PE20091627A1 - 4-hidroxipirimidina-5-carboxamidas sustituidas - Google Patents
4-hidroxipirimidina-5-carboxamidas sustituidasInfo
- Publication number
- PE20091627A1 PE20091627A1 PE2009000390A PE2009000390A PE20091627A1 PE 20091627 A1 PE20091627 A1 PE 20091627A1 PE 2009000390 A PE2009000390 A PE 2009000390A PE 2009000390 A PE2009000390 A PE 2009000390A PE 20091627 A1 PE20091627 A1 PE 20091627A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- hydroxypyrimidine
- compounds
- phenylethyl
- carbonyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/02—Heterocyclic 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
- C07D401/04—Heterocyclic 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/06—Antianaemics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/14—Heterocyclic 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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
SE REFIERE A COMPUESTOS DERIVADOS DE 4-HIDROXIPIRIMIDINA-5-CARBOXAMIDA SUSTITUIDAS DE FORMULA (I) DONDE A ES HETEROCICLILO OPCIONALMENTE SUSTITUIDO CON R9, DONDE R9 ES OH, HALOGENO, OXO, ALQUILO(C1-C6), ENTRE OTROS; R1 ES -ALQUIL(C1-C10), -ALQUIL(C1-C10)-CICLOALQUILO(C3-C10), -ALQUENIL(C2-C10), ENTRE OTROS; R2 ES H, -ALQUIL(C1-C10), -O-ALQUILARIL(C1-C10), ARILO, ENTRE OTROS; R3 ES H, OH, HALOGENO, ALCOXI(C1-C6), ENTRE OTROS; R4 ES H, -ALQUIL(C1-C10), -ALQUENIL(C2-C10), -CICLOALQUIL(C3-C10), ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 2-(4-BROMOPIRIDIN-2-IL)-4-HIDROXI-N-(1-METIL-1-FENILETIL)PIRIMIDINA-5-CARBOXAMIDA, ACIDO 2-(4-HIDROXI-5-{[(1-METIL-1-FENILETIL)AMINO]CARBONIL}PIRIMIDIN-2-IL)ISONICOTINICO, ACIDO 6-(5-{[(4-FLUOROBENCIL)AMINO]CARBONIL}-4-HIDROXIPIRIMIDIN-2-IL)NICOTINICO, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA PROLILHIDROXILASA DEL FACTOR INDUCIBLE POR HIPOXIA (HIF) PARA POTENCIAR LA PRODUCCION ENDOGENA DE ERITROPOYETINA SIENDO UTILES PARA EL TRATAMIENTO DE ANEMIA, ISQUEMIA
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US6986408P | 2008-03-18 | 2008-03-18 | |
US19291808P | 2008-09-23 | 2008-09-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20091627A1 true PE20091627A1 (es) | 2009-10-30 |
Family
ID=40627533
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2009000390A PE20091627A1 (es) | 2008-03-18 | 2009-03-17 | 4-hidroxipirimidina-5-carboxamidas sustituidas |
Country Status (13)
Country | Link |
---|---|
US (1) | US8278304B2 (es) |
EP (1) | EP2257539B1 (es) |
JP (1) | JP5557832B2 (es) |
CN (1) | CN102036981B (es) |
AR (1) | AR070925A1 (es) |
AU (1) | AU2009225869B2 (es) |
CA (1) | CA2718528C (es) |
CL (1) | CL2009000639A1 (es) |
ES (1) | ES2524883T3 (es) |
MX (1) | MX2010010209A (es) |
PE (1) | PE20091627A1 (es) |
TW (1) | TW200944511A (es) |
WO (1) | WO2009117269A1 (es) |
Families Citing this family (42)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8759345B2 (en) | 2008-04-28 | 2014-06-24 | Janssen Pharmaceutica Nv | Benzoimidazoles as prolyl hydroxylase inhibitors |
AU2009272486A1 (en) * | 2008-07-18 | 2010-01-21 | Takeda Pharmaceutical Company Limited. | Benzazepine derivatives and their use as hstamine H3 antagonists |
