1. Cell Cycle/DNA Damage Epigenetics Apoptosis Metabolic Enzyme/Protease
  2. HDAC Apoptosis Drug Metabolite
  3. DL-Sulforaphane N-acetyl-L-cysteine

DL-Sulforaphane N-acetyl-L-cysteine  (Synonyms: SFN-NAC)

目录号: HY-132242
产品使用指南

DL-Sulforaphane N-acetyl-L-cysteine (SFN-NAC) 是一种具有口服活性的 HDAC 抑制剂,也是sulforaphane (HY-13755) 代谢物且具有更长的半衰期和更好的血脑屏障通透性。DL-Sulforaphane N-acetyl-L-cysteine 通过 ERK 途径激活自噬介导的 α-微管蛋白表达下调,可用于癌症的研究。

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DL-Sulforaphane N-acetyl-L-cysteine Chemical Structure

DL-Sulforaphane N-acetyl-L-cysteine Chemical Structure

CAS No. : 334829-66-2

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1 mg ¥990
3 - 4 周
5 mg ¥4140
3 - 4 周
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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

DL-Sulforaphane N-acetyl-L-cysteine (SFN-NAC) is an orally active HDAC inhibitor and metabolite of sulforaphane (HY-13755) with longer half-life and better blood-brain barrier permeability. DL-Sulforaphane N-acetyl-L-cysteine activates autophagy-mediated downregulation of α-tubulin expression through the ERK pathway and can be used in cancer research[1][2].

体外研究
(In Vitro)

SFN-NAC (24 h) 会降低细胞活力,HA 细胞,U87MG 细胞,U373MG 细胞和 U87/TR 细胞的 IC50 值分别为 60.08 μM,35.20 μM,39.11 μM,36.20 μM[1]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Cycle Analysis[1]

Cell Line: U87MG and U373MG cells
Concentration: 0, 30 μM
Incubation Time: 24 h
Result: Induced cell-cycle arrest in the G2/M phase and triggered apoptosis at the same time.

Western Blot Analysis[1]

Cell Line: U87MG and U373MG cells
Concentration: 0, 10, 20, 30, 40, 50μM
Incubation Time: 24 h
Result: Activated ERK1/2 (Thr202/Tyr204), downregulated α-tubulin, and induced autophagy in a dose-dependent manner.

Cell Viability Assay[1]

Cell Line: HA, U87MG, U373MG and U87/TR cells
Concentration: 0, 10, 20, 30, 40, 50, 60, 70, 80, 90 μM for HA and U87MG cells or 0, 10, 20, 30, 40, 50, 60 μM for U373MG and U87/TR cells
Incubation Time: 24 h
Result: Decreased the cell viability of these cell lines in a dose-dependent manner.
体内研究
(In Vivo)

SFN-NAC (10 μmol; 6 h; Oral gavage; single dose) 显着抑制小鼠结肠粘膜中的 HDAC 活性[2]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: mice[2]
Dosage: 10 μmol
Administration: Oral gavage; 6 h; single dose
Result: Significantly inhibited HDAC activity in mouse colon mucosa.
分子量

340.48

Formula

C11H20N2O4S3

CAS 号
Unlabeled CAS

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
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  • 稀释计算器

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The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
DL-Sulforaphane N-acetyl-L-cysteine
目录号:
HY-132242
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