MA52308A - Procédés et intermédiaires pour la préparation d'antagonistes c5ar - Google Patents
Procédés et intermédiaires pour la préparation d'antagonistes c5arInfo
- Publication number
- MA52308A MA52308A MA052308A MA52308A MA52308A MA 52308 A MA52308 A MA 52308A MA 052308 A MA052308 A MA 052308A MA 52308 A MA52308 A MA 52308A MA 52308 A MA52308 A MA 52308A
- Authority
- MA
- Morocco
- Prior art keywords
- intermediaries
- preparing
- methods
- c5ar antagonists
- c5ar
- Prior art date
Links
- 101150009981 C5AR1 gene Proteins 0.000 title 1
- 102100032957 C5a anaphylatoxin chemotactic receptor 1 Human genes 0.000 title 1
- 239000005557 antagonist Substances 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/60—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/451—Non condensed piperidines, e.g. piperocaine having a carbocyclic group directly attached to the heterocyclic ring, e.g. glutethimide, meperidine, loperamide, phencyclidine, piminodine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial 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
-
- 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
- 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
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201462057107P | 2014-09-29 | 2014-09-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
MA52308A true MA52308A (fr) | 2021-02-24 |
Family
ID=55583729
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA052308A MA52308A (fr) | 2014-09-29 | 2015-09-28 | Procédés et intermédiaires pour la préparation d'antagonistes c5ar |
Country Status (19)
Country | Link |
---|---|
US (5) | US9745268B2 (fr) |
EP (2) | EP3200791B1 (fr) |
JP (1) | JP6898229B6 (fr) |
KR (2) | KR20230149873A (fr) |
CN (2) | CN113121415A (fr) |
AU (2) | AU2015324111B2 (fr) |
BR (1) | BR112017006232B1 (fr) |
CA (2) | CA2960733C (fr) |
DK (1) | DK3200791T3 (fr) |
ES (2) | ES2926828T3 (fr) |
IL (1) | IL251061B (fr) |
MA (1) | MA52308A (fr) |
MX (2) | MX368492B (fr) |
NZ (2) | NZ730123A (fr) |
PL (1) | PL3200791T3 (fr) |
PT (1) | PT3200791T (fr) |
RU (1) | RU2712233C2 (fr) |
SG (1) | SG11201702185UA (fr) |
WO (1) | WO2016053890A1 (fr) |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SI2381778T1 (sl) | 2008-12-22 | 2016-10-28 | Chemocentryx, Inc. | Antagonisti C5AR |
ES2632975T3 (es) * | 2010-06-24 | 2017-09-18 | Chemocentryx, Inc. | Antagonistas de C5aR |
JP6898229B6 (ja) * | 2014-09-29 | 2021-07-28 | ケモセントリックス,インコーポレイティド | C5aRアンタゴニスト製造における方法及び中間体 |
MA43872A (fr) | 2016-01-14 | 2021-05-19 | Chemocentryx Inc | Procédé de traitement d'une glomérulopathie à c3 |
AU2018359214A1 (en) * | 2017-10-30 | 2020-04-16 | Chemocentryx, Inc. | Deuterated compounds as immunomodulators |
SG11202011961YA (en) | 2018-06-07 | 2020-12-30 | Chemocentryx Inc | Dosing and effect of c5a antagonist with anca-associated vasculitis |
BR112021010285A2 (pt) | 2018-11-30 | 2021-08-17 | Chemocentryx, Inc. | formulações de cápsula |
KR102207333B1 (ko) * | 2019-09-09 | 2021-01-27 | 성균관대학교산학협력단 | 4중 연속 고리 화합물의 신규한 제조방법 |
CN114867473A (zh) | 2019-11-08 | 2022-08-05 | 凯莫森特里克斯股份有限公司 | 补体成分c5a受体的盐形式 |
AU2020378061A1 (en) * | 2019-11-08 | 2022-05-26 | Chemocentryx, Inc. | Free base crystalline form of a complement component C5a receptor |
