Ligand UK Development Limited

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IPC Class
A61K 31/519 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings 14
A61K 45/06 - Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca 9
C07D 487/04 - Ortho-condensed systems 9
A61K 31/197 - Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid 7
A61K 31/397 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine 6
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05 - Pharmaceutical, veterinary and sanitary products 6
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1.

TRIAZOLO[4,5-D] PYRAMIDINE DERIVATIVES AND THEIR USE AS PURINE RECEPTOR ANTAGONISTS

      
Application Number 17895037
Status Pending
Filing Date 2022-08-24
First Publication Date 2023-03-30
Owner Ligand UK Development Limited (United Kingdom)
Inventor
  • Bamford, Samantha Jane
  • Gillespie, Roger John
  • Todd, Richard Simon

Abstract

Compounds of formula (I) that are capable of acting as purine receptor antagonists, pharmaceutical compositions including the compounds, and methods of making the compounds, are disclosed. The compounds and compositions can be used in treating or preventing disorders related to purine receptor hyperfunctioning. Compounds of formula (I) that are capable of acting as purine receptor antagonists, pharmaceutical compositions including the compounds, and methods of making the compounds, are disclosed. The compounds and compositions can be used in treating or preventing disorders related to purine receptor hyperfunctioning.

IPC Classes  ?

  • C07D 487/04 - Ortho-condensed systems
  • A61K 31/443 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with oxygen as a ring hetero atom
  • A61K 31/131 - Amines, e.g. amantadine acyclic
  • A61K 31/197 - Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
  • A61K 31/519 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
  • A61K 45/06 - Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
  • C07D 405/12 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links

2.

Azetidine derivatives

      
Application Number 17148785
Grant Number 12246014
Status In Force
Filing Date 2021-01-14
First Publication Date 2021-09-02
Grant Date 2025-03-11
Owner Ligand UK Development Limited (United Kingdom)
Inventor
  • Roughley, Stephen
  • Walls, Steven
  • Hart, Terance
  • Parsons, Rachel
  • Brough, Paul
  • Graham, Christopher
  • Macias, Alba

Abstract

Compounds of formula (I) are inhibitors of fatty acid amide hydrolase, (F AAH), and which are useful in the treatment of diseases or medical conditions which benefit from inhibition of FAAH activity, such as anxiety, depression pain, inflammation, and eating, sleep, neurodegenerative and movement disorders: 3 is a divalent radical selected from optionally substituted phenylene and optionally substituted monocyclic heteroarylene radicals having 5 or 6 ring atoms.

IPC Classes  ?

  • A61K 31/396 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having three-membered rings, e.g. aziridine
  • A61K 31/397 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
  • A61K 31/4427 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems
  • A61K 31/4439 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
  • A61K 31/495 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two nitrogen atoms as the only ring hetero atoms, e.g. piperazine
  • A61K 31/497 - Non-condensed pyrazines containing further heterocyclic rings
  • A61K 31/501 - PyridazinesHydrogenated pyridazines not condensed and containing further heterocyclic rings
  • A61K 31/506 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
  • C07D 205/04 - Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
  • C07D 401/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 401/14 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
  • C07D 413/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

3.

Triazolo[4,5-d] pyramidine derivatives and their use as purine receptor antagonists

      
Application Number 17088325
Grant Number 11466019
Status In Force
Filing Date 2020-11-03
First Publication Date 2021-04-22
Grant Date 2022-10-11
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
Inventor
  • Bamford, Samantha Jane
  • Gillespie, Roger John
  • Todd, Richard Simon

Abstract

Compounds of formula (I) that are capable of acting as purine receptor antagonists, pharmaceutical compositions including the compounds, and methods of making the compounds, are disclosed. The compounds and compositions can be used in treating or preventing disorders related to purine receptor hyperfunctioning.

IPC Classes  ?

  • A61K 31/519 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
  • A61K 31/443 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with oxygen as a ring hetero atom
  • C07D 487/04 - Ortho-condensed systems
  • A61K 31/197 - Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
  • A61K 45/06 - Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
  • C07D 405/12 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links

4.

