ES2064661T3 - 11-ceto o hidroxi-3,5-dieno-esteroides como inhibidores de esteroide-5-alfa-reductasa. - Google Patents
11-ceto o hidroxi-3,5-dieno-esteroides como inhibidores de esteroide-5-alfa-reductasa.Info
- Publication number
- ES2064661T3 ES2064661T3 ES90311807T ES90311807T ES2064661T3 ES 2064661 T3 ES2064661 T3 ES 2064661T3 ES 90311807 T ES90311807 T ES 90311807T ES 90311807 T ES90311807 T ES 90311807T ES 2064661 T3 ES2064661 T3 ES 2064661T3
- Authority
- ES
- Spain
- Prior art keywords
- alpha
- dieno
- ceto
- steroids
- steroid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J1/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
- C07J1/0003—Androstane derivatives
- C07J1/0011—Androstane derivatives substituted in position 17 by a keto group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J1/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
-
- 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
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J1/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
- C07J1/0003—Androstane derivatives
- C07J1/0018—Androstane derivatives substituted in position 17 beta, not substituted in position 17 alfa
- C07J1/0022—Androstane derivatives substituted in position 17 beta, not substituted in position 17 alfa the substituent being an OH group free esterified or etherified
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J1/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
- C07J1/0051—Estrane derivatives
- C07J1/0066—Estrane derivatives substituted in position 17 beta not substituted in position 17 alfa
- C07J1/007—Estrane derivatives substituted in position 17 beta not substituted in position 17 alfa the substituent being an OH group free esterified or etherified
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J21/00—Normal steroids containing carbon, hydrogen, halogen or oxygen having an oxygen-containing hetero ring spiro-condensed with the cyclopenta(a)hydrophenanthrene skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J3/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by one carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J3/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by one carbon atom
- C07J3/005—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by one carbon atom the carbon atom being part of a carboxylic function
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J31/00—Normal steroids containing one or more sulfur atoms not belonging to a hetero ring
- C07J31/006—Normal steroids containing one or more sulfur atoms not belonging to a hetero ring not covered by C07J31/003
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J41/00—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring
- C07J41/0033—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005
- C07J41/0066—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005 the 17-beta position being substituted by a carbon atom forming part of an amide group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J41/00—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring
- C07J41/0033—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005
- C07J41/0094—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005 containing nitrile radicals, including thiocyanide radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J51/00—Normal steroids with unmodified cyclopenta(a)hydrophenanthrene skeleton not provided for in groups C07J1/00 - C07J43/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J61/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton has been modified by contraction of only one ring by one or two atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J63/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton has been modified by expansion of only one ring by one or two atoms
