Vitae Pharmaceuticals, LLC

United States of America

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2025 October 1
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IPC Class
C07D 471/04 - Ortho-condensed systems 19
C07D 487/04 - Ortho-condensed systems 10
C07D 405/14 - 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 three or more hetero rings 9
C07D 519/00 - Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups or 8
A61K 31/4353 - 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 7
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Status
Pending 4
Registered / In Force 33
Found results for  patents

1.

INHIBITORS OF THE MENIN-MLL INTERACTION

      
Application Number 19180560
Status Pending
Filing Date 2025-04-16
First Publication Date 2025-10-23
Owner Vitae Pharmaceuticals, LLC (USA)
Inventor
  • Cacatian, Salvacion
  • Claremon, David A.
  • Dillard, Lawrence Wayne
  • Dong, Chengguo
  • Fan, Yi
  • Jia, Lanqi
  • Lotesta, Stephen D.
  • Marcus, Andrew
  • Morales-Ramos, Angel
  • Singh, Suresh B.
  • Venkatraman, Shankar
  • Yuan, Jing
  • Zheng, Yajun
  • Zhuang, Linghang
  • Parent, Stephan D.
  • Houston, Travis L.

Abstract

The present invention is directed to inhibitors of the interaction of menin with MLL and MLL fusion proteins, pharmaceutical compositions containing the same, and their use in the treatment of cancer and other diseases mediated by the menin-MLL interaction.

IPC Classes  ?

  • C07D 487/10 - Spiro-condensed systems
  • A61P 35/02 - Antineoplastic agents specific for leukemia
  • 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 403/14 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing three or more hetero rings
  • C07D 405/14 - 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 three or more hetero rings
  • C07D 471/10 - Spiro-condensed systems
  • C07D 491/10 - Spiro-condensed systems
  • C07D 491/107 - Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
  • C07F 9/6561 - Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings

2.

INHIBITORS OF THE MENIN-MLL INTERACTION

      
Application Number 18289970
Status Pending
Filing Date 2022-05-13
First Publication Date 2024-12-05
Owner
  • Syndax Pharmaceuticals, Inc (USA)
  • Vitae Pharmaceuticals, LLC (USA)
Inventor
  • Cacatian, Salvacion
  • Kulkarni, Santosh S.
  • Samanta, Swapan Kumar
  • Reddy, Virsinha Venkat
  • Mcgeehan, Gerard M.
  • Miller, William H.
  • Camp, Nicholas Paul

Abstract

The present disclosure is directed to inhibitors of Formula (0), or a stereoisomer thereof, or pharmaceutically acceptable salt thereof, of the interaction of menin with MLL and MLL fusion proteins, pharmaceutical compositions containing the same, and their use in the treatment of cancer and other diseases mediated by the menin-MLL interaction. The present disclosure is directed to inhibitors of Formula (0), or a stereoisomer thereof, or pharmaceutically acceptable salt thereof, of the interaction of menin with MLL and MLL fusion proteins, pharmaceutical compositions containing the same, and their use in the treatment of cancer and other diseases mediated by the menin-MLL interaction.

IPC Classes  ?

  • C07D 471/10 - Spiro-condensed systems
  • A61K 31/506 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
  • A61K 31/53 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
  • A61K 31/5377 - 1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
  • C07D 519/00 - Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups or

3.

INHIBITORS OF THE MENIN-MLL INTERACTION

      
Application Number 18320111
Status Pending
Filing Date 2023-05-18
First Publication Date 2024-04-18
Owner Vitae Pharmaceuticals, LLC (USA)
Inventor
  • Cacatian, Salvacion
  • Claremon, David A.
  • Dong, Chengguo
  • Fan, Yi
  • Jia, Lanqi
  • Lotesta, Stephen D.
  • Singh, Suresh B.
  • Venkatraman, Shankar
  • Yuan, Jing
  • Zheng, Yajun
  • Zhuang, Linghang

Abstract

The present invention is directed to inhibitors of the interaction of menin with MLL and MLL fusion proteins, pharmaceutical compositions containing the same, and their use in the treatment of cancer and other diseases mediated by the menin-MLL interaction.

IPC Classes  ?

4.

Inhibitors of the menin-MLL interaction

      
Application Number 17902432
Grant Number 12312359
Status In Force
Filing Date 2022-09-02
First Publication Date 2023-06-08
Grant Date 2025-05-27
Owner Vitae Pharmaceuticals, LLC (USA)
Inventor
  • Cacatian, Salvacion
  • Claremon, David A.
  • Dillard, Lawrence Wayne
  • Dong, Chengguo
  • Fan, Yi
  • Jia, Lanqi
  • Lotesta, Stephen D.
  • Marcus, Andrew
  • Morales-Ramos, Angel
  • Singh, Suresh B.
  • Venkatraman, Shankar
  • Yuan, Jing
  • Zheng, Yajun
  • Zhuang, Linghang
  • Parent, Stephan D.
  • Houston, Travis L.

Abstract

The present invention is directed to inhibitors of the interaction of menin with MLL and MLL fusion proteins, pharmaceutical compositions containing the same, and their use in the treatment of cancer and other diseases mediated by the menin-MLL interaction.

IPC Classes  ?

