WO1996012496A1 - Utilisation de n-[(1s,trans)-2-hydroxycyclopentyl]-adenosine pour reduire une blessure myocardique - Google Patents
Utilisation de n-[(1s,trans)-2-hydroxycyclopentyl]-adenosine pour reduire une blessure myocardique Download PDFInfo
- Publication number
- WO1996012496A1 WO1996012496A1 PCT/EP1995/004089 EP9504089W WO9612496A1 WO 1996012496 A1 WO1996012496 A1 WO 1996012496A1 EP 9504089 W EP9504089 W EP 9504089W WO 9612496 A1 WO9612496 A1 WO 9612496A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- formula
- compound
- acceptable salt
- solvate
- physiologically acceptable
- 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.)
- Ceased
Links
- TXUZTJPPOVABRH-JYHQXFQUSA-N CCC1OC([n]2c(N)c(C(NC)=N)nc2)[IH][C@@H]1C Chemical compound CCC1OC([n]2c(N)c(C(NC)=N)nc2)[IH][C@@H]1C TXUZTJPPOVABRH-JYHQXFQUSA-N 0.000 description 1
- PSPPXRNUZVTTON-RNFRBKRXSA-N C[C@H](CC1)O[C@H]1[n]1c2ncnc(N)c2nc1 Chemical compound C[C@H](CC1)O[C@H]1[n]1c2ncnc(N)c2nc1 PSPPXRNUZVTTON-RNFRBKRXSA-N 0.000 description 1
- 0 Cc1c2nc[n]([C@@]3OI(CO)CC3)c2nc(*)n1 Chemical compound Cc1c2nc[n]([C@@]3OI(CO)CC3)c2nc(*)n1 0.000 description 1
- ORCVUFSKYJNEQI-KKJSVHSVSA-N OC[C@H]([C@H](C1)O)O[C@H]1[n]1c2ncnc(N[C@@H](CCC3)[C@H]3O)c2nc1 Chemical compound OC[C@H]([C@H](C1)O)O[C@H]1[n]1c2ncnc(N[C@@H](CCC3)[C@H]3O)c2nc1 ORCVUFSKYJNEQI-KKJSVHSVSA-N 0.000 description 1
- YEZOBWILXCIADB-OTICRUEKSA-N OC[C@H]([C@H]([C@H]1O)O)O[C@H]1N1C=NC2[IH](N[C@@H](CCC3)[C@H]3O)=NC=NC12 Chemical compound OC[C@H]([C@H]([C@H]1O)O)O[C@H]1N1C=NC2[IH](N[C@@H](CCC3)[C@H]3O)=NC=NC12 YEZOBWILXCIADB-OTICRUEKSA-N 0.000 description 1
Classifications
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7076—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines containing purines, e.g. adenosine, adenylic acid
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Molecular Biology (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Composé de la formule (1a) ou des sels ou solvates de celui-ci, acceptables sur le plan physiologique, destinés à la réduction de l'infarctus du myocarde consécutif à une ischémie myocardique sévère.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU38434/95A AU3843495A (en) | 1994-10-20 | 1995-10-18 | Use of n-{(1s,trans)-2-hydroxycyclopentyl}-adenosine for reducing myocardial injury |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9421133A GB9421133D0 (en) | 1994-10-20 | 1994-10-20 | Medicaments |
| GB9421133.1 | 1994-10-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO1996012496A1 true WO1996012496A1 (fr) | 1996-05-02 |
Family
ID=10763123
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP1995/004089 Ceased WO1996012496A1 (fr) | 1994-10-20 | 1995-10-18 | Utilisation de n-[(1s,trans)-2-hydroxycyclopentyl]-adenosine pour reduire une blessure myocardique |
Country Status (3)
| Country | Link |
|---|---|
| AU (1) | AU3843495A (fr) |
| GB (1) | GB9421133D0 (fr) |
| WO (1) | WO1996012496A1 (fr) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999017784A1 (fr) * | 1997-10-07 | 1999-04-15 | Regents Of The University Of California Corporation | Traitement de la vasculopathie peripherique obliterante et de la coronarite au moyen de conbinaisons d'heparine et d'un agoniste a2 adenosine, ou au moyen d'adenosine |
| US5972903A (en) * | 1997-10-07 | 1999-10-26 | Regents Of The University Of California Corporation | Method for promoting angiogenesis using heparin and adenosine |
