HRP20150987T1 - UPORABA sGC STIMULATORA, sGC AKTIVATORA, SAMOSTALNO I U KOMBINACIJAMA S INHIBITORIMA PDE5 ZA LIJEÄŚENJE SISTEMSKE SKLEROZE (SSc) - Google Patents
UPORABA sGC STIMULATORA, sGC AKTIVATORA, SAMOSTALNO I U KOMBINACIJAMA S INHIBITORIMA PDE5 ZA LIJEÄŚENJE SISTEMSKE SKLEROZE (SSc) Download PDFInfo
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Claims (18)
1. Spojevi prema formulama (1) do (27)
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naznačeni time da su za uporabu za prevenciju i/ili liječenje sistemske skleroze (SSc).
2. Spojevi prema formulama (1), (2), (3), (4), (5), (6), (7) i (27) naznačeni time da su za uporabu za prevenciju i/ili liječenje sistemske skleroze (SSc).
3. Spoj prema formuli (3) naznačen time da je za uporabu za prevenciju i/ili liječenje sistemske skleroze.
4. Najmanje jedan spoj prema zahtjevu 1 do 3 naznačen time da je u kombinaciji s barem jednim inhibitorom PDE5 odabranim iz skupine koja sadrži:
Tadalafil ((6R,12aR)-2,3,6,7,12,12a-Heksahidro-2-metil-6-(3,4-metilen - dioksifenil)pirazino(1',2':1,6)pirido(3,4-b)indol-1,4-dion), Vardenafil (2-(2-Etoksi-5-(4-etilpiperazin-1-il-1-sulfonil)fenil)-5-metil-7-propil-3H-imidazo (5,1-f) (1,2,4)triazin-4-on), Sildenafil (3-[2-etoksi-5-(4-metilpiperazin-1-il)sulfonil-fenil]-7- metil- 9-propil-2,4,7,8-tetrazabiciklo [4.3.0]nona -3,8,10-trien-5-on), Udenafil 5-[2-propiloksi-5-(1-metil-2-pirolidiniletilamidosulfonil)fenil]-metil-3-propil-1,6-dihidro-7H-pirazolo(4,3-d)pirimidin-7-on, Dasantafil 7-(3-Bromo-4-metoksibenzil)-1-etil-8-[[(1,2)-2-hidroksiciklopentil]amino]-3-(2-hidroksietil)-3,7-dihidro-1-purin-2,6-dion, Avanafil 4-{[(3-kloro-4-metoksifenil)metil]amino}-2-[(2S)-2-(hidroksimetil)pirolidin-1-il]-N-(pirimidin-2-ilmetil)pirimidin-5-karboksamid, Mirodenafil, Lodenafil, UK 369.003, UK 371.800, SLx 2101 od tvrtke Surface Logix, LAS 34179 Triazolo[1,2-]ksantin,6-metil-4-propil-2-[2-propoksi-5-(4-metilpiperazino)sulfonil]fenil ili soli, hidrati ili hidrati soli naznačen time da je za uporabu za prevenciju i/ili liječenje sistemske skleroze (SSc).
5. Najmanje jedan spoj prema zahtjevu 1 do 3 u kombinaciji sa sildenafilom ili vardenafilom naznačen time da je za uporabu za prevenciju i/ili liječenje sistemske skleroze (SSc).
6. Spojevi prema zahtjevu 1 do 5 su za uporabu za prevenciju i/ili liječenje sistemske skleroze (SSc), difuzne sistemske skleroze (dSSc), ograničene sistemske skleroze (lSSc), preklapajućeg tipa sistemske skleroze, nediferenciranog tipa sistemske skleroze, sistemske skleroze bez sklerodermije, fibroze kože, sklerodermije, nefrogene fibrozne dermopatije (NFD), nefrogene sistemske fibroze (NSF), stvaranja keloida.
7. Spojevi prema zahtjevu 1 do 5 naznačeni time da su za uporabu za prevenciju i/ili liječenje sistemske skleroze SSc uz popratnu fibrozu unutrašnjih organa, koji obuhvaćaju crijeva, pluća, bubrege i krvne žile.
8. Spojevi prema formulama (3), (4), (6), i/ili (7) naznačeni time da su za uporabu za prevenciju i/ili liječenje sistemske skleroze SSc.
9. Najmanje jedan spoj prema formulama (3), (4), (6) i/ili (7) u kombinaciji s vardenafilom ili sildenafilom naznačen time da je za uporabu za prevenciju i/ili liječenje sistemske skleroze SSc.
