TNSN07202A1 - Derives d'acide 7-(2h-pyrazole-3-yl)-3, 5-dihyroxy heptanoique servant d'inhibiteurs de hmg-co a reductase pour le traitement de la lipidemie - Google Patents
Derives d'acide 7-(2h-pyrazole-3-yl)-3, 5-dihyroxy heptanoique servant d'inhibiteurs de hmg-co a reductase pour le traitement de la lipidemieInfo
- Publication number
- TNSN07202A1 TNSN07202A1 TNP2007000202A TNSN07202A TNSN07202A1 TN SN07202 A1 TNSN07202 A1 TN SN07202A1 TN P2007000202 A TNP2007000202 A TN P2007000202A TN SN07202 A TNSN07202 A TN SN07202A TN SN07202 A1 TNSN07202 A1 TN SN07202A1
- Authority
- TN
- Tunisia
- Prior art keywords
- cycloalkyl
- specifically
- heteroaryl
- alkyl
- aryl
- Prior art date
Links
- -1 2H-PYRAZOLE-3-YL Chemical class 0.000 title abstract 4
- 239000003112 inhibitor Substances 0.000 title abstract 2
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical class CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 title 1
- 125000004475 heteroaralkyl group Chemical group 0.000 abstract 6
- 125000001072 heteroaryl group Chemical group 0.000 abstract 6
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 102100029077 3-hydroxy-3-methylglutaryl-coenzyme A reductase Human genes 0.000 abstract 2
- 206010004446 Benign prostatic hyperplasia Diseases 0.000 abstract 2
- 208000004403 Prostatic Hyperplasia Diseases 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical group 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- 125000006701 (C1-C7) alkyl group Chemical group 0.000 abstract 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- 101710158485 3-hydroxy-3-methylglutaryl-coenzyme A reductase Proteins 0.000 abstract 1
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 abstract 1
- 208000024827 Alzheimer disease Diseases 0.000 abstract 1
- 201000001320 Atherosclerosis Diseases 0.000 abstract 1
- 102000004190 Enzymes Human genes 0.000 abstract 1
- 108090000790 Enzymes Proteins 0.000 abstract 1
- 108090000895 Hydroxymethylglutaryl CoA Reductases Proteins 0.000 abstract 1
- 208000035150 Hypercholesterolemia Diseases 0.000 abstract 1
- 208000031226 Hyperlipidaemia Diseases 0.000 abstract 1
- 208000001132 Osteoporosis Diseases 0.000 abstract 1
- 239000003529 anticholesteremic agent Substances 0.000 abstract 1
- 239000003524 antilipemic agent Substances 0.000 abstract 1
- 206010012601 diabetes mellitus Diseases 0.000 abstract 1
- 208000006575 hypertriglyceridemia Diseases 0.000 abstract 1
- 230000000871 hypocholesterolemic effect Effects 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 230000003389 potentiating effect Effects 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Diabetes (AREA)
- Physical Education & Sports Medicine (AREA)
- Hematology (AREA)
- Rheumatology (AREA)
- Neurosurgery (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Obesity (AREA)
- Biomedical Technology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Neurology (AREA)
- Vascular Medicine (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Steroid Compounds (AREA)
Abstract
La présente invention propose des composés de formules (I), (IV) et (V) et des intermédiaires de formules (VI) et (VII) : (I), (IV), (V), (VI), (VII), formules dans lesquelles : R1 représente un atome d'hydrogène, un atome d'halogène, un groupe alkyle en C1 à C7, cycloalkyle en C3 à C8, aryle, aralkyle, hétéroaryle ou hétéroaralkyle ; plus spécifiquement, R1 représente un groupe alkyle en C1 à C7 ou cycloalkyle en C3 à C8 ; encore plus spécifiquement, R1 représente un groupe isopropyle ; le groupe alkyle cycloalkyle, aryle aralkyle, hétéroaryle ou hétéroaralkyle de R1 étant