RU2003120798A - Новые производные n-(фенилсульфонил) глицина и их применение в терапии - Google Patents
Новые производные n-(фенилсульфонил) глицина и их применение в терапииInfo
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- RU2003120798A RU2003120798A RU2003120798/04A RU2003120798A RU2003120798A RU 2003120798 A RU2003120798 A RU 2003120798A RU 2003120798/04 A RU2003120798/04 A RU 2003120798/04A RU 2003120798 A RU2003120798 A RU 2003120798A RU 2003120798 A RU2003120798 A RU 2003120798A
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- 0 C1NC=CN*1 Chemical compound C1NC=CN*1 0.000 description 1
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
- C07C311/16—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
- C07C311/18—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom to an acyclic carbon atom of a hydrocarbon radical substituted by nitrogen atoms, not being part of nitro or nitroso groups
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- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/72—Nitrogen atoms
- C07D213/73—Unsubstituted amino or imino radicals
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
- C07C311/16—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
- C07C311/19—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom to an acyclic carbon atom of a hydrocarbon radical substituted by carboxyl groups
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/26—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
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- 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
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/06—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms
- C07D233/08—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms with alkyl radicals, containing more than four carbon atoms, directly attached to ring carbon atoms
- C07D233/12—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms with alkyl radicals, containing more than four carbon atoms, directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D233/16—Radicals substituted by nitrogen atoms
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- 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
- C07D233/64—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 substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
- C07D295/125—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/13—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
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- 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
- C07D401/12—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 linked by a chain containing hetero atoms as chain links
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- Chemical & Material Sciences (AREA)
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- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pain & Pain Management (AREA)
- Public Health (AREA)
- Rheumatology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Hydrogenated Pyridines (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Claims (12)
1. Соединение N-(фенилсульфонил) глицина, отличающееся тем, что оно выбрано из группы, состоящей из
i) соединений, описываемых формулой:
в которой
W представляет собой атом хлора,
Х представляет собой атом водорода, метильную группу или атом хлора,
Y и Z представляют собой, каждый независимо от другого, атом водорода или атом хлора, или:
Х и W или Х и Y образуют совместно с атомами углерода, к которым они присоединены, фенильное ядро,
R представляет собой атом водорода, аллильную группу или C1-C4 алкильную группу, незамещенную или замещенную фенильной группой, метоксигруппой, пиридинильной группой, карбоксамидной или N-метилкарбоксамидной группой,
r1 представляет собой атом водорода, C1-C4 алкильную группу или группу (CH2)m-R’2,
n и m представляют собой, каждый независимо от другого, 1, 2, 3 или 4,
R2 и R’2 представляют собой, каждый независимо от другого, группу
группу
группу
группу
группу
группу
группу
группу
r3 представляет собой атом водорода или C1-C4 алкильную группу,
R4 представляет собой атом водорода, группу СОСН3, группу СООСН3 или C1-C4 алкильную группу,
r5 представляет собой атом водорода или C1-C4 алкильную группу, незамещенную или замещенную фенильной группой,
R6 представляет собой атом водорода или группу CONHC2H5,
R7 представляет собой атом водорода,
группу
группу
группу
группу
группу CONHCH3
r8 представляет собой атом водорода, группу NH2 или C1-C4 алкильную группу, p равно 4, 5 или 6;
ii) соли замещения соединений, соответствующих формуле I, образованных в результате их реакции с кислотой.
2. Соединение по п.1, отличающееся тем, что R представляет собой фенилметильную группу.
3. Соединение по п.1, отличающееся тем, что R представляет собой C1-C4 алкильную группу.
4. Соединение по любому из пунктов с 1 по 3, отличающееся тем, что:
r1 представляет собой атом водорода, C1-C4 алкильную группу или группу (CH2)m-R’2
m представляет собой 1, 2, 3 или 4,
R’2 представляет собой
группу
группу
группу
группу
группу
группу
R3 представляет собой атом водорода или C1-C4 алкильную группу,
R4 представляет собой атом водорода, группу СОСН3, группу СООСН3 или C1-C4 алкильную группу,
r5 представляет собой атом водорода или C1-C4 алкильную группу, которая может быть замещена фенильной группой,
R6 представляет собой атом водорода или группу CONHC2H5,
R8 представляет собой атом водорода,
p равно 4, 5 или 6.
