ES2190221T3 - Derivados de indol y su uso para el tratamiento de enfermedades malignas y otras, que se basan en proliferaciones celulares patologicas. - Google Patents
Derivados de indol y su uso para el tratamiento de enfermedades malignas y otras, que se basan en proliferaciones celulares patologicas.Info
- Publication number
- ES2190221T3 ES2190221T3 ES99927711T ES99927711T ES2190221T3 ES 2190221 T3 ES2190221 T3 ES 2190221T3 ES 99927711 T ES99927711 T ES 99927711T ES 99927711 T ES99927711 T ES 99927711T ES 2190221 T3 ES2190221 T3 ES 2190221T3
- Authority
- ES
- Spain
- Prior art keywords
- alkyl
- formula
- atom
- substituted
- general formula
- 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
- 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
- C07D401/14—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 three or more hetero rings
-
- 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
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/02—Drugs for disorders of the endocrine system of the hypothalamic hormones, e.g. TRH, GnRH, CRH, GRH, somatostatin
- A61P5/04—Drugs for disorders of the endocrine system of the hypothalamic hormones, e.g. TRH, GnRH, CRH, GRH, somatostatin for decreasing, blocking or antagonising the activity of the hypothalamic hormones
-
- 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
- C07D209/14—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D333/52—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes
- C07D333/54—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
- C07D333/56—Radicals substituted by oxygen atoms
-
- 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
- C07D403/14—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 three or more hetero rings
-
- 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
- C07D405/06—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 linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
- C07D487/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/12—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
- C07D491/14—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Endocrinology (AREA)
- Engineering & Computer Science (AREA)
- Diabetes (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Indole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Saccharide Compounds (AREA)
Abstract
Compuestos de fórmula general I: **(Fórmula)** en la que Z es un grupo de fórmula general (II) **(Fórmula)** en la que B, B¿ pueden ser un átomo de carbono, nitrógeno, oxígeno o azufre y los sistemas de anillo F y G pueden ser, independientemente entre sí, anillos penta y hexagonales tanto saturados como insaturados, X representa un grupo de fórmula general III o IV, **(Fórmula)** en la que A puede ser un átomo de N, O, S, l y n pueden tomar los números de 0 a 6, m los números 1 y 2, así como R14 y R15 conjuntamente forman un átomo de oxígeno o R14 significa un grupo hidroxilo y R15 un átomo de hidrógeno, o R14 y R15 significan átomos de hidrógeno, y en la que R16 significa un átomo de hidrógeno, un resto alquilo o arilo, un resto alquilo o arilo sustituido con halógeno, amino o azido, un resto alquiloximetilo o alquiloximetilo sustituido, R2 y R13 forman conjuntamente una unión de fórmula general V o VI **(Fórmula)** en las que el