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Physiologically active compounds

The object of the present series of experiments is to give directions for the preparation of a few of the better known organic compounds which possess pronounced physiological activity. The semimicro method is used throughout, but it can be easily adapted to the macro method by multiplying the quantities given by 4 or [Pg.317]

5 times, using flasks instead of tubes, and allowing 50 per cent more time for the reaction. [Pg.318]

Acetylsalicylic acid is prepared by acetylation of the hydroxycar-boxylic acid. Acetic anhydride or acetyl chloride may be used for the acetylation. [Pg.318]

Directions are given for both methods. The acetyl chloride method is more rapid but at the same time more expensive. [Pg.318]

The keto ester exhibits typical carbonyl properties, and reacts first with phenylhydrazine to form a phenylhydrazone shown in the above equation in brackets. The phenylhydrazone on heating loses [Pg.319]


Chapters V-X deal respectively with Heterocyclic and Alicyclic Compounds Miscellaneous Reactions Organic Reagents in Inorganic and Organic Chemistry Dyestuffs, Indicators and Related Compounds Some Physiologically-Active Compounds and Synthetic Polymers. Many of these preparations are of course intended for advanced students, but a mere perusal of the experimental details of selected preparations by those whose time for experimental work is limited may assist to impress them on the memory. Attention is particularly directed to the chapter... [Pg.1193]

Landau MA (1981) Molecular Mechanisms of Effect of Physiologically Active Compounds, (in Russian) Nauka... [Pg.48]

Posner G. H. Stereocontrolled Synthesis of Functionalized Cyclohexenes Via Diels-Alder Cycloadditions of 2-Pyrones and 2-Pyridones-Applications to Synthesis of Physiologically Active Compounds in Stereocontrolled Org. Synth. 1994 177, Ed. Trost B. M., Pb. Blackwell Oxford... [Pg.317]

It has been shown that the imidoyl chloride moiety of 2(lff)-pyrazinones can imdergo an easy addition/elimination reaction with alkyl amines [24], while reactions with anilines proceed under harsher conditions. Ullmann coupling [109-113] of 2(lff)-pyrazinones with substituted anilines could open the way to the libraries of physiologically active compounds useful in inhibiting HIV replication [7]. Polymer-bound pyrazinone was successfully... [Pg.294]

SLIPPER Institute of Physiologically Active Compounds, Russia http //camdipac.ac.ru 2D 13, 14... [Pg.396]

During a search for physiologically active compounds in South African plants, a new hasubanan ester acetal alkaloid, methylstephavanine (6), was isolated from Stephania abyssinica (19). The H-NMR spectrum of the new alkaloid 6 exhibited signals for one methylenedioxy, one N-methyl, and four methoxyl groups (19) (Table II). Its mass spectrum revealed the most abundant ion peak at m/z 229, indicating a close resemblance to the known hasubanan alkaloid, stephavanine (18). [Pg.323]

HYBOTPLUS-2000 is available from the MolPro Project. Contact Professor O. A. Raevsky, Institute of Physiologically Active Compounds, Chemo-golovka, Moscow Region, 142432, Russia e-mail raevsky ipac.ac.ru... [Pg.241]

Square-wave voltammetiy apphed to experiments with a thin-layer electrochemical cell is a valuable analytical tool for determination of small amounts of analytes [46,154-157], e.g., the determination of drugs and species with biological activity [158]. Over the past decades, SWV has been frequently applied to study physiologically active compounds embedded in a thin-film that is imposed on an electrode snrface [78,159]. Moreover, a graphite electrode modified with a thin-film... [Pg.130]

Non-crop plants associated with the crop species offer possibilities for allelopathic weed control. In this study Brassica campestris (wild mustard), which is an important weed in Santa Cruz County, and broccoli, a common crop, were intercropped, The allelopathic potential of both species and the changes in this potential throughout their life cycle were demonstrated with experiments in the laboratory. Effects of different planting densities and sowing time of canpestris on the crop yield are analyzed. Preliminary steps to separate the physiologically active compound(s) are described. The possibilities for the use of Brassica campestris in agroecosystem design as a non-crop plant that promotes pest control are described. [Pg.262]

Rhodes, M.J.C., Physiologically-active compounds in plant foods an overview, Proc. Nutr. Soc., 55, 371, 1996. [Pg.251]

Property III. Biomolecular activity—pathways leading to physiologically active compounds ( Speculative Metabolism )... [Pg.201]


See other pages where Physiologically active compounds is mentioned: [Pg.996]    [Pg.997]    [Pg.999]    [Pg.1001]    [Pg.1003]    [Pg.1005]    [Pg.1007]    [Pg.1009]    [Pg.1011]    [Pg.1013]    [Pg.401]    [Pg.827]    [Pg.1223]    [Pg.1224]    [Pg.1228]    [Pg.1230]    [Pg.1232]    [Pg.1234]    [Pg.1236]    [Pg.1238]    [Pg.175]    [Pg.214]    [Pg.267]    [Pg.303]    [Pg.391]    [Pg.236]    [Pg.261]    [Pg.239]    [Pg.42]    [Pg.123]    [Pg.996]    [Pg.997]    [Pg.999]    [Pg.1001]    [Pg.1003]    [Pg.1005]    [Pg.1007]   
See also in sourсe #XX -- [ Pg.317 , Pg.318 , Pg.319 , Pg.320 , Pg.321 , Pg.322 ]




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