ES2100544T3 - (-)-ritodrina. - Google Patents
(-)-ritodrina.Info
- Publication number
- ES2100544T3 ES2100544T3 ES93914933T ES93914933T ES2100544T3 ES 2100544 T3 ES2100544 T3 ES 2100544T3 ES 93914933 T ES93914933 T ES 93914933T ES 93914933 T ES93914933 T ES 93914933T ES 2100544 T3 ES2100544 T3 ES 2100544T3
- Authority
- ES
- Spain
- Prior art keywords
- ritodrine
- hydroxyphenyl
- remedy
- ritodrina
- ritodrines
- 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
- 229960001634 ritodrine Drugs 0.000 abstract 2
- IOVGROKTTNBUGK-SJKOYZFVSA-N (1S,2R)-ritodrine Chemical compound N([C@H](C)[C@@H](O)C=1C=CC(O)=CC=1)CCC1=CC=C(O)C=C1 IOVGROKTTNBUGK-SJKOYZFVSA-N 0.000 abstract 1
- 208000005171 Dysmenorrhea Diseases 0.000 abstract 1
- 206010013935 Dysmenorrhoea Diseases 0.000 abstract 1
- 208000005107 Premature Birth Diseases 0.000 abstract 1
- 206010036590 Premature baby Diseases 0.000 abstract 1
- 208000036029 Uterine contractions during pregnancy Diseases 0.000 abstract 1
- 206010000210 abortion Diseases 0.000 abstract 1
- 231100000176 abortion Toxicity 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 230000003389 potentiating effect Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 231100000419 toxicity Toxicity 0.000 abstract 1
- 230000001988 toxicity Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/46—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
- C07C215/56—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains further substituted by hydroxy groups
- C07C215/58—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains further substituted by hydroxy groups with hydroxy groups and the six-membered aromatic ring, or the condensed ring system containing that ring, bound to the same carbon atom of the carbon chain
- C07C215/60—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains further substituted by hydroxy groups with hydroxy groups and the six-membered aromatic ring, or the condensed ring system containing that ring, bound to the same carbon atom of the carbon chain the chain having two carbon atoms between the amino groups and the six-membered aromatic ring or the condensed ring system containing that ring
-
- 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
- A61K31/13—Amines
- A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Separation Of Suspended Particles By Flocculating Agents (AREA)
Abstract
(-)-RITODRINA, POR EJEMPLO (-)-ERITO-1-(P-HIDROXIFENIL)-2-[2-(PHIDROXIFENIL)ETILAMINO]-1-PROPANO, QUE ESTA SUSTANCIALMENTE LIBRE DEL (+)-ISOMERO, O UNA SAL DE ESTE. ESTE COMPUESTO TIENE UN POTENTE EFECTO DE INHIBIR LA CONTRACCION UTERINA CUANDO SE COMPARA CON LA (MAS MENOS)-RITODRINA Y (+)-RITODRINA Y UNA TOXICIDAD COMPARABLE A LA DE LAS OTRAS RITODINAS, Y DE ESTA MANERA SE PUEDE USAR COMO REMEDIO ALTAMENTE SEGURO PARA NACIMIENTO PREMATURO AMENAZADOS Y ABORTOS Y UN REMEDIO PARA LA DISMENORREA.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17408792 | 1992-07-01 | ||
| JP21048292 | 1992-08-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2100544T3 true ES2100544T3 (es) | 1997-06-16 |
Family
ID=26495813
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES93914933T Expired - Lifetime ES2100544T3 (es) | 1992-07-01 | 1993-06-30 | (-)-ritodrina. |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US5449694A (es) |
| EP (1) | EP0603414B1 (es) |
| JP (1) | JP2758502B2 (es) |
| KR (1) | KR0151114B1 (es) |
