AR032256A1 - Derivados de la urea como antagonistas de integrin alfa 4". - Google Patents

Derivados de la urea como antagonistas de integrin alfa 4".

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Publication number
AR032256A1
AR032256A1 ARP020100181A ARP020100181A AR032256A1 AR 032256 A1 AR032256 A1 AR 032256A1 AR P020100181 A ARP020100181 A AR P020100181A AR P020100181 A ARP020100181 A AR P020100181A AR 032256 A1 AR032256 A1 AR 032256A1
Authority
AR
Argentina
Prior art keywords
aryl
cycloalkyl
heteroaryl
4alkyl
heterocyclyl
Prior art date
Application number
ARP020100181A
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English (en)
Original Assignee
Almirall Prodesfarma Sa
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Application filed by Almirall Prodesfarma Sa filed Critical Almirall Prodesfarma Sa
Publication of AR032256A1 publication Critical patent/AR032256A1/es

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    • C07D213/02Heterocyclic 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
    • C07D213/04Heterocyclic 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
    • C07D213/24Heterocyclic 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 substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/36Radicals substituted by singly-bound nitrogen atoms
    • C07D213/40Acylated substituent nitrogen atom
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    • A61K31/16Amides, e.g. hydroxamic acids
    • A61K31/17Amides, e.g. hydroxamic acids having the group >N—C(O)—N< or >N—C(S)—N<, e.g. urea, thiourea, carmustine
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    • C07C275/00Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
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    • C07C275/40Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by nitrogen atoms not being part of nitro or nitroso groups
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    • C07C275/42Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by carboxyl groups
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Abstract

Un antagonista novedoso de integrin a4b1 y/o integrin a4b7 de la formula (1) o una sal farmacéuticamente aceptable de la misma, donde R1 es C3-10alquilo, C3-10alquenilo, C3-10alquinilo, cicloalquilo, cicloalquilo-C1-10alquilo, cicloalquilo-C2-10alquenilo, cicloalquilo-C2-10alquinilo, heterociclilo, heterociclilo-C1-10alquilo, heterociclilo-C2-10alquenilo, heterociclilo-C2-10alquinilo, arilo, arilo-C1-10alquilo, arilo-C2-10alquenilo, arilo-C2-10alquinilo, heteroarilo, heteroarilo-C1-10alquilo, heteroariloC2-10alquenilo, o heteroarilo- C2-10alquinilo; donde dichos grupos o fracciones alquilo, alquenilo y alquinilo son no sustituidos o sustituidos con desde uno a cuatro sustituyentes, los que pueden ser los mismos o diferentes y que son independientemente seleccionados desde Ra; y donde dichos grupos o fracciones cicloalquilo, heterociclilo, arilo, y heteroarilo son no sustituidos o sustituidos con desde uno a cuatro sustituyentes, los que pueden ser los mismos o diferentes y que son independientemente seleccionados desde Rb; R2 es hidrogeno, C1-6alquilo, C0-2-alquilocicloalquilo, C0-2alquilarilo, C0-2alquilheteroarilo, cicloalquil-C0-2alquilo, arilo-C0-2alquilo o heteroarilo-C0-2alquilo, donde dichos grupos o fracciones arilo y heteroarilo no son sustituidos o sustituidos desde uno hasta cuatro sustituyentes, los cuales pueden ser los mismos o diferentes y que son independientemente seleccionados desde Ra; R3 y R4 son independientemente hidrogeno o C1-4alquilo; R2 y R3 junto a los átomos a los que ellos están adjuntos pueden formar un anillo de 4 a 8 miembros; R5 es C1-6alquilo, cicloalquilo, cicloalquilo-C1-4alquilo, heterociclilo, heterociclilo-C1-4alquilo, arilo, arilo-C1-4alquilo, heteroarilo, o heteroarilo-C1-4alquilo; donde dichos grupos o fracciones alquilo son no sustituidos o sustituidos con desde uno hasta cuatro sustituyentes, los