HK6397A - Solid dispersion composition of FR-900506 substance - Google Patents
Solid dispersion composition of FR-900506 substance Download PDFInfo
- Publication number
- HK6397A HK6397A HK6397A HK6397A HK6397A HK 6397 A HK6397 A HK 6397A HK 6397 A HK6397 A HK 6397A HK 6397 A HK6397 A HK 6397A HK 6397 A HK6397 A HK 6397A
- Authority
- HK
- Hong Kong
- Prior art keywords
- substance
- solid dispersion
- dispersion composition
- water
- liters
- Prior art date
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicinal Preparation (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Reinforced Plastic Materials (AREA)
- Cosmetics (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Colloid Chemistry (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB868608080A GB8608080D0 (en) | 1986-04-02 | 1986-04-02 | Solid dispersion composition |
Publications (1)
Publication Number | Publication Date |
---|---|
HK6397A true HK6397A (en) | 1997-01-24 |
Family
ID=10595572
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HK6397A HK6397A (en) | 1986-04-02 | 1997-01-16 | Solid dispersion composition of FR-900506 substance |
Country Status (16)
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 |
ES2043766T3 (es) * | 1987-11-11 | 1994-01-01 | Pharmascience Lab | Una nueva composicion farmaceutica que comprende exifona y un polimero soluble en agua. |
FR2640137A1 (fr) * | 1988-12-08 | 1990-06-15 | Texinfine Sa | Systemes transporteurs de principes actifs lipophiles et leur procede d'obtention |
ZA905202B (en) * | 1989-07-05 | 1991-04-24 | Fujisawa Pharmaceutical Co | 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 |
WO1992001453A1 (en) * | 1990-07-19 | 1992-02-06 | Otsuka Pharmaceutical Co., Ltd. | Solid preparation |
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 |
US5565560A (en) * | 1991-05-13 | 1996-10-15 | 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 |
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 |
AU5434094A (en) * | 1992-11-18 | 1994-06-08 | Fujisawa Pharmaceutical Co., Ltd. | Prolonged-action pharmaceutical preparation |
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. |
ATE254450T1 (de) | 1995-09-19 | 2003-12-15 | Fujisawa Pharmaceutical Co | Aerosolzusammensetzungen |
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 |
SK286887B6 (sk) | 1998-03-26 | 2009-07-06 | Astellas Pharma Inc. | Farmaceutický prostriedok makrolidovej zlúčeniny s pomalým uvoľňovaním |
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 |
EP1135470A2 (en) | 1998-11-20 | 2001-09-26 | Kosan Biosciences, Inc. | Recombinant methods and materials for producing epothilone and epothilone derivatives |
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 |
US20060025388A1 (en) | 1999-04-30 | 2006-02-02 | Glick Gary D | Compositions and methods relating to novel compounds and targets thereof |
ES2214273T3 (es) * | 1999-04-30 | 2004-09-16 | The Regents Of The University Of Michigan | Utilizacion de benzodiazepinas para el tratamiento de enfermedades autoinmunes inducidas por apoptosis. |
US7144880B2 (en) * | 1999-04-30 | 2006-12-05 | Regents Of The University Of Michigan | Compositions relating to novel compounds and targets thereof |
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 |
US7063857B1 (en) | 1999-04-30 | 2006-06-20 | Sucampo Ag | Use of macrolide compounds for the treatment of dry eye |
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 |
CA2450957A1 (en) | 2001-06-22 | 2003-01-03 | Pfizer Products Inc. | Pharmaceutical compositions of dispersions of drugs and neutral polymers |
