3-phenylpropionic acid derivatives

Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...

Reexamination Certificate

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C548S222000, C514S375000

Reexamination Certificate

active

11298920

ABSTRACT:
The invention relates to new compounds, being 3-phenylpropionic acid derivatives of formula I wherein W represents COOH group or its bioisosters, or —COO—C1-C4-alkyl group; Y represents NH, N—C1-C10-alkyl, O, or S; Z represents NH, N—C1-C10-alkyl, N-aryl, N-heteroaryl, S, or O; X represents O, S, NH, N—C1-C10-alkyl, N-aryl, NSO2—C1-C10-alkyl, N—SO2-aryl, or N—SO2-heteroaryl; R1to R8each independently represent hydrogen atom or a substituent defined in the description; A is as defined in the description; n represents an integer from 0 to 4, inclusive; and pharmaceutically acceptable salts thereof. The compounds are the ligands of PPAR-gamma receptor and are useful as medicaments

REFERENCES:
patent: 5296486 (1994-03-01), Lazer et al.
patent: 6838453 (2005-01-01), Demassey et al.
patent: WO97/31907 (1997-09-01), None
patent: WO01/17994 (2001-03-01), None
patent: WO-01/85729 (2001-11-01), None
Lazer et al., Journal of Medicinal Chemistry, 1994, 37(7), pp. 913-923.
J. L. Collins et al., “N-(2-Benzoylphenyl)- L- Tyrosine PPARgamma Agonists. 2. Structure-Activity Relationship and Optimization of the Phenyl Alkyl Ether Moiety.”, J. Med. Chem. vol. 41, pp. 5037-5054, (1998). XP-002211273.
J. E. Cobb et al., “N-(2-Benzoylphenyl)-L-tyrosine PPARgamma Agonists. 3. Structure-Activity Relationship and Optimization of the N-Aryl Substituent”, J. Med. Chem. vol. 41, pp. 5055-5069 (1998). XP-002156427.

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