109 Results for "

SIRT2

" in MedChemExpress (MCE) Product Catalog:
Products (109)

109 Results for "SIRT2" in MCE Product Catalog:

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Cat. No.: HY-136713
CAS No.: 143034-06-4
Target:  

Sirtuin

Research Areas:  

Neurological Disease Cancer

Sirt1/2-IN-5 is a SIRT1/SIRT2 inhibitor with human SIRT1 IC50 0.3 μM and human SIRT2 IC50 values 1.2 μM and pIC50 5.82. Sirt1/2-IN-5 inhibits NAD +-dependent deacetylase activity of SIRT1 and SIRT2. Sirt1/2-IN-5 can be used for the research of cancer, neurodegenerative disease [2].
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Cat. No.: HY-P80320
Synonyms: SIR2L, SIR2L2, SIRT2, NAD-dependent protein deacetylase SIRTuin-2, NAD-dependent protein defatty-acylase SIRTuin-2, Regulatory protein SIR2 homolog 2, SIR2-like protein 2

Host:  

Rabbit

Application:  

WB, ICC/IF, IP, FC

Reactivity:  

Human, Rat

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Cat. No.: HY-P85521A
Synonyms: FLJ35621; FLJ37491; NAD dependent deacetylase SIRTuin 2; NAD-dependent deacetylase SIRTuin-2; NAD-dependent protein deacetylase SIRTuin-2; Regulatory protein SIR2 homolog 2; Silencing information regulator 2 like; Silent information regulator 2; Silent mating type information regulation 2; Silent mating type information regulation 2 homolog; SIR 2; SIR2; SIR2 like; SIR2 like protein 2; Sir2 related protein type 2; SIR2, S. cerevisiae, homolog-loke 2; SIR2-like protein 2; SIR2L; SIR2L2; SIRT 2; SIRT2; SIRT2_HUMAN; SIRTuin; silent mating type information regulation 2 homolog; 2; S.cerevisiae; SIRTuin 2; SIRTuin type 2; SIRTuin2.

Host:  

Mouse

Application:  

WB, ICC/IF

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P702906
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: SIRT2; SIR2L2; Prev. SIR2L; SIRTuin (Silent Mating Type Information Regulation 2, S.Cerevisiae, Homolog) 2; NAD-Dependent Protein Defatty-Acylase SIRTuin-2; NAD-Dependent Deacetylase SIRTuin-2; NAD-Dependent Protein Deacetylase SIRTuin-2; Silent Informati
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-P703015
Purity:  ≥ 85%, as determined by reducing SDS-PAGE.
Synonyms: SIRT2; SIR2L2; Prev. SIR2L; SIRTuin (Silent Mating Type Information Regulation 2, S.Cerevisiae, Homolog) 2; NAD-Dependent Protein Defatty-Acylase SIRTuin-2; NAD-Dependent Deacetylase SIRTuin-2; NAD-Dependent Protein Deacetylase SIRTuin-2; Silent Informati
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-P85521
Synonyms: FLJ35621; FLJ37491; NAD dependent deacetylase SIRTuin 2; NAD-dependent deacetylase SIRTuin-2; NAD-dependent protein deacetylase SIRTuin-2; Regulatory protein SIR2 homolog 2; Silencing information regulator 2 like; Silent information regulator 2; Silent mating type information regulation 2; Silent mating type information regulation 2 homolog; SIR 2; SIR2; SIR2 like; SIR2 like protein 2; Sir2 related protein type 2; SIR2, S. cerevisiae, homolog-loke 2; SIR2-like protein 2; SIR2L; SIR2L2; SIRT 2; SIRT2; SIRT2_HUMAN; SIRTuin; silent mating type information regulation 2 homolog; 2; S.cerevisiae; SIRTuin 2; SIRTuin type 2; SIRTuin2.

Host:  

Mouse

Application:  

WB, ICC/IF

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-101278R
CAS No.: 1429749-41-6
Research Areas:  

Cancer

Thiomyristoyl (Standard) is the analytical standard of Thiomyristoyl (HY-101278). This product is intended for research and analytical applications. Thiomyristoyl is a potent and specific SIRT2 inhibitor with an IC50 of 28 nM.
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Cat. No.: HY-182412
CAS No.: 2375182-58-2
Target:  

Sirtuin

Research Areas:  

Cancer

NH4-6 is a SIRT2 inhibitor with an IC50 of 0.032 μM against SIRT2 and an IC50 of 3 μM against SIRT1. NH4-6 inhibits the deacetylase activity of SIRT1. As a cytotoxic agent, NH4-6 reduces cancer cell viability, suppresses anchorage-independent growth of cancer cells, induces acetylation of α-tubulin, and promotes acetylation of p53. NH4-6 can be used in the research of breast cancer .
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Cat. No.: HY-184534
CAS No.: 2098493-54-8
Target:  

PROTAC Linkers

Research Areas:  

Others

N-(4-Azidobutyl)-2-chloroacetamide is a PROTAC linker that can be used for the synthesis of PROTACs, such as PROTAC Sirt2 Degrader-1 (HY-103636) .
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Cat. No.: HY-101073R
CAS No.: 1105698-15-4
Research Areas:  

