AR016510A1 - Derivados arilalquilaminicos calciliticos, una composicion farmaceutica que los comprende y el uso de dichos derivados para la manufactura de unmedicamento - Google Patents
Derivados arilalquilaminicos calciliticos, una composicion farmaceutica que los comprende y el uso de dichos derivados para la manufactura de unmedicamentoInfo
- Publication number
- AR016510A1 AR016510A1 ARP980101562A ARP980101562A AR016510A1 AR 016510 A1 AR016510 A1 AR 016510A1 AR P980101562 A ARP980101562 A AR P980101562A AR P980101562 A ARP980101562 A AR P980101562A AR 016510 A1 AR016510 A1 AR 016510A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- group
- substituted
- cycloalkyl
- ocf3
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
- C07C255/06—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms of an acyclic and unsaturated carbon skeleton
- C07C255/07—Mononitriles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/192—Radicals derived from carboxylic acids from aromatic carboxylic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
-
- 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
-
- 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
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/12—Drugs for disorders of the metabolism for electrolyte homeostasis
- A61P3/14—Drugs for disorders of the metabolism for electrolyte homeostasis for calcium homeostasis
-
- 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
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/18—Drugs for disorders of the endocrine system of the parathyroid hormones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/49—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C255/57—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and carboxyl groups, other than cyano groups, bound to the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C311/08—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
- C07C311/21—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/22—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms
- C07C311/29—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/10—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C323/17—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and singly-bound oxygen atoms bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a ring other than a six-membered aromatic ring of the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D267/00—Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D267/02—Seven-membered rings
- C07D267/08—Seven-membered rings having the hetero atoms in positions 1 and 4
- C07D267/12—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D267/16—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems condensed with two six-membered rings
- C07D267/20—[b, f]-condensed
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/20—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
- C07D295/215—Radicals derived from nitrogen analogues of carbonic acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
- C07C2603/30—Ortho- or ortho- and peri-condensed systems containing three rings containing seven-membered rings
- C07C2603/32—Dibenzocycloheptenes; Hydrogenated dibenzocycloheptenes
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Physical Education & Sports Medicine (AREA)
- Engineering & Computer Science (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Endocrinology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Immunology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Pyridine Compounds (AREA)