10. Uporaba spoja prema zahtjevima 1-9 naznačena time da je za proizvodnju lijeka za prevenciju i/ili liječenje sistemske skleroze (SSc) koji sadrži učinkovitu količinu spoja prema zahtjevima 1 do 9.
11. Uporaba spoja prema zahtjevima 1-9 naznačena time da je za proizvodnju lijeka za prevenciju i/ili liječenje sistemske skleroze (SSc), difuzne sistemske skleroze (dSSc), ograničene sistemske skleroze (lSSc), preklapajućeg tipa sistemske skleroze, nediferenciranog tipa sistemske skleroze, sistemske skleroze bez sklerodermije, fibroze kože, sklerodermije, nefrogene fibrozne dermopatije (NFD), stvaranja keloida, koji sadrži učinkovitu količinu spoja prema zahtjevima 1 do 9.
12. Uporaba spoja prema zahtjevima 1-9 naznačena time da je za proizvodnju lijeka za prevenciju i/ili liječenje sistemske skleroze SSc uz popratnu fibrozu unutrašnjih organa, koji obuhvaćaju crijeva, pluća, bubrege i krvne žile koji sadrži učinkovitu količinu spoja prema zahtjevima 1 do 9.
13. Farmaceutska formulacija koja sadrži barem jedan spoj ili jednu kombinaciju prema zahtjevima 1 do 9 naznačena time da je za uporabu za prevenciju i/ili liječenje sistemske skleroze (SSc).
14. Farmaceutska formulacija koja sadrži barem jedan spoj ili jednu kombinaciju prema zahtjevima 1 do 9 naznačena time da je za uporabu za prevenciju i/ili liječenje sistemske skleroze (SSc), difuzne sistemske skleroze (dSSc), ograničene sistemske skleroze (lSSc), preklapajućeg tipa sistemske skleroze, nediferenciranog tipa sistemske skleroze, sistemske skleroze bez sklerodermije, fibroze kože, sklerodermije, nefrogene fibrozne dermopatije (NFD), stvaranja keloida.
15. Farmaceutska formulacija koja sadrži barem jedan spoj ili jednu kombinaciju prema zahtjevima 1 do 9 naznačena time da je za uporabu za prevenciju i/ili liječenje sistemske skleroze SSc uz popratnu fibrozu unutrašnjih organa, koji obuhvaćaju crijeva, pluća, bubrege i krvne žile.
16. Komplet koji sadrži najmanje jedan stimulator i/ili aktivator sGC prema zahtjevima od 1 do 3 ili kombinacija prema zahtjevima od 4 do 5 naznačen time da je za uporabu za prevenciju i/ili liječenje sistemske skleroze (SSc).
17. Komplet prema zahtjevu 16 naznačen time da je za uporabu za prevenciju i/ili liječenje sistemske skleroze (SSc), difuzne sistemske skleroze (dSSc), ograničene sistemske skleroze (lSSc), preklapajućeg tipa sistemske skleroze, nediferenciranog tipa sistemske skleroze, sistemske skleroze bez sklerodermije, fibroze kože, sklerodermije, nefrogene fibrozne dermopatije (NFD), stvaranja keloida.
18. Komplet prema zahtjevima 16 i 17 naznačen time da je za uporabu za prevenciju i/ili liječenje sistemske skleroze SSc uz popratnu fibrozu unutrašnjih organa, koji obuhvaćaju crijeva, pluća, bubrege i krvne žile.
