NO963506L - 4-Heterocyklyl-substituerte kinazolin-derivater, fremgangsmåte for fremstilling derav og deres anvendelse som anti-kreftmidler - Google Patents
4-Heterocyklyl-substituerte kinazolin-derivater, fremgangsmåte for fremstilling derav og deres anvendelse som anti-kreftmidlerInfo
- Publication number
- NO963506L NO963506L NO963506A NO963506A NO963506L NO 963506 L NO963506 L NO 963506L NO 963506 A NO963506 A NO 963506A NO 963506 A NO963506 A NO 963506A NO 963506 L NO963506 L NO 963506L
- Authority
- NO
- Norway
- Prior art keywords
- formula
- cancer agents
- oxy
- heterocyclyl
- preparation
- Prior art date
Links
- 239000002246 antineoplastic agent Substances 0.000 title abstract 2
- 125000002294 quinazolinyl group Chemical class N1=C(N=CC2=CC=CC=C12)* 0.000 title 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 abstract 3
- -1 methylene, thio Chemical group 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- 125000004149 thio group Chemical group *S* 0.000 abstract 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000003463 hyperproliferative effect Effects 0.000 abstract 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- DRYRBWIFRVMRPV-UHFFFAOYSA-N quinazolin-4-amine Chemical class C1=CC=C2C(N)=NC=NC2=C1 DRYRBWIFRVMRPV-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- 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
- 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
- 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
- C07D487/02—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 two hetero rings
- C07D487/04—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
- C07D491/02—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 two hetero rings
- C07D491/04—Ortho-condensed systems
-
- 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
- C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US20025994A | 1994-02-23 | 1994-02-23 | |
| PCT/IB1995/000061 WO1995023141A1 (fr) | 1994-02-23 | 1995-01-27 | Derives de la quinazoline a substitution 4-heterocyclyle, procedes d'elaboration et utilisations correspondantes comme agents anticancereux |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO963506D0 NO963506D0 (no) | 1996-08-22 |
| NO963506L true NO963506L (no) | 1996-10-22 |
Family
ID=22740969
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO963506A NO963506L (no) | 1994-02-23 | 1996-08-22 | 4-Heterocyklyl-substituerte kinazolin-derivater, fremgangsmåte for fremstilling derav og deres anvendelse som anti-kreftmidler |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US5736534A (fr) |
| EP (1) | EP0746554A1 (fr) |
| JP (1) | JP2890267B2 (fr) |
| KR (1) | KR100225721B1 (fr) |
| CN (1) | CN1141633A (fr) |
| AU (1) | AU686843B2 (fr) |
| BR (1) | BR9506936A (fr) |
| CA (1) | CA2183655C (fr) |
| CO (1) | CO4340688A1 (fr) |
| CZ (1) | CZ288955B6 (fr) |
| FI (1) | FI963283A0 (fr) |
| HU (1) | HUT76291A (fr) |
| IL (1) | IL112673A0 (fr) |
| MX (1) | MX9603593A (fr) |
| NO (1) | NO963506L (fr) |
| NZ (1) | NZ278135A (fr) |
| PE (1) | PE4896A1 (fr) |
| PL (1) | PL315941A1 (fr) |
| RU (1) | RU2137762C1 (fr) |
