EPI008

Histone Deacetylase (HDAC) Inhibitor Set I

Set includes 6 inhibitors

• UNSPSC-Code: 12352200
• NACRES: NA.41

Eigenschaften

• Versandbedingung: wet ice
• Lagertemp.: −20°C

Beschreibung

Allgemeine Beschreibung

A convenient set of six selected individual HDAC (Histone Deacetylase) inhibitors.

• Apicidin

CAS Number: 183506-66-3
Molecular Formula: C₃₄H₄₉N₅O₆
Molecular Weight: 623.8

• M344

CAS Number: 251456-60-7
Molecular Formula: C₁₆H₂₅N₃O₃
Molecular Weight: 307.39

• Sodium 4-phenylbutuyrate

CAS Number: 1716-12-7
Molecular Formula: C₁₀H₁₁O₂·Na
Molecular Weight: 186.2

• Splitomycin

CAS Number: 5690-03-9
Molecular Formula: C₁₃H₁₀O₂
Molecular Weight: 198.2

• Trichostatin A

CAS Number: 58880-19-6
Molecular Formula: C₁₇H₂₂N₂O₃
Molecular Weight: 302.4

• Valproic Acid, Sodium Salt

CAS Number: 1069-66-5
Molecular Formula: C₈H₁₅O₂·Na
Molecular Weight: 166.19

Biochem./physiol. Wirkung

• Apicidin - A potent, cell permeable inhibitor of histone deacetylase (IC₅₀ = 700 pM for parasitic histone deacetylase). Inhibits HeLa cell proliferation (IC₅₀ = 50-100 nM) and induces the transcriptional activation of p21 (WAF1) in a reversible manner. Also prevents H-ras-induced invasive phenotype of MCF-10A cells possibly by down regulating MMP-2 in a reversible manner.
• M344 - An amide analog of Trichostatin A that potently Inhibits histone deacetylases (IC₅₀ = 40 nM for rat liver HDAC and IC₅₀ = 100 nM for maize HDAC). Induces differentiation and inhibits proliferation (~2 μM) of murine erythroleukemia cells.
• Sodium 4-phenylbutuyrate - Inhibitor of histone deacetylase (HDAC). Anti-neoplastic agent and transcriptional regulator. Also acts as an inducer of tumor cytostasis and differentiation.
• Splitomycin - Potent inhibitor of yeast NAD+ dependent histone deacetylase Sir2p (IC₅₀= 60 μM). Sensitizes mammalian cells to a variety of DNA-damaging agents by abrogating Sir2p activity on p53. Acts by either altering or blocking access to the acetylated histone binding pocket.
• Trichostatin A - Potent, reversible inhibitor of histone deacetylase. Mediates the activation of O6- methylguanine-DNA methyltransferase (MGMT). May be involved in cell cycle progression of several cell types, induces cell growth arrest at both G1 and G2/M phases. In some cases induces apoptosis.
• Valproic acid sodium salt - A cell-permeable histone deacetylase 1 (HDAC1) inhibitor (IC₅₀ = 400 μM) that exhibits anticancer, anti-inflammatory and neuroprotective properties. Recently it has been reported that Valproic acid enables reprogramming of primary human fibroblasts with only two factors, Oct4 and Sox2, without the need for the oncogenes c-Myc or Klf4.

Sicherheitshinweise

• Piktogramme: GHS06,GHS08
• Signalwort: Danger
• H-Sätze: H300 + H310 + H330 - H315 - H317 - H319 - H335 - H361d
• P-Sätze: P202 - P260 - P280 - P302 + P352 + P310 - P304 + P340 + P310 - P305 + P351 + P338
• Gefahreneinstufungen: Acute Tox. 1 Inhalation - Acute Tox. 2 Dermal - Acute Tox. 2 Oral - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
• Zielorgane: Respiratory system
• Lagerklassenschlüssel: 6.1A - Combustible, acute toxic Cat. 1 and 2 / very toxic hazardous materials