Primary metabolite versus Secondary metabolite: Distribution Pharmacological action - PowerPoint PPT Presentation

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Primary metabolite versus Secondary metabolite: Distribution Pharmacological action

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-Heat and oxidizing agent to oxidatively cleave C- glycosides -Quantitation: done on the principle of borntragers test, usually using Mg acetate. – PowerPoint PPT presentation

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Title: Primary metabolite versus Secondary metabolite: Distribution Pharmacological action


1
  • Side effect
  • -dependence
  • -Photosensitivity
  • -Electrolyte imbalance( hypertension and
    hypokalemia)
  • Colonic atony.
  • Colonic melanoma.
  • Contraindication
  • Pregnancy
  • Breast feeding women.
  • Children under the age of 12 years old.
  • Drug interaction
  • Other laxative.
  • Cardiac glycoside.
  • Diuretic steroid.
  • Antibiotics.

2
Pharmacodynamics and pharmacokinetics. Stomach
partial hydrolysis for O-glycoside. (so large
bulk dose is used) Small intestine Absorption
for non-polar smaller Mwt. Aglycon. Colon Activa
tion by normal flora for both O- and C- glycoside
3
Physicochemical properties , -Combined form
are soluble in aqueous alcohol and chlorinated
solvent. -Free aglycone is soluble in chlorinated
solvent and alcohols. -Detection for free
anthraquinone is done using borntragers
test. -Detection for combined anthraquinone and
dimmer is done using modified borntragers test
which uses -acid and heat to free
O-glycoside. -Acid, heat and oxidizing agent to
oxidatively cleave C- glycosides. -Heat and
oxidizing agent to oxidatively cleave C-
glycosides -Quantitation done on the principle
of borntragers test, usually using Mg acetate.
4
Natural source for anthraquinone
glycosides Senna -Botanical source Leaveas
and legumes of Cassia acutifolia
fam. Fabaceae Cassia angustifolia -Chemical
structure -Pharmacological activity
5
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6
-Aloin A -A in ß-configuration. -B in
a-configuration
Aloinoside A and B -A in ß-configuration. -B in
a-configuration.
7
  • Aloinoside A and B
  • -monoanthrone Bidesmoside, O-glycosides at C-11
    and C- glycoside at C-10.
  • -C-10 chiral centre where C- linkage of r
    Glucose unit.
  • Rhamnose is the sugar part in ß- position at
    C-11.
  • -Both are enantiomer (mirror image isomer).
  • -Aloin A is enantiomer for Aloin B, it has no
    sugar at C-11, but has CH2OH, so it is
    monodesmoside.

8
Rhubarb -Botanical source Root of Rheum
palmatum plygonaceae. -Chemical structure
-Pharmacological activity Used as laxative and
to treat ulceration of oral mucosa.
9
Flavonoid -Classification based on 1-
Degree of oxidation. 2- Position of Phenolic
group 3-Degree of unsaturation.
10
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