Fluorine in Heterocyclic Chemistry Volume 2 [[electronic resource] ] : 6-Membered Heterocycles / / edited by Valentine Nenajdenko |
Edizione | [1st ed. 2014.] |
Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2014 |
Descrizione fisica | 1 online resource (768 p.) |
Disciplina | 547.59 |
Soggetto topico |
Organic chemistry
Biomaterials Pharmacology Medicinal chemistry Organic Chemistry Pharmacology/Toxicology Medicinal Chemistry |
ISBN | 3-319-04435-4 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | Synthesis of Fluorinated Pyridines -- Fluorinated Quinolines: Synthesis, Properties and Applications -- Fluoroquinolones: Synthesis and Application -- Syntheses, Properties and Applications of Fluorinated Isoquinolines -- Fluorinated Pyrones, Chromones and Coumarins -- Chemistry of Fluorinated Diazines -- Fluorine-Containing Diazines in Medicinal Chemistry and Agrochemistry -- Fluorinated Triazines -- Chemistry of Fluorinated Purines. |
Record Nr. | UNINA-9910298651303321 |
Cham : , : Springer International Publishing : , : Imprint : Springer, , 2014 | ||
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Lo trovi qui: Univ. Federico II | ||
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Foodinformatics [[electronic resource] ] : Applications of Chemical Information to Food Chemistry / / edited by Karina Martinez-Mayorga, José Luis Medina-Franco |
Edizione | [1st ed. 2014.] |
Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2014 |
Descrizione fisica | 1 online resource (258 p.) |
Disciplina |
54
540 615.19 641.3 |
Soggetto topico |
Food—Biotechnology
Communication in chemistry Medicinal chemistry Food Science Documentation and Information in Chemistry Medicinal Chemistry |
ISBN | 3-319-10226-5 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | 1. Introduction to Molecular Similarity and Chemical Space -- 2. The Chemical Space of Flavors.- 3. Chemoinformatics Analysis and Structural Similarity Studies of Food-Related Databases -- 4. Reverse Pharmacognosy: A Tool to Accelerate the Discovery of New Bioactive Food Ingredients -- 5. Molecular Approaches to Explore Natural and Food-Compound Modulators in Cancer Epigenetics and Metabolism -- 6. Discovery of natural products that modulate the activity of PPARgamma: a source for new antidiabetics -- 7. DPP-IV, An Important Target for Anti-diabetic Functional Food Design.-8. Comparison of Different Data Analysis Tools to Study the Effect of Storage Conditions on Wine Sensory Attributes and Trace Metal Composition.- 9. Software and Online Resources: Perspectives and Potential Applications. |
Record Nr. | UNINA-9910298646303321 |
Cham : , : Springer International Publishing : , : Imprint : Springer, , 2014 | ||
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Lo trovi qui: Univ. Federico II | ||
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Functional Chitosan [[electronic resource] ] : Drug Delivery and Biomedical Applications / / edited by Sougata Jana, Subrata Jana |
Edizione | [1st ed. 2019.] |
Pubbl/distr/stampa | Singapore : , : Springer Singapore : , : Imprint : Springer, , 2019 |
Descrizione fisica | 1 online resource (XII, 489 p. 68 illus., 46 illus. in color.) |
Disciplina | 615.6 |
Soggetto topico |
Pharmaceutical technology
Nanotechnology Polymers Biomedical engineering Medicinal chemistry Pharmaceutical Sciences/Technology Polymer Sciences Biomedical Engineering/Biotechnology Medicinal Chemistry |
