WO2018151562A3 - Jnk 저해 활성을 갖는 신규한 벤즈이미다졸 유도체 및 이의 용도 - Google Patents
Jnk 저해 활성을 갖는 신규한 벤즈이미다졸 유도체 및 이의 용도 Download PDFInfo
- Publication number
- WO2018151562A3 WO2018151562A3 PCT/KR2018/001999 KR2018001999W WO2018151562A3 WO 2018151562 A3 WO2018151562 A3 WO 2018151562A3 KR 2018001999 W KR2018001999 W KR 2018001999W WO 2018151562 A3 WO2018151562 A3 WO 2018151562A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- inhibitory activity
- benzimidazole derivative
- novel benzimidazole
- jnk
- jnk inhibitory
- Prior art date
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—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
- C07D401/14—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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—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
- C07D405/14—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
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
본 발명은 JNK (C-Jun N-terminal kinase) 저해 활성을 갖는 신규한 벤즈이미다졸 유도체 및 이의 용도에 관한 것이다. 본 발명에 따른 신규 벤즈이미다졸유도체 또는 이의 약학적으로 허용가능한 염은 JNK 3 (c-Jun N-terminal kinase 3)에 대한 우수한 저해 활성을 나타내는바, 퇴행성 뇌신경계 질환의 예방 또는 치료에 있어서, 보다 근본적으로 접근하여 타겟 치료할 수 있을 것으로 기대된다.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US16/544,029 US10781201B2 (en) | 2017-02-20 | 2019-08-19 | Benzimidazole derivative having JNK inhibitory activity and use thereof |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020170022188A KR101840674B1 (ko) | 2017-02-20 | 2017-02-20 | Jnk 저해 활성을 갖는 신규한 벤즈이미다졸 유도체 및 이의 용도 |
KR10-2017-0022188 | 2017-02-20 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US16/544,029 Continuation US10781201B2 (en) | 2017-02-20 | 2019-08-19 | Benzimidazole derivative having JNK inhibitory activity and use thereof |
Publications (3)
Publication Number | Publication Date |
---|---|
WO2018151562A2 WO2018151562A2 (ko) | 2018-08-23 |
WO2018151562A3 true WO2018151562A3 (ko) | 2018-12-13 |
WO2018151562A9 WO2018151562A9 (ko) | 2019-01-10 |
Family
ID=61900488
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/KR2018/001999 WO2018151562A2 (ko) | 2017-02-20 | 2018-02-19 | Jnk 저해 활성을 갖는 신규한 벤즈이미다졸 유도체 및 이의 용도 |
Country Status (3)
Country | Link |
---|---|
US (1) | US10781201B2 (ko) |
KR (1) | KR101840674B1 (ko) |
WO (1) | WO2018151562A2 (ko) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR102514245B1 (ko) * | 2019-12-03 | 2023-03-29 | 한양대학교 에리카산학협력단 | 단백질 인산화 효소 저해 활성을 갖는 신규한 피라졸 유도체 및 이의 용도 |
KR102510351B1 (ko) * | 2020-02-28 | 2023-03-17 | 한양대학교 에리카산학협력단 | 단백질 인산화 효소 저해 활성을 갖는 신규한 이미다졸 유도체 및 이의 용도 |
KR102642716B1 (ko) * | 2021-08-18 | 2024-03-04 | 한양대학교 에리카산학협력단 | 단백질 인산화 효소 저해 활성을 갖는 신규한 이미다졸 유도체 및 이의 용도 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003000682A1 (en) * | 2001-06-25 | 2003-01-03 | Merck & Co., Inc. | (pyrimidyl)(phenyl)substituted fused heteroaryl p38 inhibiting and pkg kinase inhibiting compounds |
KR20080015475A (ko) * | 2005-07-01 | 2008-02-19 | 아이알엠 엘엘씨 | 단백질 키나제 억제제로서의 피리미딘-치환 벤즈이미다졸유도체 |
KR20140111521A (ko) * | 2013-03-11 | 2014-09-19 | 한양대학교 에리카산학협력단 | 신규 벤즈이미다졸 유도체, 이의 이성질체 또는 이의 약학적으로 허용 가능한 염, 및 이를 포함하는 약학 조성물 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100337189B1 (ko) | 1999-09-30 | 2002-05-18 | 복성해 | 인간세포의 인산화 효소 jnk의 활성 조절인자로 작용하는 마우스의 skip 단백질 및 skip 유전자 |
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2017
- 2017-02-20 KR KR1020170022188A patent/KR101840674B1/ko active IP Right Grant
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2018
- 2018-02-19 WO PCT/KR2018/001999 patent/WO2018151562A2/ko active Application Filing
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2019
- 2019-08-19 US US16/544,029 patent/US10781201B2/en active Active
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003000682A1 (en) * | 2001-06-25 | 2003-01-03 | Merck & Co., Inc. | (pyrimidyl)(phenyl)substituted fused heteroaryl p38 inhibiting and pkg kinase inhibiting compounds |
KR20080015475A (ko) * | 2005-07-01 | 2008-02-19 | 아이알엠 엘엘씨 | 단백질 키나제 억제제로서의 피리미딘-치환 벤즈이미다졸유도체 |
KR20140111521A (ko) * | 2013-03-11 | 2014-09-19 | 한양대학교 에리카산학협력단 | 신규 벤즈이미다졸 유도체, 이의 이성질체 또는 이의 약학적으로 허용 가능한 염, 및 이를 포함하는 약학 조성물 |
Non-Patent Citations (2)
Title |
---|
KIM, M. -H. ET AL.: "3D-QSAR Studies of 1,2-diaryl-1H-benzimidazole Derivatives as JNK3 Inhibitors with Protective Effects in Neuronal Cells", BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, vol. 23, no. 6, 2013, pages 1639 - 1642, XP028986080 * |
KIM, M. -H. ET AL.: "Syntheses and Biological Evaluation of 1-heteroaryl-2-aryl-1H- benzimidazole Derivatives as C-Jun N-terminal Kinase Inhibitors with Neuroprotective Effects", BIOORGANIC & MEDICINAL CHEMISTRY, vol. 21, no. 8, 2013, pages 2271 - 2285, XP028596342 * |
Also Published As
Publication number | Publication date |
---|---|
KR101840674B1 (ko) | 2018-03-21 |
WO2018151562A2 (ko) | 2018-08-23 |
US20200039959A1 (en) | 2020-02-06 |
WO2018151562A9 (ko) | 2019-01-10 |
US10781201B2 (en) | 2020-09-22 |
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