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Fluorine in Heterocyclic Chemistry Volume 2 [[electronic resource] ] : 6-Membered Heterocycles / / edited by Valentine Nenajdenko
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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Foodinformatics [[electronic resource] ] : Applications of Chemical Information to Food Chemistry / / edited by Karina Martinez-Mayorga, José Luis Medina-Franco
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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Functional Chitosan [[electronic resource] ] : Drug Delivery and Biomedical Applications / / edited by Sougata Jana, Subrata Jana
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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Fundamentals of Neurodegeneration and Protein Misfolding Disorders [[electronic resource] /] / by Martin Beckerman
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  
Cham : , : Springer International Publishing : , : Imprint : Springer, , 2015
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Grapes and Health [[electronic resource] /] / edited by John M. Pezzuto
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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Green Chemistry: Synthesis of Bioactive Heterocycles [[electronic resource] /] / edited by K. L. Ameta, Anshu Dandia
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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Haloalkyne Chemistry [[electronic resource] /] / by Huanfeng Jiang, Chuanle Zhu, Wanqing Wu
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  
Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2016
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Halogen Bonding I [[electronic resource] ] : Impact on Materials Chemistry and Life Sciences / / edited by Pierangelo Metrangolo, Giuseppe Resnati
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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Halogen Bonding II [[electronic resource] ] : Impact on Materials Chemistry and Life Sciences / / edited by Pierangelo Metrangolo, Giuseppe Resnati
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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Handbook of 200 Medicinal Plants [[electronic resource] ] : A Comprehensive Review of Their Traditional Medical Uses and Scientific Justifications / / by Shahid Akbar
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  
Cham : , : Springer International Publishing : , : Imprint : Springer, , 2020
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