ATE309207T1 - Phosphat-mimetika sowie behandlungsmethoden unter verwendung von phosphatase-inhibitoren - Google Patents
Phosphat-mimetika sowie behandlungsmethoden unter verwendung von phosphatase-inhibitorenInfo
- Publication number
- ATE309207T1 ATE309207T1 AT00961360T AT00961360T ATE309207T1 AT E309207 T1 ATE309207 T1 AT E309207T1 AT 00961360 T AT00961360 T AT 00961360T AT 00961360 T AT00961360 T AT 00961360T AT E309207 T1 ATE309207 T1 AT E309207T1
- Authority
- AT
- Austria
- Prior art keywords
- protein tyrosine
- compounds
- phosphate
- modulate
- expected
- Prior art date
Links
- 229910019142 PO4 Inorganic materials 0.000 title 1
- 102000004160 Phosphoric Monoester Hydrolases Human genes 0.000 title 1
- 108090000608 Phosphoric Monoester Hydrolases Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 title 1
- 239000010452 phosphate Substances 0.000 title 1
- 102000004190 Enzymes Human genes 0.000 abstract 2
- 108090000790 Enzymes Proteins 0.000 abstract 2
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 abstract 2
- 230000004715 cellular signal transduction Effects 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 230000000694 effects Effects 0.000 abstract 2
- 102000004169 proteins and genes Human genes 0.000 abstract 2
- 108090000623 proteins and genes Proteins 0.000 abstract 2
- -1 trifluoromethyl sulfonamido compounds Chemical class 0.000 abstract 2
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 abstract 2
- 208000035473 Communicable disease Diseases 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 208000001132 Osteoporosis Diseases 0.000 abstract 1
- 102000006335 Phosphate-Binding Proteins Human genes 0.000 abstract 1
- 108010058514 Phosphate-Binding Proteins Proteins 0.000 abstract 1
- 102000002727 Protein Tyrosine Phosphatase Human genes 0.000 abstract 1
- 230000002159 abnormal effect Effects 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 206010012601 diabetes mellitus Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 230000002519 immonomodulatory effect Effects 0.000 abstract 1
- 208000015122 neurodegenerative disease Diseases 0.000 abstract 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 108020000494 protein-tyrosine phosphatase Proteins 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C311/09—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton the carbon skeleton being further substituted by at least two halogen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/14—Sulfones; Sulfoxides having sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/16—Sulfones; Sulfoxides having sulfone or sulfoxide groups and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C317/22—Sulfones; Sulfoxides having sulfone or sulfoxide groups and singly-bound oxygen atoms bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/26—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C317/32—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/26—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C317/32—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C317/34—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having sulfone or sulfoxide groups and amino groups bound to carbon atoms of six-membered aromatic rings being part of the same non-condensed ring or of a condensed ring system containing that ring
