Indolacetaldoxim (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Indolacetaldoxim" in German language version.

refsWebsite
Global rank German rank
2nd place
3rd place
4th place
7th place
2,106th place
139th place
8,332nd place
1,213th place
8,573rd place
1,211th place
43rd place
985th place

cas.org (Global: 8,332nd place; German: 1,213th place)

commonchemistry.cas.org

chemspider.com (Global: 8,573rd place; German: 1,211th place)

doi.org (Global: 2nd place; German: 3rd place)

  • Michael Dalgaard Mikkelsen, Carsten Hørslev Hansen, Ute Wittstock, Barbara Ann Halkier: Cytochrome P450 CYP79B2 from Arabidopsis Catalyzes the Conversion of Tryptophan to Indole-3-acetaldoxime, a Precursor of Indole Glucosinolates and Indole-3-acetic Acid. In: Journal of Biological Chemistry. Band 275, Nr. 43, Oktober 2000, S. 33712–33717, doi:10.1074/jbc.M001667200.
  • Y. Mano, K. Nemoto: The pathway of auxin biosynthesis in plants. In: Journal of Experimental Botany. Band 63, Nr. 8, 1. Mai 2012, S. 2853–2872, doi:10.1093/jxb/ers091.
  • M.Soledade C Pedras, Sabine Montaut: Probing crucial metabolic pathways in fungal pathogens of crucifers: biotransformation of indole-3-acetaldoxime, 4-hydroxyphenylacetaldoxime, and their metabolites. In: Bioorganic & Medicinal Chemistry. Band 11, Nr. 14, Juli 2003, S. 3115–3120, doi:10.1016/S0968-0896(03)00241-4.
  • Erich Glawischnig, Bjarne Gram Hansen, Carl Erik Olsen, Barbara Ann Halkier: Camalexin is synthesized from indole-3-acetaldoxime, a key branching point between primary and secondary metabolism in Arabidopsis. In: Proceedings of the National Academy of Sciences. Band 101, Nr. 21, 25. Mai 2004, S. 8245–8250, doi:10.1073/pnas.0305876101, PMID 15148388, PMC 419588 (freier Volltext).
  • Majse Nafisi, Sameer Goregaoker, Christopher J. Botanga, Erich Glawischnig, Carl E. Olsen, Barbara A. Halkier, Jane Glazebrook: Arabidopsis Cytochrome P450 Monooxygenase 71A13 Catalyzes the Conversion of Indole-3-Acetaldoxime in Camalexin Synthesis. In: The Plant Cell. Band 19, Nr. 6, 31. Juli 2007, S. 2039–2052, doi:10.1105/tpc.107.051383, PMID 17573535, PMC 1955726 (freier Volltext).
  • Satoko Sugawara, Shojiro Hishiyama, Yusuke Jikumaru, Atsushi Hanada, Takeshi Nishimura, Tomokazu Koshiba, Yunde Zhao, Yuji Kamiya, Hiroyuki Kasahara: Biochemical analyses of indole-3-acetaldoxime-dependent auxin biosynthesis in Arabidopsis. In: Proceedings of the National Academy of Sciences. Band 106, Nr. 13, 31. März 2009, S. 5430–5435, doi:10.1073/pnas.0811226106, PMID 19279202, PMC 2664063 (freier Volltext).
  • J. N. Coker, W. L. Kohlhase, T. F. Martens, A. O. Rogers, G. G. Allan: A General Route to Hydantoins. In: The Journal of Organic Chemistry. Band 27, Nr. 9, September 1962, S. 3201–3204, doi:10.1021/jo01056a051.

google.de (Global: 2,106th place; German: 139th place)

books.google.de

nih.gov (Global: 4th place; German: 7th place)

ncbi.nlm.nih.gov

  • Erich Glawischnig, Bjarne Gram Hansen, Carl Erik Olsen, Barbara Ann Halkier: Camalexin is synthesized from indole-3-acetaldoxime, a key branching point between primary and secondary metabolism in Arabidopsis. In: Proceedings of the National Academy of Sciences. Band 101, Nr. 21, 25. Mai 2004, S. 8245–8250, doi:10.1073/pnas.0305876101, PMID 15148388, PMC 419588 (freier Volltext).
  • Majse Nafisi, Sameer Goregaoker, Christopher J. Botanga, Erich Glawischnig, Carl E. Olsen, Barbara A. Halkier, Jane Glazebrook: Arabidopsis Cytochrome P450 Monooxygenase 71A13 Catalyzes the Conversion of Indole-3-Acetaldoxime in Camalexin Synthesis. In: The Plant Cell. Band 19, Nr. 6, 31. Juli 2007, S. 2039–2052, doi:10.1105/tpc.107.051383, PMID 17573535, PMC 1955726 (freier Volltext).
  • Satoko Sugawara, Shojiro Hishiyama, Yusuke Jikumaru, Atsushi Hanada, Takeshi Nishimura, Tomokazu Koshiba, Yunde Zhao, Yuji Kamiya, Hiroyuki Kasahara: Biochemical analyses of indole-3-acetaldoxime-dependent auxin biosynthesis in Arabidopsis. In: Proceedings of the National Academy of Sciences. Band 106, Nr. 13, 31. März 2009, S. 5430–5435, doi:10.1073/pnas.0811226106, PMID 19279202, PMC 2664063 (freier Volltext).

pubchem.ncbi.nlm.nih.gov

wikidata.org (Global: 43rd place; German: 985th place)