CN100522954C - 含有2-苯基苯并噻唑啉衍生物的к-阿片样物质受体激动剂 - Google Patents

含有2-苯基苯并噻唑啉衍生物的к-阿片样物质受体激动剂 Download PDF

Info

Publication number
CN100522954C
CN100522954C CNB2006101392068A CN200610139206A CN100522954C CN 100522954 C CN100522954 C CN 100522954C CN B2006101392068 A CNB2006101392068 A CN B2006101392068A CN 200610139206 A CN200610139206 A CN 200610139206A CN 100522954 C CN100522954 C CN 100522954C
Authority
CN
China
Prior art keywords
phenyl
compound
methoxy
ethanoyl
propoxy
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Fee Related
Application number
CNB2006101392068A
Other languages
English (en)
Chinese (zh)
Other versions
CN1911918A (zh
Inventor
东海真树
本田崇宏
丹羽昌史
大隅八重子
藤村健一
河野慎一
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Step Pharmaceutical Co Ltd
Original Assignee
Santen Pharmaceutical Co Ltd
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
Application filed by Santen Pharmaceutical Co Ltd filed Critical Santen Pharmaceutical Co Ltd
Publication of CN1911918A publication Critical patent/CN1911918A/zh
Application granted granted Critical
Publication of CN100522954C publication Critical patent/CN100522954C/zh
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic 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
    • C07D417/02Heterocyclic 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
    • C07D417/12Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425Thiazoles
    • A61K31/428Thiazoles condensed with carbocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/04Antipruritics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/06Antigout agents, e.g. antihyperuricemic or uricosuric agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/60Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
    • C07D277/62Benzothiazoles
    • C07D277/64Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2
    • C07D277/66Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2 with aromatic rings or ring systems directly attached in position 2
CNB2006101392068A 2002-03-29 2003-03-28 含有2-苯基苯并噻唑啉衍生物的к-阿片样物质受体激动剂 Expired - Fee Related CN100522954C (zh)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP097500/2002 2002-03-29
JP2002097500 2002-03-29

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
CN038072750A Division CN1642929B (zh) 2002-03-29 2003-03-28 含有2-苯基苯并噻唑啉衍生物的κ-阿片样物质受体激动剂

Publications (2)

Publication Number Publication Date
CN1911918A CN1911918A (zh) 2007-02-14
CN100522954C true CN100522954C (zh) 2009-08-05

Family

ID=28671920

Family Applications (2)

Application Number Title Priority Date Filing Date
CNB2006101392068A Expired - Fee Related CN100522954C (zh) 2002-03-29 2003-03-28 含有2-苯基苯并噻唑啉衍生物的к-阿片样物质受体激动剂
CN038072750A Expired - Fee Related CN1642929B (zh) 2002-03-29 2003-03-28 含有2-苯基苯并噻唑啉衍生物的κ-阿片样物质受体激动剂

Family Applications After (1)

Application Number Title Priority Date Filing Date
CN038072750A Expired - Fee Related CN1642929B (zh) 2002-03-29 2003-03-28 含有2-苯基苯并噻唑啉衍生物的κ-阿片样物质受体激动剂

Country Status (10)

