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Deidrogenasi

Deidrogenasi

Le deidrogenasi sono enzimi coinvolti nelle reazioni di ossidoriduzione delle vie metaboliche, svolgendo un ruolo centrale nella produzione di energia e nella respirazione cellulare. Questi enzimi sono cruciali per processi come il ciclo dell'acido citrico, la glicolisi e l'ossidazione degli acidi grassi. Gli inibitori delle deidrogenasi sono strumenti importanti nello studio delle malattie metaboliche, del cancro e dello stress ossidativo. Presso CymitQuimica, offriamo una selezione completa di inibitori delle deidrogenasi per supportare la tua ricerca in metabolismo, biologia del cancro e biochimica.

Trovati 299 prodotti di "Deidrogenasi"

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  • CAY10566

    CAS:
    CAY10566 is a potent SCD1 inhibitor, orally bioavailable, with IC50s: HepG2 cells, 7.9nM; mouse, 4.5nM; human, 26nM.
    Formula:C18H17ClFN5O2
    Purezza:99.5% - 99.54%
    Colore e forma:Solid
    Peso molecolare:389.81
  • Olutasidenib

    CAS:
    Olutasidenib (FT-2102), an IDH1 inhibitor (IC50: 21.2/114 nM), is studied for treating AML/MDS and can cross the blood-brain barrier.
    Formula:C18H15ClN4O2
    Purezza:98.57%
    Colore e forma:Solid
    Peso molecolare:354.79
  • BAY-2402234

    CAS:
    BAY-2402234: a selective DHODH inhibitor targeting myeloid cancers with low-nanomolar potency.
    Formula:C21H18ClF5N4O4
    Purezza:98.9%
    Colore e forma:Solid
    Peso molecolare:520.84
  • IGUANA-1 free base

    CAS:
    IGUANA-1: selective ALDH1 B1 inhibitor, IC50=30 nM, hinders SW480 cell growth with IC50=2.46/0.39 μM in adherent/spheroid forms, for cancer research.
    Formula:C26H24ClN3O2
    Colore e forma:Solid
    Peso molecolare:445.94
  • LDHA-IN-3

    CAS:
    LDHA-IN-3 is a potent selenobenzene-based LDHA inhibitor with a 145.2 nM IC50, useful in cancer research.
    Formula:C13H9F3Se
    Purezza:99.71%
    Colore e forma:Solid
    Peso molecolare:301.17
  • PDK-IN-1

    CAS:
    PDK-IN-1, a PDK inhibitor, IC50: 0.03μM (PDK1), 0.1μM (HSP90), reduces tumor mass.
    Formula:C20H16BrN7O
    Colore e forma:Solid
    Peso molecolare:450.29
  • MTHFD2-IN-4


    MTHFD2-IN-4, a tricyclic coumarin derivative, serves as a potent inhibitor of MTHFD2 and has applications in cancer research [1].
    Formula:C26H21F6N2O5
    Colore e forma:Solid
    Peso molecolare:555.45
  • hDHODH-IN-13

    CAS:
    <p>hDHODH-IN-13 (compound w2), an inhibitor of human dihydroorotate dehydrogenase (hDHODH), exhibits an IC50 of 173.4 nM and has potential research applications in</p>
    Colore e forma:Soild
  • WAY-311610

    CAS:
    WAY-311610 is an HSD11B1 inhibitor targeting 11β-HSD1 enzyme with 0.34 μM IC; used for neuropathic and inflammatory pain research.
    Formula:C16H13F3N4O2
    Purezza:99.75%
    Colore e forma:Solid
    Peso molecolare:350.3
  • CM121

    CAS:
    CM121, a reversible ALDH1A2 inhibitor, targets active site with IC50=0.54μM, Kd=1.1μM, using hydrophobic interactions.
    Formula:C24H17FN4O3S
    Colore e forma:Solid
    Peso molecolare:460.48
  • MTHFD2-IN-1


    <p>MTHFD2-IN-1 (compound 12) is a potent inhibitor of methylenetetrahydrofolate dehydrogenase (MTHFD2) [1].</p>
    Formula:C24H21NO6
    Colore e forma:Solid
    Peso molecolare:419.43
  • Necroptosis-IN-3

    CAS:
    <p>Necroptosis-IN-3 (Cyclohexanecarboxamide, N-(2-thienylmethyl)-) (Compound 69) is a Necroptosis inhibitor that inhibits TNF-α induced necroptosis.</p>
    Formula:C12H17NOS
    Purezza:99.85%
    Colore e forma:Soild
    Peso molecolare:223.33
  • 18β-Glycyrrhetyl-3-O-sulfate

    CAS:
    18β-Glycyrrhetyl-3-O-sulfate (Glycyrrhetic acid 3-O-(hydrogen sulfate)), a major metabolite of Glycyrrhetinic acid (GA), serves as a potent inhibitor of type 2
    Formula:C30H46O7S
    Colore e forma:Solid
    Peso molecolare:550.75
  • Ascochlorin A

    CAS:
    Ascochlorin A, a compound with a dissociation constant (K D) of 3.29 μM, serves as a novel and potent human dihydroorotate dehydrogenase (hDHODH) inhibitor
    Formula:C23H31ClO4
    Colore e forma:Solid
    Peso molecolare:406.95
  • DHODH-IN-18

    CAS:
    DHODH-IN-18 is a human DHODH inhibitor ( IC 50 = 0.2 nM).
    Formula:C21H16ClF5N6O4
    Colore e forma:Solid
    Peso molecolare:546.84
  • MTHFD2-IN-2


    MTHFD2-IN-2 (compound 13) serves as a potent inhibitor of methylenetetrahydrofolate dehydrogenase (MTHFD2) [1].
    Formula:C22H18N4O5
    Colore e forma:Solid
    Peso molecolare:418.4
  • PDK-IN-2


    PDK-IN-2 (Compound 1F), with an IC50 of 68 nM, is a potent PDK inhibitor that downregulates the expression of PDK1 and PDK4 in cells.
    Formula:C17H23AsCl2N2O2S2
    Colore e forma:Solid
    Peso molecolare:497.33
  • 2,3-Dihydroxybenzaldehyde

    CAS:
    2,3-Dihydroxybenzaldehyde exhibits activity against NADH dehydrogenase (Km = 35 µM) and can be used in biochemical experiments and drug synthesis.
    Formula:C7H6O3
    Colore e forma:Solid
    Peso molecolare:138.12
  • DSM705

    CAS:
    DSM705: Pyrrole-based, potent nanomolar Plasmodium DHODH inhibitor with strong antimalarial efficacy; spares mammalian DHODH.
    Formula:C19H19F3N6O
    Colore e forma:Solid
    Peso molecolare:404.397
  • SCD1 inhibitor-3

    CAS:
    SCD1 inhibitor-3 (ML-270) is a highly effective and orally available compound that inhibits SCD1 with remarkable safety.
    Formula:C19H16FN7O2
    Purezza:99.5%
    Colore e forma:Solid
    Peso molecolare:393.37