DE69900841D1 - Durch enzymkatalyse erhaltene therapeutische substanzen. - Google Patents
Durch enzymkatalyse erhaltene therapeutische substanzen.Info
- Publication number
- DE69900841D1 DE69900841D1 DE69900841T DE69900841T DE69900841D1 DE 69900841 D1 DE69900841 D1 DE 69900841D1 DE 69900841 T DE69900841 T DE 69900841T DE 69900841 T DE69900841 T DE 69900841T DE 69900841 D1 DE69900841 D1 DE 69900841D1
- Authority
- DE
- Germany
- Prior art keywords
- cell
- prodrug
- endogenous
- selective substrate
- enzym
- 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.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/16—Purine radicals
- C07H19/20—Purine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
- A61K47/555—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound pre-targeting systems involving an organic compound, other than a peptide, protein or antibody, for targeting specific cells
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
- A61K47/555—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound pre-targeting systems involving an organic compound, other than a peptide, protein or antibody, for targeting specific cells
- A61K47/556—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound pre-targeting systems involving an organic compound, other than a peptide, protein or antibody, for targeting specific cells enzyme catalyzed therapeutic agent [ECTA]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/62—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being a protein, peptide or polyamino acid
- A61K47/66—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being a protein, peptide or polyamino acid the modifying agent being a pre-targeting system involving a peptide or protein for targeting specific cells
- A61K47/67—Enzyme prodrug therapy, e.g. gene directed enzyme drug therapy [GDEPT] or VDEPT
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6509—Six-membered rings
- C07F9/6512—Six-membered rings having the nitrogen atoms in positions 1 and 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/06—Pyrimidine radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/06—Pyrimidine radicals
- C07H19/10—Pyrimidine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US7226498P | 1998-01-23 | 1998-01-23 | |
US7695098P | 1998-03-05 | 1998-03-05 | |
US10863498P | 1998-11-16 | 1998-11-16 | |
PCT/US1999/001332 WO1999037753A1 (en) | 1998-01-23 | 1999-01-22 | Enzyme catalyzed therapeutic agents |
Publications (2)
Publication Number | Publication Date |
---|---|
DE69900841D1 true DE69900841D1 (de) | 2002-03-14 |
DE69900841T2 DE69900841T2 (de) | 2002-10-02 |
Family
ID=27372051
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE69900841T Expired - Lifetime DE69900841T2 (de) | 1998-01-23 | 1999-01-22 | Durch enzymkatalyse erhaltene therapeutische substanzen. |
Country Status (16)
Country | Link |
---|---|
US (3) | US6245750B1 (de) |
EP (2) | EP1167972B1 (de) |
JP (2) | JP2002500880A (de) |
CN (1) | CN1192102C (de) |
AT (1) | ATE212661T1 (de) |
AU (1) | AU753155B2 (de) |
BR (1) | BR9907736A (de) |
CA (1) | CA2317505C (de) |
DE (1) | DE69900841T2 (de) |
DK (1) | DK1045897T3 (de) |
