Cargando…

Biflavanoids : chemical and pharmacological aspects /

Biflavanoids are an important class of plant metabolites offering a range of activities, good availability and relatively low toxicity. Long thought to hold possible therapeutic potential, the recent surge in interest for natural product drug discovery has further highlighted the possibility of usin...

Descripción completa

Detalles Bibliográficos
Clasificación:Libro Electrónico
Autores principales: Lone, Shabir Hussain (Autor), Khuroo, Mohd Akbar (Autor)
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Amsterdam, Netherlands : Elsevier Ltd., 2016.
Temas:
Acceso en línea:Texto completo

MARC

LEADER 00000cam a2200000 i 4500
001 SCIDIR_ocn946997807
003 OCoLC
005 20231120112104.0
006 m o d
007 cr cnu|||unuuu
008 160420s2016 ne a ob 000 0 eng d
040 |a N$T  |b eng  |e rda  |e pn  |c N$T  |d N$T  |d YDXCP  |d OCLCF  |d OPELS  |d EBLCP  |d IDEBK  |d OCLCQ  |d OTZ  |d OCLCQ  |d U3W  |d D6H  |d MERER  |d OCLCQ  |d LQU  |d OCLCQ  |d S2H  |d OCLCO  |d LVT  |d OCLCO  |d OCLCQ  |d OCLCO 
019 |a 950461352  |a 953860061  |a 1105170370  |a 1105560283  |a 1229542287 
020 |a 9780081011904  |q (electronic bk.) 
020 |a 0081011903  |q (electronic bk.) 
020 |a 0081010303 
020 |a 9780081010303 
020 |z 9780081010303 
035 |a (OCoLC)946997807  |z (OCoLC)950461352  |z (OCoLC)953860061  |z (OCoLC)1105170370  |z (OCoLC)1105560283  |z (OCoLC)1229542287 
050 4 |a QK898.F5 
072 7 |a NAT  |x 026000  |2 bisacsh 
082 0 4 |a 582.019218  |2 23 
100 1 |a Lone, Shabir Hussain,  |e author. 
245 1 0 |a Biflavanoids :  |b chemical and pharmacological aspects /  |c Shabir Hussain Lone, Mohd Akbar Khuroo. 
264 1 |a Amsterdam, Netherlands :  |b Elsevier Ltd.,  |c 2016. 
300 |a 1 online resource :  |b illustrations 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
504 |a Includes bibliographical references. 
588 0 |a Vendor-supplied metadata. 
520 |a Biflavanoids are an important class of plant metabolites offering a range of activities, good availability and relatively low toxicity. Long thought to hold possible therapeutic potential, the recent surge in interest for natural product drug discovery has further highlighted the possibility of using them in the discovery of new drugs, and Biflavanoids: Chemical and Pharmacological Aspects provides a quick reference to the area in a focused manner, to support and encourage further research. Beginning with a focus on the structural features and occurrence of biflavanoids, Chapter 1 reviews key background information including notes on nomenclature and natural distribution. Chapter 2 then goes on to discuss methods for identification and isolation, with separation and purification using various chromatography methods reviewed, followed by identification via UV spectroscopy, NRM spectroscopy and mass spectrometry. Synthesis is the focus of Chapter 3, with a broad range of synthetic methods outlined, before the book concludes in Chapter 4 by describing the biochemical pharmacology of Biflavanoids and their anticancer, antimicrobial, antiviral, anti-inflammatory and analgesic activity. With its discussion of both the underlying chemistry and biological activity of Biflavanoids, Biflavanoids: Chemical and Pharmacological Aspects is a concise guide to this important class of compounds for all those working in the fields of medicinal chemistry and natural products drug discovery. 
505 0 |a Front Cover; Biflavanoids; Copyright Page; Contents; 1 Structural Features and Occurrence of Biflavanoids; 1.1 Introduction; 1.2 Nomenclature of Biflavanoids; 1.3 Structures of Biflavanoids; 1.4 Natural Distribution of Biflavanoids; 1.5 Conclusion; References; 2 Isolation and Identification of Biflavanoids; 2.1 Introduction; 2.2 Separation and Purification; 2.2.1 Preparative PC and TLC; 2.2.2 Column Chromatography; 2.2.3 Droplet Counter-Current Chromatography; 2.2.4 High-Pressure Liquid Chromatography; 2.3 Identification; 2.3.1 UV Spectroscopy; 2.3.2 Mass Spectrometry; 2.3.3 NMR Spectroscopy. 
505 8 |a 2.4 ConclusionReferences; 3 Synthesis of Biflavanoids; 3.1 Ullmann Coupling of Halogenated Flavones; 3.2 Synthesis of Biflavones via 1,12 Biphenyls; 3.3 Metal-Catalyzed Cross-Coupling of Flavones; 3.4 Wessely-Moser Rearrangements; 3.5 Phenol Oxidative Coupling of Flavones; 3.6 Ullmann Condensation With Flavone Salts; 3.7 Nucleophilic Substitution; 3.8 Dehydrogenation of Biflavanones Into Biflavones; 3.9 Hydrogenation of Biflavone Into Biflavanone; 3.10 Special Approaches for the Synthesis of Selective Biflavanoids; 3.10.1 Photoreductive Dimerization of Flavones. 
505 8 |a 3.10.2 Synthesis of 2,42 and 2,22 Biflavanoids Using Photoinduced Electron Transfer Reactions of Flavones With Amines3.11 Conclusion; References; 4 Biochemical Pharmacology of Biflavanoids; 4.1 General Biological Properties of Biflavanoids; 4.2 Anticancer Action of Bioflavonoids; 4.3 Antimicrobial and Antiviral Activity of Bioflavonoids; 4.4 Antiinflammatory Activity of Bioflavonoids: Cellular Mechanisms of Antiinflammatory Bioflavonoids; 4.5 Analgesic Activity of Bioflavonoids; 4.6 Antiinflammatory Activity of Synthetic Flavanoids; 4.7 Conclusion; References; Back Cover. 
650 0 |a Flavonoids. 
650 2 |a Flavonoids  |0 (DNLM)D005419 
650 6 |a Flavono�ides.  |0 (CaQQLa)201-0026353 
650 7 |a NATURE  |x Plants  |x General.  |2 bisacsh 
650 7 |a Flavonoids  |2 fast  |0 (OCoLC)fst00927101 
700 1 |a Khuroo, Mohd Akbar,  |e author. 
776 0 8 |i Print version:  |a Lone, Shabir Hussain.  |t Biflavanoids : Chemical and Pharmacological Aspects.  |d London : Elsevier Science, �2016  |z 9780081010303 
856 4 0 |u https://sciencedirect.uam.elogim.com/science/book/9780081010303  |z Texto completo