SG68683G - Enzyme inhibitory phthalazin-4-ylacetic acid derivatives,pharmaceutical compositions thereof,and process for their manufacture - Google Patents
Enzyme inhibitory phthalazin-4-ylacetic acid derivatives,pharmaceutical compositions thereof,and process for their manufactureInfo
- Publication number
- SG68683G SG68683G SG68683A SG68683A SG68683G SG 68683 G SG68683 G SG 68683G SG 68683 A SG68683 A SG 68683A SG 68683 A SG68683 A SG 68683A SG 68683 G SG68683 G SG 68683G
- Authority
- SG
- Singapore
- Prior art keywords
- phthalazin
- manufacture
- pharmaceutical compositions
- acid derivatives
- enzyme inhibitory
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
-
- 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]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/26—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings condensed with carbocyclic rings or ring systems
- C07D237/30—Phthalazines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/26—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings condensed with carbocyclic rings or ring systems
- C07D237/30—Phthalazines
- C07D237/32—Phthalazines with oxygen atoms directly attached to carbon atoms of the nitrogen-containing ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/87—Benzo [c] furans; Hydrogenated benzo [c] furans
- C07D307/88—Benzo [c] furans; Hydrogenated benzo [c] furans with one oxygen atom directly attached in position 1 or 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/04—Ortho-condensed systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Diabetes (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic 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)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB5414277 | 1977-12-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
SG68683G true SG68683G (en) | 1984-08-03 |
Family
ID=10470067
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG68683A SG68683G (en) | 1977-12-29 | 1983-11-11 | Enzyme inhibitory phthalazin-4-ylacetic acid derivatives,pharmaceutical compositions thereof,and process for their manufacture |
Country Status (31)
Country | Link |
---|---|
US (2) | US4251528A (fr) |
EP (1) | EP0002895B1 (fr) |
JP (2) | JPS5495582A (fr) |
AT (1) | AT365581B (fr) |
AU (1) | AU516264B2 (fr) |
BG (1) | BG34336A3 (fr) |
CA (1) | CA1107732A (fr) |
CS (1) | CS241015B2 (fr) |
CY (1) | CY1219A (fr) |
DD (1) | DD141021A5 (fr) |
DE (1) | DE2861170D1 (fr) |
DK (1) | DK151253C (fr) |
ES (1) | ES476496A1 (fr) |
FI (1) | FI64357C (fr) |
GR (1) | GR65303B (fr) |
HK (1) | HK22484A (fr) |
HU (1) | HU182585B (fr) |
IE (1) | IE47592B1 (fr) |
IL (1) | IL56099A0 (fr) |
IN (1) | IN150196B (fr) |
IT (1) | IT1110885B (fr) |
MY (1) | MY8500359A (fr) |
NO (1) | NO154346C (fr) |
NZ (1) | NZ189034A (fr) |
PH (1) | PH15435A (fr) |
PL (1) | PL118443B1 (fr) |
PT (1) | PT68956A (fr) |
SG (1) | SG68683G (fr) |
SU (3) | SU1087075A3 (fr) |
YU (3) | YU41607B (fr) |
ZW (1) | ZW24978A1 (fr) |
Families Citing this family (51)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IE47592B1 (en) * | 1977-12-29 | 1984-05-02 | Ici Ltd | Enzyme inhibitory phthalazin-4-ylacetic acid derivatives, pharmaceutical compositions thereof,and process for their manufacture |
CA1143733A (fr) * | 1979-07-31 | 1983-03-29 | Masao Yoshida | Obtention de 7-alcoxycarbonyl-6,8-dimethyl-4- hydroxymethyl-1-phtalazone, et de produits intermediaires |
US4762839A (en) * | 1985-06-06 | 1988-08-09 | Tanabe Seiyaku Co., Ltd. | Quinazolinone copmpounds useful for the prophyloxis and treatment of diabetic complications |
