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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 322 prodotti per "Deidrogenasi".

prodotti per pagina.
  • XEN723
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    XEN723

    CAS:
    XEN723 is a potent thiazolylimidazolidinone Stearoyl-CoA Desaturase (SCD1) inhibitor(IC50s of 45 and 524 nM in mouse and HepG2 cell, respectively).
    Formula:C21H20FN5O2S
    Purezza:99.5%
    Colore e forma:Solid
    Peso molecolare:425.479

    Ref: TM-T13356

  • TC HSD 21
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    TC HSD 21

    CAS:
    TC HSD 21 is a potent and highly selective inhibitor of 17β-hydroxysteroid dehydrogenase type 3 (IC50 = 14 nM).
    Formula:C17H12BrNO3S2
    Purezza:99.32%
    Colore e forma:Solid
    Peso molecolare:422.32

    Ref: TM-T13100

  • ML390
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    ML390

    CAS:
    ML390 exerts its potent differentiation effect on multiple leukemia models.
    Formula:C21H21F3N2O3
    Purezza:99.76%
    Colore e forma:Solid
    Peso molecolare:406.3982

    Ref: TM-T13774

  • KPLH1130
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    KPLH1130

    CAS:
    KPLH1130, a PDK inhibitor, boosts glucose tolerance and reduces inflammation in high-fat diet mice.
    Formula:C15H13N3O3
    Purezza:99.07%
    Colore e forma:Solid
    Peso molecolare:283.282

    Ref: TM-T11765

  • MF-438
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    MF-438

    CAS:
    MF-438 is an effective and orally bioavailable stearoyl-CoA desaturase 1 (SCD1) inhibitor (EC50: 2.3 nM for rSCD1).
    Formula:C19H18F3N5OS
    Purezza:98.98% - 99.50%
    Colore e forma:Solid
    Peso molecolare:421.439

    Ref: TM-T16068

  • Mutant IDH1 inhibitor
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    Mutant IDH1 inhibitor

    CAS:
    Mutant IDH1 inhibitor is an effective inhibitor of mutant IDH1 R132H (IC50: < 72 nM).
    Formula:C25H34N6O3
    Purezza:98.3%
    Colore e forma:Solid
    Peso molecolare:466.5759

    Ref: TM-T16161

  • LY 345899
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    LY 345899

    CAS:
    LY 345899 is a Folate analog and is a methylenetetrahydrofolate dehydrogenase and MTHFD2 inhibitor (IC50: 96 nM and 663 nM, respectively and a Ki: 18 nM for
    Formula:C20H21N7O7
    Purezza:99.7%
    Colore e forma:Solid
    Peso molecolare:471.4234

    Ref: TM-T15827

  • CAY10566
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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:99.54% - 99.75%
    Colore e forma:Solid
    Peso molecolare:389.811

    Ref: TM-T14878

  • Mycophenolic acid
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    Mycophenolic acid

    CAS:
    Mycophenolic acid (Mycophenolate) is an inosine monophosphate dehydrogenase(IMPDH) inhibitor with anti-proliferative activity.
    Formula:C17H20O6
    Purezza:99.27% - 99.8%
    Colore e forma:White Solid
    Peso molecolare:320.3371

    Ref: TM-T1335

  • LDH-IN-1
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    LDH-IN-1

    CAS:
    LDH-IN-1 is a pyrazole-based human lactate dehydrogenase (LDH) inhibitor(IC50s of 32 and 27 nM for LDHA and LDHB, respectively).
    Formula:C30H26N4O4S2
    Purezza:99.6%
    Colore e forma:Solid
    Peso molecolare:570.682

    Ref: TM-T11829

  • IDH-305
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    IDH-305

    CAS:
    IDH-305: Oral, mutation-specific IDH1 inhibitor, 200x selective for R132 mutants; IC50: 27/28/6.14 nM for R132H/C/WT.
    Formula:C23H22F4N6O2
    Purezza:99.68%
    Colore e forma:Solid
    Peso molecolare:490.4534

    Ref: TM-T15550

  • CBR-5884
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    CBR-5884

    CAS:
    CBR-5884: active PHGDH inhibitor, IC50=33μM, disrupts serine synthesis, selectively targets high-serine cancers.
    Formula:C14H12N2O4S2
    Purezza:99.97%
    Colore e forma:Solid
    Peso molecolare:336.386

    Ref: TM-T14884

  • NCT-502
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    NCT-502

    CAS:
    NCT-502 (N-(4,6-dimethylpyridin-2-yl)-4-[5-(trifluoromethyl)pyridin-2-yl]piperazine-1-carbothioamide) is a human phosphoglycerate dehydrogenase inhibitor,
    Formula:C18H20F3N5S
    Purezza:99.60%
    Colore e forma:Yellow Solid
    Peso molecolare:395.45

    Ref: TM-T16277

  • SCD1 inhibitor-4
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    SCD1 inhibitor-4

    CAS:
    SCD1 inhibitor-4 is stearoylCoA desaturase-1 (SCD1) inhibitor. SCD1 inhibitor-4 can be used for the research of diabetes.
    Formula:C17H16F3N5O
    Purezza:99.71%
    Colore e forma:Solid
    Peso molecolare:363.337

    Ref: TM-T10525

  • PTC299
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    PTC299

    CAS:
    PTC299 ((4-chlorophenyl) (1S)-6-chloro-1-(4-methoxyphenyl)-1,3,4,9-tetrahydropyrido[3,4-b]indole-2-carboxylate) is an orally active inhibitor of VEGFA mRNA
    Formula:C25H20Cl2N2O3
    Purezza:99.72%
    Colore e forma:White Solid
    Peso molecolare:467.344

    Ref: TM-T12574

  • Adrenosterone
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    Adrenosterone

    CAS:
    Adrenosterone (11-ketoandrostenedione) is a steroid hormone isolated from the adrenal cortex.
    Formula:C19H24O3
    Purezza:98.13% - 98.29%
    Colore e forma:Solid
    Peso molecolare:300.39

    Ref: TM-T2207

  • DHODH-IN-11
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    DHODH-IN-11

    CAS:
    DHODH-IN-11 is a leflunomide derivative and weak dihydroorotate dehydrogenase (DHODH) inhibitor with a pKa of 5.03.
    Formula:C15H11N3O2
    Purezza:98.14%
    Colore e forma:Solid
    Peso molecolare:265.2667

    Ref: TM-T11020

  • BAY-2402234
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    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:520.837

    Ref: TM-T14501

  • CVT-10216
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    CVT-10216

    CAS:
    CVT-10216 inhibits ALDH2 (IC50: 29 nM) and ALDH-1 (IC50: 1.3 μM), reducing alcohol intake and anxiety in rats.
    Formula:C24H19NO7S
    Purezza:98.76%
    Colore e forma:Solid
    Peso molecolare:465.48

    Ref: TM-T15022

  • GSK2837808A
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    GSK2837808A

    CAS:
    GSK2837808A is a potent and selective inhibitor of lactate dehydrogenase A (LDHA) (IC50s: 1.9 and 14 nM for LDHA and LDHB, respectively).
    Formula:C31H25F2N5O7S
    Purezza:99.78% - 99.78%
    Colore e forma:Solid
    Peso molecolare:649.62

    Ref: TM-T15435