- C07J63/002—Expansion of ring A by one atom, e.g. A homo steroids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J7/00—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms
- C07J7/008—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms substituted in position 21
- C07J7/0095—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms substituted in position 21 carbon in position 21 is part of carboxylic group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J71/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton is condensed with a heterocyclic ring
- C07J71/0005—Oxygen-containing hetero ring
- C07J71/001—Oxiranes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J9/00—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of more than two carbon atoms, e.g. cholane, cholestane, coprostane
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J9/00—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of more than two carbon atoms, e.g. cholane, cholestane, coprostane
- C07J9/005—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of more than two carbon atoms, e.g. cholane, cholestane, coprostane containing a carboxylic function directly attached or attached by a chain containing only carbon atoms to the cyclopenta[a]hydrophenanthrene skeleton
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Toxicology (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Urology & Nephrology (AREA)
- Reproductive Health (AREA)
- Endocrinology (AREA)
- Steroid Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
COMPUESTOS DE LA ESTRUCTURA: EN LA QUE X ES CETO O H Y OH; R ELEVADO 1 ES H O C SUB 1-8 ALCALI; R (AL CUADRADO) ES (1) A-H, (ALFA)-ACETOXI Y/O (BETA)-WCOR ELEVADO 3 DONDE W ES UNA UNION O C SUB 1-12 ALCALI Y R ELEVADO 3 ES C SUB 1-8 ALCALI, C SUB 1-8 ALKOXI DE N(R ELEVADO 4) 2 DONDE R ELEVADO 4 ES INTER ALIA, H O C SUB 1-8 ALCALI; (2) = CHWCOR ELEVADO 3 O = CHWOR ELEVADO 5 DONDE W Y R ELEVADO 3 SON COMO ARRIBA Y R ELEVADO 5 ES INTER ALIA, FENILALKILCARBONIL, BENZOIL, ALKOXICARBONIL, AMINOCARBONIL, ALKIL O ALKILCARBONIL; (3) (ALFA)-H Y (BETA)-NHCOR ELEVADO 6 DONDE R ELEVADO 6 ES ALCALI O (BETA)-N(R ELEVADO 4) SUB 2 O (4) CETO, PROCEDIMIENTOS PARA SU PREPARACION, COMPUESTOS FARMACEUTICOS QUE LOS CONTIENEN Y SU UTILIZACION EN TERAPIAS COMO INHIBIDORES DE 5-(ALFA)-REDUCTASA.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/430,152 US5041433A (en) | 1987-04-29 | 1989-11-01 | 11-keto or hydroxy 3,5-diene steroids as inhibitors of steriod 5-α-reductase |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2064661T3 true ES2064661T3 (es) | 1995-02-01 |
Family
ID=23706275
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES90311807T Expired - Lifetime ES2064661T3 (es) | 1989-11-01 | 1990-10-29 | 11-ceto o hidroxi-3,5-dieno-esteroides como inhibidores de esteroide-5-alfa-reductasa. |
Country Status (15)
Country | Link |
---|---|
US (1) | US5041433A (es) |
EP (1) | EP0427434B1 (es) |
JP (1) | JPH03169890A (es) |
KR (1) | KR100187945B1 (es) |
AT (1) | ATE115587T1 (es) |
AU (1) | AU641701B2 (es) |
CA (1) | CA2028622A1 (es) |
DE (1) | DE69015129T2 (es) |
DK (1) | DK0427434T3 (es) |
ES (1) | ES2064661T3 (es) |
GR (1) | GR3015372T3 (es) |
IE (1) | IE65562B1 (es) |
NZ (1) | NZ235871A (es) |
PT (1) | PT95750A (es) |
ZA (1) | ZA908730B (es) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5516768A (en) * | 1990-03-16 | 1996-05-14 | Smithkline Beecham Corporation | Uncompetitive inhibition of steroid and 5α-reductose |
US5300294A (en) * | 1990-06-27 | 1994-04-05 | Smithkline Beecham Corporation | Method of treating prostatic adenocarcinoma |
IT1259419B (it) * | 1991-05-24 | 1996-03-18 | Erba Carlo Spa | Steroidi 3-carbossi 17b - sostituiti insaturi utili come inibitori della testosterone 5 a reduttasi |
NZ245504A (en) * | 1991-12-20 | 1995-08-28 | Hoechst Ag | Bile acid derivatives containing an ethylenically unsaturated grouping |