facultativement substitué ; R2 représente un atome d'hydrogène, un atome d'halogène, un groupe alkyle en C1 à C7, cycloalkyle en C3 à C8, aryle aralkyle, hétéroaryle, hétéroaralkyle, NC-, R2bR2aNCO(CH2)n -, R2bR2aNS(O)n -, R2cS(O)n-, R2bR2aN(CH2)n -, R2b-J-C(O)NR2a(CH2)n -, R2b-J-SO2NR2a(CH2)n -, R2b-J-SONR2a(CH2)n, R7OOC(CH2)n – ou R7CO(CH2)n - ; plus spécifiquement, R2 représente un groupe R2bR2a NCO(CH2)n - ; encore plus spécifiquement, R2 représente un groupe R2bR2aNCO- ; le groupe alkyle, cycloalkyle, hétéroaryle ou hétéroaralkyle de R2 étant facultativement substitué ; R3 représente un atome d'hydrogène, un groupe alkyle en C1 à C6, cycloalkyle en C3 à C6, aryle, aralkyle, hétéroaryle ou hétéroaralkyle ; plus spécifiquement R3 représente un groupe aryle ; encore plus spécifiquement, R3 représente un groupe phényle ou p-fluorophényle ; le groupe alkyle, cycloalkyle, aryle aralkyle, hétéroaryle ou hétéroaralkyle de R3 étant facultativement substitué et représentant une liaison ou étant absent. Les autres substituants sont définis dans les revendications. La présente invention concerne des composés et compositions pharmaceutiques utiles comme agents hypocholestérolémiques et hypolipidémiques. Plus spécifiquement, la présente invention concerne certains puissants inhibiteurs de l'enzyme 3-hydroxy-3-méthylglutaryl-coenzyme-A-réductase (« HMG-CoA-réductase »). Les composés sont utiles pour le traitement de l'hyperlipidémie, l'hypercholestérolémie, de l'hypertriglycéridémie, de l'athérosclérose, de la maladie d'Alzheimer, de l'hypertrophie prostatique bénigne (BPH) du diabète et de l'ostéoporose.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US63048104P | 2004-11-23 | 2004-11-23 | |
| PCT/IB2005/003461 WO2006056845A1 (fr) | 2004-11-23 | 2005-11-14 | Derives d'acide 7-(2h-pyrazol-3-yl)-3, 5-dihyroxy-heptanoique comme inhibiteurs de hmg co-a reductase pour le traitement de l'hyperlipidemie |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TNSN07202A1 true TNSN07202A1 (fr) | 2008-11-21 |
Family
ID=35708411
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TNP2007000202A TNSN07202A1 (fr) | 2004-11-23 | 2007-05-22 | Derives d'acide 7-(2h-pyrazole-3-yl)-3, 5-dihyroxy heptanoique servant d'inhibiteurs de hmg-co a reductase pour le traitement de la lipidemie |
Country Status (25)
| Country | Link |
|---|---|
| US (2) | US7446121B2 (fr) |
| EP (1) | EP1819681B1 (fr) |
| JP (1) | JP2008520642A (fr) |
| KR (1) | KR20070084455A (fr) |
| AP (1) | AP2007003979A0 (fr) |
| AR (1) | AR052244A1 (fr) |
| AT (1) | ATE439347T1 (fr) |
| AU (1) | AU2005308575A1 (fr) |
| BR (1) | BRPI0518300A2 (fr) |
| CA (1) | CA2590533C (fr) |
| CR (1) | CR9102A (fr) |
| DE (1) | DE602005016009D1 (fr) |
| EA (1) | EA200700875A1 (fr) |
| ES (1) | ES2328384T3 (fr) |
| GT (1) | GT200500338A (fr) |
| IL (1) | IL182569A0 (fr) |
| MA (1) | MA30108B1 (fr) |
| MX (1) | MX2007005137A (fr) |
| NL (1) | NL1030487C2 (fr) |
| PA (1) | PA8653401A1 (fr) |
| PE (1) | PE20061057A1 (fr) |
| TN (1) | TNSN07202A1 (fr) |
| TW (1) | TW200626556A (fr) |
| UY (1) | UY29220A1 (fr) |
| WO (1) | WO2006056845A1 (fr) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AP2007003979A0 (en) * | 2004-11-23 | 2007-06-30 | Warner Lambert Co | 7-(2h-pyrazol-3-yl)-3,5-dihyroxy-heptanoic acid derivatives as hmg co-a reductase inhibitors for thetreatment of lipidemia |
| WO2006087630A2 (fr) * | 2005-02-16 | 2006-08-24 | Warner-Lambert Company Llc | Inhibiteurs oxypyrazole de l'enzyme hmg co-a reductase |
| WO2007107843A1 (fr) * | 2006-03-22 | 2007-09-27 | Pfizer Products Inc. | Procédés de traitement avec des inhibiteurs de la cetp |
