Taro Pharmaceuticals Inc.

Canada

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IPC Class
C07D 231/54 - Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems 6
A61P 29/00 - Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agentsNon-steroidal antiinflammatory drugs [NSAID] 5
C07D 401/08 - 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 carbon chain containing alicyclic rings 4
C07D 493/10 - Spiro-condensed systems 4
C07C 233/23 - Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a ring other than a six-membered aromatic ring 3
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Status
Pending 3
Registered / In Force 17

1.

TARO COMPLETE

      
Application Number 230987600
Status Pending
Filing Date 2024-02-09
Owner Taro Pharmaceuticals, Inc. (Canada)
NICE Classes  ? 05 - Pharmaceutical, veterinary and sanitary products

Goods & Services

(1) Analgesics; antacids; anti-cancer preparations; antibiotics; anticoagulants; anticonvulsants; antidepressants; antidiabetic preparations; antifungal preparations; antihypertensives; antiseptic preparations; antivirals; calcium channel blockers; corticosteroids; laxatives; nausea treatment preparations; pharmaceutical preparations for controlling cholesterol; pharmaceutical preparations for maintaining normal blood pressure and heart function; pharmaceutical preparations for reducing cholesterol; pharmaceutical preparations for the prevention and treatment of cancer; pharmaceutical preparations for the prevention and treatment of iron deficiency and anemia in humans; pharmaceutical preparations for the prevention and treatment of metabolic diseases and disorders, namely diabetes, gout, arthritis and anemia; pharmaceutical preparations for the treatment and prevention of migraines, headaches and pain; pharmaceutical preparations for the treatment of blood disorders; pharmaceutical preparations for the treatment of dermatological conditions being acne, rosacea, ichthyosis, vitiligo, urticaria and alopecia areata; pharmaceutical preparations for the treatment of dermatological diseases and disorders namely dermatitis, skin and bacterial skin infections and fungal skin infections.; pharmaceutical preparations for the treatment of digestive diseases and disorders, namely, ulcerative colitis; pharmaceutical preparations for the treatment of erectile dysfunction; pharmaceutical preparations for the treatment of gastro-intestinal diseases; pharmaceutical preparations for the treatment of inflammatory muscle diseases and disorders; pharmaceutical preparations for the treatment of muscle spasms, tremors and pain; pharmaceutical preparations for the treatment of musculoskeletal diseases, disorders and injuries namely connective tissue diseases, bone diseases and osteoporosis; pharmaceutical preparations for the treatment of smoking cessation; pharmaceutical preparations for the treatment of the central nervous system, namely, central nervous system infections, brain diseases, central nervous system movement disorders, ocular motility disorders, spinal cord diseases; pharmaceutical preparations for treating allergic rhinitis and asthma; pharmaceutical preparations for treating malignant tumors; pharmaceutical preparations for use in chemotherapy; pharmaceutical preparations namely, anti-inflammatories; psychiatric pharmaceutical preparations for the prevention and treatment of mood disorders, anxiety disorders, cognitive disorders, and schizophrenia; steroids; tumor suppressing agents

2.

TARO COMPLETE

      
Application Number 230709200
Status Registered
Filing Date 2024-01-26
Registration Date 2025-06-27
Owner Taro Pharmaceuticals, Inc. (Canada)
NICE Classes  ? 05 - Pharmaceutical, veterinary and sanitary products

