AR065813A1 - Compuesto composicion farmaceutica y metodos para tratar trastornos relacionados con pi3k y mtor y a cancer y para inhibir mtor y pi3k - Google Patents
Compuesto composicion farmaceutica y metodos para tratar trastornos relacionados con pi3k y mtor y a cancer y para inhibir mtor y pi3kInfo
- Publication number
- AR065813A1 AR065813A1 ARP080101182A ARP080101182A AR065813A1 AR 065813 A1 AR065813 A1 AR 065813A1 AR P080101182 A ARP080101182 A AR P080101182A AR P080101182 A ARP080101182 A AR P080101182A AR 065813 A1 AR065813 A1 AR 065813A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- aryl
- nhc
- optionally substituted
- heteroaryl
- Prior art date
Links
- 102000010400 1-phosphatidylinositol-3-kinase activity proteins Human genes 0.000 title abstract 3
- 108091007960 PI3Ks Proteins 0.000 title abstract 3
- 150000001875 compounds Chemical class 0.000 title abstract 2
- 101150097381 Mtor gene Proteins 0.000 title 2
- 102100023085 Serine/threonine-protein kinase mTOR Human genes 0.000 title 2
- 206010028980 Neoplasm Diseases 0.000 title 1
- 201000011510 cancer Diseases 0.000 title 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 116
- 125000005915 C6-C14 aryl group Chemical group 0.000 abstract 24
- 125000001072 heteroaryl group Chemical group 0.000 abstract 21
- 125000001424 substituent group Chemical group 0.000 abstract 20
- 229910052736 halogen Inorganic materials 0.000 abstract 16
- 150000002367 halogens Chemical class 0.000 abstract 16
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 14
- 125000000217 alkyl group Chemical group 0.000 abstract 10
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 8
- -1 N-morpholinyl Chemical group 0.000 abstract 8
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 8
- 125000000623 heterocyclic group Chemical group 0.000 abstract 8
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 8
- 229910052799 carbon Inorganic materials 0.000 abstract 6
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical class N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 abstract 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 5
- 125000004432 carbon atom Chemical group C* 0.000 abstract 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 5
- 125000005530 alkylenedioxy group Chemical group 0.000 abstract 4
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 4
- 125000004446 heteroarylalkyl group Chemical group 0.000 abstract 4
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 3
- 125000002252 acyl group Chemical group 0.000 abstract 3
- 125000000304 alkynyl group Chemical group 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 3
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 2
- 125000002911 monocyclic heterocycle group Chemical group 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000005010 perfluoroalkyl group Chemical group 0.000 abstract 2
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 1
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 abstract 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 1
- 102000013530 TOR Serine-Threonine Kinases Human genes 0.000 abstract 1
- 108010065917 TOR Serine-Threonine Kinases Proteins 0.000 abstract 1
- 150000001721 carbon Chemical group 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 229910052731 fluorine Inorganic materials 0.000 abstract 1
