CymitQuimica logo
Sirtuina

Sirtuina

Le sirtuine sono una famiglia di deacetilasi dipendenti dal NAD+ che svolgono un ruolo cruciale nella regolazione di processi cellulari come la riparazione del DNA, l'invecchiamento, il metabolismo e la resistenza allo stress. Le sirtuine influenzano la riparazione del DNA deacetilando le proteine coinvolte nelle vie di riparazione, modulandone così l'attività. Gli inibitori e gli attivatori delle sirtuine sono strumenti preziosi nella ricerca sull'invecchiamento, il cancro e le malattie metaboliche, dove la regolazione della riparazione del DNA e della longevità cellulare è di interesse. Presso CymitQuimica, offriamo una gamma di modulatori di sirtuine di alta qualità per supportare la tua ricerca sulla riparazione del DNA, l'invecchiamento cellulare e la regolazione metabolica.

Trovati 88 prodotti di "Sirtuina"

Ordinare per

Purezza (%)
0
100
|
0
|
50
|
90
|
95
|
100
prodotti per pagina.
  • Ophiopogonin D'

    CAS:
    <p>Ophiopogonin D' can activate SIRT1 in a dose-dependent manner. Ophiopogonin D' also noncompetitively inhibits UGT1A6 and UGT1A10.</p>
    Formula:C44H70O16
    Purezza:99.77%
    Colore e forma:Solid
    Peso molecolare:855.02
  • SRT 2104

    CAS:
    <p>SRT 2104 (GSK2245840) is a selective and brain-permeable SIRT1 activator.</p>
    Formula:C26H24N6O2S2
    Purezza:98.34% - 99.82%
    Colore e forma:Solid
    Peso molecolare:516.64
  • OSS_128167

    CAS:
    OSS_128167 (SIRT6-IN-1) is a specific SIRT6 inhibitor, and for SIRT6(IC50=89 μM), SIRT1(IC50=1578 μM) and SIRT2(IC50=751 μM).
    Formula:C19H14N2O6
    Purezza:97.47% - 98.6%
    Colore e forma:Solid
    Peso molecolare:366.32
  • AGK7

    CAS:
    AGK7 is an AGK2 control; it's a less selective SIRT2 inhibitor, with IC50s >5 μM for SIRT3, and >50 μM for SIRT1/2.
    Formula:C23H13Cl2N3O2
    Purezza:98.31%
    Colore e forma:Solid
    Peso molecolare:434.27
  • SRT 2183

    CAS:
    <p>SRT 2183 is a selective activator of Sirtuin-1 (SIRT1, EC1.5 : 0.36 μM).</p>
    Formula:C27H24N4O2S
    Purezza:97.86%
    Colore e forma:Solid
    Peso molecolare:468.57
  • AK-7

    CAS:
    <p>AK-7 is a brain-permeable SIRT2 inhibitor and to characterize its cholesterol-reducing properties in neuronal models with an IC50 of 15.5 μM.</p>
    Formula:C19H21BrN2O3S
    Purezza:98.43% - 99.34%
    Colore e forma:Solid
    Peso molecolare:437.35
  • Fisetin

    CAS:
    Fisetin belongs to a group of natural flavonols with anti-inflammatory, antioxidant, anti-tumor, anti-aging and neuroprotective effects. Cost effective and quality assured.
    Formula:C15H10O6
    Purezza:94.14% - 99.05%
    Colore e forma:Yellow To Brown Crystalline Powder
    Peso molecolare:286.24
  • 4'-bromo-Resveratrol

    CAS:
    <p>4'-bromo-Resveratrolis a potent inhibitor of the deacetylases sirtuin 1 (SIRT1) and 3 (SIRT3)</p>
    Formula:C14H11BrO2
    Purezza:99.00%
    Colore e forma:Solid
    Peso molecolare:291.14
  • SIRT7 inhibitor 97491

    CAS:
    SIRT7 inhibitor 97491 is an HDAC inhibitor with high specificity for SIRT7 (IC50 = 325 nM). SIRT7 inhibitor 97491 promotes apoptosis through caspase pathway.
    Formula:C15H12ClN3O
    Purezza:99.79%
    Colore e forma:Solid
    Peso molecolare:285.73
  • Tenovin-6 Hydrochloride

    CAS:
    Tenovin-6 HCl: Inhibits SIRT1 (21µM), SIRT2 (10µM), HDAC8; potent p53 activator.
    Formula:C25H35ClN4O2S
    Purezza:99.36%
    Colore e forma:Solid
    Peso molecolare:491.09
  • SRT 1460