US8937078B2 (en) | 2009-02-10 | 2015-01-20 | Janssen Pharmaceutica Nv | Quinazolinones as prolyl hydroxylase inhibitors |
AU2010266559A1 (en) | 2009-06-30 | 2011-12-15 | Merck Sharp & Dohme Corp. | Substituted 4-hydroxypyrimidine-5-carboxamides |
EP2448583B1 (en) * | 2009-06-30 | 2014-06-25 | Merck Sharp & Dohme Corp. | Substituted 4-hydroxypyrimidine-5-carboxamides |
AR077999A1 (es) * | 2009-09-02 | 2011-10-05 | Vifor Int Ag | Antagonistas de pirimidin y triazin-hepcidina |
DK2488486T3 (da) * | 2009-10-13 | 2019-11-18 | Ligand Pharm Inc | Småmolekylære forbindelser der efterligner hæmapoetisk vækstfaktor og anvendelse deraf |
US20120202787A1 (en) * | 2009-10-20 | 2012-08-09 | Pfizer Inc. | Novel Heteroaryl Imidazoles And Heteroaryl Triazoles As Gamma-Secretase Modulators |
DK2492266T3 (en) * | 2009-10-21 | 2015-12-07 | Daiichi Sankyo Co Ltd | 5-hydroxypyrimidine-4-carboxamide |
WO2011083314A1 (en) * | 2010-01-08 | 2011-07-14 | Takeda Pharmaceutical Company Limited | Benzazepine derivatives for the treatment of central nervous system disorders |
WO2011133444A1 (en) | 2010-04-21 | 2011-10-27 | Merck Sharp & Dohme Corp. | Substituted pyrimidines |
UY33469A (es) * | 2010-06-29 | 2012-01-31 | Irm Llc Y Novartis Ag | Composiciones y metodos para modular la via de señalizacion de wnt |
US8796263B2 (en) | 2010-08-13 | 2014-08-05 | Janssen Pharmaceutica Nv | 4-aminoquinazolin-2-yl-1-pyrrazole-4-carboxylic acid compounds as prolyl hydroxylase inhibitors |
CA2813708C (en) * | 2010-10-18 | 2019-09-17 | Raqualia Pharma Inc. | Arylamide derivatives as ttx-s blockers |
GB201102659D0 (en) | 2011-02-15 | 2011-03-30 | Isis Innovation | Assay |
CA2839699A1 (en) * | 2011-06-24 | 2012-12-27 | Amgen Inc. | Trpm8 antagonists and their use in treatments |
MX2013015058A (es) | 2011-06-24 | 2014-01-20 | Amgen Inc | Antagonistas de melastatina 8 de potencial receptor transitorio y su uso en tratamientos. |
GB201113101D0 (en) | 2011-07-28 | 2011-09-14 | Isis Innovation | Assay |
EP2753176A4 (en) * | 2011-09-06 | 2015-10-21 | New York Blood Ct Inc | HIV INHIBITORS |
WO2013040789A1 (en) * | 2011-09-23 | 2013-03-28 | Merck Sharp & Dohme Corp. | Substituted pyrimidines |
WO2013043624A1 (en) | 2011-09-23 | 2013-03-28 | Merck Sharp & Dohme Corp. | Substituted pyrimidines |
WO2013040790A1 (en) * | 2011-09-23 | 2013-03-28 | Merck Sharp & Dohme Corp. | Substituted pyrimidines |
WO2013043621A1 (en) | 2011-09-23 | 2013-03-28 | Merck Sharp & Dohme Corp. | Substituted pyrimidines |
EP2776023B1 (en) | 2011-10-25 | 2016-03-09 | Janssen Pharmaceutica, N.V. | Meglumine salt formulations of 1-(5,6-dichloro-1h-benzo[d]imidazol-2-yl)-1h-pyrazole-4-carboxylic acid |
CN104334528A (zh) | 2012-03-30 | 2015-02-04 | 第一三共株式会社 | (2-杂芳基氨基)琥珀酸衍生物 |
CN103450194B (zh) * | 2012-06-05 | 2015-07-08 | 首都医科大学 | 四氢-β-咔啉-3-甲酰脂肪链胺、其制备、纳米结构、免疫抑制作用及应用 |
US8952009B2 (en) | 2012-08-06 | 2015-02-10 | Amgen Inc. | Chroman derivatives as TRPM8 inhibitors |
