What Are Alkaloids
What Are Alkaloids
What Are Alkaloids
• Commonly applied to basic nitrogenous compounds of plant origin that is physiologically active.
• Among the angiosperms, the Leguminosae, Papaveraceae, Ranunculaceae, Rubiaceae, Solanaceae,
and Berberidaceae are outstanding alkaloid-yielding plants.
• The Labiatae and Rosaceae are almost free of alkaloids; the gymnosperms only rarely contain them
(Taxaceae).
• Although it has been claimed that the monocotyledons do not generally produce alkaloids, investi-
gations indicate that the Amaryllidaceae and Liliaceae are 2 of the most promising families (of a list of
11) in which to search for alkaloid-yielding plants.
• chemical rules designate that the names of all alkaloids should end in “ine."
• Alkaloids usually contain one nitrogen atom, although some, like ergotamine, may contain up to
5. The nitrogen may exist as a primary amine (RNH2), as a secondary amine (R2NH), or as a tertiary
amine (RN).
• For the most part, the alkaloids are insoluble or sparingly so in water, but the salts formed on
reaction with acids are usually freely soluble.
• The free alkaloids are usually soluble in ether, chloroform, or other relatively nonpolar,
immiscible solvents in which, however, the aikaloidal salts are insoluble. This permits a ready means for
the isolation and purification of the alkaloids as well as for their quantitative estimation.
• Most of the alkaloids are crystalline solids, although a few are amorphous. An additional few,
coniine, nicotine, and sparteine, which lack oxygen in their molecules, are liquids. Alkaloidal salts are
crystalline, and their crystal form and habit are often a useful means of rapid microscopic identification.
What is the classification of alkaloid based on the ring structure or nucleus of the chief
alkaloid group in the plant drug?
1. pyridine and piperidine Alkaloids (Arecoline, lobeline, and nicotine)
2. Tropane Alkaloids- a condensation product of pyrrolidine and piperidine
(atropine, hyoscyamine, and hyoscine)
3. quinoline Alkaloids (the cinchona alkaloids, quinine, quinidine, cinchonine, and cinchonidine)
4. isoquinoline Alkaloids (hydrastine, ( + )-tubocurarine, emetine, and the opium alkaloids)
5. indole Alkaloids (ergonovine, reserpine, and strychnine)
6. imidazole Alkaloid (pilocarpine)
7. purine bases (caffeine and theobromine)
8. steroidal Alkaloids (protoveratrine)
9. Alkaloidal Amines
• Like other amines, form double salts with compounds of mercury, gold, platinum, and other
heavy metals. These double salts are usually 'obtained as precipitates, and many of them are
microcrystallographically characteristic.
• The alkaloids usually possess a bitter taste.
PYRIDINE-PIPERIDINE ALKALOIDS
pyridine
- a tertiary base
Upon reduction it is converted into the secondary base, piperidine.
3 subgroups
(1) derivatives of piperidine, including lobeline from lobelia
(2) derivatives of nicotinic acid, including arecoline from areca
(3) derivatives of both pyridine and pyrrolidine, including nicotine from tobacco.
• The important alkaloidal drugs and their alkaloids that are classified in this group are
areca, arecoline hydrobromide, lobelia, lobeline, and nicotine.
Nicotine.
• More than 65 years ago, the Swiss chemist Trier proposed that nicotine was biosynthesized
from nicotinic acid and proline. If proline is considered a representative of the ornithine-proline-
glutamic acid group, this remarkable hypothesis may be considered correct. However, numerous
experiments conducted principally during the last 2 decades still have not clarified completely all
of the reactions involved in the production of nicotine in Nicotiana species.
• Tracer studies have shown that ornithine is incorporated into nicotine by tobacco plants.
This incorporation results in a symmetric labeling pattern of nicotine. Putrescine, N-
methylputrescine, and N-methylaminobutanal are all incorporated, and the key intermediate is
thought to be the N-methylpyrrolinium ion which, through electrophilic aromatic substitution, at-
taches to C-3 of the pyridine ring of nicotinic acid. Nicotinic acid is formed in higher plants and
certain microorganisms via quinolinic acid by the condensation of glyceraldehyde-3-phosphate
and aspartic acid. Nicotine is primarily a product of root metabolism, but the formation of small
amounts, as well as subsequent reactions such as the demethylation of nicotine, can occur in the
leaves of plants.
USE
1. Nicotine is bound to an ion exchange resin in a chewing gum base as a temporary aid to the
cigarette smoker seeking to give up smoking.
Areca
• Areca, areca nut, or betel nut is the dried, ripe seed of Areca catechu Linne (Fam.
Palmae).
• Areca is the Spanish and Portuguese term for the betel nut.
• Catechu is the East Indian name for an astringent extract or juice.
• The fruit is a nut that contains a single seed with a thin seed coat and a large ruminate
endosperm. The seeds are removed from the fruits, boiled in water containing lime, and dried.
India is a major producer of areca, but its production is mostly consumed domestically.
• Areca is mixed with lime, the leaves of Piper betle Linne’ and occasionally gambir.
• The mixture is used as a stimulant masticatory in India and the East Indies.
• In India, the mixture is known as "punsupari." Betel chewing has been practiced since early
times.
• The natives chew fresh betel nuts; dried betel nuts are used for pharmaceutic purposes. The
value of areca as a taenicide apparently has been known in the East for a long time but was not
known to western civilization until 1863.
Areca contains several alkaloids that are reduced pyridine derivatives:
• arecoline (arecaidine methyl ester)- the most abundant and physiologically most active
alkaloid, is a liquid occurring to the extent of about 0.2%. Areca also contains tannin (about 15%),
lipids, volatile oils, and gum.
• arecaidine (N-methyl guvacine)
• guvacine (tetrahydronicotinic acid)
• guvacoline (guvacine methyl ester).
• The total alkaloid content can reach 0.45%. USE AND DOSE. Areca is classified as an
ANTHELMINTIC in veterinary practice and is employed as a vermicide and taenifuge. The usual
dose in dogs is 2 to 4 g; in sheep, 4 to 8 g, based on the weight of the animal.
Lobelia
Lobelia or Indian tobacco
• consists of the dried leaves and tops of Lobelia inflata Linne’ (Fam. Lobeliaceae).
• Lobelia was named in honor of Matthias de L'Obel, a Flemish botanist (1538 to 1616); inflata
refers to the fruit, which is hollow and distended.
• Its emetic properties were first observed in 1785, and the drug was introduced into medicine
in 1807.
• The drug contains 14 alkaloids, of which lobeline is the major and most important, a pungent
volatile oil, resin, lipids, and gum.
Lobeline, (-)-lobeline, or alpha lobeline (to distinguish it from a mixture of the lobelia alkaloids
formerly designated as lobeline)
• occurs as colorless crystals that are slightly soluble in water but readily soluble in hot
alcohol.
