CL2011000480A1 - Compuestos derivados de amino-1,2,4-triazolo[1,5-a]piridina sustituidos, inhibidores de quinasa; composicion farmaceutica; y su uso para el tratamiento o prevencion de condiciones inflamatorias, inmunologicas, autoinmunes, alergicas, reumaticas, tromboticas, cancer, infecciones, padecimientos neurodegenerativos, entre otras. - Google Patents

Compuestos derivados de amino-1,2,4-triazolo[1,5-a]piridina sustituidos, inhibidores de quinasa; composicion farmaceutica; y su uso para el tratamiento o prevencion de condiciones inflamatorias, inmunologicas, autoinmunes, alergicas, reumaticas, tromboticas, cancer, infecciones, padecimientos neurodegenerativos, entre otras.

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Publication number
CL2011000480A1
CL2011000480A1 CL2011000480A CL2011000480A CL2011000480A1 CL 2011000480 A1 CL2011000480 A1 CL 2011000480A1 CL 2011000480 A CL2011000480 A CL 2011000480A CL 2011000480 A CL2011000480 A CL 2011000480A CL 2011000480 A1 CL2011000480 A1 CL 2011000480A1
Authority
CL
Chile
Prior art keywords
thrombotic
rheumatic
immunological
allergic
infections
Prior art date
Application number
CL2011000480A
Other languages
English (en)
Inventor
Kate Blease
Andrew Antony Calabrese
Jan Elsner
Sogole Bahmanyar
Paul Erdman
Bruce Fahr
Gregory Ferguson
Branden Lee
Lisa Nadolny
Garrick Packard
R J Bates
Patrick Papa
Veronique Plantevin-Krenitsky
Jennifer Riggs
Patricia Rohane
Thomas Oran Daniel
Mercedes Delgado
Sabita Sankar
John Sapienza
Yoshitaka Satoh
Victor Sloan
Randall Stevens
Lida Tehrani
Jayashree Tikhe
Eduardo Torres
Andrew Wallace
Brandon Wade Whitefield
Jingjing Zhao
Original Assignee
Signal Pharm Llc
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=41228355&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CL2011000480(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Signal Pharm Llc filed Critical Signal Pharm Llc
Publication of CL2011000480A1 publication Critical patent/CL2011000480A1/es

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    • 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
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    • 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
    • A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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    • C07D519/06—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00 containing at least one condensed beta-lactam ring system, provided for by groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00, e.g. a penem or a cepham system

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Abstract

COMPUESTOS DERIVADOS DE AMINO -1,2,4-TRIAZOL(1,5-A) PIRIDINA SUSTITUIDOS DE FORMULA;<br /> DONDE R1 Y R2 SON COMO SE DEFINE EN LA MEMORIA DESCRIPTIVA Y PLIEGO DE REIVINDICACIONES, COMPOSICION FARMACEUTICA Y SU USO PARA TRATAR O PREVENIR CONDICIONES INFLAMATORIAS, INMUNOLOGICAS, AUTOINMUNES, ALERGICAS, REUMATICAS, TROMBOTICAS, CANCER, INFECCIONES, PADECIMIENTOS NEURODEGENERATIVOS, ENTRE OTRAS.
CL2011000480A 2008-09-08 2011-03-07 Compuestos derivados de amino-1,2,4-triazolo[1,5-a]piridina sustituidos, inhibidores de quinasa; composicion farmaceutica; y su uso para el tratamiento o prevencion de condiciones inflamatorias, inmunologicas, autoinmunes, alergicas, reumaticas, tromboticas, cancer, infecciones, padecimientos neurodegenerativos, entre otras. CL2011000480A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US9521708P 2008-09-08 2008-09-08
US23047909P 2009-07-31 2009-07-31

Publications (1)

Publication Number Publication Date
CL2011000480A1 true CL2011000480A1 (es) 2011-09-16

Family

ID=41228355

Family Applications (1)

Application Number Title Priority Date Filing Date
CL2011000480A CL2011000480A1 (es) 2008-09-08 2011-03-07 Compuestos derivados de amino-1,2,4-triazolo[1,5-a]piridina sustituidos, inhibidores de quinasa; composicion farmaceutica; y su uso para el tratamiento o prevencion de condiciones inflamatorias, inmunologicas, autoinmunes, alergicas, reumaticas, tromboticas, cancer, infecciones, padecimientos neurodegenerativos, entre otras.

Country Status (22)

Country Link
US (2) US8299056B2 (es)
EP (1) EP2344494B1 (es)
JP (1) JP5689060B2 (es)
KR (1) KR20110053266A (es)
CN (2) CN104910148B (es)
AU (1) AU2009288618B2 (es)
BR (1) BRPI0918854A2 (es)
CA (1) CA2735806A1 (es)
CL (1) CL2011000480A1 (es)
CO (1) CO6531502A2 (es)
CR (1) CR20110132A (es)
EC (1) ECSP11010945A (es)
ES (1) ES2581565T3 (es)
IL (1) IL211549A (es)
MX (1) MX2011002536A (es)
NI (1) NI201100048A (es)
NZ (1) NZ591551A (es)
PE (1) PE20110387A1 (es)
RU (1) RU2552642C2 (es)
TW (1) TWI453207B (es)
WO (1) WO2010027500A1 (es)
ZA (1) ZA201101586B (es)

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EP2252617A1 (en) 2008-02-13 2010-11-24 CGI Pharmaceuticals, Inc. 6-aryl-imidaz0[l, 2-a]pyrazine derivatives, method of making, and method of use thereof
WO2009103652A1 (en) 2008-02-22 2009-08-27 F. Hoffmann-La Roche Ag Modulators for amyloid beta
US9156812B2 (en) 2008-06-04 2015-10-13 Bristol-Myers Squibb Company Crystalline form of 6-[(4S)-2-methyl-4-(2-naphthyl)-1,2,3,4-tetrahydroisoquinolin-7-yl]pyridazin-3-amine
BRPI0909945A2 (pt) * 2008-06-20 2015-07-28 Genentech Inc "composto, composição farmacêutica, método para tratar ou atenuar a gravidade de uma doença ou condição responsiva à inibição da atividade jak2 quinase em um paciente, kit para o tratamento de uma doença ou distúrbio responsivo à inibição da jak quinase"
GB0817207D0 (en) 2008-09-19 2008-10-29 Pimco 2664 Ltd therapeutic apsac compounds and their use
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