ZA200105072B - Troxerutin with high trihydroxy-ethyl-rutin content and method for preparing same. - Google Patents
Troxerutin with high trihydroxy-ethyl-rutin content and method for preparing same. Download PDFInfo
- Publication number
- ZA200105072B ZA200105072B ZA200105072A ZA200105072A ZA200105072B ZA 200105072 B ZA200105072 B ZA 200105072B ZA 200105072 A ZA200105072 A ZA 200105072A ZA 200105072 A ZA200105072 A ZA 200105072A ZA 200105072 B ZA200105072 B ZA 200105072B
- Authority
- ZA
- South Africa
- Prior art keywords
- troxerutin
- weight
- enriched
- enriched troxerutin
- water
- Prior art date
Links
- 229960003232 troxerutin Drugs 0.000 title claims description 62
- 238000000034 method Methods 0.000 title description 9
- IYVFNTXFRYQLRP-VVSTWUKXSA-N 2-[3,4-bis(2-hydroxyethoxy)phenyl]-5-hydroxy-7-(2-hydroxyethoxy)-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2r,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-4h-chromen-4-one Chemical compound O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1OC[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@H](OC=2C(C3=C(O)C=C(OCCO)C=C3OC=2C=2C=C(OCCO)C(OCCO)=CC=2)=O)O1 IYVFNTXFRYQLRP-VVSTWUKXSA-N 0.000 title description 5
- IKGXIBQEEMLURG-NVPNHPEKSA-N rutin Chemical compound O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1OC[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@H](OC=2C(C3=C(O)C=C(O)C=C3OC=2C=2C=C(O)C(O)=CC=2)=O)O1 IKGXIBQEEMLURG-NVPNHPEKSA-N 0.000 claims description 66
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 26
- 239000000843 powder Substances 0.000 claims description 6
- 238000005303 weighing Methods 0.000 claims description 3
- -1 hydroxyethyl derivatives of rutoside Chemical class 0.000 description 13
- 238000002425 crystallisation Methods 0.000 description 11
- 230000008025 crystallization Effects 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 229960004555 rutoside Drugs 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 7
- 230000008569 process Effects 0.000 description 7
- 239000002609 medium Substances 0.000 description 6
- 239000008194 pharmaceutical composition Substances 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 230000002776 aggregation Effects 0.000 description 4
- 238000004220 aggregation Methods 0.000 description 4
- 210000004369 blood Anatomy 0.000 description 4
- 239000008280 blood Substances 0.000 description 4
- 238000004090 dissolution Methods 0.000 description 4
- 210000003743 erythrocyte Anatomy 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- JMGZEFIQIZZSBH-UHFFFAOYSA-N Bioquercetin Natural products CC1OC(OCC(O)C2OC(OC3=C(Oc4cc(O)cc(O)c4C3=O)c5ccc(O)c(O)c5)C(O)C2O)C(O)C(O)C1O JMGZEFIQIZZSBH-UHFFFAOYSA-N 0.000 description 3
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 3
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- 229930195725 Mannitol Natural products 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 210000001736 capillary Anatomy 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- IVTMALDHFAHOGL-UHFFFAOYSA-N eriodictyol 7-O-rutinoside Natural products OC1C(O)C(O)C(C)OC1OCC1C(O)C(O)C(O)C(OC=2C=C3C(C(C(O)=C(O3)C=3C=C(O)C(O)=CC=3)=O)=C(O)C=2)O1 IVTMALDHFAHOGL-UHFFFAOYSA-N 0.000 description 3
