Inhibidores de la tirosina quinasa de bruton
COMPUESTOS HETEROCÍCLICOS COMO INHIBIDORES DE LA TIROSINA QUINASA DE BRUTON; COMPOSICIÓN FARMACÉUTICA QUE LOS COMPRENDE; Y SU USO PARA LA PREVENCIÓN O TRATAMIENTO DE TUMORES DE LA SANDRE Y DEL SISTEMA LINFÁTICO, ENFERMEDADES AUTOINMUNITARIAS E INFLAMATORIAS, ENTRE OTRAS ENFERMEDADES. The present inv...
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creator | SMIRNOVA, Svetlana Sergeevna GORBUNOVA, Svetlana Leonidovna SILONOV, Sergey Aleksandrovich KOZHEMYAKINA, Natalia Vladimirovna MIKHAYLOV, Leonid Evgen`evich IAKOVLEV, Pavel Andreevich POPKOVA, Aleksandra Vladimirovna KUSHAKOVA, Anna Sergeevna MOLDAVSKY, Alexander GAVRILOV, Aleksey Sergeevich ALESHUNIN, Pavel Aleksandrovich REKHARSKY, Mikhail Vladimirovich KUKUSHKINA, Anna Aleksandrovna |
description | COMPUESTOS HETEROCÍCLICOS COMO INHIBIDORES DE LA TIROSINA QUINASA DE BRUTON; COMPOSICIÓN FARMACÉUTICA QUE LOS COMPRENDE; Y SU USO PARA LA PREVENCIÓN O TRATAMIENTO DE TUMORES DE LA SANDRE Y DEL SISTEMA LINFÁTICO, ENFERMEDADES AUTOINMUNITARIAS E INFLAMATORIAS, ENTRE OTRAS ENFERMEDADES.
The present invention relates to a new compound of formula I: or pharmaceutically acceptable salt, solvate or stereoisomer thereof, wherein: V1 is C or N, V2 is C(R2) or N, whereby if V1 is C then V2 is N, if V1 is C then V2 is C(R2), or if V1 is N then V2 is C(R2); each n, k is independently 0, 1; each R2, R11 is independently H, D, Hal, CN, NR'R", C(O)NR'R", C1-C6 alkoxy; R3 is H, D, hydroxy, C(O)C1-C6 alkyl, C(O)C2-C6 alkenyl, C(O)C2-C6 alkynyl, C1-C6 alkyl; R4 is H, Hal, CN, CONR'R", hydroxy, C1-C6 alkyl, C1-C6 alkoxy; L is CH2, NH, O or chemical bond; R1 is selected from the group of the fragments, comprising: Fragment 1, Fragment 2, Fragment 3 each A1, A2, A3, A4 is independently CH, N, CHal; each A5, A6, A7, A8, A9 is independently C, CH or N; R5 is H, CN, Hal, CONR'R", C1-C6 alkyl, non-substituted or substituted by one or more halogens; each R' and R" is independently selected from the group, comprising H, C1-C6 alkyl, C1-C6 cycloalkyl, aryl; R6 is selected from the group: [formula II] each R7, R8, R9, R10 is independently vinyl, methylacetylenyl; Hal is CI, Br, I, F, which have properties of inhibitor of Bruton's tyrosine kinase (Btk), to pharmaceutical compositions containing such compounds, and their use as pharmaceuticals for treatment of diseases and disorder. |
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fullrecord | <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_CL2019001330A1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CL2019001330A1</sourcerecordid><originalsourceid>FETCH-epo_espacenet_CL2019001330A13</originalsourceid><addsrcrecordid>eNrjZNDxzMvITMpMyS9KLVZISVXISVQoySzKL87MS1QoLAWSxYkg4aSi0pL8PB4G1rTEnOJUXijNzaDs5hri7KGbWpAfn1pckJicmpdaEu_sY2RgaGlgYGhsbOBoaEycKgAdQyo_</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Inhibidores de la tirosina quinasa de bruton</title><source>esp@cenet</source><creator>SMIRNOVA, Svetlana Sergeevna ; GORBUNOVA, Svetlana Leonidovna ; SILONOV, Sergey Aleksandrovich ; KOZHEMYAKINA, Natalia Vladimirovna ; MIKHAYLOV, Leonid Evgen`evich ; IAKOVLEV, Pavel Andreevich ; POPKOVA, Aleksandra Vladimirovna ; KUSHAKOVA, Anna Sergeevna ; MOLDAVSKY, Alexander ; GAVRILOV, Aleksey Sergeevich ; ALESHUNIN, Pavel Aleksandrovich ; REKHARSKY, Mikhail Vladimirovich ; KUKUSHKINA, Anna Aleksandrovna</creator><creatorcontrib>SMIRNOVA, Svetlana Sergeevna ; GORBUNOVA, Svetlana Leonidovna ; SILONOV, Sergey