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US4457936A Expired / Lapsed US ⏱️ 0.0 years remaining

Use of hydroxyphenyl-thiazole-, -thiazoline- and -thiazolidine-carboxylic acids, for influencing the collagen metabolism

Assignee: Hoechst AG
•
Filing: 1982-04-07
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Granted: 1984-07-03
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Expires: 2002-04-07
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Abstract

Abstract What are disclosed are hydroxyphenyl-thiazole-, -thiazoline- and -thiazolidine-carboxylic acids of the formulae ##STR1## in which R 1 and R 3 , independently from each other, are hydrogen, methyl, chlorine or bromine, and R 1 and R 3 may alternatively be nitro, amino or sulfonylamido; R 2 is hydrogen, hydroxyl or methyl; R 4 is hydrogen or methyl; and R 5 is hydrogen, methyl, phenyl or --COOH; and their salts with physiologically acceptable bases, a process for the preparation thereof and their use for influencing the collagen metabolism.

Inventors

  • 👤 Eberhard Draeger
  • 👤 Henning Lubbers

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-27 14:40
CPC Classifications
C; C07; C07D; C07D277/00; C07D277/02; C07D277/08; C07D277/12; A; A61; A61P; A61P3/00; C07D277/04; C07D277/06; C07D277/20; C07D277/32; C07D277/56

Claims Analysis

Total Claims: 8
Claim 1
Independent Claim 119 words
A pharmaceutical preparation for inhibiting collagen biosynthesis which comprises an effective inhibiting amount of a carboxylic acid selected from the group of acids having the formulas ##STR25## or a soluble, physiologically acceptable carboxylate salt of such an acid, formed with a base, wherein R 1 and R 3 independently of each other are hydrogen, methyl, chlorine, or bromine, or one of R 1 or R 3 is hydrogen, methyl, chlorine, or bromine and the other is nitro, amino, or sulfonylamido; R 2 is hydrogen, hydroxyl, or methyl; R 4 is hydrogen or methyl, but not all of R 1 -R 4 are hydrogen; and R 5 is hydrogen, methyl, phenyl, or carboxyl, together with a pharmaceutically acceptable carrier therefor.
Claim 2
Dependent Claim 119 words
A pharmaceutical preparation for inhibiting collagen biosynthesis which comprises an effective inhibiting amount of a carboxylic acid selected from the group of acids having the formulas ##STR25## or a soluble, physiologically acceptable carboxylate salt of such an acid, formed with a base, wherein R 1 and R 3 independently of each other are hydrogen, methyl, chlorine, or bromine, or one of R 1 or R 3 is hydrogen, methyl, chlorine, or bromine and the other is nitro, amino, or sulfonylamido; R 2 is hydrogen, hydroxyl, or methyl; R 4 is hydrogen or methyl, but not all of R 1 -R 4 are hydrogen; and R 5 is hydrogen, methyl, phenyl, or carboxyl, together with a pharmaceutically acceptable carrier therefor.
Claim 3
Independent Claim 122 words
A method for inhibiting collagen biosynthesis in a patient requiring such treatment, which method comprises administering to said patient an effective inhibiting amount of a carboxylic acid selected from the group of acids having the formulas ##STR26## or a soluble, physiologically acceptable carboxylate salt of such an acid, formed with a base, wherein R 1 and R 3 independently of each other are hydrogen, methyl, chlorine, or bromine, or one of R 1 or R 3 is hydrogen, methyl, chlorine, or bromine and the other is nitro, amino, or sulfonylamido; R 2 is hydrogen, hydroxyl, or methyl; R 4 is hydrogen or methyl, but not all of R 1 -R 4 are hydrogen; and R 5 is hydrogen, methyl, phenyl, or carboxyl.
Claim 4
Independent Claim 122 words
A method for inhibiting collagen biosynthesis in a patient requiring such treatment, which method comprises administering to said patient an effective inhibiting amount of a carboxylic acid selected from the group of acids having the formulas ##STR26## or a soluble, physiologically acceptable carboxylate salt of such an acid, formed with a base, wherein R 1 and R 3 independently of each other are hydrogen, methyl, chlorine, or bromine, or one of R 1 or R 3 is hydrogen, methyl, chlorine, or bromine and the other is nitro, amino, or sulfonylamido; R 2 is hydrogen, hydroxyl, or methyl; R 4 is hydrogen or methyl, but not all of R 1 -R 4 are hydrogen; and R 5 is hydrogen, methyl, phenyl, or carboxyl.
Claim 5
Dependent Claim 91 words
A pharmaceutical preparation for inhibiting collagen biosynthesis which comprises an effective inhibiting amount of a carboxylic acid of the formula ##STR27## or of a soluble, physiologically acceptable, carboxylate salt of such an acid formed with a base, wherein R 1 , R 3 , and R 4 are, independently of each other, hydrogen, methyl, chlorine, or bromine, or one of R 1 or R 3 is hydrogen, methyl, chlorine, or bromine and the other is nitro; and R 2 is hydrogen, methyl, or hydroxyl; together with a pharmaceutically acceptable carrier therefor.
Claim 6
Dependent Claim 91 words
A pharmaceutical preparation for inhibiting collagen biosynthesis which comprises an effective inhibiting amount of a carboxylic acid of the formula ##STR27## or of a soluble, physiologically acceptable, carboxylate salt of such an acid formed with a base, wherein R 1 , R 3 , and R 4 are, independently of each other, hydrogen, methyl, chlorine, or bromine, or one of R 1 or R 3 is hydrogen, methyl, chlorine, or bromine and the other is nitro; and R 2 is hydrogen, methyl, or hydroxyl; together with a pharmaceutically acceptable carrier therefor.
Claim 7
Independent Claim 94 words
A method for inhibiting collagen biosynthesis in a patient requiring such treatment, which method comprises administering to said patient an effective inhibiting amount of a carboxylic acid of the formula ##STR28## or of a soluble, physiologically acceptable, carboxylate salt of such an acid formed with a base, wherein R 1 , R 3 , and R 4 are, independently of each other, hydrogen, methyl, chlorine, or bromine, or one of R 1 or R 3 is hydrogen, methyl, chlorine, or bromine and the other is nitro; and R 2 is hydrogen, methyl, or hydroxyl.
Claim 8
Independent Claim 94 words
A method for inhibiting collagen biosynthesis in a patient requiring such treatment, which method comprises administering to said patient an effective inhibiting amount of a carboxylic acid of the formula ##STR28## or of a soluble, physiologically acceptable, carboxylate salt of such an acid formed with a base, wherein R 1 , R 3 , and R 4 are, independently of each other, hydrogen, methyl, chlorine, or bromine, or one of R 1 or R 3 is hydrogen, methyl, chlorine, or bromine and the other is nitro; and R 2 is hydrogen, methyl, or hydroxyl.

References Cited (Backward Citations)

US3809754A Cited
US3882110A Cited
GB1292170A Cited
FR2062120A5 Cited
GB1382887A Cited
FR2247243A2 Cited
DE2245560A1 Cited
GB1584981A Cited
DE3002989A1 Cited
US4367233A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1987-07-03 1988-01-02 1988-07-03 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1991-07-03 1992-01-02 1992-07-03 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1995-07-03 1996-01-02 1996-07-03 $7700.00 Window Closed / Lapsed

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