ID23891A - Senyawa heterosiklik tersubstitusi tergabung - Google Patents

Senyawa heterosiklik tersubstitusi tergabung

Info

Publication number: ID23891A
Authority: ID; Indonesia
Prior art keywords: group; hydrogen atom; heterosiclic; compounds; chem
Prior art date: 1997-10-08

Application number

IDW20000649A

Other languages

English (en)

Indonesian (id)

Inventor

Takashi Fujita

Kunio Wada

Toshihiko Fujiwara

Original Assignee

Sankyo 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.)

1997-10-08

Filing date

1998-10-08

Publication date

2000-05-25

1998-10-08 Application filed by Sankyo Co filed Critical Sankyo Co

2000-05-25 Publication of ID23891A publication Critical patent/ID23891A/id

Links

150000001875 compounds Chemical class 0.000 title 1
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
230000002401 inhibitory effect Effects 0.000 abstract 2
229910052760 oxygen Inorganic materials 0.000 abstract 2
239000001301 oxygen Substances 0.000 abstract 2
229910052717 sulfur Inorganic materials 0.000 abstract 2
125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
125000003161 (C1-C6) alkylene group Chemical group 0.000 abstract 1
-1 2,4-dioxothiazolidin-5-ylmethyl group Chemical group 0.000 abstract 1
102000001381 Arachidonate 5-Lipoxygenase Human genes 0.000 abstract 1
108010093579 Arachidonate 5-lipoxygenase Proteins 0.000 abstract 1
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 abstract 1
206010022489 Insulin Resistance Diseases 0.000 abstract 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
150000002391 heterocyclic compounds Chemical class 0.000 abstract 1
229910052757 nitrogen Inorganic materials 0.000 abstract 1
125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
125000004076 pyridyl group Chemical group 0.000 abstract 1
150000003839 salts Chemical class 0.000 abstract 1
125000001424 substituent group Chemical group 0.000 abstract 1
239000011593 sulfur Substances 0.000 abstract 1
125000004434 sulfur atom Chemical group 0.000 abstract 1
208000001072 type 2 diabetes mellitus Diseases 0.000 abstract 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D235/12—Radicals substituted by oxygen atoms
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/12—Ophthalmic agents for cataracts
- 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
- 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
- A61P35/00—Antineoplastic agents
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
- A61P5/50—Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
- 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
- C07D233/56—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 only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles 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 in position 2
- C07D235/26—Oxygen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles 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 in position 2
- C07D235/28—Sulfur atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D263/44—Two oxygen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/06—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles
- C07D271/07—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D277/34—Oxygen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic 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
- C07D417/02—Heterocyclic 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
- C07D417/12—Heterocyclic 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
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic 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
- C07D417/14—Heterocyclic 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 three or more hetero rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—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
- 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

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
Veterinary Medicine (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Medicinal Chemistry (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Public Health (AREA)
Pharmacology & Pharmacy (AREA)
General Health & Medical Sciences (AREA)
Bioinformatics & Cheminformatics (AREA)
Engineering & Computer Science (AREA)
Diabetes (AREA)
Heart & Thoracic Surgery (AREA)
Cardiology (AREA)
Immunology (AREA)
Rheumatology (AREA)
Obesity (AREA)
Endocrinology (AREA)
Ophthalmology & Optometry (AREA)
Hematology (AREA)
Orthopedic Medicine & Surgery (AREA)
Emergency Medicine (AREA)
Pain & Pain Management (AREA)
Urology & Nephrology (AREA)
Vascular Medicine (AREA)
Physical Education & Sports Medicine (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Plural Heterocyclic Compounds (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Joining Of Building Structures In Genera (AREA)

IDW20000649A 1997-10-08 1998-10-08 Senyawa heterosiklik tersubstitusi tergabung ID23891A (id)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP27606397		1997-10-08

Publications (1)

Publication Number	Publication Date
ID23891A true ID23891A (id)	2000-05-25

Family

ID=17564291

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IDW20000649A ID23891A (id)	1997-10-08	1998-10-08	Senyawa heterosiklik tersubstitusi tergabung

Country Status (24)

