LTIP339A - New azaindoles, preparation process and medicinal products containing them - Google Patents
New azaindoles, preparation process and medicinal products containing themInfo
- Publication number
- LTIP339A LTIP339A LTIP339A LTIP339A LTIP339A LT IP339 A LTIP339 A LT IP339A LT IP339 A LTIP339 A LT IP339A LT IP339 A LTIP339 A LT IP339A LT IP339 A LTIP339 A LT IP339A
- Authority
- LT
- Lithuania
- Prior art keywords
- cycloalkyl
- alkyl
- optionally substituted
- phenyl
- benzyl
- Prior art date
Links
- 238000002360 preparation method Methods 0.000 title abstract 2
- 125000005334 azaindolyl group Chemical group N1N=C(C2=CC=CC=C12)* 0.000 title 1
- 229940126601 medicinal product Drugs 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 5
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 3
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- -1 R5 and R6 denote H Chemical group 0.000 abstract 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000004414 alkyl thio group Chemical group 0.000 abstract 2
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical compound CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000006350 alkyl thio alkyl group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 230000000879 anti-atherosclerotic effect Effects 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 abstract 1
- 230000000055 hyoplipidemic effect Effects 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 229930192474 thiophene Natural products 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Vascular Medicine (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Urology & Nephrology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Indole Compounds (AREA)
Abstract
These compounds correspond to the formula, <IMAGE> in which, one of the groups X1 to X4 represents nitrogen and the others a CH radical, R1 and R2 represent H, halogen, alkyl, hydroxymethyl, alkyloxymethyl, dialkylaminoalkyl, dialkylaminoalkyloxymethyl, carboxyl, ethyl carboxylate, piperidino, alkenyl, cycloalkyl, cycloalkenyl, alkylthio, benzyl, phenyl, thiophene or pyridine, optionally substituted, R3 and R4 represent H, halogen, alkyl, cycloalkyl, alkoxy or alkylthio, R5 and R6 denote H, alkyl, alkenyl, cycloalkyl, cycloalkenyl, alkoxyalkyl, alkylthioalkyl, or together form alkylene or alkyleneoxyalkylene chains, R7 denotes H, alkyl or cycloalkyl, one of the R5 to R7 radicals can also denote optionally substituted phenyl or benzyl, R8 represents H, alkyl, cycloalkyl, phenyl or benzyl, optionally substituted, R9 denotes optionally substituted phenyl, naphthyl or heterocyclyl, and their tautomeric forms, processes for their preparation and application as hypolipidaemic and anti-atheromatous medicaments.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9201701A FR2687402B1 (en) | 1992-02-14 | 1992-02-14 | NOVEL AZAINDOLES, METHODS OF PREPARATION AND MEDICAMENTS CONTAINING THEM. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| LTIP339A true LTIP339A (en) | 1994-06-15 |
