Decane

Decane is a lipid of Fatty Acyls (FA) class.

Cross Reference

There are no associated biomedical information in the current reference collection.

Current reference collection contains 4844 references associated with Decane in LipidPedia. Due to lack of full text of references or no associated biomedical terms are recognized in our current text-mining method, we cannot extract any biomedical terms related to diseases, pathways, locations, functions, genes, lipids, and animal models from the associated reference collection.

Users can download the reference list at the bottom of this page and read the reference manually to find out biomedical information.


Here are additional resources we collected from PubChem and MeSH for Decane

Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with Decane

PubChem Biomolecular Interactions and Pathways

NCBI Entrez Crosslinks

All references with Decane

Download all related citations
Per page 10 20 50 100 | Total 1520
Authors Title Published Journal PubMed Link
Chang YC et al. New Anti-Inflammatory 9,11-Secosterols with a Rare Tricyclo[5,2,1,1]decane Ring from a Formosan Gorgonian Pinnigorgia sp. 2016 Mar Drugs pmid:27898026
Han G et al. Copper-catalyzed intramolecular trifluoromethylation of N-benzylacrylamides coupled with dearomatization: access to CF3-containing 2-azaspiro[4.5]decanes. 2014 Org. Lett. pmid:24901480
Shibuta M et al. Probing of an adsorbate-specific excited state on an organic insulating surface by two-photon photoemission spectroscopy. 2014 J. Am. Chem. Soc. pmid:24451024
Sotthewes K et al. Molecular dynamics and energy landscape of decanethiolates in self-assembled monolayers on Au(111) studied by scanning tunneling microscopy. 2013 Langmuir pmid:23421806
Njauw CW et al. Molecular interactions between lecithin and bile salts/acids in oils and their effects on reverse micellization. 2013 Langmuir pmid:23441904
Kato Y et al. Discovery of 2,8-diazaspiro[4.5]decane-based trisubstituted urea derivatives as highly potent soluble epoxide hydrolase inhibitors and orally active drug candidates for treating hypertension. 2013 Bioorg. Med. Chem. Lett. pmid:24035338
Choi YJ and Lee SY Microbial production of short-chain alkanes. 2013 Nature pmid:24077097
Bennett NB and Stoltz BM A unified approach to the daucane and sphenolobane bicyclo[5.3.0]decane core: enantioselective total syntheses of daucene, daucenal, epoxydaucenal B, and 14-para-anisoyloxydauc-4,8-diene. 2013 Chemistry pmid:24302464
Ross DS Comment on "prebiotic chemistry within a simple impacting icy mixture". 2013 J Phys Chem A pmid:24224564
Goldman N and Tamblyn I Reply to "comment on 'prebiotic chemistry within a simple impacting icy mixture'". 2013 J Phys Chem A pmid:24279804