DE3684410D1 (de) * | 1985-11-07 | 1992-04-23 | Pfizer | Heterocyclische oxophthalazinylessigsaeure. |
JPS63132889A (ja) * | 1986-11-21 | 1988-06-04 | Tanabe Seiyaku Co Ltd | キナゾリノン誘導体 |
US5011840A (en) * | 1986-11-24 | 1991-04-30 | Pfizer Inc. | Imidazolidinedione derivatives in diabetes treatment |
GB8704569D0 (en) * | 1987-02-26 | 1987-04-01 | Ici America Inc | Therapeutic agent |
JPH0676391B2 (ja) * | 1987-06-09 | 1994-09-28 | フアイザー・インコーポレイテツド | ベンゾチアゾール等の複素環側鎖を有するオキソフタラジニル酢酸類の製造方法 |
US4868301A (en) * | 1987-06-09 | 1989-09-19 | Pfizer Inc. | Processes and intermediates for the preparation of oxophthalazinyl acetic acids having benzothiazole or other heterocyclic side chains |
NZ226696A (en) * | 1987-11-02 | 1991-10-25 | Merck & Co Inc | Tablet composition comprising a phthalazine acetic acid derivative as the active ingredient present in from 83-88 wt% |
DK607188A (da) * | 1987-11-02 | 1989-06-22 | Merck & Co Inc | Tablet indeholdende en phthalazineddikesyreforbindelse |
US4880928A (en) * | 1987-12-21 | 1989-11-14 | Merck & Co., Inc. | Process for the preparation of 3-((4-bromo-2-fluorophenyl)methyl)-3,4-dihydro-4-oxo-1-phthalazine-acetic acid |
US4940791A (en) * | 1988-02-29 | 1990-07-10 | Pfizer Inc. | Process for the production of phthalazineacetic acid ester derivatives and a novel hydrazine containing intermediate |
US4904782A (en) * | 1988-02-29 | 1990-02-27 | Pfizer Inc. | Process for the production of phthalazineacetic acid ester derivatives and a novel intermediate |
US4954629A (en) * | 1989-05-11 | 1990-09-04 | Pfizer Inc. | Process and intermediates for the preparation of oxophthalazinyl acetic acids and analogs thereof |
US4996204A (en) * | 1989-05-11 | 1991-02-26 | Pfizer Inc. | Pyrido[2,3-d]pyridazinones as aldose reductase inhibitors |
EP0397930A1 (fr) * | 1989-05-18 | 1990-11-22 | Merck & Co. Inc. | Procédé de préparation de l'acide 3-[(4-bromo-2-fluorophényl)méthyl]-3,4-dihydro-4-oxo-1-phtalazine acétique |
FR2647676A1 (fr) * | 1989-06-05 | 1990-12-07 | Union Pharma Scient Appl | Nouveaux derives de pyridazinone, leurs procedes de preparation, medicaments les contenant, utiles notamment comme inhibiteurs de l'aldose reductase |
US5304557A (en) * | 1989-12-15 | 1994-04-19 | Pfizer Inc. | Substituted oxoophthalazinyl acetic acids and analogs thereof |
US5037831A (en) * | 1990-05-21 | 1991-08-06 | American Home Products Corporation | Spiro-isoquinoline-pyrrolidines and analogs thereof useful as aldose reductase inhibitors |
FR2682108B1 (fr) * | 1991-10-07 | 1994-01-07 | Lipha | Acide 3,4-dihydro-4-oxo-3(prop-2-enyl)-1-phtalazineacetiques et derives, leurs preparations et medicaments les contenant. |
AU683620B2 (en) * | 1992-09-28 | 1997-11-20 | Pfizer Inc. | Substituted pyrimidines for control of diabetic complications |
EP0666851A4 (en) * | 1992-11-02 | 1995-08-30 | Merck & Co. Inc. | Substituted phthalazinones as nerotensin antagonists. |
CH683965A5 (it) * | 1993-02-19 | 1994-06-30 | Limad Marketing Exp & Imp | Composti della classe dei ftalidrazidici come sostanza attiva in agenti antinfiammatori ed antitossici. |
WO1995003053A1 (fr) * | 1993-07-26 | 1995-02-02 | Fujisawa Pharmaceutical Co., Ltd. | Oxophtalazine de traitement de la cachexie |
US6696407B1 (en) | 1997-03-21 | 2004-02-24 | The Regents Of The University Of California | Huntington's disease treatment comprising administering aldose reductase inhibitors to increase striatal CNTF |
