2D Structure

3D Structure

Lavandulol


Properties
PID PID00205
Mol. Weight 154.253 g/mol
LogP None
Water solubility 0.0102 mol/L at 20 °C
Hydrogen Bond Donor 1
Hydrogen Bond Acceptor 1
Rotatable Bonds 4
XLogP3-AA 3.0

Lavandulol

Identifiers
Formula C10H18O
PubChem CID 5464156
FEMA /
Flavor Profile None
Smiles CC(=CCC(CO)C(=C)C)C
InChl Key CZVXBFUKBZRMKR-JTQLQIEISA-N
InChl InChI=1S/C10H18O/c1-8(2)5-6-10(7-11)9(3)4/h5,10-11H,3,6-7H2,1-2,4H3/t10-/m0/s1
CAS Registry Number 498-16-8
IUPAC Systematic Name (2R)-5-methyl-2-prop-1-en-2-ylhex-4-en-1-ol

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
Wild MintBo He (薄荷)Menthae Haplocalycis HerbaCool, PungentLiver, LungView Graph
bark of Officinal magnoliaHou Pu(厚朴)Magnoliae Officinalis CortexWarm, Pungent, BitterSpleen, LiverView Graph
Chinese Ligusticum Equivalent plant: Ligusticum jeGao Ben (藁本)Ligustici Rhizoma Et RadixWarm, PungentLung, Spleen, StomachView Graph
bark of Officinal magnoliaHou Pu(厚朴)Magnoliae Officinalis CortexWarm, Pungent, BitterSpleen, LiverView Graph
bark of Officinal magnoliaHou Pu(厚朴)Magnoliae Officinalis CortexWarm, Pungent, BitterSpleen, LiverView Graph
Chinese Ligusticum Equivalent plant: Ligusticum jeGao Ben (藁本)Ligustici Rhizoma Et RadixWarm, PungentLung, Spleen, StomachView Graph
bark of Officinal magnoliaHou Pu(厚朴)Magnoliae Officinalis CortexWarm, Pungent, BitterSpleen, LiverView Graph

Pharmacological action

Lavandulol is a monoterpene alcohol found in a variety of essential oils such as lavender oil.The term refers to either of two enantiomers. The (R)-enantiomer is natural and has an aroma described as "weak floral, herbal odor with slightly lemon-like, fresh citrus fruity nuance"; the (S)-enantiomer has only a weak odor



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. Mosandl A. Authenticity assessment: a permanent challenge in food flavor and essential oil analysis[J]. Journal of chromatographic science, 2004, 42(8): 440-449.

2. Zhang, A., Wang, S., Vitullo, J., Roda, A., Mannion, C., Bergh, J. C. Olfactory discrimination among sex pheromone stereoisomers: chirality recognition by pink hibiscus mealybug males[J]. Chemical senses, 2006, 31(7): 621-626.

3. Vaello, T., Casas, J. L., Pineda, A., de Alfonso, I., Marcos-García, M. Á. Olfactory response of the Predatory Bug Orius laevigatus (Hemiptera: Anthocoridae) to the aggregation pheromone of its prey, Frankliniella occidentalis (Thysanoptera: Thripidae)[J]. Environmental entomology, 2017, 46(5): 1115-1119.

4. Kitchlu, S., Bakshi, S. K., Kaul, M. K., Bhan, M. K., Thapa, R. K., Agarwal, S. G. Tanacetum gracile Hook. f & T. A new source of lavandulol from Ladakh Himalaya (India)[J]. Flavour and fragrance journal, 2006, 21(4): 690-692.

5. Miettinen, K., Dong, L., Navrot, N., Schneider, T., Burlat, V., Pollier, J., Verpoorte, R. The seco-iridoid pathway from Catharanthus roseus[J]. Nature communications, 2014, 5: 3606.

6. Sakauchi, H., Kiyota, H., Takigawa, S. Y., Oritani, T., Kuwahara, S. Enzymatic resolution and odor description of both enantiomers of lavandulol, a fragrance of lavender oil[J]. Chemistry & biodiversity, 2005, 2(9): 1183-1186.

7. Zada, A., Dunkelblum, E., Assael, F., Franco, J. C., Silva, E. D., Protasov, A., Mendel, Z. Attraction of Planococcus ficus males to racemic and chiral pheromone baits: flight activity and bait longevity[J]. Journal of applied entomology, 2008, 132(6): 480-489.