Tucidinostat (Chidamide)

製品コードS8567 バッチS856705

印刷

化学情報

 Chemical Structure Synonyms HBI-8000, CS-055 Storage
(From the date of receipt)
3 years -20°C powder
1 years -80°C in solvent
化学式

C22H19FN4O2

分子量 390.41 CAS No. 1616493-44-7
Solubility (25°C)* 体外 DMSO 78 mg/mL (199.78 mM)
Water Insoluble
Ethanol Insoluble
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.

溶剤液(一定の濃度)を調合する

生物活性

製品説明 Tucidinostat (Chidamide, HBI-8000, CS-055) is a low nanomolar inhibitor of HDAC1, 2, 3, and 10, the HDAC isotypes well documented to be associated with the malignant phenotype with IC50 values of 95, 160, 67, 78 nM for HDAC1, 2, 3, 10 respectively.
in vitro

Chidamide inhibits class I HDACs 1-3, as well as class IIb HDAC10, at low nanomolar concentrations. Chidamide significantly induces histone H3 acetylation in both HeLa human cervical adenocarcinoma cells and human PBMC. Cell growth inhibition studies performed with 18 human-derived tumor cell lines demonstrate that chidamide and MS-275 similarly inhibit the in vitro growth of most, but not all, tumor cells in the low micromolar concentration range. However, chidamide, and to a lesser extent MS-275, is significantly less toxic to normal cells from human fetal kidney (CCC-HEK) and liver (CCC-HEL), indicating a differential cytotoxic response of normal cells versus cancerous cells to chidamide[1].

in vivo

In HCT-8 colorectal carcinoma mice xenografts, Chidamide shows in vivo antitumor activity. However, chidamide is well-tolerated at the above doses in the tumor-bearing animals, whereas the control drugs cause significant weight loss[1].

プロトコル(参考用のみ)

細胞アッセイ 細胞株 PBMC effector cells
濃度 0-400 nM
反応時間 0-400 nM
実験の流れ

Isolated PBMC effector cells are seeded into 6-well plates (6 x 106 cells/well) and treated with chidamide at different concentrations (0-400 nM) for different times (24-72 h).

動物実験 動物モデル Athymic nude mice (BALB/c-nu)
投薬量 12.5-50 mg/kg
投与方法 oral

Selleckの高級品が、幾つかの出版された研究調査結果(以下を含む)で使われた:

CYLD induces high oxidative stress and DNA damage through class I HDACs to promote radiosensitivity in nasopharyngeal carcinoma [ Cell Death Dis, 2024, 15(1):95] PubMed: 38287022
IKAROS expression drives the aberrant metabolic phenotype of macrophages in chronic HIV infection [ Clin Immunol, 2024, 260:109915] PubMed: 38286172
ADCT-602, a Novel PBD Dimer-containing Antibody-Drug Conjugate for Treating CD22-positive Hematologic Malignancies [ Mol Cancer Ther, 2024, 23(4):520-531] PubMed: 38324336
Synergistic effect of HDAC inhibitor Chidamide with Cladribine on cell cycle arrest and apoptosis by targeting HDAC2/c-Myc/RCC1 axis in acute myeloid leukemia [ Exp Hematol Oncol, 2023, 12(1):23] PubMed: 36849955
Preclinical development and evaluation of nanobody-based CD70-specific CAR T cells for the treatment of acute myeloid leukemia [ Cancer Immunol Immunother, 2023, 10.1007/s00262-023-03422-6] PubMed: 36932256
Low-Dose Chidamide Treatment Displays Sex-Specific Differences in the 3xTg-AD Mouse [ Biomolecules, 2023, 10.3390/biom13091324] PubMed: 37759724
Low-Dose Chidamide Treatment Displays Sex-Specific Differences in the 3xTg-AD Mouse [ Biomolecules, 2023, 13(9)1324] PubMed: 37759724
Single-cell profiling-guided combination therapy of c-Fos and histone deacetylase inhibitors in diffuse large B-cell lymphoma [ Clin Transl Med, 2022, 12(5):e798] PubMed: 35522945
HDAC1/3-dependent moderate liquid-liquid phase separation of YY1 promotes METTL3 expression and AML cell proliferation [ Cell Death Dis, 2022, 13(11):992] PubMed: 36424383
Targeting Class I Histone Deacetylases in Human Uterine Leiomyosarcoma [ Cells, 2022, 11(23)3801] PubMed: 36497061

長期の保管のために-20°Cの下で製品を保ってください。

人間や獣医の診断であるか治療的な使用のためにでない。

各々の製品のための特定の保管と取扱い情報は、製品データシートの上で示されます。大部分のSelleck製品は、推薦された状況の下で安定です。製品は、推薦された保管温度と異なる温度で、時々出荷されます。長期の保管のために必要とされてそれと異なる温度で、多くの製品は、短期もので安定です。品質を維持するが、夜通しの積荷のために最も経済的な貯蔵状況を用いてあなたの送料を保存する状況の下に、製品が出荷されることを、我々は確実とします。製品の受領と同時に、製品データシートの上で貯蔵推薦に従ってください。