Triazolo[4,5-d] pyramidine derivatives and their use as purine receptor antagonists

      
Application Number 16700160
Grant Number 10875868
Status In Force
Filing Date 2019-12-02
First Publication Date 2020-06-04
Grant Date 2020-12-29
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
Inventor
  • Bamford, Samantha Jane
  • Gillespie, Roger John
  • Todd, Richard Simon

Abstract

Compounds of formula (I) that are capable of acting as purine receptor antagonists, pharmaceutical compositions including the compounds, and methods of making the compounds, are. disclosed. The compounds and compositions can be used in treating or preventing disorders related to purine receptor hyperfunctioning.

IPC Classes  ?

  • C07D 405/12 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 487/04 - Ortho-condensed systems
  • A61K 31/197 - Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
  • A61K 31/519 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
  • A61K 45/06 - Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca

5.

Thienopyrimidine compounds

      
Application Number 16726308
Grant Number 11028097
Status In Force
Filing Date 2019-12-24
First Publication Date 2020-05-07
Grant Date 2021-06-08
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
Inventor
  • Jordan, Allan
  • Bedford, Simon
  • Burkhard, Klenke
  • Yule, Ian
  • Poullennec, Karine

Abstract

2B receptor antagonists: 6 taken together with the nitrogen atom to which they are attached form an optionally substituted 4- to 6-membered saturated ring.

IPC Classes  ?

  • C07D 495/04 - Ortho-condensed systems
  • C07D 495/14 - Ortho-condensed systems
  • A61K 31/519 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings

6.

Azetidine derivatives

      
Application Number 16506225
Grant Number 10918640
Status In Force
Filing Date 2019-07-09
First Publication Date 2020-01-02
Grant Date 2021-02-16
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
Inventor
  • Roughley, Stephen
  • Walls, Steven
  • Hart, Terance
  • Parsons, Rachel
  • Brough, Paul
  • Graham, Christopher
  • Macias, Alba

Abstract

Compounds of formula (I) are inhibitors of fatty acid amide hydrolase, (FAAH), and which are useful in the treatment of diseases or medical conditions which benefit from inhibition of FAAH activity, such as anxiety, depression pain, inflammation, and eating, sleep, neurodegenerative and movement disorders: 3 is a divalent radical selected from optionally substituted phenylene and optionally substituted monocyclic heteroarylene radicals having 5 or 6 ring atoms.

IPC Classes  ?

  • A61K 31/397 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
  • A61K 31/497 - Non-condensed pyrazines containing further heterocyclic rings
  • A61K 31/495 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two nitrogen atoms as the only ring hetero atoms, e.g. piperazine
  • A61K 31/506 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
  • A61K 31/4427 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems
  • C07D 401/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 401/14 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
  • C07D 205/04 - Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
  • C07D 413/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
  • A61K 31/4439 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
  • A61K 31/501 - PyridazinesHydrogenated pyridazines not condensed and containing further heterocyclic rings

7.

Triazolo[4,5-D] pyramidine derivatives and their use as purine receptor antagonists

      
Application Number 16132411
Grant Number 10538526
Status In Force
Filing Date 2018-09-15
First Publication Date 2019-01-31
Grant Date 2020-01-21
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
Inventor
  • Bamford, Samantha Jane
  • Gillespie, Roger John
  • Todd, Richard Simon

Abstract

Compounds of formula (I) that are capable of acting as purine receptor antagonists, pharmaceutical compositions including the compounds, and methods of making the compounds, are disclosed. The compounds and compositions can be used in treating or preventing disorders related to purine receptor hyperfunctioning.

IPC Classes  ?

  • A61K 31/519 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
  • C07D 487/04 - Ortho-condensed systems
  • A61K 31/197 - Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
  • A61K 45/06 - Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
  • C07D 405/12 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links

8.

1H-pyrrolo [2,3-b] pyridine derivatives and their use as kinase inhibitors

      
Application Number 16009439
Grant Number 10889582
Status In Force
Filing Date 2018-06-15
First Publication Date 2018-12-20
Grant Date 2021-01-12
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
Inventor
  • Stokes, Stephen
  • Graham, Christopher John
  • Ray, Stuart Christopher
  • Stefaniak, Emma Jayne

Abstract

1 are as defined in the claims.