  • C07D 405/14 - 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 three or more hetero rings
  • A61K 31/407 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with heterocyclic ring systems, e.g. ketorolac, physostigmine
  • A61P 3/10 - Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
  • A61P 35/00 - Antineoplastic agents
  • A61P 35/02 - Antineoplastic agents specific for leukemia
  • 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 403/14 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing three or more hetero rings
  • C07D 471/10 - Spiro-condensed systems
  • C07D 487/10 - Spiro-condensed systems
  • C07D 491/10 - Spiro-condensed systems
  • C07D 491/107 - Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
  • C07F 9/6561 - Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings

5.

Inhibitors of the menin-MLL interaction

      
Application Number 17744249
Grant Number 11919901
Status In Force
Filing Date 2022-05-13
First Publication Date 2023-01-26
Grant Date 2024-03-05
Owner
  • Syndax Pharmaceuticals, Inc. (USA)
  • Vitae Pharmaceuticals, LLC (USA)
Inventor
  • Mcgeehan, Gerard M.
  • Miller, William H.
  • Camp, Nicholas Paul
  • Cacatian, Salvacion
  • Kulkarni, Santosh S.
  • Samanta, Swapan Kumar
  • Reddy, Virsinha Venkat

Abstract

The present disclosure is directed to inhibitors of Formula (0), or a stereoisomer thereof, or pharmaceutically acceptable salt thereof, of the interaction of menin with MLL and MLL fusion proteins, pharmaceutical compositions containing the same, and their use in the treatment of cancer and other diseases mediated by the menin-MLL interaction,

IPC Classes  ?

  • C07D 405/14 - 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 three or more hetero rings
  • A61K 31/506 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
  • C07D 471/10 - Spiro-condensed systems
  • A61P 35/02 - Antineoplastic agents specific for leukemia
  • C07D 519/00 - Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups or

6.

INHIBITORS OF THE MENIN-MLL INTERACTION

      
Application Number US2022029271
Publication Number 2022/241265
Status In Force
Filing Date 2022-05-13
Publication Date 2022-11-17
Owner
  • SYNDAX PHARMACEUTICALS, INC. (USA)
  • VITAE PHARMACEUTICALS, LLC (USA)
  • SYNGENE INTERNATIONAL LIMITED (India)
Inventor
  • Mcgeehan, Gerard M.
  • Miller, William H.
  • Camp, Nicholas Paul

Abstract

The present disclosure is directed to inhibitors of Formula (0), or a stereoisomer thereof, or pharmaceutically acceptable salt thereof, of the interaction of menin with MLL and MLL fusion proteins, pharmaceutical compositions containing the same, and their use in the treatment of cancer and other diseases mediated by the menin-MLL interaction.

IPC Classes  ?

  • A61K 31/438 - 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 the ring being spiro-condensed with carbocyclic or heterocyclic ring systems
  • C07D 471/10 - Spiro-condensed systems
  • C07D 487/10 - Spiro-condensed systems

7.

INHIBITORS OF ROR GAMMA

      
Application Number 17509630
Status Pending
Filing Date 2021-10-25
First Publication Date 2022-04-14
Owner Vitae Pharmaceuticals, LLC (USA)
Inventor
  • Deng, Chaoyi
  • He, Jun
  • Xu, Bo

Abstract

The present disclosure relates to salts and crystalline forms of a compound having the formula: The present disclosure relates to salts and crystalline forms of a compound having the formula: The present disclosure relates to salts and crystalline forms of a compound having the formula: Also described are processes for the production of the salts and crystalline forms described herein.

IPC Classes  ?

8.

Dihydropyrrolopyridine inhibitors of ROR-gamma

      
Application Number 17015825
Grant Number 11535614
Status In Force
Filing Date 2020-09-09
First Publication Date 2021-08-05
Grant Date 2022-12-27
Owner Vitae Pharmaceuticals, LLC (USA)
Inventor
  • Claremon, David A.
  • Dillard, Lawrence Wayne
  • Dong, Chengguo
  • Fan, Yi
  • Jia, Lanqi
  • Liu, Zhijie
  • Lotesta, Stephen D.
  • Marcus, Andrew
  • Singh, Suresh B.
  • Tice, Colin M.
  • Yuan, Jing
  • Zhao, Wei
  • Zheng, Yajun
  • Zhuang, Linghang

Abstract

Provided are novel compounds of Formula (I): pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful in the treatment of diseases and disorders mediated by RORγ. Also provided are pharmaceutical compositions comprising the novel compounds of Formula (I) and methods for their use in treating one or more inflammatory, metabolic, autoimmune and other diseases or disorders.

IPC Classes  ?

  • C07D 471/04 - Ortho-condensed systems
  • C07D 519/00 - Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups or

9.

Inhibitors of the menin-MLL interaction

      
Application Number 16990657
Grant Number 11739085
Status In Force
Filing Date 2020-08-11
First Publication Date 2021-06-17
Grant Date 2023-08-29
Owner Vitae Pharmaceuticals, LLC (USA)
Inventor
  • Cacatian, Salvacion
  • Claremon, David A.
  • Dong, Chengguo
  • Fan, Yi
  • Jia, Lanqi
  • Lotesta, Stephen D.
  • Singh, Suresh B.
  • Venkatraman, Shankar
  • Yuan, Jing
  • Zheng, Yajun
  • Zhuang, Linghang

Abstract

The present invention is directed to inhibitors of the interaction of menin with MLL and MLL fusion proteins, pharmaceutical compositions containing the same, and their use in the treatment of cancer and other diseases mediated by the menin-MLL interaction.

