ATE537825T1 - Immunosuppressive verbindungen und zusammensetzungen - Google Patents
Immunosuppressive verbindungen und zusammensetzungenInfo
- Publication number
- ATE537825T1 ATE537825T1 AT04752678T AT04752678T ATE537825T1 AT E537825 T1 ATE537825 T1 AT E537825T1 AT 04752678 T AT04752678 T AT 04752678T AT 04752678 T AT04752678 T AT 04752678T AT E537825 T1 ATE537825 T1 AT E537825T1
- Authority
- AT
- Austria
- Prior art keywords
- compositions
- immunosuppressive compounds
- diseases
- immunosuppressant
- prevention
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 2
- 230000001506 immunosuppresive effect Effects 0.000 title 1
- 239000000203 mixture Substances 0.000 title 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 230000001404 mediated effect Effects 0.000 abstract 2
- 102000036530 EDG receptors Human genes 0.000 abstract 1
- 108091007263 EDG receptors Proteins 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 230000006806 disease prevention Effects 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 229960003444 immunosuppressant agent Drugs 0.000 abstract 1
- 230000001861 immunosuppressant effect Effects 0.000 abstract 1
- 239000003018 immunosuppressive agent Substances 0.000 abstract 1
- 230000003993 interaction Effects 0.000 abstract 1
- 210000004698 lymphocyte Anatomy 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 230000019491 signal transduction Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/23—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C323/31—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton
- C07C323/32—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton having at least one of the nitrogen atoms bound to an acyclic carbon atom of the carbon skeleton
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/26—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C317/32—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D205/04—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Immunology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US47193103P | 2003-05-19 | 2003-05-19 | |
| PCT/US2004/015701 WO2004103309A2 (en) | 2003-05-19 | 2004-05-19 | Immunosuppressant compounds and compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE537825T1 true ATE537825T1 (de) | 2012-01-15 |
Family
ID=33476902
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT04752678T ATE537825T1 (de) | 2003-05-19 | 2004-05-19 | Immunosuppressive verbindungen und zusammensetzungen |
Country Status (17)
| Country | Link |
|---|---|
| US (2) | US7462629B2 (de) |
| EP (1) | EP1638551B1 (de) |
| JP (1) | JP4575920B2 (de) |
| CN (4) | CN1787817B (de) |
| AT (1) | ATE537825T1 (de) |
| AU (2) | AU2004240649A1 (de) |
| BR (1) | BRPI0410454A (de) |
| CA (1) | CA2524054C (de) |
| CY (1) | CY1112505T1 (de) |
| DK (1) | DK1638551T3 (de) |
| ES (1) | ES2379169T3 (de) |
| MX (1) | MXPA05012459A (de) |
| PL (1) | PL1638551T3 (de) |
| PT (1) | PT1638551E (de) |
| SI (1) | SI1638551T1 (de) |
| WO (1) | WO2004103309A2 (de) |
