5 | 929106-58-1 | BM 14190-d5 | 卡維地洛-d5 | 卡維地羅-d5 | Isotope-Labeled Compounds | Adrenergic Receptor | Autophagy | Beta Receptor | Inhibitor | inhibitor | inhibit"/>

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  1. Others GPCR/G Protein Neuronal Signaling Autophagy
  2. Isotope-Labeled Compounds Adrenergic Receptor Autophagy
  3. Carvedilol-d5

Carvedilol-d5 是 Carvedilol 氘代物。Carvedilol (BM 14190) 是一種非選擇性 β/α-1 受體阻斷劑。Carvedilol 抑制脂質(zhì)過氧化,IC50 為 5 μM。Carvedilol 是一種多用途降壓劑,有潛力用于心絞痛和充血性心力衰竭的研究。Carvedilol是一種自噬 (autophagy) 誘導(dǎo)劑,可抑制 NLRP3 炎性體。

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Carvedilol-d<sub>5</sub>

Carvedilol-d5 Chemical Structure

CAS No. : 929106-58-1

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規(guī)格 價(jià)格 是否有貨 數(shù)量
1 mg ¥3238
3 - 4 周
500 μg ¥2024
3 - 4 周
5mg 詢價(jià)

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Other Forms of Carvedilol-d5:

查看 Adrenergic Receptor 亞型特異性產(chǎn)品:

  • 生物活性

  • 純度 & 產(chǎn)品資料

  • 參考文獻(xiàn)

生物活性

Carvedilol-d5 is deuterium labeled Carvedilol. Carvedilol (BM 14190) is a non-selective β/α-1 blocker[1]. Carvedilol inhibits lipid peroxidation in a dose-dependent manner with an IC50 of 5 μM. Carvedilol is a multiple action antihypertensive agent with potential use in angina and congestive heart failure[2]. Carvedilol is an autophagy inducer that inhibits the NLRP3 inflammasome[3].

產(chǎn)品應(yīng)用

1. 該化合物可作為示蹤劑。
2. 該化合物可作為 NMR、GC-MS 或 LC-MS 分析中的內(nèi)標(biāo)品,用于定量分析。

體外研究
(In Vitro)

Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].

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

分子量

411.51

Formula

C24H21D5N2O4

CAS 號
非標(biāo)記 CAS
中文名稱

卡維地洛-d5;卡維地羅-d5

運(yùn)輸條件

Room temperature in continental US; may vary elsewhere.

儲存方式

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

純度 & 產(chǎn)品資料
參考文獻(xiàn)
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產(chǎn)品名稱:
Carvedilol-d5
目錄號:
HY-B0006S2
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