WO2010046780A3 - Anti viral compounds - Google Patents
Anti viral compounds Download PDFInfo
- Publication number
- WO2010046780A3 WO2010046780A3 PCT/IB2009/007420 IB2009007420W WO2010046780A3 WO 2010046780 A3 WO2010046780 A3 WO 2010046780A3 IB 2009007420 W IB2009007420 W IB 2009007420W WO 2010046780 A3 WO2010046780 A3 WO 2010046780A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- viral compounds
- anti viral
- compounds
- hts
- hiv
- Prior art date
Links
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
- 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
-
- 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
- C07D405/02—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 two hetero rings
- C07D405/04—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 two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur 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
- 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
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Virology (AREA)
- General Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
There is provided small molecule anti-human immunodeficiency virus (anti-HIV) compounds as well as a phenotypic cell-based high throughput screening (HTS) assay for their identification.
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10744808P | 2008-10-22 | 2008-10-22 | |
US61/107,448 | 2008-10-22 | ||
US10902808P | 2008-10-28 | 2008-10-28 | |
US61/109,028 | 2008-10-28 | ||
US22883709P | 2009-07-27 | 2009-07-27 | |
US61/228,837 | 2009-07-27 |
Publications (2)
Publication Number | Publication Date |
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WO2010046780A2 WO2010046780A2 (en) | 2010-04-29 |
WO2010046780A3 true WO2010046780A3 (en) | 2011-01-13 |
Family
ID=41820529
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IB2009/007420 WO2010046780A2 (en) | 2008-10-22 | 2009-10-21 | Anti viral compounds |
Country Status (1)
Country | Link |
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WO (1) | WO2010046780A2 (en) |
Families Citing this family (64)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5775519B2 (en) * | 2009-09-25 | 2015-09-09 | ニヴァリス・セラピューティクス・インコーポレーテッド | Novel dihydropyrimidin-2 (1H) -one compounds as S-nitrosoglutathione reductase inhibitors |
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US8906933B2 (en) | 2010-09-24 | 2014-12-09 | N30 Pharmaceuticals, Inc. | Dihydropyrimidin-2(1H)-one compounds as neurokinin-3 receptor antagonists |
AU2012272898A1 (en) | 2011-06-24 | 2013-04-11 | Amgen Inc. | TRPM8 antagonists and their use in treatments |
JP2014527511A (en) | 2011-06-24 | 2014-10-16 | アムジエン・インコーポレーテツド | TRPM8 antagonists and their use in therapy |
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WO2013091089A1 (en) * | 2011-12-22 | 2013-06-27 | UNIVERSITé LAVAL | Three-dimensional cavities of dendritic cell immunoreceptor (dcir), compounds binding thereto and therapeutic applications related to inhibition of human immunodeficiency virus type-1 (hiv-1) |
JP2013199459A (en) * | 2012-03-26 | 2013-10-03 | Konica Minolta Inc | Method for producing cyanoacetic acid, method for producing cyanoacetic acid derivative and method for producing metal containing compound |
US8952009B2 (en) | 2012-08-06 | 2015-02-10 | Amgen Inc. | Chroman derivatives as TRPM8 inhibitors |
CN105793255B (en) | 2013-10-04 | 2018-11-16 | 无限药品股份有限公司 | Heterocyclic compound and application thereof |
