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PE20160839A1 - Derivados de 4-azaindol - Google Patents

Derivados de 4-azaindol

Info

Publication number
PE20160839A1
PE20160839A1 PE2016000374A PE2016000374A PE20160839A1 PE 20160839 A1 PE20160839 A1 PE 20160839A1 PE 2016000374 A PE2016000374 A PE 2016000374A PE 2016000374 A PE2016000374 A PE 2016000374A PE 20160839 A1 PE20160839 A1 PE 20160839A1
Authority
PE
Peru
Prior art keywords
halogen
alkyl
azaindol
compounds
hydroxyclohexyl
Prior art date
Application number
PE2016000374A
Other languages
English (en)
Inventor
Louise Michelle Birch
Alan James Braunton
Pineiro Jose Luis Castro
Motohiro Soejima
James Edward Kitulagoda
Andrew Payne
Afzal Khan
Original Assignee
Eisai Randd Man Co 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
Application filed by Eisai Randd Man Co Ltd filed Critical Eisai Randd Man Co Ltd
Publication of PE20160839A1 publication Critical patent/PE20160839A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • 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
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • 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
    • C07D401/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Neurology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

SE REFIERE A COMPUESTOS DERIVADOS DE 4-AZAINDOL DE FORMULAS (IA) Y (IB) DONDE R1 ES H, HALOGENO, CN, ENTRE OTROS; R2 ES H; p ES 1 O 2; R4 ES HALOGENO, ALQUILO C1-C4, ALCOXI C1-C4, ENTRE OTROS, EN LA FORMULA (IA); Y PARA LA FORMULA (IB) R1 ES ALQUILO C1-C4, ALCOXI C1-C4, ENTRE OTROS; R2 ES H; R4a ES H O HALOGENO; R4b ES H, HALOGENO, ALQUILO C1-C4, ENTRE OTROS; R4c ES H, HALOGENO, HALOALQUILO C1-C4, ENTRE OTROS; R4d ES H O HALOGENO. SON COMPUESTOS PREFERIDOS: 1-(4-FLUOROBENCIL)-N-((1S-2S)-2-HIDROXICICLOHEXIL)-7-METIL-1H-PIRROL[3,2-b]PIRIDINA-3-CARBOXAMIDA; 1-(3-FLUOROBENCIL)-N-((1S-2S)-2-HIDROXICICLOHEXIL)-1H-PIRROL[3,2-b]PIRIDINA-3-CARBOXAMIDA; ENTRE OTROS. TAMBIEN SE REFIERE A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON MODULADORES DEL RECEPTOR DE ACETILCOLINA MUSCARINICO M1 (mAChR) SIENDO UTILES EN EL TRATAMIENTO DE DEMENCIA TIPO ALZHEIMER
PE2016000374A 2013-10-01 2014-09-30 Derivados de 4-azaindol PE20160839A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB1317363.8A GB201317363D0 (en) 2013-10-01 2013-10-01 Novel compounds

Publications (1)

Publication Number Publication Date
PE20160839A1 true PE20160839A1 (es) 2016-08-20

Family

ID=49585123

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2016000374A PE20160839A1 (es) 2013-10-01 2014-09-30 Derivados de 4-azaindol

Country Status (21)

