HRP20110640T1 - Derivati cikličkih amida i njihova proizvodnja te njihova uporaba kao antitromboznih sredstava - Google Patents
Derivati cikličkih amida i njihova proizvodnja te njihova uporaba kao antitromboznih sredstava Download PDFInfo
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- HRP20110640T1 HRP20110640T1 HR20110640T HRP20110640T HRP20110640T1 HR P20110640 T1 HRP20110640 T1 HR P20110640T1 HR 20110640 T HR20110640 T HR 20110640T HR P20110640 T HRP20110640 T HR P20110640T HR P20110640 T1 HRP20110640 T1 HR P20110640T1
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- Prior art keywords
- optionally substituted
- salt
- chloronaphthalen
- sulfonyl
- hydroxypropanoyl
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- 150000003950 cyclic amides Chemical class 0.000 title abstract 2
- 239000003146 anticoagulant agent Substances 0.000 title 1
- 229960004676 antithrombotic agent Drugs 0.000 title 1
- 150000003839 salts Chemical class 0.000 claims abstract 17
- 150000001875 compounds Chemical class 0.000 claims 17
- VYODSGGBJPHDPS-OAQYLSRUSA-N (2s)-3-(6-chloronaphthalen-2-yl)sulfonyl-2-hydroxy-1-[4-(2-iminopiperidin-1-yl)piperidin-1-yl]propan-1-one Chemical compound O=C([C@@H](CS(=O)(=O)C=1C=C2C=CC(Cl)=CC2=CC=1)O)N(CC1)CCC1N1CCCCC1=N VYODSGGBJPHDPS-OAQYLSRUSA-N 0.000 claims 2
- GEHAEMCVKDPMKO-HXUWFJFHSA-N 1-[1-[(2s)-3-(6-chloronaphthalen-2-yl)sulfonyl-2-hydroxypropanoyl]piperidin-4-yl]-1,3-diazinan-2-one Chemical compound O=C([C@@H](CS(=O)(=O)C=1C=C2C=CC(Cl)=CC2=CC=1)O)N(CC1)CCC1N1CCCNC1=O GEHAEMCVKDPMKO-HXUWFJFHSA-N 0.000 claims 2
- MPARUNUPLMAFHO-LJQANCHMSA-N 1-[4-[(2s)-3-(6-chloronaphthalen-2-yl)sulfonyl-2-hydroxypropanoyl]piperazin-1-yl]-1,3-diazinan-2-one Chemical compound O=C([C@@H](CS(=O)(=O)C=1C=C2C=CC(Cl)=CC2=CC=1)O)N(CC1)CCN1N1CCCNC1=O MPARUNUPLMAFHO-LJQANCHMSA-N 0.000 claims 2
- RFFCBPYHPAOSQL-HXUWFJFHSA-N 1-[4-[(2s)-3-(6-chloronaphthalen-2-yl)sulfonyl-2-hydroxypropanoyl]piperazin-1-yl]piperidin-2-one Chemical compound O=C([C@@H](CS(=O)(=O)C=1C=C2C=CC(Cl)=CC2=CC=1)O)N(CC1)CCN1N1CCCCC1=O RFFCBPYHPAOSQL-HXUWFJFHSA-N 0.000 claims 2
- XYAFLQBDIAOLNN-UHFFFAOYSA-N 1-[4-[3-(6-chloronaphthalen-2-yl)sulfonylpropanoyl]piperazin-1-yl]-1,3-diazinan-2-one Chemical compound C1=CC2=CC(Cl)=CC=C2C=C1S(=O)(=O)CCC(=O)N(CC1)CCN1N1CCCNC1=O XYAFLQBDIAOLNN-UHFFFAOYSA-N 0.000 claims 2
- DCLWQEKIJZKZQP-XMMPIXPASA-N 2-[1-[(2s)-3-(6-chloronaphthalen-2-yl)sulfonyl-2-hydroxypropanoyl]piperidin-4-yl]-3h-isoindol-1-one Chemical compound C1C2=CC=CC=C2C(=O)N1C(CC1)CCN1C(=O)[C@H](O)CS(=O)(=O)C1=CC=C(C=C(Cl)C=C2)C2=C1 DCLWQEKIJZKZQP-XMMPIXPASA-N 0.000 claims 2
- ZNBLPBAPIPKQEP-HXUWFJFHSA-N 4-[1-[(2s)-3-(6-chloronaphthalen-2-yl)sulfonyl-2-hydroxypropanoyl]piperidin-4-yl]morpholin-3-one Chemical compound O=C([C@@H](CS(=O)(=O)C=1C=C2C=CC(Cl)=CC2=CC=1)O)N(CC1)CCC1N1CCOCC1=O ZNBLPBAPIPKQEP-HXUWFJFHSA-N 0.000 claims 2
- DJHQIIXBVWGNBK-OAQYLSRUSA-N 1-[1-[(2s)-3-(6-chloronaphthalen-2-yl)sulfonyl-2-hydroxypropanoyl]piperidin-4-yl]piperidin-2-one Chemical compound O=C([C@@H](CS(=O)(=O)C=1C=C2C=CC(Cl)=CC2=CC=1)O)N(CC1)CCC1N1CCCCC1=O DJHQIIXBVWGNBK-OAQYLSRUSA-N 0.000 claims 1
