AR055756A1 - Piperidinas sustituidas; procesos de preparacion y su uso como medicamentos - Google Patents
Piperidinas sustituidas; procesos de preparacion y su uso como medicamentosInfo
- Publication number
- AR055756A1 AR055756A1 ARP060101217A ARP060101217A AR055756A1 AR 055756 A1 AR055756 A1 AR 055756A1 AR P060101217 A ARP060101217 A AR P060101217A AR P060101217 A ARP060101217 A AR P060101217A AR 055756 A1 AR055756 A1 AR 055756A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- optionally
- hydrogen
- group
- Prior art date
Links
- 229940079593 drug Drugs 0.000 title 1
- 239000003814 drug Substances 0.000 title 1
- 238000002360 preparation method Methods 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 28
- 125000003545 alkoxy group Chemical group 0.000 abstract 18
- 229910052757 nitrogen Inorganic materials 0.000 abstract 9
- 229910052739 hydrogen Inorganic materials 0.000 abstract 8
- 239000001257 hydrogen Substances 0.000 abstract 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 8
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 7
- 125000003118 aryl group Chemical group 0.000 abstract 7
- 229910052799 carbon Inorganic materials 0.000 abstract 7
- 125000004432 carbon atom Chemical group C* 0.000 abstract 7
- 125000004414 alkyl thio group Chemical group 0.000 abstract 4
- 125000002947 alkylene group Chemical group 0.000 abstract 4
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 4
- 229910052760 oxygen Inorganic materials 0.000 abstract 4
- 239000001301 oxygen Substances 0.000 abstract 4
- 229920006395 saturated elastomer Polymers 0.000 abstract 4
- 229910052717 sulfur Inorganic materials 0.000 abstract 4
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 3
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 abstract 3
- 125000004450 alkenylene group Chemical group 0.000 abstract 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 3
- -1 carbamoyloxy Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000005842 heteroatom Chemical group 0.000 abstract 3
- 125000000623 heterocyclic group Chemical group 0.000 abstract 3
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 abstract 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 2
- 239000005977 Ethylene Substances 0.000 abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- 125000002252 acyl group Chemical group 0.000 abstract 2
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 239000011593 sulfur Chemical group 0.000 abstract 2
- 125000004434 sulfur atom Chemical group 0.000 abstract 2
- 125000000876 trifluoromethoxy group Chemical class FC(F)(F)O* 0.000 abstract 2
- 125000002023 trifluoromethyl group Chemical class FC(F)(F)* 0.000 abstract 2
- 125000002373 5 membered heterocyclic group Chemical group 0.000 abstract 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 abstract 1
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 abstract 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 1
- 125000005530 alkylenedioxy group Chemical group 0.000 abstract 1
- 125000004419 alkynylene group Chemical group 0.000 abstract 1
- 125000002431 aminoalkoxy group Chemical group 0.000 abstract 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000001769 aryl amino group Chemical group 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 125000004181 carboxyalkyl group Chemical group 0.000 abstract 1
- 150000001925 cycloalkenes Chemical class 0.000 abstract 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 abstract 1
- 125000005331 diazinyl group Chemical group N1=NC(=CC=C1)* 0.000 abstract 1
- 125000002541 furyl group Chemical group 0.000 abstract 1
- 125000006517 heterocyclyl carbonyl group Chemical group 0.000 abstract 1
- 125000002883 imidazolyl group Chemical group 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000001715 oxadiazolyl group Chemical group 0.000 abstract 1
- 125000002971 oxazolyl group Chemical group 0.000 abstract 1
- 125000004043 oxo group Chemical class O=* 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 230000003389 potentiating effect Effects 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 125000003373 pyrazinyl group Chemical group 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 1
- 125000000168 pyrrolyl group Chemical group 0.000 abstract 1
- 230000002285 radioactive effect Effects 0.000 abstract 1
- 239000002461 renin inhibitor Substances 0.000 abstract 1
- 229940086526 renin-inhibitors Drugs 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000003831 tetrazolyl group Chemical group 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
- 125000001425 triazolyl group Chemical group 0.000 abstract 1
Classifications
-
- 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
-
- 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
-
- 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
- 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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- 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
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- 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
-
- 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
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Ophthalmology & Optometry (AREA)
- Hospice & Palliative Care (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
Los compuestos son adecuados en particular como inhibidores de la renina, y son altamente potentes. Reivindicacion 1: Compuestos de la formula (1) o (2), donde: R es alquenilo C2-8, alquilo C1-8, alquinilo C2-8, alquilo-carbonilC0-8-amino-alquiloC1- 8, cicloalquiloC3-8-alquiloC0-8, alquiloC1-8-sulfonil-alquiloC1-8, carbamoil-alquiloC0-8 opcionalmente N-mono- o N,N-di-alquiladoC1-8, carboxil-alquiloC0-8 opcionalmente O-alquiladoC1-8, ureido-alquiloC1-8 o heterociclilcarbonil-alquiloC0-8 opcionalmente N- y/o N'-mono-, di- o tri-alquiladoC1-8, donde cada uno de dichos radicales puede estar sustituido, preferentemente, con 1-4 alcoxi C1-8, alcoxiC1-8-alcoxiC1-8, alcoxicarbonilC1-8-(N-alquiloC1-8)-amino, alquilo C1-8, alquiloC1-8- carbonil-(N-alquiloC1-8)-amino, alquiloC1-8-sulfanilo, alquiloC1-8-sulfinilo, aril-alcoxiC1-8, que está opcionalmente sustituido con 1 o 2 radicales arilo o alcoxi C1-8; arilo, que está opcionalmente sustituido con 1 o 2 radicales arilo o alcoxi C1- 8; aril-amino, ciano, cicloalcoxi C3-8, halogeno, heterociclil-alquiloC0-8, heterociclil-alcoxiC1-8, heterociclil-alquiloC0-8- amino, heterociclil-carbonil, hidroxilo, amino opcionalmente N-mono- o N,N-di-alquiladoC1-8, carbamoil-alquiloC1-8 opcionalmente N-mono- o N, N-di-alquiladoC1-8, carbamoiloxi opcionalmente N-mono- o N,N-di-alquiladoC1-8, sulfamoilo opcionalmente N-mono- o N,N-di-alquiladoC1-8, carbamoilo opcionalmente N-arilado o N-heterociclilo-sustituido; oxo, trifluormetoxi o trifluormetilo; R1 es arilo o heterociclilo; R2 es acenaftilo, ciclohexilo, diazinilo, furilo, imidazolilo, naftilo, oxadiazolilo, oxazolilo, fenilo, pirazinilo, piridilo, pirimidinilo, pirrolilo, oxopiridinilo, tetrazolilo, tienilo, o triazolilo, donde cada uno de dichos radicales puede estar sustituido con 1-3 grupos alcanoiloxi-alquiloC1-8, alqueniloxi C2-8, alcoxi C1-8, alcoxiC1-8-alcoxiC1-8, alcoxiC1-8-alcoxiC1-8-alquiloC1-8, alcoxiC1-8-alquiloC1-8, alcoxicarbonilo C1-8, alcoxicarboniloxiC1-8-alquiloC1-8, alquilo C1-8, carboxi-alquiloC1-8, alcoxiC1-8-alquisulfaniloC1-8, alquilsulfanilo