AR072845A1 - 5-alquil-pirimidinas y su uso en el tratamiento de enfermedades mediadas por la actividad de quinasas. - Google Patents
5-alquil-pirimidinas y su uso en el tratamiento de enfermedades mediadas por la actividad de quinasas.Info
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- AR072845A1 AR072845A1 ARP090102873A ARP090102873A AR072845A1 AR 072845 A1 AR072845 A1 AR 072845A1 AR P090102873 A ARP090102873 A AR P090102873A AR P090102873 A ARP090102873 A AR P090102873A AR 072845 A1 AR072845 A1 AR 072845A1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
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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
- C07D401/06—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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- 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
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- 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
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
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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
-
- 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
-
- 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
- C07D403/14—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 three or more hetero rings
-
- 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
- C07D409/06—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 linked by a carbon chain containing only aliphatic carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Immunology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Communicable Diseases (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Transplantation (AREA)
- Oncology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Laminated Bodies (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Abstract
Compuestos adecuados para el tratamiento adecuado de enfermedades caracterizadas por proliferacion celular excesiva o anormal, y el uso de los mismos para preparar un medicamento que tiene las propiedades mencionadas anteriormente. Reivindicacion 1: Compuestos caracterizados porque tienen la formula general (1) en la que R1 representa un grupo seleccionado entre cicloalquilo C3-8, heterocicloalquilo de 3-8 miembros, arilo C6-10 y heteroarilo de 5-12 miembros, opcionalmente sustituido con uno o más R5 iguales o diferentes; y R2 representa un grupo seleccionado entre cicloalquilo C3-8, heterocicloalquilo de 3-8 miembros, arilo C6-10 y heteroarilo de 5-12 miembros, opcionalmente sustituido con uno o más R5 iguales o diferentes; y R3 representa hidrogeno o un grupo seleccionado entre halogeno, -ORe, -NReRe, -CF3, -CN, -NC, -NO2 y alquilo C1-6; y R4 representa un grupo seleccionado entre alquilo C1-3, cicloalquilo C3-8, heterocicloalquilo de 3-8 miembros, -ORe, -NReRe, -CF3, -CN, -NC y -NO2; y cada R5 representa