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Argemone spp

Argemone grandiflora (Papaveraceae) phy 11,461 72 Argemone mexicana (Papaveraceae) cccc 40,1576 75 Argemone ochroleuca (Papaveraceae) cccc 38,2307 73 Corydalis koidzumiana (Papaveraceae) yz 94, 844 74 Corydalis spp. (Papaveraceae) phy 13,2620 74 Fumaria bella (Papaveraceae) jnp 49,178 86 Fumaria capreolata (Papaveraceae) jnp 49,178 86 Fumaria parviflora (Papaveraceae) jnp 44, 475 81 Fumaria vaillantii (Papaveraceae) phy 22,2073 83 Papaver commutatum (Papaveraceae) pm 62, 483 96... [Pg.114]

Chelidonium majus, Argemone, Bocconia, Corydalis, Eschscholzia, Glaucium, Macleaya, Papaver somniferum (opium poppy), Sanguinaria spp. (Papaveraceae), Fumaria officinalis (fumitory) (Fumariaceae)... [Pg.105]

Menispermaceae), Argemone, Chelidonium, Corydalis (Papaveraceae), Coptis, ThaEctnm (Ranunculacae), Evodia, Toddalia, fanthoxylum (Rutaceae) spp. [Pg.174]

Coelodine (Annonaceae), Berberis, Hydrastis, Mahonia, Nandina (Berberidaceae), Archangelica (Menispermaceae), Argemone, Chelidonium, Corydalis (Papaveraceae), Coptis, Thalictrum (Ranunculacae), Evodia, fanthoxylum (Rutaceae) spp. Strychnos aculeata, S. ignatii,... [Pg.178]

Argemone, Bocconia, Chelidonium majus (Papaveraceae) [root], Eschscholzia, Glaucium, Sanguinaria (Papaveraceae) spp., Z antkoxylum americanum (Rutaceae)... [Pg.228]

Juglone (= 5-Hydroxy-1,4- in Cotula (Asteraceae), Cactus (Cactaceae), Argemone (Papaveraceae), Taxodium (Taxodiaceae) spp. Juglans cinerea,J. nigra MLCK, PKA, PKC (a 3)... [Pg.313]

Argemone mexicana, Bocconia spp., Chelidonium majus [root], Eschscholtzia californica [cell culture] (Papaveraceae) ffinthoxylum zanthoxyloides (Fagara xanthoxylum) (Rutaceae) ffinthoxylum americanum, z(. spp. (Rutaceae)... [Pg.363]

Additional oxidative coupling processes among the various methylated derivatives of laudanosoline yield many other families of bases, including the pavine argemonine (88) from Argemone mexicana E berberine (89) from Hydrastis canadensis E which, despite its toxicity, has been used as an antimalarial protopine (90) and chelidonine (91) from Chelidonium majus E rhoeadine (92) and the cephalotaxus ester harringtonine (93) from Japanese plum yews ( Cephalotaxus spp.), which is a compound of some significance because it possesses potent antileukemic activity (see Fig. 3). [Pg.545]

In addition to the completely symmetrical pavine alkaloids, Stermitz et al. (518) found other pavine alkaloids of mrmitagine type (Tables X and XI) in Argemone munita, spp. rotundata. The location of the substituents of the two aromatic rings was determined on the one hand by the classic chemical method, i.e., isolation of hemipinic (Ilb) and meta-hemipinic (lla) acids after alkaline oxidation of 0,0-dimethylmunitagine and, on the other, by NMR analysis oxidative degradation of argemonine resulted only in metahemipinic acid (Ha) and its methylimide (III), respectively. [Pg.376]

Figure 1.19. Tyrosine-derived alkaloids in the Rhoeadales, Berberidales, and Ranales. The first compound synthesized is norlaudanosoline, and nine distinct types of alkaloids are encountered either in restricted taxa or widely distributed A—salutaridine B— morphine pathway restricted to Papaver section Mecones C—isothebaine pathway, characteristic of Papaver section Macrantha D—Papaver section Miltantha E—Papaver section Scapiflora F-encountered in Chelidonium (Papaveraceae-Rhoeadales) and Berberis G—characteristic for Papaver section Orthoroedes, the Corydalis dicentra and Chelidonium spp. H—cryptowoline I—Papaver section Scapiflora, genus Escholtzia, and Argemone J—Papaver sections Orthoroedes and Pilosa, Data are compiled from publications by Stermitz (1968, 1974), Santavy (1966), Santavy et al. (1965, 1966) Slavik (1955), Slavik et al. (1963), Pfeifer (1962), and Tetenyi and co-workers (1961, 1965, 1967, 1968), Bandoni, et al. (1972, 1975). The reaction pathways are according to Barton and Widdowson (1972). Only pathways A, B, and C are shown in detail the others are only suggestions. The pathways leading to the dimeric (bis) alkaloids are not shown. Figure 1.19. Tyrosine-derived alkaloids in the Rhoeadales, Berberidales, and Ranales. The first compound synthesized is norlaudanosoline, and nine distinct types of alkaloids are encountered either in restricted taxa or widely distributed A—salutaridine B— morphine pathway restricted to Papaver section Mecones C—isothebaine pathway, characteristic of Papaver section Macrantha D—Papaver section Miltantha E—Papaver section Scapiflora F-encountered in Chelidonium (Papaveraceae-Rhoeadales) and Berberis G—characteristic for Papaver section Orthoroedes, the Corydalis dicentra and Chelidonium spp. H—cryptowoline I—Papaver section Scapiflora, genus Escholtzia, and Argemone J—Papaver sections Orthoroedes and Pilosa, Data are compiled from publications by Stermitz (1968, 1974), Santavy (1966), Santavy et al. (1965, 1966) Slavik (1955), Slavik et al. (1963), Pfeifer (1962), and Tetenyi and co-workers (1961, 1965, 1967, 1968), Bandoni, et al. (1972, 1975). The reaction pathways are according to Barton and Widdowson (1972). Only pathways A, B, and C are shown in detail the others are only suggestions. The pathways leading to the dimeric (bis) alkaloids are not shown.
See other pages where Argemone spp is mentioned: [Pg.785]    [Pg.104]    [Pg.145]    [Pg.266]    [Pg.811]    [Pg.785]    [Pg.104]    [Pg.145]    [Pg.266]    [Pg.811]    [Pg.149]    [Pg.98]    [Pg.157]   
See also in sourсe #XX -- [ Pg.169 ]



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