| ZA (1) | ZA200508203B (de) |
Families Citing this family (107)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7241790B2 (en) * | 2002-07-30 | 2007-07-10 | University Of Virginia Patent Foundation | Compounds active in spinigosine 1-phosphate signaling |
| BRPI0413923A (pt) * | 2003-08-29 | 2006-11-07 | Ono Pharmaceutical Co | composto capaz de ligar o receptor de s1p e uso farmacêutico do mesmo |
| WO2005041899A2 (en) * | 2003-11-03 | 2005-05-12 | University Of Virginia Patent Foundation | Orally available sphingosine 1-phosphate receptor agonists and antagonists |
| US7718704B2 (en) * | 2004-02-24 | 2010-05-18 | Irm Llc | Immunosuppressant compounds and compositions |
| TW200538433A (en) | 2004-02-24 | 2005-12-01 | Irm Llc | Immunosuppressant compounds and compositiions |
| ATE502630T1 (de) | 2004-07-16 | 2011-04-15 | Kyorin Seiyaku Kk | Verfahren zur effektiven anwendung eines medikaments und verfahren zur prävention von nebenwirkungen |
| AU2005292984B2 (en) | 2004-10-12 | 2011-01-20 | Kyorin Pharmaceutical Co., Ltd. | Process for producing 2-amino-2-[2-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]ethyl]-1,3-propanediol hydrochloride or hydrate thereof and intermediate for the same |
| JP2008522977A (ja) * | 2004-12-06 | 2008-07-03 | ユニバーシティ オブ バージニア パテント ファンデーション | スフィンゴシン=1−リン酸のアリールアミドアナログ |
| JP4318087B2 (ja) * | 2004-12-13 | 2009-08-19 | 小野薬品工業株式会社 | アミノカルボン酸誘導体およびその医薬用途 |
| JP2008530024A (ja) * | 2005-02-08 | 2008-08-07 | ノバルティス アクチエンゲゼルシャフト | S1p受容体アゴニスト/モジュレーターおよび免疫抑制剤の組み合わせ剤による、抗リンパ球抗体誘導 |
| MX2007009848A (es) * | 2005-02-14 | 2008-03-10 | Univ Virginia | Agonistas de esfingosina 1-fosfato comprendiendo cicloalcanos y heterociclos de 5 miembros substituidos por grupos amino y fenilo. |
| CN101203512A (zh) * | 2005-04-22 | 2008-06-18 | 第一三共株式会社 | 杂环化合物 |
| JP2009506046A (ja) * | 2005-08-23 | 2009-02-12 | アイアールエム・リミテッド・ライアビリティ・カンパニー | 免疫抑制剤化合物および組成物 |
| RU2421214C2 (ru) * | 2005-10-07 | 2011-06-20 | Киорин Фармасьютикал Ко., Лтд. | Терапевтическое средство для лечения гепатита и способ лечения гепатита |
| MX2008009579A (es) * | 2006-01-27 | 2008-09-25 | Univ Virginia | Metodo para el tratamiento de dolor neuropatico. |
| TWI389683B (zh) * | 2006-02-06 | 2013-03-21 | Kyorin Seiyaku Kk | A therapeutic agent for an inflammatory bowel disease or an inflammatory bowel disease treatment using a 2-amino-1,3-propanediol derivative as an active ingredient |
| AU2007212193A1 (en) * | 2006-02-09 | 2007-08-16 | University Of Virginia Patent Foundation | Bicyclic sphingosine 1-phosphate analogs |
| JP5140593B2 (ja) * | 2006-08-08 | 2013-02-06 | 杏林製薬株式会社 | アミノアルコール誘導体及びそれらを有効成分とする免疫抑制剤 |
| US8232319B2 (en) | 2006-08-08 | 2012-07-31 | Kyorin Pharmaceutical Co., Ltd. | Amino phosphate derivative and S1P receptor modulator having same as an active ingredient |
| EP2099741A2 (de) * | 2006-11-21 | 2009-09-16 | University Of Virginia Patent Foundation | Hydrindan-analoga mit sphingosin-1-phosphatrezeptoragonistenaktivität |