Country Link
US (2) US7112598B2 (US20060205796A1-20060914-C00073.png)
EP (2) EP1496053B1 (US20060205796A1-20060914-C00073.png)
JP (1) JP5061134B2 (US20060205796A1-20060914-C00073.png)
KR (1) KR101035931B1 (US20060205796A1-20060914-C00073.png)
CN (2) CN100522954C (US20060205796A1-20060914-C00073.png)
AU (2) AU2003220894B8 (US20060205796A1-20060914-C00073.png)
CA (1) CA2480560C (US20060205796A1-20060914-C00073.png)
ES (1) ES2390052T3 (US20060205796A1-20060914-C00073.png)
NZ (1) NZ535987A (US20060205796A1-20060914-C00073.png)
WO (1) WO2003082840A1 (US20060205796A1-20060914-C00073.png)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1642590A4 (en) * 2003-07-04 2009-05-13 Santen Pharmaceutical Co Ltd MEANS TO INHIBIT THE DEGRADATION OF THE PAIN LIMIT
US7642274B2 (en) 2004-07-02 2010-01-05 Santen Pharmaceutical Co., Ltd. Inhibitor of pain threshold decrease
EP1849465A4 (en) * 2005-02-18 2008-12-24 Takeda Pharmaceutical AGENT FOR CONTROLLING THE FUNCTION OF THE GPR34 RECEPTOR
US9303027B2 (en) 2010-07-19 2016-04-05 Dr. Reddy's Laboratories Ltd. Kappa opioid receptor agonists
CN104271552B (zh) 2012-03-05 2017-08-08 雷迪博士实验室有限公司 作为kappa阿片样物质受体(kor)激动剂的取代的杂环乙酰胺
JP6275517B2 (ja) 2013-03-22 2018-02-07 あゆみ製薬株式会社 Il−2産生抑制
WO2015093567A1 (ja) 2013-12-18 2015-06-25 国立大学法人京都大学 疼痛に関する化合物及び医薬組成物
WO2018230711A1 (ja) 2017-06-16 2018-12-20 学校法人同志社 mTORインヒビターを含む、眼の症状、障害または疾患を治療または予防するための医薬およびその応用
US20200121652A1 (en) 2017-06-16 2020-04-23 The Doshisha Compounds having caspase inhibitory activity, pharmaceutical agent containing said compounds and for treating or preventing corneal endothelial symptoms, disorders, or diseases, and application of said pharmaceutical agent

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4479949A (en) * 1981-09-12 1984-10-30 Santen Pharmaceutical Co., Ltd. Benzothiazoline compounds
US4547513A (en) * 1983-12-27 1985-10-15 Santen Pharmaceutical Co., Ltd. 2-Arylbenzothiazoline derivatives and their use in treating angina cordis

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US547513A (en) * 1895-10-08 Chell
JPS4994667A (US20060205796A1-20060914-C00073.png) * 1973-01-23 1974-09-09
JPS5967276A (ja) 1982-09-01 1984-04-16 Santen Pharmaceut Co Ltd ベンゾチアゾリン誘導体
JPS6183175A (ja) * 1984-09-06 1986-04-26 Santen Pharmaceut Co Ltd ベンゾチアゾリン誘導体およびそれを主成分とする循環器官用薬剤
JPS62221679A (ja) 1986-03-19 1987-09-29 Santen Pharmaceut Co Ltd ベンゾチアゾリン誘導体
JPH066581B2 (ja) * 1986-03-19 1994-01-26 参天製薬株式会社 フエノキシアルキルアミン側鎖を有するベンゾチアゾリン誘導体
JPH08231399A (ja) * 1995-02-23 1996-09-10 Shionogi & Co Ltd モルヒネ禁断抑制作用剤
US6174891B1 (en) * 1996-11-25 2001-01-16 Toray Industries, Inc. Antipruritic agent
JP2000344821A (ja) 1999-06-01 2000-12-12 Toagosei Co Ltd オレフィン重合用触媒

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4479949A (en) * 1981-09-12 1984-10-30 Santen Pharmaceutical Co., Ltd. Benzothiazoline compounds
US4547513A (en) * 1983-12-27 1985-10-15 Santen Pharmaceutical Co., Ltd. 2-Arylbenzothiazoline derivatives and their use in treating angina cordis

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
novel calcium antagonists. synthesis and structure-activityrelationship studies of benzothiazoline derivatives. Yamamoto, K.Journal of medicinal chemistry,Vol.31 No.5. 1988
novel calcium antagonists. synthesis and structure-activityrelationship studies of benzothiazoline derivatives. Yamamoto, K.Journal of medicinal chemistry,Vol.31 No.5. 1988 *
synthesis and calcium antagonistic activity of (+)-R-and(-)-(s)-3-acetyl-2-[5-methoxy-2-[4-[N-methyl-N-(3,4,5-trimethoxyphene-thyl)amino]butoxy]phenyl]benzothiazolinehydrochloride. Fujita,M.chemical & pharmaceutical bulletin,Vol.38 No.4. 1990

