Alkaloids are nitrogen-containing organic compounds found in plants that are typically basic and have physiological effects. While traditionally defined as being derived from plants, some alkaloids come from other organisms. Alkaloids have a variety of structures but generally contain heterocyclic rings with nitrogen atoms. They can exist in different forms including as free bases, salts, and glycosides. Many plants produce alkaloids as a protective mechanism against herbivores.
The document discusses the plant Cinchona and its alkaloid content. It notes that Cinchona bark is the source of the antimalarial drug quinine. It contains quinine, quinidine, cinchonine, and cinchonidine alkaloids. Quinine was isolated from Cinchona bark in the 1820s and is still often sourced from the plant, though it can also be synthesized. Cinchona bark and its quinine content are used to treat malaria due to antipyretic and antimicrobial properties. However, the alkaloids in Cinchona bark can cause side effects like hypoglycemia, blood thinning, and heart issues if not taken
Occurrence and classification and function of alkaloidsJasmineJuliet
Alkaloids introduction, Alkaloids classification, Alkaloids function, pharmaceutical applications of alkaloids, Examples of alkaloids, Some review questions related to alkaloids.
Alkaloids are nitrogen-containing plant compounds that have physiological effects on humans and animals. They have been used for thousands of years by ancient civilizations. Alkaloids are classified based on their chemical structure, biosynthetic pathway, and physiological effects. Common examples include morphine, codeine, caffeine, and quinine. Alkaloids are typically extracted from plants using organic solvents like alcohol or chloroform and purified using precipitation, crystallization, or chromatography techniques.
classification of drugs from natural origin
alphabetical, morphological, pharmacological, chemical, taxonomical, chemotaxonomical, serotaxonomical classifications are included in the presentation
NATURAL PRODUCTS AND CHEMICAL ANALYSIS METHODSCharan Ingole
This document provides information about natural products and chemical analysis methods. It discusses natural products including their extraction from living organisms. It also describes various extraction methods for medicinal plants such as maceration, infusion, decoction, digestion, percolation, and Soxhlet extraction. Further, it covers techniques for separation and isolation of plant constituents including fractional crystallization, fractional liberation, steam distillation, fractional distillation, and sublimation. The document also discusses factors affecting the collection of medicinal plants and methods for their identification, drying, and storage in an herbarium.
Alkaloids are nitrogen-containing organic compounds found in plants that are typically basic and have physiological effects. While traditionally defined as being derived from plants, some alkaloids come from other organisms. Alkaloids have a variety of structures but generally contain heterocyclic rings with nitrogen atoms. They can exist in different forms including as free bases, salts, and glycosides. Many plants produce alkaloids as a protective mechanism against herbivores.
The document discusses the plant Cinchona and its alkaloid content. It notes that Cinchona bark is the source of the antimalarial drug quinine. It contains quinine, quinidine, cinchonine, and cinchonidine alkaloids. Quinine was isolated from Cinchona bark in the 1820s and is still often sourced from the plant, though it can also be synthesized. Cinchona bark and its quinine content are used to treat malaria due to antipyretic and antimicrobial properties. However, the alkaloids in Cinchona bark can cause side effects like hypoglycemia, blood thinning, and heart issues if not taken
Occurrence and classification and function of alkaloidsJasmineJuliet
Alkaloids introduction, Alkaloids classification, Alkaloids function, pharmaceutical applications of alkaloids, Examples of alkaloids, Some review questions related to alkaloids.
Alkaloids are nitrogen-containing plant compounds that have physiological effects on humans and animals. They have been used for thousands of years by ancient civilizations. Alkaloids are classified based on their chemical structure, biosynthetic pathway, and physiological effects. Common examples include morphine, codeine, caffeine, and quinine. Alkaloids are typically extracted from plants using organic solvents like alcohol or chloroform and purified using precipitation, crystallization, or chromatography techniques.
classification of drugs from natural origin
alphabetical, morphological, pharmacological, chemical, taxonomical, chemotaxonomical, serotaxonomical classifications are included in the presentation
NATURAL PRODUCTS AND CHEMICAL ANALYSIS METHODSCharan Ingole
This document provides information about natural products and chemical analysis methods. It discusses natural products including their extraction from living organisms. It also describes various extraction methods for medicinal plants such as maceration, infusion, decoction, digestion, percolation, and Soxhlet extraction. Further, it covers techniques for separation and isolation of plant constituents including fractional crystallization, fractional liberation, steam distillation, fractional distillation, and sublimation. The document also discusses factors affecting the collection of medicinal plants and methods for their identification, drying, and storage in an herbarium.
An introduction to glycosides By KNS & PDVPreeti Verma
The presentation is meant for academic purpose only and includes the definition, occurrence & distribution, classification, properties, chemical tests, general isolation techniques and importance of glycosides.
Alkaloids: Introduction, Property and classification OP VERMA
Alkaloids are major secondary metabolites reported in higher plants. In this PPT I have covered Introduction, Property, Clarification and identification tests.