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 |
DE60325377D1 (de) * | 2002-08-29 | 2009-01-29 | Pfizer | Motilidverbindungen |
WO2005004848A1 (en) * | 2003-07-09 | 2005-01-20 | Chong Kun Dang Pharmaceutical Corp. | The solid dispersion of tacrolimus |
JP4903568B2 (ja) * | 2003-08-29 | 2012-03-28 | ベロクシス ファーマシューティカルズ エー/エス | タクロリムスを含む固体分散体 |
BRPI0413927B8 (pt) | 2003-08-29 | 2021-05-25 | Lifecycle Pharma As | composição farmacêutica compreendendo tacrolimus, forma de dosagem, uso da composição, e, método para a preparação da composição |
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 |
CA2571710A1 (en) | 2004-06-24 | 2006-11-02 | 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 |
AU2006203946B2 (en) * | 2005-01-03 | 2009-07-23 | The Regents Of The University Of Michigan | Compositions and methods relating to novel compounds and targets thereof |
KR100678824B1 (ko) * | 2005-02-04 | 2007-02-05 | 한미약품 주식회사 | 용해성이 증가된 무정형 타크로리무스 고체분산체 및 이를포함하는 약제학적 조성물 |
WO2007053193A2 (en) | 2005-06-01 | 2007-05-10 | The Regents Of The University Of Michigan | Unsolvated benzodiazepine compositions and methods |
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 |
CA2659549C (en) | 2006-06-09 | 2013-07-30 | The Regents Of The University Of Michigan | Compositions and methods relating to novel compounds and targets thereof |
CA2664641A1 (en) * | 2006-09-26 | 2008-04-10 | Astellas Pharma, Inc. | Controlled release dosage form of tacrolimus |
US20090011018A1 (en) * | 2006-12-28 | 2009-01-08 | Astellas Pharma Inc., | Sustained release formulation for tacrolimus |
KR101164718B1 (ko) * | 2007-03-09 | 2012-07-11 | 더 리젠츠 오브 더 유니버시티 오브 미시간 | 신규 화합물 및 이의 표적에 관한 조성물 및 방법 |
ES2634153T3 (es) | 2007-05-30 | 2017-09-26 | Veloxis Pharmaceuticals A/S | Forma de dosificación oral de una vez al día que comprende tacrolimus |
US12083103B2 (en) | 2007-05-30 | 2024-09-10 | Veloxis Pharmaceuticals, Inc. | Tacrolimus for improved treatment of transplant patients |
ES2614498T3 (es) | 2007-09-14 | 2017-05-31 | The Regents Of The University Of Michigan | Inhibidores de ATPasa F1F0 y métodos relacionados |
TW200932240A (en) | 2007-10-25 | 2009-08-01 | Astellas Pharma Inc | Pharmaceutical composition containing lipophilic substance which inhibits IL-2 production |
US8188072B2 (en) | 2007-11-06 | 2012-05-29 | The Regents Of The University Of Michigan | Benzodiazepinone compounds useful in the treatment of skin conditions |
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 |
US8497307B2 (en) | 2008-09-11 | 2013-07-30 | The Regents Of The University Of Michigan | Aryl guanidine F1F0-ATPase inhibitors and related methods |
US8604023B2 (en) | 2009-04-17 | 2013-12-10 | 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 |
WO2011062766A2 (en) | 2009-11-17 | 2011-05-26 | The Regents Of The University Of Michigan | 1,4-benzodiazepine-2,5-diones and related compounds with therapeutic properties |
US9126978B2 (en) | 2009-11-17 | 2015-09-08 | The Regents Of The University Of Michigan | 1,4-benzodiazepine-2,5-diones and related compounds with therapeutic properties |
EP2575769B1 (en) | 2010-02-17 | 2016-06-15 | Veloxis Pharmaceuticals A/S | Stabilized tacrolimus composition |
PT2579860E (pt) | 2010-06-14 | 2014-05-30 | Ratiopharm Gmbh | Composição farmacêutica que contém ivabradina com libertação modificada |
MA34586B1 (fr) | 2010-08-25 | 2013-10-02 | Medis Lab | Particules cristallines de tacrolimus micronise a surface modifiee et compositions pharmaceutiques associees |
KR101243938B1 (ko) * | 2010-10-19 | 2013-03-19 | 이희엽 | 타크롤리무스를 유효성분으로 함유하는 서방형 펠렛 |