| US7834050B2 (en) | 2006-03-29 | 2010-11-16 | Duke University | Small molecule insulin mimetics absent quinones |
| WO2008059372A2 (fr) * | 2006-11-17 | 2008-05-22 | Pfizer Products Inc. | Forme cristalline d'un sel de sodium de l'acide (3r,5r)-7-[2-(4-fluoro-phényl)-4-isopropyl-5-(4-méthyl-benzylcarbamoyl)-2h-pyrazol-3-yl]-3,5-dihydroxy-heptanoïque |
| EP2630135B1 (fr) * | 2010-10-21 | 2020-03-04 | Bayer Intellectual Property GmbH | 1-(carbonyl hétérocyclique)pipéridines |
| AR087701A1 (es) * | 2011-08-31 | 2014-04-09 | Japan Tobacco Inc | Derivados de pirazol con actividad inhibidora de sglt1 |
| CA2856196C (fr) | 2011-12-06 | 2020-09-01 | Masco Corporation Of Indiana | Distribution d'ozone dans un robinet |
| WO2017112795A1 (fr) | 2015-12-21 | 2017-06-29 | Delta Faucet Company | Système de distribution de fluide comprenant un dispositif désinfectant |
| EP3778593A4 (fr) * | 2018-04-04 | 2021-12-22 | Japan Tobacco Inc. | Composé de pyrazole substitué par hétéroaryle et son utilisation médicinale |
| CN114425329B (zh) * | 2022-03-10 | 2024-04-19 | 西安凯立新材料股份有限公司 | 孕烯醇酮醋酸酯合成用催化剂及其制备方法和应用 |
| US12274680B2 (en) | 2022-09-13 | 2025-04-15 | II George William Creasy | Treatment of benign prostatic hypertrophy with capsinoids |
Family Cites Families (103)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1154810B (de) * | 1961-04-01 | 1963-09-26 | Knoll Ag | Verfahren zur Herstellung basisch substituierter Phenylacetonitrile |
| US3262977A (en) * | 1962-03-10 | 1966-07-26 | Chinoin Gyogyszer Es Vegyeszet | N-aralkyl-1, 1-diphenyl-propylamine derivatives |
| BE637389A (fr) * | 1962-09-13 | |||
| US3857952A (en) * | 1967-12-22 | 1974-12-31 | May & Baker Ltd | Certain benzene derivatives useful in treating cardiac disorders |
| CH507249A (de) * | 1968-05-31 | 1971-05-15 | Sandoz Ag | Verfahren zur Herstellung von 2-Brom-a-ergokryptin |
| US3822287A (en) * | 1969-04-17 | 1974-07-02 | Rexall Drug Chemical | Process for preparation of substituted 3,4-(diphenyl)chromans |
| US3683080A (en) * | 1970-08-28 | 1972-08-08 | Procter & Gamble | Compositions for inhibiting anomalous deposition and mobilization of calcium phosphate in animal tissue |
| BE795735A (fr) * | 1972-03-06 | 1973-06-18 | Cerm Cent Europ Rech Mauvernay | Nouvelles ethylenediamines substituees a activite cardiovasculaire |
| GB1435139A (en) * | 1972-08-17 | 1976-05-12 | Sumitomo Chemical Co | Thiazole derivatives |
| US4062950A (en) * | 1973-09-22 | 1977-12-13 | Bayer Aktiengesellschaft | Amino sugar derivatives |
| US4133814A (en) * | 1975-10-28 | 1979-01-09 | Eli Lilly And Company | 2-Phenyl-3-aroylbenzothiophenes useful as antifertility agents |
| JPS608117B2 (ja) * | 1977-02-08 | 1985-02-28 | 財団法人微生物化学研究会 | 新生理活性物質エステラスチンおよびその製造法 |
| DE2719912C3 (de) * | 1977-05-04 | 1979-12-06 | Bayer Ag, 5090 Leverkusen | Verfahren zur Isolierung von 0- |4,6-Dideoxy-4- [JJl S-O,4,6/5)-4,5,6-trihydroxy-3-hydroxymethyl-2cyclohexen-1-yl] -amino] - a -D-glucopyranosyl} -(I Pfeil nach rechts 4)-0- a D-glucopyranosyl-(l Pfeil nach rechts 4)-D-glucopyranose aus Kulturbrühen |
| DE2733747C2 (de) * | 1977-07-27 | 1979-09-27 | Hoechst Ag, 6000 Frankfurt | Verfahren zur Herstellung von 2,2 Dichlorhydrazobenzol |
| DE2860900D1 (en) * | 1977-08-22 | 1981-11-05 | Ici Plc | Triphenylalkene derivatives, process for their preparation and pharmaceutical compositions containing them |
| NO154918C (no) * | 1977-08-27 | 1987-01-14 | Bayer Ag | Analogifremgangsmaate til fremstilling av terapeutisk aktive derivater av 3,4,5-trihydroksypiperidin. |