Country Link
US (3) US9926312B2 (es)
EP (2) EP3052496B1 (es)
JP (3) JP6517790B2 (es)
KR (1) KR102248559B1 (es)
CN (1) CN105873927B (es)
AR (1) AR097866A1 (es)
AU (1) AU2014330880B2 (es)
BR (1) BR112016007016A8 (es)
CA (1) CA2924619C (es)
CL (1) CL2016000726A1 (es)
ES (2) ES2710190T3 (es)
GB (1) GB201317363D0 (es)
HK (1) HK1223090A1 (es)
IL (1) IL244609B (es)
MX (1) MX368956B (es)
PE (1) PE20160839A1 (es)
PH (1) PH12016500529A1 (es)
RU (1) RU2688938C2 (es)
SG (1) SG11201602052YA (es)
TW (1) TW201546070A (es)
WO (1) WO2015049574A1 (es)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2592078A1 (en) 2011-11-11 2013-05-15 Almirall, S.A. New cyclohexylamine derivatives having beta2 adrenergic agonist and M3 muscarinic antagonist activities
TW201517906A (zh) 2013-07-25 2015-05-16 Almirall Sa 含有maba化合物和皮質類固醇之組合
GB201317363D0 (en) 2013-10-01 2013-11-13 Eisai Ltd Novel compounds
WO2015163485A1 (en) 2014-04-23 2015-10-29 Takeda Pharmaceutical Company Limited Isoindoline-1-one derivatives as cholinergic muscarinic m1 receptor positive alloesteric modulator activity for the treatment of alzheimers disease
JP6531093B2 (ja) 2014-05-16 2019-06-12 武田薬品工業株式会社 含窒素複素環化合物
TW201617343A (zh) 2014-09-26 2016-05-16 阿爾米雷爾有限公司 具有β2腎上腺素促效劑及M3蕈毒拮抗劑活性之新穎雙環衍生物
MA43913B1 (fr) * 2015-06-08 2019-05-31 Suven Life Sciences Ltd Modulateurs allostériques positifs du récepteur m1 muscarinique
PT3347349T (pt) * 2015-09-10 2019-10-30 Suven Life Sciences Ltd Derivados de fluoroindole como moduladores alostéricos positivos para recetor m1 muscarínico
MX385975B (es) 2016-02-16 2025-03-18 Univ Vanderbilt Moduladores alostéricos positivos del receptor de acetilcolina muscarínico m1.
US10899759B2 (en) 2016-09-30 2021-01-26 Vanderbilt University Positive allosteric modulators of the muscarinic acetylcholine receptor M1
MX2020003832A (es) * 2017-10-18 2020-08-06 Suven Life Sciences Ltd Compuestos heteroarilos como moduladores alostericos positivos del receptor muscarinico m1.
KR102406885B1 (ko) * 2017-10-27 2022-06-08 수벤 라이프 사이언시스 리미티드 무스카린 m1 수용체 양성 알로스테릭 조절제로서 다환형 아미드
US12065433B2 (en) 2018-10-24 2024-08-20 Vanderbilt University Positive allosteric modulators of the muscarinic acetylcholine receptor M1
KR102347368B1 (ko) * 2020-11-03 2022-01-07 (주)케이메디켐 신규한 아자인돌 유도체, 이의 제조방법 및 이를 포함하는 인지기능 개선용 조성물
CN118440041B (zh) * 2024-07-02 2024-09-27 苏州凯瑞医药科技有限公司 一种手性4-氨基-3-羟基四氢吡喃的制备方法