IPC Classes  ?

  • A61K 45/06 - Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
  • C07D 471/04 - Ortho-condensed systems
  • A61K 31/437 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
  • A61K 31/4545 - Non-condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine

9.

Thienopyrimidine compounds

      
Application Number 15891618
Grant Number 10556911
Status In Force
Filing Date 2018-02-08
First Publication Date 2018-06-14
Grant Date 2020-02-11
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
Inventor
  • Jordan, Allan
  • Bedford, Simon
  • Burkhard, Klenke
  • Yule, Ian
  • Poullennec, Karine

Abstract

2B receptor antagonists: 6 taken together with the nitrogen atom to which they are attached form an optionally substituted 4- to 6-membered saturated ring.

IPC Classes  ?

  • C07D 495/04 - Ortho-condensed systems
  • C07D 495/14 - Ortho-condensed systems
  • A61K 31/519 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings

10.

Triazolo[4,5-D] pyramidine derivatives and their use as purine receptor antagonists

      
Application Number 15682346
Grant Number 10106547
Status In Force
Filing Date 2017-08-21
First Publication Date 2017-11-30
Grant Date 2018-10-23
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
Inventor
  • Bamford, Samantha Jane
  • Gillespie, Roger John
  • Todd, Richard Simon

Abstract

Compounds of formula (I) that are capable of acting as purine receptor antagonists, pharmaceutical compositions including the compounds, and methods of making the compounds, are disclosed. The compounds and compositions can be used in treating or preventing disorders related to purine receptor hyperfunctioning.

IPC Classes  ?

  • A01N 43/90 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
  • A61K 31/519 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
  • C07D 487/04 - Ortho-condensed systems
  • A61K 45/06 - Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
  • C07D 405/12 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
  • A61K 31/197 - Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid

11.

Thienopyrimidine compounds

      
Application Number 15436988
Grant Number 09920066
Status In Force
Filing Date 2017-02-20
First Publication Date 2017-10-12
Grant Date 2018-03-20
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
Inventor
  • Jordan, Allan
  • Bedford, Simon
  • Burkhard, Klenke
  • Yule, Ian
  • Poullennec, Karine

Abstract

2B receptor antagonists: 6 taken together with the nitrogen atom to which they are attached form an optionally substituted 4- to 6-membered saturated ring.

IPC Classes  ?

  • C07D 495/04 - Ortho-condensed systems
  • C07D 495/14 - Ortho-condensed systems
  • A61K 31/519 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings

12.

Azetidine derivatives

      
Application Number 15278386
Grant Number 10383871
Status In Force
Filing Date 2016-09-28
First Publication Date 2017-07-13
Grant Date 2019-08-20
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
Inventor
  • Roughley, Stephen
  • Walls, Steven
  • Hart, Terance
  • Parsons, Rachel
  • Brough, Paul
  • Graham, Christopher
  • Macias, Alba

Abstract

Compounds of formula (I) are inhibitors of fatty acid amide hydrolase, (FAAH), and which are useful in the treatment of diseases or medical conditions which benefit from inhibition of FAAH activity, such as anxiety, depression pain, inflammation, and eating, sleep, neurodegenerative and movement disorders: 3 is a divalent radical selected from optionally substituted phenylene and optionally substituted monocyclic heteroarylene radicals having 5 or 6 ring atoms.

IPC Classes  ?

  • A61K 31/397 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
  • A61K 31/497 - Non-condensed pyrazines containing further heterocyclic rings
  • A61K 31/495 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two nitrogen atoms as the only ring hetero atoms, e.g. piperazine
  • A61K 31/506 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
  • A61K 31/4427 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems
  • C07D 205/04 - Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
  • C07D 401/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 401/14 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
  • C07D 413/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
  • A61K 31/4439 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
  • A61K 31/501 - PyridazinesHydrogenated pyridazines not condensed and containing further heterocyclic rings

13.

