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Biblioteca

MARC Lista (tabellare)
Alcali vindicatum, or, The acid opiniator [sic] not guilty of truth [[electronic resource] ] : being an impartial enquiry into the fallacious reasons and erroneous philosophy of a late physico-medical essay touching alcali & acid : especially as they relate to the cause or cure of the small pox, scurvy, gout, rheumatism and consumption : to which is added a discourse of the nature and usefulness of an hypothesis in relation to the practice of physick : with a description of a most excellent medicine call'd tinctura sanitatis, of great use in all diseases of the head and stomack especially / / by William Coward .
Alcali vindicatum, or, The acid opiniator [sic] not guilty of truth [[electronic resource] ] : being an impartial enquiry into the fallacious reasons and erroneous philosophy of a late physico-medical essay touching alcali & acid : especially as they relate to the cause or cure of the small pox, scurvy, gout, rheumatism and consumption : to which is added a discourse of the nature and usefulness of an hypothesis in relation to the practice of physick : with a description of a most excellent medicine call'd tinctura sanitatis, of great use in all diseases of the head and stomack especially / / by William Coward .
Autore Coward William <1657?-1725.>
Pubbl/distr/stampa London, : Printed and are to be sold by the booksellers of London and Westminster, 1700
Descrizione fisica [8], 184 p
Soggetto topico Medicine
Acids
Alkaloids
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNISA-996395903603316
Coward William <1657?-1725.>  
London, : Printed and are to be sold by the booksellers of London and Westminster, 1700
Materiale a stampa
Lo trovi qui: Univ. di Salerno
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Alkaloids : Their Importance in Nature and Human Life / / edited by Joanna Kurek
Alkaloids : Their Importance in Nature and Human Life / / edited by Joanna Kurek
Pubbl/distr/stampa London : , : IntechOpen, , 2019
Descrizione fisica 1 online resource (xi, 100 pages) : illustrations
Disciplina 572.549
Soggetto topico Alkaloids
Pharmacology
ISBN 1-78984-577-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Alkaloids
Record Nr. UNINA-9910407757403321
London : , : IntechOpen, , 2019
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Alkaloids - alternatives in synthesis, modification and application / / edited by Vasil Georgiev, Atanas Pavlov
Alkaloids - alternatives in synthesis, modification and application / / edited by Vasil Georgiev, Atanas Pavlov
Autore Atanas Pavlov
Pubbl/distr/stampa IntechOpen, 2017
Descrizione fisica 1 online resource (130 pages)
Disciplina 547.72
Soggetto topico Alkaloids
Soggetto non controllato Physical Sciences
Engineering and Technology
Chemistry
Bioorganic Chemistry
Organic Chemistry
ISBN 953-51-4751-X
953-51-3392-6
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Alkaloids
Record Nr. UNINA-9910251422803321
Atanas Pavlov  
IntechOpen, 2017
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Alkaloids - secrets of life [[electronic resource] ] : alkaloid chemistry, biological significance, applications and ecological role / / Tadeusz Aniszewski
Alkaloids - secrets of life [[electronic resource] ] : alkaloid chemistry, biological significance, applications and ecological role / / Tadeusz Aniszewski
Autore Aniszewski Tadeusz
Edizione [1st ed.]
Pubbl/distr/stampa Amsterdam ; ; Oxford, : Elsevier, 2007
Descrizione fisica 1 online resource (335 p.)
Disciplina 547.7
Soggetto topico Alkaloids
Biochemistry
Soggetto genere / forma Electronic books.