enlace de trazos discontínuos significa un enlace doble o sencillo, A y R16 poseen los mismos significados que anteriormente y o puede adoptar los números 1 y 2, R2 y R13 significan restos iguales o distintos de fórmula general VII o átomos de hidrógeno, **(Fórmula)** en la que el enlace de trazos discontínuos significa un enlace doble o sencillo, A y R16 poseen los mismos significados que anteriormente y R17 significa un átomo de halógeno o un resto de fórmula general VIII **(Fórmula)** de modo que puede ser igual a 0, 1 ó 2 (cuando p=0, se trata entonces de una amina acíclica primaria e Y porta un átomo de hidrógeno adicional), Y puede ser un átomo de carbono, oxígeno o nitrógeno y cuando Y es un átomo de carbono o nitrógeno, R18 significa un átomo de hidrógeno o un resto alquilo o **(Fórmula)** arilo, un resto alquilo o arilo sustituido, heterociclo, un resto alcoxicarbonilo, un resto aminocarbonilmetilo saturado o insaturado, o un resto aminocarbonilmetilo sustituido, R2 y R13 forman conjuntamente una unión de fórmula general IX o X **(Fórmula)** en las que W representa un átomo de carbono o nitrógeno, q puede adoptar un número entre 0 y 6 y R10 y R20 pueden significar átomos de hidrógeno, restos alquilo o alquilo sustituido, en las que R1, R7 y R12 son iguales o distintos y significan átomos de hidrógeno, restos alquilo y aminoalquilo, restos fenilsulfonilo, restos alquilsililmetoximetilo, un azúcar o un azúcar sustituido, en las que R3, R4, R5, R6, R8, R9, R10 y R11 son iguales o distintos y representan respectivamente un átomo de hidrógeno, un grupo alquilo, alcoxi, alcoximetilo sustituido con alcoxi, amino, halógeno, cicloalquilo, cicloheteroalquilo, arilo o heteroarilo, un grupo nitro, un átomo de halógeno o un grupo O-alcoxi de fórmula general -O-(C=O)-R21, en la que R21 significa un grupo alquilo, alcoxi o alcoximetilo sustituido con alcoxi, amino, halógeno, cicloalquilo, cicloheteroalquilo, arilo o heteroarilo.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19819835 | 1998-05-04 | ||
| DE19838506A DE19838506C2 (de) | 1998-05-04 | 1998-08-25 | Indolderivate und deren Verwendung zur Behandlung von malignen und anderen, auf pathologischen Zellproliferationen beruhenden Erkrankungen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2190221T3 true ES2190221T3 (es) | 2003-07-16 |
Family
ID=26045937
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES99927711T Expired - Lifetime ES2190221T3 (es) | 1998-05-04 | 1999-04-22 | Derivados de indol y su uso para el tratamiento de enfermedades malignas y otras, que se basan en proliferaciones celulares patologicas. |
Country Status (21)
| Country | Link |
|---|---|
| US (2) | US6407102B1 (es) |
| EP (1) | EP1109785B1 (es) |
| JP (1) | JP2002514572A (es) |
| CN (1) | CN1151127C (es) |
| AT (1) | ATE230394T1 (es) |
| AU (1) | AU752464B2 (es) |
| BG (1) | BG104996A (es) |
| BR (1) | BR9911017A (es) |
| CA (1) | CA2330756C (es) |
| CZ (1) | CZ20003960A3 (es) |
| DE (1) | DE59903921D1 (es) |
| DK (1) | DK1109785T3 (es) |
| ES (1) | ES2190221T3 (es) |
| HU (1) | HUP0102563A3 (es) |
| IL (1) | IL139056A0 (es) |
| NO (1) | NO317261B1 (es) |
| NZ (1) | NZ507735A (es) |
| PL (1) | PL346840A1 (es) |
| SK (1) | SK16352000A3 (es) |
| TR (1) | TR200003206T2 (es) |
| WO (1) | WO1999057117A2 (es) |
