JPH0536411B2 - - Google Patents
Info
- Publication number
- JPH0536411B2 JPH0536411B2 JP62075470A JP7547087A JPH0536411B2 JP H0536411 B2 JPH0536411 B2 JP H0536411B2 JP 62075470 A JP62075470 A JP 62075470A JP 7547087 A JP7547087 A JP 7547087A JP H0536411 B2 JPH0536411 B2 JP H0536411B2
- Authority
- JP
- Japan
- Prior art keywords
- substance
- solid solution
- solution composition
- liters
- suspension
- 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
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/18—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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/141—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers
- A61K9/146—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers with organic macromolecular compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Medicinal Preparation (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Reinforced Plastic Materials (AREA)
- Cosmetics (AREA)
- Colloid Chemistry (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB868608080A GB8608080D0 (en) | 1986-04-02 | 1986-04-02 | Solid dispersion composition |
| GB8608080 | 1986-04-02 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62277321A JPS62277321A (ja) | 1987-12-02 |
| JPH0536411B2 true JPH0536411B2 (enExample) | 1993-05-31 |
Family
ID=10595572
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62075470A Granted JPS62277321A (ja) | 1986-04-02 | 1987-03-27 | Fr―900506物質の固形医薬製剤用固溶体組成物 |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US4916138A (enExample) |
| EP (1) | EP0240773B1 (enExample) |
| JP (1) | JPS62277321A (enExample) |
| KR (2) | KR950007209B1 (enExample) |
| AT (1) | ATE73327T1 (enExample) |
| CA (1) | CA1302279C (enExample) |
| DE (1) | DE3777223D1 (enExample) |
| DK (1) | DK174979B1 (enExample) |
| ES (1) | ES2032397T3 (enExample) |
| GB (1) | GB8608080D0 (enExample) |
| GR (1) | GR3004124T3 (enExample) |
| HK (1) | HK6397A (enExample) |
| IE (1) | IE59712B1 (enExample) |
| MX (1) | MX9202945A (enExample) |
| RU (1) | RU1826977C (enExample) |
| UA (1) | UA13209A (enExample) |
Families Citing this family (80)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5366971A (en) * | 1987-11-09 | 1994-11-22 | Sandoz Ltd. | Use of 11,28-dioxa-4-azatricyclo[22.3.1.04,9 ]octacos-18-ene derivatives and pharmaceutical compositions containing them |
| JPH02206A (ja) * | 1987-11-11 | 1990-01-05 | Fujisawa Pharmaceut Co Ltd | エキシホンと水溶性高分子化合物とを含有することを特徴とする新規製剤 |
| ATE84213T1 (de) * | 1987-11-11 | 1993-01-15 | Pharmascience Lab | Exifon und ein wasserloesliches polymer enthaltende pharmazeutische zubereitung. |
| FR2640137A1 (fr) * | 1988-12-08 | 1990-06-15 | Texinfine Sa | Systemes transporteurs de principes actifs lipophiles et leur procede d'obtention |
| AU635286B2 (en) * | 1989-07-05 | 1993-03-18 | Astellas Pharma Inc. | Aqueous liquid composition for external use |
| US5208228A (en) * | 1989-11-13 | 1993-05-04 | Merck & Co., Inc. | Aminomacrolides and derivatives having immunosuppressive activity |
| KR0177158B1 (ko) * | 1990-03-01 | 1999-03-20 | 후지사와 도모기찌로 | 면역억제 활성을 갖는 트리사이클릭 화합물 함유 용액 제제 |
| ES2093106T3 (es) * | 1990-07-19 | 1996-12-16 | Otsuka Pharma Co Ltd | Preparacion solida. |
| US5143918A (en) * | 1990-10-11 | 1992-09-01 | Merck & Co., Inc. | Halomacrolides and derivatives having immunosuppressive activity |
| US5147877A (en) * | 1991-04-18 | 1992-09-15 | Merck & Co. Inc. | Semi-synthetic immunosuppressive macrolides |