cuales pueden ser los mismos o diferentes y que son independientemente seleccionados desde Ra; donde dichos grupos o fracciones cicloalquilo, heterociclilo, arilo y heteroarilo son no sustituidos o sustituidos con desde uno hasta cuatro sustituyentes, los cuales pueden ser los mismos o diferentes y que son independientemente seleccionados desde Rb; L1 es ûS-, -S(O)-, -S(O)2-, -C(O)-, -C(O)O-, -C(S)-, -N(Rc)-, CH2-, -CH2N(Rc)-, -CON(Rc)-, CSN(Rc)-, -N(Rc)CO-, -N(Rc)CS-, -S(O)2N(Rc)- o ûN(Rc)S(O)2-; L2 es una union covalente, -O-, -S-, -S(O)-, -S(O)2-, -C(O)-, -C(O)O-, -OC(O)-, -C(S)-, -N(Rc)-, -CON(Rc)-, -OC(O)N(Rc), -CSN(Rc)-, N(Rc)CO-, -N(Rc)C(O)O-, -N(Rc)CS-, -S(O)2N(Rc)-, -S(O)2N(Rc)-, -N(Rc)S(O)2-, -N(Rc)CON(Rc)-, o N(Rc)CSN(Rc)-, donde si dos sustituyentes Rc están presentes ellos pueden ser lo mismos o diferentes; W es O, S, NH, N(Rc) o NCN; X es û(CH2)arilo o û(CH2)n heteroarilo-; donde dichos grupos o fracciones arilo y heteroarilo son no sustituidos o sustituidos con desde uno a cuatro sustituyentes, los cuales pueden ser los mismos o diferentes y que son independientemente seleccionados desde Rb; Y es arilo monocíclico o heteroarilo monocíclico conteniendo uno o dos heteroátomos seleccionados desde N, O y S, donde dichas fracciones arilo y heteroarilo son no sustituidos o sustituidos con desde uno a cuatro sustituyentes, los cuales pueden ser los mismos o diferentes y que son independientemente seleccionados desde Rb; Z es ûC(O)ORd, -P(O)2Ord, -S(O)2ORd, -S(O)2N(Rd)(Rd), -C(O)NH2, -C(O)N(Re)S(O)2Rd, -S(O)2N(Re)C(O)Rd, -5-tetrazolilo, o ûC(O)Rd; donde si dos grupos Rd están presentes ellos pueden ser los mismos o diferentes; Ra es ûOH, -ORe, -NO2, halogeno, -S(O)Re, -S(O)2Re, -SRe, -S(O)2ORe, -S(O)NReRe, -S(O)2NReRe, -NReRe, -O(CReRe)mNReRe, -C(O)Re, CO2Re, -CO2 (CReRe)nCONReRe, -OC(O)Re, -CN, -C(O)NReRe, -NReC(O)Re, -OC(O)NReRe, -NReC(O)ORe, -NReC(O)NReRe, -CRe(N-ORe), -CFH2, -CF2HRa, o ûCF3; donde si dos grupos Re están presentes ellos pueden ser lo mismo o diferentes; Rb es un grupo seleccionado desde: -OH, ORe, -NO2, halogeno, -S(O)Re, -S(O)2Re, -SRe, -S(O)2ORe, -S(O)NReRe, -S(O)2NReRe, -NReRe,-O(CReRe)mNReRe, -C(O)Re, -CO2Re, -CO2(CReRe)mCONReRe, -OC(O)Re, -CN, -C(O)NReRe, -NReC(O)Re, -OC(O)NReRe, -NReC(O)ORe, -NReC(O)NReRe, -CRe(N-ORe), -CFH2 ûCF2H,Ra, -CF3, C1-6alquilo, C2-4 alquenilo, C2-4alquinilo, cicloalquilo, cicloalquilo-C1-4alquilo, heterociclilo, heteociclilo-C1-4alquilo, arilo, arilo-C1-4alquilo, heteroarilo o heteroarilo C1-4alquilo; donde dichos grupos o fracciones alquilo, alquenilo, alquinilo, cicloalquilo, heterociclilo, arilo y heteroarilo son no sustituidos o sustituidos con desde uno hasta cuatro sustituyentes los cuales pueden ser los mismos o diferentes y que son independientemente seleccionados de Ra; Rc es hidrogeno, C1-10alquilo o cicloalquilo; donde dichos grupos o fracciones de alquilo o cicloalquilo son no-sustituidos o sustituidos con desde uno hasta cuatro sustituyentes los que pueden ser los mismos o diferentes y son seleccionados de Ra; Rd es hidrogeno, C1-6alquilo, cicloalquilo, cicloalquilo-C1-4alquilo, heterociclilo-C1-4alquilo, arilo, arilo-C1-4-alquilo, heteroarilo, o heteroarilo-C1-4alquilo; donde dichos grupos o fracciones de alquilo, cicloalquilo, heterociclilo, arilo y heteroarilo son no-sustituidos o sustituidos con desde uno hasta cuatro sustituyentes los que pueden ser los mismos o diferentes y son independientemente seleccionados de Ra; Re es hidrogeno o C1-4alquilo; n es un entero de 0 a 2; m es un entero de 1 a 6.
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Families Citing this family (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6960597B2 (en) 2000-06-30 2005-11-01 Orth-Mcneil Pharmaceutical, Inc. Aza-bridged-bicyclic amino acid derivatives as α4 integrin antagonists
ES2219177B1 (es) * 2003-05-05 2006-02-16 Almirall Prodesfarma, S.A. Derivados de n-(2-feniletil) sulfamida como antagonistas de la integrina alfa4.