Aleksandrovich ; KOZHEMYAKINA, Natalia Vladimirovna ; MIKHAYLOV, Leonid Evgen`evich ; IAKOVLEV, Pavel Andreevich ; POPKOVA, Aleksandra Vladimirovna ; KUSHAKOVA, Anna Sergeevna ; MOLDAVSKY, Alexander ; GAVRILOV, Aleksey Sergeevich ; ALESHUNIN, Pavel Aleksandrovich ; REKHARSKY, Mikhail Vladimirovich ; KUKUSHKINA, Anna Aleksandrovna</creatorcontrib><description>COMPUESTOS HETEROCÍCLICOS COMO INHIBIDORES DE LA TIROSINA QUINASA DE BRUTON; COMPOSICIÓN FARMACÉUTICA QUE LOS COMPRENDE; Y SU USO PARA LA PREVENCIÓN O TRATAMIENTO DE TUMORES DE LA SANDRE Y DEL SISTEMA LINFÁTICO, ENFERMEDADES AUTOINMUNITARIAS E INFLAMATORIAS, ENTRE OTRAS ENFERMEDADES.
The present invention relates to a new compound of formula I: or pharmaceutically acceptable salt, solvate or stereoisomer thereof, wherein: V1 is C or N, V2 is C(R2) or N, whereby if V1 is C then V2 is N, if V1 is C then V2 is C(R2), or if V1 is N then V2 is C(R2); each n, k is independently 0, 1; each R2, R11 is independently H, D, Hal, CN, NR'R", C(O)NR'R", C1-C6 alkoxy; R3 is H, D, hydroxy, C(O)C1-C6 alkyl, C(O)C2-C6 alkenyl, C(O)C2-C6 alkynyl, C1-C6 alkyl; R4 is H, Hal, CN, CONR'R", hydroxy, C1-C6 alkyl, C1-C6 alkoxy; L is CH2, NH, O or chemical bond; R1 is selected from the group of the fragments, comprising: Fragment 1, Fragment 2, Fragment 3 each A1, A2, A3, A4 is independently CH, N, CHal; each A5, A6, A7, A8, A9 is independently C, CH or N; R5 is H, CN, Hal, CONR'R", C1-C6 alkyl, non-substituted or substituted by one or more halogens; each R' and R" is independently selected from the group, comprising H, C1-C6 alkyl, C1-C6 cycloalkyl, aryl; R6 is selected from the group: [formula II] each R7, R8, R9, R10 is independently vinyl, methylacetylenyl; Hal is CI, Br, I, F, which have properties of inhibitor of Bruton's tyrosine kinase (Btk), to pharmaceutical compositions containing such compounds, and their use as pharmaceuticals for treatment of diseases and disorder.</description><language>spa</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; ORGANIC CHEMISTRY ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><creationdate>2019</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20190927&DB=EPODOC&CC=CL&NR=2019001330A1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20190927&DB=EPODOC&CC=CL&NR=2019001330A1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>SMIRNOVA, Svetlana Sergeevna</creatorcontrib><creatorcontrib>GORBUNOVA, Svetlana Leonidovna</creatorcontrib><creatorcontrib>SILONOV, Sergey Aleksandrovich</creatorcontrib><creatorcontrib>KOZHEMYAKINA, Natalia Vladimirovna</creatorcontrib><creatorcontrib>MIKHAYLOV, Leonid Evgen`evich</creatorcontrib><creatorcontrib>IAKOVLEV, Pavel Andreevich</creatorcontrib><creatorcontrib>POPKOVA, Aleksandra Vladimirovna</creatorcontrib><creatorcontrib>KUSHAKOVA, Anna Sergeevna</creatorcontrib><creatorcontrib>MOLDAVSKY, Alexander</creatorcontrib><creatorcontrib>GAVRILOV, Aleksey Sergeevich</creatorcontrib><creatorcontrib>ALESHUNIN, Pavel Aleksandrovich</creatorcontrib><creatorcontrib>REKHARSKY, Mikhail Vladimirovich</creatorcontrib><creatorcontrib>KUKUSHKINA, Anna Aleksandrovna</creatorcontrib><title>Inhibidores de la tirosina quinasa de bruton</title><description>COMPUESTOS HETEROCÍCLICOS COMO INHIBIDORES DE LA TIROSINA QUINASA DE BRUTON; COMPOSICIÓN FARMACÉUTICA QUE LOS COMPRENDE; Y SU USO PARA LA PREVENCIÓN O TRATAMIENTO DE TUMORES DE LA SANDRE Y DEL SISTEMA LINFÁTICO, ENFERMEDADES AUTOINMUNITARIAS E INFLAMATORIAS, ENTRE OTRAS ENFERMEDADES.