US5215894A (en) * | 1992-02-25 | 1993-06-01 | Merck & Co., Inc. | Biological process for producing 17β-N-monosubstituted carbamoyl-11-oxo-4-aza-5-α-androst-3-one testosterone-5-α reductase inhibitors |
EP0641211A1 (en) * | 1992-05-21 | 1995-03-08 | Endorecherche Inc. | INHIBITORS OF TESTOSTERONE 5$g(a)-REDUCTASE ACTIVITY |
US5641765A (en) * | 1992-11-18 | 1997-06-24 | Smithkline Beecham Corporation | 17-αand 17-βsubstituted acyl-3-carboxy-3,5-dienes and use in inhibiting 5-α-reductase |
AP9300589A0 (en) * | 1992-11-18 | 1994-01-31 | Smithkline Beecham Corp | Novel 17a and 17b substituted acyl-3-carboxy 3,5-diene steroidal compounds, pharmaceutical compositions containing these compounds, and methods for using these compounds to inhibit steroid 5-a-reductase. |
US5683995A (en) * | 1992-11-18 | 1997-11-04 | Smithkline Beecham Corporation | 17 substituted acyl-3-carboxy 3,5-diene steroidals as α-reductase inhibitors |
TW369521B (en) * | 1993-09-17 | 1999-09-11 | Smithkline Beecham Corp | Androstenone derivative |
US5637310A (en) * | 1993-12-20 | 1997-06-10 | Smithkline Beecham Corporation | Method of treating prostatic adenocarcinoma |
WO1995028413A1 (en) * | 1994-04-15 | 1995-10-26 | Smithkline Beecham Corporation | 17β-SUBSTITUTED 3-CARBOXY STEROIDS THAT INHIBIT 5-α-REDUCTASE |
US5541322A (en) * | 1994-10-14 | 1996-07-30 | Glaxo Wellcome Inc. | Synthesis of 6-azaandrostenones |
WO1999061055A1 (en) | 1998-05-22 | 1999-12-02 | The Board Of Trustees Of The Leland Stanford Junior University | Bifunctional molecules and therapies based thereon |
US20060148725A1 (en) * | 2001-12-21 | 2006-07-06 | The Miriam Hospital | Selective 11beta HSD inhibitors and methods of use thereof |
EP1587574A4 (en) * | 2001-12-21 | 2009-03-18 | Rhode Island Hospital | 11b-HSD SELECTIVE INHIBITORS AND METHODS OF USE |
US20050020550A1 (en) * | 2003-04-29 | 2005-01-27 | Morris David J. | Selective testicular 11beta-HSD inhibitors and methods of use thereof |
WO2006116718A2 (en) | 2005-04-28 | 2006-11-02 | Proteus Biomedical, Inc. | Pharma-informatics system |
WO2007035716A2 (en) | 2005-09-16 | 2007-03-29 | Raptor Pharmaceutical Inc. | Compositions comprising receptor-associated protein (rap) variants specific for cr-containing proteins and uses thereof |
CN104208718B (zh) | 2009-02-20 | 2017-12-29 | 2-Bbb医疗股份有限公司 | 基于谷胱甘肽的药物递送系统 |
MY163048A (en) | 2009-05-06 | 2017-08-15 | Laboratory Skin Care Inc | Dermal delivery compositions comprising active agent-calcium phosphate particle complexes and methods of using the same |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4191759A (en) * | 1978-04-13 | 1980-03-04 | Merck & Co., Inc. | N-substituted-17β-carbamoylandrost-4-en-3-one 5α reductase inhibitors |
US4377584A (en) * | 1978-04-13 | 1983-03-22 | Merck & Co., Inc. | 4-Aza-17β-substituted-5α-androstan-3-one-reductase inhibitors |
US4317817A (en) * | 1979-08-27 | 1982-03-02 | Richardson-Merrell Inc. | Novel steroid 5α-reductase inhibitors |
DK465481A (da) * | 1980-11-21 | 1982-05-22 | Hoffmann La Roche | Fremgangsmaade til fremstilling af d-homostemoider |
US4814324A (en) * | 1987-03-06 | 1989-03-21 | Merck & Co., Inc. | Sterol inhibitors of testosterone 5α-reductase |
US4910226A (en) * | 1987-04-29 | 1990-03-20 | Smithkline Beckman Corporation | Steroid 5-alpha-reductase inhibitors |
-
1989
- 1989-11-01 US US07/430,152 patent/US5041433A/en not_active Expired - Lifetime
-
1990
- 1990-10-26 CA CA002028622A patent/CA2028622A1/en not_active Abandoned
- 1990-10-26 AU AU65511/90A patent/AU641701B2/en not_active Ceased
- 1990-10-29 ES ES90311807T patent/ES2064661T3/es not_active Expired - Lifetime
- 1990-10-29 EP EP90311807A patent/EP0427434B1/en not_active Expired - Lifetime
- 1990-10-29 DK DK90311807.3T patent/DK0427434T3/da active