| CA1147342A (fr) * | 1977-10-12 | 1983-05-31 | Kazuo Imai | Procede de preparation de nouveaux derives de la phenylethanolamine |
| JPS5953920B2 (ja) * | 1977-12-28 | 1984-12-27 | 東洋醸造株式会社 | 新規なアミノ糖化合物およびその製法 |
| CA1121290A (fr) * | 1978-02-14 | 1982-04-06 | Yasuji Suhara | Derives amines d'un sucre |
| JPS559058A (en) * | 1978-07-06 | 1980-01-22 | Dainippon Pharmaceut Co Ltd | 1-(3-mercapto-2-methylpropanoyl)prolyl amino acid derivative |
| DE2928485A1 (de) * | 1979-07-14 | 1981-01-29 | Bayer Ag | Verwendung von harnstoffderivaten als arzneimittel bei der behandlung von fettstoffwechselstoerungen |
| ES8207217A1 (es) * | 1980-10-09 | 1982-09-01 | Hoechst Ag | Procedimiento para la preparacion de un inactivador de alfa-amilasa |
| EP0056194B1 (fr) * | 1981-01-05 | 1984-09-12 | Takeda Chemical Industries, Ltd. | Pseudo-aminosucres N-substitués, leur préparation et leur utilisation |
| US4418068A (en) * | 1981-04-03 | 1983-11-29 | Eli Lilly And Company | Antiestrogenic and antiandrugenic benzothiophenes |
| US4452813A (en) * | 1981-05-22 | 1984-06-05 | Taiho Pharmaceutical Company Limited | Sulfonate derivatives, process for preparing same and antilipemic compositions containing the derivative |
| US4410520A (en) * | 1981-11-09 | 1983-10-18 | Ciba-Geigy Corporation | 3-Amino-[1]-benzazepin-2-one-1-alkanoic acids |
| DK161312C (da) * | 1982-03-11 | 1991-12-09 | Pfizer | Analogifremgangsmaade til fremstilling af 2-aminoalkoxymethyl-4-phenyl-6-methyl-1,4-dihydropyridin-3,5-dicarboxylsyreestere eller syreadditionssalte deraf samt phthalimidoderivater til anvendelse som udgangsmateriale ved fremgangsmaaden |
| GB2126576B (en) * | 1982-06-25 | 1985-06-19 | Farmos Group Limited | Alkane and alkene derivatives |
| US4567175A (en) * | 1983-06-03 | 1986-01-28 | Tanabe Seiyaku Co., Ltd. | 8-Chloro-1,5-benzothiazepine derivatives |
| CA1247547A (fr) * | 1983-06-22 | 1988-12-28 | Paul Hadvary | Derives de leucine |
| FI844289L (fi) * | 1984-01-21 | 1985-07-22 | Hoechst Ag | Nya polypeptider med -amylashaemmande verkan, foerfarande foer deras framstaellning, deras anvaendning och farmaceutiska preparat. |
| US4613610A (en) | 1984-06-22 | 1986-09-23 | Sandoz Pharmaceuticals Corp. | Cholesterol biosynthesis inhibiting pyrazole analogs of mevalonolactone and its derivatives |
| ATE62906T1 (de) | 1984-06-22 | 1991-05-15 | Sandoz Ag | Pyrazolanaloge von mevalonolakton und abkoemmlinge davon, verfahren zu deren herstellung und deren verwendung. |
| US4631286A (en) * | 1984-10-25 | 1986-12-23 | Hoechst-Roussel Pharmaceuticals Inc. | 9-amino-1,2,3,4-tetrahydroacridin-1-ol and related compounds |
| US4634765A (en) * | 1984-12-18 | 1987-01-06 | Merrell Dow Pharmaceuticals Inc. | Homodisaccharide hypoglycemic agents |
| US5061798A (en) * | 1985-01-18 | 1991-10-29 | Smith Kline & French Laboratories, Ltd. | Benzyl pyridyl and pyridazinyl compounds |
| GB8501372D0 (en) * | 1985-01-18 | 1985-02-20 | Smith Kline French Lab | Chemical compounds |
| IL74497A (en) * | 1985-03-05 | 1990-02-09 | Proterra Ag | Pharmaceutical compositions containing phenyl carbamate derivatives and certain phenyl carbamate derivatives |
| GB8531071D0 (en) * | 1985-12-17 | 1986-01-29 | Boots Co Plc | Therapeutic compound |
| US4663318A (en) * | 1986-01-15 | 1987-05-05 | Bonnie Davis | Method of treating Alzheimer's disease |
| GB8608335D0 (en) * | 1986-04-04 | 1986-05-08 | Pfizer Ltd | Pharmaceutically acceptable salts |
| US4681893A (en) * | 1986-05-30 | 1987-07-21 | Warner-Lambert Company | Trans-6-[2-(3- or 4-carboxamido-substituted pyrrol-1-yl)alkyl]-4-hydroxypyran-2-one inhibitors of cholesterol synthesis |