| CN (1) | CN1040319C (es) |
| AT (1) | ATE148880T1 (es) |
| CA (1) | CA2116685C (es) |
| DE (1) | DE69308115T2 (es) |
| DK (1) | DK0603414T3 (es) |
| ES (1) | ES2100544T3 (es) |
| WO (1) | WO1994001392A1 (es) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH06247846A (ja) * | 1993-02-22 | 1994-09-06 | Toko Yakuhin Kogyo Kk | 塩酸リトドリンの経皮吸収製剤用組成物 |
| CA2176721A1 (en) * | 1993-11-16 | 1995-05-26 | Kristof Chwalisz | Treatment of uterine contractility disorders with a nitric oxide synthase substrate and/or donor, or a nitric oxide inhibitor |
| FR2720276B1 (fr) * | 1994-05-24 | 1997-09-05 | Christophe Boyer | Nouvelle utilisation thérapeutique des agents bétamimétiques et médicament en contenant. |
| EP0805679A1 (fr) * | 1995-11-28 | 1997-11-12 | Christophe Boyer | Utilisation therapeutique d'agents betamimetiques pour traiter les douleurs menstruelles par voie permuqueuse |
| CN1077600C (zh) * | 1998-12-04 | 2002-01-09 | 中国科学院化工冶金研究所 | 用大规模培养的麻黄细胞培养物作原料生产麻黄碱的方法 |
| CN1261405C (zh) * | 2000-11-09 | 2006-06-28 | 三井化学株式会社 | 旋光性胺衍生物及其合成方法 |
| JP4834333B2 (ja) * | 2005-06-27 | 2011-12-14 | アルプス薬品工業株式会社 | 光学活性ベンジルアミン誘導体の製造方法 |
| CN101239917B (zh) * | 2008-03-10 | 2011-05-04 | 苏州立新制药有限公司 | 一种盐酸利托君及其中间体的制备方法 |
| IT1399912B1 (it) | 2010-04-29 | 2013-05-09 | Lundbeck Pharmaceuticals Italy S Pa | Processo di preparazione di ritodrina cloridrato. |
| CN103113239B (zh) * | 2013-03-11 | 2014-04-30 | 苏州立新制药有限公司 | 盐酸利托君的制备方法 |
| CN103113237B (zh) * | 2013-03-11 | 2014-04-30 | 苏州立新制药有限公司 | 一种盐酸利托君的制备方法 |
| CN107382753B (zh) * | 2017-07-24 | 2019-08-23 | 广东众生药业股份有限公司 | 一种高纯度盐酸利托君的制备方法 |
| CN115317471A (zh) * | 2022-05-13 | 2022-11-11 | 海南久常制药有限公司 | 一种盐酸利托君原料药及其片剂制备方法 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU639846B2 (en) * | 1990-12-24 | 1993-08-05 | Duphar International Research B.V. | Method for the preparation of erythro vicinal amino-alcohols |
-
1993
- 1993-06-30 US US08/204,160 patent/US5449694A/en not_active Expired - Fee Related
- 1993-06-30 DE DE69308115T patent/DE69308115T2/de not_active Expired - Fee Related
- 1993-06-30 JP JP5519689A patent/JP2758502B2/ja not_active Expired - Lifetime
- 1993-06-30 CA CA002116685A patent/CA2116685C/en not_active Expired - Fee Related
- 1993-06-30 KR KR1019940700661A patent/KR0151114B1/ko not_active Expired - Fee Related
- 1993-06-30 WO PCT/JP1993/000896 patent/WO1994001392A1/ja not_active Ceased
- 1993-06-30 EP EP93914933A patent/EP0603414B1/en not_active Expired - Lifetime
- 1993-06-30 DK DK93914933.2T patent/DK0603414T3/da active
- 1993-06-30 AT AT93914933T patent/ATE148880T1/de active
- 1993-06-30 ES ES93914933T patent/ES2100544T3/es not_active Expired - Lifetime
- 1993-07-01 CN CN93116246A patent/CN1040319C/zh not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| DK0603414T3 (da) | 1997-04-14 |
| JP2758502B2 (ja) | 1998-05-28 |
| CN1087079A (zh) | 1994-05-25 |
| US5449694A (en) | 1995-09-12 |
| EP0603414A1 (en) | 1994-06-29 |
| EP0603414A4 (en) | 1994-11-30 |
| WO1994001392A1 (fr) | 1994-01-20 |
| KR0151114B1 (ko) | 1998-10-15 |
| EP0603414B1 (en) | 1997-02-12 |
| CN1040319C (zh) | 1998-10-21 |
| ATE148880T1 (de) | 1997-02-15 |
| DE69308115D1 (de) | 1997-03-27 |
| CA2116685A1 (en) | 1994-01-20 |
| DE69308115T2 (de) | 1997-05-28 |
| CA2116685C (en) | 1999-11-23 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG2A | Definitive protection |
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