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Gallic aldehyde

CAT: 0804-HY-W004486-01Size: 100 mgDry Ice: NoHazardous: No
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CAT#:0804-HY-W004486-01Size:100 mg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Gallic aldehyde (3,4,5-Trihydroxybenzaldehyde) is a phenolic aldehyde. Gallic aldehyde can be isolated from Geum japonicum. Gallic aldehyde inhibits the gelatinolytic activity and expression of MMP-9. Gallic aldehyde also inhibits ERK1/2, p38, and JNK. Gallic aldehyde has potent anti-HSV-1 and antioxidant activities. Gallic aldehyde also exhibits antibacterial activity against Oenococcus oeni VF[1][2][3][4].
CAS Number
13677-79-7
UNSPSC
12352005
Hazard Statement
H302, H315, H319, H335
Target
ERK; HSV; JNK; MMP; p38 MAPK
Type
Reference compound
Related Pathways
Anti-infection; MAPK/ERK Pathway; Metabolic Enzyme/Protease; Stem Cell/Wnt
Applications
COVID-19-anti-virus
Field of Research
Infection
Assay Protocol
https://www.medchemexpress.com/gallic-aldehyde.html
Purity
99.95
Solubility
DMSO : 116.67 mg/mL (ultrasonic)
Smiles
O=CC1=CC(O)=C(O)C(O)=C1
Molecular Formula
C7H6O4
Molecular Weight
154.12
Precautions
H302, H315, H319, H335
References & Citations
[1]Kadota S, et al. A New Hydrolyzable Tannin from Geum japonicum and Its Antiviral Activity[J]. Heterocycles, 1994, 38 (1) :167-175.|[2]Miwa H, et al. Liquid chromatographic determination of free and total fatty acids in milk and milk products as their 2-nitrophenylhydrazides. J Chromatogr. 1990 Dec 7;523:235-46. |[3]Thomas SC, et al. Phytotoxicity and hormesis in common mobile organic compounds in leachates of wood-derived biochars. Biochar. 2024;6 (1) :51. |[4]Arturo Anadon, et al. EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids (CEF) ; Scientific Opinion on Flavouring Group Evaluation 06, Revision 2 (FGE.06Rev2) : Straight- and branched-chain aliphatic unsaturated primary alcohols, aldehydes, carboxylic acids, and esters from chemical groups 1 and 4. EFSA Journal 2011; 9 (3) :1844. [78 pp.].
Shipping Conditions
Room Temperature
Storage Conditions
4°C (Powder, stored under nitrogen)
Scientific Category
Reference compound1
Clinical Information
No Development Reported
Isoform
ERK1; ERK2; MMP-9

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