| US4808621A (en) | 1986-07-07 | 1989-02-28 | Warner-Lambert Company | Trans-6-[2-(N-heteroaryl-3,5-disubstituted)pyrazol-4-yl)-ethyl]- or ethenyl]tetrahydro-4-hydroxypyran-2-one inhibitors of cholesterol biosynthesis |
| US4957971A (en) * | 1986-07-07 | 1990-09-18 | Warner-Lambert Company | Trans-6-(2-(N-heteroaryl-3,5-disubstituted)pyrazol-4-yl)-ethyl)-or ethenyl)tetrahydro-4-hydroxypyran-2-one inhibitors of cholesterol biosynthesis |
| DE3762617D1 (de) * | 1986-09-11 | 1990-06-13 | Nat Res Dev | Tamoxifenderivate. |
| US4816456A (en) * | 1986-10-01 | 1989-03-28 | Summers William K | Administration of monoamine acridines in cholinergic neuronal deficit states |
| FI95572C (fi) * | 1987-06-22 | 1996-02-26 | Eisai Co Ltd | Menetelmä lääkeaineena käyttökelpoisen piperidiinijohdannaisten tai sen farmaseuttisen suolan valmistamiseksi |
| US5192772A (en) * | 1987-12-09 | 1993-03-09 | Nippon Shinyaku Co. Ltd. | Therapeutic agents |
| NO177005C (no) * | 1988-01-20 | 1995-07-05 | Bayer Ag | Analogifremgangsmåte for fremstilling av substituerte pyridiner, samt mellomprodukter til bruk ved fremstillingen |
| EP0344383A1 (fr) * | 1988-06-02 | 1989-12-06 | Merrell Dow Pharmaceuticals Inc. | Inhibiteurs d'alpha-glucosidase |
| DE3836675A1 (de) * | 1988-10-28 | 1990-05-03 | Hoechst Ag | Glykosidase-inhibitor salbostatin, verfahren zu seiner herstellung und seine verwendung |
| DE3918364A1 (de) | 1989-06-06 | 1990-12-13 | Hoechst Ag | 3-desmethyl-2-methyl-mevalonsaeurederivate, verfahren zu ihrer herstellung, ihre verwendung als arzneimittel, sowie zwischenprodukte |
| US5185351A (en) * | 1989-06-14 | 1993-02-09 | Smithkline Beecham Corporation | Imidazolyl-alkenoic acids useful as angiotensin II receptor antagonists |
| FI94339C (fi) * | 1989-07-21 | 1995-08-25 | Warner Lambert Co | Menetelmä farmaseuttisesti käyttökelpoisen /R-(R*,R*)/-2-(4-fluorifenyyli)- , -dihydroksi-5-(1-metyylietyyli)-3-fenyyli-4-/(fenyyliamino)karbonyyli/-1H-pyrroli-1-heptaanihapon ja sen farmaseuttisesti hyväksyttävien suolojen valmistamiseksi |
| US5391571A (en) * | 1989-11-15 | 1995-02-21 | American Home Products Corporation | Cholesterol ester hydrolase inhibitors |
| IT1237793B (it) * | 1989-12-21 | 1993-06-17 | Zambon Spa | Composti attivi come inibitori dell'enzima hmg-coa reduttasi |
| US5196444A (en) * | 1990-04-27 | 1993-03-23 | Takeda Chemical Industries, Ltd. | 1-(cyclohexyloxycarbonyloxy)ethyl 2-ethoxy-1-[[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl]benzimidazole-7-carboxylate and compositions and methods of pharmaceutical use thereof |
| US5504078A (en) * | 1990-06-08 | 1996-04-02 | Merrell Dow Pharmaceuticals Inc. | α-glucosidase inhibitors |
| JPH054943A (ja) | 1990-08-30 | 1993-01-14 | Sagami Chem Res Center | 光学活性β,δ−ジケト酸エステル及びその還元体 |
| US5155120A (en) * | 1991-01-14 | 1992-10-13 | Pfizer Inc | Method for treating congestive heart failure |
| US5274143A (en) * | 1991-07-23 | 1993-12-28 | Hoffmann-La Roche Inc. | Process for the preparation of (R)-3-hexyl-5,6-dihydro-4-hydroxy-6-undecyl-2H-pyran-2-one and (R)-5,6-dihydro-6-undecyl-2H-pyran-2,4(3H)-dione |
| CA2098167C (fr) * | 1992-06-24 | 2006-12-19 | Dorothea Isler | Aliments pour humains et animaux contenant un inhibiteur de la lipase |
| US5629295A (en) | 1992-06-26 | 1997-05-13 | Pfizer Inc. | Steroidal glycosides for treating hypercholesterolemia |
| US5284971A (en) * | 1992-07-16 | 1994-02-08 | Syntex (U.S.A.) Inc. | 4-(3-cyclohexyl-4-hydroxy or-methoxy phenylsulfonyl) 3,5 dibromo phenyl acetic thyromimetic cholesterol-lowering agents |
| DE69314718T2 (de) * | 1992-07-21 | 1998-02-26 | Ciba Geigy Ag | Oxamidsäure-Derivate als hypocholesterämische Mittel |