- C07C317/38—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having sulfone or sulfoxide groups and amino groups bound to carbon atoms of six-membered aromatic rings being part of the same non-condensed ring or of a condensed ring system containing that ring with the nitrogen atom of at least one amino group being part of any of the groups, X being a hetero atom, Y being any atom, e.g. N-acylaminosulfones
- C07C317/40—Y being a hydrogen or a carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/44—Sulfones; Sulfoxides having sulfone or sulfoxide groups and carboxyl groups bound to the same carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/44—Sulfones; Sulfoxides having sulfone or sulfoxide groups and carboxyl groups bound to the same carbon skeleton
- C07C317/48—Sulfones; Sulfoxides having sulfone or sulfoxide groups and carboxyl groups bound to the same carbon skeleton the carbon skeleton being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
- C07C317/50—Sulfones; Sulfoxides having sulfone or sulfoxide groups and carboxyl groups bound to the same carbon skeleton the carbon skeleton being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups at least one of the nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/64—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and sulfur atoms, not being part of thio groups, bound to the same carbon skeleton
- C07C323/65—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and sulfur atoms, not being part of thio groups, bound to the same carbon skeleton containing sulfur atoms of sulfone or sulfoxide groups bound to the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/42—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- 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
- C07D231/14—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 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
- C07D231/18—One oxygen or sulfur atom
- C07D231/20—One oxygen atom attached in position 3 or 5
- C07D231/22—One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms
- C07D231/24—One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms having sulfone or sulfonic acid radicals in the molecule
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D235/16—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/18—Benzimidazoles; Hydrogenated benzimidazoles with aryl radicals directly attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
- C07D295/096—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
- C07C2601/08—Systems containing only non-condensed rings with a five-membered ring the ring being saturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (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)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Physical Education & Sports Medicine (AREA)
- Diabetes (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Biomedical Technology (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Immunology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US15097099P | 1999-08-27 | 1999-08-27 | |
US16536599P | 1999-11-12 | 1999-11-12 | |
PCT/US2000/023293 WO2001016097A1 (en) | 1999-08-27 | 2000-08-25 | Phosphate mimics and methods of treatment using phosphatase inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
ATE309207T1 true ATE309207T1 (de) | 2005-11-15 |
Family
ID=26848202
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT00961360T ATE309207T1 (de) | 1999-08-27 | 2000-08-25 | Phosphat-mimetika sowie behandlungsmethoden unter verwendung von phosphatase-inhibitoren |
Country Status (12)
Country | Link |
---|---|
