AR079668A1 - Compuestos carboxamida y su uso como inhibidores de calpaina - Google Patents

Compuestos carboxamida y su uso como inhibidores de calpaina

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AR079668A1
AR079668A1 ARP100104834A ARP100104834A AR079668A1 AR 079668 A1 AR079668 A1 AR 079668A1 AR P100104834 A ARP100104834 A AR P100104834A AR P100104834 A ARP100104834 A AR P100104834A AR 079668 A1 AR079668 A1 AR 079668A1
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alkyl
aryl
cycloalkyl
heteroaryl
radicals
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ARP100104834A
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English (en)
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Marjoleen Nijsen
Andreas Kling
Katja Jantos
Helmut Mack
Achim Moller
Wilfried Hornberger
Gisela Backfisch
Yanbin Lao
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Abbott Gmbh & Co Kg
Abbott Lab
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Publication of AR079668A1 publication Critical patent/AR079668A1/es

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Abstract

Compuestos carboxamida y su uso para la elaboracion de un medicamento. Los compuestos carboxamida son inhibidores de calpaína (cisteína proteasas dependientes del calcio). Por lo tanto, también se refiere al uso de dichos compuestos carboxamida para tratar un trastorno asociado con una actividad elevada de calpaína. Reivindicacion 1: Un compuesto carboxamida caracterizado porque es de la formula (1) en donde R1 es alquilo C1-10, alquenilo C2-10, alquinilo C2-10, donde los ultimos 3 radicales mencionados pueden estar parcial o totalmente halogenados y/o tener 1, 2 o 3 sustituyentes R1a, cicloalquilo C3-7, cicloalquil C3-7-alquilo C1-4, donde un grupo CH2 en la porcion cicloalquilo de los ultimos dos radicales mencionados puede reemplazarse por O, NH, o S, o dos átomos de C adyacentes pueden formar una union doble, donde la porcion cicloalquilo puede tener además 1, 2, 3 o 4 radicales R1b, arilo, hetarilo, aril-C1-6-alquilo, aril-C2-6-alquenilo, hetaril-C1-4-alquilo o hetaril-C2-6-alquenilo, donde arilo y hetarilo en los ultimos 6 radicales mencionados puede no estar sustituido o tener 1, 2, 3 o 4 radicales idénticos o diferentes R1c; donde R1a se selecciona en forma independiente entre sí entre OH, SH, COOH, CN, OCH2COOH, alcoxi C1-6, haloalcoxi C1-6, cicloalquiloxi C3-7, alquiltio C1-6, haloalquiltio C1-6, COORa1, CONRa2Ra3, SO2NRa2Ra3, NRa2-SO2-Ra4, NRa2-CO-Ra5, SO2-Ra4 y NRa6Ra7, R1b se selecciona en forma independiente entre sí entre OH, SH, COOH, CN, OCH2COOH, halogeno, fenilo que opcionalmente tiene 1, 2 o 3 sustituyentes R1d, alquilo C1-6, alcoxi C1-6, alquiltio C1-6, donde las porciones alquilo en los ultimos 3 sustituyentes mencionados pueden estar parcial o totalmente halogenadas y/o tener 1, 2 o 3 sustituyentes R1a, COORb1, CONRb2Rb3, SO2NRb2Rb3, NRb2-SO2-Rb4, NRb2-CO-Rb5, SO2-Rb4 y NRb6Rb7, además dos radicales R1b pueden formar juntos un grupo alquileno C1-4, o 2 radicales R1b unidos a átomos de C adyacentes de cicloalquilo pueden formar también junto con los átomos de carbono a los cuales están unidos un anillo benceno, R1c se selecciona en forma independiente entre sí entre OH, SH, halogeno, NO2, NH2, CN, COOH, OCH2COOH, alquilo C1-6, alcoxi C1-6, alcoxi C1-6-alquilo C1-4, alquiltio C1-6, donde las porciones alquilo en los ultimos 4 sustituyentes mencionados pueden estar parcial o