Families Citing this family (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HUP0102563A3 (en) | 1998-05-04 | 2003-04-28 | Zentaris Gmbh | Indole derivatives and their use in the treatment of malignant and other diseases caused by pathological cell proliferation |
| AU6111699A (en) * | 1998-10-08 | 2000-05-01 | Smithkline Beecham Plc | Novel method and compounds |
| US6719520B2 (en) | 1998-10-08 | 2004-04-13 | Smithkline Beecham Corporation | Method and compounds |
| EP1299377A2 (en) * | 2000-06-28 | 2003-04-09 | Eli Lilly And Company | Spla2 inhibitors |
| CA2416946A1 (en) | 2000-07-28 | 2003-01-22 | Sumitomo Pharmaceuticals Co., Ltd. | Pyrrole derivatives |
| TW557298B (en) * | 2000-08-14 | 2003-10-11 | Ciba Sc Holding Ag | A compound, a photopolymerizible composition, a process for producing coatings and a method for causing a photoinitiator to accumulate at the surface of coatings |
| US20030032625A1 (en) * | 2001-03-29 | 2003-02-13 | Topo Target Aps | Succinimide and maleimide derivatives and their use as topoisomerase II catalytic inhibitors |
| DE10143079A1 (de) * | 2001-09-03 | 2003-05-15 | Zentaris Ag | Cyclische Indol- und Heteroindolderivate, deren Herstellung und Verwendung als Arzneimittel |
| US20050267303A1 (en) * | 2001-09-04 | 2005-12-01 | Zentaris Ag | Cyclic indole and heteroindole derivatives and methods for making and using as pharmaceuticals |
| WO2003063861A1 (en) * | 2002-01-30 | 2003-08-07 | Sumitomo Pharmaceuticals Co., Ltd. | Fibrosis inhibitor |
| US6800655B2 (en) * | 2002-08-20 | 2004-10-05 | Sri International | Analogs of indole-3-carbinol metabolites as chemotherapeutic and chemopreventive agents |
| US7098231B2 (en) | 2003-01-22 | 2006-08-29 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
| US7223785B2 (en) | 2003-01-22 | 2007-05-29 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
| EP1747014A4 (en) * | 2004-05-03 | 2007-09-12 | Ilypsa Inc | MODULATION OF LYSOPHOSPHATIDYLCHOLINE AND TREATMENT OF CONDITIONS INDUCED BY A DIET |
| AU2006311766A1 (en) * | 2005-11-03 | 2007-05-18 | Ilypsa, Inc. | Indole compounds having C4-acidic substituents and use thereof as phospholipase-A2 inhibitors |
| WO2007056184A2 (en) * | 2005-11-03 | 2007-05-18 | Ilypsa, Inc. | Azaindole compounds and use thereof as phospholipase-a2 inhibitors |
| EP1960356A2 (en) * | 2005-11-03 | 2008-08-27 | Ilypsa, Inc. | Multivalent indole compounds and use thereof as phospholipase-a2 inhibitors |
| JP2009517341A (ja) * | 2005-11-03 | 2009-04-30 | イリプサ, インコーポレイテッド | C4−アミド置換基を有するインドール化合物およびホスホリパーゼa2インヒビターとしてのその使用 |
| CA2626961A1 (en) * | 2005-11-03 | 2007-05-18 | Ilypsa, Inc. | Phospholipase inhibitors, including multi-valent phospholipase inhibitors, and use thereof, including as lumen-localized phospholipase inhibitors |
| US20090142832A1 (en) * | 2007-11-29 | 2009-06-04 | James Dalton | Indoles, Derivatives, and Analogs Thereof and Uses Therefor |
| KR101763656B1 (ko) | 2009-06-29 | 2017-08-01 | 인사이트 홀딩스 코포레이션 | Pi3k 저해물질로서의 피리미디논 |
| CN101704828A (zh) * | 2009-11-04 | 2010-05-12 | 中国科学院昆明植物研究所 | 山橙素类双吲哚化合物,其药物组合物及其制备方法和用途 |
| TW201130842A (en) * | 2009-12-18 | 2011-09-16 | Incyte Corp | Substituted fused aryl and heteroaryl derivatives as PI3K inhibitors |
