Page 1
ALKALOIDAL AMINES
Ms. M.S.Divya Sree,
Assistant Professor,
Department of Pharmacognosy.
Page 2
Ephedra
Synonym: Ma-Huang
Biological Source: It consists of the dried young stems
of Ephedra gerardiana & Ephedra nebrodensis
belonging to family Gnetaceae.
Geographical source: China, Pakistan, north-west parts
of India, Australia, Kenya, Spain & Yugoslavia.
Page 3
Page 4
Cultivation, Collection &
Preparation
 Propagation - Seeds or layers or divisions of the root stock.
 The plants are collected after attaining the age of 4 yrs for
the extraction of alkaloid. During this period, proper
irrigation & weeding are necessary.
 The alkaloidal content of the drug varies from season to
season.
 It is found to be maximum in autumn, when plants & twigs
are dark in colour.
 Twigs are dried in sun or artificially.
Page 5
Macroscopy
 Colour – grey to greenish
 Odour – characteristic
 Taste - bitter
 Thin stems - woody, cylindrical.
 It shows internodes at a distance of about 3 - 3.5 cm.
 It bears scaly leaves.
Page 6
Microscopy
 Unicellular epidermis made up of quandrangular cells with
thick walled cuticle.
 Sunken stomata & papillae on the ridges.
 Cortex
 Non lignified fibres.
 Lignified pericyclic fibres.
 Calcium oxalate crystals
 Parenchymatous dark brown coloured pith.
Page 7
Chemical Constituents
 Contains amino alkaloids - Ephedrine, nor-
ephedrine, n-methyl ephedrine, pseudoephedrine, etc.
 Ephedrine (C10H15NO) is 1-phenyl-1-hydroxy-2-
methyl aminopropane, soluble in water, alcohol,
organic solvents and oils.
Page 8
Chemical test
o Ephedrine + water + HCl + CuSO4 and NaOH, the
solution gives violet color and when shaken with
solvent ether the organic layer shows purple and
aqueous layer shows blue color.
Page 9
Uses
Sympathomimetic effects.
Bronchodilator in Asthma, colds, flu and Hay fever
medications
Allopathic: Sinumed (dries a runny nose)
Used as an anti-inflammatory.
Page 10
Weight loss
(increases metabolism, decreases appetite – CNS
stimulant – acts on adrenergic receptors)
Also used to correct low B.P. conditions.
Page 11
COLCHICUM
Synonyms: Meadow saffron seeds, Autumn crocus.
Biological source: Dried ripe seeds of Colchicum
luteum Baker and Colchicum autumnale Linn.
Family: Liliaceae.
 Colchicum corm is also used medicinally.
Page 12
Geographical Source
• Various parts of Europe like
– England
– Holland
– Czechoslovakia
– Poland
– Yugoslavia
• Also cultivated in India.
Page 13
Page 14
Cultivation and collection
 Seed propagation
 Altitude 1000 – 3000m
 Seedlings – transplanted to open field at a distance of
1 m.
 Plants bear capsular fruits after 1 year.
Page 15
 Fruits – collected before dehiscence.
 Dark seeds are separated, processed and graded.
 Corms – isolated, adhering scales and coats are
removed.
 Corms – sliced transversely and dried below 65°C
Page 16
Macroscopy
Colchicum seeds
o Reddish brown testa
o Acrid taste
o No odor
o Very hard seeds
o 2 – 3 mm diameter
o Ovate in shape
Colchicum corms
o Yellowish brown
o Bitter and acrid taste
o No odor
o Slices 2 – 5 mm thickness
o Sub-reniform or ovate in outline
o Short fracture
o Cut surface – white and starchy,
showing grayish points
Page 17
Microscopy
Colchicum seeds
 Parenchyma
 Endosperm
 Aleurone grains
 Fixed oil
Colchicum corms
 Epidermis
 Parenchyma
 Vascular tissues
 Starch grains
Page 18
Chemical Constituents
 Chemical Constituents: 0.2 - 1% of amino alkaloids.
 Colchicine is the main constituent.
 Seeds contain upto 0.8% of colchicine and in corms
upto 0.6%, also contains demecolcine.
 Both contain tropolane or cycloheptatrienol-one ring
structure.
Page 19
Colchicine
 Amorphous, yellow - white alkaloid (darkens on
exposure to light).
 Gives a strong yellow coloration with strong mineral
acids.
 Dissolves readily in water, alcohol and chloroform,
but only slightly in ether or petroleum spirit.
Page 20
Chemical test
o Sample + 70% sulphuric acid = yellow color.
o Alcoholic solution of sample + FeCl3 gives
red color.
Page 21
Uses
Antitumor activity.
Relieve gout (used with caution – professional
supervision) and rheumatism.
Also used in biological experiments to produce
polyploidy (multiplication of the chromosomes in a
cell nucleus), hence used in horticulture and
cultivation of medicinal plants.

Alkaloidal amines ephedra, colchicum Pharmacognostic study

  • 1.
