Dehydrocurdione

上海金畔生物科技有限公司提供天然产物萜类及其苷类Terpenoids and Glycosides。

Dehydrocurdione 

Dehydrocurdione,一种 zedoary 衍生的倍半萜,在 RAW 264.7 巨噬细胞中诱导血红素加氧酶 (HO)-1,一种抗氧化酶。Dehydrocurdione 与 Keap1 相互作用,导致 Nrf2 易位,随后激活 HO-1 E2 增强子。Dehydrocurdione 抑制脂多糖诱导的 NO 释放,NO 是炎症的标志物。抗炎活性。

Dehydrocurdione

Dehydrocurdione Chemical Structure

CAS No. : 38230-32-9

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生物活性

Dehydrocurdione, a zedoary-derived sesquiterpene, induces heme oxygenase (HO)-1, an antioxidative enzyme, in RAW 264.7 macrophages. Dehydrocurdione interacts with Keap1, resulting in Nrf2 translocation followed by activation of the HO-1 E2 enhancer. Dehydrocurdione suppresses lipopolysaccharide-induced NO release, a marker of inflammation. Anti-inflammatory activity[1][2].

体外研究
(In Vitro)

Dehydrocurdione (RAW 264.7 cells) concentration-dependently increases the HO-1 mRNA level for 3 hr and the protein level for 6 hr, and both effects reached significance at a concentration of 100 μM[1].
Dehydrocurdione interacts with Keap, resulting in Nrf2 translocation followed by activation ofthe HO-1 E2 enhancer[1].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis[1]

Cell Line: RAW 264.7 cells
Concentration: 100 μM
Incubation Time: 24 hours
Result: Transiently increased the HO-1 protein level, and its effect peaked at 3-6 hr.

体内研究
(In Vivo)

Dehydrocurdione (P.o ;120 mg/kg, daily for 12 days) significantly reduces chronic adjuvant arthritis[2].
Dehydrocurdione (200 mg/kg; p.o.; Sprague-Dawley rats) dose-dependently inhibits carrageenan-induced paw edema[2].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Wistar rats[2]
Dosage: 120 mg/kg
Administration: P.o ; daily for 12 days
Result: Significantly reduces chronic adjuvant arthritis.

分子量

234.33

Formula

C15H22O2

CAS 号

38230-32-9

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.

参考文献
  • [1]. Ohnishi M, et al. Curcuma sp.-derived dehydrocurdione induces heme oxygenase-1 through a Michael reaction between its α, β-unsaturated carbonyl and Keap1. Phytother Res. 2018;32(5):892-897.

    [2]. Yoshioka T, et al. Antiinflammatory potency of dehydrocurdione, a zedoary-derived sesquiterpene. Inflamm Res. 1998;47(12):476-481.