- Medicines Containing Plant Substances (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Derivados arilalquilamínicos calcilíticos caracterizados porque comprenden un compuesto segun la formula (I) en la que: Y1 es un enlace covalente,alquilenoo alquenileno de hasta 4 átomos de C, no sustituido o sustituido con alquilo C1-4; Y2 esmetile no, no sustituido o sustituido con alquilo C1-4 o CF3; Zse selecciona del grupo formado por un enlace covalente, O, S, NH, N-alquilo C1-4, O(CH2)n, (CH2)nO, NRC=O y C=ONR, donde R es alquilo C1-4 y n es unnumero entero de 1 a 3; R3 y R4 son,independ ientemente, metilo o etilo, o juntos forman ciclopropilo; R5 es fenilo o naftilo, no sustituido o sustituido conuno o más sustituyentes seleccionados del grupo formado por OH, alquilo C1-4, CH(CH3)2, halo, halo-alquilo C1-4, alcoxi C1-4,cicloalquilo C3-6, OSO2RIV, CN,NO2, OCF3, CF3 y CH2CF3, donde RIV representa alquilo C1-4 o cicloalquilo C3-6; G es un enlace covalente o C-R6, donde R6 es H, OH u O (formando un restocarbonilo); R7 es H, OH u O-alquilo C1-4; R8 es H o alquilo C1-4;o R7 y R8 ju ntos forman un resto carbonilo; el resto -A-B- representa CH2CH2, un enlacecovalente, -CH=CH- o -C:::C-;y X se selecciona del grupo formado por las subformulas (Ia) a (Ie) donde:en la subformula (Ia): W se selecciona del grupoformadopor R1, SO2R1, C (O)R1, SO2NR1R1, C(O)NR1R1, C(O)OR1SO3R1, donde R1 y R1 se seleccionan independientemente del grupo formado por hidrogeno, alquilo C1-4,cicloalquilo C3-6, alquenilo C2-5, alquinilo C2-5, heterocicloalquilarilo y aril-alquiloC1-4; o R1 y R1 juntos fo rman un anillo heterocíclico de 3 a 7miembros, opcionalmente sustituido; donde cualquier sustituyente se selcciona del grupo formado por CN, arilo, CO2R, CO2NHR, OH, OR, NH2, halo, CF3, OCF3 yNO2, donde R representa alquiloC1-4 o cicloalquilo C3-6; X1 se selecciona del grupo formado por CN, NO2, Cl, F, Br, I, H, R, OR, CF3, OCF3 y OSO2R, dondeR representa alquilo C1-4 o cicloalquilo C3-6; X2, X3 y X4, independientemente, se seleccionan del grupo formado por CN, NO2,Cl, F, Br, I, H, R, OR, CF3, OCF3 o OSO2R, donde R representa alquilo o haloalquilo C1-4; o X1 y X2 juntos forman un anillo arílico o heteroarílico, sustituido o no sustituido; donde
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US4272497P | 1997-04-08 | 1997-04-08 | |
US6133397P | 1997-10-08 | 1997-10-08 | |
US6133097P | 1997-10-08 | 1997-10-08 | |
US6132797P | 1997-10-08 | 1997-10-08 | |
US6133197P | 1997-10-08 | 1997-10-08 | |
US6132997P | 1997-10-08 | 1997-10-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR016510A1 true AR016510A1 (es) | 2001-07-25 |
Family
ID=27556439
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP980101562A AR016510A1 (es) | 1997-04-08 | 1998-04-08 | Derivados arilalquilaminicos calciliticos, una composicion farmaceutica que los comprende y el uso de dichos derivados para la manufactura de unmedicamento |
Country Status (24)
Country | Link |
---|---|
US (1) | US6294531B1 (es) |
EP (1) | EP0973730B1 (es) |
JP (1) | JP2001523223A (es) |
KR (1) | KR20010006113A (es) |
CN (1) | CN1259120A (es) |
AR (1) | AR016510A1 (es) |
AT (1) | ATE269300T1 (es) |
AU (1) | AU721910B2 (es) |
BR (1) | BR9808491A (es) |
CA (1) | CA2286454A1 (es) |
CO (1) | CO4950536A1 (es) |
DE (1) | DE69824566T2 (es) |
DZ (1) | DZ2461A1 (es) |
ES (1) | ES2223126T3 (es) |
HU (1) | HUP0001494A3 (es) |
IL (1) | IL132205A0 (es) |
NO (1) | NO994877L (es) |
NZ (1) | NZ500055A (es) |
PE (1) | PE69299A1 (es) |
PL (1) | PL336097A1 (es) |
TR (1) | TR199902516T2 (es) |
TW (1) | TW407144B (es) |
UY (1) | UY24949A1 (es) |
WO (1) | WO1998045255A1 (es) |
Families Citing this family (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7202261B2 (en) * | 1996-12-03 | 2007-04-10 | Nps Pharmaceuticals, Inc. | Calcilytic compounds |
AR014975A1 (es) * | 1998-04-08 | 2001-04-11 | Nps Pharma Inc | Compuestos calciliticos, una composicion farmaceutica que los comprende, y el uso de los mismos para la fabricacion de un medicamento |
UA71586C2 (en) * | 1998-12-04 | 2004-12-15 | Smithkline Beecham Corp | A vitronectin receptor antagonist |