un grupo seleccionado entre Ra, Rb y Ra sustituido con uno o más Rb y/o Rc iguales o diferentes; y cada Ra independientemente entre si representa hidrogeno o un grupo opcionalmente sustituido con uno o más Rb y/o Rc iguales o diferentes, seleccionados entre alquilo C1-6, heteroalquilo de 2-6 miembros, haloalquilo C1-6, cicloalquilo C3-10, cicloalquilalquilo C4-16, arilo C6-10, arilalquilo C7-16, heteroarilo de 5-12 miembros, heteroarilalquilo de 6-18 miembros, heterocicloalquilo de 3-14 miembros y heterocicloalquilalquilo de 4-14 miembros; cada Rb representa un grupo adecuado y se selecciona independientemente entre sí entre =O, -ORc, haloalquiloxi C1-3, -OCF3, =S, -SRc, =NRc, =NORc, =NNRcRc, =NN(Rg)C(O)NRcRc, -NRcRc, -ONRcRc, -N(ORc)Rc, -N(Rg)NRcRc, halogeno, -CF3, -CN, -NC, -OCN, -SCN, -NO, -NO2, =N2, -N3, -S(O)Rc, -S(O)ORc, -S(O)2Rc, -S(O)2ORc, -S(O)NRcRc, -S(O)2NRcRc, -OS(O)Rc, -OS(O)2Rc, -OS(O)2ORc, -OS(O)NRcRc, -OS(O)2NRcRc, -C(O)Rc, -C(O)ORc, -C(O)SRc, -C(O)NRcRc, -C(O)N(Rg)NRcRc, -C(O)N(Rg)ORc, -C(NRg)NRcRc, -C(NOH)Rc, -C(NOH)NRcRc, -OC(O)Rc, -OC(O)ORc, -OC(O)SRc, -OC(O)NRcRc, -OC(NRg)NRcRc, -SC(O)Rc, -SC(O)ORc, -SC(O)NRcRc, -SC(NRg)NRcRc, -N(Rg)C(O)Rc, -N[C(O)Rc]2, -N(ORg)C(O)Rc, -N(Rg)C(NRg)Rc, -N(Rg)N(Rg)C(O)Rc, -N[C(O)Rc]NRcRc, -N(Rg)C(S)Rc, -N(Rg)S(O)Rc, -N(Rg)S(O)ORc, -N(Rg)S(O)2Rc, -N[S(O)2Rc]2, -N(Rg)S(O)2ORc, -N(Rg)S(O)2NRcRc, -N(Rg)[S(O)2]2Rc, -N(Rg)C(O)ORc, -N(Rg)C(O)SRc, -N(Rg)C(O)NRcRc, -N(Rg)C(O)NRgNRcRc, N(Rg)N(Rg)C(O)NRcRc, -N(Rg)C(S)NRcRc, -[N(Rg)C(O)]2Rc, -N(Rg)[C(O)]2Rc, -N{[C(O)]2Rc}2, -N(Rg)[C(O)]2ORc, -N(Rg)[C(O)]2NRcRc, -N{[C(O)]2ORc}2, -N{[C(O)]2NRcRc}2, -[N(Rg)C(O)]2ORc, -N(Rg)C(NRg)ORc, -N(Rg)C(NOH)Rc, -N(Rg)C(NRg)SRc, -N(Rg)C(NRg)NRcRc y -N=C(Rg)NRcRc y cada Rc independientemente entre si representa hidrogeno o un grupo opcionalmente sustituido con uno o más Rd y/o Re iguales o diferentes, seleccionados entre alquilo C1-6, heteroalquilo de 2-6 miembros, haloalquilo C1-6, cicloalquilo C3-10, cicloalquilalquilo C4-16, arilo C6-10, arilalquilo C7-16, heteroarilo de 5-12 miembros, heteroarilalquilo de 6-18 miembros, heterocicloalquilo de 3-14 miembros y heterocicloalquilalquilo de 4-14 miembros, y cada Rd representa un grupo adecuado y se selecciona independientemente entre si entre =O, -ORe, haloalquiloxi C1-3, -OCF3, =S, -SRe, =NRe, =NORe, =NNReRe, =NN(Rg)C(O)NReRe, -NReRe, -ONReRe, -N(ORe)Re, -N(Rg)NReRe, halogeno, -CF3, -CN, -NC, -OCN, -SCN, -NO, -NO2, =N2, -N3, -S(O)Re, -S(O)ORe, -S(O)2Re, -S(O)2ORe, -S(O)NReRe, -S(O)2NReRe, -OS(O)Re, -OS(O)2Re, -OS(O)2ORe, -OS(O)NReRe, -OS(O)2NReRe, -C(O)Re, -C(O)ORe, -C(O)SRe, -C(O)NReRe, -C(O)N(Rg)NReRe, -C(O)N(Rg)ORe, -C(NRg)NReRe, -C(NOH)Re, -C(NOH)NReRe, -OC(O)Re, -OC(O)ORe, -OC(O)SRe, -OC(O)NReRe, -OC(NRg)NReRe, -SC(O)Re, -SC(O)ORe, -SC(O)NReRe, -SC(NRg)NReRe, -N(Rg)C(O)Re, -N[C(O)Re]2, -N(ORg)C(O)Re, -N(Rg)C(NRg)Re, -N(Rg)N(Rg)C(O)Re, -N[C(O)Re]NReRe, -N(Rg)C(S)Re, -N(Rg)S(O)Re, -N(Rg)S(O)ORe, -N(Rg)S(O)2Re, -N[S(O)2Re]2, -N(Rg)S(O)2ORe, -N(Rg)S(O)2NReRe, -N(Rg)[S(O)2]2Re, -N(Rg)C(O)ORe, -N(Rg)C(O)SRe, -N(Rg)C(O)NReRe, -N(Rg)C(O)NRgNReRe, N(Rg)N(Rg)C(O)NReRe, -N(Rg)C(S)NReRe, -[N(Rg)C(O)]2Re, -N(Rg)[C(O)]2Re, -N{[C(O)]2Re}2, -N(Rg)[C(O)]2ORe, -N(Rg)[C(O)]2NReRe, -N{[C(O)]2ORe}2, -N{[C(O)]2NReRe}2, -[N(Rg)C(O)]2ORe, -N(Rg)C(NRg)ORe, -N(Rg)C(NOH)Re, -N(Rg)C(NRg)SRe, -N(Rg)C(NRg)NReRe