US (2) | US6596772B1 (de) |
EP (1) | EP1212296B9 (de) |
JP (1) | JP2003508382A (de) |
AT (1) | ATE309207T1 (de) |
AU (1) | AU775625B2 (de) |
CA (1) | CA2382789A1 (de) |
DE (1) | DE60023920T2 (de) |
ES (1) | ES2252058T3 (de) |
IL (1) | IL148243A0 (de) |
NZ (1) | NZ517426A (de) |
WO (1) | WO2001016097A1 (de) |
ZA (1) | ZA200201609B (de) |
Families Citing this family (93)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU3208200A (en) | 1999-01-13 | 2000-08-01 | Research Foundation Of The State University Of New York, The | A novel method for designing protein kinase inhibitors |
TWI262185B (en) * | 1999-10-01 | 2006-09-21 | Eisai Co Ltd | Carboxylic acid derivatives having anti-hyperglycemia and anti-hyperlipemia action, and pharmaceutical composition containing the derivatives |
US20090124690A1 (en) * | 2000-04-03 | 2009-05-14 | Alberte Randall S | Generation of Combinatorial Synthetic Libraries and Screening for Novel Proadhesins and Nonadhesins |
SE0102299D0 (sv) | 2001-06-26 | 2001-06-26 | Astrazeneca Ab | Compounds |
WO2003032982A1 (en) * | 2001-10-19 | 2003-04-24 | Transtech Pharma, Inc. | Bis-heteroaryl alkanes as therapeutic agents |
JP4623962B2 (ja) * | 2001-10-22 | 2011-02-02 | ザ・リサーチ・ファウンデーション・オブ・ステイト・ユニバーシティ・オブ・ニューヨーク | タンパク質キナーゼおよびホスファターゼ阻害剤、それらを設計する方法、ならびにそれらを使用する方法 |
US7005445B2 (en) | 2001-10-22 | 2006-02-28 | The Research Foundation Of State University Of New York | Protein kinase and phosphatase inhibitors and methods for designing them |
EP1446487A1 (de) * | 2001-11-13 | 2004-08-18 | Sugen, Inc. | Säuger-protein phosphatasen |
US20040014699A1 (en) * | 2002-07-18 | 2004-01-22 | Isis Pharmaceuticals, Inc. | Antisense modulation of PTPRM expression |
JPWO2004039770A1 (ja) * | 2002-10-30 | 2006-03-02 | 日本曹達株式会社 | ジフェニルスルホン誘導体を用いた記録材料及び新規ジフェニルスルホン誘導体化合物 |
DE10256182A1 (de) * | 2002-12-02 | 2004-06-24 | Merck Patent Gmbh | 2-Oxadiazolchromonderivate |
CN1747936A (zh) * | 2003-02-12 | 2006-03-15 | 特兰斯泰克制药公司 | 作为治疗试剂的取代吡咯衍生物 |
US20040186151A1 (en) * | 2003-02-12 | 2004-09-23 | Mjalli Adnan M.M. | Substituted azole derivatives as therapeutic agents |
US20040167183A1 (en) * | 2003-02-20 | 2004-08-26 | The Procter & Gamble Company | Phenethylamino sulfamic acids |
US7141596B2 (en) | 2003-10-08 | 2006-11-28 | Incyte Corporation | Inhibitors of proteins that bind phosphorylated molecules |
AU2003297904A1 (en) * | 2003-12-12 | 2005-07-14 | University Of Maryland, Baltimore | Immunomodulatory compounds that target and inhibit the py+3 binding site of tyrosene kinase p56 lck sh2 domain |
JP4898458B2 (ja) * | 2004-02-12 | 2012-03-14 | トランス テック ファーマ,インコーポレイテッド | 置換アゾール誘導体、組成物及び使用方法 |
JP2008503490A (ja) * | 2004-06-17 | 2008-02-07 | センジェント・セラピューティクス・インコーポレイテッド | チロシンホスファターゼの三置換窒素調節物質 |
US20060135483A1 (en) * | 2004-07-09 | 2006-06-22 | Cheruvallath Zacharia S | Oxygen/nitrogen heterocycle inhibitors of tyrosine phosphatases |
WO2006028970A1 (en) | 2004-09-02 | 2006-03-16 | Cengent Therapeutics, Inc. | Derivatives of thiazole and thiadiazole inhibitors of tyrosine phosphatases |
ES2318556T3 (es) | 2004-11-02 | 2009-05-01 | Pfizer, Inc. | Derivados de sulfonil bencimidazol. |
DE102005055354A1 (de) * | 2005-11-21 | 2007-10-31 | Merck Patent Gmbh | Substituierte 5-Phenyl-3,6-dihydro-2-oxo-6H-[1,3,4]thiadiazine |
US8883841B2 (en) * | 2005-11-23 | 2014-11-11 | The Board Of Regents Of The University Of Texas System | Oncogenic ras-specific cytotoxic compound and methods of use thereof |