Goods & Services

(1) Analgesics; antacids; anti-cancer preparations; antibiotics; anticoagulants; anticonvulsants; antidepressants; antidiabetic preparations; antifungal preparations; antihypertensives; antiseptic preparations; antivirals; calcium channel blockers; corticosteroids; laxatives; nausea treatment preparations; pharmaceutical preparations for controlling cholesterol; pharmaceutical preparations for maintaining normal blood pressure and heart function; pharmaceutical preparations for reducing cholesterol; pharmaceutical preparations for the prevention and treatment of cancer; pharmaceutical preparations for the prevention and treatment of iron deficiency and anemia in humans; pharmaceutical preparations for the prevention and treatment of metabolic diseases and disorders, namely diabetes, gout, arthritis and anemia; pharmaceutical preparations for the treatment and prevention of migraines, headaches and pain; pharmaceutical preparations for the treatment of blood disorders; pharmaceutical preparations for the treatment of dermatological conditions being acne, rosacea, ichthyosis, vitiligo, urticaria and alopecia areata; pharmaceutical preparations for the treatment of dermatological diseases and disorders namely dermatitis, skin and bacterial skin infections and fungal skin infections.; pharmaceutical preparations for the treatment of digestive diseases and disorders, namely, ulcerative colitis; pharmaceutical preparations for the treatment of erectile dysfunction; pharmaceutical preparations for the treatment of gastro-intestinal diseases; pharmaceutical preparations for the treatment of inflammatory muscle diseases and disorders; pharmaceutical preparations for the treatment of muscle spasms, tremors and pain; pharmaceutical preparations for the treatment of musculoskeletal diseases, disorders and injuries namely connective tissue diseases, bone diseases and osteoporosis; pharmaceutical preparations for the treatment of smoking cessation; pharmaceutical preparations for the treatment of the central nervous system, namely, central nervous system infections, brain diseases, central nervous system movement disorders, ocular motility disorders, spinal cord diseases; pharmaceutical preparations for treating allergic rhinitis and asthma; pharmaceutical preparations for treating malignant tumors; pharmaceutical preparations for use in chemotherapy; pharmaceutical preparations namely, anti-inflammatories; psychiatric pharmaceutical preparations for the prevention and treatment of mood disorders, anxiety disorders, cognitive disorders, and schizophrenia; steroids; tumor suppressing agents

3.

INDENE DERIVATIVES USEFUL IN TREATING PAIN AND INFLAMMATION

      
Application Number 18236207
Status Pending
Filing Date 2023-08-21
First Publication Date 2023-12-07
Owner TARO PHARMACEUTICALS INC. (Canada)
Inventor
  • Harwig, Curtis
  • Pettigrew, Jeremy D.
  • Cross, Jennifer
  • Seenisamy, Jeyaprakashnarayanan
  • Keregadde, Mahesh Narayan
  • Iyanar, Karthikeyan

Abstract

Compounds of formula (I): wherein, R1, R2, R3, R4a, R4b and R5 are described herein, or a stereoisomer, enantiomer or tautomer thereof or mixtures thereof, or a pharmaceutically acceptable salt or solvate thereof, are described herein, as well as other compounds. These compounds are useful in treating inflammation and/or pain. Compositions comprising a compound of the invention are also disclosed, as are methods of using the compounds to treat inflammation and/or pain.

IPC Classes  ?

  • C07D 493/10 - Spiro-condensed systems
  • A61P 29/00 - Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agentsNon-steroidal antiinflammatory drugs [NSAID]
  • C07D 231/54 - Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
  • C07D 401/08 - 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 carbon chain containing alicyclic rings
  • C07D 403/08 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a carbon chain containing alicyclic rings
  • C07D 417/08 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a carbon chain containing alicyclic rings

4.

TARO

      
Application Number 229546300
Status Pending
Filing Date 2023-11-28
Owner Taro Pharmaceuticals, Inc. (Canada)
NICE Classes  ? 05 - Pharmaceutical, veterinary and sanitary products

Goods & Services

(1) Analgesics; antacids; anti-cancer preparations; antibiotics; anticoagulants; anticonvulsants; antidepressants; antidiabetic preparations; antifungal preparations; antihypertensives; antiseptic preparations; antivirals; calcium channel blockers; corticosteroids; laxatives; nausea treatment preparations; pharmaceutical preparations for controlling cholesterol; pharmaceutical preparations for maintaining normal blood pressure and heart function; pharmaceutical preparations for reducing cholesterol; pharmaceutical preparations for the prevention and treatment of cancer; pharmaceutical preparations for the prevention and treatment of iron deficiency and anemia in humans; pharmaceutical preparations for the prevention and treatment of metabolic diseases and disorders, namely diabetes, gout, arthritis and anemia; pharmaceutical preparations for the treatment and prevention of migraines, headaches and pain; pharmaceutical preparations for the treatment of blood disorders; pharmaceutical preparations for the treatment of dermatological conditions being acne, rosacea, ichthyosis, vitiligo, urticaria and alopecia areata; pharmaceutical preparations for the treatment of dermatological diseases and disorders namely dermatitis, skin and bacterial skin infections and fungal skin infections.; pharmaceutical preparations for the treatment of digestive diseases and disorders, namely, ulcerative colitis; pharmaceutical preparations for the treatment of erectile dysfunction; pharmaceutical preparations for the treatment of gastro-intestinal diseases; pharmaceutical preparations for the treatment of inflammatory muscle diseases and disorders; pharmaceutical preparations for the treatment of muscle spasms, tremors and pain; pharmaceutical preparations for the treatment of musculoskeletal diseases, disorders and injuries namely connective tissue diseases, bone diseases and osteoporosis; pharmaceutical preparations for the treatment of smoking cessation; pharmaceutical preparations for the treatment of the central nervous system, namely, central nervous system infections, brain diseases, central nervous system movement disorders, ocular motility disorders, spinal cord diseases; pharmaceutical preparations for treating allergic rhinitis and asthma; pharmaceutical preparations for treating malignant tumors; pharmaceutical preparations for use in chemotherapy; pharmaceutical preparations namely, anti-inflammatories; psychiatric pharmaceutical preparations for the prevention and treatment of mood disorders, anxiety disorders, cognitive disorders, and schizophrenia; steroids; tumor suppressing agents