- -1 6-chloronaphthalen-2-yl Chemical group 0.000 claims 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 abstract 3
- 125000004450 alkenylene group Chemical group 0.000 abstract 2
- 208000007536 Thrombosis Diseases 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 1
- 125000004193 piperazinyl group Chemical group 0.000 abstract 1
- 125000003386 piperidinyl group Chemical group 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/68—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D211/72—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D211/74—Oxygen atoms
- C07D211/76—Oxygen atoms attached in position 2 or 6
-
- 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
- A61P35/00—Antineoplastic agents
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D413/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D417/04—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 directly linked by a ring-member-to-ring-member bond
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Vascular Medicine (AREA)
- Rheumatology (AREA)
- Urology & Nephrology (AREA)
- Pain & Pain Management (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyrrole Compounds (AREA)
Abstract
Spoj, naznačen time, da je odabran između sljedećih: 4-(1-{(2S)-3-[(6-kloronaftalen-2-il)sulfonil]-2-hidroksipropanoil}piperidin-4-il)morfolin-3-on, ili njegova sol; 1-(4-{(2S)-3-[(6-kloronaftalen-2-il)sulfonil]-2-hidroksipropanoil}piperazin-1-il)piperidin-2-on, ili njegova sol; 1-(1-{(2S)-3-[(6-kloronaftalen-2-il)sulfonil]-2-hidroksipropanoil}piperidin-4-il)tetrahidropirimidin-2(1H)-on, ili njegova sol; 1-(4-{(2S)-3-[(6-kloronaftalen-2-il)sulfonil]-2-hidroksipropanoil}piperazin-1-il)tetrahidropirimidin-2(1H)-on, ili njegova sol; 1-(1-{3-[(6-kloronaftalen-2-il)sulfonil]propanoil}piperazin-4-il)tetrahidropirimidin-2(1H)-on, ili njegova sol; (2S)-3-[(6-kloronaftalen-2-il)sulfonil]-1-(2-imino-1,4'-bipiperidin-1'-il)-1-oksopropan-2-ol, ili njegova sol; 1'-{(2S)-3-[(6-kloronaftalen-2-il)sulfonil]-2-hidroksipropanoil}-1,4'-bipiperidin-2-on, ili njegova sol; i2-(1-{(2S)-3-[(6-kloronaftalen-2-il)sulfonil]-2-hidroksipropanoil}piperidin-4-il)izoindolin-1-on, ili njegova sol. Patent sadrži još 8 patentnih zahtjeva.
Claims (9)
1. Spoj, naznačen time, da je odabran između sljedećih:
4-(1-{(2S)-3-[(6-kloronaftalen-2-il)sulfonil]-2-hidroksipropanoil}piperidin-4-il)morfolin-3-on, ili njegova sol;
1-(4-{(2S)-3-[(6-kloronaftalen-2-il)sulfonil]-2-hidroksipropanoil}piperazin-1-il)piperidin-2-on, ili njegova sol;
1-(1-{(2S)-3-[(6-kloronaftalen-2-il)sulfonil]-2-hidroksipropanoil}piperidin-4-il)tetrahidropirimidin-2(1H)-on, ili njegova sol;
1-(4-{(2S)-3-[(6-kloronaftalen-2-il)sulfonil]-2-hidroksipropanoil}piperazin-1-il)tetrahidropirimidin-2(1H)-on, ili njegova sol;
1-(1-{3-[(6-kloronaftalen-2-il)sulfonil]propanoil}piperazin-4-il)tetrahidropirimidin-2(1H)-on, ili njegova sol;
(2S)-3-[(6-kloronaftalen-2-il)sulfonil]-1-(2-imino-1,4'-bipiperidin-1'-il)-1-oksopropan-2-ol, ili njegova sol;
1'-{(2S)-3-[(6-kloronaftalen-2-il)sulfonil]-2-hidroksipropanoil}-1,4'-bipiperidin-2-on, ili njegova sol; i
2-(1-{(2S)-3-[(6-kloronaftalen-2-il)sulfonil]-2-hidroksipropanoil}piperidin-4-il)izoindolin-1-on, ili njegova sol.