Cancer

Salermide (Standard) is the analytical standard of Salermide (HY-101073). This product is intended for research and analytical applications. Salermide is an inhibitor of Sirt1 and Sirt2; can cause strong cancer-specific apoptotic cell death.
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Cat. No.: HY-101465R
CAS No.: 330461-64-8
Research Areas:  

Neurological Disease

AK-1 (Standard) is the analytical standard of AK-1 (HY-101465). This product is intended for research and analytical applications. AK-1 is a potent, specific and cell-permeable SIRT2 inhibitor, with an IC50 of 12.5 μM.
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Cat. No.: HY-100578R
CAS No.: 304896-28-4
Research Areas:  

Cancer

AGK2 (Standard) is the analytical standard of AGK2 (HY-100578). This product is intended for research and analytical applications. AGK2 is a selective SIRT2 inhibitor with an IC50 of 3.5 μM. AGK2 inhibits SIRT1 and SIRT3 with IC50s of 30 and 91 μM, respectively.
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Cat. No.: HY-108986R
CAS No.: 96969-83-4
Research Areas:  

Cancer

JFD00244 (Standard) is the analytical standard of JFD00244 (HY-108986). This product is intended for research and analytical applications. JFD00244 is a sirtuin 2 (SIRT2) inhibitor, with anti-tumor effect. JFD00244 is also a Nsp-16 inhibitor against SARS-CoV-2 [2].
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Cat. No.: HY-133849
CAS No.: 849215-53-8
Target:  

Sirtuin

Research Areas:  

Cancer

Aristoforin, a hypericin derivative, inhibits the activities of SIRT1 and SIRT2. Aristoforin induces G1 phase cell cycle arrest, scavenges hydroxyl free radicals, and exhibits protective activity against Fe 2+-induced DNA breakage. Aristoforin can be used in studies related to breast cancer and colon adenocarcinoma [2] .
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Cat. No.: HY-153509
CAS No.: 1392810-44-4
Target:  

Sirtuin

Research Areas:  

Cancer

Sirtuin-IN-1 (Compound 18) is a SIRT1/2 inhibitor (IC50s: 6.2 μM and 4.2μM for SIRT1 and SIRT2, respectively). Sirtuin-IN-1 induces G1 cell cycle arrest. Sirtuin-IN-1 exhibits potent anti-cancer activity against glioma .
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Cat. No.: HY-185682
CAS No.: 1382354-26-8
Research Areas:  

Cancer

NCO-141 is a selective SIRT2 inhibitor with an IC50 of 0.5 μM. NCO-141 induces cell apoptosis via caspase activation and mitochondrial superoxide anion production. NCO-141 induces cell autophagy by increasing LC3-II levels and autophagosome accumulation. NCO-141 is applicable to relevant research on leukemia .
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Cat. No.: HY-W744757
CAS No.: 113950-01-9
Synonyms: Niacinamide-15N; Nicotinic acid amide-15N
Nicotinamide- 15N (Niacinamide- 15N) is the deuterium labeled Nicotinamide (HY-B0150). Nicotinamide is a form of vitamin B3 or niacin. Nicotinamide Hydrochloride inhibits SIRT2 activity (IC50: 2 μM). Nicotinamide also inhibits SIRT1. Nicotinamide increases cellular NAD+, ATP, ROS levels. Nicotinamide inhibits tumor growth and improves survival. Nicotinamide also has anti-HBV activity.
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Cat. No.: HY-B0150S4
Synonyms: Niacinamide-13C,15N; Nicotinic acid amide-13C,15N
Nicotinamide- 13C, 15N (Niacinamide- 13C, 15N) is the 13C- and 15N-labeled Nicotinamide (HY-B0150). Nicotinamide is a form of vitamin B3 or niacin. Nicotinamide Hydrochloride inhibits SIRT2 activity (IC50: 2 μM). Nicotinamide also inhibits SIRT1. Nicotinamide increases cellular NAD+, ATP, ROS levels. Nicotinamide inhibits tumor growth and improves survival. Nicotinamide also has anti-HBV activity [2] .
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Cat. No.: HY-15510S
Tenovin-6-d6 is the deuterium labeled Tenovin-6 (HY-15510). Tenovin-6, an analog of Tenovin-1 (HY-13423), is an activator of p53 transcriptional activity. Tenovin-6 inhibits the protein deacetylase activities of purified human SIRT1, SIRT2, and SIRT3 with IC50s of 21 μM, 10 μM, and 67 μM, respectively. Tenovin-6 also inhibits dihydroorotate dehydrogenase (DHODH).
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Cat. No.: HY-183870
CAS No.: 1382354-18-8
NCO-90 is a selective SIRT2 inhibitor with an IC50 of 1.0 μM. NCO-90 induces Apoptosis via Caspase activation and mitochondrial superoxide anion production, and also induces Autophagic cell death by increasing LC3-II levels and autophagosome accumulation. NCO-90 exhibits anticancer activity against leukemia. NCO-90 can be used in research related to acute lymphoblastic leukemia and acute myeloid leukemia [2].
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