ISBN 1-281-00385-9
9786611003852
0-08-047533-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover; Copyright Page; Table of Contents; List of Figures; List of Tables; Preface; Chapter 1 Definition, Typology and Occurrence of Alkaloids; 1. Definition; 1.1. True alkaloids; 1.2. Protoalkaloids; 1.3. Pseudoalkaloids; 2. Occurrence in nature; 2.1. The Dogbane botanical family (Apocynaceae); 2.2. The Aster botanical family (Asteraceae); 2.3. The Logan botanical family (Loganiaceae); 2.4. The Poppy botanical family (Papaveraceae); 2.5. The Citrus botanical family (Rutaceae); 2.6. The Nightshade botanical family (Solanaceae); 2.7. The Coca botanical family (Erythroxylaceae)
2.8. The Borage botanical family (Boraginaceae)2.9. The Legume botanical family (Fabaceae); 2.10. The Monseed botanical family (Menispermaceae); 2.11. The Berberry botanical family (Berberidaceae); 2.12. The Buttercup botanical family (Ranunculaceae); 2.13. The Lily botanical family (Liliaceae); 2.14. The Coffee botanical family (Rubiaceae); 2.15. The Amaryllis botanical family (Amaryllidaceae); 2.16. The Oleaster botanical family (Elaeagnaceae); 2.17. The Caltrop botanical family (Zygophyllaceae); 2.18. Mushroom; 2.19. Moss; 2.20. Fungus and bacter; 2.21. Animals
Chapter 2 Alkaloid Chemistry1. Alkaloids as secondary metabolism molecules; 2. Synthesis and metabolism; 2.1. Skeleton diversity; 2.2. Ornithine-derived alkaloids; 2.3. Tyrosine-derived alkaloids; 2.3.1. Mescaline pathway; 2.3.2. Kreysigine and colchicine pathway; 2.3.3. Dopamine - cephaeline pathway; 2.3.4. Galanthamine pathway; 2.4. Tryptophan-derived alkaloids; 2.4.1. Psilocybin pathway; 2.4.2. Elaeagnine, harman and harmine pathway; 2.4.3. Ajmalicine, tabersonine and catharanthine pathway; 2.4.4. Vindoline, vinblastine and vincristine pathway; 2.4.5. Strychnine and brucine pathway
2.4.6. Quinine, quinidine and cinchonine synthesis pathway2.4.7. Eserine synthesis pathway; 2.4.8. Ergotamine synthesis pathway; 2.5. Nicotinic acid-derived alkaloids; 2.6. Lysine-derived alkaloids; 2.6.1. Pelletierine, lobelanine and piperine synthesis pathway; 2.6.2. The swansonine and castanospermine synthesis pathway; 2.6.3. The lupinine, lupanine, sparteine and cytisine synthesis pathway; 2.7. Methods of analysis; 2.7.1. Methodological considerations; 2.7.2. Structural approach; 2.7.2.1. Piperidine alkaloids; 2.7.2.2. Indolizidine alkaloids; 2.7.2.3. Quinolizidine alkaloids
2.7.2.4. Pyrrolizidine alkaloids2.7.2.5. Izidine alkaloids; 2.7.2.6. Pyrrolidine alkaloids; 2.7.2.7. Tropane alkaloids; 2.7.2.8. Imidazole alkaloids; 2.7.2.9. Quinazoline alkaloids; 2.7.2.10. Acridone alkaloids; 2.7.2.11. Pyridine alkaloids; 2.7.2.12. Sesquiterpene pyridine alkaloids; 2.7.2.13. Phenyl and phenylpropyl alkaloids; 2.7.2.14. Indole alkaloids; 2.7.2.15. Manzamine alkaloids; 2.8. Biogenesis of alkaloids; 2.8.1. Chemistry models; 2.8.2. Biochemistry models; 2.8.3. Molecular biology models; 2.8.4. Analytical dilemmas; 2.9. Methods of alkaloid analysis; 2.9.1. Methods in history
2.9.2. Basic methods and instruments
Record Nr. UNINA-9910457238203321
Aniszewski Tadeusz  
Amsterdam ; ; Oxford, : Elsevier, 2007
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Alkaloids - secrets of life [[electronic resource] ] : alkaloid chemistry, biological significance, applications and ecological role / / Tadeusz Aniszewski
Alkaloids - secrets of life [[electronic resource] ] : alkaloid chemistry, biological significance, applications and ecological role / / Tadeusz Aniszewski
Autore Aniszewski Tadeusz
Edizione [1st ed.]