WO2021092286A1 (fr) * | 2019-11-08 | 2021-05-14 | Chemocentryx, Inc. | Forme amorphe d'un récepteur de constituant c5a du complément |
WO2022078269A1 (fr) * | 2020-10-16 | 2022-04-21 | 苏州科睿思制药有限公司 | Forme cristalline d'avacopan, son procédé de préparation et son utilisation |
WO2022263263A1 (fr) | 2021-06-16 | 2022-12-22 | Sandoz Ag | Forme cristalline d'avacopan |
EP4137133A1 (fr) | 2021-08-19 | 2023-02-22 | Sandoz AG | Forme cristalline d'avacopan |
CN113957106B (zh) * | 2021-11-03 | 2024-04-19 | 暨明医药科技(苏州)有限公司 | 一种Avacopan及其中间体的制备方法 |
CN114262291B (zh) * | 2022-01-04 | 2023-05-19 | 重庆医科大学 | 一种阿伐可泮的合成方法 |
WO2023158722A2 (fr) | 2022-02-16 | 2023-08-24 | Teva Pharmaceuticals International Gmbh | Processus de préparation d'avacopan et de ses intermédiaires |
Family Cites Families (51)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4686100A (en) | 1985-04-02 | 1987-08-11 | The Board Of Trustees Of The Leland Stanford Junior University | Method for the treatment of adult respiratory distress syndrome |
JP2002523448A (ja) | 1998-08-28 | 2002-07-30 | サイオス インコーポレイテッド | p38−αキナーゼのインヒビター |
RU2197288C2 (ru) | 1999-08-03 | 2003-01-27 | Тверская медицинская академия | Способ лечения больных хроническим гломерулонефритом |
EP1278743A4 (fr) | 2000-05-05 | 2003-05-14 | Smithkline Beecham Corp | Nouveaux anti-infectieux |
US7105567B2 (en) | 2000-08-10 | 2006-09-12 | Mitsubishi Pharma Corporation | 3-substituted urea derivatives and medicinal use thereof |
US7855297B2 (en) | 2000-09-14 | 2010-12-21 | Mitsubishi Tanabe Pharma Corporation | Amide derivatives and medicinal use thereof |
CN1454086A (zh) | 2000-09-29 | 2003-11-05 | 神经能质公司 | 高亲和性小分子C5a受体调节物 |
SE524438C2 (sv) | 2000-10-05 | 2004-08-10 | Magnus Georg Goertz | Fjärrstyrt dörrelaterat låsarrangemang, första och andra datorpogramprodukt, bärande medium och ett datorlösbart medium |
DE10293175D2 (de) | 2001-07-19 | 2004-07-01 | Luk Lamellen & Kupplungsbau | System zum Ansteuern einer Komponente eines Getriebes eines Fahrzeuges unter Berücksichtigung eines Fluidverlustes |
WO2003015819A1 (fr) | 2001-08-17 | 2003-02-27 | Tanox, Inc. | Inhibiteur de la voie du complement se fixant a c5 et a c5a sans empecher la formation de c5b |
HUP0401900A3 (en) | 2001-09-21 | 2005-08-29 | Sanofi Aventis | 3-substituted-4-pyrimidone derivatives, pharmaceutical compositions containing them and their intermediates |
ITMI20012025A1 (it) | 2001-09-28 | 2003-03-28 | Dompe Spa | Sali di ammonio quaternari di omega-amminoalchilammidi di acidi r 2-aril-propionici e composizioni farmaceutiche che li contengono |
US20030195192A1 (en) | 2002-04-05 | 2003-10-16 | Fortuna Haviv | Nicotinamides having antiangiogenic activity |
AU2003218374A1 (en) | 2002-03-28 | 2003-10-13 | Neurogen Corporation | Substituted tetrahydroisoquinolines as c5a receptor modulators |
CA2479928A1 (fr) | 2002-03-28 | 2003-10-09 | Neurogen Corporation | Biarylamides substitues en tant que modulateurs du recepteur c5a |
CA2480082A1 (fr) | 2002-03-29 | 2003-10-16 | Neurogen Corporation | Therapie combinatoire pour le traitement de maladies faisant intervenir des composants inflammatoires |