ES (1) | ES2172303T3 (de) |
HK (2) | HK1030624A1 (de) |
IL (1) | IL137164A0 (de) |
PT (1) | PT1045897E (de) |
TW (1) | TWI244924B (de) |
WO (1) | WO1999037753A1 (de) |
Families Citing this family (63)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE59609590D1 (de) | 1995-02-01 | 2002-10-02 | Resprotect Gmbh | Verwendung von 5' substituierten nukleosiden zur hemmung von resistenzbildung bei der zytostatikabehandlung |
JP2001512830A (ja) * | 1997-08-08 | 2001-08-28 | ニューバイオティックス インコーポレイテッド | 生物療法耐性および化学療法耐性を克服するための方法および組成物 |
US6703374B1 (en) | 1997-10-30 | 2004-03-09 | The United States Of America As Represented By The Department Of Health And Human Services | Nucleosides for imaging and treatment applications |
WO1999037753A1 (en) * | 1998-01-23 | 1999-07-29 | Newbiotics, Inc. | Enzyme catalyzed therapeutic agents |
US7462605B2 (en) * | 1998-01-23 | 2008-12-09 | Celmed Oncology (Usa), Inc. | Phosphoramidate compounds and methods of use |
EP1200455B1 (de) * | 1999-07-22 | 2009-04-22 | Celmed Oncology (USA), Inc. | Enzym katalisierte therapeutische aktivierung |
WO2001007088A2 (en) * | 1999-07-22 | 2001-02-01 | Newbiotics, Inc. | Methods for treating therapy-resistant tumors |
CN1391487A (zh) * | 1999-07-22 | 2003-01-15 | 新生物公司 | 酶催化的抗一感染治疗剂 |
US6683061B1 (en) * | 1999-07-22 | 2004-01-27 | Newbiotics, Inc. | Enzyme catalyzed therapeutic activation |
US6673564B2 (en) * | 1999-10-18 | 2004-01-06 | Millennium Pharmaceuticals, Inc. | Methods for using 22045, a human cyclic nucleotide phosphodiesterase |
US20030212037A1 (en) * | 2000-12-21 | 2003-11-13 | Christopher Boyer | Use of bvdu for inhibiting the growth of hyperproliferative cells |
WO2001045690A2 (en) * | 1999-12-23 | 2001-06-28 | Newbiotics, Inc. | Use of bvdu for inhibiting the growth of hyperproliferative cells |
US20030130179A1 (en) * | 2000-07-20 | 2003-07-10 | Shepard H. Michael | Methods for identifying therapeutic targets for treating infectious disease |
AU2001277093A1 (en) * | 2000-07-20 | 2002-02-05 | Newbiotics, Inc. | Methods for identifying therapeutic targets |
ES2536972T5 (es) * | 2000-07-21 | 2022-04-06 | Gilead Sciences Inc | Profármacos de análogos de nucleótidos de fosfonato y métodos para seleccionar y preparar los mismos |
AU2002241911B9 (en) * | 2001-01-19 | 2007-01-25 | Celmed Oncology (Usa), Inc. | Methods to treat autoimmune and inflammatory conditions |
DE10108851A1 (de) * | 2001-02-23 | 2002-09-12 | Resprotect Gmbh | Verwendung von 5'-substituierten Nukleosiden und/oder deren Prodrugs zur resistenzfreien Therapie von Infektionskrankheiten |
BR0210149A (pt) * | 2001-05-09 | 2004-06-29 | Newbiotics Inc | Pródrogas ativadas por deformilase de peptìdeo |
US20030212147A1 (en) * | 2001-07-12 | 2003-11-13 | Chung Sum Man Stephen | Enzyme activated chemotherapy of liver cancer |
US20040235761A1 (en) * | 2001-08-14 | 2004-11-25 | Yousuke Furuta | Novel virus proliferaton inhibition/virucidal method and novel pyradine nucleotide/pyradine nucleoside analogue |
YU44404A (sh) * | 2001-11-23 | 2006-08-17 | Chugai Seiyaku Kabushiki Kaisha | Postupak za identifikovanje ciljnih enzima tumora |
US20030152747A1 (en) * | 2002-01-11 | 2003-08-14 | The Garland Company, Inc., An Ohio Corporation | Roofing materials |
