WO2008016643A2 - Entités chimiques, compositions et méthodes - Google Patents
Entités chimiques, compositions et méthodes Download PDFInfo
- Publication number
- WO2008016643A2 WO2008016643A2 PCT/US2007/017186 US2007017186W WO2008016643A2 WO 2008016643 A2 WO2008016643 A2 WO 2008016643A2 US 2007017186 W US2007017186 W US 2007017186W WO 2008016643 A2 WO2008016643 A2 WO 2008016643A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- optionally substituted
- ethyl
- methyl
- amino
- pyridin
- Prior art date
Links
- 0 C[C@@](CC(CNCC=*)=O)[C@](*)CNC(/C(/C(/NCCc1cccc(F)c1)=N\CC1)=C\C=C1\c1ccccc1C#N)=O Chemical compound C[C@@](CC(CNCC=*)=O)[C@](*)CNC(/C(/C(/NCCc1cccc(F)c1)=N\CC1)=C\C=C1\c1ccccc1C#N)=O 0.000 description 41
- IVCBREIIGBKFSE-GORDUTHDSA-N C/C=C/c(cc1)nc(NCCc2cc(F)ccc2)c1C(NCc1cnccc1)=O Chemical compound C/C=C/c(cc1)nc(NCCc2cc(F)ccc2)c1C(NCc1cnccc1)=O IVCBREIIGBKFSE-GORDUTHDSA-N 0.000 description 1
- JRBLZKJLELMAJA-IBBHUPRXSA-N CC(C)(C/C=N/C(c(cc1)c(NCCc2cc(F)ccc2)nc1-c1ccccc1C#N)=O)NC=O Chemical compound CC(C)(C/C=N/C(c(cc1)c(NCCc2cc(F)ccc2)nc1-c1ccccc1C#N)=O)NC=O JRBLZKJLELMAJA-IBBHUPRXSA-N 0.000 description 1
- GFKXSFIHVVNJFL-VHCIKCAMSA-N CC(C1C(NC[C@@H](CC2)NC2=O)=O)C=C(c2ccccc2C#N)N=C1NCCc1cc(F)ccc1 Chemical compound CC(C1C(NC[C@@H](CC2)NC2=O)=O)C=C(c2ccccc2C#N)N=C1NCCc1cc(F)ccc1 GFKXSFIHVVNJFL-VHCIKCAMSA-N 0.000 description 1
- QGMWCDTVHAPFMS-UHFFFAOYSA-N CC1N=CC(c2cc(C(CCC3CC(C)=CCC3)=N)c(CO)cc2C)=C1 Chemical compound CC1N=CC(c2cc(C(CCC3CC(C)=CCC3)=N)c(CO)cc2C)=C1 QGMWCDTVHAPFMS-UHFFFAOYSA-N 0.000 description 1
- TUIDWMOUUIPPCA-UHFFFAOYSA-N CC1NC1C(c(cc1)cc(C(CCC(C=CC2)=CC2F)=C)c1C(NCc1cnccc1)=O)=O Chemical compound CC1NC1C(c(cc1)cc(C(CCC(C=CC2)=CC2F)=C)c1C(NCc1cnccc1)=O)=O TUIDWMOUUIPPCA-UHFFFAOYSA-N 0.000 description 1
- HLJIHIHBDFXKJL-UHFFFAOYSA-N CCCCOCCCCC(C(C(CC(CCc1cc(F)ccc1)N)=CC1)=CC=C1N1CCCCC1)=O Chemical compound CCCCOCCCCC(C(C(CC(CCc1cc(F)ccc1)N)=CC1)=CC=C1N1CCCCC1)=O HLJIHIHBDFXKJL-UHFFFAOYSA-N 0.000 description 1
- JPWOBKNDBLMXQU-RUZDIDTESA-N CCNCCCC(N1[C@@H](CNC(c2c(NCCc3cccc(F)c3)nc(-c3ccccc3C#N)c(F)c2)=O)CCC1)=O Chemical compound CCNCCCC(N1[C@@H](CNC(c2c(NCCc3cccc(F)c3)nc(-c3ccccc3C#N)c(F)c2)=O)CCC1)=O JPWOBKNDBLMXQU-RUZDIDTESA-N 0.000 description 1
