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  1. MAPK/ERK Pathway Autophagy
  2. p38 MAPK Autophagy
  3. Ferulic acid methyl ester

Ferulic acid methyl ester  (Synonyms: 阿魏酸甲酯; Methyl ferulate)

目錄號: HY-W018643 純度: 99.89%
COA 產品使用指南

Ferulic acid methyl ester (Methyl ferulate) 是從 Stemona tuberosa 中分到的阿魏酸衍生物,具有抗氧化、抗炎作用。Ferulic acid methyl ester 能夠透過細胞膜和血腦屏障,清除自由基,可用于神經退行性疾病的研究。在原發(fā)性骨髓源性巨噬細胞中,Ferulic acid methyl ester 抑制 COX-2 的表達,降低 p-p38 和 p-JNK 的水平。

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Ferulic acid methyl ester Chemical Structure

Ferulic acid methyl ester Chemical Structure

CAS No. : 2309-07-1

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Free Sample (0.1 - 0.2 mg)   Apply now  
10 mM * 1 mL in DMSO ¥280
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500 mg ¥250
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1 g ¥400
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Customer Review

Other Forms of Ferulic acid methyl ester:

查看 p38 MAPK 亞型特異性產品:

  • 生物活性

  • 純度 & 產品資料

  • 參考文獻

生物活性

Ferulic acid methyl ester (Methyl ferulate) is a derivative of ferulic acid, isolated from Stemona tuberosa, with anti-inflammatory and antioxidant properties[1][2]. Ferulic acid methyl ester is a cell membrane and brain permeable compound, shows free radical scavenging ability, used in the research of neurodegenerative disorders[1]. Ferulic acid methyl ester inhibits COX-2 expression, blocks p-p38 and p-JNK in primary bone marrow derived-macrophages[2].

IC50 & Target[2]

p38

 

細胞效力
(Cellular Effect)
Cell Line Type Value Description References
A549 IC50
> 20 μg/mL
Compound: 17
Cytotoxicity against human A549 cells by MTT assay
Cytotoxicity against human A549 cells by MTT assay
[PMID: 29975532]
A549 IC50
> 50 μM
Compound: 1a
Cytotoxicity against human A549 cells after 72 hrs by alamar blue assay
Cytotoxicity against human A549 cells after 72 hrs by alamar blue assay
[PMID: 22954735]
Calu-1 IC50
> 50 μM
Compound: 1a
Cytotoxicity against human Calu1 cells after 72 hrs by alamar blue assay
Cytotoxicity against human Calu1 cells after 72 hrs by alamar blue assay
[PMID: 22954735]
HeLa IC50
5.55 μM
Compound: 1a
Cytotoxicity against human HeLa cells after 72 hrs by alamar blue assay
Cytotoxicity against human HeLa cells after 72 hrs by alamar blue assay
[PMID: 22954735]
HepG2 IC50
> 20 μg/mL
Compound: 17
Cytotoxicity against human HepG2 cells by MTT assay
Cytotoxicity against human HepG2 cells by MTT assay
[PMID: 29975532]
HOP-62 IC50
> 50 μM
Compound: 1a
Cytotoxicity against human HOP62 cells after 72 hrs by alamar blue assay
Cytotoxicity against human HOP62 cells after 72 hrs by alamar blue assay
[PMID: 22954735]
KB IC50
> 200 μM
Compound: 1c
Antitumor activity against KB cells by MTT assay
Antitumor activity against KB cells by MTT assay
[PMID: 17387015]
LOX IMVI IC50
> 50 μM
Compound: 1a
Cytotoxicity against human LOXIMVI cells after 72 hrs by alamar blue assay
Cytotoxicity against human LOXIMVI cells after 72 hrs by alamar blue assay
[PMID: 22954735]
M14 IC50
> 50 μM
Compound: 1a
Cytotoxicity against human M14 cells after 72 hrs by alamar blue assay
Cytotoxicity against human M14 cells after 72 hrs by alamar blue assay
[PMID: 22954735]
MDA-MB-231 IC50
> 20 μg/mL
Compound: 17
Cytotoxicity against human MDA-MB-231 cells by MTT assay
Cytotoxicity against human MDA-MB-231 cells by MTT assay
[PMID: 29975532]
NCI-H1299 IC50
> 50 μM
Compound: 1a
Cytotoxicity against human NCI-H1299 cells after 72 hrs by alamar blue assay
Cytotoxicity against human NCI-H1299 cells after 72 hrs by alamar blue assay
[PMID: 22954735]
NCI-H157 IC50
> 50 μM
Compound: 1a
Cytotoxicity against human NCI-H157 cells after 72 hrs by alamar blue assay
Cytotoxicity against human NCI-H157 cells after 72 hrs by alamar blue assay
[PMID: 22954735]
NCI-H1792 IC50
> 50 μM
Compound: 1a
Cytotoxicity against human NCI-H1792 cells after 72 hrs by alamar blue assay
Cytotoxicity against human NCI-H1792 cells after 72 hrs by alamar blue assay
[PMID: 22954735]
NCI-H460 IC50
> 50 μM
Compound: 1a
Cytotoxicity against human H460 cells after 72 hrs by alamar blue assay
Cytotoxicity against human H460 cells after 72 hrs by alamar blue assay
[PMID: 22954735]
體外研究
(In Vitro)