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MX2016006603A (en) | 2013-12-20 | 2016-09-06 | Esteve Labor Dr | Piperidine compounds having multimodal activity against pain. |
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US9775844B2 (en) | 2014-03-19 | 2017-10-03 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
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WO2016054491A1 (en) | 2014-10-03 | 2016-04-07 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
WO2017007756A1 (en) | 2015-07-06 | 2017-01-12 | Rodin Therapeutics, 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 |
US10179131B2 (en) * | 2015-07-13 | 2019-01-15 | Enanta Pharmaceuticals, Inc. | Hepatitis B antiviral agents |
WO2017048702A1 (en) | 2015-09-14 | 2017-03-23 | Infinity Pharmaceuticals, Inc. | Solid forms of isoquinolinone derivatives, process of making, compositions comprising, and methods of using the same |
TWI620748B (en) | 2016-02-05 | 2018-04-11 | National Health Research Institutes | Aminothiazole compounds and use thereof |
US10759806B2 (en) | 2016-03-17 | 2020-09-01 | Infinity Pharmaceuticals, Inc. | Isotopologues of isoquinolinone and quinazolinone compounds and uses thereof as PI3K kinase inhibitors |
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WO2017214269A1 (en) | 2016-06-08 | 2017-12-14 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
US20180072741A1 (en) | 2016-09-09 | 2018-03-15 | Incyte Corporation | Pyrazolopyrimidine compounds and uses thereof |
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WO2018049191A1 (en) | 2016-09-09 | 2018-03-15 | Incyte Corporation | Pyrazolopyridone derivatives as hpk1 modulators and uses thereof for the treatment of cancer |
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EP3570834B1 (en) | 2017-01-11 | 2021-12-22 | Alkermes, Inc. | Bicyclic inhibitors of histone deacetylase |
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US11225475B2 (en) | 2017-08-07 | 2022-01-18 | Alkermes, Inc. | Substituted pyridines as inhibitors of histone deacetylase |
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Citations (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2711746A1 (en) * | 1976-03-29 | 1977-10-06 | Nippon Shinyaku Co Ltd | NICOTINOYLAMINOTRIAZINE DERIVATIVES |
JPH02129648A (en) * | 1988-11-10 | 1990-05-17 | Canon Inc | Electrophotographic sensitive body |
WO2002070484A1 (en) * | 2001-03-05 | 2002-09-12 | Bayer Aktiengesellschaft | Substituted 2-oxy-3,5-dicyano-4-aryl-6-aminopyridines and use thereof |
WO2002070520A1 (en) * | 2001-03-07 | 2002-09-12 | Bayer Aktiengesellschaft | Substituted 2,6-diamino-3,5-dicyano-4-aryl-pyridines and their use as adenosine receptor-selective ligands |
WO2002079197A1 (en) * | 2001-03-29 | 2002-10-10 | Vertex Pharmaceuticals Incorporated | Inhibitors of c-jun n-terminal kinases (jnk) and other protein kinases |
US20020156087A1 (en) * | 1998-06-19 | 2002-10-24 | Nuss John M. | Inhibitors of glycogen synthase kinase 3 |
US20030064982A1 (en) * | 2000-09-15 | 2003-04-03 | Robert Davies | Pyrazole compounds useful as protein kinase inhibitors |
EP1302463A1 (en) * | 2000-07-18 | 2003-04-16 | Yamanouchi Pharmaceutical Co. Ltd. | Medicine comprising dicyanopyridine derivative |
WO2003049739A1 (en) * | 2001-12-07 | 2003-06-19 | Vertex Pharmaceuticals, Inc. | Pyrimidine-based compounds useful as gsk-3 inhibitors |
