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  1. Metabolic Enzyme/Protease Immunology/Inflammation Apoptosis
  2. Aldehyde Dehydrogenase (ALDH) Interleukin Related Pyroptosis Apoptosis Cuproptosis
  3. Disulfiram

Disulfiram  (Synonyms: 雙硫侖; Tetraethylthiuram disulfide; TETD)

目錄號: HY-B0240 純度: 99.78%
COA 產(chǎn)品使用指南

Disulfiram (Tetraethylthiuram disulfide) 是特異性的乙醛脫氫酶 1 型 (ALDH1) 抑制劑,對酒精具有急性敏感性。Disulfiram 有效抑制人體和小鼠細胞中脂質(zhì)體中的 GSDMD 孔形成,炎性體介導的細胞凋亡和 IL-1β 分泌。Disulfiram 是一種銅離子載體,與 Cu2+ 聯(lián)用時,可增加細胞內(nèi) ROS 水平,引發(fā)銅死亡。

MCE 的所有產(chǎn)品僅用作科學研究或藥證申報,我們不為任何個人用途提供產(chǎn)品和服務

Disulfiram Chemical Structure

Disulfiram Chemical Structure

CAS No. : 97-77-8

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規(guī)格 價格 是否有貨 數(shù)量
10 mM * 1 mL in DMSO ¥500
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1 g ¥450
In-stock
5 g   詢價  
10 g   詢價  

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Other Forms of Disulfiram:

MCE 顧客使用本產(chǎn)品發(fā)表的 68 篇科研文獻

查看 Aldehyde Dehydrogenase (ALDH) 亞型特異性產(chǎn)品:

查看 Interleukin Related 亞型特異性產(chǎn)品:

  • 生物活性

  • 實驗參考方法

  • 純度 & 產(chǎn)品資料

  • 參考文獻

生物活性

Disulfiram (Tetraethylthiuram disulfide) is a specific inhibitor of?aldehyde-dehydrogenase (ALDH1), used for the treatment of chronic alcoholism by producing an acute sensitivity to alcohol. Disulfiram inhibits gasdermin D (GSDMD) pore formation in liposomes and inflammasome-mediated pyroptosis and IL-1β secretion in human and mouse cells. Disulfiram, a copper ion carrier,?with?Cu2+ increases intracellular ROS levels and induces cuproptosis[1][2][3][4][5][6].

IC50 & Target[1]

IL-1β

 

細胞效力
(Cellular Effect)
Cell Line Type Value Description References
4T1 IC50
0.25 μM
Compound: 29; DSF
Anticancer activity against mouse 4T1 cells assessed as cell growth inhibition by MTS assay
Anticancer activity against mouse 4T1 cells assessed as cell growth inhibition by MTS assay
[PMID: 33650861]
CEM-SS IC50
> 100 μM
Compound: disulfiram
Antiviral activity against HIV-1ADA in CEM-SS cells using monocyte/macrophage cultures
Antiviral activity against HIV-1ADA in CEM-SS cells using monocyte/macrophage cultures
[PMID: 9207937]
CEM-SS IC50
3.9 μM
Compound: disulfiram
Antiviral activity against HIV-1 in CEM-SS cells using XXT assay
Antiviral activity against HIV-1 in CEM-SS cells using XXT assay
[PMID: 9207937]
HepG2 IC50
38 μM
Compound: Disulfiram
Cytotoxicity against human HepG2 cells assessed as reduction in cell viability after 72 hrs by MTT assay
Cytotoxicity against human HepG2 cells assessed as reduction in cell viability after 72 hrs by MTT assay
[PMID: 29571571]
MCF-10A IC50
10 μM
Compound: 1, DSF
Antiproliferative activity against human MCF10A cells after 72 hrs by MTT assay
Antiproliferative activity against human MCF10A cells after 72 hrs by MTT assay
[PMID: 20222671]
MCF7 IC50
0.1 μM
Compound: 1, DSF
Antiproliferative activity against human MCF7 cells expressing BCA2 and estrogen receptor after 72 hrs by MTT assay
Antiproliferative activity against human MCF7 cells expressing BCA2 and estrogen receptor after 72 hrs by MTT assay
[PMID: 20222671]
MDA-MB-231 IC50
> 10 μM
Compound: 1, DSF
Antiproliferative activity against BCA2 and ER deficient human MDA-MB-231 cells after 72 hrs by MTT assay
Antiproliferative activity against BCA2 and ER deficient human MDA-MB-231 cells after 72 hrs by MTT assay
[PMID: 20222671]
MDA-MB-231 IC50
0.32 μM
Compound: 1, DSF
Antiproliferative activity against human MDA-MB-231 cells expressing BCA2 and ERalpha after 72 hrs by MTT assay
Antiproliferative activity against human MDA-MB-231 cells expressing BCA2 and ERalpha after 72 hrs by MTT assay
[PMID: 20222671]
T47D IC50
0.17 μM
Compound: 1, DSF
Antiproliferative activity against human T47D cells expressing BCA2 and estrogen receptor after 72 hrs by MTT assay
Antiproliferative activity against human T47D cells expressing BCA2 and estrogen receptor after 72 hrs by MTT assay
[PMID: 20222671]
體外研究
(In Vitro)