| TW (1) | TW404946B (fr) |
| WO (1) | WO1995023141A1 (fr) |
| ZA (1) | ZA951458B (fr) |
Families Citing this family (132)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6645969B1 (en) | 1991-05-10 | 2003-11-11 | Aventis Pharmaceuticals Inc. | Aryl and heteroaryl quinazoline compounds which inhibit CSF-1R receptor tyrosine kinase |
| US5714493A (en) * | 1991-05-10 | 1998-02-03 | Rhone-Poulenc Rorer Pharmaceuticals, Inc. | Aryl and heteroaryl quinazoline compounds which inhibit CSF-1R receptor tyrosine kinase |
| USRE37650E1 (en) | 1991-05-10 | 2002-04-09 | Aventis Pharmacetical Products, Inc. | Aryl and heteroaryl quinazoline compounds which inhibit CSF-1R receptor tyrosine kinase |
| US5710158A (en) * | 1991-05-10 | 1998-01-20 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Aryl and heteroaryl quinazoline compounds which inhibit EGF and/or PDGF receptor tyrosine kinase |
| TW321649B (fr) * | 1994-11-12 | 1997-12-01 | Zeneca Ltd | |
| GB9424233D0 (en) * | 1994-11-30 | 1995-01-18 | Zeneca Ltd | Quinazoline derivatives |
| GB9508565D0 (en) * | 1995-04-27 | 1995-06-14 | Zeneca Ltd | Quiazoline derivative |
| GB9508538D0 (en) * | 1995-04-27 | 1995-06-14 | Zeneca Ltd | Quinazoline derivatives |
| EP0824525B1 (fr) * | 1995-04-27 | 2001-06-13 | AstraZeneca AB | Derives de quinazoline |
| GB9508537D0 (en) * | 1995-04-27 | 1995-06-14 | Zeneca Ltd | Quinazoline derivatives |
| GB9508535D0 (en) * | 1995-04-27 | 1995-06-14 | Zeneca Ltd | Quinazoline derivative |
| US5747498A (en) | 1996-05-28 | 1998-05-05 | Pfizer Inc. | Alkynyl and azido-substituted 4-anilinoquinazolines |
| US7060808B1 (en) * | 1995-06-07 | 2006-06-13 | Imclone Systems Incorporated | Humanized anti-EGF receptor monoclonal antibody |
| GB9624482D0 (en) | 1995-12-18 | 1997-01-15 | Zeneca Phaema S A | Chemical compounds |
| AU1441497A (en) * | 1996-01-23 | 1997-08-20 | Novartis Ag | Pyrrolopyrimidines and processes for their preparation |
| US5760041A (en) * | 1996-02-05 | 1998-06-02 | American Cyanamid Company | 4-aminoquinazoline EGFR Inhibitors |
| WO1997030035A1 (fr) | 1996-02-13 | 1997-08-21 | Zeneca Limited | Derives de la quinazoline utilises comme inhibiteurs du vegf |
| GB9603095D0 (en) * | 1996-02-14 | 1996-04-10 | Zeneca Ltd | Quinazoline derivatives |
| GB9603097D0 (en) * | 1996-02-14 | 1996-04-10 | Zeneca Ltd | Quinazoline compounds |
| EP0886524A2 (fr) * | 1996-03-01 | 1998-12-30 | Chiron Corporation | Apport d'agents therapeutiques a la prostate |
| ES2169355T3 (es) | 1996-03-05 | 2002-07-01 | Astrazeneca Ab | Derivados de 4-anilinoquinazolina. |
| JP3370340B2 (ja) | 1996-04-12 | 2003-01-27 | ワーナー―ランバート・コンパニー | チロシンキナーゼの不可逆的阻害剤 |
| GB9607729D0 (en) * | 1996-04-13 | 1996-06-19 | Zeneca Ltd | Quinazoline derivatives |
| GB9707800D0 (en) * | 1996-05-06 | 1997-06-04 | Zeneca Ltd | Chemical compounds |
| GB9718972D0 (en) | 1996-09-25 | 1997-11-12 | Zeneca Ltd | Chemical compounds |
| US6225318B1 (en) | 1996-10-17 | 2001-05-01 | Pfizer Inc | 4-aminoquinazolone derivatives |
| EP0837063A1 (fr) * | 1996-10-17 | 1998-04-22 | Pfizer Inc. | Dérivés de 4-aminoquinazoline |
