1. Apoptosis
  2. Apoptosis Bcl-2 Family
  3. Himachalol

Himachalol,一种倍半萜烯,是一种口服有效的解痉和抗癌成分,存在于雪松木材中。Himachalol 对黑色素瘤细胞具有抗增殖活性,并诱导细胞凋亡 (Apoptosis) (降低 Bcl-2 水平并增加 Bax 水平)。Himachalol 具有全身性降血压和外周血管扩张作用。Himachalol 可抑制卡巴胆碱引起的肠道痉挛。Himachalol 在小鼠中的 LD50 为 265 mg/kg (口服) 和 247 mg/kg (腹腔注射)。

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Himachalol

Himachalol Chemical Structure

CAS No. : 1891-45-8

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  • 生物活性

  • 纯度 & 产品资料

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生物活性

Himachalol, a sesquiterpene, is an orally active antispasmodic and anticancer constituent found in the wood of Cedrus deodara. Himachalol has anti-proliferative activity against the melanoma cells, and induces apoptosis (decreases Bcl-2 level and increases Bax level). Himachalol has systemic hypotension and peripheral vasodilation effect. Himachalol inhibits Carbachol-induced spasm of the intestine. The LD50 of Himachalol in mice is 265 mg/kg (p.o.) and 247 mg/kg (i.p.)[1][2].

分子量

222.37

Formula

C15H26O

CAS 号
结构分类
初始来源
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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Himachalol
目录号:
HY-N15424
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