AR077365A1 - Derivados de imidazol para el tratamiento de enfermedades mediadas por la inhibicion de la formacion de abeta - Google Patents
Derivados de imidazol para el tratamiento de enfermedades mediadas por la inhibicion de la formacion de abetaInfo
- Publication number
- AR077365A1 AR077365A1 ARP100102352A ARP100102352A AR077365A1 AR 077365 A1 AR077365 A1 AR 077365A1 AR P100102352 A ARP100102352 A AR P100102352A AR P100102352 A ARP100102352 A AR P100102352A AR 077365 A1 AR077365 A1 AR 077365A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkynyl
- alkenyl
- alkylaryl
- alkylheteroaryl
- Prior art date
Links
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title abstract 4
- 201000010099 disease Diseases 0.000 title abstract 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N 1H-imidazole Chemical class C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 title 1
- 230000015572 biosynthetic process Effects 0.000 title 1
- 230000005764 inhibitory process Effects 0.000 title 1
- 230000001404 mediated effect Effects 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 100
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 18
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 17
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 17
- 125000005213 alkyl heteroaryl group Chemical group 0.000 abstract 15
- 125000002877 alkyl aryl group Chemical group 0.000 abstract 12
- 229910052736 halogen Inorganic materials 0.000 abstract 7
- 150000002367 halogens Chemical class 0.000 abstract 7
- 125000000623 heterocyclic group Chemical group 0.000 abstract 7
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 6
- 208000024827 Alzheimer disease Diseases 0.000 abstract 4
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 4
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 4
- 125000001072 heteroaryl group Chemical group 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 4
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 3
- 125000006661 (C4-C6) heterocyclic group Chemical group 0.000 abstract 3
- 206010012289 Dementia Diseases 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 208000010877 cognitive disease Diseases 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 125000005842 heteroatom Chemical group 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 3
- 125000001424 substituent group Chemical group 0.000 abstract 3
- 229910052717 sulfur Inorganic materials 0.000 abstract 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 2
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 abstract 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 2
- -1 OR7 Chemical group 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000004122 cyclic group Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 208000027061 mild cognitive impairment Diseases 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 208000000044 Amnesia Diseases 0.000 abstract 1
- 102000013455 Amyloid beta-Peptides Human genes 0.000 abstract 1
- 108010090849 Amyloid beta-Peptides Proteins 0.000 abstract 1
- 206010059245 Angiopathy Diseases 0.000 abstract 1
- 208000005145 Cerebral amyloid angiopathy Diseases 0.000 abstract 1
- 206010008111 Cerebral haemorrhage Diseases 0.000 abstract 1
- 208000028698 Cognitive impairment Diseases 0.000 abstract 1
- 101100440695 Dictyostelium discoideum corB gene Proteins 0.000 abstract 1
- 201000010374 Down Syndrome Diseases 0.000 abstract 1
- 101100203602 Hypocrea jecorina (strain QM6a) sor7 gene Proteins 0.000 abstract 1
- 208000026139 Memory disease Diseases 0.000 abstract 1
- 206010033799 Paralysis Diseases 0.000 abstract 1
- 208000018737 Parkinson disease Diseases 0.000 abstract 1
- 206010036631 Presenile dementia Diseases 0.000 abstract 1
- 206010039966 Senile dementia Diseases 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 230000001054 cortical effect Effects 0.000 abstract 1
- 230000006735 deficit Effects 0.000 abstract 1
- 230000007850 degeneration Effects 0.000 abstract 1
- 230000003412 degenerative effect Effects 0.000 abstract 1
