AR042467A1 - Compuestos de 5h-pirrolo[2,1-c][1,4]benzodiazepina agonistas de vasopresina biologicamente activos - Google Patents
Compuestos de 5h-pirrolo[2,1-c][1,4]benzodiazepina agonistas de vasopresina biologicamente activosInfo
- Publication number
- AR042467A1 AR042467A1 ARP030104629A ARP030104629A AR042467A1 AR 042467 A1 AR042467 A1 AR 042467A1 AR P030104629 A ARP030104629 A AR P030104629A AR P030104629 A ARP030104629 A AR P030104629A AR 042467 A1 AR042467 A1 AR 042467A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkylene
- group
- cycloalkylene
- compounds
- heteroaryl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- 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
-
- 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
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
-
- 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
- A61P5/02—Drugs for disorders of the endocrine system of the hypothalamic hormones, e.g. TRH, GnRH, CRH, GRH, somatostatin
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
Abstract
La presente se refiere a compuestos de la fórmula (1) donde W representa ya sea un O unido por doble enlace o bien dos H unidos por simple enlace; R1 es seleccionado del grupo formado por R, R3-X-R2-, R3-S(O)-, R3-S(O)2-, -SO3R4, -S(O)2N(R )2, y D-glucuronidato, cuando W es H. O R1 es seleccionado del grupo formado por H, alquilo, cicloalquilo, arilo, arilalquilo, heteroarilo, y heteroarilalquilo, cuando W es O; R2 es seleccionado del grupo que consiste de alquileno, cicloalquileno, alquilen-X-alquileno, alquilen-X-cicloalquileno, cicloalquilen-X-alquileno, y cicloalquilen-X-cicloalquileno; R3 es seleccionado del grupo que consiste de alquilo, arilo, heteroarilo, cicloalquilo, alquenilo, cicloalquenilo, alquinilo, alquenil-X-alquileno, cicl9oalquenil-X-alquileno, y perfluoroalquilo; R4 es seleccionado del grupo que consiste de H y R3; R3 es independientemente seleccionado del grupo que consiste de H, alquilo, alquenilo, alquinilo, ciclo-alquilo, cicloalquenilo, monofluoroalquilo, perfluoroalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, hidroxialquilo (C1-6), alcoxialquilo, alquiltioalquilo, acilo, alcoxicarbonilo, -C(O)NH2, alquilaminocarbonilo, dialquilaminocarbonilo, alquilaminalquilo, y dialquilaminalquilo, y cuando dos grupos R se encuentran unidos al mismo átomo estos dos grupos juntos pueden formar un grupo alquileno; X es seleccionado del grupo que consiste de O, -NR-, -S(O)m-, -C(O)-, -OC(O)-, -C(O)O-, -NRC(O)-, y -C(O)NR-; y m es un entero seleccionado de 0, 1, y 2, y los racematos, enantiómeros, y las sales farmacéuticamente aceptables de lo mismo, un proceso para su fabricación y las formulaciones farmacéuticas que contienen a dichos compuestos las cuales son útiles como agentes anti-acuareticos en el tratamiento de la enuresis urinaria nocturna, la emergencia urinaria nocturna, y/o condiciones similares.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/320,761 US7138393B2 (en) | 1998-07-24 | 2002-12-16 | Biologically active vasopressin agonist metabolites |
Publications (1)
Publication Number | Publication Date |
---|---|
AR042467A1 true AR042467A1 (es) | 2005-06-22 |
Family
ID=32710746
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP030104629A AR042467A1 (es) | 2002-12-16 | 2003-12-15 | Compuestos de 5h-pirrolo[2,1-c][1,4]benzodiazepina agonistas de vasopresina biologicamente activos |
Country Status (15)
Country | Link |
---|---|
US (1) | US7138393B2 (es) |
EP (1) | EP1572694B1 (es) |
JP (1) | JP2006514956A (es) |
CN (1) | CN1745083A (es) |
AR (1) | AR042467A1 (es) |
AT (1) | ATE410428T1 (es) |
AU (1) | AU2003297127A1 (es) |