Pubbl/distr/stampa Amsterdam ; ; Oxford, : Elsevier, 2007
Descrizione fisica 1 online resource (335 p.)
Disciplina 547.7
Soggetto topico Alkaloids
Biochemistry
ISBN 1-281-00385-9
9786611003852
0-08-047533-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover; Copyright Page; Table of Contents; List of Figures; List of Tables; Preface; Chapter 1 Definition, Typology and Occurrence of Alkaloids; 1. Definition; 1.1. True alkaloids; 1.2. Protoalkaloids; 1.3. Pseudoalkaloids; 2. Occurrence in nature; 2.1. The Dogbane botanical family (Apocynaceae); 2.2. The Aster botanical family (Asteraceae); 2.3. The Logan botanical family (Loganiaceae); 2.4. The Poppy botanical family (Papaveraceae); 2.5. The Citrus botanical family (Rutaceae); 2.6. The Nightshade botanical family (Solanaceae); 2.7. The Coca botanical family (Erythroxylaceae)
2.8. The Borage botanical family (Boraginaceae)2.9. The Legume botanical family (Fabaceae); 2.10. The Monseed botanical family (Menispermaceae); 2.11. The Berberry botanical family (Berberidaceae); 2.12. The Buttercup botanical family (Ranunculaceae); 2.13. The Lily botanical family (Liliaceae); 2.14. The Coffee botanical family (Rubiaceae); 2.15. The Amaryllis botanical family (Amaryllidaceae); 2.16. The Oleaster botanical family (Elaeagnaceae); 2.17. The Caltrop botanical family (Zygophyllaceae); 2.18. Mushroom; 2.19. Moss; 2.20. Fungus and bacter; 2.21. Animals
Chapter 2 Alkaloid Chemistry1. Alkaloids as secondary metabolism molecules; 2. Synthesis and metabolism; 2.1. Skeleton diversity; 2.2. Ornithine-derived alkaloids; 2.3. Tyrosine-derived alkaloids; 2.3.1. Mescaline pathway; 2.3.2. Kreysigine and colchicine pathway; 2.3.3. Dopamine - cephaeline pathway; 2.3.4. Galanthamine pathway; 2.4. Tryptophan-derived alkaloids; 2.4.1. Psilocybin pathway; 2.4.2. Elaeagnine, harman and harmine pathway; 2.4.3. Ajmalicine, tabersonine and catharanthine pathway; 2.4.4. Vindoline, vinblastine and vincristine pathway; 2.4.5. Strychnine and brucine pathway
2.4.6. Quinine, quinidine and cinchonine synthesis pathway2.4.7. Eserine synthesis pathway; 2.4.8. Ergotamine synthesis pathway; 2.5. Nicotinic acid-derived alkaloids; 2.6. Lysine-derived alkaloids; 2.6.1. Pelletierine, lobelanine and piperine synthesis pathway; 2.6.2. The swansonine and castanospermine synthesis pathway; 2.6.3. The lupinine, lupanine, sparteine and cytisine synthesis pathway; 2.7. Methods of analysis; 2.7.1. Methodological considerations; 2.7.2. Structural approach; 2.7.2.1. Piperidine alkaloids; 2.7.2.2. Indolizidine alkaloids; 2.7.2.3. Quinolizidine alkaloids
2.7.2.4. Pyrrolizidine alkaloids2.7.2.5. Izidine alkaloids; 2.7.2.6. Pyrrolidine alkaloids; 2.7.2.7. Tropane alkaloids; 2.7.2.8. Imidazole alkaloids; 2.7.2.9. Quinazoline alkaloids; 2.7.2.10. Acridone alkaloids; 2.7.2.11. Pyridine alkaloids; 2.7.2.12. Sesquiterpene pyridine alkaloids; 2.7.2.13. Phenyl and phenylpropyl alkaloids; 2.7.2.14. Indole alkaloids; 2.7.2.15. Manzamine alkaloids; 2.8. Biogenesis of alkaloids; 2.8.1. Chemistry models; 2.8.2. Biochemistry models; 2.8.3. Molecular biology models; 2.8.4. Analytical dilemmas; 2.9. Methods of alkaloid analysis; 2.9.1. Methods in history
2.9.2. Basic methods and instruments
Record Nr. UNINA-9910784599503321
Aniszewski Tadeusz  
Amsterdam ; ; Oxford, : Elsevier, 2007
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Alkaloids - secrets of life : alkaloid chemistry, biological significance, applications and ecological role / / Tadeusz Aniszewski
Alkaloids - secrets of life : alkaloid chemistry, biological significance, applications and ecological role / / Tadeusz Aniszewski
Autore Aniszewski Tadeusz
Edizione [1st ed.]
