JP6129217B2 - Hifヒドロキシラーゼインヒビターとしての4−ヒドロキシ−イソキノリン化合物 - Google Patents
Hifヒドロキシラーゼインヒビターとしての4−ヒドロキシ−イソキノリン化合物 Download PDFInfo
- Publication number
- JP6129217B2 JP6129217B2 JP2014561149A JP2014561149A JP6129217B2 JP 6129217 B2 JP6129217 B2 JP 6129217B2 JP 2014561149 A JP2014561149 A JP 2014561149A JP 2014561149 A JP2014561149 A JP 2014561149A JP 6129217 B2 JP6129217 B2 JP 6129217B2
- Authority
- JP
- Japan
- Prior art keywords
- hydroxy
- amino
- isoquinoline
- carbonyl
- cyano
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Links
- LEAONNXYTDZYOY-UHFFFAOYSA-N C#Cc(nc1C(NC(CC(O)=O)c(cc2)ccc2Cl)=O)c(cc(cc2)Oc3ccccc3)c2c1O Chemical compound C#Cc(nc1C(NC(CC(O)=O)c(cc2)ccc2Cl)=O)c(cc(cc2)Oc3ccccc3)c2c1O LEAONNXYTDZYOY-UHFFFAOYSA-N 0.000 description 1
- 0 C*(C(C)(*)*C(*)=O)C(*)(*)NC(c1nc(*)c(cc(C)cc2)c2c1O)=O Chemical compound C*(C(C)(*)*C(*)=O)C(*)(*)NC(c1nc(*)c(cc(C)cc2)c2c1O)=O 0.000 description 1
- VTVAEEQPTGZMBT-UHFFFAOYSA-N CC(C)(CC(O)=O)NC(c1ncc(cc(cc2)Oc3ccccc3)c2c1O)=O Chemical compound CC(C)(CC(O)=O)NC(c1ncc(cc(cc2)Oc3ccccc3)c2c1O)=O VTVAEEQPTGZMBT-UHFFFAOYSA-N 0.000 description 1
- FJEHFGCVLOBNDL-UHFFFAOYSA-N CC(C)(CNC(c(nc(c1c2ccc(NC(NCc3ccccc3)=O)c1)C#N)c2O)=O)C(O)=O Chemical compound CC(C)(CNC(c(nc(c1c2ccc(NC(NCc3ccccc3)=O)c1)C#N)c2O)=O)C(O)=O FJEHFGCVLOBNDL-UHFFFAOYSA-N 0.000 description 1
- ZHRLUKZSPXHMRV-UHFFFAOYSA-N CC(C)(CNC(c(nc(c1c2ccc(NC(c(cc3)ccc3F)=O)c1)C#N)c2O)=O)C(O)=O Chemical compound CC(C)(CNC(c(nc(c1c2ccc(NC(c(cc3)ccc3F)=O)c1)C#N)c2O)=O)C(O)=O ZHRLUKZSPXHMRV-UHFFFAOYSA-N 0.000 description 1
- CSOPJEAVQNOFDA-UHFFFAOYSA-N CC(C)(CNC(c(nc(c1c2ccc(OCc3ccccc3)c1)C#N)c2O)=O)C(O)=O Chemical compound CC(C)(CNC(c(nc(c1c2ccc(OCc3ccccc3)c1)C#N)c2O)=O)C(O)=O CSOPJEAVQNOFDA-UHFFFAOYSA-N 0.000 description 1
- LIPLTYRTHVKYLT-UHFFFAOYSA-N CC(C)CC(CC(O)=O)CNC(c1nc(C#N)c(cc(cc2)Oc3ccccc3)c2c1O)=O Chemical compound CC(C)CC(CC(O)=O)CNC(c1nc(C#N)c(cc(cc2)Oc3ccccc3)c2c1O)=O LIPLTYRTHVKYLT-UHFFFAOYSA-N 0.000 description 1
- HOZJGVRZKLKDAT-UHFFFAOYSA-N CC(CCC(O)=O)NC(c1nc(C#N)c(cc(cc2)Oc3ccccc3)c2c1O)=O Chemical compound CC(CCC(O)=O)NC(c1nc(C#N)c(cc(cc2)Oc3ccccc3)c2c1O)=O HOZJGVRZKLKDAT-UHFFFAOYSA-N 0.000 description 1
- CIEXUDARNJDRJD-UHFFFAOYSA-N COc(cc1)ccc1Oc1cc2cnc(C(NCCCCC(O)=O)=O)c(O)c2cc1 Chemical compound COc(cc1)ccc1Oc1cc2cnc(C(NCCCCC(O)=O)=O)c(O)c2cc1 CIEXUDARNJDRJD-UHFFFAOYSA-N 0.000 description 1