2. Spoj prema zahtjevu 1, naznačen time, da je taj spoj 4-(1-{(2S)-3-[(6-kloronaftalen-2-il)sulfonil]-2-hidroksipropanoil}piperidin-4-il)morfolin-3-on, ili njegova sol.
3. Spoj prema zahtjevu 1, naznačen time, da je taj spoj 1-(4-{(2S)-3-[(6-kloronaftalen-2-il)sulfonil]-2-hidroksipropanoil}piperazin-1-il)piperidin-2-on, ili njegova sol.
4. Spoj prema zahtjevu 1, naznačen time, da je taj spoj 1-(1-{(2S)-3-[(6-kloronaftalen-2-il)sulfonil]-2-hidroksipropanoil}piperidin-4-il)tetrahidropirimidin-2(1H)-on, ili njegova sol.
5. Spoj prema zahtjevu 1, naznačen time, da je taj spoj 1-(4-{(2S)-3-[(6-kloronaftalen-2-il)sulfonil]-2-hidroksipropanoil}piperazin-1-il)tetrahidropirimidin-2(1H)-on, ili njegova sol.
6. Spoj prema zahtjevu 1, naznačen time, da je taj spoj 1-(1-{3-[(6-kloronaftalen-2-il)sulfonil]propanoil}piperazin-4-il)tetrahidropirimidin-2(1H)-on, ili njegova sol.
7. Spoj prema zahtjevu 1, naznačen time, da je taj spoj (2S)-3-[(6-kloronaftalen-2-il)sulfonil]-1-(2-imino-1,4'-bipiperidin-1'-il)-1-oksopropan-2-ol, ili njegova sol.
8. Spoj prema zahtjevu 1, naznačen time, da je taj spoj 1'-{(2S)-3-[(6-kloronaftalen-2-il)sulfonil]-2-hidroksipropanoil}-1,4'-bipiperidin-2-on, ili njegova sol.
9. Spoj prema zahtjevu 1, naznačen time, da je taj spoj 2-(1-{(2S)-3-[(6-kloronaftalen-2-il)sulfonil]-2-hidroksipropanoil}piperidin-4-il)izoindolin-1-on, ili njegova sol.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004152000 | 2004-05-21 | ||
PCT/JP2005/009711 WO2005113504A1 (en) | 2004-05-21 | 2005-05-20 | Cyclic amide derivatives, and their production and use as antithrombotic agents |
Publications (1)
Publication Number | Publication Date |
---|---|
HRP20110640T1 true HRP20110640T1 (hr) | 2011-10-31 |
Family
ID=34968275
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HR20110640T HRP20110640T1 (hr) | 2004-05-21 | 2011-09-07 | Derivati cikličkih amida i njihova proizvodnja te njihova uporaba kao antitromboznih sredstava |
Country Status (26)
Country | Link |
---|---|
US (4) | US7745623B2 (hr) |
EP (2) | EP2208726B1 (hr) |
JP (2) | JP4129047B2 (hr) |
KR (1) | KR101248637B1 (hr) |
CN (2) | CN1989104B (hr) |
AT (1) | ATE513813T1 (hr) |
AU (1) | AU2005245298B2 (hr) |
BR (1) | BRPI0511186A (hr) |
CA (1) | CA2567506C (hr) |
CY (1) | CY1111850T1 (hr) |
DK (1) | DK1748985T3 (hr) |
ES (1) | ES2368155T3 (hr) |
HK (1) | HK1100666A1 (hr) |
HR (1) | HRP20110640T1 (hr) |
IL (1) | IL178896A (hr) |
MX (1) | MXPA06013243A (hr) |
MY (1) | MY154461A (hr) |
NO (1) | NO20065929L (hr) |
NZ (1) | NZ550985A (hr) |
PL (1) | PL1748985T3 (hr) |
PT (1) | PT1748985E (hr) |
RS (1) | RS51925B (hr) |
RU (1) | RU2361861C2 (hr) |
SI (1) | SI1748985T1 (hr) |
TW (1) | TWI396686B (hr) |
WO (1) | WO2005113504A1 (hr) |
Families Citing this family (59)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1302462A4 (en) * | 2000-07-17 | 2007-07-18 | Takeda Pharmaceutical | Sulphonic derivatives, process for their preparation and their use |
WO2004048363A1 (ja) * | 2002-11-22 | 2004-06-10 | Takeda Pharmaceutical Company Limited | イミダゾール誘導体、その製造法および用途 |
TWI396686B (zh) * | 2004-05-21 | 2013-05-21 | Takeda Pharmaceutical | 環狀醯胺衍生物、以及其製品和用法 |
EP1960433A2 (en) * | 2005-11-28 | 2008-08-27 | Zymogenetics, Inc. | Il-21 receptor antagonists |
US20110045028A1 (en) * | 2006-11-30 | 2011-02-24 | Takeda Pharmaceutical Company Limited | Sustained release preparation |