    CAS:
    <p>SRT 1460 is a SIRT1 activator.</p>
    Formula:C26H29N5O4S
    Purezza:98.25%
    Colore e forma:Solid
    Peso molecolare:507.6
  • Cambinol

    CAS:
    Cambinol is a SIRT1/2 inhibitor (IC50: 56/59 μM), non-competitive with NAD, weak on SIRT5, and prompts apoptosis in lymphoma cells.
    Formula:C21H16N2O2S
    Purezza:98.02% - 99.83%
    Colore e forma:Solid
    Peso molecolare:360.43
  • Sirtinol

    CAS:
    Sirtinol is a selective SIRT1/2 inhibitor (IC50: 131/38 μM).
    Formula:C26H22N2O2
    Purezza:97.12% - 99.96%
    Colore e forma:Solid
    Peso molecolare:394.47
  • B2

    CAS:
    B2 (Linazolamide intermediate B impurity 2) promotes inclusion formation in cellular models of Huntington's disease and Parkinson's disease
    Formula:C20H17ClN4O3
    Purezza:99.66%
    Colore e forma:Solid
    Peso molecolare:396.83
  • MDL-800

    CAS:
    MDL-800 is a SIRT6 modulator with antitumor activity for the study of hepatocellular carcinoma and non-small cell lung cancer.
    Formula:C21H16BrCl2FN2O6S2
    Purezza:99.95% - 99.96%
    Colore e forma:Solid
    Peso molecolare:626.3
  • SIRT5 inhibitor 5

    CAS:
    SIRT5 inhibitor 5 is a selective and substrate-competitive SIRT5 inhibitor, which does not occupy the NAD+ binding pocket,cancer and metabolism-related disease.
    Formula:C21H14ClN3O3S
    Purezza:99.33%
    Colore e forma:Solid
    Peso molecolare:423.87
  • SIRT5 inhibitor 2

    CAS:
    SIRT5 inhibitor 2 (compound 49) has inhibitory activity through SIRT5-dependent deacetylation and cancer and neurodegenerative diseases.
    Formula:C18H12Cl2N2O3S
    Purezza:99.38% - 99.87%
    Colore e forma:Solid
    Peso molecolare:407.27
  • SIRT2-IN-9

    CAS:
    SIRT2-IN-9: selective SIRT2 inhibitor; IC50=1.3μM; halts MCF-7 cell growth; for cancer study.
    Formula:C21H22N6OS2
    Purezza:97.6%
    Colore e forma:Solid
    Peso molecolare:438.57
  • SIRT5 inhibitor 6

    CAS:
    SIRT5 inhibitor 6 is Sirtuin 5 inhibitor for sepsis-associated acute kidney injury (AKI) modulates protein succinylation and pro-inflammatory cytokine release.
    Formula:C21H28N6O4S
    Purezza:99.84%
    Colore e forma:Solid
    Peso molecolare:460.55
  • Sirt2-IN-1

    CAS:
    Sirt2-IN-1 is an inhibitor of sirtuin 2 (IC50 = 163 nM).
    Formula:C28H27N7O2S2
    Purezza:99.57% - 99.84%
    Colore e forma:Solid
    Peso molecolare:557.69
  • SIRT5 inhibitor 4

    CAS:
    SIRT5 inhibitor 4 (compound 11) is a dose-dependent and selective SIRT5 (Sirtuin5) inhibitorand no inhibitory effect on SIRT1/2/3,anticancer.
    Formula:C18H15N3O4S
    Purezza:99.97%
    Colore e forma:Solid
    Peso molecolare:369.39
  • SIRT5 inhibitor 1

    CAS:
    SIRT5 inhibitor 1 targets human Sirtuin 5 deacylase, with an IC50 of 0.11 μM, linked to aging diseases.
    Formula:C31H39FN6O6S2
    Purezza:97.8%
    Colore e forma:Solid
    Peso molecolare:674.81
  • SIRT6-IN-5

    CAS:
    SIRT6-IN-5: potent, selective SIRT6 inhibitor; IC50=34 μM; immunosuppressive, enhances chemo, boosts H3K9 acetylation, glucose uptake, curbs T-cell growth.
    Formula:C19H14N2O6
    Purezza:98.77%
    Colore e forma:Solid
    Peso molecolare:366.32
  • Sirtuin modulator 1

    CAS:
    Sirtuin modulator 1 (SRT3025 Hydrochloride) is a modulator of SIRT1 with EC1.5 of < 1 μM.
    Formula:C31H32ClN5O2S2
    Purezza:99.63%
    Colore e forma:Solid
    Peso molecolare:606.2
  • WAY-354574