AU2007211319B9 (en) | 2006-01-30 | 2012-05-31 | Vtv Therapeutics Llc | Substituted imidazole derivatives and their use as PTPase inhibitors |
JP5190892B2 (ja) * | 2006-02-28 | 2013-04-24 | 独立行政法人理化学研究所 | 新規3−(1−アミノアルキリデン)フラン−2,4(3h,5h)−ジオン誘導体、その製造方法、および、これを有効成分とする医薬組成物 |
EP2004697A2 (de) | 2006-04-07 | 2008-12-24 | The Procter & Gamble Company | An die humane proteintyrosinphosphatase-beta (hptp-beta) bindende antikörper und anwendungen davon |
US20070238700A1 (en) * | 2006-04-10 | 2007-10-11 | Winzenberg Kevin N | N-phenyl-1,1,1-trifluoromethanesulfonamide hydrazone derivative compounds and their usage in controlling parasites |
WO2007141926A1 (ja) * | 2006-06-02 | 2007-12-13 | Osaka University | 延長型アミロイドβ産生抑制剤 |
US7589212B2 (en) * | 2006-06-27 | 2009-09-15 | Procter & Gamble Company | Human protein tyrosine phosphatase inhibitors and methods of use |
US7622593B2 (en) * | 2006-06-27 | 2009-11-24 | The Procter & Gamble Company | Human protein tyrosine phosphatase inhibitors and methods of use |
CN101506180B (zh) * | 2006-06-27 | 2013-10-30 | 艾尔普罗医疗有限公司 | 人蛋白酪氨酸磷酸酶抑制剂及使用方法 |
US7795444B2 (en) | 2006-06-27 | 2010-09-14 | Warner Chilcott Company | Human protein tyrosine phosphatase inhibitors and methods of use |
US7838542B2 (en) | 2006-06-29 | 2010-11-23 | Kinex Pharmaceuticals, Llc | Bicyclic compositions and methods for modulating a kinase cascade |
US8119693B2 (en) * | 2007-05-08 | 2012-02-21 | Sanford-Burnham Medical Research Institute | Tissue non-specific alkaline phosphatase inhibitors and uses thereof for treating vascular calcification |
KR101599715B1 (ko) * | 2007-08-21 | 2016-03-08 | 세노믹스, 인코포레이티드 | 인간 t2r 쓴맛 수용체 및 이의 용도 |
WO2009049098A2 (en) * | 2007-10-09 | 2009-04-16 | Indiana University Research & Technology Corporation | Materials and methods for regulating the activity of phosphatases |
EP2227681A4 (de) * | 2007-12-31 | 2011-01-12 | Univ California | Einzelschritt-echtzeiterkennung von proteinkinase- und/oder phosphatase-aktivitäten aus sers-basis |
US7786171B2 (en) * | 2008-04-04 | 2010-08-31 | Abbott Laboratories | Amide derivatives as positive allosteric modulators and methods of use thereof |
US20120121515A1 (en) | 2009-03-13 | 2012-05-17 | Lenny Dang | Methods and compositions for cell-proliferation-related disorders |
TWI649313B (zh) | 2009-06-29 | 2019-02-01 | 阿吉歐斯製藥公司 | 治療化合物及組成物 |
KR101426125B1 (ko) | 2009-07-06 | 2014-08-06 | 에르피오 세러퓨틱스 인코포레이티드 | 암 세포의 전이 예방을 위한 화합물, 조성물 및 방법 |
US8883832B2 (en) | 2009-07-06 | 2014-11-11 | Aerpio Therapeutics Inc. | Compounds, compositions, and methods for preventing metastasis of cancer cells |
WO2011022462A2 (en) * | 2009-08-18 | 2011-02-24 | President And Fellows Of Harvard College | Neural regeneration |
EP2525790B1 (de) | 2009-10-21 | 2020-05-27 | Agios Pharmaceuticals, Inc. | Verfahren und zusammensetzungen für zellproliferationsbedingte erkrankungen |
CA2777304A1 (en) * | 2009-10-21 | 2011-04-28 | Marion Hitchcock | Substituted benzosulphonamides |
WO2011050210A1 (en) | 2009-10-21 | 2011-04-28 | Agios Pharmaceuticals, Inc. | Methods and compositions for cell-proliferation-related disorders |
US9199914B2 (en) | 2010-02-03 | 2015-12-01 | Meh Associates, Inc. | Multiple substituted fluoromethanes as selective and bioactive isosteres |
BR112013001122B1 (pt) * | 2010-07-16 | 2021-06-08 | Agios Pharmaceuticals, Inc | composto de fórmula ii, uso do composto e composição farmacêutica compreendendo dito composto |
US20140294805A1 (en) | 2010-09-03 | 2014-10-02 | Kenneth W. Bair | Novel compounds and compositions for the inhibition of nampt |
