8 | 1006718-20-2 | | 特拉唑嗪-d8 | Isotope-Labeled Compounds | Adrenergic Receptor | Beta Receptor | Inhibitor | inhibitor | inhibit"/>

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  1. Others GPCR/G Protein Neuronal Signaling
  2. Isotope-Labeled Compounds Adrenergic Receptor
  3. Terazosin-d8

Terazosin-d8 是 Terazosin 氘代物。Terazosin 是一種喹唑啉衍生物,也是一種競(jìng)爭(zhēng)性和口服活性的 α1-腎上腺素受體 (α1-adrenoceptor) 拮抗劑。Terazosin 通過舒張血管和打開膀胱來起作用。Terazosin 可用于良性前列腺增生 (BPH) 和高血壓的研究。

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Terazosin-d<sub>8</sub>

Terazosin-d8 Chemical Structure

CAS No. : 1006718-20-2

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1 mg ¥6500
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Other Forms of Terazosin-d8:

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

Terazosin-d8 is deuterium labeled Terazosin. Terazosin is a quinazoline derivative and a competitive and orally active α1-adrenoceptor antagonist. Terazosin works by relaxing blood vessels and the opening of the bladder. Terazosin has the potential for benign prostatic hyperplasia (BPH) and high blood pressure treatment[1][2][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

395.48

Formula

C19H17D8N5O4

CAS 號(hào)
非標(biāo)記 CAS
性狀

固體

顏色

White to off-white

中文名稱

特拉唑嗪-d8

運(yùn)輸條件

Room temperature in continental US; may vary elsewhere.

儲(chǔ)存方式
Powder -20°C 3 years
In solvent -80°C 6 months
-20°C 1 month
純度 & 產(chǎn)品資料
參考文獻(xiàn)
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產(chǎn)品名稱:
Terazosin-d8
目錄號(hào):
HY-B0371S
需求量:
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