- DRSKQHXSDRRWPE-KVUNNZNLSA-N CS(CC1[C@@H](C/N=C/C(c(cc2)c(CNCCc3cccc(F)c3)nc2-c2ccccc2C#N)=O)CC1)(=O)=O Chemical compound CS(CC1[C@@H](C/N=C/C(c(cc2)c(CNCCc3cccc(F)c3)nc2-c2ccccc2C#N)=O)CC1)(=O)=O DRSKQHXSDRRWPE-KVUNNZNLSA-N 0.000 description 1
- LYQGHCHCBWUXMD-KEJDIYNNSA-N C[C@@H](CNC(C1=CC=C(c2ccccc2C#N)NC1NCCc1cc(F)ccc1)=O)NC Chemical compound C[C@@H](CNC(C1=CC=C(c2ccccc2C#N)NC1NCCc1cc(F)ccc1)=O)NC LYQGHCHCBWUXMD-KEJDIYNNSA-N 0.000 description 1
- YOYPSHXARYSXSW-HLHLGKBNSA-N C[C@@](CCC1=CCCN=C1)(C1)C1C(c(cc1)c(C[C@H](C2)/C2=C/Cc2cccc(F)c2)nc1NCc1ccccn1)=O Chemical compound C[C@@](CCC1=CCCN=C1)(C1)C1C(c(cc1)c(C[C@H](C2)/C2=C/Cc2cccc(F)c2)nc1NCc1ccccn1)=O YOYPSHXARYSXSW-HLHLGKBNSA-N 0.000 description 1
- CWRATBLIJOWERP-WLTQESGOSA-N C[C@H](C(N1[C@@H](C[C@@H](CC2)[C@@H]2C(C(C(CCCCCc2cc(F)ccc2)=C(C)C2)=CC=C2c2ccccc2C#N)=O)CCC1)=O)N Chemical compound C[C@H](C(N1[C@@H](C[C@@H](CC2)[C@@H]2C(C(C(CCCCCc2cc(F)ccc2)=C(C)C2)=CC=C2c2ccccc2C#N)=O)CCC1)=O)N CWRATBLIJOWERP-WLTQESGOSA-N 0.000 description 1
- LMHDHHUBQUTCJW-SNVBAGLBSA-N C[C@H]1C=C(CCC=C)CCC1 Chemical compound C[C@H]1C=C(CCC=C)CCC1 LMHDHHUBQUTCJW-SNVBAGLBSA-N 0.000 description 1
- PJJQULXSCKPHHI-UHFFFAOYSA-N C[n]1ncc(-c(c(F)c2)nc(NCCc3cc(F)ccc3)c2C(O)=O)c1 Chemical compound C[n]1ncc(-c(c(F)c2)nc(NCCc3cc(F)ccc3)c2C(O)=O)c1 PJJQULXSCKPHHI-UHFFFAOYSA-N 0.000 description 1
- AUCABHRMIZZYPQ-IERCKHOLSA-N Cc1cc(C(NCC[C@@H](CC2)C3=C(CCCN)C3C2=O)=O)c(CNCCc2cc(F)ccc2)c(C)c1-c(cccc1)c1C#N Chemical compound Cc1cc(C(NCC[C@@H](CC2)C3=C(CCCN)C3C2=O)=O)c(CNCCc2cc(F)ccc2)c(C)c1-c(cccc1)c1C#N AUCABHRMIZZYPQ-IERCKHOLSA-N 0.000 description 1
- GUPWFAIPKGCNJQ-UHFFFAOYSA-N Cc1ccccc1C1=CC=C(C2(C3=NC3CCC(C(N(C)C)=O)N)OC2)C(NCCc2cc(F)ccc2)=NCC1 Chemical compound Cc1ccccc1C1=CC=C(C2(C3=NC3CCC(C(N(C)C)=O)N)OC2)C(NCCc2cc(F)ccc2)=NCC1 GUPWFAIPKGCNJQ-UHFFFAOYSA-N 0.000 description 1
- IIWHEPJKQOXIFA-UUSAFJCLSA-N N#Cc1ccccc1-c(cc1)nc(NCCC(C2)C=CC=C2F)c1C(NC[C@@H](CC1)NC1=O)=O Chemical compound N#Cc1ccccc1-c(cc1)nc(NCCC(C2)C=CC=C2F)c1C(NC[C@@H](CC1)NC1=O)=O IIWHEPJKQOXIFA-UUSAFJCLSA-N 0.000 description 1
- SMBXXCJFRGARKH-UHFFFAOYSA-N N#Cc1ccccc1-c(cc1)nc(NCCc2cccc(F)c2)c1C(O)=O Chemical compound N#Cc1ccccc1-c(cc1)nc(NCCc2cccc(F)c2)c1C(O)=O SMBXXCJFRGARKH-UHFFFAOYSA-N 0.000 description 1