UY32126A (es) | 2008-09-25 | 2010-04-30 | Takeda Pharmaceutical | Composición farmacéutica sólida |
JP5535931B2 (ja) | 2008-10-27 | 2014-07-02 | 武田薬品工業株式会社 | 二環性化合物 |
JPWO2010076884A1 (ja) | 2008-12-29 | 2012-06-21 | 武田薬品工業株式会社 | 新規縮合環化合物およびその用途 |
AR075158A1 (es) | 2009-01-27 | 2011-03-16 | Takeda Pharmaceutical | Derivados de pirrolopirimidinas, composiciones farmaceuticas y usos. |
AU2010242308A1 (en) | 2009-04-30 | 2011-12-01 | Takeda Pharmaceutical Company Limited | Solid preparation |
US20120172351A1 (en) | 2009-06-09 | 2012-07-05 | Nobuyuki Negoro | Novel fused cyclic compound and use thereof |
CN102548556A (zh) | 2009-07-28 | 2012-07-04 | 武田药品工业株式会社 | 片剂 |
US8221489B2 (en) * | 2009-08-20 | 2012-07-17 | Stentys | Device and method for treating a body lumen |
TW201206911A (en) | 2010-04-27 | 2012-02-16 | Takeda Pharmaceutical | Bicyclic compound |
TWI511967B (zh) | 2010-06-16 | 2015-12-11 | Takeda Pharmaceutical | 醯胺化合物之結晶 |
WO2012011591A1 (ja) | 2010-07-23 | 2012-01-26 | 武田薬品工業株式会社 | 縮合複素環化合物およびその用途 |
US20130184272A1 (en) | 2010-09-17 | 2013-07-18 | Takeda Pharmaceutical Company Limited | Diabetes therapeutic agent |
SG190925A1 (en) | 2010-11-30 | 2013-07-31 | Takeda Pharmaceutical | Bicyclic compound |
JP5945545B2 (ja) | 2011-02-17 | 2016-07-05 | 武田薬品工業株式会社 | 光学活性なジヒドロベンゾフラン誘導体の製造法 |
CN103998432A (zh) | 2011-10-24 | 2014-08-20 | 武田药品工业株式会社 | 双环化合物 |
JP6129850B2 (ja) | 2012-01-12 | 2017-05-17 | 武田薬品工業株式会社 | Mch受容体拮抗剤としてのベンゾイミダゾール誘導体 |
JP6121339B2 (ja) | 2012-02-13 | 2017-04-26 | 武田薬品工業株式会社 | 芳香環化合物 |
JP6095580B2 (ja) | 2012-02-13 | 2017-03-15 | 武田薬品工業株式会社 | 芳香環化合物 |
EP2814466B1 (en) | 2012-02-15 | 2018-12-26 | Takeda Pharmaceutical Company Limited | Tablet comprising 1-(4-methoxybutyl)-n-(2-methylpropyl)-n-[(3s,5r)-5-(morpholin-4-ylcarbonyl)piperidin-3-yl]-1h-benzimidazole-2-carboxamide or a salt thereof |
CA2864990C (en) | 2012-02-24 | 2021-03-02 | Nobuyuki Takakura | Benzofuran and benzothiophene compounds for the inhibition of ghrelin o-acyltranferase (goat) |
CN104350040B (zh) | 2012-03-29 | 2016-06-01 | 武田药品工业株式会社 | 芳环化合物 |
JPWO2013168759A1 (ja) | 2012-05-10 | 2016-01-07 | 武田薬品工業株式会社 | 芳香環化合物 |
WO2013168760A1 (ja) | 2012-05-10 | 2013-11-14 | 武田薬品工業株式会社 | 芳香環化合物 |
AR092843A1 (es) | 2012-06-05 | 2015-05-06 | Takeda Pharmaceuticals Co | Preparacion solida |
JP2015127299A (ja) | 2012-07-19 | 2015-07-09 | 武田薬品工業株式会社 | 固形製剤 |
CA2882879A1 (en) | 2012-08-24 | 2014-02-27 | Takeda Pharmaceutical Company Limited | Heterocyclic compound |
CN103936763B (zh) * | 2013-01-18 | 2017-10-31 | 中国科学院上海药物研究所 | 噁唑烷酮类化合物及其制备方法和用途 |
EP2970331B1 (en) | 2013-03-14 | 2017-05-17 | Takeda Pharmaceutical Company Limited | Spiro azetidine isoxazole derivatives and their use as sstr5 antagonists |
WO2014165816A1 (en) | 2013-04-05 | 2014-10-09 | North Carolina Central University | Compounds useful for the treatment of metabolic disorders and synthesis of the same |
JP2016523809A (ja) | 2013-07-09 | 2016-08-12 | 武田薬品工業株式会社 | 複素環化合物 |
US9776962B2 (en) | 2013-08-09 | 2017-10-03 | Takeda Pharmaceutical Company Limited | Aromatic compounds with GPR40 agonistic activity |
JO3442B1 (ar) | 2013-10-07 | 2019-10-20 | Takeda Pharmaceuticals Co | مضادات ذات نوع فرعي من مستقبل سوماتوستاتين 5 (sstr5) |
US9428470B2 (en) | 2014-02-13 | 2016-08-30 | Takeda Pharmaceutical Company Limited | Heterocyclic compound |