y -N=C(Rg)NReRe y cada Re independientemente entre si representa hidrogeno o un grupo opcionalmente sustituido con uno o mas Rf y/o Rg, iguales o similares, seleccionados entre alquilo C1-6, heteroalquilo de 2-6 miembros, haloalquilo C1-6, cicloalquilo C3-6, cicloalquilalquilo C4-16, arilo C6-10, arilalquilo C7-16, heteroarilo de 5-12 miembros, heteroarilalquilo de 6-18 miembros, heterocicloalquilo de 3-14 miembros y heterocicloalquilalquilo de 4-14 miembros, y cada Rf representa un grupo adecuado y en cada caso se selecciona independientemente entre si entre =O, -ORg, haloalquiloxi C1-3, -OCF3, =S, -SRg, =NRg, =NORg, =NNRgRg, =NN(Rh)C(O)NRgRg, -NRgRg, -ONRgRg, -N(ORg)Rg, -N(Rh)NRgRg, halogeno, -CF3, -CN, -NC, -OCN, -SCN, -NO, -NO2, =N2, -N3, -S(O)Rg, -S(O)ORg, -S(O)2Rg, -S(O)2ORg, -S(O)NRgRg, -S(O)2NRgRg, -OS(O)Rg, -OS(O)2Rg, -OS(O)2ORg, -OS(O)NRgRg, -OS(O)2NRgRg, -C(O)Rg, -C(O)ORg, -C(O)SRg, -C(O)NRgRg, -C(O)N(Rh)NRgRg, -C(O)N(Rh)ORg, -C(NRh)NRgRg, -C(NOH)Rg, -C(NOH)NRgRg, -OC(O)Rg, -OC(O)ORg, -OC(O)SRg, -OC(O)NRgRg, -OC(NRh)NRgRg, -SC(O)Rg, -SC(O)ORg, -SC(O)NRgRg, -SC(NRh)NRgRg, -N(Rh)C(O)Rg, -N[C(O)Rg]2, -N(ORh)C(O)Rg, -N(Rh)C(NRh)Rg, -N(Rh)N(Rh)C(O)Rg, -N[C(O)Rg]NRgRg, -N(Rh)C(S)Rg, -N(Rh)S(O)Rg, -N(Rh)S(O)ORg, -N(Rh)S(O)2Rg, -N[S(O)2Rg]2, -N(Rh)S(O)2ORg, -N(Rh)S(O)2NRgRg, -N(Rh)[S(O)2]2Rg, -N(Rh)C(O)ORg, -N(Rh)C(O)SRg, -N(Rh)C(O)NRgRg, -N(Rh)C(O)NRhNRgRg, N(Rh)N(Rh)C(O)NRgRg, -N(Rh)C(S)NRgRg, -[N(Rh)C(O)]2Rg, -N(Rh)[C(O)]2Rg, -N{[C(O)]2Rg}2, -N(Rh)[C(O)]2ORg, -N(Rh)[C(O)]2NRgRg, -N{[C(O)]2ORg}2, -N{[C(O)]2NRgRg}2, -[N(Rh)C(O)]2ORg, -N(Rh)C(NRh)ORg, -N(Rh)C(NOH)Rg, -N(Rh)C(NRh)SRg, -N(Rh)C(NRh)NRgRg y -N=C(Rh)NRgRg; cada Rg independientemente entre sí representa hidrogeno o un grupo opcionalmente sustituido con uno o más Rh, iguales o diferentes, seleccionados entre alquilo C1-6, heteroalquilo de 2-6 miembros, haloalquilo C1-6, cicloalquilo C3-10, cicloalquilalquilo C4-16, arilo C6-10, arilalquilo C7-16, heteroarilo de 5-12 miembros, heteroarilalquilo de 6-18 miembros, heterocicloalquilo de 3-14 miembros y heterocicloalquilalquilo de 4-14 miembros; y cada Rh se selecciona independientemente entre si entre hidrogeno, alquilo C1-6, heteroalquilo de 2-6 miembros, haloalquilo C1-6, cicloalquilo C3-10, cicloalquilalquilo C4-16, arilo C6-10, arilalquilo C7-16, heteroarilo de 5-12 miembros, heteroarilalquilo de 6-18 miembros, heterocicloalquilo de 3-14 miembros y heterocicloalquilalquilo de 4-14 miembros; opcionalmente en forma de los profármacos, los tautomeros, los racematos, los enantiomeros, los diastereoisomeros, los profármacos y las mezclas de los mismos y opcionalmente las sales farmacologicamente aceptables de los mismos.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP08161369 | 2008-07-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR072845A1 true AR072845A1 (es) | 2010-09-22 |