| WO2008064337A2 (en) * | 2006-11-21 | 2008-05-29 | University Of Virginia Patent Foundation | Benzocycloheptyl analogs having sphingosine 1-phosphate receptor activity |
| AU2007323618A1 (en) * | 2006-11-21 | 2008-05-29 | University Of Virginia Patent Foundation | Tetralin analogs having sphingosine 1-phosphate agonist activity |
| JP5411141B2 (ja) | 2007-09-10 | 2014-02-12 | カルシメディカ,インク. | 細胞内カルシウムを調節する化合物 |
| CA2703987A1 (en) * | 2007-11-08 | 2009-05-14 | Pfizer Inc. | Cyclobutyl carboxylic acid derivatives |
| GB0725101D0 (en) * | 2007-12-21 | 2008-01-30 | Glaxo Group Ltd | Compounds |
| GB0725104D0 (en) * | 2007-12-21 | 2008-01-30 | Glaxo Group Ltd | Compounds |
| TW200946105A (en) | 2008-02-07 | 2009-11-16 | Kyorin Seiyaku Kk | Therapeutic agent or preventive agent for inflammatory bowel disease containing amino alcohol derivative as active ingredient |
| US20090298894A1 (en) * | 2008-04-21 | 2009-12-03 | Asahi Kasei Pharma Corporation | Amino acid compounds |
| GB0807910D0 (en) * | 2008-04-30 | 2008-06-04 | Glaxo Group Ltd | Compounds |
| DK2307007T3 (da) * | 2008-07-23 | 2014-11-10 | Novartis Ag | Sphingosin-1-phosphat-receptormodulatorer samt deres anvendelse til behandling af muskelinflammation |
| HRP20161133T1 (hr) | 2008-07-23 | 2016-12-02 | Arena Pharmaceuticals, Inc. | DERIVATI SUSPSTITUIRANE 1,2,3,4-TETRAHIDROCIKLOPENTA[b]INDOL-3-IL-OCTENE KISELINE KORISNI U LIJEČENJU AUTOIMUNIH I UPALNIH POREMEĆAJA |
| CN105816453B (zh) | 2008-08-27 | 2021-03-05 | 艾尼纳制药公司 | 用于治疗自身免疫性病症和炎性病症的作为s1p1受体激动剂的经取代的三环酸衍生物 |
| CA2734500A1 (en) | 2008-08-27 | 2010-03-11 | Calcimedica Inc. | Compounds that modulate intracellular calcium |
| JP2012505836A (ja) * | 2008-10-17 | 2012-03-08 | アカール ファーマ ピーティーワイ リミテッド | S1p受容体モジュレーターおよびそれらの使用 |
| CA2743397C (en) * | 2008-12-18 | 2017-02-28 | Mathilde Muzerelle | Oxadiazole fused heterocyclic derivatives useful for the treatment of multiple sclerosis |
| AU2009327405A1 (en) * | 2008-12-18 | 2011-06-30 | Novartis Ag | New polymorphic form of 1- (4- { l- [ (E) -4-cyclohexyl--3-trifluoromethyl-benzyloxyimino] -ethyl) -2-ethyl-benzy l) -azetidine-3-carboxylic |
| EP2379499B1 (de) * | 2008-12-18 | 2014-04-09 | Novartis AG | Hydrochlorid Salz der 1-(4-(1-((E)-4-cyclohexyl-3-trifluoromethyl-benzyloxyimino)-ethyl)-2-ethyl-benzyl)-azetidin-3-carbonsäure |
| CN102574822A (zh) | 2009-08-04 | 2012-07-11 | 阿米拉制药公司 | 作为溶血磷脂酸受体拮抗剂的化合物 |
| UA107360C2 (en) * | 2009-08-05 | 2014-12-25 | Biogen Idec Inc | Bicyclic aryl sphingosine 1-phosphate analogs |
| US8399451B2 (en) | 2009-08-07 | 2013-03-19 | Bristol-Myers Squibb Company | Heterocyclic compounds |
| GB2474748B (en) | 2009-10-01 | 2011-10-12 | Amira Pharmaceuticals Inc | Polycyclic compounds as lysophosphatidic acid receptor antagonists |
| GB2474120B (en) | 2009-10-01 | 2011-12-21 | Amira Pharmaceuticals Inc | Compounds as Lysophosphatidic acid receptor antagonists |
| CA2780908A1 (en) * | 2009-11-24 | 2011-06-03 | Allergan, Inc. | Novel compounds as receptor modulators with therapeutic utility |