Pubbl/distr/stampa Amsterdam ; ; Oxford, : Elsevier, 2007
Descrizione fisica 1 online resource (335 p.)
Disciplina 547.7
Soggetto topico Alkaloids
Biochemistry
ISBN 1-281-00385-9
9786611003852
0-08-047533-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover; Copyright Page; Table of Contents; List of Figures; List of Tables; Preface; Chapter 1 Definition, Typology and Occurrence of Alkaloids; 1. Definition; 1.1. True alkaloids; 1.2. Protoalkaloids; 1.3. Pseudoalkaloids; 2. Occurrence in nature; 2.1. The Dogbane botanical family (Apocynaceae); 2.2. The Aster botanical family (Asteraceae); 2.3. The Logan botanical family (Loganiaceae); 2.4. The Poppy botanical family (Papaveraceae); 2.5. The Citrus botanical family (Rutaceae); 2.6. The Nightshade botanical family (Solanaceae); 2.7. The Coca botanical family (Erythroxylaceae)
2.8. The Borage botanical family (Boraginaceae)2.9. The Legume botanical family (Fabaceae); 2.10. The Monseed botanical family (Menispermaceae); 2.11. The Berberry botanical family (Berberidaceae); 2.12. The Buttercup botanical family (Ranunculaceae); 2.13. The Lily botanical family (Liliaceae); 2.14. The Coffee botanical family (Rubiaceae); 2.15. The Amaryllis botanical family (Amaryllidaceae); 2.16. The Oleaster botanical family (Elaeagnaceae); 2.17. The Caltrop botanical family (Zygophyllaceae); 2.18. Mushroom; 2.19. Moss; 2.20. Fungus and bacter; 2.21. Animals
Chapter 2 Alkaloid Chemistry1. Alkaloids as secondary metabolism molecules; 2. Synthesis and metabolism; 2.1. Skeleton diversity; 2.2. Ornithine-derived alkaloids; 2.3. Tyrosine-derived alkaloids; 2.3.1. Mescaline pathway; 2.3.2. Kreysigine and colchicine pathway; 2.3.3. Dopamine - cephaeline pathway; 2.3.4. Galanthamine pathway; 2.4. Tryptophan-derived alkaloids; 2.4.1. Psilocybin pathway; 2.4.2. Elaeagnine, harman and harmine pathway; 2.4.3. Ajmalicine, tabersonine and catharanthine pathway; 2.4.4. Vindoline, vinblastine and vincristine pathway; 2.4.5. Strychnine and brucine pathway
2.4.6. Quinine, quinidine and cinchonine synthesis pathway2.4.7. Eserine synthesis pathway; 2.4.8. Ergotamine synthesis pathway; 2.5. Nicotinic acid-derived alkaloids; 2.6. Lysine-derived alkaloids; 2.6.1. Pelletierine, lobelanine and piperine synthesis pathway; 2.6.2. The swansonine and castanospermine synthesis pathway; 2.6.3. The lupinine, lupanine, sparteine and cytisine synthesis pathway; 2.7. Methods of analysis; 2.7.1. Methodological considerations; 2.7.2. Structural approach; 2.7.2.1. Piperidine alkaloids; 2.7.2.2. Indolizidine alkaloids; 2.7.2.3. Quinolizidine alkaloids