Also Published As

Publication number Publication date
US7410987B2 (en) 2008-08-12
CN1642929A (zh) 2005-07-20
JP5061134B2 (ja) 2012-10-31
WO2003082840A1 (en) 2003-10-09
US20050113430A1 (en) 2005-05-26
EP1496053A1 (en) 2005-01-12
EP2042173A2 (en) 2009-04-01
ES2390052T3 (es) 2012-11-06
CN1911918A (zh) 2007-02-14
CN1642929B (zh) 2010-05-12
KR20040095329A (ko) 2004-11-12
NZ535987A (en) 2006-08-31
US7112598B2 (en) 2006-09-26
EP1496053B1 (en) 2012-06-20
AU2009201233B2 (en) 2012-07-05
CA2480560C (en) 2011-02-15
JP2009143940A (ja) 2009-07-02
AU2003220894B2 (en) 2009-02-05
EP2042173A3 (en) 2010-02-24
AU2003220894B8 (en) 2009-02-19
US20060205796A1 (en) 2006-09-14
CA2480560A1 (en) 2003-10-09
AU2009201233A1 (en) 2009-04-23
AU2003220894A1 (en) 2003-10-13
KR101035931B1 (ko) 2011-05-23
EP1496053A4 (en) 2008-01-16

Similar Documents

Publication Publication Date Title
CN109219604B (zh) 四氢异喹啉雌激素受体调节剂及其用途
JP5010917B2 (ja) c−Kit調節因子および使用方法
CN110167924A (zh) 用于治疗ezh2介导的癌症的组合物和方法
AP765A (en) Ziprasidone mesylate dihydrates and its uses as dopamine D2 atagonists.
NZ332219A (en) Mesylate trihydrate salt of 5-(2-(4-(1,2-benzisothiazol-3-yl)-1-piperazinyl)-ethyl)-6-chloro-1,3-dihydro-2(1H)-indol-2-one (ziprasidone), its preparation and its use as dopamine D2 antagonist
WO2012016133A2 (en) Ros1 kinase inhibitors for the treatment of glioblastoma and other p53-deficient cancers
CN101573340A (zh) 糖皮质激素受体AP-1和/或NF-κB活性的调节剂及其用途
CN100522954C (zh) 含有2-苯基苯并噻唑啉衍生物的к-阿片样物质受体激动剂
CN106536491B (zh) 作为盐皮质激素受体调节剂的苯并噁嗪酮酰胺
CN104837839A (zh) 作为多巴胺d1配体的杂芳族化合物
JP2023071905A (ja) 癌を処置するためのezh2阻害剤
KR970701719A (ko) 헤테로고리화합물과 그것의 제법 및 사용(heterocyclic compounds, their preparation and use)
US20200347031A1 (en) Novel usp7 inhibitors for treating multiple myeloma
WO2023083194A1 (zh) Wee1蛋白激酶降解剂及其用途
US5696115A (en) Method for treating nicotine withdrawal
JP4296345B2 (ja) 2−フェニルベンゾチアゾリン誘導体
CN110088098A (zh) 喹唑啉酮类parp-1抑制剂及其制备方法、药物组合物和用途
CN104520298A (zh) 用于治疗脆性x染色体综合征、帕金森病或返流疾病的二吖庚因酮衍生物
CA3180317A1 (en) Small molecule antiviral drug treatment for human papillomavirus infections
CN101432287A (zh) 用作hsp90抑制剂的吡咯并嘧啶衍生物
JP2004002352A6 (ja) 2−フェニルベンゾチアゾリン誘導体からなるκオピオイド受容体アゴニスト
CN104193731A (zh) 新型脲取代联苯类化合物及其组合物及用途
JPH04356466A (ja) 新規キノリン誘導体及びそれを有効成分として含有する制癌剤効果増強剤
NZ508304A (en) Mesylate dihydrate salt of 5-(2-(4-(1,2 benzisothiazol-3-yl)-1-piperazinyl)ethyl)-6-chloro-1,3-dihydro-2(1H)-indol-2-one ( ziprasidone) useful as dopamine D2 antagonist

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C41 Transfer of patent application or patent right or utility model
TR01 Transfer of patent right

Effective date of registration: 20160321

Address after: Tokyo, Japan, Japan

Patentee after: Step Pharmaceutical Company Limited

Address before: Osaka Japan

Patentee before: Santen Pharmaceutical Co., Ltd.

CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20090805

Termination date: 20180328

CF01 Termination of patent right due to non-payment of annual fee