ES8705459A1 - Procedimiento para la obtencion de nuevos compuestos este- roides - Google Patents
Procedimiento para la obtencion de nuevos compuestos este- roidesInfo
- Publication number
- ES8705459A1 ES8705459A1 ES544768A ES544768A ES8705459A1 ES 8705459 A1 ES8705459 A1 ES 8705459A1 ES 544768 A ES544768 A ES 544768A ES 544768 A ES544768 A ES 544768A ES 8705459 A1 ES8705459 A1 ES 8705459A1
- Authority
- ES
- Spain
- Prior art keywords
- analogues
- alpha
- group
- oriented
- open ring
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J41/00—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring
- C07J41/0033—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005
- C07J41/0094—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005 containing nitrile radicals, including thiocyanide radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/38—Drugs for disorders of the endocrine system of the suprarenal hormones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/10—Antioedematous agents; Diuretics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J1/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
- C07J1/0003—Androstane derivatives
- C07J1/0011—Androstane derivatives substituted in position 17 by a keto group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J13/00—Normal steroids containing carbon, hydrogen, halogen or oxygen having a carbon-to-carbon double bond from or to position 17
- C07J13/005—Normal steroids containing carbon, hydrogen, halogen or oxygen having a carbon-to-carbon double bond from or to position 17 with double bond in position 16 (17)
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J21/00—Normal steroids containing carbon, hydrogen, halogen or oxygen having an oxygen-containing hetero ring spiro-condensed with the cyclopenta(a)hydrophenanthrene skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J21/00—Normal steroids containing carbon, hydrogen, halogen or oxygen having an oxygen-containing hetero ring spiro-condensed with the cyclopenta(a)hydrophenanthrene skeleton
- C07J21/001—Lactones
- C07J21/003—Lactones at position 17
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J21/00—Normal steroids containing carbon, hydrogen, halogen or oxygen having an oxygen-containing hetero ring spiro-condensed with the cyclopenta(a)hydrophenanthrene skeleton
- C07J21/005—Ketals
- C07J21/008—Ketals at position 17
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J5/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond
- C07J5/0046—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond substituted in position 17 alfa
- C07J5/0053—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond substituted in position 17 alfa not substituted in position 16
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J53/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton has been modified by condensation with a carbocyclic rings or by formation of an additional ring by means of a direct link between two ring carbon atoms, including carboxyclic rings fused to the cyclopenta(a)hydrophenanthrene skeleton are included in this class
- C07J53/002—Carbocyclic rings fused
- C07J53/004—3 membered carbocyclic rings
- C07J53/007—3 membered carbocyclic rings in position 6-7
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J53/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton has been modified by condensation with a carbocyclic rings or by formation of an additional ring by means of a direct link between two ring carbon atoms, including carboxyclic rings fused to the cyclopenta(a)hydrophenanthrene skeleton are included in this class
- C07J53/002—Carbocyclic rings fused
- C07J53/004—3 membered carbocyclic rings
- C07J53/008—3 membered carbocyclic rings in position 15/16
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J71/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton is condensed with a heterocyclic ring
