382177

HDAC Inhibitor XIX, Compound 2

The HDAC Inhibitor XIX, Compound 2, also referenced under CAS 6953-61-3, controls the biological activity of HDAC. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.

• 別名: HDAC Inhibitor XIX, Compound 2, 1-Naphthohydroxamic Acid, N-Hydroxynaphthalene-1-carboxamide, Histone Deacetylase Inhibitor XIX
• 実験式（ヒル表記法）: C₁₁H₉NO₂
• CAS番号: 6953-61-3
• 分子量: 187.19
• MDL番号: MFCD00059546
• UNSPSCコード: 12352200

特性

• 品質水準: 100
• アッセイ: ≥97% (HPLC)
• フォーム: solid
• メーカー／製品名: Calbiochem^®
• 保管条件: OK to freeze; protect from light
• 色: white
• 溶解性: DMSO: 50 mg/mL
• 輸送温度: ambient
• 保管温度: 2-8°C
• InChI: 1S/C11H9NO2/c13-11(12-14)10-7-3-5-8-4-1-2-6-9(8)10/h1-7,14H,(H,12,13)
• InChI Key: JRZGPWOEHDOVMC-UHFFFAOYSA-N

詳細

詳細

A cell-permeable aryl-hydroxamate compound that selectively inhibits the activity of HDAC8 (IC₅₀ = 14 µM) over class I HDAC1 and class II HDAC6 (IC₅₀ >100 µM) without affecting the overall H4 acetylation level in BE(2)-C cultures even at concentrations as high as 20 µM. HDAC8 downregulation by either Compound 2 (10 to 40 µM) or siRNA in neuroblastoma cultures is reported to result in growth inhibition accompanied by neurite-like morphological changes. Compound 2 effectively enhances tubulin acetylation in both HeLa and HEK 293 cultures, indicating that alternative cellular enzyme(s) other than HDAC6 can be targeted for regulating tubulin acetylation.

包装

Packaged under inert gas

警告

Toxicity: Standard Handling (A)

再構成

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C.

その他情報

Oehme, I., et al. 2009. Expert Opin. Investig. Drugs18, 1605.
Oehme, I., et al. 2009. Clin. Cancer Res.15, 91.
KrennHrubec, K., et al. 2007. Bioorg. Med. Chem. Lett.17, 2874.

法的情報

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

安全性情報

• 保管分類コード: 11 - Combustible Solids
• WGK: WGK 3
• 引火点(°F): Not applicable
• 引火点(℃): Not applicable