- 235000019441 ethanol Nutrition 0.000 description 3
- 208000014617 hemorrhoid Diseases 0.000 description 3
- 239000000594 mannitol Substances 0.000 description 3
- 235000010355 mannitol Nutrition 0.000 description 3
- FDRQPMVGJOQVTL-UHFFFAOYSA-N quercetin rutinoside Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC=2C(C3=C(O)C=C(O)C=C3OC=2C=2C=C(O)C(O)=CC=2)=O)O1 FDRQPMVGJOQVTL-UHFFFAOYSA-N 0.000 description 3
- ALABRVAAKCSLSC-UHFFFAOYSA-N rutin Natural products CC1OC(OCC2OC(O)C(O)C(O)C2O)C(O)C(O)C1OC3=C(Oc4cc(O)cc(O)c4C3=O)c5ccc(O)c(O)c5 ALABRVAAKCSLSC-UHFFFAOYSA-N 0.000 description 3
- 235000005493 rutin Nutrition 0.000 description 3
- 102000004506 Blood Proteins Human genes 0.000 description 2
- 108010017384 Blood Proteins Proteins 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- RTATXGUCZHCSNG-TYSPDFDMSA-N Kaempferol-3-O-rutinoside Natural products OC1[C@H](O)[C@@H](O)C(C)O[C@H]1OCC1[C@@H](O)[C@@H](O)C(O)[C@H](OC=2C(C3=C(O)C=C(O)C=C3OC=2C=2C=CC(O)=CC=2)=O)O1 RTATXGUCZHCSNG-TYSPDFDMSA-N 0.000 description 2
- RTATXGUCZHCSNG-QHWHWDPRSA-N Nicotiflorin Chemical compound O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1OC[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@H](OC=2C(C3=C(O)C=C(O)C=C3OC=2C=2C=CC(O)=CC=2)=O)O1 RTATXGUCZHCSNG-QHWHWDPRSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000004856 capillary permeability Effects 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 229960004756 ethanol Drugs 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- MGYBYJXAXUBTQF-FSFUDZCRSA-N luteolin 7-O-rutinoside Natural products C[C@@H]1O[C@H](OC[C@H]2O[C@@H](Oc3cc(O)c4C(=O)C=C(Oc4c3)c5ccc(O)c(O)c5)[C@H](O)[C@@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@H]1O MGYBYJXAXUBTQF-FSFUDZCRSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- RTATXGUCZHCSNG-UHFFFAOYSA-N nicotiflorine Natural products OC1C(O)C(O)C(C)OC1OCC1C(O)C(O)C(O)C(OC=2C(C3=C(O)C=C(O)C=C3OC=2C=2C=CC(O)=CC=2)=O)O1 RTATXGUCZHCSNG-UHFFFAOYSA-N 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000012429 reaction media Substances 0.000 description 2
- 230000003014 reinforcing effect Effects 0.000 description 2
- 230000007928 solubilization Effects 0.000 description 2
- 238000005063 solubilization Methods 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 206010011985 Decubitus ulcer Diseases 0.000 description 1
- 206010013710 Drug interaction Diseases 0.000 description 1
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 208000005793 Restless legs syndrome Diseases 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 229930003935 flavonoid Natural products 0.000 description 1
- 150000002215 flavonoids Chemical class 0.000 description 1
- 235000017173 flavonoids Nutrition 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 230000004089 microcirculation Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 230000003285 pharmacodynamic effect Effects 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 230000000500 vasculoprotective effect Effects 0.000 description 1