- AFYLJZSLSWNUTF-UHFFFAOYSA-N NC(CC1C=CC=NC1)C(c1c(CCCC(C2)CC=CC2F)nc(C2CCCC2)cc1)=O Chemical compound NC(CC1C=CC=NC1)C(c1c(CCCC(C2)CC=CC2F)nc(C2CCCC2)cc1)=O AFYLJZSLSWNUTF-UHFFFAOYSA-N 0.000 description 1
- GFOAHABINHRDKL-SCSAIBSYSA-N NC[C@@H](CC1)NC1=O Chemical compound NC[C@@H](CC1)NC1=O GFOAHABINHRDKL-SCSAIBSYSA-N 0.000 description 1
- PHRGGDPCXVTHRA-UHFFFAOYSA-N O=C(c(cc1)c(NCCc2cc(F)ccc2)nc1Cl)NCc1cnccc1 Chemical compound O=C(c(cc1)c(NCCc2cc(F)ccc2)nc1Cl)NCc1cnccc1 PHRGGDPCXVTHRA-UHFFFAOYSA-N 0.000 description 1
- TWEOVINTSCVKEW-UHFFFAOYSA-N O=C(c(cc1)c(NCCc2cc(F)ccc2)nc1N1CCCC1)NCc1cnccc1 Chemical compound O=C(c(cc1)c(NCCc2cc(F)ccc2)nc1N1CCCC1)NCc1cnccc1 TWEOVINTSCVKEW-UHFFFAOYSA-N 0.000 description 1
- DBIIXNIOCCWVSH-SSDOTTSWSA-N O=C(c(ccc(Cl)n1)c1Cl)NC[C@@H]1NCCC1 Chemical compound O=C(c(ccc(Cl)n1)c1Cl)NC[C@@H]1NCCC1 DBIIXNIOCCWVSH-SSDOTTSWSA-N 0.000 description 1
- ZYATVYPHMGYEPI-UHFFFAOYSA-N OC(c(c(NCCc1cc(F)ccc1)n1)cc(F)c1Cl)=O Chemical compound OC(c(c(NCCc1cc(F)ccc1)n1)cc(F)c1Cl)=O ZYATVYPHMGYEPI-UHFFFAOYSA-N 0.000 description 1
- LTDGKGCHRNNCAC-UHFFFAOYSA-N OC(c(cc(c(Cl)n1)F)c1Cl)=O Chemical compound OC(c(cc(c(Cl)n1)F)c1Cl)=O LTDGKGCHRNNCAC-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/10—Drugs for disorders of the urinary system of the bladder
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
- A61P21/02—Muscle relaxants, e.g. for tetanus or cramps
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/79—Acids; Esters
- C07D213/80—Acids; Esters in position 3
-
- 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
- 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
- C07D401/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
- C07D401/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- 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
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Neurology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pain & Pain Management (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pyridine Compounds (AREA)
Abstract
L'invention concerne des entités chimiques modulant la myosine des muscles lisses et/ou la myosine non musculaire, ainsi que des entités chimiques, des compositions pharmaceutiques et des méthodes de traitement de maladies et de pathologies associées à la myosine des muscles lisses et/ou à la myosine non musculaire.
