JP7128969B2 - Pcsk9阻害剤及びその使用方法 - Google Patents
Pcsk9阻害剤及びその使用方法 Download PDFInfo
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- JP7128969B2 JP7128969B2 JP2021541173A JP2021541173A JP7128969B2 JP 7128969 B2 JP7128969 B2 JP 7128969B2 JP 2021541173 A JP2021541173 A JP 2021541173A JP 2021541173 A JP2021541173 A JP 2021541173A JP 7128969 B2 JP7128969 B2 JP 7128969B2
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- C07D417/00—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 C07D415/00
- C07D417/02—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 C07D415/00 containing two hetero rings
- C07D417/12—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 C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
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- 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
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P3/06—Antihyperlipidemics
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- A—HUMAN NECESSITIES
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- 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
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- C—CHEMISTRY; METALLURGY
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- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/78—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 2
- C07D239/84—Nitrogen atoms
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- 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
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- 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
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- 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
- C07D403/12—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 linked by a chain containing hetero atoms as chain links
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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
- C07D403/14—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
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- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—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
- C07D413/12—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 linked by a chain containing hetero atoms as chain links
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- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
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- C07D417/00—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 C07D415/00
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- 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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- 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
- C07D471/10—Spiro-condensed systems
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- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/10—Spiro-condensed systems
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- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
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- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
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- C07—ORGANIC CHEMISTRY
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- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
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- C07D498/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
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- A—HUMAN NECESSITIES
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- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
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- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Epidemiology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Gastroenterology & Hepatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pyridine Compounds (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2022080749A JP2022116083A (ja) | 2019-01-18 | 2022-05-17 | Pcsk9阻害剤及びその使用方法 |
| JP2024208167A JP2025041641A (ja) | 2019-01-18 | 2024-11-29 | Pcsk9阻害剤及びその使用方法 |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201962794234P | 2019-01-18 | 2019-01-18 | |
| US62/794,234 | 2019-01-18 | ||
| PCT/US2020/013881 WO2020150473A2 (en) | 2019-01-18 | 2020-01-16 | Pcsk9 inhibitors and methods of use thereof |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2022080749A Division JP2022116083A (ja) | 2019-01-18 | 2022-05-17 | Pcsk9阻害剤及びその使用方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2022518015A JP2022518015A (ja) | 2022-03-11 |
| JP2022518015A5 JP2022518015A5 (https=) | 2022-05-26 |
| JP7128969B2 true JP7128969B2 (ja) | 2022-08-31 |
Family
ID=71613436
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021541173A Active JP7128969B2 (ja) | 2019-01-18 | 2020-01-16 | Pcsk9阻害剤及びその使用方法 |
| JP2022080749A Pending JP2022116083A (ja) | 2019-01-18 | 2022-05-17 | Pcsk9阻害剤及びその使用方法 |
| JP2024208167A Pending JP2025041641A (ja) | 2019-01-18 | 2024-11-29 | Pcsk9阻害剤及びその使用方法 |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2022080749A Pending JP2022116083A (ja) | 2019-01-18 | 2022-05-17 | Pcsk9阻害剤及びその使用方法 |
| JP2024208167A Pending JP2025041641A (ja) | 2019-01-18 | 2024-11-29 | Pcsk9阻害剤及びその使用方法 |
Country Status (34)
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP7558942B2 (ja) | 2018-11-30 | 2024-10-01 | コメット セラピューティクス インコーポレイテッド | パンテテイン誘導体及びその使用 |
| MX2021008661A (es) * | 2019-01-18 | 2021-08-19 | Astrazeneca Ab | Inhibidores de la pcsk9 y metodos de uso de los mismos. |
| BR112021013807A2 (pt) | 2019-01-18 | 2021-11-30 | Astrazeneca Ab | Inibidores de pcsk9 e seus métodos de uso |
| CN113248501B (zh) * | 2021-06-17 | 2021-10-08 | 南京韦尔优众医药有限公司 | Cly系列化合物及其制备方法和制备药物的用途 |
| US20250026719A1 (en) * | 2021-07-06 | 2025-01-23 | Shengke Pharmaceuticals (Jiangsu) Ltd. | Novel compounds as inhibitors of pcsk9 |
| WO2023084449A1 (en) | 2021-11-12 | 2023-05-19 | Novartis Ag | Diaminocyclopentylpyridine derivatives for the treatment of a disease or disorder |
| US12084453B2 (en) | 2021-12-10 | 2024-09-10 | Incyte Corporation | Bicyclic amines as CDK12 inhibitors |
| CN114890988A (zh) * | 2022-04-28 | 2022-08-12 | 浙江工业大学 | 一种沙利度胺的化学合成方法 |
| EP4554939A1 (en) * | 2022-07-13 | 2025-05-21 | Astrazeneca AB | Pcsk9 inhibitors and methods of use thereof |
| US20240217951A1 (en) | 2022-09-23 | 2024-07-04 | Astrazeneca Ab | Pcsk9 inhibitors and methods of use thereof |
| US20240228469A1 (en) | 2022-09-23 | 2024-07-11 | Astrazeneca Ab | Pcsk9 inhibitors and methods of use thereof |
| CN120019043B (zh) * | 2022-10-14 | 2026-04-03 | 上海翰森生物医药科技有限公司 | 含氮杂环类衍生物抑制剂、其制备方法和应用 |
| US20240239767A1 (en) | 2022-12-16 | 2024-07-18 | Astrazeneca Ab | Pcsk9 inhibitors and methods of use thereof |
| CN118496204B (zh) * | 2023-02-14 | 2025-10-24 | 深圳信立泰药业股份有限公司 | 一种氘代吡啶酮化合物及其制备方法与应用 |
| CN119264042A (zh) * | 2023-07-04 | 2025-01-07 | 上海翰森生物医药科技有限公司 | 含环戊烷类衍生物抑制剂、其制备方法和应用 |
| TW202506682A (zh) | 2023-07-27 | 2025-02-16 | 大陸商上海拓界生物醫藥科技有限公司 | 二胺基環戊基取代的雜芳基衍生物及其用途和製備方法 |
| WO2025045777A1 (en) * | 2023-08-25 | 2025-03-06 | Draupnir Bio Aps | Inhibitors of pcsk9 |
| CN120398916A (zh) * | 2023-09-25 | 2025-08-01 | 深圳信立泰药业股份有限公司 | 一种式(c)的吡啶酮类化合物及其制备方法与应用 |
| WO2025168652A1 (en) | 2024-02-05 | 2025-08-14 | Astrazeneca Ab | Azd-0780 in combination with a statin for use in lowering ldl-c levels and treating cardiovacular diseases |
| WO2025168614A1 (en) * | 2024-02-05 | 2025-08-14 | Astrazeneca Ab | Pharmaceutical compositions comprising azd0780 |
| TW202602886A (zh) | 2024-03-20 | 2026-01-16 | 瑞典商阿斯特捷利康公司 | Pcsk9抑制劑及其使用方法 |
| TW202602866A (zh) | 2024-03-20 | 2026-01-16 | 瑞典商阿斯特捷利康公司 | Pcsk9抑制劑及其使用方法 |
| TW202539678A (zh) | 2024-03-20 | 2025-10-16 | 瑞典商阿斯特捷利康公司 | Pcsk9抑制劑及其使用方法 |
| WO2025214500A1 (zh) * | 2024-04-12 | 2025-10-16 | 上海翰森生物医药科技有限公司 | 含氮杂环类衍生物的自由碱晶型和酸式盐及其晶型、其制备方法和应用 |
| WO2025238159A1 (en) | 2024-05-16 | 2025-11-20 | Astrazeneca Ab | Combination therapy comprising azd0780 and ezetimibe |
| WO2026021380A1 (zh) * | 2024-07-22 | 2026-01-29 | 深圳信立泰药业股份有限公司 | PCSK9和HMG-CoA双靶化合物与应用 |
| CN121773107A (zh) * | 2024-07-30 | 2026-03-31 | 成都施贝康生物医药科技有限公司 | 一种杂环衍生物抑制剂及其制备和用途 |
| WO2026044073A1 (en) | 2024-08-22 | 2026-02-26 | Avioris Bio, Inc. | Pcsk9 inhibitors and methods of using the same |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008502736A (ja) | 2004-06-09 | 2008-01-31 | アバニール・ファーマシューティカルズ | 高脂血症および関連疾患の治療のための複素環式誘導体 |
| JP2011501952A (ja) | 2007-10-26 | 2011-01-20 | シェーリング コーポレイション | 脂質障害およびコレステロール障害を治療するための抗pcsk9および方法 |
| WO2011152508A1 (ja) | 2010-06-04 | 2011-12-08 | 興和株式会社 | 光学活性ジベンジルアミン誘導体及びその製造方法 |
| JP2022518016A (ja) | 2019-01-18 | 2022-03-11 | アストラゼネカ・アクチエボラーグ | Pcsk9阻害剤及びその使用方法 |
Family Cites Families (524)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US267A (en) | 1837-07-11 | Mcode of hanging ob suspending a band-wheel in those hobse-powebs in | ||
| US3164588A (en) | 1965-01-05 | Hjnsoj | ||
| US3962A (en) | 1845-03-21 | Fowler m | ||
| US3009911A (en) | 1961-11-21 | Derivatives of j | ||
| SE168308C1 (https=) | ||||
| US2661372A (en) | 1953-12-01 | Pharmacologically valuable stereo | ||
| US3935A (en) | 1845-02-28 | Improvement in machines for cutting sausage-meat | ||
| US3562A (en) | 1844-04-25 | Improvement in seed-planters | ||
| US3108097A (en) | 1963-10-22 | Ehnojs | ||
| US30577A (en) | 1860-11-06 | Truss-bridge | ||
