2D Structure
3D Structure
| Properties | |
|---|---|
| PID | PID00138 |
| Mol. Weight | 178.234 g/mol |
| LogP | 3.95 |
| Water solubility | In water, 0.0434 mg/L |
| Hydrogen Bond Donor | 0 |
| Hydrogen Bond Acceptor | 0 |
| Rotatable Bonds | 0 |
| XLogP3 | 4.4 |
| Identifiers | |
|---|---|
| Formula | C14H10 |
| PubChem CID | 8418 |
| FEMA | - |
| Flavor Profile | Weak Aromatic Odor |
| Smiles | c1ccc2cc3ccccc3cc2c1 |
| InChl Key | MWPLVEDNUUSJAV-UHFFFAOYSA-N |
| InChl | InChI=1S/C14H10/c1-2-6-12-10-14-8-4-3-7-13(14)9-11(12)5-1/h1-10H |
| CAS Registry Number | 120-12-7, 54261-80-2, 90640-80-5 |
| IUPAC Systematic Name | anthracene |
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/)
| English Name | Pinyin Name (Chinese Name) | Latin Name | Properties in TCM | merdians | View Graph |
|---|---|---|---|---|---|
| Rhizoma Typhonii | Bai Fu Zi(白附子) | rhizome of Giant Typhonium | Warm,Pungent,Sweet | Spleen,Liver,Heart | View Graph |
| Cassiabarktree Twig | Gui Zhi (桂枝) | Cinnamomi Ramulus | Warm, Pungent, Sweet | Lung, Bladder, Heart | View Graph |
| Dahurian Rhododendron | Man Shan Hong (满山红) | Rhododendri Daurici Folium | Cold, Pungent, Bitter | Liver, Heart, Lung | View Graph |
| Paniculate Swallowwort | Xu Chang Qing(徐长卿) | Cynanchi Paniculati Radix Et Rhizoma | Warm, Pungent | Lung, Spleen, Stomach | View Graph |
Anthracene is a solid polycyclic aromatic hydrocarbon (PAH) of formula C14H10, consisting of three fused benzene rings. It is a component of coal tar.
Anthracene is used in the production of the red dye alizarin and other dyes. Anthracene is colorless but exhibits a blue (400C500 nm peak) fluorescence
under ultraviolet radiation.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.
1. https://en.wikipedia.org/wiki/Anthracene
2. Banerjee K. Atomic Physics and Related Subjects.: Communications to Nature.: Structure of Naphthalene and Anthracene[J]. Nature, 1930, 125(3151): 456.
3. Marks M M. Bulk and anthracene in the treatment of functional constipation[J]. The American journal of digestive diseases, 1951, 18(10): 307.
4. Gao Z, Han Y, Wang F. Cooperative supramolecular polymers with anthracene‒endoperoxide photo-switching for fluorescent anti-counterfeiting[J]. Nature communications, 2018, 9(1): 3977.
5. Bowen E J, Mikiewicz E. Fluorescence of solid anthracene[J]. Nature, 1947, 159(4047): 706.
6. Ganguly S C. Fluorescence of Anthracene in Presence of Naphthacene[J]. Nature, 1943, 151(3841): 673.
7. Lönsjö O. Efficiency of a Scintillation Counter with Anthracene Phosphor for High-Energy Gamma-Rays[J]. Nature, 1952, 169(4296): 365.
8. Moore G F. Delayed excimer emission from anthracene[J]. Nature, 1966, 212(5069): 1452.
9. Wigley C B. The target cell in 7, 12-dimethylbenz (A) anthracene carcinogenesis in the mouse submandibular gland in vivo and in vitro[J]. British journal of cancer, 1973, 28(1): 85.
10. Craig D P, Hobbins P C. Polarized Ultra-Violet Absorption of Anthracene[J]. Nature, 1953, 171(4352): 566.
11. https://omlc.org/spectra/PhotochemCAD/html/022.html
12. Collin G, Höke H, Talbiersky J. Carbazole[J]. Ullmann's Encyclopedia of Industrial Chemistry, 2000.