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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T12922 | Sirtuin modulator 1 | SRT3025 Hydrochloride | Sirtuin |
Sirtuin modulator 1 (SRT3025 Hydrochloride) is a modulator of SIRT1 with EC1.5 of < 1 μM. | |||
T79903 | Sirtuin-1 inhibitor 1 | Sirtuin | |
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. | |||
T5618 | AK-1 | Sirtuin | |
AK-1 is a sirtuin 2 (SIRT2) inhibitor (IC50:12.5 µM).that prevents hippocampal neurodegeneration in Alzheimer's disease models and induces cell cycle arrest in colon carcinoma cells. | |||
T12918 | SIRT-IN-1 | Sirtuin | |
SIRT-IN-1 is a potent SIRT1/2/3 inhibitor(IC50s of 15, 10, 33 μM, respectively). | |||
T9648 | SIRT1-IN-1 | Antiviral , Sirtuin | |
SIRT1-IN-1 is a selective inhibitor of SIRT1 with an IC50 of 205 nM. SIRT1-IN-1 is an inhibitor of cytomegalovirus (CMV) with antiviral activity. | |||
T1919 | Tenovin-1 | Tenovin 1 | Mdm2 , Dehydrogenase , Sirtuin , p53 , Autophagy |
Tenovin-1 inhibits protein-deacetylating activities of SirT1 and SirT2 and protects against MDM2-mediated p53 degradation, which involves ubiquitination. | |||
T4328 | OSS_128167 | SIRT6-IN-1 | HBV , Sirtuin |
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). | |||
T6671 | Sirtinol | Apoptosis , Sirtuin , Autophagy | |
Sirtinol is a selective SIRT1/2 inhibitor (IC50: 131/38 μM). | |||
T9320 | YK-3-237 | B-[2-Methoxy-5-[(1E)-3-oxo-3-(3,4,5-trimethoxyphenyl)-1-propen-1-yl]phenyl]boronic acid | Sirtuin |
YK-3-237 (B-[2-Methoxy-5-[(1E)-3-oxo-3-(3,4,5-trimethoxyphenyl)-1-propen-1-yl]phenyl]boronic acid) reduces acetylation of mtp53 and exhibits anti-proliferative effects toward triple-negative breast cancer (TNBC) cells ca... | |||
T5096 | SRT 1720 | Sirtuin , Autophagy | |
SRT 1720 is a selective activator of human SIRT1 (EC1.5: 0.16 μM) and is >230-fold less potent for SIRT2 and SIRT3. | |||
T8346 | SRT 1460 | SRT1460 | Sirtuin |
SRT 1460 is a SIRT1 activator. | |||
T22595 | B2 | Linazolamide intermediate B impurity 2,CPNQ,5-[4-(4-Chlorobenzoyl)-1-piperazinyl]-8-nitroquinoline | Others , Sirtuin |
B2 (Linazolamide intermediate B impurity 2) promotes inclusion formation in cellular models of Huntington's disease and Parkinson's disease | |||
T7058 | Selisistat S-enantiomer | EX-527 S-enantiomer,EX-527 (S-enantiomer) | Sirtuin |
Selisistat S-enantiomer (EX-527 S-enantiomer) is an effective and specific SIRT1 inhibitor (IC50 = 98 nM) and shows >200-fold selectivity against SIRT2/3. | |||
T12920 | Sirt2-IN-1 | Sirtuin | |
Sirt2-IN-1 is an inhibitor of sirtuin 2 (IC50 = 163 nM). | |||
T77653 | Z26395438 | Sirtuin | |
Z26395438 is an inhibitor of Sirtuin-1 with IC50 of 1.6 μM. | |||
T12921 | SIRT5 inhibitor 1 | Sirtuin | |
SIRT5 inhibitor 1 is a potent and selective inhibitor of human Sirtuin 5 deacylase (IC50: 0.11 μM). sIRT5 inhibitor 1 is associated with ageing-related diseases. | |||
T21679 | 4'-bromo-Resveratrol | Sirtuin | |
4'-bromo-Resveratrolis a potent inhibitor of the deacetylases sirtuin 1 (SIRT1) and 3 (SIRT3) | |||
T16932 | SRT 2183 | Apoptosis , Sirtuin | |
SRT 2183 is a selective activator of Sirtuin-1 (SIRT1, EC1.5 : 0.36 μM). | |||
Fr13587 | 7-Chloro-4-(piperazin-1-yl)quinoline | ||
7-Chloro-4-(piperazin-1-yl)quinolone is an important scaffold in medicinal chemistry. It exhibited either alone or as hybrid with other active pharmacophores diverse pharmacological profiles. 7-Chloro-4-(piperazin-1-yl)q... | |||
T4S0800 | Demethyleneberberine | P450 , NOS , NF-κB , HIF , AMPK | |
Demethyleneberberine, which is composed of a potential antioxidant structure, could penetrate the membrane of mitochondria and accumulate in mitochondria either in vitro or in vivo.Demethyleneberberine suppresses CYP2E1,... |