5. Соединение по любому из пунктов с 1 по 4, отличающееся тем, что:
R2, представляет собой группу
группу
группу
группу
группу
R3 представляет собой атом водорода
R4 представляет собой атом водорода или C1-C4 алкильную группу, предпочтительно метильную,
R5 представляет собой атом водорода или C1-C4 алкильную группу, предпочтительно метильную,
R7 представляет собой атом водорода,
группу
группу
группу
группу
группу CONHCH3
R8 представляет собой атом водорода или группу NH2.
6. Соединение по любому из пунктов с 1 по 5, отличающееся тем, что R1 или R2 включают в свою структуру амидинильную группу.
7. Соединение по п.6, отличающееся тем, что R2 представляет собой фениламидиновую группу.
8. Соединение по п.6, отличающееся тем, что R2 включает в себя 2-имидазолильную группу.
9. Соединение по пунктам с 1 по 5, отличающееся тем, что оно выбрано из группы, включающей следующие соединения:
N-[2-[[[4-(аминоиминометил)фенил]метил][4-(1-пирролидинил)бутил]амино]-2-оксоэтил]-2-[[(2,4-дихлор-3-метилфенил)сульфонил](2-фенилэтил)амино]ацетамида дигидрохлорид,
N-[2-[[[4-(аминоиминометил)фенил]метил][3-(диметиламино)пропил]амино]-2-оксоэтил]-2-[[(2,4-дихлор-3-метилфенил)сульфонил](2-фенилэтил)амино]ацетамида дигидрохлорид,
N-[2-[[[4-(аминоиминометил)фенил]метил](4-пиперидинилэтил)амино]-2-оксоэтил]-2-[[(2,4-дихлор-3-метилфенил)сульфонил](2фенилэтил)амино]ацетамидабис-трифторацетат,
N-[2-[(4-аминобутил)(4-пиперидинилметил)амино]-2-оксоэтил]-2-[[(2,4-дихлор-3-метилфенил)сульфонил](2-фенилэтил)амино]ацетамида бис-трифторацетат,
2-[[(2,4-дихлор-3-метилфенил)сульфонил](2-фенилэтил)амино]-N-[2-[[[4-(4,5-дигидро-1H-имидазол-2-ил)фенил]метил][3-(диметиламино)пропил]амино]-2-оксоэтил]ацетамида дигидрохлорид,
2-[[(2,4-дихлор-3-метилфенил)сульфонил]метиламино]-N-[2-[[[4-(4,5-дигидро-1Н-имидазол-2-ил)фенил]метил]метиламино]-2-оксоэтил]ацетамида гидрохлорид,
2-[[(2,4-дихлор-3-метилфенил)сульфонил](2-фенилэтил)амино]-N-[2-[[3-(1Н-имидазол-5-ил)пропил][4-(1-пиррол идинил)бутил]амино]-2-оксоэтил]ацетамида дигидрохлорид.
10. Фармацевтическая композиция, отличающаяся тем, что она включает в сочетании, по меньшей мере, с одним физиологически приемлемым наполнителем по меньшей мере, одно соединение, соответствующее формуле I, по любому из пунктов с 1 по 9, или его соль замещения кислотой.
11. Применение соединения, соответствующего формуле I, по любому из пунктов с 1 по 9, или его соли замещения кислотой, для приготовления лекарственного средства, предназначенного для лечения боли.
