07551
Vanillylidenacetone
≥98.5%
Synonym(s):
4-(4-Hydroxy-3-methoxyphenyl)-3-buten-2-one
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About This Item
Recommended Products
Quality Level
assay
≥98.5%
color
yellow
mp
125-130 °C
SMILES string
COc1cc(\C=C\C(C)=O)ccc1O
InChI
1S/C11H12O3/c1-8(12)3-4-9-5-6-10(13)11(7-9)14-2/h3-7,13H,1-2H3/b4-3+
InChI key
AFWKBSMFXWNGRE-ONEGZZNKSA-N
Gene Information
human ... APP(351)
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Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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
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
Molecular and cellular biochemistry, 355(1-2), 249-256 (2011-05-14)
Oxidative stress is triggered by the wound which results in the production of reactive oxygen species (ROS), thereby delaying normal wound repair. Therefore, it is important to reduce the level of ROS to improve healing. A known antioxidant, dehydrozingerone (DHZ)
Inhibition of albumin denaturation and antiinflammatory activity of dehydrozingerone and its analogs.
Indian journal of experimental biology, 26(7), 540-542 (1988-07-01)
General pharmacology, 25(4), 651-659 (1994-07-01)
1. Dehydrozingeronolol (DZPN; 0.1, 0.5, 1.0 mg/kg, i.v.) produced a dose-dependent bradycardia response and a sustained pressor action in urethane-anesthetized normotensive rats. DZPN inhibited the tachycardia effects by (-)isoproterenol, but had no blocking effect on the arterial pressor responses induced
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