TROPANE ALKALOIDS
Tropane
• is a dicyclic compound formed by the condensation of a pyrrolidine precursor (ornithine)
with 3 acetate-derived carbon atoms. Both pyrrolidine and piperidine ring systems can be
discerned in the molecule.
tropine
• The 3-hydroxy derivative of tropane.
• Its esterification with (-)-tropic acid yields hyoscyamine (tropine tropate), which may be
racemized to form atropine.
Belladonna
Belladonna leaf, belladonna herb, or deadly nightshade leaf
• consists of the dried leaf and flowering or fruiting top of Atropa belladonna Linne’ or of its
variety ac uminata Royle ex Lindley (Fam. Solanaceae)
• Belladonna leaf yields not less than 0.35% of alkaloids.
• Atropa is from Atropos, meaning inflexible, the name of the Greek Fate who cuts the thread
of life, and probably alludes to the poisonous character of the drug.
• Belladonna is from the Italian bella, meaning beautiful, and donna, meaning lady. (The juice
of the berry, when placed in the eyes, causes dilation of the pupils, thus giving a striking
appearance.)
• The leaf yields alkaloids in concentrations ranging up to more than 1%. About three fourths
of the isolated alkaloid mixture is ( - )-hyoscyamine; the remainder is atropine. The latter compound
exists, at most, only in traces in fresh plant material.
• Atropine is formed by racemization during the extraction process. Small but varying amounts
of other bases are found in the root but not in the leaf. These include apoatropine, belladonnine,
cuscohygrine, and scopolamine.
• The yield of alkaloids averages as follows: roots, 0.6%; stems, 0.05%; leaves, 0.4%; unripe
berries, 0.19%; ripe berries, 0.21%; seeds, 0.33%.
• Belladonna leaf is commonly administered in the form of the tincture (30 mg alkaloids/100
ml) or the extract (1.25 g alkaloids/100 g). The usual dose is 0.6 to 1.0 ml of the tincture or 15 mg of
the extract, 3 or 4 times a day.
• Most of the alkaloids are derived from Egyptian henbane (Hyoscyamus muticus Linne).
Hyoscyamine
• is the tropine ester of (-)tropic acid and is asymmetric and accounts for the natural
occurrence of the optical isomer. When ( - )-hyoscyamine is extracted from the plants in which it
occurs, it usually is racemized during the process and thus converted into the ( ± )-compound, which
is atropine.
• readily hydrolyzed by boiling in dilute acids or alkalies to form these compounds
Hyoscyamine sulfate
• is the sulfate of an alkaloid usually obtained from species of Hyoscyamus Linne or other
genera of Solanaceae.
• It is extremely poisonous.
• occurs as white, odorless crystals or as a crystalline powder; it is deliquescent and is
affected by light.
Atropine
• occurs as colorless, needlelike crystals or as a white, crystalline powder
• it is optically inactive but usually contains some levorotatory hyoscyamine, the limit of which
produces an angular rotation not to exceed - 0.70°.
Atropine sulfate
• occurs as colorless crystals or as a white, crystalline powder.
• It is extremely poisonous.
• It effloresces in dry air, is slowly affected by light, and is an anticholinergic.
Scopolamine or hyoscine
• is an alkaloid that is particularly abundant in Datura fastuosa var. alba and in D. metel .
• It is an ester that, upon hydrolysis, yields tropic acid and scopoline, a base resembling
tropine.
• It occurs as an almost colorless, syrupy liquid from its chloroformic solution and as colorless
crystals from its ether solution. It is levorotatory.
• It is appliedas the free base in a transdermal system behind the ear at least 4 hours before the
antiemetic effect is required. The scopolamine is gradually released from an adhesive matrix of
mineral oil and polyisobutylene. A continuous controlled release of scopolamine flows from the
drug reservoir through a rate-controlling membrane to maintain a constant plasma level for 3
days.
Hyoscyamus or henbane
• is the dried leaf, with or without the stem and flowering or fruiting top, of Hyoscyamus
niger Linne (Fam. Solanaceae)
• contains not less than 0.04% of the alkaloids of hyoscyamus.
• Hyoscyamus is the ancient Greek and Latin name formed from 2 Greek words, meaning
hog and bean. The plant is poisonous to swine.
USE
1. Hyoscyamus is a parasympatholytic, but the crude drug is rarely employed in medicine today.
Egyptian henbane
Stramonium seed
• is the ripe seed of D. stramonium.
• The ripening capsules are gathered and dried until the seeds shake out. The seeds are
reniform, flattened, 3 to 4 mm in length, bluish black, and minutely reticulate.
• contains about 0.4% of alkaloids, principally hyoscyamine with a small proportion of
scopolamine and traces of atropine.
• Stramonium is generally regarded as a noxious weed and has frequently caused
poisoning in children when seeds were ingested. The chief toxic symptoms are those of atropine
poisoning: dilated pupils, impaired vision, dryness of the skin and secretions, extreme thirst,
hallucinations, and loss of consciousness.
Withania
• is the dried root of Withania somnifera Dunal (Fam. Solanaceae)
• Studies have shown that withania, which is closely related botanically to belladonna
and hyoscyamus, contains about a dozen biochemically heterogeneous alkaloids. Tropine and
pseudotropine are accompanied by hygrine (pyrrolidine derivative), isopelletierine (piperidine
derivative), cuscohygrine (2 pyrrolidine moieties), anaferine (2 piperidine moieties), and
anahygrine (1 pyrrolidine moiety and 1 piperidine moiety).
• The principle responsible for the sedative action of the drug has not yet been
determined
Duboisia
• consists of the dried leaves of Duboisia myoporoides R. Brown (Fam. Solanaceae)
• The drug contains ( - )-hyoscyamine, scopolamine, and a number of related alkaloids, in
addition to small amounts of nicotine and nornicotine.
• Duboisia currently is a chief source of atropine, the racemic mixture of the isomers of
hyoscyamine, which is formed during the extraction process.
• The leaves of D. leichardtii F. von Mueller, of Australia, also contain a relatively large
percentage of similar alkaloids.
• Cocaine was first isolated in 1860, but until 1884, coca was considered only as an inferior
substitute for tea. In that year, Koller discovered its local anesthetic properties.
Huanuco coca
• Contains 0.5 to 1% of ester alkaloids, derivatives of tropine and ecgonine, of which cocaine
constitutes the major part.
• Cuscohygrine is the principal nonester alkaloid in the leaf.
Truxillo coca
• has a somewhat lower content of ester alkaloids, but a much higher percentage (up to 75%)
of this quantity is cocaine.