Ferulic acid methyl ester (25 μg/mL) has no cytotoxic effects on BMDMs after treatment for 6 h, 18 h, 48 h[2].
Ferulic acid methyl ester (Methyl ferulate; 5, 10, 25 μg/mL) suppresses TNFα, IL6, IFNγ but not IL10, inhibits NO generation at 10 and 25 μg/mL, in primary bone marrow derived-macrophages (BMDMs)[2].
Ferulic acid methyl ester (25 μg/mL) inhibits COX-2 expression, blocks p-p38 and p-JNK[2].

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

Cell Viability Assay[2]

Cell Line: Primary bone marrow derived-macrophages (BMDMs)
Concentration: 25 μg/mL
Incubation Time: 6 h, 18 h, 48 h
Result: Showed no cytotoxic effects on BMDMs.

Western Blot Analysis[2]

Cell Line: RAW 246.7 cells
Concentration: 10 μg/mL and 25 μg/mL
Incubation Time: For 1 h before stimulation with LPS
Result: Significantly suppressed COX-2 expression at 25 μg/mL.
分子量

208.21

Formula

C11H12O4

CAS 號
性狀

固體

顏色

Off-white to pink

中文名稱

阿魏酸甲酯

結構分類
初始來源
運輸條件

Room temperature in continental US; may vary elsewhere.

儲存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 2 years
-20°C 1 year
溶解性數據
細胞實驗: 

DMSO 中的溶解度 : ≥ 100 mg/mL (480.28 mM; 吸濕的 DMSO 對產品的溶解度有顯著影響,請使用新開封的 DMSO)

H2O 中的溶解度 : 2 mg/mL (9.61 mM; 超聲助溶)

* "≥" means soluble, but saturation unknown.

配制儲備液
濃度 溶劑體積 質量 1 mg 5 mg 10 mg
1 mM 4.8028 mL 24.0142 mL 48.0284 mL
5 mM 0.9606 mL 4.8028 mL 9.6057 mL
查看完整儲備液配制表

* 請根據產品在不同溶劑中的溶解度選擇合適的溶劑配制儲備液;一旦配成溶液,請分裝保存,避免反復凍融造成的產品失效。
儲備液的保存方式和期限:-80°C, 2 years; -20°C, 1 year。-80°C儲存時,請在2年內使用, -20°C儲存時,請在1年內使用。

* 備注:如您選擇水作為儲備液,請稀釋至工作液后,再用 0.22 μm 的濾膜過濾除菌后使用。

  • 摩爾計算器

  • 稀釋計算器

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

質量
=
濃度
×
體積
×
分子量 *

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

This equation is commonly abbreviated as: C1V1 = C2V2

濃度 (start)

C1

×
體積 (start)

V1

=
濃度 (final)

C2

×
體積 (final)

V2

動物實驗:

請根據您的 實驗動物和給藥方式 選擇適當的溶解方案。

以下溶解方案都請先按照 In Vitro 方式配制澄清的儲備液,再依次添加助溶劑:
——為保證實驗結果的可靠性,澄清的儲備液可以根據儲存條件,適當保存;體內實驗的工作液,建議您現用現配,當天使用;
以下溶劑前顯示的百分比是指該溶劑在您配制終溶液中的體積占比;如在配制過程中出現沉淀、析出現象,可以通過加熱和/或超聲的方式助溶

  • 方案 一

    請依序添加每種溶劑: 10% DMSO    40% PEG300    5% Tween-80    45% Saline

    Solubility: ≥ 2.5 mg/mL (12.01 mM); 澄清溶液

    此方案可獲得 ≥ 2.5 mg/mL(飽和度未知)的澄清溶液。

    1 mL 工作液為例,取 100 μL 25.0 mg/mL 的澄清 DMSO 儲備液加到 400 μL PEG300 中,混合均勻;再向上述體系中加入 50 μL Tween-80,混合均勻;然后再繼續(xù)加入 450 μL 生理鹽水 定容至 1 mL。