Triazolo[4,5-D] pyramidine derivatives and their use as purine receptor antagonists

      
Application Number 15172126
Grant Number 09765080
Status In Force
Filing Date 2016-06-02
First Publication Date 2017-03-30
Grant Date 2017-09-19
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
Inventor
  • Bamford, Samantha Jane
  • Gillespie, Roger John
  • Todd, Richard Simon

Abstract

Compounds of formula (I) that are capable of acting as purine receptor antagonists, pharmaceutical compositions including the compounds, and methods of making the compounds, are. disclosed. The compounds and compositions can be used in treating or preventing disorders related to purine receptor hyperfunctioning.

IPC Classes  ?

  • C07D 471/00 - Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups
  • C07D 487/00 - Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups
  • C07D 487/04 - Ortho-condensed systems
  • C07D 405/12 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links

14.

Thienopyrimidine compounds

      
Application Number 14803214
Grant Number 09610290
Status In Force
Filing Date 2015-07-20
First Publication Date 2015-12-03
Grant Date 2017-04-04
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
Inventor
  • Jordan, Allan
  • Bedford, Simon
  • Burkhard, Klenke
  • Yule, Ian
  • Poullennec, Karine

Abstract

2B receptor antagonists: 6 taken together with the nitrogen atom to which they are attached form an optionally substituted 4- to 6-membered saturated ring.

IPC Classes  ?

  • A61K 31/519 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
  • C07D 495/04 - Ortho-condensed systems

15.

Triazolo[4,5-D] pyramidine derivatives and their use as purine receptor antagonists

      
Application Number 14618829
Grant Number 09376443
Status In Force
Filing Date 2015-02-10
First Publication Date 2015-10-15
Grant Date 2016-06-28
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
Inventor
  • Bamford, Samantha Jane
  • Gillespie, Roger John
  • Todd, Richard Simon

Abstract

Compounds of formula (I) that are capable of acting as purine receptor antagonists, pharmaceutical compositions including the compounds, and methods of making the compounds, are disclosed. The compounds and compositions can be used in treating or preventing disorders related to purine receptor hyperfunctioning.

IPC Classes  ?

  • A01N 43/90 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
  • A61K 31/519 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
  • C07D 471/00 - Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups
  • C07D 487/00 - Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups
  • C07D 487/04 - Ortho-condensed systems
  • A61K 31/197 - Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
  • A61K 45/06 - Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca

16.

Azetidine derivatives

      
Application Number 14641783
Grant Number 09475800
Status In Force
Filing Date 2015-03-09
First Publication Date 2015-07-02
Grant Date 2016-10-25
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
Inventor
  • Roughley, Stephen
  • Walls, Steven
  • Hart, Terance
  • Parsons, Rachel
  • Brough, Paul
  • Graham, Christopher
  • Macias, Alba

Abstract

Compounds of formula (I) are inhibitors of fatty acid amide hydrolase, (FAAH), and which are useful in the treatment of diseases or medical conditions which benefit from inhibition of FAAH activity, such as anxiety, depression pain, inflammation, and eating, sleep, neurodegenerative and movement disorders: 3 is a divalent radical selected from the group consisting of optionally substituted phenylene and optionally substituted monocyclic heteroarylene radicals having 5 or 6 ring atoms.

IPC Classes  ?

  • A61K 31/397 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
  • A61K 31/4427 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems
  • A61K 31/495 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two nitrogen atoms as the only ring hetero atoms, e.g. piperazine
  • C07D 413/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
  • C07D 205/04 - Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
  • C07D 401/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 401/14 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings

17.

1H-pyrrolo[2,3-B] pyridine derivatives and their use as kinase inhibitors

      
Application Number 14375353
Grant Number 10000481
Status In Force
Filing Date 2013-01-30
First Publication Date 2015-01-08
Grant Date 2018-06-19
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
Inventor
  • Stokes, Stephen
  • Graham, Christopher John
  • Ray, Stuart Christopher
  • Stefaniak, Emma Jayne

Abstract

1 are as defined in the claims.

IPC Classes  ?

  • C07D 471/04 - Ortho-condensed systems
  • A61K 45/06 - Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
  • A61K 31/437 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
  • A61K 31/4545 - Non-condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine

18.

