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Metabolism alkaloid

D-Arginine and D-ornithine metabolism D-Alanine metabolism Glutathione metabolism Alkaloid biosynthesis I Alkaloid biosynthesis II Metabolism of Complex Carbohydrates Starch and sucrose metabolism Biosynthesis and degradation of glycoprotein... [Pg.387]

The same phenomenon was observed for mitraciliatine (10) and the closed ring E alkaloids 14-19, where the percentage metabolism by O-demethylation estimated by formaldehyde production ( 1%) was much less than the degree of total metabolism (25-69%). Nevertheless, both hirsutine and mitraciliatine gave detectable amounts of a compound assumed by TLC analysis to be an 0-(17)-demethyl metabolite, whereas such was not the case with 14-19. Hirsutine and mitraciliatine were also metabolized (to unidentified products) by both rat and guinea pig liver microsomes, which did not metabolize alkaloids 4-6, 9, and 11-13. [Pg.333]

Keywords Amaryllidaceae alkaloid plant secondary metabolism alkaloid biosynthesis natural products systems biology galanthamine... [Pg.53]

Twyman RM, Verpoorte R, Memelink J, Christon P (2003) Gtmetic modification of secraid-aty metabolism alkaloids. In Thomas B, Murphy DJ, Murray B (eds) Encyclopedia of applied plant sciences. Academic, New Ymk... [Pg.245]

Another way to show that plants are actively metabolizing alkaloids is by determining the fluctuations that occur during a single day. In essence, this is catabolism of alkaloids with metabolites unknown. [Pg.190]

Dibenz[h,e]azepine-6,11-diones ent-Morphinan nomenclature, 1, 29 Morphinan, 1,2,3,4-tetrahydro-nomenclature, 1, 29 14-a-Morphinan, N-methyl-synthesis, 1, 480 Morphinans nomenclature, 1, 29 as pharmaceuticals, 1, 148 synthesis, 2, 377 Morphine, 2, 512 as analgesic, 1, 167 as metabolite of normorphine, 1, 235 as pharmaceutical, 1, 146, 147, 148 synthesis, 1, 480 Morphine alkaloids structure, 4, 534 Morphin-7-en nomenclature, 1, 29 Morphinone, dihydro-as pharmaceutical, 1, 147 Morpholine — see also 1,4-Oxazine, tetrahydrocarcinogenicity, 1, 229 corrosion inhibitor, 1, 409 metabolism, 1, 226 nomenclature, 3, 996 structure, 2, 5 synthesis, 2, 89 Morpholine, 4-aciyloyl-polymers, 1, 291 Morpholine, alkenyl-polymers, 1, 291... [Pg.704]

Smirnova and Moshkov have investigated the effects of the removal of leaves or buds and of grafting on the alkaloidal content of lupins, and Wallebroek has studied the alkaloidal and nitrogenous metabolism of Lupinus luteus seeds on germination. ... [Pg.119]

The literature of alkaloids can conveniently be divided into five sections, dealing with (1) the occurrence and distribution of these substances in plants (2) biogenesis, or the methods by which alkaloids are produced in the course of plant metabolism (3) analysis, ranging from the commercial and industrial estimation of particular alkaloids to the separation, purification and description of the individual components of the natural mixture of alkaloids, which normally occurs in plants (4) determination of structure and (5) pharmacological action. [Pg.811]

The hyoscine system occurs alone in all young plants and may continue throughout life in specimens in the northern area it may represent the original alkaloid metabolism of the plant. The hyoscyamine system appears only at the age of four to six months, and in the southern area it replaces the hyoscine system almost completely it appears to be an adapted system and may represent the adult alkaloid metabolism of the plant. Usually both systems are present in varying proportions. [Pg.814]

A -Pyrroline has been prepared in low yield by oxidation of proline with sodium hypochlorite (71), persulfate (102), and periodate (103). A -Pyrroline and A -piperideine are products of enzymic oxidation via deamination of putrescine and cadaverine or ornithine and lysine, respectively (104,105). This process plays an important part in metabolism and in the biosynthesis of various heterocyclic compounds, especially of alkaloids. [Pg.260]

The first step in this study has involved experiments which synthesize alkaloids in vitro under quasi-cellular conditions, using reactions which can proceed in the living cell and compounds which actually occur in the cell or which are supposed to be intermediates in the plant metabolism. Such synthesesaredesignatedassyntheses under physiological conditions. ... [Pg.295]

Hartmann T, Ober D (2000) Biosynthesis and Metabolism of Pyrrolizidine Alkaloids in Plants and Specialized Insect Herbivores. 209. 207-243 Haseley SR, Kamerling JP, Vliegenthart JFG (2002) Unravelling Carbohydrate Interactions with Biosensors Using Surface Plasmon Resonance (SPR) Detection. 218 93-114... [Pg.233]

In the face of the failure of rational approaches in the treatment of AzD it is perhaps not surprising that there have been many less rational ones. These include the use of vasodilators and nootropics. The former, such as hydergine, a mixture of ergot alkaloids, are intended to increase cerebral blood flow and neuronal metabolism despite some reduction in blood pressure, while the latter, like piracetam, are metabolic stimulants that increase cerebral metabolism and ATP production. Neither are of proven value in AzD. [Pg.392]

N-Nitrosamines are formed during processing and smoking of tobacco products. Proteins, agricultural chemicals and alkaloids in tobacco products serve as major precursors for volatile, nonvolatile, and tobacco-specific nitrosamines (Figure 1). In this review we will summarize the progress achieved in respect to tobacco nitrosamines since the last ACS symposium in Boston in June of 1978 (J ). Additional papers will review the metabolism of cyclic N-nitrosamines, including that of N -nitrosonornicotine 1) and the correlation between tobacco and alcohol consumption and cancer of the upper alimentary tract (J ). [Pg.247]

E) coumarins, (F) quinones, (G) flavonoids, (H) tannins, (I) alkaloids, (J) terpenoids and steroids and (K) miscellaneous and unknowns. Although many of these compounds are secondary products of plant metabolism, several are also degradation products which occur in the presence of microbial enzymes. [Pg.4]

Suzuki, T., Ashihara, H., Waller G.R.., Purine and purine alkaloid metabolism in Camellia and Coffea plant, Phytochemistry, 31,2575,1992... [Pg.21]


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See also in sourсe #XX -- [ Pg.754 ]

See also in sourсe #XX -- [ Pg.754 ]




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