AR083199A1 - Compuestos de n-heteroarilo con unidad de puente ciclico - Google Patents
Compuestos de n-heteroarilo con unidad de puente ciclicoInfo
- Publication number
- AR083199A1 AR083199A1 ARP110103572A ARP110103572A AR083199A1 AR 083199 A1 AR083199 A1 AR 083199A1 AR P110103572 A ARP110103572 A AR P110103572A AR P110103572 A ARP110103572 A AR P110103572A AR 083199 A1 AR083199 A1 AR 083199A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- amino
- hydrogen
- aminocarbonyl
- substituted
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 5
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 44
- -1 C1-6-amino alkyl Chemical group 0.000 abstract 21
- 229910052739 hydrogen Inorganic materials 0.000 abstract 21
- 239000001257 hydrogen Substances 0.000 abstract 21
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 14
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 10
- 150000002431 hydrogen Chemical group 0.000 abstract 10
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 abstract 8
- 125000003545 alkoxy group Chemical group 0.000 abstract 8
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 6
- 229910052736 halogen Inorganic materials 0.000 abstract 6
- 150000002367 halogens Chemical class 0.000 abstract 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 6
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 5
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 5
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 4
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 4
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 4
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 4
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 4
- VDFVNEFVBPFDSB-UHFFFAOYSA-N 1,3-dioxane Chemical compound C1COCOC1 VDFVNEFVBPFDSB-UHFFFAOYSA-N 0.000 abstract 4
- CZLMRJZAHXYRIX-UHFFFAOYSA-N 1,3-dioxepane Chemical compound C1CCOCOC1 CZLMRJZAHXYRIX-UHFFFAOYSA-N 0.000 abstract 4
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 abstract 4
- 125000003342 alkenyl group Chemical group 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- 125000006310 cycloalkyl amino group Chemical group 0.000 abstract 4
- 125000005366 cycloalkylthio group Chemical group 0.000 abstract 4
- HGGNZMUHOHGHBJ-UHFFFAOYSA-N dioxepane Chemical compound C1CCOOCC1 HGGNZMUHOHGHBJ-UHFFFAOYSA-N 0.000 abstract 4
- 239000003814 drug Substances 0.000 abstract 4
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 4
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 4
- 150000002825 nitriles Chemical class 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 3
- 238000011282 treatment Methods 0.000 abstract 3
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 2
- 208000006968 Helminthiasis Diseases 0.000 abstract 2
- 241001465754 Metazoa Species 0.000 abstract 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 2
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 abstract 2
- 125000004414 alkyl thio group Chemical group 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 2
- 125000001153 fluoro group Chemical group F* 0.000 abstract 2
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 208000014837 parasitic helminthiasis infectious disease Diseases 0.000 abstract 2
- 125000003396 thiol group Chemical class [H]S* 0.000 abstract 2
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 208000030852 Parasitic disease Diseases 0.000 abstract 1
- 101000585507 Solanum tuberosum Cytochrome b-c1 complex subunit 7 Proteins 0.000 abstract 1
- 125000005090 alkenylcarbonyl group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000006620 amino-(C1-C6) alkyl group Chemical group 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical group O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 abstract 1