| US6476351B1 (en) * | 1996-01-05 | 2002-11-05 | Lazare Kaplan International, Inc. | Laser marking system |
| US7414036B2 (en) | 2002-01-25 | 2008-08-19 | Muscagen Limited | Compounds useful as A3 adenosine receptor agonists |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0322242A2 (fr) * | 1987-12-23 | 1989-06-28 | Glaxo Group Limited | Dérivés d'adénosine |
| WO1992020346A1 (fr) * | 1991-05-22 | 1992-11-26 | Vanderbilt University | Methode et composition permettant de reduire la blessure du myocarde due au retablissement de la circulation |
| WO1993023418A1 (fr) * | 1992-05-14 | 1993-11-25 | Novo Nordisk A/S | Derives de la purine |
-
1994
- 1994-10-20 GB GB9421133A patent/GB9421133D0/en active Pending
-
1995
- 1995-10-18 AU AU38434/95A patent/AU3843495A/en not_active Abandoned
- 1995-10-18 WO PCT/EP1995/004089 patent/WO1996012496A1/fr not_active Ceased
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0322242A2 (fr) * | 1987-12-23 | 1989-06-28 | Glaxo Group Limited | Dérivés d'adénosine |
| WO1992020346A1 (fr) * | 1991-05-22 | 1992-11-26 | Vanderbilt University | Methode et composition permettant de reduire la blessure du myocarde due au retablissement de la circulation |
| WO1993023418A1 (fr) * | 1992-05-14 | 1993-11-25 | Novo Nordisk A/S | Derives de la purine |
Non-Patent Citations (5)
| Title |
|---|
| A. TSUCHIDA: "Pretreatment with the adenosine A1 selective agonist, 2-chloro-N6-cyclopentyladenosine (CCPA), causes a sustained limitation of infarct size in rabbits.", CARDIOVASC. RES., vol. 27, no. 4, 1993, pages 652 - 656 * |
| E.D. NORTON: "The effects of intravenous infusions of selective adenosine A1-receptor and A2-receptor agonists on myocardial reperfusion injury.", AM HEART J, vol. 123, no. 2, 1992, pages 332 - 338 * |
| J.D. THORNTON: "Intravenous pretreatment with A1-selective adenosine analogues protects the heart against infarction.", CIRCULATION, vol. 85, no. 2, 1992, pages 659 - 665 * |
| M. KARMAZYN: "Adenosine A1 receptor activation attenuates cardiac injury produced by hydrogen peroxide.", CIRC. RES., vol. 71, no. 5, 1992, pages 1107 - 1110 * |
| M.F. GURDEN: "Functional characterization of three adenosine receptor types.", BR. J. PHARMACOL., vol. 109, no. 3, 1992, pages 693 - 698 * |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6476351B1 (en) * | 1996-01-05 | 2002-11-05 | Lazare Kaplan International, Inc. | Laser marking system |
| WO1999017784A1 (fr) * | 1997-10-07 | 1999-04-15 | Regents Of The University Of California Corporation | Traitement de la vasculopathie peripherique obliterante et de la coronarite au moyen de conbinaisons d'heparine et d'un agoniste a2 adenosine, ou au moyen d'adenosine |
| US5972903A (en) * | 1997-10-07 | 1999-10-26 | Regents Of The University Of California Corporation | Method for promoting angiogenesis using heparin and adenosine |
| US6440947B1 (en) | 1997-10-07 | 2002-08-27 | The Regents Of The University Of California | Method for treating occlusive peripheral vascular disease and coronary disease |
| US7414036B2 (en) | 2002-01-25 | 2008-08-19 | Muscagen Limited | Compounds useful as A3 adenosine receptor agonists |
Also Published As
| Publication number | Publication date |
|---|---|
| GB9421133D0 (en) | 1994-12-07 |