| LT3065B LT3065B (en) | 1994-10-25 |
Family
ID=9426663
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| LTIP339A LT3065B (en) | 1992-02-14 | 1993-02-12 | New azaindoles, preparation process and medicinal products containing them |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US5338849A (en) |
| EP (1) | EP0557171B1 (en) |
| JP (1) | JPH061788A (en) |
| KR (1) | KR930017905A (en) |
| AT (1) | ATE125257T1 (en) |
| AU (1) | AU658475B2 (en) |
| CA (1) | CA2089470A1 (en) |
| CZ (1) | CZ16893A3 (en) |
| DE (1) | DE69300268T2 (en) |
| DK (1) | DK0557171T3 (en) |
| ES (1) | ES2076827T3 (en) |
| FR (1) | FR2687402B1 (en) |
| GR (1) | GR3017614T3 (en) |
| HR (1) | HRP930180A2 (en) |
| HU (1) | HUT64067A (en) |
| IL (1) | IL104573A0 (en) |
| LT (1) | LT3065B (en) |
| LV (1) | LV10453B (en) |
| MA (1) | MA22797A1 (en) |
| MX (1) | MX9300745A (en) |
| NO (1) | NO930505L (en) |
| NZ (1) | NZ245869A (en) |
| OA (1) | OA09775A (en) |
| SI (1) | SI9300076A (en) |
| SK (1) | SK9093A3 (en) |
| TN (1) | TNSN93016A1 (en) |
| ZA (1) | ZA93844B (en) |
Families Citing this family (49)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9226855D0 (en) * | 1992-12-23 | 1993-02-17 | Erba Carlo Spa | Vinylene-azaindole derivatives and process for their preparation |
| US5547966A (en) * | 1993-10-07 | 1996-08-20 | Bristol-Myers Squibb Company | Aryl urea and related compounds |
| DE69728688T2 (en) | 1996-11-19 | 2004-08-19 | Amgen Inc., Thousand Oaks | ARYL AND HETEROARYL SUBSTITUTED CONDENSED PYRROLE AS AN ANTI-FLAMMING AGENT |
| CA2306870A1 (en) | 1997-10-20 | 1999-04-29 | David Michael Goldstein | Bicyclic kinase inhibitors |
| WO1999031075A1 (en) * | 1997-12-16 | 1999-06-24 | Warner-Lambert Company | 1-substituted-1-aminomethyl-cycloalkane derivatives (=gabapentin analogues), their preparation and their use in the treatment of neurological disorders |
| US6187777B1 (en) | 1998-02-06 | 2001-02-13 | Amgen Inc. | Compounds and methods which modulate feeding behavior and related diseases |
| EP1990343B1 (en) | 1999-12-24 | 2012-04-04 | Aventis Pharma Limited | Azaindoles |
| GB0115109D0 (en) * | 2001-06-21 | 2001-08-15 | Aventis Pharma Ltd | Chemical compounds |
| CN1625555A (en) * | 2002-02-01 | 2005-06-08 | 阿斯特拉曾尼卡有限公司 | Quinazoline compounds |
| GB0207637D0 (en) * | 2002-04-02 | 2002-05-15 | Karobio Ab | Novel compound |
| SE0301372D0 (en) * | 2003-05-09 | 2003-05-09 | Astrazeneca Ab | Novel compounds |
| PL1696920T3 (en) * | 2003-12-19 | 2015-03-31 | Plexxikon Inc | Compounds and methods for development of ret modulators |
| US20070066641A1 (en) * | 2003-12-19 | 2007-03-22 | Prabha Ibrahim | Compounds and methods for development of RET modulators |
| US7507826B2 (en) | 2004-03-30 | 2009-03-24 | Vertex Pharmaceuticals Incorporated | Azaindoles useful as inhibitors of JAK and other protein kinases |
| JP2008503473A (en) * | 2004-06-17 | 2008-02-07 | プレキシコン,インコーポレーテッド | Compounds that modulate C-KIT activity |