IPC Classes  ?

10.

Inhibitors of the menin-MLL interaction

      
Application Number 16837421
Grant Number 11479557
Status In Force
Filing Date 2020-04-01
First Publication Date 2021-02-25
Grant Date 2022-10-25
Owner VITAE PHARMACEUTICALS, LLC (USA)
Inventor
  • Cacatian, Salvacion
  • Claremon, David A.
  • Dillard, Lawrence Wayne
  • Dong, Chengguo
  • Fan, Yi
  • Jia, Lanqi
  • Lotesta, Stephen D.
  • Marcus, Andrew
  • Morales-Ramos, Angel
  • Singh, Suresh B.
  • Venkatraman, Shankar
  • Yuan, Jing
  • Zheng, Yajun
  • Zhuang, Linghang
  • Parent, Stephan D.
  • Houston, Travis L.

Abstract

The present invention is directed to inhibitors of the interaction of menin with MLL and MLL fusion proteins, pharmaceutical compositions containing the same, and their use in the treatment of cancer and other diseases mediated by the menin-MLL interaction.

IPC Classes  ?

  • A61P 35/00 - Antineoplastic agents
  • A61P 35/02 - Antineoplastic agents specific for leukemia
  • C07D 487/10 - Spiro-condensed systems
  • 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 403/14 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing three or more hetero rings
  • C07D 471/10 - Spiro-condensed systems
  • C07D 491/10 - Spiro-condensed systems
  • C07D 405/14 - 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 three or more hetero rings
  • C07D 491/107 - Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
  • C07F 9/6561 - Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings

11.

Dihydropyrrolopyridine inhibitors of ROR-gamma

      
Application Number 16506518
Grant Number 10807980
Status In Force
Filing Date 2019-07-09
First Publication Date 2020-06-04
Grant Date 2020-10-20
Owner Vitae Pharmaceuticals, LLC (USA)
Inventor
  • Claremon, David A.
  • Dillard, Lawrence Wayne
  • Dong, Chengguo
  • Fan, Yi
  • Jia, Lanqi
  • Liu, Zhijie
  • Lotesta, Stephen D.
  • Marcus, Andrew
  • Singh, Suresh B.
  • Tice, Colin M.
  • Yuan, Jing
  • Zhao, Wei
  • Zheng, Yajun
  • Zhuang, Linghang

Abstract

Provided are novel compounds of Formula (I): pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful in the treatment of diseases and disorders mediated by RORγ. Also provided are pharmaceutical compositions comprising the novel compounds of Formula (I) and methods for their use in treating one or more inflammatory, metabolic, autoimmune and other diseases or disorders.

IPC Classes  ?

  • 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 31/4353 - 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
  • C07D 401/02 - 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
  • C07D 401/10 - 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 aromatic rings
  • C07D 471/04 - Ortho-condensed systems
  • C07D 519/00 - Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups or

12.

Inhibitors of ROR gamma

      
Application Number 16633334
Grant Number 11186573
Status In Force
Filing Date 2018-07-24
First Publication Date 2020-05-28
Grant Date 2021-11-30
Owner Vitae Pharmaceuticals, LLC (USA)
Inventor
  • Deng, Chaoyi
  • He, Jun
  • Xu, Bo

Abstract

The present disclosure relates to salts and crystalline forms of a compound having the formula (I): Also described are processes for the production of the salts and crystalline forms described herein.

IPC Classes  ?

13.

Dihydropyrrolopyridine inhibitors of ROR-gamma

      
Application Number 16394764
Grant Number 11001583
Status In Force
Filing Date 2019-04-25
First Publication Date 2020-03-12
Grant Date 2021-05-11
Owner Vitae Pharmaceuticals, LLC (USA)
Inventor
  • Claremon, David A.
  • Dillard, Lawrence Wayne
  • Dong, Chengguo
  • Fan, Yi
  • Lotesta, Stephen D.
  • Marcus, Andrew
  • Singh, Suresh B.
  • Tice, Colin M.
  • Yuan, Jing
  • Zhao, Wei
  • Zhuang, Linghang

Abstract

Provided are novel compounds of Formula (I): pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful in the treatment of diseases and disorders mediated by RORγ. Also provided are pharmaceutical compositions comprising the novel compounds of Formula (I) and methods for their use in treating one or more inflammatory, metabolic, autoimmune and other diseases or disorders.

IPC Classes  ?

14.

Substituted benzoimidazoles as modulators of ROR-γ

      
Application Number 16373912
Grant Number 10829448
Status In Force
Filing Date 2019-04-03
First Publication Date 2020-02-27
Grant Date 2020-11-10
Owner Vitae Pharmaceuticals, LLC (USA)
Inventor
  • Claremon, David A.
  • Dillard, Lawrence Wayne
  • Fan, Yi
  • Lotesta, Stephen D.
  • Singh, Suresh B.
  • Tice, Colin M.
  • Zhao, Wei
  • Zhuang, Linghang

Abstract

Provided are indole, benzoimidazole, pyrrolopyridine, and imidazopyridine derivatives and pharmaceutical compositions thereof, which are useful in the treatment of diseases and disorders mediated by RORγ. Such derivatives include e.g., those having the Formula II: as well as pharmaceutically acceptable salts thereof. The disclosed derivatives may be used for treating one or more inflammatory, metabolic, autoimmune and other diseases or disorders.