| AR079982A1 (es) * | 2010-01-13 | 2012-03-07 | Sanofi Aventis | Derivados de acido carboxilico heterociclicos que comprenden un anillo de oxazolopirimidina 2,5,7- sustituido., composiciones farmaceuticas y procesos para prepararlos. |
| AR079981A1 (es) * | 2010-01-13 | 2012-03-07 | Sanofi Aventis | Derivados de acido carboxilico que comprenden un anillo de oxoazolopirimidina 2,5,7- sustituido |
| CA2784565C (en) * | 2010-01-14 | 2018-03-13 | Sanofi | 2,5-substituted oxazolopyrimidine derivatives |
| PH12012501265A1 (en) * | 2010-01-14 | 2016-07-27 | Sanofi Sa | Carboxylic acid derivatives having a 2,5-substituted oxazolopyrimidine ring |
| BR112012017447B1 (pt) * | 2010-01-14 | 2019-10-29 | Sanofi Sa | derivados de ácidos carboxílicos heterocíclicos tendo um anel oxazolopirimidina 2,5-substituído, processo para a preparação dos mesmos, e composição farmacêutica |
| CA2786994C (en) | 2010-01-27 | 2018-01-16 | Arena Pharmaceuticals, Inc. | Processes for the preparation of (r)-2-(7-(4-cyclopentyl-3-(trifluoromethyl)benzyloxy)-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetic acid and salts thereof |
| CN105503882B (zh) | 2010-03-03 | 2019-07-05 | 艾尼纳制药公司 | 制备s1p1受体调节剂及其晶体形式的方法 |
| ES2548683T3 (es) | 2010-04-23 | 2015-10-20 | Bristol-Myers Squibb Company | Amidas del ácido 4-(5-isoxazolil o 5-pirrazolil-1,2,4-oxadiazol-3-il)-mandélico como agonistas de receptor de esfingosina-1-fosfato 1 |
| HUE029570T2 (en) | 2010-04-27 | 2017-03-28 | Calcimedica Inc | Intracellular calcium modifying compounds |
| EP2563759B1 (de) | 2010-04-27 | 2022-04-06 | Calcimedica, Inc. | Verbindungen als modulatoren von intrazellulärem calcium |
| US9050334B2 (en) | 2010-07-16 | 2015-06-09 | Innov88 Llc | MIF inhibitors and their uses |
| CN103180316A (zh) | 2010-08-27 | 2013-06-26 | 钙医学公司 | 调节细胞内钙的化合物 |
| WO2012040532A1 (en) | 2010-09-24 | 2012-03-29 | Bristol-Myers Squibb Company | Substituted oxadiazole compounds and their use as s1p1 agonists |
| WO2012074780A1 (en) * | 2010-12-03 | 2012-06-07 | Allergan, Inc. | Novel oxime azetidine derivatives as sphingosine 1-phosphate (s1p) receptor modulators |
| WO2012074926A1 (en) * | 2010-12-03 | 2012-06-07 | Allergan, Inc. | Novel azetidine derivatives as sphingosine 1-phosphate (s1p) receptor modulators |
| CN103347510B (zh) | 2010-12-07 | 2015-11-25 | 艾米拉医药股份有限公司 | 溶血磷脂酸受体拮抗剂及其在治疗纤维化中的用途 |
| CN103596566B (zh) | 2010-12-07 | 2017-08-25 | 阿米拉制药公司 | 多环lpa1拮抗剂及其使用 |
| PT2672823T (pt) | 2011-02-07 | 2016-11-21 | Biogen Ma Inc | Agentes que modulam s1p |
| CN103596947A (zh) | 2011-04-05 | 2014-02-19 | 艾米拉医药股份有限公司 | 用于治疗纤维化、疼痛、癌症和呼吸、过敏性、神经系统疾病或心血管疾病的基于3-或5-联苯-4-基异噁唑的化合物 |
| CN103619828A (zh) * | 2011-04-14 | 2014-03-05 | 阿勒根公司 | 作为1-磷酸鞘氨醇受体调节剂的苯基双环甲基胺衍生物 |
| US8735402B2 (en) * | 2011-07-07 | 2014-05-27 | Sanofi | Cycloalkyloxycarboxylic acid derivatives |
| US8580816B2 (en) * | 2011-07-07 | 2013-11-12 | Sanofi | Carboxylic acid derivatives having an oxazolo[5,4-b]pyridine ring |
| US20150218090A1 (en) * | 2011-10-21 | 2015-08-06 | Novartis Ag | Dosage regimen for an s1p receptor modulator or agonist |
