WO1990015607A1 - Medicament pour l'ameliorations des fonctions cerebrales - Google Patents
Medicament pour l'ameliorations des fonctions cerebrales Download PDFInfo
- Publication number
- WO1990015607A1 WO1990015607A1 PCT/JP1990/000773 JP9000773W WO9015607A1 WO 1990015607 A1 WO1990015607 A1 WO 1990015607A1 JP 9000773 W JP9000773 W JP 9000773W WO 9015607 A1 WO9015607 A1 WO 9015607A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- group
- formula
- lower alkyl
- alkyl group
- salt
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
Definitions
- the present invention relates to a cerebral function-improving agent containing a specific 2-fuunil-3-lyso-2 11-1, 4-benzothiazine derivative, for example, a decrease in cerebral function such as cerebral infarction and transient cerebral ischemia.
- the present invention relates to a brain function-improving agent effective for treating associated diseases.
- Japanese Unexamined Patent Publication (Kokai) No. 62-123181 discloses that a specific 2-phenyl-3-oxo-2H-1,4-benzothiazine derivative represented by the following general formula (I) inhibits the platelet aggregation function, although it is disclosed that it has potent antagonism and is useful as a therapeutic agent for cardiovascular diseases, there is no disclosure that this derivative is useful as a brain function improving agent.
- the present inventors have conducted intensive studies to solve the above problems, and as a result, have found that the compound of the formula (I) described in Japanese Patent Publication No. 62-123181 has an excellent brain function improving effect. Was completed.
- the present invention provides a compound represented by the formula (I):
- R is a hydrogen atom, a lower alkyl group, a halogen atom, a nitro group, a hydroxy group, a lower alkoxy group, a lower alkyloxy group, an amino group, a lower alkylamino group or a lower alkoxy group.
- R 2 represents a hydrogen atom, a lower alkyl group or a cycloalkyl group having 3 to 6 carbon atoms
- R 3 represents a hydrogen atom, a lower alkyl group.
- a brain function-improving agent comprising the compound represented by the formula or a salt thereof as an active ingredient.
- the lower alkyl group refers to an alkyl group having 1 to 6 carbon atoms such as a methyl group, an ethyl group, a propyl group, a hexyl group, etc.
- the halogen atom refers to fluorine or chlorine.
- the lower alkoxy group means methoxy, ethoxy, propoxy
- alkyl group examples include a cyclopropyl group and a cyclohexyl group, and a lower alkylenedioxy group means a group between two oxygen atoms, such as a methylenedioxy group and a c-diethylenedioxy group.
- a lower alkanol group refers to a group such as an acetyl group, a propionyl group, or a hexanol group, in which an alkylene group having up to 6 carbon atoms is present.
- ⁇ o represents an alkanol group having 6 to 6 carbon atoms.
- Examples of the salt of the compound of the formula (I) include hydrochloride, sulfate, phosphate, lactate, maleate, fumarate, oxalate, methansulfonate, and paratoluenesulfonate. And acid addition salts of pharmaceutically acceptable inorganic and organic acids, such as phosphates.
- R is a lower alkoxy group
- R 2 is a lower alkyl group
- R 4 is a lower alkyl group and a salt thereof
- R is a methoxy group
- R 2 is a methyl group
- R 3 is a methylenedioxy group
- R 4 is a methyl group.
- Optical isomers and their salts can be mentioned as having particularly favorable effects.
- the diseases according to the present invention accompanied by a decrease in cerebral function include the above-mentioned 5 disorders such as cerebral infarction and transient cerebral ischemia, as well as sequelae such as cerebral edema and cerebral hemorrhage.
- Brain injury due to trauma such as brain injury and bruise, and central deity such as dementia, psychiatry, neurosis, Alzheimer's disease Menstrual and degenerative diseases and the like can be mentioned.
- Compounds of formula (I) can be prepared by known formulation techniques together with diluents and Z or carriers such as excipients, disintegrants, stabilizers, binders and the like, as well as tablets, capsules, granules, powders, suppositories, Preparations such as injections can be made.