AU2003225047A1 (en) * | 2002-04-18 | 2003-11-03 | Celmed Oncology (Usa), Inc. | Peptide deformylase activated prodrugs |
BR0315537A (pt) | 2002-11-14 | 2005-09-27 | Celmed Oncology Usa Inc | Pró-drogas ativadas por peptìdeo desformilase |
EP1599484A2 (de) * | 2003-02-21 | 2005-11-30 | Chugai Seiyaku Kabushiki Kaisha | Verfahren zur herstellung von hexacyclischen camptothecin derivaten |
CA2536357A1 (en) * | 2003-05-29 | 2004-12-23 | The Scripps Research Institute | Targeted delivery to legumain-expressing cells |
GB0317009D0 (en) | 2003-07-21 | 2003-08-27 | Univ Cardiff | Chemical compounds |
AU2004274021B2 (en) * | 2003-09-18 | 2009-08-13 | Isis Pharmaceuticals, Inc. | 4'-thionucleosides and oligomeric compounds |
GB0401088D0 (en) | 2004-01-19 | 2004-02-18 | Univ Cardiff | Phosphoramidate derivatives |
UA88008C2 (en) * | 2004-04-09 | 2009-09-10 | Чугей Сейяку Кабусики Кайся | Water-soluble prodrugs |
US7309589B2 (en) | 2004-08-20 | 2007-12-18 | Vironix Llc | Sensitive detection of bacteria by improved nested polymerase chain reaction targeting the 16S ribosomal RNA gene and identification of bacterial species by amplicon sequencing |
GB0505781D0 (en) * | 2005-03-21 | 2005-04-27 | Univ Cardiff | Chemical compounds |
WO2006110531A2 (en) * | 2005-04-07 | 2006-10-19 | Health Research Inc. | Acyl homoserine lactones for inhibition of cell growth |
WO2006121820A1 (en) * | 2005-05-05 | 2006-11-16 | Valeant Research & Development | Phosphoramidate prodrugs for treatment of viral infection |
TW200744603A (en) * | 2005-08-22 | 2007-12-16 | Chugai Pharmaceutical Co Ltd | Novel anticancer concomitant drug |
WO2007046456A1 (ja) * | 2005-10-19 | 2007-04-26 | Chugai Seiyaku Kabushiki Kaisha | 新規水溶性プロドラッグを含有する、膵臓癌、卵巣癌または肝臓癌の予防または治療剤 |
EP1976861A2 (de) * | 2005-11-29 | 2008-10-08 | The Scripps Research Institute | Hemmung von tumorzellinvasion, metastasen und angiogenese durch targetting von legumin |
DE102006037786A1 (de) * | 2006-08-11 | 2008-03-20 | Resprotect Gmbh | Nukleoside, diese enthaltendes Arzneimittel und deren Verwendung |
US7964580B2 (en) | 2007-03-30 | 2011-06-21 | Pharmasset, Inc. | Nucleoside phosphoramidate prodrugs |
US8173621B2 (en) | 2008-06-11 | 2012-05-08 | Gilead Pharmasset Llc | Nucleoside cyclicphosphates |
SG194404A1 (en) * | 2008-12-23 | 2013-11-29 | Gilead Pharmasset Llc | Synthesis of purine nucleosides |
TWI583692B (zh) | 2009-05-20 | 2017-05-21 | 基利法瑪席特有限責任公司 | 核苷磷醯胺 |
US8618076B2 (en) | 2009-05-20 | 2013-12-31 | Gilead Pharmasset Llc | Nucleoside phosphoramidates |
WO2011005525A2 (en) | 2009-06-22 | 2011-01-13 | Health Research Inc. | Prodrug anti-cancer therapy |
BR112012024884A2 (pt) | 2010-03-31 | 2016-10-18 | Gilead Pharmasset Llc | síntese estereosseletiva de ativos contendo fósforo |
PL3290428T3 (pl) | 2010-03-31 | 2022-02-07 | Gilead Pharmasset Llc | Tabletka zawierająca krystaliczny (S)-2-(((S)-(((2R,3R,4R,5R)-5-(2,4-diokso-3,4-dihydropirymidyn-1(2H)-ylo)-4-fluoro-3-hydroksy-4-metylotetrahydrofuran-2-ylo)metoksy)(fenoksy)fosforylo)amino)propanian izopropylu |
CN103476415B (zh) | 2010-11-16 | 2017-09-22 | 南加州大学 | 用于增强成体干细胞的不对称分裂的cbp/连环蛋白拮抗剂 |