• Coca leaves were highly valued by the natives long before the Spanish conquest; the shrub
was known as "The Divine Plant of the Incas." Monardes published an extensive article on the drug in
1569.
• The natives chew the leaf, either as such or mixed with lime and are thus able to travel great
distances without experiencing fatigue and without any but the most meager food rations.
Cocaine
• is an alkaloid obtained from the leaves of Erythroxylum coca and its varieties. As explained
subsequently, much of the alkaloid is actually prepared by semisynthesis from plant-derived
ecgonine.
• Cocaine is the methyl ester of benzoylecgonine. When hydrolyzed, it splits into ecgonine,
benzoic acid, and methyl alcohol. Cinnamylcocaine splits into ecgonine, methyl alcohol, and
cinnamic acid, whereas a- and (3-truxilline split into ecgonine, methyl alcohol, and a- and (3-trux-
illic acids. (The truxillic acids are isomeric dicinnamic acids.)
• Cocaine has multiple central and peripheral nervous system actions. Over most of its
effective dose range, it is a psychomotor stimulant with a strong abuse potential. The action
responsible for the rewarding property, and hence the abuse liability, is through a prolongation of
dopamine in the synapse by blocking the dopamine reuptake mechanism. When drug access is un-
limited, cocaine has the ability to dominate behavior, reducing other behaviors such as eatingand
sleeping. It has one of the highest reinforcing potentials of any drug as measured by breaking point
studies and is the drug which animals with unlimited access are most likely to select repeatedly in
preference to food and water, to the point of death.
Cocaine hydrochloride
• is the hydrochloride of the alkaloid cocaine. It occurs as colorless crystals or as a white,
crystalline powder.
USES
1. Cocaine hydrochloride is a local anesthetic. It is applied topically to mucous membrane as a 1 to
4% solution.
2. Cocaine hydrochloride is an ingredient in Bromptom's cocktail, which is widely used to control
severe pain associated with terminal cancer. Because of its CNS stimulant properties, cocaine
counteracts the narcotic-induced sedation and respiratory depression associated with the
narcotic analgesic ingredient (morphine or methadone) used in the cocktail. It also potentiates
the analgesic effect.
• Cocaine and cocaine hydrochloride, as agents of abuse, are generally inhaled or sniffed
and are rapidly absorbed across the pharyngeal mucosa, resulting in cerebral stimulation and
euphoria.
• In addition, they are injected intravenously and subcutaneously, and cocaine free-base
is smoked.
• Inhalation of the vapors of alkaloidal cocaine, known as "free-basing," has become a
popular practice because of the rapidity of onset and the intensity of the euphoric experience. The
reason for converting cocaine hydrochloride to the free amine is that the latter substance
volatilizes at about 98°C whereas the salt volatilizes at 195°C, a temperature at which some of the
cocaine is decomposed.
• Since the cocaine is absorbed by pulmonary capillaries and moves from the lungs to
the left side of the heart and then directly to the brain, the effects are perceptible in 7 to 10 sec-
onds. Repeated use results in psychic dependence and tolerance; therefore, cocaine is classified as
a Schedule II drug under the Controlled Substances Act.
QUINOLINE ALKALOIDS
• Alkaloids containing quinoline as their basic nucleus include those obtained from cinchona
(quinine, quinidine, cinchonine, and cinchonidine).
• Cinchona and its alkaloids are the only members of this group that are therapeutically important at
present. Cinchonine, which is isomeric with cinchonidine, is the parent alkaloid of the quinine series.
Quinine and its isomer, quinidine, represent 6-methoxycinchonine.
Biosynthesis of Quinoline Alkaloids
Quinoline Derivatives. Studies with labeled geraniol and tryptophan-2-'°C indicate that quinine
is metabolically derived from the monoterpenoid-tryptophan pathway that leads to the Corynanthe-type
indole alkaloids .The most distinctive feature of quinine biosynthesis appears to be cleavage of the
benzopynole ring of the tryptophan moiety and rearrangement to form the quinuclidine nucleus and then
the quinoline nucleus. Details of the biosynthetic processes are lacking, but a , presumed biogenetic origin
involving strictosidine and corynantheal as intermediates is illustrated in Figure 8-10. Both of these
compounds are precursors.
Cuprea bark
• is obtained from Remijia purdieana Triana and R. pedunculata Fluckiger (Fam. Rubiaceae)
• It has a copper-red color, is hard, compact, and heavy, and contains numerous transversely
elongated stone cells and 2 to 6% of alkaloids, of which one third may be quinine.
• Cuprea bark is a commercial source of quinidine.
Cinchona Alkaloids
Quinidine
• is a stereoisomer of quinine and is present in cinchona barks to the extent of 0.25 to 1.25%.
• It depresses myocardial excitability, conduction velocity, and, to a lesser extent,
contractility.
Quinidine sulfate
• It is the sulfate of an alkaloid obtained from various species of Cinchona and their hybrids
and from Remijia pedunculata , or prepared from quinine.
• It occurs as fine, needlelike, white crystals that frequently cohere in masses.
• It is odorless, has a bitter taste, and darkens when exposed to light.
• It is readily soluble in water, alcohol, methanol, and chloroform.
USE AND DOSE
1. Quinidine is used to treat various cardiac arrhythmias such as premature atrial, AV junctional, and
ventricular contractions; atrial and ventricular tachycardia; atrial flutter; and atrial fibrillation. When
administered orally, the peak serum levels are slightly lower with the, gluconate and
polygalacturonate salt than with the sulfate salt.
• The usual oral dose for all available salts is 10 to 20 mg/kg/day in 4 to 6 divided doses in order
to obtain the average therapeutic serum levels of 3 to 6 mg/ml. Toxic reactions occur at levels
above 8 μg/ml. The patient should be instructed to notify the physician if skin rash, fever,
unusual bleeding or bruising, ringing in the ears, or visual disturbance occurs.
Quinidine gluconate
• Occurs as a white powder that is odorless and has a bitter taste.
• It is available in sustained release tablets.
Quinidine polygalacturonate
• Affords controlled and more uniform absorption through the intestinal mucosa than does
quinidine sulfate.
• In addition, it produces a lower incidence of gastrointestinal irritation.
Quinine
• is the diastereoisomer of quinidine.
• It occurs as white, odorless, bulky, bitter crystals or as a crystalline powder. It darkens when
exposed to light and effloresces in dry air.
• It is freely soluble in alcohol, ether, and chloroform but slightly soluble in water.
Quinine sulfate
• is the sulfate of an alkaloid obtained from the bark of Cinchona species.
• It occurs as white, odorless, bitter, fine, needlelike crystals that are usually lusterless.
• It becomes brownish when exposed to light.
• It is not readily soluble in water, alcohol, chloroform, or ether
USE
1. The drug is an antimalarial and once was the only agent available to treat this disease, which afflicts
millions of people worldwide.