- 239000011737 fluorine Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
- C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- 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]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
-
- 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
-
- 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
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Urology & Nephrology (AREA)
- Oncology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Pain & Pain Management (AREA)
- Vascular Medicine (AREA)
- Diabetes (AREA)
- Ophthalmology & Optometry (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Abstract
Análogos de imidazolopirimidina, métodos para elaborar los análogos de imidazolo-pirimidina, composiciones que comprenden un análogo de imidazolopirimidina y métodos para tratar o prevenir un trastorno relacionado con PI3K que comprende administrara un sujeto en necesidad de este una cantidad efectiva de un análogo de imidazolopirimidina, así como métodos para tratar o prevenir trastornos relacionados mTOR que comprende administrar a un sujeto en necesidad de este una cantidad efectiva de unanálogo de imidazolopirimidina. Reivindicacion 1: Un compuesto de formula (1) y sales farmacéuticamente aceptables, caracterizado porque: R1 es N-morfolinilo o N-tiomorfolinilo, en donde el átomo de azufre N-tiomorfolinilo se puede sustituir conuno o dos =O, en donde uno cualquiera o más de los átomos de hidrogeno en el anillo del N-morfolinilo o N-tiomorfolinilo se pueden sustituir independientemente con alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alcoxi C1-3, acilo C1-3, alquilcarboxiC1-3, alquilo C1-6amino, fluor, o -CN; en donde cualquiera de los dos átomos de hidrogeno adheridos al mismo átomo de carbono en R1 se pueden reemplazar por un átomo de oxígeno, en donde el átomo de oxigeno se toma junto con el carbono al cual estáadherido, forma un carbonilo (C=O); R2 es (a) alquenilo C2-10, opcionalmente sustituido con uno o más sustituyentes seleccionados independientemente de halogeno, -NH2, -NH(alquilo C1-6), -N(alquilo C1-6)(alquilo C1-6), -N(alquilo C1-3)C(O)(alquiloC1-6), -NHC(O)(alquilo C1-6), -NHC(O)H, -C(O)NH2, -C(O)NH(alquilo C1-6), -C(O)N(alquilo C1-6)(alquilo C1-6), -CN, -OH, -O(alquilo C1-6), -alquilo C1-6, -C(O)OH, -C(O)Oalquilo C1-6, -C(O)alquilo C1-6, arilo C6-14, heteroarilo C1-9, y carbociclo C3-8,dado que el sustituyente no se adhiere a un carbono del enlace doble; (b) alquinilo C2-10, opcionalmente sustituido con uno o más sustituyentes seleccionados independientemente de halogeno, -NH2, -NH(alquilo C1-6), -N(alquilo C1-6)(alquilo C1-6), -N(alquilo C1-3)C(O)(alquilo C1-6), -NHC(O)(alquilo C1-6), -NHC(O)H, -C(O)NH2, -C(O)NH(alquilo C1-6), -C(O)N(alquilo C1-6)(alquilo C1-6), -CN, -OH, -O(alquilo C1-6), -alquilo C1-6, -C(O)OH, -C(O)Oalquilo C1-6, -C(O)alquilo C1-6, arilo C6-14,heteroarilo C1-9, y carbociclo C3-8, dado que el sustituyente no se adhiere a un carbono del enlace triple; (c) arilo C6-14 opcionalmente sustituido con de 1 a 3 sustituyentes independientemente seleccionados de: halogeno, alquilo C1-6, alcoxi C1-6,opcionalmente sustituido con alcoxi C1-6, hidroxialquilo C1-6, alquenilo C2-6, alquinilo C2-6, carbociclo C3-8, arilo C6-14, heteroarilo C1-9, perfluoroalquilo C1-6, hidroxilo, NR12R12, NO2, CN, CO2H, CHO, arilo