CL2011002216A1 - Sal de adicion de una amina que contiene uno o mas grupos hidroxilo y/o carboxilicos con un derivado de acido aminonicotinico, composicion y combinacion farmaceuticas; y su uso para tratar artritis reumatoide, espondilitis anquilosante, esclerosis multiple, psoriasis, entre otras. - Google Patents

Sal de adicion de una amina que contiene uno o mas grupos hidroxilo y/o carboxilicos con un derivado de acido aminonicotinico, composicion y combinacion farmaceuticas; y su uso para tratar artritis reumatoide, espondilitis anquilosante, esclerosis multiple, psoriasis, entre otras.

Info

Publication number
CL2011002216A1
CL2011002216A1 CL2011002216A CL2011002216A CL2011002216A1 CL 2011002216 A1 CL2011002216 A1 CL 2011002216A1 CL 2011002216 A CL2011002216 A CL 2011002216A CL 2011002216 A CL2011002216 A CL 2011002216A CL 2011002216 A1 CL2011002216 A1 CL 2011002216A1
Authority
CL
Chile
Prior art keywords
hydroxyl
groups
psoriasis
derivative
pharmaceutical composition
Prior art date
Application number
CL2011002216A
Other languages
English (en)
Inventor
Carrera Francese Carrera
Garcia Juan Bautista Perez
Martin Digna Jose Garcia
Bernardini Maria Carmen Boix
Original Assignee
Almirall Sa
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
Application filed by Almirall Sa filed Critical Almirall Sa
Publication of CL2011002216A1 publication Critical patent/CL2011002216A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic 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
    • 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
    • C07D213/60Heterocyclic 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
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/79Acids; Esters
    • C07D213/80Acids; Esters in position 3
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/455Nicotinic acids, e.g. niacin; Derivatives thereof, e.g. esters, amides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/02Drugs for disorders of the nervous system for peripheral neuropathies
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic 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
    • 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
    • C07D213/60Heterocyclic 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
    • C07D213/72Nitrogen atoms
    • C07D213/74Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Neurology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Rheumatology (AREA)
  • Biomedical Technology (AREA)
  • Immunology (AREA)
  • Neurosurgery (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Pain & Pain Management (AREA)
  • Dermatology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

LA PRESENTE ÍNVENCIÓN SE REFIERE A S SALES DE ADICIÓN, FARMACÉUTICAMENTC ACEPTABLES E HIDROSOLUBLES DE (I) UNA AMÍNA QUE CONTIENE UNO O MÁS GRUPOS HIDROXILO Y/O CARBOXÍLICOS CON (II) DERIVADOS DE ÁCIDO AMINONICOTÍNICO DE FORMULA (I). DONDE RA, RB, RC Y RD ÍNDEPENDIENTEMENTE REPRESENTAN GRUPOS SELECCIONADOS DE ÁTOMOS DE HIDRÓGENO, ÁTOMOS DE HALÓGENO, GRUPOS ALQUILO CI-4 QUE PUEDEN ESTAR OPCIONALMENTE SUSTITUIDOS CON 1, 2 O 3 SUSTITUYENTES<br /> SELECCIONADOS DE ÁTOMOS DE HALÓGENO Y GRUPOS HIDROXI, Y GRUPOS ALCOXI C1-4 QUE PUEDEN ESTAR OPCIONALMENTE SUSTITUIDOS CON 1, 2 O 3 SUSTITUYENTES SELECCIONADOS DE ÁTOMOS DE HALÓGENO Y GRUPOS HIDROXI, Y SUS SOLVATOS FARMACÉUTICAMENTE ACEPTABLES.<br />  
CL2011002216A 2009-03-13 2011-09-08 Sal de adicion de una amina que contiene uno o mas grupos hidroxilo y/o carboxilicos con un derivado de acido aminonicotinico, composicion y combinacion farmaceuticas; y su uso para tratar artritis reumatoide, espondilitis anquilosante, esclerosis multiple, psoriasis, entre otras. CL2011002216A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP09382031A EP2228367A1 (en) 2009-03-13 2009-03-13 Addition salts of amines containing hydroxyl and/or carboxylic groups with amino nicotinic acid derivatives as DHODH inhibitors

Publications (1)

Publication Number Publication Date
CL2011002216A1 true CL2011002216A1 (es) 2012-03-09

Family

ID=40677683

Family Applications (1)

Application Number Title Priority Date Filing Date
CL2011002216A CL2011002216A1 (es) 2009-03-13 2011-09-08 Sal de adicion de una amina que contiene uno o mas grupos hidroxilo y/o carboxilicos con un derivado de acido aminonicotinico, composicion y combinacion farmaceuticas; y su uso para tratar artritis reumatoide, espondilitis anquilosante, esclerosis multiple, psoriasis, entre otras.