| CA2272705C (fr) * | 1996-11-27 | 2003-03-18 | Pfizer Inc. | Derives de pyrimidines bicycliques fusionnes |
| US6002008A (en) * | 1997-04-03 | 1999-12-14 | American Cyanamid Company | Substituted 3-cyano quinolines |
| US5929080A (en) * | 1997-05-06 | 1999-07-27 | American Cyanamid Company | Method of treating polycystic kidney disease |
| ZA986729B (en) * | 1997-07-29 | 1999-02-02 | Warner Lambert Co | Irreversible inhibitors of tyrosine kinases |
| ZA986732B (en) | 1997-07-29 | 1999-02-02 | Warner Lambert Co | Irreversible inhibitiors of tyrosine kinases |
| US6251912B1 (en) | 1997-08-01 | 2001-06-26 | American Cyanamid Company | Substituted quinazoline derivatives |
| ATE368665T1 (de) | 1997-08-22 | 2007-08-15 | Astrazeneca Ab | Oxindolylchinazolinderivate als angiogenesehemmer |
| US6323209B1 (en) | 1997-11-06 | 2001-11-27 | American Cyanamid Company | Method of treating or inhibiting colonic polyps |
| JPH11236333A (ja) * | 1997-12-30 | 1999-08-31 | Pfizer Prod Inc | 抗ガン剤として有用なイミダゾリン−４−オン誘導体 |
| US20030224001A1 (en) * | 1998-03-19 | 2003-12-04 | Goldstein Neil I. | Antibody and antibody fragments for inhibiting the growth of tumors |
| ZA200007412B (en) * | 1998-05-15 | 2002-03-12 | Imclone Systems Inc | Treatment of human tumors with radiation and inhibitors of growth factor receptor tyrosine kinases. |
| US6288082B1 (en) | 1998-09-29 | 2001-09-11 | American Cyanamid Company | Substituted 3-cyanoquinolines |
| US6297258B1 (en) | 1998-09-29 | 2001-10-02 | American Cyanamid Company | Substituted 3-cyanoquinolines |
| AU6159499A (en) | 1998-09-29 | 2000-04-17 | Wyeth Holdings Corporation | Substituted 3-cyanoquinolines as protein tyrosine kinases inhibitors |
| US6174903B1 (en) | 1998-12-28 | 2001-01-16 | Pfizer Inc. | Imidazolidin-4-one derivatives useful as anticancer agents |
| JP3270834B2 (ja) | 1999-01-27 | 2002-04-02 | ファイザー・プロダクツ・インク | 抗がん剤として有用なヘテロ芳香族二環式誘導体 |
| UA71945C2 (en) | 1999-01-27 | 2005-01-17 | Pfizer Prod Inc | Substituted bicyclic derivatives being used as anticancer agents |
| BRPI0017548B8 (pt) | 1999-02-10 | 2023-05-02 | Astrazeneca Ab | Composto |
| EP2042194A3 (fr) * | 1999-05-14 | 2009-04-22 | Imclone Systems, Inc. | Traitement des tumeurs humaines réfractaires avec des antagonistes de récepteur de facteur de croissance épidermique |
| US6432979B1 (en) | 1999-08-12 | 2002-08-13 | American Cyanamid Company | Method of treating or inhibiting colonic polyps and colorectal cancer |
| CN100376567C (zh) | 1999-11-05 | 2008-03-26 | 阿斯特拉曾尼卡有限公司 | 作为vegf抑制剂的喹唑啉衍生物 |
| US7160889B2 (en) | 2000-04-07 | 2007-01-09 | Astrazeneca Ab | Quinazoline compounds |
| UA73993C2 (uk) | 2000-06-06 | 2005-10-17 | Астразенека Аб | Хіназолінові похідні для лікування пухлин та фармацевтична композиція |
| AU9500201A (en) * | 2000-08-09 | 2002-02-18 | Imclone Systems Inc | Treatment of hyperproliferative diseases with epidermal growth factor receptor antagonists |
| US7115615B2 (en) | 2000-08-21 | 2006-10-03 | Astrazeneca | Quinazoline derivatives |
| AU2001292137A1 (en) | 2000-10-13 | 2002-04-22 | Astrazeneca Ab | Quinazoline derivatives |