- 230000001643 venotonic effect Effects 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H17/00—Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
- C07H17/04—Heterocyclic radicals containing only oxygen as ring hetero atoms
- C07H17/06—Benzopyran radicals
- C07H17/065—Benzo[b]pyrans
- C07H17/07—Benzo[b]pyran-4-ones
-
- 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
- A61K31/7048—Compounds having saccharide radicals and heterocyclic rings having oxygen as a ring hetero atom, e.g. leucoglucosan, hesperidin, erythromycin, nystatin, digitoxin or digoxin
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H1/00—Processes for the preparation of sugar derivatives
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Vascular Medicine (AREA)
- Epidemiology (AREA)
- Saccharide Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9815710A FR2787111B1 (fr) | 1998-12-11 | 1998-12-11 | Troxerutine a forte teneur en trihydroxy-ethyl-rutoside, a mouillabilite elevee, et procede de preparation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200105072B true ZA200105072B (en) | 2002-12-20 |
Family
ID=9533903
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200105072A ZA200105072B (en) | 1998-12-11 | 2001-06-20 | Troxerutin with high trihydroxy-ethyl-rutin content and method for preparing same. |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US6855697B1 (cs) |
| EP (1) | EP1137653B1 (cs) |
| JP (1) | JP2003505338A (cs) |
| KR (1) | KR100644478B1 (cs) |
| CN (1) | CN1196709C (cs) |
| AT (1) | ATE276265T1 (cs) |
| AU (1) | AU1569300A (cs) |
| BR (1) | BR9916130A (cs) |
| CA (1) | CA2354574C (cs) |
| CZ (1) | CZ20011998A3 (cs) |
| DE (1) | DE69920263T2 (cs) |
| ES (1) | ES2229795T3 (cs) |
| FR (1) | FR2787111B1 (cs) |
| HU (1) | HUP0104689A3 (cs) |
| IL (1) | IL143660A0 (cs) |
| PL (1) | PL195116B1 (cs) |
| RU (1) | RU2242478C2 (cs) |
| SK (1) | SK7822001A3 (cs) |
| TR (1) | TR200101695T2 (cs) |
| WO (1) | WO2000035933A1 (cs) |
| ZA (1) | ZA200105072B (cs) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1302774C (zh) * | 2003-11-07 | 2007-03-07 | 邱学良 | 一种含有曲克芦丁的泡腾片及制法 |
| RU2299070C2 (ru) * | 2005-02-08 | 2007-05-20 | Открытое акционерное общество "Химико-фармацевтический комбинат "АКРИХИН" (ОАО "АКРИХИН") | Фармацевтическая композиция для лечения заболевания вен и способ ее получения |
| RU2295970C1 (ru) * | 2006-05-23 | 2007-03-27 | Общество С Ограниченной Ответственностью "Сиа Пептайдс" | Пептид, повышающий резистентность капилляров, фармацевтическая композиция на его основе и способ ее применения |
| CN103113437A (zh) * | 2013-01-05 | 2013-05-22 | 河北联合大学 | 曲克芦丁的制备方法 |
| CN104177461B (zh) * | 2013-05-21 | 2016-11-09 | 济南新力特科技有限公司 | 三羟乙基芦丁的制备方法 |
| KR101809943B1 (ko) * | 2014-05-23 | 2017-12-18 | 지난 신라이트 테크놀로지 컴퍼니 리미티드 | 트리하이드록시에틸 루토사이드의 제조방법 |
| CN104628799B (zh) * | 2014-12-24 | 2017-10-03 | 苏州亚宝药物研发有限公司 | 一种曲克芦丁中杂质a及其分离方法 |
| CN111333602B (zh) * | 2020-04-16 | 2022-12-16 | 四川协力制药股份有限公司 | 一种曲克芦丁生产废弃母液的回收转化工艺 |
| CN112057424B (zh) * | 2020-09-18 | 2022-09-16 | 开封康诺药业有限公司 | 一种曲克芦丁冻干粉针剂及其制备方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH423808A (fr) * | 1964-03-26 | 1966-11-15 | Zyma Sa | Procédé pour la préparation d'éthers O-B-hydroxyéthylés de la rutine |