Azetidine derivatives

      
Application Number 13866059
Grant Number 09006269
Status In Force
Filing Date 2013-04-19
First Publication Date 2013-12-12
Grant Date 2015-04-14
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
Inventor
  • Roughley, Stephen
  • Walls, Steven
  • Hart, Terance
  • Parsons, Rachel
  • Brough, Paul
  • Graham, Christopher
  • Macias, Alba

Abstract

Compounds of formula (I) are inhibitors of fatty acid amide hydrolase, (FAAH), and which are useful in the treatment of diseases or medical conditions which benefit from inhibition of FAAH activity, such as anxiety, depression pain, inflammation, and eating, sleep, neurodegenerative and movement disorders: 3 is a divalent radical selected from the group consisting of optionally substituted phenylene and optionally substituted monocyclic heteroarylene radicals having 5 or 6 ring atoms.

IPC Classes  ?

  • A61K 31/397 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
  • A61K 31/4427 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems
  • A61K 31/495 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two nitrogen atoms as the only ring hetero atoms, e.g. piperazine
  • C07D 205/00 - Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
  • C07D 213/24 - Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
  • C07D 237/10 - Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D 205/04 - Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
  • C07D 401/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 401/14 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
  • C07D 413/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

19.

Triazolo [4, 5-D] pyramidine derivatives and their use as purine receptor antagonists

      
Application Number 13889921
Grant Number 08987279
Status In Force
Filing Date 2013-05-08
First Publication Date 2013-09-19
Grant Date 2015-03-24
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
Inventor
  • Bamford, Samantha Jane
  • Gillespie, Roger John
  • Todd, Richard Simon

Abstract

Compounds of formula (I) that are capable of acting as purine receptor antagonists, pharmaceutical compositions including the compounds, and methods of making the compounds, are disclosed. The compounds and compositions can be used in treating or preventing disorders related to purine receptor hyperfunctioning.

IPC Classes  ?

  • A01N 43/90 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
  • A61K 31/519 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
  • C07D 471/00 - Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups
  • C07D 487/00 - Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups
  • C07D 491/00 - Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups , , or
  • C07D 487/04 - Ortho-condensed systems
  • A61K 31/197 - Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
  • A61K 45/06 - Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca

20.

Acid addition salts, hydrates and polymorphs of 5-(2,4-dihydroxy-5-iso-propyl-phenyl)-4-(4-morpholin-4-ylmethyl-phenyl)-isoxazole-3-carboxylic acid ethylamide and formulations comprising these forms

      
Application Number 13415268
Grant Number 08487095
Status In Force
Filing Date 2012-03-08
First Publication Date 2012-07-05
Grant Date 2013-07-16
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
Inventor
  • Drysdale, Martin James
  • Dymock, Brian William
  • Krell, Christoph
  • Mutz, Michael
  • Petersen, Holger
  • Zheng, Weijia

Abstract

The present invention relates to new salt forms of 5-(2,4-dihydroxy-5-isopropyl-phenyl)-4-(4-morpholin-4-ylmethyl-phenyl)-isoxazole-3-carboxylic acid ethylamide, in particular the mesylate, hydrochloride, tartrate, phosphate and hemi fumarate salt thereof; to crystalline forms of such salts; to polymorphs of 5-(2,4-dihydroxy-5-isopropyl-phenyl)-4-(4-morpholin-4-ylmethyl-phenyl)-isoxazole-3-carboxylic acid ethylamide; to hydrates and polymorphs of the new salt forms mentioned above; to the use of the new salt forms mentioned above for the manufacture of a medicament for the treatment of a disorder mediated by Hsp90; to a method for treating a disorder mediated by Hsp90 using the new salt forms; to formulations comprising such salt forms, in particular aqueous solutions suitable for intravenous administration; and to amber glass containers being filled with such formulations.

IPC Classes  ?

  • C07D 413/10 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings

21.