    Page 1 ALKALOIDAL AMINES Ms.M.S.Divya Sree, Assistant Professor, Department of Pharmacognosy.
  • 2.
    Page 2 Ephedra Synonym: Ma-Huang BiologicalSource: It consists of the dried young stems of Ephedra gerardiana & Ephedra nebrodensis belonging to family Gnetaceae. Geographical source: China, Pakistan, north-west parts of India, Australia, Kenya, Spain & Yugoslavia.
  • 3.
  • 4.
    Page 4 Cultivation, Collection& Preparation  Propagation - Seeds or layers or divisions of the root stock.  The plants are collected after attaining the age of 4 yrs for the extraction of alkaloid. During this period, proper irrigation & weeding are necessary.  The alkaloidal content of the drug varies from season to season.  It is found to be maximum in autumn, when plants & twigs are dark in colour.  Twigs are dried in sun or artificially.
  • 5.
    Page 5 Macroscopy  Colour– grey to greenish  Odour – characteristic  Taste - bitter  Thin stems - woody, cylindrical.  It shows internodes at a distance of about 3 - 3.5 cm.  It bears scaly leaves.
  • 6.
    Page 6 Microscopy  Unicellularepidermis made up of quandrangular cells with thick walled cuticle.  Sunken stomata & papillae on the ridges.  Cortex  Non lignified fibres.  Lignified pericyclic fibres.  Calcium oxalate crystals  Parenchymatous dark brown coloured pith.
  • 7.
    Page 7 Chemical Constituents Contains amino alkaloids - Ephedrine, nor- ephedrine, n-methyl ephedrine, pseudoephedrine, etc.  Ephedrine (C10H15NO) is 1-phenyl-1-hydroxy-2- methyl aminopropane, soluble in water, alcohol, organic solvents and oils.
  • 8.
    Page 8 Chemical test oEphedrine + water + HCl + CuSO4 and NaOH, the solution gives violet color and when shaken with solvent ether the organic layer shows purple and aqueous layer shows blue color.
  • 9.
    Page 9 Uses Sympathomimetic effects. Bronchodilatorin Asthma, colds, flu and Hay fever medications Allopathic: Sinumed (dries a runny nose) Used as an anti-inflammatory.
  • 10.
    Page 10 Weight loss (increasesmetabolism, decreases appetite – CNS stimulant – acts on adrenergic receptors) Also used to correct low B.P. conditions.
  • 11.
    Page 11 COLCHICUM Synonyms: Meadowsaffron seeds, Autumn crocus. Biological source: Dried ripe seeds of Colchicum luteum Baker and Colchicum autumnale Linn. Family: Liliaceae.  Colchicum corm is also used medicinally.
  • 12.
    Page 12 Geographical Source •Various parts of Europe like – England – Holland – Czechoslovakia – Poland – Yugoslavia • Also cultivated in India.
  • 13.
  • 14.
    Page 14 Cultivation andcollection  Seed propagation  Altitude 1000 – 3000m  Seedlings – transplanted to open field at a distance of 1 m.  Plants bear capsular fruits after 1 year.
  • 15.
    Page 15  Fruits– collected before dehiscence.  Dark seeds are separated, processed and graded.  Corms – isolated, adhering scales and coats are removed.  Corms – sliced transversely and dried below 65°C
  • 16.
    Page 16 Macroscopy Colchicum seeds oReddish brown testa o Acrid taste o No odor o Very hard seeds o 2 – 3 mm diameter o Ovate in shape Colchicum corms o Yellowish brown o Bitter and acrid taste o No odor o Slices 2 – 5 mm thickness o Sub-reniform or ovate in outline o Short fracture o Cut surface – white and starchy, showing grayish points
  • 17.
    Page 17 Microscopy Colchicum seeds Parenchyma  Endosperm  Aleurone grains  Fixed oil Colchicum corms  Epidermis  Parenchyma  Vascular tissues  Starch grains
  • 18.
    Page 18 Chemical Constituents Chemical Constituents: 0.2 - 1% of amino alkaloids.  Colchicine is the main constituent.  Seeds contain upto 0.8% of colchicine and in corms upto 0.6%, also contains demecolcine.  Both contain tropolane or cycloheptatrienol-one ring structure.
  • 19.
    Page 19 Colchicine  Amorphous,yellow - white alkaloid (darkens on exposure to light).  Gives a strong yellow coloration with strong mineral acids.  Dissolves readily in water, alcohol and chloroform, but only slightly in ether or petroleum spirit.
  • 20.
    Page 20 Chemical test oSample + 70% sulphuric acid = yellow color. o Alcoholic solution of sample + FeCl3 gives red color.
  • 21.
    Page 21 Uses Antitumor activity. Relievegout (used with caution – professional supervision) and rheumatism. Also used in biological experiments to produce polyploidy (multiplication of the chromosomes in a cell nucleus), hence used in horticulture and cultivation of medicinal plants.