- Alkaloids are basic nitrogen-containing compounds found in plants, animals, and microorganisms that often have physiological effects.
- They are classified based on their biological origin, biosynthetic pathway, and chemical structure, with the main classes being proto, typical, and pseudo alkaloids.
- Common alkaloids include morphine, codeine, caffeine, and cocaine. Extraction methods take advantage of alkaloids' basic properties, using organic solvents to extract them from plant materials into aqueous solutions as salts.
Alkaloids are nitrogen-containing organic compounds produced by plants. They have diverse chemical structures but generally contain heterocyclic compounds and have physiological effects in humans and animals. Many plants produce alkaloids as protective compounds against herbivores. Some common alkaloids include morphine, codeine, caffeine, and nicotine. Alkaloids are classified based on their chemical structure, pharmacological effects, biosynthetic pathways, and plant sources. They can be detected using chemical tests like Mayer's, Wagner's, and Dragendorff's tests which produce characteristic precipitate colors.
The document discusses alkaloids, which are basic nitrogenous plant compounds that are physiologically active. Some key points:
- True alkaloids contain heterocyclic nitrogen derived from amino acids and are usually toxic. Protoalkaloids are simple amines without heterocyclic rings. Pseudoalkaloids include steroidal and terpenoid compounds.
- Over 6000 alkaloids have been discovered from plants like poppy, tobacco, and coca. They are concentrated in certain plant parts like roots, leaves, or latex.
- Alkaloids have properties like being colorless solids, bitter taste, and soluble in organic solvents. They can be classified pharmacologically or by their
The document discusses materia medica, which is the study of crude drugs obtained from plants, animals, and minerals. It covers the history and etymology of the term, describes crude drugs and their preparation and storage, and discusses various systems for classifying crude drugs based on their morphology, taxonomy, therapeutic use, and chemical constituents. The key classification systems covered are morphological, taxonomic, therapeutic, and based on active chemical constituents.
Este documento presenta información sobre los compuestos fenólicos y flavonoides. Los compuestos fenólicos son sustancias benéficas encontradas en plantas que tienen propiedades antioxidantes y antiinflamatorias. Los flavonoides son un tipo de compuesto fenólico que se encuentra en frutas y verduras y proporcionan beneficios para la salud como propiedades antioxidantes, antiinflamatorias y cardioprotectoras. El documento también clasifica diferentes tipos de flavonoides y describe sus funciones y propiedades farmacológicas.
This document discusses alkaloids, which are basic nitrogenous compounds found in plants and animals that have physiological effects in small quantities. It defines alkaloids and describes their types, including true, proto, and pseudo-alkaloids. The document outlines where alkaloids are commonly found in plants and their isolation process. It also summarizes common identification tests for alkaloids and their therapeutic uses such as analgesics and anticancer agents. Finally, it lists some examples of alkaloids and their pharmaceutical applications.
The document discusses the occurrence, classification, and biosynthesis of different types of alkaloids. It describes alkaloids as naturally occurring basic nitrogen compounds that are physiologically active but insoluble in water. Alkaloids are generally classified based on their basic chemical structures and common precursors like amino acids. The document outlines four main types of alkaloids - protoalkaloids, true alkaloids, pseudoalkaloids, and false alkaloids - and provides examples of important alkaloids like morphine, codeine, and caffeine.
- Alkaloids are basic nitrogen-containing compounds that are often obtained from plants and demonstrate physiological effects.
- They are classified based on their biological origin, biosynthetic pathway, chemical structure, and pharmacological effects.
- Common alkaloids include morphine, quinine, caffeine, and nicotine. They are extracted from plants using various organic solvents and purified.
6.lipids full notes in pdf pharmacognosy and biochemistryDr Muhammad Bilal
Lipids include fats, oils, and waxes. Fats and oils are triglycerides composed of glycerol and three fatty acids. Saturated fats from animal sources are solid at room temperature due to straight hydrocarbon chains that pack closely. Unsaturated plant oils are liquid due to double bonds that cause kinks in the chains and prevent close packing. Fixed oils are obtained from plants by expression or solvent extraction, while animal fats are separated by rendering. Lipids have many uses including soaps, coatings, and supplements.
Pharmacognosy Families By AAA Arslan, Ayyaz, AsadMuhammad Latif
This document provides information on four plants from two families: Zingiberaceae and Liliaceae. It discusses turmeric from Zingiberaceae, including its chemical formula, uses as a spice and coloring agent, and curcumin as the active constituent. It then covers three plants from Liliaceae: squill including its use as a cardiac stimulant, aloe including its use as a laxative and barbaloin as the active constituent, and colchicum including its use to treat gout and colchicine as the active constituent.
