CR7849A - Agente para la prevencion o tratamiento de neuropatias - Google Patents

Agente para la prevencion o tratamiento de neuropatias

Info

Publication number
CR7849A
CR7849A CR7849A CR7849A CR7849A CR 7849 A CR7849 A CR 7849A CR 7849 A CR7849 A CR 7849A CR 7849 A CR7849 A CR 7849A CR 7849 A CR7849 A CR 7849A
Authority
CR
Costa Rica
Prior art keywords
agent
neuropathies
prevention
treatment
preventing
Prior art date
Application number
CR7849A
Other languages
English (en)
Inventor
Momomse Yu
Sakai Nozomu
Maekama Tsuyoshi
Kawamura Toru
Sera Misayo
Original Assignee
Takeda Pharmaceutical
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Takeda Pharmaceutical filed Critical Takeda Pharmaceutical
Publication of CR7849A publication Critical patent/CR7849A/es

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/4021-aryl substituted, e.g. piretanide
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles
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    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles
    • A61K31/41551,2-Diazoles non condensed and containing further heterocyclic rings
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    • A61K31/4151,2-Diazoles
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    • A61K31/41641,3-Diazoles
    • A61K31/417Imidazole-alkylamines, e.g. histamine, phentolamine
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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Abstract

La presente invencion provee un agente para prevenir o tratar neuropatia que tiene una accion superior y baja toxicidad. Este agente comprende un compuesto representado por la formula: (I)
CR7849A 2002-11-01 2005-05-26 Agente para la prevencion o tratamiento de neuropatias CR7849A (es)

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CR7849A CR7849A (es) 2002-11-01 2005-05-26 Agente para la prevencion o tratamiento de neuropatias
CR10127A CR10127A (es) 2002-11-01 2008-07-01 Agente para la prevención o tratamiento de neuropatías (divisional exp. 7849)

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AR035016A1 (es) 1999-08-25 2004-04-14 Takeda Chemical Industries Ltd Composicion de azol promotor de produccion/secrecion de neurotrofina, compuesto prodroga del mismo, composicion farmaceutica que lo comprende y uso del mismo para preparar esta ultima.
FR2825706B1 (fr) * 2001-06-06 2003-12-12 Pf Medicament Nouveaux derives de benzothienyle ou d'indole, leur preparation et leur utilisation comme inhibiteurs de proteines prenyl transferase
JP2005518371A (ja) * 2001-12-10 2005-06-23 アムジエン・インコーポレーテツド バニロイド受容体リガンド及び治療に於けるこれらの使用
US7183276B2 (en) 2002-02-28 2007-02-27 Takeda Pharmaceutical Company Limited Azole compounds
US20060148858A1 (en) 2002-05-24 2006-07-06 Tsuyoshi Maekawa 1, 2-Azole derivatives with hypoglycemic and hypolipidemic activity

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EP1556032A1 (en) 2005-07-27
RU2005116689A (ru) 2006-01-20
CO5570666A2 (es) 2005-10-31
BR0315815A (pt) 2005-09-13
TW200416029A (en) 2004-09-01
MXPA05004505A (es) 2005-07-26
AR041867A1 (es) 2005-06-01
ZA200503967B (en) 2006-11-29
US7423159B2 (en) 2008-09-09
NZ540381A (en) 2007-11-30
CR10127A (es) 2008-08-18
NO20052626L (no) 2005-07-01
RU2337682C2 (ru) 2008-11-10
CN1731994A (zh) 2006-02-08
NO20052626D0 (no) 2005-05-31
US20080287438A1 (en) 2008-11-20
AU2003278600A1 (en) 2004-05-25
JP2008231115A (ja) 2008-10-02
US20060004069A1 (en) 2006-01-05
PE20040609A1 (es) 2004-10-29
CA2504511A1 (en) 2004-05-13
WO2004039365A1 (en) 2004-05-13
PL376733A1 (pl) 2006-01-09

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