AR016108A1 - Un derivado de bencimidazol y una composicion farmaceutica que lo contiene. - Google Patents
Un derivado de bencimidazol y una composicion farmaceutica que lo contiene.Info
- Publication number
- AR016108A1 AR016108A1 ARP980103128A ARP980103128A AR016108A1 AR 016108 A1 AR016108 A1 AR 016108A1 AR P980103128 A ARP980103128 A AR P980103128A AR P980103128 A ARP980103128 A AR P980103128A AR 016108 A1 AR016108 A1 AR 016108A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- aromatic
- alkyl
- alkenyl
- alkyloxy
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 11
- 125000000217 alkyl group Chemical group 0.000 abstract 7
- 125000003342 alkenyl group Chemical group 0.000 abstract 5
- 125000003545 alkoxy group Chemical group 0.000 abstract 5
- 125000004414 alkyl thio group Chemical group 0.000 abstract 2
- 125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 abstract 2
- 101150085511 PEDS1 gene Proteins 0.000 abstract 1
- 102100037592 Plasmanylethanolamine desaturase Human genes 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 239000008280 blood Substances 0.000 abstract 1
- 210000004369 blood Anatomy 0.000 abstract 1
- 238000004132 cross linking Methods 0.000 abstract 1
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 230000000994 depressogenic effect Effects 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 229920003199 poly(diethylsiloxane) Polymers 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D235/08—Radicals containing only hydrogen and carbon atoms
-
- 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
- C07D405/10—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 aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Diabetes (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Un derivado de benzimidazol, representado por la siguiente formula (I), o una sal del mismo: I donde R1 representa un átomo de hidrogeno, un grupo alquiloinferior, un grupo alcoxi inferior, o un grupo alquiltio inferior; R2 representa un grupo alquilo inferior aromático, que puede estar sustituido con uno o másgrupos seleccionados entre un átomo de halogeno, un grupo alquilo, un grupo haloalquilo inferior, un grupo nitro, un grupo alcoxicarbonilo inferior, un grupoaromático, un grupo alquiloxiinferior aromático, un grupo alquilo inferior cicloalquiloxi inferior, un grupo alquilo inferior aromático, un grupo alqueniloinferior aromático, un grupo alquinilo inferior aromático, un grupo alquiloxi inferior aromático, un grupo alquiloxi inferior cicloalquilo inferior, un grupoalquenilo, un grupo alcoxi inferior, un grupo alquiltio inferior, un grupo alcansulfinilo inferior, un grupo alcansulfonilo inferior, y un grupoalcansulfonilcarbamoilo inferior; R3 representa un grupo alquilo, un grupo hidroxialquilo inferior, un grupo alquenilo, un grupo aromático, un grupo aromáticohalogenado, un grupo aromático alquilo inferior, un grupo alquenilo inferior aromático, un grupo alquilo inferior aromático o un grupo alquenilo inferioraromático;y -X- es un grupo de entrecruzamiento representado por cualquiera de las siguientes formulas II a VI; composicion farmacéutica que comprende elderivado de bencimidazol que posee actividad depresora del nivel de azucar sanguíneo o actividad inhibidorade la PDES.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18769697 | 1997-06-27 | ||
