AR057983A1 - Inhibidores hterociclicos de aspartil proteasas - Google Patents
Inhibidores hterociclicos de aspartil proteasasInfo
- Publication number
- AR057983A1 AR057983A1 ARP060104660A ARP060104660A AR057983A1 AR 057983 A1 AR057983 A1 AR 057983A1 AR P060104660 A ARP060104660 A AR P060104660A AR P060104660 A ARP060104660 A AR P060104660A AR 057983 A1 AR057983 A1 AR 057983A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- arylalkyl
- aryl
- heteroaryl
- heterocycloalkyl
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 43
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 20
- 125000003118 aryl group Chemical group 0.000 abstract 20
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 17
- 125000001072 heteroaryl group Chemical group 0.000 abstract 16
- 125000004446 heteroarylalkyl group Chemical group 0.000 abstract 16
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 15
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 14
- 125000005885 heterocycloalkylalkyl group Chemical group 0.000 abstract 13
- 125000003342 alkenyl group Chemical group 0.000 abstract 12
- 125000000304 alkynyl group Chemical group 0.000 abstract 10
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 10
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 8
- 125000005843 halogen group Chemical group 0.000 abstract 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 4
- -1 -OR15 Chemical group 0.000 abstract 3
- 125000004429 atom Chemical group 0.000 abstract 3
- 125000004366 heterocycloalkenyl group Chemical group 0.000 abstract 3
- 125000001424 substituent group Chemical group 0.000 abstract 3
- 125000005018 aryl alkenyl group Chemical group 0.000 abstract 2
- 125000004350 aryl cycloalkyl group Chemical group 0.000 abstract 2
- 208000010877 cognitive disease Diseases 0.000 abstract 2
- 230000001149 cognitive effect Effects 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000004367 cycloalkylaryl group Chemical group 0.000 abstract 2
- 125000005215 cycloalkylheteroaryl group Chemical group 0.000 abstract 2
- 125000005349 heteroarylcycloalkyl group Chemical group 0.000 abstract 2
- 230000004770 neurodegeneration Effects 0.000 abstract 2
- 208000015122 neurodegenerative disease Diseases 0.000 abstract 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 2
- 102000004580 Aspartic Acid Proteases Human genes 0.000 abstract 1
- 108010017640 Aspartic Acid Proteases Proteins 0.000 abstract 1
- 101100240526 Caenorhabditis elegans nhr-20 gene Proteins 0.000 abstract 1
- 208000024172 Cardiovascular disease Diseases 0.000 abstract 1
- 229940122041 Cholinesterase inhibitor Drugs 0.000 abstract 1
- 229910003849 O-Si Inorganic materials 0.000 abstract 1
- 229910003872 O—Si Inorganic materials 0.000 abstract 1
- 239000000556 agonist Substances 0.000 abstract 1
- 125000005015 aryl alkynyl group Chemical group 0.000 abstract 1
- 125000000732 arylene group Chemical group 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000000544 cholinesterase inhibitor Substances 0.000 abstract 1
- 125000003106 haloaryl group Chemical group 0.000 abstract 1
- 125000005549 heteroarylene group Chemical group 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 239000003683 muscarinic M2 receptor antagonist Substances 0.000 abstract 1
- 125000006413 ring segment Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 1
Classifications
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- 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
-
- 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
- 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
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
-
- 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