12. Применение соединения, соответствующего формуле I, по любому из пунктов с 1 по 9, или его соли замещения кислотой, для приготовления лекарственного средства, предназначенного для лечения воспалительных заболеваний.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0100195A FR2819254B1 (fr) | 2001-01-08 | 2001-01-08 | Nouveaux composes de la n-(phenylsulfonyl) glycine, leur procede de preparation et leur utilisation pour obtenir des compostions pharmaceutiques |
FR01/00195 | 2001-01-08 |
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RU2003120798A true RU2003120798A (ru) | 2004-12-27 |
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RU2003120798/04A RU2003120798A (ru) | 2001-01-08 | 2002-01-07 | Новые производные n-(фенилсульфонил) глицина и их применение в терапии |
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US (1) | US20040063725A1 (ru) |
EP (1) | EP1351928A2 (ru) |
JP (1) | JP2004534729A (ru) |
KR (1) | KR20030070080A (ru) |
CN (1) | CN1484633A (ru) |
BR (1) | BR0206159A (ru) |
CA (1) | CA2434124A1 (ru) |
CZ (1) | CZ20031715A3 (ru) |
FR (1) | FR2819254B1 (ru) |
HU (1) | HUP0402507A2 (ru) |
IL (1) | IL156565A0 (ru) |
MX (1) | MXPA03006093A (ru) |
NO (1) | NO20033099L (ru) |
PL (1) | PL365219A1 (ru) |
RU (1) | RU2003120798A (ru) |
SK (1) | SK8282003A3 (ru) |
WO (1) | WO2002053516A2 (ru) |
Families Citing this family (42)
Publication number | Priority date | Publication date | Assignee | Title |
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MEP59808A (en) * | 2001-02-24 | 2011-05-10 | Boehringer Ingelheim Pharma | Xanthine derivative, production and use thereof as a medicament |
AU2003206945A1 (en) * | 2002-02-22 | 2003-09-09 | Max-Planck-Gesellschaft Zur Forderung Der Wissenschaften E.V. | Use of proteinase inhibitors in the treatment of autoimmune diseases |
FR2840897B1 (fr) * | 2002-06-14 | 2004-09-10 | Fournier Lab Sa | Nouveaux derives d'arylsulfonamides et leur utilisation en therapeutique |
US7407955B2 (en) | 2002-08-21 | 2008-08-05 | Boehringer Ingelheim Pharma Gmbh & Co., Kg | 8-[3-amino-piperidin-1-yl]-xanthines, the preparation thereof and their use as pharmaceutical compositions |
BRPI0408689B8 (pt) | 2003-03-25 | 2021-05-25 | Laboratoires Fournier S A | derivados de benzenosulfonamida, método para preparação e utilização disso para o tratamento da dor |
FR2853648B1 (fr) * | 2003-04-11 | 2006-08-18 | Fournier Lab Sa | Nouveaux derives de benzenesulfonamides et leur utilisation en therapeutique |
US7501426B2 (en) | 2004-02-18 | 2009-03-10 | Boehringer Ingelheim International Gmbh | 8-[3-amino-piperidin-1-yl]-xanthines, their preparation and their use as pharmaceutical compositions |
DE102004054054A1 (de) | 2004-11-05 | 2006-05-11 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Verfahren zur Herstellung chiraler 8-(3-Amino-piperidin-1-yl)-xanthine |
DE102005035891A1 (de) | 2005-07-30 | 2007-02-08 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | 8-(3-Amino-piperidin-1-yl)-xanthine, deren Herstellung und deren Verwendung als Arzneimittel |
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FR2508444A1 (fr) * | 1981-06-29 | 1982-12-31 | Irceba | Nouveaux derives sulfonyle du tryptophane utiles en tant que medicaments et leur procede de preparation |
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PT84170B (pt) * | 1986-01-24 | 1989-03-30 | Sanofi Sa | Processo para a preparacao de derivados n alfa-substituidos das n alfa-aril-sulfonilaminoacil d-amidinofenil-alaninamidas |
DE4206858A1 (de) * | 1992-03-05 | 1993-09-09 | Behringwerke Ag | Glycopeptid-derivate, verfahren zu ihrer herstellung und diese verbindungen enthaltende pharmazeutische mittel |