Glycosides play numerous important roles in living organisms. Many plants store chemicals in the form of inactive glycosides. These can be activated by enzyme hydrolysis, which causes the sugar part to be broken off, making the chemical available for use. Many such plant glycosides are used as medications. In animals and humans, poisons are often bound to sugar molecules as part of their elimination from the body.A glycoside is a molecule consisting of a sugar and a non-sugar group, called an aglycone. The sugar group is known as the glycone and can consist of a single sugar group or several sugar groups. The sugars is in its cyclic form and is covalently attached to the aglycon through the hydroxyl group of the hemiactal function.
There are many different kinds of aglycones. It can be a terpene, a flavonoid, a coumarin or practically any other natural occurring product (se figure 1)
The glycone can be attached to the aglycon in many different ways. The most common bridging atom is oxygen (O-glycoside), but it can also be sulphur (S-glycoside), nitrogen (N-glycoside) or carbon (C-glycoside). In general, one distinguishes between α-Glycosides and β-glycosides, depending on the configuration of the hemiactal hydroxyl group. The majority of the naturally occurring glycosides are β-glycosidesGenerally glycosides are more polar than the aglycones and as a result glycoside formation usually increases water solubility. This may allow the producing organism to transport and store the glycoside more efficiently
Many biologically active compounds are glycosides. The pharmacological effects are largely determined by the structure of the aglycone.
Glycosides comprise several important classes of compounds such as hormones, sweeteners, alkaloids, flavonoids and antibiotics
These slides represent a comprehensive view of history of using natural products caused to appearance of pharmacognosy as a science and show several aspects of pharmacognosy and natural products use and final their importance in discovering new drugs.
This document discusses various methods of classifying crude drugs, including alphabetical, taxonomic, morphological, chemical, pharmacological, chemotaxonomic, and serotaxonomic classification. Each method is described along with its advantages and disadvantages. Alphabetical classification arranges drugs by name, while taxonomic classification is based on the biological classification of plants. Morphological classification groups drugs based on the plant part used. Chemical and pharmacological classification consider the active chemical constituents and therapeutic effects. Chemotaxonomic and serotaxonomic classification examine chemical similarities and antigen-antibody reactions between taxa.
Este documento presenta una introducción a los alcaloides, sustancias nitrogenadas de origen vegetal con actividad fisiológica. Explica que se han identificado más de 5000 alcaloides restringidos a ciertas familias botánicas, y describe algunos alcaloides importantes como la morfina, cafeína y quinina. También resume las características químicas, propiedades y usos de los alcaloides, así como métodos para su extracción e identificación.
This document provides an introduction and objectives for a lesson on glycosides. It defines glycosides as molecules containing a sugar (glycone) and another part (aglycone) bonded via a glycosidic bond. The document then discusses the functions, nomenclature, classification, occurrence and distribution, chemical characteristics, and examples of glycosides. It also covers the extraction, isolation, purification, identification, and estimation of glycosides.
The term ‘ alkaloid ’ was coined by MEISSNER,
a German pharmacist, in 1819.
The French chemist, Derosne in 1803, isolated
narcotine . In the same year , morphine from
opium was isolated by Serturner .
Pelletier and Caventon isolated emetine in
1817 and colchicine in 1819.
From the beginning of 19th century till to date,
it has to proved to be a perpetual work to
discover new alkaloids from plants and
animals.
As per a Russian review in 1973, the numbe of
known alkaloids had reached upto 4959,
amongst which, the structures of 3293
alkaloids were elucidated.
At present, the number of alkaloids discovered
has exceeded 6000.
The document discusses primary and secondary metabolites, alkaloids, glycosides, and tannins. It defines these compounds and outlines their key properties. Alkaloids are nitrogen-containing compounds that have physiological effects. They are classified based on biosynthetic pathways, pharmacology, taxonomy, and heterocyclic ring structures. Glycosides are compounds containing a sugar and non-sugar moiety. They are classified by the type of sugar or aglycone. Tannins are polyphenolic compounds that can combine with proteins. They are classified as hydrolysable or condensed based on their chemical structures. Extraction and isolation methods are also presented.
This document provides an overview of alkaloids. It defines alkaloids as nitrogenous organic compounds that are typically bitter and have pharmacological effects. Alkaloids are found in various plants, animals, and fungi. The document discusses the distribution, extraction, classification, and examples of important alkaloids like morphine, codeine, caffeine, and quinine. It also summarizes key information about specific alkaloid-containing plants such as opium, belladonna, coca, and ipecac.
This document provides information about alkaloids, including their definition, nomenclature, physiological action, occurrence, and isolation. It defines alkaloids as basic, nitrogen-containing organic compounds produced by various organisms. Alkaloids have diverse physiological effects and are commonly found in plants, where they serve protective and metabolic functions. Methods for isolating alkaloids from plant materials involve extraction with organic solvents followed by acid/base treatments and chromatographic separation to obtain pure alkaloids.
An introduction to glycosides By KNS & PDVPreeti Verma
The presentation is meant for academic purpose only and includes the definition, occurrence & distribution, classification, properties, chemical tests, general isolation techniques and importance of glycosides.