| US2976289A (en) | 1961-03-21 | X-tetrahydro - | ||
| US3254076A (en) | 1966-05-31 | Sulfamyl hydro | ||
| US2809194A (en) | 1957-10-08 | Thiadiazine type natriuretic agents | ||
| US2783241A (en) | 1957-02-26 | S-acylimino-x-substituted-az-i | ||
| US2882271A (en) | 1959-04-14 | Xcixcxh | ||
| US2937169A (en) | 1960-05-17 | Toiutf alrtqn of h | ||
| US115905A (en) | 1871-06-13 | Improvement in trunks | ||
| US3262852A (en) | 1966-07-26 | Vasodilator and anti-anginose com- pounds containing methoxy benzyl piperazines and method of using the same | ||
| US238A (en) | 1837-06-15 | Capstan | ||
| US2161938A (en) | 1934-07-31 | 1939-06-13 | Soc Of Chemical Ind | Imidazolines |
| US2357985A (en) | 1940-07-30 | 1944-09-12 | Research Corp | Synthesis of hexoestrol |
| DE905738C (de) | 1943-06-11 | 1954-11-02 | Diwag Chemische Fabriken Ag | Verfahren zur Herstellung basischer Thymoldimethylaminoaethylaether |
| US2500444A (en) | 1944-10-10 | 1950-03-14 | Polaroid Corp | Uramidohomomeroquinene |
| AT168063B (de) | 1948-11-23 | 1951-04-10 | Richter Gedeon Vegyeszet | Verfahren zur Herstellung von neuen asymmetrischen Substitutionsprodukten des 2,4-Diamino-1,3,5-Triazins |
| DE860217C (de) | 1950-10-28 | 1952-12-18 | Albert Ag Chem Werke | Verfahren zur Herstellung von 1-Hexyl-3, 7-dimethylxanthin |
| GB740932A (en) | 1952-08-01 | 1955-11-23 | Rhone Poulenc Sa | Improvements in or relating to phenthiazine derivatives |
| US2661373A (en) | 1953-03-02 | 1953-12-01 | Kulz Ida | Certain amino alcohols and ketones |
| US2816118A (en) | 1953-11-12 | 1957-12-10 | S B Penick & Company Inc | Isolation of crystalline components from visnagan |
| FR1103113A (fr) | 1954-04-15 | 1955-10-31 | Triméthylol-alcanes et leur procédé de préparation | |
| GB769757A (en) | 1954-05-13 | 1957-03-13 | American Cyanamid Co | Improvements in or relating to the manufacture of sulfonamides |
| US2769015A (en) | 1954-10-06 | 1956-10-30 | Lab Laroche Navarron | Process of preparing 3-methyl-chromone |
| GB795174A (en) | 1954-10-13 | 1958-05-21 | Upjohn Co | Heterocyclic sulphonamides |
| GB807826A (en) | 1955-03-14 | 1959-01-21 | Thomae Gmbh Dr K | Derivatives of pyrimido[5,4-d] pyrimidine and production thereof |
| FR1165845A (fr) | 1955-05-28 | 1958-10-29 | Philips Nv | Amines secondaires portant des substituants et leur préparation |
| GB803372A (en) | 1955-11-02 | 1958-10-22 | Recordati Lab Farmacologico S | Hydroxychromone derivatives and methods of preparing the same |
| US3012042A (en) | 1956-12-21 | 1961-12-05 | Belge Produits Chimiques Sa | Benzofurans |
| NL224562A (https=) | 1957-02-05 | |||
| US2980679A (en) | 1957-04-04 | 1961-04-18 | Omikron Gagliardi Societa Di F | Process for preparing heterocyclic sulfonamides |
| GB824547A (en) | 1957-05-07 | 1959-12-02 | Recordati Lab Farmacologico S | Process for preparing flavone-7-ethyl oxyacetate |
| US3055904A (en) | 1957-11-04 | 1962-09-25 | Geigy Chem Corp | New isoindoline derivatives |
| US2965655A (en) | 1957-11-07 | 1960-12-20 | Merck & Co Inc | Process for preparing substituted 1-amino 2, 4-benzene-disulfonamides |
| US2965656A (en) | 1957-11-07 | 1960-12-20 | Merck & Co Inc | Process for preparing substituted 1-amino-2, 4-benzene-disulfonamides |
| US2980699A (en) | 1957-12-20 | 1961-04-18 | S B Penick And Company | Dihydropyranocoumarin derivatives and process for their production |
| FR1217929A (fr) | 1958-03-03 | 1960-05-06 | Ciba Geigy | Procédé de préparation du 1,1-dioxyde de la 6-chloro-7-sulfamyl-3,4-dihydro-1,2,4-benzothiadiazine et de ses sels |
| CH366523A (de) | 1958-04-14 | 1963-01-15 | Eprova Ag | Verfahren zur Herstellung der neuen 1,3,4,6- und 1,3,4,5-Tetranicotinoyl-fructose |
| NL238796A (https=) | 1958-05-07 | |||
| GB851287A (en) | 1958-07-10 | 1960-10-12 | British Drug Houses Ltd | 5-chlorotoluene-2:4-disulphonamide and alkali metal salts thereof |
| DE1102750B (de) | 1958-07-17 | 1961-03-23 | Wuelfing J A Fa | Verfahren zur Herstellung eines Salzes von Theophyllinbasen |
| GB856409A (en) | 1958-07-26 | 1960-12-14 | Chime Et Atomistique | Improvements in and relating to a new pyridazine derivative and its process of preparation |
| GB862248A (en) | 1958-08-04 | 1961-03-08 | Italseber S P A | Di-isopropylammonium salts of chloroacetic and chloropropionic acids |
| US2970082A (en) | 1958-10-07 | 1961-01-31 | Walker Lab Inc | Aluminum nicotinate compositions for hypercholesteremia |
| GB885078A (en) | 1959-01-12 | 1961-12-20 | Ciba Ltd | 3:4-dihydro-1:2:4-benzothiadiazine-1:1-dioxides and process for their manufacture |
| ES255386A1 (es) | 1959-02-04 | 1960-09-16 | Ciba Geigy | Procedimiento para preparar derivados del 3,4-dihidro-1,2,4-benzotiadiazina-1,1,-diëxido |
| US3058882A (en) | 1959-12-28 | 1962-10-16 | Hoechst Ag | N'-substituted-3-carboxy-6-halo-sulfanilamide and derivatives thereof |
| DE1102973B (de) | 1960-03-25 | 1961-03-23 | Bayer Ag | Verfahren zur Herstellung von hoch gereinigten Kallikrein-Praeparaten |
| NL291944A (https=) | 1960-05-04 | |||
| DE1265758B (de) | 1960-05-25 | 1968-04-11 | Guidotti & C Spa Labor | Verfahren zur Herstellung von o-(beta-Dialkylaminoaethoxy)-phenylketonen und deren Saeureadditionssalzen und quartaeren Salzen |
| US3081230A (en) | 1960-09-08 | 1963-03-12 | Smith Kline French Lab | Diuretic and antihypertensive triaminoarylpteridines |
| DE1302648B (https=) | 1960-09-27 | |||
| SE300218B (https=) | 1960-11-08 | 1968-04-22 | Recip Ab | |
| NL270803A (https=) | 1960-11-09 | |||
| US3255241A (en) | 1961-01-19 | 1966-06-07 | Merck & Co Inc | (2-alkylidene acyl)phenoxy-and (2-alkylidene acyl)phenylmercaptocarboxylic acids |
| US3072653A (en) | 1961-03-06 | 1963-01-08 | Warner Lamber Pharmaceutical C | 5-amino derivatives of 4-thiazolidinones and process therefor |
| DE1154810B (de) | 1961-04-01 | 1963-09-26 | Knoll Ag | Verfahren zur Herstellung basisch substituierter Phenylacetonitrile |
| FR1312427A (fr) | 1961-04-12 | 1962-12-21 | Science Union Et Compagnie Soc | Nouveaux dérivés de la pipérazine et leurs préparations |
| GB979994A (en) | 1961-07-28 | 1965-01-06 | May & Baker Ltd | Isoindolinone derivatives |
| NL281593A (https=) | 1961-07-31 | |||
| US3160641A (en) | 1961-08-07 | 1964-12-08 | Atlas Chem Ind | Purification of isosorbide |
| NL281975A (https=) | 1961-08-12 | |||
| GB984810A (en) | 1961-10-05 | 1965-03-03 | Farmaceutici Italia | Polypeptides |
| DE1236523C2 (de) | 1962-02-15 | 1975-06-12 | Sanol-Arzneimittel Dr. Schwarz Gmbh, 4019 Monheim | Verfahren zur herstellung von basischen phenylaethern und deren salzen |
| US3262977A (en) | 1962-03-10 | 1966-07-26 | Chinoin Gyogyszer Es Vegyeszet | N-aralkyl-1, 1-diphenyl-propylamine derivatives |
| BE629910A (https=) | 1962-03-22 | |||
| US3188329A (en) | 1962-04-10 | 1965-06-08 | Colgate Palmolive Co | Diuretic anils |
| US3228943A (en) | 1962-06-11 | 1966-01-11 | Lumilysergol derivatives | |
| US3338899A (en) | 1962-07-09 | 1967-08-29 | Aron Samuel | 3-phenyl-5-amino-1, 2, 4-oxadiazole compounds |
| US3265573A (en) | 1962-07-27 | 1966-08-09 | Squibb & Sons Inc | Benzothiadiazinesulfonamide-1, 1-dioxide composition |
| BE639386A (https=) | 1962-10-30 | |||
| NL300886A (https=) | 1962-11-23 | |||
| NL301580A (https=) | 1962-12-11 | |||
| NL142872C (https=) | 1963-03-28 | |||
| FR1365504A (fr) | 1963-05-24 | 1964-07-03 | Soc Ind Fab Antibiotiques Sifa | Nouveaux dérivés des thiachromanes et procédé de préparation |
| FR2790M (fr) | 1963-05-24 | 1964-10-16 | Soc Ind Fab Antibiotiques Sifa | Nouveaux dérivés des thiachromanes. |
| GB1069343A (en) | 1963-09-10 | 1967-05-17 | Ici Ltd | Propanolamine derivatives |
| US3238215A (en) | 1963-10-17 | 1966-03-01 | Sterling Drug Inc | 1-[(3-, 2-, and 1-indolyl)-lower-alkyl-, lower-alkenyl-, and lower-alkynyl]piperidines |
| NL127996C (https=) | 1963-11-19 | |||
| BR6464291D0 (pt) | 1963-11-26 | 1973-07-26 | Merrell Inc Richardson | Processo para preparar o novo composto quimico 1-1-di cloro-hexil-2-(2-piperidil)-etina |
| DE1278443C2 (de) | 1963-11-30 | 1975-07-24 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von 2,4-disulfonamid-1-chlorbenzolen |
| NL128190C (https=) | 1964-02-07 | |||
| FR1390056A (fr) | 1964-04-21 | 1965-02-19 | Holding Ceresia S A | Procédé de préparation de nouveaux dérivés du tétrahydronaphtalène et produits conformes à ceux obtenus par le présent procédé ou procédé similaire |
| NL127065C (https=) | 1964-04-22 | |||
| NL137318C (https=) | 1964-06-09 | |||
| US3422107A (en) | 1964-09-05 | 1969-01-14 | Albert Ag Chem Werke | Certain oxoalkyldimethylxanthines and a process for the preparation thereof |
| NL130749C (https=) | 1964-09-10 | |||
| GB1078852A (en) | 1964-09-30 | 1967-08-09 | Ici Ltd | Alkanolamine derivatives |
| NL6514807A (https=) | 1964-11-18 | 1966-05-20 | ||
| NL128191C (https=) | 1965-01-12 | |||
| US3929836A (en) | 1965-05-11 | 1975-12-30 | Hoffmann La Roche | 2-(2-Lower alkylamino-1-hydroxy-ethyl)-substituted benzofurans |
| FR1460571A (fr) | 1965-06-10 | 1966-03-04 | Innothera Lab Sa | Composés thiényl acétiques et leur préparation |
| DE1270544B (de) | 1965-06-19 | 1968-06-20 | Beiersdorf Ag | 4-Chlor-5-sulfamylsalicylsaeure-(2', 6'-dimethyl)-anilid und dessen Alkali- oder Ammonium-Salze sowie Verfahren zu deren Herstellung |
| DE1545575C2 (de) | 1965-12-16 | 1970-09-10 | Asta-Werke Ag, Chemische Fabrik, 4812 Brackwede | N, N'-Bis- eckige Klammer auf 3"(3', 4', 5'-trimethoxybenzoyloxy)-propyl eckige Klammer zu -homopiperazin |