| AU2001292138A1 (en) | 2000-10-13 | 2002-04-22 | Astrazeneca Ab | Quinazoline derivatives with anti-tumour activity |
| US20080008704A1 (en) * | 2001-03-16 | 2008-01-10 | Mark Rubin | Methods of treating colorectal cancer with anti-epidermal growth factor antibodies |
| WO2002085895A1 (fr) | 2001-04-19 | 2002-10-31 | Astrazeneca Ab | Derives quinazoline |
| RU2332415C2 (ru) * | 2001-04-27 | 2008-08-27 | Вертекс Фармасьютикалз Инкорпорейтед | Производные пиразола, полезные в качестве ингибиторов протеинкиназы |
| WO2003000194A2 (fr) | 2001-06-21 | 2003-01-03 | Pfizer Inc. | Derives bicycliques de pyridine et de pyrimidine utiles en tant qu'agents anticancereux |
| US20030144308A1 (en) * | 2001-09-24 | 2003-07-31 | Bauer Paul H. | Fructose 1,6-bisphosphatase inhibitors |
| CN1625555A (zh) | 2002-02-01 | 2005-06-08 | 阿斯特拉曾尼卡有限公司 | 喹唑啉化合物 |
| JP2005527511A (ja) | 2002-03-01 | 2005-09-15 | ファイザー インコーポレイテッド | 抗血管形成剤として有用なチエノピリジンのインドリル−尿素誘導体およびその使用法 |
| SE0200979D0 (sv) | 2002-03-28 | 2002-03-28 | Astrazeneca Ab | New compounds |
| US20030202973A1 (en) * | 2002-04-29 | 2003-10-30 | Dr. George Pieczenik | Treatment of refractory human tumors with epidermal growth factor receptor and HER1 mitogenic ligand (EGFRML) antagonists |
| UA77303C2 (en) | 2002-06-14 | 2006-11-15 | Pfizer | Derivatives of thienopyridines substituted by benzocondensed heteroarylamide useful as therapeutic agents, pharmaceutical compositions and methods for their use |
| ATE360015T1 (de) * | 2002-07-31 | 2007-05-15 | Critical Outcome Technologies | Protein tyrosin kinase inhibitoren |
| ATE380810T1 (de) * | 2002-10-09 | 2007-12-15 | Critical Outcome Technologies | Protein-tyrosine-kinase-inhibitoren |
| EP1622941A2 (fr) * | 2003-03-20 | 2006-02-08 | ImClone Systems Incorporated | Procede de production d'un anticorps contre le recepteur du facteur de croissance epidermique |
| PL1660095T3 (pl) * | 2003-07-25 | 2010-07-30 | Cancer Research Tech Ltd | Tricykliczne inhibitory PARP |
| CA2536321A1 (fr) | 2003-08-29 | 2005-03-10 | Pfizer Inc. | Thienopyridine-phenylacetamides et leurs derives utiles comme nouveaux agents anti-angiogeniques |
| JP4503022B2 (ja) | 2003-12-23 | 2010-07-14 | ファイザー・インク | 新規キノリン誘導体 |
| GB0330002D0 (en) | 2003-12-24 | 2004-01-28 | Astrazeneca Ab | Quinazoline derivatives |
| WO2005090407A1 (fr) * | 2004-03-19 | 2005-09-29 | Imclone Systems Incorporated | Anticorps du recepteur du facteur de croissance anti-epidermique humain |
| AP2204A (en) * | 2004-05-06 | 2011-02-07 | Warner Lambert Co | 4-phenylamino-quinazolin-6-yl-amides. |
| EP1773836B1 (fr) | 2004-05-27 | 2012-09-05 | Pfizer Products Inc. | Derives pyrrolopyrimidiniques convenant au traitement du cancer |
| AR050948A1 (es) | 2004-09-24 | 2006-12-06 | Hoffmann La Roche | Derivados de ftalazinona; su obtencion y su utilizacion en la fabricacion de medicamentos para el tratamiento del cancer. |
| US7285569B2 (en) | 2004-09-24 | 2007-10-23 | Hoff Hoffmann-La Roche Inc. | Tricycles, their manufacture and use as pharmaceutical agents |
| KR20070113286A (ko) | 2005-04-14 | 2007-11-28 | 에프. 호프만-라 로슈 아게 | 아미노피라졸 유도체, 이의 제조 및 약학 제제로서의 용도 |
