UY28501A1 - Compuestos químicos - Google Patents
Compuestos químicosInfo
- Publication number
- UY28501A1 UY28501A1 UY28501A UY28501A UY28501A1 UY 28501 A1 UY28501 A1 UY 28501A1 UY 28501 A UY28501 A UY 28501A UY 28501 A UY28501 A UY 28501A UY 28501 A1 UY28501 A1 UY 28501A1
- Authority
- UY
- Uruguay
- Prior art keywords
- chemical compounds
- dihifroxyhept
- hmg
- methylsulfonyl
- pyrimidin
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—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
- 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
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
Abstract
Se describen dos formas polimórficas de sal de calcio bis (E)-7-(4-(4-fluorofenil)-6-isopropil-2- (metil(metilsulfonil) amino)pirimidin-5-il) (3R, 5S) -3,5-dihifroxihept -6- acido enoico); los procesos para obtenerlas y su uso como inhibidores de HMG Co A reductasa.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0321127A GB0321127D0 (en) | 2003-09-10 | 2003-09-10 | Chemical compounds |
GB0404859A GB0404859D0 (en) | 2004-03-04 | 2004-03-04 | Chemical compound |
Publications (1)
Publication Number | Publication Date |
---|---|
UY28501A1 true UY28501A1 (es) | 2005-04-29 |
Family
ID=34276833
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UY28501A UY28501A1 (es) | 2003-09-10 | 2004-09-07 | Compuestos químicos |
Country Status (32)
Country | Link |
---|---|
US (4) | US20060293355A1 (es) |
EP (1) | EP1663989B1 (es) |
JP (1) | JP2007505090A (es) |
KR (1) | KR20070019943A (es) |
CN (1) | CN1878760B (es) |
AR (1) | AR045628A1 (es) |
AT (1) | ATE428701T1 (es) |
AU (1) | AU2004270467B8 (es) |
BR (1) | BRPI0414236A (es) |
CA (1) | CA2537962C (es) |
CO (1) | CO5670355A2 (es) |
CY (1) | CY1109173T1 (es) |
DE (1) | DE602004020640D1 (es) |
DK (1) | DK1663989T3 (es) |
ES (1) | ES2324042T3 (es) |
HK (1) | HK1090361A1 (es) |
HR (1) | HRP20090335T1 (es) |
IL (1) | IL174073A (es) |
IS (1) | IS2689B (es) |
MX (1) | MXPA06002761A (es) |
MY (1) | MY142615A (es) |
NO (1) | NO336358B1 (es) |
NZ (1) | NZ545785A (es) |
PL (1) | PL1663989T3 (es) |
PT (1) | PT1663989E (es) |
RU (1) | RU2363697C2 (es) |
SA (1) | SA04250297B1 (es) |
SI (1) | SI1663989T1 (es) |
TW (1) | TWI370817B (es) |
UA (1) | UA85062C2 (es) |
UY (1) | UY28501A1 (es) |
WO (1) | WO2005023779A1 (es) |
Families Citing this family (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0003305D0 (en) | 2000-02-15 | 2000-04-05 | Zeneca Ltd | Pyrimidine derivatives |
GB0011120D0 (en) | 2000-05-09 | 2000-06-28 | Avecia Ltd | Process |
NL1015744C2 (nl) | 2000-07-19 | 2002-01-22 | Dsm Nv | Werkwijze voor de bereiding van 2-(6-gesubstitueerde-1,3-dioxan-4-yl) azijnzuurderivaten. |
BR0211072A (pt) | 2001-07-13 | 2004-12-14 | Astrazeneca Uk Ltd | Processo para preparar um composto, composto, e, método para a preparação de um composto |
EP1323717A1 (en) | 2001-12-27 | 2003-07-02 | Dsm N.V. | Process for the preparation of 2-(6-Substituted-1,3-Dioxane-4-yL) acetic acid derivatives |
EP1375493A1 (en) | 2002-06-17 | 2004-01-02 | Dsm N.V. | Process for the preparation of an dioxane acetic acid ester |
