MA26906A1 - Aminoalkyl 1-lactames substituees et leur utilisation en tant qu'antagonistes du recepteur muscarinique - Google Patents
Aminoalkyl 1-lactames substituees et leur utilisation en tant qu'antagonistes du recepteur muscariniqueInfo
- Publication number
- MA26906A1 MA26906A1 MA26922A MA26922A MA26906A1 MA 26906 A1 MA26906 A1 MA 26906A1 MA 26922 A MA26922 A MA 26922A MA 26922 A MA26922 A MA 26922A MA 26906 A1 MA26906 A1 MA 26906A1
- Authority
- MA
- Morocco
- Prior art keywords
- receptor antagonists
- aminoalkyl
- muscarinic receptor
- sup
- compounds
- Prior art date
Links
- 229940121948 Muscarinic receptor antagonist Drugs 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 102000017925 CHRM3 Human genes 0.000 abstract 1
- 101150060249 CHRM3 gene Proteins 0.000 abstract 1
- 102000007205 Muscarinic M2 Receptor Human genes 0.000 abstract 1
- 108010008407 Muscarinic M2 Receptor Proteins 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 239000002464 receptor antagonist Substances 0.000 abstract 1
- 229940044551 receptor antagonist Drugs 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 229940124597 therapeutic agent Drugs 0.000 abstract 1
Classifications
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- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/24—Oxygen or sulfur atoms
- C07D207/26—2-Pyrrolidones
- C07D207/263—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
- C07D207/27—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
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- 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
- C07D417/06—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 linked by a carbon chain containing only aliphatic carbon atoms
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- 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
- C07D417/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
- C07D417/14—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 three or more hetero rings
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- Chemical & Material Sciences (AREA)
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- Health & Medical Sciences (AREA)
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- Life Sciences & Earth Sciences (AREA)
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- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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- Urology & Nephrology (AREA)
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- Obesity (AREA)
- Heart & Thoracic Surgery (AREA)
- Reproductive Health (AREA)
- Pain & Pain Management (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US20748300P | 2000-05-25 | 2000-05-25 | |
US26757901P | 2001-02-09 | 2001-02-09 |
Publications (1)
Publication Number | Publication Date |
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MA26906A1 true MA26906A1 (fr) | 2004-12-20 |
Family
ID=26902273
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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MA26922A MA26906A1 (fr) | 2000-05-25 | 2002-11-22 | Aminoalkyl 1-lactames substituees et leur utilisation en tant qu'antagonistes du recepteur muscarinique |
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US (3) | US6667301B2 (fr) |
EP (1) | EP1289965B1 (fr) |
JP (1) | JP4071000B2 (fr) |
KR (1) | KR100544000B1 (fr) |
CN (1) | CN1178922C (fr) |
AR (1) | AR028624A1 (fr) |
AT (1) | ATE307806T1 (fr) |
AU (1) | AU782191B2 (fr) |
BR (1) | BR0111061A (fr) |
CA (1) | CA2409841C (fr) |
CZ (1) | CZ302807B6 (fr) |
DE (1) | DE60114413T2 (fr) |
ES (1) | ES2251517T3 (fr) |
HR (1) | HRP20020904A2 (fr) |
HU (1) | HUP0302010A2 (fr) |
IL (1) | IL152701A0 (fr) |
MA (1) | MA26906A1 (fr) |
MX (1) | MXPA02011418A (fr) |
MY (1) | MY140835A (fr) |
NO (1) | NO20025640L (fr) |
NZ (1) | NZ522411A (fr) |
PE (1) | PE20011325A1 (fr) |