| FR5072M (cs) * | 1965-10-25 | 1967-05-16 | ||
| CH581127A5 (cs) | 1974-04-09 | 1976-10-29 | Zyma Sa | |
| US4153788A (en) * | 1974-04-09 | 1979-05-08 | Zyma S.A. | Process of preparing mono-O-β-hydroxyethyl-7 rutoside |
| CS225440B1 (cs) * | 1982-04-06 | 1984-02-13 | Frantisek Ing Kvis | Způsob přípravy směsi 0-hydroxyethylovaných derivátů rutinu |
| CN1032658A (zh) * | 1987-10-19 | 1989-05-03 | 烟台人民制药厂 | 芦丁羟乙基衍生物的精制方法 |
-
1998
- 1998-12-11 FR FR9815710A patent/FR2787111B1/fr not_active Expired - Fee Related
-
1999
- 1999-12-10 ES ES99958302T patent/ES2229795T3/es not_active Expired - Lifetime
- 1999-12-10 HU HU0104689A patent/HUP0104689A3/hu unknown
- 1999-12-10 RU RU2001119173/04A patent/RU2242478C2/ru active
- 1999-12-10 DE DE69920263T patent/DE69920263T2/de not_active Expired - Fee Related
- 1999-12-10 CA CA002354574A patent/CA2354574C/fr not_active Expired - Fee Related
- 1999-12-10 EP EP99958302A patent/EP1137653B1/fr not_active Expired - Lifetime
- 1999-12-10 AT AT99958302T patent/ATE276265T1/de not_active IP Right Cessation
- 1999-12-10 US US09/857,846 patent/US6855697B1/en not_active Expired - Fee Related
- 1999-12-10 JP JP2000588191A patent/JP2003505338A/ja active Pending
- 1999-12-10 KR KR1020017007287A patent/KR100644478B1/ko not_active Expired - Fee Related
- 1999-12-10 SK SK782-2001A patent/SK7822001A3/sk unknown
- 1999-12-10 PL PL99348200A patent/PL195116B1/pl not_active IP Right Cessation
- 1999-12-10 CZ CZ20011998A patent/CZ20011998A3/cs unknown
- 1999-12-10 BR BR9916130-3A patent/BR9916130A/pt not_active Application Discontinuation
- 1999-12-10 AU AU15693/00A patent/AU1569300A/en not_active Abandoned
- 1999-12-10 WO PCT/FR1999/003100 patent/WO2000035933A1/fr active IP Right Grant
- 1999-12-10 CN CNB998143650A patent/CN1196709C/zh not_active Expired - Fee Related
- 1999-12-10 TR TR2001/01695T patent/TR200101695T2/xx unknown
- 1999-12-10 IL IL14366099A patent/IL143660A0/xx not_active IP Right Cessation
-
2001
- 2001-06-20 ZA ZA200105072A patent/ZA200105072B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP1137653B1 (fr) | 2004-09-15 |
| BR9916130A (pt) | 2001-09-04 |
| HUP0104689A2 (hu) | 2002-04-29 |
| KR20010101173A (ko) | 2001-11-14 |
| JP2003505338A (ja) | 2003-02-12 |
| EP1137653A1 (fr) | 2001-10-04 |
| FR2787111B1 (fr) | 2001-02-23 |
| KR100644478B1 (ko) | 2006-11-10 |
| CZ20011998A3 (cs) | 2001-10-17 |
| TR200101695T2 (tr) | 2002-04-22 |
| DE69920263T2 (de) | 2005-09-29 |
| IL143660A0 (en) | 2002-04-21 |
| CA2354574C (fr) | 2009-07-28 |
| PL195116B1 (pl) | 2007-08-31 |
| WO2000035933A1 (fr) | 2000-06-22 |
| FR2787111A1 (fr) | 2000-06-16 |
| DE69920263D1 (de) | 2004-10-21 |
| CA2354574A1 (fr) | 2000-06-22 |
| CN1196709C (zh) | 2005-04-13 |
| ES2229795T3 (es) | 2005-04-16 |
| SK7822001A3 (en) | 2002-01-07 |
| US6855697B1 (en) | 2005-02-15 |
| AU1569300A (en) | 2000-07-03 |
| ATE276265T1 (de) | 2004-10-15 |
| PL348200A1 (en) | 2002-05-06 |
| CN1331697A (zh) | 2002-01-16 |
| RU2242478C2 (ru) | 2004-12-20 |
| HUP0104689A3 (en) | 2003-12-29 |
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