Applications Claiming Priority (12)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US83501006P | 2006-08-01 | 2006-08-01 | |
US83490306P | 2006-08-01 | 2006-08-01 | |
US83490406P | 2006-08-01 | 2006-08-01 | |
US83518306P | 2006-08-01 | 2006-08-01 | |
US83490106P | 2006-08-01 | 2006-08-01 | |
US60/835,183 | 2006-08-01 | ||
US60/834,903 | 2006-08-01 | ||
US60/834,904 | 2006-08-01 | ||
US60/835,010 | 2006-08-01 | ||
US60/834,901 | 2006-08-01 | ||
US83523606P | 2006-08-02 | 2006-08-02 | |
US60/835,236 | 2006-08-02 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2008016643A2 true WO2008016643A2 (fr) | 2008-02-07 |
WO2008016643A3 WO2008016643A3 (fr) | 2008-06-19 |
Family
ID=38997696
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2007/017186 WO2008016643A2 (fr) | 2006-08-01 | 2007-07-31 | Entités chimiques, compositions et méthodes |
Country Status (4)
Country | Link |
---|---|
AR (1) | AR062176A1 (fr) |
PE (1) | PE20080432A1 (fr) |
TW (1) | TW200823188A (fr) |
WO (1) | WO2008016643A2 (fr) |
Cited By (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009051112A1 (fr) * | 2007-10-15 | 2009-04-23 | Takeda Pharmaceutical Company Limited | Composés amides et leur utilisation |
US7919511B2 (en) | 2006-08-01 | 2011-04-05 | Cytokinetics, Inc. | Certain chemical entities, compositions, and methods |
WO2011042797A1 (fr) * | 2009-10-08 | 2011-04-14 | Icozen Therapeutics Pvt. Ltd. | Dérivés de pyrazole en tant que modulateurs du canal calcique activé par la libération du calcium |
US7932270B2 (en) | 2006-08-01 | 2011-04-26 | Cytokinetics, Inc. | Certain chemical entities, compositions, and methods |
US7939548B2 (en) | 2006-08-02 | 2011-05-10 | Cytokinetics, Inc. | Certain chemical entities, compositions, and methods |
US7939534B2 (en) | 2006-08-01 | 2011-05-10 | Cytokinetics, Inc. | Certain chemical entities, compositions, and methods |
JP2013506715A (ja) * | 2009-10-06 | 2013-02-28 | ミレニアム ファーマシューティカルズ, インコーポレイテッド | Pdk1インヒビターとして有用な複素環式化合物 |
US8586751B2 (en) | 2009-06-12 | 2013-11-19 | Bristol-Myers Squibb Company | Nicotinamide compounds useful as kinase modulators |
WO2015010832A1 (fr) * | 2013-07-22 | 2015-01-29 | Syngenta Participations Ag | Dérivés hétérocycliques microbiocides |
US8993612B2 (en) | 2009-10-08 | 2015-03-31 | Rhizen Pharmaceuticals Sa | Modulators of calcium release-activated calcium channel and methods for treatment of non-small cell lung cancer |
WO2016039448A1 (fr) * | 2014-09-12 | 2016-03-17 | 田辺三菱製薬株式会社 | Composé aromatique d'amide d'acide carboxylique |
US9458110B2 (en) | 2013-02-28 | 2016-10-04 | Bristol-Myers Squibb Company | Phenylpyrazole derivatives as potent ROCK1 and ROCK2 inhibitors |