| US5728704A (en) * | 1992-09-28 | 1998-03-17 | Pfizer Inc. | Substituted pyridmidines for control of diabetic complications |
| DE4243279A1 (de) | 1992-12-21 | 1994-06-23 | Bayer Ag | Substituierte Triole |
| TW381025B (en) * | 1993-08-05 | 2000-02-01 | Hoffmann La Roche | Pharmaceutical composition containing a glucosidase inhibitor and a lipase inhibitor |
| US6756388B1 (en) | 1993-10-12 | 2004-06-29 | Pfizer Inc. | Benzothiophenes and related compounds as estrogen agonists |
| US7501441B1 (en) * | 1994-09-20 | 2009-03-10 | Eli Lilly And Company | Naphthyl compounds, intermediates, processes, compositions, and methods |
| KR970706242A (ko) | 1994-10-04 | 1997-11-03 | 후지야마 아키라 | 우레아 유도체 및 ACAT-억제제로서 그의 용도(Urea derivatives and their use as ACAT-inhibitors) |
| JPH08143457A (ja) | 1994-11-21 | 1996-06-04 | Microbial Chem Res Found | 酵素阻害剤および高脂血症抑制剤 |
| US5510379A (en) * | 1994-12-19 | 1996-04-23 | Warner-Lambert Company | Sulfonate ACAT inhibitors |
| US5552412A (en) * | 1995-01-09 | 1996-09-03 | Pfizer Inc | 5-substitued-6-cyclic-5,6,7,8-tetrahydronaphthalen2-ol compounds which are useful for treating osteoporosis |
| US5510357A (en) * | 1995-02-28 | 1996-04-23 | Eli Lilly And Company | Benzothiophene compounds as anti-estrogenic agents |
| GB9504066D0 (en) | 1995-03-01 | 1995-04-19 | Pharmacia Spa | Phosphate derivatives of ureas and thioureas |
| FI974437A7 (fi) | 1995-06-06 | 1997-12-05 | Pfizer | Substituoituja N-(indoli-2-karbonyyli)amideja ja johdannaisia glykogee nifosforylaasi-inhibiittoreina |
| DE69523182T2 (de) | 1995-06-06 | 2002-02-07 | Pfizer | Substituierte n-(indol-2-carbonyl)-glycinamide und derivate als glycogen phosphorylase inhibitoren |
| WO1996040640A1 (fr) | 1995-06-07 | 1996-12-19 | Pfizer Inc. | DERIVES DE BIPHENYL-2-ACIDE CARBOXYLIQUE-TETRAHYDRO-ISOQUINOLEINE-6-YL AMIDES, PREPARATION DE CES AMIDES ET UTILISATION EN TANT QU'INHIBITEURS DE LA PROTEINE DE TRANSFERT DE TRIGLYCERIDE MICROSOMAL ET/OU DE LA SECRETION D'APOLIPOPROTEINES B (Apo B) |
| GEP20002029B (en) * | 1995-07-17 | 2000-04-10 | Warner Lambert Company Us | (54) Crystalline [R-(R*,R*,]–2-(4-Fluorophenyl)-Beta,Delta-Dihydroxy-5-(1-Methyl-Ethyl)-3-Phenyl–4-{Phenylamino) Carbonyl} - 1H - Pyrrole - 1 - Heptanoic Acid Hemi Calcium Salt (Atorvastatin) |
| JPH09173638A (ja) * | 1995-12-25 | 1997-07-08 | Hudson Soft Co Ltd | 相対時間による派生シナリオ起動方法 |
| TW513409B (en) * | 1996-06-07 | 2002-12-11 | Eisai Co Ltd | Polymorphs of donepezil hydrochloride |
| WO1997046526A1 (fr) * | 1996-06-07 | 1997-12-11 | Eisai Co., Ltd. | Polymorphes stables d'hydrochlorure de 1-benzyl-4-[(5,6-dimethoxy-1-indanon)-2-yl]methyl-piperidine), dit hydrochlorure de donepezil et procede pour leur production |
| TW506836B (en) * | 1996-06-14 | 2002-10-21 | Janssen Pharmaceutica Nv | Fast-dissolving galanthamine hydrobromide tablet |
| JPH10310578A (ja) * | 1996-11-13 | 1998-11-24 | Yoshitomi Pharmaceut Ind Ltd | 3−フェニルピラゾール化合物 |
| EA001539B1 (ru) | 1996-11-27 | 2001-04-23 | Пфайзер Инк. | Амиды, ингибирующие секрецию аполипопротеина в (аро в) и/или микросомного протеина переноса триглицеридов (мтр) |
| PE107899A1 (es) | 1997-09-09 | 1999-11-17 | Glaxo Group Ltd | Derivados de pirrolopirrolona como inhibidores de elastasa leucocitaria |
| ES2218869T3 (es) * | 1997-12-05 | 2004-11-16 | Eisai Co., Ltd. | Cristales polimorficos de donepezil y un proceso para produccion de dichos cristales. |
| EP1054860B1 (fr) | 1997-12-19 | 2007-04-25 | Pfizer Ireland Pharmaceuticals | Procede de synthese de 1,3-diols |
| PA8471201A1 (es) * | 1998-06-16 | 2000-09-29 | Pfizer Prod Inc | Combinaciones terapeuticas que comprenden un modulador del receptor de estrogenos selectivo y hormona paratiroidea |