在誘導凋亡癌細胞死亡之前,Disulfiram -銅復合物有效抑制培養(yǎng)的乳腺癌 MDA-MB-231 和 MCF10DCIS.com 細胞中的蛋白酶體活性,但不抑制正常的永生化 MCF-10A 細胞[1]。Disulfiram (DS) 是一種臨床上使用的抗酒精中毒藥物,以劑量依賴性方式強烈抑制本構(gòu)和 5-FU 誘導的 NF-活化。DisuLfiram 抑制 NF-kappaB 核轉(zhuǎn)位和 DNA 結(jié)合活性,但對 5-FU 誘導的 IkappaBalpha 降解沒有影響。Disulfiram 顯著增強 5-FU 對 DLD-1 和 RKO (WT) 細胞系的凋亡作用,并協(xié)同增強 5-FU 對兩種細胞系的細胞毒性。DisuLfiram 還在體外有效消除 5-FU 耐藥細胞系 H630 (5-FU) 中的 5-FU 化學耐藥性[2]。Oseltamivir 降低了活細胞的數(shù)量,添加 CuCl2 顯著增強了 DSF 誘導的細胞死亡,使其低于對照的 10%[3]。Disulfiram 與 Cu2+ 或 Zn2+ 聯(lián)合用于黑素瘤細胞可降低細胞周期蛋白 A 的表達,并在低于單獨 Disulfiram 的濃度下減少體外增殖[4]。
DisuLfiram (0.1 nM-10 μM;72 h) + Cu2+ 組合增強對卵巢癌細胞系的細胞毒性[1]

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

體內(nèi)研究
(In Vivo)

Disulfiram 顯著抑制腫瘤生長(74%),這與攜帶 MDA-MB-231 腫瘤異種移植物的小鼠體內(nèi)蛋白酶體抑制和凋亡誘導有關[1]。
蛋白酶體抑制是通過腫瘤組織蛋白酶體活性水平降低以及泛素化蛋白和天然蛋白酶體底物 p27 和 Bax[1] 的積累來衡量的。
細胞凋亡表現(xiàn)為 caspase 激活和凋亡細胞核形成[1]
Disulfiram 阻斷 P-糖蛋白擠出泵,抑制轉(zhuǎn)錄因子核因子-kappaB,使腫瘤對化療敏感,減少血管生成,抑制小鼠腫瘤生長[4]。
Disulfiram 抑制移植到嚴重聯(lián)合免疫缺陷小鼠體內(nèi)的黑色素瘤的生長和血管生成,這些作用通過補充 Zn2+ 得到加強[4]。

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

Clinical Trial
分子量

296.54

Formula

C10H20N2S4

CAS 號
性狀

固體

顏色

White to yellow

中文名稱

雙硫侖;二硫龍;二硫化四乙基秋蘭姆

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 1 year
-20°C 6 months
溶解性數(shù)據(jù)
細胞實驗: 

DMSO 中的溶解度 : 75 mg/mL (252.92 mM; 超聲助溶; 吸濕的 DMSO 對產(chǎn)品的溶解度有顯著影響,請使用新開封的 DMSO)

配制儲備液
濃度 溶劑體積 質(zhì)量 1 mg 5 mg 10 mg
1 mM 3.3722 mL 16.8611 mL 33.7223 mL
5 mM 0.6744 mL 3.3722 mL 6.7445 mL
查看完整儲備液配制表

* 請根據(jù)產(chǎn)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(chǎn)品失效
儲備液的保存方式和期限:-80°C, 1 year; -20°C, 6 months。-80°C儲存時,請在1年內(nèi)使用, -20°C儲存時,請在6個月內(nèi)使用。

  • 摩爾計算器

  • 稀釋計算器

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

質(zhì)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(jù)您的 實驗動物和給藥方式 選擇適當?shù)娜芙夥桨浮?

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(jié)果的可靠性,澄清的儲備液可以根據(jù)儲存條件,適當保存;體內(nèi)實驗的工作液,建議您現(xiàn)用現(xiàn)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(xiàn)沉淀、析出現(xiàn)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: ≥ 2.08 mg/mL (7.01 mM); 澄清溶液

    此方案可獲得 ≥ 2.08 mg/mL(飽和度未知)的澄清溶液。

    1 mL 工作液為例,取 100 μL 20.8 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: ≥ 2.08 mg/mL (7.01 mM); 澄清溶液

    此方案可獲得 ≥ 2.08 mg/mL(飽和度未知)的澄清溶液。

    1 mL 工作液為例,取 100 μL 20.8 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。

以下溶解方案,請直接配制工作液。建議現(xiàn)用現(xiàn)配,在短期內(nèi)盡快用完。 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(xiàn)沉淀、析出現(xiàn)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: Corn Oil

