PE20030186A1 - FUSED CYCLIC COMPOUNDS AS MODULATORS OF THE NUCLEAR HORMONE RECEPTOR - Google Patents
FUSED CYCLIC COMPOUNDS AS MODULATORS OF THE NUCLEAR HORMONE RECEPTORInfo
- Publication number
- PE20030186A1 PE20030186A1 PE2001000651A PE2001000651A PE20030186A1 PE 20030186 A1 PE20030186 A1 PE 20030186A1 PE 2001000651 A PE2001000651 A PE 2001000651A PE 2001000651 A PE2001000651 A PE 2001000651A PE 20030186 A1 PE20030186 A1 PE 20030186A1
- Authority
- PE
- Peru
- Prior art keywords
- cr7r7
- alkyl
- link
- modulators
- heterocycle
- 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
- C07D487/08—Bridged systems
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/407—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
-
- 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
- A61K31/655—Azo (—N=N—), diazo (=N2), azoxy (>N—O—N< or N(=O)—N<), azido (—N3) or diazoamino (—N=N—N<) compounds
-
- 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
- A61K31/66—Phosphorus compounds
- A61K31/675—Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/08—Bridged systems
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
SE REFIERE A COMPUESTOS CICLICOS FUSIONADOS DE FORMULA I DONDE G ES ARILO, HETEROCICLO, HETEROARILO OPCIONALMENTE SUSTITUIDO CON H, CN, R1R2NC=O, HOCR3R3', R1R1'P=O, ENTRE OTROS; E ES C=Z2, CR7R7', SO2, P=OR2; Z1 Y Z2 SON O, S, NH, NR6; A1 Y A2 SON CR7, N; Y ES J-J'-J"; J Y J" SON (CR7R7')n; n ES 0-3; J' ES UN ENLACE, O, S, SO, SO2, NH, NR6, NR1C0, CR7R7', C=CR8R8', R2P=O, OPOOR2, ENTRE OTROS; W ES CR7R7'-CR7R7', R8C=CR8', N=CR8, N=N, ENTRE OTROS; Q ES H, ALQUILO, ALQUENILO, ENTRE OTROS; M ES UN ENLACE, O, CR7R7', NR10, M' ES UN ENLACE, NR10, AL MENOS UNO DE M Y M' ES UN ENLACE; L ES UN ENLACE, (CR7R7')n, NH, NR5, N(CR7R7')n, n ES 0-3; R1 Y R1' SON H, ALQUILO, HETEROCICLO, ENTRE OTROS; R2 ES ALQUILO, CICLOALQUILO, HETEROCICLO, ENTRE OTROS; R6 ES ALQUILO, CICLOALQUILO, HETEROCICLO, ENTRE OTROS; R7 Y R7' SON H, ALQUILO, CICLOALQUILO, HETEROCILO, ENTRE OTROS; R8 Y R8' SON H, ALQUILO, HETEROCICLO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS (5O,8O,8aO)-8,8a-DIHIDRO-2-[3-(TRIFLUOROMETIL)FENIL]-5,8-METANOIMIDAZO[1,5-a]PIRIDIN-1,3(2H,5H)-DIONA, (5O,8O,8aO)-8,8a-DIHIDRO-2-[1-NAFTALENIL]-5,8-METANOIMIDAZO[1,5-a]PIRIDIN-1,3(2H,5H)-DIONA, ENTRE OTROS. TAMBIEN SE REFIERE A UNA COMPOSICION QUE COMPRENDE ADEMAS OTRO AGENTE ANTICANCEROSO. LOS COMPUESTOS SON MIMETICOS ESTEROIDES Y MODULADORES DE LA FUNCION DEL RECEPTOR DE HORMONAS NUCLEARES DE ENLACE A ESTEROIDES Y PUEDEN SER UTILES PARA EL TRATAMIENTO DE ENFERMEDADES PROLIFERATIVAS, CANCER, HIPERTROFIA BENIGNA DE PROSTATA, ENFERMEDAD CARDIACA,REFERS TO FUSED CYCLICAL COMPOUNDS OF FORMULA I WHERE G IS ARYL, HETEROCICLO, HETEROARYL OPTIONALLY SUBSTITUTED WITH H, CN, R1R2NC = O, HOCR3R3 ', R1R1'P = O, AMONG OTHERS; E IS C = Z2, CR7R7 ', SO2, P = OR2; Z1 AND Z2 ARE O, S, NH, NR6; A1 AND A2 ARE CR7, N; Y IS J-J'-J "; J AND J" ARE (CR7R7 ') n; n IS 0-3; J 'IS A LINK, O, S, SO, SO2, NH, NR6, NR1C0, CR7R7', C = CR8R8 ', R2P = O, OPOOR2, AMONG OTHERS; W IS CR7R7'-CR7R7 ', R8C = CR8', N = CR8, N = N, AMONG OTHERS; Q IS H, RENTAL, ALKENYL, AMONG OTHERS; M IS A LINK, OR, CR7R7 ', NR10, M' IS A LINK, NR10, AT LEAST ONE OF M AND M 'IS A LINK; L IS A LINK, (CR7R7 ') n, NH, NR5, N (CR7R7') n, n IS 0-3; R1 