AR035330A1 - Uso de metabolito de (-) -cis-6-fenil-5- (4-(2-pirrolidin-1-iletoxi) fenil)-5, 6, 7, 8-tetrahidronaftalen-2-ol, metabolitos y composiciones que los contienen - Google Patents
Uso de metabolito de (-) -cis-6-fenil-5- (4-(2-pirrolidin-1-iletoxi) fenil)-5, 6, 7, 8-tetrahidronaftalen-2-ol, metabolitos y composiciones que los contienenInfo
- Publication number
- AR035330A1 AR035330A1 ARP010101626A ARP010101626A AR035330A1 AR 035330 A1 AR035330 A1 AR 035330A1 AR P010101626 A ARP010101626 A AR P010101626A AR P010101626 A ARP010101626 A AR P010101626A AR 035330 A1 AR035330 A1 AR 035330A1
- Authority
- AR
- Argentina
- Prior art keywords
- phenyl
- disease
- cancer
- formula
- metabolite
- Prior art date
Links
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- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member 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
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- C07D295/08—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 with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
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- Gynecology & Obstetrics (AREA)
Abstract
Uso de un metabolito de (-)-cis-6-fenil-5-[4-(2-pirrolidin-1-iletoxi)fenil]-5,6,7,8-tetrahidronaftalen-2-ol de la fórmula (1) para la preparación de medicamentos caracterizado porque es para el tratamiento de osteoporosis, cáncer de mama, hiperlipidemia, arteriosclerosis, enfermedad de Alzheimer, cataratas, pérdida de libido, disfunción sexual masculina, cáncer de colon, verrugas dérmicas, enfermedad autoinmune, alopecia, acné, enfermedad cardiovascular, diabetes, endometriosis, disfunción sexual femenina, hiperglucemia, obesidad, trastorno obsesivo compulsivo, síndrome premenstrual, carcinoma prostático, hiperplasia prostática benigna, hipertensión pulmonar, dano por reperfusión, artritis reumatoide, osteoartritis, seborrea, ginecomastia senil, deficiencia de testosterona, síndrome de Turner, fibrosis uterina, vaginitis atrófica, incontinencia, cáncer de útero, hirsutismo, bulimia, anorexia, deseo sexual hipoactivo, trastorno de la excitación sexual, dispareunia, vaginismo, prolapso, infecciones del tracto urinario, apoplejía, infarto de miocardio, insuficiencia renal aguda o crónica, enfermedad oclusiva arterial periférica, fenómeno de Raynaud, cánceres de ovario, hígado y práncreas, así como de cáncer desmoide, glioma y carcinoma de células renales, o promover la curación de heridas, incrementar la frecuencia de los orgasmos o reducción del pH vaginal, fórmula (1), donde R1 se selecciona de fórmulas (2), (3) y (4) o -NH(CH2)3COR6; R5 se selecciona de H o CH3; R2, R3, R4 y R7 son iguales o diferentes y se seleccionan de H y OR5; y R6 se selecciona de -OH - -NHCH2COOH, siempre que: (a) si R1 es fórmula (2) o -NH(CH2)3COOH y (b) R2 es OH u OCH3 y R3 y R7 son H, o si R1 es como se definió (a) anteriormente, y (c) R2 y R7 son H y R3 es OH u OCH3, entonces R4 no es H o un isómero óptico, estereoisómero, regioisómero o isómero configuracional o isómero geométrico de éste o un tautómero o una sal farmacéuticamente aceptable de éste. Estos compuestos de la presente se pueden utilizar como patrones en ensayos analíticos o como intermedio para la síntesis química o biosíntesis posterior de entidades químicas. La presente se refiere también a composiciones farmacéuticas para el tratamiento de enfermedades y a su uso en la preparación de las mismas.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US26719800P | 2000-04-07 | 2000-04-07 |
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|---|---|
| AR035330A1 true AR035330A1 (es) | 2004-05-12 |
Family
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP010101626A AR035330A1 (es) | 2000-04-07 | 2001-04-05 | Uso de metabolito de (-) -cis-6-fenil-5- (4-(2-pirrolidin-1-iletoxi) fenil)-5, 6, 7, 8-tetrahidronaftalen-2-ol, metabolitos y composiciones que los contienen |
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| CN (1) | CN1209353C (es) |
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| AR (1) | AR035330A1 (es) |
| AT (1) | ATE333450T1 (es) |
| AU (2) | AU2001240985B2 (es) |
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| BR (1) | BR0109838A (es) |
| CA (1) | CA2405070A1 (es) |
| CR (1) | CR6766A (es) |
| CZ (1) | CZ20023223A3 (es) |
| DE (1) | DE60121557T2 (es) |
| DK (1) | DK1268453T3 (es) |
| EA (1) | EA004866B1 (es) |
| EE (1) | EE200200580A (es) |
| ES (1) | ES2266169T3 (es) |
| HK (1) | HK1052511B (es) |
| HR (1) | HRP20020802A2 (es) |
| HU (1) | HUP0300419A3 (es) |
| IL (1) | IL152082A0 (es) |
| IS (1) | IS6549A (es) |
| MA (1) | MA26890A1 (es) |
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| NO (1) | NO20024767L (es) |
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| PA (1) | PA8514901A1 (es) |
| PE (1) | PE20011183A1 (es) |
| PL (1) | PL358593A1 (es) |
| PT (1) | PT1268453E (es) |
| SK (1) | SK14092002A3 (es) |
| TN (1) | TNSN01052A1 (es) |
| TR (1) | TR200202310T2 (es) |
| UY (1) | UY26656A1 (es) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5631365A (en) | 1993-09-21 | 1997-05-20 | Schering Corporation | Hydroxy-substituted azetidinone compounds useful as hypocholesterolemic agents |
