FI952179A - Uusia 3,3-difenyylipropyyliamiineja, niiden käyttö ja valmistus - Google Patents
Uusia 3,3-difenyylipropyyliamiineja, niiden käyttö ja valmistus Download PDFInfo
- Publication number
- FI952179A FI952179A FI952179A FI952179A FI952179A FI 952179 A FI952179 A FI 952179A FI 952179 A FI952179 A FI 952179A FI 952179 A FI952179 A FI 952179A FI 952179 A FI952179 A FI 952179A
- Authority
- FI
- Finland
- Prior art keywords
- compounds
- diphenylpropylamines
- methyl
- preparation
- formula
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
- C07C217/54—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
- C07C217/56—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms
- C07C217/62—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms linked by carbon chains having at least three carbon atoms between the amino groups and the six-membered aromatic ring or the condensed ring system containing that ring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/46—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
- C07C215/48—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by hydroxy groups
- C07C215/54—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by hydroxy groups linked by carbon chains having at least three carbon atoms between the amino groups and the six-membered aromatic ring or the condensed ring system containing that ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Luminescent Compositions (AREA)
- Photoreceptors In Electrophotography (AREA)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE9203318A SE9203318D0 (sv) | 1992-11-06 | 1992-11-06 | Novel 3,3-diphenylpropylamines, their use and preparation |
SE9203318 | 1992-11-06 | ||
SE9300927 | 1993-11-05 | ||
PCT/SE1993/000927 WO1994011337A1 (en) | 1992-11-06 | 1993-11-05 | Novel 3,3-diphenylpropylamines, their use and preparation |
Publications (3)
Publication Number | Publication Date |
---|---|
FI952179A0 FI952179A0 (fi) | 1995-05-05 |
FI952179A true FI952179A (fi) | 1995-05-05 |
FI120256B FI120256B (fi) | 2009-08-31 |
Family
ID=20387730
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FI952179A FI120256B (fi) | 1992-11-06 | 1995-05-05 | Menetelmä uusien terapeuttisesti aktiivisten 3,3-difenyylipropyyliamiinien valmistamiseksi ja välituotteita |
Country Status (15)
Country | Link |
---|---|
US (4) | USRE40851E1 (fi) |
EP (1) | EP0667852B1 (fi) |
JP (1) | JP3343256B2 (fi) |
AT (1) | ATE164828T1 (fi) |
AU (1) | AU672458B2 (fi) |
CA (1) | CA2148827C (fi) |
DE (1) | DE69317898T2 (fi) |
DK (1) | DK0667852T3 (fi) |
ES (1) | ES2117155T3 (fi) |
FI (1) | FI120256B (fi) |
HK (1) | HK1006349A1 (fi) |
HU (1) | HU224916B1 (fi) |
NO (1) | NO305477B1 (fi) |
SE (1) | SE9203318D0 (fi) |
WO (1) | WO1994011337A1 (fi) |
Families Citing this family (70)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SE9203318D0 (sv) * | 1992-11-06 | 1992-11-06 | Kabi Pharmacia Ab | Novel 3,3-diphenylpropylamines, their use and preparation |
WO1998000140A1 (en) * | 1996-07-01 | 1998-01-08 | Sepracor, Inc. | Methods and compositions for treating urinary incontinence using enantiomerically enriched (r)-trihexyphenidyl |