PE20151860A1 (es) * | 2013-03-29 | 2015-12-16 | Takeda Pharmaceutical | Derivados de 6-(5-hidroxi-1h-pirazol-1-il)nicotinamida y su uso como inhidores de la phd |
US10226449B2 (en) | 2013-12-20 | 2019-03-12 | 3-V Biosciences, Inc. | Heterocyclic modulators of lipid synthesis and combinations thereof |
JP2017114765A (ja) * | 2014-04-25 | 2017-06-29 | 大正製薬株式会社 | トリアゾリルで置換されたヘテロアリール化合物 |
US10137107B2 (en) | 2014-09-19 | 2018-11-27 | New York Blood Center, Inc. | Substituted phenylpyrrolecarboxamides with therapeutic activity in HIV |
KR102307037B1 (ko) * | 2014-09-29 | 2021-09-30 | 더 스크립스 리서치 인스티튜트 | 심폐 장애들의 치료를 위한 스핑고신-1-포스페이트 수용체 조절제들 |
WO2016054804A1 (en) * | 2014-10-10 | 2016-04-14 | Merck Sharp & Dohme Corp. | Substituted pyrimidines as inhibitors of hif prolyl hydroxylase |
CN111349077B (zh) * | 2019-02-02 | 2022-06-28 | 杭州华东医药集团新药研究院有限公司 | 一种哒嗪衍生物及其制备方法和医药用途 |
GB201908511D0 (en) * | 2019-06-13 | 2019-07-31 | Adorx Therapeutics Ltd | Hydroxamate compounds |
KR20230049673A (ko) * | 2020-09-25 | 2023-04-13 | 상하이 메이유에 바이오테크 디벨롭먼트 컴퍼니 리미티드 | 피리미딘 카르복스아미드 화합물 및 이의 용도 |
AU2021404895A1 (en) | 2020-12-21 | 2023-06-29 | Intervet International B.V. | A process for the preparation of n-(bis(4-methoxyphenyl)methyl)-6-oxo-2-(pyridazin-3-yl)-1,6-dihydropyrimidine-5-carboxamide |
CN114835687B (zh) * | 2021-04-02 | 2023-09-05 | 北京华森英诺生物科技有限公司 | AhR抑制剂 |
TW202321211A (zh) | 2021-08-10 | 2023-06-01 | 美商艾伯維有限公司 | 菸鹼醯胺ripk1抑制劑 |
EP4413000A1 (en) | 2021-10-04 | 2024-08-14 | FoRx Therapeutics AG | N,n-dimethyl-4-(7-(n-(1-methylcyclopropyl)sulfamoyl)-imidazo[1,5-a]pyridin-5-yl)piperazine-1-carboxamide derivatives and the corresponding pyrazolo[1,5-a]pyridine derivatives as parg inhibitors for the treatment of cancer |
GB202301059D0 (en) * | 2023-01-25 | 2023-03-08 | Univ Oxford Innovation Ltd | PHD inhibitors |
GB202301050D0 (en) * | 2023-01-25 | 2023-03-08 | Univ Oxford Innovation Ltd | PHD Inhibitors |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2853220A1 (de) * | 1978-12-09 | 1980-07-03 | Hoechst Ag | Neue amino-pyrimidin-carbanilide, verfahren zu ihrer herstellung, diese verbindungen enthaltende arzneimittel und ihre verwendung |
EP0557879B1 (de) * | 1992-02-22 | 1997-01-08 | Hoechst Aktiengesellschaft | 4-Amino-2-ureido-pyrimidin-5-carbonsäureamide, Verfahren zu deren Herstellung, diese Verbindungen enthaltende Arzneimittel und deren Verwendung |
AU767558B2 (en) * | 1999-09-16 | 2003-11-13 | Mitsubishi Tanabe Pharma Corporation | Aromatic nitrogenous six-membered ring compounds |
WO2001027105A1 (fr) * | 1999-10-12 | 2001-04-19 | Takeda Chemical Industries, Ltd. | Composes de pyrimidine-5-carboxamide, procede de preparation et d'utilisation desdits composes |
US7273868B2 (en) * | 2000-04-28 | 2007-09-25 | Tanabe Seiyaku Co., Ltd. | Pyrazine derivatives |
JP2004501191A (ja) * | 2000-06-28 | 2004-01-15 | テバ ファーマシューティカル インダストリーズ リミティド | カルベジロール |
AU2002230217B2 (en) * | 2001-02-15 | 2005-02-17 | Tanabe Seiyaku Co., Ltd. | Tablets quickly disintegrated in oral cavity |
PL372944A1 (en) * | 2001-02-20 | 2005-08-08 | Bristol-Myers Squibb Company | 2,4-disubstituted pyrimidine-5-carboxamide derivatives as kcnq potassium channel modulators |