2.7.2.4. Pyrrolizidine alkaloids2.7.2.5. Izidine alkaloids; 2.7.2.6. Pyrrolidine alkaloids; 2.7.2.7. Tropane alkaloids; 2.7.2.8. Imidazole alkaloids; 2.7.2.9. Quinazoline alkaloids; 2.7.2.10. Acridone alkaloids; 2.7.2.11. Pyridine alkaloids; 2.7.2.12. Sesquiterpene pyridine alkaloids; 2.7.2.13. Phenyl and phenylpropyl alkaloids; 2.7.2.14. Indole alkaloids; 2.7.2.15. Manzamine alkaloids; 2.8. Biogenesis of alkaloids; 2.8.1. Chemistry models; 2.8.2. Biochemistry models; 2.8.3. Molecular biology models; 2.8.4. Analytical dilemmas; 2.9. Methods of alkaloid analysis; 2.9.1. Methods in history
2.9.2. Basic methods and instruments
Record Nr. UNINA-9910825324003321
Aniszewski Tadeusz  
Amsterdam ; ; Oxford, : Elsevier, 2007
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Ancistrocladus naphthylisoquinoline alkaloids / / edited by A. Douglas Kinghorn, Heinz Falk, Simon Gibbons, Yoshinori Asakawa, Ji-Kai Liu, Verena M Dirsch
Ancistrocladus naphthylisoquinoline alkaloids / / edited by A. Douglas Kinghorn, Heinz Falk, Simon Gibbons, Yoshinori Asakawa, Ji-Kai Liu, Verena M Dirsch
Edizione [1st ed. 2023.]
Pubbl/distr/stampa Cham : , : Springer International Publishing : , : Imprint : Springer, , 2023
Descrizione fisica 1 online resource (344 pages) : illustrations (black and white, and colour)
Disciplina 769
572.549
Collana Progress in the Chemistry of Organic Natural Products
Soggetto topico Alkaloids
Botanical chemistry
ISBN 3-031-10457-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto 1. Introduction -- 2. Naphthylisoquinoline Alkaloids, a Fascinating Class of Axially Chiral Biaryl Natural Products -- 3. Ancistrocladus, a Genus of Woody Lianas of the Monotypic Plant Family Ancistrocladaceae Widely Occurring in India, Sri Lanka, and Southeast Asia -- 4.The Indian Liana Ancistrocladus heyneanus and Ancistrocladus hamatus from Sri Lanka: Early Studies and More Recent Discoveries -- Full Absolute Stereostructures of Naphthylisoquinoline Alkaloids Directly from Crude Extracts: Characterization of New Metabolites from Ancistrocladus griffithii by the HPLC-MS/MS-NMR-ECD Triad -- 6. Ancistrobenomine A, the First Naphthylisoquinoline Alkaloid with a Hydroxymethylene Function at C-3, and Related 5,1'-Coupled Compounds -- 7. Ancistrocladus cochinchinensis from Central Vietnam, a Distinct Ancistrocladus Taxon? — Metabolite Pattern und Phylogenetic Relationship to Ancistrocladus aff. tectorius from China -- 8.Widespread Throughout Southeast Asia: Ancistrocladus tectorius, a Rich Source of Unique, Structurally Most Diverse Mono- and Dimeric Naphthylisoquinoline Alkaloids -- 9. Tables of the Naphthylisoquinoline Alkaloids and Related Compounds Isolated from Asian Ancistrocladus Species.
