WO2005016326A3 - Analogues de la thalidomide utilises comme inhibiteurs potentiels de l'angiogenese - Google Patents
Analogues de la thalidomide utilises comme inhibiteurs potentiels de l'angiogenese Download PDFInfo
- Publication number
- WO2005016326A3 WO2005016326A3 PCT/US2004/022242 US2004022242W WO2005016326A3 WO 2005016326 A3 WO2005016326 A3 WO 2005016326A3 US 2004022242 W US2004022242 W US 2004022242W WO 2005016326 A3 WO2005016326 A3 WO 2005016326A3
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- WO
- WIPO (PCT)
- Prior art keywords
- thalidomide
- analogs
- angiogenesis inhibitors
- potential angiogenesis
- subject
- Prior art date
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
-
- 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
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/235—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids having an aromatic ring attached to a carboxyl group
- A61K31/24—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids having an aromatic ring attached to a carboxyl group having an amino or nitro group
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/4035—Isoindoles, e.g. phthalimide
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- 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
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/575—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of three or more carbon atoms, e.g. cholane, cholestane, ergosterol, sitosterol
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/64—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
- C07C233/65—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/18—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/18—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D209/20—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals substituted additionally by nitrogen atoms, e.g. tryptophane
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/80—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D211/84—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen directly attached to ring carbon atoms
- C07D211/86—Oxygen atoms
- C07D211/88—Oxygen atoms attached in positions 2 and 6, e.g. glutarimide
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Emergency Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US48651503P | 2003-07-11 | 2003-07-11 | |
US60/486,515 | 2003-07-11 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2005016326A2 WO2005016326A2 (fr) | 2005-02-24 |
WO2005016326A3 true WO2005016326A3 (fr) | 2005-06-16 |
Family
ID=34193060
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2004/022242 WO2005016326A2 (fr) | 2003-07-11 | 2004-07-09 | Analogues de la thalidomide utilises comme inhibiteurs potentiels de l'angiogenese |
Country Status (1)
Country | Link |
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WO (1) | WO2005016326A2 (fr) |
Families Citing this family (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7320991B2 (en) | 2001-02-27 | 2008-01-22 | The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services, National Institutes Of Health | Analogs of thalidomide as potential angiogenesis inhibitors |
US8952895B2 (en) | 2011-06-03 | 2015-02-10 | Apple Inc. | Motion-based device operations |
CA2808646C (fr) | 2003-09-17 | 2016-08-23 | The Government Of The United States Of America, As Represented By The Secretary Of The Department Of Health And Human Services | Analogues de la thalidomide comme modulateurs tnf-alpha |
CA2648216C (fr) | 2006-04-13 | 2016-06-07 | Michael Gutschow | Composes tetrahalogenes utilises comme inhibiteurs d'angiogenese |
WO2008007979A1 (fr) * | 2006-07-12 | 2008-01-17 | Auckland Uniservices Limited | Dérivés de l'acide benzoïque ayant des propriétés immunomodulatrices et anticancéreuses |
WO2012031603A2 (fr) | 2010-09-09 | 2012-03-15 | Danish Medical Consults Aps | Administration d'inhibiteurs d'angiogenèse par les voies aériennes |
