EPI009

Histone Deacetylase (HDAC) Inhibitor Set II

Set includes 7 inhibitors

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

Propriétés

• Conditions d'expédition: wet ice
• Température de stockage: −20°C

Description

Description générale

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

• CI-994

CAS Number: 112522-64-2
Molecular Formula: C₁₅H₁₅N₃O₂
Molecular Weight: 269.3

• Panobinostat (LBH589)

CAS Number: 404950-80-7
Molecular Formula: C₂₁H₂₃N₃O₂
Molecular Weight: 349.43

• SAHA

CAS Number: 149647-78-9
Molecular Formula: C₁₄H₂₀N₂O₃
Molecular Weight: 264.3

• SBHA

CAS Number: 38937-66-5
Molecular Formula: C₈H₁₆N₂O₄
Molecular Weight: 204.22

• Scriptaid

CAS Number: 287383-59-9
Molecular Formula: C₁₈H₁₈N₂O₄
Molecular Weight: 326.35

• Trichostatin A

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

• Tubacin

CAS Number: 537049-40-4
Molecular Formula: C₄₁H₄₃N₃O₇S
Molecular Weight: 721.86

Actions biochimiques/physiologiques

• CI-994 - Cell-permeable. A histone deacetylase (HDAC) inhibitor: K_i values are 0.41, 0.75, >100 and >100 μM for HDAC1, HDAC3, HDAC6 and HDAC8, respectively. Displays significant antitumor activity in vitro and in vivo against a broad spectrum of murine and human tumor models.
• Panobinostat (LBH589) - Highly potent inhibitor of both histone deacetylase 1 (HDAC1) activity and tumour cell proliferation in vitro. The IC₅₀ values of HDAC isozymes HDAC1-IP Ac-H4, HDAC8, MALunselective, B61HDAC1 and B12HDAC6 are 0.23±0.06, 283±29, 75±4, 47±5 and 89±12 nM, respectively. And to A2780 proliferation, IC₅₀ value is 4.6±1.8 nM.
• SAHA - Potent, reversible inhibitor of histone deacetylase 1 (HDAC1) and 3 (HDAC3). Induces cell growth arrest at both G1 and G2 phases. Induces apoptosis.
• SBHA - Competitive histone deacetylase (HDAC) inhibitor that has been shown to inhibit HDAC1 (IC₅₀ = 0.25 μM) and HDAC3 (IC₅₀ = 0.30 μM). SBHA causes cell differentiation, cell cycle arrest, or apoptosis. SBHA also enhances cytotoxicity induced by Oxaliplatin in the colorectal cancer cell lines.
• Scriptaid - A relatively non-toxic Inhibitor of histone deacetylase (HDAC). Facilitates transcriptional activation (TGF-ß/Smad4) in both stable and transient receptor assays in a concentration-dependent manner. At ~2 μg/ml (6-8 μM) concentrations, results in a greater than 100-fold increase in histone acetylation in PANC-1 cells.
• 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.
• Tubacin - Tubacin (Tubulin acetylation inducer) is a highly potent, selective, reversible, and cell-permeable inhibitor of histone deacetylase 6 (HDAC6, IC₅₀ = 4 nM). Displays 1000-fold more selectivity for HDAC6 over other HDACs. It inhibits α-tubulin deacetylation in mammalian cells. Unlike trichostatin A (TSA), which is a broad spectrum HDAC inhibitor, tubacin is specific for the tubulin deacetylase activity of HDAC6. Tubacin causes increased acetylation of α-tubulin, accumulation of polyubiquitinated proteins, and apoptosis. It does not affect global histone deacetylation, gene-expression profiling, or cell cycle progression mediated α-tubulin deacetylation in mammalian cells.

Informations sur la sécurité

• Pictogrammes: GHS06,GHS08,GHS05
• Mention d'avertissement: Danger
• Mentions de danger: H301 + H331,H315,H318,H341,H360,H373
• Conseils de prudence: P202 - P280 - P301 + P310 - P302 + P352 - P304 + P340 + P311 - P305 + P351 + P338
• Classification des risques: Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1 - Muta. 2 - Repr. 1A - Skin Irrit. 2 - STOT RE 2 Inhalation
• Code de la classe de stockage: 6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): 188.6 °F - closed cup
• Point d'éclair (°C): 87 °C - closed cup