Country	Link
US (1)	US6432993B1 (fr)
EP (1)	EP1022272B1 (fr)
KR (1)	KR100666887B1 (fr)
CN (1)	CN1255386C (fr)
AT (1)	ATE267814T1 (fr)
AU (1)	AU740704B2 (fr)
BR (1)	BR9813848B1 (fr)
CA (1)	CA2305807C (fr)
CZ (1)	CZ302475B6 (fr)
DE (1)	DE69824194T2 (fr)
DK (1)	DK1022272T3 (fr)
ES (1)	ES2221203T3 (fr)
HU (1)	HU228193B1 (fr)
ID (1)	ID23891A (fr)
IL (1)	IL135537A (fr)
MX (1)	MXPA00003546A (fr)
NO (1)	NO318070B1 (fr)
NZ (1)	NZ503794A (fr)
PL (1)	PL200859B1 (fr)
PT (1)	PT1022272E (fr)
RU (1)	RU2196141C2 (fr)
TR (1)	TR200000946T2 (fr)
TW (1)	TW475931B (fr)
WO (1)	WO1999018081A1 (fr)

Families Citing this family (54)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AU757729B2 (en)	1999-04-07	2003-03-06	Sankyo Company Limited	Amine derivatives
WO2000061582A1 (fr) *	1999-04-08	2000-10-19	Sankyo Company, Limited	Derives imidazole condenses substitues
PL352383A1 (en)	1999-06-28	2003-08-25	Sankyo Co	Semi-finished products for synthesis of derivatives of benzimidazole and method of obtaining same
JP2001072671A (ja) *	1999-06-28	2001-03-21	Sankyo Co Ltd	ベンズイミダゾール化合物の合成中間体およびその製造方法
EP1197211A4 (fr) *	1999-07-19	2004-09-01	Sankyo Co	Agents preventifs et therapeutiques du cancer
FI20000542A7 (fi) *	2000-03-09	2001-09-10	Nokia Corp	Siirtokapasiteettien sovittaminen pakettivälitteisessä verkossa
WO2002013864A1 (fr) *	2000-08-16	2002-02-21	Sankyo Company, Limited	Preparation medicinale de prevention et traitement du cancer
US6452014B1 (en) *	2000-12-22	2002-09-17	Geron Corporation	Telomerase inhibitors and methods of their use
WO2003033494A1 (fr) *	2001-10-17	2003-04-24	Sankyo Company, Limited	Derive de benzimidazole
WO2003032988A1 (fr) *	2001-10-17	2003-04-24	Sankyo Company, Limited	Composition pharmaceutique
WO2003053440A1 (fr) *	2001-12-11	2003-07-03	Sankyo Company, Limited	Composition medicinale
TW200403055A (en) *	2002-06-25	2004-03-01	Sankyo Co	Pharmaceutical composition of a peroxisome proliferator-activated receptor (PPAR) gamma atcivetor and a diuretic
WO2004013109A1 (fr) *	2002-08-02	2004-02-12	Sankyo Company, Limited	Derive de resorcinol
US7232828B2 (en)	2002-08-10	2007-06-19	Bethesda Pharmaceuticals, Inc.	PPAR Ligands that do not cause fluid retention, edema or congestive heart failure
US7371759B2 (en)	2003-09-25	2008-05-13	Bristol-Myers Squibb Company	HMG-CoA reductase inhibitors and method
US7420059B2 (en)	2003-11-20	2008-09-02	Bristol-Myers Squibb Company	HMG-CoA reductase inhibitors and method
US7572805B2 (en)	2004-07-14	2009-08-11	Bristol-Myers Squibb Company	Pyrrolo(oxo)isoquinolines as 5HT ligands
EP1798216A4 (fr)	2004-09-28	2008-12-03	Sankyo Co	Intermédiaire de synthèse d un dérivé de 1-méthyl-1h-benzimidazole 6-substitué et méthode de synthèse dudit intermédiaire
US7517991B2 (en)	2004-10-12	2009-04-14	Bristol-Myers Squibb Company	N-sulfonylpiperidine cannabinoid receptor 1 antagonists
US20060106014A1 (en) *	2004-10-14	2006-05-18	Sekhar Boddupalli	Methods for treating diabetes
WO2006076598A2 (fr)	2005-01-12	2006-07-20	Bristol-Myers Squibb Company	Composes heterocycliques bicycliques en tant que modulateurs des recepteurs de canabinoides
US7368458B2 (en)	2005-01-12	2008-05-06	Bristol-Myers Squibb Company	Bicyclic heterocycles as cannabinoid receptor modulators
WO2006076569A2 (fr)	2005-01-12	2006-07-20	Bristol-Myers Squibb Company	Heterocycles bicycliques servant de modulateurs aux recepteurs cannabinoides
US20060160850A1 (en)	2005-01-18	2006-07-20	Chongqing Sun	Bicyclic heterocycles as cannabinoid receptor modulators
EP1846410B1 (fr)	2005-02-10	2009-01-21	Bristol-Myers Squibb Company	Dihydroquinazolinones utilisees comme modulateurs de la 5ht
RU2418788C2 (ru) *	2005-03-10	2011-05-20	Сги Фармасьютиклз, Инк.	Некоторые замещенные амиды, способ их получения и способ их применения