• Quinine's antimalarial action is believed to be the intercalation of the quinoline moiety
into the DNA of the Plasmodium parasite, thereby reducing the effectiveness of DNA to act as a
template. Intercalating agents such as quinine are rigid planar polycyclic molecules that insert
between the adjacent stacked base pairs of the double helix of DNA. This results in DNA that has
increased length, and because or a greater electrostatic interaction between the intercalated
molecule and the two DNA strands, there is an inhibition of the strand separation that is required
for replication and transcription of the genetic code. It suppresses but does not cure vivax
malaria and was once almost abandoned in this country in favor of chloroquine or other, newer,
synthetic antimalarials.
• Recently, it has regained considerable importance in the treatment of chloroquine-
resistant falciparum malaria in combination with pyrimethamine and sulfadiazine or tetracycline.
• The usual dose is 650 mg every 8 hours for 10 to 14 days. The patient should be
instructed to notify the physician if ringing in the ears or visual disturbance occurs.
2. Quinine has a skeletal muscle relaxant effect, increasing the refractory period by direct action on the
muscle fiber, decreasing the excitability of the motor end-plate by a curariform action, and affecting
the distribution of calcium within the muscle fiber.
• Therefore, it is used for the prevention and treatment of nocturnal recumbency leg cramps in
a dose of 260 to 300 mg at bedtime.
• Daily doses of 0.2 to 0.4 g as a tonic or as an analgesic in the treatment of colds were used
extensively in the past
ISOQUINOLINE ALKALOIDS
• Although the more important opium alkaloids (morphine, codeine, thebaine) exhibit a
phenanthrene nucleus, the majority of its alkaloids have the isoquinoline ring structure.
• These phenanthrene alkaloids are derived biosynthetically from benzyli-soquinoline
intermediates. For this reason, opium is included in this group. Sanguinaria, another member of the
Papaveraceae, also contains isoquinoline alkaloids.
• The important drugs and their alkaloids in this group are ipecac, emetine, hydrastis,
hydrastine, sanguinaria, curare, tubocurarine, berberine, and opium and its alkaloids.
Ipecac
• consists of the dried rhizome and roots of Cephaelis ipecacuanha (Brotero) A. Richard,
known in commerce as Rio or Brazilian ipecac, or of Cephaelis acuminata Karsten, known in
commerce as Cartagena, Nicaragua, or Panama ipecac (Fam. Rubiaceae).
• Ipecac yields not less than 2% of the ether-soluble alkaloids of ipecac.
• Cephaelis is from 2 Greek words, meaning head and to collect or roll up, and refers to the
inflorescence;
• ipecacuanha is Portuguese from the Brazilian Indian ipekaaguene, meaning a, creeping
plant that causes vomiting;
• acuminata refers to the acute apex of the leaf.
• The drug was first mentioned by a Jesuit friar in 1601. It was introduced into Europe by Le
Gras in 1672 and by 1690 was well-known in medicine.
• Ipecac contains 5 alkaloids (2 to 2.5%).
• The 3 principal alkaloids are emetine, cephaeline, and psychotrine, contained chiefly in the
bark which makes up about 90% of the drug. About 40% of starch is present.
USES AND DOSE
1. Ipecac, in the form of syrup, is used in the treatment of drug overdose and in certain poisonings.
2. It produces emesis through a local irritant effect on the gastrointestinal mucosa and a central
medullary effect by stimulation of the chemoreceptor trigger zone.
• The usual dose in adults and children older than one year of age is 15 ml, followed by
one to 2 glasses of water and may be repeated once in 20 minutes if emesis does not occur.
The syrup should be recovered by gastric lavage if emesis does not occur after the second
dose.
• Ipecac syrup should not be confused with ipecac fluidextract, which is 14 times stronger.
Ipecac mixed with opium (as Dover's powder) acts as a diaphoretic. Ipecac syrup is included in
poison antidote kits because of its emetic properties
Emetine or methylcephaeline
• Is an alkaloid obtained from ipecac or prepared synthetically by methylation of cephaeline.
• It was discovered by Pelletier and Magendie in 1817.
Emetine hydrochloride
• is a hydrated hydrochloride of emetine.
• It occurs as a white, odorless, crystalline powder that becomes yellowish when exposed to
light.
• It is freely soluble in water and alcohol.
USES AND DOSE
1. Emetine hydrochloride is an antiamebic and acts primarily in the intestinal wall and the liver.
• It inhibits polypeptide chain elongation, thereby blocking protein synthesis.
• The usual dose is, intramuscularly or subcutaneously, 1 mg per kg of body weight, but
not exceeding 65 mg daily, for not more than 5 days.
• The drug is not administered orally because it produces nausea and vomiting.
2. Emetine hydrochloride has been used extensively as an antiprotozoal agent, particularly in the treat-
ment of amebic dysentery, pyorrhea alveolaris, and other amebic diseases.
3. It possesses expectorant and emetic properties.
Hydrastis or goldenseal
• consists of the dried rhizome and roots of Hydrastis cana densis Linne (Fam.
Ranunculaceae).
• Hydrastis is Greek and means to accomplish or act with water; the specific name refers to
the habitat.
• The plant is a perennial herb with a short horizontal rhizome that bears numerous long,
slender roots: Internally, the rhizome and roots show a golden yellow color.
• Hydrastis was known to the Cherokee Indians, who used it as a dye and an internal remedy.
These Indians introduced its use to the early American settlers.
Hydrastine
• is readily soluble in chloroform, alcohol, and ether but almost insoluble in water. It
crystallizes in prisms, melting at 131 to 132° C.
Hydrastine hydrochloride
• occurs as a white or creamy white powder that is odorless, bitter, and hydroscopic.
Berberine
• is readily soluble in water but almost insoluble in ether.
• The salts of berberine form bright yellow crystals.
Sanguinaria or bloodroot
• is the dried rhizome of Sanguinaria canadensis Linne (Fam. Papaveraceae).
• The generic name is from sanguinarius, meaning bloody, and refers to the color of the juice;
• canadensis refers to the plant habitat in Canada.
• Bloodroot was used by the Indians to stain their faces and was also used as an acrid emetic.
• Its use in homemade cough remedies seems to have been adopted by the early settlers.
• Sanguinaria contains alkaloids of the protopine series, including sanguinarine (about 1%),
chelerythrine, protopine, and, allocryptopine. These alkaloids are colorless but tend to form colored
salts.
• Sanguinarine yields reddish salts with nitric or sulfuric acids; yellowish salts are formed with
chelerythrine.
• All alkaloids of sanguinaria are found in other members of the Papaveraceae and, like
berberine and hydrastine, are isoquinoline derivatives. Species of the families Ranunculaceae,
Berberidaceae, Menispermaceae, and Papaveraceae contain alkaloids of this type.