5.

Indene derivatives useful in treating pain and inflammation

      
Application Number 17751035
Grant Number 11773108
Status In Force
Filing Date 2022-05-23
First Publication Date 2022-09-29
Grant Date 2023-10-03
Owner Taro Pharmaceuticals Inc. (Canada)
Inventor
  • Harwig, Curtis
  • Pettigrew, Jeremy D.
  • Cross, Jennifer
  • Seenisamy, Jeyaprakashnarayanan
  • Keregadde, Mahesh Narayan
  • Iyanar, Karthikeyan

Abstract

5 are described herein, or a stereoisomer, enantiomer or tautomer thereof or mixtures thereof, or a pharmaceutically acceptable salt or solvate thereof, are described herein, as well as other compounds. These compounds are useful in treating inflammation and/or pain. Compositions comprising a compound of the invention are also disclosed, as are methods of using the compounds to treat inflammation and/or pain.

IPC Classes  ?

  • C07D 493/10 - Spiro-condensed systems
  • C07D 231/54 - Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
  • C07D 401/08 - 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 carbon chain containing alicyclic rings
  • C07D 403/08 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a carbon chain containing alicyclic rings
  • C07D 417/08 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a carbon chain containing alicyclic rings
  • A61P 29/00 - Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agentsNon-steroidal antiinflammatory drugs [NSAID]

6.

Indene derivatives useful in treating pain and inflammation

      
Application Number 17045626
Grant Number 11420962
Status In Force
Filing Date 2019-04-05
First Publication Date 2021-05-27
Grant Date 2022-08-23
Owner TARO PHARMACEUTICALS INC. (Canada)
Inventor
  • Harwig, Curtis
  • Pettigrew, Jeremy D.
  • Cross, Jennifer
  • Seenisamy, Jeyaprakashnarayanan
  • Keregadde, Mahesh Narayan
  • Kher, Samir Satish

Abstract

5 are described herein, or a stereoisomer, enantiomer or tautomer thereof or mixtures thereof, or a pharmaceutically acceptable salt or solvate thereof, are described herein, as well as other compounds. These compounds are useful in treating inflammation and/or pain. Compositions comprising a compound of the invention are also disclosed, as are methods of using the compounds to treat inflammation and/or pain.

IPC Classes  ?

  • C07D 263/56 - BenzoxazolesHydrogenated benzoxazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
  • C07D 231/54 - Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
  • C07D 239/74 - QuinazolinesHydrogenated quinazolines with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached to ring carbon atoms of the hetero ring
  • C07D 241/42 - Benzopyrazines with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
  • C07D 261/20 - Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings condensed with carbocyclic rings or ring systems
  • C07D 209/08 - IndolesHydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
  • C07D 277/64 - Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2
  • C07D 285/14 - ThiadiazolesHydrogenated thiadiazoles condensed with carbocyclic rings or ring 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
  • A61P 29/00 - Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agentsNon-steroidal antiinflammatory drugs [NSAID]
  • 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
  • C07D 239/84 - Nitrogen atoms
  • C07D 401/08 - 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 carbon chain containing alicyclic rings
  • C07D 403/04 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings directly linked by a ring-member-to-ring- member bond
  • C07D 403/08 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a carbon chain containing alicyclic rings
  • 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

7.