CA2818853A1 (en) | 2010-11-30 | 2012-06-07 | Gilead Pharmasset Llc | 2'-spirocyclo-nucleosides for use in therapy of hcv or dengue virus |
CN103501824A (zh) * | 2011-02-18 | 2014-01-08 | Uab研究基金会 | 与嘌呤核苷磷酸化酶或核苷水解酶的前体药物的改进的治疗用途相关的应用 |
RU2614406C2 (ru) | 2011-03-01 | 2017-03-28 | Нукана Биомед Лимитед | Фосфороамидатные производные 5-фтор-2'-дезоксиуридина для применения для лечения рака |
AU2012308295B2 (en) | 2011-09-16 | 2017-10-26 | Gilead Pharmasset Llc | Methods for treating HCV |
US8889159B2 (en) | 2011-11-29 | 2014-11-18 | Gilead Pharmasset Llc | Compositions and methods for treating hepatitis C virus |
SG10201510322UA (en) | 2012-11-16 | 2016-01-28 | Univ Cardiff | Process for preparing nucleoside prodrugs |
LT2950786T (lt) | 2013-01-31 | 2020-03-10 | Gilead Pharmasset Llc | Dviejų antivirusinių junginių preparatų kompozicija |
EP2984098A2 (de) | 2013-04-12 | 2016-02-17 | Achillion Pharmaceuticals, Inc. | Deuterierte nukleosid-prodrugs zur behandlung von hcv |
ES2792503T3 (es) | 2013-08-27 | 2020-11-11 | Gilead Pharmasset Llc | Formulación combinada de dos compuestos antivirales |
US9828409B2 (en) * | 2014-03-19 | 2017-11-28 | Minghong Zhong | Bridged-cyclo-ProTides as prodrugs of therapeutic nucleosides and nucleotides |
SI3119794T1 (en) | 2014-06-25 | 2018-02-28 | NuCana plc | FORMULATION, COMPOSITION OF GEMCITABIN PREPARED |
SI3160978T1 (sl) | 2014-06-25 | 2020-11-30 | NuCana plc | Gemcitabin predzdravila |
EP3204004A4 (de) | 2014-10-08 | 2018-05-30 | Epigenetics Pharma LLC | Vitamin-e-nukleosidprodrugs |
GB201709471D0 (en) | 2017-06-14 | 2017-07-26 | Nucana Biomed Ltd | Diastereoselective synthesis of hosphate derivatives |
CN109207551B (zh) * | 2017-07-07 | 2023-05-26 | 上海睿智化学研究有限公司 | 一种筛选叶酸代谢相关药物的方法 |
KR102545956B1 (ko) * | 2022-10-19 | 2023-06-22 | 주식회사 카이팜 | 브리부딘을 유효성분으로 포함하는 오스카 유도 질환의 예방 또는 치료용 조성물 |
Family Cites Families (93)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB982776A (en) * | 1962-01-24 | 1965-02-10 | Wellcome Found | 2-deoxyuridines and their use in pharmaceutical compositions having anti-immune activity |
JPS5017989B1 (de) * | 1970-12-24 | 1975-06-25 | ||
US4267171A (en) | 1979-07-02 | 1981-05-12 | The Regents Of The University Of California | C-5 Substituted cytosine nucleosides |
US4247544A (en) | 1979-07-02 | 1981-01-27 | The Regents Of The University Of California | C-5 Substituted uracil nucleosides |
US4668777A (en) | 1981-03-27 | 1987-05-26 | University Patents, Inc. | Phosphoramidite nucleoside compounds |
JPS5843993A (ja) | 1981-09-09 | 1983-03-14 | Yamasa Shoyu Co Ltd | 1−β−D−アラビノフラノシル−(E)−5−(2−ハロゲノビニル)ウラシル−5′−りん酸およびその製造法 |
EP0095294A1 (de) | 1982-05-22 | 1983-11-30 | Beecham Group Plc | Deoxyuridin-Derivate, ihre Herstellungsverfahren und ihre medizinische Anwendung |
DE3229169A1 (de) | 1982-08-05 | 1984-02-09 | Robugen GmbH Pharmazeutische Fabrik, 7300 Esslingen | Verwendung von 5-alkylpyrimidinnukleosiden und deren derivate als zytostatika |
US4816570A (en) | 1982-11-30 | 1989-03-28 | The Board Of Regents Of The University Of Texas System | Biologically reversible phosphate and phosphonate protective groups |