• Sanguinaria of good quality contains not more than 5% of the roots of the plant. Shriveled
rhizomes that are gray and free from starch should be rejected.
USES AND DOSE
1. Sanguinaria has stimulating expectorant and emetic properties.
• The usual dose is 125 mg.
Curare or South American arrow poison
• is a crude dried extract from the bark and stems of Strychnos castelnaei Weddell, S. toxifera
Bentham, S. crevauxii G. Planchon (Fam.Loganiaceae) and from Chondodendron tomentosum Ruiz
et Pavon (Fam. Menispermaceae).
• The term "curare" is derived from woorari or urari, Indian words for poison. Curare varies in
composition among the Indian tribes. Each tribe modifies the formula in accordance with tribal
custom.
• The young bark is scraped off the plants, mixed with other substances, and boiled in water and
strained or extracted by crude percolation with water. It is evaporated to a paste over a fire or in
the sun.
• The earliest available preparations were named according to the containers in which the drug was
packaged: calabash (gourd), tube (bamboo), or pot (clay pot) curare.
• It is a brownish or black, shiny, resinoid mass with a bitter taste.
• It is readily soluble in cold water and in dilute alcohol.
• ( + )-Tubocurarine, the most important constituent, is a quaternary compound that contains a bis-
benzylisoquinoline structure. The crude extract exhibits a paralyzing effect on voluntary muscle
(curariform effect) by blocking nerve impulses to skeletal muscles at the myoneural junction.
• It also produces a toxic action on blood vessels as well as a histamine like effect.
• Curare was brought to England by Sir Walter Raleigh in 1595, but it has only recently come into
prominence in medical circles. Claude Bernard, Kolliker, Langley, and other investigators studied
the effect of curare on mechanisms of neuromuscular activity; however, its heterogeneous na-
ture, its variability, and its uncertain supply limited its use in therapeutics.
Indian opium
• is produced in the states of Madhya Pradesh, Rajasthan, and Uttar Pradesh.
• At present it is the only licit source of opium.
• The 5-kg cakes are shipped in polyethylene bags.
• Indian opium yields about 10% of anhydrous morphine.
More than 30 different alkaloids have been obtained from opium and its extracts, some of which are
alteration products of the alkaloids occurring naturally in drug. The most important of these is
• morphine- which exist to the extent of (4 to 21%
• Codeine- (.8 – 25%)
• Noscapine (formerly narcotine)- (4-8%)
• Papaverine (0.5- 2.5%)
• Thebaine (0.5- 2%)
• Other alkaloids include narceine, protopeine, laudanine, codamine, cryptopine, lanthopine, and
meconidine
• Opium also contains from 3-5% of meconic acid, which exist free or in combination with
morphine, codeine, and other alkaloids. It forms rhombic prisms that are soluble in water and
alcohol and give a red color in solutions of ferric chloride. The color is not altered when HCL is
added.
• Opium in its normal, air dried condition yields not less than 9.5% of anhydrous morphine
USES of Opium
1. A pharmaceutic necessity for the production of powdered opium
2. It acts chiefly on the CNS; its action first stimulates and then depresses nerve response
3. It serves as an analgesic, a hypnotic and a narcotic
4. It checks excessive peristalsis and contracts the pupil of the eye
ALKALOIDS OF OPIUM
MORPHINE
• Most important of the opium alkaloids
• Morphine and related alkaloids are morphinan isoquinoline derivatives.
• The molecule contains a phenolic and alcoholic hydroxyl group
• The alkaloids and its salts occur as white silky crystals, sometimes in cubic masses or as
fine crystalline powder.
• It is stable in air, odorless, and bitter-tasting
• A prototype of opiate analgesic drugs which acts at several sites in the CNS to produce
analgesia
• It has agonist activity at mu (µ)and kappa(K) opiate receptor subtypes
• Analgesia at the supraspinal level as well as euphoria, respiratory depression, and physical
dependence results from agonist activity at µ receptor.
• Agonist activity at the kappa receptor is responsible for analgesia at supraspinal level,
miosis, and sedation
• Classed as narcotic analgesics, they are strongly hypnotic and narcotic
• Their use tends to induce nausea, vomiting, constipation and habit formation.
• Centrally acting analgesics, in most cases have certain structural features in common.
They are the ff:
• A central carbon atom with no hydrogen substitution ( quaternary)
1. a phenyl group or isostere attached to this carbon atom
2. a tertiary nitrogen atom
3. a two carbon bridge separating the tertiary and the central carbon atom
• Morphine and the related opium alkaloids that have analgesic activity possess
these structural features. In the case of morphine, the central carbon atom is C-13; the phenyl ring
attached to C-13 is composed of carbon atoms 1 to 4 and 11 to 12: and the tertiary nitrogen atom
is linked via a two-carbon bridge (C-15, C-16) to the central carbon atom.
CODEINE
• Is the most widely used opium alkaloid.
• It may be either obtained from opium (0.2 to 0.7%) or prepared from morphine by methylation
or from thebaine by appropriate reduction and demethylation.
• methyl morphine
• Codeine and its salts occur as fine needles or as white crystalline powders that effloresce in
air.
• Codeine and its salts are narcotic analgesics and antitussive; they are used as sedatives,
especially in allaying coughs.
• Although its action is similar to that of morphine, codeine is considerably less toxic and
involves much less dander of habit formation.
DIACETYLMORPHINE OR HEROIN
• It is formed by the acetylation of morphine; the hydrogen atoms of both the phenolic
and alcoholic hydroxyl groups are replaced by acetyl groups.
• Heroin’s action is similar but more pronounced than that of morphine.
• Because of its potency and the danger of habit formation, its manufacture in the
United States is forbidden by law, and its use in medicine has been discontinued.
PAPAVERINE
• Occurs naturally in opium to the extent of about 1%, but it may also be produced synthetically.
Papaverine hydrochloride
• Occurs as white crystals or as a white crystalline powder. It is odorless but has a slightly bitter
taste.
• It is a smooth muscle relaxant.
• It is used principally for the relief of cerebral and peripheral ischemia complicated by
arrhythmias
INDOLE ALKALOIDS
RAUWOLFIA SRPENTINA
• Is the dried root of Rauwolfia serpentina (Fam. Apocynaceae)
• It contains not less than 0.155 of he reserpine- rescinnamine group of alkaloids, calculated
as reserpine
• Three series of alkaloids have been reported
(1) weakly basic indole alkaloids
The principal alkaloids are reserine, rescinnamine, and deserpidine are tertiary indole alkaloids
that have a carbocylic structure in ring E and are of the corynane type
Other tertiary indole alkaloids exhibit a heterocyclic structure in ring E: -yohimbine (identical with
ajmalicine, tetrahydroserpentine, and raubasine) and reserpiline
(2) Indoline alkaloids of intermediate basicity
Ajmaline, isoajmaline, rauwolfinine- these bases do not have tranquilizing action
(3) Strong anhydronium bases
Serpentine, serpentinine and alstoine
• Exert their hypotensive effects by depletion of catecholamine and serotonin stores in many
organs, including the brain and adrenal medulla, and by the reduction of uptake of catecholamines
by adrenergic neurons.