The present invention relates to a new compound of formula I: or pharmaceutically acceptable salt, solvate or stereoisomer thereof, wherein: V1 is C or N, V2 is C(R2) or N, whereby if V1 is C then V2 is N, if V1 is C then V2 is C(R2), or if V1 is N then V2 is C(R2); each n, k is independently 0, 1; each R2, R11 is independently H, D, Hal, CN, NR'R", C(O)NR'R", C1-C6 alkoxy; R3 is H, D, hydroxy, C(O)C1-C6 alkyl, C(O)C2-C6 alkenyl, C(O)C2-C6 alkynyl, C1-C6 alkyl; R4 is H, Hal, CN, CONR'R", hydroxy, C1-C6 alkyl, C1-C6 alkoxy; L is CH2, NH, O or chemical bond; R1 is selected from the group of the fragments, comprising: Fragment 1, Fragment 2, Fragment 3 each A1, A2, A3, A4 is independently CH, N, CHal; each A5, A6, A7, A8, A9 is independently C, CH or N; R5 is H, CN, Hal, CONR'R", C1-C6 alkyl, non-substituted or substituted by one or more halogens; each R' and R" is independently selected from the group, comprising H, C1-C6 alkyl, C1-C6 cycloalkyl, aryl; R6 is selected from the group: [formula II] each R7, R8, R9, R10 is independently vinyl, methylacetylenyl; Hal is CI, Br, I, F, which have properties of inhibitor of Bruton's tyrosine kinase (Btk), to pharmaceutical compositions containing such compounds, and their use as pharmaceuticals for treatment of diseases and disorder.</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>HUMAN NECESSITIES</subject><subject>HYGIENE</subject><subject>MEDICAL OR VETERINARY SCIENCE</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><subject>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2019</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZNDxzMvITMpMyS9KLVZISVXISVQoySzKL87MS1QoLAWSxYkg4aSi0pL8PB4G1rTEnOJUXijNzaDs5hri7KGbWpAfn1pckJicmpdaEu_sY2RgaGlgYGhsbOBoaEycKgAdQyo_</recordid><startdate>20190927</startdate><enddate>20190927</enddate><creator>SMIRNOVA, Svetlana Sergeevna</creator><creator>GORBUNOVA, Svetlana Leonidovna</creator><creator>SILONOV, Sergey Aleksandrovich</creator><creator>KOZHEMYAKINA, Natalia Vladimirovna</creator><creator>MIKHAYLOV, Leonid Evgen`evich</creator><creator>IAKOVLEV, Pavel Andreevich</creator><creator>POPKOVA, Aleksandra Vladimirovna</creator><creator>KUSHAKOVA, Anna Sergeevna</creator><creator>MOLDAVSKY, Alexander</creator><creator>GAVRILOV, Aleksey Sergeevich</creator><creator>ALESHUNIN, Pavel Aleksandrovich</creator><creator>REKHARSKY, Mikhail Vladimirovich</creator><creator>KUKUSHKINA, Anna Aleksandrovna</creator><scope>EVB</scope></search><sort><creationdate>20190927</creationdate><title>Inhibidores de la tirosina quinasa de bruton</title><author>SMIRNOVA, Svetlana Sergeevna ; GORBUNOVA, Svetlana Leonidovna ; SILONOV, Sergey Aleksandrovich ; KOZHEMYAKINA, Natalia Vladimirovna ; MIKHAYLOV, Leonid Evgen`evich ; IAKOVLEV, Pavel Andreevich ; POPKOVA, Aleksandra Vladimirovna ; KUSHAKOVA, Anna Sergeevna ; MOLDAVSKY, Alexander ; GAVRILOV, Aleksey Sergeevich ; ALESHUNIN, Pavel Aleksandrovich ; REKHARSKY, Mikhail Vladimirovich ; KUKUSHKINA, Anna Aleksandrovna</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CL2019001330A13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>spa</language><creationdate>2019</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>HUMAN NECESSITIES</topic><topic>HYGIENE</topic><topic>MEDICAL OR VETERINARY