| US3360518A (en) | 1966-01-03 | 1967-12-26 | Wallace & Tiernan Inc | Tetrahydro-halo-sulfamyl quinazolinones |
| CH472404A (de) | 1966-03-04 | 1969-05-15 | Sandoz Ag | Verfahren zur Herstellung neuer Indolderivate |
| CH469002A (de) | 1966-06-21 | 1969-02-28 | Sandoz Ag | Verfahren zur Herstellung neuer Indolderivate |
| FR5733M (https=) | 1966-09-27 | 1968-01-22 | ||
| FR6087M (https=) | 1967-01-10 | 1968-06-04 | ||
| US3961071A (en) | 1967-02-06 | 1976-06-01 | Boehringer Ingelheim Gmbh | Therapeutic compositions and method |
| US3940489A (en) | 1967-02-06 | 1976-02-24 | Boehringer Ingelheim Gmbh | Therapeutic compositions and method |
| GB1160925A (en) | 1967-02-08 | 1969-08-06 | Menarini Sas | 2-Substituted Benzofuran Derivatives |
| DE1668055B2 (de) | 1967-03-10 | 1973-09-06 | Farbwerke Hoechst AG, vormals Mei ster Lucius & Bruning, 6000 Frankfurt | Basisch substituierte cyclopentylphenolaether, deren salze mit physiologisch vertraeglichen saeuren und verfahren zu deren herstellung |
| DE1670827C3 (de) | 1967-03-20 | 1974-10-24 | Bayer Ag, 5090 Leverkusen | 4-(2'-Nitrophenyl)-2,6-dimethyl-3,5-dicarbmethoxy-1,4-dihydropyridin |
| US3563997A (en) | 1967-12-04 | 1971-02-16 | Yoshitomi Pharmaceutical | Certain thieno(2,3-c)pyridines |
| US3511836A (en) | 1967-12-13 | 1970-05-12 | Pfizer & Co C | 2,4,6,7-tetra substituted quinazolines |
| US3857952A (en) | 1967-12-22 | 1974-12-31 | May & Baker Ltd | Certain benzene derivatives useful in treating cardiac disorders |
| NL6903138A (https=) | 1968-03-02 | 1969-09-04 | ||
| GB1203691A (en) | 1968-03-06 | 1970-09-03 | Science Union & Cie | New disubstituted n-amino indoline derivatives and process for preparing them |
| GB1218591A (en) | 1968-04-03 | 1971-01-06 | Delalande Sa | Derivatives of n-(3,4,5-trimethoxy cennamoyl) piperazine and their process of preparation |
| US4045482A (en) | 1968-11-12 | 1977-08-30 | Yamanouchi Pharmaceutical Co. Ltd. | 4-(3-Isopropylamino-2-hydroxypropoxy indene |
| DE1815922C3 (de) | 1968-12-20 | 1979-04-26 | Boehringer Mannheim Gmbh, 6800 Mannheim | 5-Phenyltetrazol-Derivate |
| FR8120M (https=) | 1968-12-26 | 1970-08-03 | ||
| GB1285038A (en) | 1969-02-21 | 1972-08-09 | Ici Ltd | Alkanolamine derivatives |
| US3836671A (en) | 1969-02-21 | 1974-09-17 | Ici Ltd | Alkanolamine derivatives for producing beta-adrenergic blockade |
| US3655663A (en) | 1969-04-21 | 1972-04-11 | Burton K Wasson | 4-(3-secondary amino-2-hydroxy-proxy) 1 2 5-thiadiazoles |
| US3663570A (en) | 1969-04-28 | 1972-05-16 | Sankyo Co | Coumarin derivatives |
| GB1262785A (en) | 1969-04-29 | 1972-02-09 | Orsymonde | Improvements in or relating to phloroglucinol derivatives |
| CA956632A (en) | 1969-05-16 | 1974-10-22 | Yoshitomi Pharmaceutical Industries | Phenoxy-aminopropanol derivatives |
| US4012444A (en) | 1969-07-08 | 1977-03-15 | Allen & Hanburys Limited | 5-[1-Hydroxy-2-(1-methyl-3-phenylpropyl)aminoethyl] salicylamide and physiologically acceptable acid addition salts thereof |
| US3634583A (en) | 1969-07-24 | 1972-01-11 | Leo Pharm Prod Ltd | Pharmaceutical composition for the treatment of oedematous conditions and hypertension |
| BE757001A (fr) | 1969-10-10 | 1971-03-16 | Cerpha | Derives heterocycliques d'acides phenoxy acetique et leur preparation |
| US4018824A (en) | 1969-11-28 | 1977-04-19 | Teikoku Hormone Mfg. Co., Ltd. | 1-Aryloxy-3-aminopropane derivatives |
| US3935259A (en) | 1970-01-08 | 1976-01-27 | Ciba-Geigy Corporation | New amines and processes for their manufacture |
| US4038313A (en) | 1970-01-08 | 1977-07-26 | Ciba-Geigy Corporation | Cycloalkylureido phenoxy propanolamines |
| SE354851B (https=) | 1970-02-18 | 1973-03-26 | Haessle Ab | |
| US3770724A (en) | 1970-03-31 | 1973-11-06 | Roussel Uclaf | Process for preparing pentacyclic alkaloids |
| GB1308191A (en) | 1970-04-06 | 1973-02-21 | Science Union & Cie | Thiochroman derivatives and a process for preparing them |
| US3663597A (en) | 1970-05-05 | 1972-05-16 | American Home Prod | Process for the purification of cyclandelate |
| FR2092133B1 (https=) | 1970-05-06 | 1974-03-22 | Orsymonde | |
| US3669968A (en) | 1970-05-21 | 1972-06-13 | Pfizer | Trialkoxy quinazolines |
| US4059622A (en) | 1970-05-27 | 1977-11-22 | Imperial Chemical Industries Limited | Alkanolamine derivatives |
| FR2092895B1 (https=) | 1970-06-29 | 1973-07-13 | Lafon Victor | |
| DE2117571C3 (de) | 1971-04-10 | 1979-10-11 | Bayer Ag, 5090 Leverkusen | Unsymmetrische 1,4-Dihydropyridin-33-dicarbonsäureester, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Arzneimittel |
| CA989411A (en) | 1971-05-13 | 1976-05-18 | Kakenyaku Kako Co. | Benzofuran derivatives and preparation thereof |
| DE2815926A1 (de) | 1978-04-13 | 1979-10-18 | Boehringer Mannheim Gmbh | Neue carbazolyl-(4)-oxy-propanolamin-derivate, verfahren zu ihrer herstellung und diese verbindungen enthaltende arzneimittel |
| US3773939A (en) | 1971-11-24 | 1973-11-20 | Janssen Pharmaceutica Nv | N-arallyl-n'-aralkyl piperazine pharmaceutical compositions |
| JPS5229318B2 (https=) | 1972-03-30 | 1977-08-01 | ||
| US3910924A (en) | 1972-04-13 | 1975-10-07 | Otsuka Pharma Co Ltd | 3,4-Dihydrocarbostyril derivatives and a process for preparing the same |
| ZA732937B (en) | 1972-05-05 | 1974-03-27 | Maggioni & C Spa | Non mercurial diuretics |
| GB1435139A (en) | 1972-08-17 | 1976-05-12 | Sumitomo Chemical Co | Thiazole derivatives |
| US3985758A (en) | 1973-02-20 | 1976-10-12 | Yamanouchi Pharmaceutical Co., Ltd. | 1,4-Dihydropyridine derivatives |
| GB1390748A (en) | 1973-04-09 | 1975-04-16 | Continental Pharma | Alkyl and cycloalkylthiophenylalkylaminoalkanols their salts and the preparation thereof |
| DE2319278C2 (de) | 1973-04-17 | 1986-02-20 | Bayer Ag, 5090 Leverkusen | Pharmazeutisches Mittel |
| US3857981A (en) | 1973-06-20 | 1974-12-31 | Armour & Co | Preserving red color in red meats |
| US4062950A (en) | 1973-09-22 | 1977-12-13 | Bayer Aktiengesellschaft | Amino sugar derivatives |
| US4146643A (en) | 1973-12-18 | 1979-03-27 | Sandoz Ltd. | Increasing vigilance or treating cerebral insufficiency with substituted vincamines |
| AT334385B (de) | 1973-12-20 | 1976-01-10 | Chemie Linz Ag | Verfahren zur herstellung von neuen phenoxypropylaminderivaten und deren salzen |
| NL175059C (nl) | 1974-02-23 | Boehringer Mannheim Gmbh | Bereiding van bloeddrukverlagende stoffen en van preparaten die ze bevatten. | |
| GB1501632A (en) | 1974-06-28 | 1978-02-22 | Cm Ind | Aromatic ketones having cardiovascular activity |
| GB1477664A (en) | 1974-04-17 | 1977-06-22 | Christiaens Sa A | Pyridine derivatives |
| DE2419970C3 (de) | 1974-04-25 | 1980-06-12 | Hoechst Ag, 6000 Frankfurt | 3-<l-Pyrrolidinyl)-4-phenoxy-5sulfamoylbenzoesäure und Verfahren zu ihrer Herstellung |
| DE2521113A1 (de) | 1974-05-15 | 1976-03-18 | Maggioni & C Spa | Cycloaliphatische derivate von 3.3-diphenylpropylamin |
| JPS5612114B2 (https=) | 1974-06-07 | 1981-03-18 | ||
| US4338322A (en) | 1975-07-02 | 1982-07-06 | Fujisawa Pharmaceutical Co., Ltd. | 1,4-Dihydropyridine derivatives, pharmaceutical compositions containing same and methods of effecting vasodilation using same |
| US4129565A (en) | 1975-07-11 | 1978-12-12 | Nisshin Flour Milling Co., Ltd. | Isocarbostyril derivatives |
| US4340541A (en) | 1975-08-15 | 1982-07-20 | Sandoz Ltd. | 4-(2-Benzoyloxy-3-tert.-butylaminopropoxy-2-methyl indole |
| US4035750A (en) | 1975-10-14 | 1977-07-12 | Eastman Kodak Company | Electrophotographic apparatus having improved photoconductor regenerative structure and procedure |
| US4105776A (en) | 1976-06-21 | 1978-08-08 | E. R. Squibb & Sons, Inc. | Proline derivatives and related compounds |
| US4154839A (en) | 1975-11-05 | 1979-05-15 | Bayer Aktiengesellschaft | 2,6-Dimethyl-3-carboxymethoxy-4-(2-nitrophenyl)-5-carbisobutoxy-1,4-dihydropyridine |
| FR2330383A1 (fr) | 1975-11-06 | 1977-06-03 | Synthelabo | Nouveaux ethers de phenols substitues, leurs sels, leur preparation et les medicaments qui les renferment |
| US4046889A (en) | 1976-02-13 | 1977-09-06 | E. R. Squibb & Sons, Inc. | Azetidine-2-carboxylic acid derivatives |
| GB1544872A (en) | 1976-06-25 | 1979-04-25 | Sterling Drug Inc | 4-hydroxyphenylalkanolamine derivatives and preparation thereof |
| DE2645710C2 (de) | 1976-10-09 | 1985-06-27 | Merck Patent Gmbh, 6100 Darmstadt | Phenoxy-amino-propanole, Verfahren zu ihrer Herstellung und pharmazeutische Zubereitung |
| JPS608117B2 (ja) | 1977-02-08 | 1985-02-28 | 財団法人微生物化学研究会 | 新生理活性物質エステラスチンおよびその製造法 |
| DE2719912C3 (de) | 1977-05-04 | 1979-12-06 | Bayer Ag, 5090 Leverkusen | Verfahren zur Isolierung von 0- |4,6-Dideoxy-4- [JJl S-O,4,6/5)-4,5,6-trihydroxy-3-hydroxymethyl-2cyclohexen-1-yl] -amino] - a -D-glucopyranosyl} -(I Pfeil nach rechts 4)-0- a D-glucopyranosyl-(l Pfeil nach rechts 4)-D-glucopyranose aus Kulturbrühen |
| US4466972A (en) | 1977-06-20 | 1984-08-21 | Sandoz Ltd. | Benzoxadiazoles and benzothiadiazoles, their preparation and pharmaceutical compositions containing them |
| DE2733747C2 (de) | 1977-07-27 | 1979-09-27 | Hoechst Ag, 6000 Frankfurt | Verfahren zur Herstellung von 2,2 Dichlorhydrazobenzol |
| NO154918C (no) | 1977-08-27 | 1987-01-14 | Bayer Ag | Analogifremgangsmaate til fremstilling av terapeutisk aktive derivater av 3,4,5-trihydroksypiperidin. |