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DE102010021637A DE102010021637A1 (de) | 2010-05-26 | 2010-05-26 | Substituierte 5-Fluor-1H-Pyrazolopyridine und ihre Verwendung |
EP10170413 | 2010-07-22 | ||
PCT/EP2011/058433 WO2011147810A1 (en) | 2010-05-26 | 2011-05-24 | THE USE OF sGC STIMULATORS, sGC ACTIVATORS, ALONE AND COMBINATIONS WITH PDE5 INHIBITORS FOR THE TREATMENT OF SYSTEMIC SCLEROSIS (SSc). |
EP11722786.8A EP2576548B1 (en) | 2010-05-26 | 2011-05-24 | THE USE OF sGC STIMULATORS, sGC ACTIVATORS, ALONE AND COMBINATIONS WITH PDE5 INHIBITORS FOR THE TREATMENT OF SYSTEMIC SCLEROSIS (SSc) |
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CA (2) | CA2800709C (hr) |
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Families Citing this family (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10189856B2 (en) | 2010-05-26 | 2019-01-29 | Adverio Pharma Gmbh | Use of sGC stimulators, sGC activators, alone and combinations with PDE5 inhibitors for the treatment of systemic sclerosis (SSc) |
DE102010021637A1 (de) * | 2010-05-26 | 2011-12-01 | Bayer Schering Pharma Aktiengesellschaft | Substituierte 5-Fluor-1H-Pyrazolopyridine und ihre Verwendung |
EP2637659B1 (en) | 2010-11-09 | 2016-05-18 | Ironwood Pharmaceuticals, Inc. | Sgc stimulators |
EP2594270A3 (en) * | 2011-11-18 | 2013-07-31 | BIP Patents | The use of sGC stimulators, sGC activators, alone and combinations with PDE5 inhibitors for the treatment of systemic sclerosis (SSc) |
CN102491974B (zh) * | 2011-12-12 | 2013-08-07 | 南京药石药物研发有限公司 | 1-(2-氟苄基)-1H-吡唑并[3,4-b]吡啶-3-甲脒盐酸盐的合成方法 |
EP2797915B1 (en) | 2011-12-27 | 2016-07-13 | Ironwood Pharmaceuticals, Inc. | 2-benzyl-3-(oxazole/thiazole)-5-(pyrimidin-2-yl)-1(H)-pyrazole derivatives as stimulators of the soluble guanylate cyclase (sGC) for the treatment of e.g. hypertension or heart failure |
JP6140738B2 (ja) * | 2012-03-06 | 2017-05-31 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH | 置換アザ二環およびその使用 |
MX338887B (es) * | 2012-09-07 | 2016-05-04 | Boehringer Ingelheim Int | Alcoxipirazoles como activadores de guanilato ciclasa soluble. |
EP2897953B8 (en) * | 2012-09-19 | 2019-06-26 | Cyclerion Therapeutics, Inc. | Sgc stimulators |
WO2014128109A1 (en) | 2013-02-21 | 2014-08-28 | Bayer Pharma Aktiengesellschaft | Forms of methyl {4,6-diamino-2-[1-(2-fluorobenzyl)-1h-pyrazolo[3,4-b]pyridino-3-yl]pyrimidino-5-yl}methyl carbamate |
KR102283996B1 (ko) | 2013-03-15 | 2021-07-29 | 더 스크립스 리서치 인스티튜트 | 연골형성의 유도를 위한 화합물 및 방법 |
EP3024455A1 (en) | 2013-07-25 | 2016-06-01 | Bayer Pharma Aktiengesellschaft | Sgc stimulators or sgc activators and pde5 inhibitors in combination with additional treatment for the therapy of cystic fibrosis |
EP3059224B1 (en) | 2013-10-15 | 2019-03-20 | TOA Eiyo Ltd. | 4-aminomethylbenzoic acid derivative |
WO2015106268A1 (en) | 2014-01-13 | 2015-07-16 | Ironwood Pharmaceuticals, Inc. | USE OF sGC STIMULATORS FOR THE TREATMENT OF NEUROMUSCULAR DISORDERS |
ES2755183T3 (es) | 2014-06-13 | 2020-04-21 | Inventiva | Compuestos ppar para uso en el tratamiento de enfermedades fibróticas |
TW201625584A (zh) | 2014-07-02 | 2016-07-16 | 諾華公司 | 茚滿及吲哚啉衍生物及其作為可溶性鳥苷酸環化酶活化劑之用途 |
AU2015292833B2 (en) | 2014-07-22 | 2019-11-28 | Boehringer Ingelheim International Gmbh | Heterocyclic carboxylic acids as activators of soluble guanylate cyclase |
CA2984983A1 (en) * | 2015-05-06 | 2016-11-10 | Bayer Pharma Aktiengesellschaft | The use of sgc stimulators, sgc activators, alone and combinations with pde5 inhibitors for the treatment of digital ulcers (du) concomitant to systemic sclerosis (ssc) |