FR2701480B1 (fr) * | 1993-02-15 | 1995-05-24 | Sanofi Elf | Composés à groupe sulfamoyle et amidino, leur procédé de préparation et les compositions pharmaceutiques les contenant. |
US5714497A (en) * | 1993-02-15 | 1998-02-03 | Sanofi | Compounds bearing sulphamoyl and amidino radicals, their preparation process and pharmaceutical compositions containing them |
FR2735128B1 (fr) * | 1995-06-07 | 1997-07-25 | Fournier Ind & Sante | Nouveaux composes de benzenesulfonamide, leur procede de preparation et utilisation en therapeutique. |
FR2743073B1 (fr) * | 1995-12-29 | 1998-02-20 | Fournier Ind & Sante | Nouveaux composes de 1-benzenesulfonylpyrrolidine, procede de preparation et utilisation en therapeutique |
FR2743562B1 (fr) * | 1996-01-11 | 1998-04-03 | Sanofi Sa | Derives de n-(arylsulfonyl) aminoacides, leur preparation, les compositions pharmaceutiques en contenant |
FR2751650B1 (fr) * | 1996-07-24 | 1998-10-09 | Fournier Ind & Sante | Nouveaux composes de n-benzenesulfonyl-l-proline, procede de preparation et utilisation en therapeutique |
FR2756562B1 (fr) * | 1996-12-04 | 1999-01-08 | Fournier Ind & Sante | Nouveaux composes de n-benzenesulfonyl-l-proline, procede de preparation et utilisation en therapeutique |
FR2765222B1 (fr) * | 1997-06-27 | 1999-12-31 | Fournier Ind & Sante | Nouveaux composes de n-benzenesulfonyl-l-proline, procede de preparation et utilisation en therapeutique |
EP1364960A4 (en) * | 2001-02-02 | 2005-05-18 | Chugai Pharmaceutical Co Ltd | PEPTIDE DERIVATIVES |
-
2001
- 2001-01-08 FR FR0100195A patent/FR2819254B1/fr not_active Expired - Fee Related
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2002
- 2002-01-07 IL IL15656502A patent/IL156565A0/xx unknown
- 2002-01-07 BR BR0206159-7A patent/BR0206159A/pt active Pending
- 2002-01-07 SK SK828-2003A patent/SK8282003A3/sk unknown
- 2002-01-07 WO PCT/FR2002/000033 patent/WO2002053516A2/fr not_active Application Discontinuation
- 2002-01-07 KR KR10-2003-7008532A patent/KR20030070080A/ko not_active Application Discontinuation
- 2002-01-07 JP JP2002554636A patent/JP2004534729A/ja active Pending
- 2002-01-07 RU RU2003120798/04A patent/RU2003120798A/ru not_active Application Discontinuation
- 2002-01-07 EP EP02710082A patent/EP1351928A2/fr not_active Withdrawn
- 2002-01-07 MX MXPA03006093A patent/MXPA03006093A/es unknown
- 2002-01-07 PL PL02365219A patent/PL365219A1/xx not_active Application Discontinuation
- 2002-01-07 CZ CZ20031715A patent/CZ20031715A3/cs unknown
- 2002-01-07 HU HU0402507A patent/HUP0402507A2/hu unknown
- 2002-01-07 CN CNA028035194A patent/CN1484633A/zh active Pending
- 2002-01-07 US US10/451,617 patent/US20040063725A1/en not_active Abandoned
- 2002-01-07 CA CA002434124A patent/CA2434124A1/fr not_active Abandoned
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2003
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CN1484633A (zh) | 2004-03-24 |
JP2004534729A (ja) | 2004-11-18 |
MXPA03006093A (es) | 2005-02-14 |
EP1351928A2 (fr) | 2003-10-15 |
FR2819254A1 (fr) | 2002-07-12 |
WO2002053516A2 (fr) | 2002-07-11 |
FR2819254B1 (fr) | 2003-04-18 |
CA2434124A1 (fr) | 2002-07-11 |
IL156565A0 (en) | 2004-01-04 |
WO2002053516A3 (fr) | 2002-10-10 |
KR20030070080A (ko) | 2003-08-27 |
NO20033099D0 (no) | 2003-07-07 |
CZ20031715A3 (cs) | 2003-11-12 |
US20040063725A1 (en) | 2004-04-01 |
SK8282003A3 (en) | 2003-12-02 |
BR0206159A (pt) | 2003-12-23 |
HUP0402507A2 (hu) | 2005-03-29 |
PL365219A1 (en) | 2004-12-27 |
NO20033099L (no) | 2003-09-02 |
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