totalmente halogenadas y/o tener 1, 2 o 3 sustituyentes R1a, cicloalquilo C3-7, cicloalquil C3-7-alquilo C1-4, cicloalquiloxi C3-7, donde la porcion cicloalquilo de los ultimos tres radicales mencionados puede tener 1, 2, 3 o 4 radicales R1b, arilo, hetarilo, O-arilo, O-CH2-arilo, donde los ultimos tres radicales mencionados no están sustituidos en la porcion arilo o pueden tener 1, 2, 3 o 4 radicales R1d, COORc1, CONRc2Rc3, SO2NRc2Rc3, NRc2-SO2-Rc4 NRc2-CO-Rc5, SO2-Rc4, -(CH2)pNRc6Rc7 con p = 0, 1, 2, 3, 4, 5 o 6 y O-(CH2)qNRc6Rc7 con q = 2, 3, 4, 5 o 6; donde Ra1, Rb1 y Rc1 son en forma independiente entre sí H, alquilo C1-6, haloalquilo C1-6, alquilo C1-6 que tiene 1, 2 o 3 sustituyentes R1a, o alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-7, cicloalquil C3-7-alquilo C1-4, heterocicloalquil C3-7-alquilo C1-4, alcoxi C1-6-alquilo C1-4, arilo, aril-C1-4-alquilo, hetarilo o hetaril-C1-4-alquilo, donde arilo y hetarilo en los ultimos 4 radicales mencionados no están sustituidos o tienen 1, 2 o 3 sustituyentes R1d, Ra2, Rb2 y Rc2 son en forma independiente entre si H, alquilo C1-6, haloalquilo C1-6, alquilo C1-6 que tiene 1, 2 o 3 sustituyentes R1a, o alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-7, cicloalquil C3-7-alquilo C1-4, heterocicloalquil C3-7-alquilo C1-4, alcoxi C1-6-alquilo C1-4, arilo, aril-C1-4-alquilo, hetarilo o hetaril-C1-4-alquilo, donde arilo y hetarilo en tos ultimos 4 radicales mencionados no están sustituidos o tienen 1, 2 o 3 sustituyentes R1d, y Ra3, Rb3 y Rc3 son en forma independiente entre si H, alquilo C1-6, haloalquilo C1-6, alquilo C1-6 que tiene 1, 2 o 3 sustituyentes R1a, o alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-7, cicloalquil C3-7-alquilo C1-4, heterocicloalquil C3-7-alquilo C1-4, alcoxi C1-6-alquilo C1-4, arilo, aril-C1-4-alquilo, hetarilo o hetaril-C1-4-alquilo, donde arilo y hetarilo en los ultimos 4 radicales mencionados no están sustituidos o tienen 1 2 o 3 sustituyentes R1d, o los dos radicales Ra2 y Ra3, o Rb2 y Rb3 o Rc2 y Rc3 forman junto con el átomo de N un heterociclo con nitrogeno de entre 3 y 7 miembros opcionalmente sustituido que puede tener opcionalmente 1, 2 o 3 heteroátomos adicionales idénticos o diferentes del grupo de O, N, S como miembros del anillo, Ra4, Rb4 y Rc4 son en forma independiente entre sí alquilo C1-6, haloalquilo C1-6, alquilo C1-6 que tiene 1, 2 o 3 sustituyentes R1a, o alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-7, cicloalquil C3-7-alquilo C1-4, heterocicloalquil C3-7-alquilo C1-4, alcoxi C1-6-alquilo C1-4, arilo, aril-C1-4-alquilo, hetarilo o hetaril-C1-4-alquilo, donde arilo y hetarilo en los ultimos 4 radicales mencionados no están sustituidos o tienen 1, 2 o 3 sustituyentes R1d, Ra5, Rb5 y Rc5 tienen en forma independiente entre sí uno de los significados mencionados para Ra1, Rb1 y Rc1; Ra6, Rb6 y Rc6 son en forma independiente entre sí H, alquilo C1-6, alcoxi C1-6, haloalquilo C1-6, alquilo C1-6 que tiene 1, 2 o 3 sustituyentes R1a, o alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-7, cicloalquil C3-7-alquilo C1-4, heterocicloalquil C3-7-alquilo C1-4, alcoxi C1-6-alquilo C1-4, CO-alquilo C1-6, CO-O-alquilo C1-6, SO2-alquilo C1-6, arilo, hetarilo, O-arilo, OCH2-arilo, aril-C1-4-alquilo, hetaril-C1-4-alquilo, CO-arilo, CO-hetarilo, CO-(aril-C1-4-alquilo), CO-(hetaril-C1-4-alquilo), CO-Oarilo, CO-O-hetarilo, CO-O-(aril-C1-4-alquilo), CO-O(hetaril-C1-4-alquilo), SO2-arilo, SO2-hetarilo, SO2-(aril-C1-4-alquilo) o