| EP2809645A1 (de) * | 2012-02-03 | 2014-12-10 | Novartis AG | Verfahren zur herstellung eines n-(4-cyclohexyl-3-trifluormethyl-benzyloxy-)acetimidinsäure-ethylesters |
| US9512116B2 (en) | 2012-10-12 | 2016-12-06 | Calcimedica, Inc. | Compounds that modulate intracellular calcium |
| KR20190136125A (ko) | 2012-12-21 | 2019-12-09 | 국립연구개발법인 양자과학기술연구개발기구 | 뇌 안에 축적된 타우 단백질을 이미징하기 위한 신규한 화합물 |
| WO2014127033A1 (en) * | 2013-02-13 | 2014-08-21 | Allergan, Inc. | Azetidine derivatives as sphingosine 1-phosphate (s1p) receptor modulators |
| JP6294872B2 (ja) | 2013-04-26 | 2018-03-14 | 国立大学法人京都大学 | 脳動脈瘤の形成および/または増大の抑制若しくは縮小用医薬組成物 |
| CN103408501B (zh) * | 2013-08-14 | 2016-03-09 | 合肥医工医药有限公司 | 苄基嘧啶衍生物、其制备方法及其医药用途 |
| US9951026B2 (en) | 2013-09-17 | 2018-04-24 | Pharmakea, Inc. | Heterocyclic vinyl autotaxin inhibitor compounds |
| US9714240B2 (en) | 2013-09-17 | 2017-07-25 | Pharmakea, Inc. | Vinyl autotaxin inhibitor compounds |
| EP3049405A4 (de) | 2013-09-26 | 2017-03-08 | Pharmakea Inc. | Autotaxin-inhibitorverbindungen |
| KR102367876B1 (ko) | 2013-11-22 | 2022-02-24 | 사브레 테라퓨틱스 엘엘씨 | 오토탁신 억제제 화합물 |
| EP3527569B1 (de) | 2014-02-03 | 2021-08-25 | Vitae Pharmaceuticals, LLC | Dihydropyrrolopyridininhibitoren von ror-gamma zur behandlung von augentrockenheit |
| TWI675032B (zh) | 2014-10-14 | 2019-10-21 | 美商維它藥物公司 | ROR-γ之二氫吡咯并吡啶抑制劑 |
| US9845308B2 (en) | 2014-11-05 | 2017-12-19 | Vitae Pharmaceuticals, Inc. | Isoindoline inhibitors of ROR-gamma |
| US9663515B2 (en) | 2014-11-05 | 2017-05-30 | Vitae Pharmaceuticals, Inc. | Dihydropyrrolopyridine inhibitors of ROR-gamma |
| AU2016205361C1 (en) | 2015-01-06 | 2021-04-08 | Arena Pharmaceuticals, Inc. | Methods of treating conditions related to the S1P1 receptor |
| WO2016144703A1 (en) | 2015-03-06 | 2016-09-15 | Pharmakea, Inc. | Fluorinated lysyl oxidase-like 2 inhibitors and uses thereof |
| EA036337B1 (ru) | 2015-05-27 | 2020-10-28 | Сабре Терапьютикс Ллс | Ингибиторы аутотаксина и их применения |
| PL3310760T3 (pl) | 2015-06-22 | 2023-03-06 | Arena Pharmaceuticals, Inc. | Krystaliczna sól L-argininy kwasu (R)-2-(7-(4-cyklopentylo-3-(trifluorometylo)benzyloksy)- 1,2,3,4-tetrahydrocyklo-penta[b]indol-3-ilo)octowego do zastosowania w zaburzeniach związanych z receptorem S1P1 |
| ES2856931T3 (es) | 2015-08-05 | 2021-09-28 | Vitae Pharmaceuticals Llc | Moduladores de ROR-gamma |
| JP2018525429A (ja) * | 2015-08-28 | 2018-09-06 | アッヴィ・インコーポレイテッド | S1p調節剤としての縮合複素環化合物 |
| EP3868750A1 (de) | 2015-11-20 | 2021-08-25 | Vitae Pharmaceuticals, LLC | Modulatoren von ror-gamma |
| TW202220968A (zh) | 2016-01-29 | 2022-06-01 | 美商維它藥物有限責任公司 | ROR-γ調節劑 |
| KR20190017950A (ko) * | 2016-06-10 | 2019-02-20 | 아이오 테라퓨틱스, 인크. | 암 면역요법을 위한 수용체 선택적 레티노이드 및 렉시노이드 화합물 및 면역 조절제 |
| US9481674B1 (en) | 2016-06-10 | 2016-11-01 | Vitae Pharmaceuticals, Inc. | Dihydropyrrolopyridine inhibitors of ROR-gamma |
| MX390964B (es) | 2016-09-07 | 2025-03-21 | Pharmakea Inc | Formas cristalinas de un inhibidor tipo lisil oxidasa 2 y metodos de realizacion. |