| US7498342B2 (en) * | 2004-06-17 | 2009-03-03 | Plexxikon, Inc. | Compounds modulating c-kit activity |
| EP2264033A1 (en) | 2004-07-27 | 2010-12-22 | SGX Pharmaceuticals, Inc. | 3,5-DIPHENYL-SUBSTITUTED PYRROLO[2,3b]PYRIDINES USEFUL AS KINASE INHIBITORS |
| BRPI0513899A (en) * | 2004-07-27 | 2008-05-20 | Sgx Pharmaceuticals Inc | fused ring heterocyclic kinase modulators |
| US7626021B2 (en) * | 2004-07-27 | 2009-12-01 | Sgx Pharmaceuticals, Inc. | Fused ring heterocycle kinase modulators |
| US7361764B2 (en) | 2004-07-27 | 2008-04-22 | Sgx Pharmaceuticals, Inc. | Pyrrolo-pyridine kinase modulators |
| EP1787991B2 (en) * | 2004-07-28 | 2020-06-24 | Takeda Pharmaceutical Company Limited | PYRROLO[2,3-c]PYRIDINE COMPOUND, PROCESS FOR PRODUCING THE SAME, AND USE |
| US20060183758A1 (en) * | 2005-02-17 | 2006-08-17 | Cb Research And Development, Inc. | Method for synthesis of AZA-annelated pyrroles, thiophenes, and furans |
| CA2608733A1 (en) * | 2005-05-17 | 2007-02-01 | Plexxikon, Inc. | Pyrrol (2,3-b) pyridine derivatives protein kinase inhibitors |
| DK2395004T3 (en) * | 2005-06-22 | 2016-03-21 | Plexxikon Inc | Pyrrolo [2,3-b] pyridine derivatives as protein kinase inhibitors |
| TW201412738A (en) | 2006-01-17 | 2014-04-01 | Vertex Pharma | Azaindoles useful as inhibitors of janus kinases |
| WO2008063888A2 (en) | 2006-11-22 | 2008-05-29 | Plexxikon, Inc. | Compounds modulating c-fms and/or c-kit activity and uses therefor |
| WO2008079909A1 (en) * | 2006-12-21 | 2008-07-03 | Plexxikon, Inc. | Pyrrolo [2,3-b] pyridines as kinase modulators |
| NZ577798A (en) | 2006-12-21 | 2012-04-27 | Vertex Pharma | 5-cyano-4- (pyrrolo [2, 3b] pyridine-3-yl) -pyrimidine derivatives useful as protein kinase inhibitors |
| PE20081581A1 (en) * | 2006-12-21 | 2008-11-12 | Plexxikon Inc | PIRROLO [2,3-b] PYRIDINES COMPOUNDS AS KINASE MODULATORS |
| WO2008080015A2 (en) | 2006-12-21 | 2008-07-03 | Plexxikon, Inc. | Compounds and methods for kinase modulation, and indications therefor |
| US20100190777A1 (en) | 2007-07-17 | 2010-07-29 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| FR2946342B1 (en) | 2009-06-05 | 2011-06-24 | Galderma Res & Dev | NOVEL DIOXO-IMIDAZOLIDINE DERIVATIVES, ENZYME INHIBITORS SOAT-1, PHARMACEUTICAL AND COSMETIC COMPOSITIONS CONTAINING SAME |
| FR2946345B1 (en) | 2009-06-05 | 2011-05-20 | Galderma Res & Dev | NOVEL DIOXO-IMIDAZOLIDINE DERIVATIVES, ENZYME INHIBITORS SOAT-1, PHARMACEUTICAL AND COSMETIC COMPOSITIONS CONTAINING SAME |
| FR2946346B1 (en) | 2009-06-05 | 2011-05-20 | Galderma Res & Dev | NOVEL DIOXO-IMIDAZOLIDINE DERIVATIVES, ENZYME INHIBITORS SOAT-1, PHARMACEUTICAL AND COSMETIC COMPOSITIONS CONTAINING SAME |
| FR2946340B1 (en) | 2009-06-05 | 2011-06-24 | Galderma Res & Dev | NOVEL N-PHENYL ACETAMIA, INHIBITORS OF ENZYME SOAT-1, PHARMACEUTICAL AND COSMETIC COMPOSITIONS CONTAINING SAME |
| HUE027598T2 (en) * | 2009-04-03 | 2016-10-28 | Hoffmann La Roche | Propane-i-sulfonic acid {3-[5-(4-chloro-phenyl)-1h-pyrrolo[2,3-b]pyridine-3-carbonyl]-2,4-difluoro-phenyl}-amide compositions and uses thereof |
