JPS6137726A - 血小板活性化因子によつて誘発される病気の治療用組成物 - Google Patents
血小板活性化因子によつて誘発される病気の治療用組成物Info
- Publication number
- JPS6137726A JPS6137726A JP15711385A JP15711385A JPS6137726A JP S6137726 A JPS6137726 A JP S6137726A JP 15711385 A JP15711385 A JP 15711385A JP 15711385 A JP15711385 A JP 15711385A JP S6137726 A JPS6137726 A JP S6137726A
- Authority
- JP
- Japan
- Prior art keywords
- paf
- gingolide
- induced
- dose
- injection
- 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.)
- Granted
Links
- 201000010099 disease Diseases 0.000 title claims description 14
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title claims description 14
- 230000001225 therapeutic effect Effects 0.000 title claims description 7
- 239000000203 mixture Substances 0.000 title claims 6
- 230000010118 platelet activation Effects 0.000 title 1
- 229930184727 ginkgolide Natural products 0.000 claims description 7
- 239000007921 spray Substances 0.000 claims description 7
- 238000001990 intravenous administration Methods 0.000 claims description 6
- 230000003213 activating effect Effects 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims 1
- SQOJOAFXDQDRGF-WJHVHIKBSA-N ginkgolide B Natural products O=C1[C@@H](C)[C@@]2(O)[C@@H]([C@H](O)[C@]34[C@@H]5OC(=O)[C@]23O[C@H]2OC(=O)[C@H](O)[C@@]42[C@H](C(C)(C)C)C5)O1 SQOJOAFXDQDRGF-WJHVHIKBSA-N 0.000 claims 1
- SQOJOAFXDQDRGF-MMQTXUMRSA-N ginkgolide-b Chemical compound O[C@H]([C@]12[C@H](C(C)(C)C)C[C@H]3OC4=O)C(=O)O[C@H]2O[C@]24[C@@]13[C@@H](O)[C@@H]1OC(=O)[C@@H](C)[C@]21O SQOJOAFXDQDRGF-MMQTXUMRSA-N 0.000 claims 1
- 208000009144 Pure autonomic failure Diseases 0.000 description 42
- 150000001875 compounds Chemical class 0.000 description 24
- 238000012360 testing method Methods 0.000 description 23
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- 239000007924 injection Substances 0.000 description 19
- 238000011282 treatment Methods 0.000 description 16
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- 241000700159 Rattus Species 0.000 description 12
- 238000000034 method Methods 0.000 description 11
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- 102100034937 Poly(A) RNA polymerase, mitochondrial Human genes 0.000 description 10
- 230000002401 inhibitory effect Effects 0.000 description 10
- HVAUUPRFYPCOCA-AREMUKBSSA-N 2-O-acetyl-1-O-hexadecyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCCOC[C@@H](OC(C)=O)COP([O-])(=O)OCC[N+](C)(C)C HVAUUPRFYPCOCA-AREMUKBSSA-N 0.000 description 8
- 241000282414 Homo sapiens Species 0.000 description 8
- 108010003541 Platelet Activating Factor Proteins 0.000 description 8
- 208000007536 Thrombosis Diseases 0.000 description 8
- 241000700198 Cavia Species 0.000 description 7
- 230000009471 action Effects 0.000 description 7
- 230000005764 inhibitory process Effects 0.000 description 7
- 230000002829 reductive effect Effects 0.000 description 7
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 239000003814 drug Substances 0.000 description 6
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- 241000282412 Homo Species 0.000 description 4
- UCTWMZQNUQWSLP-UHFFFAOYSA-N adrenaline Chemical compound CNCC(O)C1=CC=C(O)C(O)=C1 UCTWMZQNUQWSLP-UHFFFAOYSA-N 0.000 description 4
- 230000002776 aggregation Effects 0.000 description 4
- 238000004220 aggregation Methods 0.000 description 4
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- XTWYTFMLZFPYCI-KQYNXXCUSA-N 5'-adenylphosphoric acid Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O XTWYTFMLZFPYCI-KQYNXXCUSA-N 0.000 description 3
- XTWYTFMLZFPYCI-UHFFFAOYSA-N Adenosine diphosphate Natural products C1=NC=2C(N)=NC=NC=2N1C1OC(COP(O)(=O)OP(O)(O)=O)C(O)C1O XTWYTFMLZFPYCI-UHFFFAOYSA-N 0.000 description 3
