MA34917B1 - Dérivés substitués de l'acide 3-hétéroaroylamino-propionique et leur utilisation comme composés pharmaceutiques - Google Patents
Dérivés substitués de l'acide 3-hétéroaroylamino-propionique et leur utilisation comme composés pharmaceutiquesInfo
- Publication number
- MA34917B1 MA34917B1 MA36196A MA36196A MA34917B1 MA 34917 B1 MA34917 B1 MA 34917B1 MA 36196 A MA36196 A MA 36196A MA 36196 A MA36196 A MA 36196A MA 34917 B1 MA34917 B1 MA 34917B1
- Authority
- MA
- Morocco
- Prior art keywords
- compounds
- heteroaroylamino
- substituted
- propionic acid
- acid derivatives
- Prior art date
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- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/44—Radicals substituted by doubly-bound oxygen, sulfur, or nitrogen atoms, or by two such atoms singly-bound to the same carbon atom
- C07D213/46—Oxygen atoms
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- 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
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
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- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the nitrogen-containing ring
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- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
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- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
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Abstract
LA PRÉSENTE INVENTION CONCERNE DES COMPOSÉS DE FORMULE (I), DANS LAQUELLE A, D, E, L, G, R10, R30, R40, R50 ET R60 ONT LES SIGNIFICATIONS INDIQUÉES DANS LES REVENDICATIONS, LESDITS COMPOSÉS ÉTANT DES COMPOSÉS PHARMACEUTIQUES ACTIFS DE VALEUR. CE SONT DES INHIBITEURS DE LA PROTÉASE CATHEPSINE A, ET ILS SONT UTILES DANS LE TRAITEMENT DE MALADIES TELLES QUE L'ATHÉROSCLÉROSE, UNE INSUFFISANCE CARDIAQUE, DES MALADIES RÉNALES, DES MALADIES HÉPATIQUES OU DES MALADIES INFLAMMATOIRES, PAR EXEMPLE. L'INVENTION CONCERNE EN OUTRE DES PROCÉDÉS DE PRÉPARATION DES COMPOSÉS DE FORMULE I, LEUR UTILISATION ET DES COMPOSITIONS PHARMACEUTIQUES LES COMPRENANT.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP11305078 | 2011-01-26 | ||
PCT/EP2012/051189 WO2012101197A1 (fr) | 2011-01-26 | 2012-01-26 | Dérivés substitués de l'acide 3-hétéroaroylamino-propionique et leur utilisation comme composés pharmaceutiques |
Publications (1)
Publication Number | Publication Date |
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MA34917B1 true MA34917B1 (fr) | 2014-02-01 |
Family
ID=44041622
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA36196A MA34917B1 (fr) | 2011-01-26 | 2012-01-26 | Dérivés substitués de l'acide 3-hétéroaroylamino-propionique et leur utilisation comme composés pharmaceutiques |
Country Status (29)
Country | Link |
---|---|
US (3) | US8669370B2 (fr) |
EP (1) | EP2667870B1 (fr) |
JP (1) | JP5957467B2 (fr) |
KR (1) | KR20140007399A (fr) |
CN (1) | CN103442712B (fr) |
AR (1) | AR085013A1 (fr) |
AU (1) | AU2012210513B2 (fr) |
BR (1) | BR112013016508A2 (fr) |
CA (1) | CA2822120C (fr) |
CL (1) | CL2013002129A1 (fr) |
CO (1) | CO6761373A2 (fr) |
CY (1) | CY1118844T1 (fr) |
DK (1) | DK2667870T3 (fr) |
ES (1) | ES2604556T3 (fr) |
HK (1) | HK1187253A1 (fr) |