AU2012219323A1 (en) | 2011-02-18 | 2013-09-05 | President And Fellows Of Harvard College | Molecular switch for neuronal outgrowth |
FI3406251T3 (fi) | 2011-05-03 | 2024-02-21 | Agios Pharmaceuticals Inc | Pyruvaattikinaasin aktivaattoreita terapeuttista käyttöä varten |
CN102827073A (zh) | 2011-06-17 | 2012-12-19 | 安吉奥斯医药品有限公司 | 治疗活性组合物和它们的使用方法 |
CN102827170A (zh) | 2011-06-17 | 2012-12-19 | 安吉奥斯医药品有限公司 | 治疗活性组合物和它们的使用方法 |
DK2800743T3 (en) | 2012-01-06 | 2018-06-14 | Agios Pharmaceuticals Inc | THERAPEUTIC ACTIVE RELATIONS AND PROCEDURES FOR USE THEREOF |
US9474779B2 (en) * | 2012-01-19 | 2016-10-25 | Agios Pharmaceuticals, Inc. | Therapeutically active compositions and their methods of use |
US10206967B2 (en) | 2012-04-09 | 2019-02-19 | Case Western Reserve University | Compositions and methods for treating heart disease and/or injury |
US10729777B2 (en) | 2012-04-09 | 2020-08-04 | Case Western Reserve University | Compositions and methods for inhibiting the activity of LAR family phosphatases |
EP2841086B1 (de) * | 2012-04-09 | 2018-09-26 | Case Western Reserve University | Zusammensetzungen zur behandlung von nervenverletzung durch hemmung der aktivität der lar-phosphatasefamilie |
US10786541B2 (en) | 2012-04-09 | 2020-09-29 | Case Western Reserve University | Compositions and methods for treating heart disease and/or injury |
CA2888360A1 (en) | 2012-10-15 | 2014-04-24 | Agios Pharmaceuticals, Inc. | Therapeutic compounds and compositions |
WO2015003355A2 (en) | 2013-07-11 | 2015-01-15 | Agios Pharmaceuticals, Inc. | Therapeutically active compounds and their methods of use |
AU2014287121B2 (en) | 2013-07-11 | 2018-11-15 | Agios Pharmaceuticals, Inc. | 2,4- or 4,6-diaminopyrimidine compounds as IDH2 mutants inhibitors for the treatment of cancer |
WO2015003360A2 (en) | 2013-07-11 | 2015-01-15 | Agios Pharmaceuticals, Inc. | Therapeutically active compounds and their methods of use |
US9579324B2 (en) | 2013-07-11 | 2017-02-28 | Agios Pharmaceuticals, Inc | Therapeutically active compounds and their methods of use |
US20150031627A1 (en) | 2013-07-25 | 2015-01-29 | Agios Pharmaceuticals, Inc | Therapeutically active compounds and their methods of use |
RS58960B1 (sr) | 2013-09-09 | 2019-08-30 | Peloton Therapeutics Inc | Aril etri i njihova primena |
US9884843B2 (en) | 2013-12-16 | 2018-02-06 | Peloton Therapeutics, Inc. | Cyclic sulfone and sulfoximine analogs and uses thereof |
CN106255498B (zh) | 2014-03-14 | 2020-06-26 | 阿吉奥斯制药公司 | 治疗活性化合物的药物组合物 |
US10258672B2 (en) | 2014-10-09 | 2019-04-16 | Case Western Reserve University | Compositions and methods of treating root avulsion injury |
WO2016144825A1 (en) | 2015-03-11 | 2016-09-15 | Peloton Therapeutics, Inc. | Aromatic compounds and uses thereof |
US10278942B2 (en) | 2015-03-11 | 2019-05-07 | Peloton Therapeutics, Inc. | Compositions for use in treating pulmonary arterial hypertension |
WO2016144826A1 (en) | 2015-03-11 | 2016-09-15 | Peloton Therapeutics, Inc. | Substituted pyridines and uses thereof |
US10512626B2 (en) | 2015-03-11 | 2019-12-24 | Peloton Therapeautics, Inc. | Compositions for use in treating glioblastoma |
WO2016168510A1 (en) | 2015-04-17 | 2016-10-20 | Peloton Therapeutics, Inc. | Combination therapy of a hif-2-alpha inhibitor and an immunotherapeutic agent and uses thereof |
ES2959690T3 (es) | 2015-06-11 | 2024-02-27 | Agios Pharmaceuticals Inc | Procedimientos de uso de activadores de piruvato cinasa |