BR (1) | BR0317383A (es) |
CA (1) | CA2508764A1 (es) |
DE (1) | DE60324018D1 (es) |
DK (1) | DK1572694T3 (es) |
ES (1) | ES2312859T3 (es) |
MX (1) | MXPA05006241A (es) |
TW (1) | TW200413355A (es) |
WO (1) | WO2004060894A1 (es) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0210397D0 (en) * | 2002-05-07 | 2002-06-12 | Ferring Bv | Pharmaceutical formulations |
RU2472539C2 (ru) | 2007-08-06 | 2013-01-20 | Аллерган, Инк. | Способы и устройства для доставки препарата десмопрессина |
US20100286045A1 (en) | 2008-05-21 | 2010-11-11 | Bjarke Mirner Klein | Methods comprising desmopressin |
PT3085381T (pt) * | 2008-05-21 | 2018-05-18 | Ferring Bv | Desmopressina orodispersível para aumentar o período inicial de sono não perturbado pela noctúria |
US11963995B2 (en) | 2008-05-21 | 2024-04-23 | Ferring B.V. | Methods comprising desmopressin |
MX2011005119A (es) * | 2008-11-18 | 2011-05-30 | Hoffmann La Roche | Alquilciclohexileteres de dihidrotetraazabenzoazulenos. |
US9532959B2 (en) | 2010-07-08 | 2017-01-03 | Wellesley Pharmaceuticals, Llc | Pharmaceutical formulation for reducing frequency of urination and method of use thereof |
US10010514B2 (en) | 2010-07-08 | 2018-07-03 | Wellesley Pharmaceuticals, Llc | Pharmaceutical formulation for reducing frequency of urination and method of use thereof |
US10278925B2 (en) | 2012-01-04 | 2019-05-07 | Wellesley Pharmaceuticals, Llc | Delayed-release formulations, methods of making and use thereof |
US10105330B2 (en) | 2012-01-04 | 2018-10-23 | Wellesley Pharmaceuticals, Llc | Extended, delayed and immediate release formulation method of manufacturing and use thereof |
AU2012363788B2 (en) * | 2012-01-04 | 2017-03-09 | Wellesley Pharmaceuticals, Llc | Delayed-release formulation for reducing the frequency of urination and method of use thereof |
KR20180025993A (ko) * | 2012-01-04 | 2018-03-09 | 웰즐리 파마슈티컬스 엘엘씨 | 배뇨 빈도를 감소시키기 위한 연장-방출형 제제 및 이의 사용 방법 |
US10105328B2 (en) | 2014-06-06 | 2018-10-23 | Wellesley Pharmaceuticals, Llc | Composition for reducing frequency of urination, method of making and use thereof |
Family Cites Families (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1251767B (de) | 1964-02-28 | 1968-04-18 | Dr Karl Thomae Gesellschaft mit beschrankter Haftung Biberach/Riß | Verfahren zur Herstellung von neuen m 6 Stellung substituierten 5 6 Dihydro-5oxo HH pyrido[2,3-b] [l,5]benzodiazepinen |
US4680298A (en) | 1983-05-31 | 1987-07-14 | Schering Corporation | Tricyclic anti-allergy and use as anti-inflammatory agents |
US4766108A (en) * | 1986-12-04 | 1988-08-23 | Smith Kline Beckman Corporation | Tyr-Arg-vasopressin antagonists |
US5055448A (en) * | 1987-06-25 | 1991-10-08 | Medical College Of Ohio | Linear derivatives of arginine vasopressin antagonists |
US4839355A (en) | 1987-09-09 | 1989-06-13 | Sterling Drug Inc. | Tricyclic-pyridinylquinoline compounds, their preparation and use |
US5070187A (en) * | 1989-11-03 | 1991-12-03 | Trustees Of Boston University | Pharmacologically effective antagonists of arginine-vasopressin |
CA2048003A1 (en) | 1990-08-21 | 1992-02-22 | Serge Burner | Tricyclic pyridone derivatives |
US5516774A (en) * | 1993-07-29 | 1996-05-14 | American Cyanamid Company | Tricyclic diazepine vasopressin antagonists and oxytocin antagonists |
US5512563A (en) * | 1993-07-29 | 1996-04-30 | American Cyanamid Company | Tricyclic benzazepine vasopressin antagonists |
US5420270A (en) * | 1993-10-07 | 1995-05-30 | G. D. Searle & Co. | Aryl substituted dibenzoxazepine compounds, pharmaceutical compositions and methods of use |
ATE239710T1 (de) | 1994-06-15 | 2003-05-15 | Otsuka Pharma Co Ltd | Benzoheterocyclische derivate verwendbar als vasopressin- oder oxytocin-modulatoren |