- ZONUPWOYJLMWNR-UHFFFAOYSA-N N#Cc([n+]([O-])c1C(NCCCC(O)=O)=O)c(cc(cc2)Oc3ccccc3)c2c1O Chemical compound N#Cc([n+]([O-])c1C(NCCCC(O)=O)=O)c(cc(cc2)Oc3ccccc3)c2c1O ZONUPWOYJLMWNR-UHFFFAOYSA-N 0.000 description 1
- UTAGYFGEPUYWLP-UHFFFAOYSA-N N#Cc(c1c2ccc(-c3ccccc3)c1)nc(C(NCCC(O)=O)=O)c2O Chemical compound N#Cc(c1c2ccc(-c3ccccc3)c1)nc(C(NCCC(O)=O)=O)c2O UTAGYFGEPUYWLP-UHFFFAOYSA-N 0.000 description 1
- WZJDYOWVFHSRTF-LJQANCHMSA-N N#Cc(c1c2ccc(Oc3ccccc3)c1)nc(C(N[C@H](CCc1ccccc1)CC(O)=O)=O)c2O Chemical compound N#Cc(c1c2ccc(Oc3ccccc3)c1)nc(C(N[C@H](CCc1ccccc1)CC(O)=O)=O)c2O WZJDYOWVFHSRTF-LJQANCHMSA-N 0.000 description 1
- QFVGBJOTYFRVOI-LBPRGKRZSA-N N#Cc(c1cc(Oc2ccccc2)ccc11)nc(C(NC[C@H](CC(O)=O)O)=O)c1O Chemical compound N#Cc(c1cc(Oc2ccccc2)ccc11)nc(C(NC[C@H](CC(O)=O)O)=O)c1O QFVGBJOTYFRVOI-LBPRGKRZSA-N 0.000 description 1
- RRUOOJXGLKPFSE-UHFFFAOYSA-N N#Cc(nc1C(NCC(C(O)=O)c(cccc2)c2F)=O)c(cc(cc2)Oc3ccccc3)c2c1O Chemical compound N#Cc(nc1C(NCC(C(O)=O)c(cccc2)c2F)=O)c(cc(cc2)Oc3ccccc3)c2c1O RRUOOJXGLKPFSE-UHFFFAOYSA-N 0.000 description 1
- IOROJGTUVPLIBU-UHFFFAOYSA-N N#Cc(nc1C(NCC2(CC(O)=O)CCCCC2)=O)c(cc(cc2)Oc3ccccc3)c2c1O Chemical compound N#Cc(nc1C(NCC2(CC(O)=O)CCCCC2)=O)c(cc(cc2)Oc3ccccc3)c2c1O IOROJGTUVPLIBU-UHFFFAOYSA-N 0.000 description 1
- BDBHWOUZJXGIQO-UHFFFAOYSA-N NC(NC(CCNC(c(nc(c1cc(Oc2ccccc2)ccc11)C#N)c1O)=O)C(O)=O)=O Chemical compound NC(NC(CCNC(c(nc(c1cc(Oc2ccccc2)ccc11)C#N)c1O)=O)C(O)=O)=O BDBHWOUZJXGIQO-UHFFFAOYSA-N 0.000 description 1
- FIVYBSPPKFZCNQ-UHFFFAOYSA-N OC(C1(CNC(c(ncc2c3ccc(Oc4ccccc4)c2)c3O)=O)CCC1)=O Chemical compound OC(C1(CNC(c(ncc2c3ccc(Oc4ccccc4)c2)c3O)=O)CCC1)=O FIVYBSPPKFZCNQ-UHFFFAOYSA-N 0.000 description 1
- PBBJYCCOUZDWCZ-UHFFFAOYSA-N OC(C1(CNC(c(ncc2c3ccc(Oc4ccccc4)c2)c3O)=O)CCOCC1)=O Chemical compound OC(C1(CNC(c(ncc2c3ccc(Oc4ccccc4)c2)c3O)=O)CCOCC1)=O PBBJYCCOUZDWCZ-UHFFFAOYSA-N 0.000 description 1
- CXCKWUPISMEDBQ-UHFFFAOYSA-N OC(CCCCNC(c1ncc(cc(cc2)-c(cc3)ccc3F)c2c1O)=O)=O Chemical compound OC(CCCCNC(c1ncc(cc(cc2)-c(cc3)ccc3F)c2c1O)=O)=O CXCKWUPISMEDBQ-UHFFFAOYSA-N 0.000 description 1
- FTCUDOFYRBMPLE-UHFFFAOYSA-N OC(CCCNC(c1ncc(cc(cc2)Oc3ccccc3)c2c1O)=O)=O Chemical compound OC(CCCNC(c1ncc(cc(cc2)Oc3ccccc3)c2c1O)=O)=O FTCUDOFYRBMPLE-UHFFFAOYSA-N 0.000 description 1
- VNDPTXLBKNLABX-UHFFFAOYSA-N OC(CCNC(c1ncc(cc(cc2)NC(Nc3ccccc3)=O)c2c1O)=O)=O Chemical compound OC(CCNC(c1ncc(cc(cc2)NC(Nc3ccccc3)=O)c2c1O)=O)=O VNDPTXLBKNLABX-UHFFFAOYSA-N 0.000 description 1