-
- 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
- C07D487/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Virology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Heart & Thoracic Surgery (AREA)
- Psychiatry (AREA)
- Oncology (AREA)
- AIDS & HIV (AREA)
- Cardiology (AREA)
- Molecular Biology (AREA)
- Hospice & Palliative Care (AREA)
- Communicable Diseases (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Se divulga el método para inhibir las aspartil proteasas, y en particular, los métodos para tratar enfermedades cardiovasculares, enfermedades cognitivas y neurodegenerativas. Además se divulgan métodos para tratar enfermedades cognitivas o neurodegenerativas utilizando los compuestos de formula (1) en combinacion con un inhibidor de colinesterasa o un agonista m1 o antagonista m2 muscarínicos. Reivindicacion 1: Un compuesto que tiene la formula estructural formula (1), o su estereoisomero, tautomero, o sal aceptable para uso farmacéutico, donde W es -S(O)-, -S(O)2-, -C(=O)-, -O-, -C(=S)-, -C(R6)(R7)-, -N(R5)-, -P(O)(OR15)- o -C(=N(R5))-; Ar es arileno o heteroarileno, donde Ar está independientemente no sustituido o sustituido con 1 a 5 grupos R14; R1, R2 y R5 se seleccionan independientemente del grupo integrado por H, alquilo, arilalquilo, heteroarilalquilo, cicloalquilalquilo, heterocicloalquilalquilo, arilcicloalquilalquilo, heteroarilcicloalquilalquilo, arilheterocicloalquilalquilo, heteroarilheterocicloalquilalquilo, cicloalquilo, ariIcicloalquilo heteroarilcicloalquilo, heterocicloalquilo, arilheterocicloalquilo, heteroarilheterocicloalquilo, alquenilo, arilalquenilo, cicloalquenilo, arilcicloalquenllo, heteroarilcicloalquenilo, heterocicloalquenilo, arilheterocicloalquenilo, heteroarilheterocicloalquenilo, alquinilo, arilalquinilo. arilo, cicloalquilarilo, heterocicloalquilarilo, heterocicloalquenilarilo, heteroarilo, cicloalquilheteroarilo, heterocicloalquilheteroarilo, cicloalquenilarilo, heterocicloalquenilarilo, -OR15, -CN, -C(O)R8, -C(O)OR9, .-S(O)R10, -S(O)2R10, -C(O)N(R11)(R12), -S(O)N(R11)(R12), -S(O)2N(R11)(R12), -NO2, -N=C(R8)2 y -N(R8)2; R3, R4, R6 y R7 se seleccionan independientemente del grupo integrado por H, alquilo, arilalquilo, heteroarilalquilo, cicloalquilalquilo, heterocicloalquilalquilo, arilcicloalquilalquilo, heteroarilcicloalquilalquilo, arilheterocicloalquilalquilo, heteroarilheterocicloalquilalquilo, cicloalquilo, arilcicloalquilo, heteroarilcicloalquilo, heterocicloalquilo, arilheterocicloalquilo, heteroarilheterocicloalquilo, alquenilo, arilalquenilo, cicloalquenilo, arilcicloalquenilo, heteroarilcicloalquenilo, heterocicloalquenilo, arilheterocicloalquenilo, heteroarilheterocicloalquenilo, alquinilo, arilalquinilo, arilo, cicloalquilarilo, heterocicloalquilarilo, heterocicloalquenilarilo, heteroarilo, cicloalquilheteroarilo, heterocicloalquilheteroarilo, cicloalquenilarilo, heterocicloalquenilarilo, -CH2-O-Si(R9)(R10)(R19), -CN, -C(O)R8, -C(O)OR9 o -C(O)N(R11)(R12); u opcionalmente, R3, R4, R6 y R7, junto con el átomo de carbono al cual están unidos forman un anillo cicloalquilo de 3 a 8 miembros opcionalmente sustituido con 1 a 4 restos R14 donde 1-5 de los átomos del anillo pueden ser reemplazados por -O-; -S-; -N(R5)-; -C(O)-; -S(O)-, o -S(O)2-; R8 se selecciona independientemente del grupo integrado por H, alquilo. alquenilo, alquinilo, cicloalquilo, cicloalquilalquilo, cicloalquenilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, -OR15, -N(R15)(R16), -N(R15)C(O)R16, -N(R15)S(O)R16, -N(R15)S(O)2R16, - N(R15)S(O)2N(R16)(R17), -N(R15)S(O)N(R16)(R17), -N(R15)C(O)N(R16)(R17) y -N(R15)C(O)OR16; R9 se selecciona independientemente del grupo integrado por