AU6473898A (en) * | 1997-03-21 | 1998-10-20 | Regents Of The University Of California, The | Methods for modulating neurotrophic factor-associated activity using aldose reductase inhibitors |
EP1598054B1 (fr) * | 1997-04-15 | 2011-03-16 | Csir | Méthodes non-thérapeutiques pour réduire l'appétit |
CN1205207C (zh) * | 1998-03-31 | 2005-06-08 | 药品发现学会公司 | 取代的吲哚链烷酸 |
TNSN99224A1 (fr) * | 1998-12-01 | 2005-11-10 | Inst For Pharm Discovery Inc | Methodes de reduction des niveaux de glucose et triglyceride en serum et pour suppression de l'antigenese utilisant les acides la indolealkanoique |
GB2396815B (en) * | 1999-10-27 | 2004-09-08 | Phytopharm Plc | A composition comprising a pregnenone derivative and an NSAID |
DE19963607B4 (de) * | 1999-12-23 | 2005-12-15 | Schering Ag | Verfahren zur Herstellung von 4-(Heteroaryl-methyl) halogen-1(2H)-phthalazinonen |
GB2363985B (en) | 2000-06-30 | 2004-09-29 | Phytopharm Plc | Extracts,compounds & pharmaceutical compositions having anti-diabetic activity and their use |
AU2002215160A1 (en) * | 2000-11-30 | 2002-06-11 | Pfizer Products Inc. | Combination of gaba agonists and aldose reductase inhibitors |
DE60204611T2 (de) | 2001-02-28 | 2006-05-11 | Pfizer Products Inc., Groton | Sulfonyl-pyridazinon-derivate zur Verwendung als Aldose-reduktase-inhibitoren |
AU2002226634B2 (en) * | 2001-03-30 | 2007-01-25 | Pfizer Products Inc. | Pyridazinone aldose reductase inhibitors |
HUP0303920A3 (en) * | 2001-04-30 | 2004-07-28 | Pfizer Prod Inc | Pharmaceutical compositions containing combinations of aldose reductase inhibitor pyridazinons and cyclooxygenase 2 inhibitors |
AU761191B2 (en) | 2001-05-24 | 2003-05-29 | Pfizer Products Inc. | Therapies for tissue damage resulting from ischemia |
US20050209237A1 (en) * | 2002-04-30 | 2005-09-22 | Brazzell Romulus K | Method for decreasing capillary permeability in the retina |
KR20050026002A (ko) * | 2002-07-26 | 2005-03-14 | 디 인스티튜트스 포 파마슈티컬 디스커버리, 엘엘씨 | 치환된 인돌알칸산 유도체 및 이를 함유하는 당뇨 합병증치료용 제형 |
US7572910B2 (en) * | 2003-02-20 | 2009-08-11 | Pfizer, Inc. | Pyridazinone aldose reductase inhibitors |
US20110092566A1 (en) * | 2004-11-19 | 2011-04-21 | Srivastava Satish K | Treatment of cancer with aldose reductase inhibitors |
JP4838582B2 (ja) * | 2004-12-27 | 2011-12-14 | 岐阜プラスチック工業株式会社 | 台車用本体 |
JP2010520913A (ja) | 2007-03-12 | 2010-06-17 | サズセ アーペーエス | ルイボスの抗糖尿病性抽出物 |
CA2685202C (fr) | 2007-03-23 | 2017-11-28 | The Board Of Regents Of The University Of Texas System | Methodes de traitement de l'asthme allergique |
US20090270490A1 (en) * | 2008-04-24 | 2009-10-29 | The Board Of Regents Of The University Of Texas System | Methods involving aldose reductase inhibition |
AU2011348074B2 (en) | 2010-12-23 | 2016-04-28 | The Board Of Regents Of The University Of Texas System | Methods for treating COPD |
CA2895162C (fr) | 2012-12-14 | 2021-03-09 | D. Lynn Kirkpatrick | Procedes et compositions pour l'inhibition de cnksr1 |
US10227356B2 (en) | 2015-04-20 | 2019-03-12 | Phusis Therapeutics, Inc. | Compounds, compositions and methods for inhibiting CNKSR1 |
EP3862160A4 (fr) * | 2018-10-04 | 2022-08-10 | Nitto Denko Corporation | Feuille de protection amovible résistante à la chaleur et procédé de liage par thermo-compression |
JP6751974B1 (ja) * | 2019-10-16 | 2020-09-09 | 株式会社コバヤシ | 離型フィルム及び離型フィルムの製造方法 |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3833579A (en) * | 1935-11-11 | 1974-09-03 | Inoue Michiro | 4-carbamoyl phthalazones |
JPS5116430B2 (fr) * | 1971-08-05 | 1976-05-24 | ||
GB1398549A (en) * | 1972-11-06 | 1975-06-25 | Boots Co Ltd | Phthalazine derivatives and their use in pharmaceutical compo sitions |