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- 206010010904 Convulsion Diseases 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- 235000011201 Ginkgo Nutrition 0.000 description 2
- NTYJJOPFIAHURM-UHFFFAOYSA-N Histamine Chemical compound NCCC1=CN=CN1 NTYJJOPFIAHURM-UHFFFAOYSA-N 0.000 description 2
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- 239000007903 gelatin capsule Substances 0.000 description 2
- 229960001340 histamine Drugs 0.000 description 2
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- 229940021182 non-steroidal anti-inflammatory drug Drugs 0.000 description 2
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- 230000029058 respiratory gaseous exchange Effects 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- QZAYGJVTTNCVMB-UHFFFAOYSA-N serotonin Chemical compound C1=C(O)C=C2C(CCN)=CNC2=C1 QZAYGJVTTNCVMB-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000008733 trauma Effects 0.000 description 2
- 239000002966 varnish Substances 0.000 description 2
- SGTNSNPWRIOYBX-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-{[2-(3,4-dimethoxyphenyl)ethyl](methyl)amino}-2-(propan-2-yl)pentanenitrile Chemical compound C1=C(OC)C(OC)=CC=C1CCN(C)CCCC(C#N)(C(C)C)C1=CC=C(OC)C(OC)=C1 SGTNSNPWRIOYBX-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 206010002091 Anaesthesia Diseases 0.000 description 1
- 206010002199 Anaphylactic shock Diseases 0.000 description 1
- 206010003178 Arterial thrombosis Diseases 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000218631 Coniferophyta Species 0.000 description 1
- 206010011968 Decreased immune responsiveness Diseases 0.000 description 1
- 102100029493 EKC/KEOPS complex subunit TP53RK Human genes 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- XQLWNAFCTODIRK-UHFFFAOYSA-N Gallopamil Chemical compound C1=C(OC)C(OC)=CC=C1CCN(C)CCCC(C#N)(C(C)C)C1=CC(OC)=C(OC)C(OC)=C1 XQLWNAFCTODIRK-UHFFFAOYSA-N 0.000 description 1
- 101000872147 Homo sapiens Biogenesis of lysosome-related organelles complex 1 subunit 6 Proteins 0.000 description 1
- 101000693011 Homo sapiens Pancreatic alpha-amylase Proteins 0.000 description 1
- 101100245176 Homo sapiens TP53RK gene Proteins 0.000 description 1
- 238000012404 In vitro experiment Methods 0.000 description 1
- 241001124553 Lepismatidae Species 0.000 description 1
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- 108700023400 Platelet-activating factor receptors Proteins 0.000 description 1
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- 208000027418 Wounds and injury Diseases 0.000 description 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
- OIPILFWXSMYKGL-UHFFFAOYSA-N acetylcholine Chemical compound CC(=O)OCC[N+](C)(C)C OIPILFWXSMYKGL-UHFFFAOYSA-N 0.000 description 1
- 229960004373 acetylcholine Drugs 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000004931 aggregating effect Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000037005 anaesthesia Effects 0.000 description 1
- 208000003455 anaphylaxis Diseases 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 229940125715 antihistaminic agent Drugs 0.000 description 1
- 239000000739 antihistaminic agent Substances 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000001045 blue dye Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
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- 239000013256 coordination polymer Substances 0.000 description 1
- 229940109248 cromoglycate Drugs 0.000 description 1
- IMZMKUWMOSJXDT-UHFFFAOYSA-N cromoglycic acid Chemical compound O1C(C(O)=O)=CC(=O)C2=C1C=CC=C2OCC(O)COC1=CC=CC2=C1C(=O)C=C(C(O)=O)O2 IMZMKUWMOSJXDT-UHFFFAOYSA-N 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000007123 defense Effects 0.000 description 1
