AR074130A1 - Inhibidores de la diacilglicerol aciltransferasa - Google Patents
Inhibidores de la diacilglicerol aciltransferasaInfo
- Publication number
- AR074130A1 AR074130A1 ARP090104454A ARP090104454A AR074130A1 AR 074130 A1 AR074130 A1 AR 074130A1 AR P090104454 A ARP090104454 A AR P090104454A AR P090104454 A ARP090104454 A AR P090104454A AR 074130 A1 AR074130 A1 AR 074130A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- cycloalkyl
- aryl
- heteroaryl
- group
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title 1
- 125000003118 aryl group Chemical group 0.000 abstract 22
- 125000000623 heterocyclic group Chemical group 0.000 abstract 20
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 19
- 125000001072 heteroaryl group Chemical group 0.000 abstract 18
- 125000000217 alkyl group Chemical group 0.000 abstract 17
- 101100495917 Arabidopsis thaliana ATRX gene Proteins 0.000 abstract 12
- 125000005843 halogen group Chemical group 0.000 abstract 8
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 7
- 125000003342 alkenyl group Chemical group 0.000 abstract 6
- 125000000304 alkynyl group Chemical group 0.000 abstract 6
- 229910052739 hydrogen Inorganic materials 0.000 abstract 6
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 4
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 4
- -1 cycloalkenylalkyl Chemical group 0.000 abstract 4
- 125000001188 haloalkyl group Chemical group 0.000 abstract 4
- 125000004446 heteroarylalkyl group Chemical group 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 229910052757 nitrogen Inorganic materials 0.000 abstract 4
- 229910052760 oxygen Inorganic materials 0.000 abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 3
- 229910003827 NRaRb Inorganic materials 0.000 abstract 3
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 3
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 3
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 3
- 229910052717 sulfur Inorganic materials 0.000 abstract 3
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 abstract 2
- 208000008589 Obesity Diseases 0.000 abstract 2
- 125000002618 bicyclic heterocycle group Chemical group 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 230000003247 decreasing effect Effects 0.000 abstract 2
- 206010012601 diabetes mellitus Diseases 0.000 abstract 2
- 239000008103 glucose Substances 0.000 abstract 2
- 125000004415 heterocyclylalkyl group Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 235000020824 obesity Nutrition 0.000 abstract 2
- 125000004043 oxo group Chemical group O=* 0.000 abstract 2
- 208000024172 Cardiovascular disease Diseases 0.000 abstract 1
- 208000032928 Dyslipidaemia Diseases 0.000 abstract 1
- 208000017170 Lipid metabolism disease Diseases 0.000 abstract 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 150000002391 heterocyclic compounds Chemical class 0.000 abstract 1
- 150000002431 hydrogen Chemical class 0.000 abstract 1
- 208000030159 metabolic disease Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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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
