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
-
- 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)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Diabetes (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (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 |
|---|---|---|---|
| US11600008P | 2008-11-19 | 2008-11-19 | |
| US11598708P | 2008-11-19 | 2008-11-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| 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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| JPWO2012124744A1 (ja) * | 2011-03-14 | 2014-07-24 | 大正製薬株式会社 | 含窒素縮合複素環化合物 |
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| RU2014149136A (ru) | 2012-05-08 | 2016-07-10 | Мерк Шарп И Доум Корп. | ТЕТРАГИДРОНАФТИРИДИНОВЫЕ И РОДСТВЕННЫЕ БИЦИКЛИЧЕСКИЕ СОЕДИНЕНИЯ ДЛЯ ИНГИБИРОВАНИЯ RORγ АКТИВНОСТИ И ЛЕЧЕНИЯ ЗАБОЛЕВАНИЯ |
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| KR20160068956A (ko) | 2013-10-15 | 2016-06-15 | 얀센 파마슈티카 엔.브이. | RORyT의 퀴놀리닐 조절제 |
| US9403816B2 (en) | 2013-10-15 | 2016-08-02 | Janssen Pharmaceutica Nv | Phenyl linked quinolinyl modulators of RORγt |
| US10555941B2 (en) | 2013-10-15 | 2020-02-11 | Janssen Pharmaceutica Nv | Alkyl linked quinolinyl modulators of RORγt |
| WO2015095792A1 (en) | 2013-12-20 | 2015-06-25 | Merck Sharp & Dohme Corp. | Carbamate benzoxaxine propionic acids and acid derivatives for modulation of rorgamma activity and the treatment of disease |
| WO2015095795A1 (en) | 2013-12-20 | 2015-06-25 | Merck Sharp & Dohme Corp. | TETRAHYDRONAPHTHYRIDINE, BENZOXAZINE, AZA-BENZOXAZINE, AND RELATED BICYCLIC COMPOUNDS FOR INHIBITION OF RORgamma ACTIVITY AND THE TREATMENT OF DISEASE |
| WO2015095788A1 (en) | 2013-12-20 | 2015-06-25 | Merck Sharp & Dohme Corp. | 2-ACYLAMIDOMETHYL AND SULFONYLAMIDOMETHYL BENZOXAZINE CARBAMATES FOR INHIBITION OF RORgamma ACTIVITY AND THE TREATMENT OF DISEASE |
| CA2935880A1 (en) * | 2014-01-10 | 2015-07-16 | Aurigene Discovery Technologies Limited | Indazole compounds as irak4 inhibitors |
| EP3466955B1 (en) | 2014-01-13 | 2020-12-16 | Aurigene Discovery Technologies Limited | Method of preparing oxazolo[4,5-b]pyridine and thiazolo[4,5-b]pyridine derivatives as irak4 inhibitors for treating cancer |
| WO2015131035A1 (en) | 2014-02-27 | 2015-09-03 | Lycera Corporation | Adoptive cellular therapy using an agonist of retinoic acid receptor-related orphan receptor gamma & related therapeutic methods |
| WO2015171558A2 (en) | 2014-05-05 | 2015-11-12 | Lycera Corporation | BENZENESULFONAMIDO AND RELATED COMPOUNDS FOR USE AS AGONISTS OF RORγ AND THE TREATEMENT OF DISEASE |
| WO2015171610A2 (en) | 2014-05-05 | 2015-11-12 | Lycera Corporation | Tetrahydroquinoline sulfonamide and related compounds for use as agonists of rory and the treatment of disease |
| WO2016130818A1 (en) | 2015-02-11 | 2016-08-18 | Merck Sharp & Dohme Corp. | SUBSTITUTED PYRAZOLE COMPOUNDS AS RORgammaT INHIBITORS AND USES THEREOF |
| JP2018515491A (ja) | 2015-05-05 | 2018-06-14 | リセラ・コーポレイションLycera Corporation | RORγの作動薬及び疾患の療法として使用するジヒドロ−2H−ベンゾ[b][1,4]オキサジンスルホンアミド及び関連化合物 |
| HK1253734A1 (zh) | 2015-06-11 | 2019-06-28 | The Regents Of The University Of Michigan | 用作RORγ激动剂和用於治疗疾病的芳基二氢-2H-苯并[B][1,4]恶嗪磺酰胺和相关化合物 |
| KR20180070697A (ko) | 2015-10-27 | 2018-06-26 | 머크 샤프 앤드 돔 코포레이션 | Ror감마t 저해제로서의 치환된 인다졸 화합물 및 이의 용도 |
| CA3002846A1 (en) | 2015-10-27 | 2017-05-04 | Merck Sharp & Dohme Corp. | Substituted bicyclic pyrazole compounds as rorgammat inhibitors and uses thereof |
| AU2016344118A1 (en) | 2015-10-27 | 2018-05-10 | Merck Sharp & Dohme Corp. | Heteroaryl substituted benzoic acids as rorgammat inhibitors and uses thereof |
| CN106176776A (zh) * | 2016-07-04 | 2016-12-07 | 华北制药集团新药研究开发有限责任公司 | 葡萄糖激酶激动活性化合物的医药用途 |
| BR112019018991A2 (pt) | 2017-03-31 | 2020-04-14 | Aurigene Discovery Technologies Limited | compostos e composições para tratar distúrbios hematológicos |
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| JP7198386B2 (ja) * | 2019-04-03 | 2022-12-28 | 広州白雲山医薬集団股分有限公司白雲山制薬総廠 | Ret阻害剤としての窒素含有スピロ環誘導体 |
| US12178821B2 (en) | 2021-04-08 | 2024-12-31 | Curis, Inc. | Combination therapies for the treatment of cancer |
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| CN101835757B (zh) | 2007-05-22 | 2014-03-05 | 玛德瑞哥制药公司 | 二酰甘油酰基转移酶抑制剂 |
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| US20090076275A1 (en) * | 2007-09-19 | 2009-03-19 | David Robert Bolin | Diacylglycerol acyltransferase inhibitors |
| CA2719507C (en) * | 2008-03-31 | 2018-03-27 | Metabolex, Inc. | Oxymethylene aryl compounds and uses thereof |
| EP2346853A2 (en) * | 2008-11-19 | 2011-07-27 | Schering Corporation | Inhibitors of diacylglycerol acyltransferase |
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- 2009-11-17 AU AU2009316786A patent/AU2009316786A1/en not_active Abandoned
- 2009-11-17 CN CN2009801549757A patent/CN102281919A/zh active Pending
- 2009-11-17 WO PCT/US2009/064738 patent/WO2010059602A2/en not_active Ceased
- 2009-11-17 EP EP09752998.6A patent/EP2367598B1/en not_active Not-in-force
- 2009-11-17 JP JP2011536587A patent/JP2012509274A/ja active Pending
- 2009-11-17 CA CA2743609A patent/CA2743609A1/en not_active Abandoned
- 2009-11-17 MX MX2011005234A patent/MX2011005234A/es not_active Application Discontinuation
- 2009-11-18 AR ARP090104454A patent/AR074130A1/es not_active Application Discontinuation
- 2009-11-18 TW TW098139170A patent/TW201031657A/zh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| WO2010059602A2 (en) | 2010-05-27 |
| CA2743609A1 (en) | 2010-05-27 |
| AU2009316786A1 (en) | 2010-05-27 |
| EP2367598B1 (en) | 2014-04-09 |
| WO2010059602A3 (en) | 2010-07-15 |
| CN102281919A (zh) | 2011-12-14 |
| EP2367598A2 (en) | 2011-09-28 |
| MX2011005234A (es) | 2011-06-01 |
| US8716312B2 (en) | 2014-05-06 |
| TW201031657A (en) | 2010-09-01 |
| JP2012509274A (ja) | 2012-04-19 |
| US20110224137A1 (en) | 2011-09-15 |
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