Record Nr. UNINA-9910733715503321
Cham : , : Springer International Publishing : , : Imprint : Springer, , 2023
Materiale a stampa
Lo trovi qui: Univ. Federico II
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The cigarette papers / / Stanton A. Glantz ... [et al.] [[electronic resource]]
The cigarette papers / / Stanton A. Glantz ... [et al.] [[electronic resource]]
Pubbl/distr/stampa Berkeley, : University of California Press, c1996
Descrizione fisica 1 online resource (xix, 539 p. ) : ill. ;
Disciplina 362.29/6
Altri autori (Persone) GlantzStanton A
BeroLisa
HanauerPeter
SladeJohn
BarnesDeborah E
Soggetto topico Smoking - Health aspects
Tobacco industry - United States
Tobacco use - Health aspects
Industry
Nicotine - adverse effects
Smoking
Cigarettes
Habits
Technology, Industry, and Agriculture
Pyridines
Solanaceae
Solanaceous Alkaloids
Technology
Angiosperms
Behavior
Alkaloids
Heterocyclic Compounds, 1-Ring
Heterocyclic Compounds
Embryophyta
Behavior and Behavior Mechanisms
Psychology
Streptophyta
Viridiplantae
Plants
Eukaryota
Nicotine
Business & Economics
Industries
ISBN 0-520-92099-6
0-585-06878-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Looking through a keyhole at the tobacco industry -- Smoking and disease: the tobacco industry's earliest responses -- Addiction and cigarettes as nicotine delivery devices -- The search for a "safe" cigarette -- Public relations in the "safe" cigarette era -- Agricultural chemicals and cigarette additives -- Legal concerns facing the industry -- Lawyer management of scientific research -- Stonewalling : politics and public relations -- Environmental tobacco smoke and the nonsmokers' rights movement -- Where do we go from here?
Record Nr. UNINA-9910495962303321
Berkeley, : University of California Press, c1996
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Modern alkaloids [[electronic resource] ] : structure, isolation, synthesis and biology / / edited by Ernesto Fattorusso and Orazio Taglialatela-Scafati
Modern alkaloids [[electronic resource] ] : structure, isolation, synthesis and biology / / edited by Ernesto Fattorusso and Orazio Taglialatela-Scafati
Pubbl/distr/stampa Weinheim, : Wiley-VCH, c2008
Descrizione fisica 1 online resource (691 p.)
Disciplina 572.549
Altri autori (Persone) FattorussoErnesto
Taglialatela-ScafatiOrazio
Soggetto topico Alkaloids - Structure
Alkaloids
ISBN 1-281-31181-2
9786611311810
3-527-62107-5
3-527-62108-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Modern Alkaloids; Contents; Preface; List of Contributors; I Bioactive Alkaloids: Structure and Biology; 1 Ecological Roles of Alkaloids; 1.1 Introduction: Defense Strategies in Plants; 1.2 Ecological Roles of Alkaloids; 1.3 Modes of Action; 1.3.1 Unspecific Interactions; 1.3.2 Specific Interactions; 1.3.3 Cytotoxicity of Alkaloids; 1.4 Evolution of Alkaloidal Defense Systems; 1.5 Conclusions; 2 Antitumor Alkaloids in Clinical Use or in Clinical Trials; 2.1 Introduction; 2.2 Antitumor Alkaloids in Clinical Use; 2.2.1 Vinca Alkaloids; 2.2.1.1 Vinblastine (VLB, 1); 2.2.1.2 Vincristine (VCR, 2)