SCIENCE</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><topic>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</topic><toplevel>online_resources</toplevel><creatorcontrib>SMIRNOVA, Svetlana Sergeevna</creatorcontrib><creatorcontrib>GORBUNOVA, Svetlana Leonidovna</creatorcontrib><creatorcontrib>SILONOV, Sergey Aleksandrovich</creatorcontrib><creatorcontrib>KOZHEMYAKINA, Natalia Vladimirovna</creatorcontrib><creatorcontrib>MIKHAYLOV, Leonid Evgen`evich</creatorcontrib><creatorcontrib>IAKOVLEV, Pavel Andreevich</creatorcontrib><creatorcontrib>POPKOVA, Aleksandra Vladimirovna</creatorcontrib><creatorcontrib>KUSHAKOVA, Anna Sergeevna</creatorcontrib><creatorcontrib>MOLDAVSKY, Alexander</creatorcontrib><creatorcontrib>GAVRILOV, Aleksey Sergeevich</creatorcontrib><creatorcontrib>ALESHUNIN, Pavel Aleksandrovich</creatorcontrib><creatorcontrib>REKHARSKY, Mikhail Vladimirovich</creatorcontrib><creatorcontrib>KUKUSHKINA, Anna Aleksandrovna</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>SMIRNOVA, Svetlana Sergeevna</au><au>GORBUNOVA, Svetlana Leonidovna</au><au>SILONOV, Sergey Aleksandrovich</au><au>KOZHEMYAKINA, Natalia Vladimirovna</au><au>MIKHAYLOV, Leonid Evgen`evich</au><au>IAKOVLEV, Pavel Andreevich</au><au>POPKOVA, Aleksandra Vladimirovna</au><au>KUSHAKOVA, Anna Sergeevna</au><au>MOLDAVSKY, Alexander</au><au>GAVRILOV, Aleksey Sergeevich</au><au>ALESHUNIN, Pavel Aleksandrovich</au><au>REKHARSKY, Mikhail Vladimirovich</au><au>KUKUSHKINA, Anna Aleksandrovna</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Inhibidores de la tirosina quinasa de bruton</title><date>2019-09-27</date><risdate>2019</risdate><abstract>COMPUESTOS HETEROCÍCLICOS COMO INHIBIDORES DE LA TIROSINA QUINASA DE BRUTON; COMPOSICIÓN FARMACÉUTICA QUE LOS COMPRENDE; Y SU USO PARA LA PREVENCIÓN O TRATAMIENTO DE TUMORES DE LA SANDRE Y DEL SISTEMA LINFÁTICO, ENFERMEDADES AUTOINMUNITARIAS E INFLAMATORIAS, ENTRE OTRAS ENFERMEDADES.
The present invention relates to a new compound of formula I: or pharmaceutically acceptable salt, solvate or stereoisomer thereof, wherein: V1 is C or N, V2 is C(R2) or N, whereby if V1 is C then V2 is N, if V1 is C then V2 is C(R2), or if V1 is N then V2 is C(R2); each n, k is independently 0, 1; each R2, R11 is independently H, D, Hal, CN, NR'R", C(O)NR'R", C1-C6 alkoxy; R3 is H, D, hydroxy, C(O)C1-C6 alkyl, C(O)C2-C6 alkenyl, C(O)C2-C6 alkynyl, C1-C6 alkyl; R4 is H, Hal, CN, CONR'R", hydroxy, C1-C6 alkyl, C1-C6 alkoxy; L is CH2, NH, O or chemical bond; R1 is selected from the group of the fragments, comprising: Fragment 1, Fragment 2, Fragment 3 each A1, A2, A3, A4 is independently CH, N, CHal; each A5, A6, A7, A8, A9 is independently C, CH or N; R5 is H, CN, Hal, CONR'R", C1-C6 alkyl, non-substituted or substituted by one or more halogens; each R' and R" is independently selected from the group, comprising H, C1-C6 alkyl, C1-C6 cycloalkyl, aryl; R6 is selected from the group: [formula II] each R7, R8, R9, R10 is independently vinyl, methylacetylenyl; Hal is CI, Br, I, F, which have properties of inhibitor of Bruton's tyrosine kinase (Btk), to pharmaceutical compositions containing such compounds, and their use as pharmaceuticals for treatment of diseases and disorder.</abstract><oa>free_for_read</oa></addata></record> |
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title | Inhibidores de la tirosina quinasa de bruton |
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