| CA1147342A (en) | 1977-10-12 | 1983-05-31 | Kazuo Imai | Process of producing novel phenylethanolamine derivatives |
| US4188390A (en) | 1977-11-05 | 1980-02-12 | Pfizer Inc. | Antihypertensive 4-amino-2-[4-(1,4-benzodioxan-2-carbonyl) piperazin-1-yl or homopiperazin-1-yl]quinazolines |
| IT1088554B (it) | 1977-11-17 | 1985-06-10 | F I D I A Spa | Procedimento sellettivo per la preparazione di derivati della 7-indrossi cumarina |
| JPS5953920B2 (ja) | 1977-12-28 | 1984-12-27 | 東洋醸造株式会社 | 新規なアミノ糖化合物およびその製法 |
| JPS55301A (en) | 1978-02-14 | 1980-01-05 | Yamanouchi Pharmaceut Co Ltd | 1,4-dihydropyridine-3,5-dicarboxylic ester derivative and its preparation |
| CA1121290A (en) | 1978-02-14 | 1982-04-06 | Yasuji Suhara | Amino sugar derivatives |
| IT1094076B (it) | 1978-04-18 | 1985-07-26 | Acraf | Cicloalchiltriazoli |
| US4172896A (en) | 1978-06-05 | 1979-10-30 | Dainippon Pharmaceutical Co., Ltd. | Methane-sulfonamide derivatives, the preparation thereof and composition comprising the same |
| SE429652B (sv) | 1978-06-30 | 1983-09-19 | Haessle Ab | 2.6-dimetyl-4-(2.3-diklorfenyl)-1.4-dihydropyridin-3.5-dikarboxylsyra-3-metylester-5-etylester |
| JPS559058A (en) | 1978-07-06 | 1980-01-22 | Dainippon Pharmaceut Co Ltd | 1-(3-mercapto-2-methylpropanoyl)prolyl amino acid derivative |
| DE2845770A1 (de) | 1978-10-19 | 1980-04-30 | Schering Ag | Neue prostacyclin-derivate und verfahren zu ihrer herstellung |
| IL58849A (en) | 1978-12-11 | 1983-03-31 | Merck & Co Inc | Carboxyalkyl dipeptides and derivatives thereof,their preparation and pharmaceutical compositions containing them |
| US4231938A (en) | 1979-06-15 | 1980-11-04 | Merck & Co., Inc. | Hypocholesteremic fermentation products and process of preparation |
| DE2928485A1 (de) | 1979-07-14 | 1981-01-29 | Bayer Ag | Verwendung von harnstoffderivaten als arzneimittel bei der behandlung von fettstoffwechselstoerungen |
| US4508729A (en) | 1979-12-07 | 1985-04-02 | Adir | Substituted iminodiacids, their preparation and pharmaceutical compositions containing them |
| US4444784A (en) | 1980-08-05 | 1984-04-24 | Merck & Co., Inc. | Antihypercholesterolemic compounds |
| JPS56110665A (en) | 1980-02-08 | 1981-09-01 | Yamanouchi Pharmaceut Co Ltd | Sulfamoyl-substituted phenetylamine derivative and its preparation |
| SE8004087L (sv) | 1980-06-02 | 1981-12-03 | Haessle Ab | Nya parasubstituerade 3-fenoxi-1-alkylaminopropanol-2-er med betareceptorblockerande egenskaper, samt forfarande for deras framstellning, farmaceutiska beredningar innehallande desamma, och metod att behandla akut ... |
| DK149080C (da) | 1980-06-06 | 1986-07-28 | Sankyo Co | Fremgangsmaade til fremstilling af derivater af ml-236b-carboxylsyre |
| US4394382A (en) | 1980-06-17 | 1983-07-19 | Kowa Company, Ltd. | Dihydrobenzopyran compounds and pharmaceutical composition comprising said compounds |
| US4450171A (en) | 1980-08-05 | 1984-05-22 | Merck & Co., Inc. | Antihypercholesterolemic compounds |
| US4344949A (en) | 1980-10-03 | 1982-08-17 | Warner-Lambert Company | Substituted acyl derivatives of 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acids |
| ES8207217A1 (es) | 1980-10-09 | 1982-09-01 | Hoechst Ag | Procedimiento para la preparacion de un inactivador de alfa-amilasa |
| US4470972A (en) | 1981-04-28 | 1984-09-11 | Schering Corporation | 7-Carboxyalkylaminoacyl-1,4-dithia-7-azaspiro[4.4]-nonane-8-carboxylic acids |
| ZA817261B (en) | 1980-10-23 | 1982-09-29 | Schering Corp | Carboxyalkyl dipeptides,processes for their production and pharmaceutical compositions containing them |
| US4337201A (en) | 1980-12-04 | 1982-06-29 | E. R. Squibb & Sons, Inc. | Phosphinylalkanoyl substituted prolines |
| FR2496699B1 (fr) | 1980-12-22 | 1985-06-21 | Siderurgie Fse Inst Rech | Lance de soufflage de gaz oxydant, notamment d'oxygene, pour le traitement des metaux en fusion |
| EP0056194B1 (en) | 1981-01-05 | 1984-09-12 | Takeda Chemical Industries, Ltd. | N-substituted pseudo-aminosugars, their production and use |
| US4452813A (en) | 1981-05-22 | 1984-06-05 | Taiho Pharmaceutical Company Limited | Sulfonate derivatives, process for preparing same and antilipemic compositions containing the derivative |
| JPS57209270A (en) | 1981-06-19 | 1982-12-22 | Chugai Pharmaceut Co Ltd | Proline derivative |
| US4410520A (en) | 1981-11-09 | 1983-10-18 | Ciba-Geigy Corporation | 3-Amino-[1]-benzazepin-2-one-1-alkanoic acids |
| IE55867B1 (en) | 1981-12-29 | 1991-02-14 | Hoechst Ag | New derivatives of bicyclic aminoacids,processes for their preparation,agents containing these compounds and their use,and new bicyclic aminoacids as intermediates and processes for their preparation |
| US4555502A (en) | 1982-09-30 | 1985-11-26 | Merck & Co., Inc. | Aminoacyl-containing dipeptide derivatives useful as antihypertensives |
| DK161312C (da) | 1982-03-11 | 1991-12-09 | Pfizer | Analogifremgangsmaade til fremstilling af 2-aminoalkoxymethyl-4-phenyl-6-methyl-1,4-dihydropyridin-3,5-dicarboxylsyreestere eller syreadditionssalte deraf samt phthalimidoderivater til anvendelse som udgangsmateriale ved fremgangsmaaden |
| US4448784A (en) | 1982-04-12 | 1984-05-15 | Hoechst-Roussel Pharmaceuticals, Inc. | 1-(Aminoalkylphenyl and aminoalkylbenzyl)-indoles and indolines and analgesic method of use thereof |
| ATE50987T1 (de) | 1982-05-10 | 1990-03-15 | Takeda Chemical Industries Ltd | Dihydropyridinderivate, deren herstellung und verwendung. |
| JPS6058233B2 (ja) | 1982-05-24 | 1985-12-19 | 田辺製薬株式会社 | 2−オキソイミダゾリジン誘導体及びその製法 |
| US4452790A (en) | 1982-06-23 | 1984-06-05 | E. R. Squibb & Sons, Inc. | Phosphonyl hydroxyacyl amino acid derivatives as antihypertensives |
| US4463176A (en) | 1982-09-13 | 1984-07-31 | Mead Johnson & Company | Process for resolution of optical isomers |
| AU557175B2 (en) | 1982-10-15 | 1986-12-11 | Kyowa Hakko Kogyo Co. Ltd. | 2,6-dimethyl-4-(3-nitro phenyl)-1,4-dihydro pyridine-3,5- dicarboxylic acid esters |
| US4739073A (en) | 1983-11-04 | 1988-04-19 | Sandoz Pharmaceuticals Corp. | Intermediates in the synthesis of indole analogs of mevalonolactone and derivatives thereof |
| US4567175A (en) | 1983-06-03 | 1986-01-28 | Tanabe Seiyaku Co., Ltd. | 8-Chloro-1,5-benzothiazepine derivatives |
| CA1247547A (en) | 1983-06-22 | 1988-12-28 | Paul Hadvary | Leucine derivatives |
| US4678783B1 (en) | 1983-11-04 | 1995-04-04 | Asahi Chemical Ind | Substituted isoquinolinesulfonyl compounds |
| US4654362A (en) | 1983-12-05 | 1987-03-31 | Janssen Pharmaceutica, N.V. | Derivatives of 2,2'-iminobisethanol |
| FI844289L (fi) | 1984-01-21 | 1985-07-22 | Hoechst Ag | Nya polypeptider med -amylashaemmande verkan, foerfarande foer deras framstaellning, deras anvaendning och farmaceutiska preparat. |
| GB8403866D0 (en) | 1984-02-14 | 1984-03-21 | Recordati Chem Pharm | Diphenylalkylaminoalkyl esters |
| JPS60222472A (ja) | 1984-03-30 | 1985-11-07 | Kanebo Ltd | 新規なピペラジン誘導体および該化合物を有効成分とする医薬組成物 |
| US4699905A (en) | 1984-04-10 | 1987-10-13 | Sankyo Company, Limited | Perhydrothiazepine derivatives, their preparation and their therapeutic use |
| US4672068A (en) | 1984-05-04 | 1987-06-09 | Fujirebio Kabushiki Kaisha | Antihypertensive 1,4-dihydropyridines having a conjugated ester |
| NZ212895A (en) | 1984-08-22 | 1988-07-28 | Glaxo Spa | 1,4-dihydropyridine derivatives and pharmaceutical compositions |
| US4634765A (en) | 1984-12-18 | 1987-01-06 | Merrell Dow Pharmaceuticals Inc. | Homodisaccharide hypoglycemic agents |
| KR890004196B1 (ko) | 1985-07-29 | 1989-10-27 | 산텐세이야꾸가부시끼가이샤 | 신규 벤조티아진 유도체의 제조방법 |
| US4885284A (en) | 1986-01-22 | 1989-12-05 | Nissan Chemical Industries Ltd. | Dihydropyridine-5-phosphonic acid cyclic propylene ester |
| US4847271A (en) | 1986-01-27 | 1989-07-11 | Merck & Co., Inc. | Antihypercholesterolemic β-lactones |
| GB8608335D0 (en) | 1986-04-04 | 1986-05-08 | Pfizer Ltd | Pharmaceutically acceptable salts |
| US5138069A (en) | 1986-07-11 | 1992-08-11 | E. I. Du Pont De Nemours And Company | Angiotensin II receptor blocking imidazoles |
| CA1319144C (en) | 1986-11-14 | 1993-06-15 | Quirico Branca | Tetrahydronaphthalene derivatives |
| US5041432A (en) | 1987-01-30 | 1991-08-20 | E. I. Du Pont De Nemours And Company | Steroid derivatives useful as hypocholesterolemics |
| ATE61588T1 (de) | 1987-08-03 | 1991-03-15 | Delagrange Lab | 1,4-dihydropyridine, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel. |
| CA1336714C (en) | 1987-08-20 | 1995-08-15 | Yoshihiro Fujikawa | Quinoline type mevalonolactone inhibitors of cholesterol biosynthesis |
| JP2569746B2 (ja) | 1987-08-20 | 1997-01-08 | 日産化学工業株式会社 | キノリン系メバロノラクトン類 |
| US5192772A (en) | 1987-12-09 | 1993-03-09 | Nippon Shinyaku Co. Ltd. | Therapeutic agents |
| US4804770A (en) | 1988-04-29 | 1989-02-14 | E. R. Squibb & Sons, Inc. | Process for preparing a keto-phosphonate intermediate useful in preparing HMG-CoA reductase inhibitors |
| EP0344383A1 (en) | 1988-06-02 | 1989-12-06 | Merrell Dow Pharmaceuticals Inc. | Novel alpha-Glucosidase inhibitors |
| JP2853227B2 (ja) | 1988-10-13 | 1999-02-03 | ノバルテイス・アクチエンゲゼルシヤフト | 7置換‐ヘプト‐6‐エン酸、ヘプタン酸及び誘導体並びにそれらの中間体の製法 |
| DE3836675A1 (de) | 1988-10-28 | 1990-05-03 | Hoechst Ag | Glykosidase-inhibitor salbostatin, verfahren zu seiner herstellung und seine verwendung |
| WO1990005132A1 (fr) | 1988-11-11 | 1990-05-17 | Banyu Pharmaceutical Co., Ltd. | Derives d'allylamine substitues, procede de preparation et utilisation |