C1-8, alquilsulfaniloC1-8-alcoxi, alquilsulfaniloC1-8-alcoxiC1-8-alquiloC1-8, alquilsulfaniloC1-8-alquiloC1-8, ciano, ciano- alquiloC1-8, cicloalquiloC3-8-alcoxiC0-6-alcoxiC1-8, alcoxiC1-6-alquiloC0-6-cicloalquilo-C3-8-alcoxiC0-6-alquiloC1-8; cicloalquiloC3-8-alcoxiC0-6-alquiloC1-8; halo-alquiloC1-8, halogeno, hidroxi-alquiloC1-8; hidroxilo, oxido; trifluormetoxi o trifluormetilo; o un grupo de alquilendioxi C1-8, y/o con un radical L1-T1-L2-T2-L3-T3-L4-T4-L5-U; L1, L2, L3, L4 y L5 son, de manera independiente, un enlace, alquileno C1-8, alquenileno C2-8 o alquinileno C2-8; cicloalqueno C3-8, o están ausentes; T1, T2, T3 y T4 son, de manera independiente: a) un enlace, o están ausentes, o son uno de los grupos: b) -CH(OH)-; c) -CH(OR6)-; d) -CH(NR5R6)-; e) -CO-; f) -CR7R8-; g) -O- o -NR6-; h) -S (O)0-2-; i) -SO2NR6-; j) -NR6SO2-; k) -CONR6-; i) -NR6CO-; m) -O-CO-; n) -CO-O-; o) -O-CO-O-; p) -O-CO-NR6-; q) -N(R6)-CO-N(R6)-; r) -N(R6)-CO-O-; s) pirrolidinileno, piperidinileno o piperazinileno; t) -C(R11)(R12)-; donde los enlaces que comienzan a partir de b)-t) llevan a un átomo de carbono aromático o saturado del grupo adyacente, si el enlace comienza a partir de un heteroátomo, y donde no están presentes más de dos grupos b)-f), tres grupo g)-h) y un grupo i)-t; R3 es hidrogeno, hidroxilo, alcoxi C1-8 o alqueniloxi C2-8; R4 es hidrogeno, alquenilo C2-8, alcoxi C1-8, alcoxiC1-8-alquiloC1-8, alcoxiC1-8-alcoxiC1-8, alquilo C1-8, opcionalmente (N-alquiloC1-8)-alcoxicarboniloC1-8-amino-alcoxiC1-8, opcionalmente (N-alquiloC1-8)-alquilcarboniloC1-8-amino-alcoxiC1-8, opcionalmente (N-mono- o N,N-di-alquiloC1-8)-amino-alcoxiC1-8, bencilo, cicloalquiloxi C3-8, cicloalquiloxiC3-8-alcoxiC1-8, heterociclil-alcoxiC0-8, heterocicliloxi-alcoxiC1-8, hidroxi, hidroxi-alcoxiC1-8-alcoxiC1-8, hidroxi-alquiloC1-8, oxo o un grupo R4a-Z1-X1- donde R4a es; a) H-; b) alquiloC1-8-; c) alqueniloC2-8-; d) hidroxi-alquiloC1-8-; e) polihidroxi-alquiloC1-8-; f) alquiloC1-8-O-alquiloC1-8-; g) arilo; h) heterociclilo; i) arilalquilo-; j) heterociclilalquilo-; k) ariloxialquilo-; l) heterocicloxialquilo- ; m) (R5, R6)N-(CH2)1-3-; n) (R5, R6)N-; o) alquiloC1-8-S(O)0-2-; p) aril-S(O)0-2-; heterociclil-S(O)0-2-; r) HO-SO3- o sus sales; s) H2N-C(NH)-NH-; (t) NC-; y los enlaces que comienzan a partir de n)-t) conducen a un átomo de carbono del grupo adyacente, y este átomo de carbono está saturado si el enlace comienza a partir de un heteroátomo; Z1: a) es un enlace; está ausente; o es uno de los grupos: b) -alquilenoC1-8-; c) -alquilenilenoC2-8-; d) -O-, -N(R11)-, S(O)0-2-; e) -CO-; f) -O-CO-; g) -O-CO-O-; h) -O-CO-N(R11)-; i) -N(R11)-CO-O-; j) -CO-N(R11)-; k) -N(R11)-CO-; l) -N(R11)-CO-N(R11)-; m) -CH(OR9)-; y los enlaces que comienzan a partir de d) y f)-m) conducen a un átomo de carbono del grupo adyacente, y este átomo de carbono está saturado si el enlace comienza a partir de un heteroátomo; X1: a) es un enlace; está ausente; o es uno de los grupos: b) -O-; c) -N(R11)-; d) -S(O)0-2-; e) -(CH2)1-3-; o R3 y R4 en la formula (1) juntos son un enlace; R5 y R6 son, de manera independiente, hidrogeno, alquilo C1-8, alquenilo C2-8, aril-alquiloC1-8 o acilo, o junto con el átomo de nitrogeno a que están unidos, son un anillo heterocíclico de 5 o 6 miembros que puede contener un átomo de nitrogeno, oxígeno o azufre adicional, o un grupo -SO- o -SO2-, y el átomo de nitrogeno adicional puede estar opcionalmente sustituido con radicales alquilo C1-8; R7 y R8, junto con el átomo de carbono al que están unidos, son un anillo 3-7 miembros que puede contener uno o dos átomos de -O- o -S- o grupos -SO- o -SO2-; R 9 es hidrogeno, alquilo C1-8, alcoxiC1-8-alquiloC1-8, acilo o arilalquilo; R10 es carboxialquilo, alcoxicarbonilalquilo, alquilo o hidrogeno; R11 es hidrogeno o alquilo C1-8; R12 es hidrogeno o alquilo C1-8; Q es etileno o está ausente (formula (1)) o es etileno o metileno (formula (2)); U es hidrogeno, alquilo C1-8, ciano, cicloalquilo C3-8 opcionalmente sustituido, arilo o heterociclilo; W es oxígeno o azufre; X es un enlace, oxígeno o azufre, o es un grupo >CH-R11, >CHOR9, -O-CO-, >CO, >C=NOR10, -O-CHR11- o -O-CHR11-CO-NR9-, y el enlace que comienza a partir de un átomo de oxígeno o azufre conduce a un átomo de carbono saturado del grupo de Z, o a R1; Z es alquileno C1-8, alquenileno C2-8, hidroxi-alquilidenoC1-8, -O-, -S-, -O-alq-, -S-alq-, -alq-O-, -alq-S- o -alq-NR9-, donde alq es alquileno C1-8; y donde: a) si Z es -O- o -S-, X es >CH-R11, y/o bien R2 contiene un sustituyente L1-T1-L2-T2-L3-T3-L4-T4-L5-U; o R4 es un sustituyente diferente de hidrogeno, como se define con anterioridad; b) si Z es -O-alq- o -S-alq-, X es >CH-R11; y c) si X es un enlace, Z es alquenileno C2-8, -alq-O- o -alq-S-; m es 0 o 1; n es 0 o 1; o una sal o profármaco de dicho compuesto; o donde uno o más átomos se reemplazan por sus isotopos estables, no radiactivos.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US66655605P | 2005-03-31 | 2005-03-31 | |
| US75085305P | 2005-12-16 | 2005-12-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR055756A1 true AR055756A1 (es) | 2007-09-05 |
Family
ID=36586065
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP060101217A AR055756A1 (es) | 2005-03-31 | 2006-03-29 | Piperidinas sustituidas; procesos de preparacion y su uso como medicamentos |
| ARP080100485A AR065188A2 (es) | 2005-03-31 | 2008-02-05 | Piperidinas sustituidas, preparacion farmaceutica y uso de dichas piperidinas para preparar medicamentos |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP080100485A AR065188A2 (es) | 2005-03-31 | 2008-02-05 | Piperidinas sustituidas, preparacion farmaceutica y uso de dichas piperidinas para preparar medicamentos |
Country Status (13)
| Country | Link |
|---|---|
| US (2) | US20100029628A1 (es) |
| EP (1) | EP1863803B1 (es) |
| JP (2) | JP2008534558A (es) |
| AR (2) | AR055756A1 (es) |
| AT (1) | ATE479681T1 (es) |
| BR (2) | BRPI0608758A2 (es) |
| CA (1) | CA2601702A1 (es) |
| DE (1) | DE602006016573D1 (es) |
| IL (2) | IL186130A0 (es) |
| PL (1) | PL1863803T3 (es) |
| PT (1) | PT1863803E (es) |
| TW (2) | TW200833687A (es) |
| WO (1) | WO2006103277A2 (es) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101010323B (zh) | 2004-08-25 | 2010-06-16 | 埃科特莱茵药品有限公司 | 作为肾素抑制剂的双环壬烯衍生物 |
| TW200833687A (en) * | 2005-03-31 | 2008-08-16 | Speedel Experimenta Ag | Substituted piperidines |
| NZ564689A (en) | 2005-05-27 | 2011-02-25 | Actelion Pharmaceuticals Ltd | Novel piperidine carboxylic acid amide derivatives |
| GB0514203D0 (en) | 2005-07-11 | 2005-08-17 | Novartis Ag | Organic compounds |
| EP2018380B1 (en) | 2006-05-19 | 2011-10-19 | Abbott Laboratories | Cns active fused bicycloheterocycle substituted azabicyclic alkane derivatives |
| JP2009539806A (ja) * | 2006-06-08 | 2009-11-19 | シュペーデル・エクスペリメンタ・アーゲー | ２，５−二置換ピペリジン |
| TW200821303A (en) * | 2006-08-08 | 2008-05-16 | Speedel Experimenta Ag | Organic compounds |
| EP1958634A3 (en) * | 2007-02-14 | 2008-09-24 | Speedel Experimenta AG | Substituted piperidines as inhibitors of beta-secretase, cathepsin D, plasmepsin II and/or HIV protease |
| TW200922596A (en) * | 2007-10-25 | 2009-06-01 | Speedel Experimenta Ag | 4,4-disubstituted piperidines |
| EA201000720A1 (ru) * | 2007-11-02 | 2010-10-29 | Новартис Аг | 4,4-дизамещённые пиперидины как ингибиторы ренина |
| AU2008339351B2 (en) | 2007-12-19 | 2013-02-28 | Sumitomo Dainippon Pharma Co., Ltd. | Bicyclic heterocyclic derivative |
| JP2011511039A (ja) * | 2008-02-08 | 2011-04-07 | ノバルティス アーゲー | レニン阻害剤としての置換ピペリジン |
