Molecules inhibiting a metabolic pathway involving the Syk protein tyrosine kinase and method for identifying said molecules

Patent metadata

Field	Value
Publication number	US-9504676-B2
Application number	US-201314059406-A
Country	US
Kind code	B2
Filing date	Oct 21, 2013
Priority date	Apr 9, 2008
Publication date	Nov 29, 2016
Grant date	Nov 29, 2016

Abstract

The present invention relates to the C-13 molecule (methyl 2-{5-[(3-benzyl-4-oxo-2-thioxo-1,3-thiazolidin-5-ylidene)methyl]-2-furyl}-benzoate) and to organic molecules functionally equivalent to the C-13 molecule, capable of inhibiting the binding of an antibody or antibody fragment with the human Syk protein tyrosine kinase, to the use of these molecules for the production of medicaments for the prevention or treatment of diseases dependent on metabolic pathways involving Syk, and also to a method for identifying such molecules.

First claim

The invention claimed is:

1. A method for treating a type I hypersensitivity reaction or an autoimmune disease dependent on metabolic pathways involving spleen tyrosine kinase (Syk) in a human, which comprises administering a compound to the human, wherein said compound is
(a) compound C-13having the following formula

(b) an organic compound functionally equivalent to compound C-13 having a molecular weight between 50 and 2500 Daltons, selected from substituted compounds of C-13, wherein one or more atoms belonging to a carbon chain, an aromatic group, a cycle or a heterocycle of C-13 substituted via a covalent bond by one or a plurality of halogens, and/or by one or a plurality of aromatic, cyclic, heterocyclic, alkyl, alkoxy, carboxyl, carbonyl, primary, secondary or tertiary amine, amide or sulphonamide groups; or
(c) a stereo-isomer, racemate or pharmacologically acceptable salt of C-13 or of said functionally equivalent compound; wherein said functionally equivalent compound binds with Syk tyrosine kinase protein at a site located outside the catalytic domain of such protein, on a three-dimensional cavity situated between both SH2 domains and inter-domain A of Syk, wherein said three-dimensional cavity comprises the arginine residue situated in position 68 and the two glutamic acid residues situated in positions 121 and 155 of human Syk tyrosine kinase protein, the sequence of which is set forth in SEQ ID No: 1; and
wherein said functionally equivalent compound is capable of inhibiting by at least 10% in vitro binding of antibody fragment G4G11 (SEQ) ID No: 2), with human Syk tyrosine kinase protein.

2. The method according to claim 1 , wherein said three-dimensional cavity further comprises the serine residue situated in position 9, the glutamine residue situated in position 43, the phenylalanine residue situated in position 51, the isoleucine residue situated in position 66, the glutamate residues situated in positions 67 and 69, the leucine residue situated in position 70, the asparagine residue situated in position 71, the glycine residue situated in position 72, the threonine residue situated in position 73, the tyrosine residue situated in position 74 and the alanine residue situated in position 75.

3. The method according to claim 1 , wherein said compound inhibits IgE-dependent mast cell degranulation.

4. The method according to claim 1 , wherein said compound is capable of inhibiting, by 50% in vitro, mast cell degranulation at a concentration (IC50) between 1 ng/ml and 1 mg/ml.

5. The method according to claim 1 , wherein said metabolic pathway involving Syk is a mast cell or basophil activation pathway.

6. The method according to claim 1 , wherein said type I hypersensitivity reaction is allergic asthma, allergic conjunctivitis, allergic rhinitis, anaphylaxis, angioedema, urticaria, eosinophilia, or an allergy to an antibiotic.

7. The method according to claim 1 , wherein said autoimmune disease is rheumatoid arthritis.

8. The method according to claim 1 , wherein said compound is used in combination with a further therapeutic molecule.

9. The method according to claim 1 , wherein said compound is administered orally, sublingually, nasally, ocularly, locally, intravenously, intraperitoneally, subcutaneously, by aerosol or by inhalation.

10. The method according to claim 1 , wherein said compound is administered to an adult, a child or a newborn human patient.

11. The method according to claim 1 , wherein said compound is administered at doses between 0.01 mg/kg and 200 mg/kg.

Assignees

• Dariavach Piona
• Martineau Pierre Emile Ulysse
• Villoutreix Bruno
• Centre Nat Rech Scient

Inventors

• Dariavach Piona
• Martineau Pierre Emile Ulysse
• Villoutreix Bruno

Classifications

• A61P43/00

  Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

• A61P37/00

  Drugs for immunological or allergic disorders · CPC title

• A61P37/02

  Immunomodulators · CPC title

• A61P35/00

  Antineoplastic agents · CPC title

• A61P7/10

  Antioedematous agents; Diuretics · CPC title