| US5185351A (en) | 1989-06-14 | 1993-02-09 | Smithkline Beecham Corporation | Imidazolyl-alkenoic acids useful as angiotensin II receptor antagonists |
| FI94339C (fi) | 1989-07-21 | 1995-08-25 | Warner Lambert Co | Menetelmä farmaseuttisesti käyttökelpoisen /R-(R*,R*)/-2-(4-fluorifenyyli)- , -dihydroksi-5-(1-metyylietyyli)-3-fenyyli-4-/(fenyyliamino)karbonyyli/-1H-pyrroli-1-heptaanihapon ja sen farmaseuttisesti hyväksyttävien suolojen valmistamiseksi |
| US5064856A (en) | 1989-07-31 | 1991-11-12 | Merck & Co., Inc. | Novel hmg-coa synthase inhibitors |
| US5391571A (en) | 1989-11-15 | 1995-02-21 | American Home Products Corporation | Cholesterol ester hydrolase inhibitors |
| DE122007000050I1 (de) | 1990-02-19 | 2007-11-08 | Novartis Ag | Acylverbindungen |
| US5270317A (en) | 1990-03-20 | 1993-12-14 | Elf Sanofi | N-substituted heterocyclic derivatives, their preparation and the pharmaceutical compositions in which they are present |
| US5102915A (en) | 1990-03-22 | 1992-04-07 | Merrell Dow Pharmaceuticals Inc. | Cyclopropyl squalene derivatives and their use as inhibitors of cholesterol synthesis |
| US5051534A (en) | 1990-03-22 | 1991-09-24 | Merrell Dow Pharmaceuticals Inc. | Novel cyclopropyl squalene derivatives and their use as inhibitors of cholesterol synthesis |
| US5064864A (en) | 1990-03-30 | 1991-11-12 | Merrell Dow Pharmaceuticals Inc. | Di- and tetra-fluoro analogs of squalene as inhibitors of squalene epoxidase |
| US5011859A (en) | 1990-03-30 | 1991-04-30 | Merrell Dow Pharmaceuticals Inc. | Di- and tetra-fluoro analogs of squalene as inhibitors of squalene epoxidase |
| US5196444A (en) | 1990-04-27 | 1993-03-23 | Takeda Chemical Industries, Ltd. | 1-(cyclohexyloxycarbonyloxy)ethyl 2-ethoxy-1-[[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl]benzimidazole-7-carboxylate and compositions and methods of pharmaceutical use thereof |
| US5504078A (en) | 1990-06-08 | 1996-04-02 | Merrell Dow Pharmaceuticals Inc. | α-glucosidase inhibitors |
| US5120729A (en) | 1990-06-20 | 1992-06-09 | Merck & Co., Inc. | Beta-lactams as antihypercholesterolemics |
| ZA915659B (en) | 1990-07-25 | 1992-05-27 | Merrell Dow Pharma | Novel piperidyl ethers and thioethers as inhibitors of cholesterol biosynthesis |
| US5026554A (en) | 1990-09-13 | 1991-06-25 | Merck & Co., Inc. | Method of inhibiting fungal growth using squalene synthetase inhibitors |
| US5177080A (en) | 1990-12-14 | 1993-01-05 | Bayer Aktiengesellschaft | Substituted pyridyl-dihydroxy-heptenoic acid and its salts |
| US5084461A (en) | 1991-03-27 | 1992-01-28 | Merrell Dow Pharmaceuticals Inc. | Azadecalin amides and thioamides as inhibitors of cholesterol biosynthesis |
| JP2648897B2 (ja) | 1991-07-01 | 1997-09-03 | 塩野義製薬株式会社 | ピリミジン誘導体 |
| US5274143A (en) | 1991-07-23 | 1993-12-28 | Hoffmann-La Roche Inc. | Process for the preparation of (R)-3-hexyl-5,6-dihydro-4-hydroxy-6-undecyl-2H-pyran-2-one and (R)-5,6-dihydro-6-undecyl-2H-pyran-2,4(3H)-dione |
| WO1993012069A1 (fr) | 1991-12-16 | 1993-06-24 | Yamanouchi Pharmaceutical Co., Ltd. | Nouveau derive d'alcool amine ou son sel |
| WO1993011782A1 (en) | 1991-12-19 | 1993-06-24 | Southwest Foundation For Biomedical Research | Cetp inhibitor polypeptide, antibodies against the synthetic polypeptide and prophylactic and therapeutic anti-atherosclerosis treatments |
| CA2098167C (en) | 1992-06-24 | 2006-12-19 | Dorothea Isler | Foodstuffs and feedstuffs containing a lipase inhibitor |
| US5629295A (en) | 1992-06-26 | 1997-05-13 | Pfizer Inc. | Steroidal glycosides for treating hypercholesterolemia |
| US5350758A (en) | 1992-07-08 | 1994-09-27 | Merrell Dow Pharmaceuticals Inc. | Piperidyl sulfonamides and sulfoxamides as inhibitors of cholesterol biosynthesis |
| GB9217295D0 (en) | 1992-08-14 | 1992-09-30 | Wellcome Found | Controlled released tablets |
| US5728704A (en) | 1992-09-28 | 1998-03-17 | Pfizer Inc. | Substituted pyridmidines for control of diabetic complications |
| FR2697250B1 (fr) | 1992-10-28 | 1995-01-20 | Fournier Ind & Sante | Dérivés de beta,beta-diméthyl-4-pipéridineéthanol et de 1,2,3,6-tétrahydro-beta,beta-diméthyl-4-pyridineéthanol, leur procédé de préparation et leur utilisation en thérapeutique. |
| FR2697252B1 (fr) | 1992-10-28 | 1994-12-09 | Fournier Ind & Sante | Dérivés de 1,2,3,5,6,7,8,8a-octahydro-5,5,8a-triméthyl-(8abeta)-6-isoquinolineamine, leur procédé de préparation et leur utilisation en thérapeutique. |
| DE4309553A1 (de) | 1993-03-24 | 1994-09-29 | Bayer Ag | Verfahren zur Herstellung von 3R,5S-(+)-Natrium-erythro-(E)-7-(4-(4-flurophenyl)-2,6-diisopropyl-5-methoxymethyl-pyrid-3-yl)-3,5-dihydroxy-hept-6-enoat |
| US5541231A (en) | 1993-07-30 | 1996-07-30 | Glaxo Wellcome Inc. | Stabilized Pharmaceutical |
| US5358970A (en) | 1993-08-12 | 1994-10-25 | Burroughs Wellcome Co. | Pharmaceutical composition containing bupropion hydrochloride and a stabilizer |
| GB9315856D0 (en) | 1993-07-30 | 1993-09-15 | Wellcome Found | Stabilized pharmaceutical |
| TW381025B (en) | 1993-08-05 | 2000-02-01 | Hoffmann La Roche | Pharmaceutical composition containing a glucosidase inhibitor and a lipase inhibitor |
| PT765313E (pt) | 1994-06-17 | 2003-11-28 | Hoffmann La Roche | Derivados de n,n'-bis(quinolin-4-il)-diamina a sua preparacao e a sua utilizacao como agentes anti-malaria |
| KR970706242A (ko) | 1994-10-04 | 1997-11-03 | 후지야마 아키라 | 우레아 유도체 및 ACAT-억제제로서 그의 용도(Urea derivatives and their use as ACAT-inhibitors) |
| JPH08143457A (ja) | 1994-11-21 | 1996-06-04 | Microbial Chem Res Found | 酵素阻害剤および高脂血症抑制剤 |
| WO1996018616A1 (en) | 1994-12-12 | 1996-06-20 | Merck & Co., Inc. | Substituted 2-aminopyridines as inhibitors of nitric oxide synthase |
| US5510379A (en) | 1994-12-19 | 1996-04-23 | Warner-Lambert Company | Sulfonate ACAT inhibitors |
| GB9504066D0 (en) | 1995-03-01 | 1995-04-19 | Pharmacia Spa | Phosphate derivatives of ureas and thioureas |
| EP0738510A3 (fr) | 1995-04-20 | 2005-12-21 | L'oreal | Utilisation d'un inhibiteur d'HMG-coenzyme A-reductase pour lutter contre le vieillissement de la peau et pour traiter l'acné. Composition comprenant au moins un inhibiteur HMG-coenzyme A reductase et au moins un actif possédant des propriétes desquamantes |
| DE69523182T2 (de) | 1995-06-06 | 2002-02-07 | Pfizer | Substituierte n-(indol-2-carbonyl)-glycinamide und derivate als glycogen phosphorylase inhibitoren |
| FI974437A7 (fi) | 1995-06-06 | 1997-12-05 | Pfizer | Substituoituja N-(indoli-2-karbonyyli)amideja ja johdannaisia glykogee nifosforylaasi-inhibiittoreina |
| WO1996040640A1 (en) | 1995-06-07 | 1996-12-19 | Pfizer Inc. | BIPHENYL-2-CARBOXYLIC ACID-TETRAHYDRO-ISOQUINOLIN-6-YL AMIDE DERIVATIVES, THEIR PREPARATION AND THEIR USE AS INHIBITORS OF MICROSOMAL TRIGLYCERIDE TRANSFER PROTEIN AND/OR APOLIPOPROTEIN B (Apo B) SECRETION |
| NZ325248A (en) | 1995-12-23 | 1999-09-29 | Pfizer Res & Dev | Quinoline and quinazoline compounds useful in therapy |
| JPH105585A (ja) | 1996-06-27 | 1998-01-13 | Toagosei Co Ltd | リチウムイオン吸着剤 |
| SE9603285D0 (sv) | 1996-09-10 | 1996-09-10 | Astra Ab | New compounds |
| US5874438A (en) | 1996-10-11 | 1999-02-23 | Bayer Aktiengesellschaft | 2,2'-bridged bis-2,4-diaminoquinazolines |
| EA001539B1 (ru) | 1996-11-27 | 2001-04-23 | Пфайзер Инк. | Амиды, ингибирующие секрецию аполипопротеина в (аро в) и/или микросомного протеина переноса триглицеридов (мтр) |
| DE69839355T2 (de) | 1997-07-29 | 2009-06-04 | Alcon Laboratories, Inc., Fort Worth | Ophthalmische Zusammensetzungen enthaltend Galaktomannanpolymere und Borat |
| AU2483599A (en) | 1998-01-29 | 1999-08-16 | Sepracor, Inc. | Pharmaceutical uses of optically pure (-)-bupropion |
| US6197786B1 (en) | 1998-09-17 | 2001-03-06 | Pfizer Inc | 4-Carboxyamino-2-substituted-1,2,3,4-tetrahydroquinolines |
| GT199900147A (es) | 1998-09-17 | 1999-09-06 | 1, 2, 3, 4- tetrahidroquinolinas 2-sustituidas 4-amino sustituidas. | |
| US8889112B2 (en) | 1999-09-16 | 2014-11-18 | Ocularis Pharma, Llc | Ophthalmic formulations including selective alpha 1 antagonists |
| US6683113B2 (en) | 1999-09-23 | 2004-01-27 | Pharmacia Corporation | (R)-chiral halogenated substituted N,N-Bis-benzyl aminioalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity |
| US20040138284A1 (en) | 2000-02-11 | 2004-07-15 | Matthias Wiesner | Indol-3-yl derivatives |
| GB0014022D0 (en) | 2000-06-08 | 2000-08-02 | Novartis Ag | Organic compounds |
| WO2002020500A2 (en) | 2000-09-01 | 2002-03-14 | Icos Corporation | Materials and methods to potentiate cancer treatment |
| EP1217000A1 (en) | 2000-12-23 | 2002-06-26 | Aventis Pharma Deutschland GmbH | Inhibitors of factor Xa and factor VIIa |
| BR0207285A (pt) | 2001-02-15 | 2004-02-10 | Pfizer Producs Inc | Agonistas de ppar |
| JP2004520397A (ja) | 2001-02-15 | 2004-07-08 | ファイザー・プロダクツ・インク | 増殖性アクチベータ受容体(ppar)化合物 |
| EP1491541B1 (en) | 2001-03-30 | 2007-01-24 | Pfizer Products Inc. | Pyridazinone aldose reductase inhibitors |
| CZ20033309A3 (cs) | 2001-06-07 | 2004-05-12 | Eliálillyáandácompany | Modulátory receptorů aktivovaných peroxizomálními proliferátory }PPARB |
| CN104744461A (zh) | 2001-09-21 | 2015-07-01 | 百时美施贵宝公司 | 含有内酰胺的化合物及其衍生物作为Xa因子的抑制剂 |
| AU2003209321A1 (en) | 2002-01-18 | 2003-07-30 | Pharmacia Corporation | Substituted pyridazinones as inhibitors of p38 |
| US6875780B2 (en) | 2002-04-05 | 2005-04-05 | Warner-Lambert Company | Compounds that modulate PPAR activity and methods for their preparation |