| JP2009504759A (ja) * | 2005-08-16 | 2009-02-05 | メモリ ファーマセチカル コーポレーション | ホスホジエステラーゼ１０阻害剤 |
| WO2007098169A1 (fr) * | 2006-02-21 | 2007-08-30 | Amgen Inc. | Derives de cinnoline en tant qu'inhibiteurs de phosphodiesterase 10 |
| AU2007221049A1 (en) * | 2006-02-28 | 2007-09-07 | Amgen Inc. | Cinnoline and quinazoline derivates as phosphodiesterase 10 inhibitors |
| US20090099175A1 (en) * | 2006-03-01 | 2009-04-16 | Arrington Mark P | Phosphodiesterase 10 inhibitors |
| EP2017263A4 (fr) | 2006-05-09 | 2011-11-30 | Daiichi Sankyo Co Ltd | Derive acide carboxylique inferieur d'heteroarylamide |
| RU2320649C9 (ru) * | 2006-12-29 | 2008-12-27 | Государственное образовательное учреждение высшего профессионального образования "Российский государственный университет Дружбы народов" (РУДН) | СПОСОБ ПОЛУЧЕНИЯ ПРОИЗВОДНЫХ 4,5,6,9-ТЕТРАГИДРОТИЕНО[3,2-d]АЗОЦИНОВ |
| CA2673683C (fr) | 2007-01-11 | 2014-07-29 | Critical Outcome Technologies, Inc. | Composes et methode de traitement un cancer |
| US20080190689A1 (en) * | 2007-02-12 | 2008-08-14 | Ballard Ebbin C | Inserts for engine exhaust systems |
| CA2710039C (fr) | 2007-12-26 | 2018-07-03 | Critical Outcome Technologies, Inc. | Semicarbazones, thiosemicarnazones et composes associes, et methodes de traitement du cancer |
| DE102008022221A1 (de) | 2008-05-06 | 2009-11-12 | Universität des Saarlandes | Inhibitoren der humanen Aldosteronsynthase CYP11B2 |
| US20110086834A1 (en) * | 2008-06-26 | 2011-04-14 | Amgen Inc. | Alkynyl alcohols as kinase inhibitors |
| CA2730890C (fr) | 2008-07-17 | 2018-05-15 | Critical Outcome Technologies Inc. | Composes inhibiteurs et procedes de traitement du cancer |
| US8541404B2 (en) | 2009-11-09 | 2013-09-24 | Elexopharm Gmbh | Inhibitors of the human aldosterone synthase CYP11B2 |
| CA2794952C (fr) | 2010-04-01 | 2018-05-15 | Critical Outcome Technologies Inc. | Composes et methodes pour le traitement du vih |
| CN102786512A (zh) * | 2012-05-31 | 2012-11-21 | 中国人民解放军军事医学科学院毒物药物研究所 | N-芳基不饱和稠环叔胺类化合物及其制备方法和抗肿瘤应用 |
| CN108245521B (zh) * | 2018-01-24 | 2020-01-03 | 浙江工业大学 | 二丙氨基乙酰氨基苯并氮杂*基喹唑啉类化合物在制备治疗白血病药物中的应用 |
| CN108276385B (zh) * | 2018-01-24 | 2019-12-06 | 浙江工业大学 | 异丁酰氨基喹唑啉类化合物及其制备与应用 |
| CN108125958B (zh) * | 2018-01-24 | 2020-08-21 | 浙江工业大学 | 邻甲苯氨基乙酰氨基氯代苯并氮杂*基喹唑啉类化合物在制备治疗白血病药物中的应用 |
| CN108276384B (zh) * | 2018-01-24 | 2019-12-06 | 浙江工业大学 | 乙酰氨基苯并[d]氮杂卓基喹唑啉类化合物及其制备与应用 |
| CN108324719B (zh) * | 2018-01-24 | 2020-08-21 | 浙江工业大学 | 邻甲苯氨基乙酰氨基甲氧苯基苯并氮杂*基喹唑啉类化合物在制备治疗宫颈癌药物中的应用 |
| CN108117542B (zh) * | 2018-01-24 | 2019-12-24 | 浙江工业大学 | 丙酰氨基甲氧苯基苯并[d]氮杂卓基喹唑啉类化合物及制备和应用 |
| CN108164510B (zh) * | 2018-01-24 | 2020-08-21 | 浙江工业大学 | 氯乙酰氨基苯并[d]氮杂*基喹唑啉类化合物及其制备方法和应用 |
| CN108125961B (zh) * | 2018-01-24 | 2020-05-26 | 浙江工业大学 | 吗啉基乙酰氨基甲氧苯基苯并氮杂*基喹唑啉类化合物在制备治疗白血病药物中的应用 |
| CN108143736B (zh) * | 2018-01-24 | 2020-08-21 | 浙江工业大学 | 丁酰氨基苯并[d]氮杂*基喹唑啉类在制备治疗肺癌药物中的应用 |
| CN108186649B (zh) * | 2018-01-24 | 2020-05-26 | 浙江工业大学 | 丙酰氨基氯代苯并[d]氮杂*基喹唑啉类在制备治疗白血病药物中的应用 |
| CN108125959B (zh) * | 2018-01-24 | 2019-12-31 | 浙江工业大学 | 二甲氧基苯氨基乙酰氨基喹唑啉类化合物在制备治疗白血病药物中的应用 |
| CN108078994B (zh) * | 2018-01-24 | 2020-01-03 | 浙江工业大学 | 6-(2-吗啉基乙酰氨基)喹唑啉类化合物在制备治疗肺癌药物中的应用 |