AND R1 'ARE H, ALKYL, HETEROCYCLE, AMONG OTHERS; R2 IS ALKYL, CYCLOALKYL, HETEROCYCLE, AMONG OTHERS; R6 IS ALKYL, CYCLOALKYL, HETEROCYCLE, AMONG OTHERS; R7 AND R7 'ARE H, ALKYL, CYCLOALKYL, HETEROCYL, AMONG OTHERS; R8 AND R8 'ARE H, ALKYL, HETEROCICLO, AMONG OTHERS. PREFERRED COMPOUNDS ARE (5O, 8O, 8aO) -8,8a-DIHYDRO-2- [3- (TRIFLUOROMETHYL) PHENYL] -5,8-METHANOIMIDAZO [1,5-a] PYRIDIN-1,3 (2H, 5H) -DIONA, (5O, 8O, 8aO) -8,8a-DIHYDRO-2- [1-NAPHTHALENYL] -5,8-METHANOIMIDAZO [1,5-a] PYRIDIN-1,3 (2H, 5H) -DIONA, AMONG OTHERS. IT ALSO REFERS TO A COMPOSITION THAT ALSO INCLUDES ANOTHER ANTI-CANCER AGENT. THE COMPOUNDS ARE STEROID MIMETICS AND MODULATORS OF THE FUNCTION OF THE STEROID-BINDING NUCLEAR HORMONE RECEPTOR AND MAY BE USEFUL FOR THE TREATMENT OF PROLIFERATIVE DISEASES, CANCER, BENIGN PRADOSTATE HYPERTROPHY, ILLNESS
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US21439200P | 2000-06-28 | 2000-06-28 | |
| US28443801P | 2001-04-18 | 2001-04-18 | |
| US28461701P | 2001-04-18 | 2001-04-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20030186A1 true PE20030186A1 (en) | 2003-03-23 |
Family
ID=27395986
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2001000651A PE20030186A1 (en) | 2000-06-28 | 2001-08-23 | FUSED CYCLIC COMPOUNDS AS MODULATORS OF THE NUCLEAR HORMONE RECEPTOR |
Country Status (9)
| Country | Link |
|---|---|
| KR (1) | KR20030014407A (en) |
| CN (1) | CN1443187A (en) |
| AR (1) | AR031709A1 (en) |
| CZ (1) | CZ20024250A3 (en) |
| IL (1) | IL152890A0 (en) |
| PE (1) | PE20030186A1 (en) |
| PL (1) | PL366565A1 (en) |
| TR (1) | TR200202702T2 (en) |
| UY (1) | UY26809A1 (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9409856B2 (en) | 2005-11-28 | 2016-08-09 | Gtx, Inc. | Estrogen receptor ligands and methods of use thereof |
| EP2455362A1 (en) * | 2005-11-28 | 2012-05-23 | GTX, Inc. | Nuclear receptor binding agents |
| US8546451B2 (en) | 2005-11-28 | 2013-10-01 | Gtx, Inc. | Estrogen receptor ligands and methods of use thereof |
| CN102875556B (en) * | 2011-07-12 | 2016-03-30 | 天津药明康德新药开发有限公司 | (4S)-1-replaces-2,5-diazabicyclos [2,2,1] heptane derivative and preparation method |
| CN110184346A (en) * | 2019-07-11 | 2019-08-30 | 德阳市人民医院 | The diagnosis marker of Male Osteoporosis |
-
2001
- 2001-06-20 IL IL15289001A patent/IL152890A0/en unknown
- 2001-06-20 CZ CZ20024250A patent/CZ20024250A3/en unknown
- 2001-06-20 TR TR2002/02702T patent/TR200202702T2/en unknown
- 2001-06-20 PL PL01366565A patent/PL366565A1/en not_active Application Discontinuation
- 2001-06-20 CN CN01811976A patent/CN1443187A/en active Pending
- 2001-06-20 KR KR1020027017857A patent/KR20030014407A/en not_active Withdrawn
- 2001-06-28 AR ARP010103100A patent/AR031709A1/en unknown
- 2001-06-28 UY UY26809A patent/UY26809A1/en not_active Application Discontinuation
- 2001-08-23 PE PE2001000651A patent/PE20030186A1/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| UY26809A1 (en) | 2002-01-31 |
| TR200202702T2 (en) | 2004-12-21 |
| IL152890A0 (en) | 2003-06-24 |
| CN1443187A (en) | 2003-09-17 |
| KR20030014407A (en) | 2003-02-17 |
| CZ20024250A3 (en) | 2003-10-15 |
| PL366565A1 (en) | 2005-02-07 |
| AR031709A1 (en) | 2003-10-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Grant, registration | ||
| FD | Application declared void or lapsed |