ISBN | 981-15-0263-3 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | Chapter 1. Chitosan and its Derivatives: a New Versatile Bio-polymer for Various Applications -- Chapter 2. Application of Chitosan in Oral Drug Delivery -- Chapter 3. Transdermal Delivery of Chitosan Based Systems -- Chapter 4 . Chitosan Based Ocular Drug Delivery systems -- Chapter 5. Functional Chitosan Carriers for Oral Colon-Specific Drug Delivery -- Chapter 6. Chitosan-based Hydrogels for Drug Delivery -- Chapter 7. Recent Advances of Chitosan based Systems for Delivery of Anticancer Drugs -- Chapter 8. Chitosan-based systems for Gene Delivery -- Chapter 9. Chitosan-based Interpenetrating Polymer Networks: Drug Delivery Application -- Chapter 10. Chitosan-based Systems in Tissue Engineering -- Chapter 11. Chitosan based Nanoformulation as Carriers of Small Molecules for Tissue Regeneration -- Chapter 12. Chitosan based Systems for Theranostic Applications -- Chapter 13. Grafted Chitosan Systems for Biomedical Applications -- Chapter 14. Chitosan-based Systems for Controlled Delivery of Antimicrobial Peptides for Biomedical Application -- Chapter 15. Antibacterial Activity of Chitosan based Systems. |
Record Nr. | UNINA-9910383825003321 |
Singapore : , : Springer Singapore : , : Imprint : Springer, , 2019 | ||
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Lo trovi qui: Univ. Federico II | ||
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Fundamentals of Neurodegeneration and Protein Misfolding Disorders [[electronic resource] /] / by Martin Beckerman |
Autore | Beckerman Martin |
Edizione | [1st ed. 2015.] |
Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2015 |
Descrizione fisica | 1 online resource (XXII, 378 p. 122 illus., 103 illus. in color.) |
Disciplina | 616.3995 |
Collana | Biological and Medical Physics, Biomedical Engineering |
Soggetto topico |
Neurosciences
Biophysics Biological physics Proteins Biomedical engineering Neurology Medicinal chemistry Biological and Medical Physics, Biophysics Protein Science Biomedical Engineering and Bioengineering Neurology Medicinal Chemistry |
ISBN | 3-319-22117-5 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | Introduction -- Protein Folding, Part I: Basic Principles -- Protein Folding, Part II: Energy Landscapes and Protein Dynamics -- Protein Misfolding and Aggregation -- Protein Quality Control, Part I: Molecular Chaperones and the Ubiquitin-Proteasome System -- Protein Quality Control, Part II: Autophagy and Aging -- Prion Diseases -- Alzheimer’s Disease -- Parkinson’s Disease -- Huntington’s Disease and other Unstable Repeat Disorders -- Amyotrophic Lateral Sclerosis and Frontotemporal Lobar Degeneration. |
Record Nr. | UNINA-9910298458503321 |
Beckerman Martin
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Cham : , : Springer International Publishing : , : Imprint : Springer, , 2015 | ||
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Lo trovi qui: Univ. Federico II | ||
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Grapes and Health [[electronic resource] /] / edited by John M. Pezzuto |
Edizione | [1st ed. 2016.] |
Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2016 |
Descrizione fisica | 1 online resource (X, 235 p. 39 illus., 13 illus. in color.) |
Disciplina | 572 |
Soggetto topico |
Nutrition
Food—Biotechnology Medicinal chemistry Nutrition Food Science Medicinal Chemistry |
ISBN | 3-319-28995-0 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | Grape Anatomy and Physiology -- Standardized Grape Powder for Basic and Clinical Research -- Grape Polyphenosis in the Prevention of Cardiovascular Disease -- Grapes and Atherosclerosis -- - Grapes and Inflammation -- Grapes and Cancer -- Grapes and Gastrointestinal Health: Implications with Intestinal and Systemic Diseases -- Grapes and the Brain -- Grapes and Joint Health -- Grapes and Urinary Bladder Function -- Grapes and Vision. |
Record Nr. | UNINA-9910254026103321 |
Cham : , : Springer International Publishing : , : Imprint : Springer, , 2016 | ||
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Lo trovi qui: Univ. Federico II | ||
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Green Chemistry: Synthesis of Bioactive Heterocycles [[electronic resource] /] / edited by K. L. Ameta, Anshu Dandia |