- IGBKLAZQWUSTAU-INIZCTEOSA-N O[C@@H](CCNC(c1ncc(cc(cc2)Oc3ccccc3)c2c1O)=O)C(O)=O Chemical compound O[C@@H](CCNC(c1ncc(cc(cc2)Oc3ccccc3)c2c1O)=O)C(O)=O IGBKLAZQWUSTAU-INIZCTEOSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the nitrogen-containing ring
- C07D217/26—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- 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
- C07D401/02—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
- C07D401/04—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
-
- 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
- C07D401/02—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
- C07D401/12—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
-
- 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
- C07D405/02—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
- C07D405/12—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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—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
- C07D409/12—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
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Hospice & Palliative Care (AREA)
- Neurology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261609022P | 2012-03-09 | 2012-03-09 | |
| US61/609,022 | 2012-03-09 | ||
| PCT/US2013/029912 WO2013134660A1 (en) | 2012-03-09 | 2013-03-08 | 4 -hydroxy- isoquinoline compounds as hif hydroxylase inhibitors |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017047346A Division JP2017101089A (ja) | 2012-03-09 | 2017-03-13 | Hifヒドロキシラーゼインヒビターとしての4−ヒドロキシ−イソキノリン化合物 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015509543A JP2015509543A (ja) | 2015-03-30 |
| JP2015509543A5 JP2015509543A5 (enExample) | 2016-04-28 |
| JP6129217B2 true JP6129217B2 (ja) | 2017-05-17 |
Family
ID=48014301
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014561149A Active JP6129217B2 (ja) | 2012-03-09 | 2013-03-08 | Hifヒドロキシラーゼインヒビターとしての4−ヒドロキシ−イソキノリン化合物 |
| JP2017047346A Pending JP2017101089A (ja) | 2012-03-09 | 2017-03-13 | Hifヒドロキシラーゼインヒビターとしての4−ヒドロキシ−イソキノリン化合物 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017047346A Pending JP2017101089A (ja) | 2012-03-09 | 2017-03-13 | Hifヒドロキシラーゼインヒビターとしての4−ヒドロキシ−イソキノリン化合物 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US9409892B2 (enExample) |
| EP (1) | EP2834220B1 (enExample) |
| JP (2) | JP6129217B2 (enExample) |
| CN (1) | CN104470899B (enExample) |
| AU (1) | AU2013229922B2 (enExample) |
| CA (1) | CA2866556C (enExample) |
| IL (1) | IL234544A (enExample) |