| US7001926B2 (en) | 2000-03-10 | 2006-02-21 | Oxigene, Inc. | Tubulin binding agents and corresponding prodrug constructs |
| US7091240B2 (en) | 2000-03-10 | 2006-08-15 | Oxigene, Inc. | Tubulin binding ligands and corresponding prodrug constructs |
| CZ20002567A3 (cs) * | 2000-07-11 | 2001-12-12 | Léčiva, A.S. | Tableta vyrobitelná přímým tabletováním, obsahující aktivní látku kyselinu 4-amino-1-hydroxybutyliden-1,1-bisfosfonovou, a způsob její výroby |
| EP1192945A3 (en) * | 2000-09-21 | 2004-03-03 | Pfizer Products Inc. | Use of an estrogen agonist/antagonist for treating osteoarthritis |
| AU781168B2 (en) * | 2001-01-26 | 2005-05-12 | Pfizer Products Inc. | Method of treating certain cancers using an estrogen agonist/antagonist |
| AU2003207567B2 (en) * | 2002-01-18 | 2008-01-24 | Merck Sharp & Dohme Corp. | Edg receptor agonists |
| WO2003076930A1 (en) * | 2002-03-14 | 2003-09-18 | Warner-Lambert Company Llc | Method for characterizing metabolites using hydrogen/deuterium exchange |
| CA2536946A1 (en) * | 2003-08-26 | 2005-03-03 | Board Of Regents, The University Of Texas System | Estrogen receptor modulators and uses thereof |
| US7456214B2 (en) | 2004-05-03 | 2008-11-25 | Baylor University | Chromene-containing compounds with anti-tubulin and vascular targeting activity |
| AU2012200714B2 (en) * | 2004-08-13 | 2014-04-17 | Wyeth Llc | Tanaproget derivatives, metabolites, and uses thereof |
| MX2007001812A (es) * | 2004-08-13 | 2007-03-26 | Wyeth Corp | Derivados de tanaproget, metabolitos, y usos de los mismos. |
| CA2611035C (en) * | 2005-06-22 | 2010-09-14 | Pfizer Products Inc. | Stereoselective hydrogenation process for preparing cis-6-phenyl-5-[4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-2-methoxy-5,6,7,8-tetrahydronaphthalene hydrochloride |
| US7902147B2 (en) * | 2007-11-05 | 2011-03-08 | Duke University | Chronic lymphocytic leukemia prognosis and treatment |
| TW201043595A (en) * | 2009-03-13 | 2010-12-16 | Organon Nv | Tetrahydronaphthalen-2-ol derivatives |
| US9845291B2 (en) | 2014-12-18 | 2017-12-19 | Genentech, Inc. | Estrogen receptor modulators and uses thereof |
| WO2017168174A1 (en) | 2016-04-02 | 2017-10-05 | N4 Pharma Uk Limited | New pharmaceutical forms of sildenafil |
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|---|---|---|---|---|
| US3522319A (en) * | 1964-01-23 | 1970-07-28 | Ciba Geigy Corp | Phenol substituted tetrahydronaphthalenes useful as estrogenics |
| 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 |
| UA51676C2 (uk) | 1995-11-02 | 2002-12-16 | Пфайзер Інк. | (-)цис-6(s)-феніл-5(r)[4-(2-піролідин-1-ілетокси)феніл]-5,6,7,8-тетрагідронафталін-2-ол d-тартрат, спосіб його одержання, спосіб лікування захворювань, що піддаються лікуванню агоністами естрогену, та фармацевтична композиція |
| TW442286B (en) | 1996-02-28 | 2001-06-23 | Pfizer | New therapeutic uses of estrogen agonists |
| IL120266A (en) | 1996-02-28 | 2005-05-17 | Pfizer | Use of estrogen antagonists and estrogen agonists in the preparation of medicaments for inhibiting pathological conditions |
| US6358951B1 (en) * | 1998-08-21 | 2002-03-19 | Pfizer Inc. | Growth hormone secretagogues |
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2001
- 2001-03-19 HR HR20020802A patent/HRP20020802A2/hr not_active Application Discontinuation
- 2001-03-19 WO PCT/IB2001/000427 patent/WO2001077093A1/en not_active Ceased
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- 2001-03-19 EA EA200200949A patent/EA004866B1/ru not_active IP Right Cessation
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- 2001-03-19 PL PL01358593A patent/PL358593A1/xx not_active Application Discontinuation
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- 2001-03-19 HK HK03104866.0A patent/HK1052511B/zh not_active IP Right Cessation
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- 2001-03-19 CA CA002405070A patent/CA2405070A1/en not_active Abandoned
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- 2001-03-19 EP EP01912069A patent/EP1268453B1/en not_active Expired - Lifetime
- 2001-03-19 AP APAP/P/2002/002641A patent/AP2002002641A0/en unknown
- 2001-03-19 AT AT01912069T patent/ATE333450T1/de not_active IP Right Cessation
- 2001-03-19 AU AU4098501A patent/AU4098501A/xx active Pending
- 2001-03-19 JP JP2001575567A patent/JP2004510693A/ja not_active Withdrawn
- 2001-03-19 KR KR1020027013379A patent/KR20020089434A/ko not_active Ceased
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- 2001-04-05 PE PE2001000320A patent/PE20011183A1/es not_active Application Discontinuation
- 2001-04-05 AR ARP010101626A patent/AR035330A1/es unknown
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- 2002-09-17 IS IS6549A patent/IS6549A/is unknown
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- 2002-10-02 MA MA26847A patent/MA26890A1/fr unknown
- 2002-10-02 CR CR6766A patent/CR6766A/es not_active Application Discontinuation
- 2002-10-03 NO NO20024767A patent/NO20024767L/no not_active Application Discontinuation
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