| CN108014114B (zh) * | 2018-01-24 | 2020-08-21 | 浙江工业大学 | 氯乙酰氨基喹唑啉类化合物在制备治疗肺癌药物中的应用 |
| CN109251196B (zh) * | 2018-01-24 | 2020-11-13 | 浙江工业大学 | 氨基苯并[d]氮杂*基喹唑啉类化合物及其制备方法和应用 |
| CN108129461B (zh) * | 2018-01-24 | 2020-08-21 | 浙江工业大学 | 苯甲酰氨基苯并[d]氮杂*基喹唑啉类化合物及制备和应用 |
| CN108129460B (zh) * | 2018-01-24 | 2020-10-09 | 浙江工业大学 | 甲氧苯基苯并[d]氮杂*基喹唑啉类化合物及制备和应用 |
| CN108014115B (zh) * | 2018-01-24 | 2020-10-02 | 浙江工业大学 | 特戊酰氨基甲氧苯基苯并[d]氮杂*基喹唑啉类化合物在制备治疗肺癌药物中的应用 |
| CN108125960B (zh) * | 2018-01-24 | 2020-08-21 | 浙江工业大学 | 异丁酰氨基苯并[d]氮杂*基喹唑啉类化合物在制备治疗肺癌药物中的应用 |
| CN108245520B (zh) * | 2018-01-24 | 2019-12-24 | 浙江工业大学 | 乙酰氨基喹唑啉类化合物在制备治疗肺癌药物中的应用 |
| CN108324718B (zh) * | 2018-01-24 | 2020-10-09 | 浙江工业大学 | 环己基甲氧基甲酰氨基氯代苯并氮杂*基喹唑啉类化合物在治疗白血病药物中的应用 |
| CN108309984B (zh) * | 2018-01-24 | 2020-02-21 | 浙江工业大学 | 丙酰氨基喹唑啉类化合物在制备治疗宫颈癌药物中的应用 |
| CN108125962B (zh) * | 2018-01-24 | 2020-08-21 | 浙江工业大学 | 苯并[d]氮杂*基喹唑啉类化合物在制备治疗肺癌药物中的应用 |
| CN108078995B (zh) * | 2018-01-24 | 2020-01-03 | 浙江工业大学 | 苯甲酰氨基喹唑啉类化合物在制备治疗肺癌药物中的应用 |
| CN108276386B (zh) * | 2018-01-24 | 2020-10-09 | 浙江工业大学 | 环己基甲氧基甲酰氨基喹唑啉类化合物及制备和应用 |
| CN108014113B (zh) * | 2018-01-24 | 2020-10-09 | 浙江工业大学 | 丁酰氨基二甲氧基苯并[d]氮杂*基喹唑啉类化合物在制备治疗宫颈癌药物中的应用 |
| CN108078993B (zh) * | 2018-01-24 | 2020-02-21 | 浙江工业大学 | 6-硝基喹唑啉类化合物在制备治疗肺癌药物中的应用 |
| CN108295076B (zh) * | 2018-01-24 | 2020-05-22 | 浙江工业大学 | 丙酰氨基二甲氧基苯并[d]氮杂*基喹唑啉类在制备治疗肺癌药物中的应用 |
| CN108014116B (zh) * | 2018-01-24 | 2020-08-21 | 浙江工业大学 | 氨基二甲氧基苯并[d]氮杂*基喹唑啉类化合物在制备治疗肺癌药物中的应用 |
| CN108245519B (zh) * | 2018-01-24 | 2020-02-21 | 浙江工业大学 | 丁酰氨基喹唑啉类化合物在制备治疗白血病药物中的应用 |
| CN108329300B (zh) * | 2018-01-24 | 2020-10-09 | 浙江工业大学 | 硝基苯并[d]氮杂*基喹唑啉类化合物及其制备方法和应用 |
| CN108078992B (zh) * | 2018-01-24 | 2020-08-21 | 浙江工业大学 | 特戊酰氨基二甲氧基苯并[d]氮杂*基喹唑啉类化合物在制备治疗白血病药物中的应用 |
| CN108324717B (zh) * | 2018-01-24 | 2020-08-21 | 浙江工业大学 | 特戊酰氨基氯代苯并[d]氮杂*基喹唑啉类化合物在制备治疗宫颈癌药物中的应用 |
| CN108250185B (zh) * | 2018-01-24 | 2020-08-21 | 浙江工业大学 | 6-(2-(邻甲苯氨基)乙酰氨基)喹唑啉类化合物及制备和应用 |
| CN108014112B (zh) * | 2018-01-24 | 2020-10-09 | 浙江工业大学 | 邻甲苯氨基乙酰氨基苯并[d]氮杂*基喹唑啉类化合物在制备治疗肺癌药物中的应用 |
| CN108047206B (zh) * | 2018-01-24 | 2019-11-29 | 浙江工业大学 | 特戊酰氨基苯并[d]氮杂*基喹唑啉类化合物及制备和应用 |
| CN108042546B (zh) * | 2018-01-24 | 2020-10-09 | 浙江工业大学 | 吗啉基乙酰氨基苯并[d]氮杂*基喹唑啉类化合物在制备治疗宫颈癌药物中的应用 |
| CN108084162B (zh) * | 2018-01-24 | 2019-11-29 | 浙江工业大学 | 二甲氧基苯氨基乙酰氨基苯并[d]氮杂*基喹唑啉类化合物及制备和应用 |
| CN108017621B (zh) * | 2018-01-24 | 2020-08-21 | 浙江工业大学 | 吗啉基乙酰氨基二甲氧基苯并[d]氮杂*基喹唑啉类化合物及制备和应用 |
| CN108033949B (zh) * | 2018-01-24 | 2019-11-29 | 浙江工业大学 | 6-(2-二丙氨基乙酰氨基)喹唑啉类化合物及制备和应用 |
| EP4605089A1 (fr) * | 2022-10-20 | 2025-08-27 | Mekanistic Therapeutics LLC | Composés utiles dans la modulation de egfr et pi3k |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4012513A (en) * | 1971-11-03 | 1977-03-15 | Imperial Chemical Industries Limited | Indole derivatives for providing analgesic and anti-inflammatory effects |
| BE790679A (fr) * | 1971-11-03 | 1973-04-27 | Ici Ltd | Derives de l'indole |
| US4343940A (en) * | 1979-02-13 | 1982-08-10 | Mead Johnson & Company | Anti-tumor quinazoline compounds |