| US5250678A (en) | 1991-05-13 | 1993-10-05 | Merck & Co., Inc. | O-aryl, O-alkyl, O-alkenyl and O-alkynylmacrolides having immunosuppressive activity |
| US5162334A (en) * | 1991-05-13 | 1992-11-10 | Merck & Co., Inc. | Amino O-alkyl, O-alkenyl and O-alkynlmacrolides having immunosuppressive activity |
| US5565560A (en) * | 1991-05-13 | 1996-10-15 | Merck & Co., Inc. | O-Aryl,O-alkyl,O-alkenyl and O-alkynylmacrolides having immunosuppressive activity |
| US5189042A (en) * | 1991-08-22 | 1993-02-23 | Merck & Co. Inc. | Fluoromacrolides having immunosuppressive activity |
| US5208241A (en) * | 1991-09-09 | 1993-05-04 | Merck & Co., Inc. | N-heteroaryl, n-alkylheteroaryl, n-alkenylheteroaryl and n-alkynylheteroarylmacrolides having immunosuppressive activity |
| ATE183083T1 (de) * | 1992-11-18 | 1999-08-15 | Fujisawa Pharmaceutical Co | Pharmazeutische zubereitung mit verlängerter wirkung |
| DE4316537A1 (de) * | 1993-05-18 | 1994-11-24 | Basf Ag | Zubereitungen in Form fester Lösungen |
| US5693648A (en) * | 1994-09-30 | 1997-12-02 | Merck & Co., Inc. | O-aryl, O-alkyl, O-alkenyl and O-alkynyl-macrolides having immunosuppressive activity |
| BE1009856A5 (fr) | 1995-07-14 | 1997-10-07 | Sandoz Sa | Composition pharmaceutique sous la forme d'une dispersion solide comprenant un macrolide et un vehicule. |
| WO1997010806A1 (en) | 1995-09-19 | 1997-03-27 | Fujisawa Pharmaceutical Co., Ltd. | Aerosol compositions |
| TW426516B (en) * | 1996-12-06 | 2001-03-21 | Fujisawa Pharmaceutical Co | An oral pharmaceutical composition in solid dispersion containing water-insoluble tricyclic compounds |
| EP0978288A4 (en) * | 1997-04-11 | 2006-07-12 | Astellas Pharma Inc | DRUG COMPOSITION |
| KR100440553B1 (ko) * | 1998-03-26 | 2004-07-15 | 후지사와 야꾸힝 고교 가부시키가이샤 | 서방성 제제 |
| US6350786B1 (en) * | 1998-09-22 | 2002-02-26 | Hoffmann-La Roche Inc. | Stable complexes of poorly soluble compounds in ionic polymers |
| US6410301B1 (en) | 1998-11-20 | 2002-06-25 | Kosan Biosciences, Inc. | Myxococcus host cells for the production of epothilones |
| US6303342B1 (en) * | 1998-11-20 | 2001-10-16 | Kason Biosciences, Inc. | Recombinant methods and materials for producing epothilones C and D |
| US20040176358A1 (en) * | 1999-04-30 | 2004-09-09 | The Regents Of The University Of Michigan | Compositions and methods relating to novel compounds and targets thereof |
| US20030119029A1 (en) * | 1999-04-30 | 2003-06-26 | Regents Of The University Of Michigan | Compositions and methods relating to novel benzodiazepine compounds and targets thereof |
| US7063857B1 (en) | 1999-04-30 | 2006-06-20 | Sucampo Ag | Use of macrolide compounds for the treatment of dry eye |
| IL146222A0 (en) * | 1999-04-30 | 2002-07-25 | Univ Michigan | Therapeutic applications of pro-apoptotic benzodiazepines |
| US20060025388A1 (en) | 1999-04-30 | 2006-02-02 | Glick Gary D | Compositions and methods relating to novel compounds and targets thereof |
| US7144880B2 (en) | 1999-04-30 | 2006-12-05 | Regents Of The University Of Michigan | Compositions relating to novel compounds and targets thereof |
| US20050113460A1 (en) * | 1999-04-30 | 2005-05-26 | The Regents Of The University Of Michigan | Compositions and methods relating to novel compounds and targets thereof |
| AU2001238476A1 (en) | 2000-02-18 | 2001-08-27 | Kosan Biosciences, Inc. | Motocide compounds |
| US6750047B2 (en) * | 2000-08-21 | 2004-06-15 | Kosan Biosciences, Inc. | Fermentation and purification of migrastatin and analog |
| GB0108498D0 (en) * | 2001-04-04 | 2001-05-23 | Novartis Ag | Organic Compounds |
