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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-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.
PC-25498

SIRT2 inhibitor AF8

SIRT2 inhibitor

SIRT2 inhibitor AF8 is a potent, subtype selective SIRT2 inhibitor with IC50 of 0.06 uM.
PC-25497

SIRT2 inhibitor 24a

SIRT2 inhibitor

SIRT2 inhibitor 24a is a potent, subtype selective SIRT2 inhibitor with IC50 of 0.85 uM.
PC-25496

SIRT2 inhibitor RW-78

SIRT2 inhibitor

SIRT2 inhibitor RW-78 is a potent, ubtype selective, NAD+ independent SIRT2 inhibitor with IC50 of 26 nM, has high selective against SIRT1, 3 and 5, shows cellular target engagement via NanoBRET assays in HEK293T cells with EC50 of 15 nM.

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