- 238000002483 medication Methods 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 abstract 1
- RBNBDIMXFJYDLQ-UHFFFAOYSA-N thieno[3,2-d]pyrimidine Chemical group C1=NC=C2SC=CC2=N1 RBNBDIMXFJYDLQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 abstract 1
- 125000000464 thioxo group Chemical group S=* 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
-
- 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/10—Anthelmintics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
-
- 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
- C07D487/08—Bridged systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Tropical Medicine & Parasitology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Se refiere a determinados compuestos de N-heteroarilo que son en general útiles como medicamentos, más específicamente como medicamentos para animales. El medicamento puede usarse preferiblemente para tratar infecciones helmínticas y el tratamiento de parasitosis, tales como las provocadas por infecciones helmínticas. También se refiere a usos de los compuestos para elaborar medicamentos y tratamientos que comprenden la administración de los compuestos a animales que necesitan dichos tratamientos. También se refiere a la preparación de los compuestos de N-heteroarilo. Asimismo, se refiere a composiciones farmacéuticas y kits que comprenden los compuestos.Reivindicación 1: Un compuesto de la fórmula (1) y sus solvatos, N-óxidos, sales y profármacos farmacéuticamente aceptables, donde R1 es halógeno, amino, alquilo C1-6-amino, di-(alquilo C1-6)amino, alquilo C1-6-amino-alquilo C1-6, di-(alquilo C1-6)amino-alquilo C1-6, alquilo C1-6, hidroxi-alquilo C1-6, alquiloxi C1-6, alquiltio C1-6, alquenilo C2-6, alquinilo C2-6, alquiloxi C1-6-alquilo C1-6, alquiltio C1-6-alquilo C1-6, alquilo C1-6-carbonilo, alquiloxi C1-6-carbonilo, alquenilo C2-6-carbonilo, SF5, alquilo C1-6-sulfonilo donde cada uno de los radicales que contienen carbonos opcionalmente está sustituido con uno o varios átomos de halógeno, preferiblemente átomos de flúor; R2 es hidrógeno, halógeno, amino, alquilo C1-6-amino, di-(alquilo C1-6)amino, alquilo C1-6-amino-alquilo C1-6, di-(alquilo C1-6)amino-alquilo C1-6, alquilo C1-6, hidroxi-alquilo C1-6, alquiloxi C1-6, alquiltio C1-6, alquenilo C2-6, alquinilo C2-6, alquiloxi C1-6-alquilo C1-6, alquiltio C1-6-alquilo C1-6, alquilo C1-6-carbonilo, alquiloxi C1-6-carbonilo, alquenilo C2-6-carbonilo, donde cada uno de los radicales que contienen carbonos opcionalmente está sustituido con uno o varios átomos de halógeno, preferiblemente átomos de flúor, preferiblemente R2 es hidrógeno; R3 es hidrógeno, alquilo C1-6 o cicloalquilo, preferiblemente hidrógeno; R4 es hidrógeno, alquilo C1-6 o cicloalquilo, preferiblemente hidrógeno; R5 es hidrógeno, alquilo C1-6 o cicloalquilo; R6 es hidrógeno, alquilo C1-6, cicloalquilo, hidroxi, alquiloxi C1-6, fenil-alquiloxi C1-6, hidroxi-alquilo C1-6, alquiloxi C1-6-alquilo C1-6, fenil-alquiloxi C1-6-alquilo C1-6, tiol-alquilo C1-6, alquiltio C1-6-alquilo C1-6, fenil-alquiltio C1-6-alquilo C1-6, hidroxicarbonilo, hidroxicarbonil-alquilo C1-6, alquiloxi C1-6- carbonilo, alquiloxi C1-6-carbonil-alquilo C1-6, aminocarbonilo, aminocarbonil-alquilo C1-6, alquilo C1-6-aminocarbonilo, alquilo C1-6-aminocarbonilo-(alquilo C1-6), di(alquilo C1-6)aminocarbonilo, di(alquilo C1-6)aminocarbonilo-(alquilo C1-6), alquilo C1-6-amino-alquilo C1-6, di(alquilo C1-6)amino-alquilo C1-6, fenilo, fenil-alquilo C1-6, donde cada grupo fenilo está opcionalmente sustituido con hidroxi, alquiloxi C1-6 o cicloalquiloxi; R7 es hidrógeno, alquilo C1-6 o cicloalquilo; o R6 y R7 juntos representan un grupo oxo o un grupo tioxo o R6 o R7 se unen junto con R4 o R5 para formar un