| JP7635798 | 1998-03-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR016108A1 true AR016108A1 (es) | 2001-06-20 |
Family
ID=26417500
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP980103128A AR016108A1 (es) | 1997-06-27 | 1998-06-26 | Un derivado de bencimidazol y una composicion farmaceutica que lo contiene. |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US6420409B1 (es) |
| EP (1) | EP1020452A4 (es) |
| KR (1) | KR20010014166A (es) |
| CN (1) | CN1135224C (es) |
| AR (1) | AR016108A1 (es) |
| AU (1) | AU748541B2 (es) |
| BR (1) | BR9811273A (es) |
| CA (1) | CA2294505A1 (es) |
| HU (1) | HUP0002324A3 (es) |
| IL (1) | IL133674A0 (es) |
| RU (1) | RU2243968C2 (es) |
| TR (1) | TR199903277T2 (es) |
| TW (1) | TW453999B (es) |
| WO (1) | WO1999000373A1 (es) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR9810456A (pt) * | 1997-06-27 | 2001-09-25 | Fujisawa Pharmaceutical Co | Composto de sulfonamida, método para sua obtenção e seu uso farmacêutico |
| EP1070705A4 (en) * | 1998-04-06 | 2002-04-17 | Fujisawa Pharmaceutical Co | INDOLE DERIVATIVES |
| EP1132087A4 (en) * | 1998-11-13 | 2002-06-26 | Fujisawa Pharmaceutical Co | REMEDIES FOR POLYKYSTIC OVARY SYNDROME |
| US6869950B1 (en) * | 1998-12-24 | 2005-03-22 | Fujisawa Pharmaceutical Co., Ltd. | Benzimidazole derivatives |
| US6432989B1 (en) | 1999-08-27 | 2002-08-13 | Pfizer Inc | Use of CRF antagonists to treat circadian rhythm disorders |
| US6525067B1 (en) | 1999-11-23 | 2003-02-25 | Pfizer Inc | Substituted heterocyclic derivatives |
| EP1149583A3 (en) * | 2000-04-13 | 2001-11-14 | Pfizer Products Inc. | Combinations of corticotropin releasing factor antagonists and growth hormone secretagogues |
| US6821978B2 (en) | 2000-09-19 | 2004-11-23 | Schering Corporation | Xanthine phosphodiesterase V inhibitors |
| US6943171B2 (en) | 2001-11-09 | 2005-09-13 | Schering Corporation | Polycyclic guanine derivative phosphodiesterase V inhibitors |
| CA2468827A1 (en) * | 2001-12-03 | 2003-06-12 | Takeda Chemical Industries, Ltd. | Insulin resistance improving agents |
| FR2833948B1 (fr) * | 2001-12-21 | 2004-02-06 | Sod Conseils Rech Applic | Nouveaux derives de benzimidazole et leur utilisation en tant que medicament |
| US20030181461A1 (en) * | 2002-01-25 | 2003-09-25 | Lautt Wilfred Wayne | Use of phosphodiesterase antagonists to treat insulin resistance |
| NZ560368A (en) * | 2002-05-03 | 2008-11-28 | Israel Inst Biolog Res | Methods and compostions for treatment of central and peripheral nervous system disorders and novel compounds useful therefor |
| AU2003902860A0 (en) * | 2003-06-06 | 2003-06-26 | Daicel Chemical Industries, Ltd | Benzimidazole compounds |
| SE0302573D0 (sv) * | 2003-09-26 | 2003-09-26 | Astrazeneca Ab | Benzimidazole derivatives, compositions containing them, preparation thereof and uses thereof |
| GB0400781D0 (en) * | 2004-01-14 | 2004-02-18 | Novartis Ag | Organic compounds |
| TW200533336A (en) * | 2004-03-02 | 2005-10-16 | Fujisawa Pharmaceutical Co | Concomitant drugs |
| US20070232673A1 (en) * | 2006-01-19 | 2007-10-04 | Roth Gregory P | 2-Imino-benzimidazoles |
| WO2011063339A1 (en) * | 2009-11-23 | 2011-05-26 | Cardioxyl Pharmaceuticals, Inc. | Nitroxyl donors for the treatment of pulmonary hypertension |
