2D Structure

3D Structure

1-Methylnaphthalene


Properties
PID PID00130
Mol. Weight 142.201 g/mol
LogP 3.87
Water solubility In water, 25.8 mg/L
Hydrogen Bond Donor 0
Hydrogen Bond Acceptor 0
Rotatable Bonds 0
XLogP3-AA 3.9

1-Methylnaphthalene

Identifiers
Formula C11H10
PubChem CID 7002
FEMA 3193
Flavor Profile /
Smiles Cc1cccc2ccccc12
InChl Key QPUYECUOLPXSFR-UHFFFAOYSA-N
InChl InChI=1S/C11H10/c1-9-5-4-7-10-6-2-3-8-11(9)10/h2-8H,1H3
CAS Registry Number 1321-94-4, 90-12-0
IUPAC Systematic Name 1-methylnaphthalene

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
Chinese Thorowax Equivalent plant: Bupleurum scorzChai Hu(柴胡)Bupleuri RadixMinor cold, Pungent, BitterLiver, Gallbladder, LungView Graph
Catclaw Buttercup RootMao Zhua Cao (猫爪草)Ranunculi Ternati RadixWarm, Pungent, SweetLung, Bladder, HeartView Graph
Paniculate SwallowwortXu Chang Qing(徐长卿)Cynanchi Paniculati Radix Et RhizomaWarm, PungentLung, Spleen, StomachView Graph
Alpinia katsumadaiCao Dou Kou(草豆蔻)Katsumada GalangalWarm,PungentSpleen, Stomach, Kidney, LungView Graph

Pharmacological action

1-Methylnaphthalene is an organic compound with the formula CH3C10H7. It is a colorless liquid. It is isomeric with 2-methylnaphthalene.



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. https://en.wikipedia.org/wiki/1-Methylnaphthalene

2. Shaddix C R, Brezinsky K, Glassman I. Oxidation of 1-methylnaphthalene[C]//Symposium (International) on Combustion. Elsevier, 1992, 24(1): 683-690.

3. Yang, Q., Cai, S., Dong, S., Chen, L., Chen, J., Cai, T. Biodegradation of 3-methyldiphenylether (MDE) by Hydrogenophaga atypical strain QY7-2 and cloning of the methy-oxidation gene mdeABCD[J]. Scientific reports, 2016, 6: 39270.

4. ados Santos, H. F., Duarte, G. A. S., da Costa Rachid, C. T., Chaloub, R. M., Calderon, E. N., de Barros Marangoni, L. F., Rosado, A. S. Impact of oil spills on coral reefs can be reduced by bioremediation using probiotic microbiota[J]. Scientific reports, 2015, 5: 18268.

5. Berna, J., Leigh, D. A., Lubomska, M., Mendoza, S. M., Pérez, E. M., Rudolf, P., Zerbetto, F. Macroscopic transport by synthetic molecular machines[J]. Nature materials, 2005, 4(9): 704.

6. Wang, Yinliang, Yincan Jin, Qi Chen, Ming Wen, Hanbo Zhao, Hongxia Duan, and Bingzhong Ren. Selectivity and ligand-based molecular modeling of an odorant-binding protein from the leaf beetle Ambrostoma quadriimpressum (Coleoptera: Chrysomelidae) in relation to habitat-related volatiles. Scientific reports 7.1 (2017): 15374.

7. Chen, Chia-Li, Mary Kacarab, Ping Tang, and David R. Cocker III. SOA formation from naphthalene, 1-methylnaphthalene, and 2-methylnaphthalene photooxidation. Atmospheric environment 131 (2016): 424-433.