SO2-(hetaril-C1-4-alquilo), donde arilo y hetarilo en los ultimos 18 radicales mencionados no están sustituidos o tienen 1, 2 o 3 sustituyentes R1d, Ra7, Rb7 y Rc7 son en forma independiente entre sí H, alquilo C1-6, haloalquilo C1-6, alquilo C1-6 que tiene 1, 2 o 3 sustituyentes R1a, o alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-7, cicloalquil C3-7-alquilo C1-4, heterocicloalquil C3-7-alquilo C1-4, alcoxi C1-6-alquilo C1-6, arilo, aril-C1-4-alquilo, hetarilo o hetaril-C1-4-alquilo, donde arilo y hetarilo en los ultimos 4 radicales mencionados no están sustituidos o tienen 1, 2 o 3 sustituyentes R1d, o los dos radicales Ra6 y Ra7, o Rb6 y Rb7 o Rc6 y Rc7 forman junto con el átomo de N un heterociclo con nitrogeno de entre 3 y 7 miembros opcionalmente sustituido que puede tener opcionalmente 1, 2 o 3 heteroátomos adicionales idénticos o diferentes del grupo de O, N y S como miembros del anillo, o dos radicales R1b o dos radicales R1c unidos a átomos de C adyacentes forman junto con los átomos de C a los cuales están unidos un carbociclo de 4, 5, 6 o 7 miembros opcionalmente sustituido o un heterociclo opcionalmente sustituido que tiene 1, 2 o 3 heteroátomos idénticos o diferentes del grupo de O, N y S como miembros del anillo; R1d se selecciona entre halogeno, OH, SH, NO2, COOH, C(O)NH2, CHO, CN, NH2, OCH2COOH, alquilo C1-6, haloalquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, alquiltio C1-6, haloalquiltio C1-6, CO-alquilo C1-6, CO-O-alquilo C1-6, NH-alquilo C1-6, NHCHO, NH-C(O)alquilo C1-6, y SO2-alquilo C1-6; R2 es cicloalquilo C3-7, cicloalquil C3-7-alquilo C1-4, donde un grupo CH2 en la porcion cicloalquilo de los ultimos dos radicales mencionados puede reemplazarse por O, NH, o S, o dos átomos de C adyacentes pueden formar una union doble, donde la porcion cicloalquilo puede tener adicionalmente 1, 2, 3 o 4 radicales R2b; arilo, O-arilo, O-CH2-arilo, hetarilo, aril-C1-6-alquilo, aril-C2-6-alquenilo, hetaril-C1-4-alquilo o hetaril-C2-6-alquenilo, donde arilo y hetarilo en los ultimos 8 radicales mencionados pueden no estar sustituidos o tener 1, 2, 3 o 4 radicales R2c idénticos o diferentes; donde R2b tiene uno de los significados indicados para R1b, y R2c tiene uno de los significados indicados para R1c; R3 es haloalquilo C1-4 o alquilo C1-6, alquenilo C3-6, alquinilo C3-6, cicloalquilo C3-6, cicloalquil C3-6-alquilo C1-2, heterocicloalquil C3-6-alquilo C1-2, alcoxi C1-4-alquilo C1-2, donde alquilo, alquenilo, alcoxi, alquinilo, cicloalquilo, heterocicloalquilo en los ultimos 7 radicales mencionados no están sustituidos o tienen 1, 2 o 3 sustituyentes Rxa, arilo, aril-C1-4-alquilo, hetarilo o hetaril-C1-4-alquilo, donde arilo y hetarilo en los ultimos 4 radicales mencionados no están sustituidos o tienen 1, 2 o 3 sustituyentes Rxd, donde Rxa tiene uno de los significados indicados para R1a, y Rxd tiene uno de los significados indicados para R1d; R4 y R5 se seleccionan en forma independiente entre si entre halogeno, NH2, CN, CF3, CHF2, CH2F, O-CF3, O-CHF2, O-CH2F, COOH, OCH2COOH, alquilo C1-2, alcoxi C1-2, alcoxi C1-2-alquilo C1-2, alquiltio C1-2, CH2NRR', donde R y R' se seleccionan en forma independiente entre sí entre hidrogeno y alquilo C1-4; m es 0,1 o 2; n es 0,1 o 2; y los tautomeros del mismo, los hidratos del mismo, las prodrogas del mismo y las sales farmacéuticamente adecuadas del mismo.