TW200726765A (en)	2005-06-17	2007-07-16	Bristol Myers Squibb Co	Triazolopyridine cannabinoid receptor 1 antagonists
US7629342B2 (en)	2005-06-17	2009-12-08	Bristol-Myers Squibb Company	Azabicyclic heterocycles as cannabinoid receptor modulators
US7452892B2 (en)	2005-06-17	2008-11-18	Bristol-Myers Squibb Company	Triazolopyrimidine cannabinoid receptor 1 antagonists
US7632837B2 (en)	2005-06-17	2009-12-15	Bristol-Myers Squibb Company	Bicyclic heterocycles as cannabinoid-1 receptor modulators
US7317012B2 (en)	2005-06-17	2008-01-08	Bristol-Myers Squibb Company	Bicyclic heterocycles as cannabinoind-1 receptor modulators
US7795436B2 (en)	2005-08-24	2010-09-14	Bristol-Myers Squibb Company	Substituted tricyclic heterocycles as serotonin receptor agonists and antagonists
AR056155A1 (es)	2005-10-26	2007-09-19	Bristol Myers Squibb Co	Antagonistas del receptor 1 de la hormona de concentracion de melanina no basica
US7553836B2 (en)	2006-02-06	2009-06-30	Bristol-Myers Squibb Company	Melanin concentrating hormone receptor-1 antagonists
NZ570381A (en) *	2006-02-09	2011-02-25	Daiichi Sankyo Co Ltd	Anti-cancer pharmaceutical composition
CA2649288C (fr)	2006-04-19	2015-11-24	Novartis Ag	Composes a base de benzoxazole et de benzothiazole 6-0 substitues et procedes d'inhibition de signalisation csf-1r
TW201336497A (zh) *	2007-02-08	2013-09-16	Daiichi Sankyo Co Ltd	噻唑啶二酮化合物之結晶型及其製法
JP5294419B2 (ja)	2007-04-05	2013-09-18	第一三共株式会社	縮合二環式ヘテロアリール誘導体
US20090011994A1 (en)	2007-07-06	2009-01-08	Bristol-Myers Squibb Company	Non-basic melanin concentrating hormone receptor-1 antagonists and methods
US8722710B2 (en)	2007-09-26	2014-05-13	Deuterx, Llc	Deuterium-enriched pioglitazone
PE20091928A1 (es)	2008-05-29	2009-12-31	Bristol Myers Squibb Co	Tienopirimidinas hidroxisustituidas como antagonistas de receptor-1 de hormona concentradora de melanina no basicos
TW201008936A (en)	2008-07-31	2010-03-01	Daiichi Sankyo Co Ltd	Crystalline forms of thiazolidinedione compound and its manufacturing method
JPWO2010013768A1 (ja) *	2008-07-31	2012-01-12	第一三共株式会社	チアゾリジンジオン化合物の結晶及びその製造方法
MX2011009852A (es)	2009-03-27	2011-09-29	Bristol Myers Squibb Co	Metodos para prevenir episodios cardiovasculares adversos mayores con inhibidores de dipeptidil peptidasa iv.
WO2011065420A1 (fr)	2009-11-26	2011-06-03	第一三共株式会社	Procédé de fabrication d'un dérivé de 1-méthyl-1h-benzimidazole substitué en 6 et intermédiaire de fabrication issu de ce procédé
US8207351B2 (en) *	2010-04-30	2012-06-26	International Business Machines Corporation	Cyclic carbonyl compounds with pendant carbonate groups, preparations thereof, and polymers therefrom
EP2892896B1 (fr)	2012-09-05	2016-06-29	Bristol-Myers Squibb Company	Antagonistes du récepteur 1 de l'hormone de concentration de pyrrolone ou pyrrolidinone mélanine
US9499482B2 (en)	2012-09-05	2016-11-22	Bristol-Myers Squibb Company	Pyrrolone or pyrrolidinone melanin concentrating hormone receptor-1 antagonists
US20140221369A1 (en) *	2013-02-01	2014-08-07	Deuterx, Llc	5-deutero-2,4-thiazolidinedione and 5-deutero-2,4-oxazolidinedione derivatives and compositions comprising and methods of using the same
WO2014152843A1 (fr)	2013-03-14	2014-09-25	Deuterx, Llc	2,4-thiazolidinediones enrichies en deutérium et méthodes de traitement
EP3094328B1 (fr)	2014-01-15	2020-08-19	Poxel SA	Méthodes de traitement de troubles neurologiques, métaboliques et autres à l'aide de pioglitazone énantiopure enrichie en deutérium
MA53175A (fr)	2018-07-19	2021-05-26	Astrazeneca Ab	Méthodes de traitement de hfpef au moyen de dapagliflozine et compositions comprenant celle-ci
US11767317B1 (en)	2020-06-30	2023-09-26	Poxel Sa	Methods of synthesizing enantiopure deuterium-enriched pioglitazone
US11319313B2 (en)	2020-06-30	2022-05-03	Poxel Sa	Crystalline forms of deuterium-enriched pioglitazone

