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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
MeSH Review

Isatis

 
 
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High impact information on Isatis

  • Different amounts of isatan B were produced under red and far red light in the two Isatis species [1].
  • Tryptanthrin is a pharmacologically active compound in the anti-inflammatory herb Isatis tinctoria, with potent inhibitory activity on prostaglandin and leukotriene synthesis and on inducible NO synthase [2].
  • Quantitative determination of the dual COX-2/5-LOX inhibitor tryptanthrin in Isatis tinctoria by ESI-LC-MS [3].
  • Isatis tinctoria L. is an old European and Chinese dye plant and anti-inflammatory herb from which the potent cyclooxygenase-2 and 5-lipoxygenase inhibitor tryptanthrin (1) (indolo-[2,1-b]-quinazoline-6,12-dione) was recently isolated as one of the active principles [3].
  • A new indigoid derivative, bisindigotin (1), with 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-antagonistic activity was isolated from the ethanol extract of the Chinese medicinal herb Isatis indigotica [4].
 

Associations of Isatis with chemical compounds

  • Indole is presumably a product of indole-3-glycerol phosphate catabolism in Isatis tinctoria [5].
  • We recently clarified the nature of indigo precursors in woad (Isatis tinctoria L.), by identifying the major indoxyl glycoside as isatan A (indoxyl-3-O-(6'-O-malonyl-beta-D-ribohexo-3-ulopyranoside)), and by correcting the structure of the related isatan B (indoxyl-3-O-beta-D-ribohexo-3-ulopyranoside) [6].
  • Four alkaloids, previously identified in Isatis species, were tested for their inhibitory effect on histamine release [7].
  • The activity in the lipophilic fractions of the Isatis extract could be linked to an unsaturated fatty acid, alpha-linolenic acid [8].
  • The results showed that Isatis indigotica root extract significantly and dose-dependently inhibited the writhing responses of mice and decreased the licking time in both the early and late phases of the formalin test [9].
 

Gene context of Isatis

References

  1. Light quality influences indigo precursors production and seed germination in Isatis tinctoria L. and Isatis indigotica Fort. Tozzi, S., Lercari, B., Angelini, L.G. Photochem. Photobiol. (2005) [Pubmed]
  2. Tryptanthrin content in Isatis tinctoria leaves--a comparative study of selected strains and post-harvest treatments. Oberthür, C., Hamburger, M. Planta Med. (2004) [Pubmed]
  3. Quantitative determination of the dual COX-2/5-LOX inhibitor tryptanthrin in Isatis tinctoria by ESI-LC-MS. Danz, H., Baumann, D., Hamburger, M. Planta Med. (2002) [Pubmed]
  4. Bisindigotin, a TCDD antagonist from the Chinese medicinal herb Isatis indigotica. Wei, X.Y., Leung, C.Y., Wong, C.K., Shen, X.L., Wong, R.N., Cai, Z.W., Mak, N.K. J. Nat. Prod. (2005) [Pubmed]
  5. Identification of an indigo precursor from leaves of Isatis tinctoria (Woad). Maugard, T., Enaud, E., Choisy, P., Legoy, M.D. Phytochemistry (2001) [Pubmed]
  6. The content of indigo precursors in Isatis tinctoria leaves--a comparative study of selected accessions and post-harvest treatments. Oberthür, C., Graf, H., Hamburger, M. Phytochemistry (2004) [Pubmed]
  7. Inhibitory activity of indolin-2-one derivatives on compound 48/80-induced histamine release from mast cells. Rüster, G.U., Hoffmann, B., Hamburger, M. Die Pharmazie. (2004) [Pubmed]
  8. HPLC based activity profiling for 5-lipoxygenase inhibitory activity in Isatis tinctoria leaf extracts. Oberthür, C., Jäggi, R., Hamburger, M. Fitoterapia (2005) [Pubmed]
  9. Studies on the antinociceptive, anti-inflammatory and anti pyretic effects of Isatis indigotica root. Ho, Y.L., Chang, Y.S. Phytomedicine (2002) [Pubmed]
  10. Identification and isolation of the cyclooxygenase-2 inhibitory principle in Isatis tinctoria. Danz, H., Stoyanova, S., Wippich, P., Brattström, A., Hamburger, M. Planta Med. (2001) [Pubmed]
  11. Nutritional support for chronic myelogenous and other leukemias: a review of the scientific literature. Steriti, R. Alternative medicine review : a journal of clinical therapeutic. (2002) [Pubmed]
 
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