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- 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
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- 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
- A61P3/06—Antihyperlipidemics
-
- 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
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- 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
- 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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/10—Spiro-condensed systems
-
- 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
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Diabetes (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Child & Adolescent Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
La presente se relaciona con composiciones farmacéuticas que comprenden los compuestos heterociclos y con el uso de los compuestos para el tratamiento o prevencion de una enfermedad cardiovascular, un trastorno metabolico, obesidad, un trastorno relacionado con la obesidad, dislipidemia, diabetes, una complicacion de la diabetes, tolerancia disminuida a la glucosa o glucosa disminuida en ayunas. Reivindicacion 1: Un compuesto, o una sal aceptable para uso farmacéutico del mismo, compuesto que está representado por la formula (1) en la cual cada A es seleccionado de manera independiente entre C(R3) y N; o, por otro lado el resto de formula (2) es uno de los restos del grupo de formulas (3); X es seleccionado de manera independiente entre C(R3), N, N(R4), O y S, siempre que no más de un X sea S o O, y por lo menos un X o un Y sea N, O, o S; Y es seleccionado de manera independiente entre C y N; Z es independientemente un enlace, O o NR4; R1 es seleccionado de heterocicloalquilo con contenido de 1-4 heteroátomos que pueden ser iguales o diferentes y es seleccionado del grupo constituido por O, S y N, donde dicho heterocicloalquilo no está sustituido o está opcionalmente sustituido de manera independiente con uno o más restos, que pueden ser iguales o diferentes, donde cada sustituyente es independientemente seleccionado del grupo constituido por alquilo, alcoxi, alcoxialquilo, haloalcoxi, alquenilo, alquinilo, cicloalquilo, cicloalquilalquilo, cicloalquenilo, cicloalquenilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, halo, -CN, -ORc, =O, -C(O)Rc, -C(O)ORc, -C(O)N(Rc)(Rd), -SF5, -OSF5, -Si(Rc)3, -SRc, -S(O)N(Rc(Rd), -CH(Rc)(Rd), -S(O)2N(Rc)(Rd), -C(=NORc)Rd, -P(O)(ORc)(ORd), -N(Rc)(Rd), -alquil-N(Rc)(Rd), -N(Rc)C(O)Rd, -CH2-N(Rc)C(O)Rd, -CH2-N(Rc)C(O)N(Rd)(Rb), -CH2-Rc, -CH2N(Rc)(Rd), -N(Rc)S(O)Rd, -N(Rc)S(O)2Rd, -CH2-N(Rc)S(O)2Rd, -N(Rc)S(O)2N(Rd)(Rb), -N(Rc)S(O)N(Rd)(Rb), -N(Rc)C(O)N(Rd)(Rb), -CH2-N(Rc)C(O)N(Rd)(Rb), -N(Rc)C(O)ORd, -CH2-N(Rc)C(O)ORd, -S(O)Rc, =NORc, -N3, -NO2 y -S(O)2Rc, en donde cada Rb, Rc y Rd está seleccionado, de modo independiente; o alternativamente, dicho heterocicloalquilo puede estar fusionado a arilo, donde dicho arilo puede no estar sustituido, o estar sustituido opcionalmente, de manera independiente, con uno o más restos, que pueden ser iguales o diferentes, donde cada sustituyente es independientemente