The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
Chemical Compound Review

Ferutinin     [(3R,3aR,4S,8aR)-3-hydroxy- 6,8a-dimethyl-3...

Synonyms: CHEMBL465040, SureCN12512403, NSC-606959, NSC606959, ZINC02564854, ...
 
 
Welcome! If you are familiar with the subject of this article, you can contribute to this open access knowledge base by deleting incorrect information, restructuring or completely rewriting any text. Read more.
 

Disease relevance of Jaeschkeanadiol p-hydroxybenzoate

 

High impact information on Jaeschkeanadiol p-hydroxybenzoate

 

Biological context of Jaeschkeanadiol p-hydroxybenzoate

  • Ferutinin establishes a transmembrane potential in BLM equal to the Nernst's potential [2].
  • In conclusion, if repetitively administered, ferutinin was able to stimulate sexual behavior after acute ingestion, but exerted a negative influence on the sexual capacity of potent male rats, whereas teferdin only improved copulatory performance of sluggish/impotent animals [3].
 

Anatomical context of Jaeschkeanadiol p-hydroxybenzoate

 

Associations of Jaeschkeanadiol p-hydroxybenzoate with other chemical compounds

 

Gene context of Jaeschkeanadiol p-hydroxybenzoate

  • The estrogenic activity of a series of analogues of the daucane ester ferutinin (1a) modified at the acyl moiety was investigated in a yeast screen containing the human estrogen receptor alpha [5].

References

  1. Calcium ionophoretic and apoptotic effects of ferutinin in the human Jurkat T-cell line. Macho, A., Blanco-Molina, M., Spagliardi, P., Appendino, G., Bremner, P., Heinrich, M., Fiebich, B.L., Muñoz, E. Biochem. Pharmacol. (2004) [Pubmed]
  2. Ionophoretic properties of ferutinin. Zamaraeva, M.V., Hagelgans, A.I., Abramov, A.Y., Ternovsky, V.I., Merzlyak, P.G., Tashmukhamedov, B.A., Saidkhodzjaev, A.I. Cell Calcium (1997) [Pubmed]
  3. Activity of single components of Ferula hermonis on male rat sexual behavior. Zanoli, P., Rivasi, M., Zavatti, M., Brusiani, F., Vezzalini, F., Baraldi, M. Int. J. Impot. Res. (2005) [Pubmed]
  4. Ferutinin stimulates nitric oxide synthase activity in median eminence of the rat. Colman-Saizarbitoria, T., Boutros, P., Amesty, A., Bahsas, A., Mathison, Y., Garrido, M.d.e.l. .R., Israel, A. Journal of ethnopharmacology. (2006) [Pubmed]
  5. Daucane phytoestrogens: a structure-activity study. Appendino, G., Spagliardi, P., Cravotto, G., Pocock, V., Milligan, S. J. Nat. Prod. (2002) [Pubmed]
 
WikiGenes - Universities