| DK2442809T3 (en) | 2009-06-17 | 2016-12-19 | Vertex Pharma | Inhibitors of the replication of influenza virus |
| US8329724B2 (en) | 2009-08-03 | 2012-12-11 | Hoffmann-La Roche Inc. | Process for the manufacture of pharmaceutically active compounds |
| ES2633317T3 (en) | 2009-11-06 | 2017-09-20 | Plexxikon, Inc. | Compounds and methods for kinase modulation, and indications for it |
| JP5810157B2 (en) * | 2010-07-09 | 2015-11-11 | ザ・ウォルター・アンド・エリザ・ホール・インスティテュート・オブ・メディカル・リサーチ | Protein kinase inhibitors and methods of treatment |
| AU2011343642A1 (en) | 2010-12-16 | 2013-05-02 | Vertex Pharmaceuticals Incorporated | Inhibitors of influenza viruses replication |
| MA34948B1 (en) | 2011-02-07 | 2014-03-01 | Plexxikon Inc | COMPOUNDS AND METHODS FOR MODULATING KINASE, AND INDICATIONS THEREOF |
| TWI558702B (en) | 2011-02-21 | 2016-11-21 | 普雷辛肯公司 | Solid forms of a pharmaceutically active substance |
| UA118010C2 (en) | 2011-08-01 | 2018-11-12 | Вертекс Фармасьютікалз Інкорпорейтед | INFLUENCES OF INFLUENZA VIRUS REPLICATION |
| US9150570B2 (en) | 2012-05-31 | 2015-10-06 | Plexxikon Inc. | Synthesis of heterocyclic compounds |
| RS57541B1 (en) | 2013-11-13 | 2018-10-31 | Vertex Pharma | Methods of preparing inhibitors of influenza viruses replication |
| EP3068776B1 (en) | 2013-11-13 | 2019-05-29 | Vertex Pharmaceuticals Incorporated | Inhibitors of influenza viruses replication |
| JP6704416B2 (en) | 2015-05-13 | 2020-06-03 | バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated | Methods for preparing inhibitors of influenza virus replication |
| MA42422A (en) | 2015-05-13 | 2018-05-23 | Vertex Pharma | INHIBITORS OF INFLUENZA VIRUS REPLICATION |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1261179A (en) * | 1959-02-04 | 1961-05-19 | Chimiotherapie Lab Franc | 12-aza deserpidine and its preparation process |
| US3354174A (en) * | 1964-02-19 | 1967-11-21 | Sterling Drug Inc | 1-and 2-benzimidazolyl-lower-alkylamidoximes, amidines-, and guanidines |
| IL83821A0 (en) * | 1986-09-10 | 1988-02-29 | Sandoz Ag | Azaindole and indolizine derivatives,their production and pharmaceutical compositions containing them |
| EP0279263B1 (en) * | 1987-02-10 | 1993-08-04 | Abbott Laboratories | Indole, benzofuran, benzothiophene containing lipoxygenase inhibiting compounds |
| US5153226A (en) * | 1989-08-31 | 1992-10-06 | Warner-Lambert Company | Acat inhibitors for treating hypocholesterolemia |
| WO1991004027A1 (en) * | 1989-09-15 | 1991-04-04 | Pfizer Inc. | New n-aryl and n-heteroarylamide and urea derivatives as inhibitors of acyl coenzyme a: cholesterol acyl transferase (acat) |
| DE4022414A1 (en) * | 1990-07-13 | 1992-01-16 | Bayer Ag | SUBSTITUTED PYRROLO-PYRIDINE |
| FR2674522B1 (en) * | 1991-03-26 | 1993-07-16 | Lipha | NOVEL INDOLE DERIVATIVES, PREPARATION METHODS AND MEDICAMENTS CONTAINING THEM. |
-
1992
- 1992-02-14 FR FR9201701A patent/FR2687402B1/en not_active Expired - Fee Related