    CAS:
    WAY-354574 is an active compound that targets the deacetylase Sirtuin, utilized in research focused on Huntington's disease (HD) [1].
    Formula:C20H23ClN2O3S
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:406.93
  • Sirtuin-1 inhibitor 1

    CAS:
    <p>Sirtuin-1 inhibitor 1 is an inhibitor against deacetylase-1 (Sirtuin-1) and can be used to study senescence and cell death in the organism.</p>
    Formula:C20H17N3O2
    Purezza:99.1%
    Colore e forma:Solid
    Peso molecolare:331.37
  • Epigenetic factor-IN-1

    CAS:
    <p>Epigenetic factor-IN-1 (40569Z) is an epigenetic factor inhibitor that exhibits potent binding affinity for SIRT7.</p>
    Formula:C32H34FN5O6S2
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:667.77
  • SRT3657

    CAS:
    <p>SRT3657 is a brain-permeable SIRT1 activator, has neuroprotective effect.</p>
    Formula:C40H54N8O6S
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:774.97
  • SIRT5 inhibitor 7

    CAS:
    SIRT5 inhibitor 7 , a substrate-competitive and selective SIRT5 inhibitor, significantly attenuated renal dysfunction and pathological damage in AKI mice.
    Formula:C28H32ClN7O3S
    Purezza:99.77%
    Colore e forma:Solid
    Peso molecolare:582.12
  • SIRT-IN-1

    CAS:
    <p>SIRT-IN-1 is a potent SIRT1/2/3 inhibitor(IC50s of 15, 10, 33 μM, respectively).</p>
    Formula:C19H27N5O2S
    Purezza:99.29%
    Colore e forma:Solid
    Peso molecolare:389.52
  • SIRT6-IN-3

    CAS:
    SIRT6-IN-3 (compound 8a), a selective SIRT6 inhibitor (IC50 = 7.49 μM), impedes the proliferation of pancreatic ductal adenocarcinoma (PDAC) cells and prompts
    Formula:C21H30Br3ClN6S
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:673.73
  • SIRT-IN-6

    CAS:
    <p>SIRT-IN-6 (Compound 14) is a pan-inhibitor of SIRT1/2/3 with an IC50 value of &gt;50 μM. It shows potential as a research agent for studies involving metabolic disorders, inflammation, cancer, and neurodegenerative diseases.</p>
    Formula:C7H4ClN3OS
    Colore e forma:Solid
    Peso molecolare:213.644
  • SIRT1-IN-5

    CAS:
    SIRT1-IN-5 (215) is a modulator of NAD-dependent deacetylase SIRT1 with potential applications in cancer and cellular signaling research.
    Formula:C21H17N3O3S
    Purezza:99.97%
    Colore e forma:Solid
    Peso molecolare:391.44
  • MC3138

    CAS:
    MC3138 is a selective SIRT5 activator showing anti-tumor effects in PDAC cells.
    Formula:C25H25NO6
    Purezza:99.57%
    Colore e forma:Solid
    Peso molecolare:435.47
  • Sirtuin-IN-2


    Sirtuin-IN-2 (compound 20) is an inhibitor of Sirtuin5, a key target in leukemia and breast cancer.
    Formula:C28H46N8O6S
    Colore e forma:Solid
    Peso molecolare:622.78
  • SIRT6 activator 2

    CAS:
    SIRT6 activator2 (compound 31) is a sirtuin6 activator known for its anti-lipid accumulation properties. It significantly downregulates LXR, SREBP-1c, and their target genes, making it valuable for research into lipid metabolism-related diseases.
    Formula:C23H23N3O6
    Colore e forma:Solid
    Peso molecolare:437.45
  • DCHC

    CAS:
    <p>DCHC is an activator of SIRT1, but it does not induce SIRT1 expression. This compound can be utilized in studies related to mitochondrial damage.</p>
    Formula:C15H8Cl2O3
    Colore e forma:Solid
    Peso molecolare:307.128
  • MDL-811

    CAS:
    <p>MDL-811, an allosteric activator of SIRT6, markedly enhances the deacetylation of histone H3 at lysine residues 9, 18, and 56 (H3K9Ac, H3K18Ac, and H3K56Ac),</p>
    Formula:C25H25BrCl2FN3O5S2
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:681.42

    Ref: TM-T81831

    5mg
    Fuori produzione
    50mg
    Fuori produzione
    Prodotto fuori produzione