US9828345B2 (en) | 2013-02-28 | 2017-11-28 | Bristol-Myers Squibb Company | Phenylpyrazole derivatives as potent ROCK1 and ROCK2 inhibitors |
US9951069B1 (en) | 2017-01-11 | 2018-04-24 | Rodin Therapeutics, Inc. | Bicyclic inhibitors of histone deacetylase |
US10336762B2 (en) | 2017-02-16 | 2019-07-02 | Gilead Sciences, Inc. | Pyrrolo[1,2-b]pyridazine derivatives |
US10421756B2 (en) | 2015-07-06 | 2019-09-24 | Rodin Therapeutics, Inc. | Heterobicyclic N-aminophenyl-amides as inhibitors of histone deacetylase |
CN111393376A (zh) * | 2020-05-11 | 2020-07-10 | 安徽赛迪生物科技有限公司 | 一种2-氯嘧啶-4-甲酸的合成方法 |
US10875866B2 (en) | 2018-07-13 | 2020-12-29 | Gilead Sciences, Inc. | Pyrrolo[1,2-B]pyridazine derivatives |
US10919902B2 (en) | 2015-07-06 | 2021-02-16 | Alkermes, Inc. | Hetero-halo inhibitors of histone deacetylase |
WO2021092322A1 (fr) * | 2019-11-06 | 2021-05-14 | Remedy Plan, Inc. | Traitements anticancéreux ciblant des cellules souches cancéreuses |
EP3868749A1 (fr) | 2016-03-23 | 2021-08-25 | Syngenta Participations Ag | Composés herbicides |
US11225475B2 (en) | 2017-08-07 | 2022-01-18 | Alkermes, Inc. | Substituted pyridines as inhibitors of histone deacetylase |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4140853A (en) * | 1975-04-18 | 1979-02-20 | Schering Aktiengesellschaft | Process for the preparation of aminopyridines |
WO2005108391A1 (fr) * | 2004-04-22 | 2005-11-17 | Eli Lilly And Company | Amides en tant qu'inhibiteurs de la bace |
-
2007
- 2007-07-31 WO PCT/US2007/017186 patent/WO2008016643A2/fr active Application Filing
- 2007-08-01 PE PE2007000999A patent/PE20080432A1/es not_active Application Discontinuation
- 2007-08-01 TW TW096128145A patent/TW200823188A/zh unknown
- 2007-08-01 AR ARP070103397A patent/AR062176A1/es unknown
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4140853A (en) * | 1975-04-18 | 1979-02-20 | Schering Aktiengesellschaft | Process for the preparation of aminopyridines |
WO2005108391A1 (fr) * | 2004-04-22 | 2005-11-17 | Eli Lilly And Company | Amides en tant qu'inhibiteurs de la bace |
Cited By (48)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7919511B2 (en) | 2006-08-01 | 2011-04-05 | Cytokinetics, Inc. | Certain chemical entities, compositions, and methods |
US7939534B2 (en) | 2006-08-01 | 2011-05-10 | Cytokinetics, Inc. | Certain chemical entities, compositions, and methods |
US7932270B2 (en) | 2006-08-01 | 2011-04-26 | Cytokinetics, Inc. | Certain chemical entities, compositions, and methods |
US7939548B2 (en) | 2006-08-02 | 2011-05-10 | Cytokinetics, Inc. | Certain chemical entities, compositions, and methods |
WO2009051112A1 (fr) * | 2007-10-15 | 2009-04-23 | Takeda Pharmaceutical Company Limited | Composés amides et leur utilisation |
