2. Signaling Pathways
  3. Cell Cycle/DNA Damage
    Epigenetics
  4. Sirtuin

Sirtuin

Sirtuin

Related Products

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Sirtuin (Sir2 proteins) are a class of proteins that possess either mono-ADP-ribosyltransferase, or deacylase activity, including deacetylase, desuccinylase, demalonylase, demyristoylase and depalmitoylase activity. Sirtuins regulate important biological pathways in bacteria, archaeaand eukaryotes. Sirtuins have been implicated in influencing a wide range of cellular processes like aging, transcription, apoptosis, inflammation and stress resistance, as well as energy efficiency and alertness during low-calorie situations. Sirtuins can also control circadian clocks and mitochondrial biogenesis.

Sirtuin Isoform Specific Products:

Sirtuin Isoform Comparison
Cat. No. Product Name Effect Purity Chemical Structure
  • HY-147233
    MIND4-19
    		Inhibitor 99.93%
    MIND4-19 is a potent SIRT2 inhibitor with an IC50 value of 7.0 μM. MIND4-19 can be used for researching Huntington's disease.
    MIND4-19
  • HY-19758A
    Sirtuin modulator 1
    		Modulator 99.85%
    Sirtuin modulator 1 is a modulator of SIRTl, a homolog of SIRT3, with EC1.5 of < 1 μM, extracted from patent WO 2010071853 A1, Compound No.4.
    Sirtuin modulator 1
  • HY-B0150S2
    Nicotinamide-13C6
    		Inhibitor 99.8%
    Nicotinamide-13C6 is the 13C-labeled Nicotinamide. Nicotinamide is a form of vitamin B3 that plays essential roles in cell physiology through facilitating NAD+ redox homeostasis and providing NAD+ as a substrate to a class of enzymes that catalyze non-redox reactions. Nicotinamide is an inhibitor of SIRT1.
    Nicotinamide-<sup>13</sup>C<sub>6</sub>
  • HY-N3504
    Ophiopogonin D'
    		Activator 99.85%
    Ophiopogonin D', isolated from the tubers of Ophiopogon japonicus, is a rare naturally occurring C29 steroidal glycoside. Ophiopogonin D' shows cytotoxic activity against two human tumor cell lines MG-63 and SNU387 with IC50s of 3.09 μM and 3.63 μM, respectively. Ophiopogonin D' activates SIRT1 in a dose-dependent manner.
    Ophiopogonin D'
  • HY-RS12954
    Sirt7 Mouse Pre-designed siRNA Set A
    		Inhibitor

    Sirt7 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Sirt7 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.
    Sirt7 Mouse Pre-designed siRNA Set A
    Sirt7 Mouse Pre-designed siRNA Set A
  • HY-123033C
    Nicotinamide riboside malate
    		Activator 98.04%
    Nicotinamide riboside malate, an orally active NAD+ precursor, increases NAD+ levels and activates SIRT1 and SIRT3. Nicotinamide riboside malate is a source of vitamin B3 (niacin) and enhances oxidative metabolism, protection against high fat diet-induced metabolic abnormalities. Nicotinamide riboside malate reduces cognitive deterioration in a transgenic mouse model of Alzheimer’s disease.
    Nicotinamide riboside malate
  • HY-N0182A
    Fisetin quarterhydrate
    		Activator 98.64%
    Fisetin quarterhydrate is a natural flavonol found in many fruits and vegetables with various benefits, such as antioxidant, anticancer, neuroprotection effects.
    Fisetin quarterhydrate
  • HY-RS12953
    SIRT7 Human Pre-designed siRNA Set A
    		Inhibitor

