JP2003523460A5 - - Google Patents
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- Publication number
- JP2003523460A5 JP2003523460A5 JP2001561068A JP2001561068A JP2003523460A5 JP 2003523460 A5 JP2003523460 A5 JP 2003523460A5 JP 2001561068 A JP2001561068 A JP 2001561068A JP 2001561068 A JP2001561068 A JP 2001561068A JP 2003523460 A5 JP2003523460 A5 JP 2003523460A5
- Authority
- JP
- Japan
- Prior art keywords
- uronic acid
- percentage
- heparin
- molecular weight
- desulfation
- 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
- 239000002253 acid Substances 0.000 description 48
- HTTJABKRGRZYRN-UHFFFAOYSA-N Heparin Chemical class OC1C(NC(=O)C)C(O)OC(COS(O)(=O)=O)C1OC1C(OS(O)(=O)=O)C(O)C(OC2C(C(OS(O)(=O)=O)C(OC3C(C(O)C(O)C(O3)C(O)=O)OS(O)(=O)=O)C(CO)O2)NS(O)(=O)=O)C(C(O)=O)O1 HTTJABKRGRZYRN-UHFFFAOYSA-N 0.000 description 21
- 125000003700 epoxy group Chemical group 0.000 description 15
- 229920000669 heparin Polymers 0.000 description 11
- 229960002897 heparin Drugs 0.000 description 11
- 150000007513 acids Chemical class 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 7
- 239000000243 solution Substances 0.000 description 6
- IAJILQKETJEXLJ-LECHCGJUSA-N iduronic acid Chemical group O=C[C@@H](O)[C@H](O)[C@@H](O)[C@H](O)C(O)=O IAJILQKETJEXLJ-LECHCGJUSA-N 0.000 description 5
- 150000004676 glycans Chemical group 0.000 description 4
- 150000002338 glycosides Chemical group 0.000 description 4
- 229920001542 oligosaccharide Polymers 0.000 description 4
- 150000002482 oligosaccharides Chemical class 0.000 description 4
- IAJILQKETJEXLJ-UHFFFAOYSA-N Galacturonsaeure Natural products O=CC(O)C(O)C(O)C(O)C(O)=O IAJILQKETJEXLJ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 125000003172 aldehyde group Chemical group 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 229920001282 polysaccharide Polymers 0.000 description 3
- 239000005017 polysaccharide Substances 0.000 description 3
- 108090000790 Enzymes Proteins 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 229920002683 Glycosaminoglycan Polymers 0.000 description 2
- 206010027476 Metastases Diseases 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- 206010028980 Neoplasm Diseases 0.000 description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 230000033115 angiogenesis Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 230000009401 metastasis Effects 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 239000008194 pharmaceutical composition Substances 0.000 description 2
- 238000007142 ring opening reaction Methods 0.000 description 2
- JQWHASGSAFIOCM-UHFFFAOYSA-M sodium periodate Chemical compound [Na+].[O-]I(=O)(=O)=O JQWHASGSAFIOCM-UHFFFAOYSA-M 0.000 description 2
- 238000000108 ultra-filtration Methods 0.000 description 2
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- 206010012689 Diabetic retinopathy Diseases 0.000 description 1
- 206010016654 Fibrosis Diseases 0.000 description 1
- 102100024025 Heparanase Human genes 0.000 description 1
- 108010022901 Heparin Lyase Proteins 0.000 description 1
- 108090000856 Lyases Proteins 0.000 description 1
- 102000004317 Lyases Human genes 0.000 description 1
- 241000872931 Myoporum sandwicense Species 0.000 description 1
- 201000004681 Psoriasis Diseases 0.000 description 1