US9346776B2 (en) | 2014-02-13 | 2016-05-24 | Takeda Pharmaceutical Company Limited | Fused heterocyclic compound |
JP2017529401A (ja) * | 2014-09-26 | 2017-10-05 | チャーンジョウ インシュヨン ファーマシューティカル カンパニー,リミティド | Ns4b阻害剤としてのベンゾフラン類似体 |
CN107108530B (zh) | 2014-12-23 | 2020-12-15 | 克洛星有限公司 | 2-卤素-4,6-二烷氧基-1,3,5-三嗪的工业生产方法以及其在胺存在下的用途 |
AR111199A1 (es) | 2017-03-31 | 2019-06-12 | Takeda Pharmaceuticals Co | Compuesto aromático agonista de gpr40 |
JOP20180028A1 (ar) | 2017-03-31 | 2019-01-30 | Takeda Pharmaceuticals Co | مركب ببتيد |
CA3058578A1 (en) | 2017-03-31 | 2018-10-04 | Takeda Pharmaceutical Company Limited | Aromatic compound |
US11207312B2 (en) | 2017-07-17 | 2021-12-28 | Merck Sharp & Dohme Corp. | Metallo-beta-lactamase inhibitors and methods of use thereof |
KR20210008834A (ko) | 2018-03-23 | 2021-01-25 | 카모트 테라퓨틱스, 인크. | G-단백질 결합 수용체의 조절제 |
EP3650440A4 (en) | 2018-08-27 | 2020-11-25 | Scohia Pharma, Inc. | BENZOIC ESTER COMPOUND |
JP2022503793A (ja) | 2018-09-24 | 2022-01-12 | 武田薬品工業株式会社 | Gip受容体アゴニストペプチド化合物及びその使用 |
EP3856339A1 (en) | 2018-09-24 | 2021-08-04 | Takeda Pharmaceutical Company Limited | Gip receptor agonist peptide compounds and uses thereof |
AR121649A1 (es) | 2020-03-25 | 2022-06-22 | Takeda Pharmaceuticals Co | Dosificación qw de compuestos peptídicos agonistas del receptor de gip y sus usos |
KR20230005184A (ko) | 2020-03-25 | 2023-01-09 | 다케다 야쿠힌 고교 가부시키가이샤 | Gip 수용체 작용제 펩티드 화합물의 qd 투약 및 이의 용도 |
BR112023023559A2 (pt) | 2021-05-13 | 2024-02-06 | Carmot Therapeutics Inc | Moduladores de receptores acoplados à proteína g |
WO2023169456A1 (en) | 2022-03-09 | 2023-09-14 | Gasherbrum Bio , Inc. | Heterocyclic glp-1 agonists |
WO2023179542A1 (en) | 2022-03-21 | 2023-09-28 | Gasherbrum Bio , Inc. | 5,8-dihydro-1,7-naphthyridine derivatives as glp-1 agonists for the treatment of diabetes |
WO2023198140A1 (en) | 2022-04-14 | 2023-10-19 | Gasherbrum Bio, Inc. | Heterocyclic glp-1 agonists |
WO2024125602A1 (en) | 2022-12-15 | 2024-06-20 | Gasherbrum Bio, Inc. | Salts and solid forms of a compound having glp-1 agonist activity |
WO2024131869A1 (en) | 2022-12-22 | 2024-06-27 | Gasherbrum Bio, Inc. | Heterocyclic glp-1 agonists |
WO2024138048A1 (en) | 2022-12-22 | 2024-06-27 | Gasherbrum Bio, Inc. | Heterocyclic glp-1 agonists |
WO2024169952A1 (en) | 2023-02-16 | 2024-08-22 | Gasherbrum Bio, Inc. | Heterocyclic glp-1 agonists |
Family Cites Families (87)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US270488A (en) * | 1883-01-09 | Drilling apparatus | ||
US2201270A (en) * | 1936-04-17 | 1940-05-21 | Mcintyre John Taylor | Apparatus for allaying dust from rock drills |
US2946565A (en) * | 1953-06-16 | 1960-07-26 | Jersey Prod Res Co | Combination drilling and testing process |
US2849214A (en) * | 1954-09-02 | 1958-08-26 | Gulf Research Development Co | Borehole drilling apparatus for preventing lost circulation |
US3497020A (en) * | 1968-05-20 | 1970-02-24 | Archer W Kammerer Jr | System for reducing hydrostatic pressure on formations |
JPS5011391B1 (hr) * | 1970-07-21 | 1975-04-30 | ||
SE355840B (hr) * | 1971-09-08 | 1973-05-07 | Atlas Copco Ab | |
FR2228301B1 (hr) * | 1973-05-03 | 1977-10-14 | Ibm | |
US4147786A (en) * | 1976-02-02 | 1979-04-03 | Ciba-Geigy Corporation | 1-Indolylalkyl-3-or 4-trimethyleneurido-piperidines |
FI782133A (fi) | 1977-07-08 | 1979-01-09 | Ciba Geigy Ag | Piperidino-propanoler och foerfarande foer deras framstaellning |