Family
ID=40202900
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP090102873A AR072845A1 (es) | 2008-07-29 | 2009-07-28 | 5-alquil-pirimidinas y su uso en el tratamiento de enfermedades mediadas por la actividad de quinasas. |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US8916548B2 (es) |
| EP (1) | EP2323992B1 (es) |
| JP (1) | JP5599791B2 (es) |
| KR (1) | KR20110041536A (es) |
| CN (1) | CN102112450A (es) |
| AR (1) | AR072845A1 (es) |
| AU (1) | AU2009275957A1 (es) |
| BR (1) | BRPI0916679A2 (es) |
| CA (1) | CA2731909A1 (es) |
| CL (1) | CL2011000195A1 (es) |
| CO (1) | CO6341617A2 (es) |
| DK (1) | DK2323992T3 (es) |
| EA (1) | EA201100255A1 (es) |
| EC (1) | ECSP11010786A (es) |
| ES (1) | ES2597903T3 (es) |
| HU (1) | HUE029837T2 (es) |
| IL (1) | IL210343A0 (es) |
| MA (1) | MA32505B1 (es) |
| MX (1) | MX2011000729A (es) |
| NZ (1) | NZ590558A (es) |
| PE (1) | PE20110196A1 (es) |
| PL (1) | PL2323992T3 (es) |
| TW (1) | TW201010984A (es) |
| UY (1) | UY32009A (es) |
| WO (1) | WO2010012740A1 (es) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2009275957A1 (en) | 2008-07-29 | 2010-02-04 | Boehringer Ingelheim International Gmbh | 5-alkynyl-pyrimidines |
| AR072538A1 (es) | 2008-07-29 | 2010-09-01 | Boehringer Ingelheim Int | Derivados de indolinonas, composiciones farmacéuticas y usos |
| AR076332A1 (es) * | 2009-04-21 | 2011-06-01 | Boehringer Ingelheim Int | Derivados heterociclicos de 5-alquinil-piridinas, composiciones farmaceuticas que los comprenden y uso de los mismos para el tratamiento y/o prevencion del cancer, procesos inflamatorios, autoinmunes, y/o infecciones. |
| UY33198A (es) * | 2010-01-26 | 2011-08-31 | Boehringer Ingelheim Int | 5-alquinil-pirimidinas. |
| US8633183B2 (en) * | 2010-01-26 | 2014-01-21 | Boehringer Ingelheim International Gmbh | 5-alkynyl-pyrimidines |
| US8466162B2 (en) * | 2011-01-26 | 2013-06-18 | Boehringer Ingelheim International Gmbh | 5-alkynyl-pyridines |
| TW201245176A (en) * | 2011-01-26 | 2012-11-16 | Boehringer Ingelheim Int | New 5-alkynyl-pyridines |
| US8912200B2 (en) * | 2011-07-28 | 2014-12-16 | Nerviano Medical Sciences S.R.L. | Alkynyl substituted pyrimidinyl-pyrroles active as kinases inhibitors |
| UA110995C2 (uk) * | 2011-10-07 | 2016-03-10 | Ф. Хоффманн-Ля Рош Аг | Етинільні похідні як модулятори метаботропного глутаматного рецептора |
| JP6430512B2 (ja) * | 2013-12-11 | 2018-11-28 | セルジーン クオンティセル リサーチ,インク. | リジン特異的デメチラーゼ−1の阻害剤 |