US4948882A (en) | 1983-02-22 | 1990-08-14 | Syngene, Inc. | Single-stranded labelled oligonucleotides, reactive monomers and methods of synthesis |
RO88451A2 (ro) | 1984-06-05 | 1986-01-30 | Intreprinderea De Antibiotice,Ro | Derivati ai acidului 7-aminocefalosporanic si procedeu de preparare aacestora |
US5070082A (en) | 1986-10-23 | 1991-12-03 | American Cyanamid Company | Solubilized pro-drugs |
US5116827A (en) * | 1986-10-23 | 1992-05-26 | American Cyanamid Company | Quinolinecarboxylic acid derivatives as solubilized pro-drugs |
US5077282A (en) * | 1986-10-23 | 1991-12-31 | American Cyanamid Company | Solubilized pro-drugs |
US5212291A (en) * | 1986-10-23 | 1993-05-18 | American Cyanamid Company | Anthracycline derivatives as solubilized pro-drugs |
US5077283A (en) * | 1986-10-23 | 1991-12-31 | American Cyanamid Company | Solubilized imidazole pro-drugs |
US4963533A (en) | 1986-10-24 | 1990-10-16 | Stichting Rega Vzw (Rega) | Therapeutic application of dideoxycytidinene |
US5116822A (en) | 1986-10-24 | 1992-05-26 | Stichting Rega Vzw | Therapeutic application of dideoxycytidinene |
NL8700366A (nl) | 1987-02-13 | 1988-09-01 | Stichting Rega V Z W | Combinatie van fu met bvdu als middel tegen adenocarcinoom. |
US5085983A (en) | 1988-08-19 | 1992-02-04 | City Of Hope | Detection of human tumor progression and drug resistance |
US4975278A (en) | 1988-02-26 | 1990-12-04 | Bristol-Myers Company | Antibody-enzyme conjugates in combination with prodrugs for the delivery of cytotoxic agents to tumor cells |
JPH01301690A (ja) | 1987-10-08 | 1989-12-05 | Stichting Rega Vzw | 抗hiv活性をもつ3’−アジド−2,6−ジアミノプリン−2’,3’−ジデオキシリボシド |
JPH01265099A (ja) | 1987-10-08 | 1989-10-23 | Stichting Rega Vzw | 抗hiv活性をもつ3’,−フルオロプリン−2’,3’−ジデオキシリボシド類 |
US4963263A (en) | 1988-03-24 | 1990-10-16 | Terrapin Technologies, Inc. | Method of identity analyte-binding peptides |
US5133866A (en) | 1988-03-24 | 1992-07-28 | Terrapin Technologies, Inc. | Method to identify analyte-bending ligands |
US5300425A (en) | 1987-10-13 | 1994-04-05 | Terrapin Technologies, Inc. | Method to produce immunodiagnostic reagents |
US5217869A (en) | 1987-10-13 | 1993-06-08 | Terrapin Technologies, Inc. | Method to produce immunodiagnostic reagents |
US5338659A (en) | 1991-04-02 | 1994-08-16 | Terrapin Technologies, Inc. | Method for determining analyte concentration by cross-reactivity profiling |
EP0316592A3 (de) | 1987-11-13 | 1990-09-19 | Stichting REGA V.Z.W. | 3'-Fluor-2',3'-dideoxyuridin und seine therapeutische Verwendung |
CA1317291C (en) | 1987-12-14 | 1993-05-04 | Naeem Botros Hanna | Antitumor 6-sulfenamide, 6-sulfinamide and 6-sulfonamide purines, purine nucleosides, purine nucleotides and related compounds |
EP0448550B1 (de) * | 1988-02-24 | 1994-08-10 | INSTITUT DE RECHERCHES CHIMIQUES ET BIOLOGIQUES APPLIQUEES (I.R.C.E.B.A.) Société à responsabilité limitée dite: | Derivate von deoxy-2'-uridin substituiert in der 5, 3' oder 5' stellung durch acylierte alpha-amino-gruppen, verfahren zur herstellung und arzneimittel daraus |
WO1990003978A1 (en) | 1988-10-03 | 1990-04-19 | Stichting Rega Vzw | 5-halogeno-3'-fluoro-2',3'-dideoxyuridine compounds and their therapeutic application |