- C07J71/0005—Oxygen-containing hetero ring
- C07J71/001—Oxiranes
- C07J71/0015—Oxiranes at position 9(11)
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Toxicology (AREA)
- Diabetes (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Steroid Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
METODO DE OBTENER NUEVOS COMPUESTOS ESTEROIDES. CONSISTE EN TRATAR UN COMPUESTO DE FORMULA (II) CON UN AGENTE DE OXIDACION, EN PRESENCIA DE UN DISOLVENTE ORGANICO INERTE, A PRESION NORMAL Y A UNA TEMPERATURA ENTRE C10 Y 50JC, PARA OBTENER NUEVOS COMPUESTOS ESTEROIDES DE FORMULA (I) DONDE A-A- SIGNIFICA EL GRUPO -CH2-CH2- O CHFCH-; R1 ES H; R2 ES UN ALCOXI INFERIOR-CARBONILO A-ORIENTADO Y OTROS; X ES DOS ATOMOS DE HIDROGENO U OXO; E Y1 E Y2 JUNTOS FORMAN EL PUENTE OXIGENO -O- Y OTROS. TIENEN APLICACIONES FARMACEUTICAS COMO DIURETICOS.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH198183 | 1983-04-13 |
Publications (2)
Publication Number | Publication Date |
---|---|
ES544768A0 ES544768A0 (es) | 1987-05-01 |
ES8705459A1 true ES8705459A1 (es) | 1987-05-01 |
Family
ID=4223123
Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES531517A Granted ES531517A0 (es) | 1983-04-13 | 1984-04-11 | Procedimiento para la obtencion de nuevos compuestos esteroides |
ES544769A Expired ES8705460A1 (es) | 1983-04-13 | 1985-07-01 | Procedimiento para la obtencion de nuevos compuestos este- roides |
ES544768A Expired ES8705459A1 (es) | 1983-04-13 | 1985-07-01 | Procedimiento para la obtencion de nuevos compuestos este- roides |
ES544770A Expired ES8705461A1 (es) | 1983-04-13 | 1985-07-01 | Procedimiento para la obtencion de nuevos compuestos este- roides |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES531517A Granted ES531517A0 (es) | 1983-04-13 | 1984-04-11 | Procedimiento para la obtencion de nuevos compuestos esteroides |
ES544769A Expired ES8705460A1 (es) | 1983-04-13 | 1985-07-01 | Procedimiento para la obtencion de nuevos compuestos este- roides |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES544770A Expired ES8705461A1 (es) | 1983-04-13 | 1985-07-01 | Procedimiento para la obtencion de nuevos compuestos este- roides |
Country Status (23)
Country | Link |
---|---|
US (1) | US4559332A (es) |
EP (1) | EP0122232B1 (es) |
JP (1) | JPS59231100A (es) |
AR (4) | AR241918A1 (es) |
AT (1) | ATE39256T1 (es) |
AU (1) | AU565017B2 (es) |
CA (1) | CA1220781A (es) |
DD (2) | DD251144A5 (es) |
DE (2) | DE3475622D1 (es) |
DK (1) | DK163988C (es) |
ES (4) | ES531517A0 (es) |
FI (1) | FI77669C (es) |
GR (1) | GR81834B (es) |
HU (1) | HU191406B (es) |
IE (1) | IE57541B1 (es) |
IL (1) | IL71504A (es) |
LU (1) | LU91072I2 (es) |
NL (1) | NL300144I1 (es) |
NO (1) | NO159800C (es) |
NZ (1) | NZ207826A (es) |
PH (1) | PH19997A (es) |
PT (1) | PT78413B (es) |
ZA (1) | ZA842710B (es) |
Families Citing this family (103)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4670551A (en) * | 1984-06-21 | 1987-06-02 | Ciba-Geigy Corporation | Epoxy steroids |
WO1992012991A1 (en) * | 1991-01-29 | 1992-08-06 | Shionogi Seiyaku Kabushiki Kaisha | Triterpene derivative |
US6245755B1 (en) | 1992-04-21 | 2001-06-12 | Curators Of The Unversity Of Missouri | Use of aldosterone antagonists to inhibit myocardial fibrosis |
US6150347A (en) * | 1992-04-21 | 2000-11-21 | The Curators Of The University Of Missouri | Use of aldosterone antagonists to inhibit myocardial fibrosis |
JPH05329410A (ja) * | 1992-05-29 | 1993-12-14 | Sekisui Plastics Co Ltd | マスキング材 |
US6642268B2 (en) | 1994-09-13 | 2003-11-04 | G.D. Searle & Co. | Combination therapy employing ileal bile acid transport inhibiting benzothipines and HMG Co-A reductase inhibitors |
US6262277B1 (en) * | 1994-09-13 | 2001-07-17 | G.D. Searle And Company | Intermediates and processes for the preparation of benzothiepines having activity as inhibitors of ileal bile acid transport and taurocholate uptake |