GB0218781D0 (en) | 2002-08-13 | 2002-09-18 | Astrazeneca Ab | Chemical process |
DE60330050D1 (de) | 2002-12-16 | 2009-12-24 | Astrazeneca Uk Ltd | Verfahren zur herstellung von pyrimidinverbindungen |
GB0312896D0 (en) * | 2003-06-05 | 2003-07-09 | Astrazeneca Ab | Chemical process |
UY28501A1 (es) * | 2003-09-10 | 2005-04-29 | Astrazeneca Uk Ltd | Compuestos químicos |
GB0322552D0 (en) | 2003-09-26 | 2003-10-29 | Astrazeneca Uk Ltd | Therapeutic treatment |
GB0324791D0 (en) | 2003-10-24 | 2003-11-26 | Astrazeneca Ab | Chemical process |
GB0428328D0 (en) | 2004-12-24 | 2005-02-02 | Astrazeneca Uk Ltd | Chemical process |
GB0514078D0 (en) * | 2005-07-08 | 2005-08-17 | Astrazeneca Uk Ltd | Chemical process |
JP2008539278A (ja) * | 2006-09-18 | 2008-11-13 | テバ ファーマシューティカル インダストリーズ リミティド | 結晶性ロスバスタチンカルシウム |
TW200831469A (en) * | 2006-12-01 | 2008-08-01 | Astrazeneca Uk Ltd | Chemical process |
WO2010081861A1 (en) * | 2009-01-14 | 2010-07-22 | Krka, Tovarna Zdravil, D.D., Novo Mesto | Process for the preparation of rosuvastatin |
BRPI1005147A2 (pt) * | 2009-01-15 | 2019-09-24 | Egis Gyogyszergyar Nyilvanosan Muekoedoe Reszvenytarsasag | processo de preparação de sais de rosuvastatina |
HUP0900285A2 (en) | 2009-05-07 | 2011-01-28 | Egis Gyogyszergyar Nyilvanosan Mukoedoe Reszvenytarsasag | Rosuvastatin salts and preparation thereof |
WO2011074016A1 (en) | 2009-12-17 | 2011-06-23 | Matrix Laboratories Ltd | Novel polymorphic forms of rosuvastatin calcium and process for preparation of the same |
HU230737B1 (hu) | 2010-11-16 | 2018-01-29 | EGIS Gyógyszergyár Nyrt | Eljárás rosuvastatin só előállítására |
WO2012069394A1 (en) | 2010-11-22 | 2012-05-31 | Basf Se | Multicomponent system of rosuvastatin calcium salt and sorbitol |
DE202012011888U1 (de) | 2011-04-18 | 2013-03-21 | Basf Se | Kristallines Mehrkomponentensystem von Rosuvastatin-Calciumsalz und Vanillin |
WO2014050874A1 (ja) * | 2012-09-27 | 2014-04-03 | 東和薬品株式会社 | ロスバスタチンカルシウムの新規結晶形態およびその製造方法 |
RO129060B1 (ro) | 2013-04-25 | 2014-11-28 | Antibiotice S.A. | Compoziţie farmaceutică stabilă cu rosuvastatină calcică amorfă |
JP6596339B2 (ja) | 2014-02-06 | 2019-10-23 | 株式会社エーピーアイ コーポレーション | ロスバスタチンカルシウム及びその中間体の製造方法 |
PL3445751T3 (pl) | 2016-04-18 | 2023-09-18 | Morepen Laboratories Limited | Nowa polimorficzna postać krystalicznej rozuwastatyny wapniowej i nowe procesy otrzymywania krystalicznej i amorficznej rozuwastatyny wapniowej |
CN105837516B (zh) * | 2016-05-16 | 2018-07-10 | 山东新时代药业有限公司 | 一种瑞舒伐他汀钙晶型及其制备方法 |
US11446757B2 (en) | 2017-09-13 | 2022-09-20 | Jfe Steel Corporation | Double-sided friction stir welding method for metal sheets and double-sided friction stir welding device |
Family Cites Families (56)
Publication number | Priority date | Publication date | Assignee | Title |
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US4645858A (en) * | 1982-03-22 | 1987-02-24 | G. D. Searle & Co. | Pentanedioic acid derivatives |