Country Status (35)

Country Link
US (1) US20120014918A1 (es)
EP (2) EP2228367A1 (es)
JP (1) JP5674685B2 (es)
KR (1) KR101674699B1 (es)
CN (1) CN102348689B (es)
AR (1) AR075738A1 (es)
AU (1) AU2010223528B2 (es)
BR (1) BRPI1006766B8 (es)
CA (1) CA2754804C (es)
CL (1) CL2011002216A1 (es)
CO (1) CO6420337A2 (es)
CY (1) CY1114418T1 (es)
DK (1) DK2406225T3 (es)
EA (1) EA022350B1 (es)
EC (1) ECSP11011365A (es)
ES (1) ES2428746T3 (es)
HK (1) HK1162487A1 (es)
HR (1) HRP20130851T1 (es)
IL (1) IL214519A (es)
ME (1) ME01564B (es)
MX (1) MX2011009146A (es)
MY (1) MY155140A (es)
NZ (1) NZ594493A (es)
PE (1) PE20120171A1 (es)
PL (1) PL2406225T3 (es)
PT (1) PT2406225E (es)
RS (1) RS52949B (es)
SG (1) SG173823A1 (es)
SI (1) SI2406225T1 (es)
SM (1) SMT201300104B (es)
TW (1) TWI428127B (es)
UA (1) UA105786C2 (es)
UY (1) UY32467A (es)
WO (1) WO2010102826A1 (es)
ZA (1) ZA201105744B (es)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2319596B1 (es) 2006-12-22 2010-02-08 Laboratorios Almirall S.A. Nuevos derivados de los acidos amino-nicotinico y amino-isonicotinico.
UY31272A1 (es) 2007-08-10 2009-01-30 Almirall Lab Nuevos derivados de ácido azabifenilaminobenzoico
EP2135610A1 (en) 2008-06-20 2009-12-23 Laboratorios Almirall, S.A. Combination comprising DHODH inhibitors and methotrexate
EP2239256A1 (en) 2009-03-13 2010-10-13 Almirall, S.A. Sodium salt of 5-cyclopropyl-2-{[2-(2,6-difluorophenyl)pyrimidin-5-yl]amino}benzoic acid as DHODH inhibitor
EP2314577A1 (en) 2009-10-16 2011-04-27 Almirall, S.A. Process for manufacturing 2-[(3,5-difluoro-3'-methoxy-1,1'-biphenyl-4-yl)amino]nicotinic acid
EP2444088A1 (en) * 2010-10-22 2012-04-25 Almirall, S.A. Amino derivatives for the treatment of proliferative skin disorders
EP2594271A1 (en) * 2011-11-21 2013-05-22 Almirall, S.A. 2-[(3,5-difluoro-3'-methoxy-1,1'-biphenyl-4-yl)amino]nicotinic acid for the treatment of psoriasis.
KR101251851B1 (ko) 2011-11-30 2013-04-10 현대자동차주식회사 Isg 시스템 및 이의 제어방법
TW201350467A (zh) * 2012-05-08 2013-12-16 Teva Pharma N-乙基-4-羥基-1-甲基-5-(甲基(2,3,4,5,6-五羥基己基)胺基)-2-側氧-n-苯基-1,2-二氫喹啉-3-甲醯胺
TW201400117A (zh) * 2012-06-05 2014-01-01 Teva Pharma 使用拉喹莫德治療眼發炎疾病
EP3308770A1 (en) * 2013-04-12 2018-04-18 Actavis Group PTC EHF Pemetrexed formulation
WO2018136009A1 (en) 2017-01-20 2018-07-26 Aslan Pharmaceuticals Pte Ltd Combination therapy
WO2018136010A1 (en) 2017-01-20 2018-07-26 Aslan Pharmaceuticals Pte Ltd Combination therapy
EP3590920A4 (en) * 2017-03-02 2021-01-06 Shanghai Institute of Materia Medica, Chinese Academy of Sciences AROMATIC FORMIATE 2-FTO INHIBITOR (SUBSTITUTED BENZENE MATRIX), PROCESS OF PREPARATION AND APPLICATIONS
AU2019359036A1 (en) 2018-10-09 2021-06-03 Aslan Pharmaceuticals Pte Ltd Malonate salt of varlitinib
KR20220035022A (ko) * 2018-12-21 2022-03-21 르 라보레또레 쎄르비에르 유기 화합물의 결정질 및 염 형태 및 그의 제약 조성물
EP4228640A1 (en) * 2020-10-15 2023-08-23 ASLAN Pharmaceuticals Pte Ltd Treatment of autoimmune diseases with a dihydroorotate hehydrogenase (dhodh) inhibitor
CN114907267A (zh) * 2021-02-08 2022-08-16 中国科学院上海药物研究所 用于抗肿瘤的药物组合