Indene derivatives useful in treating pain and inflammation

      
Application Number 17045675
Grant Number 11352367
Status In Force
Filing Date 2019-04-05
First Publication Date 2021-02-04
Grant Date 2022-06-07
Owner TARO PHARMACEUTICALS INC. (Canada)
Inventor
  • Harwig, Curtis
  • Pettigrew, Jeremy D.
  • Cross, Jennifer
  • Seenisamy, Jeyaprakashnarayanan
  • Keregadde, Mahesh Narayan
  • Iyanar, Karthikeyan

Abstract

5 are described herein, or a stereoisomer, enantiomer or tautomer thereof or mixtures thereof, or a pharmaceutically acceptable salt or solvate thereof, are described herein, as well as other compounds. These compounds are useful in treating inflammation and/or pain. Compositions comprising a compound of the invention are also disclosed, as are methods of using the compounds to treat inflammation and/or pain.

IPC Classes  ?

  • C07D 493/10 - Spiro-condensed systems
  • C07D 231/54 - Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
  • C07D 401/08 - 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 carbon chain containing alicyclic rings
  • C07D 403/08 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a carbon chain containing alicyclic rings
  • C07D 417/08 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a carbon chain containing alicyclic rings
  • A61P 29/00 - Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agentsNon-steroidal antiinflammatory drugs [NSAID]

8.

SHIP1 modulators and methods related thereto

      
Application Number 15676726
Grant Number 10174046
Status In Force
Filing Date 2017-08-14
First Publication Date 2018-06-07
Grant Date 2019-01-08
Owner TARO PHARMACEUTICALS INC. (Canada)
Inventor
  • Mackenzie, Lloyd F.
  • Macrury, Thomas B.
  • Harwig, Curtis
  • Bogucki, David
  • Raymond, Jeffery R.
  • Pettigrew, Jeremy D.

Abstract

Compounds of formula (II): wherein 13 are described herein, or a stereoisomer, enantiomer or tautomer thereof or mixtures thereof, or a pharmaceutically acceptable salt or solvate thereof, are described herein, as well as other compounds. These compounds have activity as SHIP1 modulators, and thus may be useful in treating a variety of diseases, disorders or conditions that would benefit from SHIP1 modulation. Compositions comprising a compound of the invention are also disclosed, as are methods of SHIP1 modulation by administration of such compounds to an animal in need thereof.

IPC Classes  ?

  • C07D 493/10 - Spiro-condensed systems
  • A61K 31/416 - 1,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
  • C07D 213/75 - Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
  • C07D 213/82 - AmidesImides in position 3
  • C07D 215/227 - Oxygen atoms attached in position 2 or 4 only one oxygen atom which is attached in position 2
  • C07C 275/22 - Derivatives of urea, i.e. compounds containing any of the groups the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing rings other than six-membered aromatic rings
  • C07D 221/18 - Ring systems of four or more rings
  • C07D 231/54 - Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
  • C07C 215/26 - Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated and containing rings other than six-membered aromatic rings
  • C07C 215/38 - Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated and containing six-membered aromatic rings with rings other than six-membered aromatic rings being part of the carbon skeleton
  • C07C 335/10 - Derivatives of thiourea having nitrogen atoms of thiourea groups bound to acyclic carbon atoms of an unsaturated carbon skeleton
  • C07C 233/23 - Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a ring other than a six-membered aromatic ring
  • C07D 261/20 - Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings condensed with carbocyclic rings or ring systems
  • C07D 277/24 - Radicals substituted by oxygen atoms
  • C07D 277/28 - Radicals substituted by nitrogen atoms
  • C07C 255/30 - Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the same unsaturated acyclic carbon skeleton
  • C07D 211/58 - Nitrogen atoms attached in position 4
  • C07D 213/30 - Oxygen atoms
  • C07D 307/42 - Singly bound oxygen atoms
  • C07D 333/16 - Radicals substituted by singly bound hetero atoms other than halogen by oxygen atoms
  • C07D 231/56 - BenzopyrazolesHydrogenated benzopyrazoles
  • C07D 277/64 - Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2
  • C07C 35/21 - Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring polycyclic, at least one hydroxy group bound to a non-condensed ring
  • C07C 35/23 - Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring polycyclic, at least one hydroxy group bound to a condensed ring system with a hydroxy group on a condensed ring system having two rings
  • C07D 213/38 - Radicals substituted by singly-bound nitrogen atoms having only hydrogen or hydrocarbon radicals attached to the substituent nitrogen atom
  • C07D 221/16 - Ring systems of three rings containing carbocyclic rings other than six-membered
  • C07D 307/52 - Radicals substituted by nitrogen atoms not forming part of a nitro radical
  • C07D 333/20 - Radicals substituted by singly bound hetero atoms other than halogen by nitrogen atoms

9.