- 238000000586 desensitisation Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 231100000673 dose–response relationship Toxicity 0.000 description 1
- 230000000001 effect on platelet aggregation Effects 0.000 description 1
- 230000002866 effect on thrombosis Effects 0.000 description 1
- 230000003511 endothelial effect Effects 0.000 description 1
- KAQKFAOMNZTLHT-VVUHWYTRSA-N epoprostenol Chemical compound O1C(=CCCCC(O)=O)C[C@@H]2[C@@H](/C=C/[C@@H](O)CCCCC)[C@H](O)C[C@@H]21 KAQKFAOMNZTLHT-VVUHWYTRSA-N 0.000 description 1
- 229960001123 epoprostenol Drugs 0.000 description 1
- CJAONIOAQZUHPN-KKLWWLSJSA-N ethyl 12-[[2-[(2r,3r)-3-[2-[(12-ethoxy-12-oxododecyl)-methylamino]-2-oxoethoxy]butan-2-yl]oxyacetyl]-methylamino]dodecanoate Chemical compound CCOC(=O)CCCCCCCCCCCN(C)C(=O)CO[C@H](C)[C@@H](C)OCC(=O)N(C)CCCCCCCCCCCC(=O)OCC CJAONIOAQZUHPN-KKLWWLSJSA-N 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 238000002594 fluoroscopy Methods 0.000 description 1
- 229960000457 gallopamil Drugs 0.000 description 1
- 102000056984 human BLOC1S6 Human genes 0.000 description 1
- 230000028993 immune response Effects 0.000 description 1
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- 238000011534 incubation Methods 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000007928 intraperitoneal injection Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000000644 isotonic solution Substances 0.000 description 1
- 210000004731 jugular vein Anatomy 0.000 description 1
- YEESKJGWJFYOOK-IJHYULJSSA-N leukotriene D4 Chemical compound CCCCC\C=C/C\C=C/C=C/C=C/[C@H]([C@@H](O)CCCC(O)=O)SC[C@H](N)C(=O)NCC(O)=O YEESKJGWJFYOOK-IJHYULJSSA-N 0.000 description 1
- 150000002617 leukotrienes Chemical class 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 210000000440 neutrophil Anatomy 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000003359 percent control normalization Methods 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- 102000030769 platelet activating factor receptor Human genes 0.000 description 1
- 201000003144 pneumothorax Diseases 0.000 description 1
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- -1 rompin Chemical compound 0.000 description 1
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- 239000002904 solvent Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 229960004072 thrombin Drugs 0.000 description 1
- 230000001732 thrombotic effect Effects 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 210000003437 trachea Anatomy 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- 230000002792 vascular Effects 0.000 description 1
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- 230000002227 vasoactive effect Effects 0.000 description 1
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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
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/365—Lactones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
Landscapes
- Health & Medical Sciences (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Medicines Containing Plant Substances (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8418424 | 1984-07-19 | ||
| GB848418424A GB8418424D0 (en) | 1984-07-19 | 1984-07-19 | Inhibition of platelets aggregation |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6137726A true JPS6137726A (ja) | 1986-02-22 |
| JPH0529009B2 JPH0529009B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1993-04-28 |
Family
ID=10564125
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15711385A Granted JPS6137726A (ja) | 1984-07-19 | 1985-07-18 | 血小板活性化因子によつて誘発される病気の治療用組成物 |
Country Status (9)