| ES2333645T3 (es) * | 2001-06-22 | 2010-02-25 | Bend Research, Inc. | Composiciones farmaceuticas de dispersiones de medicamentos y polimeros neutros. |
| GB0123400D0 (en) | 2001-09-28 | 2001-11-21 | Novartis Ag | Organic compounds |
| US6989131B2 (en) * | 2002-03-12 | 2006-01-24 | Uop Llc | Catalytic reactor with integral evaporator |
| CN100363359C (zh) * | 2002-08-29 | 2008-01-23 | 菲塞股份有限公司 | 运动内酯化合物 |
| BRPI0412329A (pt) * | 2003-07-09 | 2006-09-05 | Chong Kun Dang Pharm Corp | dispersão sólida de tacrolimus e método de processar a mesma |
| SI1663216T1 (sl) * | 2003-08-29 | 2012-03-30 | Veloxis Pharmaceuticals As | Sestavek z modificiranim sproščanjem ki vsebuje takrolimus |
| AU2004267909B2 (en) | 2003-08-29 | 2008-12-18 | Veloxis Pharmaceuticals, Inc. | Modified release compositions comprising tacrolimus |
| US20050272723A1 (en) * | 2004-04-27 | 2005-12-08 | The Regents Of The University Of Michigan | Methods and compositions for treating diseases and conditions associated with mitochondrial function |
| US20090275099A1 (en) * | 2004-04-27 | 2009-11-05 | Regents Of The University Of Michigan | Methods and compositions for treating diseases and conditions associated with mitochondrial function |
| US20110104186A1 (en) | 2004-06-24 | 2011-05-05 | Nicholas Valiante | Small molecule immunopotentiators and assays for their detection |
| US20060014677A1 (en) * | 2004-07-19 | 2006-01-19 | Isotechnika International Inc. | Method for maximizing efficacy and predicting and minimizing toxicity of calcineurin inhibitor compounds |
| US20060052369A1 (en) * | 2004-09-07 | 2006-03-09 | The Regents Of The University Of Michigan | Compositions and methods relating to novel compounds and targets thereof |
| US7638624B2 (en) * | 2005-01-03 | 2009-12-29 | The Regents Of The University Of Michigan | Compositions and methods relating to novel benzodiazepine compounds and derivatives |
| KR100678824B1 (ko) * | 2005-02-04 | 2007-02-05 | 한미약품 주식회사 | 용해성이 증가된 무정형 타크로리무스 고체분산체 및 이를포함하는 약제학적 조성물 |
| EP1893218A4 (en) | 2005-06-01 | 2011-01-12 | Univ Michigan | UNLOCKED BENZODIAZEPINE COMPOSITIONS AND METHOD |
| US20070105844A1 (en) * | 2005-10-26 | 2007-05-10 | Regents Of The University Of Michigan | Therapeutic compositions and methods |
| CA2628193C (en) | 2005-11-01 | 2012-08-14 | The Regents Of The University Of Michigan | Novel 1,4-benzodiazepine-2,5-diones with therapeutic properties |
| GB0602632D0 (en) * | 2006-02-08 | 2006-03-22 | Pliva Istrazivacki Inst D O O | Preparation Of A Solid Dosage From Comprising Tacrolimus And/Or Sirolimus |
| US7759338B2 (en) * | 2006-04-27 | 2010-07-20 | The Regents Of The University Of Michigan | Soluble 1,4 benzodiazepine compounds and stable salts thereof |
| EP2037741B1 (en) | 2006-06-09 | 2013-11-27 | The Regents Of The University Of Michigan | Benzodiazepine derivatives for use in the treatment of immune, inflammatory and proliferative disorders |
| WO2008041553A1 (en) | 2006-09-26 | 2008-04-10 | Astellas Pharma Inc. | Tacrolimus sustained-release preparation |
| EP2119442A4 (en) * | 2006-12-28 | 2010-12-15 | Astellas Pharma Inc | PHARMACEUTICAL COMPOSITION WITH TACROLIMUS MAINTAINED RELEASE |
| CN101662940A (zh) * | 2007-03-09 | 2010-03-03 | 密执安州立大学董事会 | 与新化合物及其靶标有关的组合物和方法 |
| SI2167033T1 (sl) | 2007-05-30 | 2017-08-31 | Veloxis Pharmaceuticals A/S | Odmerna oblika, ki obsega takrolimus, za dajanje enkrat na dan |
| US12083103B2 (en) | 2007-05-30 | 2024-09-10 | Veloxis Pharmaceuticals, Inc. | Tacrolimus for improved treatment of transplant patients |
