SK15352000A3 - Spôsob výroby cyklických peptidov viazaných k polymérnemu nosiču - Google Patents
Spôsob výroby cyklických peptidov viazaných k polymérnemu nosiču Download PDFInfo
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- SK15352000A3 SK15352000A3 SK1535-2000A SK15352000A SK15352000A3 SK 15352000 A3 SK15352000 A3 SK 15352000A3 SK 15352000 A SK15352000 A SK 15352000A SK 15352000 A3 SK15352000 A3 SK 15352000A3
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- Slovakia
- Prior art keywords
- asp
- lys
- leu
- val
- amino acid
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- 229960003692 gamma aminobutyric acid Drugs 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000003862 glucocorticoid Substances 0.000 description 1
- ZDXPYRJPNDTMRX-UHFFFAOYSA-N glutamine Natural products OC(=O)C(N)CCC(N)=O ZDXPYRJPNDTMRX-UHFFFAOYSA-N 0.000 description 1
- 108010049041 glutamylalanine Proteins 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 230000035876 healing Effects 0.000 description 1
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 description 1
- 108010040030 histidinoalanine Proteins 0.000 description 1
- 230000003054 hormonal effect Effects 0.000 description 1
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- 239000005556 hormone Substances 0.000 description 1
- 102000058004 human PTH Human genes 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
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- 125000001841 imino group Chemical group [H]N=* 0.000 description 1
- 229960003444 immunosuppressant agent Drugs 0.000 description 1
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- 238000011065 in-situ storage Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
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- 238000005342 ion exchange Methods 0.000 description 1
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- 238000002955 isolation Methods 0.000 description 1
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- 201000006370 kidney failure Diseases 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- AMXOYNBUYSYVKV-UHFFFAOYSA-M lithium bromide Chemical compound [Li+].[Br-] AMXOYNBUYSYVKV-UHFFFAOYSA-M 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 125000004370 n-butenyl group Chemical group [H]\C([H])=C(/[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 description 1
- 230000004962 physiological condition Effects 0.000 description 1
- OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 description 1
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- 229920001155 polypropylene Polymers 0.000 description 1
- 239000005373 porous glass Substances 0.000 description 1
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- 239000002244 precipitate Substances 0.000 description 1
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- 201000009395 primary hyperaldosteronism Diseases 0.000 description 1
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- IVRIRQXJSNCSPQ-UHFFFAOYSA-N propan-2-yl carbonochloridate Chemical compound CC(C)OC(Cl)=O IVRIRQXJSNCSPQ-UHFFFAOYSA-N 0.000 description 1
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 description 1
- 125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- MHZSEPBBOTVGFW-UHFFFAOYSA-N pyrrolidin-1-ylphosphane Chemical compound PN1CCCC1 MHZSEPBBOTVGFW-UHFFFAOYSA-N 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 108020003175 receptors Proteins 0.000 description 1