C6-14-O-, arilo (C6-14)alquil-O-,opcionalmente sustituido con de 1 a 3 alcoxi C1-6, -C(O)NR12R12, NHC(O)R13, -NHC(O)NR12R12, -NHC(O)OR13, -NH(SO2)-(alquilo C1-6), y -(SO2)-(alquilo C1-6); en donde cualquiera de los dos átomos de hidrogeno en los átomos de carbono adyacentes delarilo C6-14 se pueden reemplazar por un grupo alquilenodioxi de modo que el grupo alquilenodioxi, cuando se toma junto con los dos átomos de carbono a los cuales está adherido, forman un heterociclo de 5- a 7- miembros que contiene dos átomos deoxigeno; (d) o heteroarilo C1-9 opcionalmente sustituido con de 1 a 3 sustituyentes independientemente seleccionados de: halogeno, alquilo C1-6, alcoxi C1-6, opcionalmente sustituido con alcoxi C1-6, hidroxialquilo C1-6, alquenilo C2-6, alquinilo C2-6, carbociclo C3-8, arilo C6-14, heteroarilo C1-9, perfluoroalquilo C1-6, hidroxilo, NR12R12, NO2, CN, CO2H, CHO, arilo C6-14-O-, arilo (C6-14)alquil-O-, opcionalmente sustituido con de 1 a 3 alcoxi C1-6, -C(O)NR12R12, NHC(O)R13, -NHC(O)NR12R12, -NHC(O)OR13, -NH(SO2)-(alquilo C1-6), y -(SO2)-(alquilo C1-6); en donde cualquiera de los dos átomos de hidrogeno en los átomos de carbono adyacentes del heteroarilo C1-9 se pueden reemplazar por un grupo alquilenodioxi de modo que el grupoalquilenodioxi, cuando se toma junto con los dos átomos de carbono a los cuales está adherido, forman un heterociclo de 5- a 7- miembros que contiene dos átomos de oxigeno; cada R12 es cada uno independientemente -H, -alquilo C1-6, alcoxi C1-6,arilo C6-14, heteroarilo C1-9, o -carbociclo C3-8, o dos radicales R12, cuando se toma junto con el nitrogeno al cual ellos están adheridos, pueden formar un heterociclo que contiene nitrogeno de 3- a 7- miembros en donde hasta dos de los átomos decarbono del heterociclo se pueden reemplazar por -N(R8)-, -O-, -S-, -S(O)- o - S(O)2-; R13 es independientemente -alquilo C1-6, arilo C6-14, heteroarilo C1-9, o -carbociclo C3-8; R8 es hidrogeno, alquilo C1-6, arilo C6-14, o heteroarilo C1-9; R3 esH, alquilo C1-6, opcionalmente sustituido con uno o más sustituyentes seleccionados independientemente de halogeno; NH2, -NH(alquilo C1-6), -N(alquilo C1-6)(alquilo C1-6), -N(alquilo C1-3)C(O)(alquilo C1-6), -NHC(O)(alquilo C1-6), -NHC(O)H, -C(O)NH2, -C(O)NH(alquilo C1-6), -C(O)N(alquilo C1-6)(alquilo C1-6), -CN, -OH, -O(alquilo C1-6), -alquilo C1-6, -C(O)OH, -C(O)Oalquilo C1-6, -C(O)alquilo C1-6, arilo C6-14, heteroarilo C1-9, y carbociclo C3-8, c) alquenilo -C2-10, opcionalmentesustituido con uno o más sustituyentes seleccionados independientemente de halogeno, -NH2, -NH(alquilo C1-6), -N(alquilo C1-6)(alquilo C1-6), -N(alquilo C1-3)C(O)(alquilo C1-6), -NHC(O)(alquilo C1-6), -NHC(O)H, -C(O)NH2, -C(O)NH(alquilo C1-6), -C(O)N(alquilo C1-6)(alquilo C1-6), -CN, -OH, -O(alquilo C1-6), -alquilo C1-6, -C(O)OH, -C(O)Oalquilo C1-6, -C(O)alquilo C1-6, arilo C6-14, heteroarilo C1-9, y carbociclo C3-8, dado que el sustituyente no se adhiere a un carbono del enlace doble; (d)alquinilo C2-10 opcionalmente sustituido con uno o más sustituyentes seleccionados independientemente de halogeno, -NH2, -NH(alquilo C1-6), -N(alquilo C1-6)(alquilo C1-6), -N(alquilo C1-3)C(O)(alquilo C1-6), -NHC(O)(alquilo C1-6), -NHC(O)H, -C(O)NH2, -C(O)NH(alquilo C1-6), -C(O)N(alquilo C1-6)(alquilo C1-6), -CN, -OH, -O(alquilo C1-6), -alquilo C1-6, -C(O)OH, -C(O)Oalquilo