seleccionado del grupo constituido por alquilo, alcoxi, alcoxialquilo, haloalcoxi, alquenilo, alquinilo, cicloalquilo, cicloalquilalquilo, cicloalquenilo, cicloalquenilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, heterociclilo, heterociclilalquilo, halo, -CN, -ORc, -C(O)Rc, -C(O)ORc, -C(O)N(Rc)(Rd), -SF5, -OSF5, -Si(Rc)3, -SRc, -S(O)N(Rc(Rd), -CH(Rc)(Rd), -S(O)2N(Rc)(Rd), -C(=NORc)Rd, -P(O)(ORc)(ORd), -N(Rc)(Rd), -alquil-N(Rc)(Rd), -N(Rc)C(O)Rd, -CH2-N(Rc)C(O)Rd, -CH2-N(Rc)C(O)N(Rd)(Rb), -CH2-Rc, -CH2N(Rc)(Rd), -N(Rc)S(O)Rd, -N(Rc)S(O)2Rd, -CH2-N(Rc)S(O)2Rd, -N(Rc)S(O)2N(Rd)(Rb), -N(Rc)S(O)N(Rd)(Rb), -N(Rc)C(O)N(Rd)(Rb), -CH2-N(Rc)C(O)N(Rd)(Rb), -N(Rc)C(O)ORd, -CH2-N(Rc)C(O)ORd, -S(O)Rc, -N3, -NO2 y -S(O)2Rc, en donde cada Rb, Rc y Rd está seleccionado, de modo independiente; o alternativamente, dicho heterociclilo puede estar fusionado a arilo, donde cada uno de dichos heterocicloalquilo y arilo puede no estar sustituido, o estar sustituido opcionalmente, de manera independiente, con uno o más restos, que pueden ser iguales o diferentes, donde cada sustituyente es independientemente seleccionado del grupo constituido por alquilo, alcoxi, alcoxialquilo, haloalcoxi, alquenilo, alquinilo, cicloalquilo, cicloalquilalquilo, cicloalquenilo, cicloalquenilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, halo, -CN, -ORc, =O, -C(O)Rc, -C(O)ORc, -C(O)N(Rc)(Rd), -SF5, -OSF5, -Si(Rc)3, -SRc, -S(O)N(Rc(Rd), -CH(Rc)(Rd), -S(O)2N(Rc)(Rd), -C(=NORc)Rd, -P(O)(ORc)(ORd), -N(Rc)(Rd), -alquil-N(Rc)(Rd), -N(Rc)C(O)Rd, -CH2-N(Rc)C(O)Rd, -CH2-N(Rc)C(O)N(Rd)(Rb), -CH2-Rc, -CH2N(Rc)(Rd), -N(Rc)S(O)Rd, -N(Rc)S(O)2Rd, -CH2-N(Rc)S(O)2Rd, -N(Rc)S(O)2N(Rd)(Rb), -N(Rc)S(O)N(Rd)(Rb), -N(Rc)C(O)N(Rd)(Rb), -CH2-N(Rc)C(O)N(Rd)(Rb), -N(Rc)C(O)ORd, -CH2-N(Rc)C(O)ORd, -S(O)Rc, =NORc, -N3, -NO2 y -S(O)2Rc, en donde cada Rb, Rc y Rd está seleccionado, de modo independiente; R3 es seleccionado del grupo que comprende H, alquilo inferior, hidroxi, halo, O-alquilo, O-haloalquilo, O-cicloalquilo, S-alquilo, S-haloalquilo, CN, CF3, -SF5, -OSF5, Si(Rc)3, cicloalquilo, heterociclilo, haloalquilo, arilo, heteroarilo, N-alquilo, N-haloalquilo, NH2, y N-cicloalquilo; R4 es seleccionado del grupo que comprende H, alquilo inferior, cicloalquilo, heterociclilo, haloalquilo, arilo, y heteroarilo; R5 es seleccionado del grupo que comprende alquilo inferior, cicloalquilo, heterociclilo, haloalquilo, arilo, y heteroarilo; y R10 es uno de (i) un anillo de heterociclilo de 4-8 miembros que tiene de 1 a 3 átomos de N en el anillo, o (ii) un arillo de heterociclilo bicíclico que tiene de 1 a 3 átomos de N en el anillo, o (iii) un grupo arilo, o (iv) un grupo heteroarilo, donde dicho grupo arilo o heteroarilo correspondiente a R10 no está sustituido o está opcionalmente sustituido de manera independiente con uno o más restos G donde dichos restos G pueden ser iguales o diferentes y donde cada resto G es independientemente seleccionado del grupo expuesto más delante, y donde dicho anillo de heterociclilo correspondiente a R10 está a su vez no sustituido o opcionalmente sustituido, de (i) un átomo de N del anillo o (ii) un átomo de carbono de anillo de dicho anillo