US9796697B2 (en) | 2015-06-12 | 2017-10-24 | Peloton Therapeutics, Inc. | Tricyclic inhibitors of HIF-2-alpha and uses thereof |
CA3002067C (en) | 2015-10-15 | 2023-11-28 | Agios Pharmaceuticals, Inc. | Combination therapy for treating malignancies |
SG10202111435UA (en) | 2015-10-15 | 2021-12-30 | Les Laboratoires Servier Sas | Combination therapy for treating malignancies |
EP4302834A2 (de) | 2016-07-12 | 2024-01-10 | Revolution Medicines, Inc. | 2,5-disubstituierte 3-methyl pyrazine und 2,5,6-trisubstituierte 3-methylpyrazine als allosterische shp2-inhibitoren |
KR102348155B1 (ko) * | 2016-07-18 | 2022-01-06 | 오에이티 아그리오 가부시키가이샤 | 신규한 벤질아미드 화합물, 이를 제조하는 방법, 및 살진드기제 |
CA3030680C (en) * | 2016-08-19 | 2021-11-02 | Nippon Soda Co., Ltd. | Method for producing fluorine-containing sulfonylamide compound |
CN106645723A (zh) * | 2016-11-04 | 2017-05-10 | 中国人民解放军第二军医大学 | Shp2蛋白在制备肝癌对索拉菲尼疗效评估试剂盒中的应用 |
BR112019014527A2 (pt) | 2017-01-23 | 2020-02-27 | Revolution Medicines, Inc. | Compostos de piridina como inibidores de shp2 alostéricos |
WO2018136265A1 (en) | 2017-01-23 | 2018-07-26 | Revolution Medicines, Inc. | Bicyclic compounds as allosteric shp2 inhibitors |
MX2020002608A (es) | 2017-09-07 | 2020-09-18 | Revolution Medicines Inc | Composiciones que comprenden inhibidores de shp2 y metodos para tratar el cáncer. |
KR20200070295A (ko) | 2017-10-12 | 2020-06-17 | 레볼루션 메디슨즈, 인크. | 알로스테릭 shp2 억제제로서의 피리딘, 피라진 및 트리아진 화합물 |
EP3724189B1 (de) | 2017-12-15 | 2023-10-04 | Revolution Medicines, Inc. | Polyzyklischen verbindungen als allosterischen shp2 hemmer |
BR112020021967A2 (pt) | 2018-05-03 | 2021-01-26 | Jiangsu Hengrui Medicine Co., Ltd. | derivados de benzimidazol como moduladores de receptor gama órfão relacionado a retinoides (ror¿) e usos farmacêuticos dos mesmos |
US10980788B2 (en) | 2018-06-08 | 2021-04-20 | Agios Pharmaceuticals, Inc. | Therapy for treating malignancies |
CN112745268B (zh) * | 2019-10-31 | 2022-09-16 | 江苏恒瑞医药股份有限公司 | 苯并咪唑衍生物的晶型及制备方法 |
CN114502535B (zh) * | 2019-10-31 | 2024-04-12 | 江苏恒瑞医药股份有限公司 | 一种RORγ调节剂的酸加成盐 |
WO2021253017A2 (en) * | 2020-06-07 | 2021-12-16 | Ramasamy Sundaram | Compositions and methods for detoxifying bacterial endotoxins and hydrogen sulfide by recombinant fusion enzymes |
CN115637189B (zh) * | 2022-11-14 | 2023-08-29 | 俄美达(武汉)有限公司 | 一种基于多孔性碳材的镁合金切削液的制备方法 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE758241A (fr) * | 1969-11-03 | 1971-04-30 | Agfa Gevaert Nv | Bereiding van 2-alkyl-thiazolen en 2-alkyl-selenazolen met een geanelleerde aromatische ring |
US4177057A (en) * | 1977-10-25 | 1979-12-04 | United States Borax & Chemical Corporation | Herbicidal benzimidazoles |
US5710173A (en) * | 1995-06-07 | 1998-01-20 | Sugen, Inc. | Thienyl compounds for inhibition of cell proliferative disorders |
CA2293400A1 (en) * | 1997-06-13 | 1998-12-17 | Gerald Mcmahon | Novel heteroaryl compounds for the modulation of protein tyrosine enzyme related cellular signal transduction |
-
2000
- 2000-08-25 AT AT00961360T patent/ATE309207T1/de not_active IP Right Cessation
- 2000-08-25 DE DE60023920T patent/DE60023920T2/de not_active Expired - Fee Related
- 2000-08-25 EP EP00961360A patent/EP1212296B9/de not_active Expired - Lifetime
- 2000-08-25 IL IL14824300A patent/IL148243A0/xx unknown
- 2000-08-25 JP JP2001519667A patent/JP2003508382A/ja not_active Withdrawn
- 2000-08-25 US US09/645,879 patent/US6596772B1/en not_active Expired - Fee Related