C1-6, -C(O)alquilo C1-6, arilo C6-14, heteroarilo C1-9, y carbociclo C3-8, dado que el sustituyente no se adhiere aun carbono del enlace triple, (e) arilo C6-14, opcionalmente sustituido con uno o más sustituyentes seleccionados independientemente de halogeno, -NH2,-NH(alquilo C1-6), -N(alquilo C1-6)(alquilo C1-6), -N(alquilo C1-3)C(O)(alquilo C1-6), -NHC(O)(alquilo C1-6), -NHC(O)H, -C(O)NH2, -C(O)NH(alquilo C1-6), -C(O)N(alquilo C1-6)(alquilo C1-6), -CN, -OH, -O(alquilo C1-6), -alquilo C1-6, -C(O)OH, -C(O)Oalquilo C1-6, -C(O)alquilo C1-6, arilo C6-14, heteroarilo C1-9, y carbociclo C3-8, (f)heteroarilo C1-9 opcionalmente sustituido con uno o más sustituyentes seleccionados independientemente de halogeno, -NH2, -NH(alquilo C1-6), -N(alquilo C1-6)(alquilo C1-6), -N(alquilo C1-3)C(O)(alquilo C1-6), -NHC(O)(alquilo C1-6), -NHC(O)H, -C(O)NH2, -C(O)NH(alquilo C1-6), -C(O)N(alquilo C1-6)(alquilo C1-6), -CN, -OH, -O(alquilo C1-6), -alquilo C1-6, -C(O)OH, -C(O)Oalquilo C1-6, -C(O)alquilo C1-6, arilo C6-14, heteroarilo C1-9, y carbociclo C3-8, (g) carbonilo C3-8, opcionalmentesustituido con uno o más sustituyentes seleccionados independientemente de halogeno, -NH2, -NH(alquilo C1-6), -N(alquilo C1-6)(alquilo C1-6), -N(alquilo C1-3)C(O)(alquilo C1-6), -NHC(O)(alquilo C1-6), -NHC(O)H, -C(O)NH2, -C(O)NH(alquilo C1-6), -C(O)N(alquilo C1-6)(alquilo C1-6), -CN, -OH, -O(alquilo C1-6), -alquilo C1-6, -C(O)OH, -C(O)Oalquilo C1-6, -C(O)alquilo C1-6, arilo C6-14, heteroarilo C1-9, y carbociclo C3-8, (h) heterociclil(alquilo C1-6) opcionalmente sustituido con (arilo C6-14)alquilo; (i) heterociclo monocíclico de 3- a 7-miembros opcionalmente sustituido con uno o más sustituyentes independientemente seleccionados de: alquilo C1-6, alcoxi C1-6carbonilo, acilo C1-8, arilo C6-14alquilo, en donde la porcion del anillodel grupo arilo C6-14alquilo se sustituye opcionalmente por 1 a 3 sustituyentes independientemente seleccionados de: halogeno, alquilo C1-6, NH2, alquilo C1-6amino, dialquilo C1-6amino, alcoxi C1-6 en donde el alcoxi C1-6 se sustituye opcionalmentecon NH2, alquilo C1-6amino, o dialquilo C1-6amino, heterociclo C1-9, arilo C6-14, y heteroarilo C1-9; heteroarilalquilo C1-6, en donde la porcion del anillo del grupo heteroarilalquilo C1-6 se sustituye opcionalmente por 1 a 3 sustituyentesindependientemente seleccionados de: halogeno, alquilo C1-6, NH2, alquilo C1-6amino, dialquilo C1-6amino, alcoxi C1-6, en donde el alcoxi C1-6 se sustituye opcionalmente con NH2, alquilo C1-6amino, o dialquilo C1-6amino, heterociclo C1-9, arilo C6-14, y heteroarilo C1-9, -C(O)OH, halogeno, -NH2, -NH(alquilo C1-6), -N(alquilo C1-6)(alquilo C1-6), -N(alquilo C1-3)C(O)(alquilo C1-6), -NHC(O)(alquilo C1-6), -NHC(O)H, -C(O)NH2, -C(O)NH(alquilo C1-6), -C(O)N(alquilo C1-6)(alquilo C1-6), -CN, -OH, -O(alquilo C1-6), arilo C6-14, heteroarilo C1-9, y carbociclo C3-8, (j) heterociclo monocíclico de 3- a 7-miembros que contiene nitrogeno opcionalmente sustituido con uno o más sustituyentes independientemente seleccionados de: alquilo C1-6, alcoxiC1-6carbonilo, acilo C1-8, arilo C6-14alquilo, en donde la porcion del anillo del grupo arilo C6-14alquilo se sustituye opcionalmente por 1 a 3 sustituyentes independientemente seleccionados de: halogeno, alquilo C1-6, NH2, alquilo C1-6amino,dialquilo C1-6amino, alcoxi C1-6, en donde el alcoxi C1-6 se