PE20001456A1 (es) * | 1999-02-02 | 2001-01-28 | Smithkline Beecham Corp | Compuestos calcioliticos |
AU750584B2 (en) * | 1999-02-17 | 2002-07-25 | Merck & Co., Inc. | Dibenzo-azepine derivatives as alphav integrin receptor antagonists |
JP2001026506A (ja) * | 1999-04-28 | 2001-01-30 | Takeda Chem Ind Ltd | スルホンアミド誘導体 |
US6586617B1 (en) | 1999-04-28 | 2003-07-01 | Sumitomo Chemical Takeda Agro Company, Limited | Sulfonamide derivatives |
AR030684A1 (es) * | 2000-01-24 | 2003-09-03 | Smithkline Beecham Corp | Compuestos calciliticos, uso de dichos compuestos en la manufactura de medicamentos, e intermediarios utiles en la preparacion de dichos compuestos |
US20030018203A1 (en) | 2002-07-17 | 2003-01-23 | Largo Maria Amparo | Calcilytic compounds |
FR2812875B1 (fr) | 2000-08-08 | 2003-12-12 | Centre Nat Rech Scient | Nouvelles diamines possedant une activite modulatrice des casr et leur mode de preparation |
WO2002012189A1 (fr) * | 2000-08-09 | 2002-02-14 | Mitsubishi Pharma Corporation | Composes amide bicycliques condenses et utilisations medicales associees |
AU2001277752A1 (en) | 2000-08-11 | 2002-02-25 | Japan Tobacco Inc. | Calcium receptor antagonists |
AU2002230579A1 (en) * | 2000-10-25 | 2002-05-06 | Smithkline Beecham Corp | Calcilytic compounds |
US7176322B2 (en) | 2002-05-23 | 2007-02-13 | Amgen Inc. | Calcium receptor modulating agents |
US6908935B2 (en) | 2002-05-23 | 2005-06-21 | Amgen Inc. | Calcium receptor modulating agents |
MY143244A (en) | 2002-11-26 | 2011-04-15 | Smithkline Beecham Corp | Calcilytic compounds |
WO2004069793A2 (en) | 2003-01-28 | 2004-08-19 | Bristol-Myers Squibb Company | Novel 2-substituted cyclic amines as calcium sensing receptor modulators |
US7205322B2 (en) | 2003-02-12 | 2007-04-17 | Bristol-Myers Squibb Company | Thiazolidine compounds as calcium sensing receptor modulators |
DK1619180T3 (da) | 2003-04-23 | 2010-03-29 | Japan Tobacco Inc | CaSR-antagonist |
JPWO2004106280A1 (ja) * | 2003-05-28 | 2006-07-20 | 日本たばこ産業株式会社 | CaSRアンタゴニスト |
US7265145B2 (en) | 2003-05-28 | 2007-09-04 | Bristol-Myers Squibb Company | Substituted piperidines and pyrrolidines as calcium sensing receptor modulators and method |
RS52715B (en) | 2005-04-13 | 2013-08-30 | Astex Therapeutics Limited | HYDROXYBENZAMIDE DERIVATIVES AND THEIR APPLICATIONS AS HSP90 INHIBITORS |
WO2007056388A2 (en) * | 2005-11-07 | 2007-05-18 | The General Hospital Corporation | Compositions and methods for modulating poly (adp-ribose) polymerase activity |
US7754725B2 (en) | 2006-03-01 | 2010-07-13 | Astex Therapeutics Ltd. | Dihydroxyphenyl isoindolymethanones |
EP2073802A1 (en) | 2006-10-12 | 2009-07-01 | Astex Therapeutics Limited | Pharmaceutical combinations |
GB0620259D0 (en) | 2006-10-12 | 2006-11-22 | Astex Therapeutics Ltd | Pharmaceutical compounds |
JP5528807B2 (ja) | 2006-10-12 | 2014-06-25 | アステックス、セラピューティックス、リミテッド | 複合薬剤 |
US8916552B2 (en) | 2006-10-12 | 2014-12-23 | Astex Therapeutics Limited | Pharmaceutical combinations |
EP2081891A2 (en) | 2006-10-12 | 2009-07-29 | Astex Therapeutics Limited | Pharmaceutical compounds having hsp90 inhibitory or modulating activity |
JP5518478B2 (ja) | 2006-10-12 | 2014-06-11 | アステックス、セラピューティックス、リミテッド | 医薬化合物 |
BRPI0721700A2 (pt) | 2007-05-29 | 2013-02-13 | Shanghai Inst Materia Medica | usos de compostos heptacÍclicos, os referidos compostos, e composiÇÕes compreendendo os mesmos |
GB0806527D0 (en) | 2008-04-11 | 2008-05-14 | Astex Therapeutics Ltd | Pharmaceutical compounds |
WO2010103429A1 (en) | 2009-03-10 | 2010-09-16 | Pfizer Inc. | 1,1-(Dimethyl-Ethylamino)-2-Hydroxy-Propoxy]-Ethyl}-3-Methyl-Biphenyl-4- Carboxylic Acid Derivatives As Calcium Receptor Antagonists |
GB201217330D0 (en) | 2012-09-28 | 2012-11-14 | Univ Cardiff | Therapeutic for treating inflammatory lung disorders |