ES2617446T3 (es) | 2010-09-27 | 2017-06-19 | Morphosys Ag | Anticuerpo anti-cd38 y lenalidomida o bortezomib para el tratamiento del mieloma múltiple y nhl |
US8927725B2 (en) | 2011-12-02 | 2015-01-06 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Thio compounds |
ES2644022T3 (es) | 2013-03-14 | 2017-11-27 | Bristol-Myers Squibb Company | Combinación de un agonista de DR5 y un antagonista de anti-PD-1 y métodos de uso |
US9694084B2 (en) | 2014-12-23 | 2017-07-04 | Dana-Farber Cancer Institute, Inc. | Methods to induce targeted protein degradation through bifunctional molecules |
CN107257800B (zh) | 2014-12-23 | 2020-06-30 | 达纳-法伯癌症研究所股份有限公司 | 通过双功能分子诱导靶蛋白降解的方法 |
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US20200199097A1 (en) * | 2017-08-21 | 2020-06-25 | Nanjing Noratech Pharmaceuticals Co., Ltd | Pomalidomide derivative and preparation method therefor |
US10513515B2 (en) | 2017-08-25 | 2019-12-24 | Biotheryx, Inc. | Ether compounds and uses thereof |
CN107698648B (zh) * | 2017-08-30 | 2020-08-14 | 大连理工大学 | 含胆甾醇的萘酰亚胺类衍生物及其合成和应用 |
KR20210032430A (ko) | 2018-07-11 | 2021-03-24 | 에이치 리 모피트 캔서 센터 앤드 리서어치 인스티튜트 아이엔씨 | 세레블론-기반 메커니즘에 대한 이량체 면역-조절 화합물 |
US11236103B2 (en) | 2018-07-27 | 2022-02-01 | Biotheryx, Inc. | Bifunctional compounds |
WO2020041331A1 (fr) | 2018-08-20 | 2020-02-27 | Arvinas Operations, Inc. | Composé chimère ciblant la protéolyse (protac) ayant une activité de liaison à l'ubiquitine ligase e3 et ciblant une protéine alpha-synucléine pour le traitement de maladies neurodégénératives |
CN111499610A (zh) * | 2019-01-31 | 2020-08-07 | 南京诺瑞特医药科技有限公司 | 泊马度胺前体药物盐的多晶型物 |
SG11202111343TA (en) | 2019-05-03 | 2021-11-29 | Morphosys Ag | Anti-cd19 therapy in patients having a limited number of nk cells |
EP3999182A1 (fr) | 2019-07-17 | 2022-05-25 | Arvinas Operations, Inc. | Composés ciblant la protéine tau et procédés d'utilisation associés |
KR20220103969A (ko) | 2019-10-31 | 2022-07-25 | 모르포시스 아게 | 백혈병 또는 림프종의 치료를 위해 레날리도마이드와 조합된 항-cd19 요법 |
CN114786723A (zh) | 2019-10-31 | 2022-07-22 | 莫佛塞斯公司 | 序贯抗cd19疗法 |
WO2021222150A2 (fr) | 2020-04-28 | 2021-11-04 | Anwita Biosciences, Inc. | Polypeptides d'interleukine-2 et protéines de fusion de ceux-ci, ainsi que leurs compositions pharmaceutiques et leurs applications thérapeutiques |
EP3915556A1 (fr) | 2020-05-27 | 2021-12-01 | Franz Josef Vonnahme | Application rectale de thalidomide chez des patients atteints de rectite radique chronique hémorragique |
CN117327059A (zh) * | 2020-07-08 | 2024-01-02 | 北京泰德制药股份有限公司 | 抑制并诱导蛋白降解的化合物 |
CN118388454A (zh) | 2021-04-16 | 2024-07-26 | 阿尔维纳斯运营股份有限公司 | Bcl6蛋白水解的调节剂和其相关使用方法 |
WO2024054591A1 (fr) | 2022-09-07 | 2024-03-14 | Arvinas Operations, Inc. | Composés de dégradation de fibrosarcome rapidement accéléré (raf) et procédés d'utilisation associés |
Citations (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB962857A (en) * | 1961-12-04 | 1964-07-08 | Distillers Co Yeast Ltd | Process for the production of imides |
US3314953A (en) * | 1964-03-16 | 1967-04-18 | Richardson Merrell Inc | 1-substituted-3-phthalimido-2, 5-dioxopyrrolidines |
GB1075420A (en) * | 1965-05-08 | 1967-07-12 | Gruenenthal Chemie | Cyclic imide compounds and a process for their production |
US3560495A (en) * | 1965-05-08 | 1971-02-02 | Ernst Frankus | 1-heterocyclic amino methyl or 1-heterocyclic hydrazino methyl-3-phthalimido or (3',6'-dithia-3',4',5',6'-tetrahydrophthalimido)-pyrrolidinediones-2,5 or piperidinediones-2,6 |
US4092147A (en) * | 1975-11-12 | 1978-05-30 | American Cyanamid Company | Method for controlling the relative stem growth of plants |
US4291048A (en) * | 1978-07-06 | 1981-09-22 | Joseph Gold | Method of treating tumors and cancerous cachexia with L-tryptophan |
DE3332633A1 (de) * | 1983-09-09 | 1985-04-04 | Luitpold-Werk Chemisch-pharmazeutische Fabrik GmbH & Co, 8000 München | Substituierte carbonsaeurederivate, verfahren zu ihrer herstellung, und arzneimittel |