WO2005019193A2 (en) * 2003-08-20 2005-03-03 Smithkline Beecham Corporation Phenylurea derivatives useful in the treatment of conditions mediated by polo-like kinases (plk)
CA2813757C (en) 2005-08-18 2014-04-08 Nissan Chemical Industries, Ltd. Thiophene compound having sulfonyl group and process for producing the same
WO2007060409A1 (en) * 2005-11-23 2007-05-31 Astrazeneca Ab L-alanine derivatives
KR100588821B1 (ko) * 2006-01-06 2006-06-12 모악개발 주식회사 균일 팽창이 가능한 패커를 구비하는 하수관로 부분보수장치
US20080045521A1 (en) * 2006-06-09 2008-02-21 Astrazeneca Ab Phenylalanine derivatives
WO2008093065A1 (en) * 2007-01-29 2008-08-07 Astrazeneca Ab L-ALANINE DERIVATIVES AS α5βL ANTAGONISTS
WO2008094992A2 (en) 2007-01-31 2008-08-07 Vertex Pharmaceuticals Incorporated 2-aminopyridine derivatives useful as kinase inhibitors
ES2320955B1 (es) 2007-03-02 2010-03-16 Laboratorios Almirall S.A. Nuevos derivados de 3-((1,2,4)triazolo(4,3-a)piridin-7-il)benzamida.
WO2008125811A1 (en) * 2007-04-11 2008-10-23 Astrazeneca Ab N-[HETEROARYLCARBONYL]-S-THIENYL-L-ALANINE DERIVATIVES AS α5β1 ANTAGONISTS
EP2108641A1 (en) 2008-04-11 2009-10-14 Laboratorios Almirall, S.A. New substituted spiro[cycloalkyl-1,3'-indo]-2'(1'H)-one derivatives and their use as p38 mitogen-activated kinase inhibitors
EP2113503A1 (en) 2008-04-28 2009-11-04 Laboratorios Almirall, S.A. New substituted indolin-2-one derivatives and their use as p39 mitogen-activated kinase inhibitors
EP2328896B1 (en) 2008-07-23 2013-10-23 Vertex Pharmaceuticals Incorporated Tri-cyclic pyrazolopyridine kinase inhibitors
AU2009274011B2 (en) 2008-07-23 2014-12-18 Vertex Pharmaceuticals Incorporated Pyrazolopyridine kinase inhibitors
US8569337B2 (en) 2008-07-23 2013-10-29 Vertex Pharmaceuticals Incorporated Tri-cyclic pyrazolopyridine kinase inhibitors
EP2313372B1 (en) * 2008-08-06 2013-04-10 Vertex Pharmaceuticals Incorporated Aminopyridine kinase inhibitors
KR101038486B1 (ko) * 2008-09-03 2011-06-01 쌍용건설 주식회사 패커를 이용한 비굴착식 하수관로 보수 장치 및 방법
TW201034689A (en) * 2008-12-05 2010-10-01 Molecular Insight Pharm Inc CA-IX specific radiopharmaceuticals for the treatment and imaging of cancer
CN102459259A (zh) 2009-05-06 2012-05-16 沃泰克斯药物股份有限公司 吡唑并吡啶类
FI20095678A0 (fi) * 2009-06-16 2009-06-16 Biotie Therapies Oy Ureasubstituoituja sulfoniamidijohdannaisia
EP2322176A1 (en) 2009-11-11 2011-05-18 Almirall, S.A. New 7-phenyl-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one derivatives
EP2550272A1 (en) 2010-01-27 2013-01-30 Vertex Pharmaceuticals Incorporated Pyrazolopyrazine kinase inhibitors
JP2013518114A (ja) 2010-01-27 2013-05-20 バーテックス ファーマシューティカルズ インコーポレイテッド ピラゾロピリミジンキナーゼ阻害剤
CA2787315A1 (en) 2010-01-27 2011-08-04 Vertex Pharmaceuticals Incorporated Pyrazolopyridine kinase inhibitors
EP2611777B1 (en) * 2010-09-03 2016-05-11 Forma TM, LLC. N-(4-{[pyridin-3-yl-methyl)carbamoyl]amino}benzene-sulfone derivatives as nampt inhibitors for therapy of diseases such as cancer
US10266488B2 (en) 2013-10-10 2019-04-23 Eastern Virginia Medical School 4-((2-hydroxy-3-methoxybenzyl)amino)benzenesulfonamide derivatives as potent and selective inhibitors of 12-lipoxygenase
EP3873897B1 (en) 2018-10-30 2024-08-14 Gilead Sciences, Inc. N-benzoyl-phenylalanine derivatives as alpha4beta7 integrin inhibitors for treating inflammatory diseases