HR (1) | HRP20161545T1 (fr) |
HU (1) | HUE029781T2 (fr) |
IL (3) | IL227025A (fr) |
LT (1) | LT2667870T (fr) |
MA (1) | MA34917B1 (fr) |
MX (3) | MX2013007608A (fr) |
PL (1) | PL2667870T3 (fr) |
PT (1) | PT2667870T (fr) |
RU (1) | RU2632897C2 (fr) |
SG (2) | SG191826A1 (fr) |
SI (1) | SI2667870T1 (fr) |
UY (1) | UY33874A (fr) |
WO (1) | WO2012101197A1 (fr) |
ZA (1) | ZA201304463B (fr) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8669370B2 (en) | 2011-01-26 | 2014-03-11 | Sanofi | Substituted 3-heteroaroylamino-propionic acid derivatives and their use as pharmaceuticals |
CA2835220A1 (fr) * | 2011-05-31 | 2012-12-06 | Theravance, Inc. | Inhibiteurs de neprilysine |
WO2014053533A1 (fr) | 2012-10-05 | 2014-04-10 | Sanofi | Utilisation de dérivés substitués de l'acide 3-hétéroaroylamino-propionique en tant que produits pharmaceutiques destinés à la prévention/au traitement de la fibrillation auriculaire |
AU2013354278B2 (en) * | 2012-12-07 | 2017-10-12 | F. Hoffmann-La Roche Ag | Novel pyridine derivatives |
KR20150136508A (ko) | 2013-03-28 | 2015-12-07 | 사노피 | 바이아릴-프로피온산 유도체 및 약제로서의 그의 용도 |
EP2978754B1 (fr) | 2013-03-28 | 2017-05-10 | Sanofi | Dérivés de l'acide propionique biaryle-et leur utilisation comme produits pharmaceutiques |
BR112016016289B1 (pt) * | 2014-01-14 | 2023-02-07 | Takeda Pharmaceutical Company Limited | Heteroaris e usos dos mesmos |
US20200085810A1 (en) * | 2018-07-26 | 2020-03-19 | Hoffmann-La Roche Inc. | Compounds for use in treating kidney disorders |
CN115093400B (zh) * | 2021-09-18 | 2023-09-05 | 北京华森英诺生物科技有限公司 | AhR抑制剂及其用途和制备方法 |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AR204813A1 (es) | 1972-05-08 | 1976-03-05 | Yamanouchi Pharma Co Ltd | Proceso para la preparacion de derivados de ampilicina |
TW406076B (en) * | 1993-12-30 | 2000-09-21 | Hoechst Ag | Substituted heterocyclic carboxamides, their preparation and their use as pharmaceuticals |
US5801195A (en) | 1994-12-30 | 1998-09-01 | Celgene Corporation | Immunotherapeutic aryl amides |
WO2003003008A1 (fr) * | 2001-06-29 | 2003-01-09 | 7Tm Pharma A/S | Bibliotheques chimiques utiles aux procedes de decouvertes de medicaments |
US20040072802A1 (en) | 2002-10-09 | 2004-04-15 | Jingwu Duan | Beta-amino acid derivatives as inhibitors of matrix metalloproteases and TNF-alpha |
JP2004203871A (ja) * | 2002-12-13 | 2004-07-22 | Yamanouchi Pharmaceut Co Ltd | 医薬組成物 |
AU2003292218A1 (en) | 2002-12-23 | 2004-07-14 | Sanofi-Aventis Deutschland Gmbh | PYRAZOLE-DERIVATIVES AS FACTOR Xa INHIBITORS |
JP2005145839A (ja) * | 2003-11-12 | 2005-06-09 | Japan Science & Technology Agency | 新規なカテプシンa阻害剤 |
AU2006205220B2 (en) | 2005-01-10 | 2012-09-13 | Exelixis, Inc. | Heterocyclic carboxamide compounds as steroid nuclear receptors ligands |
AR058051A1 (es) | 2005-09-21 | 2008-01-23 | Astrazeneca Ab | Quinolinas de alquilnitrilo.proceso de obtencion y composiciones farmaceuticas. |
US7511063B2 (en) | 2006-08-16 | 2009-03-31 | Schering Corporation | High affinity quinoline-based kinase ligands |
BRPI0721298A2 (pt) | 2006-12-29 | 2014-03-25 | Abbott Gmbh & Co Kg | Composto de carboxamida e seus usos como inibidores de calpaína |
JP5504171B2 (ja) | 2007-12-26 | 2014-05-28 | サノフイ | P2y12アンタゴニストとしてのヘテロサイクリックピラゾール−カルボキサミド |