DE3741509A1 (de) * | 1987-12-08 | 1989-06-22 | Hoechst Ag | Verfahren zur herstellung optisch aktiver 3-desmethylmevalonsaeurederivate sowie zwischenprodukte |
EP0367895A1 (en) | 1988-10-06 | 1990-05-16 | Sandoz Ag | Pyrimidinyl-substituted hydroxyacids, lactones and esters and pharmaceutical compositions containing them |
US5026698A (en) * | 1988-11-02 | 1991-06-25 | Nissan Chemical Industries, Ltd. | Thienopyridine type mevalonolactones |
JP2648897B2 (ja) * | 1991-07-01 | 1997-09-03 | 塩野義製薬株式会社 | ピリミジン誘導体 |
WO1993008823A1 (en) | 1991-11-06 | 1993-05-13 | Tanabe Seiyaku Co., Ltd. | Guanidinyl and related cell adhesion modulation compounds |
US5278313A (en) * | 1992-03-27 | 1994-01-11 | E. R. Squibb & Sons, Inc. | Process for the preparation of 1,3-dioxane derivatives useful in the preparation of HMG-COA reductase inhibitors |
EP0577040B1 (de) * | 1992-07-02 | 1997-09-24 | Hoechst Aktiengesellschaft | Verfahren zur Herstellung von (3R,5S)6-Hydroxy-3,5-0-isopropyliden-3,5-dihydroxy-hexansäure-tert.-butylester |
ES2167587T3 (es) | 1995-07-17 | 2002-05-16 | Warner Lambert Co | Forma cristalina de la sal hemicalcica del acido (r-(r*,r*))-2-(4-fluorofenil)-beta,delta-dihidroxi-5-(1-metiletil)-3-fenil-4-((fenilamino)carbonil)-1h-pirrol-1-heptanoico (atorvastatina). |
FR2741620B1 (fr) | 1995-11-28 | 1997-12-26 | Oreal | Procede de preparation de composes a groupement beta-hydroxy -delta-lactone analogues de la (+) compactine et de la (+) mevinoline |
US6278001B1 (en) * | 1995-11-28 | 2001-08-21 | L'oréal | Method for preparing (+) compactin and (+) mevinolin analog compounds having a β-hydroxy-δ-lactone grouping |
EP0907639B1 (en) | 1996-06-24 | 2003-03-12 | Novartis AG | Polymorphic compounds |
SA99191255B1 (ar) | 1998-11-30 | 2006-11-25 | جي دي سيرل اند كو | مركبات سيليكوكسيب celecoxib |
CZ299566B6 (cs) * | 1998-12-10 | 2008-09-03 | Kaneka Corporation | Zpusob výroby simvastatinu |
GB9900339D0 (en) * | 1999-01-09 | 1999-02-24 | Zeneca Ltd | Chemical compounds |
GB9903472D0 (en) * | 1999-02-17 | 1999-04-07 | Zeneca Ltd | Chemical process |
WO2001022962A1 (en) | 1999-09-30 | 2001-04-05 | Merck & Co., Inc. | Anti-hypercholesterolemic drug combination |
PT1235799E (pt) | 1999-11-17 | 2005-05-31 | Teva Pharma | Forma polimorfica de atorvastatina-calcio |
GB0001621D0 (en) | 2000-01-26 | 2000-03-15 | Astrazeneca Ab | Pharmaceutical compositions |
GB0003305D0 (en) * | 2000-02-15 | 2000-04-05 | Zeneca Ltd | Pyrimidine derivatives |
AU2000254249A1 (en) | 2000-03-28 | 2001-10-08 | Biocon India Limited | Synthesis of (r-(r*,r*))-2-(4-fluorophenyl)-beta,delta-dihydroxy-5-(1- |
GB0011120D0 (en) * | 2000-05-09 | 2000-06-28 | Avecia Ltd | Process |
GB0011163D0 (en) | 2000-05-10 | 2000-06-28 | Astrazeneca Ab | Chemical compound |
NL1015744C2 (nl) * | 2000-07-19 | 2002-01-22 | Dsm Nv | Werkwijze voor de bereiding van 2-(6-gesubstitueerde-1,3-dioxan-4-yl) azijnzuurderivaten. |
PL361230A1 (en) | 2000-10-05 | 2004-10-04 | Biogal Gyogyszergyar Rt. | Pravastatin sodium substantially free of pravastatin lactone and epi-pravastatin, and compositions containing same |