sustituye opcionalmente con NH2, alquilo C1-6amino, o dialquilo C1-6amino, heterociclo C1-9, arilo C6-14, y heteroarilo C1-9, (ii) heteroarilalquilo C1-6 en donde la porcion del anillo delgrupo heteroarilalquilo C1-6 se sustituye opcionalmente por 1 a 3 sustituyentes independientemente seleccionados de: halogeno, alquilo C1-6, NH2, alquilo C1-6amino, dialquilo C1-6amino, alcoxi C1-6, en donde el alcoxi C1-6 se sustituye opcionalmentecon NH2, alquilo C1-6amino, o dialquilo C1-6amino, heterociclo C1-9, arilo C6-14, y heteroarilo C1-9, -C(O)OH, halogeno, -NH2, -NH(alquilo C1-6), -N(alquilo C1-6)(alquilo
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US91930007P | 2007-03-21 | 2007-03-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR065813A1 true AR065813A1 (es) | 2009-07-01 |
Family
ID=39535224
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP080101182A AR065813A1 (es) | 2007-03-21 | 2008-03-19 | Compuesto composicion farmaceutica y metodos para tratar trastornos relacionados con pi3k y mtor y a cancer y para inhibir mtor y pi3k |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US20080233127A1 (es) |
| EP (1) | EP2125815A2 (es) |
| JP (1) | JP2010522209A (es) |
| CN (1) | CN101730697A (es) |
| AR (1) | AR065813A1 (es) |
| AU (1) | AU2008228758A1 (es) |
| BR (1) | BRPI0809140A2 (es) |
| CA (1) | CA2681326A1 (es) |
| CL (1) | CL2008000790A1 (es) |
| MX (1) | MX2009010067A (es) |
| PE (1) | PE20090060A1 (es) |
| TW (1) | TW200902531A (es) |
| WO (1) | WO2008116129A2 (es) |
Families Citing this family (53)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1577816A3 (en) * | 1996-09-04 | 2006-08-02 | Intertrust Technologies Corp. | Trusted infrastructure support systems, methods and techniques for secure electronic commerce and rights management |
| AU2008282728B2 (en) | 2007-08-02 | 2012-04-19 | Amgen Inc. | Pl3 kinase modulators and methods of use |
| CN104119336B (zh) | 2007-10-05 | 2016-08-24 | 维拉斯通股份有限公司 | 嘧啶取代的嘌呤衍生物 |
| CN101835779B (zh) * | 2007-10-26 | 2014-01-29 | 霍夫曼-拉罗奇有限公司 | 作为pi3激酶抑制剂的嘌呤衍生物 |
| US7820665B2 (en) | 2007-12-19 | 2010-10-26 | Amgen Inc. | Imidazopyridazine inhibitors of PI3 kinase for cancer treatment |
| WO2009146406A1 (en) * | 2008-05-30 | 2009-12-03 | Genentech, Inc. | Purine pi3k inhibitor compounds and methods of use |
| AU2009276339B2 (en) * | 2008-07-31 | 2012-06-07 | Genentech, Inc. | Pyrimidine compounds, compositions and methods of use |
| TWI378933B (en) * | 2008-10-14 | 2012-12-11 | Daiichi Sankyo Co Ltd | Morpholinopurine derivatives |
| US8785457B2 (en) | 2009-03-13 | 2014-07-22 | Cellzome Limited | Pyrimidine derivatives as mTOR inhibitors |
| US8461158B2 (en) | 2009-03-27 | 2013-06-11 | Pathway Therapeutics Inc. | Pyrimidinyl and 1,3,5-triazinyl benzimidazole sulfonamides and their use in cancer therapy |
| US8754080B2 (en) | 2009-04-03 | 2014-06-17 | Verastem, Inc. | Pyrimidine substituted purine compounds as kinase (S) inhibitors |
| JPWO2010125799A1 (ja) | 2009-04-27 | 2012-10-25 | 塩野義製薬株式会社 | Pi3k阻害活性を有するウレア誘導体 |
| SG175708A1 (en) * | 2009-05-27 | 2011-12-29 | Genentech Inc | Bicyclic pyrimidine pi3k inhibitor compounds selective for p110 delta, and methods of use |
| SG176959A1 (en) * | 2009-06-24 | 2012-01-30 | Genentech Inc | Oxo-heterocycle fused pyrimidine compounds, compositions and methods of use |