| EP1505966A4 (en) | 2002-05-10 | 2006-08-30 | Bristol Myers Squibb Co | 1,1-DISUBSTITUTED CYCLOALKYL DERIVATIVES AS FACTOR XA HEMMER |
| EP1542948A4 (en) | 2002-08-23 | 2008-12-17 | Univ Connecticut | NEW BIPHENYL AND BIPHENYLENE CANNABINOIDS |
| AU2003286711A1 (en) | 2002-10-25 | 2004-05-13 | Vertex Pharmaceuticals Incorporated | Indazolinone compositions useful as kinase inhibitors |
| EP1578715B1 (en) * | 2002-12-20 | 2011-03-02 | Bayer Pharmaceuticals Corporation | Indane acetic acid derivatives and their use as pharmaceutical agents, intermediates, and method of preparation |
| US20050197350A1 (en) | 2003-03-31 | 2005-09-08 | Taisho Pharmaceutical Co., Ltd. | Novel quinoline, tetrahydroquinazoline, and pyrimidine derivatives and methods of treatment related to the use thereof |
| TW200503747A (en) | 2003-04-22 | 2005-02-01 | Avanir Pharmaceuticals | Peptide mediators of reverse cholesterol transport for the treatment of hypercholesterolemia |
| US6933289B2 (en) | 2003-07-01 | 2005-08-23 | Allergan, Inc. | Inhibition of irritating side effects associated with use of a topical ophthalmic medication |
| EP1654002B2 (en) | 2003-08-07 | 2014-01-29 | Allergan, Inc. | Compositions for delivery of therapeutics into the eyes |
| US20050059744A1 (en) | 2003-09-12 | 2005-03-17 | Allergan, Inc. | Methods and compositions for the treatment of pain and other alpha 2 adrenergic-mediated conditions |
| BRPI0515500A (pt) | 2004-09-20 | 2008-07-29 | Xenon Pharmaceuticals Inc | derivados piridazina para inibição de estearoil-coa-desaturase |
| WO2006035967A1 (en) | 2004-09-30 | 2006-04-06 | Taisho Pharmaceutical Co., Ltd. | Pyridine derivatives and their use as medicaments for treating diseases related to mch receptor |
| US7381732B2 (en) | 2004-10-26 | 2008-06-03 | Bristol-Myers Squibb Company | Pyrazolobenzamides and derivatives as factor Xa inhibitors |
| WO2006051311A1 (en) | 2004-11-12 | 2006-05-18 | Galapagos Nv | Nitrogen heteroaromatic compounds which bind to the active site of protein kinase enzymes |
| GB0428082D0 (en) | 2004-12-22 | 2005-01-26 | Welcome Trust The Ltd | Therapeutic compounds |
| EP1853573A1 (en) * | 2005-02-25 | 2007-11-14 | Rigel Pharmaceuticals, Inc. | Benzisothiazoles useful for treating or preventing hcv infection |
| WO2006126081A2 (en) | 2005-05-24 | 2006-11-30 | Pharmacia & Upjohn Company Llc | Pyridino [2 , 3-b] pyrazinones as pde-5 inhibitors |
| NZ564222A (en) | 2005-06-14 | 2011-10-28 | Taigen Biotechnology Co Ltd | Pyrimidine compounds |
| US20070203236A1 (en) | 2006-01-11 | 2007-08-30 | Smith Jeffrey W | Novel antagonists of the human fatty acid synthase thioesterase |
| JP2007291087A (ja) | 2006-03-29 | 2007-11-08 | Taisho Pharmaceut Co Ltd | ピリジン誘導体及びその使用に関連する治療法 |
| HRP20130044T1 (hr) | 2006-07-25 | 2013-02-28 | Cephalon, Inc. | Derivati piridizinona |
| WO2008046216A1 (en) | 2006-10-18 | 2008-04-24 | Methylgene, Inc. | Kinase inhibitors and uses thereof |
| EP2121619A2 (en) | 2006-11-24 | 2009-11-25 | AC Immune S.A. | Compounds for the treatment of diseases associated with amyloid or amyloid-like proteins |
| KR101442288B1 (ko) | 2006-12-13 | 2014-09-19 | 지보당 네덜란드 서비시즈 비.브이. | 카복실산과 퓨린, 피리미딘, 뉴클레오사이드 또는 뉴클레오타이드의 향미 조절 유도체 |
| US7803809B2 (en) | 2008-11-12 | 2010-09-28 | Amgen Inc. | Substituted pyrano [2,3-b] pyridinamine compounds as beta-secretase modulators and methods of use |
| CN102099036B (zh) | 2008-06-03 | 2015-05-27 | 英特芒尼公司 | 用于治疗炎性疾患和纤维化疾患的化合物和方法 |
| WO2010048149A2 (en) | 2008-10-20 | 2010-04-29 | Kalypsys, Inc. | Heterocyclic modulators of gpr119 for treatment of disease |
| SG175390A1 (en) | 2009-04-29 | 2011-12-29 | Amarin Corp Plc | Pharmaceutical compositions comprising epa and a cardiovascular agent and methods of using the same |
| US20110009628A1 (en) | 2009-07-08 | 2011-01-13 | Haiyan Liu | Compounds and Compositions for Modulating Lipid Levels and Methods of Preparing Same |
| WO2011008931A2 (en) | 2009-07-15 | 2011-01-20 | Cystic Fibrosis Foundation Therapeutics, Inc. | Arylpyrimidine compounds and combination therapy comprising same for treating cystic fibrosis & related disorders |
| SG178106A1 (en) | 2009-08-05 | 2012-03-29 | Versitech Ltd | Antiviral compounds and methods of making and using thereof |
| US20120219558A1 (en) | 2009-09-25 | 2012-08-30 | Yan Ni | Antagonists of pcsk9 |
| CN102596249A (zh) | 2009-10-30 | 2012-07-18 | 默沙东公司 | Ax1和ax189 pcsk9拮抗剂和变体 |
| IN2012DN03824A (https=) | 2009-10-30 | 2015-08-28 | Merck Sharp & Dohme | |
| AR079336A1 (es) | 2009-12-11 | 2012-01-18 | Irm Llc | Antagonistas de la pro-proteina convertasa-subtilisina/quexina tipo 9 (pcsk9) |
| EP2558491B1 (en) | 2010-04-13 | 2018-07-04 | Bristol-Myers Squibb Company | Fibronectin based scaffold domain proteins that bind pcsk9 |
| AU2011253058A1 (en) | 2010-05-13 | 2012-12-06 | Amgen Inc. | Heteroaryloxycarbocyclyl compounds as PDE10 inhibitors |
| WO2011147199A1 (en) | 2010-05-28 | 2011-12-01 | Versitech Limited | Compounds and methods for treating viral infections |
| US8450316B2 (en) | 2010-06-24 | 2013-05-28 | Trustees Of Tufts College | Niacin mimetics, and methods of use thereof |
| WO2011163612A1 (en) | 2010-06-24 | 2011-12-29 | Trustees Of Tufts College | Niacin mimetics, and methods of use thereof |
| US9050334B2 (en) | 2010-07-16 | 2015-06-09 | Innov88 Llc | MIF inhibitors and their uses |
| WO2012016133A2 (en) | 2010-07-29 | 2012-02-02 | President And Fellows Of Harvard College | Ros1 kinase inhibitors for the treatment of glioblastoma and other p53-deficient cancers |
| WO2012054438A1 (en) | 2010-10-22 | 2012-04-26 | Schering Corporation | Anti-pcsk9 |
| US8987271B2 (en) | 2010-12-22 | 2015-03-24 | Eutropics Pharmaceuticals, Inc. | 2,2′-biphenazine compounds and methods useful for treating disease |
| CN103261230A (zh) | 2010-12-22 | 2013-08-21 | 霍夫曼-拉罗奇有限公司 | 抗pcsk9抗体及使用方法 |
| SG192117A1 (en) | 2011-01-28 | 2013-08-30 | Sanofi Sa | Human antibodies to pcsk9 for use in methods of treating particular groups of subjects |
| CN103339110A (zh) | 2011-01-28 | 2013-10-02 | 诺瓦提斯公司 | 作为cdk9抑制剂的取代的杂-联芳基化合物及其用途 |
| WO2012109530A1 (en) | 2011-02-11 | 2012-08-16 | Irm Llc | Pcsk9 antagonists |
| WO2012142498A2 (en) | 2011-04-13 | 2012-10-18 | Innovimmune Biotherapeutics, Inc. | Mif inhibitors and their uses |
| JOP20200043A1 (ar) | 2011-05-10 | 2017-06-16 | Amgen Inc | طرق معالجة أو منع الاضطرابات المختصة بالكوليسترول |
| WO2012162635A1 (en) | 2011-05-26 | 2012-11-29 | Sunovion Pharmaceuticals Inc. | Metabotropic glutamate receptors 5 modulators and methods of use thereof |
| WO2012170607A2 (en) | 2011-06-10 | 2012-12-13 | Novartis Ag | Use of pcsk9 antagonists |
| WO2012168491A1 (en) | 2011-06-10 | 2012-12-13 | Novartis Ag | Pharmaceutical formulations of pcsk9 antagonists |
| WO2012177741A1 (en) | 2011-06-20 | 2012-12-27 | Genentech, Inc. | Pcsk9-binding polypeptides and methods of use |
| BR112014000392A2 (pt) | 2011-07-14 | 2017-02-21 | Pfizer | tratamento com anticorpos anti-pcsk9 |
| US8815909B2 (en) | 2011-07-18 | 2014-08-26 | Bristol-Myers Squibb Company | Diaminocyclohexane compounds and uses thereof |
| AR087305A1 (es) | 2011-07-28 | 2014-03-12 | Regeneron Pharma | Formulaciones estabilizadas que contienen anticuerpos anti-pcsk9, metodo de preparacion y kit |
| JP5741850B2 (ja) | 2011-09-13 | 2015-07-01 | コニカミノルタ株式会社 | 光学フィルム、それを含む偏光板および液晶表示装置 |
| AR087715A1 (es) | 2011-09-16 | 2014-04-09 | Lilly Co Eli | Anticuerpos anti pcsk9 y usos de los mismos |
| HUE069234T2 (hu) | 2011-09-16 | 2025-02-28 | Regeneron Pharma | Eljárások lipoprotein(a)-szint csökkentésére proprotein-konvertáz szubtilizin/kexin 9 (PCSK9) inhibitorának beadásával |
| US9879093B2 (en) | 2011-12-20 | 2018-01-30 | Adaerata, Limited Partnershp | Single domain antibodies as inhibitors of PCSK9 |
| MX367352B (es) | 2012-01-06 | 2019-08-16 | Gemphire Therapeutics Inc | Metodos para reducir el riesgo de padecer una enfermedad cardiovascular. |
| TW201348231A (zh) * | 2012-02-29 | 2013-12-01 | Amgen Inc | 雜雙環化合物 |
| PT2822936T (pt) * | 2012-03-07 | 2021-12-02 | Univ Of Delhi | Derivados da aminoquinolina e suas utilizações |
| JPWO2013137371A1 (ja) * | 2012-03-15 | 2015-08-03 | 興和株式会社 | 新規ピリミジン化合物及びそれらを含有する医薬 |
| WO2013148284A1 (en) | 2012-03-29 | 2013-10-03 | Genentech, Inc. | Antibodies that bind to a pcsk9 cleavage site and methods of use |
| EP2844733B1 (en) | 2012-04-18 | 2020-07-15 | Hemoshear, LLC | In vitro model for pathological or physiologic conditions |
| EA039663B1 (ru) | 2012-05-03 | 2022-02-24 | Амген Инк. | Применение антитела против pcsk9 для снижения сывороточного холестерина лпнп и лечения связанных с холестерином расстройств |
| US9255154B2 (en) | 2012-05-08 | 2016-02-09 | Alderbio Holdings, Llc | Anti-PCSK9 antibodies and use thereof |
| KR20150059638A (ko) | 2012-05-25 | 2015-06-01 | 카타베이시스 파마슈티칼즈, 인코포레이티드 | 전구단백질 전환효소 섭틸리신/켁신 9형 저하 방법 |
| EP2861624A1 (en) | 2012-06-15 | 2015-04-22 | F. Hoffmann-La Roche AG | Anti-pcsk9 antibodies, formulations, dosing, and methods of use |
| CA2877766A1 (en) | 2012-07-03 | 2014-01-09 | Majambu Mbikay | Quercetin-3-glucoside and uses thereof |
| BR112014030284B1 (pt) | 2012-07-18 | 2021-11-30 | Sunshine Lake Pharma Co., Ltd | Composto, composição farmacêutica, e, uso de um composto ou de uma composição farmacêutica |