US6777552B2 (en) * | 2001-08-16 | 2004-08-17 | Teva Pharmaceutical Industries, Ltd. | Processes for preparing calcium salt forms of statins |
HUP0303555A3 (en) | 2000-11-16 | 2005-08-29 | Teva Pharma | Hydrolysis of [r(r |
IL156055A0 (en) | 2000-11-30 | 2003-12-23 | Teva Pharma | Novel crystal forms of atorvastatin hemi calcium and processes for their preparation as well as novel processes for preparing other forms |
NL1017548C2 (nl) | 2001-03-09 | 2002-09-10 | Synthon Bv | Een lactonisatie proces. |
IN190564B (es) | 2001-04-11 | 2003-08-09 | Cadila Heathcare Ltd | |
WO2002098854A2 (en) | 2001-06-06 | 2002-12-12 | Bristol-Myers Squibb Company | Process for preparing chiral diol sulfones and dihydroxy acid hmg coa reductase inhibitors |
BR0211072A (pt) * | 2001-07-13 | 2004-12-14 | Astrazeneca Uk Ltd | Processo para preparar um composto, composto, e, método para a preparação de um composto |
NZ529913A (en) | 2001-08-16 | 2005-03-24 | Teva Pharma | Processes for preparing calcium salt forms of statins |
EP1423365A1 (en) | 2001-08-22 | 2004-06-02 | Ciba Specialty Chemicals Holding Inc. | Process for the preparation of indole derivatives |
JP2005512516A (ja) | 2001-09-24 | 2005-05-12 | メルク エンド カムパニー インコーポレーテッド | スタチン薬物の組合せのスクリーニング方法および選択方法 |
AR033485A1 (es) | 2001-09-25 | 2003-12-26 | Otsuka Pharma Co Ltd | Sustancia medicinal de aripiprazol de baja higroscopicidad y proceso para la preparacion de la misma |
EP1323717A1 (en) * | 2001-12-27 | 2003-07-02 | Dsm N.V. | Process for the preparation of 2-(6-Substituted-1,3-Dioxane-4-yL) acetic acid derivatives |
KR100511533B1 (ko) | 2002-04-09 | 2005-08-31 | 임광민 | 키랄 중간체, 그의 제조방법 및 그를 이용한 HMG-CoA환원저해제의 제조방법 |
BR0311195A (pt) | 2002-05-21 | 2005-02-22 | Ranbaxy Lab Ltd | Processo de preparação de rosuvastatina |
EP1375493A1 (en) | 2002-06-17 | 2004-01-02 | Dsm N.V. | Process for the preparation of an dioxane acetic acid ester |
DE10228103A1 (de) | 2002-06-24 | 2004-01-15 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
GB0218781D0 (en) | 2002-08-13 | 2002-09-18 | Astrazeneca Ab | Chemical process |
DE60330050D1 (de) | 2002-12-16 | 2009-12-24 | Astrazeneca Uk Ltd | Verfahren zur herstellung von pyrimidinverbindungen |
GB0312896D0 (en) * | 2003-06-05 | 2003-07-09 | Astrazeneca Ab | Chemical process |
US7563748B2 (en) | 2003-06-23 | 2009-07-21 | Cognis Ip Management Gmbh | Alcohol alkoxylate carriers for pesticide active ingredients |
UY28501A1 (es) * | 2003-09-10 | 2005-04-29 | Astrazeneca Uk Ltd | Compuestos químicos |
GB0321827D0 (en) * | 2003-09-18 | 2003-10-15 | Astrazeneca Uk Ltd | Chemical compounds |
GB0324791D0 (en) * | 2003-10-24 | 2003-11-26 | Astrazeneca Ab | Chemical process |
DE10352659B4 (de) | 2003-11-11 | 2007-09-13 | Ratiopharm Gmbh | Verfahren zur Herstellung von Statinen und Tetrahydropyranonderivate zur Verwendung in dem Verfahren |
WO2005054207A1 (en) * | 2003-12-04 | 2005-06-16 | Glenmark Pharmaceuticals Limited | Process for the preparation of pyrimidine derivatives |
US7241800B2 (en) * | 2004-03-17 | 2007-07-10 | Mai De Ltd. | Anhydrous amorphous form of fluvastatin sodium |
