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Linda J Chernesky

age ~58

from Libertyville, IL

Also known as:
  • Linda Jean Chernesky
  • Linda J Dorn
  • Linda Chernesky Living
  • Linda J Chemesky
  • Chernesky J Lenda

Linda Chernesky Phones & Addresses

  • Libertyville, IL
  • Lake Zurich, IL
  • Arlington Heights, IL
  • Palatine, IL
  • Wheeling, IL
  • Wauconda, IL
  • Lane, IL
  • Hawthorn Wds, IL

Us Patents

  • Heteroatom Substituted Propanyl Derivatives Having 5-Lipoxygenase Inhibitory Activity

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  • US Patent:
    55167950, May 14, 1996
  • Filed:
    Sep 12, 1994
  • Appl. No.:
    8/304745
  • Inventors:
    Joseph F. Dellaria - Lindenhurst IL
    Linda J. Chernesky - Arlington Heights IL
  • Assignee:
    Abbott Laboratories - Abbott Park IL
  • International Classification:
    A61K 31335
    C07D31726
  • US Classification:
    514467
  • Abstract:
    Compounds of the structure ##STR1## where R. sup. 1 is alkyl of one to four carbon atoms and R. sup. 2 is selected from (a) alkenyl of one to four carbon atoms, (b) ##STR2## (c) ##STR3## and (d) ##STR4## are potent inhibitors of lipoxygenase enzymes and thus inhibit the biosynthesis of leukotrienes. These compounds are useful in the treatment or amelioration of allergic and inflammatory disease states.
  • Pyran-4-Ylmethyl Substituted Arylalkylaryl-, Arylalkenylylaryl-, And Arylalkynylarylurea Inhibitors Of 5-Lipoxygenase

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  • US Patent:
    54847869, Jan 16, 1996
  • Filed:
    Aug 24, 1993
  • Appl. No.:
    8/111090
  • Inventors:
    Joseph F. Dellaria - Lindenhurst IL
    Anwer Basha - Lake Forest IL
    Lawrence A. Black - Vernon Hills IL
    Linda J. Chernesky - Arlington Heights IL
    Wendy Lee - Chicago IL
  • Assignee:
    Abbott Laboratories - Abbott Park IL
  • International Classification:
    A61K 3135
    A61K 31495
    C07D31500
    C07D23904
  • US Classification:
    514256
  • Abstract:
    Compounds of structure ##STR1## where W is selected from ##STR2## where Q is oxygen or sulfur, R. sup. 5 and R. sup. 6 are independently selected from hydrogen and alkyl, or R. sup. 5 and R. sup. 6, together with the nitrogen atoms to which they are attached, define a radical of formula ##STR3## L. sup. 1 and L. sup. 2 are independently selected from a valence bond, alkylene, propenylene, and propynylene, R. sup. 1, R. sup. 2, R. sup. 3, and R. sup. 4 are independently selected from alkyl, alkoxy, haloalkyl, halogen, cyano, amino, alkoxycarbonyl, and dialkylaminocarbonyl, Y is oxygen, >NR. sup. 9 where R. sup. 9 is hydrogen or alkyl, or ##STR4## where n=0, 1, or 2, and A is selected from ##STR5## inhibit the biosynthesis of leukotrienes. These compounds are useful in the treatment or amelioration of allergic and inflammatory disease states.
  • (Trans-1,4-Dialkoxycyclohexyl) Substituted Arylalkylaryl-Arylalkenylaryl-, And Arylalkynylarylurea Inhibitors Of 5-Lipoxygenase

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  • US Patent:
    54079594, Apr 18, 1995
  • Filed:
    Nov 12, 1993
  • Appl. No.:
    8/152115
  • Inventors:
    Joseph F. Dellaria - Lindenhurst IL
    Anwer Basha - Lake Forest IL
    Lawrence A. Black - Vernon Hills IL
    Linda J. Chernesky - Arlington Heights IL
    Wendy Lee - Chicago IL
  • Assignee:
    Abbott Laboratories - Abbott Park IL
  • International Classification:
    A61K 3117
    C07C27506
    C07C27530
  • US Classification:
    514598
  • Abstract:
    Compounds of structure ##STR1## where W is selected from the group consisting of ##STR2## where Q is oxygen or sulfur, R. sup. 7 and R. sup. 8 are independently selected from hydrogen and alkyl, or R. sup. 7 and R. sup. 8, together with the nitrogen atoms to which they are attached, define a radical of formula ##STR3## L. sup. 1 and L. sup. 2 are independently selected from a valence bond, alkylene, propenylene, and propynylene; R. sup. 1, R. sup. 2, R. sup. 3, and R. sup. 4 are independently selected from alkyl, alkoxy, haloalkyl, halogen, cyano, amino, alkoxycarbonyl, and dialkylaminocarbonyl; Y is oxygen, >NR. sup. 11, where R. sup. 11 is hydrogen or alkyl, or ##STR4## where n=0, 1, or 2; and R. sup. 5 and R. sup. 6 are alkyl, inhibit the biosynthesis of leukotrienes. These compounds are useful in the treatment or amelioration of allergic and inflammatory disease states.
  • ((4-Alkoxypyran-4-Yl) Substituted) Ether, Arylalkyl-, Arylalkenyl-, And Arylalkynyl)Urea Inhibitors Of 5-Lipoxygenase