| NZ (1) | NZ700760A (enExample) |
| SG (1) | SG11201405574UA (enExample) |
| WO (1) | WO2013134660A1 (enExample) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102718708A (zh) | 2003-06-06 | 2012-10-10 | 菲布罗根有限公司 | 含氮杂芳基化合物及其在增加内源性促红细胞生成素中的用途 |
| CN105037323A (zh) | 2008-11-14 | 2015-11-11 | 菲布罗根有限公司 | 作为hif羟化酶抑制剂的苯并噻喃衍生物 |
| US8883823B2 (en) | 2012-07-16 | 2014-11-11 | Fibrogen, Inc. | Crystalline forms of a prolyl hydroxylase inhibitor |
| ES2631655T3 (es) | 2012-07-16 | 2017-09-01 | Fibrogen, Inc. | Procedimiento para fabricar compuestos de isoquinolina |
| KR20220164068A (ko) | 2012-07-16 | 2022-12-12 | 피브로겐, 인크. | 프롤릴 하이드록실라제 억제제 [(4-하이드록시-1-메틸-7-페녹시-아이소퀴놀린-3-카보닐)-아미노]-아세트산의 결정형 |
| LT3003284T (lt) | 2013-06-06 | 2020-04-27 | Fibrogen, Inc. | Hif hidroksilazės inhibitoriaus farmacinės kompozicijos |
| WO2015054579A1 (en) * | 2013-10-11 | 2015-04-16 | Isis Pharmaceuticals, Inc. | Treatment of acute kidney injury with phd1 modulators |
| WO2016034108A1 (zh) | 2014-09-02 | 2016-03-10 | 广东东阳光药业有限公司 | 喹啉酮类化合物及其应用 |
| CN106146395B (zh) | 2015-03-27 | 2019-01-01 | 沈阳三生制药有限责任公司 | 3-羟基吡啶化合物、其制备方法及其制药用途 |
| CN106146490B (zh) * | 2015-03-27 | 2018-10-23 | 沈阳三生制药有限责任公司 | 被芳氧基或杂芳氧基取代的5-羟基-1,7-萘啶化合物、其制备方法及其制药用途 |
| CN105367435A (zh) * | 2015-12-03 | 2016-03-02 | 张伟 | 一种β-丙氨酸叔丁酯盐酸盐的制备方法 |
| CN107188875B (zh) * | 2016-03-15 | 2020-11-10 | 联化科技股份有限公司 | 一种取代苯酞类化合物的制备方法及其中间体 |
| CN106478503A (zh) * | 2016-09-29 | 2017-03-08 | 上海勋和医药科技有限公司 | Roxadustat中间体的制备方法 |
| JP2019529522A (ja) | 2016-10-10 | 2019-10-17 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | RORγ調節因子としての三環式スルホン類 |
| CN107954931B (zh) * | 2016-10-17 | 2021-06-22 | 上海医药集团青岛国风药业股份有限公司 | 一种诺得司他的制备方法 |
| WO2018140186A1 (en) | 2017-01-28 | 2018-08-02 | Kingchem Life Science Llc | A process for preparing 5-phenoxy-1(3h)isobenzofuranone |
| TW201920108A (zh) * | 2017-09-25 | 2019-06-01 | 日商武田藥品工業有限公司 | N-(氰基取代之苄基或吡啶基甲基)-3-羥基吡啶醯胺衍生物 |
| CN108084090B (zh) * | 2017-12-20 | 2020-03-17 | 北京六合宁远科技有限公司 | 一种药物中间体含氮杂环的溴代化合物的合成方法 |
| CN112679431B (zh) * | 2019-10-18 | 2023-05-05 | 上海迪赛诺化学制药有限公司 | 一种制备异喹啉酮类化合物的方法 |
| US20230112619A1 (en) * | 2019-10-18 | 2023-04-13 | Shanghai Desano Chemical Pharmaceutical Co., Ltd. | Method for preparing isoquinolinone compounds |
| CN112679430B (zh) * | 2019-10-18 | 2023-05-05 | 上海迪赛诺化学制药有限公司 | 一种制备异喹啉酮类化合物的方法 |
| CN113754569B (zh) * | 2020-06-04 | 2024-07-02 | 四川国为制药有限公司 | 一种中间体化合物及其制备方法和用途 |