| JP5416122B2 (ja) | 2007-09-14 | 2014-02-12 | ザ リージェンツ オブ ザ ユニバーシティ オブ ミシガン | F1F0−ATPaseインヒビターおよび関連の方法 |
| TW200932240A (en) | 2007-10-25 | 2009-08-01 | Astellas Pharma Inc | Pharmaceutical composition containing lipophilic substance which inhibits IL-2 production |
| RU2010122902A (ru) | 2007-11-06 | 2011-12-20 | Дзе Риджентс оф дзе Юниверсити оф Мичиган (US) | Бензодиапениноновые соединения, применимые в лечении кожных состояний |
| CL2008000374A1 (es) * | 2008-02-05 | 2008-04-04 | Igloo Zone Chile S A | Composicion farmaceutica que comprende un polvo para suspension oral de tacrolimus o una de sus sales, hidratos o solvatos y excipientes farmaceuticamente aceptables; procedimiento de preparacion de dicha composicion farmaceutica; y uso para la preve |
| KR101003042B1 (ko) | 2008-03-17 | 2010-12-21 | 종근당바이오 주식회사 | 고순도 타크로리무스의 정제 방법 |
| US8222272B2 (en) * | 2008-04-11 | 2012-07-17 | Roxane Laboratories, Inc. | Pharmaceutical formulation and process comprising a solid dispersion of macrolide (tacrolimus) |
| US12403095B2 (en) | 2008-05-30 | 2025-09-02 | Veloxis Pharmaceuticals, Inc. | Stabilized tacrolimus composition |
| JP5567573B2 (ja) | 2008-09-11 | 2014-08-06 | ザ リージェンツ オブ ザ ユニバーシティ オブ ミシガン | アリールグアニジンf1f0−atpアーゼ阻害剤およびそれと関連する方法 |
| WO2010121164A2 (en) | 2009-04-17 | 2010-10-21 | The Regents Of The University Of Michigan | 1,4-benzodiazepinone compounds and their use in treating cancer |
| US8673897B2 (en) | 2009-09-18 | 2014-03-18 | The Regents Of The University Of Michigan | Benzodiazepinone compounds and methods of treatment using same |
| AU2010322287B2 (en) | 2009-11-17 | 2014-04-03 | The Regents Of The University Of Michigan | 1,4-benzodiazepine-2,5-diones and related compounds with therapeutic properties |
| CN102753179A (zh) | 2009-11-17 | 2012-10-24 | 密执安大学评议会 | 具有治疗性能的1,4-苯并二氮杂*-2,5-二酮和相关化合物 |
| LT2575769T (lt) | 2010-02-17 | 2016-10-10 | Veloxis Pharmaceuticals A/S | Stabilizuota takrolimuzo kompozicija |
| US20130116239A1 (en) | 2010-06-14 | 2013-05-09 | ratiopharm GnbH | Ivabradine-containing pharmaceutical composition with modified release |
| WO2012026896A1 (en) | 2010-08-25 | 2012-03-01 | Les Laboratoires Medis Sa | Surface modified micronized tacrolimus crystalline particles and pharmaceutical compositions thereof |
| KR101243938B1 (ko) * | 2010-10-19 | 2013-03-19 | 이희엽 | 타크롤리무스를 유효성분으로 함유하는 서방형 펠렛 |
| BR112014021506B1 (pt) | 2012-04-11 | 2020-06-16 | Dow Global Technologies Llc | Composição líquida, uso de uma composição líquida, dispersão de sólidos, processo para revestir uma forma de dosagem e processo para a manufatura de cápsulas |
| KR20160058840A (ko) | 2013-09-25 | 2016-05-25 | 다우 글로벌 테크놀로지스 엘엘씨 | 유기 액체 희석제 및 특정의 하이드록시알킬 메틸셀룰로오스를 포함하는 조성물 |
| WO2016078481A1 (zh) | 2014-11-21 | 2016-05-26 | 杭州领业医药科技有限公司 | 一种含他克莫司的药物组合物及其制备方法 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL130099C (enExample) * | 1963-10-11 | |||
| DE1492034A1 (de) * | 1965-05-18 | 1969-02-20 | Merck Ag E | Verfahren zur Herstellung fester haltbarer Zubereitungen von empfindlichen,in Wasser schwer loeslichen Wirkstoffen,vorzugsweise Arzneimitteln |
| US3852421A (en) * | 1970-03-23 | 1974-12-03 | Shinetsu Chemical Co | Excipient and shaped medicaments prepared therewith |
| GB1322306A (en) * | 1971-04-15 | 1973-07-04 | Meiji Seika Co | Stabilized antibiotic preparation and manufacturing process therefor |
| US4127647A (en) * | 1975-04-08 | 1978-11-28 | Meiji Seika Kaisha, Ltd. | Process for preparation of stable amorphous macrolide antibiotic solids |
