AR053902A1 - Inhibidores de aspartil proteasa heterociclicos macrociclicos - Google Patents
Inhibidores de aspartil proteasa heterociclicos macrociclicosInfo
- Publication number
- AR053902A1 AR053902A1 ARP060102460A ARP060102460A AR053902A1 AR 053902 A1 AR053902 A1 AR 053902A1 AR P060102460 A ARP060102460 A AR P060102460A AR P060102460 A ARP060102460 A AR P060102460A AR 053902 A1 AR053902 A1 AR 053902A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- group
- heteroarylalkyl
- cycloalkylalkyl
- heterocycloalkyl
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 11
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 11
- 125000003118 aryl group Chemical group 0.000 abstract 11
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 11
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 11
- 125000001072 heteroaryl group Chemical group 0.000 abstract 11
- 125000004446 heteroarylalkyl group Chemical group 0.000 abstract 11
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 11
- 125000003342 alkenyl group Chemical group 0.000 abstract 10
- 125000000217 alkyl group Chemical group 0.000 abstract 10
- 125000005843 halogen group Chemical group 0.000 abstract 10
- 125000005885 heterocycloalkylalkyl group Chemical group 0.000 abstract 10
- 125000004350 aryl cycloalkyl group Chemical group 0.000 abstract 6
- 229910052799 carbon Inorganic materials 0.000 abstract 6
- 125000004432 carbon atom Chemical group C* 0.000 abstract 6
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 6
- 125000001188 haloalkyl group Chemical group 0.000 abstract 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 125000004946 alkenylalkyl group Chemical group 0.000 abstract 1
- 125000004450 alkenylene group Chemical group 0.000 abstract 1
- 125000004419 alkynylene group Chemical group 0.000 abstract 1
- 125000000732 arylene group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000002993 cycloalkylene group Chemical group 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000001475 halogen functional group Chemical group 0.000 abstract 1
- 125000005549 heteroarylene group Chemical group 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- -1 heterocycloalkyalkyl Chemical group 0.000 abstract 1
- 125000006588 heterocycloalkylene group Chemical group 0.000 abstract 1
- 125000006413 ring segment Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/08—Bridged systems
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- 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
- 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
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Tropical Medicine & Parasitology (AREA)
- Virology (AREA)
- Hospice & Palliative Care (AREA)
- AIDS & HIV (AREA)
- Molecular Biology (AREA)
- Psychiatry (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Reivindicacion 1: Un compuesto que tiene la formula estructural (1), o una sal, solvato o éster farmacéuticamente aceptable del mismo, en donde: W es un enlace, -C(=S)(C(R3)(R4))a, -(C(R3)(R4))aC(=S)-, S(O)1-2(C(R3)(R4))a-, -(C(R3)(R4))aS(O)1-2, - C(=O)(C(R3)(R4))a-, -(C(R3)(R4))aC(=O)-, -O(C(R3)(R4))a-, -(C(R3)(R4))aO-, -(C(R3(R4))a-, -N(R5)(C(R3)(R4))a-, -(C(R3)(R4))aN(R5)- o -C(=N(R5))(C(R3)(R4))a-, -(C(R3)(R4))aC(=N(R5))-; en donde a es 0-2; U es un enlace, -S(O)1-2-, -C(=O)-, -O-, - P(O)(OR6)-, -(C(R3)(R4))b-, -N(R5)- o -C(=N(R5))-; en donde b es 0-2; siempre que cuando W sea -S(O)-, -S(O)2-, -O-, o -N(R5)-, U no sea -S(O)-, -S(O)2-, -O-, o -N(R5)-; R1 y R5 están independientemente seleccionados a partir del grupo consistente en H, alquilo, alquenilo, alquinilo, cicloalquilo, cicloalquilalquilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, arilciclalquilo, -OR19, -CN, -C(O)R20, -C(O)OR19, -S(O)1-2R21, -C(O)N(R22)(R23), -S(O)1-2N(R22)(R23), -NO2, -N=C(R22)(R23) y -N(R22)(R23); o R5 es un grupo de formulas (2) a (5), en donde R26 numera 0 a 5 sustituyentes, m es 0 a 6 y n es 1 a 5; R2, R3, R4, R6, R7, R8, R9, R10, R11, R12, R13, R14, R15, R16, R17 y R18 están independientemente seleccionados a partir del grupo consistente en H, alquilo, alquenilo, alquinilo, cicloalquilo, cicloalquilalquilo, heterocicloalquilo, heterocicloalquialquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, arilcicloalquilo, halo, -CF3, -SH, -OR19, -CN, -C(O)R20, -C(O)OR19, -S(O)0-2R21, -S(O)1-2N(R22)(R23), -C(O)N(R22)(R23), -N(R22)C(O)R20, -N(R22)C(O)N(R22)(R23), -N(R22)C(O)OR19, -N(R22)S(O)1-2R21, -NO2, -N=C(R22)(R23) y -N(R22)(R23); en donde c, d, e, f, g y h son 0- 4; X, Y y Z están independientemente seleccionados a partir del grupo consistente en -O-, -N(R5)- , -C(O)-, -S(O)0-2-, -C(O)N(R22)-, -N(R22)C(O)-, -S(O)1-2N(R22)-, -N(R22)S(O)1-2- o un enlace; L(s) y M(t) están independientemente seleccionados a partir del grupo consiste en cicloalquileno, heterocicloalquileno, alquenileno, alquinileno, arileno, heteroarileno, o un enlace; en donde los átomos del anillo e L y M están opcionalmente sustituidos con 1 a 5 grupos R24 independientemente seleccionados a partir del grupo consistente en H, alquilo alquenilo, alquinilo, cicloalquilo, cicloalquilalquilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, arilcicloalquilo, halo, -CF3, -SH, - OR19, -CN, -C(O)R20, -C(O)OR19, -S(O)0-2R21, -S(O)1-2N(R22)(R23), -C (O)N(R22)(R23), -N(R22)C(O)R20, -N(R22)C(O)N(R22)(R23), -N(R22)C(O)OR19, -N(R22)S(O)1-2R21, -NO2, -N=C(R22)(R23) y -N(R22)(R23); en donde s es 1 o 2 y t es 1 o 2; R19 es H, alquilo, alquenilo, alquinilo, arilo, cicloalquilo, cicloalquilalquilo, heteroarilo, arilalquilo, heteroarilalquilo, heterocicloalquilo o heterocicloalquilalquilo; R20 es H, alquilo, alquenilo, alquinilo, arilo, cicloalquilo, cicloalquilalquilo, heteroarilo, arilalquilo, heteroarilalquilo, heterocicloalquilo, heterocicloalquilalquilo o -N(R23)(R24); R21 es alquilo, alquenilo, alquinilo, arilo, cicloalquilo, cicloalquilalquilo, heteroarilo, arilalquilo, heteroarilalquilo, heterocicloalquilo o heterocicloalquilalquilo; R22 y R23 son H, alquilo, alquenilo, alquinilo, arilo, cicloalquilo, cicloalquilalquilo, heteroarilo, arilalquilo, heteroarilalquilo, heterocicloalquilo o heterocicloalquilalquilo; siempre que i) cuando U es un enlace, -O- o -N(R5)-, entonces R2 no está seleccionado a partir del grupo consistente en halo, -SH, -OR19, -S(O)0-2R21, -S(O)1-2N(R22)(R23), -N(R22)C(O)R20, -N(R22)C(O)N(R22)(R23), -N(R22)C(O)OR19, -N(R22)S(O)1-2R21, -NO2, -N=C(R22)(R23) y -N(R22)(R23); ii) cuando W es -O(C(R3)(R4))a- o -N(R5)(C(R3)(R4))a- y a es O, entonces R2 no está seleccionado a partir del grupo consistente en halo, -SH, -OR19, -S(O)0-2R21, -S(O)1-2N(R22)(R23), -N(R22)C(O)R20, -N(R22)C(O)N(R22)(R23), -N(R22)C(O)OR19, -N(R22)S(O)1- 2R21, -NO2, -N=C(R22)(R23) y -N(R22)(R23); iii) cuando W es -O(C(R3)(R4))a- o -N(R5)(C(R3)(R4))a- y a es 1 o 2, entonces R3 y R4 sobre el átomo de carbono adyacente al heteroátomo de W, no están seleccionados a partir del grupo consistente en halo, - SH, -OR19, -S(O)0-2R21, -S(O)1-2N(R22)(R23), -N(R22)C(O)R20, -N(R22)C(O)N(R22)(R23), -N(R22)C(O)OR19, -N(R22)S(O)1-2R21, -NO2, -N=C(R22)(R23) y -N(R22)(R23); iv) cuando U es un enlace, -O- o -N(R5)- y c es 0, entonces Z no es -O-, -N(R5)-, -S(O)0-2- , -N(R22)C(O)-, -S(O)1-2N(R22)- o -N(R22)S(O)1-2-; v) cuando W es -O(C(R3)(R4))a- o -N(R5)(C(R3)(R4))a- y a y c son 0, entonces Z no es -O-, -N(R5)-, -S(O)0-2-, -N(R22)C(O)-, -S(O)1-2N(R22)- o -N(R22)S(O)1-2-; vi) cuando Z es -O- o -N(R5)-, entonces R7, R8, R9 y R10 sobre el átomo de carbono adyacente a Z no están seleccionados a partir del grupo consistente en halo, -SH, -OR19, -S(O)0-2R21, -S(O)1-2N(R22)(R23), -N(R22)C(O)R20, -N(R22)C(O)N(R22)(R23), -N(R22)C(O)OR19, -N(R22)S(O)1-2R21, -NO2, - N=C(R22)(R23) y -N(R22)(R23); (vii) cuando Y es -O- o -N(R5)-, entonces R11, R12, R13 y R14 sobre el átomo de carbono adyacente a Y no están seleccionados a partir del grupo consistente en halo, -SH, -OR19, -S(O)0-2R21, -S(O)1-2N(R22)(R23), - N(R22)C(O)R20, -N(R22)C(O)N(R22)(R23), -N(R22)C(O)OR19, -N(R22)S(O)1-2R21, -NO2, -N=C(R22)(R23) y -N(R22)(R23); viii) cuando X es -O- o -N(R5)-, entonces R15, R16, R17, y R18 sobre el átomo de carbono adyacente a X no están seleccionados a partir del grupo consistente en halo, -SH, -OR19, -S(O)0-2R21, -S(O)1-2N(R22)(R23), -N(R22)C(O)R20, -N(R22)C(O)N(R22)(R23), -N(R22)C(O)OR19, -N(R22)S(O)1-2R21, -NO2, -N=C(R22)(R23) y -N(R22)(R23); ix) cuando d y e son ambos cero y M es un enlace, entonces Z o Y no pueden ser ambos -O-; x) cuando f y g son ambos cero y L es un enlace, entonces Y o X no pueden ser ambos -O-; xi) cuando h es 1, entonces X no es -O- o -N(R5)-; xii) X, L, M, Y, Z y los átomos de carbono de -(C(R17)(R18))h-, - (C(R15)(R16))g-, -(C(R13)(R14))r, -(C(R11)(R12))e-, -(C(R9)(R10))d- y -(C(R7)(R8))c-, conjuntamente con W, el carbono de -C(R2)- y el átomo de nitrogeno al cual W está unido forman un anillo de al menos 5 átomos; xiii) cuando W es un enlace, entonces el anillo formado por X, L, M, Y, Z y los átomos de carbono de -(C(R17)(R18)h, -(C(R15)(R16))g-, -(C(R13)(R14))f-, -(C(R11)(R12))e-, -(C(R9)(R10))d-, -(C(R7)(R8))c-, W, el carbono de -C(R2)- y el átomo de nitrogeno unido a W, posee un tamano de anillo superior a 9 átomos; y en donde cada uno de los grupos alquilo, alquenilo, alquinilo, cicloalquilo, cicloalquilalquilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, arilcicloalquilo en las definiciones precedentes está independientemente no sustituido o sustituido con 1 a 5 residuos R26 independientemente seleccionados a partir del grupo consistente en alquilo, alquenilo, alquinilo, cicloalquilo, cicloalquilalquilo, cicloalquenilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, arilcicloalquilo, halo, haloalquilo, haloalcoxi, -CN, -CF3, -SH, -OR19, -CN, -CH(R22)R23), -C(O)R20, -C(O)OR19, - C(=NOR19)R22, -P(O)(OR19)(OR19), -S(O)0-2R21, -S(O)1-2N(R22)(R23), -C(O)N(R22)(R23), -N(R22)C(O)R20, -alquil-N(R22)C(O)R20, -N(R22)C(O)N(R22)(R23), -alquil-N(R22)C(O)N(R22)(R23), -CH2-R22, -N(R22)C(O)OR19, -N(R22)S(O)1-2R21, -N(R22)S(O)1-2, N(R22)(R23), -N3, -NO2, -N=C(R22)(R23), =NOR19-N(R22)(R23) y -alquil-N(R22)(R23); en donde cada uno del alquilo, alquenilo, alquinilo, cicloalquilo, cicloalquilalquilo, cicloalquenilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, arilcicloalquilo, halo, haloalquilo y haloalcoxi en el grupo R26 precedente está independientemente no sustituido o sustituido con 1 a 5 residuos R27 independientemente seleccionados a partir del grupo consistente en alquilo, alquenilo, alquinilo, cicloalquilo, cicloalquilalquilo, cicloalquenilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, arilcicloalquilo, halo, haloalquilo, haloalcoxi, -CN, - CF3, -SH, -OR19, -CN, -CH(R22)(R23), -C(O)R20, -C(O)OR19, -C(=NOR19)R22, -P(O)(OR19)(OR19), -S(O)0-2R21, -S(O)1-2N(R22)(R23), -C(O)N(R22)(R23), -N(R22)C(O)R20, -alquil-N(R22)C(O)R20, -N(R22)C(O)N(R22)(R23) , -alquil-N(R22)C(O)N(R22)(R23), -CH2-R22, - N(R22)C(O)OR19, -N(R22)S(O)1-2R21, -N(R22)S(O)1-2N(R22)(R23), -N3, -NO2, -N=C(R22)(R23), =NOR19-N(R22)(R23) y-alquil-N(R22)(R23).
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US69054205P | 2005-06-14 | 2005-06-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR053902A1 true AR053902A1 (es) | 2007-05-23 |
Family
ID=37309231
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP060102460A AR053902A1 (es) | 2005-06-14 | 2006-06-12 | Inhibidores de aspartil proteasa heterociclicos macrociclicos |
Country Status (10)
| Country | Link |
|---|---|
| US (2) | US7812013B2 (es) |
| EP (1) | EP1902057B1 (es) |
| JP (1) | JP2008543841A (es) |
| CN (1) | CN101193892A (es) |
| AR (1) | AR053902A1 (es) |
| CA (1) | CA2609562A1 (es) |
| MX (1) | MX2007016185A (es) |
| PE (1) | PE20070078A1 (es) |
| TW (1) | TW200716645A (es) |
| WO (1) | WO2006138195A1 (es) |
Families Citing this family (57)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7763609B2 (en) * | 2003-12-15 | 2010-07-27 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| US7592348B2 (en) | 2003-12-15 | 2009-09-22 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| US7700603B2 (en) | 2003-12-15 | 2010-04-20 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| WO2006041405A1 (en) * | 2004-10-15 | 2006-04-20 | Astrazeneca Ab | Substituted amino-pyrimidones and uses thereof |
| EP1802587A4 (en) * | 2004-10-15 | 2010-02-17 | Astrazeneca Ab | SUBSTITUTED AMINO BINDINGS AND THEIR APPLICATIONS |
| US20080287399A1 (en) * | 2004-12-14 | 2008-11-20 | Astrazeneca Ab | Substituted Aminopyridines and Uses Thereof |
| ES2436795T3 (es) * | 2005-06-14 | 2014-01-07 | Merck Sharp & Dohme Corp. | Inhibidores heterocíclicos de aspartil proteasa, preparación y uso de los mismos |
| CN101193892A (zh) * | 2005-06-14 | 2008-06-04 | 先灵公司 | 大环杂环天冬氨酰基蛋白酶抑制剂 |
| CA2609582A1 (en) | 2005-06-14 | 2006-12-28 | Schering Corporation | Aspartyl protease inhibitors |
| US7759354B2 (en) | 2005-06-14 | 2010-07-20 | Schering Corporation | Bicyclic guanidine derivatives as asparyl protease inhibitors, compositions, and uses thereof |
| CN101360720A (zh) * | 2005-11-15 | 2009-02-04 | 阿斯利康(瑞典)有限公司 | 新颖的2-氨基嘧啶酮衍生物及其用途 |
| CN101360721A (zh) * | 2005-11-15 | 2009-02-04 | 阿斯利康(瑞典)有限公司 | 新颖的2-氨基嘧啶酮衍生物或2-氨基吡啶酮衍生物及其用途 |
| TW200804290A (en) * | 2005-11-15 | 2008-01-16 | Astrazeneca Ab | Compounds and uses thereof |
| CN101360722A (zh) * | 2005-11-15 | 2009-02-04 | 阿斯利康(瑞典)有限公司 | 新颖的2-氨基嘧啶衍生物及其用途 |
| WO2007058601A1 (en) * | 2005-11-21 | 2007-05-24 | Astrazeneca Ab | Novel 2-amino-imidazole-4-one compounds and their use in the manufacture of a medicament to be used in the treatment of cognitive impairment, alzheimer’s disease, neurodegeneration and dementia |
| TW200734311A (en) * | 2005-11-21 | 2007-09-16 | Astrazeneca Ab | New compounds |
| AR058381A1 (es) * | 2005-12-19 | 2008-01-30 | Astrazeneca Ab | Compuestos derivados de 2-aminopiridin-4-onas y una composicion farmaceutica |
| CN101460480A (zh) * | 2006-04-05 | 2009-06-17 | 阿斯利康(瑞典)有限公司 | 2-氨基嘧啶-4-酮类化合物及其用于治疗或预防Aβ相关病理的用途 |
| EP2644600B1 (en) | 2006-06-12 | 2017-01-11 | Merck Sharp & Dohme Corp. | Heterocyclic aspartyl protease inhibitors |
| US20080051420A1 (en) * | 2006-06-14 | 2008-02-28 | Astrazeneca Ab | New Compounds 317 |
| TW200815447A (en) * | 2006-06-14 | 2008-04-01 | Astrazeneca Ab | Novel compounds IV |
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| US20100063121A1 (en) | 2010-03-11 |
| EP1902057A1 (en) | 2008-03-26 |
| US20060281729A1 (en) | 2006-12-14 |
| CN101193892A (zh) | 2008-06-04 |
| TW200716645A (en) | 2007-05-01 |
| PE20070078A1 (es) | 2007-03-08 |
| US7812013B2 (en) | 2010-10-12 |
| EP1902057B1 (en) | 2013-10-23 |
| CA2609562A1 (en) | 2006-12-28 |
| JP2008543841A (ja) | 2008-12-04 |
| MX2007016185A (es) | 2008-03-07 |
| US8557798B2 (en) | 2013-10-15 |
| WO2006138195A1 (en) | 2006-12-28 |
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