H, alquilo, cicloalquilo, cicloalquilalquilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo y heteroarilalquilo; R10 se selecciona independientemente del grupo integrado por H, alquilo. alquenilo, cicloalquilo, cicloalquilalquilo, cicloalquenilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo y -N(R15)(R16); R11 y R12 se seleccionan independientemente del grupo integrado por H, alquilo, cicloalquilo, cicloalquilalquilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, -C(O)R8, -C(O)OR8, -S(O)R10, -S(O)2R10, -C(O)N(R15)(R16), -S(O)N(R15)(R16) y -S(O)2N(R15)(R16); R14 es 1-5 sustituyentes independientemente seleccionados del grupo integrado por alquilo, alquenilo, alquinilo, cicloalquilo, cicloalquilalquilo, cicloalquenilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, halo, -CN, -OR15, -C(O)R15, -C(O)OR15, -C(O)N(R15)(R16), -SR15, -S(O)N(R15)(R16), -S(O)2N(R15)(R16), -C(=NOR15)R16, -P(O)(OR15)(OR16), -N(R15)(R16), -N(R15)C(O)R16, -N(R15)S(O)R16, -N(R15)S(O)2R16, -N(R15)S(O)2N(R16)(R17), -N(R15)C(O)N(R16)(R17) y -N(R15)C(O)OR16; R15, R16 y R17 se seleccionan independientemente del grupo integrado por H, alquilo, alquenilo, alquinilo, cicloalquilo, cicloalquilalquilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, arilcicloalquilo, arilheterocicloalquilo, R18-alquilo, R18-cicloalquilo, R18-cicloalquilalquilo, R18- heterocicloalquilo, R18-heterocicloalquilalquilo, R18-arilo, R18-arilalquilo, R18-heteroarilo y R18-heteroarilalquilo; o R15, R16 y R17 son seleccionadas del grupo de estructuras (2), donde R23 totaliza 0 a 5 sustituyentes, m es 0 a 6 y n es 1 a 5; R18 es 1-5 sustituyentes independientemente seleccionados del grupo integrado por alquilo, alquenilo, arilo, arilalquilo, arilalquenilo, arilalquinilo, -NO2, halo, heteroarilo, HO-alquiloxialquilo, -CF3, -CN, alquil-CN, -C(O)R19, -C(O)OH, -C(O)OR19, -C(O)NHR20, -C(O)NH2, -C(O)N(alquilo)2, -C(O)N(alquil)(arilo), -C(O)N(alquil)(heteroarilo), -SR19, -S(O)2R20, -S(O)NH2, -S(O)NH(alquilo), -S(O)N(alquil)(alquilo), -S(O)NH(arilo), -S(O)2NH2, -S(O)2NHR19, -S(O)2NH(heterocicloalquilo), - S(O)2N(alquilo)2, -S(O)2N(alquil)(arilo), -OCF3, -OH, -OR20, -O-heterocicloalquilo, -O-cicloalquilalquilo, -O-heterocicloalquilalquilo, -NH2, -NHR20, -N(alquil)2, -N(arilalquilo)2, -N(arilalquil)-(heteroarilalquilo), -NHC(O)R20, -NHC(O)NH2, - NHC(O)NH(alquilo), -NHC(O)N(alquil)(alquilo), -N(alquil)C(O)NH(alquilo), -N(alquil)C(O)N(alquil)(alquilo), -NHS(O)2R20, .-NHS(O)2NH(alquilo), -NHS(O)2N(alquil)(alquilo), -N(alquil)S(O)2NH(alquilo) y -N(alquil)S(O)2N(alquil)(alquilo); o dos restos R18 sobre átomos adyacentes pueden unirse en forma conjunta para formar las estructuras del grupo de formulas (3); R19 es alquilo, cicloalquilo, arilo, arilalquilo o heteroarilalquilo; R20 es alquilo, cicloalquilo, arilo, arilo halo sustituido, arilalquilo, heteroarilo o heteroarilalquilo; y donde cada uno de los grupos alquilo, cicloalquilo, cicloalquilalquilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo heteroarilo, heteroarilalquilo, alquenilo y alquinilo en R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R11, R12 y R14 está independientemente no sustituido o sustituido con 1 a 5 grupos R21 independientemente seleccionados del grupo integrado por alquilo, alquenilo, alquinilo, cicloalquilo, cicloalquilalquilo, cicloalquenilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, halo, -CN, -OR15, -C(O)R15, -C(O)OR15, -C(O)N(R15)(R16), -SR15, -S(O)N(R15)(R16), -CH(R15)(R16), -S(O)2N(R15)(R16), -C(=NOR15)R16, - P(O)(OR15)(OR16), -N(R15)(R16), -alquil-N(R15)(R16), -N(R15)C(O)R16, -CH2-N(R15)C(O)R16, -CH2-R15; -N(R15)S(O)R16, -N(R15)S(O)2R16, -CH2-N(R15)S(O)2R16, -N(R15)S(O)2N(R16)(R17), -N(R15)S(O)N(R16)(R17), -N(R15)C(O)N(R16)(R17), -CH2- N(R15)C(O)N(R16)(R17), -N(R15)C(O)OR16, -CH2-N(R15)C(O)OR16, -S(O)R15, =NOR15, -N3, -NO2 