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3839344A (en) * 1973-03-28 1974-10-01 Schering Corp N-methyl d-glucamine salt of 2(2'-methyl-3'-trifluoromethylanilino)nicotinic acid
GB9804343D0 (en) 1998-02-27 1998-04-22 Univ Cardiff Chemical compounds
EP1225886A2 (en) * 1999-06-10 2002-07-31 Warner-Lambert Company Method of inhibiting amyloid protein aggregation and imaging amyloid deposits
SI1381356T1 (sl) 2001-04-05 2008-12-31 Aventis Pharma Inc Uporaba (Z)-2-ciano-3-hidroksi-but-2-enojska kislina-(4'-trifluorometilfenil)-amida za zdravljenje multiple skleroze
WO2003006424A1 (en) 2001-07-10 2003-01-23 4Sc Ag Novel compounds as anti-inflammatory, immunomodulatory and anti-proliferatory agents
JP2004099586A (ja) * 2002-05-21 2004-04-02 Sumitomo Pharmaceut Co Ltd ジヒドロオロテートデヒドロゲナーゼ阻害剤
US7071355B2 (en) 2002-12-23 2006-07-04 4 Sc Ag Compounds as anti-inflammatory, immunomodulatory and anti-proliferatory agents
WO2004056747A1 (en) 2002-12-23 2004-07-08 4Sc Ag Dhodh-inhibitors and method for their identification
CN1993125A (zh) 2004-05-21 2007-07-04 Uab研究基金会 涉及嘧啶合成抑制剂的组合物和方法
WO2006022442A1 (ja) 2004-08-24 2006-03-02 Santen Pharmaceutical Co., Ltd. ジヒドロオロテートデヒドロゲナーゼ阻害活性を有する新規複素環アミド誘導体
EP1804782A1 (en) 2004-10-19 2007-07-11 Aventis Pharmaceuticals Inc. Use of (z)-2-cyano-3-hydroxy-but-2-enoic acid-(4'-trifluoromethylphenyl)-amide for treating inflammatory bowel disease
JP2007015952A (ja) * 2005-07-06 2007-01-25 Shionogi & Co Ltd ナフタレン誘導体
ES2303758B1 (es) 2006-02-20 2009-08-13 Laboratorios Almirall S.A. Nuevos derivados de piridin-3-amina.
ES2301380B1 (es) 2006-08-09 2009-06-08 Laboratorios Almirall S.A. Nuevos derivados de 1,7-naftiridina.
ES2319596B1 (es) 2006-12-22 2010-02-08 Laboratorios Almirall S.A. Nuevos derivados de los acidos amino-nicotinico y amino-isonicotinico.
UY31272A1 (es) * 2007-08-10 2009-01-30 Almirall Lab Nuevos derivados de ácido azabifenilaminobenzoico

