1. Others Anti-infection Metabolic Enzyme/Protease
  2. Fungal Isotope-Labeled Compounds Cytochrome P450
  3. Tebuconazole-d6

Tebuconazole-d6 是氘代标记的 Tebuconazole (HY-B0852)。Tebuconazole 是一种具有口服活性的农用唑类杀菌剂,也能抑制 CYP51 ,对于白色念珠菌 CYP51 (CaCYP51) 和人 CYP51 截短体 (Δ60HsCYP51) 的 IC50 值分别为 0.9 和 1.3 μM。Tebuconazole 诱导 HepG2 细胞中的脂质积累和氧化应激。Tebuconazole 可降低 MAC-T 细胞活力和增殖,诱导内质网应激介导的细胞凋亡,并增加 MAC-T 细胞的氧化应激水平。

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Tebuconazole-d<sub>6</sub> Chemical Structure

Tebuconazole-d6 Chemical Structure

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Other Forms of Tebuconazole-d6:

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Tebuconazole-d6 is a deuterium labeled Tebuconazole (HY-B0852). Tebuconazole is an orally active agricultural azole fungicide which can also inhibit CYP51 with IC50s of 0.9 and 1.3 μM for Candida albicans CYP51 (CaCYP51) and truncated Homo sapiens CYP51 (Δ60HsCYP51), respectively. Tebuconazole induces lipid accumulation and oxidative stress in HepG2 Cells. Tebuconazole decreases MAC-T cells viability and proliferation, induces ER-stress-mediated apoptosis and increases oxidative stress levels in MAC-T cells[1][2][3][4][5][6].

体外研究
(In Vitro)

氢、碳和其他元素的稳定重同位素已被掺入药物分子中,主要用作药物开发过程中定量的示踪剂。氘化因其可能影响药物的药代动力学和代谢特征而受到关注。

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

分子量

313.86

Formula

C16H16D6ClN3O

非标记 CAS
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

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

纯度 & 产品资料
参考文献
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Tebuconazole-d6
目录号:
HY-B0852S2
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