Alkaloids: Introduction, Property and classification OP VERMA
Alkaloids are major secondary metabolites reported in higher plants. In this PPT I have covered Introduction, Property, Clarification and identification tests.
- Alkaloids are basic nitrogen-containing compounds found in plants, animals, and microorganisms that often have physiological effects.
- They are classified based on their biological origin, biosynthetic pathway, and chemical structure, with the main classes being proto, typical, and pseudo alkaloids.
- Common alkaloids include morphine, codeine, caffeine, and cocaine. Extraction methods take advantage of alkaloids' basic properties, using organic solvents to extract them from plant materials into aqueous solutions as salts.
Alkaloids are nitrogen-containing organic compounds produced by plants. They have diverse chemical structures but generally contain heterocyclic compounds and have physiological effects in humans and animals. Many plants produce alkaloids as protective compounds against herbivores. Some common alkaloids include morphine, codeine, caffeine, and nicotine. Alkaloids are classified based on their chemical structure, pharmacological effects, biosynthetic pathways, and plant sources. They can be detected using chemical tests like Mayer's, Wagner's, and Dragendorff's tests which produce characteristic precipitate colors.
The document discusses alkaloids, which are basic nitrogenous plant compounds that are physiologically active. Some key points:
- True alkaloids contain heterocyclic nitrogen derived from amino acids and are usually toxic. Protoalkaloids are simple amines without heterocyclic rings. Pseudoalkaloids include steroidal and terpenoid compounds.
- Over 6000 alkaloids have been discovered from plants like poppy, tobacco, and coca. They are concentrated in certain plant parts like roots, leaves, or latex.
- Alkaloids have properties like being colorless solids, bitter taste, and soluble in organic solvents. They can be classified pharmacologically or by their
The document discusses materia medica, which is the study of crude drugs obtained from plants, animals, and minerals. It covers the history and etymology of the term, describes crude drugs and their preparation and storage, and discusses various systems for classifying crude drugs based on their morphology, taxonomy, therapeutic use, and chemical constituents. The key classification systems covered are morphological, taxonomic, therapeutic, and based on active chemical constituents.
Este documento presenta información sobre los compuestos fenólicos y flavonoides. Los compuestos fenólicos son sustancias benéficas encontradas en plantas que tienen propiedades antioxidantes y antiinflamatorias. Los flavonoides son un tipo de compuesto fenólico que se encuentra en frutas y verduras y proporcionan beneficios para la salud como propiedades antioxidantes, antiinflamatorias y cardioprotectoras. El documento también clasifica diferentes tipos de flavonoides y describe sus funciones y propiedades farmacológicas.
This document discusses alkaloids, which are basic nitrogenous compounds found in plants and animals that have physiological effects in small quantities. It defines alkaloids and describes their types, including true, proto, and pseudo-alkaloids. The document outlines where alkaloids are commonly found in plants and their isolation process. It also summarizes common identification tests for alkaloids and their therapeutic uses such as analgesics and anticancer agents. Finally, it lists some examples of alkaloids and their pharmaceutical applications.
The document discusses the occurrence, classification, and biosynthesis of different types of alkaloids. It describes alkaloids as naturally occurring basic nitrogen compounds that are physiologically active but insoluble in water. Alkaloids are generally classified based on their basic chemical structures and common precursors like amino acids. The document outlines four main types of alkaloids - protoalkaloids, true alkaloids, pseudoalkaloids, and false alkaloids - and provides examples of important alkaloids like morphine, codeine, and caffeine.
- Alkaloids are basic nitrogen-containing compounds that are often obtained from plants and demonstrate physiological effects.
- They are classified based on their biological origin, biosynthetic pathway, chemical structure, and pharmacological effects.
- Common alkaloids include morphine, quinine, caffeine, and nicotine. They are extracted from plants using various organic solvents and purified.
6.lipids full notes in pdf pharmacognosy and biochemistryDr Muhammad Bilal
Lipids include fats, oils, and waxes. Fats and oils are triglycerides composed of glycerol and three fatty acids. Saturated fats from animal sources are solid at room temperature due to straight hydrocarbon chains that pack closely. Unsaturated plant oils are liquid due to double bonds that cause kinks in the chains and prevent close packing. Fixed oils are obtained from plants by expression or solvent extraction, while animal fats are separated by rendering. Lipids have many uses including soaps, coatings, and supplements.
Pharmacognosy Families By AAA Arslan, Ayyaz, AsadMuhammad Latif
This document provides information on four plants from two families: Zingiberaceae and Liliaceae. It discusses turmeric from Zingiberaceae, including its chemical formula, uses as a spice and coloring agent, and curcumin as the active constituent. It then covers three plants from Liliaceae: squill including its use as a cardiac stimulant, aloe including its use as a laxative and barbaloin as the active constituent, and colchicum including its use to treat gout and colchicine as the active constituent.