grupo alquileno C1-3 que está opcionalmente sustituido con uno o varios radicales seleccionados del grupo de alquilo C1-6, cicloalquilo; m es un número entero de 1 a 3; n es un número entero de 1 a 3; X es un grupo carbonilo, tiocarbonilo o sulfonilo, preferiblemente un grupo carbonilo; A es un enlace o NR8, donde R8 es hidrógeno o alquilo C1-6, preferiblemente hidrógeno; E es un enlace o NR9, donde R9 es hidrógeno o alquilo C1-6, preferiblemente hidrógeno; B es N o CR10, donde R10 es hidrógeno o alquilo C1-6, preferiblemente hidrógeno; D es N o CR11, donde R11 es hidrógeno o alquilo C1-6, preferiblemente hidrógeno; Y1 es CR12 o N, donde C está sustituido con R12 que es hidrógeno, halógeno, alquilo C1-6, alquenilo C1-6, cicloalquilo, haloalquilo C1-6, alcoxi C1-6, cicloalquiloxi, haloalcoxi C1-6, nitrilo, nitro, amino, alquilo C1-6-amino, cicloalquilamino, (alquilo C1-6)-(cicloalquil)amino, di(alquilo C1-6)amino, N-pirrolidinilo, N-piperidinilo, N-morfolinilo, alquiltio C1-6, cicloalquiltio, haloalquiltio C1-6, alquilo C1-6-carbonilo, haloalquilo C1-6-carbonilo, alquilo C1-6-carbonilamino, aminocarbonilo, alquilo C1-6-aminocarbonilo, di(alquilo C1-6)aminocarbonilo, alcoxi C1-6-carbonilo, fenilo, dioxolano tal como 1,3-dioxolano, dioxano tal como 1,3-dioxano, o dioxepano tal como 1,3-dioxepano, cada uno de dichos anillos no está sustituido o está sustituido con alquilo C1-6; Y2 es CR13 o N, donde C está sustituido con R13 que es hidrógeno, halógeno, alquilo C1-6, alquenilo C1-6, cicloalquilo, cicloalquiloxi, haloalquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, nitrilo, nitro, amino, alquilo C1-6-amino, cicloalquilamino, (alquilo C1-6)-(cicloalquil)amino, di(alquilo C1-6)amino, N-pirrolidinilo, N-piperidinilo, N-morfolinilo, tiol, hidroxi, alquiltio C1-6, cicloalquiltio, haloalquiltio C1-6, alquilo C1-6-carbonilo, haloalquilo C1-6-carbonilo, aminocarbonilo, alquilo C1-6-aminocarbonilo, di(alquilo C1-6)aminocarbonilo, alquilo C1-6-carbonilamino, alcoxi C1-6-carbonilo, dioxolano tal como 1,3-dioxolano, dioxano tal como 1,3-dioxano, o dioxepano tal como 1,3-dioxepano, cada uno de dichos anillos no está sustituido o está sustituido con alquilo C1-6; Y3 es CR14 o N, donde C está sustituido con R14 que es hidrógeno, halógeno, alquilo C1-6, alquenilo C1-6, cicloalquilo, cicloalquiloxi, haloalquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, nitrilo, nitro, amino, alquilo C1-6-amino, cicloalquilamino, (alquilo C1-6)-(cicloalquil)amino, di(alquilo C1-6)amino, N-pirrolidinilo, N-piperidinilo, N-morfolinilo, tiol, hidroxi, alquiltio C1-6, cicloalquiltio, haloalquiltio C1-6, alquilo C1-6-carbonilo, haloalquilo C1-6-carbonilo, alquilo C1-6-carbonilamino, aminocarbonilo, alquilo C1-6-aminocarbonilo, di(alquilo C1-6)aminocarbonilo, alcoxi C1-6-carbonilo, dioxolano tal como 1,3-dioxolano, dioxano tal como 1,3-dioxano, o dioxepano tal como 1,3-dioxepano, cada uno de dichos anillos no está sustituido o está sustituido con alquilo C1-6; Y4 es CR15 o N, donde C está sustituido con R15 que es hidrógeno, halógeno, alquilo C1-6, alquenilo C1-6, cicloalquilo, cicloalquiloxi, haloalquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, nitrilo, nitro, amino, alquilo C1-6-amino, cicloalquilamino, (alquilo C1-6)-(cicloalquil)amino, di(alquilo C1-6)amino, N-pirrolidinilo, N-piperidinilo, N-morfolinilo, alquiltio C1-6, cicloalquiltio, haloalquiltio C1-6, alquilo C1-6-carbonilo, haloalquilo C1-6-carbonilo, alquilo C1-6-carbonilamino, aminocarbonilo, alquilo C1-6-aminocarbonilo, di(alquilo C1-6)aminocarbonilo, alcoxi C1-6-carbonilo, fenilo, dioxolano tal como 1,3-dioxolano, dioxano tal como 1,3-dioxano, o dioxepano tal como 1,3-dioxepano, cada uno de dichos anillos no está sustituido o está sustituido con alquilo C1-6; o Y1 e Y2 y/o Y3 e Y4 se unen entre sí para formar un sistema de anillos, y donde por lo menos uno de B y D es un átomo de nitrógeno, y donde R1 y R2 son ambos diferentes de un grupo metilo perfluorado si el grupo de la fórmula (2) representa un grupo tienopirimidina sustituido con alquilo C1-6.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP10181551 | 2010-09-29 | ||