EP0948964B1 (en) * | 1996-12-02 | 2003-04-02 | Kyorin Pharmaceutical Co., Ltd. | Novel n-substituted pyrrolidine derivatives and process for preparing the same |
SE9701144D0 (sv) * | 1997-03-27 | 1997-03-27 | Pharmacia & Upjohn Ab | Novel compounds, their use and preparation |
EP0957073A1 (en) * | 1998-05-12 | 1999-11-17 | Schwarz Pharma Ag | Novel derivatives of 3,3-diphenylpropylamines |
PT1039882E (pt) | 1998-08-27 | 2011-01-03 | Pfizer Health Ab | Formulação terapêutica para administrar tolterodina com libertação controlada |
SK6412002A3 (en) | 1999-11-11 | 2002-09-10 | Pharmacia Ab | Pharmaceutical formulation containing tolterodine and its use |
DE19955190A1 (de) * | 1999-11-16 | 2001-06-21 | Sanol Arznei Schwarz Gmbh | Stabile Salze neuartiger Derivate von 3,3-Diphenylpropylaminen |
SE9904850D0 (sv) * | 1999-12-30 | 1999-12-30 | Pharmacia & Upjohn Ab | Novel process and intermediates |
WO2001070689A1 (fr) | 2000-03-24 | 2001-09-27 | Meiji Seika Kaisha, Ltd. | DERIVES DE LA DIPHENYLALKYLAMINE UTILES COMME AGONISTES DU RECEPTEUR DE L'OPIOIDE $g(d) |
DE10028443C1 (de) * | 2000-06-14 | 2002-05-29 | Sanol Arznei Schwarz Gmbh | Verfahren zur Herstellung von 3,3-Diarylpropylaminen, (R,S)- und (R)-4-Phenyl-2-chromanon-6-carbonsäure sowie (R)-4-Phenyl-2-chromanon-carbonsäure-cinchonidinsalz und deren Verwendung zur Herstellung eines rechtsdrehenden Hydroxybenzylalkohols und von pharmazeutischen Zusammensetzungen |
DE10033016A1 (de) | 2000-07-07 | 2002-01-24 | Sanol Arznei Schwarz Gmbh | Verfahren zur Herstellung von 3,3-Diarylpropylaminen |
PE20020547A1 (es) | 2000-10-24 | 2002-06-12 | Upjohn Co | Uso de la tolterodina en tratamientos del asma |
NZ528377A (en) * | 2001-03-27 | 2005-05-27 | Galen Chemicals Ltd | Intravaginal drug delivery devices for the administration of an antimicrobial agent |
US20030027856A1 (en) * | 2001-06-29 | 2003-02-06 | Aberg A.K. Gunnar | Tolterodine metabolites |
US20030060513A1 (en) * | 2001-09-27 | 2003-03-27 | Arneric Stephen P. | Pharmaceutical composition |
MXPA04003865A (es) * | 2001-10-26 | 2004-07-08 | Upjohn Co | Compuestos de amonio cuaternario y sus usos como agentes antimuscarinicos. |
JP2005511582A (ja) * | 2001-11-05 | 2005-04-28 | ファルマシア アンド アップジョン カンパニー リミティド ライアビリティー カンパニー | 抗ムスカリン・エアゾール |
WO2003039524A1 (en) * | 2001-11-09 | 2003-05-15 | Pharmacia Ab | Anti-muscarinic agent and estrogen-agonist for treating unstable or overactive bladder |
WO2003053428A1 (en) * | 2001-12-20 | 2003-07-03 | Pharmacia Corporation | Controlled release dosage form having improved drug release properties |
IL163666A0 (en) | 2002-02-22 | 2005-12-18 | New River Pharmaceuticals Inc | Active agent delivery systems and methods for protecting and administering active agents |
US7005449B2 (en) | 2002-04-23 | 2006-02-28 | Pharmacia & Upjohn Company | Tolterodine salts |
CN1668585A (zh) * | 2002-07-08 | 2005-09-14 | 兰贝克赛实验室有限公司 | 用作蝇蕈碱受体拮抗剂的3,6-二取代氮杂双环[3.1.0]己烷衍生物 |
US7825132B2 (en) | 2002-08-23 | 2010-11-02 | Novartis Vaccines And Diagnostics, Inc. | Inhibition of FGFR3 and treatment of multiple myeloma |
US7838527B2 (en) * | 2002-11-13 | 2010-11-23 | Novartis Vaccines And Diagnostics, Inc. | Methods of treating cancer and related methods |
DE10315917A1 (de) * | 2003-04-08 | 2004-11-18 | Schwarz Pharma Ag | Hochreine Basen von 3,3-Diphenylpropylaminmonoestern |