- KZWHEHSUEBTKJM-SLPGGIOYSA-N [(2r,3r,4s,5r)-3,4,5,6-tetrahydroxy-1-oxohexan-2-yl]sulfamic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](C=O)NS(O)(=O)=O KZWHEHSUEBTKJM-SLPGGIOYSA-N 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- IAJILQKETJEXLJ-RSJOWCBRSA-N aldehydo-D-galacturonic acid Chemical compound O=C[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)C(O)=O IAJILQKETJEXLJ-RSJOWCBRSA-N 0.000 description 1
- 230000002001 anti-metastasis Effects 0.000 description 1
- 230000000259 anti-tumor effect Effects 0.000 description 1
- 239000004019 antithrombin Substances 0.000 description 1
- 239000003637 basic solution Substances 0.000 description 1
- 210000002808 connective tissue Anatomy 0.000 description 1
- 238000006477 desulfuration reaction Methods 0.000 description 1
- 230000023556 desulfurization Effects 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 230000004761 fibrosis Effects 0.000 description 1
- 150000002301 glucosamine derivatives Chemical class 0.000 description 1
- 239000003102 growth factor Substances 0.000 description 1
- 108010037536 heparanase Proteins 0.000 description 1
- 108010083213 heparitinsulfate lyase Proteins 0.000 description 1
- 239000008241 heterogeneous mixture Substances 0.000 description 1
- 210000003630 histaminocyte Anatomy 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- 230000014508 negative regulation of coagulation Effects 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 150000004804 polysaccharides Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 210000000952 spleen Anatomy 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate group Chemical group S(=O)(=O)([O-])[O-] QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 230000019635 sulfation Effects 0.000 description 1
- 238000005670 sulfation reaction Methods 0.000 description 1
- 210000001541 thymus gland Anatomy 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT2000RM000041A IT1316986B1 (it) | 2000-01-25 | 2000-01-25 | Derivati glicosamminoglicani parzialmente desolfatati nonanticoagulanti ad attivita' antiangiogenica. |
| ITRM2000A000041 | 2000-01-25 | ||
| IT2000A000041 | 2000-01-25 | ||
| PCT/IT2001/000034 WO2001055221A1 (en) | 2000-01-25 | 2001-01-24 | Derivatives of partially desulphated glycosaminoglycans endowed with antiangiogenic activity and devoid of anticoagulating effect |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2003523460A JP2003523460A (ja) | 2003-08-05 |
| JP2003523460A5 true JP2003523460A5 (enExample) | 2012-10-18 |
| JP5371167B2 JP5371167B2 (ja) | 2013-12-18 |
Family
ID=11454382
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001561068A Expired - Fee Related JP5371167B2 (ja) | 2000-01-25 | 2001-01-24 | 抗脈管形成活性を有し、かつ、抗凝固作用がない、部分脱硫酸グリコサミノグリカンの誘導体 |
Country Status (21)
| Country | Link |
|---|---|
| US (4) | US20030013682A1 (enExample) |
| EP (1) | EP1268558B1 (enExample) |
| JP (1) | JP5371167B2 (enExample) |
| KR (1) | KR100812406B1 (enExample) |
| CN (1) | CN100540570C (enExample) |
| AT (1) | ATE348115T1 (enExample) |
| AU (1) | AU782632B2 (enExample) |
| BR (1) | BR0107696A (enExample) |
| CA (1) | CA2397964C (enExample) |
| CY (1) | CY1108001T1 (enExample) |
| CZ (1) | CZ303030B6 (enExample) |
| DE (1) | DE60125154T2 (enExample) |
| DK (1) | DK1268558T3 (enExample) |
| ES (1) | ES2277911T3 (enExample) |
| HU (1) | HU229509B1 (enExample) |
| IT (1) | IT1316986B1 (enExample) |
| MX (1) | MXPA02007195A (enExample) |
| PL (1) | PL209479B1 (enExample) |
| PT (1) | PT1268558E (enExample) |
| SK (1) | SK287566B6 (enExample) |
| WO (1) | WO2001055221A1 (enExample) |