de heterociclilo, con uno o más restos G, donde dichos restos G pueden ser iguales o diferentes, donde cada resto G es independientemente seleccionado del grupo constituido por (a) -(CHR20)n-C(O)-NRaRb, con la condicion de que no sea un anillo de heterociclilo de 5 o 6 miembros cuando R20 es hidrogeno y R10 puede ser un anillo de heterociclilo de 5 o 6 miembros cuando G está presente en forma de grupo oxo; (b) -(CHR20)n-C(O)-O-R5, con la condicion de que R10 no sea un anillo de heterociclilo de 5 o 6 miembros cuando R20 es hidrogeno; (c) -(CHR20)n-C(O)-OH, con la condicion de que R10 no sea un anillo de heterociclilo de 5 o 6 miembros cuando R20 es hidrogeno; (d) -(CHR20)n-C(O)-Ra; (e) -(CHR20)n-S(O)2-Ra; (f) -(CHR20)n-S(O)2-(CH2)n-Ra; (g) -(CHR20)n-S(O)2-NRaRb; (h) -(CHR20)n-Ra; (i) -(CHR20)n-O-Ra; (j) -NH-C(O)-O-Ra solo de C y no de N; (k) -NH-C(O)-Ra solo de C y no de N; (l) -NH-C(O)-NRaRb solo de C y no de N; (m) -(CHR20)n-C(O)-NH-NH-C(O)-Ra; (n) -O-P(O)-(Ra)2 solo de C y no de N; (o) -O-CH(Ra)2 solo de C y no de N; (p) un grupo oxo solo de C y no de N; (q) -C(O)-(CHR20)n-C(O)-O-Ra; (r) -C(O)-(CHR20)n-Ra; (s) un grupo espirociclilo; (t) -C(O)-(cicloalquil)-C(O)-N(Rb)-Ra con la condicion de que R10 no sea un anillo de heterociclilo de 5 o 6 miembros; (u) -C(O)-(cicloalquil)-C(O)-OR5, con la condicion de que R10 no sea un anillo de heterociclilo de 5 o 6 miembros; (v) -C(O)-(cicloalquil)-C(O)OH, con la condicion de que R10 no sea un anillo de heterociclilo de 5 o 6 miembros; (w) bioisostero de -C(O)-(cicloalquil)-C(O)OH con la condicion de que R10 no sea un anillo de heterociclilo de 5 o 6 miembros; (x) -C(O)-(aril)-C(O)OH; e (y) -C(O)-(heteroaril)-C(O)OH, donde Ra es seleccionado del grupo que consiste en hidrogeno, hidroxi, CN, halo, alquilo, alquenilo, alquinilo, arilo, (aril)alquil-, heteroarilo, (heteroaril)alquil-, heterociclilo, (heterociclil)alquil-, cicloalquilo, (cicloalquil)alquil-, espirociclilo o un heterociclilo bicíclico, donde cada uno de dichos alquilo, alquenilo, alquinilo, arilo, heteroarilo, heterociclilo y cicloalquilo no está sustituido o está opcionalmente sustituido de manera independiente con uno o más restos que pueden ser iguales o diferentes, donde cada resto es seleccionado de manera independiente del grupo constituido por O-haloalquilo, S-haloalquilo, CN, NO2, CF3, cicloalquilo, heterociclilo, haloalquilo, arilo, heteroarilo, N-alquilo, N-haloalquilo, y N-cicloalquilo; alquilo, alquenilo, alquinilo, cicloaIquilalquilo, cicloalquenilo, heterociclilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, halo, -ORc, -C(O)Rc, -C(O)ORc, -C(O)N(Rc)(Rd), -SF5, -OSF5, -Si(Rc)3, -SRc, -S(O)N(Rc(Rd), -CH(Rc)(Rd), -S(O)2N(Rc)(Rd), -C(=NORc)Rd, -P(O)(ORc)(ORd), -N(Rc)(Rd), -alquil-N(Rc)(Rd), -N(Rc)C(O)Rd, -CH2-N(Rc)C(O)Rd, -CH2-N(Rc)C(O)N(Rd)(Rb), -CH2-Rc, -CH2N(Rc)(Rd), -N(Rc)S(O)Rd, -N(Rc)S(O)2Rd, -CH2-N(Rc)S(O)2Rd, -N(Rc)S(O)2N(Rd)(Rb), -N(Rc)S(O)N(Rd)(Rb), -N(Rc)C(O)N(Rd)(Rb), -CH2-N(Rc)C(O)N(Rd)(Rb), -N(Rc)C(O)ORd, -CH2-N(Rc)C(O)ORd, -S(O)Rc, =NORc, -N3, -NO2 y -S(O)2Rc, en donde cada Rb, Rc y Rd está seleccionado, de manera independiente; Rb es H, alquilo inferior, cicloalquilo, arilo, heteroarilo