IPC Classes  ?

  • A61K 31/4184 - 1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
  • C07D 235/04 - BenzimidazolesHydrogenated benzimidazoles
  • C07D 209/10 - IndolesHydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
  • C07D 405/14 - 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 three or more hetero rings
  • C07D 401/06 - 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 only aliphatic carbon atoms
  • C07D 235/10 - Radicals substituted by halogen atoms or nitro radicals
  • C07D 235/12 - Radicals substituted by oxygen atoms
  • 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 405/06 - 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 carbon chain containing only aliphatic carbon atoms
  • C07D 471/04 - Ortho-condensed systems
  • C07D 235/26 - Oxygen atoms
  • 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

15.

Benzimidazole derivatives as modulators of ROR-gamma

      
Application Number 16073503
Grant Number 10829481
Status In Force
Filing Date 2017-01-27
First Publication Date 2019-11-21
Grant Date 2020-11-10
Owner Vitae Pharmaceuticals, LLC (USA)
Inventor
  • Claremon, David A.
  • Dillard, Lawrence Wayne
  • Fan, Yi
  • Lotesta, Stephen D.
  • Singh, Suresh B.
  • Tice, Colin M.
  • Zhao, Wei
  • Zhuang, Linghang

Abstract

Provided are novel compounds of Formula I: pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful in the treatment of diseases and disorders mediated by RORy. Also provided are pharmaceutical compositions comprising the novel compounds of Formula I and methods for their use in treating one or more inflammatory, metabolic, autoimmune and other diseases or disorders.

IPC Classes  ?

  • C07D 405/14 - 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 three or more hetero rings
  • C07D 405/10 - 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 carbon chain containing aromatic rings

16.

Modulators of ROR-gamma

      
Application Number 15776836
Grant Number 11008340
Status In Force
Filing Date 2016-11-17
First Publication Date 2019-10-24
Grant Date 2021-05-18
Owner Vitae Pharmaceuticals, LLC (USA)
Inventor
  • Claremon, David A.
  • Dillard, Lawrence Wayne
  • Fan, Yi
  • Jia, Lanqi
  • Singh, Suresh B.
  • Tice, Colin M.
  • Xu, Zhenrong
  • Yuan, Jing
  • Zhuang, Linghang

Abstract

Provided are novel compounds of Formula I: pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful in the treatment of diseases and disorders mediated by RORγ. Also provided are pharmaceutical compositions comprising the novel compounds of Formula I and methods for their use in treating one or more inflammatory, metabolic, autoimmune and other diseases or disorders.

IPC Classes  ?

  • C07D 513/04 - Ortho-condensed systems
  • C07D 217/04 - Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ringAlkylene-bis-isoquinolines with hydrocarbon or substituted hydrocarbon radicals attached to the ring nitrogen atom
  • C07D 217/24 - Oxygen atoms
  • C07D 231/56 - BenzopyrazolesHydrogenated benzopyrazoles
  • C07D 239/88 - Oxygen atoms
  • C07D 401/06 - 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 only aliphatic carbon atoms
  • 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 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 471/04 - Ortho-condensed systems

17.

Inhibitors of the menin-MLL interaction

      
Application Number 16333852
Grant Number 10899758
Status In Force
Filing Date 2017-09-15
First Publication Date 2019-07-04
Grant Date 2021-01-26
Owner VITAE PHARMACEUTICALS, LLC (USA)
Inventor
  • Cacatian, Salvacion
  • Claremon, David A.
  • Dong, Chengguo
  • Fan, Yi
  • Jia, Lanqi
  • Lotesta, Stephen D.
  • Singh, Suresh B.
  • Venkatraman, Shankar
  • Yuan, Jing
  • Zheng, Yajun
  • Zhuang, Linghang

Abstract

The present invention is directed to inhibitors of the interaction of menin with MLL and MLL fusion proteins, pharmaceutical compositions containing the same, and their use in the treatment of cancer and other diseases mediated by the menin-MLL interaction.

IPC Classes  ?

18.

Inhibitors of the menin-MLL interaction

      
Application Number 16308739
Grant Number 10683302
Status In Force
Filing Date 2017-06-08
First Publication Date 2019-05-16
Grant Date 2020-06-16
Owner VITAE PHARMACEUTICALS, LLC (USA)
Inventor
  • Cacatian, Salvacion
  • Claremon, David A.
  • Dillard, Lawrence Wayne
  • Dong, Chengguo
  • Fan, Yi
  • Jia, Lanqi
  • Lotesta, Stephen D.
  • Marcus, Andrew
  • Morales-Ramos, Angel
  • Singh, Suresh B.
  • Venkatraman, Shankar
  • Yuan, Jing
  • Zheng, Yajun
  • Zhuang, Linghang
  • Parent, Stephan D.
  • Houston, Travis L.

Abstract

The present invention is directed to inhibitors of the interaction of menin with MLL and MLL fusion proteins, pharmaceutical compositions containing the same, and their use in the treatment of cancer and other diseases mediated by the menin-MLL interaction.

IPC Classes  ?

  • C07D 405/14 - 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 three or more hetero 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 403/14 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing three or more hetero rings
  • C07D 471/10 - Spiro-condensed systems
  • C07D 487/10 - Spiro-condensed systems
  • C07D 491/10 - Spiro-condensed systems
  • A61P 35/02 - Antineoplastic agents specific for leukemia
  • C07D 491/107 - Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
  • C07F 9/6561 - Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings

19.

Dihydropyrrolopyridine inhibitors of ROR-gamma

      
Application Number 16025155
Grant Number 10399976
Status In Force
Filing Date 2018-07-02
First Publication Date 2018-12-27
Grant Date 2019-09-03
Owner Vitae Pharmaceuticals, LLC (USA)
Inventor
  • Claremon, David A.
  • Dillard, Lawrence Wayne
  • Dong, Chengguo
  • Fan, Yi
  • Jia, Lanqi
  • Liu, Zhijie
  • Lotesta, Stephen D.
  • Marcus, Andrew
  • Singh, Suresh B.
  • Tice, Colin M.
  • Yuan, Jing
  • Zhao, Wei
  • Zheng, Yajun
  • Zhuang, Linghang

Abstract

Provided are novel compounds of Formula (I): . Also provided are pharmaceutical compositions comprising the novel compounds of Formula (I) and methods for their use in treating one or more inflammatory, metabolic, autoimmune and other diseases or disorders.

IPC Classes  ?

  • 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 31/4353 - 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
  • C07D 471/04 - Ortho-condensed systems
  • C07D 519/00 - Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups or

20.

Substituted indoles as modulators of ROR-gamma

      
Application Number 15749322
Grant Number 10301261
Status In Force
Filing Date 2016-08-03
First Publication Date 2018-08-09
Grant Date 2019-05-28
Owner Vitae Pharmaceuticals, LLC (USA)
Inventor
  • Claremon, David A.
  • Dillard, Lawrence Wayne
  • Fan, Yi
  • Lotesta, Stephen D.
  • Singh, Suresh B.
  • Tice, Colin M.
  • Zhao, Wei
  • Zhuang, Linghang

Abstract

Provided are novel compounds of Formula I: pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful in the treatment of diseases and disorders mediated by RORy. Also provided are pharmaceutical compositions comprising the novel compounds of Formula I and methods for their use in treating one or more inflammatory, metabolic, autoimmune and other diseases or disorders.

IPC Classes  ?

  • A61K 31/404 - Indoles, e.g. pindolol
  • C07D 209/04 - IndolesHydrogenated indoles
  • C07D 209/10 - IndolesHydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
  • C07D 405/14 - 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 three or more hetero rings
  • C07D 401/06 - 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 only aliphatic carbon atoms
  • C07D 235/10 - Radicals substituted by halogen atoms or nitro radicals
  • C07D 235/12 - Radicals substituted by oxygen atoms
  • 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 405/06 - 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 carbon chain containing only aliphatic carbon atoms
  • C07D 471/04 - Ortho-condensed systems
  • C07D 235/26 - Oxygen atoms
  • 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

21.

Dihydropyrrolopyridine inhibitors of RORγ

      
Application Number 15709903
Grant Number 10087184
Status In Force
Filing Date 2017-09-20
First Publication Date 2018-08-09
Grant Date 2018-10-02
Owner VITAE PHARMACEUTICALS, LLC (USA)
Inventor
  • Claremon, David A.
  • Dillard, Lawrence Wayne
  • Dong, Chengguo
  • Fan, Yi
  • Jia, Lanqi
  • Lotesta, Stephen D.
  • Marcus, Andrew
  • Singh, Suresh B.
  • Tice, Colin M.
  • Yuan, Jing
  • Zhao, Wei
  • Zheng, Yajun
  • Zhuang, Linghang

Abstract

Provided are novel compounds of Formula (I): γ. Also provided are pharmaceutical compositions comprising the novel compounds of Formula (I) and methods for their use in treating one or more inflammatory, metabolic, autoimmune and other diseases or disorders.

IPC Classes  ?

  • 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 31/4353 - 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
  • C07D 471/04 - Ortho-condensed systems

22.

Dihydropyrrolopyridine inhibitors of ROR-gamma

      
Application Number 15455481
Grant Number 10047085
Status In Force
Filing Date 2017-03-10
First Publication Date 2017-09-14
Grant Date 2018-08-14
Owner VITAE PHARMACEUTICALS, LLC (USA)
Inventor
  • Claremon, David A.
  • Dillard, Lawrence Wayne
  • Dong, Chengguo
  • Fan, Yi
  • Jia, Lanqi
  • Liu, Zhijie
  • Lotesta, Stephen D.
  • Marcus, Andrew
  • Singh, Suresh B.
  • Tice, Colin M.
  • Yuan, Jing
  • Zhao, Wei
  • Zheng, Yajun
  • Zhuang, Linghang

Abstract

Provided are novel compounds of Formula (I): pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful in the treatment of diseases and disorders mediated by RORγ. Also provided are pharmaceutical compositions comprising the novel compounds of Formula (I) and methods for their use in treating one or more inflammatory, metabolic, autoimmune and other diseases or disorders.

IPC Classes  ?

  • 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 31/4353 - 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
  • C07D 471/04 - Ortho-condensed systems
  • C07D 519/00 - Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups or

23.

Piperazine derivatives as liver X receptor modulators

      
Application Number 15502356
Grant Number 10144715
Status In Force
Filing Date 2015-08-04
First Publication Date 2017-08-10
Grant Date 2018-12-04
Owner VITAE PHARMACEUTICALS, LLC (USA)
Inventor
  • Claremon, David A.
  • Dong, Chengguo
  • Fan, Yi
  • Leftheris, Katerina
  • Lotesta, Stephen D.
  • Singh, Suresh B.
  • Tice, Colin M.
  • Zhao, Wei
  • Zheng, Yajun
  • Zhuang, Linghang

Abstract

Provided are novel compounds of Formula (I): pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are liver X receptor modulators, and which are useful in the treatment of diseases and disorders associated with the liver X receptor. Also provided are the compounds of Formula (I) and pharmaceutical compositions thereof for treating atherosclerosis, cardiovascular disease, Alzheimer's disease, dermatitis, dyslipidemia, cancer and other diseases or disorders.

IPC Classes  ?

  • C07D 241/04 - Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
  • 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 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 401/04 - 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 directly linked by a ring-member-to-ring- member bond
  • C07D 401/06 - 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 only aliphatic carbon atoms
  • C07D 403/14 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing three or more hetero rings
  • C07D 405/06 - 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 carbon chain containing only aliphatic carbon atoms
  • C07D 413/04 - 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 directly linked by a ring-member-to-ring- member bond
  • C07D 417/04 - 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 directly linked by a ring-member-to-ring- member bond
  • C07D 417/14 - 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 three or more hetero rings
  • C07D 497/04 - Ortho-condensed systems
  • C07D 513/04 - Ortho-condensed systems

24.

Liver X receptor modulators

      
Application Number 15182749
Grant Number 09814715
Status In Force
Filing Date 2016-06-15
First Publication Date 2017-05-18
Grant Date 2017-11-14
Owner VITAE PHARMACEUTICALS, LLC (USA)
Inventor
  • Dong, Chengguo
  • Fan, Yi
  • Leftheris, Katerina
  • Lotesta, Stephen D.
  • Singh, Suresh B.
  • Tice, Colin M.
  • Zhao, Wei
  • Zheng, Yajun
  • Zhuang, Linghang

Abstract

Provided herein are novel compounds and pharmaceutically acceptable salts thereof that are liver X receptor modulators. Also provided are compositions comprising compounds of the invention and a carrier. Additionally, use of the compounds herein and methods for treating a disease or disorder associated with the liver X receptor are further described.

IPC Classes  ?

  • A61K 31/506 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
  • A61K 31/4985 - Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
  • C07D 487/04 - Ortho-condensed systems

25.

Dihydropyrrolopyridine inhibitors of ROR-gamma

      
Application Number 15277836
Grant Number 09796710
Status In Force
Filing Date 2016-09-27
First Publication Date 2017-03-23
Grant Date 2017-10-24
Owner VITAE PHARMACEUTICALS, LLC (USA)
Inventor
  • Claremon, David A.
  • Dillard, Lawrence Wayne
  • Dong, Chengguo
  • Fan, Yi
  • Jia, Lanqi
  • Lotesta, Stephen D.
  • Marcus, Andrew
  • Singh, Suresh B.
  • Tice, Colin M.
  • Yuan, Jing
  • Zhao, Wei
  • Zheng, Yajun
  • Zhuang, Linghang

Abstract

Provided are novel compounds of Formula (I): . Also provided are pharmaceutical compositions comprising the novel compounds of Formula (I) and methods for their use in treating one or more inflammatory, metabolic, autoimmune and other diseases or disorders.

IPC Classes  ?

  • 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 31/4353 - 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

26.

Thiazolopyrrolidine inhibitors of ROR- γ

      
Application Number 14888129
Grant Number 09868748
Status In Force
Filing Date 2014-05-01
First Publication Date 2017-01-12
Grant Date 2018-01-16
Owner VITAE PHARMACEUTICALS, LLC (USA)
Inventor
  • Claremon, David A.
  • Dillard, Lawrence Wayne
  • Dong, Chengguo
  • Fan, Yi
  • Jia, Lanqi
  • Lotesta, Stephen D.
  • Marcus, Andrew
  • Singh, Suresh B.
  • Tice, Colin M.
  • Yuan, Jing
  • Zhao, Wei
  • Zheng, Yajun
  • Zhuang, Linghang

Abstract

Provided are novel compounds of Formula (I): pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful in the treatment of diseases and disorders mediated by RORγ. Also provided are pharmaceutical compositions comprising the novel compounds of Formula (I) and methods for their use in treating one or more inflammatory, metabolic, autoimmune and other diseases or disorders.

IPC Classes  ?

  • C07D 513/04 - Ortho-condensed systems
  • C07D 519/00 - Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups or

27.

Liver X receptor modulators

      
Application Number 15204422
Grant Number 09707232
Status In Force
Filing Date 2016-07-07
First Publication Date 2017-01-12
Grant Date 2017-07-18
Owner VITAE PHARMACEUTICALS, LLC (USA)
Inventor
  • Dong, Chengguo
  • Fan, Yi
  • Leftheris, Katerina
  • Lotesta, Stephen D.
  • Singh, Suresh B.
  • Tice, Colin M.
  • Zhao, Wei
  • Zheng, Yajun
  • Zhuang, Linghang

Abstract

Provided herein are novel compounds and pharmaceutically acceptable salts thereof that are liver X receptor modulators. Also provided are compositions comprising compounds of the invention and a carrier. Additionally, use of the compounds herein and methods for treating a disease or disorder associated with the liver X receptor are further described.

IPC Classes  ?

  • C07D 487/04 - Ortho-condensed systems
  • A61K 31/4985 - Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
  • A61K 31/506 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
  • C07F 7/18 - Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages

28.

Dihydropyrrolopyridine inhibitors of ROR-gamma

      
Application Number 15178796
Grant Number 09481674
Status In Force
Filing Date 2016-06-10
First Publication Date 2016-11-01
Grant Date 2016-11-01
Owner VITAE PHARMACEUTICALS, LLC (USA)
Inventor
  • Claremon, David A.
  • Yuan, Jing
  • Zhao, Wei
  • Zheng, Yajun

Abstract

Provided are novel compounds of Formula (I): pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful in the treatment of diseases and disorders mediated by RORγ. Also provided are pharmaceutical compositions comprising the novel compounds of Formula (I) and methods for their use in treating one or more inflammatory, metabolic, autoimmune and other diseases or disorders.

IPC Classes  ?

29.

Dihydropyrrolopyridine inhibitors of ROR-gamma

      
Application Number 14990430
Grant Number 09624217
Status In Force
Filing Date 2016-01-07
First Publication Date 2016-07-14
Grant Date 2017-04-18
Owner VITAE PHARMACEUTICALS, LLC (USA)
Inventor
  • Claremon, David A.
  • Dillard, Lawrence Wayne
  • Dong, Chengguo
  • Fan, Yi
  • Jia, Lanqi
  • Liu, Zhijie
  • Lotesta, Stephen D.
  • Marcus, Andrew
  • Singh, Suresh B.
  • Tice, Colin M.
  • Yuan, Jing
  • Zhao, Wei
  • Zheng, Yajun
  • Zhuang, Linghang

Abstract

Provided are novel compounds of Formula (I): pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful in the treatment of diseases and disorders mediated by RORγ. Also provided are pharmaceutical compositions comprising the novel compounds of Formula (I) and methods for their use in treating one or more inflammatory, metabolic, autoimmune and other diseases or disorders.

IPC Classes  ?

  • C07D 401/02 - 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
  • C07D 401/10 - 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 aromatic rings
  • 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 31/4353 - 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
  • C07D 471/04 - Ortho-condensed systems
  • C07D 519/00 - Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups or

30.

Isoindoline inhibitors of ROR-gamma

      
Application Number 14933468
Grant Number 09845308
Status In Force
Filing Date 2015-11-05
First Publication Date 2016-05-05
Grant Date 2017-12-19
Owner VITAE PHARMACEUTICALS, LLC (USA)
Inventor
  • Claremon, David A.
  • Dillard, Lawrence Wayne
  • Dong, Chengguo
  • Fan, Yi
  • Jia, Lanqi
  • Lotesta, Stephen D.
  • Marcus, Andrew
  • Singh, Suresh B.
  • Tice, Colin M.
  • Yuan, Jing
  • Zhao, Wei
  • Zheng, Yajun
  • Zhuang, Linghang

Abstract

Provided are novel compounds of Formula (I): pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful in the treatment of diseases and disorders mediated by RORγ. Also provided are pharmaceutical compositions comprising the novel compounds of Formula (I) and methods for their use in treating one or more inflammatory, metabolic, autoimmune and other diseases or disorders.

IPC Classes  ?

  • 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 209/44 - Iso-indolesHydrogenated iso-indoles
  • C07D 403/12 - 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 chain containing hetero atoms as chain links
  • 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 405/14 - 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 three or more hetero rings

31.

Dihydropyrrolopyridine inhibitors of ROR-gamma

      
Application Number 14933524
Grant Number 09663515
Status In Force
Filing Date 2015-11-05
First Publication Date 2016-05-05
Grant Date 2017-05-30
Owner VITAE PHARMACEUTICALS, LLC (USA)
Inventor
  • Claremon, David A.
  • Dillard, Lawrence Wayne
  • Dong, Chengguo
  • Fan, Yi
  • Lotesta, Stephen D.
  • Marcus, Andrew
  • Singh, Suresh B.
  • Tice, Colin M.
  • Yuan, Jing
  • Zhao, Wei
  • Zhuang, Linghang

Abstract

Provided are novel compounds of Formula (I): pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful in the treatment of diseases and disorders mediated by RORγ. Also provided are pharmaceutical compositions comprising the novel compounds of Formula (I) and methods for their use in treating one or more inflammatory, metabolic, autoimmune and other diseases or disorders.

IPC Classes  ?

32.