Family Cites Families (55)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9420521D0 (en) 1994-10-12 1994-11-30 Smithkline Beecham Plc Novel compounds
US6063930A (en) 1996-04-03 2000-05-16 Merck & Co., Inc. Substituted imidazole compounds useful as farnesyl-protein transferase inhibitors
US7868204B2 (en) 2001-09-14 2011-01-11 Methylgene Inc. Inhibitors of histone deacetylase
JP2005516901A (ja) 2001-11-19 2005-06-09 ニューロジェン コーポレイション 1H−ピロロ[3,2−b]ピリジン−3−カルボン酸アミド化合物
GB0222743D0 (en) 2002-10-01 2002-11-06 Celltech R&D Ltd Chemical compounds
AR043633A1 (es) 2003-03-20 2005-08-03 Schering Corp Ligandos de receptores de canabinoides
DE602004027171D1 (de) 2003-04-11 2010-06-24 High Point Pharmaceuticals Llc Verbindungen mit Aktivität an der 11Beta-Hydroxasteroiddehydrogenase
JP2006522744A (ja) 2003-04-11 2006-10-05 ノボ ノルディスク アクティーゼルスカブ グルココルチコイド受容体アゴニスト療法に伴う副作用を最小化するための、11β−ヒドロキシステロイドデヒドロゲナーゼ1型阻害剤およびグルココルチコイド受容体アゴニストを使用する併用療法
JP2006522750A (ja) 2003-04-11 2006-10-05 ノボ ノルディスク アクティーゼルスカブ 代謝性症候群ならびに関連の疾患および障害を治療するために、11β−ヒドロキシステロイドデヒドロゲナーゼ1型阻害剤および抗高血圧剤を使用する併用療法
EP1853261B1 (de) 2005-03-03 2017-01-11 Universität des Saarlandes Selektive hemmstoffe humaner corticoidsynthasen
FR2890072A1 (fr) * 2005-09-01 2007-03-02 Fournier S A Sa Lab Nouveaux composesde pyrrolopyridine
WO2007084667A2 (en) 2006-01-19 2007-07-26 Osi Pharmaceutical, Inc. Fused heterobicyclic kinase inhibitors
US7964728B2 (en) 2006-07-06 2011-06-21 Solvay Pharmaceuticals B.V. Azaindole derivatives with a combination of partial nicotinic acetyl-choline receptor agonism and dopamine reuptake inhibition
WO2008067566A1 (en) 2006-11-30 2008-06-05 Amira Pharmaceuticals, Inc. Compositions and treatments comprising 5-lipoxygenase-activating protein inhibitors and nitric oxide modulators
NZ582056A (en) 2007-08-10 2012-08-31 Lundbeck & Co As H Bicyclic heteroaryl compounds for treating conditions related to p2x7 receptor activation
KR20100065167A (ko) 2007-08-29 2010-06-15 쉐링 코포레이션 바이러스 감염 치료용 2,3-치환된 아자인돌 유도체
AU2009206580A1 (en) 2008-01-25 2009-07-30 Merck Sharp & Dohme Corp. Quinolizidinone M1 receptor positive allosteric modulators
CA2712701A1 (en) 2008-01-31 2009-08-06 Henning Steinhagen Cyclic azaindole-3-carboxamides, their preparation and their use as pharmaceuticals
WO2009121033A2 (en) 2008-03-27 2009-10-01 University Of Southern California Substituted nitrogen heterocycles and synthesis and uses thereof
US20100305120A1 (en) 2008-04-04 2010-12-02 Biomarin Iga Limited Compounds for treating muscular dystrophy
US8012992B2 (en) 2008-06-30 2011-09-06 Allergan, Inc. Aza-indoles and related compounds having sphingosine-1-phosphate (S1P) receptor antagonist biological activity
EP2326631A4 (en) 2008-08-18 2012-03-21 Univ Yale MIF MODULATORS
WO2010033980A2 (en) 2008-09-22 2010-03-25 Isis Innovation Ltd. 4-azaindole bisphosphonates
CN102292323B (zh) 2008-11-20 2014-12-24 默沙东公司 芳基甲基苯并喹唑啉酮 m1受体正向变构调节剂
CA2744507A1 (en) 2008-12-05 2010-06-10 F.Hoffmann-La Roche Ag Pyrrolopyrazinyl urea kinase inhibitors
EP2370407B1 (en) 2008-12-19 2014-06-18 Bristol-Myers Squibb Company Carbazole and carboline kinase inhibitors
AU2010216263A1 (en) 2009-02-23 2011-07-14 Merck Sharp & Dohme Corp. Pyrazolo [4,3-c] cinnolin-3-one M1 receptor positive allosteric modulators
EP2421366B1 (en) 2009-04-20 2013-08-28 Merck Sharp & Dohme Corp. Heterocyclic fused cinnoline m1 receptor positive allosteric modulators
JP2012211085A (ja) 2009-08-12 2012-11-01 Kyowa Hakko Kirin Co Ltd ヘッジホッグシグナル阻害剤
CA2771939A1 (en) * 2009-08-26 2011-03-03 Nycomed Gmbh Methylpyrrolopyridinecarboxamides
HUE026296T2 (en) 2009-08-31 2016-06-28 Merck Sharp & Dohme Positive allosteric pyranyl arylmethyl benzoquinazolinone M1 receptor modulators
US8664387B2 (en) * 2009-12-14 2014-03-04 Merck Sharp & Dohme Corp. Pyridoquinazolinone M1 receptor positive allosteric modulators
ES2575154T3 (es) * 2009-12-17 2016-06-24 Merck Sharp & Dohme Corp. Moduladores alostéricos positivos del receptor M1 de quinolina amida
EP2515656B1 (en) 2009-12-21 2014-08-06 Merck Sharp & Dohme Corp. Aminobenzoquinazolinone m1 receptor positive allosteric modulators
CN102770431A (zh) 2009-12-23 2012-11-07 赛诺菲 [4[4-(5-氨基甲基-2-氟-苯基)-哌啶-1-基]-(1h-吡咯并吡啶-基)-甲酮及其合成
WO2011149801A1 (en) 2010-05-28 2011-12-01 Merck Sharp & Dohme Corp. Naphthalene carboxamide m1 receptor positive allosteric modulators
EP2582241B1 (en) * 2010-06-15 2016-04-06 Merck Sharp & Dohme Corp. Heterocyclic fused phenanthrolinone m1 receptor positive allosteric modulators
EP2582676B1 (en) * 2010-06-15 2016-12-14 Merck Sharp & Dohme Corp. Tetrahydroquinoline amide m1 receptor positive allosteric modulators
EP2588104B1 (en) 2010-07-01 2014-12-10 Merck Sharp & Dohme Corp. Isoindolone m1 receptor positive allosteric modulators
WO2012016133A2 (en) 2010-07-29 2012-02-02 President And Fellows Of Harvard College Ros1 kinase inhibitors for the treatment of glioblastoma and other p53-deficient cancers
WO2012047702A1 (en) 2010-10-04 2012-04-12 Merck Sharp & Dohme Corp. Dihydrobenzoquinazolinone m1 receptor positive allosteric modulators
AR084433A1 (es) 2010-12-22 2013-05-15 Ironwood Pharmaceuticals Inc Inhibidores de la faah y composiciones farmaceuticas que los contienen
WO2012112933A1 (en) 2011-02-18 2012-08-23 The Scripps Research Institute Directed differentiation of oligodendrocyte precursor cells to a myelinating cell fate
US9464065B2 (en) 2011-03-24 2016-10-11 The Scripps Research Institute Compounds and methods for inducing chondrogenesis
US20130072473A1 (en) 2011-05-09 2013-03-21 Proteostasis Therapeutics, Inc. Compounds for treating protein folding disorders
EP2709621B1 (en) 2011-05-17 2016-11-02 Merck Sharp & Dohme Corp. N-linked quinolineamide m1 receptor positive allosteric modulators
EP2709451B1 (en) 2011-05-17 2015-12-30 Merck Sharp & Dohme Corp. N-linked lactam m1 receptor positive allosteric modulators
EP2709624B1 (en) 2011-05-17 2016-04-27 Merck Sharp & Dohme Corp. N-methyl tetrahydroquinoline m1 receptor positive allosteric modulators
US9586964B2 (en) 2011-10-28 2017-03-07 Vanderbilt University Substituted 2-(4-heterocyclylbenzyl)isoindolin-1-one analogs as positive allosteric modulators of the muscarinic acetylcholine receptor M1
CN104039789B (zh) 2011-12-22 2016-09-07 默克专利股份有限公司 四氮杂-环戊二烯并[a]茚基及其作为正向变构调节剂的用途
WO2013106795A1 (en) 2012-01-12 2013-07-18 Vanderbilt University Substituted 4-(1h~pyrazol-4.yl)benzyl analogues as positive allosteric modulators of machr m1 receptors
US9163020B2 (en) * 2013-07-17 2015-10-20 Global Alliance For Tb Drug Development Azaindole compounds, synthesis thereof, and methods of using the same
TW201512197A (zh) * 2013-08-30 2015-04-01 Hoffmann La Roche 吡咯并吡啶或吡唑并吡啶衍生物
CA2918925A1 (en) * 2013-09-27 2015-04-02 F. Hoffmann-La Roche Ag Indol and indazol derivatives
GB201317363D0 (en) 2013-10-01 2013-11-13 Eisai Ltd Novel compounds

