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  2. GPCR/G Protein
  3. Prostaglandin Receptor
  4. U-46619

U-46619  (Synonyms: 9,11-Methanoepoxy PGH2)

目錄號: HY-108566 純度: ≥99.0%
COA 產(chǎn)品使用指南

U-46619 (9,11-Methanoepoxy PGH2) 是一種穩(wěn)定的 Thromboxane A2 (HY-113350) (TXA2) 的類似物，可作為有效的 TXA2 (TP) 激動劑。 U-46619 也是一種 RhoA 激動劑。 U-46619 通過 TXA2 受體激活來刺激 RhoA 的激活。

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U-46619 Chemical Structure

U-46619 Chemical Structure

CAS No. : 56985-40-1

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規(guī)格 價格 是否有貨 數(shù)量
1 mg (28.5 mM * 100 μL in Methyl acetate) ￥3300
In-stock
5 mg (28.5 mM * 500 μL in Methyl acetate) 現(xiàn)貨 詢價

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Customer Review

查看 Prostaglandin Receptor 亞型特異性產(chǎn)品:

  • 生物活性

  • 純度 & 產(chǎn)品資料

  • 參考文獻

生物活性

U-46619 (9,11-Methanoepoxy PGH2) is a stable analogue of Thromboxane A2 (HY-113350) (TXA2) and acts as a potent TXA2 (TP) agonist. U-46619 also is a RhoA agonist. U-46619 stimulates the activation of RhoA through TXA2 receptor activation[1][4][5].

IC50 & Target

TXA2/TP

 

體外研究
(In Vitro)

U-46619 (1 nM-10 μM) causes platelets shape change and aggregation in a concentration-dependent manner, and with EC50s of 0.58 μM and 0.013 μM for aggregation and shape change, respectively[1].
? U-46619 (10 nM-10 μM) increases internal Ca2+ concentration ([Ca2+]i) and activates phosphoinositide (PI) hydrolysis in a concentration-dependent manner with a similar concentration-dependency[1].
? U-46619 (3 nM-10 μM) also activates GTPase concentration-dependently in the membranes derived from platelets[1].
? U-46619 improves the differentiation efficiency of human induced pluripotent stem cells into endothelial cells by activating both p38MAPK and ERK1/2 signaling pathways[2].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.
體內研究
(In Vivo)

U-46619 (5 μg/kg; i.v.) increases blood pressure in male spontaneously hypertensive rats (SHR)[3].

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

Animal Model: 12-15 weeks-old male and female SHR[2]
Dosage: 5 μg/kg
Administration: Intravenous injection
Result: Induceed a significant increase of MABP after 1 min in male SHR.
分子量

350.49

Formula

C21H34O4
CAS 號
性狀

液體

顏色

Colorless to light yellow

運輸條件

Room temperature in continental US; may vary elsewhere.
儲存方式

Solution, -20°C, 2 years
溶解性數(shù)據(jù)
細胞實驗： 

DMSO 中的溶解度 : 100 mg/mL (285.31 mM; 超聲加熱助溶; 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)

  • 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

只
由于實驗過程有損耗，建議您多配一只動物的量
計算結果
工作液所需濃度 : mg/mL
純度 & 產(chǎn)品資料

純度: ≥99.0%

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, 6 months; -20°C, 1 month。-80°C儲存時，請在6個月內使用，-20°C儲存時，請在1個月內使用。

可選溶劑 濃度 溶劑體積 質量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 2.8531 mL 14.2657 mL 28.5315 mL 71.3287 mL
5 mM 0.5706 mL 2.8531 mL 5.7063 mL 14.2657 mL
10 mM 0.2853 mL 1.4266 mL 2.8531 mL 7.1329 mL
15 mM 0.1902 mL 0.9510 mL 1.9021 mL 4.7552 mL
20 mM 0.1427 mL 0.7133 mL 1.4266 mL 3.5664 mL
25 mM 0.1141 mL 0.5706 mL 1.1413 mL 2.8531 mL
30 mM 0.0951 mL 0.4755 mL 0.9510 mL 2.3776 mL
40 mM 0.0713 mL 0.3566 mL 0.7133 mL 1.7832 mL
50 mM 0.0571 mL 0.2853 mL 0.5706 mL 1.4266 mL
60 mM 0.0476 mL 0.2378 mL 0.4755 mL 1.1888 mL
80 mM 0.0357 mL 0.1783 mL 0.3566 mL 0.8916 mL
100 mM 0.0285 mL 0.1427 mL 0.2853 mL 0.7133 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：
U-46619
目錄號：
HY-108566
需求量：