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- 238000001953 recrystallisation Methods 0.000 description 1
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- 239000012925 reference material Substances 0.000 description 1
- 238000004007 reversed phase HPLC Methods 0.000 description 1
- 229940043230 sarcosine Drugs 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- IZTQOLKUZKXIRV-YRVFCXMDSA-N sincalide Chemical class C([C@@H](C(=O)N[C@@H](CCSC)C(=O)NCC(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC=1C=CC=CC=1)C(N)=O)NC(=O)[C@@H](N)CC(O)=O)C1=CC=C(OS(O)(=O)=O)C=C1 IZTQOLKUZKXIRV-YRVFCXMDSA-N 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- BAZAXWOYCMUHIX-UHFFFAOYSA-M sodium perchlorate Chemical compound [Na+].[O-]Cl(=O)(=O)=O BAZAXWOYCMUHIX-UHFFFAOYSA-M 0.000 description 1
- 229910001488 sodium perchlorate Inorganic materials 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
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- 238000003756 stirring Methods 0.000 description 1
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- 238000010998 test method Methods 0.000 description 1
- UGNWTBMOAKPKBL-UHFFFAOYSA-N tetrachloro-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(Cl)=C(Cl)C1=O UGNWTBMOAKPKBL-UHFFFAOYSA-N 0.000 description 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 1
- RWRDLPDLKQPQOW-UHFFFAOYSA-N tetrahydropyrrole Substances C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- HNKJADCVZUBCPG-UHFFFAOYSA-N thioanisole Chemical compound CSC1=CC=CC=C1 HNKJADCVZUBCPG-UHFFFAOYSA-N 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- FGMPLJWBKKVCDB-UHFFFAOYSA-N trans-L-hydroxy-proline Natural products ON1CCCC1C(O)=O FGMPLJWBKKVCDB-UHFFFAOYSA-N 0.000 description 1
- 125000004044 trifluoroacetyl group Chemical group FC(C(=O)*)(F)F 0.000 description 1
- CWMFRHBXRUITQE-UHFFFAOYSA-N trimethylsilylacetylene Chemical compound C[Si](C)(C)C#C CWMFRHBXRUITQE-UHFFFAOYSA-N 0.000 description 1
- JBWKIWSBJXDJDT-UHFFFAOYSA-N triphenylmethyl chloride Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(Cl)C1=CC=CC=C1 JBWKIWSBJXDJDT-UHFFFAOYSA-N 0.000 description 1
- 230000002227 vasoactive effect Effects 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 108010027345 wheylin-1 peptide Proteins 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K17/00—Carrier-bound or immobilised peptides; Preparation thereof
- C07K17/02—Peptides being immobilised on, or in, an organic carrier
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06139—Dipeptides with the first amino acid being heterocyclic
- C07K5/06182—Dipeptides with the first amino acid being heterocyclic and Pristinamycin II; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/04—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length on carriers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/575—Hormones
- C07K14/635—Parathyroid hormone, i.e. parathormone; Parathyroid hormone-related peptides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/50—Cyclic peptides containing at least one abnormal peptide link
- C07K7/54—Cyclic peptides containing at least one abnormal peptide link with at least one abnormal peptide link in the ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Molecular Biology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Medicinal Chemistry (AREA)
