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Tranylcypromine hydrochloride
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Tranylcypromine hydrochloride图片
CAS NO:1986-47-6
包装与价格:
包装价格(元)
100mg电议
250mg电议
500mg电议
1 g电议

产品名称
SKF 385 hydrochloride
产品介绍
Tranylcypromine hydrochloride (SKF 385 hydrochloride) 是 lysine-specific demethylase 1(LSD1/BHC110)和 monoamine oxidase(MAO)的不可逆抑制剂。Tranylcypromine hydrochloride 抑制 LSD1,MAO A 和 MAO B 的IC50值分别为 20.7,2.3 和 0.95 μM。Tranylcypromine hydrochloride 可用于忧郁症的研究。
生物活性

Tranylcypromine hydrochloride (SKF 385 hydrochloride) is an irreversible inhibitor of lysine-specific demethylase 1(LSD1/BHC110)andmonoamine oxidase(MAO). Tranylcypromine hydrochloride inhibits LSD1, MAO A and MAO B withIC50s of 20.7, 2.3 and 0.95 μM, respectively. Tranylcypromine hydrochloride can be used for the research of depression[1][2][3].

IC50& Target

MAO-A

2.3 μM (IC50)

MAO-B

0.95 μM (IC50)

体外研究
(In Vitro)

Tranylcypromine hydrochlorid (50 μM-5 mM; 1 h or 12-14 h) inhibits histone and nucleosomal demethylation[1].
Tranylcypromine hydrochlorid (2 μM; 3 h) shows a specific derepression of OCT4 transcription[1].
Tranylcypromine hydrochlorid (0-100 μM; 15 min) shows IC50values of 20.7, 2.3 and 0.95 μM for LSD1, MAO A and MAO B, respectively[2].
Tranylcypromine hydrochlorid (0-800 μM) shows Kivalues of 242.7, 101.9 and 16 μM for LSD1, MAO A and MAO B, respectively[2].

Western Blot Analysis[1]

Cell Line:Sf21 insect cell line
Concentration:50 μM, 200 μM, 1 mM and 5 mM
Incubation Time:12-14 hours or 1 hour
Result:Showed inhibitory activities of histone H3K4 demethylation and nucleosomal demethylation.

RT-PCR[1]

Cell Line:P19 EC cell line
Concentration:2 μM
Incubation Time:3 hours
Result:Decreased Oct4 mRNA levels.
体内研究
(In Vivo)

Tranylcypromine hydrochlorid (3 mg/kg; i.p. once daily for 3 days) decreases LPS-mediated microglial activation and proinflammatory cytokine COX-2 and IL-6 levels in wild-type mice[3].
Tranylcypromine hydrochlorid (3 mg/kg; i.p. once daily for 7 days) down-regulates Aβ-mediate microglial activation in 5xFAD mice[3].

Animal Model:Wild-type mice[3]
Dosage:3 mg/kg
Administration:Intraperitoneal injection; 3 mg/kg once daily for 3 days
Result:Significantly down-regulated LPS-stimulated microglial activation in the cortex and Hippocampus, and LPS-induced astrocyte activation only in the cortex. Reduced LPS-induced COX-2 levels in hippocampus CA1, decreased LPS-evoked IL-6 levels in the cortex and hippocampus CA1 and suppressed LPS-mediated IL-1β levels in the cortex.
Animal Model:5xFAD mice[3]
Dosage:3 mg/kg
Administration:Intraperitoneal injection; 3 mg/kg once daily for 7 days
Result:Differentially regulated microglial and astrocyte activation in this mouse model of AD.
分子量

169.65

性状

Solid

Formula

C9H12ClN

CAS 号

1986-47-6

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, sealed storage, away from moisture

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

溶解性数据
In Vitro: 

H2O : 100 mg/mL(589.45 mM;Need ultrasonic)

DMSO : 100 mg/mL(589.45 mM;Need ultrasonic)

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM5.8945 mL29.4724 mL58.9449 mL
5 mM1.1789 mL5.8945 mL11.7890 mL
10 mM0.5894 mL2.9472 mL5.8945 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80℃, 6 months; -20℃, 1 month (sealed storage, away from moisture)。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.

    请依序添加每种溶剂: 10% DMSO    40%PEG300   5%Tween-80   45% saline

    Solubility: ≥ 2.5 mg/mL (14.74 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (14.74 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;向上述体系中加入50 μL Tween-80,混合均匀;然后继续加入 450 μL生理盐水定容至 1 mL。

    将 0.9 g 氯化钠,完全溶解于 100 mL ddH2O 中,得到澄清透明的生理盐水溶液
  • 2.

    请依序添加每种溶剂: 10% DMSO    90% (20%SBE-β-CDin saline)

    Solubility: ≥ 2.5 mg/mL (14.74 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (14.74 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL20% 的 SBE-β-CD 生理盐水水溶液中,混合均匀。

    将 2 g 磺丁基醚 β-环糊精加入 5 mL 生理盐水中,再用生理盐水定容至 10 mL,完全溶解,澄清透明
  • 3.

    请依序添加每种溶剂: 10% DMSO    90%corn oil

    Solubility: ≥ 2.5 mg/mL (14.74 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (14.74 mM,饱和度未知) 的澄清溶液,此方案不适用于实验周期在半个月以上的实验。

    以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中,混合均匀。

*以上所有助溶剂都可在本网站选购。