2D Structure

3D Structure

2-Methoxy-4-Vinylphenol


Properties
PID PID00051
Mol. Weight 150.177 g/mol
LogP 2.25
Water solubility 0.049 mol/L at 20 °C
Hydrogen Bond Donor 1
Hydrogen Bond Acceptor 2
Rotatable Bonds 2
XLogP3 2.4

2-Methoxy-4-Vinylphenol

Identifiers
Formula C9H10O2
PubChem CID 332
FEMA 2675
Flavor Profile Clove, Curry, Spice
Smiles C=Cc1ccc(O)c(OC)c1
InChl Key YOMSJEATGXXYPX-UHFFFAOYSA-N
InChl InChI=1S/C9H10O2/c1-3-7-4-5-8(10)9(6-7)11-2/h3-6,10H,1H2,2H3
CAS Registry Number 7786-61-0, 31853-85-7
IUPAC Systematic Name 4-ethenyl-2-methoxyphenol

Organ Location Map/System Distribution of Pungent Flavor Compounds’ Targets


Note: Known Targets (Gene) from 6952 literatures, DrugBank (http://www.drugbank.ca/), STITCH (http://stitch.embl.de/), ChEMBL (https://www.ebi.ac.uk/chembl/), Therapeutic Target Database (http://bidd.nus.edu.sg/group/ttd/), and Comparative Toxicogenomics Database (CTD, http://ctdbase.org/)


Related Pungent TCM

English Name Pinyin Name (Chinese Name) Latin Name Properties in TCM merdians View Graph
Clove TreeDing Xiang (丁香)Caryophylli FlosWarm,PungentSpleen, Stomach, Kidney, LungView Graph

Pharmacological action

2-Methoxy-4-vinylphenol is an aromatic substance used as a flavoring agent. It is one of the compounds responsible for the natural aroma of buckwheat. The aroma of pure substance was described as: apple, spicy, peanut, wine-like or clove and curry.



Note: Click anywhere in the blank, you can drag the whole dynamic diagram. Click on a node, you can drag his location to see it more clearly. The blue circle represents pharmacology, toxicology, or daily use. Orange hexagon represents the pungent compounds.

References

1. Jeong J B, Hong S C, Jeong H J, et al. Anti-inflammatory effect of 2-methoxy-4-vinylphenol via the suppression of NF-κB and MAPK activation, and acetylation of histone H3[J]. Archives of pharmacal research, 2011, 34(12): 2109-2116.

2. Yu G Q, Li D Z, Lu Y L, et al. Deciphering the Odorant Binding, Activation, and Discrimination Mechanism of Dhelobp21 from Dastarus Helophoroides[J]. Scientific reports, 2018, 8(1): 13506.

3. Davidovich-Rikanati R, Sitrit Y, Tadmor Y, et al. Enrichment of tomato flavor by diversion of the early plastidial terpenoid pathway[J]. Nature biotechnology, 2007, 25(8): 899.

4. de Lerma N L, Peinado R A, Puig-Pujol A, et al. Influence of two yeast strains in free, bioimmobilized or immobilized with alginate forms on the aromatic profile of long aged sparkling wines[J]. Food chemistry, 2018, 250: 22-29.

5. Xu J, Wu H, Wang Z, et al. Microbial dynamics and metabolite changes in Chinese Rice Wine fermentation from sorghum with different tannin content[J]. Scientific reports, 2018, 8(1): 4639.

6. Fierascu I, Georgiev M I, Ortan A, et al. Phyto-mediated metallic nano-architectures via Melissa officinalis L.: synthesis, characterization and biological properties[J]. Scientific Reports, 2017, 7(1): 12428.

7. Neff J C, Townsend A R, Gleixner G, et al. Variable effects of nitrogen additions on the stability and turnover of soil carbon[J]. Nature, 2002, 419(6910): 915.

8. Janes D, Kantar D, Kreft S, Prosen H (2008). "Identification of buckwheat (Fagopyrum esculentum Moench) aroma compounds with GC-MS". Food Chemistry. 112: 120–124.

9. https://en.wikipedia.org/wiki/2-Methoxy-4-vinylphenol