Crystalline solid forms of the acetate salt of (1S,3S,4R)-4-((3AS,4R,5S,7AS)-4-(aminomethyl)-7A-methyl-1-methyleneoctahydro-1H-inden-5-YL)-3- (hydroxymethyl)-4-methylcyclohexanol

      
Application Number 15885387
Grant Number 10065920
Status In Force
Filing Date 2018-01-31
First Publication Date 2018-06-07
Grant Date 2018-09-04
Owner TARO PHARMACEUTICALS INC. (Canada)
Inventor
  • Mackenzie, Lloyd F.
  • Raymond, Jeffery R.
  • Harwig, Curtis
  • Fernandez Casares, Ana

Abstract

The present invention is generally directed to novel crystalline forms of the acetate salt of (1S,3S,4R)-4-((3aS,4R,5S,7aS)-4-(aminomethyl)-7a-methyl-1-methyleneoctahydro-1H-inden-5-yl)-3-(hydroxymethyl)-4-methylcyclohexanol and processes for their preparation.

IPC Classes  ?

  • C07C 215/42 - Compounds containing amino and hydroxy groups bound to the same carbon skeleton having amino groups or hydroxy groups bound to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton

10.

Synthesis of a substituted indene derivative

      
Application Number 15411863
Grant Number 10053415
Status In Force
Filing Date 2017-01-20
First Publication Date 2018-03-29
Grant Date 2018-08-21
Owner TARO PHARMACEUTICALS INC. (Canada)
Inventor
  • Harwig, Curtis
  • Seenisamy, Jeyaprakashnarayanan
  • Keregadde, Mahesh Narayan
  • Chetia, Lakshindra

Abstract

This invention is directed to methods of preparing AQX-1125 having the formula: This invention is also directed to intermediates utilized in the methods of preparing AQX-1125.

IPC Classes  ?

  • C07C 209/30 - Preparation of compounds containing amino groups bound to a carbon skeleton by reduction of nitrogen-to-oxygen or nitrogen-to-nitrogen bonds

11.

SHIP1 modulators and methods related thereto

      
Application Number 14772737
Grant Number 10100056
Status In Force
Filing Date 2014-02-27
First Publication Date 2017-09-07
Grant Date 2018-10-16
Owner TARO PHARMACEUTICALS INC. (Canada)
Inventor
  • Mackenzie, Lloyd F.
  • Harwig, Curtis
  • Bogucki, David
  • Raymond, Jeffery R.
  • Pettigrew, Jeremy D.

Abstract

7 are defined herein, or stereoisomers or pharmaceutically acceptable salts thereof, are described herein. Such compounds have activity as SHIP1 modulators, and thus may be used to treat any of a variety of diseases, disorders or conditions that would benefit from SHIP1 modulation. Compositions comprising a compound of formula (I) in combination with a pharmaceutically acceptable carrier or diluent are also disclosed, as are methods of SHIP1 modulation by administration of such compounds to an animal in need thereof.

IPC Classes  ?

  • C07D 473/34 - Nitrogen atom attached in position 6, e.g. adenine
  • C07D 207/335 - Radicals substituted by nitrogen atoms not forming part of a nitro radical
  • C07D 207/06 - Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with radicals, containing only hydrogen and carbon atoms, attached to ring carbon atoms
  • C07D 213/38 - Radicals substituted by singly-bound nitrogen atoms having only hydrogen or hydrocarbon radicals attached to the substituent nitrogen atom
  • C07D 231/12 - Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
  • C07D 249/08 - 1,2,4-TriazolesHydrogenated 1,2,4-triazoles
  • C07D 233/60 - Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms with hydrocarbon radicals, substituted by oxygen or sulfur atoms, attached to ring nitrogen atoms
  • C07D 209/08 - IndolesHydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
  • C07D 317/46 - Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
  • C07D 295/096 - Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
  • C07D 213/64 - One oxygen atom attached in position 2 or 6
  • C07D 239/34 - One oxygen atom
  • C07D 241/18 - Oxygen or sulfur atoms
  • C07C 279/08 - Derivatives of guanidine, i.e. compounds containing the group the singly-bound nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of guanidine groups bound to acyclic carbon atoms of a carbon skeleton being further substituted by singly-bound oxygen atoms
  • C07C 215/42 - Compounds containing amino and hydroxy groups bound to the same carbon skeleton having amino groups or hydroxy groups bound to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
  • C07C 233/23 - Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a ring other than a six-membered aromatic ring
  • C07C 311/04 - Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms to acyclic carbon atoms of hydrocarbon radicals substituted by singly-bound oxygen atoms
  • C07C 225/10 - Compounds containing amino groups and doubly-bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly-bound oxygen atoms not being part of a —CHO group, e.g. amino ketones having amino groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being saturated and containing rings with doubly-bound oxygen atoms bound to carbon atoms not being part of rings
  • C07C 233/74 - Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a ring other than a six-membered aromatic ring
  • C07C 255/31 - Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing rings other than six-membered aromatic rings
  • C07C 275/24 - Derivatives of urea, i.e. compounds containing any of the groups the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing six-membered aromatic rings