US5596018A (en) | 1988-12-28 | 1997-01-21 | Toray Industries, Inc. | Antiviral agents against aids-causing virus |
US5433955A (en) | 1989-01-23 | 1995-07-18 | Akzo N.V. | Site specific in vivo activation of therapeutic drugs |
US5264618A (en) | 1990-04-19 | 1993-11-23 | Vical, Inc. | Cationic lipids for intracellular delivery of biologically active molecules |
SK280313B6 (sk) | 1990-04-24 | 1999-11-08 | �Stav Organick� Chemie A Biochemie Av �R | N-(3-fluór-2-fosfonylmetoxypropyl)deriváty purínov |
WO1991017424A1 (en) | 1990-05-03 | 1991-11-14 | Vical, Inc. | Intracellular delivery of biologically active substances by means of self-assembling lipid complexes |
GB9010242D0 (en) | 1990-05-08 | 1990-06-27 | British Telecomm | Optical signal regenerator and optical communications system incorporating same |
US5137724A (en) | 1990-05-23 | 1992-08-11 | Stichting Rega Vzw | Combinations of TS-inhibitors and viral TK-inhibitors in antiherpetic medicines |
US5627165A (en) | 1990-06-13 | 1997-05-06 | Drug Innovation & Design, Inc. | Phosphorous prodrugs and therapeutic delivery systems using same |
US5608046A (en) * | 1990-07-27 | 1997-03-04 | Isis Pharmaceuticals, Inc. | Conjugated 4'-desmethyl nucleoside analog compounds |
US5556942A (en) * | 1991-04-29 | 1996-09-17 | Terrapin Technologies, Inc. | Glutathione S-transferase-activated compounds |
CA2107914C (en) | 1991-04-29 | 2007-04-03 | Lawrence M. Kauvar | Method to profile and treat abnormal cells |
US5645988A (en) | 1991-05-08 | 1997-07-08 | The United States Of America As Represented By The Department Of Health And Human Services | Methods of identifying drugs with selective effects against cancer cells |
SK279262B6 (sk) | 1991-05-16 | 1998-08-05 | Glaxo Group Limited | Protivírusová zmes, farmaceutický prostriedok s je |
DK0530407T3 (da) | 1991-09-04 | 1996-07-29 | Stichting Rega V Z W | Substituerede nukleosidderivater, fremgangsmåder til fremstilling heraf og farmaceutiske sammensætninger indeholdende disse |
US5233031A (en) * | 1991-09-23 | 1993-08-03 | University Of Rochester | Phosphoramidate analogs of 2'-deoxyuridine |
US5879700A (en) | 1991-10-15 | 1999-03-09 | Hostetler; Karl Y. | Nucleoside analogue phosphates for topical use |
US5274162A (en) * | 1991-12-13 | 1993-12-28 | Arnold Glazier | Antineoplastic drugs with bipolar toxification/detoxification functionalities |
WO1993013740A2 (en) | 1991-12-31 | 1993-07-22 | Worcester Foundation For Experimental Biology | Antiparasitic oligonucleotides active against drug resistant malaria |
US5430148A (en) | 1992-03-31 | 1995-07-04 | Agouron Pharmaceuticals, Inc. | Antiproliferative quinazolines |
US5668828A (en) * | 1992-05-08 | 1997-09-16 | Sanconix, Inc. | Enhanced frequency agile radio |
US6057305A (en) | 1992-08-05 | 2000-05-02 | Institute Of Organic Chemistry And Biochemistry Of The Academy Of Sciences Of The Czech Republic | Antiretroviral enantiomeric nucleotide analogs |
US5516631A (en) | 1992-10-13 | 1996-05-14 | La Jolla Cancer Research Foundation | Method of inhibiting replication of hyperproliferative cells |
IL105244A (en) * | 1993-03-31 | 2003-07-31 | Dpharm Ltd | Prodrugs with enhanced penetration into cells |