| US9540449B2 (en) | 2012-08-13 | 2017-01-10 | Regeneron Pharmaceuticals, Inc. | Anti-PCSK9 antibodies with pH-dependent binding characteristics |
| UA116217C2 (uk) | 2012-10-09 | 2018-02-26 | Санофі | Пептидна сполука як подвійний агоніст рецепторів glp1-1 та глюкагону |
| AR092924A1 (es) | 2012-10-09 | 2015-05-06 | Sanofi Sa | Derivados de pirrolidinona como moduladores de gpr119 para el tratamiento de diabetes, obesidad, dislipidemia y trastornos relacionados |
| AU2013366692B2 (en) | 2012-12-21 | 2017-11-23 | Sanofi | Dual GLP1/GIP or trigonal GLP1/GIP/Glucagon agonists |
| WO2014107739A1 (en) | 2013-01-07 | 2014-07-10 | Eleven Biotherapeutics, Inc. | Antibodies against pcsk9 |
| TWI644899B (zh) | 2013-02-04 | 2018-12-21 | 健生藥品公司 | Flap調節劑 |
| EP2951157A1 (en) | 2013-02-04 | 2015-12-09 | Merck Patent GmbH | Positive allosteric modulators of mglur3 |
| WO2014127316A2 (en) | 2013-02-15 | 2014-08-21 | Srx Cardio, Llc | Proprotein convertase subtilisin/kexin type 9 (pcsk9) allosteric binding ligands to mudulate serum low density lipoprotein (ldl) levels |
| ME03336B (me) * | 2013-03-12 | 2019-10-20 | Vertex Pharma | Inhibitori dnk-pk |
| HK1213194A1 (zh) | 2013-03-14 | 2016-06-30 | Daiichi Sankyo Co., Ltd. | 用於新型的结合蛋白质pcsk9 |
| WO2014150983A2 (en) | 2013-03-15 | 2014-09-25 | Amgen Inc. | Human antigen binding proteins that bind to proprotein convertase subtilisin kexin type 9 |
| EP2968985A2 (en) | 2013-03-15 | 2016-01-20 | Amgen, Inc. | Human antigen binding proteins that bind to proprotein convertase subtilisin kexin type 9 |
| EP2968266B1 (en) | 2013-03-15 | 2019-05-01 | Shifa Biomedical Corporation | Anti-proprotein convertase subtilisin kexin type 9 (anti-pcsk9) compounds in the treatment and/or prevention of cardiovascular diseases |
| EP2961765A4 (en) | 2013-03-15 | 2016-11-09 | Adaerata Ltd Partnership | SMALL MOLECULAR PCSK9 MODULATORS AND METHOD OF USE THEREOF |
| CN105473141A (zh) | 2013-03-15 | 2016-04-06 | 实发生物医学公司 | 治疗和/或预防心血管疾病的抗pcsk9化合物和方法 |
| EP2986599A1 (en) | 2013-04-17 | 2016-02-24 | Pfizer Inc. | N-piperidin-3-ylbenzamide derivatives for treating cardiovascular diseases |
| TWI682780B (zh) | 2013-05-30 | 2020-01-21 | 美商再生元醫藥公司 | 醫藥組成物用於製造治療與pcsk9功能獲得性突變有關之體染色體顯性高膽固醇血症的藥物之用途 |
| US10111953B2 (en) | 2013-05-30 | 2018-10-30 | Regeneron Pharmaceuticals, Inc. | Methods for reducing remnant cholesterol and other lipoprotein fractions by administering an inhibitor of proprotein convertase subtilisin kexin-9 (PCSK9) |
| US10494442B2 (en) | 2013-06-07 | 2019-12-03 | Sanofi Biotechnology | Methods for inhibiting atherosclerosis by administering an inhibitor of PCSK9 |
| US9776995B2 (en) | 2013-06-12 | 2017-10-03 | Amgen Inc. | Bicyclic sulfonamide compounds as sodium channel inhibitors |
| CA2916259C (en) | 2013-06-28 | 2024-02-20 | Amgen Inc. | Methods for treating homozygous familial hypercholesterolemia |
| AR092240A1 (es) | 2013-08-26 | 2015-04-08 | Sunshine Lake Pharma Co Ltd | Derivados heterociclicos nitrogenados y su aplicacion en farmacos |
| CN105658232A (zh) | 2013-08-30 | 2016-06-08 | 阿尔莫生物科技股份有限公司 | 使用白细胞介素-10治疗疾病和病症的方法 |
| ES2914978T3 (es) | 2013-10-11 | 2022-06-20 | Sanofi Biotechnology | Uso de un inhibidor de PCSK9 para tratar hiperlipidemia |
| CN104558685B (zh) | 2013-10-24 | 2017-09-29 | 中国石油化工股份有限公司 | 一种磷氮膨胀型阻燃剂及其合成方法 |
| JP2017019724A (ja) | 2013-10-25 | 2017-01-26 | 第一三共株式会社 | 置換ピリジン化合物および他の医薬の組み合わせ |
| CN118105480A (zh) | 2013-11-12 | 2024-05-31 | 赛诺菲生物技术公司 | 用于与pcsk9抑制剂一起使用的给药方案 |
| HK1224186A1 (zh) | 2013-11-20 | 2017-08-18 | Cymabay Therapeutics, Inc. | 纯阖家族型高胆固醇血症的治疗 |
| EP3080148A2 (en) | 2013-12-11 | 2016-10-19 | Glycotope GmbH | Glycosylated glycophorin peptides |
| EP3080152A1 (en) | 2013-12-13 | 2016-10-19 | Sanofi | Non-acylated exendin-4 peptide analogues |
| TW201609798A (zh) | 2013-12-13 | 2016-03-16 | 賽諾菲公司 | Exendin-4胜肽類似物 |
| WO2015086733A1 (en) | 2013-12-13 | 2015-06-18 | Sanofi | Dual glp-1/glucagon receptor agonists |
| WO2015086728A1 (en) | 2013-12-13 | 2015-06-18 | Sanofi | Exendin-4 peptide analogues as dual glp-1/gip receptor agonists |
| TW201609800A (zh) | 2013-12-13 | 2016-03-16 | 賽諾菲公司 | 做為雙重glp-1/升糖素受體促效劑之艾塞那肽-4胜肽類似物 |
| EP3080154B1 (en) | 2013-12-13 | 2018-02-07 | Sanofi | Dual glp-1/gip receptor agonists |
| EA201691320A1 (ru) | 2014-02-14 | 2016-11-30 | Ридженерон Фармасьютикалз, Инк. | Способы лечения пациентов с гиперхолестеринемией, которая устойчива к терапии умеренными дозами статинов |
| WO2015140079A1 (en) | 2014-03-17 | 2015-09-24 | Sanofi | Methods for treating subjects with primary hypercholesterolemia that is not adequately controlled |
| LT3119757T (lt) | 2014-03-17 | 2018-07-10 | Pfizer Inc. | Diacilglicerolio aciltransferazės 2 inhibitoriai, skirti panaudoti metabolinių ir susijusių ligų gydyme |
| AR099937A1 (es) | 2014-04-04 | 2016-08-31 | Sanofi Sa | Compuestos de isoindolinona como moduladores de gpr119 para el tratamiento de diabetes, obesidad, dislipidemia y trastornos relacionados |
| JP2017515797A (ja) | 2014-04-04 | 2017-06-15 | サノフイ | 糖尿病、肥満、脂質異常症および関連障害の治療のためのgpr119モジュレーターとしての置換インダノン化合物 |
| TW201625605A (zh) | 2014-04-04 | 2016-07-16 | 賽諾菲公司 | 用於治療糖尿病、肥胖、血脂異常及相關病症之作為gpr119調節劑的經取代之稠合雜環類 |
| TW201625670A (zh) | 2014-04-07 | 2016-07-16 | 賽諾菲公司 | 衍生自exendin-4之雙重glp-1/升糖素受體促效劑 |
| TW201625668A (zh) | 2014-04-07 | 2016-07-16 | 賽諾菲公司 | 作為胜肽性雙重glp-1/昇糖素受體激動劑之艾塞那肽-4衍生物 |
| TW201625669A (zh) | 2014-04-07 | 2016-07-16 | 賽諾菲公司 | 衍生自艾塞那肽-4(Exendin-4)之肽類雙重GLP-1/升糖素受體促效劑 |
| US20170183306A1 (en) | 2014-05-30 | 2017-06-29 | Universite Paris Decartes | Cyclic compounds having a 1,3 diamino-functionality for use in the treatment of hiv infection |
| WO2015187295A2 (en) | 2014-06-02 | 2015-12-10 | Armo Biosciences, Inc. | Methods of lowering serum cholesterol |
| US9932381B2 (en) | 2014-06-18 | 2018-04-03 | Sanofi | Exendin-4 derivatives as selective glucagon receptor agonists |
| TWI677489B (zh) | 2014-06-20 | 2019-11-21 | 美商基利科學股份有限公司 | 多環型胺甲醯基吡啶酮化合物之合成 |
| WO2015200438A1 (en) | 2014-06-24 | 2015-12-30 | Eleven Biotherapeutics, Inc. | High affinity antibodies against pcsk9 |
| CA2955304C (en) | 2014-07-16 | 2023-12-12 | Sanofi Biotechnology | Methods for treating high cardiovascular risk patients with hypercholesterolemia |
| JP2017528498A (ja) | 2014-09-25 | 2017-09-28 | アラクセス ファーマ エルエルシー | Kras g12c変異体タンパク質のインヒビター |
| WO2016054388A1 (en) | 2014-10-03 | 2016-04-07 | University Of Pittsburgh - Of The Commonwealth System Of Higher Education | Glutaminase inhibitors |
| WO2016055901A1 (en) | 2014-10-08 | 2016-04-14 | Pfizer Inc. | Substituted amide compounds |
| NZ734082A (en) | 2015-01-20 | 2019-01-25 | Boehringer Ingelheim Animal Health Usa Inc | Anthelmintic compounds, compositions and method of using thereof |
| WO2016127102A2 (en) | 2015-02-06 | 2016-08-11 | Ernesto Abel-Santos | Inhibiting germination of clostridium perfringens spores to reduce necrotic enteritis |
| EA039310B1 (ru) | 2015-02-26 | 2022-01-12 | Санофи Байотекнолоджи | Способы снижения сердечно-сосудистого риска |
| BR112017019378A2 (pt) | 2015-03-18 | 2019-02-19 | Zealand Pharma A/S | análogos de amilina |
| EP3271405A1 (en) | 2015-03-20 | 2018-01-24 | Aarhus Universitet | Inhibitors of pcsk9 for treatment of lipoprotein metabolism disorders |
| DK3283507T3 (da) | 2015-04-16 | 2020-01-02 | Zealand Pharma As | Acyleret glucagonanalog |
| HK1257929A1 (zh) | 2015-11-06 | 2019-11-01 | Gemphire Therapeutics Inc. | 治疗混合性血脂异常 |
| TW201731867A (zh) | 2015-12-02 | 2017-09-16 | 賽諾菲公司 | Fgf21變異體 |
| AU2016366560A1 (en) | 2015-12-11 | 2018-06-28 | The Trustees Of The University Of Pennsylvania | Gene therapy for treating familial hypercholesterolemia |
| MX381314B (es) * | 2016-01-20 | 2025-03-12 | Janssen Sciences Ireland Uc | Pirimidinas sustituidas con arilo para su uso en la infeccion por virus influenza |
| HK1257556A1 (zh) | 2016-02-26 | 2019-10-25 | 耀石治疗公司 | 对正接受降脂疗法的纯合型家族性高胆固醇血症患者的治疗 |
| PL3429591T3 (pl) | 2016-03-16 | 2023-07-17 | Kura Oncology, Inc. | Podstawione pochodne tieno[2,3-d]pirymidyny jako inhibitory meniny-mll i metody ich zastosowania |
| JP2019513802A (ja) | 2016-04-14 | 2019-05-30 | ルシー マイケル | 組み合わせ組成物およびその使用方法 |
| TW201808888A (zh) | 2016-05-05 | 2018-03-16 | 嘉來克生命科學有限責任公司 | 整合應激途徑之調節劑 |
| WO2018007999A1 (en) | 2016-07-08 | 2018-01-11 | Staten Biotechnology B.V. | Anti-apoc3 antibodies and methods of use thereof |
| US10960020B2 (en) | 2016-09-15 | 2021-03-30 | The Brigham And Women's Hospital, Inc. | Modulation of PCSK9 and LDLR through DRP1 inhibition |
| EP4397311A3 (en) | 2016-10-18 | 2024-10-16 | Novartis AG | Methods for preventing cardiovascular events through proprotein convertase subtilisin kexin 9 (pcsk9) protein reduction |
| US20200038481A1 (en) | 2016-11-10 | 2020-02-06 | Csl Limited | Reconstituted high density lipoprotein treatment of myocardial infarction |
| JOP20190112A1 (ar) | 2016-11-14 | 2019-05-14 | Amgen Inc | علاجات مدمجة لتصلب الشرايين، شاملة مرض قلبي وعائي تصلبي |
| WO2018106820A1 (en) | 2016-12-07 | 2018-06-14 | Kura Oncology, Inc. | Methods of promoting beta cell proliferation |
| WO2018106818A1 (en) | 2016-12-07 | 2018-06-14 | Kura Oncology, Inc. | Methods of promoting beta cell proliferation |
| AR110351A1 (es) | 2016-12-13 | 2019-03-20 | Bristol Myers Squibb Co | COMPUESTOS DE HETEROARILO SUSTITUIDOS CON FOSFINÓXIDO ALQUILAMIDA COMO MODULADORES DE RESPUESTAS DE IL-12, IL-23 Y/O IFNa |