Also Published As

Publication number Publication date
EP3489237B1 (en) 2020-05-13
ES2710190T3 (es) 2019-04-23
HK1223090A1 (zh) 2017-07-21
RU2016116775A3 (es) 2018-06-27
MX368956B (es) 2019-10-23
JP2020143100A (ja) 2020-09-10
CN105873927A (zh) 2016-08-17
TW201546070A (zh) 2015-12-16
BR112016007016A8 (pt) 2020-02-27
CA2924619A1 (en) 2015-04-09
RU2688938C2 (ru) 2019-05-23
AU2014330880B2 (en) 2019-01-31
US20150094328A1 (en) 2015-04-02
KR102248559B1 (ko) 2021-05-04
MX2016004014A (es) 2016-09-21
SG11201602052YA (en) 2016-04-28
JP2019112433A (ja) 2019-07-11
AU2014330880A1 (en) 2016-04-07
IL244609A0 (en) 2016-04-21
IL244609B (en) 2019-12-31
US10072005B2 (en) 2018-09-11
PH12016500529A1 (en) 2016-05-16
EP3052496A1 (en) 2016-08-10
BR112016007016A2 (pt) 2017-08-01
EP3052496B1 (en) 2018-11-28
US20180208593A1 (en) 2018-07-26
EP3489237A1 (en) 2019-05-29
US9926312B2 (en) 2018-03-27
GB201317363D0 (en) 2013-11-13
CL2016000726A1 (es) 2016-09-23
ES2807221T3 (es) 2021-02-22
CN105873927B (zh) 2017-11-28
CA2924619C (en) 2021-12-07
JP6517790B2 (ja) 2019-05-22
JP6899944B2 (ja) 2021-07-07
JP2016531890A (ja) 2016-10-13
KR20160072133A (ko) 2016-06-22
RU2016116775A (ru) 2017-11-09
WO2015049574A1 (en) 2015-04-09
AR097866A1 (es) 2016-04-20
US20160244445A1 (en) 2016-08-25

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