US6268392B1 (en) | 1994-09-13 | 2001-07-31 | G. D. Searle & Co. | Combination therapy employing ileal bile acid transport inhibiting benzothiepines and HMG Co-A reductase inhibitors |
WO1996040255A2 (en) * | 1995-06-07 | 1996-12-19 | G.D. Searle & Co. | Method to treat cardiofibrosis with a combination therapy of an angiotensin ii antagonist and an epoxy-steroidal aldosterone antagonist |
WO1996040257A1 (en) * | 1995-06-07 | 1996-12-19 | G.D. Searle & Co. | Epoxy-steroidal aldosterone antagonist and angiotensin ii antagonist combination therapy for treatment of congestive heart failure |
ATE365171T1 (de) * | 1995-12-11 | 2007-07-15 | Searle Llc | Verfahren zur herstellung einer epoxyverbindung |
US20050159594A1 (en) * | 1995-12-11 | 2005-07-21 | Pharmacia Corporation | Eplerenone crystal form exhibiting enhanced dissolution rate |
US20050267302A1 (en) * | 1995-12-11 | 2005-12-01 | G.D. Searle & Co. | Eplerenone crystalline form exhibiting enhanced dissolution rate |
US20020045746A1 (en) * | 1995-12-11 | 2002-04-18 | Barton Kathleen P. | Eplerenone crystalline form |
EP1167381A3 (en) * | 1995-12-11 | 2004-09-29 | G.D. Searle & Co. | Process for preparation of 7 alpha-carboxyl 9,11-epoxy steroids and Intermediates useful therein |
US20020038021A1 (en) * | 1995-12-11 | 2002-03-28 | Barton Kathleen P. | Eplerenone crystalline form exhibiting enhanced dissolution rate |
AU747959B2 (en) * | 1995-12-11 | 2002-05-30 | G.D. Searle & Co. | Processes and intermediates for the preparation of 9, 11-epoxy steroids |
US6887991B1 (en) | 1996-12-11 | 2005-05-03 | G. D. Searle & Company | Processes for preparation of 9, 11-epoxy steroids and intermediates useful therein |
ES2293944T3 (es) * | 1996-12-11 | 2008-04-01 | G.D. Searle Llc. | Procedimiento de epoxidacion. |
EP1223174A3 (en) * | 1996-12-11 | 2005-03-16 | G.D. Searle & Co. | Processes for preparation of 3-keto-7alpha-alkoxycarbonyl-delta-4,5- steroids and intermediates useful therein |
US6368835B1 (en) * | 1998-05-29 | 2002-04-09 | Kyowa Hakko Kogyo Co., Ltd. | Process for producing a lactone using corynebacterium sp. NK-1 (FERM BP-6329) |
CZ20011590A3 (cs) * | 1998-11-06 | 2003-01-15 | G. D. Searle & Co. | Léčivo pro léčení kardiovaskulárních poruch a kompozice s obsahem inhibitoru enzymu konvertujícího angiotensin, antagonisty aldosteronu, kličkového diuretika a digoxinu |
UA74141C2 (uk) * | 1998-12-09 | 2005-11-15 | Дж.Д. Сірл Енд Ко. | Фармацевтична композиція на основі тонкоподрібненого еплеренону (варіанти), спосіб її одержання та спосіб лікування розладів, опосередкованих альдостероном (варіанти) |
ES2201827T3 (es) | 1998-12-23 | 2004-03-16 | G.D. Searle Llc | Combinaciones de inhibidores de la proteina de transferencia de ester de colesterilo y de derivados de acido fibrico para indicaciones cardiovasculares. |
JP2002533411A (ja) * | 1998-12-23 | 2002-10-08 | ジー.ディー.サール エルエルシー | 心臓血管に適用するための組み合わせ |
EP1140184B1 (en) * | 1998-12-23 | 2003-06-04 | G.D. Searle LLC. | Combinations of cholesteryl ester transfer protein inhibitors and nicotinic acid derivatives for cardiovascular indications |
CZ20012342A3 (cs) | 1998-12-23 | 2001-12-12 | G. D. Searle Llc | Kombinace inhibitorů transportu ľlučové kyseliny v ileu a derivátů kyseliny fibrové pro kardiovaskulární indikace |
WO2000038726A1 (en) * | 1998-12-23 | 2000-07-06 | G.D. Searle Llc | Combinations of ileal bile acid transport inhibitors and cholesteryl ester transfer protein inhibitors for cardiovascular indications |
US6462091B1 (en) | 1998-12-23 | 2002-10-08 | G.D. Searle & Co. | Combinations of cholesteryl ester transfer protein inhibitors and HMG coA reductase inhibitors for cardiovascular indications |
PT1140185E (pt) | 1998-12-23 | 2003-10-31 | Searle Llc | Combinacoes de inibidores de proteina de transferencia de ester de colesterilo com agentes sequestrantes de acido biliar para indicacoes cardiovasculares |