2.2.1.3 Vindesine (VDS, 3)2.2.1.4 Vinorelbine (VRLB, 4); 2.2.1.5 Vinflunine (VFL, 5); 2.2.2 Camptothecin and Analogs; 2.2.2.1 Camptothecin (CPT, 6); 2.2.2.2 Irinotecan (CPT-11); 2.2.2.3 Topotecan; 2.2.2.4 Exatecan; 2.2.2.5 Gimatecan; 2.2.2.6 Karenitecin; 2.2.2.7 Lurtotecan; 2.2.2.8 Rubitecan (9-nitrocamptothecin); 2.2.3 Taxanes; 2.2.3.1 Paclitaxel; 2.2.3.2 Docetaxel; 2.3 Antitumor Alkaloids in Clinical Trials; 2.3.1 Ecteinascidin-743 (Yondelis, Trabectedin); 2.3.2 7-Hydroxystaurosporine (UCN-01); 2.3.3 Ellipticine and Analogs; 2.3.4 Acronycine and Analogs; 2.3.5 Colchicine and Analogs
2.3.6 Ukrain2.4 Alkaloids Used for MDR Reversal; 2.4.1 Cinchona Alkaloids; 2.4.2 Dofequidar Fumarate (MS-209); 2.5 Alkaloids Used for Cancer Prevention; 2.6 Conclusions; 2.7 Acknowledgments; 3 Alkaloids and the Bitter Taste; 3.1 Introduction; 3.2 The Bitter Taste Chemoreception Mechanism; 3.3 Bitter Alkaloids in Food; 3.4 The Bitter Taste of Alkaloids in Other Drugs and Poisons; 3.5 Alkaloids and Taste in Insects; 3.6 The Bitter Taste of Alkaloids: Should We Avoid, Mask, or Understand?; 3.7 Acknowledgments; 4 Capsaicin and Capsaicinoids; 4.1 Introduction
4.2 What Is an Alkaloid? Is Capsaicin an Alkaloid?4.3 Diversity, Biosynthesis, and Metabolism of Capsaicinoids; 4.4 Quantization of Capsaicinoids and Their Distribution in Chili Pepper; 4.5 Isolation and Synthesis of Capsaicin; 4.6 TRV1 as the Biological Target of Capsaicin and the Ecological Raison d'être of Capsaicinoids: A Molecular View; 4.7 Naturally Occurring Analogs and Antagonists of Capsaicin and Endogenous Vanilloids; 4.8 Structure-Activity Relationships of Capsaicinoids; 4.9 Molecular Gastronomy of Hot Food; 4.9.1 Biomedical Relevance of Capsaicin-Induced Trigeminal Responses
4.9.2 Effect of Capsaicin on Taste4.9.3 Gustatory Sweating; 4.9.4 Gustatory Rhinitis; 4.9.5 Hot Food Mitridatism; 4.9.6 Effect of Capsaicin on Digestion; 4.9.7 Capsaicin and Stomach Cancer; 4.9.8 The Effect of Age and Sex on the Sensitivity to Capsaicin; 4.9.9 Capsaicin as a Slimming Agent; 4.9.10 Quenching Capsaicin; 4.9.11 Chilies and Olive Oil; 4.9.12 Who Should Avoid Chilies?; 4.9.13 How can the Pungency of Chilies be Moderated?; 4.9.14 Psychology of Pepper Consumption; 4.10 Conclusions; 4.11 Acknowledgments; 5 Glycosidase-Inhibiting Alkaloids: Isolation, Structure, and Application
5.1 Introduction
Record Nr. UNINA-9910144278503321
Weinheim, : Wiley-VCH, c2008
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Modern alkaloids [[electronic resource] ] : structure, isolation, synthesis and biology / / edited by Ernesto Fattorusso and Orazio Taglialatela-Scafati
Modern alkaloids [[electronic resource] ] : structure, isolation, synthesis and biology / / edited by Ernesto Fattorusso and Orazio Taglialatela-Scafati
Pubbl/distr/stampa Weinheim, : Wiley-VCH, c2008
Descrizione fisica 1 online resource (691 p.)