| GB1593261A (en) * | 1976-07-23 | 1981-07-15 | Inveresk Res Int | Controlled release suppository |
| GB1579818A (en) * | 1977-06-07 | 1980-11-26 | Yamanouchi Pharma Co Ltd | Nifedipine-containing solid preparation composition |
| DE3013839A1 (de) * | 1979-04-13 | 1980-10-30 | Freunt Ind Co Ltd | Verfahren zur herstellung einer aktivierten pharmazeutischen zusammensetzung |
| CA1146866A (en) * | 1979-07-05 | 1983-05-24 | Yamanouchi Pharmaceutical Co. Ltd. | Process for the production of sustained release pharmaceutical composition of solid medical material |
| US4259314A (en) * | 1979-12-10 | 1981-03-31 | Hans Lowey | Method and composition for the preparation of controlled long-acting pharmaceuticals |
| US4369172A (en) * | 1981-12-18 | 1983-01-18 | Forest Laboratories Inc. | Prolonged release therapeutic compositions based on hydroxypropylmethylcellulose |
| US4389393A (en) * | 1982-03-26 | 1983-06-21 | Forest Laboratories, Inc. | Sustained release therapeutic compositions based on high molecular weight hydroxypropylmethylcellulose |
| JPS6038322A (ja) * | 1983-08-11 | 1985-02-27 | Fujisawa Pharmaceut Co Ltd | ジヒドロピリジンa物質含有易溶性固形製剤 |
| US4894366A (en) * | 1984-12-03 | 1990-01-16 | Fujisawa Pharmaceutical Company, Ltd. | Tricyclo compounds, a process for their production and a pharmaceutical composition containing the same |
-
1986
- 1986-04-02 GB GB868608080A patent/GB8608080D0/en active Pending
-
1987
- 1987-03-14 AT AT87103716T patent/ATE73327T1/de not_active IP Right Cessation
- 1987-03-14 DE DE8787103716T patent/DE3777223D1/de not_active Expired - Lifetime
- 1987-03-14 EP EP87103716A patent/EP0240773B1/en not_active Expired - Lifetime
- 1987-03-14 ES ES198787103716T patent/ES2032397T3/es not_active Expired - Lifetime
- 1987-03-18 DK DK198701404A patent/DK174979B1/da not_active IP Right Cessation
- 1987-03-27 JP JP62075470A patent/JPS62277321A/ja active Granted
- 1987-04-01 UA UA4202275A patent/UA13209A/uk unknown
- 1987-04-01 IE IE84387A patent/IE59712B1/en not_active IP Right Cessation
- 1987-04-01 KR KR1019870003087A patent/KR950007209B1/ko not_active Expired - Lifetime
- 1987-04-01 CA CA000533582A patent/CA1302279C/en not_active Expired - Lifetime
- 1987-04-01 RU SU4202275A patent/RU1826977C/ru active
- 1987-07-01 KR KR1019870007053A patent/KR950007210B1/ko not_active Expired - Lifetime
-
1988
- 1988-07-25 US US07/224,235 patent/US4916138A/en not_active Expired - Lifetime
-
1992
- 1992-03-24 GR GR910402151T patent/GR3004124T3/el unknown
- 1992-06-17 MX MX9202945A patent/MX9202945A/es unknown
-
1997
- 1997-01-16 HK HK6397A patent/HK6397A/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| ES2032397T3 (es) | 1993-02-16 |
| KR950007210B1 (ko) | 1995-07-04 |
| KR890001626A (ko) | 1989-03-28 |
| GR3004124T3 (enExample) | 1993-03-31 |
| DK140487D0 (da) | 1987-03-18 |
| ATE73327T1 (de) | 1992-03-15 |
| KR950007209B1 (ko) | 1995-07-04 |
| DK174979B1 (da) | 2004-04-05 |
| UA13209A (uk) | 1997-02-28 |
| IE870843L (en) | 1987-10-02 |
| US4916138A (en) | 1990-04-10 |
| EP0240773B1 (en) | 1992-03-11 |
| IE59712B1 (en) | 1994-03-23 |
| KR870010073A (ko) | 1987-11-30 |
| JPS62277321A (ja) | 1987-12-02 |
| MX9202945A (es) | 1992-07-01 |
| HK6397A (en) | 1997-01-24 |
| DE3777223D1 (de) | 1992-04-16 |
| RU1826977C (ru) | 1993-07-07 |
| EP0240773A1 (en) | 1987-10-14 |
| GB8608080D0 (en) | 1986-05-08 |
| DK140487A (da) | 1987-10-03 |
| CA1302279C (en) | 1992-06-02 |
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