JP4599164B2 - ３位が複素環式基によって置換されたピリドインドロン誘導体、それらの製造法およびそれらの治療用途 - Google Patents
３位が複素環式基によって置換されたピリドインドロン誘導体、それらの製造法およびそれらの治療用途 Download PDFInfo
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- JP4599164B2 JP4599164B2 JP2004546105A JP2004546105A JP4599164B2 JP 4599164 B2 JP4599164 B2 JP 4599164B2 JP 2004546105 A JP2004546105 A JP 2004546105A JP 2004546105 A JP2004546105 A JP 2004546105A JP 4599164 B2 JP4599164 B2 JP 4599164B2
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- indol
- pyrido
- dihydro
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- 229960000624 procarbazine Drugs 0.000 description 1
- 238000011321 prophylaxis Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003586 protic polar solvent Substances 0.000 description 1
- 230000006825 purine synthesis Effects 0.000 description 1
- 150000003212 purines Chemical class 0.000 description 1
- 150000003230 pyrimidines Chemical class 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 206010038038 rectal cancer Diseases 0.000 description 1
- 201000001275 rectum cancer Diseases 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 210000001625 seminal vesicle Anatomy 0.000 description 1
- 229960003440 semustine Drugs 0.000 description 1
- 201000000849 skin cancer Diseases 0.000 description 1
- 201000002314 small intestine cancer Diseases 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 201000011549 stomach cancer Diseases 0.000 description 1
- 229960001052 streptozocin Drugs 0.000 description 1
- ZSJLQEPLLKMAKR-GKHCUFPYSA-N streptozocin Chemical compound O=NN(C)C(=O)N[C@H]1[C@@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O ZSJLQEPLLKMAKR-GKHCUFPYSA-N 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 230000007428 synaptic transmission, GABAergic Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 229960001603 tamoxifen Drugs 0.000 description 1
- 229940063683 taxotere Drugs 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 201000003120 testicular cancer Diseases 0.000 description 1
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- 229960003433 thalidomide Drugs 0.000 description 1
- 201000002510 thyroid cancer Diseases 0.000 description 1
- 229960003087 tioguanine Drugs 0.000 description 1
- 229940044693 topoisomerase inhibitor Drugs 0.000 description 1
- 230000004565 tumor cell growth Effects 0.000 description 1
- 210000003932 urinary bladder Anatomy 0.000 description 1
- 210000003741 urothelium Anatomy 0.000 description 1
- 210000004291 uterus Anatomy 0.000 description 1
- 229960005486 vaccine Drugs 0.000 description 1
- 201000010653 vesiculitis Diseases 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0213270A FR2846330B1 (fr) | 2002-10-23 | 2002-10-23 | Derives de pyridoindolone substitues en -3 par groupe heterocyclique, leur preparation et leur application en therapeutique |
| PCT/FR2003/003111 WO2004037821A1 (fr) | 2002-10-23 | 2003-10-21 | Derives de pyridoindolone substitues en -3 par un groupe heterocyclique, leur preparation et leur application en therapeutique |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2006505577A JP2006505577A (ja) | 2006-02-16 |
| JP2006505577A5 JP2006505577A5 (enExample) | 2006-12-07 |
| JP4599164B2 true JP4599164B2 (ja) | 2010-12-15 |
Family
ID=32088226
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004546105A Expired - Fee Related JP4599164B2 (ja) | 2002-10-23 | 2003-10-21 | ３位が複素環式基によって置換されたピリドインドロン誘導体、それらの製造法およびそれらの治療用途 |