CN116574039A (zh) * | 2023-05-17 | 2023-08-11 | 上海大学 | 一种多取代胺基苯甲腈类化合物及其制备方法 |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE298506C (es) | ||||
GB1199632A (en) * | 1967-09-07 | 1970-07-22 | Ici Ltd | Alkanolamine Derivatives |
GB1199037A (en) | 1967-09-27 | 1970-07-15 | Ici Ltd | Alkanolamine Derivatives |
US4165384A (en) | 1974-11-01 | 1979-08-21 | Aktiebolaget Hassle | Amide substituted phenoxy propanol amines |
CA1262729A (en) * | 1983-10-19 | 1989-11-07 | Leo Alig | Phenoxypropanolamines |
US5166218A (en) * | 1983-10-19 | 1992-11-24 | Hoffmann-La Roche Inc. | Phenoxypropanolamines and pharmaceutical compositions thereof |
DD298506A5 (de) * | 1988-12-30 | 1992-02-27 | Ernst-Moritz-Arndt-Universitaet Greifswald,De | Verfahren zur herstellung halogensubstituierter 1-phenoxy-3-alkylamino-propan-2-ole |
DE4017019A1 (de) * | 1990-05-26 | 1991-11-28 | Hoechst Ag | Verwendung von substituierten ss-hydroxyethylaminen als potente hemmstoffe der exoenzyme von pilzen |
EP0901459B1 (en) * | 1996-04-09 | 2005-06-29 | Nps Pharmaceuticals, Inc. | Calcilytic compounds |
-
1998
- 1998-04-03 UY UY24949A patent/UY24949A1/es not_active Application Discontinuation
- 1998-04-05 DZ DZ980071A patent/DZ2461A1/xx active
- 1998-04-06 PE PE1998000256A patent/PE69299A1/es not_active Application Discontinuation
- 1998-04-08 EP EP98914581A patent/EP0973730B1/en not_active Expired - Lifetime
- 1998-04-08 TR TR1999/02516T patent/TR199902516T2/xx unknown
- 1998-04-08 KR KR1019997009191A patent/KR20010006113A/ko not_active Application Discontinuation
- 1998-04-08 AT AT98914581T patent/ATE269300T1/de not_active IP Right Cessation
- 1998-04-08 AR ARP980101562A patent/AR016510A1/es not_active Application Discontinuation
- 1998-04-08 CO CO98019757A patent/CO4950536A1/es unknown
- 1998-04-08 IL IL13220598A patent/IL132205A0/xx unknown
- 1998-04-08 US US09/402,310 patent/US6294531B1/en not_active Expired - Fee Related
- 1998-04-08 DE DE69824566T patent/DE69824566T2/de not_active Expired - Lifetime
- 1998-04-08 CN CN98805849A patent/CN1259120A/zh active Pending
- 1998-04-08 WO PCT/US1998/006928 patent/WO1998045255A1/en active IP Right Grant
- 1998-04-08 AU AU68900/98A patent/AU721910B2/en not_active Ceased
- 1998-04-08 CA CA002286454A patent/CA2286454A1/en not_active Abandoned
- 1998-04-08 JP JP54305598A patent/JP2001523223A/ja not_active Ceased
- 1998-04-08 NZ NZ500055A patent/NZ500055A/en not_active IP Right Cessation
- 1998-04-08 PL PL98336097A patent/PL336097A1/xx unknown
- 1998-04-08 ES ES98914581T patent/ES2223126T3/es not_active Expired - Lifetime
- 1998-04-08 HU HU0001494A patent/HUP0001494A3/hu unknown
- 1998-04-08 BR BR9808491-7A patent/BR9808491A/pt not_active Application Discontinuation
- 1998-07-22 TW TW087105217A patent/TW407144B/zh not_active IP Right Cessation
-
1999
- 1999-10-07 NO NO994877A patent/NO994877L/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
TR199902516T2 (xx) | 2000-02-21 |
CA2286454A1 (en) | 1998-10-15 |
AU6890098A (en) | 1998-10-30 |
IL132205A0 (en) | 2001-03-19 |
NO994877D0 (no) | 1999-10-07 |
PE69299A1 (es) | 1999-09-26 |
PL336097A1 (en) | 2000-06-05 |
TW407144B (en) | 2000-10-01 |
ATE269300T1 (de) | 2004-07-15 |
KR20010006113A (ko) | 2001-01-26 |
ES2223126T3 (es) | 2005-02-16 |
JP2001523223A (ja) | 2001-11-20 |
AU721910B2 (en) | 2000-07-20 |
EP0973730A4 (en) | 2000-08-23 |
DZ2461A1 (fr) | 2003-01-18 |
HUP0001494A2 (hu) | 2000-10-28 |
UY24949A1 (es) | 2001-04-30 |
NZ500055A (en) | 2001-12-21 |
EP0973730B1 (en) | 2004-06-16 |
US6294531B1 (en) | 2001-09-25 |
EP0973730A1 (en) | 2000-01-26 |
CO4950536A1 (es) | 2000-09-01 |
DE69824566D1 (de) | 2004-07-22 |
HUP0001494A3 (en) | 2002-01-28 |
CN1259120A (zh) | 2000-07-05 |
DE69824566T2 (de) | 2005-08-18 |
BR9808491A (pt) | 2000-05-23 |
NO994877L (no) | 1999-10-07 |
WO1998045255A1 (en) | 1998-10-15 |
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