PL (1) | PL204753B1 (fr) |
RU (1) | RU2241702C2 (fr) |
TW (1) | TWI306095B (fr) |
UY (1) | UY26729A1 (fr) |
WO (1) | WO2001090081A1 (fr) |
YU (1) | YU88902A (fr) |
Families Citing this family (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001090081A1 (fr) * | 2000-05-25 | 2001-11-29 | F. Hoffmann-La Roche Ag | 1-aminoalkyle-lactames substitues et leur utilisation en tant qu'antagonistes de recepteur muscarinique |
AU2002345664C1 (en) * | 2001-06-11 | 2008-03-06 | Xenoport, Inc. | Prodrugs of gaba analogs, compositions and uses thereof |
US7186855B2 (en) | 2001-06-11 | 2007-03-06 | Xenoport, Inc. | Prodrugs of GABA analogs, compositions and uses thereof |
US8048917B2 (en) | 2005-04-06 | 2011-11-01 | Xenoport, Inc. | Prodrugs of GABA analogs, compositions and uses thereof |
US6818787B2 (en) | 2001-06-11 | 2004-11-16 | Xenoport, Inc. | Prodrugs of GABA analogs, compositions and uses thereof |
CN100358870C (zh) | 2001-12-03 | 2008-01-02 | 弗·哈夫曼-拉罗切有限公司 | 作为毒蕈碱受体拮抗剂的氨基四氢萘衍生物 |
AU2002352125A1 (en) | 2001-12-03 | 2003-06-17 | F. Hoffmann-La Roche Ag | 4-piperidinyl alkylamine derivatives as muscarinic receptor antagonists |
DE60230683D1 (de) | 2002-07-08 | 2009-02-12 | Ranbaxy Lab Ltd | 3,6-disubstituierte azabicyclo-3.1.0 hexan-derivat |
EP1618091A1 (fr) | 2003-04-09 | 2006-01-25 | Ranbaxy Laboratories, Ltd. | Derives d'azabicyclo hexane substitues en tant qu'antagonistes de recepteurs muscariniques |
CN100436414C (zh) | 2003-04-11 | 2008-11-26 | 兰贝克赛实验室有限公司 | 作为毒蕈碱受体拮抗剂的氮杂双环衍生物 |
WO2006050514A1 (fr) | 2004-11-04 | 2006-05-11 | Xenoport, Inc. | Formes posologiques orales a liberation prolongee d'un promedicament du nom de gabapentine |
CA2616918A1 (fr) | 2005-07-01 | 2007-01-11 | Jenrin Discovery | Inhibiteurs mao-b utiles dans le traitement de l'obesite |
US20090221664A1 (en) | 2005-10-19 | 2009-09-03 | Abhijit Ray | Pharmaceutical compositions of muscarinic receptor antagonists |
TWI423967B (zh) * | 2008-02-21 | 2014-01-21 | Dainippon Sumitomo Pharma Co | 醯胺衍生物及含有其之醫藥組合物 |
US8008291B2 (en) * | 2008-02-29 | 2011-08-30 | Mimetica Pty Ltd | 3-aminoalkyl-1,4-diazepan-2-one melanocortin-5 receptor antagonists |
MX2010009486A (es) * | 2008-02-29 | 2011-02-22 | Mimetica Pty Ltd | Antagonistas de tipo 1,4-diazepan 2 ona 3-sustituida del receptor de melanocortina-5. |
PL2300461T3 (pl) * | 2008-05-01 | 2013-09-30 | Vitae Pharmaceuticals Inc | Cykliczne inhibitory dehydrogenazy 11beta-hydroksysteroidów 1 |
EP2687525B1 (fr) * | 2008-07-25 | 2015-09-23 | Boehringer Ingelheim International GmbH | Inhibiteurs cycliques de la 11-bêta-hydroxystéroïde déshydrogénase 1 |
AU2009276090A1 (en) | 2008-07-28 | 2010-02-04 | F. Hoffmann-La Roche Ag | Diazepan and piperazine derivatives modulators of chemokine receptors |
US9737047B2 (en) | 2011-03-22 | 2017-08-22 | Ccd Holdings Llc | Method for the treatment, control, minimization, and prevention of bovine mastitis |
US8757092B2 (en) | 2011-03-22 | 2014-06-24 | Eco-Composites Llc | Animal bedding and associated method for preparing the same |
MA39950B1 (fr) * | 2014-06-06 | 2019-08-30 | Astellas Pharma Inc | Dérivé de 2-acylaminothiazole pour le traitement des maladies des voies urinaires et de la vessie |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
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US3054794A (en) | 1958-01-17 | 1962-09-18 | Us Vitamin Pharm Corp | Process for preparing 3-(aminoalkyl)-oxazolidine-2, 4-diones |
US3354178A (en) | 1965-04-09 | 1967-11-21 | Sterling Drug Inc | Nu-(4-amino-2-butynyl)-nu-alkylcarboxamides |
US4065471A (en) | 1965-04-09 | 1977-12-27 | Sterling Drug Inc. | N-(4-Amino-2-butynyl)imides |
AT345806B (de) | 1975-03-06 | 1978-10-10 | Thomae Gmbh Dr K | Verfahren zur herstellung neuer substituierter arylalkylamine und deren salze |
US4087541A (en) | 1975-03-06 | 1978-05-02 | Boehringer Ingelheim Gmbh | 2-(Aralkylaminoalkyl)phthalimidines |