• Their sedative and tranquilizing properties are thought to be related to depletion of
amines in the CNS
Reserpine
• Is a white or pale buff to slightly yellow, odorless, crystalline powder that darkens slowly when
exposed to light and rapidly when in solution.
• An antihypertensive and antipsychotic agent
• Obtained in commercial quantities from four different species of Rauwolfia; R. serentina , R.
micrantha , R. tetraphylla and R. vomitoria.
Rescinnamine
• Is an alkaloid that occurs in several species of Rauwolfia.
• Its appearance, properties, and solubility are somewhat similar to those of reserpine
• Chemically, it is the methyl reserpate ester of 3, 4, 5- trimethoxycinnamic acid
• It is used to treat mild essential hypertension
Deserpidine
Canescine, recanescine
Alkaloid obtained from the root of Rauwolfia canescens
Chemically, it is 11- desmethoxyreserpine
• Same uses as Rauwolfia serpentina and reserpine and is claimed to have fewer side effects
YOHIMBINE
• An indole alkaloid of corynane type obtained from the bark of West African tree Pausinystalia
yohimbe (Fam. Rubiaceae)
• The bark contains about 6% of a mixture of alkaloids, the principal one f which is yohimbine
• Treated impotence in patients with vascular or diabetic problems
• Its peripheral autonomic nervous system effect is to increase cholinergic and decrease
adrenergic activity
• In male sexual performance, erection is linked to increased cholinergic activity which results in
increased penile blood flow, decreased penile blood outflow, or both, causing erectile stimulation.
CATHARANTHUS OR VINCA
• It is the dried whole plant of Catharanthus roseus (Fam. Apocynaceae), formerly designated
Vinca rosea Linne’
• Botanically it is closely related to Vinca minor Linne’, the common periwinkle
• During he course of a modern scientific investigation prompted by the folklore reputation of
this plant as an oral hypoglycemic agent, the ability of certain fractions to produce
granulocytopenia and bone marrow depression I rats was observed by the Canadian group of
Noble, Beer and Cutts. Continued study led to the isolation of an alkaloid, vinblastine, which
produced severe leukopenia in rats
• Four bisindole compounds vinblastine, vinleurosine, vinrosidine, and vincristine, possess
demonstrable oncolytic activity
• Nearly 500 kg of catharanthus are utilized to produced 1 g of vincristine
CATHARANTUS ALKALOIDS
• More than 90 different alkaloids have been isolated from catharanthus
• They generally indole and dihydroindole derivatives, some of which occur in other members of
the Apocynaceae. This includes ajmalicine, tetrahydroalstonine, serpentine and lochnerine.
• The alkaloids with antineoplastic activity belong to a new class of bisindole derivatives
VINDESINE
• Is a semisynthetic derivative of vinbastine where the cetyl group at position 4 of the vindoline
has been removed.
• Even though it is derived from vinblastine, it has antineoplastic activity more closely
resembling that of vincristine.
• Clinical trials indicate that it has good activity in difficult-to-treat or refractory cancer types,
and there appears to be a lack of cross resistance with vincristine and vinblastine
VINORELBINE TARTRATE
• Is a semi synthetic derivative of vinblastine which is prepared by removing the ethyl side chain
a position 4’ of the catharanthine moiety, and the 4’- hydroxyl is removed as water to introduce a
unsaturation at 3’4’.
• The derivative is a 3’-noranhydrovinblastine.
• It is indicated as a single agent or in combination with cisplatin for the first line treatment of
non-small cell lung cancer
NUX VOMICA
• Is a dried ripe seed of Strychnos nux vomica Linne’ (Fam. Loganiaceae)
• Strychnos is the Greek name for a number of poisonous plants
• Nux vomica is from two Latin words and means a nut that causes vomiting
• Contains alkaloids, 1.5 to 5%, consisting chiefly of strychnine and brucine , the former
comprising from one third to one half of the total amount
• Nux vomica and the seeds of the closely related Strychnos ignatii (ignatia or St. Ignatius
bean)serve as a commercial source of strychnine and brucine. The former alkaloid is commonly
marketed as strychnine sulfate or strychnine phosphate.
PHYSOSTIGMINE OR ESERINE
• An alkaloid usually obtained from the dried, ripe seed of P. venenosum
• It occurs as a white, odorless, microcrystalline powder that may acquire a red tint when
exposed to heat, light, air, or contact with traces of metal. This color change may indicate
hydrolysis to eseroline and oxidation to rubreserpine. These degradation products are irritating to
the eye and lack substantial pharmacologic activity.
• Should be preserved in tight, light-resistant containers in quantities not exceeding 1 g.
• A reversible inhibitor of the cholinesterases and thus enhances the effects of endogenous
acetylcholine.
• In the eye, increase in cholinergic activity leads to miosis, contraction of the ciliary muscle,
and a decrease in intraocular pressure caused by an increases out-flow of the aqueous humor.
• USE: Employed in ophthalmology to treat glaucoma.
ERGOT ALKALOIDS
ERGONOVINE MALEATE OR ERGOMETRINE MALEATE
• Occurs as a white or faintly yellow, odorless, microcrystalline powder.
• It is affected by light and is readily soluble in water but less soluble in alcohol
• The accepted chemical name of isolysergic acid isomer of ergonovine is ergometrinine
• The oxytocic effect of the drug, either rally, SC, or IM, is sometimes noted within 5 minutes
after giving the dose, and its effect is more marked than that of either ergotoxine or ergotamine.
However, the vasoconstrictor action is much less marked.
• An oxytocic and produces much faster stimulation of the uterine muscles than do other ergot
alkaloids. The gravid uterus is very sensitive to this effect, and small doses of alkaloid can be given
immediately postpartum to increase the frequency and amplitude of uterine contractions as well as
to increase the basal tone of the uterine smooth muscle, resulting in a decrease in blood loss from
the postpartum uterus.
METHYLERGONOVINE MALEATE
• It is a semi synthetic homolog of ergonovine prepared from lysergic acid and 2-aminobutnol
• It occurs as a white to pinkish tan microcrystalline powder
• An oxytocic reputed to be slightly more active and longer acting than ergonovine
ERGOTAMINE TARTRATE
• Occurs as a colorless crystals or as white , crystalline powder, sparingly soluble in water or in
alcohol
• Possess oxytocic activity, but it is not employed for that effect
• It is used to prevent or abort vascular headaches, including migraine and cluster headaches.
