WO2008009963A3 - Pyrimidine derivatives as modulators of parathyroid hormone receptors - Google Patents
Pyrimidine derivatives as modulators of parathyroid hormone receptors Download PDFInfo
- Publication number
- WO2008009963A3 WO2008009963A3 PCT/GB2007/002767 GB2007002767W WO2008009963A3 WO 2008009963 A3 WO2008009963 A3 WO 2008009963A3 GB 2007002767 W GB2007002767 W GB 2007002767W WO 2008009963 A3 WO2008009963 A3 WO 2008009963A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- parathyroid hormone
- pyrimidine derivatives
- modulators
- hormone receptors
- pth
- Prior art date
Links
Classifications
-
- 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
- C07D403/12—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 linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/26—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/34—One oxygen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (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)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The present invention is concerned with pyrimidine derivatives, their intermediates, uses thereof and processes for their production. In particular, the present invention relates to parathyroid hormone (PTH) and parathyroid hormone related protein (PTHrp) receptor ligands, (PTH-I or PTH/PTHrp receptor ligands). The invention also relates to methods of preparing such ligands and to compounds which are useful as intermediates in such methods.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0614579.1A GB0614579D0 (en) | 2006-07-21 | 2006-07-21 | Pyrimidine derivatives |
GB0614579.1 | 2006-07-21 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2008009963A2 WO2008009963A2 (en) | 2008-01-24 |
WO2008009963A3 true WO2008009963A3 (en) | 2008-05-08 |
Family
ID=36998543
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/GB2007/002767 WO2008009963A2 (en) | 2006-07-21 | 2007-07-20 | Pyrimidine derivatives as modulators of parathyroid hormone receptors |
Country Status (2)
Country | Link |
---|---|
GB (1) | GB0614579D0 (en) |
WO (1) | WO2008009963A2 (en) |
Cited By (1)
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US9273077B2 (en) | 2008-05-21 | 2016-03-01 | Ariad Pharmaceuticals, Inc. | Phosphorus derivatives as kinase inhibitors |
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CL2008000467A1 (en) | 2007-02-14 | 2008-08-22 | Janssen Pharmaceutica Nv | COMPOUNDS DERIVED FROM 2-AMINOPIRIMIDINE, HISTAMINE RECEIVER MODULATORS H4; YOUR PREPARATION PROCEDURE; PHARMACEUTICAL COMPOSITION THAT INCLUDES SUCH COMPOUNDS; AND ITS USE TO TREAT A SELECTED INFLAMMATORY DISORDER OF ALEGIA, ASMA |
EP2300013B2 (en) | 2008-05-21 | 2024-11-13 | Takeda Pharmaceutical Company Limited | Phosphorous derivatives as kinase inhibitors |
GB0815369D0 (en) * | 2008-08-22 | 2008-10-01 | Summit Corp Plc | Compounds for treatment of duchenne muscular dystrophy |
US8586751B2 (en) | 2009-06-12 | 2013-11-19 | Bristol-Myers Squibb Company | Nicotinamide compounds useful as kinase modulators |
WO2012151561A1 (en) | 2011-05-04 | 2012-11-08 | Ariad Pharmaceuticals, Inc. | Compounds for inhibiting cell proliferation in egfr-driven cancers |
US9981918B2 (en) | 2011-08-30 | 2018-05-29 | Chdi Foundation, Inc. | Kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof |
AU2013204563B2 (en) | 2012-05-05 | 2016-05-19 | Takeda Pharmaceutical Company Limited | Compounds for inhibiting cell proliferation in EGFR-driven cancers |
US9611283B1 (en) | 2013-04-10 | 2017-04-04 | Ariad Pharmaceuticals, Inc. | Methods for inhibiting cell proliferation in ALK-driven cancers |
EP3094631B1 (en) | 2014-01-16 | 2019-01-09 | FMC Corporation | Pyrimidinyloxy benzene derivatives as herbicides |
EP3169684B1 (en) | 2014-07-17 | 2019-06-26 | CHDI Foundation, Inc. | Combination of kmo inhibitor 6-(3-chloro-4-cyclopropoxyphenyl)pyrimidine-4-carboxylic acid with antiviral agent for treating hiv related neurological disorders |
WO2016043260A1 (en) * | 2014-09-19 | 2016-03-24 | 塩野義製薬株式会社 | Cyclic guanidine or amidine compound |
ES2872553T3 (en) | 2015-03-06 | 2021-11-02 | Pharmakea Inc | Lysyl oxidase type-2 inhibitors and uses thereof |
JP6697809B2 (en) | 2015-03-06 | 2020-05-27 | ファーマケア,インク. | Fluorinated lysyl oxidase-like 2 inhibitors and their use |