    Solubility: 30 mg/mL (101.17 mM); 澄清溶液; 超聲助溶

  • 方案 二

    請依序添加每種溶劑: 50% PEG300    50% Saline

    Solubility: 10 mg/mL (33.72 mM); 懸濁液; 超聲助溶

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(shù)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(nèi)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(wǎng)站選購。 ,Tween 80,均可在 MCE 網(wǎng)站選購。
計算結(jié)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(chǎn)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(shù)支持聯(lián)系。
動物實驗體內(nèi)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(chǎn)品資料

純度: 99.78%

參考文獻
Cell Assay
[4]

The effect of disulfiram (0.15-5.0 μM) or sodium diethyldithiocarbamate (1.0 μM) on proliferation of malignant cell lines is studied in cultures stimulated with 10% FBS. Cell numbers are quantitated 24 to 72 hours later, as outlined below. In some experiments, disulfiram is added immediately after cells are plated. In other experiments, cells are plated and allowed to grow for 24 to 72 hours before fresh medium with disulfiram is added and cell numbers are assayed 24 to 72 hours later. Synergy is studied between disulfiram and?N,N′-bis(2-chloroethyl-N-nitrosourea (carmustine, 1.0-1,000 μM) or cisplatin (0.1-100 μg/mL) added to medium. The effect of metal ions on disulfiram is studied with 0.2 to 10 μM Cu2+?(provided as CuSO4), Zn2+?(as ZnCl2), Ag+?(as silver lactate), or Au3+?(as HAuCl4·3H2O) ions added to growth medium, buffered to physiologic pH. To provide a biologically relevant source of copper, medium is supplemented with human ceruloplasmin at doses replicating low and high normal adult serum concentrations (250 and 500 mg/mL).

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

Animal Administration
[4]

Adult female CB17-SCID mice are housed in a protected laminar flow facility with access to water and either a standard diet containing 87 ppm zinc or a zinc-supplemented diet containing 1,000 ppm Zn2+?as zinc acetate. Mice are injected s.c. in the right groin with 5×106?cells from a highly aggressive malignant melanoma obtained from a Carolinas Medical Center patient. The frozen tumor is passaged twice in SCID mice to adapt it to?in vivo?growth before use in these experiments. On the day of tumor injection, all mice began daily administration of drug. Drug is given in a total volume of 0.2 mL by gastric gavage via smooth Teflon-tipped needles inserted transorally into the stomach. Four groups are studied: tumor control (n=10; 0.2 mL olive oil daily; zinc diet of 87 ppm); zinc-supplemented control (n=10; 0.2 mL olive oil daily; zinc diet of 1,000 ppm); disulfiram (n=10; 200 mg/kg/d disulfiram in 0.2 mL olive oil; zinc diet of 87 ppm); and zinc-supplemented diet + disulfiram (n=10; 200 mg/kg/d disulfiram in 0.2 mL olive oil; zinc diet of 1,000 ppm). Mice are examined daily, the tumor is measured in two dimensions, and the tumor volume is estimated using the formula for an elipse. When estimated tumor volume approached 500 mm3?within any animal, all mice are euthanized. Tumors are excised, weighed, fixed in formalin, sectioned, and stained or immunostained for factor VIII. Slides are coded and examined by a blinded observer who identified vessels as deposits of red cells. For each slide, the number of vessels is counted in four different fields representative of the tumor. The average number of vessels per field is averaged per biopsy specimen and used to evaluate tumor vascularity.

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

參考文獻

完整儲備液配制表

* 請根據(jù)產(chǎn)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(chǎn)品失效。
儲備液的保存方式和期限:-80°C, 1 year; -20°C, 6 months。-80°C儲存時,請在1年內(nèi)使用, -20°C儲存時,請在6個月內(nèi)使用。

可選溶劑 濃度 溶劑體積 質(zhì)量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 3.3722 mL 16.8611 mL 33.7223 mL 84.3057 mL
5 mM 0.6744 mL 3.3722 mL 6.7445 mL 16.8611 mL
10 mM 0.3372 mL 1.6861 mL 3.3722 mL 8.4306 mL
15 mM 0.2248 mL 1.1241 mL 2.2482 mL 5.6204 mL
20 mM 0.1686 mL 0.8431 mL 1.6861 mL 4.2153 mL
25 mM 0.1349 mL 0.6744 mL 1.3489 mL 3.3722 mL
30 mM 0.1124 mL 0.5620 mL 1.1241 mL 2.8102 mL
40 mM 0.0843 mL 0.4215 mL 0.8431 mL 2.1076 mL
50 mM 0.0674 mL 0.3372 mL 0.6744 mL 1.6861 mL
60 mM 0.0562 mL 0.2810 mL 0.5620 mL 1.4051 mL
80 mM 0.0422 mL 0.2108 mL 0.4215 mL 1.0538 mL
100 mM 0.0337 mL 0.1686 mL 0.3372 mL 0.8431 mL
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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產(chǎn)品名稱:
Disulfiram
目錄號:
HY-B0240
需求量: