Fochon Biosciences, Ltd.

China

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2024 4
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IPC Class
A61P 35/00 - Antineoplastic agents 16
C07D 471/04 - Ortho-condensed systems 16
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
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 8
C07D 487/04 - Ortho-condensed systems 8
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Status
Pending 12
Registered / In Force 16
Found results for  patents

1.

GLP-1R AGONISTS AND USES THEREOF

      
Application Number CN2024072529
Publication Number 2024/153070
Status In Force
Filing Date 2024-01-16
Publication Date 2024-07-25
Owner FOCHON BIOSCIENCES, LTD. (China)
Inventor
  • Xu, Hua
  • Zhou, Chenglin
  • Zhao, Xingdong
  • Wang, Weibo

Abstract

Provided are certain GLP-1R agonists of formula (I), pharmaceutical compositions thereof, and methods of use thereof.

IPC Classes  ?

  • C07D 471/04 - Ortho-condensed systems
  • C07D 487/04 - Ortho-condensed systems
  • C07D 491/048 - Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
  • C07D 495/04 - Ortho-condensed systems
  • C07D 495/00 - Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
  • C07D 273/02 - Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups having two nitrogen atoms and only one oxygen atom
  • C07D 307/78 - Benzo [b] furansHydrogenated benzo [b] furans
  • C07D 333/54 - Benzo [b] thiophenesHydrogenated benzo [b] thiophenes with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
  • A61K 31/343 - Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
  • 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
  • A61K 31/403 - 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 carbocyclic rings, e.g. carbazole
  • A61K 31/381 - Heterocyclic compounds having sulfur as a ring hetero atom having five-membered rings
  • A61K 31/4245 - Oxadiazoles
  • A61P 3/04 - AnorexiantsAntiobesity agents
  • A61P 3/06 - Antihyperlipidemics
  • A61P 3/10 - Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
  • A61P 9/06 - Antiarrhythmics
  • A61P 9/10 - Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
  • A61P 9/12 - Antihypertensives
  • A61P 25/16 - Anti-Parkinson drugs
  • A61P 25/28 - Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
  • A61P 1/16 - Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics

2.

COMPOUNDS AS PROTEIN KINASE INHIBITORS

      
Application Number CN2023131038
Publication Number 2024/099437
Status In Force
Filing Date 2023-11-10
Publication Date 2024-05-16
Owner FOCHON BIOSCIENCES, LTD. (China)
Inventor
  • Xu, Hua
  • He, Chengxi
  • Zhou, Zuwen
  • Rong, Yue
  • Zhang, Huajie
  • Zhou, Chenglin
  • Zhao, Xingdong
  • Dong, Wenjing
  • Jiang, Lihua
  • Lin, Shu
  • Wang, Weibo

Abstract

Provided are certain PI3K inhibitors, pharmaceutical compositions thereof, and methods of use thereof.

IPC Classes  ?

  • C07D 471/04 - Ortho-condensed systems
  • C07D 405/04 - 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 directly linked by a ring-member-to-ring- member bond
  • 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 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 239/90 - Oxygen atoms with acyclic radicals attached in position 2 or 3
  • A61K 31/519 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
  • A61P 35/00 - Antineoplastic agents

3.

COMPOUNDS AS BCL-2 INHIBITORS

      
Application Number CN2023112491
Publication Number 2024/032755
Status In Force
Filing Date 2023-08-11
Publication Date 2024-02-15
Owner FOCHON BIOSCIENCES, LTD. (China)
Inventor
  • He, Chengxi
  • Tan, Rui
  • Zhou, Chenglin
  • Zhao, Xingdong
  • Wang, Weibo

Abstract

Provided are certain BCL-2 inhibitors, pharmaceutical compositions thereof, and methods of use thereof.

IPC Classes  ?

  • C07D 471/04 - Ortho-condensed systems
  • C07D 498/14 - Ortho-condensed systems
  • C07D 498/12 - Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero 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 31/4375 - 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 six-membered ring having nitrogen as a ring hetero atom, e.g. quinolizines, naphthyridines, berberine, vincamine
  • 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
  • A61K 31/538 - 1,4-Oxazines, e.g. morpholine ortho- or peri-condensed with carbocyclic ring systems
  • A61K 31/553 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and at least one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
  • A61P 35/00 - Antineoplastic agents
  • A61P 35/02 - Antineoplastic agents specific for leukemia
  • A61P 35/04 - Antineoplastic agents specific for metastasis
  • A61P 37/00 - Drugs for immunological or allergic disorders
  • A61P 37/02 - Immunomodulators
  • A61P 37/06 - Immunosuppressants, e.g. drugs for graft rejection
  • A61P 37/08 - Antiallergic agents
  • A61P 25/00 - Drugs for disorders of the nervous system
  • A61P 25/28 - Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia

4.

COMPOUNDS AS BCL-2 INHIBITORS

      
Application Number CN2023112601
Publication Number 2024/032776
Status In Force
Filing Date 2023-08-11
Publication Date 2024-02-15
Owner FOCHON BIOSCIENCES, LTD. (China)
Inventor
  • Zhou, Chenglin
  • Zhao, Xingdong
  • Wang, Weibo

Abstract

Provided are certain BCL-2 inhibitors, pharmaceutical compositions thereof, and methods of use thereof.

IPC Classes  ?

  • C07D 471/04 - Ortho-condensed systems
  • C07D 498/04 - Ortho-condensed systems
  • C07D 498/14 - Ortho-condensed systems
  • C07D 498/22 - Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains four or more hetero rings
  • 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
  • A61K 31/538 - 1,4-Oxazines, e.g. morpholine ortho- or peri-condensed with carbocyclic ring systems
  • A61P 35/00 - Antineoplastic agents
  • A61P 37/00 - Drugs for immunological or allergic disorders

5.

SUBSTITUTED PYRROLO [2, 3-b] PYRIDINE AND PYRAZOLO [3, 4-b] PYRIDINE DERIVATIVES AS PROTEIN KINASE INHIBITORS

      
Application Number 18253252
Status Pending
Filing Date 2021-11-16
First Publication Date 2023-12-21
Owner Fochon Biosciences, Ltd. (China)
Inventor
  • Tan, Haohan
  • Liu, Qihong
  • Wang, Yunling
  • Jiang, Lihua
  • Lin, Shu
  • Zhao, Xingdong
  • Wang, Weibo

Abstract

Provided are certain BTK inhibitors, pharmaceutical compositions thereof, and methods of use thereof.

IPC Classes  ?

6.

COMPOUNDS AS BCL-2 INHIBITORS

      
Application Number CN2023094781
Publication Number 2023/231777
Status In Force
Filing Date 2023-05-17
Publication Date 2023-12-07
Owner
  • FOCHON PHARMACEUTICALS, LTD. (China)
  • FOCHON BIOSCIENCES, LTD. (China)
Inventor
  • Xu, Hua
  • Huang, Zhuo
  • Jia, Xiaodong
  • Zhang, Weipeng
  • Tan, Rui
  • Zheng, Anquan
  • Wang, Binglei
  • Tan, Haohan
  • Gao, Fan
  • Rong, Yue
  • Liu, Hongbin
  • Yu, Jinhua
  • Zhou, Chenglin
  • Liu, Yanxin
  • Lin, Shu
  • Zhao, Xingdong
  • Wang, Weibo

Abstract

Provided are certain BCL-2 inhibitors, pharmaceutical compositions thereof, and methods of use thereof.

IPC Classes  ?

  • C07D 471/04 - Ortho-condensed systems
  • C07D 471/10 - Spiro-condensed systems
  • 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 498/14 - 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 31/496 - Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
  • A61K 31/499 - Spiro-condensed pyrazines or piperazines
  • A61P 35/00 - Antineoplastic agents
  • A61P 37/00 - Drugs for immunological or allergic disorders

7.

COMPOUNDS AS SARS-COV-2 INHIBITORS

      
Application Number CN2023078655
Publication Number 2023/165459
Status In Force
Filing Date 2023-02-28
Publication Date 2023-09-07
Owner FOCHON BIOSCIENCES , LTD. (China)
Inventor
  • He, Chengxi
  • Xu, Hua
  • Liu, Qihong
  • Liu, Bin
  • Qi, Yangli
  • Zhou, Zuwen
  • Tan, Rui
  • Huang, Zhuo
  • Tan, Haohan
  • Chen, Zhifang
  • Li, Zhifu
  • Wang, Yunling
  • Chen, Ling
  • Wang, Xianlong
  • Yang, Lijun
  • Dong, Wenjing
  • Lin, Shu
  • Zhao, Xingdong
  • Wang, Weibo

Abstract

Provided are certain antiviral agents, pharmaceutical compositions thereof, and methods of use thereof.

IPC Classes  ?

  • 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 419/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms containing three or more hetero rings
  • A61K 31/513 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
  • 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
  • A61P 31/12 - Antivirals

8.

COMPOUNDS AS PROTEIN KINASE INHIBITORS

      
Application Number 17998998
Status Pending
Filing Date 2021-05-14
First Publication Date 2023-06-08
Owner Fochon Biosciences, Ltd. (China)
Inventor
  • Zhou, Zuwen
  • Tan, Rui
  • Xu, Hua
  • Liu, Qihong
  • Zhang, Huajie
  • Liu, Bin
  • Zhang, Weipeng
  • Li, Zhifu
  • Liu, Yanxin
  • Lin, Shu
  • Zhao, Xingdong
  • Wang, Weibo

Abstract

Provided are certain PI3K inhibitors, pharmaceutical compositions thereof, and methods of use thereof.

IPC Classes  ?

  • 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
  • A61P 35/00 - Antineoplastic agents

9.

COMPOUNDS AS BCL-2 INHIBITORS

      
Application Number 17998234
Status Pending
Filing Date 2021-05-07
First Publication Date 2023-05-25
Owner FOCHON BIOSCIENCES, LTD. (China)
Inventor
  • Zhang, Weipeng
  • Liu, Hongbin
  • Tan, Rui
  • Li, Zhifu
  • Rong, Yue
  • Liu, Qihong
  • Chen, Zhifang
  • Chen, Ling
  • Xu, Hua
  • Zhou, Zuwen
  • Yu, Jinhua
  • Tan, Haohan
  • Liu, Bin
  • Wang, Yunling
  • Yang, Lijun
  • He, Chengxi
  • Jiang, Lihua
  • Lin, Shu
  • Zhao, Xingdong
  • Wang, Weibo

Abstract

Provided are certain Bcl-2 inhibitors, pharmaceutical compositions thereof, and methods of use thereof.

IPC Classes  ?

  • C07D 471/04 - Ortho-condensed systems
  • C07D 498/14 - Ortho-condensed systems
  • C07D 471/14 - 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

10.

COMPOUNDS AS SARS-COV-2 INHIBITORS

      
Application Number CN2022132823
Publication Number 2023/088418
Status In Force
Filing Date 2022-11-18
Publication Date 2023-05-25
Owner FOCHON BIOSCIENCES, LTD. (China)
Inventor
  • He, Chengxi
  • Xu, Hua
  • Yu, Jinhua
  • Liu, Qihong
  • Qi, Yangli
  • Huang, Zhuo
  • Jiang, Lihua
  • Lin, Shu
  • Zhao, Xingdong
  • Wang, Weibo

Abstract

Provided are certain antiviral agents, pharmaceutical compositions thereof, and methods of use thereof.

IPC Classes  ?

  • C07D 487/06 - Peri-condensed systems
  • C07D 401/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 209/18 - Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
  • C07D 209/02 - Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
  • 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
  • A61K 31/403 - 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 carbocyclic rings, e.g. carbazole
  • 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 31/14 - Antivirals for RNA viruses

11.

COMPOUNDS USEFUL AS KINASE INHIBITORS

      
Application Number 17906178
Status Pending
Filing Date 2021-03-10
First Publication Date 2023-05-11
Owner Fochon Biosciences, Ltd. (China)
Inventor
  • He, Chengxi
  • Wang, Xianlong
  • Rong, Yue
  • Tan, Rui
  • Zhang, Huajie
  • Tan, Haohan
  • Liu, Yanxin
  • Lin, Shu
  • Li, Tongshuang
  • Zhao, Xingdong
  • Wang, Weibo

Abstract

Provided are certain BTK inhibitors, pharmaceutical compositions thereof, and methods of use thereof.

IPC Classes  ?

12.

COMPOUNDS AS PROTEIN KINASE INHIBITORS

      
Application Number CN2022129918
Publication Number 2023/078401
Status In Force
Filing Date 2022-11-04
Publication Date 2023-05-11
Owner FOCHON BIOSCIENCES, LTD. (China)
Inventor
  • Tan, Haohan
  • Li, Zhifu
  • Liu, Bin
  • Wang, Yunling
  • He, Chengxi
  • Liu, Qihong
  • Xu, Hua
  • Qi, Yangli
  • Liu, Yanxin
  • Lin, Shu
  • Zhao, Xingdong
  • Wang, Weibo

Abstract

Provided are certain PI3K inhibitors, pharmaceutical compositions thereof, and methods of use thereof.

IPC Classes  ?

  • C07D 471/04 - Ortho-condensed systems
  • C07D 487/04 - Ortho-condensed systems
  • 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
  • A61P 35/00 - Antineoplastic agents

13.

COMPOUNDS AS CDK2/4/6 INHIBITORS

      
Application Number 17905072
Status Pending
Filing Date 2021-02-26
First Publication Date 2023-05-04
Owner Fochon Biosciences, Ltd. (China)
Inventor
  • Zhang, Huajie
  • Xu, Hua
  • He, Chengxi
  • Chen, Ling
  • Yang, Lijun
  • Jiang, Lihua
  • Lin, Shu
  • Zhao, Xingdong
  • Wang, Weibo

Abstract

Provided are certain CDK2/4/6 inhibitors, pharmaceutical compositions thereof, and methods of use thereof.

IPC Classes  ?

  • C07D 475/00 - Heterocyclic compounds containing pteridine 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
  • A61K 45/06 - Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca

14.

COMPOUNDS AS ERK INHIBITORS

      
Application Number CN2022100072
Publication Number 2022/268065
Status In Force
Filing Date 2022-06-21
Publication Date 2022-12-29
Owner FOCHON BIOSCIENCES, LTD. (China)
Inventor
  • Li, Tongshuang
  • Liu, Qihong
  • Li, Zhifu
  • Zou, Zongyao
  • Lin, Shu
  • Zhao, Xingdong
  • Wang, Weibo

Abstract

Provided are certain ERK inhibitors, pharmaceutical compositions thereof, and methods of use thereof.

IPC Classes  ?

  • C07D 487/04 - Ortho-condensed systems
  • A61K 31/4162 - 1,2-Diazoles condensed with heterocyclic ring systems
  • A61K 31/506 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
  • A61P 35/00 - Antineoplastic agents

15.

COMPOUNDS AS BCL-2 INHIBITORS

      
Document Number 03238781
Status Pending
Filing Date 2022-11-10
Open to Public Date 2022-11-10
Owner FOCHON BIOSCIENCES, LTD. (China)
Inventor
  • Liu, Hongbin
  • Xu, Hua
  • Zhang, Weipeng
  • Tan, Rui
  • Yu, Jinhua
  • Wang, Yunling
  • Qi, Yangli
  • Rong, Yue
  • Huang, Zhuo
  • Chen, Ling
  • Zhou, Chenglin
  • Jiang, Lihua
  • Lin, Shu
  • Zhao, Xingdong
  • Wang, Weibo

Abstract

Provided are certain BCL-2 inhibitors, pharmaceutical compositions thereof, and methods of use thereof.

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 31/444 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. amrinone
  • C07D 471/10 - Spiro-condensed systems
  • C07D 497/04 - Ortho-condensed systems
  • C07D 498/14 - Ortho-condensed systems

16.

COMPOUNDS AS PARP INHIBITORS

      
Application Number CN2022088989
Publication Number 2022/228387
Status In Force
Filing Date 2022-04-25
Publication Date 2022-11-03
Owner FOCHON BIOSCIENCES, LTD. (China)
Inventor
  • Xu, Hua
  • Wang, Xianlong
  • Zhou, Zuwen
  • Li, Zhifu
  • Liu, Qihong
  • Tan, Haohan
  • Rong, Yue
  • Liu, Hongbin
  • Jiang, Lihua
  • Lin, Shu
  • Zhao, Xingdong
  • Wang, Weibo

Abstract

Provided are certain PARP inhibitors, pharmaceutical compositions thereof, and methods of use thereof.

IPC Classes  ?

  • C07D 471/04 - Ortho-condensed systems
  • 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 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
  • 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
  • A61K 31/495 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two nitrogen atoms as the only ring hetero atoms, e.g. piperazine
  • A61P 35/00 - Antineoplastic agents

17.

SUBSTITUTED PYRROLO [2, 3-B] PYRIDINE AND PYRAZOLO [3, 4-B] PYRIDINE DERIVATIVES AS PROTEIN KINASE INHIBITORS

      
Document Number 03198254
Status Pending
Filing Date 2021-11-16
Open to Public Date 2022-05-27
Owner FOCHON BIOSCIENCES, LTD. (China)
Inventor
  • Tan, Haohan
  • Liu, Qihong
  • Wang, Yunling
  • Jiang, Lihua
  • Lin, Shu
  • Zhao, Xingdong
  • Wang, Weibo

Abstract

Provided are certain BTK inhibitors, pharmaceutical compositions thereof, and methods of use thereof.

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
  • A61P 35/00 - Antineoplastic agents

18.

COMPOUNDS AS PROTEIN KINASE INHIBITORS

      
Document Number 03178569
Status Pending
Filing Date 2021-05-14
Open to Public Date 2021-11-25
Owner FOCHON BIOSCIENCES, LTD. (China)
Inventor
  • Zhou, Zuwen
  • Tan, Rui
  • Xu, Hua
  • Liu, Qihong
  • Zhang, Huajie
  • Liu, Bin
  • Zhang, Weipeng
  • Li, Zhifu
  • Liu, Yanxin
  • Lin, Shu
  • Zhao, Xingdong
  • Wang, Weibo

Abstract

Provided are certain PI3K inhibitors, pharmaceutical compositions thereof, and methods of use thereof.

IPC Classes  ?

19.

COMPOUNDS AS BCL-2 INHIBITORS

      
Document Number 03177906
Status Pending
Filing Date 2021-05-07
Open to Public Date 2021-11-11
Owner FOCHON BIOSCIENCES, LTD. (China)
Inventor
  • Zhang, Weipeng
  • Liu, Hongbin
  • Tan, Rui
  • Li, Zhifu
  • Rong, Yue
  • Liu, Qihong
  • Chen, Zhifang
  • Chen, Ling
  • Xu, Hua
  • Zhou, Zuwen
  • Yu, Jinhua
  • Tan, Haohan
  • Liu, Bin
  • Wang, Yunling
  • Yang, Lijun
  • He, Chengxi
  • Jiang, Lihua
  • Lin, Shu
  • Zhao, Xingdong
  • Wang, Weibo

Abstract

Provided are certain Bcl-2 inhibitors, pharmaceutical compositions thereof, and methods of use thereof.

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
  • C07D 471/10 - Spiro-condensed systems

20.

Macrocyclic compounds as TRK kinases inhibitors

      
Application Number 17042385
Grant Number 11555042
Status In Force
Filing Date 2019-03-27
First Publication Date 2021-05-13
Grant Date 2023-01-17
Owner Fochon Biosciences, Ltd. (China)
Inventor
  • Zhang, Huajie
  • Liu, Qihong
  • He, Chengxi
  • Zhang, Weipeng
  • Tan, Rui
  • Liu, Bin
  • Fu, Hong
  • Tan, Haohan
  • Yang, Lijun
  • Liu, Hongbin
  • Wang, Yunling
  • Gao, Yuwei
  • Zou, Zongyao
  • Liu, Yanxin
  • Lin, Shu
  • Li, Tongshuang
  • Zhao, Xingdong
  • Wang, Weibo

Abstract

Provided are certain TRK inhibitors, pharmaceutical compositions thereof, and methods of use thereof.

IPC Classes  ?

  • C07D 498/12 - Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
  • 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
  • A61K 31/519 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
  • A61P 29/00 - Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agentsNon-steroidal antiinflammatory drugs [NSAID]
  • A61P 35/00 - Antineoplastic agents
  • C07D 498/22 - Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains four or more hetero rings
  • C07D 487/22 - Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups in which the condensed system contains four or more hetero rings
  • C07D 498/20 - Spiro-condensed systems

21.

Sulfoximine, sulfonimidamide, sulfondiimine and diimidosulfonamide compounds as inhibitors of indoleamine 2,3-dioxygenase

      
Application Number 16464435
Grant Number 11168078
Status In Force
Filing Date 2017-11-28
First Publication Date 2021-03-11
Grant Date 2021-11-09
Owner FOCHON BIOSCIENCES, LTD. (China)
Inventor
  • Chen, Zhifang
  • Tan, Rui
  • Liu, Qihong
  • Yang, Lijun
  • Li, Zhifu
  • Tan, Haohan
  • Liu, Hongbin
  • Zhao, Xingdong
  • Lin, Min
  • Sun, Jing
  • Wang, Weibo

Abstract

Provided are certain IDO inhibitors or pharmaceutically acceptable salts thereof which can inhibit enzymatic activity of indoleamine 2,3-dioxygenase (IDO) and may be useful for the treatment of diseases and disorders mediated by IDO. In addition, pharmaceutical compositions thereof and methods of use thereof are also provided.

IPC Classes  ?

  • A61K 31/4245 - Oxadiazoles
  • C07D 411/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 271/08 - 1,2,5-OxadiazolesHydrogenated 1,2,5-oxadiazoles
  • C07D 409/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

22.

Substituted 2-azabicyclo[3.1.0]hexanes as TRK kinases inhibitors

      
Application Number 16980487
Grant Number 11459332
Status In Force
Filing Date 2019-03-13
First Publication Date 2021-01-28
Grant Date 2022-10-04
Owner Fochon Biosciences, Ltd. (China)
Inventor
  • Liu, Hongbin
  • Tan, Haohan
  • He, Chengxi
  • Wang, Xianlong
  • Liu, Qihong
  • Li, Zhifu
  • Zhou, Zuwen
  • Gao, Yuwei
  • Jiang, Lihua
  • Linghu, Li
  • Lin, Shu
  • Zhao, Xingdong
  • Wang, Weibo

Abstract

Provided are certain TRK inhibitors of formula (I): pharmaceutical compositions thereof, and methods of use thereof.

IPC Classes  ?

  • A61K 31/403 - 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 carbocyclic rings, e.g. carbazole
  • C07D 209/02 - Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
  • C07D 487/04 - 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
  • A61K 45/06 - Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca

23.

SUBSTITUTED PYRROLO [2, 3-B] PYRIDINE AND PYRAZOLO [3, 4-B] PYRIDINE DERIVATIVES AS PROTEIN KINASE INHIBITORS

      
Document Number 03137985
Status Pending
Filing Date 2020-06-01
Open to Public Date 2020-12-03
Owner FOCHON BIOSCIENCES, LTD. (China)
Inventor
  • Tan, Haohan
  • Liu, Qihong
  • Liu, Bin
  • Li, Zhifu
  • Wang, Xianlong
  • Zhou, Zuwen
  • Zhang, Weipeng
  • Wang, Yunling
  • Zhou, Chenglin
  • Gao, Yuwei
  • Jiang, Lihua
  • Liu, Yanxin
  • Zou, Zongyao
  • Lin, Shu
  • Yu, Kai
  • Li, Tongshuang
  • Zhao, Xingdong
  • Wang, Weibo

Abstract

Provided are certain BTK inhibitors, pharmaceutical compositions thereof, and methods of use thereof.

IPC Classes  ?

  • 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
  • A61K 31/519 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
  • A61P 35/00 - Antineoplastic agents
  • C07D 471/04 - Ortho-condensed systems
  • C07D 487/04 - Ortho-condensed systems

24.

MACROCYCLIC COMPOUNDS AS TRK KINASES INHIBITORS

      
Document Number 03093140
Status Pending
Filing Date 2019-03-27
Open to Public Date 2019-10-03
Owner FOCHON BIOSCIENCES, LTD. (China)
Inventor
  • Zhang, Huajie
  • Liu, Qihong
  • He, Chengxi
  • Zhang, Weipeng
  • Tan, Rui
  • Liu, Bin
  • Fu, Hong
  • Tan, Haohan
  • Yang, Lijun
  • Liu, Hongbin
  • Wang, Yunling
  • Gao, Yuwei
  • Zou, Zongyao
  • Liu, Yanxin
  • Lin, Shu
  • Li, Tongshuang
  • Zhao, Xingdong
  • Wang, Weibo

Abstract

Provided are certain TRK ithibitors, pharmaceutical compositions thereof, and methods of use thereof.

IPC Classes  ?

  • C07D 487/04 - Ortho-condensed systems
  • A61K 31/519 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
  • A61P 29/00 - Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agentsNon-steroidal antiinflammatory drugs [NSAID]
  • A61P 35/00 - Antineoplastic agents
  • C07D 498/22 - Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains four or more hetero rings
  • 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

25.

SUBSTITUTED (2-AZABICYCLO[3.1.0]HEXAN-2-YL)PYRAZOLO[1,5-.ALPHA.]PYRIMIDINE AND IMIDAZO[1,2-B]PYRIDAZINE COMPOUNDS AS TRK KINASES INHIBITORS

      
Document Number 03092416
Status Pending
Filing Date 2019-03-13
Open to Public Date 2019-09-19
Owner FOCHON BIOSCIENCES, LTD. (China)
Inventor
  • Liu, Hongbin
  • Tan, Haohan
  • He, Chengxi
  • Wang, Xianlong
  • Liu, Qihong
  • Li, Zhifu
  • Zhou, Zuwen
  • Gao, Yuwei
  • Jiang, Lihua
  • Linghu, Li
  • Lin, Shu
  • Zhao, Xingdong
  • Wang, Weibo

Abstract

Provided are certain TRK inhibitors, pharmaceutical compositions thereof, and methods of use thereof.

IPC Classes  ?

  • C07D 487/04 - Ortho-condensed systems
  • A61K 31/519 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
  • A61P 35/00 - Antineoplastic agents
  • 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

26.

Certain protein kinase inhibitor

      
Application Number 15569709
Grant Number 10450316
Status In Force
Filing Date 2016-04-28
First Publication Date 2018-10-11
Grant Date 2019-10-22
Owner FOCHON BIOSCIENCES, LTD. (China)
Inventor
  • Zhao, Xingdong
  • Li, Tongshuang
  • Tan, Haohan
  • Chen, Zhifang
  • Chen, Ling
  • Liu, Qihong
  • Rong, Yue
  • Yang, Lijun
  • Wang, Xianlong
  • Tan, Rui
  • Zhou, Zuwen
  • Liu, Bin
  • Lin, Min
  • Jiang, Lihua
  • Liu, Yanxin
  • Linghu, Li
  • Sun, Jing
  • Wang, Weibo

Abstract

Provided are certain CDK4/6 inhibitors with the structure of formula (I), pharmaceutical compositions thereof, and methods of use therefor. The compounds are of the class of pyrimidin-2 amine derivatives, useful for the treatment of hyper-proliferative diseases.

IPC Classes  ?

  • C07D 487/04 - Ortho-condensed systems
  • 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 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
  • A61K 45/06 - Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
  • A61K 31/506 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
  • C07D 487/10 - Spiro-condensed systems
  • C07D 471/14 - 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
  • A61P 35/00 - Antineoplastic agents
  • A61K 31/5383 - 1,4-Oxazines, e.g. morpholine ortho- or peri-condensed with heterocyclic ring systems

27.

Certain protein kinase inhibitors

      
Application Number 15523315
Grant Number 10328060
Status In Force
Filing Date 2015-11-01
First Publication Date 2018-02-08
Grant Date 2019-06-25
Owner FOCHON BIOSCIENCES, LTD. (China)
Inventor
  • Zhao, Xingdong
  • Ding, Jian
  • Meng, Linghua
  • Geng, Meiyu
  • Li, Tongshuang
  • Zhou, Zuwen
  • Chen, Ling
  • Liu, Qihong
  • Wang, Xianlong
  • Yang, Lijun
  • Rong, Yue
  • Tan, Rui
  • Yu, Chuiliang
  • Jiang, Lihua
  • Liu, Yanxin
  • Linghu, Li
  • Sun, Jing
  • Wang, Weibo

Abstract

Provided are certain PI3K inhibitors, pharmaceutical compositions thereof, and methods of use therefor.

IPC Classes  ?

  • 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
  • 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 45/06 - Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
  • A61K 31/4375 - 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 six-membered ring having nitrogen as a ring hetero atom, e.g. quinolizines, naphthyridines, berberine, vincamine
  • A61K 31/505 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim
  • A61K 31/52 - Purines, e.g. adenine

28.

PHOSPHOINOSITIDE 3-KINASE INHIBITORS

      
Document Number 02966252
Status In Force
Filing Date 2015-11-01
Open to Public Date 2016-05-06
Grant Date 2023-10-24
Owner
  • SHANGHAI INSTITUTE OF MATERIA MEDICA CHINESE ACADEMY OF SCIENCES (China)
  • FOCHON BIOSCIENCES, LTD. (China)
Inventor
  • Zhao, Xingdong
  • Ding, Jian
  • Meng, Linghua
  • Geng, Meiyu
  • Li, Tongshuang
  • Zhou, Zuwen
  • Chen, Ling
  • Liu, Qihong
  • Wang, Xianlong
  • Yang, Lijun
  • Rong, Yue
  • Tan, Rui
  • Yu, Chuiliang
  • Jiang, Lihua
  • Liu, Yanxin
  • Linghu, Li
  • Sun, Jing
  • Wang, Weibo

Abstract

Provided are certain phosphoinositide 3-kinase (PI3K) inhibitors, pharmaceutical compositions thereof, and methods of use thereof For example, disclosed are compounds represented by formula I, or a pharmaceutically acceptable salt thereof The compounds of formula I can modulate PI3K , and inhibit the activity of PI3K. Accordingly, compounds of formula I can be used to treat, for example, cell proliferative disorders. (see formula I)

IPC Classes  ?

  • C07D 221/04 - Ortho- or peri-condensed ring systems
  • A61K 31/4355 - 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 oxygen as a ring hetero atom
  • A61K 31/4365 - 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 having sulfur as a ring hetero atom, e.g. ticlopidine
  • 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 35/00 - Antineoplastic agents
  • A61P 43/00 - Drugs for specific purposes, not provided for in groups
  • C07D 221/00 - Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups
  • C07D 513/04 - Ortho-condensed systems