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. |