EP0000485A1 (de) | 1977-07-08 | 1979-02-07 | Ciba-Geigy Ag | Piperidino-propanole, ihre Herstellung und pharmazeutische Präparate die diese enthalten |
US4329348A (en) | 1979-02-26 | 1982-05-11 | Ciba-Geigy Corporation | N-Oxacyclic-alkylpiperidines as psychostimulants |
US4630691A (en) * | 1983-05-19 | 1986-12-23 | Hooper David W | Annulus bypass peripheral nozzle jet pump pressure differential drilling tool and method for well drilling |
US4534426A (en) * | 1983-08-24 | 1985-08-13 | Unique Oil Tools, Inc. | Packer weighted and pressure differential method and apparatus for Big Hole drilling |
US4567954A (en) * | 1983-12-02 | 1986-02-04 | Norton Christensen, Inc. | Replaceable nozzles for insertion into a drilling bit formed by powder metallurgical techniques and a method for manufacturing the same |
US4695575A (en) * | 1984-11-13 | 1987-09-22 | Janssen Pharmaceutica, N.V. | 4-[(bicycle heterocyclyl)-methyl and -hetero]-piperidines |
ZA928276B (en) | 1991-10-31 | 1993-05-06 | Daiichi Seiyaku Co | Aromatic amidine derivates and salts thereof. |
US5902272A (en) * | 1992-01-07 | 1999-05-11 | Arthrocare Corporation | Planar ablation probe and method for electrosurgical cutting and ablation |
HU218419B (hu) | 1992-03-06 | 2000-08-28 | E.R. Squibb And Sons, Inc. | Mikroszomális triglicerid transzfer protein (MTP) nagy molekulatömegű alegységének rekombináns úton történő előállítására és a protein és inhibitorainak kimutatására szolgáló eljárások |
US5595872A (en) | 1992-03-06 | 1997-01-21 | Bristol-Myers Squibb Company | Nucleic acids encoding microsomal trigyceride transfer protein |
US5355967A (en) * | 1992-10-30 | 1994-10-18 | Union Oil Company Of California | Underbalance jet pump drilling method |
GB9321557D0 (en) | 1992-11-03 | 1993-12-08 | Zeneca Ltd | Carboxamide derivatives |
GB9312806D0 (en) | 1993-06-22 | 1993-08-04 | Boots Co Plc | Therapeutic agents |
GB9317104D0 (en) | 1993-08-17 | 1993-09-29 | Zeneca Ltd | Therapeutic heterocycles |
TW394760B (en) | 1993-09-07 | 2000-06-21 | Hoffmann La Roche | Novel Carboxamides, process for their preparation and pharmaceutical composition containing the same |
ZA951617B (en) * | 1994-03-04 | 1997-02-27 | Lilly Co Eli | Antithrombotic agents. |
US5456326A (en) * | 1994-04-18 | 1995-10-10 | Exxon Production Research Company | Apparatus and method for installing open-ended tubular members axially into the earth |
IL115420A0 (en) | 1994-09-26 | 1995-12-31 | Zeneca Ltd | Aminoheterocyclic derivatives |
JP2002515008A (ja) | 1994-10-27 | 2002-05-21 | メルク エンド カンパニー インコーポレーテッド | ムスカリン・アンタゴニスト |
ATE233240T1 (de) | 1994-12-02 | 2003-03-15 | Yamanouchi Pharma Co Ltd | Neues amidinonaphthylderivat oder dessen salz |
GB9508786D0 (en) * | 1995-04-29 | 1995-06-21 | Zeneca Ltd | Substituted heterocycles |
DE69533991T2 (de) | 1995-05-29 | 2006-04-13 | Pfizer Inc. | Dipeptide, die die ausschüttung von wachstumshormonen stimulieren |
US5612353A (en) | 1995-06-07 | 1997-03-18 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Substituted (sulfinic acid, sulfonic acid, sulfonylamino or sulfinylamino) N-[(aminoiminomethyl)phenylalkyl]-azaheterocyclylamide compounds |
US5849759A (en) | 1995-12-08 | 1998-12-15 | Berlex Laboratories, Inc. | Naphthyl-substituted benzimidazole derivatives as anti-coagulants |