DK1140190T3 (da) | 1998-12-23 | 2002-12-23 | Searle Llc | Kombinationer af ileumgaldesyretransport-inhibitorer og galdesyre-sekvestreringsmidler til cardiovaskulære indikatorer |
US20030096798A1 (en) * | 1999-11-09 | 2003-05-22 | Williams Gordon H. | Methods for the treatment or prophylaxis of aldosterone-mediated pathogenic effects in a subject using an epoxy-steroidal aldosterone antagonist |
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DK1175220T3 (da) * | 1999-12-08 | 2005-08-29 | Pharmacia Corp | Nanopartikulære eplerenonkompositioner |
CN100413881C (zh) * | 1999-12-08 | 2008-08-27 | 法马西亚公司 | 依匹乐酮晶形 |
EP1505072A3 (en) * | 1999-12-08 | 2006-06-21 | Pharmacia Corporation | Eplerenone crystalline form exhiniting enhanced dissolution rate |
US20030083493A1 (en) * | 1999-12-08 | 2003-05-01 | Barton Kathleen P. | Eplerenone drug substance having high phase purity |
EP1527782A1 (en) * | 1999-12-08 | 2005-05-04 | Pharmacia Corporation | Nanoparticulate eplerenone compositions |
HUP0203032A3 (en) * | 1999-12-08 | 2003-04-28 | Pharmacia Corp Chicago | Eplerenone crystalline form exhibiting enhanced dissolution rate, process for their preparation and pharmaceutical compositions containing them and their use |
JP2003528830A (ja) | 2000-03-10 | 2003-09-30 | ファルマシア・コーポレーション | テトラヒドロベンゾチエピン類の製造方法 |
AU2001247331A1 (en) * | 2000-03-10 | 2001-09-24 | Pharmacia Corporation | Combination therapy for the prophylaxis and treatment of hyperlipidemic conditions and disorders |
AU2001261434A1 (en) * | 2000-05-11 | 2001-11-26 | Pharmacia Corporation | Aldosterone antagonist composition for release during aldosterone acrophase |
AU1604001A (en) * | 2000-06-13 | 2001-12-24 | Pharmacia Corp | Use of an aldosterone antagonist for the treatment or prohpylaxis of aldosterone-mediated pathogenic effects |
US6716829B2 (en) | 2000-07-27 | 2004-04-06 | Pharmacia Corporation | Aldosterone antagonist and cyclooxygenase-2 inhibitor combination therapy to prevent or treat inflammation-related cardiovascular disorders |
JP2004511435A (ja) * | 2000-07-27 | 2004-04-15 | ファルマシア・コーポレーション | うっ血性心不全の処置のための、エポキシ−ステロイド型アルドステロン拮抗薬とβ−アドレナリン作動性拮抗薬の併用療法 |
EP1313485B1 (en) * | 2000-08-28 | 2005-10-12 | Pharmacia Corporation | Use of an aldosterone receptor antagonist to improve cognitive function |
CA2427615A1 (en) * | 2000-10-30 | 2002-06-13 | Pharmacia Corporation | Aspergillus ochraceus 11 alpha hydroxylase and oxidoreductase |
NZ525726A (en) * | 2000-11-09 | 2004-10-29 | Astrazeneca Ab | Oral pharmaceutical composition containing a block copolymer |
US8168616B1 (en) | 2000-11-17 | 2012-05-01 | Novartis Ag | Combination comprising a renin inhibitor and an angiotensin receptor inhibitor for hypertension |
US20040077625A1 (en) * | 2001-07-25 | 2004-04-22 | Tremont Samuel J. | Novel 1,4-benzothiazepine and 1,5-benzothiazepine compounds as inhibitors of apical sodium codependent bile acid transport abd taurocholate uptake |
US20030220310A1 (en) * | 2001-07-27 | 2003-11-27 | Schuh Joseph R. | Epoxy-steroidal aldosterone antagonist and calcium channel blocker combination therapy for treatment of congestive heart failure |
WO2003040127A1 (en) * | 2001-11-02 | 2003-05-15 | G.D. Searle Llc | Novel mono- and di-fluorinated benzothiepine compounds as inhibitors of apical sodium co-dependent bile acid transport (asbt) and taurocholate uptake |
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US6852753B2 (en) | 2002-01-17 | 2005-02-08 | Pharmacia Corporation | Alkyl/aryl hydroxy or keto thiepine compounds as inhibitors of apical sodium co-dependent bile acid transport (ASBT) and taurocholate uptake |
AU2003222010A1 (en) * | 2002-03-18 | 2003-10-08 | Pharmacia Corporation | Combination of an aldosterone receptor antagonist and a bile acid sequestering agent |
AU2003222009A1 (en) * | 2002-03-18 | 2003-10-08 | Pharmacia Corporation | Combination of an aldosterone receptor antagonist and nicotinic acid or a nicotinic acid derivative |
