UY37018A - Inhibidores bicíclicos de pad4 - Google Patents
Inhibidores bicíclicos de pad4Info
- Publication number
- UY37018A UY37018A UY0001037018A UY37018A UY37018A UY 37018 A UY37018 A UY 37018A UY 0001037018 A UY0001037018 A UY 0001037018A UY 37018 A UY37018 A UY 37018A UY 37018 A UY37018 A UY 37018A
- Authority
- UY
- Uruguay
- Prior art keywords
- pad4
- bicyclic inhibitors
- inhibitors
- bicyclic
- compositions
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- 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
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- A61K31/435—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
- A61K31/4353—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
- A61K31/437—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
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- A61K31/435—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
- A61K31/4353—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
- A61K31/4375—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 heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
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- A61K31/435—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
- A61K31/439—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 forming part of a bridged ring system, e.g. quinuclidine
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- 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
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- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
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Abstract
La presente invención proporciona compuestos útiles como inhibidores de PAD4, composiciones de estos y métodos para tratar trastornos relacionados con PAD4.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US201562264925P | 2015-12-09 | 2015-12-09 |
Publications (1)
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UY37018A true UY37018A (es) | 2017-06-30 |
Family
ID=59013640
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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UY0001037018A UY37018A (es) | 2015-12-09 | 2016-12-09 | Inhibidores bicíclicos de pad4 |
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US (1) | US9963448B2 (es) |
EP (2) | EP3386590B1 (es) |
JP (1) | JP6932136B2 (es) |
KR (1) | KR20180098574A (es) |
CN (1) | CN109069869B (es) |
AR (1) | AR107032A1 (es) |
AU (1) | AU2016366398A1 (es) |
BR (1) | BR112018011709A2 (es) |
CA (1) | CA3007639A1 (es) |
EA (1) | EA201891251A1 (es) |
ES (1) | ES2877543T3 (es) |
IL (1) | IL259794A (es) |
MX (1) | MX2018006632A (es) |
SG (1) | SG11201804668UA (es) |
TW (1) | TW201726674A (es) |
UY (1) | UY37018A (es) |
WO (1) | WO2017100594A1 (es) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA3199601A1 (en) * | 2015-05-21 | 2016-11-24 | Glaxosmithkline Intellectual Property Development Limited | Benzoimidazole derivatives as pad4 inhibitors |
KR20180110160A (ko) | 2016-02-23 | 2018-10-08 | 패들락 테라퓨틱스, 인코포레이티드 | Pad4의 헤테로아릴 억제제 |
CN109790162B (zh) | 2016-07-27 | 2022-06-28 | 帕德罗科治疗公司 | Pad4的共价抑制剂 |
JP7118951B2 (ja) | 2016-09-12 | 2022-08-16 | パドロック・セラピューティクス・インコーポレイテッド | Pad4のヘテロアリール阻害剤 |
EP3760628A4 (en) * | 2018-02-26 | 2021-10-13 | Nanjing Transthera Biosciences Co., Ltd. | PEPTIDYLARGININE DEIMINASE INHIBITOR AND ITS USES |
US20220348562A1 (en) * | 2018-08-08 | 2022-11-03 | Bristol-Myers Squibb Company | Benzimidazole inhibitors of pad enzymes |
EP3833671B1 (en) * | 2018-08-08 | 2022-08-24 | Bristol-Myers Squibb Company | Substituted thienopyrroles as pad4 inhibitors |
AU2019318415A1 (en) * | 2018-08-08 | 2021-03-25 | Bristol-Myers Squibb Company | Substituted benzimidazoles as PAD4 inhibitors |
US11524959B1 (en) | 2018-08-08 | 2022-12-13 | Bristol-Myers Squibb Company | Indole and azaindole inhibitors of pad enzymes |
WO2020194160A1 (en) | 2019-03-28 | 2020-10-01 | Lupin Limited | Macrocyclic compounds as sting agonists |