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2017537142A (ja) * | 2014-10-30 | 2017-12-14 | チェンデュ バイユ ファーマシューティカル カンパニー リミテッドＣｈｅｎｇｄｕ Ｂａｉｙｕ Ｐｈａｒｍａｃｅｕｔｉｃａｌ Ｃｏ．，Ｌｔｄ． | ギンコライドＢと第Ｘａ因子阻害剤とを含有する薬物組成物及びその製造方法と用途 |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4879285A (en) * | 1986-08-22 | 1989-11-07 | Royal North Shore Hospital And Area Health Service | Fertility control |
| DE3710921C2 (de) * | 1986-10-21 | 1996-09-26 | Korth Ruth | Verwendung der Gingkolide BN 52020, BN 52021 und BN 52063 zur Behandlung von Arteriosklerose |
| CN1030415A (zh) | 1987-02-20 | 1989-01-18 | 山之内制药株式会社 | 饱和的杂环碳酰胺衍生物和它的制备方法 |
| DE3707532C2 (de) * | 1987-03-09 | 1998-05-28 | Bauer Johann | Verwendung einer Kombination von Extr. Gingko biloba oder mindestens einem Gingkolid und Acetylsalicylsäure oder DL-Lysin-mono-acetylsalicylat oder Diflunisal zur Behandlung von Verbrennungen, Verbrühungen, Strahlenschäden und Erfrierungen |
| DE3726864A1 (de) * | 1987-08-12 | 1989-02-23 | Bauer Johann | Verwendung von ginkgo bilobae extrakten zur bekaempfung von entzuendlichen prozessen |
| DE4034090B4 (de) * | 1990-10-20 | 2004-05-13 | Korth, Ruth-Maria, Dr.med. | Verwendung von Ginkgoliden und Triazolothienodiazepinen zur Behandlung der Blutplättchenaggregation in Gegenwart von LDL und LA-paf |
| EP0540766A1 (en) * | 1991-11-04 | 1993-05-12 | Korth, Ruth-Maria, Dr. med | Treatment of eosinophil-mediated diseases with Paf antagonists and procedure for determining their efficacy. |
| DE4017818C2 (de) * | 1990-06-06 | 2001-02-15 | Korth Ruth Maria | Verfahren zur Überprüfung von Substanzen auf ihre Wirksamkeit als paf-Acether-Antagonisten |
| US5530023A (en) * | 1987-10-20 | 1996-06-25 | Korth; Ruth | Production of binding sites for PAF, PAF analogues and PAF antagonists in endothelial cells |
| EP0540767B9 (en) * | 1991-11-04 | 2004-12-22 | Korth, Ruth-Maria, Dr. med | Treatment and prevention of mental diseases mediated by elevated lyso paf levels with paf antagonists |
| US5895785A (en) * | 1987-10-20 | 1999-04-20 | Ruth Korth | Treatment and prevention of disorders mediated by LA-paf or endothelial cells |
| DE3735525C2 (de) * | 1987-10-20 | 1997-02-20 | Korth Ruth Maria | Verfahren zur Bestimmung der Wirksamkeit von paf-Acether-Rezeptor-Antagonisten |
| GB8725871D0 (en) * | 1987-11-04 | 1987-12-09 | Scras | Ginkgolide derivatives |
| GB8725872D0 (en) * | 1987-11-04 | 1987-12-09 | Scras | Indenofuran derivative |
| FR2627387B1 (fr) * | 1988-02-24 | 1992-06-05 | Fabre Sa Pierre | Procede d'obtention d'un extrait de feuilles de ginkgo biloba |
| DE3840832A1 (de) * | 1988-12-03 | 1990-06-07 | Mueller Robert Dr | Aeusserlich anzuwendendes praeparat |
| US5002965A (en) * | 1989-05-09 | 1991-03-26 | Societe De Conseils De Recherches Et D'applications Scientifiques (S.C.R.A.S.) | Use of ginkgolides to prevent reperfusion injury in organ transplantation |
| ES2095316T3 (es) * | 1990-05-31 | 1997-02-16 | Allergan Inc | Uso de antagonistas del factor activador de plaquetas como agentes antipruriticos. |
| US6277846B1 (en) | 1990-05-31 | 2001-08-21 | Allergan Sales, Inc. | Use of platelet activating factor antagonists as anti-pruritic agents |
| DE69132379T2 (de) * | 1990-06-06 | 2001-03-01 | Ruth-Maria Korth | Behandlung von Erkrankungen mit Paf-Antagonisten und Verfahren zur Bestimmung deren Wirksamkeit |
| GB9107425D0 (en) * | 1991-04-09 | 1991-05-22 | Scras | Preparation of ginkgolide b |
| GB9408044D0 (en) * | 1994-04-22 | 1994-06-15 | Sod Conseils Rech Applic | Conversion of ginkgolide c to ginkgolide b |
| US6274621B1 (en) * | 1995-11-09 | 2001-08-14 | Societe De Conseils De Recherches Et D'applications Scientifiques, Sas | Ginkgolides for inhibition of membrane expression of benzodiazepine receptors |