ATE365732T1 (de) | 2003-10-31 | 2007-07-15 | Warner Lambert Co | Pyrimidine als inhibitoren von phosphoinositid-3- kinasen (pi3k) |
US7091202B2 (en) * | 2004-09-15 | 2006-08-15 | Bristol-Myers Squibb Company | 4-arylspirocycloalkyl-2-aminopyrimidine carboxamide KCNQ potassium channel modulators |
ZA200802411B (en) * | 2005-09-15 | 2009-09-30 | Orchid Res Lab Ltd | Novel pyrimidine carboxamides |
BRPI0620668A2 (pt) * | 2005-12-14 | 2011-11-22 | Du Pont | composto da fórmula 1, composição que compreende composto, composição de controle de pragas invertebradas, composição de pulverização, composição de isca, dispositivo de armadilha, métodos de controle de pragas invertebradas, método de controle de baratas, formigas ou cupins e método de proteção de sementes contra pragas invertebradas |
JP5161793B2 (ja) * | 2006-01-27 | 2013-03-13 | フィブロジェン, インコーポレイテッド | 低酸素症誘導因子(hif)を安定化するシアノイソキノリン化合物 |
WO2007136990A2 (en) * | 2006-05-16 | 2007-11-29 | Smithkline Beecham Corporation | Prolyl hydroxylase inhibitors |
PE20080209A1 (es) * | 2006-06-23 | 2008-05-15 | Smithkline Beecham Corp | Derivados de glicina como inhibidores de prolil hidroxilasa |
EP4095127A1 (en) * | 2006-06-26 | 2022-11-30 | Akebia Therapeutics Inc. | Prolyl hydroxylase inhibitors and methods of use |
US20100029609A1 (en) * | 2006-09-08 | 2010-02-04 | Frederic Berst | Biaryl sulfonamide derivatives |
-
2009
- 2009-03-09 CN CN200980118093.5A patent/CN102036981B/zh active Active
- 2009-03-09 MX MX2010010209A patent/MX2010010209A/es not_active Application Discontinuation
- 2009-03-09 CA CA2718528A patent/CA2718528C/en active Active
- 2009-03-09 AU AU2009225869A patent/AU2009225869B2/en active Active
- 2009-03-09 WO PCT/US2009/036501 patent/WO2009117269A1/en active Application Filing
- 2009-03-09 EP EP09722697.1A patent/EP2257539B1/en active Active
- 2009-03-09 ES ES09722697.1T patent/ES2524883T3/es active Active
- 2009-03-09 JP JP2011500864A patent/JP5557832B2/ja active Active
- 2009-03-12 US US12/381,468 patent/US8278304B2/en active Active
- 2009-03-17 AR ARP090100958A patent/AR070925A1/es unknown
- 2009-03-17 PE PE2009000390A patent/PE20091627A1/es not_active Application Discontinuation
- 2009-03-17 CL CL2009000639A patent/CL2009000639A1/es unknown
- 2009-03-17 TW TW098108639A patent/TW200944511A/zh unknown
Also Published As
Publication number | Publication date |
---|---|
CL2009000639A1 (es) | 2009-07-17 |
AU2009225869A1 (en) | 2009-09-24 |
CN102036981B (zh) | 2015-04-08 |
ES2524883T3 (es) | 2014-12-15 |
AU2009225869B2 (en) | 2014-01-23 |
EP2257539A1 (en) | 2010-12-08 |
AR070925A1 (es) | 2010-05-12 |
US20090239876A1 (en) | 2009-09-24 |
CA2718528C (en) | 2016-10-25 |
CA2718528A1 (en) | 2009-09-24 |
EP2257539B1 (en) | 2014-09-10 |
JP5557832B2 (ja) | 2014-07-23 |
CN102036981A (zh) | 2011-04-27 |
MX2010010209A (es) | 2010-10-05 |
JP2011515402A (ja) | 2011-05-19 |
US8278304B2 (en) | 2012-10-02 |
WO2009117269A1 (en) | 2009-09-24 |
TW200944511A (en) | 2009-11-01 |
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