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MX2015013945A - Derivados de urea utiles como inhibidores de quinasa. - Google Patents

Derivados de urea utiles como inhibidores de quinasa.

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Publication number
MX2015013945A
MX2015013945A MX2015013945A MX2015013945A MX2015013945A MX 2015013945 A MX2015013945 A MX 2015013945A MX 2015013945 A MX2015013945 A MX 2015013945A MX 2015013945 A MX2015013945 A MX 2015013945A MX 2015013945 A MX2015013945 A MX 2015013945A
Authority
MX
Mexico
Prior art keywords
kinase inhibitors
urea derivatives
derivatives useful
members
inflammatory diseases
Prior art date
Application number
MX2015013945A
Other languages
English (en)
Other versions
MX363950B (es
Inventor
Premji Meghani
Aaron Rigby
Matthew Colin Thor Fyfe
Stephen Malcolm Thom
Thomas Matthew Baker
Gareth William Harbottle
Vedran Hasimbegovic
Colin Sambrook-Smith
Original Assignee
Respivert Ltd
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
Priority claimed from GB201305945A external-priority patent/GB201305945D0/en
Priority claimed from GBGB1322678.2A external-priority patent/GB201322678D0/en
Priority claimed from GB201402647A external-priority patent/GB201402647D0/en
Application filed by Respivert Ltd filed Critical Respivert Ltd
Publication of MX2015013945A publication Critical patent/MX2015013945A/es
Publication of MX363950B publication Critical patent/MX363950B/es

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C317/00—Sulfones; Sulfoxides
    • C07C317/44—Sulfones; Sulfoxides having sulfone or sulfoxide groups and carboxyl groups bound to the same carbon skeleton
    • C07C317/48—Sulfones; Sulfoxides having sulfone or sulfoxide groups and carboxyl groups bound to the same carbon skeleton the carbon skeleton being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
    • 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
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    • 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
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    • 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
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    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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    • A61K31/535—Heterocyclic 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
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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    • C07C311/08—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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    • C07C317/28—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to acyclic carbon atoms of the carbon skeleton
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    • C07D211/84—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen directly attached to ring carbon atoms
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    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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Abstract

Se proporcionan compuestos de fórmula I, (ver Fórmula) en donde R1A R1E, R2 a R5, L y X1 a X3 tienen los significados dados en la descripción, que los compuestos tienen actividad antiinflamatoria (por ejemplo, a través de la inhibición de uno o más de los miembros de: la familia de enzimas de proteína quinasa activadas por mitógeno p38; quinasa Syk; y los miembros de la familia Src de tirosina quinasas) y tienen uso en terapia, que incluyen combinaciones farmacéuticas, especialmente en el tratamiento de enfermedades inflamatorias, incluyendo enfermedades inflamatorias del pulmón, ojo e intestinos.
MX2015013945A 2013-04-02 2014-04-01 Derivados de urea utiles como inhibidores de quinasa. MX363950B (es)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
GB201305945A GB201305945D0 (en) 2013-04-02 2013-04-02 New compounds
GBGB1322678.2A GB201322678D0 (en) 2013-12-20 2013-12-20 New compounds
GB201402647A GB201402647D0 (en) 2014-02-14 2014-02-14 New compounds
PCT/GB2014/051022 WO2014162126A1 (en) 2013-04-02 2014-04-01 Urea derivatives useful as kinase inhibitors

Publications (2)

Publication Number Publication Date
MX2015013945A true MX2015013945A (es) 2015-12-11
MX363950B MX363950B (es) 2019-04-08

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Family Applications (2)

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MX2015013945A MX363950B (es) 2013-04-02 2014-04-01 Derivados de urea utiles como inhibidores de quinasa.
MX2015013944A MX363949B (es) 2013-04-02 2014-04-01 Inhibidor de quinasa.

Family Applications After (1)

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