Edizione | [1st ed. 2014.] |
Pubbl/distr/stampa | New Delhi : , : Springer India : , : Imprint : Springer, , 2014 |
Descrizione fisica | 1 online resource (418 p.) |
Disciplina | 547.59 |
Soggetto topico |
Bioorganic chemistry
Medicinal chemistry Inorganic chemistry Bioorganic Chemistry Medicinal Chemistry Inorganic Chemistry |
ISBN | 81-322-1850-7 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | Synthesis of Heterocycles through Multi-component Reactions in Water -- Sustainable Approaches towards the Synthesis of Quinoxalines -- Eco-friendly Synthesis of Bioactive Heterocycles -- Ammonium and Phosphonium Based Ionic Liquid: Green and Reusable Catalysts -- An Approach towards Green Switch through Nano catalysis for the Synthesis of Biodynamic Heterocycles -- Microwave Induced Synthesis of Various Quinoline Derivatives: Green Methodologies in Organic Synthesis -- Imidazolium Ionic Liquids: An Environment Friendly Medium for Various Applications -- Water: A Benign Solvent for the Synthesis of Various Organic Moieties -- Synthesis and synthetic applications of Biologically interesting Rhodanine and Rhodanine-based Scaffolds -- Molecular Iodine: Mild, Green and Nontoxic Lewis Acid Catalyst for the Synthesis of Heterocyclic Compounds -- Microwave Radiations: A Tool for the Synthesis of Heterocycles in an Eco-friendly Manner -- Green Chemistry Approach using Heterogeneous Catalysts in the Heterocyclic Synthesis -- Synthesis and Biological Evaluation of Some Quinazoline Heterocyclic Derivatives. |
Record Nr. | UNINA-9910298636003321 |
New Delhi : , : Springer India : , : Imprint : Springer, , 2014 | ||
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Lo trovi qui: Univ. Federico II | ||
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Haloalkyne Chemistry [[electronic resource] /] / by Huanfeng Jiang, Chuanle Zhu, Wanqing Wu |
Autore | Jiang Huanfeng |
Edizione | [1st ed. 2016.] |
Pubbl/distr/stampa | Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2016 |
Descrizione fisica | 1 online resource (86 p.) |
Disciplina | 660 |
Collana | SpringerBriefs in Green Chemistry for Sustainability |
Soggetto topico |
Organic chemistry
Optical materials Electronic materials Medicinal chemistry Organic Chemistry Optical and Electronic Materials Medicinal Chemistry |
ISBN | 3-662-49001-3 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Preface; Contents; Abbreviations; 1 Introduction; Abstract; References; 2 Preparation of Haloalkynes; Abstract; References; 3 Reactions of Haloalkynes; Abstract; 3.1 Transformations of Carbon-Halo Bond Motif; 3.1.1 Construction of Carbon-Carbon Bond; 3.1.1.1 Construction of C(sp)--C(sp) Bond; C(sp)--C(sp) Homo-Coupling; C(sp)--C(sp) Cross-Coupling; 3.1.1.2 Construction of C(sp)--C(sp2) Bond; C(sp)--C(sp2) Cross-Coupling; Alkynylation Reactions; 3.1.1.3 Construction of C(sp)--C(sp3) Bond; 3.1.2 Construction of Carbon-Nitrogen Bond; 3.1.3 Construction of Carbon-Sulfur Bond
3.1.4 Construction of Carbon-Phosphorus Bond3.2 Transformations of Carbon-Carbon Triple Bond Motif; 3.2.1 Nucleophilic Additions; 3.2.1.1 Halogen Nucleophiles; 3.2.1.2 Boron Nucleophiles; 3.2.1.3 Carbon Nucleophiles; 3.2.1.4 Nitrogen Nucleophiles; 3.2.1.5 Oxygen Nucleophiles; 3.2.1.6 Sulfur Nucleophiles; 3.2.2 Cycloadditions; 3.2.2.1 [2 + 2] Cycloaddition; 3.2.2.2 [3 + 2] Cycloaddition; 3.2.2.3 [4 + 2] and [2 + 2 + 2] Cycloadditions; 3.3 Transformations Involved Both Carbon-Halo Bond and Carbon-Carbon Triple Bond Motif; 3.3.1 Initially Reacted at the Carbon-Halo Bond 3.3.2 Initially Reacted at the Carbon-Carbon Triple BondReferences; 4 Conclusions and Outlook; Abstract |
Record Nr. | UNINA-9910254042503321 |
Jiang Huanfeng
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Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2016 | ||