12.

SHIP1 modulators and methods related thereto

      
Application Number 14772731
Grant Number 09765085
Status In Force
Filing Date 2014-02-27
First Publication Date 2017-08-31
Grant Date 2017-09-19
Owner TARO PHARMACEUTICALS INC. (Canada)
Inventor
  • Mackenzie, Lloyd F.
  • Macrury, Thomas B.
  • Harwig, Curtis
  • Bogucki, David
  • Raymond, Jeffery R.
  • Pettigrew, Jeremy D.

Abstract

13 are described herein, or a stereoisomer, enantiomer or tautomer thereof or mixtures thereof, or a pharmaceutically acceptable salt or solvate thereof, are described herein, as well as other compounds. These compounds have activity as SHIP1 modulators, and thus may be useful in treating a variety of diseases, disorders or conditions that would benefit from SHIP1 modulation. Compositions comprising a compound of the invention are also disclosed, as are methods of SHIP1 modulation by administration of such compounds to an animal in need thereof.

IPC Classes  ?

  • C07D 231/54 - Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
  • A61K 31/416 - 1,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
  • C07D 493/10 - Spiro-condensed systems
  • C07D 213/75 - Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
  • C07D 213/82 - AmidesImides in position 3
  • C07D 215/227 - Oxygen atoms attached in position 2 or 4 only one oxygen atom which is attached in position 2
  • C07C 275/22 - Derivatives of urea, i.e. compounds containing any of the groups the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing rings other than six-membered aromatic rings
  • C07D 221/18 - Ring systems of four or more rings
  • C07C 215/26 - Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated and containing rings other than six-membered aromatic rings
  • C07C 215/38 - Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated and containing six-membered aromatic rings with rings other than six-membered aromatic rings being part of the carbon skeleton
  • C07C 335/10 - Derivatives of thiourea having nitrogen atoms of thiourea groups bound to acyclic carbon atoms of an unsaturated carbon skeleton
  • C07C 233/23 - Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a ring other than a six-membered aromatic ring
  • C07D 261/20 - Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings condensed with carbocyclic rings or ring systems
  • C07D 277/24 - Radicals substituted by oxygen atoms
  • C07D 277/28 - Radicals substituted by nitrogen atoms
  • C07C 255/30 - Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the same unsaturated acyclic carbon skeleton
  • C07D 211/58 - Nitrogen atoms attached in position 4
  • C07D 213/30 - Oxygen atoms
  • C07D 307/42 - Singly bound oxygen atoms
  • C07D 333/16 - Radicals substituted by singly bound hetero atoms other than halogen by oxygen atoms
  • C07D 231/56 - BenzopyrazolesHydrogenated benzopyrazoles
  • C07D 277/64 - Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2
  • C07C 35/21 - Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring polycyclic, at least one hydroxy group bound to a non-condensed ring
  • C07C 35/23 - Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring polycyclic, at least one hydroxy group bound to a condensed ring system with a hydroxy group on a condensed ring system having two rings
  • C07D 213/38 - Radicals substituted by singly-bound nitrogen atoms having only hydrogen or hydrocarbon radicals attached to the substituent nitrogen atom
  • C07D 221/16 - Ring systems of three rings containing carbocyclic rings other than six-membered
  • C07D 307/52 - Radicals substituted by nitrogen atoms not forming part of a nitro radical
  • C07D 333/20 - Radicals substituted by singly bound hetero atoms other than halogen by nitrogen atoms

13.