y -S(O)2R15; y donde cada uno de los grupos alquilo, cicloalquenilo, cicloalquilo, cicloalquilalquilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, alquenilo y alquinilo en R21 está independientemente no sustituido o sustituido con 1 a 5 grupos R22 independientemente seleccionados del grupo integrado por alquilo, cicloalquilo, cicloalquenilo, heterocicloalquilo, arilo, heteroarilo, halo, -CF3, -CN, -OR15, -C(O)R15, -C(O)OR15, -alquil-C(O)OR15, C(O)N(R15)(R16), -SR15, -S(O)N(R15)(R16), -S(O)2N(R15)(R16), -C(=NOR15)R16, -P(O)(OR15)(OR16), -N(R15)(R16), -alquil-N(R15)(R16), -N(R15)C(O)R16, - CH2-N(R15)C(O)R16, -N(R15)S(O)R16, -N(R15)S(O)2R16, -CH2-N(R15)S(O)2R16, -N(R15)S(O)2N(R16)(R17), -N(R15)S(O)N(R16)(R17), -N(R15)C(O)N(R16)(R17), -CH2-N(R15)C(O)N(R16)(R17), -N(R15)C(O)OR16, -CH2-N(R15)C(O)OR16, -N3, =NOR15, -NO2, -S(O)R15 y - S(O)2R15; o dos restos R21 o dos R22 sobre átomos adyacentes pueden unirse en forma conjunta para formar un resto del grupo de formulas (3); y cuando R21 o R22 se seleccionan del grupo integrado por -C(=NOR15)R16, -N(R15)C(O)R16, -CH2-N(R15)C(O)R16, -N(R15)S(O)R16, -N(R15)S(O)2N(R16)(R17), -N(R15)S(O)N(R16)(R17), -N(R15)C(O)N(R16)(R17), -CH2-N(R15)C(O)N(R16)(R17), -N(R15)C(O)OR16 y -CH2-N(R15)C(O)OR16, R15 y R16 juntos pueden ser una cadena C2 a C4 donde, opcionalmente, uno, dos o tres carbonos del anillo pueden ser reemplazados por -C(O)- o -N(H)- y R15 y R16, junto con los átomos a los cuales están unidos, forman un anillo de 5 a 7 miembros, opcionalmente sustituido con R23; R23 es 1 a 5 grupos independientemente seleccionados del grupo integrado por alquilo, alquenilo, alquinilo, cicloalquilo, cicloalquilalquilo, cicloalquenilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, halo, -CN, -OR24, -C(O)R24, -C(O)OR24, -C(O)N(R24)(R25), -SR24, -S(O)N(R24)(R25), -S(O)2N(R24)(R25), -C(=NOR24)R25, -P(O)(OR24)(OR25), -N(R24)(R25), -alquil-N(R24)(R25), -N(R24)C(O)R25, -CH2-N(R24)C(O)R25, -N(R24)S(O)R25, -N(R24)S(O)2R25, -CH2-N(R24)S(O)2R25, -N(R24)S(O)2N(R25)(R26), - N(R24)S(O)N(R25)(R26), -N(R24)C(O)N(R25)(R26), -CH2-N(R24)C(O)N(R25)(R26), -N(R24)C(O)OR25, -CH2-N(R24)C(O)OR25, -S(O)R24 y -S(O)2R24 y donde cada uno de los grupos alquilo, cicloalquilo, cicloalquilalquilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, alquenilo y alquinilo en R23 está independientemente no sustituido o sustituido con 1 a 5 grupos R27 independientemente seleccionados del grupo integrado por alquilo, cicloal
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US73062205P | 2005-10-27 | 2005-10-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR057983A1 true AR057983A1 (es) | 2008-01-09 |
Family
ID=37873175
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP060104660A AR057983A1 (es) | 2005-10-27 | 2006-10-25 | Inhibidores hterociclicos de aspartil proteasas |
Country Status (12)
| Country | Link |
|---|---|
| US (3) | US7763606B2 (es) |
| EP (1) | EP1940828B1 (es) |
| JP (1) | JP2009513656A (es) |
| CN (1) | CN101296926A (es) |
| AR (1) | AR057983A1 (es) |
| AT (1) | ATE478070T1 (es) |
| CA (1) | CA2626976A1 (es) |
| DE (1) | DE602006016314D1 (es) |
| ES (1) | ES2349433T3 (es) |
| PE (1) | PE20070531A1 (es) |
| TW (1) | TW200803847A (es) |
| WO (1) | WO2007050721A2 (es) |
Families Citing this family (50)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7700603B2 (en) | 2003-12-15 | 2010-04-20 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| US7592348B2 (en) | 2003-12-15 | 2009-09-22 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| US7763609B2 (en) | 2003-12-15 | 2010-07-27 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| EP1802587A4 (en) * | 2004-10-15 | 2010-02-17 | Astrazeneca Ab | SUBSTITUTED AMINO BINDINGS AND THEIR APPLICATIONS |