| CN104945420A (zh) | 2009-06-29 | 2015-09-30 | 因塞特公司 | 作为pi3k抑制剂的嘧啶酮类 |
| EP2532659A1 (en) | 2009-07-07 | 2012-12-12 | Pathway Therapeutics, Inc. | Pyrimidinyl and 1,3,5-triazinyl benzimidazoles and their use in cancer therapy |
| CN102711766B (zh) * | 2009-11-12 | 2014-06-04 | 霍夫曼-拉罗奇有限公司 | N-9-取代的嘌呤化合物、组合物和使用方法 |
| US8828990B2 (en) * | 2009-11-12 | 2014-09-09 | Genentech, Inc. | N-7 substituted purine and pyrazolopyrimine compounds, compositions and methods of use |
| US8759359B2 (en) | 2009-12-18 | 2014-06-24 | Incyte Corporation | Substituted heteroaryl fused derivatives as PI3K inhibitors |
| WO2011107585A1 (en) | 2010-03-04 | 2011-09-09 | Cellzome Limited | Morpholino substituted urea derivatives as mtor inhibitors |
| WO2011130342A1 (en) | 2010-04-14 | 2011-10-20 | Incyte Corporation | FUSED DERIVATIVES AS ΡI3Κδ INHIBITORS |
| US9062055B2 (en) | 2010-06-21 | 2015-06-23 | Incyte Corporation | Fused pyrrole derivatives as PI3K inhibitors |
| CA2802808A1 (en) | 2010-07-14 | 2012-01-19 | F. Hoffmann-La Roche Ag | Purine compounds selective for pi3k p110 delta, and methods of use |
| AU2011302124B2 (en) | 2010-09-14 | 2016-03-17 | Exelixis, Inc. | Inhibitors of PI3K-delta and methods of their use and manufacture |
| AU2011343712B2 (en) | 2010-12-16 | 2015-09-17 | Genentech, Inc. | Tricyclic PI3k inhibitor compounds and methods of use |
| CA2822070C (en) | 2010-12-20 | 2019-09-17 | Incyte Corporation | N-(1-(substituted-phenyl)ethyl)-9h-purin-6-amines as pi3k inhibitors |
| US9108984B2 (en) | 2011-03-14 | 2015-08-18 | Incyte Corporation | Substituted diamino-pyrimidine and diamino-pyridine derivatives as PI3K inhibitors |
| US9126948B2 (en) | 2011-03-25 | 2015-09-08 | Incyte Holdings Corporation | Pyrimidine-4,6-diamine derivatives as PI3K inhibitors |
| BR112013024907A2 (pt) | 2011-03-28 | 2016-12-20 | Mei Pharma Inc | composto, composição farmacêutica, método para o tratamento, prevenção ou atenuação de um ou mais sintomas de um distúrbio, doença ou condição mediada por pi3k em um sujeito, método para modular a atividade enzimática de pi3k |
| JP2014510122A (ja) | 2011-04-04 | 2014-04-24 | セルゾーム リミテッド | mTOR阻害剤としてのジヒドロピロロピリミジン誘導体 |
| AR087760A1 (es) | 2011-09-02 | 2014-04-16 | Incyte Corp | Heterociclilaminas como inhibidores de pi3k |
| CA2849189A1 (en) | 2011-09-21 | 2013-03-28 | Cellzome Limited | Morpholino substituted urea or carbamate derivatives as mtor inhibitors |
| CN103946222B (zh) | 2011-10-07 | 2016-12-28 | 塞尔佐姆有限公司 | 作为mtor抑制剂的吗啉代取代的双环嘧啶脲或氨基甲酸衍生物 |
| US8906910B2 (en) | 2011-12-20 | 2014-12-09 | Glaxosmithkline Llc | Imidazopyridine derivatives as PI3 kinase |
| AR090548A1 (es) | 2012-04-02 | 2014-11-19 | Incyte Corp | Azaheterociclobencilaminas biciclicas como inhibidores de pi3k |
| CN104350144B (zh) | 2012-05-23 | 2017-08-04 | 弗·哈夫曼-拉罗切有限公司 | 获得和使用内胚层和肝细胞的组合物和方法 |
| CN103588792B (zh) * | 2013-03-04 | 2016-03-23 | 中国科学院上海药物研究所 | 吡啶并嘧啶或嘧啶并嘧啶类化合物、其制备方法、药物组合物及其用途 |
| US10077277B2 (en) | 2014-06-11 | 2018-09-18 | Incyte Corporation | Bicyclic heteroarylaminoalkyl phenyl derivatives as PI3K inhibitors |
| PT3831833T (pt) | 2015-02-27 | 2023-02-06 | Incyte Corp | Processos para a preparação de um inibidor pi3k |
| PT3277682T (pt) | 2015-03-30 | 2019-07-09 | Daiichi Sankyo Co Ltd | Derivados de 6-morfolinil-2-pirazolil-9h-purina e utilização dos mesmos como inibidores de pi3k |