- 1990-10-29 NZ NZ235871A patent/NZ235871A/en unknown
- 1990-10-29 AT AT90311807T patent/ATE115587T1/de not_active IP Right Cessation
- 1990-10-29 DE DE69015129T patent/DE69015129T2/de not_active Expired - Fee Related
- 1990-10-31 IE IE392090A patent/IE65562B1/en unknown
- 1990-10-31 ZA ZA908730A patent/ZA908730B/xx unknown
- 1990-10-31 JP JP2297020A patent/JPH03169890A/ja active Pending
- 1990-10-31 PT PT95750A patent/PT95750A/pt not_active Application Discontinuation
- 1990-11-01 KR KR1019900017704A patent/KR100187945B1/ko not_active IP Right Cessation
-
1995
- 1995-03-13 GR GR940403878T patent/GR3015372T3/el unknown
Also Published As
Publication number | Publication date |
---|---|
AU641701B2 (en) | 1993-09-30 |
IE65562B1 (en) | 1995-11-01 |
CA2028622A1 (en) | 1991-05-02 |
EP0427434A2 (en) | 1991-05-15 |
AU6551190A (en) | 1991-07-18 |
US5041433A (en) | 1991-08-20 |
EP0427434A3 (en) | 1992-03-04 |
IE903920A1 (en) | 1991-05-08 |
NZ235871A (en) | 1991-12-23 |
PT95750A (pt) | 1991-09-13 |
ATE115587T1 (de) | 1994-12-15 |
DE69015129D1 (de) | 1995-01-26 |
JPH03169890A (ja) | 1991-07-23 |
EP0427434B1 (en) | 1994-12-14 |
ZA908730B (en) | 1991-11-27 |
DE69015129T2 (de) | 1995-05-04 |
GR3015372T3 (en) | 1995-06-30 |
KR910009725A (ko) | 1991-06-28 |
KR100187945B1 (ko) | 1999-06-01 |
DK0427434T3 (da) | 1995-05-08 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
ES2064661T3 (es) | 11-ceto o hidroxi-3,5-dieno-esteroides como inhibidores de esteroide-5-alfa-reductasa. | |
EP0613883A4 (en) | HYDROXAMIC ACID DERIVATIVE. | |
PT80157B (en) | Methods of treating viral diseases with pyridazinamines anti-virally active pyridazinamines | |
HUT67285A (en) | Cyclic ureas and analogues and pharmaceutical compositions | |
EP0151824A3 (en) | N-(4-piperidinyl) bicyclic condesed 2-imidazolamine derivatives | |
ES2094721T3 (es) | Analogos de la camptotecina solubles en agua. | |
PT727419E (pt) | Compostos intermediarios para a preparacao de inibidores da protease retroviral | |
ES2123654T3 (es) | Carbapenems que contienen un grupo fenilo substituido con carboxi, procesos para su preparacion, productos intermedios y uso como antibioticos. | |
TW268005B (es) | ||
ES2063146T3 (es) | Composiciones farmaceuticas que contienen acido n-(3,4-dimetoxicinamoil)-antranilico. | |
ZA911728B (en) | Benzisothiazolinone-1-dioxide derivatives as elastase inhibitors | |
FI935777A0 (fi) | Inhibitorer foer HIV-proteas anvaendbara vid behandling av AIDS | |
PT100583A (pt) | Metodo de tratamento e/ou profilaxia utilizando,por exemplo, derivados de benzopirano, composicoes que os contem, compostos utilizados e processos para a sua preparacao | |
EP0199400A3 (en) | Substituted n-û(4-piperidinyl)alkyl¨ bicyclic condensed ozazol- and thiazolamines | |
ES2074462T3 (es) | Derivados 3-piperazinil-benzazoles antipsicoticos. | |
NZ218170A (en) | Piperidine derivatives and pharmaceutical compositions | |
ATE92960T1 (de) | Alpha-1-antitrypsin-varianten, besonders verwendbar als kallikrein-inhibitoren. | |
GR3031095T3 (en) | 3-ALKYLOXY-, ARYLOXY-, OR ARYLALKYLOXYBENZO b]THIOPHENE-2-CARBOXAMIDES AS INHIBITORS OF CELL ADHESION. | |
ES2000681A6 (es) | Un procedimiento para preparar nuevos compuestos de bencilpiperazina | |
FI923662A (fi) | Terapeutiska medel | |
ZA906666B (en) | 3-substituted nitro-steroid derivatives as 5-alpha-reductase inhibitors | |
ZA911994B (en) | Novel ascorbic acid derivatives | |
HUT54688A (en) | Process for producing compounds utilizable for treating ulcus and pharmaceutical compositions containing them as active components | |
AR241434A1 (es) | Procedimiento para la preparacion de 3-(piperidinil)-1h-indazoles. | |
EP0653207A4 (en) | AIDS VIRUS INFECTIVE COMPOSITION. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG2A | Definitive protection |
Ref document number: 427434 Country of ref document: ES |