MXPA04009037A (es) * | 2002-03-20 | 2005-01-25 | Pharmacia Corp | Formulacion de eplerenona de almacenamiento estable. |
WO2003082895A2 (en) * | 2002-03-22 | 2003-10-09 | Pharmacia & Upjohn Company | Process to prepare eplerenone |
US7235655B2 (en) * | 2002-03-22 | 2007-06-26 | Pharmacia & Upjohn Company | Processes to prepare eplerenone |
US20070066579A1 (en) * | 2002-08-16 | 2007-03-22 | White Michael J | 5-androsten-3beta-ol steroid intermediates and processs for their preparation |
ATE339437T1 (de) * | 2002-08-16 | 2006-10-15 | Pharmacia & Upjohn Co Llc | 5-androsten-3-olsteroidzwischenprodukte und verfahren zu deren herstellung |
PL376919A1 (pl) * | 2002-11-06 | 2006-01-09 | Pharmacia & Upjohn Company Llc | Sposoby wytwarzania 7-karboksy-podstawionych steroidów |
DE60312029T2 (de) * | 2002-11-07 | 2007-06-21 | Pharmacia & Upjohn Co. Llc, Kalamazoo | Verfahren zur herstellung c-7 substituierter 5-androstene |
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EP1842543A1 (en) | 2006-04-05 | 2007-10-10 | Speedel Pharma AG | Pharmaceutical composition coprising an aldosterone synthase inhibitor and a mineralcorticoid receptor antagonist |
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DE102006028032A1 (de) * | 2006-06-14 | 2007-12-20 | Henkel Kgaa | Aufhell- und/oder Färbemittel mit Nitrilen |
EP2124959A4 (en) * | 2006-12-21 | 2011-09-14 | Alphapharm Pty Ltd | PHARMACEUTICAL COMPOSITION |
CA2582496A1 (en) * | 2007-03-20 | 2008-09-20 | Apotex Pharmachem Inc. | Improved process for the preparation and purification of eplerenone |
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CN101863951B (zh) * | 2009-04-15 | 2012-06-06 | 浙江省天台县奥锐特药业有限公司 | 依普利酮的制备方法 |
SG176010A1 (en) | 2009-05-28 | 2011-12-29 | Novartis Ag | Substituted aminobutyric derivatives as neprilysin inhibitors |
AU2010251967B9 (en) | 2009-05-28 | 2014-04-03 | Novartis Ag | Substituted aminopropionic derivatives as neprilysin inhibitors |
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RU2016101363A (ru) * | 2010-02-08 | 2018-11-21 | Прэари Фармасьютикалз, Ллк | Способ лечения заболеваний, связанных с глюкокортикоидной нечувствительностью |
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JP6180930B2 (ja) | 2010-06-16 | 2017-08-16 | アンスティチュ ナショナル ドゥ ラ サンテ エ ドゥ ラ ルシェルシュ メディカル | 創傷治癒過程における再上皮化を刺激するための方法及び組成物 |
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JP6295277B2 (ja) | 2013-02-14 | 2018-03-14 | ノバルティス アーゲー | Nep(中性エンドペプチダーゼ)阻害剤としての置換ビスフェニルブタン酸ホスホン酸誘導体 |
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US3095412A (en) * | 1961-12-19 | 1963-06-25 | Searle & Co | 9alpha, 11alpha-epoxy and 11beta-chloro-9alpha-hydroxy 17alpha-(2-carboxyethyl)-17beta-hydroxyandrost-4-en-3-one gamma-lactones and delta1 and delta6 analogs |
GB1041534A (en) * | 1963-04-24 | 1966-09-07 | Merck & Co Inc | 20-spiroxane compounds |
US3729491A (en) * | 1970-06-15 | 1973-04-24 | Searle & Co | 3,5-dioxo-a-nor-b-homo steroidal spirolactones |
GB1368006A (en) * | 1972-08-24 | 1974-09-25 | Searle & Co | 4alpha,7alpha-carbonyl-5-cyano-17-hzydroxy-3-oxo-5beta,17alpha- pregnane-21-carboxylic acid ypsilon-lactone |
US3849404A (en) * | 1973-03-09 | 1974-11-19 | Searle & Co | Purification of 6,7-dihydro-17-hydroxy-3-oxo-3'h-cyclopropa(6,7)-17alpha-pregna-4,6-diene-21-carboxylic acid gamma-lactones |
DE2652761C2 (de) * | 1976-11-16 | 1985-11-21 | Schering AG, 1000 Berlin und 4709 Bergkamen | 15,16-Methylen-Spirolactone, Verfahren zu deren Herstellung und diese enthaltende Arzneimittel |
DE2922500A1 (de) * | 1979-05-31 | 1980-12-04 | Schering Ag | 6 beta .7 beta |
DE3111951A1 (de) * | 1981-03-23 | 1982-09-30 | Schering Ag, 1000 Berlin Und 4619 Bergkamen | 7(alpha)-alkoxycarbonyl-15ss-methylen-4-androstene, verfahren zu ihrer herstellung und verwendung als arzneimittel |
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