AU2003214520A1 (en) * | 2003-04-09 | 2004-11-01 | Ranbaxy Laboratories Limited | Substituted azabicyclo hexane derivatives as muscarinic receptor antagonists |
WO2004089900A1 (en) * | 2003-04-11 | 2004-10-21 | Ranbaxy Laboratories Limited | Azabicyclo derivatives as muscarinic receptor antagonists |
BRPI0409653A (pt) | 2003-04-25 | 2006-04-25 | Pharmacia & Upjohn Co Llc | 3,3-difenilpropilaminas (tolterodina) substituìdas com halogênio com atividade antimuscarìnica |
WO2004105692A2 (en) * | 2003-05-23 | 2004-12-09 | Bridge Pharma, Inc. | Smooth muscle spasmolytic agents |
WO2005012227A2 (en) * | 2003-08-05 | 2005-02-10 | Ranbaxy Laboratories Limited | Process for preparation of 2-(3-diisopropylamino-1-phenylpropyl)-4-hydroxymethyl-phenol, a metabolite of tolterodine |
ES2235648B1 (es) * | 2003-12-22 | 2006-11-01 | Ragactives, S.L. | Procedimiento para la obtencion de tolterodina. |
EP1701932B1 (en) * | 2003-12-24 | 2012-07-18 | Cipla Ltd. | Tolterodine, compositions and uses thereof, and preparation of the same |
US7875624B2 (en) | 2004-02-20 | 2011-01-25 | Novartis Vaccines And Diagnostics, Inc. | Modulating and measuring cellular adhesion |
EP1629834A1 (en) | 2004-08-27 | 2006-03-01 | KRKA, D.D., Novo Mesto | Sustained release pharmaceutical composition of tolterodine |
US20100035954A1 (en) * | 2004-12-15 | 2010-02-11 | Mohammad Salman | Acid addition salts of muscarinic receptor antagonists |
TW200637804A (en) * | 2005-01-10 | 2006-11-01 | Teva Pharma | Substantially pure tolterodine tartrate and process for preparing thereof |
WO2006117754A1 (en) * | 2005-05-03 | 2006-11-09 | Ranbaxy Laboratories Limited | 3,6-disubstituted azabicyclo [3.1.0] hexane derivatives as muscarinic receptor antagonists |
KR101319122B1 (ko) | 2005-05-13 | 2013-10-23 | 노파르티스 아게 | 약물 저항성 암을 치료하는 방법 |
AU2006327882A1 (en) * | 2005-12-20 | 2007-06-28 | Pfizer Products Inc. | Pharmaceutical combination for the treatment of LUTS comprising a PDE5 inhibitor and a muscarinic antagonist |
MX2008011963A (es) | 2006-03-20 | 2008-10-01 | Pfizer Ltd | Derivados de amina. |
CN101454273B (zh) * | 2006-05-31 | 2013-08-21 | 施瓦茨制药有限公司 | 取代的羟甲基苯酚的合成方法 |
EP1862449A1 (en) * | 2006-05-31 | 2007-12-05 | Schwarz Pharma Ltd. | A shortened synthesis of substituted hydroxymethyl phenols |
IES20060424A2 (en) * | 2006-06-08 | 2007-10-31 | Schwarz Pharma Ltd | Accelerated synthesis of (3-Diisopropylamino-1-phenylpropyl)-4-(hydroxymethyl)phenol and its phenolic monoesters |
CA2648333C (en) | 2006-06-09 | 2014-04-29 | Schwarz Pharma Ltd | Synthesis of phenolic esters of hydroxymethyl phenols |
KR101488740B1 (ko) | 2006-06-12 | 2015-02-03 | 유씨비 파마 게엠베하 | 새로운 키랄 중간체, 그 키랄 중간체의 제조방법 및 톨테로딘, 페소테로딘 또는 그 활성대사물질의 제조에서 그키랄 중간체의 사용 |
IES20060435A2 (en) | 2006-06-12 | 2007-12-12 | Schwarz Pharma Ltd | Shortened synthesis using paraformaldehyde or trioxane |
EP2044001B1 (en) * | 2006-06-20 | 2016-11-23 | LEK Pharmaceuticals d.d. | Process for preparation of 3-(2-hydroxy-5-substituted phenyl)-n-alkyl-3-phenylpropylamines |
WO2009037569A2 (en) * | 2007-09-21 | 2009-03-26 | Actavis Group Ptc Ehf | An improved process for the preparation of fesoterodine |