- the compound of the formula (I) can be usually administered orally or parenterally by intravenous injection and the like, and the dose is determined depending on symptoms, dosage form, etc. 5500 mgZ days, preferably 100-100 mgZ, which may be administered once or several times daily.
- the compound of formula (I) was orally administered to rats, and its acute toxicity was examined. As a result, it was confirmed that the compound of formula (I) was highly safe.
- the compound of formula (I) markedly prolonged the survival time of solid death based on brain tissue damage under hypoxia, and showed a potent cerebral protective effect (anti-hypoxia effect).
- the compound of formula (I) markedly ameliorated cerebral energy metabolism disorders and learning and memory disorders in ischemic cerebral ischemia disorders.
- the compound of formula (I) enhanced acetylcholine synthase (ChAT) activity in brain-impaired animals. Therefore, the compound of the formula (I) is excellent as a cerebral dysfunction improving agent, that is, a therapeutic agent for a disease accompanied by a decrease in cerebral function, and also as an ischemic cerebral disease therapeutic agent. is there.
- N 2 gas was introduced at a rate of 5 l / min.
- the time from the start of ventilation to the stop of breathing was measured.
- a representative compound of the present invention is (+) — 3, 4 — dihydro 2 — [5 — methoxy 2 — C 3-[N-methyl-N— [2 — [(3,4—methyloxy) phenyl] amino] probo] phenyl] —4—methyl-3—oxo-1 2H—1,4—benzotin Jin fumarate (Compound A) was used. The results are shown in Table 1 / o
- ATP was measured using ATP-UVtest (Sigma)
- lactate was measured using 1 actate-UVtest (Boehringer-Manhai Iriyamanouchi)
- pyruvate was measured using Pyruvate UVtest (Beilinga-Mannheim Yamanouchi).
- test drug was suspended in a 0.5% aqueous methylcellulose solution and orally administered 30 minutes before ligation.
- the results are shown in Tables 2 and 3.
- the water maze test was performed according to the ischemic load7. Black water was seen in a cylindrical water tank with a diameter of 1.2 m, and the water temperature was maintained at 20: 1. At the midpoint between the center of the aquarium and the wall, an “invisible” (hereinafter referred to as a “stand”) was installed from above the water surface submerged to 2 on below the water surface.
- the water maze test was performed once a day (one session) and for three consecutive days (three sessions).
- the platform was set up and placed on it for 30 seconds to learn if there was an escape from cold water.
- the animals were released four times from four points on the aquarium wall that were set in advance, and the total time (swimming time, seconds) of four trials until climbing to the platform was measured 5 times.
- the animals were left on the table again for 30 seconds to complete the session.
- the total time required for the four trials is limited to a maximum of 180 seconds.
- the session is over.
- the second and third sessions were conducted under the same conditions as the first session except for the first free swim> o.
- Table 4 shows the results.
- the experimental equipment consisted of a bright room with a grid on the floor and a dark room to which an electric shock could be applied through the grid on the floor, with animals free at the border between the two rooms.
- the rat was put in a bright room with the guillotine door closed, and the time until the guillotine door was opened and moved to a dark room 30 seconds later was measured. After confirming that you have moved into the dark room, close the guillotine door and give an electric shock of 0.8 ⁇ for 2 seconds (Shock gener at or / Scrambler SG S-002T, Muromachi Kikai).
- the mean I5 response latency was shorter in the disease control group than in the sham-operated group, indicating that passive avoidance was impaired ( ⁇ 0.01).
- the mean response latency of the group to which Compound ⁇ ⁇ was administered was significantly longer than that of the control group, and the passive avoidance disorder due to cerebral ischemia was remarkably improved. It was shown to have an inhibitory effect.
- Compound A was administered orally to rats, the results of studying the acute toxicity, LD 50 of that was 2 9 3 mgZkg.