Also Published As

Publication number Publication date
PL2406225T3 (pl) 2013-12-31
MY155140A (en) 2015-09-15
HRP20130851T1 (hr) 2013-10-25
TWI428127B (zh) 2014-03-01
ZA201105744B (en) 2012-04-25
AR075738A1 (es) 2011-04-20
CN102348689B (zh) 2014-05-14
PE20120171A1 (es) 2012-03-01
KR20110126694A (ko) 2011-11-23
IL214519A (en) 2015-03-31
HK1162487A1 (en) 2012-08-31
IL214519A0 (en) 2011-09-27
UY32467A (es) 2010-05-31
DK2406225T3 (da) 2013-09-30
CN102348689A (zh) 2012-02-08
EP2406225A1 (en) 2012-01-18
TW201034669A (en) 2010-10-01
US20120014918A1 (en) 2012-01-19
JP2012520252A (ja) 2012-09-06
WO2010102826A1 (en) 2010-09-16
BRPI1006766B8 (pt) 2021-05-25
ES2428746T3 (es) 2013-11-11
EA022350B1 (ru) 2015-12-30
BRPI1006766B1 (pt) 2021-03-23
UA105786C2 (uk) 2014-06-25
AU2010223528A1 (en) 2011-08-25
MX2011009146A (es) 2011-09-15
CY1114418T1 (el) 2016-08-31
JP5674685B2 (ja) 2015-02-25
PT2406225E (pt) 2013-09-19
AU2010223528B2 (en) 2017-02-16
SG173823A1 (en) 2011-09-29
EA201101297A1 (ru) 2012-04-30
RS52949B (en) 2014-02-28
EP2406225B1 (en) 2013-06-26
CA2754804A1 (en) 2010-09-16
EP2228367A1 (en) 2010-09-15
KR101674699B1 (ko) 2016-11-09
CA2754804C (en) 2018-07-24
ME01564B (me) 2014-09-20
ECSP11011365A (es) 2011-10-31
SMT201300104B (it) 2013-11-08
CO6420337A2 (es) 2012-04-16
SI2406225T1 (sl) 2013-10-30
NZ594493A (en) 2013-11-29

Similar Documents

Publication Publication Date Title
CL2011002216A1 (es) Sal de adicion de una amina que contiene uno o mas grupos hidroxilo y/o carboxilicos con un derivado de acido aminonicotinico, composicion y combinacion farmaceuticas; y su uso para tratar artritis reumatoide, espondilitis anquilosante, esclerosis multiple, psoriasis, entre otras.
DOP2015000158A (es) Inhibidores de prmt5 y sus usos
NI201400107A (es) Compuestos de heterociclilo como inhibidores de mek
AR070221A1 (es) Derivados de ftalazinona inhibidores de polimerasas, composiciones farmaceuticas que los contienen y usos de los mismos para prevenir y/o tratar tumores cancerigenos,lesiones isquemicas y otras enfermedades asociadas.
NI201200184A (es) Morfolinopirimidinas y su uso en terapia
ECSP12012057A (es) Pirrolidinonas heteroaromáticas fusionadas
UY30977A1 (es) Derivados de isoindolinas 4&#39; -o-sustituidas. composiciones que las contienen y metodos para sus usos.
CO7111284A2 (es) Nucleósidos de espirooxetano de uracilo
SV2011004077A (es) Derivados aminobutiricos sustituidos como inhibidores de neprilisina
AR088029A1 (es) Compuestos de pirimidina sustituidos, composiciones farmaceuticas que los contienen y uso de los mismos para el tratamiento del dolor, accidentes cerebrovasculares, epilepsia y otras enfermedades del sistema nervioso central
AR077292A1 (es) Derivados de piperazin - quinolin sulfonamidas y composiciones farmaceuticas
PE20141078A1 (es) Compuestos de ester boronato y composiciones farmaceuticas de los mismos
UY31083A1 (es) Derivados de sulfoximinas para la inhibicion de b-secretasa
UY31048A1 (es) Nuevos compuestos de pirimidina y usos de los mismos
EA201390163A1 (ru) Гетеробициклические производные в качетстве ингибиторов hcv
AR078049A1 (es) Moduladores de lxr
CU20130116A7 (es) Derivados de heteroarilo como moduladores de nachr alfa 7
UY33655A (es) Co-cristales y sales de inhibidores de ccr30
CL2017002354A1 (es) Compuestos derivados de heteroarilos bicíclicos fusionados con actividad como inhibidores de phd.
MA41337A (fr) Dérivés de l&#39;hydroxyalkyl pipérazine utilisés comme modulateurs du récepteur cxcr3
UY33490A (es) Ésteres de quinolina nuevos útiles para el tratamiento de trastornos cutáneos.
UY37191A (es) Derivados de dibenzofurano para uso como inhibidores de bromodominio
CL2011002213A1 (es) Sal de adicion cristalina de (i) trometamina con (ii) un derivado de acido azabifenilaminobenzoico; composicion farmaceutica que comprende a la sal y otros agentes terapeuticos; combinacion farmaceutica; y su uso para el tratamiento de artritis reumatoide, artritis psoriasica, espondilitis anquilosante, esclerosis multiple, entre otras
UY33279A (es) Una pirimidina sustituida como un antagonista del receptor de la prostaglandina d2
AR077429A1 (es) Compuestos hidroxiasenapina sus derivados y composiciones farmaceuticas que comprenden los mismos