MA26438A1 - Derives 6,5-heterobicycliques substitues, procede pour leur preparation et compositions pharmaceutiques les contenant. - Google Patents

Derives 6,5-heterobicycliques substitues, procede pour leur preparation et compositions pharmaceutiques les contenant.

Info

Publication number
MA26438A1
MA26438A1 MA24779A MA24779A MA26438A1 MA 26438 A1 MA26438 A1 MA 26438A1 MA 24779 A MA24779 A MA 24779A MA 24779 A MA24779 A MA 24779A MA 26438 A1 MA26438 A1 MA 26438A1
Authority
MA
Morocco
Prior art keywords
substituted
preparation
pharmaceutical compositions
compositions containing
heterobicyclic derivatives
Prior art date
Application number
MA24779A
Other languages
English (en)
Inventor
Liang Chen Yuhpyng
Original Assignee
Pfizer
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=21823717&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA26438(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Pfizer filed Critical Pfizer
Publication of MA26438A1 publication Critical patent/MA26438A1/fr

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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
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    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
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    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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    • A61P5/38—Drugs for disorders of the endocrine system of the suprarenal hormones
    • A61P5/42—Drugs for disorders of the endocrine system of the suprarenal hormones for decreasing, blocking or antagonising the activity of mineralocorticosteroids
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    • 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
MA24779A 1996-08-28 1997-08-27 Derives 6,5-heterobicycliques substitues, procede pour leur preparation et compositions pharmaceutiques les contenant. MA26438A1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US2503996P 1996-08-28 1996-08-28

Publications (1)

Publication Number Publication Date
MA26438A1 true MA26438A1 (fr) 2004-12-20

Family

ID=21823717

Family Applications (1)

Application Number Title Priority Date Filing Date
MA24779A MA26438A1 (fr) 1996-08-28 1997-08-27 Derives 6,5-heterobicycliques substitues, procede pour leur preparation et compositions pharmaceutiques les contenant.

Country Status (36)

Country Link
EP (1) EP0923582B1 (fr)
JP (2) JP3621706B2 (fr)
KR (1) KR20000035934A (fr)
CN (1) CN1227554A (fr)
AP (1) AP762A (fr)
AR (1) AR015103A1 (fr)
AT (1) ATE340176T1 (fr)
AU (1) AU735401B2 (fr)
BG (1) BG103189A (fr)
BR (1) BR9711970A (fr)
CA (1) CA2263566C (fr)
CO (1) CO4600634A1 (fr)
CZ (1) CZ68199A3 (fr)
DE (1) DE69736711T2 (fr)
DZ (1) DZ2300A1 (fr)
EA (1) EA002769B1 (fr)
ES (1) ES2273369T3 (fr)
GT (1) GT199700095A (fr)
HR (1) HRP970454B1 (fr)
HU (1) HUP9903965A3 (fr)
ID (1) ID18249A (fr)
IL (1) IL127566A0 (fr)
IS (1) IS4963A (fr)
MA (1) MA26438A1 (fr)
NO (1) NO313636B1 (fr)
NZ (1) NZ333302A (fr)
OA (1) OA10977A (fr)
PA (1) PA8436201A1 (fr)
PE (1) PE108898A1 (fr)
PL (1) PL332040A1 (fr)
SK (1) SK23399A3 (fr)
TN (1) TNSN97145A1 (fr)
TR (1) TR199900389T2 (fr)
TW (1) TW575573B (fr)
WO (1) WO1998008847A1 (fr)
ZA (1) ZA977687B (fr)

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US6313124B1 (en) 1997-07-23 2001-11-06 Dupont Pharmaceuticals Company Tetrazine bicyclic compounds
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US6060478A (en) * 1996-07-24 2000-05-09 Dupont Pharmaceuticals Azolo triazines and pyrimidines
US6191131B1 (en) 1997-07-23 2001-02-20 Dupont Pharmaceuticals Company Azolo triazines and pyrimidines
EP0970082A2 (fr) 1997-02-18 2000-01-12 Neurocrine Biosciences, Inc. Antagonistes crf biazacycliques
EP0977759A1 (fr) * 1997-04-22 2000-02-09 Janssen Pharmaceutica N.V. Thiophenopyridines antagonistes du crf
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CA2326319A1 (fr) 1998-04-02 1999-10-14 Neurogen Corporation Derives de 5,6,7,8-tetrahydro-9h pyrimidino[2,3-b]indole et de 5,6,7,8-tetrahydro-9h-pyrimidino[4,5-b]indole a substitution aminoalkyl: des ligands specifiques du crf1
US6472402B1 (en) 1998-04-02 2002-10-29 Neurogen Corporation Aminoalkyl substituted 5,6,7,8-Tetrahydro-9H-Pyridino [2,3-B]indole derivatives
AU3213699A (en) * 1998-04-03 1999-10-25 Du Pont Pharmaceuticals Company Thiazolo(4,5-d)pyrimidines and pyridines as corticotropin releasing factor (CRF)antagonists
US6194574B1 (en) 1998-06-09 2001-02-27 Neurogen Corporation Pyrido[2,3-b]indolizine derivatives and aza analogues thereof: CRF1 specific ligands
US6509338B1 (en) 1998-06-22 2003-01-21 Bristol-Myers Squibb Company Pyrazolo[1,5-A]triazine corticotropin releasing factor antagonists
AU5777299A (en) * 1998-08-21 2000-03-14 Du Pont Pharmaceuticals Company Isoxazolo(4,5-d)pyrimidines as CRF antagonists
JP2002529469A (ja) 1998-11-12 2002-09-10 ニューロクライン バイオサイエンシーズ， インコーポレイテッド Ｃｒｆレセプターアンタゴニストおよびそれに関する方法
US6531475B1 (en) * 1998-11-12 2003-03-11 Neurocrine Biosciences, Inc. CRF receptor antagonists and methods relating thereto
ES2180338T3 (es) * 1998-11-12 2003-02-01 Neurocrine Biosciences Inc Antagonistas del receptor de crf y metodos relacionados.
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