o heterocicloalquilo; Rc es H, alquilo inferior, cicloalquilo, arilo, heteroarilo o heterocicloalquilo; Rd es H, alquilo inferior, cicloalquilo, arilo, heteroarilo o heterocicloalquilo; donde cada uno de dichos alquilo, cicloalquilo, arilo, heteroarilo o heterocicloalquilo de Rb, Rc, y Rd puede no estar sustituido, o estar sustituido opcionalmente, de manera independiente. con 1-2 sustituyentes seleccionados de manera independiente de halo, NH2, CF3, CN, o-alquilo, NH-alquilo, N(alquil)2, y Si(alquil)3; R20 es H, -OH, halo, o -CF3; y m es 1-3; n es 0-3.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US11600008P | 2008-11-19 | 2008-11-19 | |
US11598708P | 2008-11-19 | 2008-11-19 |
Publications (1)
Publication Number | Publication Date |
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AR074130A1 true AR074130A1 (es) | 2010-12-22 |
Family
ID=42110031
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP090104454A AR074130A1 (es) | 2008-11-19 | 2009-11-18 | Inhibidores de la diacilglicerol aciltransferasa |
Country Status (10)
Country | Link |
---|---|
US (1) | US8716312B2 (es) |
EP (1) | EP2367598B1 (es) |
JP (1) | JP2012509274A (es) |
CN (1) | CN102281919A (es) |
AR (1) | AR074130A1 (es) |
AU (1) | AU2009316786A1 (es) |
CA (1) | CA2743609A1 (es) |
MX (1) | MX2011005234A (es) |
TW (1) | TW201031657A (es) |
WO (1) | WO2010059602A2 (es) |
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JP6728061B2 (ja) | 2014-05-05 | 2020-07-22 | リセラ・コーポレイションLycera Corporation | RORγアゴニストとして用いるテトラヒドロキノリンスルホンアミド及び関連化合物ならびに疾患の治療 |
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EP3292119A4 (en) | 2015-05-05 | 2018-10-03 | Lycera Corporation | DIHYDRO-2H-BENZO[b][1,4]OXAZINE SULFONAMIDE AND RELATED COMPOUNDS FOR USE AS AGONISTS OF RORy AND THE TREATMENT OF DISEASE |
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2009
- 2009-11-17 US US13/129,843 patent/US8716312B2/en not_active Expired - Fee Related
- 2009-11-17 EP EP09752998.6A patent/EP2367598B1/en not_active Not-in-force
- 2009-11-17 CA CA2743609A patent/CA2743609A1/en not_active Abandoned
- 2009-11-17 CN CN2009801549757A patent/CN102281919A/zh active Pending
- 2009-11-17 WO PCT/US2009/064738 patent/WO2010059602A2/en active Application Filing
- 2009-11-17 JP JP2011536587A patent/JP2012509274A/ja active Pending
- 2009-11-17 MX MX2011005234A patent/MX2011005234A/es not_active Application Discontinuation
- 2009-11-17 AU AU2009316786A patent/AU2009316786A1/en not_active Abandoned
- 2009-11-18 AR ARP090104454A patent/AR074130A1/es not_active Application Discontinuation
- 2009-11-18 TW TW098139170A patent/TW201031657A/zh unknown
Also Published As
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US20110224137A1 (en) | 2011-09-15 |
CA2743609A1 (en) | 2010-05-27 |
US8716312B2 (en) | 2014-05-06 |
TW201031657A (en) | 2010-09-01 |
CN102281919A (zh) | 2011-12-14 |
EP2367598B1 (en) | 2014-04-09 |
EP2367598A2 (en) | 2011-09-28 |
JP2012509274A (ja) | 2012-04-19 |
WO2010059602A2 (en) | 2010-05-27 |
MX2011005234A (es) | 2011-06-01 |
WO2010059602A3 (en) | 2010-07-15 |
AU2009316786A1 (en) | 2010-05-27 |
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