US8329691B2 (en) | 2007-10-15 | 2012-12-11 | Takeda Pharmaceutical Company Limited | Amide compounds and use of the same |
US8586751B2 (en) | 2009-06-12 | 2013-11-19 | Bristol-Myers Squibb Company | Nicotinamide compounds useful as kinase modulators |
US10030016B2 (en) | 2009-10-06 | 2018-07-24 | Sunesis Pharmaceuticals, Inc. | Heterocyclic compounds useful as PDK1 inhibitors |
US9546165B2 (en) | 2009-10-06 | 2017-01-17 | Sunesis Pharmaceuticals, Inc. | Heterocyclic compounds useful as PDK1 inhibitors |
JP2013506715A (ja) * | 2009-10-06 | 2013-02-28 | ミレニアム ファーマシューティカルズ, インコーポレイテッド | Pdk1インヒビターとして有用な複素環式化合物 |
US10668051B2 (en) | 2009-10-08 | 2020-06-02 | Rhizen Pharmaceuticals Sa | Modulators of calcium release-activated calcium channel |
US8377970B2 (en) | 2009-10-08 | 2013-02-19 | Rhizen Pharmaceuticals Sa | Modulators of calcium release-activated calcium channel |
CN104788430B (zh) * | 2009-10-08 | 2019-10-22 | 理森制药股份公司 | 吡唑衍生物钙释放激活钙通道调节剂及非小细胞肺癌的治疗方法 |
US8993612B2 (en) | 2009-10-08 | 2015-03-31 | Rhizen Pharmaceuticals Sa | Modulators of calcium release-activated calcium channel and methods for treatment of non-small cell lung cancer |
CN104788430A (zh) * | 2009-10-08 | 2015-07-22 | 理森制药股份公司 | 吡唑衍生物钙释放激活钙通道调节剂及非小细胞肺癌的治疗方法 |
WO2011042797A1 (fr) * | 2009-10-08 | 2011-04-14 | Icozen Therapeutics Pvt. Ltd. | Dérivés de pyrazole en tant que modulateurs du canal calcique activé par la libération du calcium |
CN102834382B (zh) * | 2009-10-08 | 2016-08-03 | 理森制药股份公司 | 作为钙释放激活钙通道调节剂的吡唑衍生物 |
US10246450B2 (en) | 2009-10-08 | 2019-04-02 | Rhizen Pharmaceuticals Sa | Modulators of calcium release-activated calcium channel |
EA024630B1 (ru) * | 2009-10-08 | 2016-10-31 | Ризен Фармасьютикалз С.А. | Производные пиразола как ингибиторы ионных каналов, активируемых высвобождением кальция (crac) |
US8921364B2 (en) | 2009-10-08 | 2014-12-30 | Rhizen Pharmaceuticals Sa | Modulators of calcium release-activated calcium channel |
US9758514B2 (en) | 2009-10-08 | 2017-09-12 | Rhizen Pharmaceuticals Sa | Modulators of calcium release-activated calcium channel |
US10174034B2 (en) | 2009-10-08 | 2019-01-08 | Rhizen Pharmaceuticals Sa | Modulators of calcium release-activated calcium channel and methods for treatment of non-small cell lung cancer |
US9944631B2 (en) | 2009-10-08 | 2018-04-17 | Rhizen Pharmaceuticals Sa | Modulators of calcium release-activated calcium channel |
CN110627724A (zh) * | 2009-10-08 | 2019-12-31 | 理森制药股份公司 | 吡唑衍生物钙释放激活钙通道调节剂及非小细胞肺癌的治疗方法 |
CN102834382A (zh) * | 2009-10-08 | 2012-12-19 | 理森制药股份公司 | 作为钙释放激活钙通道调节剂的吡唑衍生物 |
US9828345B2 (en) | 2013-02-28 | 2017-11-28 | Bristol-Myers Squibb Company | Phenylpyrazole derivatives as potent ROCK1 and ROCK2 inhibitors |