MOA: Direct vasoconstriction of the dilated carotid artery bed with a concomitant decrease in the
amplitude of pulsations
It may inhibit receptor uptake of norepinephrine at sympathetic nerve endings, increasing the
vasoconstrictive action, and the drug is also an antagonist of serotonin activity
• It is used with caffeine for the treatment of migraine headache. Both act as cerebral
vasoconstrictors; caffeine is believed to enhance the action of ergotamine
DIHYDROERGOTAMINE MESYLATE
• A salt of a semi synthetic alkaloid prepared from ergotamine by hydrogenation of the ∆ 9 double bond
in the lysergic acid nucleus
• Employed in the treatment of migraine because it is more effective and better tolerated than the
parent alkaloid
ERGOTOXINE
• Formerly employed as reference standard in the form of ergotoxine ethanesulfonate, which
was discontinued because it was a variable mixture of three closely related alkaloids, ergocristne,
ergokrytine and ergocornine. A mixture of equal parts of these component alkaloids is
hydrogenated to eliminate the ∆ 9 double bond of the lysergic acid nucleus and to yield an
equivalent mixture of dihydroergocristine, dihydroergokryptine, and dihydroergocrnine.
• ERGOLOID MESYLATES- the methanesulfonates of the three mixtures, marketed for the relief of
symptoms of idiopathic decline in mental capacity in geriatric individuals
- They produce vasorelaxation, increased cerebral blood flow, lowering of systemic blood pressure,
and bradycardia.
METHYSERGIDE MALEATE
• The salt of methylergonovine that has an additional methyl group attached to the nitrogen at
position 1 of the lysergic acid nucleus.
• It is prepared by semisynthesis from lysergic acid
• A serotonin antagonist employed in the prophylaxis of vascular headache.
• The patient should be advised to take medicine with meals and to notify the physician if cold,
numb, or painful hands, leg cramps, abdominal or chest pain, or change in skin color occurs
Aside from Claviceps species and the members of Convolvulaceae, ergot alkaloids have been reported
only in few other fungi
Aspergillus fumigates Balansia cyperi
B. obtecta Penicillium chermesinum
P. gorlenkoanum P. kapuscinski
P. roquefortii Rhizopus arrhizus
Sphacelia typhina
IMIDAZOLE ALKALOIDS
PILOCARPINE
• Pilcarpus or jaborandi consists of the leaflets of Pilocarpus jaborandi Holmes(Pernambuco
jaborandi), or of P. pinnatofolius(Paraguay jaborandi) (Fam. Rutaceae)
• The lactone of pilocarpic acid
• An acid with glyoxaline nucleus
• It is an oily syrupy liquid, though its salts crystallize easily
• It may obtained by treating the powdered leaves with sodium carbonate, extracting with
benzene, and then shaking the benzene extract with dilute HCl or HNO 3. The aqueous solution is
then made alkaline and shaken with chloroform; the chloroform solution is then shaken with acid,
and the alkaloidal salt is allowed to crystallize
• Directly stimulates the muscarinic receptors in the eye, causing constriction of the pupil and
contraction of the ciliary muscle
• In narrow angle glaucoma, miosis opens the anterior chamber angle to improve the outflow of
aqueous humor
• In chronic open-angle glaucoma, the increase in outflow is independent of the miotic effect.
Contraction of the ciliary muscle enhances the outflow of aqueous humor via indirect effects on the
trabecular system
PILOCARPINE HCl
• Obtained from the dried leaf of Pilocarpus jaborandi or of P. microphyllus
• It is hygroscopic
PILOCARPINE NITRATE
• It is stable in air but is affected by light.
• Occurs as colorless, translucent, odorless, faintly bitter crystals, shiny, white crystals
• Applied topically as 0.25 to 10% solution of pilocarpine HCl or as a 0.5 to 6% solution of
pilocarpine nitrate to the conjunctiva. The patient should advise to wash hands immediately after
application.
• Also available in an ocular therapeutic system that provides continuous release over one week
following placement in the conjunctival cul-de-sac.
STEROIDAL ALKALOIDS
• Derived biosynthetically from six isoprene units and could be classified as triterpenoids or
steroids; however they also contain nitrogen giving them basic properties. The nitrogen may be
part of a ring system, usually incorporated at a late stage in biosynthesis, or it may be as an N-
methyl substituted amino group.
• Found in the plant families Apocynaceae, Buxaceae, Liliaceae, and Solanaceae
GROUP I – consisting of esters of the steroidal bases (alkamines) with organic acids, includes:
Cevadine Neoprotoveratrine
Germidine Protovratrine
Germitrine Veratridine
Neogermitrine
GROUP II – are glucosides of the alkamines includes:
pseudojervine
veratrosine
GROUP III – alkamines themselves
Germine rubijervine
Jervine veratramine
ALKALOIDAL AMINES
• The alkaloids in this group do not contain heterocyclic nitrogen atoms.
• Many are simple derivatives of phenyllethylamine and, such, are derived from the common
amino acids, phenylalanine or tyrosine.
• Some of the alkaloids in this category whose biosynthesis has been studied utilizing
labeled precursors include mescaline in the peyote cactus (Lophophora williamsii), ephedrine in
Ephedra distachya , cathinone in the khat plant (Catha edulis), and colchicine in the autumn crocus
(Colchicum autumnale).
In the biosynthesis of colchicines, ring A and five carbon atoms of the seven-membered ring B of
colchicines derive from phenylalanine. Tyrosine cannot replace phenylalanine as a precursor for
this part of the molecule. Radioactivity from tyrosine-3-14C is incorporated into the C-12 position
of the tropolone ring C. Many of the details of the biosynthetic pathway are unknown; a
phenethylisoquinoline intermediate is suspected, and androcymbine also occurs in Colchicum.
Labeled acetate is readily incorporated into the acetyl group of the molecule, presumably during
terminal phase of biosynthesis.
Other alkaloidal amines are tryptamine derivatives and, as such, are biosynthesized from
tryptophan. Examples include gramine in Hordeum vulgare, psilocybin in the Mexican
hallucinogenic mushroom, Psilocybe semperviva, and serotonin and bufotenine in number of plant
and animal species.
The drugs and their alkaloids classified as alkaloidal amines are ephedrine, colchicum seed,
colchicum corm, colchicines, khat, and peyote.
Ephedra or ma huang
• Is the entire plant or the over ground portion of Ephedra sinica Stapf(Fam. Gnetaceae). In
Chinese characters, “ma” means astringent and “huang” means yellow, probably referring to the
taste and color of the drug.