| MX2019002612A (es) | 2016-09-07 | 2019-08-21 | Pharmakea Inc | Usos de un inhibidor de lisil-oxidasa tipo 2. |
| JP2020507610A (ja) | 2017-02-16 | 2020-03-12 | アリーナ ファーマシューティカルズ, インコーポレイテッド | 腸管外症状を伴う炎症性腸疾患の治療のための化合物および方法 |
| KR20190116416A (ko) | 2017-02-16 | 2019-10-14 | 아레나 파마슈티칼스, 인크. | 원발 담즙성 담관염을 치료하기 위한 화합물 및 방법 |
| WO2019018975A1 (en) | 2017-07-24 | 2019-01-31 | Vitae Pharmaceuticals, Inc. | INHIBITORS OF ROR GAMMA |
| MA49685A (fr) | 2017-07-24 | 2021-04-14 | Vitae Pharmaceuticals Llc | INHIBITEURS DE ROR gamma |
| JP7293343B2 (ja) * | 2018-05-09 | 2023-06-19 | アプリノイア セラピューティクス リミテッド | ヘテロアリール化合物及びその使用 |
| AU2019280822A1 (en) | 2018-06-06 | 2021-01-07 | Arena Pharmaceuticals, Inc. | Methods of treating conditions related to the S1P1 receptor |
| CN110776450B (zh) * | 2018-07-27 | 2022-09-27 | 广东东阳光药业有限公司 | 一种辛波莫德晶型及其制备方法 |
| EP3847158A1 (de) | 2018-09-06 | 2021-07-14 | Arena Pharmaceuticals, Inc. | Verbindungen zur verwendung bei der behandlung von autoimmun- und entzündlichen erkrankungen |
| CN113072474A (zh) * | 2018-12-06 | 2021-07-06 | 上海济煜医药科技有限公司 | 作为免疫调节剂的化合物及其制备方法和应用 |
| JP7464920B2 (ja) * | 2018-12-06 | 2024-04-10 | シャンハイ ジェミンケア ファーマシューティカル カンパニー,リミティド | 免疫調節としての芳香環誘導体及びその製造方法と使用 |
| CN111484434A (zh) * | 2019-01-29 | 2020-08-04 | 东莞市东阳光仿制药研发有限公司 | 一种辛波莫德晶型及其制备方法 |
| WO2020173346A1 (zh) * | 2019-02-25 | 2020-09-03 | 广东东阳光药业有限公司 | 一种辛波莫德的制备方法 |
| CA3161455A1 (en) | 2019-11-13 | 2021-05-20 | Aprinoia Therapeutics Limited | Compounds for degrading tau protein aggregates and uses thereof |
| US12331048B2 (en) | 2022-10-31 | 2025-06-17 | Ventus Therapeutics U.S., Inc. | Pyrido-[3,4-d]pyridazine amine derivatives useful as NLRP3 inhibitors |
| CN119776509A (zh) * | 2023-10-08 | 2025-04-08 | 华东师范大学 | Ndufa10基因和S1pr4基因突变在肌病诊断、预测和治疗中的用途 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH540247A (de) * | 1967-04-21 | 1973-09-28 | Ciba Geigy Ag | Verfahren zur Herstellung von heterocyclischen, Asthylendoppelbindungen enthaltenden Verbindungen |
| IL109161A0 (en) * | 1993-03-31 | 1994-06-24 | Cell Therapeutics Inc | Amino alcohol derivatives, methods for the preparation thereof, and pharmaceutical compositions containing the same |
| AU3325295A (en) * | 1994-08-24 | 1996-03-14 | Eli Lilly And Company | Pyrrolidinyl di-carboxylic acid derivatives as metabotropic glutamate receptor antagonists |
| US6110922A (en) * | 1998-12-29 | 2000-08-29 | Abbott Laboratories | Cell adhesion-inhibiting antiinflammatory and immune-suppressive compounds |
| EP1195165A4 (de) * | 1999-07-12 | 2005-08-10 | Ono Pharmaceutical Co | Fibrose inhibitore die als aktiven bestandteil sphingosin-a-phosphat oder dessen rezeptoragonisten enthalten |
| US20040235794A1 (en) * | 2001-09-04 | 2004-11-25 | Shinji Nakade | Remedies for respiratory diseases comprising sphingosine-1-phosphate receptor controller |
| AU2002363236A1 (en) * | 2001-10-30 | 2003-05-12 | Millennium Pharmaceuticals, Inc. | Compounds, pharmaceutical compositions and methods of use therefor |