HUE052337T2 (hu) * | 2015-07-23 | 2021-04-28 | Bayer Pharma AG | Oldható guanilát-cikláz stimulátorai/aktivátorai a neutrális endopeptidáz egy inhibitorával (NEP-inhibitor) és/vagy egy angiotenzin All-antagonistával kombinációban és ezek alkalmazása |
EP3359258A4 (en) * | 2015-10-07 | 2019-08-21 | AiViva Biopharma, Inc. | COMPOSITIONS AND METHOD FOR THE TREATMENT OF FIBROTIC SKIN DISEASES |
AU2016371762A1 (en) | 2015-12-14 | 2018-06-21 | Cyclerion Therapeutics, Inc. | Use of sGC stimulators for the treatment of gastrointestinal sphincter dysfunction |
RU2018126349A (ru) | 2015-12-18 | 2020-01-20 | Новартис Аг | Индановые производные и их применение в качестве активаторов растворимой гуанилатциклазы |
CN108697678A (zh) | 2016-02-01 | 2018-10-23 | 铁木医药有限公司 | sGC刺激剂在非酒精性脂肪性肝炎(NASH)治疗中的应用 |
WO2018111795A2 (en) | 2016-12-13 | 2018-06-21 | Ironwood Pharmaceuticals, Inc. | Use of sgc stimulators for the treatment of esophageal motility disorders |
US20190388407A1 (en) | 2017-02-12 | 2019-12-26 | Aiviva Biopharma, Inc. | Multikinase inhibitors of vegf and tfg beta and uses thereof |
WO2018188590A1 (en) | 2017-04-11 | 2018-10-18 | Sunshine Lake Pharma Co., Ltd. | Fluorine-substituted indazole compounds and uses thereof |
CN108690016B (zh) * | 2017-04-11 | 2022-08-12 | 广东东阳光药业有限公司 | 吡唑并吡啶类化合物及其用途 |
US11508483B2 (en) | 2018-05-30 | 2022-11-22 | Adverio Pharma Gmbh | Method of identifying a subgroup of patients suffering from dcSSc which benefits from a treatment with sGC stimulators and sGC activators in a higher degree than a control group |
JP7542518B2 (ja) | 2018-07-11 | 2024-08-30 | ティセント セラピューティクス インコーポレーテッド | ミトコンドリア(mitochonrial)障害の処置のためのsGC刺激剤の使用 |
CN111638329B (zh) * | 2020-06-09 | 2021-06-01 | 南方医科大学 | 一种用于检测布鲁氏菌病elispot检测试剂盒及其应用 |
EP3925953A1 (en) * | 2020-06-16 | 2021-12-22 | Adverio Pharma GmbH | Process for preparing methyl {4,6-diamino-2-[5-fluoro-1-(2-fluorobenzyl)-1h-pyrazolo[3,4-b]pyridin-3-yl]pyrimidin-5-yl}carbamate |
CN115160312B (zh) * | 2022-06-29 | 2023-12-26 | 常州制药厂有限公司 | 一种维立西呱关键中间体及其制备方法 |
Family Cites Families (36)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5380945A (en) | 1989-06-21 | 1995-01-10 | Abbott Laboratories | Guanidino compounds as regulators of nitric oxide synthase |
DE19642255A1 (de) * | 1996-10-14 | 1998-04-16 | Bayer Ag | Verwendung von 1-Benzyl-3-(substituierten-hetaryl) -kondensierten Pyrazol-Derivaten |
US6331543B1 (en) | 1996-11-01 | 2001-12-18 | Nitromed, Inc. | Nitrosated and nitrosylated phosphodiesterase inhibitors, compositions and methods of use |
EP1095016B1 (en) | 1998-07-08 | 2005-11-09 | Sanofi-Aventis Deutschland GmbH | Sulfur substituted sulfonylaminocarboxylic acid n-arylamides, their preparation, their use and pharmaceutical preparations comprising them |
DE19834047A1 (de) | 1998-07-29 | 2000-02-03 | Bayer Ag | Substituierte Pyrazolderivate |
DE19834044A1 (de) | 1998-07-29 | 2000-02-03 | Bayer Ag | Neue substituierte Pyrazolderivate |
DE19943636A1 (de) | 1999-09-13 | 2001-03-15 | Bayer Ag | Neuartige Dicarbonsäurederivate mit pharmazeutischen Eigenschaften |
DE19943635A1 (de) | 1999-09-13 | 2001-03-15 | Bayer Ag | Neuartige Aminodicarbonsäurederivate mit pharmazeutischen Eigenschaften |
DE19943634A1 (de) | 1999-09-13 | 2001-04-12 | Bayer Ag | Neuartige Dicarbonsäurederivate mit pharmazeutischen Eigenschaften |
US6538023B1 (en) | 2000-09-15 | 2003-03-25 | Tsuyoshi Ohnishi | Therapeutic uses of green tea polyphenols for sickle cell disease |