Liver X receptor modulators

      
Application Number 14721262
Grant Number 09416135
Status In Force
Filing Date 2015-05-26
First Publication Date 2015-11-26
Grant Date 2016-08-16
Owner VITAE PHARMACEUTICALS, LLC (USA)
Inventor
  • Dong, Chengguo
  • Fan, Yi
  • Leftheris, Katerina
  • Lotesta, Stephen D.
  • Singh, Suresh B.
  • Tice, Colin M.
  • Zhao, Wei
  • Zheng, Yajun
  • Zhuang, Linghang

Abstract

Provided herein are novel compounds and pharmaceutically acceptable salts thereof that are liver X receptor modulators. Also provided are compositions comprising compounds of the invention and a carrier. Additionally, use of the compounds herein and methods for treating a disease or disorder associated with the liver X receptor are further described.

IPC Classes  ?

  • C07D 487/04 - Ortho-condensed systems
  • A61K 31/4985 - Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
  • C07F 7/18 - Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages

33.

Liver X receptor modulators

      
Application Number 14657179
Grant Number 09388190
Status In Force
Filing Date 2015-03-13
First Publication Date 2015-09-03
Grant Date 2016-07-12
Owner VITAE PHARMACEUTICALS, LLC (USA)
Inventor
  • Dong, Chengguo
  • Fan, Yi
  • Leftheris, Katerina
  • Lotesta, Stephen D.
  • Singh, Suresh B.
  • Tice, Colin M.
  • Zhao, Wei
  • Zheng, Yajun
  • Zhuang, Linghang

Abstract

Provided herein are novel compounds and pharmaceutically acceptable salts thereof that are liver X receptor modulators. Also provided are compositions comprising compounds of the invention and a carrier. Additionally, use of the compounds herein and methods for treating a disease or disorder associated with the liver X receptor are further described.

IPC Classes  ?

  • C07D 487/04 - Ortho-condensed systems
  • A61K 31/4985 - Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems

34.

Dihydropyrrolopyridine inhibitors of ROR-gamma

      
Application Number 14609798
Grant Number 09266886
Status In Force
Filing Date 2015-01-30
First Publication Date 2015-08-06
Grant Date 2016-02-23
Owner VITAE PHARMACEUTICALS, LLC (USA)
Inventor
  • Lotesta, Stephen D.
  • Marcus, Andrew
  • Yuan, Jing

Abstract

Provided are novel compounds of Formula (I): pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful in the treatment of diseases and disorders mediated by RORγ. Also provided are pharmaceutical compositions comprising the novel compounds of Formula (I) and methods for their use in treating one or more inflammatory, metabolic, autoimmune and other diseases or disorders.

IPC Classes  ?

  • C07D 401/02 - 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
  • C07D 401/10 - 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 aromatic rings
  • 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 31/4353 - 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
  • C07D 471/04 - Ortho-condensed systems

35.

Liver X receptor modulators

      
Application Number 14547804
Grant Number 09006245
Status In Force
Filing Date 2014-11-19
First Publication Date 2015-03-19
Grant Date 2015-04-14
Owner VITAE PHARMACEUTICALS, LLC (USA)
Inventor
  • Leftheris, Katerina
  • Zhuang, Linghang

Abstract

Provided herein are novel compounds and pharmaceutically acceptable salts thereof that are liver X receptor modulators. Also provided are compositions comprising compounds of the invention and a carrier. Additionally, use of the compounds herein and methods for treating a disease or disorder associated with the liver X receptor are further described.

IPC Classes  ?

  • C07D 487/04 - Ortho-condensed systems
  • A61K 31/4985 - Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems

36.

Liver X receptor modulators

      
Application Number 14385671
Grant Number 09073931
Status In Force
Filing Date 2013-03-14
First Publication Date 2015-03-05
Grant Date 2015-07-07
Owner VITAE PHARMACEUTICALS, LLC (USA)
Inventor
  • Leftheris, Katerina
  • Zhuang, Linghang

Abstract

Provided herein are novel compounds and pharmaceutically acceptable salts thereof that are liver X receptor modulators. Also provided are compositions comprising compounds of the invention and a carrier. Additionally, use of the compounds herein and methods for treating a disease or disorder associated with the liver X receptor are further described.

IPC Classes  ?

  • C07D 487/04 - Ortho-condensed systems
  • A61K 31/4985 - Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems

37.

Liver X receptor modulators

      
Application Number 14385688
Grant Number 09006244
Status In Force
Filing Date 2013-03-14
First Publication Date 2015-02-19
Grant Date 2015-04-14
Owner VITAE PHARMACEUTICALS, LLC (USA)
Inventor
  • Dong, Chengguo
  • Fan, Yi
  • Leftheris, Katerina
  • Lotesta, Stephen D.
  • Singh, Suresh B.
  • Tice, Colin M.
  • Zhao, Wei
  • Zheng, Yajun
  • Zhuang, Linghang

Abstract

Provided herein are novel compounds and pharmaceutically acceptable salts thereof that are liver X receptor modulators. Also provided are compositions comprising compounds of the invention and a carrier. Additionally, use of the compounds herein and methods for treating a disease or disorder associated with the liver X receptor are further described.

IPC Classes  ?

  • C07D 487/04 - Ortho-condensed systems
  • A61K 31/4985 - Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems