AR035260A1 - Derivados de piperidina amino sustituidas, composiciones farmaceuticas y el uso de dichos derivados para la preparacion de medicamentos como inhibidores de la gama secretasa, y para el tratamiento de la enfermedad de alzheimer - Google Patents
Derivados de piperidina amino sustituidas, composiciones farmaceuticas y el uso de dichos derivados para la preparacion de medicamentos como inhibidores de la gama secretasa, y para el tratamiento de la enfermedad de alzheimerInfo
- Publication number
- AR035260A1 AR035260A1 ARP020102925A ARP020102925A AR035260A1 AR 035260 A1 AR035260 A1 AR 035260A1 AR P020102925 A ARP020102925 A AR P020102925A AR P020102925 A ARP020102925 A AR P020102925A AR 035260 A1 AR035260 A1 AR 035260A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- independently selected
- group
- different
- same
- Prior art date
Links
- 208000024827 Alzheimer disease Diseases 0.000 title abstract 2
- 102000002659 Amyloid Precursor Protein Secretases Human genes 0.000 title abstract 2
- 108010043324 Amyloid Precursor Protein Secretases Proteins 0.000 title abstract 2
- 239000003814 drug Substances 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- LWMPFIOTEAXAGV-UHFFFAOYSA-N piperidin-1-amine Chemical compound NN1CCCCC1 LWMPFIOTEAXAGV-UHFFFAOYSA-N 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 42
- 125000000217 alkyl group Chemical group 0.000 abstract 16
- 125000003118 aryl group Chemical group 0.000 abstract 9
- 125000001072 heteroaryl group Chemical group 0.000 abstract 9
- 229910052736 halogen Inorganic materials 0.000 abstract 6
- 150000002367 halogens Chemical class 0.000 abstract 6
- 229910052757 nitrogen Inorganic materials 0.000 abstract 6
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 6
- 125000002947 alkylene group Chemical group 0.000 abstract 5
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 5
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 4
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 3
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 3
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 3
- 125000004475 heteroaralkyl group Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
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
- C07D401/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
- C07D211/56—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
- C07D211/56—Nitrogen atoms
- C07D211/58—Nitrogen atoms attached in position 4
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
- C07D211/60—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D211/62—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals attached in position 4
-
- 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
- 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
- C07D403/06—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 carbon chain containing only aliphatic carbon atoms
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyrrole Compounds (AREA)
Abstract
Derivados de piperidina amino sustituidas, que comprenden un compuesto de la fórmula (1) o las sales o solvatos farmacéuticamente aceptables del mismo, en el cual: Ar1 y Ar2 son independientemente seleccionados entre arilo y heteroarilo; Y es un enlace, o Y representa un grupo -(C(R3)2)1-3-; Cada R1 es independientemente seleccionado entre: alquilo (C1-6); arilo; arilo sustituido con uno o más sustituyentes independientemente seleccionados entre halógeno, CF3, alquilo (C1-6), alcoxi (C1-6), OCF3, NH2 o CN; heteroarilo; heteroarilo sustituido con uno o más sustituyentes independientemente seleccionados entre halógeno, CF3, alquilo (C1-6), alcoxi (C1-6), OCF3, NH2 o CN; halógeno; -CF3; -OCF3; -CN; -NO2; -NH2; -C(O)NHalquilo (C1-6); -C(O)N(alquilo (C1-6))2, donde cada grupo alquilo (C1-6) es igual o diferente de los demás; -C(O)N(alquilo (C1-6))2, donde cada grupo alquilo (C1-6) es igual o diferente de los demás y dichos grupos alquilo (C1-6) tomados junto con el nitrógeno al cual están unidos forman un anillo; -NHC(O)alquilo (C1-6), -NHC(O)Oalquilo (C1-6), -NHC(O)NHalquilo (C1-6), -NHSO2alquilo (C1-6); -OH; -OC(O)alquilo (C1-6); -Oalquilo (C1-6); -Oarilo; u -Oaralquilo (C1-6); Cada R2 es independientemente seleccionado entre: alquilo (C1-6); halógeno; -CF3; -OCF3; -CN; -NO2; -NH2; -C(O)Oalquilo (C1-6); -C(O)NHalquilo (C1-6), -N(alquilo (C1-6))2- donde cada sustituyente alquilo (C1-6) es igual o diferente de los demás; -N(alquilo (C1-6))2, donde cada sustituyente alquilo (C1-6) es igual o diferente de los demás y los sustituyentes alquilo (C1-6), junto con el átomo de nitrógeno al cual están unidos forman un anillo; -NHC(O)alquilo (C1-6); -NHC(O)Oalquilo (C1-6); -NHC(O)NHalquilo (C1-6); -NHSO2alquilo (C1-6); -OH; -OC(O)alquilo (C1-6); -Oalquilo (C1-6); -Oarilo; Oar-alquilo (C1-6); arilo; arilo sustituido con uno o más sustituyentes independientemente seleccionados entre: halógeno, CF3, alquilo (C1-6), alcoxi (C1-6), OCF3, NH2 o CN; heteroarilo; heteroarilo sustituido con uno o más sustituyentes independientemente seleccionados entre halógeno, CF3, alquilo (C1-6), alcoxi (C1-6) OCF3, NH2 o CN; -C(O)N(alquilo (C1-6))2 donde cada grupo alquilo es independientemente seleccionado; -C(O)N(alquilo (C1-6))2 donde cada grupo alquilo es independientemente seleccionado y donde los grupos alquilo, tomados junto con el átomo de nitrógeno, forman un anillo heterocicloalquilo; o un grupo seleccionado entre los restos de fórmulas (2) a (6); Cada R3 es independientemente seleccionado entre H y alquilo (C1-3); Cada R4 es independientemente seleccionado entre: alquilo (C1-3); -OH; u -Oalquilo (C1-3); R5 es seleccionado entre: hidrógeno; alquilo (C1-6); arilo; heteroarilo; -alquilen(C1-3)-Oalquilo(C1-3); -alquilen(C1-6)-S(O)0-2alquilo(C1-3); -alquilen(C1-8)-S(O)0-2NHalquilo(C1-3); -C(O)alquilo (C1-6); C(O)arilo; -C(O)aralquilo (C1-3), -C(O)heteroarilo; -C(O)heteroaralquilo (C1-3); -C(O)Oalquilo (C1-6); -C(O)NHalquilo (C1-6); -C(O)N(alquilo (C1-6))2, donde cada grupo alquilo C1-6 es igual o diferente de los demás; -C(O)N(alquilo (C1-6))2, donde cada grupo alquilo C1-6 es igual o diferente de los demás y donde los grupos alquilo C1-6, tomados junto con el nitrógeno al cual están unidos, forman un anillo de heterocicloalquilo; -C(O)alquilen(C1-3)-NHalquilo(C1-3); -C(O)alquilen(C1-3)-N(alquilo (C1-3))2; donde cada grupo alquilo es seleccionado independientemente; -SO2alquilo (C1-6); -SO2NHalquilo (C1-6); -SO2N(alquilo (C1-6))2; donde cada grupo alquilo C1-6 es igual o diferente de los demás; -SO2N(alquilo (C1-6))2, donde cada grupo alquilo C1-6 es igual o diferente de los demás y donde los grupos alquilo C1-6, tomados junto con el nitrógeno al cual están unidos, forman un anillo de heterocicloalquilo o un grupo de la fórmula (7), (8), (9) o (10); R6 es -H o alquilo (C1-6); X es seleccionado entre CH2, O, S, SO, SO2 o N-R7; R7 es seleccionado entre alquilo (C1-6), cicloalquilo (C3-6), alquilen(C1-3)-cicloalquilo(C3-6); arilo, aralquilo (C1-3), heteroarilo, heteroaralquilo (C1-3), -C(O)alquilo (C1-6), -C(O)arilo; -C(O)aralquilo (C1-3), -C(O)heteroarilo; -C(O)heteroaralquilo (C1-3), -C(O)Oalquilo (C1-6), -C(O)NHalquilo (C1-6), -C(O)N(alquilo (C1-6))2, donde cada grupo C1-6 es igual o diferente a los demás; -C(O)N(alquilo (C1-6))2, donde cada grupo alquilo C1-6 es igual o diferente a los demás y donde los grupos alquilo C1-6, tomados junto con el nitrógeno al cual están unidos, forman un anillo heterocicloalquilo; -C(O)alquilen(C1-3)-NHalquilo(C1-3), -C(O)alquilen(C1-3)-N(alquilo (C1-3))2, donde los grupos alquilo C1-3 son iguales o diferentes; o -alquilen(C1-3)-O-alquilo(C1-3); n y p son independientemente seleccionados entre 0 a 3 para formar un anillo de 4 a 7 miembros; r representa de 0 a 3; q representa de 0 a 3 y t representa de 0 a 3. También se describen composiciones farmacéuticas y el uso de dichos compuestos para la preparación de medicamentos para inhibir la gama secretasa y para el tratamiento de la enfermedad de Alzheimer.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US31006801P | 2001-08-03 | 2001-08-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR035260A1 true AR035260A1 (es) | 2004-05-05 |
Family
ID=23200871
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP020102925A AR035260A1 (es) | 2001-08-03 | 2002-08-01 | Derivados de piperidina amino sustituidas, composiciones farmaceuticas y el uso de dichos derivados para la preparacion de medicamentos como inhibidores de la gama secretasa, y para el tratamiento de la enfermedad de alzheimer |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US7122675B2 (es) |
| EP (1) | EP1411944A1 (es) |
| JP (1) | JP2005504042A (es) |
| CN (1) | CN1780621A (es) |
| AR (1) | AR035260A1 (es) |
| CA (1) | CA2455861A1 (es) |
| MX (1) | MXPA04001016A (es) |
| WO (1) | WO2003013527A1 (es) |
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| US7521481B2 (en) | 2003-02-27 | 2009-04-21 | Mclaurin Joanne | Methods of preventing, treating and diagnosing disorders of protein aggregation |
| US7067509B2 (en) * | 2003-03-07 | 2006-06-27 | Neurocrine Biosciences, Inc. | Melanin-concentrating hormone receptor antagonists and compositions and methods related thereto |
| CA2526487A1 (en) | 2003-06-30 | 2005-01-06 | Daiichi Pharmaceutical Co., Ltd. | Heterocyclic methyl sulfone derivative |
| WO2005014540A1 (en) | 2003-08-08 | 2005-02-17 | Schering Corporation | Cyclic amine base-1 inhibitors having a heterocyclic substituent |
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| NZ547528A (en) | 2003-10-29 | 2008-11-28 | Elan Pharm Inc | N-substituted benzene sulfonamides |
| ATE552851T1 (de) | 2004-02-03 | 2012-04-15 | Univ Michigan | Zusammensetzungen zur behandlung von brust- und bauchspeicheldrüsenkrebs |
| US20050232927A1 (en) * | 2004-02-03 | 2005-10-20 | The Regents Of The University Of Michigan | Compositions and methods for characterizing, regulating, diagnosing, and treating cancer |
| JP2007531742A (ja) * | 2004-04-05 | 2007-11-08 | シェーリング コーポレイション | 新規のγセクレターゼインヒビター |
| CN1968924B (zh) * | 2004-06-15 | 2011-08-03 | 默沙东公司 | 作为β-分泌酶抑制剂用于治疗阿尔茨海默氏病的吡咯烷-3-基化合物 |
| EP1789404B1 (en) * | 2004-06-30 | 2010-03-24 | Schering Corporation | Substituted n-arylsulfonylheterocyclic amines as gamma-secretase inhibitors |
| ATE491693T1 (de) | 2004-07-22 | 2011-01-15 | Schering Corp | Substituierte amide als inhibitoren der beta- sekretase |
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| US8133857B2 (en) * | 2006-03-07 | 2012-03-13 | The Brigham and Women's FHospital, Inc. | NOTCH inhibition in the treatment of atherosclerosis |
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| ATE554085T1 (de) | 2006-11-30 | 2012-05-15 | Probiodrug Ag | Neue inhibitoren von glutaminylcyclase |
| EP2106439B1 (en) | 2007-01-24 | 2014-11-12 | The Regents of the University of Michigan | Compositions and methods for treating and diagnosing pancreatic cancer |
| EA200901140A1 (ru) | 2007-03-01 | 2010-04-30 | Пробиодруг Аг | Новое применение ингибиторов глутаминилциклазы |
| WO2008124118A1 (en) | 2007-04-09 | 2008-10-16 | Purdue Pharma L.P. | Benzenesulfonyl compounds and the use therof |
| JP5667440B2 (ja) | 2007-04-18 | 2015-02-12 | プロビオドルグ エージー | グルタミニルシクラーゼ阻害剤としてのチオ尿素誘導体 |
| EP1997805A1 (en) * | 2007-06-01 | 2008-12-03 | Commissariat à l'Energie Atomique | Compounds with antiparasitic activity, applications thereof to the treatment of infectious diseases caused by apicomplexans |
| US8765736B2 (en) | 2007-09-28 | 2014-07-01 | Purdue Pharma L.P. | Benzenesulfonamide compounds and the use thereof |
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| US9181233B2 (en) | 2010-03-03 | 2015-11-10 | Probiodrug Ag | Inhibitors of glutaminyl cyclase |
| US8269019B2 (en) | 2010-03-10 | 2012-09-18 | Probiodrug Ag | Inhibitors |
| JP5945532B2 (ja) | 2010-04-21 | 2016-07-05 | プロビオドルグ エージー | グルタミニルシクラーゼの阻害剤としてのベンゾイミダゾール誘導体 |
| US8530670B2 (en) | 2011-03-16 | 2013-09-10 | Probiodrug Ag | Inhibitors |
| WO2013059302A1 (en) | 2011-10-17 | 2013-04-25 | Nationwide Children's Hospital, Inc. | Products and methods for aortic abdominal aneurysm |
| WO2016059220A1 (en) | 2014-10-16 | 2016-04-21 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Tcr-activating agents for use in the treatment of t-all |
| WO2017023999A1 (en) * | 2015-08-03 | 2017-02-09 | Emory University | Methylsulfonamide derivatives and uses related thereto |
| PL3461819T3 (pl) | 2017-09-29 | 2020-11-30 | Probiodrug Ag | Inhibitory cyklazy glutaminylowej |
| WO2020016377A1 (en) | 2018-07-19 | 2020-01-23 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Combination for treating cancer |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5646167A (en) * | 1993-01-06 | 1997-07-08 | Ciba-Geigy Corporation | Arylsulfonamido-substituted hydroxamix acids |
| US5559128A (en) * | 1995-04-18 | 1996-09-24 | Merck & Co., Inc. | 3-substituted piperidines promote release of growth hormone |
| CZ20013000A3 (cs) | 1999-02-26 | 2002-02-13 | Merck & Co., Inc. | Nové sulfonamidové sloučeniny a jejich pouľití |
| FR2802206B1 (fr) * | 1999-12-14 | 2005-04-22 | Sod Conseils Rech Applic | Derives de 4-aminopiperidine et leur utilisation en tant que medicament |
| CA2406652A1 (en) * | 2000-04-20 | 2001-11-01 | Nps Allelix Corp. | Aminopiperidines for use as glyt-1 inhibitors |
| CN1458923A (zh) * | 2000-09-25 | 2003-11-26 | 埃科特莱茵药品有限公司 | 抗疟用取代氨基-氮杂-环烷类化合物 |
| JP2005504042A (ja) * | 2001-08-03 | 2005-02-10 | シェーリング コーポレイション | γセクレターゼインヒビターのようなスルホンアミド誘導体 |
-
2002
- 2002-08-01 JP JP2003518536A patent/JP2005504042A/ja active Pending
- 2002-08-01 CA CA002455861A patent/CA2455861A1/en not_active Abandoned
- 2002-08-01 CN CNA028193520A patent/CN1780621A/zh active Pending
- 2002-08-01 WO PCT/US2002/024293 patent/WO2003013527A1/en not_active Ceased
- 2002-08-01 AR ARP020102925A patent/AR035260A1/es unknown
- 2002-08-01 MX MXPA04001016A patent/MXPA04001016A/es unknown
- 2002-08-01 EP EP02761207A patent/EP1411944A1/en not_active Withdrawn
- 2002-08-01 US US10/210,803 patent/US7122675B2/en not_active Expired - Fee Related
-
2005
- 2005-09-09 US US11/223,545 patent/US20060009467A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| US20060009467A1 (en) | 2006-01-12 |
| WO2003013527A1 (en) | 2003-02-20 |
| CA2455861A1 (en) | 2003-02-20 |
| CN1780621A (zh) | 2006-05-31 |
| EP1411944A1 (en) | 2004-04-28 |
| US20030216380A1 (en) | 2003-11-20 |
| MXPA04001016A (es) | 2004-05-27 |
| JP2005504042A (ja) | 2005-02-10 |
| US7122675B2 (en) | 2006-10-17 |
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