| AU2010328230B2 (en) | 2009-12-07 | 2016-06-02 | Cardioxyl Pharmaceuticals, Inc. | Bis-acylated hydroxylamine derivatives |
| US20110144067A1 (en) * | 2009-12-07 | 2011-06-16 | Toscano John P | N-Acyloxysulfonamide and N-Hydroxy-N-Acylsulfonamide Derivatives |
| JP5990106B2 (ja) * | 2011-01-28 | 2016-09-07 | 佐藤製薬株式会社 | 縮環化合物 |
| SG11201804359SA (en) * | 2015-12-11 | 2018-06-28 | Teijin Pharma Ltd | Aminoazole derivative |
| WO2017192728A1 (en) | 2016-05-03 | 2017-11-09 | Virginia Commonwealth University | Heteroatom -doped porous carbons for clean energy applications and methods for their synthesis |
| US12234205B1 (en) | 2024-05-22 | 2025-02-25 | King Saud University | Sulfonylhydrazide derivatives as anticancer agents |
Family Cites Families (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE676196C (de) | 1936-08-21 | 1939-05-30 | I G Farbenindustrie Akt Ges | Verfahren zur Herstellung von Imidazolverbindungen |
| US3152142A (en) | 1962-05-24 | 1964-10-06 | Dow Chemical Co | Benzimidazole compounds |
| FR2291749A1 (fr) | 1974-11-20 | 1976-06-18 | Delalande Sa | Nouveaux benzimidazoles acetiques, leur procede de preparation et leur application en therapeutique |
| JPS51133267A (en) | 1975-05-08 | 1976-11-18 | Lilly Co Eli | Substituted 11sulphonyl benzimidazole |
| US4179505A (en) | 1977-03-30 | 1979-12-18 | Janssen Pharmaceutica N.V. | 5-[4-(Diarylmethyl)-1-piperazinylalkyl]benzimidazole derivatives |
| US4243806A (en) | 1979-06-13 | 1981-01-06 | Janssen Pharmaceutica N.V. | 5-[4-(Diarylmethyl)-1-piperazinylalkyl]benzimidazole derivatives |
| GB2053215B (en) | 1979-06-25 | 1983-04-07 | May & Baker Ltd | Benzimidazole derivatives |
| JPS625966A (ja) | 1985-07-03 | 1987-01-12 | Nippon Shinyaku Co Ltd | ベンズイミダゾ−ル誘導体 |
| NZ221729A (en) | 1986-09-15 | 1989-07-27 | Janssen Pharmaceutica Nv | Imidazolyl methyl-substituted benzimidazole derivatives and pharmaceutical compositions |
| ZA899367B (en) * | 1988-12-22 | 1990-08-29 | Yamanouchi Pharma Co Ltd | 4,5,6,7-tetrahydrobenzimidazole derivatives |
| CA2004911A1 (en) | 1988-12-22 | 1990-06-22 | Mitsuaki Ohta | 4,5,6,7-tetrahydrobenzimidazole derivatives |
| DE3928177A1 (de) * | 1989-04-08 | 1991-02-28 | Thomae Gmbh Dr K | Benzimidazole, diese verbindungen enthaltende arzneimittel und verfahren zu ihrer herstellung |
| AU7759591A (en) | 1990-04-13 | 1991-11-11 | Smithkline Beecham Corporation | Substituted benzimidazoles |
| 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 |
| US5703110A (en) | 1990-04-27 | 1997-12-30 | Takeda Chemical Industries, Ltd. | Benzimidazole derivatives, their production and use |
| DE4023369A1 (de) * | 1990-07-23 | 1992-01-30 | Thomae Gmbh Dr K | Benzimidazole, diese verbindungen enthaltende arzneimittel und verfahren zu ihrer herstellung |
| RU1836357C (ru) | 1990-07-23 | 1993-08-23 | Др.Карл Томэ ГмбХ | Производные бензимидазола, их изомеры, смеси изомеров, гидраты или их физиологически переносимые соли, обладающие антагонистическими в отношении ангиотензина свойствами |
| PT98674B (pt) * | 1990-08-15 | 1999-01-29 | British Bio Technology | Processo para a preparacao de compostos que sao antagonistas do factor de activacao de plaquetas por exemplo derivados de imidazole e de seus intermedriarios |