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7781416B2 (en) | 2000-01-25 | 2010-08-24 | Sigma-Tau Research Switzerland S.A. | Derivatives of partially desulphated glycosaminoglycans as heparanase inhibitors, endowed with antiangiogenic activity and devoid of anticoagulating effect |
| IT1316986B1 (it) | 2000-01-25 | 2003-05-26 | Sigma Tau Ind Farmaceuti | Derivati glicosamminoglicani parzialmente desolfatati nonanticoagulanti ad attivita' antiangiogenica. |
| CA2457719C (en) | 2001-09-12 | 2012-01-03 | Benito Casu | Derivatives of partially desulphated glycosaminoglycans as heparanase inhibitors, endowed with antiangiogenic activity and devoid of anticoagulating effect |
| AU2008202261B2 (en) * | 2001-09-12 | 2011-07-28 | Leadiant Biosciences S.A. | Derivatives of partially desulphated glycosaminoglycans as heparanase inhibitors, endowed with antiangiogenic activity and devoid of anticoagulating effect |
| EP1765874A1 (en) | 2004-03-26 | 2007-03-28 | Glycogenesys, Inc. | Modified pectins, compositions and methods related thereto |
| WO2009007224A1 (en) * | 2007-07-10 | 2009-01-15 | Sigma-Tau Industrie Farmaceutiche Riunite S.P.A. | Low molecular weight heparin derivatives having neuroprotective activity |
| KR101561860B1 (ko) * | 2007-11-02 | 2015-10-20 | 모멘타 파머슈티컬스 인코포레이티드 | 비항응고성 다당류 조성물 |
| US8592393B2 (en) * | 2007-11-02 | 2013-11-26 | Momenta Pharmaceuticals, Inc. | Polysaccharide compositions and methods of use for the treatment and prevention of disorders associated with progenitor cell mobilization |
| US8569262B2 (en) * | 2007-11-02 | 2013-10-29 | Momenta Pharmaceuticals, Inc. | Polysaccharide compositions and methods of use for the treatment and prevention of disorders associated with progenitor cell mobilization |
| EP2205642B1 (en) | 2007-11-02 | 2016-01-27 | Momenta Pharmaceuticals, Inc. | Non-anticoagulant polysaccharide compositions |
| BR112012026542A2 (pt) | 2010-04-16 | 2016-07-12 | Momenta Pharmaceuticals Inc | abordagem seletiva de tecido |
| US8431826B2 (en) | 2010-05-14 | 2013-04-30 | James Robert Howard | Capacitive power and ground plane structure utilizing fractal elements for the reduction of radiated emissions |
| WO2011159770A2 (en) | 2010-06-17 | 2011-12-22 | Momenta Pharmaceuticals, Inc. | Methods and compositions for modulating hair growth |
| WO2013095215A1 (en) | 2011-12-19 | 2013-06-27 | Dilaforette Ab | Low anticoagulant heparins |
| PT2794665T (pt) | 2011-12-19 | 2018-01-24 | Dilafor Ab | Glicosaminoglicanos não anticoagulativos que compreendem unidade repetitiva de dissacáridos e sua utilização médica |
| DK2797942T3 (en) | 2011-12-28 | 2018-12-10 | Galectin Therapeutics Inc | Composition of Hitherto-Unknown Carbohydrate Drugs for the Treatment of Human Diseases |
| CN104619329B (zh) | 2012-06-06 | 2018-01-26 | 卡莱克汀医疗有限公司 | 用于治疗与升高的诱导型一氧化氮合酶相关联的疾病的半乳糖‑鼠李糖半乳糖醛酸酯组合物 |
| US9507912B2 (en) | 2012-08-31 | 2016-11-29 | Nuvectra Corporation | Method and system of simulating a pulse generator on a clinician programmer |
| CN104812244B (zh) | 2012-09-17 | 2018-10-30 | 卡莱克汀医疗有限公司 | 增强癌症治疗中特异性免疫疗法的方法 |
| US8828971B2 (en) | 2012-10-10 | 2014-09-09 | Galectin Therapeutics, Inc. | Galactose-pronged carbohydrate compounds for the treatment of diabetic nephropathy and associated disorders |
| US9339515B2 (en) | 2013-02-20 | 2016-05-17 | Galectin Therapeutics, Inc. | Method for treatment of pulmonary fibrosis |
| WO2014193818A1 (en) | 2013-05-28 | 2014-12-04 | Momenta Pharmaceuticals, Inc. | Pharmaceutical compositions |