| FR2763592B1 (fr) * | 1997-05-20 | 1999-07-16 | Sod Conseils Rech Applic | Nouveaux derives glycosyles des ginkgolides, leur application en tant que medicaments et compositions pharmaceutiques les contenant |
| KR100258018B1 (ko) * | 1997-12-23 | 2000-07-01 | 유승필 | 티클로피딘과 은행잎 추출물을 함유한 약제조성물 |
| DE19802697A1 (de) | 1998-01-24 | 1999-07-29 | Bayer Ag | Selektive Herbizide auf Basis von N-Aryl-triazolin(thi)onen und N-Arylsulfonylamino(thio)carbonyltriazolin(thi)onen |
| US7078434B1 (en) | 1999-08-12 | 2006-07-18 | Societe De Conseils De Recherches Et D'applications Scientifiques Sas | Use of Ginkgo extract |
| AU2004242777B2 (en) * | 2003-05-30 | 2011-05-12 | Ranbaxy Laboratories Limited | Substituted pyrrole derivatives and their use as HMG-Co inhibitors |
| BRPI0618379A2 (pt) * | 2005-11-08 | 2011-08-30 | Ranbaxy Lab Ltd | processo para preparação do hemi-sal de cálcio do ácido (3r,5r) -7-[2-(4-fluorofenil)-5-isopropil-3-fenil-4-[(4-hidroxime tilfenilamino) carbonil]-pirrol-1-il] -3, 5-diidroxi heptanóico |
| CL2007000667A1 (es) * | 2006-03-14 | 2008-03-14 | Ranbaxi Lab Ltd | Composicion farmaceutica que comprende al acido 7-[2-(4-fluorofenil)-5-isopropil-3-fenil-4-[(4-hidroximetilfenilamino)carbonil]pirrol-1-il]-3,5-dihidroxi-heptanoico o una sal y al menos un agente estabilizante; procedimiento de preparacion, util en e |
| WO2008010087A2 (en) * | 2006-07-14 | 2008-01-24 | Ranbaxy Laboratories Limited | Polymorphic forms of an hmg-coa reductase inhibitor and uses thereof |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2117429C3 (de) * | 1971-04-08 | 1982-04-01 | Fa. Dr. Willmar Schwabe, 7500 Karlsruhe | Verfahren zur Herstellung eines Injektions- bzw. Infusionspräparates mit einem Gehalt an einem Wirkstoffgemisch aus den Blättern von Ginkgo biloba |
| FR2518406A1 (fr) * | 1981-12-22 | 1983-06-24 | Prodipharm | Nouveau procede d'obtention de substances vaso-actives extraites de feuilles de ginkgo |
-
1984
- 1984-07-19 GB GB848418424A patent/GB8418424D0/en active Pending
-
1985
- 1985-01-23 US US06/693,716 patent/US4734280A/en not_active Expired - Lifetime
- 1985-03-12 BE BE0/214631A patent/BE901915A/fr unknown
- 1985-04-18 DE DE19853514054 patent/DE3514054A1/de active Granted
- 1985-07-11 GB GB08517577A patent/GB2162062B/en not_active Expired
- 1985-07-12 BE BE0/215337A patent/BE902874A/fr not_active IP Right Cessation
- 1985-07-18 FR FR8510993A patent/FR2567758B1/fr not_active Expired - Lifetime
- 1985-07-18 JP JP15711385A patent/JPS6137726A/ja active Granted
-
1988
- 1988-03-01 MY MYPI88000209A patent/MY102586A/en unknown
- 1988-12-06 SG SG859/88A patent/SG85988G/en unknown
-
1989
- 1989-07-27 HK HK601/89A patent/HK60189A/xx not_active IP Right Cessation
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2017537142A (ja) * | 2014-10-30 | 2017-12-14 | チェンデュ バイユ ファーマシューティカル カンパニー リミテッドＣｈｅｎｇｄｕ Ｂａｉｙｕ Ｐｈａｒｍａｃｅｕｔｉｃａｌ Ｃｏ．，Ｌｔｄ． | ギンコライドＢと第Ｘａ因子阻害剤とを含有する薬物組成物及びその製造方法と用途 |
Also Published As
| Publication number | Publication date |
|---|---|
| SG85988G (en) | 1989-05-26 |
| FR2567758B1 (fr) | 1990-10-19 |
| US4734280A (en) | 1988-03-29 |
| GB2162062B (en) | 1988-07-20 |
| DE3514054C2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1991-06-06 |
| JPH0529009B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1993-04-28 |
| MY102586A (en) | 1992-07-31 |
| FR2567758A1 (fr) | 1986-01-24 |
| BE901915A (fr) | 1985-07-01 |
| DE3514054A1 (de) | 1986-01-23 |
| GB8418424D0 (en) | 1984-08-22 |
| GB2162062A (en) | 1986-01-29 |
| BE902874A (fr) | 1985-11-04 |
| HK60189A (en) | 1989-08-04 |
| GB8517577D0 (en) | 1985-08-14 |
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