07551
香草醛缩丙酮
≥98.5%
别名:
4-(4-羟基-3-甲氧苯基)-3-丁烯-2-酮
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关于此项目
经验公式（希尔记法）:
C11H12O3
化学文摘社编号:
分子量:
192.21
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
214-096-9
MDL number:
Assay:
≥98.5%
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Pharmacological actions and acute toxicity of methyl- and phenyl-3-methoxy-4-hydroxy styryl ketones.
G B Singh et al.
Arzneimittel-Forschung, 37(6), 708-712 (1987-06-01)
Some pharmacological actions and acute toxicity effects of methyl- and phenyl-3-methoxy-4-hydroxy styryl ketones have been described in experimental animals. The compounds antagonised the contractions evoked by a variety of agonists on several smooth muscle preparations in vitro. They produced inhibitory
Jin Tatsuzaki et al.
Journal of Asian natural products research, 12(3), 227-232 (2010-04-15)
Dehydrozingerone analogs and related compounds were screened as potential antitumor promoters by using the in vitro short-term 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced Epstein-Barr virus early antigen activation assay. Among the 40 synthesized compounds, the prenylated analogs 16 and 34-36 showed the most significant
I Rahath Kubra et al.
Journal of food science, 78(1), M64-M69 (2013-01-03)
The efficacy of Dehydrozingerone (DZ; dehydroderivative of zingerone) as an antifungal agent and its mode of action against food spoilage fungal pathogens was studied and presented. DZ is a constituent of ginger (Zingiber officinale rhizomes) and structural half analogue of
Inhibition of albumin denaturation and antiinflammatory activity of dehydrozingerone and its analogs.
G Elias et al.
Indian journal of experimental biology, 26(7), 540-542 (1988-07-01)
D V Rajakumar et al.
Die Pharmazie, 49(7), 516-519 (1994-07-01)
The antioxidant property of dehydrozingerone and its analogs were investigated in the ferric-ascorbate induced lipid peroxidation model in rat brain homogenate. All the non phenolic compounds were either inactive or less active, while phenolic compounds with substitution at both meta
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