| US5614519A (en) | 1991-02-06 | 1997-03-25 | Karl Thomae Gmbh | (1-(2,3 or 4-N-morpholinoalkyl)-imidazol-4-yl)-benizimidazol-1-yl-methyl]-biphenyls useful as angiotensin-II antagonists |
| US5594003A (en) | 1991-02-06 | 1997-01-14 | Dr. Karl Thomae Gmbh | Tetrahydroimidazo[1,2-a]pyridin-2-yl-(benzimidazol-1-yl)-methyl-biphenyls useful as angiotensin-II antagonists |
| SI9210098B (sl) | 1991-02-06 | 2000-06-30 | Dr. Karl Thomae | Benzimidazoli, zdravila, ki te spojine vsebujejo, in postopek za njihovo pripravo |
| US5602127A (en) | 1991-02-06 | 1997-02-11 | Karl Thomae Gmbh | (Alkanesultam-1-yl)-benzimidazol-1-yl)-1yl)-methyl-biphenyls useful as angiotensin-II antagonists |
| DE4224133A1 (de) * | 1992-07-22 | 1994-01-27 | Thomae Gmbh Dr K | Benzimidazole, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung |
| US5407835A (en) | 1991-07-31 | 1995-04-18 | Abbott Laboratories | Reagents and methods for the quantification of amitriptyline or nortriptyline in biological fluids |
| GB9121776D0 (en) | 1991-10-14 | 1991-11-27 | Fujisawa Pharmaceutical Co | Benzimidazole derivatives and process for preparation thereof |
| DE4237557A1 (de) | 1992-11-06 | 1994-05-11 | Bayer Ag | Substituierte Benzimidazole |
| JPH0853424A (ja) | 1994-08-11 | 1996-02-27 | Kureha Chem Ind Co Ltd | ベンズイミダゾールスルホン酸アミド誘導体 |
| GB9423910D0 (en) | 1994-11-26 | 1995-01-11 | Pfizer Ltd | Therapeutic agents |
| DK0882718T3 (da) | 1995-12-28 | 2005-12-12 | Astellas Pharma Inc | Benzimidazolderivater |
-
1998
- 1998-06-25 TW TW087110304A patent/TW453999B/zh not_active IP Right Cessation
- 1998-06-26 EP EP98929723A patent/EP1020452A4/en not_active Withdrawn
- 1998-06-26 BR BR9811273-2A patent/BR9811273A/pt not_active IP Right Cessation
- 1998-06-26 WO PCT/JP1998/002885 patent/WO1999000373A1/ja not_active Ceased
- 1998-06-26 US US09/446,749 patent/US6420409B1/en not_active Expired - Fee Related
- 1998-06-26 RU RU2000101811/04A patent/RU2243968C2/ru not_active IP Right Cessation
- 1998-06-26 CA CA002294505A patent/CA2294505A1/en not_active Abandoned
- 1998-06-26 TR TR1999/03277T patent/TR199903277T2/xx unknown
- 1998-06-26 HU HU0002324A patent/HUP0002324A3/hu unknown
- 1998-06-26 AU AU79346/98A patent/AU748541B2/en not_active Ceased
- 1998-06-26 IL IL13367498A patent/IL133674A0/xx unknown
- 1998-06-26 KR KR1019997012237A patent/KR20010014166A/ko not_active Withdrawn
- 1998-06-26 CN CNB988085798A patent/CN1135224C/zh not_active Expired - Fee Related
- 1998-06-26 AR ARP980103128A patent/AR016108A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU7934698A (en) | 1999-01-19 |
| BR9811273A (pt) | 2000-07-18 |
| US6420409B1 (en) | 2002-07-16 |
| HUP0002324A3 (en) | 2001-07-30 |
| EP1020452A1 (en) | 2000-07-19 |
| KR20010014166A (ko) | 2001-02-26 |
| CA2294505A1 (en) | 1999-01-07 |
| EP1020452A4 (en) | 2003-04-02 |
| WO1999000373A1 (en) | 1999-01-07 |
| CN1268123A (zh) | 2000-09-27 |
| HUP0002324A2 (hu) | 2001-05-28 |
| AU748541B2 (en) | 2002-06-06 |
| IL133674A0 (en) | 2001-04-30 |
| HK1028246A1 (en) | 2001-02-09 |
| RU2243968C2 (ru) | 2005-01-10 |
| TR199903277T2 (xx) | 2000-07-21 |
| WO1999000373A8 (en) | 2000-07-20 |
| TW453999B (en) | 2001-09-11 |
| CN1135224C (zh) | 2004-01-21 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FB | Suspension of granting procedure |