| GT199900147A (es) * | 1998-09-17 | 1999-09-06 | 1, 2, 3, 4- tetrahidroquinolinas 2-sustituidas 4-amino sustituidas. | |
| US6197786B1 (en) * | 1998-09-17 | 2001-03-06 | Pfizer Inc | 4-Carboxyamino-2-substituted-1,2,3,4-tetrahydroquinolines |
| ATE254928T1 (de) * | 1999-03-31 | 2003-12-15 | Eisai Co Ltd | Stabilisierte zusammensetzung mit nootropen wirkstoffen |
| GB9914977D0 (en) * | 1999-06-25 | 1999-08-25 | Glaxo Group Ltd | Chemical compounds |
| US6479552B2 (en) * | 1999-09-23 | 2002-11-12 | G.D. Searle & Co. | Use of substituted N, N-disubstituted diamino compounds for inhibiting cholesteryl ester transfer protein activity |
| US6683113B2 (en) * | 1999-09-23 | 2004-01-27 | Pharmacia Corporation | (R)-chiral halogenated substituted N,N-Bis-benzyl aminioalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity |
| US20030171377A1 (en) * | 2001-08-29 | 2003-09-11 | Bigge Christopher Franklin | Antidiabetic agents |
| US6875780B2 (en) * | 2002-04-05 | 2005-04-05 | Warner-Lambert Company | Compounds that modulate PPAR activity and methods for their preparation |
| PT1567493E (pt) * | 2002-11-26 | 2009-04-09 | Pfizer Prod Inc | Activadores de ppar |
| WO2004056359A1 (fr) * | 2002-12-20 | 2004-07-08 | Pfizer Products Inc. | Formes posologiques comprenant un inhibiteur de la cetp et un inhibiteur de la hmg-coa reductase |
| US7250444B2 (en) * | 2003-08-11 | 2007-07-31 | Pfizer Inc. | Pyrrole-based HMG-CoA reductase inhibitors |
| KR20060133013A (ko) * | 2004-04-16 | 2006-12-22 | 워너-램버트 캄파니 엘엘씨 | 신규 이미다졸 |
| AP2007003979A0 (en) * | 2004-11-23 | 2007-06-30 | Warner Lambert Co | 7-(2h-pyrazol-3-yl)-3,5-dihyroxy-heptanoic acid derivatives as hmg co-a reductase inhibitors for thetreatment of lipidemia |
-
2005
- 2005-11-14 AP AP2007003979A patent/AP2007003979A0/xx unknown
- 2005-11-14 EP EP05801166A patent/EP1819681B1/fr not_active Expired - Lifetime
- 2005-11-14 DE DE602005016009T patent/DE602005016009D1/de not_active Expired - Lifetime
- 2005-11-14 WO PCT/IB2005/003461 patent/WO2006056845A1/fr not_active Ceased
- 2005-11-14 KR KR1020077011587A patent/KR20070084455A/ko not_active Ceased
- 2005-11-14 EA EA200700875A patent/EA200700875A1/ru unknown
- 2005-11-14 BR BRPI0518300-6A patent/BRPI0518300A2/pt not_active Application Discontinuation
- 2005-11-14 ES ES05801166T patent/ES2328384T3/es not_active Expired - Lifetime
- 2005-11-14 AU AU2005308575A patent/AU2005308575A1/en not_active Abandoned
- 2005-11-14 JP JP2007542152A patent/JP2008520642A/ja active Pending
- 2005-11-14 CA CA2590533A patent/CA2590533C/fr not_active Expired - Fee Related
- 2005-11-14 AT AT05801166T patent/ATE439347T1/de not_active IP Right Cessation
- 2005-11-14 MX MX2007005137A patent/MX2007005137A/es not_active Application Discontinuation
- 2005-11-18 US US11/283,264 patent/US7446121B2/en not_active Expired - Fee Related
- 2005-11-21 AR ARP050104871A patent/AR052244A1/es unknown
- 2005-11-21 UY UY29220A patent/UY29220A1/es not_active Application Discontinuation
- 2005-11-21 PE PE2005001361A patent/PE20061057A1/es not_active Application Discontinuation
- 2005-11-22 NL NL1030487A patent/NL1030487C2/nl not_active IP Right Cessation
- 2005-11-22 TW TW094140920A patent/TW200626556A/zh unknown
- 2005-11-22 GT GT200500338A patent/GT200500338A/es unknown
- 2005-11-23 PA PA20058653401A patent/PA8653401A1/es unknown
-
2007
- 2007-04-16 IL IL182569A patent/IL182569A0/en unknown
- 2007-05-03 CR CR9102A patent/CR9102A/es not_active Application Discontinuation
- 2007-05-22 TN TNP2007000202A patent/TNSN07202A1/fr unknown