GB9602294D0 (en) | 1996-02-05 | 1996-04-03 | Zeneca Ltd | Heterocyclic compounds |
IL129877A (en) | 1996-11-27 | 2004-08-31 | Aventis Pharm Prod Inc | A pharmaceutical preparation containing a component having an Xa antagonist activity and an antifouling agent |
DE69835430T2 (de) | 1997-05-30 | 2007-03-08 | Takeda Pharmaceutical Co. Ltd. | Sulfonamidderivate, ihre herstellung und verwendung |
FR2764511B1 (fr) | 1997-06-13 | 2000-09-08 | Sanofi Sa | Compositions pour le traitement et la prevention de la thrombose arterielle et utilisation d'un inhibiteur du facteur xa seul et/ou en combinaison avec un antiagregant plaquettaire |
GB9715895D0 (en) | 1997-07-29 | 1997-10-01 | Zeneca Ltd | Heterocyclic compounds |
US6348478B1 (en) | 1997-11-20 | 2002-02-19 | Teijin Limited | Biphenylamidine derivatives |
IL135408A0 (en) | 1997-11-21 | 2001-05-20 | Schering Corp | Substituted oximes as neurokinin antagonists |
WO1999033805A1 (fr) | 1997-12-26 | 1999-07-08 | Mochida Pharmaceutical Co., Ltd. | Composes aromatiques presentant des groupements amino cycliques ou leur sels |
CA2317017A1 (en) | 1998-02-05 | 1999-08-12 | Takeda Chemical Industries, Ltd. | Sulfonamide derivatives, their production and use |
EP1070714B1 (en) * | 1998-04-10 | 2004-08-04 | Japan Tobacco Inc. | Amidine compounds |
US6129152A (en) * | 1998-04-29 | 2000-10-10 | Alpine Oil Services Inc. | Rotating bop and method |
GB9809349D0 (en) | 1998-05-02 | 1998-07-01 | Zeneca Ltd | Heterocyclic derivatives |
US6423519B1 (en) * | 1998-07-15 | 2002-07-23 | Gpc Biotech Inc. | Compositions and methods for inhibiting fungal growth |
CA2340100A1 (en) | 1998-08-11 | 2000-02-24 | Daiichi Pharmaceutical Co., Ltd. | Novel sulfonyl derivatives |
JP2000080046A (ja) * | 1998-09-03 | 2000-03-21 | Dai Ichi Seiyaku Co Ltd | 多臓器障害の予防・治療剤 |
EP1115396A4 (en) | 1998-09-25 | 2002-05-22 | Sunol Molecular Corp | PHARMACEUTICALLY ACTIVE COMPOUNDS, AND METHODS OF USE THEREOF |
CA2355886C (en) | 1998-12-23 | 2006-10-31 | Schering Corporation | Substituted oximes and hydrazones as neurokinin antagonists |
US6204265B1 (en) * | 1998-12-23 | 2001-03-20 | Schering Corporation | Substituted oximes and hydrazones as neurokinin antagonists |
US7217714B1 (en) | 1998-12-23 | 2007-05-15 | Agouron Pharmaceuticals, Inc. | CCR5 modulators |
CA2383492A1 (en) | 1999-06-22 | 2000-12-28 | Takeda Chemical Industries, Ltd. | Acylhydrazine derivatives, their production and use |
DE60015541T2 (de) | 1999-06-30 | 2005-12-08 | Mochida Pharmaceutical Co. Ltd. | Trizyklische verbindungen mit einer spiro-einheit |
DE60041584D1 (de) | 1999-07-28 | 2009-04-02 | Aventis Pharma Inc | Substituierte oxoazaheterozyclische verbindungen |
AU7354900A (en) | 1999-09-09 | 2001-04-10 | Merck & Co., Inc. | Inhibitors of prenyl-protein transferase |
EP1242366A1 (en) | 1999-12-15 | 2002-09-25 | Axys Pharmaceuticals, Inc. | Salicylamides as serine protease and factor xa inhibitors |
US6723091B2 (en) * | 2000-02-22 | 2004-04-20 | Gyrus Medical Limited | Tissue resurfacing |
US6629974B2 (en) * | 2000-02-22 | 2003-10-07 | Gyrus Medical Limited | Tissue treatment method |
AR033517A1 (es) | 2000-04-08 | 2003-12-26 | Astrazeneca Ab | Derivados de piperidina, proceso para su preparacion y uso de estos derivados en la fabricacion de medicamentos |
JP2002201178A (ja) * | 2000-07-17 | 2002-07-16 | Takeda Chem Ind Ltd | スルホン誘導体、その製造法及び用途 |
