Studies in Natural Products Chemistry: Structure and Chemistry (Part D)

Передня обкладинка
Elsevier, 24 лип. 1995 р. - 680 стор.

Rapid advances in chromatographic procedures, spectroscopic techniques and pharmacological assay methods have resulted in the discovery of an increasing number of new and interesting natural products from terrestrial and marine sources. The present volume contains comprehensive reviews on some of the major advances in this field which have taken place in recent years. The reviews include those on: novel metabolites from marine gastropods; the chemistry of marine natural products of the Halenaquinol family; secondary metabolites from Echinoderms and Bryozoans; triterpenoids and aromatic compounds from medicinal plants; chemistry and activity of sesquiterpenes from the genus Lactarius; the chemistry of bile alcohols; antifungal sesquiterpene dialdehydes; annonaceous acetogenins; nargenicin macrolides; and lignans and diarylheptanoids. Tropane alkaloids and phenolides formed by root cultures are also reviewed. Articles on natural Diels-Alder type adducts, the use of computer aided overlay for modelling the substrate binding domain of HLADH, applications of 170 NMR spectroscopy to natural product chemistry and the role of biological raw materials in synthesis are included. Volume 17 provides material of interest to natural products chemists.

З цієї книги

Зміст

Theoretical studies of CD spectra
33
Chapter 3 Bryozoan secondary metabolites and their chemical ecology
73
Chapter 4 Structure and biological activity of triteipenoids and aromatic compounds from medicinal plants
113
Chemistry and biological activity
153
Disorders of choylesterol sidechain oxidation in cerebrotendinous xanthomatosis
207
Chapter 7 Antifungal sesquiteipene dialdehydes from the Warburgia plants and their synergists
233
Chapter 8 Determination of relative and absolute configuration in the Annonaceous acetogenins
251
Chapter 9 The chemistry of the nargenicin macrolides
283
Chapter 11 The chemistiy of natural diarylheptanoids
357
Chapter 12 Tropane alkaloids in root cultures of Solanaccous plants
395
Chapter 13 Phenolics in root cultures of medicinal plants
421
Chapter 14 Chemistry and biosynthesis of natural DielsAlder type adducts from Moraceous plants
451
Chapter 15 Modelling the substrate binding domain of horse liver alcohol dehydrogenase HLADH by computer aided substrate overlay
479
Chapter 16 Applications of 17O NMR spectroscopy to natural products chemistry
549
Chapter 17 The role of biological raw materials in synthesis
601
Subject Index
655

Chapter 10 Some aspects of the chemistry of lignans
311

Інші видання - Показати все

Загальні терміни та фрази

Популярні уривки

Сторінка 69 - This work was supported in part by grants from the Ministry of Education, Science and Culture...
Сторінка 224 - VM: Familial diseases with storage of sterols other than cholesterol: cerebrotendinous xanthomatosis and sitosterolemia with xanthomatosis, in The Metabolic Basis of Inherited Disease, 5th ed.
Сторінка 249 - Fungal sterols and the mode of action of the polyene antibiotics.
Сторінка 226 - SM (1973). The metabolism of cholestanol, cholesterol and bile acids in cerebrotendinous xanthomatosis. J. Clin. Invest., 52, 2822-35 4.
Сторінка 231 - Leitersdorf E, Reshef A, Meiner V, Levitzki R, Schwartz SP, Dann EJ, Berkman N, Cali JJ, Klapholz L, Berginer VM 1993 Frameshift and splice-junction mutations in the sterol 27-hydroxylase gene cause cerebrotendinous xanthomatosis in Jews of Moroccan origin. J Clin Invest 91:2488-2496.
Сторінка 229 - Diagnosis of cerebrotendinous xanthomatosis (CTX) and effect of chenodeoxycholic acid therapy by analysis of urine using capillary gas chromatography. Clin. Chim. Acta.
Сторінка xii - University of Medicine & Dentistry of New Jersey New Jersey Medical School...
Сторінка 357 - Research Group for Alkaloid Chemistry of the Hungarian Academy of Sciences, Technical University, Budapest (Received...
Сторінка 28 - JT Baker and V. Murphy, Handbook of Marine Science, Compounds from Marine Organisms, Vol.
Сторінка 248 - CS Barnes and JW Loder: The structure of polygodial: a new sesquiterpene dialdehyde from Polygonum hydropiper L.

Про автора (1995)

Atta-ur-Rahman, Professor Emeritus, International Center for Chemical and Biological Sciences (H. E. J. Research Institute of Chemistry and Dr. Panjwani Center for Molecular Medicine and Drug Research), University of Karachi, Pakistan, was the Pakistan Federal Minister for Science and Technology (2000-2002), Federal Minister of Education (2002), and Chairman of the Higher Education Commission with the status of a Federal Minister from 2002-2008. He is a Fellow of the Royal Society of London (FRS) and an UNESCO Science Laureate. He is a leading scientist with more than 1283 publications in several fields of organic chemistry.

Бібліографічна інформація