EP2238127B1 (fr) | 2007-12-26 | 2012-08-15 | Sanofi | Dérivés de pyrazole-carboxamide utiles en tant qu'antagonistes de p2y12 |
US20110306597A1 (en) | 2008-06-18 | 2011-12-15 | James Michael Crawforth | Nicotinamide Derivatives |
US8501749B2 (en) | 2009-01-30 | 2013-08-06 | Boehringer Ingelheim International Gmbh | Azaquinazolinediones chymase inhibitors |
NZ596304A (en) * | 2009-05-28 | 2014-01-31 | Novartis Ag | Substituted aminopropionic derivatives as neprilysin inhibitors |
US8669370B2 (en) | 2011-01-26 | 2014-03-11 | Sanofi | Substituted 3-heteroaroylamino-propionic acid derivatives and their use as pharmaceuticals |
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2012
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- 2012-01-26 KR KR20137022435A patent/KR20140007399A/ko not_active Application Discontinuation
- 2012-01-26 JP JP2013550878A patent/JP5957467B2/ja not_active Expired - Fee Related
- 2012-01-26 PT PT127011260T patent/PT2667870T/pt unknown
- 2012-01-26 SG SG2013051347A patent/SG191826A1/en unknown
- 2012-01-26 MX MX2013007608A patent/MX2013007608A/es active IP Right Grant
- 2012-01-26 HU HUE12701126A patent/HUE029781T2/en unknown
- 2012-01-26 MX MX2014010972A patent/MX340370B/es unknown
- 2012-01-26 SI SI201230780A patent/SI2667870T1/sl unknown
- 2012-01-26 CN CN201280015338.3A patent/CN103442712B/zh not_active Expired - Fee Related
- 2012-01-26 AU AU2012210513A patent/AU2012210513B2/en not_active Ceased
- 2012-01-26 CA CA2822120A patent/CA2822120C/fr not_active Expired - Fee Related
- 2012-01-26 SG SG10201600592WA patent/SG10201600592WA/en unknown
- 2012-01-26 WO PCT/EP2012/051189 patent/WO2012101197A1/fr active Application Filing
- 2012-01-26 DK DK12701126.0T patent/DK2667870T3/en active
- 2012-01-26 MX MX2014010974A patent/MX347157B/es unknown
- 2012-01-26 PL PL12701126T patent/PL2667870T3/pl unknown
- 2012-01-26 RU RU2013139349A patent/RU2632897C2/ru not_active IP Right Cessation
- 2012-01-26 BR BR112013016508A patent/BR112013016508A2/pt not_active IP Right Cessation
- 2012-01-26 MA MA36196A patent/MA34917B1/fr unknown
- 2012-01-26 ES ES12701126.0T patent/ES2604556T3/es active Active
- 2012-01-26 EP EP12701126.0A patent/EP2667870B1/fr active Active
- 2012-01-26 LT LTEP12701126.0T patent/LT2667870T/lt unknown
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2013
- 2013-06-18 ZA ZA2013/04463A patent/ZA201304463B/en unknown
- 2013-06-18 IL IL227025A patent/IL227025A/en active IP Right Grant
- 2013-07-25 CL CL2013002129A patent/CL2013002129A1/es unknown
- 2013-08-23 CO CO13200355A patent/CO6761373A2/es unknown
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2014
- 2014-01-09 HK HK14100230.4A patent/HK1187253A1/zh not_active IP Right Cessation
- 2014-01-17 US US14/157,703 patent/US9029559B2/en not_active Expired - Fee Related
- 2014-03-10 US US14/202,804 patent/US9120783B2/en not_active Expired - Fee Related
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2016
- 2016-11-21 HR HRP20161545TT patent/HRP20161545T1/hr unknown
- 2016-11-23 CY CY20161101210T patent/CY1118844T1/el unknown
- 2016-12-26 IL IL249826A patent/IL249826A0/en unknown
- 2016-12-26 IL IL249825A patent/IL249825A0/en unknown
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