Glycosides play numerous important roles in living organisms. Many plants store chemicals in the form of inactive glycosides. These can be activated by enzyme hydrolysis, which causes the sugar part to be broken off, making the chemical available for use. Many such plant glycosides are used as medications. In animals and humans, poisons are often bound to sugar molecules as part of their elimination from the body.A glycoside is a molecule consisting of a sugar and a non-sugar group, called an aglycone. The sugar group is known as the glycone and can consist of a single sugar group or several sugar groups. The sugars is in its cyclic form and is covalently attached to the aglycon through the hydroxyl group of the hemiactal function.
There are many different kinds of aglycones. It can be a terpene, a flavonoid, a coumarin or practically any other natural occurring product (se figure 1)
The glycone can be attached to the aglycon in many different ways. The most common bridging atom is oxygen (O-glycoside), but it can also be sulphur (S-glycoside), nitrogen (N-glycoside) or carbon (C-glycoside). In general, one distinguishes between α-Glycosides and β-glycosides, depending on the configuration of the hemiactal hydroxyl group. The majority of the naturally occurring glycosides are β-glycosidesGenerally glycosides are more polar than the aglycones and as a result glycoside formation usually increases water solubility. This may allow the producing organism to transport and store the glycoside more efficiently
Many biologically active compounds are glycosides. The pharmacological effects are largely determined by the structure of the aglycone.
Glycosides comprise several important classes of compounds such as hormones, sweeteners, alkaloids, flavonoids and antibiotics
These slides represent a comprehensive view of history of using natural products caused to appearance of pharmacognosy as a science and show several aspects of pharmacognosy and natural products use and final their importance in discovering new drugs.
This document discusses various methods of classifying crude drugs, including alphabetical, taxonomic, morphological, chemical, pharmacological, chemotaxonomic, and serotaxonomic classification. Each method is described along with its advantages and disadvantages. Alphabetical classification arranges drugs by name, while taxonomic classification is based on the biological classification of plants. Morphological classification groups drugs based on the plant part used. Chemical and pharmacological classification consider the active chemical constituents and therapeutic effects. Chemotaxonomic and serotaxonomic classification examine chemical similarities and antigen-antibody reactions between taxa.
Este documento presenta una introducción a los alcaloides, sustancias nitrogenadas de origen vegetal con actividad fisiológica. Explica que se han identificado más de 5000 alcaloides restringidos a ciertas familias botánicas, y describe algunos alcaloides importantes como la morfina, cafeína y quinina. También resume las características químicas, propiedades y usos de los alcaloides, así como métodos para su extracción e identificación.
This document provides an introduction and objectives for a lesson on glycosides. It defines glycosides as molecules containing a sugar (glycone) and another part (aglycone) bonded via a glycosidic bond. The document then discusses the functions, nomenclature, classification, occurrence and distribution, chemical characteristics, and examples of glycosides. It also covers the extraction, isolation, purification, identification, and estimation of glycosides.
The term ‘ alkaloid ’ was coined by MEISSNER,
a German pharmacist, in 1819.
The French chemist, Derosne in 1803, isolated
narcotine . In the same year , morphine from
opium was isolated by Serturner .
Pelletier and Caventon isolated emetine in
1817 and colchicine in 1819.
From the beginning of 19th century till to date,
it has to proved to be a perpetual work to
discover new alkaloids from plants and
animals.
As per a Russian review in 1973, the numbe of
known alkaloids had reached upto 4959,
amongst which, the structures of 3293
alkaloids were elucidated.
At present, the number of alkaloids discovered
has exceeded 6000.
The document discusses primary and secondary metabolites, alkaloids, glycosides, and tannins. It defines these compounds and outlines their key properties. Alkaloids are nitrogen-containing compounds that have physiological effects. They are classified based on biosynthetic pathways, pharmacology, taxonomy, and heterocyclic ring structures. Glycosides are compounds containing a sugar and non-sugar moiety. They are classified by the type of sugar or aglycone. Tannins are polyphenolic compounds that can combine with proteins. They are classified as hydrolysable or condensed based on their chemical structures. Extraction and isolation methods are also presented.
This document provides an overview of alkaloids. It defines alkaloids as nitrogenous organic compounds that are typically bitter and have pharmacological effects. Alkaloids are found in various plants, animals, and fungi. The document discusses the distribution, extraction, classification, and examples of important alkaloids like morphine, codeine, caffeine, and quinine. It also summarizes key information about specific alkaloid-containing plants such as opium, belladonna, coca, and ipecac.
This document provides information about alkaloids, including their definition, nomenclature, physiological action, occurrence, and isolation. It defines alkaloids as basic, nitrogen-containing organic compounds produced by various organisms. Alkaloids have diverse physiological effects and are commonly found in plants, where they serve protective and metabolic functions. Methods for isolating alkaloids from plant materials involve extraction with organic solvents followed by acid/base treatments and chromatographic separation to obtain pure alkaloids.