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH06779B2 (ja) *	1985-06-10	1994-01-05	武田薬品工業株式会社	チアゾリジオン誘導体およびそれを含んでなる医薬組成物
US5143930A (en)	1990-02-07	1992-09-01	Sankyo Company, Limited	Thiazolidine derivatives with anti-diabetic activity, their preparation and their use
GB9017218D0 (en)	1990-08-06	1990-09-19	Beecham Group Plc	Novel compounds
WO1992003425A1 (fr)	1990-08-23	1992-03-05	Pfizer Inc.	Derives d'hydroxy-uree hypoglycemique
GB9023584D0 (en)	1990-10-30	1990-12-12	Beecham Group Plc	Novel compounds
GB9023585D0 (en)	1990-10-30	1990-12-12	Beecham Group Plc	Novel compounds
CZ289317B6 (cs)	1994-04-11	2002-01-16	Sankyo Company Limited	Heterocyklická sloučenina, farmaceutický prostředek ji obsahující a její pouľití
IL118474A (en) *	1995-06-01	2001-08-08	Sankyo Co	Benzimideol derivatives and pharmaceutical preparations containing them
JP3291164B2 (ja) *	1995-06-02	2002-06-10	日石三菱株式会社	接触分解ガソリンの脱硫方法
JP3651816B2 (ja) *	1995-07-03	2005-05-25	三共株式会社	動脈硬化症予防および治療剤
IL118778A (en)	1995-07-03	1999-07-14	Sankyo Co	Pharmaceutical compositions for the treatment of arteriosclerosis and xanthoma containing an hmg-coa reductase inhibitor
IL120443A (en)	1996-03-18	2000-07-16	Sankyo Co	Use of an insulin sensitizer for the manufacture of a medicament for the treatment or prophylaxis of pancreatitis
JPH1072371A (ja) *	1996-08-28	1998-03-17	Sankyo Co Ltd	回腸型胆汁酸トランスポーター阻害剤

1998
- 1998-10-08 TW TW087116711A patent/TW475931B/zh not_active IP Right Cessation
- 1998-10-08 EP EP98947789A patent/EP1022272B1/fr not_active Expired - Lifetime
- 1998-10-08 BR BRPI9813848-0A patent/BR9813848B1/pt not_active IP Right Cessation
- 1998-10-08 AT AT98947789T patent/ATE267814T1/de active
- 1998-10-08 TR TR2000/00946T patent/TR200000946T2/xx unknown
- 1998-10-08 MX MXPA00003546A patent/MXPA00003546A/es active IP Right Grant
- 1998-10-08 HU HU0003859A patent/HU228193B1/hu unknown
- 1998-10-08 DE DE1998624194 patent/DE69824194T2/de not_active Expired - Lifetime
- 1998-10-08 DK DK98947789T patent/DK1022272T3/da active
- 1998-10-08 WO PCT/JP1998/004548 patent/WO1999018081A1/fr not_active Ceased
- 1998-10-08 CN CNB988116928A patent/CN1255386C/zh not_active Expired - Fee Related
- 1998-10-08 CA CA002305807A patent/CA2305807C/fr not_active Expired - Fee Related
- 1998-10-08 KR KR1020007003711A patent/KR100666887B1/ko not_active Expired - Fee Related
- 1998-10-08 IL IL135537A patent/IL135537A/en not_active IP Right Cessation
- 1998-10-08 PL PL339771A patent/PL200859B1/pl not_active IP Right Cessation
- 1998-10-08 ID IDW20000649A patent/ID23891A/id unknown
- 1998-10-08 AU AU94587/98A patent/AU740704B2/en not_active Ceased
- 1998-10-08 RU RU2000109326/04A patent/RU2196141C2/ru not_active IP Right Cessation
- 1998-10-08 ES ES98947789T patent/ES2221203T3/es not_active Expired - Lifetime
- 1998-10-08 NZ NZ503794A patent/NZ503794A/xx not_active IP Right Cessation
- 1998-10-08 CZ CZ20001219A patent/CZ302475B6/cs not_active IP Right Cessation
- 1998-10-08 PT PT98947789T patent/PT1022272E/pt unknown
2000
- 2000-04-07 US US09/543,667 patent/US6432993B1/en not_active Expired - Lifetime
- 2000-04-07 NO NO20001816A patent/NO318070B1/no not_active IP Right Cessation

