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Combinatorial chemistry
Presented by: Manju Jakhar
M.Pharm (Pharmacology)
1st Semester
DEFINITION:-
• Combinatorial chemistry is a technique by which large numbers of different
but structurally similar molecules are produced rapidly and submitted for
pharmacological assay.
• This technique uses the same reaction conditions with the same reaction
vessels to produce a large range of analogues.
• Technique invented in the late 1980s and early 1990s to enable tasks to be
applied to many molecules simultaneously.
TYPES OF COMBINATORIAL SYNTHESIS
Combinatorial chemistry is of two types: -
(1) Solid phase combinatorial chemistry
(The compound library have been synthesized on solid phase such as resin bead)
(2) Solution phase combinatorial chemistry
(The compound library have been synthesized in solvent in the reaction flask)
1.SOLID PHASE TECHNIQUES
• Reactants are bound to a polymeric surface and modified whilst still attached. Final product
is released at the end of the synthesis.
Advantages
• Specific reactants can be bound to specific beads
• Beads can be mixed and reacted in the same reaction vessel
• Products formed are distinctive for each bead and physically distinct
• Excess reagents can be used to drive reactions to completion
• Excess reagents and by products are easily removed
• Reaction intermediates are attached to bead and do not need to be isolated and purified
• Individual beads can be separated to isolate individual products
• Polymeric support can be regenerated and re-used after cleaving the product
• Automation is possible.
Requirements
• A resin bead or a functionalised surface to act as a solid support
• An anchor or linker
• A bond linking the substrate to the linker. The bond must be stable to the reaction
conditions used in the synthesis
• A means of cleaving the product from the linker at the end
• Protecting groups for functional groups not involved in the synthesis
beads
 Anchor or Linker
Types of Resin & Linkers
Protecting groups
• few protecting groups used in solid phase synthesis.
 For amines.:-
• Boc ( t-butoxycarbonyl )
• Fmoc (9-fluorenylmetoxy carbonyl)
• Tmsec (2 [ trimethylsilyl ] ethoxycarbonyl)
 For carboxylic acids:-
• Tert Bu ester(t-butyl ester)
• Fm ester(9-fluronyl methyl ester)
• Tmse ester(2 [trimethylsilyl] ethyl) 17
Equipment for Solid Phase Peptide Synthesis
2.Parallel Synthesis
3.Mixed Combinatorial Synthesis
• To use a standard route to produce a large variety of different analouges where
each reaction vessel or tube contains a mixture of products.
• The identities of the structures in each vessels are not known with certainty.
• Useful for finding a lead compound.
• Each mixture is tested for activity.
• Inactive mixture are stored in combinatorial libraries.
• Active mixtures are studied further to identify active component.
Equipment for mixed combinatorial synthesis:-
Combinatorial chemistry. in drug discovery
Combinatorial chemistry. in drug discovery

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Combinatorial chemistry. in drug discovery

  • 1. Combinatorial chemistry Presented by: Manju Jakhar M.Pharm (Pharmacology) 1st Semester
  • 2. DEFINITION:- • Combinatorial chemistry is a technique by which large numbers of different but structurally similar molecules are produced rapidly and submitted for pharmacological assay. • This technique uses the same reaction conditions with the same reaction vessels to produce a large range of analogues. • Technique invented in the late 1980s and early 1990s to enable tasks to be applied to many molecules simultaneously.
  • 3.
  • 4.
  • 5.
  • 6.
  • 7.
  • 8.
  • 9. TYPES OF COMBINATORIAL SYNTHESIS Combinatorial chemistry is of two types: - (1) Solid phase combinatorial chemistry (The compound library have been synthesized on solid phase such as resin bead) (2) Solution phase combinatorial chemistry (The compound library have been synthesized in solvent in the reaction flask)
  • 10. 1.SOLID PHASE TECHNIQUES • Reactants are bound to a polymeric surface and modified whilst still attached. Final product is released at the end of the synthesis. Advantages • Specific reactants can be bound to specific beads • Beads can be mixed and reacted in the same reaction vessel • Products formed are distinctive for each bead and physically distinct • Excess reagents can be used to drive reactions to completion • Excess reagents and by products are easily removed • Reaction intermediates are attached to bead and do not need to be isolated and purified • Individual beads can be separated to isolate individual products • Polymeric support can be regenerated and re-used after cleaving the product • Automation is possible.
  • 11. Requirements • A resin bead or a functionalised surface to act as a solid support • An anchor or linker • A bond linking the substrate to the linker. The bond must be stable to the reaction conditions used in the synthesis • A means of cleaving the product from the linker at the end • Protecting groups for functional groups not involved in the synthesis
  • 13.  Anchor or Linker
  • 14. Types of Resin & Linkers
  • 15. Protecting groups • few protecting groups used in solid phase synthesis.  For amines.:- • Boc ( t-butoxycarbonyl ) • Fmoc (9-fluorenylmetoxy carbonyl) • Tmsec (2 [ trimethylsilyl ] ethoxycarbonyl)  For carboxylic acids:- • Tert Bu ester(t-butyl ester) • Fm ester(9-fluronyl methyl ester) • Tmse ester(2 [trimethylsilyl] ethyl) 17
  • 16. Equipment for Solid Phase Peptide Synthesis
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  • 22. 3.Mixed Combinatorial Synthesis • To use a standard route to produce a large variety of different analouges where each reaction vessel or tube contains a mixture of products. • The identities of the structures in each vessels are not known with certainty. • Useful for finding a lead compound. • Each mixture is tested for activity. • Inactive mixture are stored in combinatorial libraries. • Active mixtures are studied further to identify active component.
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  • 30. Equipment for mixed combinatorial synthesis:-