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Evolution of camalexin and structurally related indolic compounds.Thomas Rauhut et al.Phytochemistry, 70(15-16), 1638-1644 (2009-06-16) Structural identification of Diindole agonists of the aryl hydrocarbon receptor derived from degradation of indole-3-pyruvic acid.Goutam Chowdhury et al.Chemical research in toxicology, 22(12), 1905-1912 (2009-10-29) Biosynthesis of the halogenated auxin, 4-chloroindole-3-acetic acid.Nathan D Tivendale et al.Plant physiology, 159(3), 1055-1063 (2012-05-11) Biochemical and behavioural studies on indole-pyruvic acid: a keto-analogue of tryptophan.L Bacciottini et al.Pharmacological research communications, 19(11), 803-817 (1987-11-01) Indole-3-pyruvic and -propionic acids, kynurenic acid, and related metabolites as luminophores and free-radical scavengers.R Hardeland et al.Advances in experimental medicine and biology, 467, 389-395 (2000-03-18) The biochemical mechanism of auxin biosynthesis by an arabidopsis YUCCA flavin-containing monooxygenase.Xinhua Dai et al.The Journal of biological chemistry, 288(3), 1448-1457 (2012-11-29) A new gene for auxin synthesis.Klaus Palme et al.Cell, 133(1), 31-32 (2008-04-09) Indole-3-acetic acid biosynthetic pathway and aromatic amino acid aminotransferase activities in Pantoea dispersa strain GPK.G B Kulkarni et al.Letters in applied microbiology, 56(5), 340-347 (2013-03-02) YUC and TAA1/TAR proteins function in the same pathway for auxin biosynthesis.Nancy R Hofmann The Plant cell, 23(11), 3869-3869 (2011-11-24) Structural insight into the inhibition of human kynurenine aminotransferase I/glutamine transaminase K.Qian Han et al.Journal of medicinal chemistry, 52(9), 2786-2793 (2009-04-03) Functional characterization of the CKRC1/TAA1 gene and dissection of hormonal actions in the Arabidopsis root.Zhao-Yang Zhou et al.The Plant journal : for cell and molecular biology, 66(3), 516-527 (2011-01-25) Cyclic ketones and substituted α-keto acids as alternative substrates for novel Biginelli-like scaffold synthesesAbelman, Matthew M, et al. 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