US5502037A (en) | 1993-07-09 | 1996-03-26 | Neuromed Technologies, Inc. | Pro-cytotoxic drug conjugates for anticancer therapy |
US5798340A (en) | 1993-09-17 | 1998-08-25 | Gilead Sciences, Inc. | Nucleotide analogs |
AU7661794A (en) | 1993-09-21 | 1995-04-10 | Amersham International Plc | Reagents comprising chimeric molecules of nucleic acids and nucleic acid analogs |
US5908919A (en) | 1993-10-01 | 1999-06-01 | Terrapin Technologies | Urethane mediated, GST specific molecular release systems |
GB9323008D0 (en) | 1993-11-05 | 1994-01-05 | Connors Thomas | Improvements relating to cancer therapy |
US5457187A (en) * | 1993-12-08 | 1995-10-10 | Board Of Regents University Of Nebraska | Oligonucleotides containing 5-fluorouracil |
US5521161A (en) | 1993-12-20 | 1996-05-28 | Compagnie De Developpment Aguettant S.A. | Method of treating HIV in humans by administration of ddI and hydroxycarbamide |
GB9415167D0 (en) * | 1994-07-27 | 1994-09-14 | Springer Caroline J | Improvements relating to cancer therapy |
US5556992A (en) * | 1994-09-02 | 1996-09-17 | Universite De Montreal | Novel rhodamine derivatives for photodynamic therapy of cancer and in vitro purging of the leukemias |
IL115156A (en) | 1994-09-06 | 2000-07-16 | Univ Georgia | Pharmaceutical compositions for the treatment of cancer comprising 1-(2-hydroxymethyl-1,3-dioxolan-4-yl) cytosines |
US5968910A (en) | 1994-11-30 | 1999-10-19 | Jan M. R. Balzarini | Compositions containing two or three inhibitors of different HIV reverse transcriptases |
DE59609590D1 (de) | 1995-02-01 | 2002-10-02 | Resprotect Gmbh | Verwendung von 5' substituierten nukleosiden zur hemmung von resistenzbildung bei der zytostatikabehandlung |
US5705336A (en) * | 1995-03-07 | 1998-01-06 | The United States Of America As Represented By The Department Of Health And Human Services | Assay for sensitivity of tumors to DNA-platinating chemotherapy |
GB9505025D0 (en) | 1995-03-13 | 1995-05-03 | Medical Res Council | Chemical compounds |
IN186549B (de) | 1995-04-19 | 2001-09-29 | Kumiai Chemical Co Ltd | |
US5856464A (en) * | 1995-06-07 | 1999-01-05 | Lajolla Pharmaceutical Company | Selective capping solution phase oligonucleotide synthesis |
US5998151A (en) * | 1995-12-01 | 1999-12-07 | The United States Of America As Represented By The Department Of Health And Human Services | Methods for predicting the efficacy of a chemotherapeutic regimen for gastrointestinal cancers using antibodies specific for thymidylate synthase |
US5981507A (en) | 1995-12-14 | 1999-11-09 | Advanced Magnetics, Inc. | Polymeric carriers linked to nucleotide analogues via a phosphoramide bond |
US5880097A (en) | 1996-01-04 | 1999-03-09 | Terrapin Techologies, Inc. | Tethered prodrugs |
JP2000504670A (ja) * | 1996-01-31 | 2000-04-18 | ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア | 腫瘍細胞の成長を抑制する方法 |
RU2111970C1 (ru) | 1996-06-25 | 1998-05-27 | Иван Игоревич Федоров | 3'-оксимино-2',3'-дидезоксинуклеозиды |
GB9708611D0 (en) | 1997-04-28 | 1997-06-18 | Univ Cardiff | Chemical compounds |
WO1999006072A1 (en) | 1997-07-30 | 1999-02-11 | Boehringer Mannheim Corporation | Cyclized prodrugs |