- 2000-08-25 AU AU73321/00A patent/AU775625B2/en not_active Ceased
- 2000-08-25 WO PCT/US2000/023293 patent/WO2001016097A1/en active IP Right Grant
- 2000-08-25 ES ES00961360T patent/ES2252058T3/es not_active Expired - Lifetime
- 2000-08-25 NZ NZ517426A patent/NZ517426A/en unknown
- 2000-08-25 CA CA002382789A patent/CA2382789A1/en not_active Abandoned
-
2002
- 2002-02-26 ZA ZA200201609A patent/ZA200201609B/en unknown
-
2003
- 2003-07-14 US US10/618,083 patent/US20040138255A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
AU775625B2 (en) | 2004-08-05 |
WO2001016097A1 (en) | 2001-03-08 |
DE60023920T2 (de) | 2006-07-20 |
ES2252058T3 (es) | 2006-05-16 |
EP1212296B1 (de) | 2005-11-09 |
NZ517426A (en) | 2004-04-30 |
EP1212296B9 (de) | 2006-05-10 |
US6596772B1 (en) | 2003-07-22 |
ZA200201609B (en) | 2003-07-30 |
EP1212296A1 (de) | 2002-06-12 |
US20040138255A1 (en) | 2004-07-15 |
CA2382789A1 (en) | 2001-03-08 |
IL148243A0 (en) | 2002-09-12 |
JP2003508382A (ja) | 2003-03-04 |
AU7332100A (en) | 2001-03-26 |
DE60023920D1 (de) | 2005-12-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
ATE309207T1 (de) | Phosphat-mimetika sowie behandlungsmethoden unter verwendung von phosphatase-inhibitoren | |
ATE402698T1 (de) | Verwendung von ppar-gamma aktivatoren zur behandlung von hautkrankheiten | |
DK0966465T3 (da) | Inhibitorer af IMPDH-enzymer | |
DK1162995T3 (da) | Enzymer til behandling af diabetes mellitus type I | |
DE69737814D1 (de) | Gekürzte lösliche typ-i-rezeptoren für tumor-nekrose-faktor | |
BR9811988A (pt) | Derivados de n-alcanoilfenilalanina | |
MX9606404A (es) | Composiciones farmaceuticas y metodos para formular trasnduccion de señales. | |
ATE298248T1 (de) | T-zell inhibierende rezeptorzusammensetzungen sowie deren verwendung | |
ATE413386T1 (de) | Ppar-gamma modulatoren | |
ATE286053T1 (de) | Naphthyridinone zur hemmung der durch protein- tyrosin-kinase und zellzyklus kinase hervorgerufenen zellvermehrung | |
DE69830513D1 (de) | HEMMUNG DER p38 KINASE UNTER VERWENDUNG VON SYMMETRISCHEN UND ASYMMETRISCHEN DIPHENYLHARNSTOFFEN | |
EP1247803A3 (de) | Indolinon-Verbindungen und deren Verwendung als Protein- Kinase-Modulatoren | |
EP1488792A3 (de) | Quinazolinverbindungen mit CSF-1R Rezeptor Tyrosinkinase inhibierender Wirkung | |
ATE292623T1 (de) | 2-indolinonderivate als modulatoren der proteinkinase-ativität | |
EP2409704A3 (de) | c-Met-Modulatoren und Verwendungsverfahren | |
ATE353640T1 (de) | Antagoniste zur behandlung von cd11/cd18 adhäsionsrezeptor-vermittelten krankheiten | |
WO2000008202A3 (en) | 3-methylidenyl-2-indolinone modulators of protein kinase | |
PT655890E (pt) | Celulas recombinantes, construcoes de adn, vectores e metodos para expressao de enzimas degradantes de fitato em proporcoes desejadas | |
MY129998A (en) | Saccharin derivative proteolytic enzyme inhibitors | |
DK1192247T3 (da) | Sphingosinkinaseenzym | |
DE69825286D1 (de) | Verwendung von cholinesterasehemmern zur behandlung von aufmerksamkeitsmangel-störungen | |
AU2001280812A1 (en) | Gsk3 polypeptides | |
DE69826717D1 (de) | Target zur behandlung von atherosklerose, fettleibigkeit und diabetis typ ii | |
WO1998024887A3 (en) | Parasitic nematode transglutaminase proteins, nucleic acid molecules, and uses thereof | |
WO2001066709A3 (en) | Sphingomyelinase enzymes and uses relating thereto |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
RER | Ceased as to paragraph 5 lit. 3 law introducing patent treaties |