KR101188333B1 (ko) * | 2008-02-20 | 2012-10-09 | 에스케이케미칼주식회사 | 안정성이 우수하고 경피제로 유용한 톨테로딘 결정성산부가염 |
US20090214665A1 (en) * | 2008-02-26 | 2009-08-27 | Lai Felix S | Controlled Release Muscarinic Receptor Antagonist Formulation |
KR20120014583A (ko) * | 2009-05-11 | 2012-02-17 | 라티오팜 게엠베하 | 타르타르산 염 형태의 데스페소테로딘 |
IT1394217B1 (it) | 2009-05-15 | 2012-06-01 | Chemi Spa | Metodo di preparazione di fesoterodina e/o fesoterodina fumarato. |
IT1394219B1 (it) | 2009-05-15 | 2012-06-01 | Chemi Spa | Metodo di preparazione di fesoterodina fumarato di elevata purezza. |
ES2456866T3 (es) * | 2009-07-27 | 2014-04-23 | Crystal Pharma, S.A.U. | Procedimiento para la obtención de 3,3-difenilpropilaminas |
IT1396373B1 (it) | 2009-10-29 | 2012-11-19 | Dipharma Francis Srl | Procedimento per la preparazione di fesoterodina. |
IL210279A0 (en) | 2009-12-25 | 2011-03-31 | Dexcel Pharma Technologies Ltd | Extended release compositions for high solubility, high permeability acdtive pharmaceutical ingredients |
EP2364966A1 (en) | 2010-03-09 | 2011-09-14 | LEK Pharmaceuticals d.d. | Process for preparation of 3-(2-hydroxy-5-substituted phenyl)-3-phenylpropylamines, intermediates for making hydroxytolterodine |
US20110282094A1 (en) | 2010-05-11 | 2011-11-17 | Intas Pharmaceuticals Limited | Process for preparation of phenolic monoesters of hydroxymethyl phenols |
WO2011145019A1 (en) * | 2010-05-17 | 2011-11-24 | Orchid Chemicals And Pharmaceuticals Limited | Improved process for diphenylpropylamine derivatives |
IT1401451B1 (it) | 2010-06-10 | 2013-07-26 | Chemi Spa | Nuovo processo di preparazione di 2-idrossi-4-fenil-3,4-diidro-2h-cromen-6-il-metanolo e (r)-2-[3-(diisopropilammino)-1-fenilpropil]-4-(idrossimetil)fenolo. |
IT1403094B1 (it) | 2010-12-09 | 2013-10-04 | Dipharma Francis Srl | Procedimento per la preparazione di fesoterodina o un suo sale |
TWI590821B (zh) | 2011-01-18 | 2017-07-11 | 輝瑞有限公司 | 固體分子分散液 |
US9422228B2 (en) | 2012-05-04 | 2016-08-23 | Crystal Pharma, S.A.U. | Process for the preparation of optically pure fesoterodine derivatives |
CA2875342C (en) | 2012-06-14 | 2017-06-13 | Ratiopharm Gmbh | Desfesoterodine salts |
ITMI20121232A1 (it) | 2012-07-16 | 2014-01-17 | Cambrex Profarmaco Milano Srl | Procedimento per la preparazione di 2-(3-n,n-diisopropilamino-1-fenilpropil)-4-idrossimetil-fenolo e suoi derivati |
GB201402556D0 (en) | 2014-02-13 | 2014-04-02 | Crystec Ltd | Improvements relating to inhalable particles |
WO2016148444A1 (ko) * | 2015-03-17 | 2016-09-22 | 제이더블유중외제약 주식회사 | 신규 데스페소테로딘 유도체, 이의 약제학적으로 허용되는 염 및 이를 포함하는 약제학적 조성물 |
WO2017137955A1 (en) | 2016-02-14 | 2017-08-17 | Celestis Pharmaceuticals Pvt. Ltd. | Novel (r) and rac 3-(2-(allyloxy)-5-methylphenyl)-n,n-diisopropyl-3- phenylpropan-1-amine and its use for synthesis of (r) and rac-2-(3- (diisopropylamino)-1-phenylpropyl)-4-(hydroxymethyl)phenol |
CN110372571B (zh) | 2018-04-12 | 2022-11-15 | 中国科学院大连化学物理研究所 | 一种2-(2,2-二芳基乙基)-环胺衍生物或盐及合成和应用与组合物 |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DK111894A (fi) | 1962-11-15 | |||
GB1169944A (en) * | 1966-08-25 | 1969-11-05 | Geistlich Soehne Ag | Novel 3,3-Diphenylpropylamines and processes for the preparation thereof |