DD123741A5 (fr) | 1975-03-06 | 1977-01-12 | ||
US4083407A (en) * | 1977-02-07 | 1978-04-11 | The Dow Chemical Company | Spacer composition and method of use |
US4490369A (en) | 1981-05-19 | 1984-12-25 | Dr. Karl Thomae Gesellschaft Mit Beschrankter Haftung | Benzazepine derivatives, their pharmaceutical compositions and method of use |
US4729994A (en) | 1986-08-20 | 1988-03-08 | Mcneilab, Inc. | Benzothiazepine vasodilators having aralkyl substitution |
DE3631013A1 (de) | 1986-09-12 | 1988-03-24 | Thomae Gmbh Dr K | Neue naphthylderivate, diese verbindungen enthaltende arzneimittel und verfahren zu ihrer herstellung |
FI892362A (fi) | 1988-06-01 | 1989-12-02 | Eisai Co Ltd | Buten- eller propensyraderivat. |
US5177089A (en) | 1988-06-01 | 1993-01-05 | Eisai Co., Ltd. | Butenoic or propenoic acid derivative |
US5998452A (en) | 1993-06-23 | 1999-12-07 | Chugai Seiyaku Kabushiki Kaisha | Benzene derivatives, compositions and methods for treating ischemic diseases |
SE9303274D0 (sv) | 1993-10-07 | 1993-10-07 | Astra Ab | Novel phenylethyl and phenylproplamines |
US6319920B1 (en) * | 1998-02-27 | 2001-11-20 | Syntex (U.S.A.) Llc | 2-arylethyl-(piperidin-4-ylmethyl)amine derivatives |
WO2001090081A1 (fr) * | 2000-05-25 | 2001-11-29 | F. Hoffmann-La Roche Ag | 1-aminoalkyle-lactames substitues et leur utilisation en tant qu'antagonistes de recepteur muscarinique |
-
2001
- 2001-05-16 WO PCT/EP2001/005584 patent/WO2001090081A1/fr active IP Right Grant
- 2001-05-16 AU AU10122/02A patent/AU782191B2/en not_active Ceased
- 2001-05-16 ES ES01980030T patent/ES2251517T3/es not_active Expired - Lifetime
- 2001-05-16 MX MXPA02011418A patent/MXPA02011418A/es active IP Right Grant
- 2001-05-16 HU HU0302010A patent/HUP0302010A2/hu unknown
- 2001-05-16 EP EP01980030A patent/EP1289965B1/fr not_active Expired - Lifetime
- 2001-05-16 KR KR1020027015885A patent/KR100544000B1/ko not_active IP Right Cessation
- 2001-05-16 CA CA002409841A patent/CA2409841C/fr not_active Expired - Fee Related
- 2001-05-16 PL PL361282A patent/PL204753B1/pl unknown
- 2001-05-16 AT AT01980030T patent/ATE307806T1/de active
- 2001-05-16 RU RU2002133208/04A patent/RU2241702C2/ru not_active IP Right Cessation
- 2001-05-16 YU YU88902A patent/YU88902A/sh unknown
- 2001-05-16 CZ CZ20024200A patent/CZ302807B6/cs not_active IP Right Cessation
- 2001-05-16 BR BR0111061-6A patent/BR0111061A/pt active Search and Examination
- 2001-05-16 IL IL15270101A patent/IL152701A0/xx unknown
- 2001-05-16 NZ NZ522411A patent/NZ522411A/en unknown
- 2001-05-16 CN CNB018100430A patent/CN1178922C/zh not_active Expired - Fee Related
- 2001-05-16 JP JP2001586270A patent/JP4071000B2/ja not_active Expired - Fee Related
- 2001-05-16 DE DE60114413T patent/DE60114413T2/de not_active Expired - Lifetime
- 2001-05-21 PE PE2001000457A patent/PE20011325A1/es not_active Application Discontinuation
- 2001-05-22 US US09/862,286 patent/US6667301B2/en not_active Expired - Lifetime
- 2001-05-23 MY MYPI20012428A patent/MY140835A/en unknown
- 2001-05-24 UY UY26729A patent/UY26729A1/es not_active Application Discontinuation
- 2001-05-24 AR ARP010102491A patent/AR028624A1/es not_active Application Discontinuation
- 2001-05-25 TW TW090112671A patent/TWI306095B/zh not_active IP Right Cessation
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2002
- 2002-11-14 HR HRP20020904 patent/HRP20020904A2/hr not_active Application Discontinuation
- 2002-11-22 NO NO20025640A patent/NO20025640L/no not_active Application Discontinuation
- 2002-11-22 MA MA26922A patent/MA26906A1/fr unknown
-
2003
- 2003-10-14 US US10/685,124 patent/US7094778B2/en not_active Expired - Fee Related
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2006
- 2006-08-22 US US11/508,581 patent/US7361648B2/en not_active Expired - Fee Related
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