JP6185559B2 (ja) * | 2012-04-11 | 2017-08-23 | ダウ グローバル テクノロジーズ エルエルシー | 有機希釈剤およびセルロースエーテルを含む組成物 |
CN105530918A (zh) * | 2013-09-25 | 2016-04-27 | 陶氏环球技术有限责任公司 | 包含有机液体稀释剂和特定羟烷基甲基纤维素的组合物 |
US20170072058A1 (en) * | 2014-11-21 | 2017-03-16 | Solipharma Llc | Pharmaceutical composition containing tacrolimus and preparation methods thereof |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL130099C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 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 EP EP87103716A patent/EP0240773B1/en not_active Expired - Lifetime
- 1987-03-14 ES ES198787103716T patent/ES2032397T3/es not_active Expired - Lifetime
- 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
- 1987-03-18 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 |
---|---|
KR950007209B1 (ko) | 1995-07-04 |
ES2032397T3 (es) | 1993-02-16 |
GR3004124T3 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1993-03-31 |
IE870843L (en) | 1987-10-02 |
DK140487D0 (da) | 1987-03-18 |
JPH0536411B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1993-05-31 |
DK140487A (da) | 1987-10-03 |
KR950007210B1 (ko) | 1995-07-04 |
DK174979B1 (da) | 2004-04-05 |
ATE73327T1 (de) | 1992-03-15 |
GB8608080D0 (en) | 1986-05-08 |
CA1302279C (en) | 1992-06-02 |
KR870010073A (ko) | 1987-11-30 |
RU1826977C (ru) | 1993-07-07 |
DE3777223D1 (de) | 1992-04-16 |
US4916138A (en) | 1990-04-10 |
EP0240773B1 (en) | 1992-03-11 |
IE59712B1 (en) | 1994-03-23 |
EP0240773A1 (en) | 1987-10-14 |
UA13209A (uk) | 1997-02-28 |
JPS62277321A (ja) | 1987-12-02 |
MX9202945A (es) | 1992-07-01 |
KR890001626A (ko) | 1989-03-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0240773B1 (en) | Solid dispersion composition of fr-900506 substance | |
KR930010708B1 (ko) | 트리사이클로 화합물의 제조방법 | |
EP0349061A2 (en) | Immunosuppressant agent | |
EP0353678B1 (en) | FR-901154 and FR-901155 substances, a process for their production | |
EP0349049A3 (en) | Immunosuppressant compound | |
CA2066499A1 (en) | Lipophilic macrolide useful as an immunosuppressant | |
JPH078873B2 (ja) | 免疫抑制剤として有効な新規の親油性マクロライド | |
EP0388962A2 (en) | BMY-41950 antitumor antibiotic | |
EP1751272A2 (en) | Production of tacrolimus (fk-506) using new streptomyces species | |
KR19990087816A (ko) | 신규 테르페닐 화합물 및 이를 함유한 약제 | |
CZ279307B6 (cs) | Rebeccamycinový analog, způsob jeho přípravy a farmaceutický prostředek, který ho obsahuje | |
EP0358508A2 (en) | Novel immunosuppressant compound | |
EP0378321A2 (en) | Microbial transformation product of L-683-590 | |
GB2278844A (en) | Microbial transformation product having immunosuppressive activity | |
RU2228337C2 (ru) | Ванкорезмицин (варианты), его использование, штамм amycolatopsis вида hil-006734 для его получения | |
US5359060A (en) | Phosponated derivatives of macrolides | |
EP0818464B1 (en) | Methylsulfomycin l, a process for its production and its use | |
CA2131373C (en) | 2-aminosugar derivatives of macrolides | |
JPH07500352A (ja) | マクロライドの糖誘導体 | |
US6004995A (en) | Macrolide compound 0406 | |
EP0501399A1 (en) | Physiologically active kanglemycin C, process for preparing the same and use thereof | |
EP0378320A2 (en) | Microbial transformation product | |
EP0369503A1 (en) | Method for the control of pneumocystis carinii | |
BAROW et al. | WIN 66306, A NEW NEUROKININ ANTAGONIST PRODUCED BY AN Aspergillus species: FERMENTATION, ISOLATION AND PHYSICO-CHEMICAL PROPERTIES | |
WO1992011275A1 (en) | 13-dimethyl fr-900506 derivative and the use as an immunosuppressive agent |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PF | Patent in force | ||
PE | Patent expired |
Effective date: 20070313 |