ATE184593T1 - Aminosäurederivate und ihre verwendung als phospholipase-a2-inhibitoren - Google Patents

Aminosäurederivate und ihre verwendung als phospholipase-a2-inhibitoren

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Publication number
ATE184593T1
ATE184593T1 AT95906504T AT95906504T ATE184593T1 AT E184593 T1 ATE184593 T1 AT E184593T1 AT 95906504 T AT95906504 T AT 95906504T AT 95906504 T AT95906504 T AT 95906504T AT E184593 T1 ATE184593 T1 AT E184593T1
Authority
AT
Austria
Prior art keywords
pct
fatty acid
acid derivative
phospholipase
inhibitors
Prior art date
Application number
AT95906504T
Other languages
English (en)
Inventor
Shigehiro Takase
Nobuharu Shigematsu
Seiji Yoshimura
Satoshi Okada
Keiji Hemmi
Hirokazu Tanaka
Takanao Otsuka
Yasuhisa Tsurumi
Masanori Okamoto
Masakuni Okuhara
Naoki Fukami
Original Assignee
Fujisawa Pharmaceutical Co
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
Priority claimed from GB9401268A external-priority patent/GB9401268D0/en
Priority claimed from GB9421962A external-priority patent/GB9421962D0/en
Application filed by Fujisawa Pharmaceutical Co filed Critical Fujisawa Pharmaceutical Co
Application granted granted Critical
Publication of ATE184593T1 publication Critical patent/ATE184593T1/de

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    • 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
    • C07D213/24—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 substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/36—Radicals substituted by singly-bound nitrogen atoms
    • C07D213/40—Acylated substituent nitrogen atom
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    • C07C271/06—Esters of carbamic acids
    • C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C271/22—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by carboxyl groups
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    • C07C271/06—Esters of carbamic acids
    • C07C271/40—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings
    • C07C271/42—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C271/54—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by carboxyl groups
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    • C07C275/16—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms of an acyclic and saturated carbon skeleton being further substituted by carboxyl groups
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    • C07C311/30—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/37—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
    • C07C311/38—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring having sulfur atoms of sulfonamide groups and amino groups bound to carbon atoms of six-membered rings of the same carbon skeleton
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    • C07D215/38—Nitrogen atoms
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    • C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
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    • C07D217/06—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines with the ring nitrogen atom acylated by carboxylic or carbonic acids, or with sulfur or nitrogen analogues thereof, e.g. carbamates
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    • 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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    • C07D241/40—Benzopyrazines
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    • C07D263/54—Benzoxazoles; Hydrogenated benzoxazoles
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    • C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
    • C07D317/50—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to atoms of the carbocyclic ring
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    • 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

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AT95906504T 1994-01-24 1995-01-23 Aminosäurederivate und ihre verwendung als phospholipase-a2-inhibitoren ATE184593T1 (de)

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AU708306B2 (en) * 1995-07-24 1999-07-29 Fujisawa Pharmaceutical Co., Ltd. Esters and amides as PLA2 inhibitors
KR19990035780A (ko) * 1995-07-24 1999-05-25 후지야마 아키라 Ｐｌａ２ 억제제로서의 에스테르 및 아미드
AU2001272234B2 (en) * 2000-07-24 2006-06-01 The University Of Queensland Compounds and inhibitors of phospholipases
CA2417127A1 (en) 2000-07-24 2002-01-31 The University Of Queensland Compounds and inhibitors of phospholipases
WO2003101177A2 (en) * 2002-06-04 2003-12-11 Sequenom, Inc. Diagnosing predisposition to fat deposition and therapeutic methods for reducing fat deposition and treatment of associated conditions
AUPS282602A0 (en) 2002-06-07 2002-06-27 Garvan Institute Of Medical Research Method of inhibiting cell proliferation
EP1581095A4 (de) * 2002-06-27 2006-10-18 Harkness Pharmaceuticals Inc Therapeutische methoden zur reduzierung der fettablagerung und zur behandlung von damit einhergehenden erkrankungen
US7045547B2 (en) * 2002-08-20 2006-05-16 University Of Delaware Acyl-CoA dehydrogenase allenic inhibitors
US20050008607A1 (en) * 2003-06-05 2005-01-13 L'oreal Composition containing a carbonyl amine
WO2007022443A2 (en) * 2005-08-17 2007-02-22 The Regents Of The University Of California Systemic and intrathecal effects of a novel series of phospholipase a2 inhibitors on hyperalgesia and spinal pge2 release
US8420852B2 (en) 2007-07-06 2013-04-16 The Regents Of The University Of California Phospholipase A2 inhibitors and their use in treating neurological injury and disease
EP2923710A1 (de) 2014-03-27 2015-09-30 Universitätsklinikum Heidelberg Bakterielle Phospholipase-Inhibitoren als Modulatoren von Dickdarmbakterienflora

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EP0336356A3 (de) * 1988-04-05 1991-09-25 Abbott Laboratories Tryptophan-Derivate, verwendbar als CCK-Gegner
JP2831800B2 (ja) * 1990-02-23 1998-12-02 日本エマルジョン株式會社 油溶性ｎ―長鎖アシル酸性アミノ酸エステル、その混合物及びこれらを含む香粧品
EP0533882B1 (de) * 1991-04-03 2001-02-07 Korea Research Institute Of Chemical Technology 2-chinolinonderivate, verfahren zu deren herstellung und diese enthaltende fungizide und insektizide
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