HETEROCYCLIC SUBSTITUTED PYRIDINE COMPOUNDS WITH CXCR3 ANTAGONIST ACTIVITY

The present application discloses a compound, or enantiomers, stereoisomers, rotamers, tautomers, racemates or prodrug of said compound, or pharmaceutically acceptable salts, solvates or esters of said compound, or of said prodrug, said compound having the general structure shown in Formula 1: or a...

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Main Authors ROSENBLUM, STUART, B, SHIH, NENG-YANG, MCGUINESS, BRAIN, F, HOBBS, DOUGLAS, W, KOZLOWSKI, JOSEPH, A
Format Patent
LanguageEnglish
French
Published 27.09.2007
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Abstract The present application discloses a compound, or enantiomers, stereoisomers, rotamers, tautomers, racemates or prodrug of said compound, or pharmaceutically acceptable salts, solvates or esters of said compound, or of said prodrug, said compound having the general structure shown in Formula 1: or a pharmaceutically acceptable salt, solvate or ester thereof. Also disclosed is a method of treating chemokine mediated diseases, such as, palliative therapy, curative therapy, prophylactic therapy of certain diseases and conditions such as inflammatory diseases (non-limiting example(s) include, psoriasis), autoimmune diseases (non-limiting example(s) include, rheumatoid arthritis, multiple sclerosis), graft rejection (non-limiting example(s) include, allograft rejection, zenograft rejection), infectious diseases (e.g, tuberculoid leprosy), fixed drug eruptions, cutaneous delayed-type hypersensitivity responses, ophthalmic inflammation, type I diabetes, viral meningitis and tumors using a compound of Formula 1. La présente invention concerne un composé, ou des énantiomères, des stéréoisomères, des rotamères, des tautomères, des racémates ou un promédicament dudit composé, ou des sels, des solvates ou des esters pharmaceutiquement acceptables dudit composé ou dudit promédicament, ledit composé ayant la structure générale présentée dans la formule 1 : ou un sel, un solvate ou un ester de celui-ci pharmaceutiquement acceptable. L'invention concerne également un procédé de traitement des maladies induites par des chimiokines tel qu'un traitement palliatif, un traitement curatif ou un traitement prophylactique de certaines maladies et de certains états tels que des maladies inflammatoires (le ou les exemples non limitants incluent le psoriasis), des maladies auto-immunes (le ou les exemples non limitants incluent la polyarthrite rhumatoïde, la sclérose en plaques), le rejet du greffon (le ou les exemples non limitants incluent le rejet d'un greffon homologue, le rejet d'un greffon hétérologue), les maladies infectieuses (par exemple la lèpre tuberculoïde), les dermatites médicamenteuses fixes, les réponses d'hypersensibilité cutanée de type retardé, les inflammations ophtalmiques, le diabète de type I, la méningite virale et les tumeurs en utilisant un composé de formule 1.
AbstractList The present application discloses a compound, or enantiomers, stereoisomers, rotamers, tautomers, racemates or prodrug of said compound, or pharmaceutically acceptable salts, solvates or esters of said compound, or of said prodrug, said compound having the general structure shown in Formula 1: or a pharmaceutically acceptable salt, solvate or ester thereof. Also disclosed is a method of treating chemokine mediated diseases, such as, palliative therapy, curative therapy, prophylactic therapy of certain diseases and conditions such as inflammatory diseases (non-limiting example(s) include, psoriasis), autoimmune diseases (non-limiting example(s) include, rheumatoid arthritis, multiple sclerosis), graft rejection (non-limiting example(s) include, allograft rejection, zenograft rejection), infectious diseases (e.g, tuberculoid leprosy), fixed drug eruptions, cutaneous delayed-type hypersensitivity responses, ophthalmic inflammation, type I diabetes, viral meningitis and tumors using a compound of Formula 1. La présente invention concerne un composé, ou des énantiomères, des stéréoisomères, des rotamères, des tautomères, des racémates ou un promédicament dudit composé, ou des sels, des solvates ou des esters pharmaceutiquement acceptables dudit composé ou dudit promédicament, ledit composé ayant la structure générale présentée dans la formule 1 : ou un sel, un solvate ou un ester de celui-ci pharmaceutiquement acceptable. L'invention concerne également un procédé de traitement des maladies induites par des chimiokines tel qu'un traitement palliatif, un traitement curatif ou un traitement prophylactique de certaines maladies et de certains états tels que des maladies inflammatoires (le ou les exemples non limitants incluent le psoriasis), des maladies auto-immunes (le ou les exemples non limitants incluent la polyarthrite rhumatoïde, la sclérose en plaques), le rejet du greffon (le ou les exemples non limitants incluent le rejet d'un greffon homologue, le rejet d'un greffon hétérologue), les maladies infectieuses (par exemple la lèpre tuberculoïde), les dermatites médicamenteuses fixes, les réponses d'hypersensibilité cutanée de type retardé, les inflammations ophtalmiques, le diabète de type I, la méningite virale et les tumeurs en utilisant un composé de formule 1.
Author MCGUINESS, BRAIN, F
SHIH, NENG-YANG
ROSENBLUM, STUART, B
KOZLOWSKI, JOSEPH, A
HOBBS, DOUGLAS, W
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DocumentTitleAlternate COMPOSES DE PYRIDINE AVEC SUBSTITUTION HETEROCYCLIQUE AYANT UNE ACTIVITE ANTAGONISTE DE CXCR3
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Snippet The present application discloses a compound, or enantiomers, stereoisomers, rotamers, tautomers, racemates or prodrug of said compound, or pharmaceutically...
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SubjectTerms CHEMISTRY
HETEROCYCLIC COMPOUNDS
HUMAN NECESSITIES
HYGIENE
MEDICAL OR VETERINARY SCIENCE
METALLURGY
ORGANIC CHEMISTRY
PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS
Title HETEROCYCLIC SUBSTITUTED PYRIDINE COMPOUNDS WITH CXCR3 ANTAGONIST ACTIVITY
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