Also Published As

Publication number	Publication date
BR9813848B1 (pt)	2011-07-12
ES2221203T3 (es)	2004-12-16
NO318070B1 (no)	2005-01-31
IL135537A (en)	2006-08-20
IL135537A0 (en)	2001-05-20
EP1022272A4 (fr)	2002-07-17
EP1022272B1 (fr)	2004-05-26
HUP0003859A3 (en)	2005-09-28
CN1255386C (zh)	2006-05-10
DE69824194T2 (de)	2005-01-13
NO20001816D0 (no)	2000-04-07
AU740704B2 (en)	2001-11-15
MXPA00003546A (es)	2002-08-06
DE69824194D1 (de)	2004-07-01
CN1280570A (zh)	2001-01-17
DK1022272T3 (da)	2004-09-27
AU9458798A (en)	1999-04-27
BR9813848A (pt)	2000-10-03
PL200859B1 (pl)	2009-02-27
WO1999018081A1 (fr)	1999-04-15
CZ20001219A3 (cs)	2000-08-16
KR20010030961A (ko)	2001-04-16
NZ503794A (en)	2002-09-27
KR100666887B1 (ko)	2007-01-10
CA2305807A1 (fr)	1999-04-15
HK1027354A1 (en)	2001-01-12
PT1022272E (pt)	2004-08-31
TR200000946T2 (tr)	2000-07-21
EP1022272A1 (fr)	2000-07-26
HU228193B1 (en)	2013-01-28
NO20001816L (no)	2000-06-07
CA2305807C (fr)	2008-01-22
US6432993B1 (en)	2002-08-13
PL339771A1 (en)	2001-01-02
TW475931B (en)	2002-02-11
RU2196141C2 (ru)	2003-01-10
CZ302475B6 (cs)	2011-06-08
HUP0003859A2 (hu)	2001-08-28
ATE267814T1 (de)	2004-06-15

Publication	Publication Date	Title
ID23891A (id)	2000-05-25	Senyawa heterosiklik tersubstitusi tergabung
DK1357111T3 (da)	2009-11-02	2-pyridonderivater med affinitet for cannabinoid type 2-receptor
ATE401312T1 (de)	2008-08-15	Pyrimidin-5-carboxamid-derivate
DK1325910T3 (da)	2008-11-10	Aliphatiske nitrogenholdige femleddede ringforbindelser
ATE271045T1 (de)	2004-07-15	Sauerstoffhaltige heterocyclische verbindungen
DE69813605D1 (de)	2003-05-22	Benzofuranderivate
DK0695755T3 (da)	1999-06-28	Pyrrolocarbazoler
ATE164844T1 (de)	1998-04-15	Azolverbindungen, ihre herstellung und verwendung als antimykotische mittel
DK0841327T3 (da)	2002-01-21	Triazolantisvampemiddel
ATE504572T1 (de)	2011-04-15	Derivate von aromatische heterocyclen enthaltende integraseinhibitoren
ATE161820T1 (de)	1998-01-15	Carboxylatderivate mit einer die phospholipase a2 hemmenden aktivität
ATE284884T1 (de)	2005-01-15	Triazolderivate mit amidbindungen
ATE119523T1 (de)	1995-03-15	Isochinolinderivate und ihre salze als proteasehemmer.
ZA915926B (en)	1992-03-25	Pesticidal heterocyclic compounds
EA200200462A1 (ru)	2002-10-31	Производные 2-арилхинолина, их получение и терапевтическое применение