| PE20191716A1 (es) | 2017-02-08 | 2019-12-05 | Bristol Myers Squibb Co | Polipeptidos de relaxina modificada que comprenden un mejorador farmacocinetico y sus usos |
| CA3072274C (en) | 2017-02-08 | 2024-01-02 | Brooke Schumm | Intra-operative radiation therapy capsule with cylindrical shell radiation containment shutter system |
| AR110988A1 (es) | 2017-02-21 | 2019-05-22 | Sanofi Sa | Compuestos de azetidina como moduladores de gpr119 para el tratamiento de la diabetes, la obesidad, la dislipidemia y trastornos relacionados |
| WO2018165718A1 (en) * | 2017-03-17 | 2018-09-20 | Cardio Therapeutics Pty Ltd | Heterocyclic inhibitors of pcsk9 |
| WO2018175746A1 (en) | 2017-03-24 | 2018-09-27 | Kura Oncology, Inc. | Methods for treating hematological malignancies and ewing's sarcoma |
| CN110506056A (zh) | 2017-04-21 | 2019-11-26 | 斯塔滕生物技术有限公司 | 抗apoc3抗体和其使用方法 |
| JP7252908B2 (ja) | 2017-06-14 | 2023-04-05 | トレベナ・インコーポレイテッド | S1p1活性を調節するための化合物およびその使用法 |
| JP6928986B2 (ja) | 2017-06-26 | 2021-09-01 | 深▲チェン▼市塔吉瑞生物医薬有限公司Shenzhen TargetRx, Inc. | キナーゼ活性を阻害するためのインダゾール系化合物、その組成物および使用 |
| CN109384712B (zh) | 2017-08-14 | 2021-05-07 | 北京宽厚医药科技有限公司 | 靶向nk1受体拮抗剂及其在化疗所致恶心、呕吐治疗中的应用 |
| WO2019079701A1 (en) | 2017-10-20 | 2019-04-25 | Dana-Farber Cancer Institute, Inc. | HETEROBIFUNCTIONAL COMPOUNDS HAVING IMPROVED SPECIFICITY FOR BRD4 BROMODOMAINE |
| JP2021501210A (ja) | 2017-10-30 | 2021-01-14 | モントリオール ハート インスティテュート | 血漿コレステロールの上昇を処置する方法 |
| PE20210119A1 (es) | 2017-10-31 | 2021-01-19 | Staten Biotechnology B V | Anticuerpos anti-apoc3 y metodos de uso de estos |
| UY37957A (es) | 2017-11-02 | 2019-05-31 | Abbvie Inc | Moduladores de la vía de estrés integrada |
| EA202091269A1 (ru) | 2017-11-21 | 2020-08-07 | Бристол-Маерс Сквибб Компани | Сульфон-, пиридин-, алкил-, амид-замещенные гетероарильные соединения |
| WO2019111225A1 (en) | 2017-12-08 | 2019-06-13 | Avaliv Therapeutics | Compounds and methods for the treatment of non‑alcoholic steatohepatitis |
| SG11202005146VA (en) | 2017-12-18 | 2020-06-29 | Regeneron Pharma | Bispecific antigen binding molecules that bind leptin receptor and/or gp130, and methods of use thereof |
| JP7466448B2 (ja) * | 2018-01-17 | 2024-04-12 | バーテックス ファーマシューティカルズ インコーポレイテッド | Dna-pk阻害剤 |
| US11513131B2 (en) | 2018-01-22 | 2022-11-29 | Global Genomics Group, LLC | Low density lipoprotein triglycerides (LDL-TG) as a biomarker of cardiovascular disease and uses thereof |
| WO2019147650A1 (en) | 2018-01-23 | 2019-08-01 | Gila Therapeutics, Inc. | Peptide yy pharmaceutical formulations, compositions, and methods |
| CA3093469A1 (en) | 2018-03-09 | 2019-09-12 | The Brigham And Women's Hospital, Inc. | Combination therapy for cardiovascular diseases |
| CN111936486B (zh) | 2018-03-22 | 2023-09-22 | 百时美施贵宝公司 | 用作IL-12、IL-23和/或IFNα响应的调节剂的包含吡啶的杂环化合物 |
| CN110384801B (zh) | 2018-04-20 | 2021-09-14 | 中国科学院上海药物研究所 | miRNA552簇的微小RNA在治疗LDLC相关代谢性疾病中的应用 |
| ES2969982T3 (es) | 2018-04-24 | 2024-05-23 | Vertex Pharma | Compuestos de pteridinona y usos de los mismos |
| US20190374526A1 (en) | 2018-06-06 | 2019-12-12 | Merck Sharp & Dohme Corp. | Substituted Heterocyclic Compounds as Inhibitors of PRDM9 |
| US11442072B2 (en) | 2018-07-10 | 2022-09-13 | Jenny and Antti Wihuri Foundation | Method for measuring LDL aggregation |
| US11254660B2 (en) | 2018-08-31 | 2022-02-22 | Pfizer Inc. | Combinations for treatment of NASH/NAFLD and related diseases |
| KR20210070300A (ko) | 2018-10-03 | 2021-06-14 | 스태튼 바이오테크놀로지 비.브이. | 사람 및 시노몰구스 ApoC3에 대해 특이적인 항체 및 이의 사용 방법 |
| JP7631193B2 (ja) | 2018-10-22 | 2025-02-18 | アルミス インコーポレイテッド | Tyk2阻害剤およびその使用 |
| KR20260037169A (ko) | 2018-11-09 | 2026-03-17 | 노파르티스 아게 | apo(a)를 표적화하는 콘쥬게이션된 안티센스 화합물로 심혈관 사건의 위험을 감소시키는 방법 |
| US12399188B2 (en) | 2018-12-06 | 2025-08-26 | Zora Biosciences Oy | Biomarkers for cardiovascular events |
| BR112021013807A2 (pt) | 2019-01-18 | 2021-11-30 | Astrazeneca Ab | Inibidores de pcsk9 e seus métodos de uso |
| CN111484480B (zh) | 2019-01-29 | 2023-08-11 | 上海翰森生物医药科技有限公司 | 一种多环类衍生物抑制剂、其制备方法和应用 |
| CA3128368A1 (en) | 2019-02-01 | 2020-08-06 | Memorial Sloan Kettering Cancer Center | Senolytic car-t cells targeting upar, a cell surface and secreted senescence biomarker |
| US20200390858A1 (en) | 2019-04-17 | 2020-12-17 | Ngm Biopharmaceuticals, Inc. | Combination Therapy for Modulating Bile Acid Homeostasis and Treatment of Bile Acid Disorders and Diseases |
| WO2020234726A1 (en) | 2019-05-20 | 2020-11-26 | Pfizer Inc. | Combinations comprising benzodioxol as glp-1r agonists for use in the treatment of nash/nafld and related diseases |
| WO2021119321A1 (en) | 2019-12-10 | 2021-06-17 | Regeneron Pharmaceuticals, Inc. | Use of a pcsk9 inhibitor to treat homozygous familial hypercholesterolemia |
| WO2021209808A1 (en) | 2020-04-16 | 2021-10-21 | Abionyx Pharma Sa | Cer-001 therapy for treating kidney disease |
| CN113713107B (zh) | 2020-05-26 | 2022-09-23 | 中国科学院上海药物研究所 | miRNA552簇的微小RNA在治疗糖脂代谢病中的应用 |
| CA3179316A1 (en) | 2020-05-29 | 2021-12-02 | Andrew W. HAMER | Pcsk9 inhibitors and methods of use thereof to treat cholesterol-related disorders |
| WO2021250069A1 (en) | 2020-06-10 | 2021-12-16 | Christian-Albrechts-Universität Zu Kiel | Pharmaceutical compound for the treatment of atherosclerotic cardiovascular disease |
| US20240002354A1 (en) | 2020-08-05 | 2024-01-04 | Rezubio Pharmaceuticals Co., Ltd | Antidiabetic compounds and compositions |
| EP4243805A1 (en) | 2020-08-07 | 2023-09-20 | Gbiotech S.À.R.L. | Combination therapies for treating coronavirus infection |
| US12472171B2 (en) | 2020-08-19 | 2025-11-18 | Biogen Ma Inc. | Methods for treating hypercholesterolemia |
| KR20230069969A (ko) | 2020-09-15 | 2023-05-19 | 리제너론 파마슈티칼스 인코포레이티드 | 통증에 대한 lepr 아고니스트의 사용 |
| AU2020472970A1 (en) | 2020-10-20 | 2023-06-22 | Halo Therapeutics Ltd | Agonists of free fatty acid receptor 1 and their use in diseases associated with said receptor |
| AU2021373780A1 (en) | 2020-11-05 | 2023-06-08 | Amgen Inc. | METHODS FOR TREATING ATHEROSCLEROTIC CARDIOVASCULAR DISEASE WITH LPA-TARGETED RNAi CONSTRUCTS |
| EP4011877A3 (en) | 2020-12-11 | 2023-01-11 | Institut de Cardiologie de Montréal | Method of treating elevated plasma cholesterol |
| US20240044924A1 (en) | 2020-12-11 | 2024-02-08 | Helsingin Yliopisto | Method for determining a likelihood of a subject to respond to lipid lowering therapy |
| EP4294257B1 (en) | 2021-02-22 | 2025-11-05 | Regeneron Pharmaceuticals, Inc. | Method for diagnosing and treating partial lipodystrophy |
| US20250281495A1 (en) | 2021-02-25 | 2025-09-11 | Icahn School Of Medicine At Mount Sinai | Methods for inhibiting inflammation and progression of atherosclerotic plaques and cardiovascular events in patients with cerebro- and cardio-vascular disease |
| CA3212583A1 (en) | 2021-03-27 | 2022-10-06 | Daniel Gooding | Compositions having improved bioavailability of therapeutics |
| AU2022299514A1 (en) | 2021-06-24 | 2024-01-18 | Sirnaomics, Inc. | Products and compositions |
| AU2022297535A1 (en) | 2021-06-25 | 2024-01-04 | Amgen Inc. | Treatment of cardiovascular disease with trem-1 antigen binding proteins |
| EP4370519A1 (en) | 2021-07-14 | 2024-05-22 | Eternygen UK Ltd. | 5,6,7,8-tetrahydro-2,6- and 2,7-naphthyridine derivatives for use in the treatment of diseases responsive to citrate transporter modulation |
| WO2023052783A1 (en) | 2021-09-30 | 2023-04-06 | Sitryx Therapeutics Limited | Novel compounds |
| WO2023079294A1 (en) | 2021-11-05 | 2023-05-11 | Sitryx Therapeutics Limited | Phthalazine derivatives as pyruvate kinase modulators |
| JP2024546039A (ja) | 2021-11-12 | 2024-12-17 | シェンチェン ジンタイ テクノロジー カンパニー リミテッド | アスパラギン酸誘導体並びに肝線維症及び非アルコール性肝炎などの代謝性疾患の治療におけるその使用 |
| CN114277032A (zh) | 2021-12-31 | 2022-04-05 | 华中科技大学同济医学院附属协和医院 | 一种低密度脂蛋白受体基因突变体及其应用 |
| US20250223281A1 (en) | 2022-01-14 | 2025-07-10 | Rezubio Pharmaceuticals Co., Ltd | Antidiabetic compounds and compositions |
| TW202345865A (zh) | 2022-01-24 | 2023-12-01 | 大陸商上海舶望製藥有限公司 | 抑制LPA(Apo(a))蛋白表達的組合物和方法 |
| CN116617390A (zh) | 2022-02-11 | 2023-08-22 | 武汉大学 | Asgr1抑制剂在促进胆固醇外排和治疗非酒精性脂肪性肝病中的应用 |
| US20250177377A1 (en) | 2022-03-11 | 2025-06-05 | University Of Florida Research Foundation, Incorporated | Targeting ptchd1 and neuronal cholesterol to enhance safety of opioid analgesics |
| US20230338419A1 (en) | 2022-03-21 | 2023-10-26 | The Trustees Of The University Of Pennsylvania | Methods and apparatus for diagnosis and detection of cardiac allograft vasculopathy |
| CN116948030B (zh) | 2022-04-25 | 2024-11-19 | 武汉大学 | 抗asgr1单克隆抗体及其应用 |
| CN117045715B (zh) | 2022-05-13 | 2025-06-06 | 浙江养生堂天然药物研究所有限公司 | 红肉苹果和樱桃李组合物及其在抗动脉粥样硬化方面的应用 |
| CN115581694A (zh) | 2022-11-10 | 2023-01-10 | 正大青春宝药业有限公司 | 洋川芎内脂i在制备治疗高血脂症药物中的应用 |
| CN117180404A (zh) | 2023-10-24 | 2023-12-08 | 清华大学 | Cholesin在调节胆固醇稳态中的用途 |
| CN117482076A (zh) | 2023-11-24 | 2024-02-02 | 中国人民解放军陆军军医大学第二附属医院 | 甲硫氨酸类化合物在制备pcsk9抑制剂中的应用 |
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Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008502736A (ja) | 2004-06-09 | 2008-01-31 | アバニール・ファーマシューティカルズ | 高脂血症および関連疾患の治療のための複素環式誘導体 |
| JP2011501952A (ja) | 2007-10-26 | 2011-01-20 | シェーリング コーポレイション | 脂質障害およびコレステロール障害を治療するための抗pcsk9および方法 |
| WO2011152508A1 (ja) | 2010-06-04 | 2011-12-08 | 興和株式会社 | 光学活性ジベンジルアミン誘導体及びその製造方法 |
| JP2022518016A (ja) | 2019-01-18 | 2022-03-11 | アストラゼネカ・アクチエボラーグ | Pcsk9阻害剤及びその使用方法 |
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