Health benefits of plant alkaloids A Lecture By Mr Allah Dad Khan Former DG ...Mr.Allah Dad Khan
Health benefits of plant alkaloids A Lecture By Mr Allah Dad Khan Former DG Agriculture Extension Khyber Pakhtun Khwa Province & Visiting Professor Agriculture University Peshawar Pakistan
This document discusses alkaloids, which are nitrogen-containing compounds found in plants. It describes their characteristics, sources, structures, properties, uses, biosynthesis, tests to identify them, and classifications. Key points include: alkaloids are bitter and derived from amino acids; they are found in various plant families and parts; they have pharmacological effects like analgesia and serve defensive roles in plants; and examples like nicotine, areca, lobeline, and tropane alkaloids like atropine and hyoscyamine are described.
This document discusses alkaloids, which are nitrogenous plant compounds that have physiological effects. It describes their characteristics, sources, uses, and importance in pharmacy. Key points include: alkaloids are bitter and derived from amino acids; sources include various plant families; uses include analgesic, narcotic, and mydriatic effects; important alkaloids include morphine, codeine, nicotine, and atropine. Tests are outlined to identify the presence of alkaloids. The document also classifies and describes important alkaloid groups such as tropane and solanaceous alkaloids.
This document provides information about alkaloids, including their characteristics, sources, uses, and classification. Some key points include:
- Alkaloids are nitrogen-containing compounds found in plants that are usually bitter and have physiological effects. They are derived from amino acids.
- Major sources of alkaloids include plants from the Papaveraceae, Solanaceae, and Rutaceae families.
- Alkaloids have various pharmacological actions and uses including as analgesics, narcotics, and anticholinergics.
- Common alkaloids and their sources are discussed like nicotine from tobacco, arecoline from areca nut, and hyoscyamine from belladonna.
- Tests
The document discusses alkaloids, which are nitrogen-containing plant compounds. It defines alkaloids and explains that they are difficult to define precisely due to overlapping properties with other amines. It then covers the distribution of various alkaloids in different plant parts, their chemical properties, pharmacological actions, classification based on ring structure, extraction methods, and chemical tests to identify alkaloids.
Alkaloids-New S 2020.pdfyrhfeettsswartttemoyourtri
The document defines alkaloids as basic heterocyclic nitrogenous compounds of plant origin that are physiologically active. However, some alkaloids deviate from this definition by not being basic or having nitrogen outside a heterocyclic ring. Alkaloids are classified as true, proto, or pseudo depending on their origin and structure. They are commonly found in dicots but rare in lower plants, and are distributed in various plant parts and families. In addition to acting as insect deterrents, alkaloids may function as nitrogen sources, growth regulators, or energy sources for plants. The document outlines extraction, purification, and classification methods for alkaloids. It provides examples of specific alkaloid-containing plants and
This ppt contains a suitable contents. This notes is effective for B.Pharm & D.Pharm students. In this notes we all the related topic of secondary metabolites. In this notes we all sub topics of secondary metabolites such as Alkaloids, Glycosides, Terpenoids, Taninns, Resins, Flavonoids, etc.
The document discusses alkaloids, which are basic organic compounds found in plants that contain at least one nitrogen atom. It defines alkaloids and describes their properties, occurrence in plants, and functions. The document then covers various topics related to alkaloids including their classification into heterocyclic and non-heterocyclic types based on their ring structure, general extraction methods, and in-depth examinations of specific alkaloid-containing plants and their active constituents like cocaine from coca leaves and colchicine from autumn crocus.
This document discusses alkaloids, which are nitrogen-containing organic compounds found primarily in plants. Certain plant families like poppies, buttercups, nightshades, and amaryllis are particularly rich in alkaloids. Alkaloids have diverse physiological effects and are basic in nature with at least one nitrogen atom in a heterocyclic ring. They are classified based on their source, physiological response, discoverer, taxonomy, pharmacology, biosynthesis or chemical structure. The main chemical classifications are heterocyclic alkaloids which have nitrogen-containing rings and nonheterocyclic alkaloids which are biological amines.
Primary metabolites directly involve normal growth and development and perform essential physiological functions. Examples include ethanol, lactic acid, sugars, fatty acids and amino acids. Secondary metabolites are not directly involved in normal growth and development but represent chemical adaptations to stresses or serve defensive/protective functions. Examples include alkaloids, glycosides, flavonoids and volatile oils. The shikimic acid pathway appears important for biosynthesis of phenylpropane derivatives like phenylalanine and tyrosine in plants. It involves conversion of chorismic acid to prephenic acid or anthranilic acid. Alkaloids are basic compounds found in plants containing nitrogen in a heterocyclic ring. They have complex molecular structures and significant pharmacological activity
Alkaloids are classified based on their biosynthetic precursors, which include amino acids like ornithine, tryptophan, lysine, phenylalanine, tyrosine, and histidine. Other precursors include purines. Major classes include tropane alkaloids from ornithine, indole alkaloids from tryptophan, quinoline alkaloids from tryptophan, papaver alkaloids from tyrosine, and purine alkaloids like caffeine, theobromine, and theophylline not derived from amino acids. Biosynthesis involves reactions like decarboxylation and transamination of amino acid precursors.