- 230000006806 disease prevention Effects 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 239000012458 free base Substances 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 150000002460 imidazoles Chemical class 0.000 abstract 1
- 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 abstract 1
- 230000006984 memory degeneration Effects 0.000 abstract 1
- 208000023060 memory loss Diseases 0.000 abstract 1
- 230000004770 neurodegeneration Effects 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 230000000750 progressive effect Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 208000024891 symptom Diseases 0.000 abstract 1
- 230000002792 vascular Effects 0.000 abstract 1
Classifications
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- 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
- C07D401/04—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 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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
- C07D233/88—Nitrogen atoms, e.g. allantoin
-
- 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
-
- 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
- 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
- C07D401/14—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 three or more hetero rings
-
- 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
- C07D403/10—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 aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Neurosurgery (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (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)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Derivados de imidazol y sus composiciones farmacéuticas. Asimismo, su uso para el tratamiento y/o la prevencion de patologías relacionadas con Abeta, tales como síndrome de Down, angiopatía beta-amiloide tal como, aunque no a modo de limitacion, angiopatía amiloide cerebral o hemorragia cerebral hereditaria, trastornos asociados con el deterioro cognitivo, tales como, aunque no a modo de limitacion, MCI (deterioro cognitivo leve), enfermedad de Alzheimer, pérdida de la memoria, síntomas de déficit de atencion asociados con la enfermedad de Alzheimer, neurodegeneracion asociada con enfermedades tales como la enfermedad de Alzheimer o demencia, incluyendo demencia de origen mixto vascular y degenerativo, demencia pre-senil, demencia senil y demencia asociada con enfermedad de Parkinson, parálisis supranuclear progresiva o degeneracion basal cortical. Reivindicacion 1: Un compuesto de acuerdo con la formula (1) donde A se selecciona de alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquilarilo C1-6, alquilheteroarilo C1-6, alquil C0-6-cicloalquilo C3-8, alquil C0-6-cicloalquenilo C3-6, alquil C0-6-cicloalquinilo C6 o alquil C0-6-heterociclilo C3-8, donde dicho A está opcionalmente sustituido con uno o varios R1; B es arilo o heteroarilo, donde dicho arilo o heteroarilo está opcionalmente sustituido con uno o varios R2; C se selecciona de hidrogeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquil C0-6-cicloalquilo C3-6, alquil C0-6-cicloalquenilo C3-6, alquil C0-6-cicloalquinilo C6, alquilarilo C0-6, alquilheteroarilo C0-6, alquilheterociclilo C0-6, alquil C0-6OR4, alquil C0-6CO2R4, alquil C0-6N(R4)2, halogeno, alquil C0-6CN, alquil C0-6COR4, CHO, NO2, alquil C0-6CON(R4)2, O(CO)OR4, O(CO)R4, O(CO)N(R4)2, NR4(CO)OR4, alquil C0-6NR4(CO)R4, NR4(CO)N(R4)2, NR4(CO)(CO)R4, NR4(CO)(CO)N(R4)2, alquil C0-6SR4, alquil C0-6OSO2R4, alquil C0-6SO3R4, alquil C0-6SO2R4, alquil C0-6SOR4, alquil C0-6(SO2)N(R4)2, alquil C0-6(SO)N(R4)2, alquil C0-6NR4(SO2)N(R4)2, alquil C0-6NR4(SO)R4, SF5 y OSF5, donde dicho alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquil C0-6-cicloalquilo C3-6, alquilarilo C0-6, alquilheteroarilo C0-6 o alquilheterociclilo C0-6 está opcionalmente sustituido con uno o varios R3; R1 se selecciona de alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquil C0-6-cicloalquilo C3-6, alquil C0-6-cicloalquenilo C3-6, alquil C0-6-cicloalquinilo C6, alquilarilo C0-6, alquilheteroarilo C0-6, alquilheterociclilo C0-6, alquil C0-6CO2R4, alquil C0-6N(R4)2, alquil C0-6OR4, halogeno, alquil C0-6CN, alquil C0-6COR4, CHO, NO2, alquil C0-6CON(R4)2, O(CO)OR4, O(CO)R4, O(CO)N(R4)2, NR4(CO)OR4, alquil