JP2001512830A (ja) * | 1997-08-08 | 2001-08-28 | ニューバイオティックス インコーポレイテッド | 生物療法耐性および化学療法耐性を克服するための方法および組成物 |
AU729377B2 (en) | 1997-10-23 | 2001-02-01 | Asterias Biotherapeutics, Inc. | Methods and materials for the growth of primate-derived primordial stem cells in feeder-free culture |
US6703374B1 (en) | 1997-10-30 | 2004-03-09 | The United States Of America As Represented By The Department Of Health And Human Services | Nucleosides for imaging and treatment applications |
DK1027365T3 (da) | 1997-10-30 | 2005-05-30 | Us Gov Health & Human Serv | Antitumor-uridinanaloger |
WO1999037753A1 (en) * | 1998-01-23 | 1999-07-29 | Newbiotics, Inc. | Enzyme catalyzed therapeutic agents |
GB9821121D0 (en) | 1998-09-29 | 1998-11-25 | James Robinson Ltd | Grey colouring photochromic fused pyrans |
NZ512171A (en) | 1998-12-11 | 2004-07-30 | Medarex Inc | Prodrug compound comprising a therapeutic agent, an oligopeptide with a non-genetically encoded amino acid, a stabilizing group and optionally a linker group |
EP1200455B1 (de) * | 1999-07-22 | 2009-04-22 | Celmed Oncology (USA), Inc. | Enzym katalisierte therapeutische aktivierung |
US6683061B1 (en) * | 1999-07-22 | 2004-01-27 | Newbiotics, Inc. | Enzyme catalyzed therapeutic activation |
AU6607200A (en) | 1999-07-23 | 2001-02-13 | Westinghouse Electric Company Llc | Pulsed gamma neutron activation analysis (pgnaa) method and apparatus for nondestructive assay of containerized contaminants |
US6294546B1 (en) * | 1999-08-30 | 2001-09-25 | The Broad Of Trustees Of The Leland Stanford Junior University | Uses of diterpenoid triepoxides as an anti-proliferative agent |
GB0009486D0 (en) | 2000-04-17 | 2000-06-07 | Univ Cardiff | Chemical compounds |
GB0011203D0 (en) | 2000-05-09 | 2000-06-28 | Univ Cardiff | Chemical compounds |
WO2002039952A2 (en) * | 2000-11-16 | 2002-05-23 | Newbiotics, Inc. | Synergistic ecta compositions |
AU2002241911B9 (en) * | 2001-01-19 | 2007-01-25 | Celmed Oncology (Usa), Inc. | Methods to treat autoimmune and inflammatory conditions |
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Also Published As
Publication number | Publication date |
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EP1167972A2 (de) | 2002-01-02 |
TWI244924B (en) | 2005-12-11 |
HK1039520A1 (zh) | 2002-04-26 |
JP2001220397A (ja) | 2001-08-14 |
US6245750B1 (en) | 2001-06-12 |
IL137164A0 (en) | 2001-07-24 |
US20010034440A1 (en) | 2001-10-25 |
EP1045897B1 (de) | 2002-01-30 |
DE69900841T2 (de) | 2002-10-02 |
EP1167972A3 (de) | 2006-05-24 |
BR9907736A (pt) | 2000-10-17 |
CN1192102C (zh) | 2005-03-09 |
CN1291228A (zh) | 2001-04-11 |
DK1045897T3 (da) | 2002-05-13 |
CA2317505C (en) | 2011-01-04 |
US7601703B2 (en) | 2009-10-13 |
EP1045897A1 (de) | 2000-10-25 |
EP1167972B1 (de) | 2017-03-08 |
CA2317505A1 (en) | 1999-07-29 |
WO1999037753A1 (en) | 1999-07-29 |
HK1030624A1 (en) | 2001-05-11 |
US6339151B1 (en) | 2002-01-15 |
PT1045897E (pt) | 2002-07-31 |
JP3265304B2 (ja) | 2002-03-11 |
EP1045897A4 (de) | 2000-10-25 |
ES2172303T3 (es) | 2002-09-16 |
AU753155B2 (en) | 2002-10-10 |
JP2002500880A (ja) | 2002-01-15 |
AU2464699A (en) | 1999-08-09 |
ATE212661T1 (de) | 2002-02-15 |
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