The document discusses several plants and plant products used as medicines, including their biological sources, chemical constituents, properties, uses, and commercial applications. It provides details on alkaloids, describing their physical and chemical properties as well as classification. Examples of important alkaloid-containing plants discussed include vinca, rauwolfia, belladonna, opium, and tea.
The document discusses several plants and plant products used as medicines, including their biological sources, chemical constituents, properties, uses, and commercial applications. It provides details on alkaloids, describing their physical and chemical properties as well as classes and tests. Examples of important alkaloid-containing plants are discussed in depth, such as vinca, rauwolfia, belladonna, opium, and tea.
This document discusses alkaloids, which are basic, nitrogen-containing compounds found in plants. It defines alkaloids and notes that the definition is not fully satisfactory. It describes the various ways alkaloids exist in plants, such as in free form, as glycosides, amides, and esters. The document outlines different classification systems for alkaloids including taxonomic, pharmacological, biosynthetic, and chemical classifications. It also discusses the isolation and purification process for extracting alkaloids from plants.
The document discusses the isolation and properties of alkaloids such as atropine and quinine. It provides a history of alkaloid discovery and defines alkaloids as basic heterocyclic nitrogenous compounds found primarily in plants. Methods for isolating alkaloids from plant materials using extraction with organic solvents and precipitation are described. Key tests and properties of atropine and quinine such as appearance, solubility, chemical tests, and uses are outlined. The isolation of atropine from plants such as belladonna involves extraction with petroleum ether followed by precipitation. Quinine is isolated from cinchona bark using extraction with benzene followed by acid-base separation.
The document discusses the isolation and properties of alkaloids including atropine and quinine. It provides a history of alkaloid discovery and defines alkaloids as basic heterocyclic nitrogenous compounds found primarily in plants that are physiologically active. Methods of alkaloid isolation from plant materials and chemical tests for identification are described. Key details about the biological sources, isolation, properties, identification and uses of atropine and quinine are also summarized.
This document provides an overview of resins and resin combinations. It defines resins as solid or semi-solid amorphous products derived mostly from plants. Resins can occur alone or in combination with other plant metabolites like volatile oils, gums, or oils and gums. The document discusses the properties, types, occurrence, extraction and identification of resins. It provides examples of specific resins and their constituents and uses, including cannabis, capsicum, myrrh, asafoetida, balsam of tolu, balsam of peru, benzoin, turmeric and ginger.
This document defines and describes different types of drugs obtained from plants, including organized and unorganized drugs. It discusses rhizomes, roots, resins, alkaloids, and glycosides that are used as drugs. It then focuses on describing resins, including their physical and chemical properties, distribution in plants, occurrence in secretory structures, and classification based on constituents. Finally, it describes the main chemical components of resins - resin acids, resin alcohols including resinotannols and resinols, and resenes.
How to Build a Module in Odoo 17 Using the Scaffold MethodCeline George
Odoo provides an option for creating a module by using a single line command. By using this command the user can make a whole structure of a module. It is very easy for a beginner to make a module. There is no need to make each file manually. This slide will show how to create a module using the scaffold method.
বাংলাদেশের অর্থনৈতিক সমীক্ষা ২০২৪ [Bangladesh Economic Review 2024 Bangla.pdf] কম্পিউটার , ট্যাব ও স্মার্ট ফোন ভার্সন সহ সম্পূর্ণ বাংলা ই-বুক বা pdf বই " সুচিপত্র ...বুকমার্ক মেনু 🔖 ও হাইপার লিংক মেনু 📝👆 যুক্ত ..
আমাদের সবার জন্য খুব খুব গুরুত্বপূর্ণ একটি বই ..বিসিএস, ব্যাংক, ইউনিভার্সিটি ভর্তি ও যে কোন প্রতিযোগিতা মূলক পরীক্ষার জন্য এর খুব ইম্পরট্যান্ট একটি বিষয় ...তাছাড়া বাংলাদেশের সাম্প্রতিক যে কোন ডাটা বা তথ্য এই বইতে পাবেন ...
তাই একজন নাগরিক হিসাবে এই তথ্য গুলো আপনার জানা প্রয়োজন ...।
বিসিএস ও ব্যাংক এর লিখিত পরীক্ষা ...+এছাড়া মাধ্যমিক ও উচ্চমাধ্যমিকের স্টুডেন্টদের জন্য অনেক কাজে আসবে ...
Exploiting Artificial Intelligence for Empowering Researchers and Faculty, In...Dr. Vinod Kumar Kanvaria
Exploiting Artificial Intelligence for Empowering Researchers and Faculty,
International FDP on Fundamentals of Research in Social Sciences
at Integral University, Lucknow, 06.06.2024
By Dr. Vinod Kumar Kanvaria
How to Manage Your Lost Opportunities in Odoo 17 CRMCeline George
Odoo 17 CRM allows us to track why we lose sales opportunities with "Lost Reasons." This helps analyze our sales process and identify areas for improvement. Here's how to configure lost reasons in Odoo 17 CRM
How to Add Chatter in the odoo 17 ERP ModuleCeline George
In Odoo, the chatter is like a chat tool that helps you work together on records. You can leave notes and track things, making it easier to talk with your team and partners. Inside chatter, all communication history, activity, and changes will be displayed.