| JP6132302B2 (ja) * | 2013-05-28 | 2017-05-24 | リーディアント・バイオサイエンシーズ・ソシエタ・アノニマＬｅａｄｉａｎｔ Ｂｉｏｓｃｉｅｎｃｅｓ Ｓ．Ａ． | 抗血管新生活性を有し、抗凝血効果を有さない、ヘパラナーゼ阻害剤としての部分的に脱硫酸化されたグリコサミノグリカンの誘導体 |
| ITLO20130005A1 (it) * | 2013-10-31 | 2015-05-01 | He E Biochimiche G Ronzonr S R | Derivati di glucosamminoglicani n-desolfatati e loro uso come farmaci |
| ITLO20130006A1 (it) | 2013-11-06 | 2015-05-07 | He E Biochimiche G Ronzoni S R | Derivati carbossilati di glucosamminoglicani e loro uso come farmaci |
| CN103724458B (zh) * | 2014-01-17 | 2016-03-30 | 福州大学 | 含n-非取代葡萄糖胺肝素六糖的制备及其纯化 |
| HUE042681T2 (hu) | 2015-03-06 | 2019-07-29 | Leadiant Biosciences Sa In Liquidazione | Myeloma multiplex roneparstat kombinációs terápiája |
| JP2016014148A (ja) * | 2015-09-10 | 2016-01-28 | シグマ−タウ・リサーチ・スウィッツァーランド・ソシエテ・アノニム | 抗血管新生活性を有し、抗凝血効果を有さない、ヘパラナーゼ阻害剤としての部分的に脱硫酸化されたグリコサミノグリカンの誘導体 |
| CN107177015A (zh) * | 2016-03-11 | 2017-09-19 | 梁颖 | 一种重乙酰化肝素修饰物及其制备方法和应用 |
| WO2018107200A1 (en) | 2016-12-13 | 2018-06-21 | Beta Therapeutics Pty Ltd | Heparanase inhibitors and use thereof |
| US11787783B2 (en) | 2016-12-13 | 2023-10-17 | Beta Therapeutics Pty Ltd | Heparanase inhibitors and use thereof |
| CN108424474B (zh) * | 2017-02-15 | 2023-07-25 | 清华大学 | 去抗凝肝素衍生物及其用于炎症性肠病的治疗 |
| US11225531B2 (en) | 2018-02-02 | 2022-01-18 | Shenzhen Hepalink Pharmaceutical Group Co., Ltd. | Glycosaminoglycan derivative and preparation method therefor and use thereof |
| EP3705126A1 (en) | 2019-03-05 | 2020-09-09 | Leadiant Biosciences S.p.A. | Roneparstat for the treatment of amyloidosis |
| WO2021128253A1 (zh) * | 2019-12-27 | 2021-07-01 | 深圳市海普瑞药业集团股份有限公司 | 一种糖胺聚糖衍生物及其应用 |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4500519A (en) * | 1978-11-06 | 1985-02-19 | Choay S.A. | Mucopolysaccharides having biological properties, preparation and method of use |
| US5262403A (en) | 1986-03-10 | 1993-11-16 | Board Of Regents, The University Of Texas System | Glycosaminoglycan derivatives and their use as inhibitors of tumor invasiveness of metastatic profusion-II |
| IL79255A0 (en) | 1986-06-26 | 1986-09-30 | Hadassah Med Org | Composition for metastasis prevention |
| WO1988001280A1 (en) * | 1986-08-21 | 1988-02-25 | Board Of Regents, The University Of Texas System | Glycosaminoglycan derivatives and their use as inhibitors of tumor invasiveness or metastatic profusion |
| FR2614026B1 (fr) * | 1987-04-16 | 1992-04-17 | Sanofi Sa | Heparines de bas poids moleculaire, a structure reguliere, leur preparation et leurs applications biologiques |
| US5280016A (en) * | 1991-03-29 | 1994-01-18 | Glycomed Incorporated | Non-anticoagulant heparin derivatives |
| JPH05157344A (ja) * | 1991-12-09 | 1993-06-22 | Mitsubishi Heavy Ind Ltd | 空気調和機の吹出口 |
| JPH0512822A (ja) | 1991-12-16 | 1993-01-22 | Seiko Epson Corp | カートリツジ |
| JPH06157344A (ja) * | 1992-02-07 | 1994-06-03 | Childrens Medical Center Corp:The | 血管新生阻害のための医薬製剤及び血管新生阻害方法 |
| US5668118A (en) * | 1992-07-24 | 1997-09-16 | Cavalier Pharmaceuticals | Method of synthesis of 2-O-desulfated Heparin and use thereof for inhibition of elastase and Cathepspin G |
| US5696100A (en) * | 1992-12-22 | 1997-12-09 | Glycomed Incorporated | Method for controlling O-desulfation of heparin and compositions produced thereby |
| US5296471A (en) | 1992-12-22 | 1994-03-22 | Glycomed Incorporated | Method for controlling o-desulfation of heparin and compositions produced thereby |
| IT1264709B1 (it) | 1993-07-12 | 1996-10-04 | Italfarmaco Spa | Derivati eparinici ad attivita' antimetastatica |