| PH23565A (en) * | 1986-09-05 | 1989-08-25 | Sumitomo Chemical Co | Novel pyrimidinylpyrimidine derivatives and a plant disease protectant containing them as the active ingredient |
| US5252573A (en) * | 1988-12-15 | 1993-10-12 | Imperial Chemical Industries Plc | Anti-tumor agents |
| CA2102780C (fr) * | 1991-05-10 | 2007-01-09 | Alfred P. Spada | Composes de type bis-monoaryle, aryle bicyclique et (ou) heteroaryle inhibant l'activite de tyrosine kinase des recepteurs de l'egf et (ou) du pdgf |
| NZ243082A (en) * | 1991-06-28 | 1995-02-24 | Ici Plc | 4-anilino-quinazoline derivatives; pharmaceutical compositions, preparatory processes, and use thereof |
| PT100905A (pt) * | 1991-09-30 | 1994-02-28 | Eisai Co Ltd | Compostos heterociclicos azotados biciclicos contendo aneis de benzeno, ciclo-hexano ou piridina e de pirimidina, piridina ou imidazol substituidos e composicoes farmaceuticas que os contem |
| GB9300059D0 (en) * | 1992-01-20 | 1993-03-03 | Zeneca Ltd | Quinazoline derivatives |
| GB9323290D0 (en) * | 1992-12-10 | 1994-01-05 | Zeneca Ltd | Quinazoline derivatives |
| GB9314893D0 (en) * | 1993-07-19 | 1993-09-01 | Zeneca Ltd | Quinazoline derivatives |
-
1995
- 1995-01-27 PL PL95315941A patent/PL315941A1/xx unknown
- 1995-01-27 BR BR9506936A patent/BR9506936A/pt not_active Application Discontinuation
- 1995-01-27 US US08/682,565 patent/US5736534A/en not_active Expired - Fee Related
- 1995-01-27 AU AU29727/95A patent/AU686843B2/en not_active Ceased
- 1995-01-27 JP JP7522227A patent/JP2890267B2/ja not_active Expired - Lifetime
- 1995-01-27 WO PCT/IB1995/000061 patent/WO1995023141A1/fr not_active Ceased
- 1995-01-27 EP EP95905737A patent/EP0746554A1/fr not_active Withdrawn
- 1995-01-27 CA CA002183655A patent/CA2183655C/fr not_active Expired - Fee Related
- 1995-01-27 HU HU9602305A patent/HUT76291A/hu unknown
- 1995-01-27 RU RU96119255A patent/RU2137762C1/ru active
- 1995-01-27 CN CN95191723A patent/CN1141633A/zh active Pending
- 1995-01-27 CZ CZ19962413A patent/CZ288955B6/cs not_active IP Right Cessation
- 1995-01-27 KR KR1019960704612A patent/KR100225721B1/ko not_active Expired - Fee Related
- 1995-01-27 MX MX9603593A patent/MX9603593A/es not_active IP Right Cessation
- 1995-02-06 TW TW084100928A patent/TW404946B/zh not_active IP Right Cessation
- 1995-02-16 IL IL11267395A patent/IL112673A0/xx unknown
- 1995-02-17 PE PE1995262160A patent/PE4896A1/es not_active Application Discontinuation
- 1995-02-22 ZA ZA951458A patent/ZA951458B/xx unknown
- 1995-02-22 CO CO95006643A patent/CO4340688A1/es unknown
-
1996
- 1996-08-19 NZ NZ278135A patent/NZ278135A/en unknown
- 1996-08-22 FI FI963283A patent/FI963283A0/fi unknown
- 1996-08-22 NO NO963506A patent/NO963506L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| NZ278135A (en) | 1998-03-25 |
| JPH09501953A (ja) | 1997-02-25 |
| RU2137762C1 (ru) | 1999-09-20 |
| HUT76291A (en) | 1997-07-28 |
| WO1995023141A1 (fr) | 1995-08-31 |
| CZ241396A3 (en) | 1997-07-16 |
| NO963506D0 (no) | 1996-08-22 |
| AU686843B2 (en) | 1998-02-12 |
| PL315941A1 (en) | 1996-12-09 |
| CN1141633A (zh) | 1997-01-29 |
| FI963283A7 (fi) | 1996-08-22 |
| AU2972795A (en) | 1995-09-11 |