US9458110B2 (en) | 2013-02-28 | 2016-10-04 | Bristol-Myers Squibb Company | Phenylpyrazole derivatives as potent ROCK1 and ROCK2 inhibitors |
WO2015010832A1 (fr) * | 2013-07-22 | 2015-01-29 | Syngenta Participations Ag | Dérivés hétérocycliques microbiocides |
WO2016039448A1 (fr) * | 2014-09-12 | 2016-03-17 | 田辺三菱製薬株式会社 | Composé aromatique d'amide d'acide carboxylique |
US11858939B2 (en) | 2015-07-06 | 2024-01-02 | Alkermes, Inc. | Hetero-halo inhibitors of histone deacetylase |
US10919902B2 (en) | 2015-07-06 | 2021-02-16 | Alkermes, Inc. | Hetero-halo inhibitors of histone deacetylase |
US10421756B2 (en) | 2015-07-06 | 2019-09-24 | Rodin Therapeutics, Inc. | Heterobicyclic N-aminophenyl-amides as inhibitors of histone deacetylase |
EP3868749A1 (fr) | 2016-03-23 | 2021-08-25 | Syngenta Participations Ag | Composés herbicides |
US11225479B2 (en) | 2017-01-11 | 2022-01-18 | Alkermes, Inc. | Bicyclic inhibitors of histone deacetylase |
US10519149B2 (en) | 2017-01-11 | 2019-12-31 | Rodin Therapeutics, Inc. | Bicyclic inhibitors of histone deacetylase |
US9951069B1 (en) | 2017-01-11 | 2018-04-24 | Rodin Therapeutics, Inc. | Bicyclic inhibitors of histone deacetylase |
US10696673B2 (en) | 2017-01-11 | 2020-06-30 | Rodin Therapeutics, Inc. | Bicyclic inhibitors of histone deacetylase |
US10793567B2 (en) | 2017-01-11 | 2020-10-06 | Rodin Therapeutics, Inc. | Bicyclic inhibitors of histone deacetylase |
US11286256B2 (en) | 2017-01-11 | 2022-03-29 | Alkermes, Inc. | Bicyclic inhibitors of histone deacetylase |
US10336762B2 (en) | 2017-02-16 | 2019-07-02 | Gilead Sciences, Inc. | Pyrrolo[1,2-b]pyridazine derivatives |
US11225475B2 (en) | 2017-08-07 | 2022-01-18 | Alkermes, Inc. | Substituted pyridines as inhibitors of histone deacetylase |
US11912702B2 (en) | 2017-08-07 | 2024-02-27 | Alkermes, Inc. | Substituted pyridines as inhibitors of histone deacetylase |
US11535622B2 (en) | 2018-07-13 | 2022-12-27 | Gilead Sciences, Inc. | Pyrrolo[1,2-b] pyridazine derivatives |
US10875866B2 (en) | 2018-07-13 | 2020-12-29 | Gilead Sciences, Inc. | Pyrrolo[1,2-B]pyridazine derivatives |
WO2021092322A1 (fr) * | 2019-11-06 | 2021-05-14 | Remedy Plan, Inc. | Traitements anticancéreux ciblant des cellules souches cancéreuses |
CN114929672A (zh) * | 2019-11-06 | 2022-08-19 | 治疗方案股份有限公司 | 靶向癌症干细胞的癌症治疗 |
CN111393376B (zh) * | 2020-05-11 | 2022-05-13 | 安徽赛迪生物科技有限公司 | 一种2-氯嘧啶-4-甲酸的合成方法 |
CN111393376A (zh) * | 2020-05-11 | 2020-07-10 | 安徽赛迪生物科技有限公司 | 一种2-氯嘧啶-4-甲酸的合成方法 |
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WO2008016643A3 (fr) | 2008-06-19 |
AR062176A1 (es) | 2008-10-22 |
PE20080432A1 (es) | 2008-05-29 |
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