-
1993
- 1993-02-01 IL IL104573A patent/IL104573A0/en unknown
- 1993-02-04 US US08/013,427 patent/US5338849A/en not_active Expired - Fee Related
- 1993-02-08 ZA ZA93844A patent/ZA93844B/en unknown
- 1993-02-09 NZ NZ245869A patent/NZ245869A/en unknown
- 1993-02-10 CZ CZ93168A patent/CZ16893A3/en unknown
- 1993-02-10 OA OA60340A patent/OA09775A/en unknown
- 1993-02-11 MX MX9300745A patent/MX9300745A/en unknown
- 1993-02-12 TN TNTNSN93016A patent/TNSN93016A1/en unknown
- 1993-02-12 AU AU33005/93A patent/AU658475B2/en not_active Ceased
- 1993-02-12 CA CA002089470A patent/CA2089470A1/en not_active Abandoned
- 1993-02-12 EP EP93400366A patent/EP0557171B1/en not_active Expired - Lifetime
- 1993-02-12 HU HU9300372A patent/HUT64067A/en unknown
- 1993-02-12 AT AT93400366T patent/ATE125257T1/en not_active IP Right Cessation
- 1993-02-12 DE DE69300268T patent/DE69300268T2/en not_active Expired - Fee Related
- 1993-02-12 DK DK93400366.6T patent/DK0557171T3/en active
- 1993-02-12 JP JP5023965A patent/JPH061788A/en active Pending
- 1993-02-12 MA MA23089A patent/MA22797A1/en unknown
- 1993-02-12 SI SI19939300076A patent/SI9300076A/en unknown
- 1993-02-12 SK SK9093A patent/SK9093A3/en unknown
- 1993-02-12 NO NO93930505A patent/NO930505L/en unknown
- 1993-02-12 HR HR930180A patent/HRP930180A2/en not_active Application Discontinuation
- 1993-02-12 ES ES93400366T patent/ES2076827T3/en not_active Expired - Lifetime
- 1993-02-12 LT LTIP339A patent/LT3065B/en not_active IP Right Cessation
- 1993-02-12 LV LVP-93-119A patent/LV10453B/en unknown
- 1993-02-13 KR KR1019930001980A patent/KR930017905A/en not_active Withdrawn
-
1995
- 1995-10-04 GR GR950402727T patent/GR3017614T3/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| LV10453A (en) | 1995-02-20 |
| ZA93844B (en) | 1994-08-08 |
| LT3065B (en) | 1994-10-25 |
| HU9300372D0 (en) | 1993-04-28 |
| NZ245869A (en) | 1995-05-26 |
| MA22797A1 (en) | 1993-10-01 |
| DK0557171T3 (en) | 1995-12-04 |
| SK9093A3 (en) | 1993-09-08 |
| HUT64067A (en) | 1993-11-29 |
| NO930505L (en) | 1993-08-16 |
| TNSN93016A1 (en) | 1994-03-17 |
| CZ16893A3 (en) | 1993-12-15 |
| MX9300745A (en) | 1993-09-01 |
| US5338849A (en) | 1994-08-16 |
| CA2089470A1 (en) | 1993-08-15 |
| OA09775A (en) | 1993-11-30 |
| DE69300268D1 (en) | 1995-08-24 |
| NO930505D0 (en) | 1993-02-12 |
| KR930017905A (en) | 1993-09-20 |
| JPH061788A (en) | 1994-01-11 |
| FR2687402A1 (en) | 1993-08-20 |
| EP0557171A1 (en) | 1993-08-25 |
| SI9300076A (en) | 1993-09-30 |
| IL104573A0 (en) | 1993-06-10 |
| AU3300593A (en) | 1993-08-19 |
| ATE125257T1 (en) | 1995-08-15 |
| LV10453B (en) | 1995-10-20 |
| EP0557171B1 (en) | 1995-07-19 |
| HRP930180A2 (en) | 1995-10-31 |
| ES2076827T3 (en) | 1995-11-01 |
| DE69300268T2 (en) | 1996-04-04 |
| FR2687402B1 (en) | 1995-06-30 |
| GR3017614T3 (en) | 1996-01-31 |
| AU658475B2 (en) | 1995-04-13 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM9A | Lapsed patents |
Effective date: 19960212 |