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Steroid Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP90909377A EP0429676B1 (en) | 1989-06-16 | 1990-06-14 | Drug for improving brain function |
DE69028603T DE69028603T2 (de) | 1989-06-16 | 1990-06-14 | Arzneimittel für bessere gehirnwirkung |
KR1019910700073A KR0133553B1 (ko) | 1989-06-16 | 1990-06-14 | 뇌기능 개선제 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1/153646 | 1989-06-16 | ||
JP15364689 | 1989-06-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1990015607A1 true WO1990015607A1 (fr) | 1990-12-27 |
Family
ID=15567085
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP1990/000773 WO1990015607A1 (fr) | 1989-06-16 | 1990-06-14 | Medicament pour l'ameliorations des fonctions cerebrales |
Country Status (8)
Country | Link |
---|---|
US (1) | US5182276A (ja) |
EP (1) | EP0429676B1 (ja) |
KR (1) | KR0133553B1 (ja) |
AT (1) | ATE142881T1 (ja) |
CA (1) | CA2032487A1 (ja) |
DE (1) | DE69028603T2 (ja) |
DK (1) | DK0429676T3 (ja) |
WO (1) | WO1990015607A1 (ja) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5182276A (en) * | 1989-06-16 | 1993-01-26 | Santen Pharmaceutical Co., Ltd. | Nootropic agent |
WO2024012554A1 (zh) * | 2022-07-14 | 2024-01-18 | 上海日馨医药科技股份有限公司 | Tpk激动剂及使用其治疗神经退行性疾病的方法 |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EA019020B1 (ru) * | 2011-07-12 | 2013-12-30 | Институт Химических Проблем Им. М.Ф. Нагиева Национальной Академии Наук Азербайджана | Способ лечения нарушений гемостаза при ушибах головного мозга |
Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5518707B1 (ja) * | 1970-10-12 | 1980-05-21 | ||
JPS59148771A (ja) * | 1983-02-09 | 1984-08-25 | Santen Pharmaceut Co Ltd | ベンゾチアジン誘導体 |
JPS60156679A (ja) * | 1983-12-27 | 1985-08-16 | ヘキスト・アクチエンゲゼルシヤフト | ベンゾチアジン誘導体 |
JPS60166674A (ja) * | 1984-02-09 | 1985-08-29 | Santen Pharmaceut Co Ltd | ベンゾチアジン誘導体 |
WO1986005490A1 (en) * | 1985-03-19 | 1986-09-25 | Santen Pharmaceutical Co., Ltd. | 2-arylbenzothiazine derivatives |
WO1987000838A1 (en) * | 1985-07-29 | 1987-02-12 | Santen Pharmaceutical Co., Ltd. | Novel benzothiazine derivatives |
JPS62258370A (ja) * | 1986-04-28 | 1987-11-10 | ヘキスト・アクチエンゲゼルシヤフト | ベンゾチアジノン誘導体 |
JPS62258371A (ja) * | 1986-04-28 | 1987-11-10 | ヘキスト・アクチエンゲゼルシヤフト | ベンゾチアジノン誘導体およびその製造法 |
JPS6357579A (ja) * | 1986-08-27 | 1988-03-12 | Santen Pharmaceut Co Ltd | 3−チオキソ−ベンゾチアジン誘導体 |
JPS6357578A (ja) * | 1986-08-27 | 1988-03-12 | Santen Pharmaceut Co Ltd | ベンゾチアジン誘導体 |
JPS63104969A (ja) * | 1986-10-23 | 1988-05-10 | Santen Pharmaceut Co Ltd | 含硫黄複素環化合物 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3166554A (en) * | 1965-01-19 | Certificate of correction | ||
US3725403A (en) * | 1970-10-20 | 1973-04-03 | Squibb & Sons Inc | Benzothiazine derivatives |
