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化驗
≥90% (LC/MS-ELSD)
形狀
solid
應用
metabolomics
vitamins, nutraceuticals, and natural products
儲存溫度
−20°C
SMILES 字串
CC(C)c1ccc2c(CC[C@H]3[C@@](C)(CCC[C@]23C)C(O)=O)c1
InChI
1S/C20H28O2/c1-13(2)14-6-8-16-15(12-14)7-9-17-19(16,3)10-5-11-20(17,4)18(21)22/h6,8,12-13,17H,5,7,9-11H2,1-4H3,(H,21,22)/t17-,19-,20-/m1/s1
InChI 密鑰
NFWKVWVWBFBAOV-MISYRCLQSA-N
一般說明
脱氢枞酸(DHA 或 DAA)是一种具有生物活性的双萜类植物化学物质,存在于各种松属物种中。它是树脂酸和松香酸(AA)的衍生物。
應用
脱氢枞酸可用作以下应用的参考标准物:
- 使用傅里叶变换红外光谱(FTIR)研究松树脂的老化过程
- 通过拉曼光谱分析和红外光谱相结合的方法研究松属植物成分随年龄的变化
- 估计在地中海白松(Pinus halepensis)的化学防御中作为代替物对生物胁迫的抗性。
生化/生理作用
脱氢枞酸(DHA)具有抗癌症、抗衰老、抗菌、抗溃疡、胃保护和细胞毒性等多种生物活性。它是一种有效的抗炎剂和过氧化物酶体增殖物激活受体 α 和 γ(PPAR α/γ)的双重激活剂。DHA 具有抗衰老作用,是一种去乙酰化酶 1(SIRT 1)激活化合物。它对耐多药菌株具有抗菌特性。脱氢枞酸及其衍生物具有胃保护作用和细胞毒性作用。
訊號詞
Danger
危險聲明
危險分類
Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1
儲存類別代碼
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
水污染物質分類(WGK)
WGK 1
閃點(°F)
Not applicable
閃點(°C)
Not applicable
其他客户在看
Bioorganic & medicinal chemistry letters, 18(19), 5201-5205 (2008-09-16)
A series of dehydroabietic acid (DHAA, 2) derivatives was synthesized and evaluated as BK channel openers in an assay system of CHO-K1 cells expressing hBKalpha channels. Systematic modifications of the peripheral functionality of ring C of DHAA showed that the
Journal of natural products, 70(2), 154-159 (2007-02-24)
Dehydroabietic acid (DHA) (1) is one of the main compounds in Scots pine wood responsible for aquatic and microbial toxicity. The degradation of 1 by Trametes versicolor and Phlebiopsis gigantea in liquid stationary cultures was followed by HPLC-DAD-ELSD. Both fungi
Materials (Basel, Switzerland), 11(9) (2018-09-16)
Infectious disease caused by pathogenic bacteria continues to be the primary challenge to humanity. Antimicrobial resistance and microbial biofilm formation in part, lead to treatment failures. The formation of biofilms by nosocomial pathogens such as Staphylococcus aureus (S. aureus), Pseudomonas
Organic letters, 11(1), 153-156 (2008-12-11)
A new class of dehydroabietic amine-substituted primary amine-thiourea bifunctional catalysts were designed and synthesized. The doubly stereocontrolled organocatalytic conjugate addition of a variety of heterocycles-bearing ketones to nitroalkenes was investigated for the first time, affording (S)- or (R)-gamma-nitro heteroaromatic ketones
Pharmacological research, 52(5), 429-437 (2005-08-30)
Dehydroabietic acid derivatives have been reported to display antisecretory and antipepsin effect in animal models. Some 19 dehydroabietic acid diterpenes were prepared and assessed for gastroprotective activity in the HCl/EtOH-induced gastric lesions in mice as well as for cytotoxicity in
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