- Biophysics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Biochemistry (AREA)
- Endocrinology (AREA)
- Toxicology (AREA)
- Zoology (AREA)
- Gastroenterology & Hepatology (AREA)
- Analytical Chemistry (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US8189798P | 1998-04-15 | 1998-04-15 | |
| PCT/US1999/008435 WO1999052933A1 (en) | 1998-04-15 | 1999-04-15 | Process for the preparation of resin-bound cyclic peptides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SK15352000A3 true SK15352000A3 (sk) | 2001-04-09 |
Family
ID=22167111
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK1535-2000A SK15352000A3 (sk) | 1998-04-15 | 1999-04-15 | Spôsob výroby cyklických peptidov viazaných k polymérnemu nosiču |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US6569993B1 (ru) |
| EP (1) | EP1093458A4 (ru) |
| JP (1) | JP2002511483A (ru) |
| KR (1) | KR20010085236A (ru) |
| CN (2) | CN1163504C (ru) |
| AP (1) | AP1117A (ru) |
| AU (1) | AU744812B2 (ru) |
| BG (1) | BG104903A (ru) |
| BR (1) | BR9909634A (ru) |
| CA (1) | CA2325572A1 (ru) |
| CZ (1) | CZ20003798A3 (ru) |
| EA (1) | EA200001071A1 (ru) |
| HU (1) | HUP0101629A2 (ru) |
| IL (1) | IL138338A0 (ru) |
| NO (1) | NO20005165L (ru) |
| OA (1) | OA11501A (ru) |
| PL (1) | PL347103A1 (ru) |
| SK (1) | SK15352000A3 (ru) |
| UA (1) | UA72460C2 (ru) |
| WO (1) | WO1999052933A1 (ru) |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL138338A0 (en) | 1998-04-15 | 2001-10-31 | Aventis Pharm Prod Inc | Process for the preparation of resin-bound cyclic peptides |
| GB9912911D0 (en) * | 1999-06-04 | 1999-08-04 | Zeneca Ltd | Chemical process |
| MXPA02010375A (es) * | 2000-04-19 | 2003-04-25 | Schering Corp | Inhibidores macrociclicos de la ns3-serina proteasa del virus de la hepatitis c que comprenden porciones alquil y arilalanina p2. |
| US6756480B2 (en) | 2000-04-27 | 2004-06-29 | Amgen Inc. | Modulators of receptors for parathyroid hormone and parathyroid hormone-related protein |
| US20040082783A1 (en) * | 2002-08-06 | 2004-04-29 | Schafmeister Christian E. | Bis (amino acid) molecular scaffolds |
| CN1906209A (zh) | 2003-11-05 | 2007-01-31 | 达纳-法伯癌症研究所股份有限公司 | 稳定的α螺旋肽及其用途 |
| GB0408958D0 (en) * | 2004-04-22 | 2004-05-26 | Pharma Mar Sa | Convergent synthesis for kahalalide compounds |
| TW200626611A (en) * | 2004-09-20 | 2006-08-01 | Lonza Ag | Peptide cyclisation |
| GB0505199D0 (en) * | 2005-03-14 | 2005-04-20 | Southampton Polypeptides | Process |
| PL2084183T3 (pl) | 2006-10-13 | 2010-10-29 | Lilly Co Eli | Pegylowane pth jako modulatory receptora pth i ich zastosowania |
| DK2118123T3 (en) | 2007-01-31 | 2016-01-25 | Dana Farber Cancer Inst Inc | Stabilized p53 peptides and uses thereof |
| CN101235080B (zh) * | 2007-01-31 | 2010-09-08 | 中国科学院上海有机化学研究所 | 一种达托霉素的合成方法 |
| ES2610531T3 (es) | 2007-03-28 | 2017-04-28 | President And Fellows Of Harvard College | Polipéptidos cosidos |
| US20090275519A1 (en) | 2008-02-08 | 2009-11-05 | Aileron Therapeutics, Inc. | Therapeutic peptidomimetic macrocycles |
| US20110144303A1 (en) * | 2008-04-08 | 2011-06-16 | Aileron Therapeutics, Inc. | Biologically Active Peptidomimetic Macrocycles |