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Lo trovi qui: Univ. Federico II | ||
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Halogen Bonding I [[electronic resource] ] : Impact on Materials Chemistry and Life Sciences / / edited by Pierangelo Metrangolo, Giuseppe Resnati |
Edizione | [1st ed. 2015.] |
Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2015 |
Descrizione fisica | 1 online resource (IX, 280 p. 191 illus., 83 illus. in color.) |
Disciplina | 546 |
Collana | Topics in Current Chemistry |
Soggetto topico |
Inorganic chemistry
Organic chemistry Medicinal chemistry Inorganic Chemistry Organic Chemistry Medicinal Chemistry |
ISBN | 3-319-14057-4 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | From the Contents: The nature and directionality of halogen bonding; the sigma hole -- Solid-state NMR study of halogen-bonded adducts -- Infrared and Raman measurements of halogen bonding in cryogenic solutions -- Halogen bonding in the gas phase -- Halogen bonding in solution -- Unconventional motifs for halogen bonding. |
Record Nr. | UNINA-9910298625903321 |
Cham : , : Springer International Publishing : , : Imprint : Springer, , 2015 | ||
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Lo trovi qui: Univ. Federico II | ||
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Halogen Bonding II [[electronic resource] ] : Impact on Materials Chemistry and Life Sciences / / edited by Pierangelo Metrangolo, Giuseppe Resnati |
Edizione | [1st ed. 2015.] |
Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2015 |
Descrizione fisica | 1 online resource (IX, 208 p. 130 illus., 66 illus. in color.) |
Disciplina | 546.73 |
Collana | Topics in Current Chemistry |
Soggetto topico |
Inorganic chemistry
Organic chemistry Medicinal chemistry Inorganic Chemistry Organic Chemistry Medicinal Chemistry |
ISBN | 3-319-15732-9 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Intro -- Preface -- References -- Contents -- Characteristics of a sigma-Hole and the Nature of a Halogen Bond -- 1 Introduction -- 2 Methods -- 2.1 Isolated Subsystems -- 2.2 SAPT Decomposition -- 2.3 Complexes -- 3 Results and Discussion -- 3.1 Halogenated Molecules -- 3.2 Complexes -- 4 Conclusions -- References -- Anion Recognition in Solution via Halogen Bonding -- 1 Introduction -- 2 Interactions of Anions with Monodentate Halogen Bond Donors -- 2.1 Molecular Halogen or Interhalogen Donors -- 2.2 Monodentate Haloorganic Donors -- 3 Multidentate Halogen Bond Donors as Anion Receptors -- 4 Anion Recognition with Cationic Halogen Bond Donors -- 5 Anion Recognition Through Combinations of Halogen and Hydrogen Bonding -- 6 Summary, Conclusions, and Outlook -- References -- Halogen Bonding in Solution -- 1 Introduction -- 2 Neutral, Two-Center Halogen Bond Complexes -- 3 Charged, Two-Center Halogen Bond Complexes -- 4 Neutral, Three-Center Halogen Bond Complexes -- 5 Charged, Three-Center Halogen Bond Complexes -- 6 Conclusions and Outlook -- 7 Addendum -- References -- Halonium Ions as Halogen Bond Donors in the Solid State [XL2]Y Complexes -- 1 Introduction -- 1.1 Halogen Bond: The Long Lost Brother of the Hydrogen Bond -- 1.2 . or Simply a Charge Transfer Interaction? -- 2 Halonium-Nitrogen Complexes -- 2.1 Aromatic sp2 Nitrogen -- 2.2 Halonium to sp and Other sp2 Nitrogens -- 2.3 Halonium to sp3 Nitrogens -- 3 Halonium-Sulfur Complexes -- 4 Halonium-Selenium and Halonium-Tellurium Complexes -- References -- Organizing Radical Species in the Solid State with Halogen Bonding -- 1 Introduction -- 2 Radicals as Halogen Bond Donors -- 2.1 Halogenated Trioxytriangulene Radical -- 2.2 TTF Radical Cations Salts: Toward Chiral Conductors -- 2.2.1 IodoTTFs with Non-centrosymmetric ClO4- Anion -- 2.2.2 IodoTTFs with Halogen Bonding to Chiral Anions.