JPS5651465A (en) * | 1979-10-02 | 1981-05-09 | Yoshitomi Pharmaceut Ind Ltd | Benzothiazine derivative |
EP0186310A1 (en) * | 1984-11-28 | 1986-07-02 | Takeda Chemical Industries, Ltd. | 1,4-Benzothiazine Derivatives, their production and use |
US4654372A (en) * | 1986-01-10 | 1987-03-31 | Warner-Lambert Company | Method for using verapamil for treating stroke |
US5182276A (en) * | 1989-06-16 | 1993-01-26 | Santen Pharmaceutical Co., Ltd. | Nootropic agent |
-
1990
- 1990-06-14 US US07/623,657 patent/US5182276A/en not_active Expired - Fee Related
- 1990-06-14 EP EP90909377A patent/EP0429676B1/en not_active Expired - Lifetime
- 1990-06-14 CA CA002032487A patent/CA2032487A1/en not_active Abandoned
- 1990-06-14 KR KR1019910700073A patent/KR0133553B1/ko not_active IP Right Cessation
- 1990-06-14 WO PCT/JP1990/000773 patent/WO1990015607A1/ja active IP Right Grant
- 1990-06-14 DE DE69028603T patent/DE69028603T2/de not_active Expired - Fee Related
- 1990-06-14 DK DK90909377.5T patent/DK0429676T3/da active
- 1990-06-14 AT AT90909377T patent/ATE142881T1/de active
Patent Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5518707B1 (ja) * | 1970-10-12 | 1980-05-21 | ||
JPS59148771A (ja) * | 1983-02-09 | 1984-08-25 | Santen Pharmaceut Co Ltd | ベンゾチアジン誘導体 |
JPS60156679A (ja) * | 1983-12-27 | 1985-08-16 | ヘキスト・アクチエンゲゼルシヤフト | ベンゾチアジン誘導体 |
JPS60166674A (ja) * | 1984-02-09 | 1985-08-29 | Santen Pharmaceut Co Ltd | ベンゾチアジン誘導体 |
WO1986005490A1 (en) * | 1985-03-19 | 1986-09-25 | Santen Pharmaceutical Co., Ltd. | 2-arylbenzothiazine derivatives |
WO1987000838A1 (en) * | 1985-07-29 | 1987-02-12 | Santen Pharmaceutical Co., Ltd. | Novel benzothiazine derivatives |
JPS62258370A (ja) * | 1986-04-28 | 1987-11-10 | ヘキスト・アクチエンゲゼルシヤフト | ベンゾチアジノン誘導体 |
JPS62258371A (ja) * | 1986-04-28 | 1987-11-10 | ヘキスト・アクチエンゲゼルシヤフト | ベンゾチアジノン誘導体およびその製造法 |
JPS6357579A (ja) * | 1986-08-27 | 1988-03-12 | Santen Pharmaceut Co Ltd | 3−チオキソ−ベンゾチアジン誘導体 |
JPS6357578A (ja) * | 1986-08-27 | 1988-03-12 | Santen Pharmaceut Co Ltd | ベンゾチアジン誘導体 |
JPS63104969A (ja) * | 1986-10-23 | 1988-05-10 | Santen Pharmaceut Co Ltd | 含硫黄複素環化合物 |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5182276A (en) * | 1989-06-16 | 1993-01-26 | Santen Pharmaceutical Co., Ltd. | Nootropic agent |
WO2024012554A1 (zh) * | 2022-07-14 | 2024-01-18 | 上海日馨医药科技股份有限公司 | Tpk激动剂及使用其治疗神经退行性疾病的方法 |
Also Published As
Publication number | Publication date |
---|---|
DK0429676T3 (ja) | 1997-03-10 |
EP0429676B1 (en) | 1996-09-18 |
CA2032487A1 (en) | 1990-12-17 |
KR920700645A (ko) | 1992-08-10 |
DE69028603D1 (de) | 1996-10-24 |
EP0429676A1 (en) | 1991-06-05 |
EP0429676A4 (en) | 1992-05-20 |
DE69028603T2 (de) | 1997-02-13 |
ATE142881T1 (de) | 1996-10-15 |
US5182276A (en) | 1993-01-26 |
KR0133553B1 (ko) | 1998-04-23 |
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