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| CN112125901A (zh) * | 2014-09-05 | 2020-12-25 | 赛尔基因昆蒂赛尔研究公司 | 赖氨酸特异性脱甲基酶-1的抑制剂 |
| CN104744376A (zh) * | 2015-03-14 | 2015-07-01 | 长沙深橙生物科技有限公司 | 一种2-异丙基嘧啶衍生物的制备方法 |
| CN104803921A (zh) * | 2015-03-14 | 2015-07-29 | 长沙深橙生物科技有限公司 | 一种苯取代嘧啶衍生物的制备方法 |
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| DE3832570A1 (de) | 1988-09-24 | 1990-03-29 | Hoechst Ag | 7-substituierte derivate der 3,5-dihydroxyhept-6-insaeure, verfahren zur ihrer herstellung, ihre verwendung als arzneimittel, sowie zwischenprodukte |
| WO1994014780A1 (en) | 1992-12-18 | 1994-07-07 | The Wellcome Foundation Limited | Pyrimidine, pyridine, pteridinone and indazole derivatives as enzyme inhibitors |
| US5622954A (en) | 1994-05-11 | 1997-04-22 | Fmc Corporation | 5[W(substituted aryl)alkenylene and alkynylene]-2,4-diaminopyrimidines as pesticides |
| EP1261327B1 (en) | 2000-02-25 | 2005-04-27 | F.Hoffmann-La Roche Ag | Adenosine receptor modulators |
| JP5154728B2 (ja) * | 2000-07-24 | 2013-02-27 | クレニツキー・ファーマシューティカルズ,インコーポレイテッド | 神経栄養活性を有する置換5−アルキニルピリミジン |
| RU2006100484A (ru) * | 2003-06-13 | 2006-06-10 | Центарис ГмбХ, Германи (DE) | Соединения, обладающие ингибирующей активностью в отношении фосфатидилинозит-3-киназы, фармацевтическая композиция, способ определения эффективности этих соединений, способ лечения нарушений (варианты) и способ изменения передачи сигнала в клетках |
| ATE402705T1 (de) | 2003-12-24 | 2008-08-15 | Astrazeneca Ab | Pyrimidine mit tie2 (tek) aktivität |
| HRP20161751T1 (hr) * | 2004-05-13 | 2017-04-07 | Icos Corporation | Kinazolinoni kao inhibitori humane fosfatidilinozitol 3-kinaze delta |
| US7776869B2 (en) * | 2004-10-18 | 2010-08-17 | Amgen Inc. | Heteroaryl-substituted alkyne compounds and method of use |
| US20100048543A1 (en) | 2005-02-01 | 2010-02-25 | Astrazeneca Ab | Pyrimidine compounds having ties (tek) inhibitory activity |
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| JP2008534565A (ja) | 2005-03-31 | 2008-08-28 | アストラゼネカ アクチボラグ | Tie2阻害活性のあるアミノピリミジン誘導体 |
| EP2364974A1 (en) * | 2005-10-07 | 2011-09-14 | Exelixis, Inc. | N-(3-Phenylamino-quinoxalin-2-yl)-benzenesulfonamide derivatives as phosphatidylinositol 3-kinase inhibitors |
| JO2660B1 (en) * | 2006-01-20 | 2012-06-17 | نوفارتيس ايه جي | Pi-3 inhibitors and methods of use |
| EP2057129A1 (en) | 2006-08-24 | 2009-05-13 | AstraZeneca AB | Morpholino pyrimidine derivatives useful in the treatment of proliferative disorders |
| ES2618057T3 (es) | 2006-12-29 | 2017-06-20 | Janssen Sciences Ireland Uc | Pirimidinas 5,6-sustituidas inhibidoras del VIH |
| EP2022785A1 (en) | 2007-06-20 | 2009-02-11 | Bayer Schering Pharma Aktiengesellschaft | Alkynylpyrimidines as Tie2 kinase inhibitors |
| AU2009275957A1 (en) | 2008-07-29 | 2010-02-04 | Boehringer Ingelheim International Gmbh | 5-alkynyl-pyrimidines |
| US8633183B2 (en) | 2010-01-26 | 2014-01-21 | Boehringer Ingelheim International Gmbh | 5-alkynyl-pyrimidines |
