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Glutaminasi

Glutaminasi

Gli inibitori della glutaminasi sono composti che inibiscono la glutaminasi, un enzima che catalizza la conversione della glutamina in glutammato, un passaggio cruciale nel metabolismo cellulare, specialmente nelle cellule tumorali. La glutaminasi svolge un ruolo chiave nel fornire energia e precursori biosintetici per le cellule in rapida proliferazione. Gli inibitori della glutaminasi sono importanti per esplorare le dipendenze metaboliche nelle cellule tumorali e sviluppare potenziali strategie terapeutiche. Presso CymitQuimica, offriamo inibitori della glutaminasi per supportare la tua ricerca nel metabolismo del cancro, nella bioenergetica cellulare e nella scoperta di nuove terapie.

Trovati 44 prodotti di "Glutaminasi"

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  • α-Glucosidase-IN-5

    CAS:
    α-Glucosidase-IN-5 (compound 8) is isolated from a twig extract of Polyalthia cinnamomea which is a potent α-glucosidase inhibitor with an IC50 of 57.9 µM.
    Formula:C15H13NO3
    Colore e forma:Solid
    Peso molecolare:255.27
  • Glutaminase-IN-4

    CAS:
    Glutaminase-IN-4 (compound 2a) is a glutaminase (GLS) inhibitor (IC50: 2.3 μM).
    Formula:C23H22N6O2S2
    Colore e forma:Solid
    Peso molecolare:478.59
  • NC9 TG2 inhibitor

    CAS:
    NC9 is an irreversible inhibitor of transglutaminase 2 (TG2) and also inhibits Factor XIIIA (FXIIIA).
    Formula:C35H47N5O8S
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:697.84
  • AA10 TG2 inhibitor

    CAS:
    AA10 is an irreversible inhibitor of transglutaminase 2 (TG2).
    Formula:C32H36N4O5
    Colore e forma:Solid
    Peso molecolare:556.65
  • VA4 TG2 inhibitor

    CAS:
    VA4 is a novel irreversible TG2 transamidase site-specific inhibitor.
    Formula:C33H41N5O6S
    Colore e forma:Solid
    Peso molecolare:635.77
  • GLS1 Inhibitor

    CAS:
    GLS1 inhibitor blocks glutaminase 1 (IC50=0.021 μM), hinders NCI H1703 NSCLC cell growth in vitro (GI50=0.011 μM), and suppresses tumors in mice.
    Formula:C19H21N7O2S
    Colore e forma:Solid
    Peso molecolare:411.48
  • CP4d inhibitor

    CAS:
    CP4d is a novel reversible tg2 transamidase site-specific inhibitor
    Formula:C18H13N5O5
    Colore e forma:Solid
    Peso molecolare:379.33
  • JHU-083

    CAS:
    JHU-083 is a glutaminase antagonist that improves cognition and normalizes aberrant hippocampal glutaminase activity in APOE4 mice.
    Formula:C14H24N4O4
    Purezza:97.89% - 99.53%
    Colore e forma:Solid
    Peso molecolare:312.37
  • THDP-17

    CAS:
    THDP-17 is a inhibitor of glutaminase. THDP-17 shows a partial uncompetitive inhibition in vitro.
    Formula:C12H16N2S
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:220.33
  • AA9 TG2 inhibitor

    CAS:
    <p>AA9 is a novel transglutaminase (TG2) inhibitor.</p>
    Formula:C32H36N4O5
    Colore e forma:Solid
    Peso molecolare:556.65
  • GLS1 Inhibitor-3

    CAS:
    GLS1 Inhibitor-3 (compound C147) is a potent inhibitor of GLS1 (IC50: 27.98 nM) and exhibits anti-proliferative effects.
    Formula:C30H32N10O2S
    Colore e forma:Solid
    Peso molecolare:596.71
  • Duazomycin

    CAS:
    Duazomycin, an antitumor substance and glutamine antagonist, is used as a chemotherapeutic agent.
    Formula:C8H11N3O4
    Colore e forma:Solid
    Peso molecolare:213.19
  • UPGL00004

    CAS:
    <p>UPGL00004: potent GAC inhibitor, IC50=29 nM, Kd=27 nM, suppresses triple-negative breast cancer cell growth.</p>
    Formula:C25H26N8O2S2
    Purezza:97.93%
    Colore e forma:Solid
    Peso molecolare:534.66
  • TG-2-IN-1

    CAS:
    TG-2-IN-1 (Compound D003) is a transglutaminase-2 ( TGM-2 ) inhibitor. TG-2-IN-1 can be used in myopia research[1].
    Formula:C8H13ClN2OS
    Purezza:98.43%
    Colore e forma:Solid
    Peso molecolare:220.72
  • TG2-IN-3h

    CAS:
    TG2-IN-3h is a highly selective, potent, cell-permeable fluorescent irreversible tissue transglutaminase (tg2) inhibitor
    Formula:C21H26N4O4S
    Purezza:99.34% - 99.76%
    Colore e forma:Solid
    Peso molecolare:430.52
  • Sirpiglenastat

    CAS:
    Sirpiglenastat (DRP-104) is a glutamine antagonist, a prodrug of DON, with antitumor activity that acts by suppressing the adaptive immune system.
    Formula:C22H27N5O5
    Purezza:98.01% - 98.37%
    Colore e forma:Solid
    Peso molecolare:441.48
  • IPN60090

    CAS:
    IPN60090: potent oral GLS1 inhibitor, IC50 of 31 nM, potential for anticancer and immunomodulation.
    Formula:C24H27F3N8O3
    Purezza:99.76%
    Colore e forma:Solid
    Peso molecolare:532.52
  • KCC009

    CAS:
    KCC009 is a potent and selective Transglutaminase 2 Inhibitor.
    Formula:C21H22BrN3O5
    Colore e forma:Solid
    Peso molecolare:476.32
  • ZED-1227

    CAS:
    <p>ZED-1227 (TAK-227) is a TG2 inhibitor with anticancer activity that blocks inflammation-induced TG2 expression and activation for the treatment of Celiac Diseas</p>
    Formula:C26H36N6O6
    Purezza:99.04%
    Colore e forma:Solid
    Peso molecolare:528.6
  • TGase2-IN-1

    CAS:
    TGase2-IN-1 (Compound 22) is an orally effective TGase2 inhibitor with an IC50 of 1.12 µM. It inhibits TGase2 in human retinal microvascular endothelial cells with a strikingly lower IC50 of 0.07 µM. The oral bioavailability of TGase2-IN-1 is 74.6%. Additionally, it can suppress retinal vascular leakage in a mouse model of diabetes induced by Streptozotocin.
    Formula:C23H25N3O3
    Colore e forma:Solid
    Peso molecolare:391.46