    SIRT7 Human Pre-designed siRNA Set A contains three designed siRNAs for SIRT7 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
    SIRT7 Human Pre-designed siRNA Set A
    SIRT7 Human Pre-designed siRNA Set A
  • HY-153104
    CrBKA
    		98.46%
    CrBKA is a fluorogenic small-molecule substrate of SIRT6 with weak activity.
    CrBKA
  • HY-123033
    Nicotinamide riboside
    		Activator
    Nicotinamide riboside, an orally active NAD+ precursor, increases NAD+ levels and activates SIRT1 and SIRT3. Nicotinamide riboside is a source of vitamin B3 (niacin) and enhances oxidative metabolism, protection against high fat diet-induced metabolic abnormalities. Nicotinamide riboside reduces cognitive deterioration in a transgenic mouse model of Alzheimer’s disease.
    Nicotinamide riboside
  • HY-161920
    SIRT3-IN-1
    		Inhibitor ≥98.0%
    SIRT3-IN-1 (compound 17f) is a SIRT3 inhibitor, with IC50 of 0.043 μM. SIRT3-IN-1 can be used in the research of acute leukemia (AML).
    SIRT3-IN-1
  • HY-N2740
    Agalloside
    		≥98.0%
    Agalloside is a neural stem cell differentiation activator that can be found in Aquilaria agallocha.
    Agalloside
  • HY-155725
    Z26395438
    		Inhibitor 99.59%
    Z26395438 (compound 1) is a potent Sirtuin-1 inhibitor, with an IC50 value of 1.6 μM.
    Z26395438
  • HY-Q49697
    Sirtuin modulator 3
    		Modulator 99.32%
    Sirtuin modulator 3 (compound 129) is a N-phenyl benzamide derivative, acts as a sirtuin modulator.
    Sirtuin modulator 3
  • HY-RS12948
    Sirt5 Mouse Pre-designed siRNA Set A
    		Inhibitor

    Sirt5 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Sirt5 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.
    Sirt5 Mouse Pre-designed siRNA Set A
    Sirt5 Mouse Pre-designed siRNA Set A
  • HY-W020111
    7-Chloro-4-(piperazin-1-yl)quinoline
    		Inhibitor 98.63%
    7-Chloro-4-(piperazin-1-yl)quinolone is an important scaffold in medicinal chemistry. 7-Chloro-4-(piperazin-1-yl)quinolone is a potent sirtuin inhibitor and also inhibits the serotonin uptake (IC50 of 50 μM). 7-Chloro-4-(piperazin-1-yl)quinolone exhibits antimalarial activity on D10 and K1 strains of P. falciparum with IC50s of 1.18 μM and 0.97 μM, respectively.
    7-Chloro-4-(piperazin-1-yl)quinoline
  • HY-130479
    AdipoR agonist 1
    		Activator ≥98.0%
    AdipoR agonist 1 (Compound 112254) is an agonist for adiponectin receptor (AdipoR), which activates the transcriptional regulators like peroxisome proliferator-activated receptors (PPARs), peroxisome proliferator-activated receptor gamma coactivator 1α (PGC-1α), sirtuin 1 (SIRT1), and adenylate-activated protein kinase (AMPK). AdipoR agonist 1 is utilized in preventive doping research.
    AdipoR agonist 1
  • HY-47822
    WAY-354574
    		≥98.0%
    WAY-354574 is an active molecule targeting deacetylase (Sirtuin) for the study of Huntington's disease (HD).
    WAY-354574
  • HY-15452R
    Selisistat (Standard)
    		Inhibitor
    Selisistat (Standard) is the analytical standard of Selisistat. This product is intended for research and analytical applications. Selisistat (EX-527) is a potent and selective SirT1 (Sir2 in Drosophila melanogaster) inhibitor with an IC50 of 123 nM for SirT1. Selisistat alleviates pathology in multiple animal and cell models of Huntington's disease.
    Selisistat (Standard)
  • HY-111303
    CHIC35
    		Inhibitor
    CHIC35, an analog of EX-527, is a potent and selective inhibitor of SIRT1 (IC50=0.124 μM). CHIC35 shows potential selective inhibition against SIRT1 over SIRT2 (IC50=2.8 μM) or SIRT3 (IC50>100 μM). CHIC35 has anti-inflammatory effects and can be used for CHARGE syndrome research.
    CHIC35
Cat. No. Product Name / Synonyms Application Reactivity
Sirtuin Isoform Comparison

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