2.2.3 Chiral IodoTTF Salts -- 2.3 Paramagnetic Metal Complexes with Halogenated Ligands -- 2.3.1 Halopyridine Complexes of Metal Halides -- 2.3.2 Spin Crossover Cooperativity and Halogen Bonding -- 3 Radicals as Halogen Bond Acceptors -- 3.1 Nitronyl Radicals -- 3.2 Metal Complexes with Essentially Metallic Spin Density -- 3.3 Metal Complexes with Non-innocent Ligands -- 4 Halogen-Bonded Charge Transfer Salts -- 5 Summary, Conclusions, and Outlook -- References -- Halogen Bonding in the Design of Organic Phosphors -- 1 Introduction -- 2 New Strategy of Introducing Metal-Free Heavy Atom Perturber by Halogen Bonding in Defined Stoichiometry -- 2.1 Halogen Bonding Acceptors as Phosphors -- 2.2 Donors as Heavy Atom Perturbing Sources -- 2.3 Advantages of Halogen Bonding -- 3 Phosphorescent Cocrystals Assembled by the New Strategy -- 3.1 Structural Features of Cocrystals -- 3.1.1 Cocrystals by PAHs and Haloperfluorobenzenes -- 3.1.2 Cocrystals by Fluorene and Its Heterocyclic Analogues and Haloperfluorobenzenes -- 3.2 Phosphorescent Properties of Cocrystals -- 3.2.1 Emission from PAHs in Cocrystals -- 3.2.2 Emission from Fluorene or Its Heterocyclic Analogues in Cocrystals -- 4 Concluding Remarks -- References -- Halogen-Bonded Photoresponsive Materials -- 1 Preface -- 2 Introduction to Azobenzene -- 3 Photoinduced Surface Patterning in Azopolymers: What Does Halogen Bonding Have to Offer? -- 4 Photoactive Halogen-Bonded Liquid Crystals -- 5 Halogen-Bonded Crystals That Move -- 6 Conclusions -- References -- Halogen Bonds in Organic Synthesis and Organocatalysis -- 1 Hydrogen Bonding in Non-covalent Organocatalysis -- 2 Halogen Bonding in Organic Synthesis and Non-covalent Organocatalysis -- 2.1 Further Directional Interaction: Halogen Bonding -- 2.2 Overview and Scope -- 2.3 Solely-Halogen-Based Halogen-Bond Donors -- 2.3.1 Elemental Halogens. 2.3.2 Interhalogen Compounds -- 2.4 N-X-Based Halogen-Bond Donors -- 2.5 C-X-Based Halogen-Bond Donors -- 2.5.1 Monodentate Halogen-Bond Donors -- 2.5.2 Multidentate Halogen-Bond Donors -- Proof-of-Principle Reaction -- Isothermal Calorimetric Titrations -- Halopyridinium-Based Halogen-Bond Donors as Activators -- Triazolium-Based Halogen-Bond Donors as Activators -- Polyfluorinated Azo-Bridged Halogen-Bond Donors -- Polyfluorinated Halogen-Bond Donors as Organocatalysts -- 3 Summary and Outlook -- References -- Index. |
Record Nr. | UNINA-9910298608903321 |
Cham : , : Springer International Publishing : , : Imprint : Springer, , 2015 | ||
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Lo trovi qui: Univ. Federico II | ||
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Handbook of 200 Medicinal Plants [[electronic resource] ] : A Comprehensive Review of Their Traditional Medical Uses and Scientific Justifications / / by Shahid Akbar |
Autore | Akbar Shahid |
Edizione | [1st ed. 2020.] |
Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2020 |
Descrizione fisica | 1 online resource (2,076 pages) |
Disciplina | 581.634 |
Soggetto topico |
Pharmacology
Pharmacy Medicinal chemistry Pharmacology/Toxicology Medicinal Chemistry Plantes medicinals Farmacologia |
Soggetto genere / forma | Llibres electrònics |
ISBN | 3-030-16807-7 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | Abelmoschus maschatus -- Abrus precatorius -- Abutilon indicum -- Acacia catechu -- Acacia nilotica (A. arabica) -- Achillea millefolium -- Achyranthes aspera -- Aconitum napellus -- Acorus calamus -- Adiantum venustum (Adiantun capillus-veneris) -- Aegle marmelos -- Agrimonia eupatorium.