| CA3235718A1 (en) * | 2021-10-28 | 2023-05-04 | Insilico Medicine Ip Limited | Prolyl hydroxylase domain-containing protein (phd) inhibitors and uses thereof |
| CN118715015A (zh) * | 2021-12-17 | 2024-09-27 | 阿克比治疗有限公司 | 选择性phd1抑制剂化合物、组合物和使用方法 |
| EP4448493A1 (en) * | 2021-12-17 | 2024-10-23 | Akebia Therapeutics, Inc. | Picolinamide compounds as selective phd1 inhibitors, compositions, and methods of use |
| CA3248087A1 (en) * | 2022-01-13 | 2023-07-20 | Fibrogen, Inc. | TREATMENT OF CONGESTIVE HEART FAILURE |
| WO2024138317A1 (zh) * | 2022-12-26 | 2024-07-04 | 中国科学院广州生物医药与健康研究院 | 一种甲状腺激素受体β激动剂化合物及其制备方法和应用 |
| WO2024222890A1 (en) * | 2023-04-28 | 2024-10-31 | Insilico Medicine Ip Limited | Prolyl hydroxylase domain-containing protein (phd) inhibitors, combinations and uses thereof |
| KR20250174914A (ko) * | 2023-04-28 | 2025-12-15 | 인실리코 메디신 아이피 리미티드 | 결정질 프롤릴 하이드록실라제 도메인 포함 단백질(phd) 억제제 및 이의 용도 |
| CN121057737A (zh) * | 2023-04-28 | 2025-12-02 | 英矽智能科技知识产权有限公司 | 含脯氨酰羟化酶结构域的蛋白质(phd)抑制剂结晶及其用途 |
| CN117486797A (zh) * | 2023-11-23 | 2024-02-02 | 传健生物医药(厦门)有限公司 | 一种罗沙司他关键中间体及罗沙司他的制备方法 |
| WO2025252553A1 (en) | 2024-06-04 | 2025-12-11 | Syngenta Crop Protection Ag | Pesticidally-active 2,2-dihalocyclopropyl compounds |
Family Cites Families (51)
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2013
- 2013-03-08 JP JP2014561149A patent/JP6129217B2/ja active Active
- 2013-03-08 CA CA2866556A patent/CA2866556C/en active Active
- 2013-03-08 US US14/383,874 patent/US9409892B2/en active Active
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- 2013-03-08 EP EP13712970.6A patent/EP2834220B1/en active Active
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- 2013-03-08 WO PCT/US2013/029912 patent/WO2013134660A1/en not_active Ceased
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| CA2866556C (en) | 2020-01-07 |
| EP2834220B1 (en) | 2016-11-09 |
| SG11201405574UA (en) | 2014-10-30 |
| US9409892B2 (en) | 2016-08-09 |
| HK1206743A1 (en) | 2016-01-15 |
| JP2015509543A (ja) | 2015-03-30 |
| CA2866556A1 (en) | 2013-09-12 |
| AU2013229922B2 (en) | 2017-09-28 |
| CN104470899A (zh) | 2015-03-25 |
| NZ700760A (en) | 2016-08-26 |
| WO2013134660A1 (en) | 2013-09-12 |
| EP2834220A1 (en) | 2015-02-11 |
| AU2013229922A1 (en) | 2014-10-23 |
| US20150038528A1 (en) | 2015-02-05 |
| CN104470899B (zh) | 2017-12-26 |
| JP2017101089A (ja) | 2017-06-08 |
| IL234544A (en) | 2017-03-30 |
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