| US38846310P | 2010-09-30 | 2010-09-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR083199A1 true AR083199A1 (es) | 2013-02-06 |
Family
ID=44719929
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP110103572A AR083199A1 (es) | 2010-09-29 | 2011-09-28 | Compuestos de n-heteroarilo con unidad de puente ciclico |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8883791B2 (es) |
| EP (1) | EP2621923B1 (es) |
| AR (1) | AR083199A1 (es) |
| BR (1) | BR112013006953A2 (es) |
| ES (1) | ES2624845T3 (es) |
| HU (1) | HUE034347T2 (es) |
| PL (1) | PL2621923T3 (es) |
| WO (1) | WO2012041872A1 (es) |
Families Citing this family (47)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9260441B2 (en) * | 2012-03-28 | 2016-02-16 | Intervet Inc. | Heteroaryl compounds with cyclic bridging unit |
| US9428477B2 (en) * | 2012-04-27 | 2016-08-30 | Nippon Zoki Pharmaceutical Co., Ltd. | Trans-2-decenoic acid derivative and drug containing same |
| BR112015021524A2 (pt) * | 2013-03-04 | 2017-07-18 | Advanced Medical Res Institute Of Canada | derivados de sulfonil quinolina e usos dos mesmos |
| US9227978B2 (en) | 2013-03-15 | 2016-01-05 | Araxes Pharma Llc | Covalent inhibitors of Kras G12C |
| JO3805B1 (ar) | 2013-10-10 | 2021-01-31 | Araxes Pharma Llc | مثبطات كراس جي12سي |
| AR098136A1 (es) | 2013-10-21 | 2016-05-04 | Merck Patent Gmbh | Compuestos de heteroarilo como inhibidores de btk y usos de los mismos |
| EP3145904A1 (en) * | 2014-05-21 | 2017-03-29 | Intervet International B.V. | Improved process for preparing substituted crotonic acids |
| GB201410816D0 (en) * | 2014-06-17 | 2014-07-30 | Ucb Biopharma Sprl And Katholieke Universiteit Leuven | Therapeutic agents |
| GB201410817D0 (en) * | 2014-06-17 | 2014-07-30 | Ucb Biopharma Sprl And Katholieke Universiteit Leuven K U Leuven R & D | Therapeutic agents |
| GB201410815D0 (en) * | 2014-06-17 | 2014-07-30 | Ucb Biopharma Sprl And Katholieke Universiteit Leuven | Therapeutic agents |
| NZ729137A (en) | 2014-08-04 | 2022-07-29 | Nuevolution As | Optionally fused heterocyclyl-substituted derivatives of pyrimidine useful for the treatment of inflammatory, metabolic, oncologic and autoimmune diseases |
| JO3556B1 (ar) | 2014-09-18 | 2020-07-05 | Araxes Pharma Llc | علاجات مدمجة لمعالجة السرطان |
| WO2016049524A1 (en) | 2014-09-25 | 2016-03-31 | Araxes Pharma Llc | Inhibitors of kras g12c mutant proteins |
| BR112017021869A2 (pt) | 2015-04-10 | 2018-12-11 | Araxes Pharma Llc | compostos quinazolina substituídos e métodos de uso dos mesmos |
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- 2011-09-28 BR BR112013006953A patent/BR112013006953A2/pt not_active IP Right Cessation
- 2011-09-28 WO PCT/EP2011/066805 patent/WO2012041872A1/en not_active Ceased
- 2011-09-28 HU HUE11761594A patent/HUE034347T2/en unknown
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- 2011-09-28 AR ARP110103572A patent/AR083199A1/es unknown
- 2011-09-28 PL PL11761594T patent/PL2621923T3/pl unknown
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| ES2624845T3 (es) | 2017-07-17 |
| PL2621923T3 (pl) | 2017-08-31 |
| WO2012041872A1 (en) | 2012-04-05 |
| BR112013006953A2 (pt) | 2016-07-26 |
| EP2621923A1 (en) | 2013-08-07 |
| EP2621923B1 (en) | 2017-03-29 |
| HUE034347T2 (en) | 2018-02-28 |
| US8883791B2 (en) | 2014-11-11 |
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