-Alhagi maurorum -- Alkanna tinctoria -- Allium cepa -- Allium sativum -- Aloe vera -- Alpinia galangal -- Alpinia officinarum -- Alstonia scholaris -- Althaea officinalis -- Ammi majus -- Anacardium occidentale -- Anacyclus pyrethrum -- Andrographis paniculata -- Anethum graveolens -- Anthemis nobilis -- Apium graveolens -- Argemone Mexicana -- Aristolochia bracteolata -- Aristolochia fontanesii (A. longa) -- Aristolochia indica -- Aristolochia rotunda -- Artemisia absinthium -- Artemisia vulgaris -- Asparagus adscendens -- Asparagus officinalis -- Asparagus racemosus -- Atropa belladonna -- Azadirachta indica -- Bacopa monnieri -- Bauhinia tomentosa -- Berberis Aristata -- Berberis vulgaris -- Bombyx mori -- Borago officinalis -- Boswellia serrata -- Brassica nigra -- Butea monosperma -- Caccinia macranthera var. glauca (C. glauca) -- Caesalpinia bonduc (Caesalpinia bonducella) -- Cannabis sativa -- Capparis spinosa -- Cardiospermum halicacabum -- Carthamus tinctorius -- Carum carvi -- Cassia fistula -- Catharanthus roseus -- Celastrus paniculatus -- Centaurea behen -- Centella asiatica -- Chamaecrista absus (Cassia absus) -- Chamaemelum nobile (Anthemis nobilis) -- Cheilocostus speciosus (Costus Speciosus) -- Cichorium intybus -- Cinnamomum camphora -- Cinnamomum cassia -- Cinnamomum verum (C. zeylanicum) -- Citrullus colocynthis -- Clitoria ternatea -- Colchicum autumnale -- Colchicum luteum -- Commiphora gileadensis (C. opobalsamum) -- Commiphora myrrha -- Commiphora wightii (C. mukul) -- Convolvulus scammonia -- Cotoneaster nummularius -- Crocus sativus -- Croton tiglium -- Cullen corylifolium (Psoralea corylifolia) -- Cuminum cyminum -- Curcuma aromatica -- Curcuma longa -- Curcuma zedoaria -- Cuscuta chinensis -- Cuscuta reflexa -- Cydonia oblonga -- Cymbopogon schoenanthus -- Cyperus rotundus -- Datura stramonium -- Delphinium denudatum -- Dolichousnea longissimi (Usnea longissima) -- Doronicum pardalianches -- Embelia ribes -- Euphorbia hirta -- Euphorbia resinifera -- Ferula assa-foetida -- Ficus carica -- Ficus racemosa -- Foeniculum vulgare -- Fumaria officinalis -- Gentiana lutea -- Glycyrrhiza glabra -- Gymnema sylvestre -- Helleborus niger -- Hemidesmus Indicus -- Hibiscus rosa-sinensis -- Holarrhena pubescens (Holarrhena antidysenterica) -- Hyoscyamus niger -- Hyssopus officinalis -- Illicium verum -- Iris germanica -- Juniperus communi -- Justicia adhatoda (Adhatoda vasica) -- Lactuca sativa -- Lavandula stoechas -- Lawsonia inermis -- Lepidium sativum -- Linum usitatissimum -- Lupinus albus -- Malva sylvestris -- Marrubium vulgare -- Matricaria chamomilla -- Melia azedarach -- Melilotus officinalis -- Melissa officinalis -- Mesua ferrea -- Momordica charantia -- Moringa oleifera -- Myristica fragrans -- Myrtus communis -- Nageia nagi -- Nepeta cataria -- Nigella sativa -- Ocimum basilicum -- Ocimum gratissimum -- Ocimum tenuiflorum (Ocimum sanctum -- Operculina turpethum -- Paeonia emodi -- Pandanus odorifer (Pandanus Odoratissimus) -- Papaver somniferum -- Persicaria bistorta -- Phyllanthus emblica (Emblica officinalis) -- Picrorhiza kurroa -- Pimpinella anisum -- Piper cubeba -- Piper nigrum -- Pistacia lentiscus -- Plantago major -- Plantago ovata -- Plumbago zeylanica -- Polygonum aviculare -- Portulaca oleracea -- Quercus infectoria -- Rauvolfia serpentina -- Rheum emodi -- Rheum officinale -- Ricinus communis -- Rubia cordifolia -- Rumex vesicarius -- Ruta graveolens -- Salix caprea -- Salvia officinalis -- Santalum album -- Saussurea lappa -- Semecarpus anacardium -- Senna alexandrina -- Senna occidentalis -- Senna tora -- Sida cordifolia -- Smilax china;- Solanum americanum (S. nigrum) -- Sterculia urens -- Strychnos nux-vomica -- Swertia chirata -- Symplocos racemosa -- Syzygium cumini (Eugenia jambolana) -- Tamarindus indica -- Taraxacum officinale -- Taxus baccata -- Tephrosia purpurea -- Terminalia bellirica -- Terminalia chebula -- Thymus vulgaris -- Tinospora cordifolia -- Trachyspermum ammi (Ptychotis coptica) -- Tribulus terrestris -- Trigonella foenum-graecum -- Tussilago farfara -- Valeriana jatamansi (Nardostachys jatamansi) -- Verbena officinalis -- Vernonia anthelmintica (Baccharoides anthelmintica) -- Vigna unguiculata (Dolichos biflorus) -- Viola odorata -- Viscum album -- Withania somnifera -- Wrightia tinctoria -- Zingiber officinale -- Zingiber zerumbet -- Ziziphus jujuba -- Abbreviations -- Glossary -- Ayurvedic Terms of Diseases -- List of Referenced Books -- Index. |
Record Nr. | UNINA-9910409697403321 |
Akbar Shahid
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Cham : , : Springer International Publishing : , : Imprint : Springer, , 2020 | ||
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Lo trovi qui: Univ. Federico II | ||
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