Azetidine derivatives as FAAH inhibitors

      
Application Number 12920181
Grant Number 08450346
Status In Force
Filing Date 2009-02-27
First Publication Date 2012-02-02
Grant Date 2013-05-28
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
Inventor
  • Roughley, Stephen
  • Walls, Steven
  • Hart, Terance
  • Parsons, Rachel
  • Brough, Paul
  • Graham, Christopher
  • Macias, Alba

Abstract

3 is a divalent radical selected from the group consisting of optionally substituted phenylene and optionally substituted monocyclic heteroarylene radicals having 5 or 6 ring atoms.

IPC Classes  ?

  • A61K 31/397 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
  • A61K 31/4427 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems
  • A61K 31/495 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two nitrogen atoms as the only ring hetero atoms, e.g. piperazine
  • C07D 205/00 - Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
  • C07D 213/24 - Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
  • C07D 237/10 - Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms

22.

Triazolo[4,5-D]pyramidine derivatives and their use as purine receptor antagonists

      
Application Number 12997721
Grant Number 08450328
Status In Force
Filing Date 2009-06-25
First Publication Date 2011-07-14
Grant Date 2013-05-28
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
Inventor
  • Bamford, Samantha Jane
  • Gillespie, Roger John
  • Todd, Richard Simon

Abstract

Compounds of formula (I) that are capable of acting as purine receptor antagonists, pharmaceutical compositions including the compounds, and methods of making the compounds, are disclosed. The compounds and compositions can be used in treating or preventing disorders related to purine receptor hyperfunctioning.

IPC Classes  ?

  • A01N 43/90 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
  • A61K 31/519 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
  • C07D 471/00 - Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups

23.

Thienopyrimidine compounds

      
Application Number 12678378
Grant Number 09120807
Status In Force
Filing Date 2008-09-19
First Publication Date 2011-05-19
Grant Date 2015-09-01
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
Inventor
  • Jordan, Allan
  • Bedford, Simon
  • Burkhard, Klenke
  • Yule, Ian
  • Poullennec, Karine

Abstract

6 taken together with the nitrogen atom to which they are attached form an optionally substituted 4- to 6-membered saturated ring.

IPC Classes  ?

  • C07D 495/04 - Ortho-condensed systems
  • A61K 31/519 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings

24.

Acid addition salts, hydrates and polymorphs of 5-(2,4-dihydroxy-5-isopropyl-phenyl)-4-(4-morpholin-4-ylmethyl-phenyl)-isoxazole-3-carboxylic acid ethylamide and formulations comprising these forms

      
Application Number 12529090
Grant Number 08163747
Status In Force
Filing Date 2008-02-28
First Publication Date 2010-04-15
Grant Date 2012-04-24
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
Inventor
  • Drysdale, Martin James
  • Dymock, Brian William
  • Krell, Christoph
  • Mutz, Michael
  • Petersen, Holger
  • Zheng, Weijia

Abstract

The present invention relates to new salt forms of 5-(2,4-dihydroxy-5-isopropyl-phenyl)-4-(4-morpholin-4-ylmethyl-phenyl)-isoxazole-3-carboxylic acid ethylamide, in particular the mesylate, hydrochloride, tartrate, phosphate and hemi fumarate salt thereof; to crystalline forms of such salts; to polymorphs of 5-(2,4-dihydroxy-5-isopropyl-phenyl)-4-(4-morpholin-4-ylmethyl-phenyl)-isoxazole-3-carboxylic acid ethylamide; to hydrates and polymorphs of the new salt forms mentioned above; to the use of the new salt forms mentioned above for the manufacture of a medicament for the treatment of a disorder mediated by Hsp90; to a method for treating a disorder mediated by Hsp90 using the new salt forms; to formulations comprising such salt forms, in particular aqueous solutions suitable for intravenous administration; and to amber glass containers being filled with such formulations.

IPC Classes  ?

  • A61K 31/535 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and at least one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
  • C07D 413/10 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings

25.