| US20090062282A1 (en) * | 2004-10-15 | 2009-03-05 | Astrazeneca Ab | Substituted Amino-Pyrimidones and Uses Thereof |
| EP1831170A4 (en) * | 2004-12-14 | 2009-10-14 | Astrazeneca Ab | SUBSTITUTED AMINOPYRIDINES AND THEIR USE |
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| CH511863A (de) | 1967-04-13 | 1971-08-31 | Ciba Geigy Ag | Verfahren zur Herstellung von 2,4-Benzdiazepinen |
| EP0118171B1 (en) | 1983-03-04 | 1989-03-22 | Arco Chemical Technology, Inc. | Production of polyurethane-forming components having free-isocyanate or hydroxy groups |
| US4550169A (en) * | 1983-11-21 | 1985-10-29 | American Cyanamid Company | Platinum chelates of 2-hydrazino-azoles |
| CA2104060A1 (en) | 1992-11-10 | 1994-05-11 | Robert Ed Johnson | Aryl-fused and hetaryl-fused-2,4-diazepine and 2,4-diazocine antiarrhythmic agents |
| AU2002306734A1 (en) | 2001-03-15 | 2002-10-03 | The Johns Hopkins University | Inhibitors of plasmepsins |
| EP1480941B1 (en) * | 2002-03-04 | 2011-01-26 | Ambrilia Biopharma Inc. | Urea derivatives as hiv aspartyl protease inhibitors |
| JP4790624B2 (ja) * | 2003-11-21 | 2011-10-12 | ジョンズ ホプキンス ユニバーシティ | 生体分子パーティションモチーフ及びそれらの使用 |
| MY149978A (en) | 2003-12-15 | 2013-11-15 | Merck Sharp & Dohme | Heterocyclic aspartyl protease inhibitors |
| US7592348B2 (en) | 2003-12-15 | 2009-09-22 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| AU2006259572A1 (en) | 2005-06-14 | 2006-12-28 | Schering Corporation | Aspartyl protease inhibitors |
| EP1891021B1 (en) * | 2005-06-14 | 2019-01-23 | Merck Sharp & Dohme Corp. | Aspartyl protease inhibitors |
| US8110682B2 (en) * | 2005-06-14 | 2012-02-07 | Schering Corporation | Preparation and use of compounds as aspartyl protease inhibitors |
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2006
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- 2006-10-25 CN CNA2006800398031A patent/CN101296926A/zh active Pending
- 2006-10-25 JP JP2008537928A patent/JP2009513656A/ja not_active Ceased
- 2006-10-25 WO PCT/US2006/041716 patent/WO2007050721A2/en not_active Ceased
- 2006-10-25 PE PE2006001297A patent/PE20070531A1/es not_active Application Discontinuation
- 2006-10-25 AR ARP060104660A patent/AR057983A1/es not_active Application Discontinuation
- 2006-10-25 CA CA002626976A patent/CA2626976A1/en not_active Abandoned
- 2006-10-25 EP EP06817385A patent/EP1940828B1/en active Active
- 2006-10-25 US US11/586,151 patent/US7763606B2/en active Active
- 2006-10-25 AT AT06817385T patent/ATE478070T1/de not_active IP Right Cessation
- 2006-10-25 ES ES06817385T patent/ES2349433T3/es active Active
- 2006-10-26 TW TW095139559A patent/TW200803847A/zh unknown
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2010
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|---|---|
| ATE478070T1 (de) | 2010-09-15 |
| JP2009513656A (ja) | 2009-04-02 |
| US7763606B2 (en) | 2010-07-27 |
| TW200803847A (en) | 2008-01-16 |
| PE20070531A1 (es) | 2007-07-13 |
| EP1940828B1 (en) | 2010-08-18 |
| HK1119680A1 (en) | 2009-03-13 |
| WO2007050721A2 (en) | 2007-05-03 |
| CA2626976A1 (en) | 2007-05-03 |
| US8202854B2 (en) | 2012-06-19 |
| EP1940828A2 (en) | 2008-07-09 |
| US20110280867A1 (en) | 2011-11-17 |
| CN101296926A (zh) | 2008-10-29 |
| WO2007050721A3 (en) | 2007-06-14 |
| US8012960B2 (en) | 2011-09-06 |
| US20100247519A1 (en) | 2010-09-30 |
| US20070099898A1 (en) | 2007-05-03 |
| DE602006016314D1 (de) | 2010-09-30 |
| ES2349433T3 (es) | 2011-01-03 |
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