AR205004A1 (es) * | 1973-10-30 | 1976-03-31 | Ishikawa M | Procedimiento para preparar derivados de 6,8-dialquil-7-alcoxi-carbonil-4-hidroximetil-1-ftalazona y la 7,8-lactona |
DE2451117A1 (de) * | 1973-10-31 | 1975-05-22 | Boots Co Ltd | Therapeutisch wirksame verbindungen |
GB1502312A (en) | 1975-03-20 | 1978-03-01 | Ici Ltd | Quinolone derivatives |
IE43079B1 (en) * | 1975-03-20 | 1980-12-17 | Ici Ltd | Quinolone derivatives |
JPS5214788A (en) * | 1975-07-21 | 1977-02-03 | Fuji Photo Film Co Ltd | Process for preparing phthalazinone and its derivatives |
NL7702763A (nl) * | 1976-03-18 | 1977-09-20 | Takio Shimamoto En Masayuki Is | Werkwijze voor de bereiding van thromboxaan- -antagonisten en van preparaten die deze stof- fen bevatten. |
IE47592B1 (en) * | 1977-12-29 | 1984-05-02 | Ici Ltd | Enzyme inhibitory phthalazin-4-ylacetic acid derivatives, pharmaceutical compositions thereof,and process for their manufacture |
US4293553A (en) * | 1978-08-11 | 1981-10-06 | Masayuki Ishikawa | 1-Phthalazone derivatives, and use thereof |
-
1978
- 1978-11-27 IE IE2337/78A patent/IE47592B1/en not_active IP Right Cessation
- 1978-11-28 NZ NZ189034A patent/NZ189034A/xx unknown
- 1978-11-28 IN IN860/DEL/78A patent/IN150196B/en unknown
- 1978-11-29 AU AU42040/78A patent/AU516264B2/en not_active Expired
- 1978-11-29 US US05/964,725 patent/US4251528A/en not_active Expired - Lifetime
- 1978-11-30 IL IL56099A patent/IL56099A0/xx not_active IP Right Cessation
- 1978-11-30 DK DK541878A patent/DK151253C/da not_active IP Right Cessation
- 1978-12-01 DE DE7878300720T patent/DE2861170D1/de not_active Expired
- 1978-12-01 CY CY1219A patent/CY1219A/xx unknown
- 1978-12-01 EP EP78300720A patent/EP0002895B1/fr not_active Expired
- 1978-12-06 PH PH21901A patent/PH15435A/en unknown
- 1978-12-12 GR GR57849A patent/GR65303B/el unknown
- 1978-12-14 FI FI783844A patent/FI64357C/fi not_active IP Right Cessation
- 1978-12-16 PL PL1978222157A patent/PL118443B1/pl unknown
- 1978-12-20 SU SU782698853A patent/SU1087075A3/ru active
- 1978-12-20 PT PT68956A patent/PT68956A/pt not_active IP Right Cessation
- 1978-12-21 JP JP15695378A patent/JPS5495582A/ja active Granted
- 1978-12-21 CA CA318,345A patent/CA1107732A/fr not_active Expired
- 1978-12-22 HU HU78IE856A patent/HU182585B/hu not_active IP Right Cessation
- 1978-12-26 BG BG7841857A patent/BG34336A3/xx unknown
- 1978-12-28 ZW ZW249/78A patent/ZW24978A1/xx unknown
- 1978-12-28 NO NO784397A patent/NO154346C/no unknown
- 1978-12-28 IT IT52480/78A patent/IT1110885B/it active
- 1978-12-28 CS CS789084A patent/CS241015B2/cs unknown
- 1978-12-29 YU YU3127/78A patent/YU41607B/xx unknown
- 1978-12-29 AT AT0937678A patent/AT365581B/de not_active IP Right Cessation
- 1978-12-29 ES ES476496A patent/ES476496A1/es not_active Expired
- 1978-12-29 DD DD78210284A patent/DD141021A5/de not_active IP Right Cessation
-
1980
- 1980-10-06 US US06/194,211 patent/US4393062A/en not_active Expired - Lifetime
-
1981
- 1981-12-04 SU SU813359216A patent/SU1272984A3/ru active
- 1981-12-04 SU SU813359636A patent/SU1072803A3/ru active
-
1982
- 1982-10-14 YU YU2321/82A patent/YU42807B/xx unknown
- 1982-10-14 YU YU2320/82A patent/YU42054B/xx unknown
-
1983
- 1983-11-11 SG SG68683A patent/SG68683G/en unknown
-
1984
- 1984-03-15 HK HK224/84A patent/HK22484A/xx unknown
-
1985
- 1985-12-30 MY MY359/85A patent/MY8500359A/xx unknown
-
1987
- 1987-10-28 JP JP62270508A patent/JPS63119469A/ja active Granted
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