214
13
Otles S, Yalcin B (2012) Phenolic compounds analysis of root, stalk, and leaves of nettle.
ScientificWorldJournal 2012:564367. https://doi.org/10.1100/2012/564367
Panter KE, Keeler RF (1989) Chapter 5—Piperidine alkaloids of poison hemlock (Conium maculatum). In:
Toxicants of plant origin, vol I. CRC Press, Boca Raton
Raduner S et al (2006) Alkylamides from Echinacea are a new class of cannabinomimetics. Cannabinoid
type 2 receptor-dependent and -independent immunomodulatory effects. J Biol Chem 281:14192–
14206. https://doi.org/10.1074/jbc.M601074200
Raharjo TJ, Widjaja I, Roytrakul S, Verpoorte R (2004) Comparative proteomics of Cannabis sativa plant
tissues. J Biomol Tech 15:97–106
Rein KS, Snyder RV (2006) The biosynthesis of polyketide metabolites by dinoflagellates. Adv Appl
Microbiol 59:93–125. https://doi.org/10.1016/S0065-2164(06)59004-5
Reynolds T (2005) Hemlock alkaloids from Socrates to poison aloes. Phytochemistry 66:1399–1406.
https://doi.org/10.1016/j.phytochem.2005.04.039
Rios MY, Aguilar-Guadarrama AB, Gutierrez Mdel C (2007) Analgesic activity of affinin, an alkamide
from Heliopsis longipes (Compositae). J Ethnopharmacol 110:364–367. https://doi.org/10.1016/j.
jep.2006.09.041
Rizhsky L et al (2016) Integrating metabolomics and transcriptomics data to discover a biocatalyst that
can generate the amine precursors for alkamide biosynthesis. Plant J 88:775–793. https://doi.
org/10.1111/tpj.13295
Sirikantaramas S, Taura F, Tanaka Y, Ishikawa Y, Morimoto S, Shoyama Y (2005) Tetrahydrocannabinolic acid
synthase, the enzyme controlling marijuana psychoactivity, is secreted into the storage cavity of the
glandular trichomes. Plant Cell Physiol 46:1578–1582. https://doi.org/10.1093/pcp/pci166
Stewart C Jr, Mazourek M, Stellari GM, O’Connell M, Jahn M (2007) Genetic control of pungency in C. chinense via the Pun1 locus. J Exp Bot 58:979–991. https://doi.org/10.1093/jxb/erl243
Stout JM, Boubakir Z, Ambrose SJ, Purves RW, Page JE (2012) The hexanoyl-CoA precursor for cannabinoid
biosynthesis is formed by an acyl-activating enzyme in Cannabis sativa trichomes. Plant J 71:353–365.
https://doi.org/10.1111/j.1365-313X.2012.04949.x
Teaster ND et al (2007) N-Acylethanolamine metabolism interacts with abscisic acid signaling in
Arabidopsis thaliana seedlings. Plant Cell 19:2454–2469. https://doi.org/10.1105/tpc.106.048702
Tretyn A, Kendrick RE (1991) Acetylcholine in plants: presence, metabolism and mechanism of action. Bot
Rev 57(1):33–73. https://doi.org/10.1007/BF02858764
Van Wagoner RM, Satake M, Wright JL (2014) Polyketide biosynthesis in dinoflagellates: what makes it
different? Nat Prod Rep 31:1101–1137. https://doi.org/10.1039/c4np00016a
Woelkart K, Salo-Ahen OM, Bauer R (2008) CB receptor ligands from plants. Curr Top Med Chem 8:173–186
Chapter 13 · Minor Groups of Secondary Metabolites
13
Otles S, Yalcin B (2012) Phenolic compounds analysis of root, stalk, and leaves of nettle.
ScientificWorldJournal 2012:564367. https://doi.org/10.1100/2012/564367
Panter KE, Keeler RF (1989) Chapter 5—Piperidine alkaloids of poison hemlock (Conium maculatum). In:
Toxicants of plant origin, vol I. CRC Press, Boca Raton
Raduner S et al (2006) Alkylamides from Echinacea are a new class of cannabinomimetics. Cannabinoid
type 2 receptor-dependent and -independent immunomodulatory effects. J Biol Chem 281:14192–
14206. https://doi.org/10.1074/jbc.M601074200
Raharjo TJ, Widjaja I, Roytrakul S, Verpoorte R (2004) Comparative proteomics of Cannabis sativa plant
tissues. J Biomol Tech 15:97–106
Rein KS, Snyder RV (2006) The biosynthesis of polyketide metabolites by dinoflagellates. Adv Appl
Microbiol 59:93–125. https://doi.org/10.1016/S0065-2164(06)59004-5
Reynolds T (2005) Hemlock alkaloids from Socrates to poison aloes. Phytochemistry 66:1399–1406.
https://doi.org/10.1016/j.phytochem.2005.04.039
Rios MY, Aguilar-Guadarrama AB, Gutierrez Mdel C (2007) Analgesic activity of affinin, an alkamide
from Heliopsis longipes (Compositae). J Ethnopharmacol 110:364–367. https://doi.org/10.1016/j.
jep.2006.09.041
Rizhsky L et al (2016) Integrating metabolomics and transcriptomics data to discover a biocatalyst that
can generate the amine precursors for alkamide biosynthesis. Plant J 88:775–793. https://doi.
org/10.1111/tpj.13295
Sirikantaramas S, Taura F, Tanaka Y, Ishikawa Y, Morimoto S, Shoyama Y (2005) Tetrahydrocannabinolic acid
synthase, the enzyme controlling marijuana psychoactivity, is secreted into the storage cavity of the
glandular trichomes. Plant Cell Physiol 46:1578–1582. https://doi.org/10.1093/pcp/pci166
Stewart C Jr, Mazourek M, Stellari GM, O’Connell M, Jahn M (2007) Genetic control of pungency in C. chinense via the Pun1 locus. J Exp Bot 58:979–991. https://doi.org/10.1093/jxb/erl243
Stout JM, Boubakir Z, Ambrose SJ, Purves RW, Page JE (2012) The hexanoyl-CoA precursor for cannabinoid
biosynthesis is formed by an acyl-activating enzyme in Cannabis sativa trichomes. Plant J 71:353–365.
https://doi.org/10.1111/j.1365-313X.2012.04949.x
Teaster ND et al (2007) N-Acylethanolamine metabolism interacts with abscisic acid signaling in
Arabidopsis thaliana seedlings. Plant Cell 19:2454–2469. https://doi.org/10.1105/tpc.106.048702
Tretyn A, Kendrick RE (1991) Acetylcholine in plants: presence, metabolism and mechanism of action. Bot
Rev 57(1):33–73. https://doi.org/10.1007/BF02858764
Van Wagoner RM, Satake M, Wright JL (2014) Polyketide biosynthesis in dinoflagellates: what makes it
different? Nat Prod Rep 31:1101–1137. https://doi.org/10.1039/c4np00016a
Woelkart K, Salo-Ahen OM, Bauer R (2008) CB receptor ligands from plants. Curr Top Med Chem 8:173–186
Chapter 13 · Minor Groups of Secondary Metabolites