WO2021057910A1 (zh) * | 2019-09-27 | 2021-04-01 | 南京药捷安康生物科技有限公司 | 肽酰精氨酸脱亚胺酶抑制剂及其用途 |
KR20220137694A (ko) * | 2020-02-06 | 2022-10-12 | 브리스톨-마이어스 스큅 컴퍼니 | 면역억제제로서 유용한 마크로시클릭 pad4 억제제 |
CR20220550A (es) | 2020-04-30 | 2022-12-15 | Gilead Sciences Inc | Inhibidores macrocíclicos de las peptidilarginina deiminasas |
US11878965B2 (en) | 2020-12-22 | 2024-01-23 | Gilead Sciences, Inc. | Inhibitors of peptidylarginine deiminases |
CN112618546B (zh) * | 2020-12-22 | 2022-03-01 | 陈昊 | Pad4抑制剂在制备放射治疗增敏药物方面的应用 |
WO2024109945A1 (en) * | 2022-11-24 | 2024-05-30 | Helios Huaming Biopharma Co., Ltd. | Selenium containing heterocycle compounds and use thereof |
Family Cites Families (12)
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ITMI20012060A1 (it) * | 2001-10-05 | 2003-04-05 | Recordati Chem Pharm | Nuovi eterocilcli n-acilati |
US6897208B2 (en) | 2001-10-26 | 2005-05-24 | Aventis Pharmaceuticals Inc. | Benzimidazoles |
JP2006513159A (ja) | 2002-11-01 | 2006-04-20 | メルク エンド カムパニー インコーポレーテッド | アンドロゲン受容体モジュレーターとしてのカルボニルアミノ−ベンズイミダゾール誘導体 |
US20110052562A1 (en) | 2007-12-19 | 2011-03-03 | The Scripps Research Institute | Benzimidazoles and analogs as rho kinase inhibitors |
US8710039B2 (en) * | 2010-11-01 | 2014-04-29 | The Penn State Research Foundation | Therapeutic compositions and methods |
JP5721484B2 (ja) | 2011-03-17 | 2015-05-20 | 富士フイルム株式会社 | 重合性液晶組成物、それを用いた高分子材料および光学異方性フィルム、並びに重合性液晶化合物 |
WO2013052263A2 (en) | 2011-09-16 | 2013-04-11 | Microbiotix, Inc. | Antifungal compounds |
WO2013157021A1 (en) | 2012-04-20 | 2013-10-24 | Advinus Therapeutics Limited | Bicyclic compounds, compositions and medicinal applications thereof |
EP2858983B1 (en) | 2012-06-11 | 2018-04-18 | UCB Biopharma SPRL | Tnf-alpha modulating benzimidazoles |
MX2014015769A (es) | 2012-06-29 | 2015-04-10 | Pfizer | 7h-pirrolo[2,3-d]pirimidinas 4-(amino-substituidas)novedosas como inhibidores de lrrk2. |
ES2609126T3 (es) * | 2012-07-26 | 2017-04-18 | Glaxo Group Limited | 2-(Azaindol-2-il)benzimidazoles como inhibidores de PAD4 |
CA3199601A1 (en) * | 2015-05-21 | 2016-11-24 | Glaxosmithkline Intellectual Property Development Limited | Benzoimidazole derivatives as pad4 inhibitors |
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2016
- 2016-12-07 AR ARP160103778A patent/AR107032A1/es unknown
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- 2016-12-09 WO PCT/US2016/065857 patent/WO2017100594A1/en active Application Filing
- 2016-12-09 CA CA3007639A patent/CA3007639A1/en not_active Abandoned
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- 2016-12-09 MX MX2018006632A patent/MX2018006632A/es unknown
- 2016-12-09 KR KR1020187019382A patent/KR20180098574A/ko not_active Application Discontinuation
- 2016-12-09 EP EP16873928.2A patent/EP3386590B1/en active Active
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- 2016-12-09 US US15/374,159 patent/US9963448B2/en active Active
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- 2016-12-09 JP JP2018549402A patent/JP6932136B2/ja active Active
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2018
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EP3386590A4 (en) | 2019-10-16 |
US9963448B2 (en) | 2018-05-08 |
CN109069869A (zh) | 2018-12-21 |
EA201891251A1 (ru) | 2018-12-28 |
US20170166565A1 (en) | 2017-06-15 |
WO2017100594A1 (en) | 2017-06-15 |
BR112018011709A2 (pt) | 2018-12-04 |
IL259794A (en) | 2018-08-30 |
CN109069869B (zh) | 2022-09-13 |
AU2016366398A1 (en) | 2018-07-19 |
TW201726674A (zh) | 2017-08-01 |
JP6932136B2 (ja) | 2021-09-08 |
MX2018006632A (es) | 2018-11-09 |
ES2877543T3 (es) | 2021-11-17 |
JP2019505568A (ja) | 2019-02-28 |
EP3386590A1 (en) | 2018-10-17 |
CA3007639A1 (en) | 2017-06-15 |
AR107032A1 (es) | 2018-03-14 |
EP3386590B1 (en) | 2021-06-02 |
SG11201804668UA (en) | 2018-06-28 |
KR20180098574A (ko) | 2018-09-04 |
EP3885342A1 (en) | 2021-09-29 |
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