| WO2003051837A2 (de) * | 2001-12-14 | 2003-06-26 | Zentaris Gmbh | Tetrahydrocarbazolderivate als liganden für g-protein gekoppelte rezeptoren (gpcr) |
| ATE441654T1 (de) * | 2002-01-18 | 2009-09-15 | Merck & Co Inc | Edg-rezeptoragonisten |
| US20050070506A1 (en) | 2002-01-18 | 2005-03-31 | Doherty George A. | Selective s1p1/edg1 receptor agonists |
| DE10207844A1 (de) * | 2002-02-15 | 2003-09-04 | Schering Ag | 1-Phenyl-2-heteroaryl-substituierte Benzimidazolderivate, deren Verwendung zur Herstellung von Arzneimitteln sowie diese Derivate enthaltende pharmazeutische Präparate |
| US20030207924A1 (en) * | 2002-03-07 | 2003-11-06 | Xue-Min Cheng | Compounds that modulate PPAR activity and methods of preparation |
| HRP20040952A2 (en) * | 2002-04-26 | 2005-06-30 | F. Hoffmann - La Roche Ag | Isoquinoline derivatives |
| JP2007186422A (ja) * | 2004-01-28 | 2007-07-26 | Astellas Pharma Inc | アリールスルフィド誘導体 |
-
2004
- 2004-05-19 CN CN2004800131943A patent/CN1787817B/zh not_active Expired - Fee Related
- 2004-05-19 CA CA2524054A patent/CA2524054C/en not_active Expired - Fee Related
- 2004-05-19 PT PT04752678T patent/PT1638551E/pt unknown
- 2004-05-19 CN CN2004800139502A patent/CN1791592B/zh not_active Expired - Fee Related
- 2004-05-19 EP EP04752678A patent/EP1638551B1/de not_active Expired - Lifetime
- 2004-05-19 AT AT04752678T patent/ATE537825T1/de active
- 2004-05-19 DK DK04752678.5T patent/DK1638551T3/da active
- 2004-05-19 US US10/849,450 patent/US7462629B2/en not_active Expired - Fee Related
- 2004-05-19 PL PL04752678T patent/PL1638551T3/pl unknown
- 2004-05-19 BR BRPI0410454-4A patent/BRPI0410454A/pt not_active IP Right Cessation
- 2004-05-19 AU AU2004240649A patent/AU2004240649A1/en not_active Abandoned
- 2004-05-19 SI SI200431832T patent/SI1638551T1/sl unknown
- 2004-05-19 CN CN2004800132486A patent/CN1791395B/zh not_active Expired - Lifetime
- 2004-05-19 JP JP2006533219A patent/JP4575920B2/ja not_active Expired - Fee Related
- 2004-05-19 CN CN2004800188602A patent/CN1816544B/zh not_active Expired - Fee Related
- 2004-05-19 ES ES04752678T patent/ES2379169T3/es not_active Expired - Lifetime
- 2004-05-19 WO PCT/US2004/015701 patent/WO2004103309A2/en not_active Ceased
- 2004-05-19 MX MXPA05012459A patent/MXPA05012459A/es active IP Right Grant
- 2004-05-19 US US10/849,079 patent/US7060697B2/en not_active Expired - Fee Related
-
2005
- 2005-10-11 ZA ZA200508203A patent/ZA200508203B/en unknown
-
2008
- 2008-07-11 AU AU2008203088A patent/AU2008203088A1/en not_active Abandoned
-
2012
- 2012-03-16 CY CY20121100286T patent/CY1112505T1/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US20050009786A1 (en) | 2005-01-13 |
| ES2379169T3 (es) | 2012-04-23 |
| CN1787817B (zh) | 2011-09-07 |
| WO2004103309A2 (en) | 2004-12-02 |
| SI1638551T1 (sl) | 2012-04-30 |
| US7462629B2 (en) | 2008-12-09 |
| CN1791592A (zh) | 2006-06-21 |
| CN1816544A (zh) | 2006-08-09 |
| US20050014724A1 (en) | 2005-01-20 |
| AU2004240649A1 (en) | 2004-12-02 |