| US8759359B2 (en) * | 2009-12-18 | 2014-06-24 | Incyte Corporation | Substituted heteroaryl fused derivatives as PI3K inhibitors |
| EP2558463A1 (en) | 2010-04-14 | 2013-02-20 | Incyte Corporation | Fused derivatives as i3 inhibitors |
| WO2011163195A1 (en) | 2010-06-21 | 2011-12-29 | Incyte Corporation | Fused pyrrole derivatives as pi3k inhibitors |
| EP3660016A1 (en) | 2010-12-20 | 2020-06-03 | Incyte Holdings Corporation | N-(1-(substituted-phenyl)ethyl)-9h-purin-6-amines as pi3k inhibitors |
| US9108984B2 (en) | 2011-03-14 | 2015-08-18 | Incyte Corporation | Substituted diamino-pyrimidine and diamino-pyridine derivatives as PI3K inhibitors |
| WO2012135009A1 (en) | 2011-03-25 | 2012-10-04 | Incyte Corporation | Pyrimidine-4,6-diamine derivatives as pi3k inhibitors |
| PT3513793T (pt) | 2011-09-02 | 2021-05-10 | Incyte Holdings Corp | Heterociclilaminas como inibidores de pi3k |
| AR090548A1 (es) | 2012-04-02 | 2014-11-19 | Incyte Corp | Azaheterociclobencilaminas biciclicas como inhibidores de pi3k |
| WO2015191677A1 (en) | 2014-06-11 | 2015-12-17 | Incyte Corporation | Bicyclic heteroarylaminoalkyl phenyl derivatives as pi3k inhibitors |
| SG10201907576SA (en) | 2015-02-27 | 2019-09-27 | Incyte Corp | Salts of pi3k inhibitor and processes for their preparation |
| US9732097B2 (en) | 2015-05-11 | 2017-08-15 | Incyte Corporation | Process for the synthesis of a phosphoinositide 3-kinase inhibitor |
| US9988401B2 (en) | 2015-05-11 | 2018-06-05 | Incyte Corporation | Crystalline forms of a PI3K inhibitor |
| CN106317169B (zh) * | 2015-06-23 | 2019-07-02 | 首都医科大学 | 双吲哚-二肽衍生物,其合成,抗血栓活性和制备抗血栓剂的应用 |
| CN109790191B (zh) * | 2016-08-05 | 2022-04-08 | 香港大学 | 铂配合物及其使用方法 |
| SG11202011680YA (en) | 2018-06-01 | 2020-12-30 | Incyte Corp | Dosing regimen for the treatment of pi3k related disorders |
| EA202192575A1 (ru) | 2019-03-21 | 2022-01-14 | Онксео | Соединения dbait в сочетании с ингибиторами киназ для лечения рака |
| WO2020245208A1 (en) | 2019-06-04 | 2020-12-10 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Use of cd9 as a biomarker and as a biotarget in glomerulonephritis or glomerulosclerosis |
| CN114761006A (zh) | 2019-11-08 | 2022-07-15 | Inserm(法国国家健康医学研究院) | 对激酶抑制剂产生耐药性的癌症的治疗方法 |
| WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
| WO2026006328A1 (en) * | 2024-06-26 | 2026-01-02 | Arizona Board Of Regents On Behalf Of Arizona State University | Compositions and methods for mode-selective modulation of transient receptor potential vanilloid-1 (trpv1) |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3598583A (en) * | 1968-08-09 | 1971-08-10 | Itek Corp | Indomethylene dye bases and their utilization in photographic processes and compositions |
| FR2688220A1 (fr) * | 1992-03-06 | 1993-09-10 | Adir | Nouveaux derives de thiazolidine-2,4-dione, leur procede de preparation et les compositions pharmaceutiques qui les contiennent. |
| WO1994024117A1 (fr) * | 1993-04-22 | 1994-10-27 | Nippon Shinyaku Co., Ltd. | Derive de l'acide benzofurancarboxylique et composition pharmaceutique |
| US5656643A (en) | 1993-11-08 | 1997-08-12 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Bis mono-and bicyclic aryl and heteroaryl compounds which inhibit EGF and/or PDGF receptor tyrosine kinase |
| CA2179650C (en) * | 1993-12-23 | 2007-10-30 | William Francis Heath, Jr. | Bisindolemaleimides and their use as protein kinase c inhibitors |