Crystalline solid forms of the acetate salt of (1S,3S,4R)-4-((3aS,4R,5S,7aS)-4-(aminomethyl)-7a-methyl-1-methyleneoctahydro-1H-inden-5-yl)-3-(hydroxymethyl)-4-methylcyclohexanol

      
Application Number 15191134
Grant Number 09944590
Status In Force
Filing Date 2016-06-23
First Publication Date 2016-12-29
Grant Date 2018-04-17
Owner TARO PHARMACEUTICALS INC. (Canada)
Inventor
  • Mackenzie, Lloyd F.
  • Raymond, Jeffery R.
  • Harwig, Curtis
  • Fernandez Casares, Ana

Abstract

The present invention is generally directed to novel crystalline forms of the acetate salt of (1S,3S,4R)-4-((3aS,4R,5S,7aS)-4-(aminomethyl)-7a-methyl-1-methyleneoctahydro-1H-inden-5-yl)-3-(hydroxymethyl)-4-methylcyclohexanol and processes for their preparation.

IPC Classes  ?

  • C07C 215/42 - Compounds containing amino and hydroxy groups bound to the same carbon skeleton having amino groups or hydroxy groups bound to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton

14.

Process for preparing a crystalline form of halobetasol propionate

      
Application Number 13735428
Grant Number 09365609
Status In Force
Filing Date 2013-01-07
First Publication Date 2013-08-22
Grant Date 2016-06-14
Owner TARO PHARMACEUTICALS INC. (Canada)
Inventor
  • Gutman, Daniella
  • Chernyak, Shimon

Abstract

The present invention provides a process for preparing a crystalline form of halobetasol propionate, comprising the step of crystallizing halobetasol propionate from absolute ethanol or a mixture of ethanol and water, wherein the crystalline form of halobetasol propionate is characterized by an x-ray powder diffraction pattern having peaks at 10.0, 11.6, 12.9, 13.4, 14.5, 16.4, 17.6, and 23.5±0.2 degrees 2θ.

IPC Classes  ?

  • A61K 31/56 - Compounds containing cyclopenta[a]hydrophenanthrene ring systemsDerivatives thereof, e.g. steroids
  • C07J 5/00 - Normal steroids containing carbon, hydrogen, halogen, or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane, and substituted in position 21 by only one singly bound oxygen atom
  • C07J 7/00 - Normal steroids containing carbon, hydrogen, halogen, or oxygen, substituted in position 17 beta by a chain of two carbon atoms

15.

Stable liquid desoximethasone compositions with reduced oxidized impurity

      
Application Number 13605622
Grant Number 08715624
Status In Force
Filing Date 2012-09-06
First Publication Date 2012-12-27
Grant Date 2014-05-06
Owner TARO PHARMACEUTICALS INC. (Canada)
Inventor
  • Rao, Srinivasa
  • Dixit, Suresh
  • Yacobi, Avraham
  • Bailey, Arthur

Abstract

4 alcohol; and d) a stabilizing agent selected from the group consisting of an oleaginous vehicle and a propellant, wherein the stabilizing agent is in an amount sufficient to reduce the formation of less than about 1 wt % 17-carboxy-9α-fluoro-11β-hydroxy-16α-methyl-androsta-1,4-diene-3-one under an accelerated storage condition.

IPC Classes  ?

  • A61K 9/08 - Solutions
  • A61K 31/573 - Compounds containing cyclopenta[a]hydrophenanthrene ring systemsDerivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone substituted in position 21, e.g. cortisone, dexamethasone, prednisone or aldosterone
  • A61K 9/12 - AerosolsFoams
  • A61K 9/14 - Particulate form, e.g. powders

16.

Oral suspension of prednisolone acetate

      
Application Number 13483273
Grant Number 08461139
Status In Force
Filing Date 2012-05-30
First Publication Date 2012-09-20
Grant Date 2013-06-11
Owner TARO PHARMACEUTICALS INC. (Canada)
Inventor
  • Asotra, Satish
  • Gao, Shen
  • Yacobi, Avraham

Abstract

The present invention relates to novel oral suspension formulation comprising prednisolone acetate, a pharmaceutically acceptable vehicle and a thickening agent. The present invention further provides a method of treating patients in need of prednisolone with the novel formulation.

IPC Classes  ?