JPH0881460A (ja) | 1994-09-08 | 1996-03-26 | Yamanouchi Pharmaceut Co Ltd | 新規なテトラヒドロベンゾジアゼピン誘導体又はその塩 |
AR002459A1 (es) | 1995-01-17 | 1998-03-25 | American Cyanamid Co | Antagonistas de vasopresina de benzacepina triciclicos, una composicion farmaceutica que los contiene, un metodo para tratar enfermedades y unprocedimiento para su preparacion. |
US5536718A (en) * | 1995-01-17 | 1996-07-16 | American Cyanamid Company | Tricyclic benzazepine vasopressin antagonists |
US5521173A (en) * | 1995-01-17 | 1996-05-28 | American Home Products Corporation | Tricyclic benzazepine vasopressin antagonists |
TW359669B (en) | 1995-12-15 | 1999-06-01 | Otsuka Pharma Co Ltd | Benzazepine derivatives |
US5880122A (en) * | 1996-11-01 | 1999-03-09 | American Home Products Corporation | 3-Carboxamide derivatives of 5H-pyrrolo 2,1-c! 1,4!-benzodiazepines |
AU727654B2 (en) | 1997-06-13 | 2000-12-21 | Yamanouchi Pharmaceutical Co., Ltd. | Tricyclic pyrazole derivative |
US6194407B1 (en) * | 1997-07-30 | 2001-02-27 | American Home Products Corporation | Tricyclic pyrido vasopressin agonists |
BR9811585A (pt) | 1997-07-30 | 2000-09-26 | American Home Prod | Agonistas de vasopressinas tricìclicas |
EP1149104B1 (en) | 1999-02-04 | 2002-12-11 | Wyeth | Pyrrolobenzodiazepine carboxyamide vasopressin agonists |
US6297234B1 (en) | 1999-02-04 | 2001-10-02 | American Home Products Corporation | Arylthiophene vasopressin agonists |
CN1399542A (zh) | 1999-09-27 | 2003-02-26 | 美国氰胺公司 | 药用载体制剂 |
CA2385971A1 (en) | 1999-09-27 | 2001-04-05 | American Cyanamid Company | Vasopressin agonist formulation and process |
GB0000079D0 (en) | 2000-01-05 | 2000-02-23 | Ferring Bv | Novel antidiuretic agents |
GB0015601D0 (en) | 2000-06-26 | 2000-08-16 | Ferring Bv | Novel antidiuretic agents |
-
2002
- 2002-12-16 US US10/320,761 patent/US7138393B2/en not_active Expired - Fee Related
-
2003
- 2003-12-09 TW TW092134683A patent/TW200413355A/zh unknown
- 2003-12-15 AR ARP030104629A patent/AR042467A1/es not_active Application Discontinuation
- 2003-12-16 DK DK03814820T patent/DK1572694T3/da active
- 2003-12-16 WO PCT/US2003/039897 patent/WO2004060894A1/en active Application Filing
- 2003-12-16 EP EP03814820A patent/EP1572694B1/en not_active Expired - Lifetime
- 2003-12-16 DE DE60324018T patent/DE60324018D1/de not_active Expired - Lifetime
- 2003-12-16 JP JP2004565510A patent/JP2006514956A/ja active Pending
- 2003-12-16 CA CA002508764A patent/CA2508764A1/en not_active Abandoned
- 2003-12-16 CN CNA2003801095935A patent/CN1745083A/zh active Pending
- 2003-12-16 AT AT03814820T patent/ATE410428T1/de not_active IP Right Cessation
- 2003-12-16 ES ES03814820T patent/ES2312859T3/es not_active Expired - Lifetime
- 2003-12-16 AU AU2003297127A patent/AU2003297127A1/en not_active Withdrawn
- 2003-12-16 BR BR0317383-6A patent/BR0317383A/pt not_active IP Right Cessation
- 2003-12-16 MX MXPA05006241A patent/MXPA05006241A/es active IP Right Grant
Also Published As
Publication number | Publication date |
---|---|
US20030134845A1 (en) | 2003-07-17 |
ES2312859T3 (es) | 2009-03-01 |
CA2508764A1 (en) | 2004-07-22 |
MXPA05006241A (es) | 2005-08-19 |
EP1572694A1 (en) | 2005-09-14 |
EP1572694B1 (en) | 2008-10-08 |
TW200413355A (en) | 2004-08-01 |
JP2006514956A (ja) | 2006-05-18 |
BR0317383A (pt) | 2005-11-16 |
ATE410428T1 (de) | 2008-10-15 |
CN1745083A (zh) | 2006-03-08 |
DE60324018D1 (de) | 2008-11-20 |
US7138393B2 (en) | 2006-11-21 |
DK1572694T3 (da) | 2009-02-02 |
AU2003297127A1 (en) | 2004-07-29 |
WO2004060894A1 (en) | 2004-07-22 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FA | Abandonment or withdrawal |