• It has been used as a medicine in China for more than 5000 years. Its used in modern
medicine began in 1923 with the discovery of the valuable properties of ephedrine.
• The plant is a low, dioecious, practically leafless shrub that grows 60 to 90cm high. The
stem is green, erect, small ribbed, and channeled. It is 1.5mm in diameter and usually terminates
in a sharp point. At the nodes, which are 4 to 6 m apart, the leaves appear as whitish, triangular,
scarious sheaths. Small blossom appear in the summer.
Ephedrine or (-)-erythro-α-[1-(methylamino)ethyl]benzyl alcohol
Ephedrine hydrochloride
• Also occurs s fine, white, odorless crystals or as a powder and is affected by light.
• It has the same pharmacologic properties as ephedrine and is used as a sympathomimetic.
Both of these salts are readily soluble in water and in hot alcohol but not in ether.
Allied Plants.
• In addition to Ephedra sinica (the source of ma huang) and E. equisetina Bunge (the chief
source of the extracted alkaloid), E. distachya Linne also yields ephedrine.
COLCHICINE
• is the dried, ripe see of colchicum autumnale Linne (Fam. Liliaceae). Colchicum corm is
the dried corm of the same species.
• Dioscorides mentions Colchicum. The arabs recommended the used of the corm for gout in
medieval times, but he drug was abandoned because of its toxicity. It again came into used in
Europe about the middle of the 17th century.
• Colchicum contains the alkaloid colchicines, up to 0.8 percent in the seed and 0.6 percent
in the corm.
Colchicine
PURINE BASES
• Purines are derivatives of a heterocyclic nucleus consisting of the 6-membered pyrimidine ring
fused to the 5-membered imidazole ring.
• The pharmaceutically important bases of this group are all methylated derivatives of 2,6-
dioxypurine (xanthine)
Caffeine – 1, 3, 7-trimethylxanthine
Theophylline – 1, 3-dimethylxanthine
Theobromine – 3, 7- dimethylxanthine
• The methylxanthines competitively inhibit phosphodiesterase, which results to increase of
cyclic adenosine monophosphate with a subsequent release of endogenous epinephrine. This
results to:
- direct relaxation of the smooth muscles of the bronchi and pulmonary blood vessels
- a stimulation of the CNS
- an inuction of diuresis
- increase in gastric acid secretion
- Inhibition of uterine contractions and a weak positivechronotropic and inotropic effect on
the heart
Caffeine containing drugs
KOLA, COLA OR KLANUTS
• Dried cotyledon of Cola nitida or of other species of Cola (Fam. Sterculiaceae)
• It yields not less than 1% of anhydrous caffeine
• It is used in the manufacture of nonalcoholic beverages
• The fresh nut is chewed as a stimulant, similar to the betel nut
• Contain caffeine, up to 3.5%, and Theobromine, less that 1%.
• In the fresh nuts, these purine derivatives are bound to the tannin kolacatechin
• During the drying process, the complex is split, yielding free caffeine and Theobromine and
converting the colorless kolacatechin to the red- brown cola red
• Possesses the central stimulating action of caffeine
• It is an ingredient in several carbonated beverages
CAFFEINE
• Synthesized from the same precursors in Coffea arabica as are the purine bases in all other
biologic systems that have been investigated
• Carbon atoms 2 and 8 derive either from formate or from any compound that can give rise to
an active 1-carbon fragment (serine, glycine, formaldehyde, and methanol). These same
compounds, as well as methionine, are active precursors of the N- methyl groups of the molecule.
Carbon atom 6 is derived from the carbon dioxide, and carbons 4 and 5, together with the nitrogen
at 7, are derived from glycine. The nitrogen atom at position 1 derives from aspartic acid, but
those in positions 3 and 9 originate from the amide nitrogen of glutamine.
• 1,3,7-trimethylxanthine occurs in coffee, tea, cacao, guarana, kola and mate
• Although it is prepared synthetically, it is usually prepared from tea, tea dust, or tea
sweepings, or recovered from coffee roasters
• Caffeine is anhydrous or contains one molecule of water of hydration
• Occurs as white powder or as white, glistening needles matted together in fleecy masses
• It has bitter taste
• It may be sublimed without decomposition when heated
• The solubility in water is markedly increase by the presence of citric acid, benzoates,
salicylates, and bromides; medicinal compound of this class are citrated caffeine and caffeine and
sodium benzoate. The latter is most suitable for IM injection as an analeptic in the treatment of
poisoning, as a stimulant in acute circulatory failure and as diuretic
• Caffeine and its related compounds are CNS stimulants
THEOPHYLLINE
THEA OR TEA
• Consist of the prepared leaves and leaf buds of Camellia sinensis (Fam. Theaceae)
GREEN TEA
• Prepared in china and Japan by rapidly drying the freshly picked leaves in copper pans over a
mild artificial heat. The leaves are often rolled in the palm of the hand as they dry.
BLACK TEA
• Prepared in Sri Lanka and India by heaping the fresh leaves until fermentation has begun.
They are then rapidly dried artificially with heat.
• Occurs as more or less crumpled, bright green or blackish green, mass.
• Its odor is agreeable and aromatic. Its taste is pleasantly astringent and bitter.
• Contains 1 to 45 of caffeine (theine) and small amounts of adenine, Theobromine, Theophylline
and xanthine; about 15% of gallotannic acid and about 0.75% of a yellow volatile oil that is solid at
ordinary temperatures and has a strongly aromatic odor and taste.
• The stimulating action of tea is essentially that of the contained caffeine; its astringent
properties are owing the tannin content. Tea leaf waste and tea dust represent important sources
for the extraction of caffeine
THEOPHYLLINE OR 1, 3- DIMETHYLXANTHINE
• Isomeric with thebromine and was first isolated from tea in 1885
• Prepared synthetically from caffeine or by other means
• Occurs as a white, odorless, bitter crystalline powder that is soluble in about 120 parts of
water. It is rendered more soluble when combined with basic compounds
• Utilized principally as smooth muscle relaxants for the symptomatic relief or prevention of
bronchial asthma and for the treatment of reversible bronchospasm associated with chronic
bronchitis and emphysema. It also possess diuretic properties
THEOBROMINE OR 3, 7- DIMETHYLXANTHINE
• Compound prepared from the dried, ripe seed of Theobroma cacao (Fam. Sterculiaceae) or is
made synthetically
• Occurs as a white crystalline powder with a bitter taste and sublimes at about 260C
• The base is slightly soluble in cold water or in alcohol but is readily soluble when mixed with
salts that form basic solutions, such as calcium salicylate, sodium acetate, or sodium salicylate
• A diuretic and a smooth muscle relaxant
• It has little stimulant action on the CNS