C0-6NR4(CO)R4, NR4(CO)N(R4)2, NR4(CO)(CO)R4, NR4(CO)(CO)N(R4)2, alquil C0-6SR4, alquil C0-6OSO2R4, alquil C0-6SO3R4, alquil C0-6SO2R4, alquil C0-6SOR4, alquil C0-6(SO2)N(R4)2, alquil C0-6(SO)N(R4)2, alquil C0-6NR4(SO2)N(R4)2, alquil C0-6NR4(SO)R4, SF5 y OSF5, donde dicho alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquil C0-6-cicloalquilo C3-6, alquilarilo C0-6, alquilheteroarilo C0-6 o alquilheterociclilo C0-6 está opcionalmente sustituido con uno o varios R3; o dos R1 pueden formar, junto con los átomos a los cuales están unidos, un anillo cíclico o heterocíclico opcionalmente sustituido con uno o varios R6; R2 se selecciona de alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquil C0-6-cicloalquilo C3-6, alquil C0-6-cicloalquenilo C3-6, alquil C0-6-cicloalquinilo C6, alquilarilo C0-6, alquilheteroarilo C0-6, alquilheterociclilo C0-6, alquil C0-6CO2R4, alquil C0-6N(R4)2, halogeno, alquil C0-6CN, alquil C0-6COR4, CHO, NO2, alquil C0-6CON(R4)2, O(CO)OR4, O(CO)R4, O(CO)N(R4)2, NR4(CO)OR4, alquil C0-6NR4(CO)R4, NR4(CO)N(R4)2, NR4(CO)(CO)R4, NR4(CO)(CO)N(R4)2, alquil C0-6SR4, alquil C0-6OSO2R4, alquil C0-6SO3R4, alquil C0-6SO2R4, alquil C0-6SOR4, alquil C0-6(SO2)N(R4)2, alquil C0-6(SO)N(R4)2, alquil C0-6NR4(SO2)N(R4)2, alquil C0-6NR4(SO)R4, y alquil C0-6OR4, donde dicho alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquil C0-6-cicloalquilo C3-6, alquilarilo C0-6, alquilheteroarilo C0-6 o alquilheterociclilo C0-6 está opcionalmente sustituido con uno o varios R3; o dos R2 pueden formar, junto con los átomos a los cuales están unidos, un anillo cíclico o heterocíclico opcionalmente sustituido con uno o varios R6; R3 se selecciona de halogeno, NO2, CHO, alquil C0-6CN, alquil C0-6OR4, haloalquilo C1-6, alquil C0-6N(R4)2, NR4C(O)R4, alquil C0-6CO2R4, alquil C0-6CON(R4)2, alquil C0-6NR4(CO)R4, O(CO)N(R4)2, NR4(CO)OR4, NR4(CO)N(R4)2, O(CO)OR4, O(CO)R4, alquil C0-6COR4, NR4(CO)(CO)R4, NR4(CO)(CO)N(R4)2, alquil C0-6SR4, alquil C0-6(SO2)N(R4)2, Oalquil C2-6NR4(SO2)R4, alquil C0-6(SO)N(R4)2, OSO2R4, SO3R4, alquil C0-6NR4(SO2)N(R4)2, alquil C0-6NR4(SO)R4, alquil C0-6SO2R4, alquil C0-6SOR4, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquil C0-6-cicloalquilo C3-6, alquil C0-6-cicloalquenilo C3-6, alquil C0-6-cicloalquinilo C6, alquilarilo C0-6, alquilheteroarilo C0-6, y alquilheterociclilo C0-6, donde dicho alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquil C0-6-cicloalquilo C3-6, alquilarilo C0-6, alquilheteroarilo C0-6 o alquilheterociclilo C0-6 está opcionalmente sustituido con uno o varios R6; R4 se selecciona de hidrogeno, alquilo C1-6, haloalquilo C1-3, alquenilo C2-6, alquinilo C2-6, alquil C0-6-cicloalquilo C3-6, alquil C0-6-cicloalquenilo C3-6, alquil C0-6-cicloalquinilo C6, alquilarilo C0-6, alquilheteroarilo C0-6, alquilheterociclilo C0-6, alquil C1-6OR5 y alquil C1-6N(R5)2, donde dicho alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquil C0-6-cicloalquilo C3-6, alquilarilo C0-6, alquilheteroarilo C0-6 o alquilheterociclilo C0-6 está opcionalmente sustituido con uno o varios R6; o dos R4 pueden formar juntos un anillo heterocíclico de 4 a 6 miembros que contiene uno o varios heteroátomos seleccionados de N, O o S, donde dicho anillo heterocíclico está opcionalmente sustituido con uno o varios R6; R5 se selecciona de hidrogeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquil C0-6-cicloalquilo C3-6, alquil C0-6-cicloalquenilo C3-6, alquil C0-6-cicloalquinilo C3-6, alquilarilo C0-6, alquilheterociclilo C0-6 y alquilheteroarilo C0-6, donde dicho alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquil C0-6-cicloalquilo C3-6, alquilarilo C0-6, alquilheteroarilo C0-6 o alquilheterociclilo C0-6 está opcionalmente sustituido con uno o varios R6; o dos R5 pueden formar juntos un anillo heterocíclico de 4 a 6 miembros que contiene uno o varios heteroátomos seleccionados de N, O o S, donde dicho anillo heterocíclico está opcionalmente sustituido con uno o varios R6; R6 se selecciona de oxo, halogeno, nitro, CN, OR7, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquilarilo C0-6, alquilheteroarilo C0-6, alquil C0-6-cicloalquilo