GB1169945A (en) | 1966-08-25 | 1969-11-05 | Geistlich Soehne Ag | Pharmaceutical Compositions containing Diphenylalkyl-amine Derivatives |
US4139537A (en) | 1976-06-29 | 1979-02-13 | Cooper Laboratories, Inc. | 3-Aryloxy-1-(2- or 4-iminodihydro-1-pyridyl)-2-propanol antiarrhythmic compounds |
SE8800207D0 (sv) | 1988-01-22 | 1988-01-22 | Kabivitrum Ab | Nya aminer, deras anvendning och framstellning |
US5382600A (en) * | 1988-01-22 | 1995-01-17 | Pharmacia Aktiebolag | 3,3-diphenylpropylamines and pharmaceutical compositions thereof |
SE9203318D0 (sv) * | 1992-11-06 | 1992-11-06 | Kabi Pharmacia Ab | Novel 3,3-diphenylpropylamines, their use and preparation |
US5472958A (en) * | 1994-08-29 | 1995-12-05 | Abbott Laboratories | 2-((nitro)phenoxymethyl) heterocyclic compounds that enhance cognitive function |
PE20020547A1 (es) * | 2000-10-24 | 2002-06-12 | Upjohn Co | Uso de la tolterodina en tratamientos del asma |
-
1992
- 1992-11-06 SE SE9203318A patent/SE9203318D0/xx unknown
-
1993
- 1993-11-05 HU HU9501329A patent/HU224916B1/hu unknown
- 1993-11-05 DE DE69317898T patent/DE69317898T2/de not_active Expired - Lifetime
- 1993-11-05 EP EP93924876A patent/EP0667852B1/en not_active Expired - Lifetime
- 1993-11-05 US US11/402,337 patent/USRE40851E1/en not_active Expired - Lifetime
- 1993-11-05 ES ES93924876T patent/ES2117155T3/es not_active Expired - Lifetime
- 1993-11-05 JP JP51197794A patent/JP3343256B2/ja not_active Expired - Lifetime
- 1993-11-05 US US11/017,635 patent/USRE39667E1/en not_active Expired - Lifetime
- 1993-11-05 WO PCT/SE1993/000927 patent/WO1994011337A1/en active IP Right Grant
- 1993-11-05 AU AU54380/94A patent/AU672458B2/en not_active Expired
- 1993-11-05 DK DK93924876T patent/DK0667852T3/da active
- 1993-11-05 AT AT93924876T patent/ATE164828T1/de active
- 1993-11-05 CA CA002148827A patent/CA2148827C/en not_active Expired - Lifetime
-
1995
- 1995-05-05 NO NO951775A patent/NO305477B1/no not_active IP Right Cessation
- 1995-05-05 US US08/432,113 patent/US5559269A/en not_active Ceased
- 1995-05-05 FI FI952179A patent/FI120256B/fi not_active IP Right Cessation
-
1996
- 1996-07-22 US US08/684,638 patent/US5686464A/en not_active Expired - Lifetime
-
1998
- 1998-06-17 HK HK98105466A patent/HK1006349A1/xx not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
NO305477B1 (no) | 1999-06-07 |
HU9501329D0 (en) | 1995-06-28 |
DE69317898D1 (de) | 1998-05-14 |
AU5438094A (en) | 1994-06-08 |
NO951775L (no) | 1995-05-05 |
AU672458B2 (en) | 1996-10-03 |
DK0667852T3 (da) | 1999-01-11 |
EP0667852A1 (en) | 1995-08-23 |
HUT72742A (en) | 1996-05-28 |
FI952179A0 (fi) | 1995-05-05 |
US5686464A (en) | 1997-11-11 |
HK1006349A1 (en) | 1999-02-19 |
CA2148827C (en) | 2005-01-04 |
EP0667852B1 (en) | 1998-04-08 |
HU224916B1 (en) | 2006-04-28 |
CA2148827A1 (en) | 1994-05-26 |
ES2117155T3 (es) | 1998-08-01 |
JP3343256B2 (ja) | 2002-11-11 |
US5559269A (en) | 1996-09-24 |
NO951775D0 (no) | 1995-05-05 |
DE69317898T2 (de) | 1998-10-15 |
JPH08503208A (ja) | 1996-04-09 |
SE9203318D0 (sv) | 1992-11-06 |
USRE40851E1 (en) | 2009-07-14 |
WO1994011337A1 (en) | 1994-05-26 |
FI120256B (fi) | 2009-08-31 |
USRE39667E1 (en) | 2007-05-29 |
ATE164828T1 (de) | 1998-04-15 |
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