  • A61K 31/537 - 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 spiro-condensed or forming part of bridged ring systems
  • A61P 5/00 - Drugs for disorders of the endocrine system
  • A61P 29/00 - Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agentsNon-steroidal antiinflammatory drugs [NSAID]
  • A61P 17/00 - Drugs for dermatological disorders
  • A61P 25/00 - Drugs for disorders of the nervous system
  • A61P 1/00 - Drugs for disorders of the alimentary tract or the digestive system
  • A61P 7/00 - Drugs for disorders of the blood or the extracellular fluid
  • A61P 35/00 - Antineoplastic agents
  • A61P 7/10 - Antioedematous agentsDiuretics
  • A61P 37/08 - Antiallergic agents
  • C07J 5/00 - Normal steroids containing carbon, hydrogen, halogen, or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane, and substituted in position 21 by only one singly bound oxygen atom

17.

Oral suspension of prednisolone acetate

      
Application Number 12870144
Grant Number 08206727
Status In Force
Filing Date 2010-08-27
First Publication Date 2010-12-23
Grant Date 2012-06-26
Owner TARO PHARMACEUTICALS INC. (Canada)
Inventor
  • Asotra, Satish
  • Gao, Shen
  • Yacobi, Avraham

Abstract

The present invention relates to novel oral suspension formulation comprising prednisolone acetate, a pharmaceutically acceptable vehicle and a thickening agent. The present invention further provides a method of treating patients in need of prednisolone with the novel formulation.

IPC Classes  ?

  • A61K 31/573 - Compounds containing cyclopenta[a]hydrophenanthrene ring systemsDerivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone substituted in position 21, e.g. cortisone, dexamethasone, prednisone or aldosterone
  • A61P 11/00 - Drugs for disorders of the respiratory system
  • A61P 5/00 - Drugs for disorders of the endocrine system
  • A61P 17/00 - Drugs for dermatological disorders
  • A61P 35/00 - Antineoplastic agents

18.

Stable liquid desoximethasone compositions with reduced oxidized impurity

      
Application Number 11921106
Grant Number 08277780
Status In Force
Filing Date 2006-05-26
First Publication Date 2009-04-23
Grant Date 2012-10-02
Owner TARO PHARMACEUTICALS INC. (Canada)
Inventor
  • Rao, Srinivasa
  • Dixit, Suresh
  • Yacobi, Avraham
  • Bailey, Arthur

Abstract

4 alcohol; and d) a stabilizing agent selected from the group consisting of an oleaginous vehicle and a propellant, wherein the stabilizing agent is in an amount sufficient to reduce the formation of less than about 1 wt % 17-carboxy-9α-fluoro-11β-hydroxy-16a-methyl-androsta-1,4-diene-3-one under an accelerated storage condition.

IPC Classes  ?

  • A61K 9/12 - AerosolsFoams
  • A61K 8/02 - Cosmetics or similar toiletry preparations characterised by special physical form

19.

Oral suspension of prednisolone acetate

      
Application Number 11457197
Grant Number 07799331
Status In Force
Filing Date 2006-07-13
First Publication Date 2007-02-08
Grant Date 2010-09-21
Owner TARO PHARMACEUTICALS INC. (Canada)
Inventor
  • Asotra, Satish
  • Gao, Shen
  • Yacobi, Avraham

Abstract

The present invention relates to novel oral suspension formulation comprising prednisolone acetate, a pharmaceutically acceptable vehicle and a thickening agent. The present invention further provides a method of treating patients in need of prednisolone with the novel formulation.

IPC Classes  ?

  • A61K 31/57 - Compounds containing cyclopenta[a]hydrophenanthrene ring systemsDerivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone
  • A61K 9/00 - Medicinal preparations characterised by special physical form
  • A61K 9/14 - Particulate form, e.g. powders

20.

Indene derivatives as pharmaceutical agents

      
Application Number 10825084
Grant Number 07601874
Status In Force
Filing Date 2004-04-15
First Publication Date 2005-01-06
Grant Date 2009-10-13
Owner TARO PHARMACEUTICALS INC. (Canada)
Inventor
  • Raymond, Jeffery R
  • Han, Kang
  • Zhou, Yuanlin
  • He, Yuehua
  • Noren, Bradley
  • Yee, James Gee Ken

Abstract

Compounds of formula (Ia): 6 are defined herein, as well as other indene derivatives are disclosed herein. Pharmaceutical compositions containing the compounds and methods of using the compounds are also disclosed.

IPC Classes  ?