Country Status (13)
| Country | Link |
|---|---|
| EP (1) | EP1556380B1 (enExample) |
| JP (1) | JP4599164B2 (enExample) |
| AR (1) | AR041690A1 (enExample) |
| AT (1) | ATE323091T1 (enExample) |
| AU (1) | AU2003292285A1 (enExample) |
| CY (1) | CY1105158T1 (enExample) |
| DE (1) | DE60304596T2 (enExample) |
| DK (1) | DK1556380T3 (enExample) |
| ES (1) | ES2263033T3 (enExample) |
| FR (1) | FR2846330B1 (enExample) |
| PT (1) | PT1556380E (enExample) |
| TW (1) | TW200418853A (enExample) |
| WO (1) | WO2004037821A1 (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2823975B1 (fr) | 2001-04-27 | 2003-05-30 | Sanofi Synthelabo | Nouvelle utilisation de pyridoindolone |
| FR2846329B1 (fr) | 2002-10-23 | 2004-12-03 | Sanofi Synthelabo | Derives de pyridoindolone substitues en -3 par un phenyle, leur preparation et leur application en therapeutique |
| FR2869316B1 (fr) | 2004-04-21 | 2006-06-02 | Sanofi Synthelabo | Derives de pyridoindolone substitues en -6, leur preparation et leur application en therapeutique. |
| FR2892416B1 (fr) * | 2005-10-20 | 2008-06-27 | Sanofi Aventis Sa | Derives de 6-heteroarylpyridoindolone, leur preparation et leur application en therapeutique |
| JP7214879B2 (ja) * | 2019-02-01 | 2023-01-30 | メッドシャイン ディスカバリー インコーポレイテッド | ｃ－Ｍｅｔ阻害剤としてのピリミジニルを含むトリシクリル系化合物 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4263304A (en) * | 1978-06-05 | 1981-04-21 | Sumitomo Chemical Company, Limited | 7 H-indolo[2,3-c]isoquinolines |
| FR2765581B1 (fr) * | 1997-07-03 | 1999-08-06 | Synthelabo | Derives de 3-aryl-1,9-dihydro-2h-pyrido[2,3-b]indol-2-one, leur preparation et leur application en therapeutique |
| FR2765582B1 (fr) * | 1997-07-03 | 1999-08-06 | Synthelabo | Derives de 3-alkyl-1,9-dihydro-2h-pyrido[2,3-b]indol-2-one leur preparation et leur application en therapeutique |
-
2002
- 2002-10-23 FR FR0213270A patent/FR2846330B1/fr not_active Expired - Fee Related
-
2003
- 2003-10-21 DE DE60304596T patent/DE60304596T2/de not_active Expired - Lifetime
- 2003-10-21 PT PT03767851T patent/PT1556380E/pt unknown
- 2003-10-21 JP JP2004546105A patent/JP4599164B2/ja not_active Expired - Fee Related
- 2003-10-21 ES ES03767851T patent/ES2263033T3/es not_active Expired - Lifetime
- 2003-10-21 DK DK03767851T patent/DK1556380T3/da active
- 2003-10-21 AT AT03767851T patent/ATE323091T1/de active
- 2003-10-21 EP EP03767851A patent/EP1556380B1/fr not_active Expired - Lifetime
- 2003-10-21 AU AU2003292285A patent/AU2003292285A1/en not_active Abandoned
- 2003-10-21 WO PCT/FR2003/003111 patent/WO2004037821A1/fr not_active Ceased
- 2003-10-22 AR ARP030103841A patent/AR041690A1/es unknown
- 2003-10-22 TW TW092129284A patent/TW200418853A/zh unknown
-
2006
- 2006-07-12 CY CY20061100971T patent/CY1105158T1/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| FR2846330B1 (fr) | 2004-12-03 |
| ATE323091T1 (de) | 2006-04-15 |
| EP1556380B1 (fr) | 2006-04-12 |
| DE60304596T2 (de) | 2007-05-10 |
| FR2846330A1 (fr) | 2004-04-30 |
| ES2263033T3 (es) | 2006-12-01 |
| DE60304596D1 (de) | 2006-05-24 |
| AU2003292285A1 (en) | 2004-05-13 |
| AR041690A1 (es) | 2005-05-26 |
| JP2006505577A (ja) | 2006-02-16 |
| PT1556380E (pt) | 2006-08-31 |
| TW200418853A (en) | 2004-10-01 |
| WO2004037821A1 (fr) | 2004-05-06 |
| DK1556380T3 (da) | 2006-08-14 |
| CY1105158T1 (el) | 2010-03-03 |
| EP1556380A1 (fr) | 2005-07-27 |
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