DE10054278A1 (de) * | 2000-11-02 | 2002-05-08 | Bayer Ag | Verwendung von Stimulatoren der löslichen Guanylatcyclase zur Behandlung von Osteoporose |
AR031176A1 (es) | 2000-11-22 | 2003-09-10 | Bayer Ag | Nuevos derivados de pirazolpiridina sustituidos con piridina |
CA2433425A1 (en) * | 2000-12-29 | 2002-09-06 | Alteon, Inc. | Method for treating fibrotic diseases or other indications iiic |
DE10110749A1 (de) | 2001-03-07 | 2002-09-12 | Bayer Ag | Substituierte Aminodicarbonsäurederivate |
DE10110750A1 (de) | 2001-03-07 | 2002-09-12 | Bayer Ag | Neuartige Aminodicarbonsäurederivate mit pharmazeutischen Eigenschaften |
GB0202254D0 (en) * | 2002-01-31 | 2002-03-20 | Pfizer Ltd | Prevention of scarring |
DE10220570A1 (de) | 2002-05-08 | 2003-11-20 | Bayer Ag | Carbamat-substituierte Pyrazolopyridine |
WO2005113490A1 (en) | 2004-05-21 | 2005-12-01 | Icagen, Inc. | Sulfone-containing prodrugs |
DE102004038328A1 (de) * | 2004-08-06 | 2006-03-16 | Bayer Healthcare Ag | Neue Verwendungen von 2-Phenyl-substituierten Imidazotriazinon-Derivaten |
DE102005016345A1 (de) | 2005-04-09 | 2006-10-12 | Bayer Healthcare Ag | Neue Verwendung von 2-Phenyl-substituierten Imidazotriazinon-Derivaten |
DE102005047945A1 (de) * | 2005-07-16 | 2007-01-18 | Bayer Healthcare Ag | Verwendung von Aktivatoren der löslichen Guanylatzyklase zur Behandlung von Raynaud Phänomenen |
EP1906957A1 (en) | 2005-07-18 | 2008-04-09 | Bayer HealthCare AG | Novel use of activators and stimulators of soluble guanylate cyclase for the prevention or treatment of renal disorders |
AU2008250643A1 (en) | 2007-05-12 | 2008-11-20 | Bayer Schering Pharma Aktiengesellschaft | sGC stimulators, sGC activators and combinations for the treatment of urological disorders |
DE102007026392A1 (de) | 2007-06-06 | 2008-12-11 | Bayer Healthcare Ag | Lösungen für die Perfusion und Konservierung von Organen und Geweben |
KR20100059952A (ko) | 2007-09-06 | 2010-06-04 | 머크 샤프 앤드 돔 코포레이션 | 가용성 구아닐레이트 사이클라제 활성제 |
WO2009068652A1 (en) * | 2007-11-30 | 2009-06-04 | Smithkline Beecham Corporation | 2, 6-disubstituted pyridines and 2, 4-disubstituted pyrimidines as soluble guanylate cyclase activators |
WO2009071504A1 (en) * | 2007-12-03 | 2009-06-11 | Smithkline Beecham Corporation | 2,6-disubstituted pyridines as soluble guanylate cyclase activators |
US8461348B2 (en) | 2008-04-04 | 2013-06-11 | Takeda Pharmaceutical Company Limited | Heterocyclic derivative and use thereof |
US8158636B2 (en) | 2008-05-19 | 2012-04-17 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
US8633318B2 (en) | 2008-09-16 | 2014-01-21 | Proximagen Ltd | Compounds for treatment or prevention of inflammation, an inflammatory disease, or an immune or an autoimmune disorder |
CA2743864A1 (en) | 2008-11-25 | 2010-06-10 | Merck Sharp & Dohme Corp. | Soluble guanylate cyclase activators |
KR20110117655A (ko) | 2009-01-17 | 2011-10-27 | 바이엘 파마 악티엔게젤샤프트 | 발기 부전의 치료를 위한 sgc 자극제 또는 sgc 활성화제와 pde5 억제제의 조합물 |
DK2421519T3 (en) | 2009-04-23 | 2017-02-06 | Univ Zuerich | NMDA RECEPTOR BLOCKERS FOR THE TREATMENT OF SEAL CELL ANAEMS |
DK2512479T3 (en) * | 2009-12-18 | 2016-06-06 | Exodos Life Sciences Ltd Partnership | Compositions for the treatment of peripheral vascular disease |
CN104800219A (zh) | 2010-02-05 | 2015-07-29 | 阿德弗里奥药品有限责任公司 | 用于治疗囊性纤维化的单独和与PDE5抑制剂组合的sGC刺激剂或sGC激活剂 |
US10189856B2 (en) | 2010-05-26 | 2019-01-29 | Adverio Pharma Gmbh | Use of sGC stimulators, sGC activators, alone and combinations with PDE5 inhibitors for the treatment of systemic sclerosis (SSc) |
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