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2009
- 2009-07-28 AU AU2009275957A patent/AU2009275957A1/en not_active Abandoned
- 2009-07-28 WO PCT/EP2009/059763 patent/WO2010012740A1/en not_active Ceased
- 2009-07-28 ES ES09781207.7T patent/ES2597903T3/es active Active
- 2009-07-28 HU HUE09781207A patent/HUE029837T2/en unknown
- 2009-07-28 BR BRPI0916679A patent/BRPI0916679A2/pt not_active IP Right Cessation
- 2009-07-28 AR ARP090102873A patent/AR072845A1/es unknown
- 2009-07-28 DK DK09781207.7T patent/DK2323992T3/en active
- 2009-07-28 KR KR1020117003951A patent/KR20110041536A/ko not_active Withdrawn
- 2009-07-28 JP JP2011520491A patent/JP5599791B2/ja active Active
- 2009-07-28 PL PL09781207T patent/PL2323992T3/pl unknown
- 2009-07-28 MX MX2011000729A patent/MX2011000729A/es unknown
- 2009-07-28 EA EA201100255A patent/EA201100255A1/ru unknown
- 2009-07-28 TW TW098125388A patent/TW201010984A/zh unknown
- 2009-07-28 UY UY0001032009A patent/UY32009A/es not_active Application Discontinuation
- 2009-07-28 US US13/055,949 patent/US8916548B2/en active Active
- 2009-07-28 NZ NZ590558A patent/NZ590558A/xx not_active IP Right Cessation
- 2009-07-28 EP EP09781207.7A patent/EP2323992B1/en active Active
- 2009-07-28 PE PE2011000088A patent/PE20110196A1/es not_active Application Discontinuation
- 2009-07-28 CN CN2009801301499A patent/CN102112450A/zh active Pending
- 2009-07-28 CA CA2731909A patent/CA2731909A1/en not_active Abandoned
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2010
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2011
- 2011-01-26 MA MA33560A patent/MA32505B1/fr unknown
- 2011-01-27 CO CO11009242A patent/CO6341617A2/es not_active Application Discontinuation
- 2011-01-27 EC EC2011010786A patent/ECSP11010786A/es unknown
- 2011-01-28 CL CL2011000195A patent/CL2011000195A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JP2011529468A (ja) | 2011-12-08 |
| NZ590558A (en) | 2012-12-21 |
| EP2323992A1 (en) | 2011-05-25 |
| WO2010012740A1 (en) | 2010-02-04 |
| AU2009275957A1 (en) | 2010-02-04 |
| KR20110041536A (ko) | 2011-04-21 |
| CO6341617A2 (es) | 2011-11-21 |
| BRPI0916679A2 (pt) | 2015-11-17 |
| HUE029837T2 (en) | 2017-04-28 |
| EA201100255A1 (ru) | 2011-08-30 |
| JP5599791B2 (ja) | 2014-10-01 |
| UY32009A (es) | 2010-02-26 |
| EP2323992B1 (en) | 2016-07-20 |
| MX2011000729A (es) | 2011-03-15 |
| ES2597903T3 (es) | 2017-01-24 |
| US20110281838A1 (en) | 2011-11-17 |
| ECSP11010786A (es) | 2011-02-28 |
| DK2323992T3 (en) | 2016-10-31 |
| PL2323992T3 (pl) | 2017-01-31 |
| MA32505B1 (fr) | 2011-07-03 |
| CL2011000195A1 (es) | 2011-07-08 |
| CN102112450A (zh) | 2011-06-29 |
| TW201010984A (en) | 2010-03-16 |
| CA2731909A1 (en) | 2010-02-04 |
| US8916548B2 (en) | 2014-12-23 |
| IL210343A0 (en) | 2011-03-31 |
| PE20110196A1 (es) | 2011-04-03 |
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