| TW404946B (en) | 2000-09-11 |
| IL112673A0 (en) | 1995-05-26 |
| CO4340688A1 (es) | 1996-07-30 |
| US5736534A (en) | 1998-04-07 |
| CA2183655A1 (fr) | 1995-08-31 |
| BR9506936A (pt) | 1997-09-09 |
| CA2183655C (fr) | 2001-03-06 |
| KR970701183A (ko) | 1997-03-17 |
| JP2890267B2 (ja) | 1999-05-10 |
| EP0746554A1 (fr) | 1996-12-11 |
| HU9602305D0 (en) | 1996-10-28 |
| PE4896A1 (es) | 1996-03-09 |
| MX9603593A (es) | 1997-03-29 |
| FI963283A0 (fi) | 1996-08-22 |
| KR100225721B1 (ko) | 1999-10-15 |
| CZ288955B6 (cs) | 2001-10-17 |
| ZA951458B (en) | 1996-08-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2183655A1 (fr) | Derives de la quinazoline a substitution 4-heterocyclyle, procedes d'elaboration et utilisations correspondantes comme agents anticancereux | |
| NO331002B1 (no) | Tioxantinderivater og farmasoytiske preparater med tioxantinderivater | |
| NO962386L (no) | Heterocykliske ring-kondenserte pyrimidin-derivater | |
| IT1229570B (it) | Derivati fluorurati di acidi biliari, loro preparazione e composizioni farmaceutiche che li contengono. | |
| NO980954L (no) | Nye-4-(oksyalkoksyfenyl)-3-oksy-piperidiner for behandling av hjerte- og nyreinsuffisiens | |
| ATE284860T1 (de) | Neue verwendung von phenylheteroalkylamin- derivaten | |
| IE782337L (en) | Phthalazine-acetic acid derivatives. | |
| NO954427L (no) | Hiv-proteaseinhibitorer som er anvendbare for behandling av AIDS | |
| NO20055565L (no) | Anvendelse av derivater av 2,4-dihydro-[1,2,4]triazol-3-thion som inhibitorer av enzymet myeloperoksidase (MPO) | |
| TW429250B (en) | Novel heterocyclic derivatives and pharmaceutical use thereof | |
| NO943093L (no) | Fremgangsmåte for fremstilling av clavulansyre | |
| NO890723D0 (no) | Fremgangsmaate for fremstilling av terapeutisk aktive 3-alkenyl-1-azabicyklo(3.2.0)hept2-en-2-karboksylsyrederivater. | |
| NO904839L (no) | Fremgangsmaate for fremstilling av benzoxazinderivater. | |
| IT1223313B (it) | Derivati di acidi biliari loro preparazione e composizioni farmaceutiche che li contengono | |
| SE9701304D0 (sv) | Compounds | |
| ATE61588T1 (de) | 1,4-dihydropyridine, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel. | |
| CA2111223A1 (fr) | Derives de benzo- et de pyridopyrane ayant une activite anxiolytique et anticonvulsive | |
| NO160297C (no) | Analogifremgangsmaate for fremstilling av terapeutisk virksomme 2-oksoazetidinderivater | |
| GB8814587D0 (en) | Condensed pyrazole 3-oxo-propanenitrile derivatives & process for their preparation | |
| AU3623299A (en) | Benzofuroxan derivatives and their use in treating angina pectoris | |
| DE69720966D1 (de) | Benzo[c]chinolizin derivate,deren herstellung und verwendung als 5-alfa-reduktase inhibitoren | |
| NO20013921L (no) | Heterocykliske derivater som inhibitorer av faktor Xa | |
| HUP0204217A2 (en) | Novel a-500359 derivatives | |
| TR199903296T2 (en) | Bile�ikler. | |
| AU658175B2 (en) | Use of 2-iminothiazolidin-4-one derivatives as novel pharmaceutical active ingredients |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FC2A | Withdrawal, rejection or dismissal of laid open patent application |