| EA033106B1 (ru) * | 2015-04-21 | 2019-08-30 | Гуйчжоу Бэйлинг Груп Фармасьютикал Ко., Лтд. | Производное пуринил-n-гидроксипиримидинформамида, способы его получения и его применения |
| WO2016183060A1 (en) | 2015-05-11 | 2016-11-17 | Incyte Corporation | Process for the synthesis of a phosphoinositide 3-kinase inhibitor |
| US9988401B2 (en) | 2015-05-11 | 2018-06-05 | Incyte Corporation | Crystalline forms of a PI3K inhibitor |
| KR102399639B1 (ko) | 2016-12-02 | 2022-05-18 | 다이이찌 산쿄 가부시키가이샤 | 신규 엔도-β-N-아세틸글루코사미니다아제 |
| US11304953B2 (en) | 2017-05-23 | 2022-04-19 | Mei Pharma, Inc. | Combination therapy |
| WO2019018562A1 (en) | 2017-07-19 | 2019-01-24 | Ideaya Biosciences, Inc. | AMIDO COMPOUND AS MODULATORS OF AHR |
| KR20200041358A (ko) | 2017-08-14 | 2020-04-21 | 메이 파마, 아이엔씨. | 병용 요법 |
| KR102884803B1 (ko) | 2018-06-01 | 2025-11-12 | 인사이트 코포레이션 | Pi3k 관련 장애의 치료를 위한 투여 요법 |
| CN112707907B (zh) * | 2019-10-24 | 2023-05-23 | 张飞 | 嘌呤衍生物及其中间体与制备抗癌症药物的应用 |
| CN111875606B (zh) * | 2020-07-20 | 2023-04-07 | 武汉工程大学 | 一种基于虚拟对接获得的嘌呤类化合物及其制备方法和应用 |
| CN113116895B (zh) * | 2020-12-31 | 2023-08-18 | 天津医科大学肿瘤医院 | 用于治疗神经母细胞瘤的喹啉衍生物 |
| WO2025090871A1 (en) * | 2023-10-27 | 2025-05-01 | University Of Virginia Patent Foundation | Electrophilic purine compounds for modification of proteins |
| CN117503743B (zh) * | 2023-12-08 | 2024-04-16 | 南京鼓楼医院 | 一种nlrp3炎症小体抑制剂及其在制备预防或治疗细胞焦亡的药物中的应用 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60260579A (ja) * | 1984-01-13 | 1985-12-23 | Yoshitomi Pharmaceut Ind Ltd | プリン誘導体 |
| JPS6210085A (ja) * | 1985-07-05 | 1987-01-19 | Yoshitomi Pharmaceut Ind Ltd | トリフルオロメチルプリン誘導体 |
| KR100774855B1 (ko) * | 2000-04-27 | 2007-11-08 | 아스텔라스세이야쿠 가부시키가이샤 | 축합 헤테로아릴 유도체 |
| TW200510394A (en) * | 2003-05-29 | 2005-03-16 | Synta Pharmaceuticals Corp | Heterocyclic compounds for preventing and treating disorders associated with excessive bone loss |
| FR2880626B1 (fr) * | 2005-01-13 | 2008-04-18 | Aventis Pharma Sa | Derives de la purine, compositions les contenant et utilisation |
| GB2431156A (en) * | 2005-10-11 | 2007-04-18 | Piramed Ltd | 1-cyclyl-3-substituted- -benzenes and -azines as inhibitors of phosphatidylinositol 3-kinase |
-
2008
- 2008-03-07 US US12/044,500 patent/US20080233127A1/en not_active Abandoned
- 2008-03-19 PE PE2008000503A patent/PE20090060A1/es not_active Application Discontinuation
- 2008-03-19 CL CL200800790A patent/CL2008000790A1/es unknown
- 2008-03-19 AR ARP080101182A patent/AR065813A1/es unknown
- 2008-03-21 AU AU2008228758A patent/AU2008228758A1/en not_active Abandoned
- 2008-03-21 JP JP2009554756A patent/JP2010522209A/ja not_active Withdrawn
- 2008-03-21 TW TW097110236A patent/TW200902531A/zh unknown
- 2008-03-21 BR BRPI0809140-4A patent/BRPI0809140A2/pt not_active Application Discontinuation
- 2008-03-21 WO PCT/US2008/057771 patent/WO2008116129A2/en not_active Ceased
- 2008-03-21 EP EP08744161A patent/EP2125815A2/en not_active Withdrawn
- 2008-03-21 MX MX2009010067A patent/MX2009010067A/es unknown
- 2008-03-21 CA CA002681326A patent/CA2681326A1/en not_active Abandoned
- 2008-03-21 CN CN200880009067A patent/CN101730697A/zh active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| WO2008116129A3 (en) | 2009-02-12 |
| CN101730697A (zh) | 2010-06-09 |
| US20080233127A1 (en) | 2008-09-25 |
| PE20090060A1 (es) | 2009-01-18 |
| TW200902531A (en) | 2009-01-16 |
| JP2010522209A (ja) | 2010-07-01 |