US7161004B2 (en) * | 2004-06-21 | 2007-01-09 | Dr. Reddy's Laboratories Limited | Processes to produce intermediates for rosuvastatin |
WO2006000020A1 (en) | 2004-06-29 | 2006-01-05 | European Nickel Plc | Improved leaching of base metals |
GB0428328D0 (en) * | 2004-12-24 | 2005-02-02 | Astrazeneca Uk Ltd | Chemical process |
EP1895898B1 (en) | 2005-06-29 | 2011-02-16 | Compumedics Limited | Sensor assembly with conductive bridge |
TW200831469A (en) * | 2006-12-01 | 2008-08-01 | Astrazeneca Uk Ltd | Chemical process |
-
2004
- 2004-09-07 UY UY28501A patent/UY28501A1/es not_active Application Discontinuation
- 2004-09-08 AU AU2004270467A patent/AU2004270467B8/en not_active Ceased
- 2004-09-08 SI SI200431145T patent/SI1663989T1/sl unknown
- 2004-09-08 CA CA2537962A patent/CA2537962C/en active Active
- 2004-09-08 ES ES04768376T patent/ES2324042T3/es active Active
- 2004-09-08 JP JP2006525882A patent/JP2007505090A/ja active Pending
- 2004-09-08 EP EP04768376A patent/EP1663989B1/en active Active
- 2004-09-08 PT PT04768376T patent/PT1663989E/pt unknown
- 2004-09-08 NZ NZ545785A patent/NZ545785A/en not_active IP Right Cessation
- 2004-09-08 MX MXPA06002761A patent/MXPA06002761A/es active IP Right Grant
- 2004-09-08 WO PCT/GB2004/003829 patent/WO2005023779A1/en active Application Filing
- 2004-09-08 AT AT04768376T patent/ATE428701T1/de active
- 2004-09-08 RU RU2006111354/04A patent/RU2363697C2/ru not_active IP Right Cessation
- 2004-09-08 US US10/571,254 patent/US20060293355A1/en not_active Abandoned
- 2004-09-08 PL PL04768376T patent/PL1663989T3/pl unknown
- 2004-09-08 BR BRPI0414236-5A patent/BRPI0414236A/pt not_active Application Discontinuation
- 2004-09-08 DE DE602004020640T patent/DE602004020640D1/de active Active
- 2004-09-08 DK DK04768376T patent/DK1663989T3/da active
- 2004-09-08 KR KR1020067004952A patent/KR20070019943A/ko not_active Application Discontinuation
- 2004-09-08 CN CN2004800308267A patent/CN1878760B/zh active Active
- 2004-09-08 UA UAA200602622A patent/UA85062C2/uk unknown
- 2004-09-09 MY MYPI20043667A patent/MY142615A/en unknown
- 2004-09-10 AR ARP040103249A patent/AR045628A1/es unknown
- 2004-09-10 TW TW093127580A patent/TWI370817B/zh not_active IP Right Cessation
- 2004-09-18 SA SA04250297A patent/SA04250297B1/ar unknown
-
2006
- 2006-03-02 IL IL174073A patent/IL174073A/en active IP Right Grant
- 2006-03-14 NO NO20061181A patent/NO336358B1/no not_active IP Right Cessation
- 2006-03-15 CO CO06026185A patent/CO5670355A2/es not_active Application Discontinuation
- 2006-03-30 IS IS8385A patent/IS2689B/is unknown
- 2006-09-28 HK HK06110818A patent/HK1090361A1/xx unknown
-
2009
- 2009-06-10 HR HR20090335T patent/HRP20090335T1/xx unknown
- 2009-06-24 CY CY20091100661T patent/CY1109173T1/el unknown
- 2009-11-10 US US12/615,935 patent/US20100222373A1/en not_active Abandoned
-
2011
- 2011-03-01 US US13/038,245 patent/US8436167B2/en active Active
-
2013
- 2013-04-08 US US13/858,553 patent/US20130225622A1/en not_active Abandoned
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