WO1994020085A1 (fr) * | 1993-03-01 | 1994-09-15 | The Children's Medical Center Corporation | Procedes et compositions pour inhiber l'angiogenese |
WO1997012625A1 (fr) * | 1995-10-03 | 1997-04-10 | Cytran, Ltd. | Compositions pharmaceutiques a base de dipeptide angiostatique et leur procede d'utilisation |
WO1997037988A1 (fr) * | 1996-04-09 | 1997-10-16 | Grünenthal GmbH | Promedicaments acyles de la n-hydroxymethylthalidomide a effet immunomodulateur |
WO1998025895A1 (fr) * | 1996-12-13 | 1998-06-18 | Eli Lilly And Company | Inhibiteurs de l'activite enzymatique de l'antigene psa |
US5783605A (en) * | 1995-02-27 | 1998-07-21 | Kuo; Sheng-Chu | Helper inducers for differentiation therapy and chemoprevention of cancer |
US5789434A (en) * | 1994-11-15 | 1998-08-04 | Bayer Corporation | Derivatives of substituted 4-biarylbutyric acid as matrix metalloprotease inhibitors |
WO1999013873A1 (fr) * | 1997-09-15 | 1999-03-25 | Klavdia Stepanovna Evlanenkova | Agent permettant de traiter des malades souffrant de tumeurs |
WO2002064083A2 (fr) * | 2000-11-30 | 2002-08-22 | The Children's Medical Center Corporation | Synthese de 3-amino-thalidomide et de ses enantiomeres |
WO2003014315A2 (fr) * | 2001-08-06 | 2003-02-20 | The Children's Medical Center Corporation | Synthese et activite antitumorale d'analogues de thalidomide substitues par azote |
WO2003097052A2 (fr) * | 2002-05-17 | 2003-11-27 | Celgene Corporation | Methodes et compositions faisant appel a des composes immunomodulateurs pour le traitement et la prise en charge des cancers et d'autres maladies |
WO2004085422A1 (fr) * | 2003-03-27 | 2004-10-07 | Tian Jin Hemay Bio-Tech Co., Ltd. | Derives de thalidomide hydrosoluble |
-
2004
- 2004-07-09 WO PCT/US2004/022242 patent/WO2005016326A2/fr active Application Filing
Patent Citations (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB962857A (en) * | 1961-12-04 | 1964-07-08 | Distillers Co Yeast Ltd | Process for the production of imides |
US3314953A (en) * | 1964-03-16 | 1967-04-18 | Richardson Merrell Inc | 1-substituted-3-phthalimido-2, 5-dioxopyrrolidines |
GB1075420A (en) * | 1965-05-08 | 1967-07-12 | Gruenenthal Chemie | Cyclic imide compounds and a process for their production |
US3560495A (en) * | 1965-05-08 | 1971-02-02 | Ernst Frankus | 1-heterocyclic amino methyl or 1-heterocyclic hydrazino methyl-3-phthalimido or (3',6'-dithia-3',4',5',6'-tetrahydrophthalimido)-pyrrolidinediones-2,5 or piperidinediones-2,6 |
US4092147A (en) * | 1975-11-12 | 1978-05-30 | American Cyanamid Company | Method for controlling the relative stem growth of plants |
US4291048A (en) * | 1978-07-06 | 1981-09-22 | Joseph Gold | Method of treating tumors and cancerous cachexia with L-tryptophan |
DE3332633A1 (de) * | 1983-09-09 | 1985-04-04 | Luitpold-Werk Chemisch-pharmazeutische Fabrik GmbH & Co, 8000 München | Substituierte carbonsaeurederivate, verfahren zu ihrer herstellung, und arzneimittel |
WO1994020085A1 (fr) * | 1993-03-01 | 1994-09-15 | The Children's Medical Center Corporation | Procedes et compositions pour inhiber l'angiogenese |
US5789434A (en) * | 1994-11-15 | 1998-08-04 | Bayer Corporation | Derivatives of substituted 4-biarylbutyric acid as matrix metalloprotease inhibitors |
US5783605A (en) * | 1995-02-27 | 1998-07-21 | Kuo; Sheng-Chu | Helper inducers for differentiation therapy and chemoprevention of cancer |
WO1997012625A1 (fr) * | 1995-10-03 | 1997-04-10 | Cytran, Ltd. | Compositions pharmaceutiques a base de dipeptide angiostatique et leur procede d'utilisation |
WO1997037988A1 (fr) * | 1996-04-09 | 1997-10-16 | Grünenthal GmbH | Promedicaments acyles de la n-hydroxymethylthalidomide a effet immunomodulateur |
WO1998025895A1 (fr) * | 1996-12-13 | 1998-06-18 | Eli Lilly And Company | Inhibiteurs de l'activite enzymatique de l'antigene psa |
WO1999013873A1 (fr) * | 1997-09-15 | 1999-03-25 | Klavdia Stepanovna Evlanenkova | Agent permettant de traiter des malades souffrant de tumeurs |