| CL2008000790A1 (es) | 2008-05-30 |
| CA2681326A1 (en) | 2008-09-25 |
| BRPI0809140A2 (pt) | 2014-08-26 |
| MX2009010067A (es) | 2009-10-12 |
| AU2008228758A1 (en) | 2008-09-25 |
| EP2125815A2 (en) | 2009-12-02 |
| WO2008116129A2 (en) | 2008-09-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AR065813A1 (es) | Compuesto composicion farmaceutica y metodos para tratar trastornos relacionados con pi3k y mtor y a cancer y para inhibir mtor y pi3k | |
| ES2622881T3 (es) | Compuestos de N-heteroarilo | |
| AR045470A1 (es) | Derivados de acido fenoxiacetico | |
| AR060316A1 (es) | Azaindoles de utilidad como inhibidores de janus quinasas | |
| AR085039A1 (es) | DERIVADOS DE PURINA, COMPOSICIONES FARMACEUTICAS QUE LOS COMPRENDEN Y SU USO EN LA PREPARACION DE MEDICAMENTOS PARA TRATAR ENFERMEDADES MODULADAS POR LA INHIBICION DE LA PI3K DE CLASE I Y/O mTOR | |
| RU2010100945A (ru) | Способы и композиции для стимулирования нейрогенеза и ингибирования дегенерации нейронов с использованием изотиазолопиримидинонов | |
| AR051195A1 (es) | Piridinas como inhibidores de plk | |
| MX2019014982A (es) | Derivados de 7h-imidazo[1-5-a]pirazin-8-ona como inhibidores de la fosfodiesterasa 9(pde9); y el uso de los mismos en el tratamiento de trastornos neurodegenerativos. | |
| AR069510A1 (es) | Arilo y heteroarilo imidazo[1,5-a]pirazinas fusionadas como inhibidores de la fosfodiesterasa 10 | |
| MX367713B (es) | Uso de derivados de pirazolopirimidina para el tratamiento de trastornos relacionados con la fosfoinositida 3-cinasa delta. | |
| RU2017104856A (ru) | Функционализированные и замещенные индолы в качестве противораковых средств | |
| EA201790088A1 (ru) | Ингибиторы syk | |
| RU2013153388A (ru) | Способы применения активаторов пируваткиназы | |
| AR064010A1 (es) | Inhibidores de la actividad de la akt | |
| AR080328A1 (es) | Tienopirimidinas que contienen un grupo alquilo sustituido inhibidoras de quinasas mnk1 y/o mnk2, composiciones farmaceuticas que las contienen y uso de las mismas para el tratamiento de trastornos metabolicos tales como diabetes y obesidad, y trastornos hiperproliferativos, entre otros | |
| AR067329A1 (es) | Analogos dipeptidos como inhibidores del factor de coagulacion | |
| AR075396A1 (es) | Derivados de quinazolinas y composiciones farmaceuticas | |
| EA201490491A1 (ru) | Производные 2-амино-4-(пиридин-2-ил)-5,6-дигидро-4h-1,3-оксазинов и их использование в качестве ингибиторов bace-1 и/или bace-2 | |
| PE20181519A1 (es) | Compuestos de benzaldehido sustituidos y metodos para su uso en incrementar la oxigenacion del tejido | |
| AR083161A1 (es) | Inhibidores macrociclicos de la replicacion del virus de la hepatitis c, composiciones farmaceuticas que los comprenden, su uso en medicamentos, intermediarios de su sintesis y metodos de preparacion de los mismos | |
| AR086100A1 (es) | Compuestos de cromenona y composiciones farmaceuticas que los contienen | |
| RU2007146173A (ru) | Пиридо [2,3-d] пиримидины, полезные в качестве ингибиторов вич, и способы их получения | |
| AR087017A1 (es) | Pirrolotriazinas sustituidas con hidroximetilarilo y sus usos | |
| PE20141553A1 (es) | Compuestos de triazolopiridina como inhibidores de la ped10a | |
| EA201171415A1 (ru) | Ингибиторы белков семейства iap |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FB | Suspension of granting procedure |