| US8022068B2 (en) | 2008-02-08 | 2011-09-20 | Novartis Ag | Substituted piperidines as renin inhibitors |
| US8889714B2 (en) | 2008-05-05 | 2014-11-18 | Actelion Pharmaceuticals Ltd. | 3,4-substituted piperidine derivatives as renin inhibitors |
| EP2163245A1 (en) | 2008-09-10 | 2010-03-17 | Novartis Ag | Renin inhibitors for the treatment of psoriasis |
| WO2010132873A2 (en) | 2009-05-15 | 2010-11-18 | Northwestern University | Chiral pyrrolidine core compounds en route to inhibitors of nitric oxide synthase |
| JP5331883B2 (ja) | 2009-06-24 | 2013-10-30 | 大日本住友製薬株式会社 | Ｎ−置換−環状アミノ誘導体 |
| WO2016112387A1 (en) * | 2015-01-09 | 2016-07-14 | J.W. Speaker Corporation | Tracking and lighting systems and methods for a vehicle |
| DE102015013191A1 (de) * | 2015-10-10 | 2017-04-13 | Daimler Ag | Verfahren zum Betrieb einer Leuchteinheit und Leuchteinheit |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3648251B2 (ja) * | 1995-09-07 | 2005-05-18 | エフ．ホフマン−ラ ロシュ アーゲー | 心及び腎不全を治療するための新規４−（オキシアルコキシフェニル）−３−オキシ−ピペリジン |
| US6376672B1 (en) * | 1999-04-27 | 2002-04-23 | Hoffmann-La Roche Inc. | Naphthalenylmethoxypiperidines as renin inhibitors |
| US6197959B1 (en) * | 1999-04-27 | 2001-03-06 | Hoffmann-La Roche Inc. | Piperidine derivatives |
| US20040204455A1 (en) * | 2003-04-10 | 2004-10-14 | Cody Wayne Livingston | Piperidine derivative rennin inhibitors |
| TW200833687A (en) * | 2005-03-31 | 2008-08-16 | Speedel Experimenta Ag | Substituted piperidines |
-
2006
- 2006-03-29 TW TW097113173A patent/TW200833687A/zh unknown
- 2006-03-29 AR ARP060101217A patent/AR055756A1/es unknown
- 2006-03-29 TW TW095110894A patent/TW200716622A/zh unknown
- 2006-03-30 AT AT06725445T patent/ATE479681T1/de active
- 2006-03-30 DE DE602006016573T patent/DE602006016573D1/de active Active
- 2006-03-30 WO PCT/EP2006/061197 patent/WO2006103277A2/en active Application Filing
- 2006-03-30 BR BRPI0608758-2A patent/BRPI0608758A2/pt not_active IP Right Cessation
- 2006-03-30 US US11/887,227 patent/US20100029628A1/en not_active Abandoned
- 2006-03-30 CA CA002601702A patent/CA2601702A1/en not_active Abandoned
- 2006-03-30 BR BRPI0621969-1A patent/BRPI0621969A2/pt not_active IP Right Cessation
- 2006-03-30 EP EP06725445A patent/EP1863803B1/en not_active Not-in-force
- 2006-03-30 PT PT06725445T patent/PT1863803E/pt unknown
- 2006-03-30 PL PL06725445T patent/PL1863803T3/pl unknown
- 2006-03-30 JP JP2008503525A patent/JP2008534558A/ja active Pending
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2007
- 2007-09-20 IL IL186130A patent/IL186130A0/en unknown
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2008
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- 2008-02-11 IL IL189429A patent/IL189429A0/en unknown
- 2008-03-14 US US12/076,221 patent/US7687495B2/en not_active Expired - Fee Related
- 2008-03-18 JP JP2008069369A patent/JP2008201787A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| PT1863803E (pt) | 2010-11-18 |
| US20080171748A1 (en) | 2008-07-17 |
| US7687495B2 (en) | 2010-03-30 |
| JP2008534558A (ja) | 2008-08-28 |
| TW200833687A (en) | 2008-08-16 |
| WO2006103277A2 (en) | 2006-10-05 |
| BRPI0621969A2 (pt) | 2011-07-19 |
| PL1863803T3 (pl) | 2011-02-28 |
| WO2006103277A3 (en) | 2006-12-28 |
| IL189429A0 (en) | 2008-06-05 |
| ATE479681T1 (de) | 2010-09-15 |
| TW200716622A (en) | 2007-05-01 |
| AR065188A2 (es) | 2009-05-20 |
| BRPI0608758A2 (pt) | 2009-07-07 |
| JP2008201787A (ja) | 2008-09-04 |
| EP1863803B1 (en) | 2010-09-01 |
| DE602006016573D1 (de) | 2010-10-14 |
| US20100029628A1 (en) | 2010-02-04 |
| CA2601702A1 (en) | 2006-10-05 |
| IL186130A0 (en) | 2008-01-20 |
| EP1863803A2 (en) | 2007-12-12 |
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