WO2002064083A2 (fr) * | 2000-11-30 | 2002-08-22 | The Children's Medical Center Corporation | Synthese de 3-amino-thalidomide et de ses enantiomeres |
WO2003014315A2 (fr) * | 2001-08-06 | 2003-02-20 | The Children's Medical Center Corporation | Synthese et activite antitumorale d'analogues de thalidomide substitues par azote |
WO2003097052A2 (fr) * | 2002-05-17 | 2003-11-27 | Celgene Corporation | Methodes et compositions faisant appel a des composes immunomodulateurs pour le traitement et la prise en charge des cancers et d'autres maladies |
WO2004085422A1 (fr) * | 2003-03-27 | 2004-10-07 | Tian Jin Hemay Bio-Tech Co., Ltd. | Derives de thalidomide hydrosoluble |
Non-Patent Citations (14)
Title |
---|
"THE MERCK INDEX", 2001, MERCK & CO., XP002322662 * |
DATABASE CA [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; 7 October 2004 (2004-10-07), ZHANG, HESHENG: "Preparation of water-soluble thalidomide derivatives", XP002308491, retrieved from STN Database accession no. 2004:817880 * |
DATABASE WPI Section Ch Week 199919, Derwent World Patents Index; Class B02, AN 1998-592576 * |
DATABASE WPI Section Ch Week 200470, Derwent World Patents Index; Class B02, AN 2004-719020 * |
DE A U ET AL: "POSSIBLE ANTINEOPLASTIC AGENTS: III SYNTHESIS OF 6-ALKYL-2- U4'METHOXYPHTHALIMIDO AND 6-ALKYL-3-U3'-4'-DIMETHOXYPHENYL GLUTARIMIDES", JOURNAL OF THE INDIAN CHEMICAL SOCIETY, THE INDIAN CHEMICAL SOCIETY, CALCUTTA, IN, vol. 53, no. 11, 1 November 1976 (1976-11-01), pages 1122 - 1125, XP000675187, ISSN: 0019-4522 * |
DE A U ET AL: "POSSIBLE ANTINEOPLASTIC AGENTS: PART IV - SYNTHESIS & ANTINEOPLASTIC POTENCY OF N-SUBSTITUTED ALPHA-(4,5-DIMETHOXYPHTHALIMIDO)GLUTARIMIDES & N-SUBSTITUTED BETA-(4-BROMOPHENYL)GLUTARIMIDES", INDIAN JOURNAL OF CHEMISTRY, SECTION B: ORGANIC, INCL. MEDICINAL, PUBLICATIONS & INFORMATIONS DIRECTORATE, NEW DELHI, IN, vol. 16B, no. 6, 1 June 1978 (1978-06-01), pages 510 - 512, XP000675183, ISSN: 0019-5103 * |
FOLKES L K ET AL: "Oxidative activation of indole-3-acetic acids to cytotoxic species- a potential new role for plant auxins in cancer therapy.", BIOCHEMICAL PHARMACOLOGY. 15 JAN 2001, vol. 61, no. 2, 15 January 2001 (2001-01-15), pages 129 - 136, XP008044869, ISSN: 0006-2952 * |
HESS, S. ET AL: "Synthesis and immunological activity of water-soluble thalidomide prodrugs", BIOORGANIC & MEDICINAL CHEMISTRY , 9(5), 1279-1291 CODEN: BMECEP; ISSN: 0968-0896, 2001, XP001202654 * |
KARBOWNIK M ET AL: "Indole-3-propionic acid, a melatonin-related molecule, protects hepatic microsomal membranes from iron-induced oxidative damage: relevance to cancer reduction.", JOURNAL OF CELLULAR BIOCHEMISTRY. 2001, vol. 81, no. 3, 2001, pages 507 - 513, XP008044870, ISSN: 0730-2312 * |
LENTZSCH S ET AL: "S-3-amino-phthalimido-glutarimide inhibits angiogenesis and growth of B-cell neoplasias in mice", CANCER RESEARCH, AMERICAN ASSOCIATION FOR CANCER RESEARCH, BALTIMORE, MD, US, vol. 62, 15 April 2002 (2002-04-15), pages 2300 - 2305, XP002959459, ISSN: 0008-5472 * |
LEPPER, ERIN R. ET AL: "Comparative Molecular Field Analysis and Comparative Molecular Similarity Indices Analysis of Thalidomide Analogues as Angiogenesis Inhibitors", JOURNAL OF MEDICINAL CHEMISTRY , 47(9), 2219-2227 CODEN: JMCMAR; ISSN: 0022-2623, 2004, XP001202667 * |
NG, SYLVIA S. W. ET AL: "Antiangiogenic Activity of N-substituted and Tetrafluorinated Thalidomide Analogues", CANCER RESEARCH , 63(12), 3189-3194 CODEN: CNREA8; ISSN: 0008-5472, 15 June 2003 (2003-06-15), XP001202664 * |
SEDLAK M ET AL: "Preparation, 1H and 13C NMR spectra of substituted 2-benzoylaminocarboxamides", COLLECTION OF CZECHOSLOVAK CHEMICAL COMMUNICATIONS, ACADEMIC PRESS, LONDON, GB, vol. 60, 1995, pages 150 - 160, XP002136842, ISSN: 0010-0765 * |
SUZUKI, MAMORU ET AL: "Use of a new protecting group in an attempted synthesis of cyclopropyldihydroxyphenylalanine", JOURNAL OF ORGANIC CHEMISTRY , 48(24), 4769-71 CODEN: JOCEAH; ISSN: 0022-3263, 1983, XP008044808 * |
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