CA2969816C (en) | 2015-03-18 | 2022-03-01 | E I Du Pont De Nemours And Company | Substituted pyrimidinyloxy pyridine derivatives as herbicides |
TWI828952B (en) | 2015-06-05 | 2024-01-11 | 美商艾佛艾姆希公司 | Pyrimidinyloxy benzene derivatives as herbicides |
EP3939973A1 (en) | 2015-07-06 | 2022-01-19 | Alkermes, Inc. | Hetero-halo inhibitors of histone deacetylase |
EP3319968A1 (en) | 2015-07-06 | 2018-05-16 | Rodin Therapeutics, Inc. | Heterobicyclic n-aminophenyl-amides as inhibitors of histone deacetylase |
BR112018000687B1 (en) | 2015-07-13 | 2021-05-04 | Fmc Corporation | compost, herbicide compositions, herbicide mixtures and methods for controlling the growth of unwanted vegetation |
EA201990621A1 (en) | 2016-09-07 | 2019-09-30 | Фармакеа, Инк. | CRYSTALLIC FORMS OF LYSYLOXIDASE-LIKE PROTEIN 2 INHIBITOR AND METHODS FOR PRODUCING |
EP3509594A4 (en) | 2016-09-07 | 2020-05-06 | Pharmakea, Inc. | Uses of a lysyl oxidase-like 2 inhibitor |
AU2018207402B2 (en) | 2017-01-11 | 2023-09-28 | Alkermes, Inc. | Bicyclic inhibitors of histone deacetylase |
US11427549B2 (en) | 2017-05-02 | 2022-08-30 | Fmc Corporation | Pyrimidinyloxy benzo-fused compounds as herbicides |
TW201843148A (en) * | 2017-05-08 | 2018-12-16 | 國立大學法人京都大學 | Compound, light emitting material and organic light emitting element |
WO2019032528A1 (en) | 2017-08-07 | 2019-02-14 | Rodin Therapeutics, Inc | Bicyclic inhibitors of histone deacetylase |
EP3713926B1 (en) | 2017-11-21 | 2023-06-07 | Bayer Aktiengesellschaft | 2-hetarylpyrimidine-4-carboxamides as aryl hydrocarbon receptor anatgonists |
CA3082858A1 (en) | 2017-11-21 | 2019-05-31 | Bayer Aktiengesellschaft | 2-phenylpyrimidine-4-carboxamides as ahr inhibitors |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003099776A1 (en) * | 2002-05-23 | 2003-12-04 | Amgen Inc. | Calcium receptor modulating arylalkylamines |
WO2005075458A1 (en) * | 2004-02-10 | 2005-08-18 | Sanofi-Aventis | Pyrimidine derivatives as orexin receptors antagonists |
WO2006071538A2 (en) * | 2004-12-13 | 2006-07-06 | Neurogen Corporation | Substituted biaryl analogues |
-
2006
- 2006-07-21 GB GBGB0614579.1A patent/GB0614579D0/en not_active Ceased
-
2007
- 2007-07-20 WO PCT/GB2007/002767 patent/WO2008009963A2/en active Application Filing
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003099776A1 (en) * | 2002-05-23 | 2003-12-04 | Amgen Inc. | Calcium receptor modulating arylalkylamines |
WO2005075458A1 (en) * | 2004-02-10 | 2005-08-18 | Sanofi-Aventis | Pyrimidine derivatives as orexin receptors antagonists |
WO2006071538A2 (en) * | 2004-12-13 | 2006-07-06 | Neurogen Corporation | Substituted biaryl analogues |
Non-Patent Citations (4)
Title |
---|
GHOSH D ET AL: "2,4-bis(aryloxy)pyrimidines as antimierobial agents.", JOURNAL OF MEDICINAL CHEMISTRY NOV 1968, vol. 11, no. 6, November 1968 (1968-11-01), pages 1237 - 1238, XP002470439, ISSN: 0022-2623 * |
KIM D H ET AL: "Synthesis of pyrido[1,2 a]pyrimido[4,5 d]pyrimidin 5 ones. Cyclization reaction of 4 [(3 hydroxy 2 pyridyl)amino] 2 phenyl 5 pyrimidinecarboxylic acid with acetic anhydride", JOURNAL OF HETEROCYCLIC CHEMISTRY 1975, vol. 12, no. 3, 1975, pages 477 - 480, XP002470440, ISSN: 0022-152X * |
SAKAI NORIO ET AL: "New approach to the practical synthesis of tri- or tetrasubstituted pyrimidine derivatives: a four-component coupling reaction from a functionalized silane, two types of aromatic nitriles, and acetals.", ORGANIC LETTERS 13 OCT 2005, vol. 7, no. 21, 13 October 2005 (2005-10-13), pages 4705 - 4708, XP002470438, ISSN: 1523-7060 * |
TRANTOLO D J ET AL: "Inhibitors of Bacillus subtilis DNA Polymerase III. Influence of Modifications in the Pyrimidine Ring of Anilino- and (Benzylamino)pyrimidines", JOURNAL OF MEDICINAL CHEMISTRY, AMERICAN CHEMICAL SOCIETY. WASHINGTON, US, vol. 29, no. 5, 1986, pages 676 - 681, XP002269094, ISSN: 0022-2623 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9273077B2 (en) | 2008-05-21 | 2016-03-01 | Ariad Pharmaceuticals, Inc. | Phosphorus derivatives as kinase inhibitors |
Also Published As
Publication number | Publication date |
---|---|
GB0614579D0 (en) | 2006-08-30 |
WO2008009963A2 (en) | 2008-01-24 |
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