mopivabil


    Mopivabil is the angiotensin II receptor antagonist[1].
    Formula:C14H20O3
    Color and Shape:Solid
    Molecular weight:236.31

    Ref: TM-T60323

    25mg
    964.00€
    50mg
    1,251.00€
    100mg
    1,972.00€
  • U 75875

    CAS:
    U 75875 is a protease inhibitor.
    Formula:C45H61N7O7
    Color and Shape:Solid
    Molecular weight:812.01

    Ref: TM-T34976

    25mg
    2,583.00€
    50mg
    3,402.00€
    100mg
    4,680.00€
  • AZ0108

    CAS:
    AZ0108, an oral PARP1,2,6 inhibitor, selectively blocks centrosome clustering, is viable for in vivo studies, and doesn't inhibit PARP3/TNKS1.
    Formula:C24H20F4N6O2
    Color and Shape:Solid
    Molecular weight:500.45

    Ref: TM-T70138

    25mg
    2,853.00€
    50mg
    3,763.00€
    100mg
    5,220.00€