| JPH08295688A (ja) * | 1995-04-28 | 1996-11-12 | Sharp Corp | ビスアゾ化合物、その中間体及びそれらの製造方法、並びにビスアゾ化合物を含有する電子写真感光体 |
| DE19547263C2 (de) * | 1995-12-07 | 1999-04-29 | Cardiotec Inc | Amidinohydrazone vom Benzo[b]furan abgeleiteter Ketone, Verfahren zu deren Herstellung und diese Verbindungen enthaltende Arzneimittel |
| HUP0102563A3 (en) | 1998-05-04 | 2003-04-28 | Zentaris Gmbh | Indole derivatives and their use in the treatment of malignant and other diseases caused by pathological cell proliferation |
-
1999
- 1999-04-22 HU HU0102563A patent/HUP0102563A3/hu unknown
- 1999-04-22 ES ES99927711T patent/ES2190221T3/es not_active Expired - Lifetime
- 1999-04-22 EP EP99927711A patent/EP1109785B1/de not_active Expired - Lifetime
- 1999-04-22 CA CA002330756A patent/CA2330756C/en not_active Expired - Fee Related
- 1999-04-22 AU AU44975/99A patent/AU752464B2/en not_active Ceased
- 1999-04-22 TR TR2000/03206T patent/TR200003206T2/xx unknown
- 1999-04-22 BR BR9911017-2A patent/BR9911017A/pt not_active IP Right Cessation
- 1999-04-22 SK SK1635-2000A patent/SK16352000A3/sk unknown
- 1999-04-22 JP JP2000547087A patent/JP2002514572A/ja not_active Withdrawn
- 1999-04-22 IL IL13905699A patent/IL139056A0/xx not_active IP Right Cessation
- 1999-04-22 PL PL99346840A patent/PL346840A1/xx not_active Application Discontinuation
- 1999-04-22 CZ CZ20003960A patent/CZ20003960A3/cs unknown
- 1999-04-22 AT AT99927711T patent/ATE230394T1/de not_active IP Right Cessation
- 1999-04-22 WO PCT/DE1999/001214 patent/WO1999057117A2/de not_active Ceased
- 1999-04-22 DK DK99927711T patent/DK1109785T3/da active
- 1999-04-22 DE DE59903921T patent/DE59903921D1/de not_active Expired - Fee Related
- 1999-04-22 CN CNB998058033A patent/CN1151127C/zh not_active Expired - Fee Related
- 1999-05-04 US US09/305,115 patent/US6407102B1/en not_active Expired - Fee Related
-
2000
- 2000-10-24 NZ NZ507735A patent/NZ507735A/xx unknown
- 2000-10-27 NO NO20005448A patent/NO317261B1/no unknown
- 2000-11-28 BG BG104996A patent/BG104996A/xx unknown
-
2002
- 2002-05-03 US US10/137,653 patent/US6812243B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| DE59903921D1 (de) | 2003-02-06 |
| CZ20003960A3 (cs) | 2002-04-17 |
| EP1109785B1 (de) | 2003-01-02 |
| JP2002514572A (ja) | 2002-05-21 |
| TR200003206T2 (tr) | 2001-07-23 |
| ATE230394T1 (de) | 2003-01-15 |
| WO1999057117A2 (de) | 1999-11-11 |
| AU4497599A (en) | 1999-11-23 |
| HK1038354A1 (en) | 2002-03-15 |
| CN1151127C (zh) | 2004-05-26 |
| CN1310705A (zh) | 2001-08-29 |
| SK16352000A3 (sk) | 2002-07-02 |
| IL139056A0 (en) | 2001-11-25 |
| DK1109785T3 (da) | 2003-04-22 |
| BR9911017A (pt) | 2001-02-06 |
| NZ507735A (en) | 2003-04-29 |
| EP1109785A2 (de) | 2001-06-27 |
| AU752464B2 (en) | 2002-09-19 |
| HUP0102563A3 (en) | 2003-04-28 |
| PL346840A1 (en) | 2002-02-25 |
| NO20005448D0 (no) | 2000-10-27 |
| US20030008898A1 (en) | 2003-01-09 |
| NO20005448L (no) | 2000-10-27 |
| HUP0102563A2 (hu) | 2001-11-28 |
| NO317261B1 (no) | 2004-09-27 |
| US6812243B2 (en) | 2004-11-02 |
| CA2330756A1 (en) | 1999-11-11 |
| US6407102B1 (en) | 2002-06-18 |
| CA2330756C (en) | 2007-10-02 |
| BG104996A (en) | 2001-07-31 |
| WO1999057117A3 (de) | 2001-04-12 |
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