- 2007-05-23 MA MA29934A patent/MA30108B1/fr unknown
-
2008
- 2008-10-08 US US12/247,434 patent/US20090170852A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| WO2006056845A1 (fr) | 2006-06-01 |
| DE602005016009D1 (de) | 2009-09-24 |
| ES2328384T3 (es) | 2009-11-12 |
| IL182569A0 (en) | 2007-07-24 |
| TW200626556A (en) | 2006-08-01 |
| KR20070084455A (ko) | 2007-08-24 |
| EP1819681A1 (fr) | 2007-08-22 |
| CA2590533C (fr) | 2010-09-07 |
| AP2007003979A0 (en) | 2007-06-30 |
| PA8653401A1 (es) | 2006-09-08 |
| MA30108B1 (fr) | 2009-01-02 |
| US20060111422A1 (en) | 2006-05-25 |
| PE20061057A1 (es) | 2006-11-09 |
| MX2007005137A (es) | 2007-06-22 |
| US7446121B2 (en) | 2008-11-04 |
| CR9102A (es) | 2007-05-30 |
| AU2005308575A1 (en) | 2006-06-01 |
| BRPI0518300A2 (pt) | 2008-11-11 |
| AR052244A1 (es) | 2007-03-07 |
| NL1030487A1 (nl) | 2006-05-24 |
| ATE439347T1 (de) | 2009-08-15 |
| JP2008520642A (ja) | 2008-06-19 |
| UY29220A1 (es) | 2006-06-30 |
| GT200500338A (es) | 2006-06-22 |
| EA200700875A1 (ru) | 2007-12-28 |
| US20090170852A1 (en) | 2009-07-02 |
| NL1030487C2 (nl) | 2007-01-08 |
| EP1819681B1 (fr) | 2009-08-12 |
| CA2590533A1 (fr) | 2006-06-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| TNSN07202A1 (fr) | Derives d'acide 7-(2h-pyrazole-3-yl)-3, 5-dihyroxy heptanoique servant d'inhibiteurs de hmg-co a reductase pour le traitement de la lipidemie | |
| AP804A (en) | APO-B-secretion/MTP inhibitory amides. | |
| TW200519088A (en) | Aryl or heteroaryl amide compounds | |
| WO2005105732A8 (fr) | Composes methylaryl- ou heteroarylamides substitues | |
| FR2954317A1 (fr) | Nouveaux derives phenoliques, et leur utilisation pharmaceutique ou cosmetique | |
| DE69520502D1 (de) | (azetidinyl-1-ylalkyl)lactame und zwischenprodukte als tachykinin antagonisten | |
| MY123062A (en) | Organometallic addition to ketones | |
| CA2481461A1 (fr) | Derives de n-[phenyl(piperidin-2-yl) methyl] benzamide, leur preparation et leur application en therapeutique | |
| YU34796A (sh) | Supstituisani n(indol-2-karbonil) гћві -alaninamid, njihovi derivati i farmaceutske smeše koje ih sadrže | |
| GB2401606A (en) | Pyranones useful as atm inhibitors | |
| MA26983A1 (fr) | Derives biaryliques de nicotinamide utiles comme inhibiteurs d'iso-enzymes pde4 | |
| ZA200607542B (en) | MTP inhibiting aryl piperidines or piperazines substituted with 5-membered heterocycles | |
| GB9900339D0 (en) | Chemical compounds | |
| TNSN06360A1 (fr) | 4-phenylamino-quinazoline-6-yl-amides | |
| CA2621040C (fr) | Derives de 4-phenyl-6-substitue-pyrimidine-2-carbonitrile | |
| HRP20090474T1 (hr) | Postupak i intermedijeri za sintezu kaspofungina | |
| HUP0203526A2 (hu) | D4-antagonistákként alkalmazható tienoizoxazolil- és tienilpirazolil-fenoxi-helyettesített propilszármazékok, eljárás az előállításukra és ezeket tartalmazó gyógyszerkészítmények | |
| DK1694641T3 (da) | Prostaglandinsyntese | |
| DE69612967D1 (en) | Optisch aktive thiazolidinonderivate | |
| RU2384573C2 (ru) | Пиразол- и фенилпроизводные в качестве ингибиторов ppar | |
| DK0854866T3 (da) | Fremgangsmåde til fremstilling af 2-(pyrid-2-yloxymethyl)-phenylacetater som pesticidmellemprodukter | |
| EP2516400A1 (fr) | Dérivés phénoliques, et leur utilisation pharmaceutique ou cosmétique | |
| HRP20020347B1 (en) | Phenyl-and pyridyl-tetrahydro-pyridines having tnf inhibiting activity | |
| AU6506894A (en) | Perhydroisoindole derivatives, preparation thereof and pharmaceutical compositions containing same | |
| Petrini et al. | α-Amido sulfones from natural α-amino acids and their reaction with carbon nucleophiles |