WO2004024691A1 (en) * | 2002-09-16 | 2004-03-25 | Glaxo Group Limited | Cox-2 inhibiting pyridine derivatives |
WO2004076412A2 (en) * | 2003-02-26 | 2004-09-10 | Sugen, Inc. | Aminoheteroaryl compounds as protein kinase inhibitors |
WO2005054199A1 (en) * | 2003-12-03 | 2005-06-16 | Cytopia Research Pty Ltd | Tubulin inhibitors |
WO2008033455A2 (en) * | 2006-09-13 | 2008-03-20 | The Institutes For Pharmaceutical Discovery, Llc | Biphenyl and heteroaryl phenyl derivatives as protein tyrosine phosphatases inhibitors |
EP2141164A1 (en) * | 2008-07-01 | 2010-01-06 | Mutabilis | New 1,2,4-triazine derivatives and biological applications thereof |
-
2009
- 2009-10-21 WO PCT/IB2009/007420 patent/WO2010046780A2/en active Application Filing
Patent Citations (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2346349A1 (en) * | 1976-03-29 | 1977-10-28 | Nippon Shinyaku Co Ltd | NICOTINOYLAMINOTRIAZINE DERIVATIVES AND NEW PRODUCTS THUS OBTAINED FOR DIURETIC AND ANTI-ULCER ACTIVITIES |
DE2711746A1 (en) * | 1976-03-29 | 1977-10-06 | Nippon Shinyaku Co Ltd | NICOTINOYLAMINOTRIAZINE DERIVATIVES |
JPH02129648A (en) * | 1988-11-10 | 1990-05-17 | Canon Inc | Electrophotographic sensitive body |
US20020156087A1 (en) * | 1998-06-19 | 2002-10-24 | Nuss John M. | Inhibitors of glycogen synthase kinase 3 |
EP1302463A1 (en) * | 2000-07-18 | 2003-04-16 | Yamanouchi Pharmaceutical Co. Ltd. | Medicine comprising dicyanopyridine derivative |
US20030064982A1 (en) * | 2000-09-15 | 2003-04-03 | Robert Davies | Pyrazole compounds useful as protein kinase inhibitors |
WO2002070484A1 (en) * | 2001-03-05 | 2002-09-12 | Bayer Aktiengesellschaft | Substituted 2-oxy-3,5-dicyano-4-aryl-6-aminopyridines and use thereof |
WO2002070520A1 (en) * | 2001-03-07 | 2002-09-12 | Bayer Aktiengesellschaft | Substituted 2,6-diamino-3,5-dicyano-4-aryl-pyridines and their use as adenosine receptor-selective ligands |
WO2002079197A1 (en) * | 2001-03-29 | 2002-10-10 | Vertex Pharmaceuticals Incorporated | Inhibitors of c-jun n-terminal kinases (jnk) and other protein kinases |
WO2003049739A1 (en) * | 2001-12-07 | 2003-06-19 | Vertex Pharmaceuticals, Inc. | Pyrimidine-based compounds useful as gsk-3 inhibitors |
WO2004024691A1 (en) * | 2002-09-16 | 2004-03-25 | Glaxo Group Limited | Cox-2 inhibiting pyridine derivatives |
WO2004076412A2 (en) * | 2003-02-26 | 2004-09-10 | Sugen, Inc. | Aminoheteroaryl compounds as protein kinase inhibitors |
WO2005054199A1 (en) * | 2003-12-03 | 2005-06-16 | Cytopia Research Pty Ltd | Tubulin inhibitors |
WO2008033455A2 (en) * | 2006-09-13 | 2008-03-20 | The Institutes For Pharmaceutical Discovery, Llc | Biphenyl and heteroaryl phenyl derivatives as protein tyrosine phosphatases inhibitors |
EP2141164A1 (en) * | 2008-07-01 | 2010-01-06 | Mutabilis | New 1,2,4-triazine derivatives and biological applications thereof |
Non-Patent Citations (15)
Title |
---|
BRAD H. HENKE, DAVID H. DREWRY, STACEY A. JONES, EUGENE L. STEWART, SUSAN L. WEAVER, ROBERT W. WIETHE: "2-Amino-4,6-diarylpyridines as novel ligands for the estrogen receptor", BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, vol. 11, 2001, pages 1939 - 1942, XP002575776 * |
BRITT-MARIE SWAHN, YAFENG XUE, ERWAN ARZEL, ELISABETH KALLIN, ANGELIKA MAGNUS ET AL: "Design and synthesis of 2'-anilino-4,4'-bipyridines as selective inhibitors of c-Jun N-terminal kinase-3", BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, vol. 16, 2006, pages 1397 - 1401, XP002575780 * |