Executive Directors Chat Leveraging AI for Diversity, Equity, and InclusionTechSoup
Let’s explore the intersection of technology and equity in the final session of our DEI series. Discover how AI tools, like ChatGPT, can be used to support and enhance your nonprofit's DEI initiatives. Participants will gain insights into practical AI applications and get tips for leveraging technology to advance their DEI goals.
Strategies for Effective Upskilling is a presentation by Chinwendu Peace in a Your Skill Boost Masterclass organisation by the Excellence Foundation for South Sudan on 08th and 09th June 2024 from 1 PM to 3 PM on each day.
This presentation includes basic of PCOS their pathology and treatment and also Ayurveda correlation of PCOS and Ayurvedic line of treatment mentioned in classics.
3. Introduction
The term alkaloid (alkali like) was coined by Carl F.W. Meissner in 1819, derived from the Arabic word “Al qualja” means
ashes of plants
Group of natural occurring simple or complex nitrogen containing compounds
Basic in nature
Secondary metabolites abundantly found in plants and lesser extent in micro-organisms and animals
Families rich in alkaloids are: Apocynaceae, Rubiaceae, Solanaceae, Papaveraceae
In addition to carbon, hydrogen and nitrogen, may also contain oxygen,sulfur and other elements
Usually derivatives of amino acids
Produce various physiological function in organisms like- anti-bacterial, anti-inflammatory, analgesic, anti-neoplastic,
hypnotic, psychotropic, local anaesthetic etc
5. Classification
Hegnauer’s classification
True Alkaloids:- They contain nitrogen atom in heterocyclic system and derived from amino acids
Example: Atropine, Morphine, Nicotine
Proto alkaloids:- They do not contain nitrogen atom in heterocyclic system but derived from amino acids
Example: Mescaline, Epinephrine, Ephedrine
Pseudo alkaloids:- They contain nitrogen atom in heterocyclic system but not the derivative of amino acids
Example: Caffeine, Theobromine, Coniine
9. Classification
Taxonomical classification
Alkaloids are classified based on biological sources. Examples: Quinine from the bark of Cinchona calisaya, Rauwolfia from
roots of Rauwolfia serpentina, Morphine from dried latex of Papaver somniferum, etc.
10. Nomenclature
There is no unique method for naming alkaloids
Many individual names are formed by adding the suffix "ine" to the species or genus name For example, atropine is isolated
from the plant Atropa belladonna
If several alkaloids are extracted from one plant then their names often contain suffixes "idine", "anine", "aline", "inine" etc.
Naming alkaloids as the second Latin name the plant extract from him like Belladonine from belladonna
Naming alkaloids according to the physiological effect (therapeutic) ex. Narcotic (Narcotine) , emetic ( emetine)
Naming alkaloids according to the Discoverer ex. Pelletierine from Pelletier
There are also at least 86 alkaloids whose names contain the root "vin" because they are extracted from vinca plants such
as Vinca rosea (Catharanthus roseus); these are called vinca alkaloids
11. Extraction & Purification
Stas-Otto method
Plant’s Material (Dried & Powdered)
Moist with water
Treat with lime
Extract with organic solvent
Filtration
Filtrate
Add water
Organic layer of alkali
Add water & Acid
Salt form in aqueous layer
Purification
Purified by chromatography
12. REFERENCES
1. Libretexts (2020) Alkaloids, Chemistry LibreTexts. Available at:
https://chem.libretexts.org/Courses/University_of_California_Davis/UCD_Chem_231A%3A_Methods_of_
Organic_Synthesis/Under_construction/1_Ideas/Alkaloids (Accessed: 05 October 2023).
2. (n.d.). Jiwaji University. http://www.jiwaji.edu/pdf/ecourse/pharmaceutical/Alkaloids-
Classification%20&%20Identification.pdf
3. Introductory Chapter: Alkaloids -Their Importance in Nature and for Human Life. (n.d.). IntechOpen -
Open Science Open Minds |IntechOpen. https://www.intechopen.com/chapters/66742
4. Classification of Alkaloids - Solution Parmacy. (n.d.). Solution
Parmacy. https://solutionpharmacy.in/classification-of-alkaloids/
5. Contributors to Wikimedia projects. (2001, October 24). Alkaloid - Wikipedia. Wikipedia, the free
encyclopedia. https://en.wikipedia.org/wiki/Alkaloid#In_medicine
6. Extraction Method of Alkaloids - Solution Parmacy. (n.d.). Solution
Parmacy. https://solutionpharmacy.in/extraction-method-of-alkaloids/