US20040014744A1 (en) | 2002-04-05 | 2004-01-22 | Fortuna Haviv | Substituted pyridines having antiangiogenic activity |
JP2005536533A (ja) * | 2002-08-08 | 2005-12-02 | ベーリンガー インゲルハイム ファーマシューティカルズ インコーポレイテッド | 置換ベンゾイミダゾール化合物 |
AU2003265625A1 (en) | 2002-08-21 | 2004-03-11 | Neurogen Corporation | Amino methyl imidazoles as c5a receptor modulators |
US7455837B2 (en) | 2002-11-05 | 2008-11-25 | The Regents Of The University Of Michigan | Compositions and methods for the diagnosis and treatment of sepsis |
FR2846654A1 (fr) | 2002-11-05 | 2004-05-07 | Servier Lab | Nouveaux derives de la 2,3-dihydro-4(1h)-pyridinone, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
AU2003291403A1 (en) | 2002-11-08 | 2004-06-03 | Neurogen Corporation | 3-substituted-6-aryl pyridined as ligands of c5a receptors |
AU2003902354A0 (en) | 2003-05-15 | 2003-05-29 | Harkin, Denis W. | Treatment of haemorrhagic shock |
WO2004110996A1 (fr) | 2003-06-19 | 2004-12-23 | Pfizer Products Inc. | Antagoniste de nk1 |
WO2005007087A2 (fr) | 2003-07-03 | 2005-01-27 | Neurogen Corporation | Derives (heterocycloalkyl)methyle substitues de type azole utilises comme modulateurs des recepteurs c5a |
GB0325956D0 (en) | 2003-11-06 | 2003-12-10 | Addex Pharmaceuticals Sa | Novel compounds |
AU2005267289A1 (en) | 2004-06-24 | 2006-02-02 | Incyte Corporation | N-substituted piperidines and their use as pharmaceuticals |
EP1621536A1 (fr) * | 2004-07-27 | 2006-02-01 | Aventis Pharma S.A. | Dérivés d'urées cycliques aminés, leur préparation et utilisation pharmaceutique en tant qu'inhibiteurs de Kinase |
WO2006071958A1 (fr) | 2004-12-29 | 2006-07-06 | Millennium Pharmaceuticals, Inc. | Composes utilises comme antagonistes du recepteur de la chimiokine |
KR20070113233A (ko) | 2005-02-18 | 2007-11-28 | 아스트라제네카 아베 | 항균성 피페리딘 유도체 |
US7880004B2 (en) | 2005-09-15 | 2011-02-01 | Bristol-Myers Squibb Company | Met kinase inhibitors |
WO2007051062A2 (fr) | 2005-10-28 | 2007-05-03 | Chemocentryx, Inc. | Dihydropyridines substituees et leurs methodes d'utilisation |
ES2597843T3 (es) | 2005-11-24 | 2017-01-23 | Dompé Farmaceutici S.P.A. | Derivados de (R)-arilalquilamino y composiciones farmacéuticas que los contienen |
MX340784B (es) | 2006-03-15 | 2016-07-26 | Alexion Pharma Inc | Inhibidores de complemento para usarse en el tratamiento de pacientes con hemoglobinuria paroxística nocturna. |
WO2008022060A2 (fr) | 2006-08-14 | 2008-02-21 | Novartis Ag | composés organiques et leurs utilisations |
US8198266B2 (en) | 2006-10-31 | 2012-06-12 | Inserm (Institut National De La Sante Et De La Recherche Medicale) | Use of an EGFR antagonist for the treatment of glomerolonephritis |
JP2010531873A (ja) | 2007-06-29 | 2010-09-30 | トレント ファーマシューティカルズ リミテッド | Hsp誘導剤としての新規の置換ピペリドン |
CA2737219C (fr) | 2008-08-11 | 2017-02-28 | Tracy Keller | Analogues d'halofuginone pour l'inhibition d'arnt synthetases et leurs utilisations |
WO2010025510A1 (fr) | 2008-09-03 | 2010-03-11 | Xenome Ltd | Bibliothèques de conjugués peptidiques et leurs méthodes de fabrication |
US20100074863A1 (en) | 2008-09-17 | 2010-03-25 | Yat Sun Or | Anti-infective pyrrolidine derivatives and analogs |
CN109045296A (zh) | 2008-11-10 | 2018-12-21 | 阿雷克森制药公司 | 用于治疗补体相关障碍的方法和组合物 |
