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Cat. No. Product Name Information
PC-42642

SRT1720

SIRT1 activator

SRT1720 (SRT-1720) is a potent, selective SIRT1 activator with EC1.5 of 0.16 uM.
PC-45037

AK-7

SIRT2 inhibitor

AK-7 is a potent, selective and brain-permeable SIRT2 inhibitor with IC50 of 15.5 uM.
PC-42395

AK-1

SIRT2 inhibitor

AK-1 is a potent, selective and brain-permeable SIRT2 inhibitor with IC50 of 12.5 uM.
PC-42309

Salermide

SIRT1/SIRT2 inhibitor

Salermide is a potent Sirtuin inhibitor with IC50 of 76 and 45 uM for SIRT1 and SIRT2, respectively.
PC-25603

SIRT3 activator 31

SIRT3 agonist

SIRT3 activator 31 is a specific, cellular active small molecule activator of mitochondrial SIRT3 with binding KD of 32 uM, binds stronger to Sirt3 than to Sirt5.
PC-25602

MC3215

SIRT5 agonist

MC3215 is a specific, cellular active small molecule activator of mitochondrial SIRT5 with binding KD of 28 uM, increases in vitro Sirt5 deacetylase activity and elicits similar effects to Sirt5 overexpression.
PC-25601

MC2606

SIRT1 agonist

MC2606 is a potent, selective activator of SIRT1, MC2606 (1 uM) induces H4K16 deacetylation in HaCaT cells.
PC-25567

SIRT3 activator SZC-6

SIRT3 activator

SIRT3 activator SZC-6 is a selective small molecule SIRT3 activator, increases SIRT3 deacetylation activitywith EC50 of 23.2 uM, binds directly to SIRT3 with SPR KD of 15 uM.
PC-25519

Kuwanon C

SIRT1 inhibitor, OATP2B1 inhibitor

Kuwanon C (KWN-C, Mulberrin) is an effective inhibitor of organic anion-transporting polypeptide 2B1 (OATP2B1)-mediated estrone-3-sulfate (E3S) uptake with IC50 of 1.8 uM, also inhibits SIRT1 activity via targeting activity of the TGF-β1-Smad2/3-JNK1 signaling pathway.
PC-25501

Tenovin-6 hydrochloride

SIRT2 inhibitor

Tenovin-6 hydrochloride is a small-molecule p53 activator, inhibits purified human SirT1 deacetylase activity in vitro with IC50 of 21 μM and human SirT2 activity with IC50 of 10 μM.
PC-25500

Tenovin-6

SIRT2 inhibitor

Tenovin-6 is a small-molecule p53 activator, inhibits purified human SirT1 deacetylase activity in vitro with IC50 of 21 μM and human SirT2 activity with IC50 of 10 μM.
PC-25499

SIRT2 inhibitor KPM-2

SIRT2 inhibitor

KPM-2 is a potent, selective, substrate-competitive sirtuin-2 (SIRT2) inhibitor with IC50 of 55 nM, >25-fold selective over SIRT1 and SIRT3.

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