FENTON HEIRTZLER, MARKUS NEUBURGER, KLAUS KULIKE: "Insights on the synthesis and organisational phenomena of twisted pyrazine-pyridine hybrids", J. CHEM. SOC. PERKIN TRANSACTIONS 1, vol. 2002, no. 6, 2002, pages 809 - 820, XP002575779 * |
FENTON R. HEIRTZLER: "Preparation of non-symmetrical 2,3-bis-(2,2'-oligopyridyl)pyrazines via 1,2-disubstituted ethanones", SYNLETT, vol. 1999, no. 8, 1999, pages 1203 - 1206, XP002575778 * |
FRANCOISE GELLIBERT, ANNE-CHARLOTTE DE GOUVILLE, JAMES WOOLVEN, NEIL MATHEWS, VAN-LOC NGUYEN ET AL.: "Discovery of 4-{4-[3-(pyridin-2-yl)-1H-pyrazol-4-yl]pyridin-2-yl}-N-(tetrahydro-2H-pyran-4-yl)benzamide (GW788388): A potent , selective and orally active transforming growth factor-beta type I receptor inhibitor", J. MED. CHEM., vol. 49, no. 7, 16 March 2006 (2006-03-16), pages 2210 - 2221, XP002575772 * |
G. G. MOSKALENKO, V. F. SEDOVA: "Synthesis of substituted 2- and 4-hydroxyaminopyrimidines", CHEMISTRY OF HETEROCYCLIC COMPOUNDS, vol. 22, no. 11, 1986, pages 1232 - 1236, XP002575774 * |
ION NICOLESCU-DUVAZ, ESTEBAN ROMAN, STEVEN R. WHITTAKER, FRANK FRIEDLOS, RUTH KIRK ET AL: "Novel inhibitors of B-RAF based on a disubstituted pyrazine scaffold. Generation of a nanomolar lead", J. MED. CHEM., vol. 49, no. 1, 2006, pages 407 - 416, XP002575784 * |
ISABELLE PRÉVOT-HALTER, THOMAS I. SMITH, JEAN WEISS: "Assembling organic receptors around transition metal templates: Functionalized catechols and dioxomolybdenum(VI) for the recognition of dicarboxylic acids", J. ORG. CHEM., vol. 62, no. 7, 1997, pages 2186 - 2192, XP002575777 * |
JOHN LIMANTO, RICHARD A. DESMOND, DONALD R. GAUTHIER, PAUL N. DEVINE, ROBERT A. REAMER, R. P. VOLANTE: "A regioselective approach to 5-substituted-3-amino-1,2,4-triazines", ORGANIC LETTERS, vol. 5, no. 13, 23 May 2003 (2003-05-23), pages 2271 - 2274, XP002575786 * |
JULIO ALVAREZ-BUILLA, JUAN LOPEZ BENITO, MA. GLORIA QUINTANILLA: "Reinvestigation of Thesing's synthesis of 2-pyridones using 1-(methylthio-thiocarbonylmethyl)pyridinium iodide", J. PRAKT. CHEM., vol. 328, no. 2, 1986, pages 245 - 252, XP002575775 * |
L. RUHLMANN, C. COSTA-COQUELARD, J. HAO, S. JIANG, C. HE, L. SUN, I. LAMPRE: "Association of ruthenium complexes [Ru(bpy)3]2+ or [Ru(bpy)2(Mebpy-py)]2+ with Dawson polyanions alpha-[P2W18O62]6- or alpha2-[FeIII(H2O)P2W17O61]7-", CAN. J. CHEM., vol. 86, no. 11, 15 October 2008 (2008-10-15), pages 1034 - 1043, XP002575782 * |
MILES CONGREVE, DAVID AHARONY, JEFFREY ALBERT, OWEN CALLAGHAN, JAMES CAMPBELL ET AL: "Application of fragment screening by X-ray crystallography to the discovery of aminopyridines as inhibitors of beta-secretase", J. MED. CHEM., vol. 50, no. 6, 2007, pages 1124 - 1132, XP002575785 * |
ROLAND SPITZNER, MARKUS LESINSKI, MONIKA RICHTER, WERNER SCHROTH: "Nukleophile Substitutionen und Eliminierungen von Aminofunktionen via Pyridiniumsalze", MONATSHEFTE FÜR CHEMIE, vol. 118, 1987, pages 485 - 502, XP002575773 * |
SANTOSH S. KULKARNI, AMY HAUCK NEWMAN: "Design and synthesis of novel heterobiaryl amides as metabotropic glutamate receptor subtype 5 antagonists", BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, vol. 17, 2007, pages 2074 - 2079, XP002575781 * |
THOMAS BARK, THOMAS WEYHERMÜLLER, FENTON HEIRTZLER: "Self-assembly of a helical dicopper(I) metallophane", CHEM. COMMUN., vol. 14, 1998, pages 1475 - 1476, XP002575783 * |
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