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  • US Patent:
    54460620, Aug 29, 1995
  • Filed:
    Nov 12, 1993
  • Appl. No.:
    8/152569
  • Inventors:
    Joseph F. Dellaria - Lindenhurst IL
    Anwer Basha - Lake Forest IL
    Lawrence A. Black - Vernon Hills IL
    Linda J. Chernesky - Arlington Heights IL
    Wendy Lee - Chicago IL
  • Assignee:
    Abbott Laboratories - Abbott Park IL
  • International Classification:
    A61K 3135
    C07D30910
    C07D40510
  • US Classification:
    514459
  • Abstract:
    Compounds of the structure ##STR1## where W is selected from ##STR2## where Q is oxygen or sulfur, R. sup. 6 and R. sup. 7 are hydrogen or alkyl, or R. sup. 6 and R. sup. 7, together with the nitrogen atoms to which they are attached, define a radical of formula ##STR3## Z is --CH. sub. 2 --, oxygen, sulfur, or --NR. sup. 9, L. sup. 1 and L. sup. 2 are selected from a valence bond, alkylene, propenylene, and propynylene; R. sup. 1 and R. sup. 2 are independently selected from alkyl, alkoxy, haloalkyl, halogen, cyano, amino, alkoxycarbonyl, and dialkylaminocarbonyl; Y is selected from oxygen, >NR. sup. 10, and ##STR4## L. sup. 3 is selected from alkylene of one to three carbon atoms, propenylene, propynylene, ##STR5## and R. sup. 3, R. sup. 4, and R. sup. 5 are hydrogen or alkyl of one to four carbon atoms inhibit the synthesis of leukotrienes. These compounds are useful in the treatment or amelioration of allergic and inflammatory disease states.
  • (4-Alkoxypyran-4-Yl) Substituted Arylalkylaryl-, Aryalkenylaryl-, And Aryalkynylarylurea Inhibitors Of 5-Lipoxygenase

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  • US Patent:
    54321948, Jul 11, 1995
  • Filed:
    May 9, 1994
  • Appl. No.:
    8/236001
  • Inventors:
    Joseph F. Dellaria - Lindenhurst IL
    Anwer Basha - Lake Forest IL
    Lawrence A. Black - Vernon Hills IL
    Linda J. Chernesky - Arlington Heights IL
    Wendy Lee - Chicago IL
  • Assignee:
    Abbott Laboratories - Abbott Park IL
  • International Classification:
    A61K 3135
    C07D30910
  • US Classification:
    514460
  • Abstract:
    Compounds of the structure ##STR1## wherein W is selected from ##STR2## where Q is oxygen or sulfur, R. sup. 6 and R. sup. 7 are hydrogen or alkyl, or R. sup. 6 and R. sup. 7, together with the nitrogen atoms to which they are attached, define a radical of formula ##STR3## R. sup. 8 is selected from hydrogen, alkyl, haloalkyl, optionally substituted phenyl, hydroxyalkyl, aminoalkyl, carboxyalkyl, (alkoxycarbonyl)alkyl, and (alkylaminocarbonyl)alkyl; Z is --CH. sub. 2 --, oxygen, sulfur, or --NR. sup. 9 where R. sup. 9 is hydrogen or alkyl, L. sup. 1 and L. sup. 2 are selected from a valence bond, alkylene, propenylene, and propynylene, R. sup. 1, R. sup. 2, R. sup. 3, and R. sup. 4 are independently selected from alkyl, haloalkyl, halogen, cyano, amino, alkoxycarbonyl, and dialkylaminocarbonyl, Y is selected from oxygen, --NR. sup. 10, where R. sup.
  • 1, 2-Dialkoxyethanes As 5-Lipoxygenase Inhibitors

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  • US Patent:
    54750091, Dec 12, 1995
  • Filed:
    Sep 12, 1994
  • Appl. No.:
    8/304066
  • Inventors:
    Linda J. Chernesky - Arlington Heights IL
    Joseph F. Dellaria - Lindenhurst IL
  • Assignee:
    Abbott Laboratories - Abbott Park IL
  • International Classification:
    A61K 3147
    C07D21514
  • US Classification:
    514312
  • Abstract:
    Compounds of the structure ##STR1## where Ar. sup. 1 is selected from optionally substituted carbocyclic aryl; optionally substituted 5- or 6-membered heterocyclic aryl; optionally substituted 10-membered bicyclic heterocyclic aryl containing one or two nitrogen atoms; optionally substituted benzo[b]furyl; optionally substituted benzo[b]thienyl; ##STR2## L. sup. 1 is a valence bond, alkylene, propenylene, or propynylene; Y is oxygen, >NR. sup. 5, or >S(O)n; Ar. sup. 2 is optionally substituted phenyl; L. sup. 2 is ##STR3## and R. sup. 1 and R. sup. 2 are alkyl, or taken together define a group of formula ##STR4## are potent inhibitors of lipoxygenase enzymes and thus inhibit the biosynthesis of leukotrienes. These compounds are useful in the treatment or amelioration of allergic and inflammatory disease states.

Classmates

Linda Chernesky Photo 1

Linda Bower (Chernesky)

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Schools:
Central High School Scranton PA 1964-1968

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