| US5583121A (en) * | 1994-01-12 | 1996-12-10 | Michigan State University | Non-anticoagulant chemically modified heparinoids for treating hypovolemic shock and related shock syndromes |
| CA2189038A1 (en) * | 1994-05-06 | 1995-11-09 | Kevin R. Holme | O-desulfated heparin derivatives, methods of making and uses thereof |
| IL114951A (en) * | 1995-08-15 | 1999-08-17 | Hadasit Med Res Service | Quinazolinone-containing pharmaceutical compositions for prevention of neovascularization |
| US5854221A (en) * | 1996-12-12 | 1998-12-29 | The Children's Medical Center Corporation | Endothelial cell proliferation inhibitor and method of use |
| CA2237273C (en) * | 1996-01-15 | 2009-01-13 | Janssen Pharmaceutica N.V. | Angiogenesis inhibiting pyridazinamines |
| JP4051099B2 (ja) * | 1997-01-31 | 2008-02-20 | 生化学工業株式会社 | 低分子化ヘパリン、その製造法及び医薬組成物 |
| IT1296581B1 (it) | 1997-11-28 | 1999-07-14 | Istituto Scient Di Chimica E B | Materiali polimerici non trombogenici e ad esaltata compatibilita' con fluidi e tessuti organici |
| IT1296998B1 (it) * | 1997-12-19 | 1999-08-03 | Derivati Organici Lab | Composizione costituita da frazioni di eparina avente caratteristiche riproducibili con peso molecolare medio di 5200 d |
| US7781416B2 (en) * | 2000-01-25 | 2010-08-24 | Sigma-Tau Research Switzerland S.A. | Derivatives of partially desulphated glycosaminoglycans as heparanase inhibitors, endowed with antiangiogenic activity and devoid of anticoagulating effect |
| IT1316986B1 (it) | 2000-01-25 | 2003-05-26 | Sigma Tau Ind Farmaceuti | Derivati glicosamminoglicani parzialmente desolfatati nonanticoagulanti ad attivita' antiangiogenica. |
-
2000
- 2000-01-25 IT IT2000RM000041A patent/IT1316986B1/it active
-
2001
- 2001-01-24 BR BR0107696-5A patent/BR0107696A/pt not_active IP Right Cessation
- 2001-01-24 ES ES01906098T patent/ES2277911T3/es not_active Expired - Lifetime
- 2001-01-24 HU HU0204196A patent/HU229509B1/hu not_active IP Right Cessation
- 2001-01-24 JP JP2001561068A patent/JP5371167B2/ja not_active Expired - Fee Related
- 2001-01-24 PT PT01906098T patent/PT1268558E/pt unknown
- 2001-01-24 PL PL357209A patent/PL209479B1/pl unknown
- 2001-01-24 US US10/182,185 patent/US20030013682A1/en not_active Abandoned
- 2001-01-24 CN CNB018040942A patent/CN100540570C/zh not_active Expired - Fee Related
- 2001-01-24 CZ CZ20022308A patent/CZ303030B6/cs not_active IP Right Cessation
- 2001-01-24 EP EP01906098A patent/EP1268558B1/en not_active Expired - Lifetime
- 2001-01-24 DK DK01906098T patent/DK1268558T3/da active
- 2001-01-24 DE DE60125154T patent/DE60125154T2/de not_active Expired - Lifetime
- 2001-01-24 SK SK1067-2002A patent/SK287566B6/sk not_active IP Right Cessation
- 2001-01-24 CA CA2397964A patent/CA2397964C/en not_active Expired - Fee Related
- 2001-01-24 WO PCT/IT2001/000034 patent/WO2001055221A1/en not_active Ceased
- 2001-01-24 AU AU34064/01A patent/AU782632B2/en not_active Ceased
- 2001-01-24 MX MXPA02007195A patent/MXPA02007195A/es active IP Right Grant
- 2001-01-24 KR KR1020027009395A patent/KR100812406B1/ko not_active Expired - Fee Related
- 2001-01-24 AT AT01906098T patent/ATE348115T1/de active
-
2004
- 2004-10-19 US US10/967,255 patent/US20050107331A1/en not_active Abandoned
-
2005
- 2005-01-04 US US11/028,512 patent/US7790700B2/en not_active Expired - Fee Related
-
2007
- 2007-02-01 CY CY20071100140T patent/CY1108001T1/el unknown
-
2010
- 2010-08-05 US US12/851,166 patent/US8222231B2/en not_active Expired - Fee Related
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