C3-6, alquilheterociclilo C0-6, haloalquilo C1-6, Oalquil C2-6N(R7)2, N(R7)2, CON(R7)2, NR7(CO)R7, O(CO)alquilo C1-6, (CO)Oalquilo C1-6, COR7, SON(R7)2, (SO2)N(R7)2, NR7SO2R7, NR7SOR7, SO2R7, SOR7, (CO)alquil C1-6N(R7)2, (SO2)alquil C1-6N(R7)2, OSO2R7 y SO3R7, donde dicho alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquilarilo C0-6, alquilheteroarilo C0-6, alquilheterociclilo C0-6 o alquil C0-6-cicloalquilo C3-6 está opcionalmente sustituido con uno o varios sustituyentes seleccionados independientemente de halo, nitro, ciano, OR7, alquilo C1-6 o haloalquilo C1-6; R7 se selecciona de hidrogeno, alquilo C1-6, haloalquilo C1-3, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-6, cicloalquenilo C3-6, cicloalquinilo C6, arilo, heteroarilo y heterociclilo, donde dicho alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-6 arilo, heteroarilo o heterociclilo está opcionalmente sustituido con uno a tres sustituyentes seleccionados independientemente de hidroxi, ciano, halogeno y Oalquilo C1-3; o dos R7 pueden formar juntos un anillo heterocíclico de 4 a 6 miembros que contiene uno o varios heteroátomos seleccionados de N, O o S, donde dicho anillo heterocíclico está opcionalmente sustituido con uno o varios sustituyentes seleccionados independientemente de hidroxi, Oalquilo C1-3, ciano y halogeno; en forma de base libre o de una sal farmacéuticamente aceptable de dicho compuesto.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US22253509P | 2009-07-02 | 2009-07-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR077365A1 true AR077365A1 (es) | 2011-08-24 |
Family
ID=43411290
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP100102352A AR077365A1 (es) | 2009-07-02 | 2010-07-01 | Derivados de imidazol para el tratamiento de enfermedades mediadas por la inhibicion de la formacion de abeta |
Country Status (4)
| Country | Link |
|---|---|
| AR (1) | AR077365A1 (es) |
| TW (1) | TW201103893A (es) |
| UY (1) | UY32750A (es) |
| WO (1) | WO2011002408A1 (es) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| UA108363C2 (uk) | 2009-10-08 | 2015-04-27 | Похідні імінотіадіазиндіоксиду як інгібітори bace, композиція на їх основі і їх застосування | |
| US8415483B2 (en) | 2010-12-22 | 2013-04-09 | Astrazeneca Ab | Compounds and their use as BACE inhibitors |
| US20120165346A1 (en) * | 2010-12-22 | 2012-06-28 | Astrazeneca Ab | Compounds and their use as BACE inhibitors |
| WO2013054108A1 (en) | 2011-10-10 | 2013-04-18 | Astrazeneca Ab | Mono-fluoro beta-secretase inhibitors |
| US9000185B2 (en) * | 2012-06-20 | 2015-04-07 | Astrazeneca Ab | Cycloalkyl ether compounds and their use as BACE inhibitors |
| US9000183B2 (en) | 2012-06-20 | 2015-04-07 | Astrazeneca Ab | Cyclohexane-1,2′-indene-1′,2″-imidazol compounds and their use as BACE inhibitors |
| US9000184B2 (en) | 2012-06-20 | 2015-04-07 | Astrazeneca Ab | Cyclohexane-1,2′-naphthalene-1′,2″-imidazol compounds and their use as BACE inhibitors |
| US9000182B2 (en) * | 2012-06-20 | 2015-04-07 | Astrazeneca Ab | 2H-imidazol-4-amine compounds and their use as BACE inhibitors |
| US10548882B2 (en) * | 2012-06-21 | 2020-02-04 | Astrazeneca Ab | Camsylate salt |
| CN114989103B (zh) * | 2022-06-09 | 2024-07-09 | 杭州科巢生物科技有限公司 | 一种2-甲氧基-3-(1-甲基-1h-1,2,4-三唑-3-基)苯胺的制备方法 |
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| JP2009520686A (ja) * | 2005-11-21 | 2009-05-28 | アストラゼネカ・アクチエボラーグ | 新規な2−アミノ−イミダゾール−4−オン化合物並びに認知障害、アルツハイマー病、神経変性及び認知症の治療に使用する医薬の製造におけるその使用 |
| TW200734311A (en) * | 2005-11-21 | 2007-09-16 | Astrazeneca Ab | New compounds |
| WO2008076044A1 (en) * | 2006-12-20 | 2008-06-26 | Astrazeneca Ab | Novel 2-amino-5, 5-diaryl-imidazol-4-ones |
| TW200831484A (en) * | 2006-12-20 | 2008-08-01 | Astrazeneca Ab | New compounds |
| TW200902503A (en) * | 2007-05-15 | 2009-01-16 | Astrazeneca Ab | New compounds |
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- 2010-07-02 WO PCT/SE2010/050760 patent/WO2011002408A1/en not_active Ceased
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| TW201103893A (en) | 2011-02-01 |
| WO2011002408A1 (en) | 2011-01-06 |
| UY32750A (es) | 2011-01-31 |
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