| CA2737921C (en) * | 2008-09-22 | 2019-01-15 | Aileron Therapeutics, Inc. | Methods for preparing purified alpha-helical peptidomimetic macrocycle compositions with low metal ppm levels |
| CA2744088A1 (en) | 2009-01-14 | 2010-07-22 | Aileron Therapeutics, Inc. | Peptidomimetic macrocycles |
| US20130072439A1 (en) | 2009-09-22 | 2013-03-21 | Huw M. Nash | Peptidomimetic macrocycles |
| ES2711526T3 (es) | 2010-08-13 | 2019-05-06 | Aileron Therapeutics Inc | Macrociclos peptidomiméticos |
| RU2639523C2 (ru) | 2011-10-18 | 2017-12-21 | Эйлерон Терапьютикс, Инк. | Пептидомиметические макроциклы и их применение |
| MX362492B (es) | 2012-02-15 | 2019-01-21 | Aileron Therapeutics Inc | Macrociclos peptidomiméticos. |
| JP6450192B2 (ja) | 2012-02-15 | 2019-01-09 | エイルロン セラピューティクス，インコーポレイテッド | トリアゾール架橋した、およびチオエーテル架橋したペプチドミメティック大環状化合物 |
| AU2013337388B2 (en) | 2012-11-01 | 2018-08-02 | Aileron Therapeutics, Inc. | Disubstituted amino acids and methods of preparation and use thereof |
| SG11201702175YA (en) | 2014-09-24 | 2017-04-27 | Aileron Therapeutics Inc | Peptidomimetic macrocycles and formulations thereof |
| KR20170058424A (ko) | 2014-09-24 | 2017-05-26 | 에일러론 테라퓨틱스 인코포레이티드 | 펩티드모방 거대고리 및 이의 용도 |
| EP3294318A4 (en) | 2015-03-20 | 2019-04-03 | Aileron Therapeutics, Inc. | PEPTIDOMIMETIC MACROCYCLES AND USES THEREOF |
| CN106146648B (zh) * | 2015-03-26 | 2020-06-12 | 深圳翰宇药业股份有限公司 | 一种甲状旁腺激素类似物的合成方法 |
| US10059741B2 (en) | 2015-07-01 | 2018-08-28 | Aileron Therapeutics, Inc. | Peptidomimetic macrocycles |
| JP2018528217A (ja) | 2015-09-10 | 2018-09-27 | エルロン・セラピューティクス・インコーポレイテッドＡｉｌｅｒｏｎ Ｔｈｅｒａｐｅｕｔｉｃｓ，Ｉｎｃ． | Ｍｃｌ−１のモジュレーターとしてのペプチド模倣大環状分子 |
| CN110551178B (zh) * | 2018-06-01 | 2020-07-21 | 深圳翰宇药业股份有限公司 | 一种含脯氨酸的首尾环肽合成方法 |
| CN112538103B (zh) * | 2020-12-28 | 2022-10-25 | 合肥科生景肽生物科技有限公司 | 制备生长激素释放抑制素的方法 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3782010T2 (de) * | 1986-12-04 | 1993-02-18 | Toyo Jozo Kk | Vom calcitonin-gen abgeleitete peptidderivate. |
| US5674839A (en) * | 1987-05-22 | 1997-10-07 | Competitive Technologies, Inc. | Cyclic analogs of alpha-MSH fragments |
| US4959352A (en) * | 1987-09-18 | 1990-09-25 | Hoffmann-La Roche Inc. | Cyclic growth hormone releasing factor analogs and method for the manufacture thereof |
| US5169862A (en) * | 1989-07-07 | 1992-12-08 | Peptide Technologies Corporation | Analogs of viscosin and their uses |
| CA2045495A1 (en) * | 1989-11-08 | 1991-05-09 | Masutaka Ohsaki | Peptides and processes for producing cyclic peptides |
| US5064939A (en) * | 1990-02-06 | 1991-11-12 | The Salk Institute For Biological Studies | Cyclic gnrh antagonists |
| US6183722B1 (en) * | 1991-11-27 | 2001-02-06 | Diatide, Inc. | Somatostatin analogs |
| JPH0621079A (ja) | 1992-06-29 | 1994-01-28 | Nippon Telegr & Teleph Corp <Ntt> | 半導体装置 |
| US6008058A (en) * | 1993-06-18 | 1999-12-28 | University Of Louisville | Cyclic peptide mixtures via side chain or backbone attachment and solid phase synthesis |
| GB2282813A (en) * | 1993-10-15 | 1995-04-19 | Merck & Co Inc | Annular antigen scaffolds comprising thioether linkages |
| US5556940A (en) * | 1994-06-20 | 1996-09-17 | National Research Council Of Canada | Parathyroid hormone analogues for the treatment of osteoporosis |
| US5569742A (en) * | 1994-06-22 | 1996-10-29 | The Salk Institute For Biological Studies | Centrally truncated NPY cyclic peptides |
