Generation of compound libraries utilizing molecular imprints including a double or anti-idiotypic approach

• US 20050042677A1
• Filed: 09/27/2002
• Published: 02/24/2005
• Est. Priority Date: 09/28/2001
• Status: Abandoned Application

• Current Assignee: Klaus Mosbach
• Original Assignee: Klaus Mosbach
• Inventors: Ye, Lei, Mosbach, Klaus
• Application Number:
  US10/490,632
• Publication Number:
  US 20050042677A1
• Time in Patent Office: Days
• US Class Current: 435/7.100
• CPC Class Codes: C40B 40/04 Libraries containing only organic compounds

Abstract

The present invention relates to a method of producing new chemical entities comprising the steps of: (i) taking a chemical entity as the template to prepare a molecularly imprinted polymer (MIP), (ii) removing the template from the MIP, (iii) using the specific binding sites of the MIP to direct, or facilitate, the syntheses of new chemical entities for the generation of compound libraries using molecularly imprinted polymers, and to a use of such compound libraries.

Claims

1. A method of producing new chemical entities comprising the steps of:

(i) taking a chemical entity as the template to prepare a molecularly imprinted polymer (MIP),

(ii) removing the template from the MIP, and

(iii) using the specific binding sites of the MIP to direct, or facilitate, the synthesis of new chemical entities,

wherein a focused compound library is generated by screening more than one reactant and wherein hit products are those that are obtainable only via the site directed synthesis provided by the imprinted polymer.

2. A method according to claim 1, wherein the chemical entity that is chosen as the template has desired physical, chemical, biochemical or physiological properties.

3. A method according to claim 1, wherein the chemical entity that is chosen as the template is an enzyme inhibitor, an agonist or antagonist, or an affinity ligand.

4. A method according to claim 1, wherein the imprinted polymer is an organic polymer or an inorganic polymer.

5. A method according to claim 1, wherein the new chemical entities produced are the same as, or different from, the original template.

6. A method according to claim 1, wherein the syntheses of the new chemical entities are carried out by organic reactions.

7. A method according to claim 1, wherein the syntheses of the new chemical entities are carried out by polymerization reactions.

8. A method according to claim 1, wherein the syntheses of the new chemical entities is are carried out separately.

9. A method according to claim 1, wherein the syntheses of several new chemical entities are carried out simultaneously in one pot.

10. A method according to claim 1, wherein the hit products that are identified are subjected to scale up synthesis.

11. A method for iterative lead optimization, wherein a new template is chosen from one of the hit products of claim 1 for the preparation of a new MIP, which subsequently is used to generate a new focused compound library.

12. A method according to claim 1, comprising the further step of using said hit products to replace the original template.

14. A method according to claim 2, wherein the chemical entity that is chosen as the template is an enzyme inhibitor, an agonist or antagonist, or an affinity ligand.

15. A method for iterative lead optimization, wherein a new template is chosen from one of the hit products of claim 7 for the preparation of a new MIP, which subsequently is used to generate a new focused compound library.

16. A method for iterative lead optimization, wherein a new template is chosen from one of the hit products of claim 8 for the preparation of a new MIP, which subsequently is used to generate a new focused compound library.

17. A method for iterative lead optimization, wherein a new template is chosen from one of the hit products of claim 9 for the preparation of a new MIP, which subsequently is used to generate a new focused compound library.

18. A method for iterative lead optimization, wherein a new template is chosen from one of the hit products of claim 10 for the preparation of a new MIP, which subsequently is used to generate a new focused compound library.

19. A method according to claim 8, comprising the further step of using said hit products to replace the original template.

20. A method according to claim 9, comprising the further step of using said hit products to replace the original template.

21. A method according to claim 10, comprising the further step of using said hit products to replace the original template.

22. A method according to claim 11, comprising the further step of using said hit products to replace the original template.

13. (Canceled)