2-amino-7,8-dihydro-6H-pyrido[4,3-d]pyrimidin-5-ones

      
Application Number 11541462
Grant Number 07671059
Status In Force
Filing Date 2006-09-28
First Publication Date 2007-05-31
Grant Date 2010-03-02
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
Inventor
  • Machajewski, Timothy D.
  • Shafer, Cynthia M.
  • Mcbride, Christopher
  • Antonios-Mccrea, William
  • Doughan, Brandon M.
  • Levine, Barry H.
  • Xia, Yi
  • Mckenna, Maureen
  • Wang, X. Michael
  • Mendenhall, Kris
  • Zhou, Yasheen
  • Brinner, Kristin
  • Gao, Zhenhai
  • Poon, Daniel
  • Barsanti, Paul
  • Lin, Xiaodong
  • Costales, Abran
  • Rico, Alice
  • Brammeier, Nathan
  • Pick, Teresa
  • Renhowe, Paul A.

Abstract

Disclosed are 2-amino-7,8-dihydro-6H-pyrido[4,3-d]pyrimidin-5-one compounds, their stereoisomers, tautomers, pharmaceutically acceptable salts, and prodrugs thereof; compositions that include a pharmaceutically acceptable carrier and one or more of the 2-amino-7,8-dihydro-6H-pyrido[4,3-d]pyrimidin-5-one compounds, either alone or in combination with at least one additional therapeutic agent. Disclosed also are methods of using the 2-amino-7,8-dihydro-6H-pyrido[4,3-d]pyrimidin-5-one compounds, either alone or in combination with at least one additional therapeutic agent, in the prophylaxis or treatment of cellular proliferative, viral, autoimmune, cardiovascular, and central nervous system diseases.

IPC Classes  ?

  • A61K 31/519 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
  • A61K 31/5355 - Non-condensed oxazines containing further heterocyclic rings
  • C07D 471/04 - Ortho-condensed systems
  • C07D 487/04 - Ortho-condensed systems
  • C07D 413/06 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
  • A61P 35/00 - Antineoplastic agents

26.

FROVA

      
Application Number 133372500
Status Registered
Filing Date 2007-01-23
Registration Date 2008-01-25
Owner Ligand UK Development Limited (United Kingdom)
NICE Classes  ? 05 - Pharmaceutical, veterinary and sanitary products

Goods & Services

(1) Pharmaceutical preparations for the treatment of headaches.

27.

FROVA

      
Application Number 132573400
Status Registered
Filing Date 2006-11-20
Registration Date 2008-07-08
Owner Ligand UK Development Limited (United Kingdom)
NICE Classes  ?
  • 05 - Pharmaceutical, veterinary and sanitary products
  • 16 - Paper, cardboard and goods made from these materials

Goods & Services

(1) Pharmaceutical preparations, namely, analgesics. (2) Printed educational materials on the subject of pain medications and pain management.

28.

FROVA

      
Serial Number 76668676
Status Registered
Filing Date 2006-11-07
Registration Date 2007-08-21
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
NICE Classes  ?
  • 05 - Pharmaceutical, veterinary and sanitary products
  • 16 - Paper, cardboard and goods made from these materials

Goods & Services

Pharmaceutical preparations, namely analgesics Printed educational materials on the subject of pain medications and pain management

29.

FROVA

      
Serial Number 78017693
Status Registered
Filing Date 2000-07-20
Registration Date 2004-03-30
Owner LIGAND UK DEVELOPMENT LIMITED (United Kingdom)
NICE Classes  ? 05 - Pharmaceutical, veterinary and sanitary products

Goods & Services

Pharmaceutical preparations for the treatment of headaches

30.

MIGARD

      
Application Number 687878
Status Registered
Filing Date 1997-12-24
Registration Date 1997-12-24
Owner Ligand UK Development Limited (United Kingdom)
NICE Classes  ? 05 - Pharmaceutical, veterinary and sanitary products

Goods & Services

Pharmaceutical preparations and substances; pharmaceutical preparations and substances for the treatment of migraine, cluster headache and tension headache.

31.

MIGARD

      
Application Number 000694299
Status Registered
Filing Date 1997-11-25
Registration Date 1999-04-06
Owner Ligand UK Development Limited (United Kingdom)
NICE Classes  ? 05 - Pharmaceutical, veterinary and sanitary products

Goods & Services

Pharmaceutical preparations and substances; pharmaceutical preparations and substances for the treatment of migraine, cluster headache and tension headache.