| AU3843495A (en) | 1996-05-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4378347A (en) | Composition for treating the heart for myocardial infarction | |
| US4296100A (en) | Method of treating the heart for myocardial infarction | |
| Yun et al. | Role of prostaglandins in the control of renin secretion in the dog. | |
| CA2061270C (fr) | Methode et appareil pour traiter les blessures de reperfusion | |
| US5849763A (en) | Use of levobupivacaine as an anesthetic agent | |
| Trouve et al. | Nitrendipine: an antidote to cardiac and lethal toxicity of cocaine | |
| EP0627921A1 (fr) | Procede d'inhibition de la carcinogenese a l'aide d'un traitement a la deshydroepiandrosterone et ses analogues | |
| Herzog et al. | Short-term low dose intracoronary diltiazem administered at the onset of reperfusion reduces myocardial infarct size | |
| EP0344880B1 (fr) | Compositions pharmaceutiques à activité anticancéreuse | |
| DE69711649T2 (de) | P1, p4-dithio-p2,p3-monochloromethylen 5',5'''-diadenosin-p1,p4-tetraphosphat verwendet als anti-thrombose mittel | |
| Didolkar et al. | Comparison of regional versus systemic chemotherapy with adriamycin | |
| EP0610336B1 (fr) | Traitement des troubles neurologiques a l'aide d'un compose inhibant l'interleukin-1 | |
| Perla et al. | Prevention of histamine and surgical shock by cortical hormone (desoxycorticosterone acetate and cortin) and saline | |
| JP3253302B2 (ja) | 3−ジアルキルアミノエトキシベンゾイル−ベンゾフランを含有する非経口溶液 | |
| HU206186B (en) | Process for producing pharmaceutical compositions comprising amino acid derivatives having ace-inhibiting effect | |
| WO1996012496A1 (fr) | Utilisation de n-[(1s,trans)-2-hydroxycyclopentyl]-adenosine pour reduire une blessure myocardique | |
| CN113577051A (zh) | 一种维拉帕米在制备保护软骨细胞缓解骨关节炎的产品中的应用 | |
| RU2432948C2 (ru) | Применение активаторов растворимой гуанилатциклазы для лечения нарушений кровоснабжения | |
| RU2252754C2 (ru) | Применение карипорида для уменьшения нежелательных воздействий макролидных антибиотиков при ишемии и реперфузии сердца | |
| US5585355A (en) | Method for increasing blood-ocular barrier permeability with permeabilizer peptides | |
| Stanford | The stress response to trauma and critical illness | |
| EP0366033A2 (fr) | Méthode pour modifier le dysfonctionnement post-ischémique du myocarde en utilisant un inhibiteur de l'ACE seul ou en combinaison avec un agent thrombolytique, et la combinaison | |
| CA2160689C (fr) | Nouvelle methode de traitement | |
| US5232950A (en) | Method for using ketamine for prevention or reduction of the effects of stroke in a subject having increased risk for stroke | |
| CN114796217B (zh) | 一种含有西洛他唑的组合物在制备治疗脑血管病药物中的应用 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AK | Designated states |
Kind code of ref document: A1 Designated state(s): AL AM AT AU BB BG BR BY CA CH CN CZ DE DK EE ES FI GB GE HU IS JP KE KG KP KR KZ LK LR LT LU LV MD MG MK MN MW MX NO NZ PL PT RO RU SD SE SG SI SK TJ TM TT UA UG US UZ VN |
|
| AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): KE MW SD SZ UG AT BE CH DE DK ES FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN ML MR NE SN TD TG |
|
| DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
| REG | Reference to national code |
Ref country code: DE Ref legal event code: 8642 |
|
| 122 | Ep: pct application non-entry in european phase | ||
| NENP | Non-entry into the national phase |
Ref country code: CA |