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WO2012076639A1 (en) * 2010-12-09 2012-06-14 Abbott Gmbh & Co. Kg Carboxamide compounds and their use as calpain inhibitors v
EP2834230A1 (en) 2012-04-03 2015-02-11 AbbVie Deutschland GmbH & Co KG Carboxamide compounds and their use as calpain inhibitors v
ES2834959T3 (es) 2012-12-06 2021-06-21 Celgene Quanticel Res Inc Inhibidores de histona desmetilasa
WO2017061614A1 (ja) 2015-10-08 2017-04-13 神戸ウェルネスサイエンス株式会社 筋肉損傷や筋肉疲労の抑制剤
WO2017156071A1 (en) 2016-03-09 2017-09-14 Blade Therapeutics, Inc. Cyclic keto-amide compounds as calpain modulators and methods of production and use thereof
US11292801B2 (en) 2016-07-05 2022-04-05 Blade Therapeutics, Inc. Calpain modulators and therapeutic uses thereof
CN110023304A (zh) 2016-09-28 2019-07-16 布莱德治疗公司 钙蛋白酶调节剂及其治疗用途
CA3095164A1 (en) * 2018-03-28 2019-10-03 Blade Therapeutics, Inc. Calpain modulators and therapeutic uses thereof

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4826835A (en) 1985-10-23 1989-05-02 Rorer Pharmaceutical Corporation Pyridyl-pyridazinone and pyridyl-pyrazolinone compounds and their use in the treatment of congestive heart failure
US4743608A (en) 1986-07-15 1988-05-10 Rorer Pharmaceutical Corporation Pyridone-pyridyl-imidazolyl and triazolyl compounds and their use as cardiotonic agents
ES2180600T3 (es) * 1994-10-19 2003-02-16 Novartis Ag Eteres de isosteros substrato de aspartato proteasa antivirales.
DE19642591A1 (de) 1996-10-15 1998-04-16 Basf Ag Neue Piperidin-Ketocarbonsäure-Derivate, deren Herstellung und Anwendung
DE19650975A1 (de) 1996-12-09 1998-06-10 Basf Ag Neue heterocyclisch substituierte Benzamide und deren Anwendung
CA2274464C (en) 1996-12-11 2007-01-02 Basf Aktiengesellschaft Ketobenzamides as calpain inhibitors
US6083944A (en) 1997-10-07 2000-07-04 Cephalon, Inc. Quinoline-containing α-ketoamide cysteine and serine protease inhibitors
JP4782924B2 (ja) 1998-04-20 2011-09-28 アボット ゲゼルシャフト ミット ベシュレンクテル ハフツング ウント コンパニー コマンディトゲゼルシャフト 新規の置換アミド、それらの製造および使用
JP2002512240A (ja) 1998-04-20 2002-04-23 ビーエーエスエフ アクチェンゲゼルシャフト 複素環式置換基を有する新規アミド、その製造方法およびその使用
DE19818614A1 (de) 1998-04-20 1999-10-21 Basf Ag Neue substituierte Amide, deren Herstellung und Anwendung
DE19817459A1 (de) 1998-04-20 1999-10-21 Basf Ag Neue heterozyklische substituierte Amide, Herstellung und Anwendung
BR9909773A (pt) 1998-04-20 2000-12-19 Basf Ag Amida heterociclicamente substituìda, uso da mesma, e, preparação farmacêutica para uso oral, parenteral e intraperitoneal
DE59913973D1 (de) 1998-05-25 2006-12-21 Abbott Gmbh & Co Kg Heterocyclische substituierte Amide, deren Herstellung und Verwendung
DE10114762A1 (de) 2001-03-26 2002-10-02 Knoll Gmbh Verwendung von Cysteinprotease-Inhibitoren
BRPI0308208B8 (pt) * 2002-03-05 2021-05-25 Axys Pharm Inc compostos inibidores de catepsina cisteína protease e composições farmacêuticas compreendendo os mesmos
EP2402331A1 (en) 2005-08-02 2012-01-04 Vertex Pharmaceuticals Incorporated Inhibitors of serine proteases
TWI405571B (zh) 2006-12-29 2013-08-21 Abbott Gmbh & Co Kg 羰醯胺化合物及其作為鈣蛋白酶(calpain)抑制劑之用途
EP2125113A2 (en) 2007-02-26 2009-12-02 Achillion Pharmaceuticals, Inc. Tertiary amine substituted peptides useful as inhibitors of hcv replication
TWI519530B (zh) 2009-02-20 2016-02-01 艾伯維德國有限及兩合公司 羰醯胺化合物及其作為鈣蛋白酶(calpain)抑制劑之用途
US8236798B2 (en) 2009-05-07 2012-08-07 Abbott Gmbh & Co. Kg Carboxamide compounds and their use as calpain inhibitors

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