| AU2008203088A1 (en) | 2008-08-07 |
| HK1090559A1 (en) | 2006-12-29 |
| PL1638551T3 (pl) | 2012-05-31 |
| WO2004103309A3 (en) | 2005-03-03 |
| CN1791592B (zh) | 2012-07-04 |
| ZA200508203B (en) | 2007-02-28 |
| EP1638551B1 (de) | 2011-12-21 |
| CA2524054A1 (en) | 2004-12-02 |
| CN1816544B (zh) | 2011-06-08 |
| CN1791395B (zh) | 2012-09-26 |
| US7060697B2 (en) | 2006-06-13 |
| MXPA05012459A (es) | 2006-02-22 |
| DK1638551T3 (da) | 2012-04-02 |
| EP1638551A4 (de) | 2008-12-31 |
| JP2006528987A (ja) | 2006-12-28 |
| CN1787817A (zh) | 2006-06-14 |
| JP4575920B2 (ja) | 2010-11-04 |
| CA2524054C (en) | 2012-04-24 |
| BRPI0410454A (pt) | 2006-06-13 |
| EP1638551A2 (de) | 2006-03-29 |
| CN1791395A (zh) | 2006-06-21 |
| PT1638551E (pt) | 2012-03-28 |
| CY1112505T1 (el) | 2015-12-09 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| BRPI0410454A (pt) | composições e compostos imunossupressores | |
| TW200505442A (en) | Immunosuppressant compounds and compositions | |
| TW200505428A (en) | Immunosuppressant compounds and compositions | |
| WO2004113330A8 (en) | Immunosuppressant compounds and compositions | |
| WO2005082089A3 (en) | Immunosuppressant compounds and compositions | |
| WO2004071442A3 (en) | Novel bicyclic compounds and compositions | |
| TW200700068A (en) | Phthalazine, aza-and diaza-phthalazine compounds and methods of use | |
| IL190654A (en) | Methods of Methyl-Sulfonamido-Propanamido, Processes for Preparation and Medicines Containing Them | |
| ATE384050T1 (de) | Benzazepinderivate als histamin-h3-antagonisten | |
| ATE549311T1 (de) | Amino-propanolderivative als modulatoren des sphingosin-1-phosphat-rezeptors | |
| TW200612905A (en) | Novel sulfamate and sulfamide derivatives useful for the treatment of epilepsy and related disorders | |
| TW200611702A (en) | Novel sulfamate and sulfamide derivatives useful for the treatment of epilepsy and related disorders | |
| TW200716120A (en) | Pyrazolo-pyrimidine derivatives as mGluR2 antagonists | |
| ATE433966T1 (de) | Methylendipiperidinderivate | |
| ATE478863T1 (de) | Heterotetracyclische verbindungen als tpo- mimetica | |
| TW200514781A (en) | Novel compounds | |
| FR2872165B1 (fr) | Nouveaux derives de pyrimido-benzimidazole | |
| MX2007006754A (es) | Derivados de indenilo y uso de los mismos para el tratamiento de trastornos neurologicos. | |
| ATE467636T1 (de) | Pyrazoloä3 , 4-düazepinderivate als histamin-h3- antagonisten | |
| ES2333026T3 (es) | Derivados de ciclohexil-1,4-diamina sustituidos. | |
| TW200801005A (en) | Acetylenic piperazines as metabotropic glutamate receptor antagonists | |
| HRP20050603A2 (en) | Novel anticonvulsant derivative salts | |
| ATE417042T1 (de) | Substituierte 2,5-diaminomethyl-1h-pyrrole | |
| ATE365556T1 (de) | Verwendung von 3-aza-aoxa-dibenzo(e,h)azulenen zur herstellung von pharmazeutischen formulierung für die behandlung und prävention von erkrankungen und störungen des zentralen nervensystems | |
| UA84701C2 (ru) | Замещенные индолы, способ их получения, их использования |