| US5717062A (en) * | 1995-06-07 | 1998-02-10 | Beth Israel Hospital Association | Cyclic analogs of PTH and PTHrP |
| WO1997002289A1 (en) * | 1995-07-06 | 1997-01-23 | Zeneca Limited | Peptide inhibitors of fibronectine |
| US6169071B1 (en) * | 1996-07-12 | 2001-01-02 | Mcgill University | Compounds and methods for modulating cell adhesion |
| US5939383A (en) * | 1996-11-15 | 1999-08-17 | Remacle; Jose | Cyclic peptides bearing a tail designed for subsequent chemical coupling and process for preparing same |
| CA2290443A1 (en) * | 1997-05-14 | 1998-11-19 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Peptide parathyroid hormone analogs |
| WO1999031121A2 (en) * | 1997-12-15 | 1999-06-24 | Peptor Ltd. | Branched building units for synthesizing cyclic peptides |
| IL138338A0 (en) | 1998-04-15 | 2001-10-31 | Aventis Pharm Prod Inc | Process for the preparation of resin-bound cyclic peptides |
-
1999
- 1999-04-15 IL IL13833899A patent/IL138338A0/xx unknown
- 1999-04-15 PL PL99347103A patent/PL347103A1/xx not_active Application Discontinuation
- 1999-04-15 WO PCT/US1999/008435 patent/WO1999052933A1/en not_active Application Discontinuation
- 1999-04-15 CZ CZ20003798A patent/CZ20003798A3/cs unknown
- 1999-04-15 SK SK1535-2000A patent/SK15352000A3/sk unknown
- 1999-04-15 BR BR9909634-0A patent/BR9909634A/pt not_active IP Right Cessation
- 1999-04-15 EP EP99917595A patent/EP1093458A4/en not_active Withdrawn
- 1999-04-15 UA UA2000116453A patent/UA72460C2/uk unknown
- 1999-04-15 AP APAP/P/2000/001972A patent/AP1117A/en active
- 1999-04-15 AU AU35679/99A patent/AU744812B2/en not_active Ceased
- 1999-04-15 EA EA200001071A patent/EA200001071A1/ru unknown
- 1999-04-15 CN CNB998119709A patent/CN1163504C/zh not_active Expired - Fee Related
- 1999-04-15 KR KR1020007011446A patent/KR20010085236A/ko not_active Application Discontinuation
- 1999-04-15 JP JP2000543489A patent/JP2002511483A/ja active Pending
- 1999-04-15 HU HU0101629A patent/HUP0101629A2/hu unknown
- 1999-04-15 CA CA002325572A patent/CA2325572A1/en not_active Abandoned
- 1999-04-15 CN CNA2004100386677A patent/CN1552737A/zh active Pending
- 1999-11-18 US US09/442,989 patent/US6569993B1/en not_active Expired - Fee Related
-
2000
- 2000-10-13 NO NO20005165A patent/NO20005165L/no not_active Application Discontinuation
- 2000-10-13 OA OA1200000283A patent/OA11501A/en unknown
- 2000-11-02 BG BG104903A patent/BG104903A/bg unknown
Also Published As
| Publication number | Publication date |
|---|---|
| UA72460C2 (en) | 2005-03-15 |
| BR9909634A (pt) | 2001-10-16 |
| AU744812B2 (en) | 2002-03-07 |
| EP1093458A1 (en) | 2001-04-25 |
| JP2002511483A (ja) | 2002-04-16 |
| PL347103A1 (en) | 2002-03-25 |
| CZ20003798A3 (cs) | 2001-08-15 |
| AU3567999A (en) | 1999-11-01 |
| NO20005165L (no) | 2000-12-15 |
| CA2325572A1 (en) | 1999-10-21 |
| IL138338A0 (en) | 2001-10-31 |
| HUP0101629A2 (en) | 2003-03-28 |
| US6569993B1 (en) | 2003-05-27 |
| WO1999052933A1 (en) | 1999-10-21 |
| CN1552737A (zh) | 2004-12-08 |
| AP1117A (en) | 2002-11-02 |
| OA11501A (en) | 2004-05-14 |
| KR20010085236A (ko) | 2001-09-07 |
| EA200001071A1 (ru) | 2001-08-27 |
| CN1323313A (zh) | 2001-11-21 |
| CN1163504C (zh) | 2004-08-25 |
| NO20005165D0 (no) | 2000-10-13 |
| AP2000001972A0 (en) | 2000-12-31 |
| BG104903A (bg) | 2001-07-31 |
| EP1093458A4 (en) | 2001-07-18 |
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