EP1302462A4 (en) * | 2000-07-17 | 2007-07-18 | Takeda Pharmaceutical | Sulphonic derivatives, process for their preparation and their use |
US6511973B2 (en) * | 2000-08-02 | 2003-01-28 | Bristol-Myers Squibb Co. | Lactam inhibitors of FXa and method |
WO2002026720A2 (en) | 2000-09-29 | 2002-04-04 | Millennium Pharmaceuticals, Inc. | PIPERAZINE BASED INHIBITORS OF FACTOR Xa |
EP1331892B1 (en) * | 2000-10-18 | 2006-07-05 | Mattioli Engineering Limited | Apparatus for plasma skin resurfacing |
FR2819511A1 (fr) | 2001-01-18 | 2002-07-19 | Servier Lab | Nouveaux composes azepane, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
JPWO2002068407A1 (ja) | 2001-02-28 | 2004-06-24 | 山之内製薬株式会社 | ベンゾイミダゾール化合物 |
ES2298386T3 (es) | 2001-07-26 | 2008-05-16 | Eli Lilly And Company | 1-glicinil-4-(1-metilpiperidin-4-il)piperazinas y -piperidinas como antagonistas del factor xa. |
US6877571B2 (en) * | 2001-09-04 | 2005-04-12 | Sunstone Corporation | Down hole drilling assembly with independent jet pump |
WO2003022214A2 (en) | 2001-09-06 | 2003-03-20 | Millennium Pharmaceuticals, Inc. | Piperazine and homopiperazine compounds |
PL204263B1 (pl) | 2001-09-21 | 2009-12-31 | Bristol Myers Squibb Co | Pochodna 1H-pirazolo[3,4-c]pirydyny i jej zastosowanie oraz kompozycja farmaceutyczna i jej zastosowanie |
EP2243776A1 (en) * | 2001-10-12 | 2010-10-27 | High Point Pharmaceuticals, LLC | Substituted piperidines and their use for the treatment of diseases related to the histamine H3 receptor |
DE10155075A1 (de) * | 2001-11-09 | 2003-05-22 | Merck Patent Gmbh | Cyclische Sulfonamide |
DE60330847D1 (de) * | 2002-03-28 | 2010-02-25 | Mitsubishi Tanabe Pharma Corp | Benzofuranderivat |
TW200307667A (en) * | 2002-05-06 | 2003-12-16 | Bristol Myers Squibb Co | Sulfonylaminovalerolactams and derivatives thereof as factor Xa inhibitors |
DE10229070A1 (de) | 2002-06-28 | 2004-01-15 | Merck Patent Gmbh | Phenylderivate 5 |
US20040006490A1 (en) | 2002-07-08 | 2004-01-08 | Gingrich Mark A. | Prescription data exchange system |
EP1558606A4 (en) * | 2002-10-02 | 2008-05-07 | Bristol Myers Squibb Co | DIAMINOALKYL CONTAINING LACTAM, BETA AMINO ACIDS, ALPHA AMINO ACIDS AND DERIVATIVES THEREOF AS FACTOR XA INHIBITORS |
WO2004035579A1 (ja) | 2002-10-15 | 2004-04-29 | Takeda Pharmaceutical Company Limited | イミダゾピリジン誘導体、その製造法および用途 |
WO2004048363A1 (ja) * | 2002-11-22 | 2004-06-10 | Takeda Pharmaceutical Company Limited | イミダゾール誘導体、その製造法および用途 |
MXPA05008878A (es) * | 2003-02-21 | 2005-10-05 | Pfizer | Derivados de aminotiazol sustituidos con cicloalquilo que contiene n y composiciones farmaceuticas para inhibir la proliferacion celular, y metodos para su uso. |
US6899188B2 (en) * | 2003-03-26 | 2005-05-31 | Sunstone Corporation | Down hole drilling assembly with concentric casing actuated jet pump |
WO2005087266A1 (en) | 2004-03-05 | 2005-09-22 | Vddi Pharmaceuticals | Combination therapy for inhibition of platelet aggregation |
TWI396686B (zh) | 2004-05-21 | 2013-05-21 | Takeda Pharmaceutical | 環狀醯胺衍生物、以及其製品和用法 |
US7988933B2 (en) | 2006-09-01 | 2011-08-02 | Siemens Healthcare Diagnostics Inc. | Identification system for a clinical sample container |
KR100906250B1 (ko) | 2006-09-04 | 2009-07-07 | 주식회사 엘지화학 | 바인더로서 고중합도 폴리비닐알콜과 폴리비닐피롤리돈의혼합물을 포함하는 전극 합제 및 이를 포함하는 리튬이차전지 |
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