PL3873900T3 (pl) 2018-10-30 2025-06-02 Gilead Sciences, Inc. Imidazo[1,2-a]pirydynowe pochodne jako inhibitory integryny alpha4beta7 do leczenia chorób zapalnych
LT3873884T (lt) 2018-10-30 2025-03-10 Gilead Sciences, Inc. 3-(chinolin-8-il)-1,4-dihidropirido[3,4-d]pirimidin-2,4-diono dariniai kaip alfa4beta7 integrino inhibitoriai, skirti uždegiminių ligų gydymui
KR102659859B1 (ko) 2018-10-30 2024-04-25 길리애드 사이언시즈, 인코포레이티드 알파4β7 인테그린의 억제를 위한 화합물
EP4013499A1 (en) 2019-08-14 2022-06-22 Gilead Sciences, Inc. Compounds for inhibition of alpha 4 beta 7 integrin
WO2022093552A2 (en) * 2020-10-16 2022-05-05 Saint Louis Univeristy Rev-erb agonists

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4740611A (en) * 1986-10-30 1988-04-26 The Standard Oil Company N,N'-disubstituted ureas
US4705864A (en) * 1986-11-10 1987-11-10 The Standard Oil Company Aryl oxime derivatives of hydantoins
WO1992008464A1 (en) * 1990-11-15 1992-05-29 Tanabe Seiyaku Co. Ltd. Substituted urea and related cell adhesion modulation compounds
GB9310713D0 (en) * 1993-05-24 1993-07-07 Zeneca Ltd Aryl substituted heterocycles
DK0900211T3 (da) * 1996-04-23 2003-10-27 Upjohn Co Thiadiazolyl(thio)urinstoffer, der er nyttige som matrixmetalloproteaseinhibitorer
ES2271971T3 (es) 1996-07-25 2007-04-16 Biogen Idec Ma Inc. Inhibidores de la adhesion celular.
NZ333038A (en) * 1996-08-22 2000-10-27 Warner Lambert Co Non-peptide bombesin receptor antagonists
AU728435B2 (en) 1997-05-29 2001-01-11 Merck & Co., Inc. Sulfonamides as cell adhesion inhibitors
ATE249421T1 (de) 1997-06-23 2003-09-15 Tanabe Seiyaku Co Inhibitoren der alpha4-beta1 vermittelten zelladhäsion
US6353023B1 (en) 1997-08-28 2002-03-05 Pharmacia & Upjohn Company Inhibitors of protein tyrosine phosphatase
WO1999020617A1 (en) * 1997-10-21 1999-04-29 Active Biotech Ab Antiinflammatory thiadiazolyl ureas which act as lfa-1 and mac-1 inhibitors
TR200001312T2 (tr) 1997-11-10 2000-09-21 Bristol-Myers Squibb Company Benzotiyazol protein tirozin kinaz önleyicileri.
US6645939B1 (en) 1997-11-24 2003-11-11 Merck & Co., Inc. Substituted β-alanine derivatives as cell adhesion inhibitors
JP2001524465A (ja) 1997-11-24 2001-12-04 メルク エンド カムパニー インコーポレーテッド 細胞接着阻害剤としての置換β−アラニン誘導体
ATE298338T1 (de) 1997-12-17 2005-07-15 Merck & Co Inc Integrin-rezeptor-antagonisten
EP0975589A2 (en) 1998-01-21 2000-02-02 ZymoGenetics, Inc. Dialkyl ureas as calcitonin mimetics
DE69927050T2 (de) * 1998-12-16 2006-06-29 Bayer Healthcare Ag Biphenylverbindungen und biphenyl-analoge als intergrin-antagonisten
CA2359114A1 (en) 1999-01-25 2000-07-27 Elan Pharmaceuticals, Inc. Compounds which inhibit leukocyte adhesion mediated by vla-4
WO2000051974A1 (en) 1999-03-01 2000-09-08 Elan Pharmaceuticals, Inc. Alpha-aminoacetic acid derivatives useful as alpha 4 beta 7 - receptor antagonists
DE19909979A1 (de) 1999-03-06 2000-09-07 Bayer Ag Verfahren zur Herstellung von Glycokonjugaten von 20(S)-Camptothecin
CZ303312B6 (cs) 1999-05-07 2012-07-25 Texas Biotechnology Corporation Deriváty karboxylové kyseliny, které inhibují vazbu integrinu na jejich receptory
US6518283B1 (en) 1999-05-28 2003-02-11 Celltech R&D Limited Squaric acid derivatives
AU6909300A (en) * 1999-08-20 2001-03-19 Merck & Co., Inc. Substituted ureas as cell adhesion inhibitors

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