SI2381778T1 (sl) | 2008-12-22 | 2016-10-28 | Chemocentryx, Inc. | Antagonisti C5AR |
US20110275639A1 (en) * | 2008-12-22 | 2011-11-10 | Chemocentryx, Inc. | C5aR ANTAGONISTS |
WO2011035143A2 (fr) | 2009-09-17 | 2011-03-24 | The Regents Of The University Of Michigan | Procédés et compositions pour inhiber des maladies et des états à médiation par rho |
ES2632975T3 (es) * | 2010-06-24 | 2017-09-18 | Chemocentryx, Inc. | Antagonistas de C5aR |
KR20150033652A (ko) | 2012-06-20 | 2015-04-01 | 노파르티스 아게 | 보체 경로 조절제 및 그의 용도 |
WO2014180961A1 (fr) | 2013-05-08 | 2014-11-13 | Novo Nordisk A/S | Utilisation d'antagonistes de c5ar |
JP6898229B6 (ja) * | 2014-09-29 | 2021-07-28 | ケモセントリックス,インコーポレイティド | C5aRアンタゴニスト製造における方法及び中間体 |
MA43872A (fr) | 2016-01-14 | 2021-05-19 | Chemocentryx Inc | Procédé de traitement d'une glomérulopathie à c3 |
CN109310686B (zh) | 2016-04-04 | 2022-06-21 | 凯莫森特里克斯股份有限公司 | 可溶性C5aR拮抗剂 |
EP4262800A1 (fr) | 2020-12-21 | 2023-10-25 | ChemoCentryx, Inc. | Traitement de la glomérulopathie à c3 à l'aide d'un inhibiteur de c5a |
-
2015
- 2015-09-28 JP JP2017516679A patent/JP6898229B6/ja active Active
- 2015-09-28 CN CN202110432100.1A patent/CN113121415A/zh active Pending
- 2015-09-28 MX MX2017003789A patent/MX368492B/es active IP Right Grant
- 2015-09-28 CA CA2960733A patent/CA2960733C/fr active Active
- 2015-09-28 KR KR1020237035689A patent/KR20230149873A/ko active Application Filing
- 2015-09-28 RU RU2017114960A patent/RU2712233C2/ru active
- 2015-09-28 NZ NZ730123A patent/NZ730123A/en unknown
- 2015-09-28 CN CN201580052937.6A patent/CN106999481B/zh active Active
- 2015-09-28 ES ES20160995T patent/ES2926828T3/es active Active
- 2015-09-28 DK DK15845610.3T patent/DK3200791T3/da active
- 2015-09-28 EP EP15845610.3A patent/EP3200791B1/fr active Active
- 2015-09-28 WO PCT/US2015/052697 patent/WO2016053890A1/fr active Application Filing
- 2015-09-28 PT PT158456103T patent/PT3200791T/pt unknown
- 2015-09-28 ES ES15845610T patent/ES2802428T3/es active Active
- 2015-09-28 AU AU2015324111A patent/AU2015324111B2/en active Active
- 2015-09-28 PL PL15845610T patent/PL3200791T3/pl unknown
- 2015-09-28 CA CA3220371A patent/CA3220371A1/fr active Pending
- 2015-09-28 EP EP20160995.5A patent/EP3682879B1/fr active Active
- 2015-09-28 MA MA052308A patent/MA52308A/fr unknown
- 2015-09-28 BR BR112017006232-1A patent/BR112017006232B1/pt active IP Right Grant
- 2015-09-28 NZ NZ767823A patent/NZ767823A/en unknown
- 2015-09-28 KR KR1020177011789A patent/KR102593431B1/ko active IP Right Grant
- 2015-09-28 SG SG11201702185UA patent/SG11201702185UA/en unknown
- 2015-09-28 US US14/867,669 patent/US9745268B2/en active Active
-
2017
- 2017-03-09 IL IL251061A patent/IL251061B/en active IP Right Grant
- 2017-03-23 MX MX2019011911A patent/MX2019011911A/es unknown
- 2017-07-25 US US15/659,468 patent/US10266492B2/en active Active
-
2019
- 2019-03-21 US US16/360,195 patent/US10532982B2/en active Active
- 2019-12-06 US US16/706,296 patent/US20200354320A1/en not_active Abandoned
-
2021
- 2021-06-22 AU AU2021204209A patent/AU2021204209B2/en active Active
-
2022
- 2022-02-08 US US17/667,289 patent/US11845729B2/en active Active
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