Disciplina 572.549
Altri autori (Persone) FattorussoErnesto
Taglialatela-ScafatiOrazio
Soggetto topico Alkaloids - Structure
Alkaloids
ISBN 1-281-31181-2
9786611311810
3-527-62107-5
3-527-62108-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Modern Alkaloids; Contents; Preface; List of Contributors; I Bioactive Alkaloids: Structure and Biology; 1 Ecological Roles of Alkaloids; 1.1 Introduction: Defense Strategies in Plants; 1.2 Ecological Roles of Alkaloids; 1.3 Modes of Action; 1.3.1 Unspecific Interactions; 1.3.2 Specific Interactions; 1.3.3 Cytotoxicity of Alkaloids; 1.4 Evolution of Alkaloidal Defense Systems; 1.5 Conclusions; 2 Antitumor Alkaloids in Clinical Use or in Clinical Trials; 2.1 Introduction; 2.2 Antitumor Alkaloids in Clinical Use; 2.2.1 Vinca Alkaloids; 2.2.1.1 Vinblastine (VLB, 1); 2.2.1.2 Vincristine (VCR, 2)
2.2.1.3 Vindesine (VDS, 3)2.2.1.4 Vinorelbine (VRLB, 4); 2.2.1.5 Vinflunine (VFL, 5); 2.2.2 Camptothecin and Analogs; 2.2.2.1 Camptothecin (CPT, 6); 2.2.2.2 Irinotecan (CPT-11); 2.2.2.3 Topotecan; 2.2.2.4 Exatecan; 2.2.2.5 Gimatecan; 2.2.2.6 Karenitecin; 2.2.2.7 Lurtotecan; 2.2.2.8 Rubitecan (9-nitrocamptothecin); 2.2.3 Taxanes; 2.2.3.1 Paclitaxel; 2.2.3.2 Docetaxel; 2.3 Antitumor Alkaloids in Clinical Trials; 2.3.1 Ecteinascidin-743 (Yondelis, Trabectedin); 2.3.2 7-Hydroxystaurosporine (UCN-01); 2.3.3 Ellipticine and Analogs; 2.3.4 Acronycine and Analogs; 2.3.5 Colchicine and Analogs
2.3.6 Ukrain2.4 Alkaloids Used for MDR Reversal; 2.4.1 Cinchona Alkaloids; 2.4.2 Dofequidar Fumarate (MS-209); 2.5 Alkaloids Used for Cancer Prevention; 2.6 Conclusions; 2.7 Acknowledgments; 3 Alkaloids and the Bitter Taste; 3.1 Introduction; 3.2 The Bitter Taste Chemoreception Mechanism; 3.3 Bitter Alkaloids in Food; 3.4 The Bitter Taste of Alkaloids in Other Drugs and Poisons; 3.5 Alkaloids and Taste in Insects; 3.6 The Bitter Taste of Alkaloids: Should We Avoid, Mask, or Understand?; 3.7 Acknowledgments; 4 Capsaicin and Capsaicinoids; 4.1 Introduction
4.2 What Is an Alkaloid? Is Capsaicin an Alkaloid?4.3 Diversity, Biosynthesis, and Metabolism of Capsaicinoids; 4.4 Quantization of Capsaicinoids and Their Distribution in Chili Pepper; 4.5 Isolation and Synthesis of Capsaicin; 4.6 TRV1 as the Biological Target of Capsaicin and the Ecological Raison d'être of Capsaicinoids: A Molecular View; 4.7 Naturally Occurring Analogs and Antagonists of Capsaicin and Endogenous Vanilloids; 4.8 Structure-Activity Relationships of Capsaicinoids; 4.9 Molecular Gastronomy of Hot Food; 4.9.1 Biomedical Relevance of Capsaicin-Induced Trigeminal Responses
4.9.2 Effect of Capsaicin on Taste4.9.3 Gustatory Sweating; 4.9.4 Gustatory Rhinitis; 4.9.5 Hot Food Mitridatism; 4.9.6 Effect of Capsaicin on Digestion; 4.9.7 Capsaicin and Stomach Cancer; 4.9.8 The Effect of Age and Sex on the Sensitivity to Capsaicin; 4.9.9 Capsaicin as a Slimming Agent; 4.9.10 Quenching Capsaicin; 4.9.11 Chilies and Olive Oil; 4.9.12 Who Should Avoid Chilies?; 4.9.13 How can the Pungency of Chilies be Moderated?; 4.9.14 Psychology of Pepper Consumption; 4.10 Conclusions; 4.11 Acknowledgments; 5 Glycosidase-Inhibiting Alkaloids: Isolation, Structure, and Application
5.1 Introduction
Record Nr. UNINA-9910830380003321
Weinheim, : Wiley-VCH, c2008
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