    生理鹽水的配制:將 0.9 g 氯化鈉,溶解于 ddH?O 并定容至 100 mL,可以得到澄清透明的生理鹽水溶液。
  • 方案 二

    請依序添加每種溶劑: 10% DMSO    90% (20% SBE-β-CD in Saline)

    Solubility: ≥ 2.5 mg/mL (12.01 mM); 澄清溶液

    此方案可獲得 ≥ 2.5 mg/mL(飽和度未知)的澄清溶液。

    1 mL 工作液為例,取 100 μL 25.0 mg/mL 的澄清 DMSO 儲備液加到 900 μL 20% 的 SBE-β-CD 生理鹽水水溶液 中,混合均勻。

    2 g SBE-β-CD(磺丁基醚 β-環(huán)糊精)粉末定容于 10 mL 的生理鹽水中,完全溶解至澄清透明。
動物溶解方案計算器
請輸入動物實驗的基本信息:

給藥劑量

mg/kg

動物的平均體重

g

每只動物的給藥體積

μL

動物數量

由于實驗過程有損耗,建議您多配一只動物的量
請輸入您的動物體內配方組成:
%
DMSO +
+
%
Tween-80 +
%
Saline
如果您的動物是免疫缺陷鼠或者體弱鼠,建議 DMSO 中的在最后工作液體系中的占比盡量不超過 2%。
方案所需 助溶劑 包括:DMSO ,均可在 MCE 網站選購。 ,Tween 80,均可在 MCE 網站選購。
計算結果
工作液所需濃度 : mg/mL
儲備液配制方法 : mg 藥物溶于 μL  DMSO(母液濃度為 mg/mL)。
您所需的儲備液濃度超過該產品的實測溶解度,以下方案僅供參考,如有需要,請與 MCE 中國技術支持聯系。
動物實驗體內工作液的配制方法 : 取 μL DMSO 儲備液,加入 μL 。 μL ,混合均勻至澄清,再加 μL Tween 80,混合均勻至澄清,再加 μL 生理鹽水
連續(xù)給藥周期超過半月以上,請謹慎選擇該方案。
請確保第一步儲備液溶解至澄清狀態(tài),從左到右依次添加助溶劑。您可采用超聲加熱 (超聲清洗儀,建議頻次 20-40 kHz),渦旋吹打等方式輔助溶解。
純度 & 產品資料

純度: 99.95%

參考文獻

完整儲備液配制表

* 請根據產品在不同溶劑中的溶解度選擇合適的溶劑配制儲備液;一旦配成溶液,請分裝保存,避免反復凍融造成的產品失效。
儲備液的保存方式和期限:-80°C, 2 years; -20°C, 1 year。-80°C儲存時,請在2年內使用, -20°C儲存時,請在1年內使用。

可選溶劑 濃度 溶劑體積 質量 1 mg 5 mg 10 mg 25 mg
H2O / DMSO 1 mM 4.8028 mL 24.0142 mL 48.0284 mL 120.0711 mL
5 mM 0.9606 mL 4.8028 mL 9.6057 mL 24.0142 mL
DMSO 10 mM 0.4803 mL 2.4014 mL 4.8028 mL 12.0071 mL
15 mM 0.3202 mL 1.6009 mL 3.2019 mL 8.0047 mL
20 mM 0.2401 mL 1.2007 mL 2.4014 mL 6.0036 mL
25 mM 0.1921 mL 0.9606 mL 1.9211 mL 4.8028 mL
30 mM 0.1601 mL 0.8005 mL 1.6009 mL 4.0024 mL
40 mM 0.1201 mL 0.6004 mL 1.2007 mL 3.0018 mL
50 mM 0.0961 mL 0.4803 mL 0.9606 mL 2.4014 mL
60 mM 0.0800 mL 0.4002 mL 0.8005 mL 2.0012 mL
80 mM 0.0600 mL 0.3002 mL 0.6004 mL 1.5009 mL
100 mM 0.0480 mL 0.2401 mL 0.4803 mL 1.2007 mL

* 備注:如您選擇水作為儲備液,請稀釋至工作液后,再用 0.22 μm 的濾膜過濾除菌后使用。

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產品名稱:
Ferulic acid methyl ester
目錄號:
HY-W018643
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