PE20040913A1 - Enantiomeros (r) y (s) de derivados del acido tiofeno hidroxamico como inhibidores de desacetilasa histona (hdac) - Google Patents
Enantiomeros (r) y (s) de derivados del acido tiofeno hidroxamico como inhibidores de desacetilasa histona (hdac)Info
- Publication number
- PE20040913A1 PE20040913A1 PE2003001262A PE2003001262A PE20040913A1 PE 20040913 A1 PE20040913 A1 PE 20040913A1 PE 2003001262 A PE2003001262 A PE 2003001262A PE 2003001262 A PE2003001262 A PE 2003001262A PE 20040913 A1 PE20040913 A1 PE 20040913A1
- Authority
- PE
- Peru
- Prior art keywords
- thiophene
- hydroxamic
- inhibitors
- desacetilase
- hdac
- Prior art date
Links
- 239000002253 acid Substances 0.000 title abstract 5
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 title abstract 4
- 239000003112 inhibitor Substances 0.000 title abstract 3
- NEAQRZUHTPSBBM-UHFFFAOYSA-N 2-hydroxy-3,3-dimethyl-7-nitro-4h-isoquinolin-1-one Chemical class C1=C([N+]([O-])=O)C=C2C(=O)N(O)C(C)(C)CC2=C1 NEAQRZUHTPSBBM-UHFFFAOYSA-N 0.000 title abstract 2
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical compound C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 title abstract 2
- 108010033040 Histones Proteins 0.000 title abstract 2
- 229930192474 thiophene Natural products 0.000 title abstract 2
- 102000003964 Histone deacetylase Human genes 0.000 title 1
- 108090000353 Histone deacetylase Proteins 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- 240000001546 Byrsonima crassifolia Species 0.000 abstract 1
- -1 HYDROXAMIC HYDROXYL Chemical class 0.000 abstract 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical group 0.000 abstract 1
- 229940126601 medicinal product Drugs 0.000 abstract 1
- 230000035755 proliferation Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 230000000707 stereoselective effect Effects 0.000 abstract 1
- 210000004881 tumor cell Anatomy 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur 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
- C07D333/38—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
SE REFIERE A LOS ENANTIOMEROS (R) Y (S) DE DERIVADOS DEL ACIDO TIOFENO HIDROXAMICO DE FORMULA I, INCLUYENDO SUS SALES FISIOLOGICAMENTE ACEPTABLES, EN DONDE Ar ES UN GRUPO ARILO O HETEROARILO QUE PUEDE ESTAR SUSTITUIDO HASTA 3 VECES O NO POR HALOGENO, FENILO, ALQUILO, ENTRE OTROS; R1 ES H, FENILO, ALQUILO O ALQUENILO QUE PUEDEN ESTAR SUSTITUIDO UNA O VARIAS VECES O NO SUSTITUIDO POR HALOGENO, OH, NO2, NH2, ENTRE OTROS; O R1 Y Ar FORMAN UN ANILLO DE TETRAHIDRONAFTALENO, INDANO o DIBENZOSUBERANO; R2 ES H o ALQUILO; n ES 1, 2 o 3. SON COMPUESTOS PREFERIDOS: 2-HIDROXIAMIDA 5-[(1-TIOFENO-2-IL-ETIL)-AMIDA] DEL ACIDO (R)-TIOFENO-2,5-DICARBOXILICO; 2-HIDROXIAMIDA 5-[(1-TIOFENO-2-IL-ETIL)-AMIDA] DEL ACIDO (S)-TIOFENO-2,5-DICARBOXILICO; 2-HIDROXIAMIDA 5-{[1-(5-METIL-TIOFENO-2-IL)-ETIL]-AMIDA} DEL ACIDO (R)-TIOFENO-2,5-DICARBOXILICO; ENTRE OTROS. TAMBIEN SE REFIERE A UN PROCEDIMIENTO PARA LA ELABORACION ESTEREOSELECTIVA DE ESTOS COMPUESTOS Y UN MEDICAMENTO QUE LOS CONTIENE. ESTOS COMPUESTOS SON INHIBIDORES DE LA DESACETILASA HISTONA (HDAC) SON UTILES COMO INHIBIDORES DE LA PROLIFERACION DE CELULAS TUMORALES
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP02028038 | 2002-12-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20040913A1 true PE20040913A1 (es) | 2005-01-18 |
Family
ID=32524005
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2003001262A PE20040913A1 (es) | 2002-12-16 | 2003-12-11 | Enantiomeros (r) y (s) de derivados del acido tiofeno hidroxamico como inhibidores de desacetilasa histona (hdac) |
Country Status (18)
Country | Link |
---|---|
US (1) | US7098241B2 (es) |
EP (1) | EP1575933A1 (es) |
JP (1) | JP2006513181A (es) |
KR (1) | KR100781929B1 (es) |
CN (1) | CN100391954C (es) |
AR (1) | AR042459A1 (es) |
AU (1) | AU2003293882A1 (es) |
BR (1) | BR0317348A (es) |
CA (1) | CA2507629A1 (es) |
CL (1) | CL2003002611A1 (es) |
GT (1) | GT200300285A (es) |
PA (1) | PA8592101A1 (es) |
PE (1) | PE20040913A1 (es) |
PL (1) | PL377696A1 (es) |
RU (1) | RU2348625C2 (es) |
TW (1) | TW200418825A (es) |
UY (1) | UY28127A1 (es) |
WO (1) | WO2004054999A1 (es) |
Families Citing this family (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AP1753A (en) * | 2001-06-11 | 2007-07-18 | Shire Biochem Inc | Thiophene derivatives as antiviral agents for flavvivirus infection |
US7154002B1 (en) | 2002-10-08 | 2006-12-26 | Takeda San Diego, Inc. | Histone deacetylase inhibitors |
US7250514B1 (en) | 2002-10-21 | 2007-07-31 | Takeda San Diego, Inc. | Histone deacetylase inhibitors |
CN100413861C (zh) | 2002-12-10 | 2008-08-27 | 维勒凯姆制药股份有限公司 | 用于治疗或预防黄病毒感染的化合物 |
US7381825B2 (en) | 2003-03-17 | 2008-06-03 | Takeda San Diego, Inc. | Histone deacetylase inhibitors |
US20050261347A1 (en) * | 2003-10-24 | 2005-11-24 | Wyeth | Dihydrobenzofuranyl alkanamine derivatives and methods for using same |
US7435837B2 (en) * | 2003-10-24 | 2008-10-14 | Wyeth | Dihydrobenzofuranyl alkanamine derivatives and methods for using same |
EP1778683A1 (en) * | 2004-06-14 | 2007-05-02 | F.Hoffmann-La Roche Ag | Thiophene derivatives, their manufacture and use as pharmaceutical agents |
JP2008501665A (ja) * | 2004-06-14 | 2008-01-24 | エフ.ホフマン−ラ ロシュ アーゲー | チオフェンヒドロキサム酸誘導体及びhdac阻害剤としてのこれらの使用 |
US7638553B2 (en) * | 2004-06-14 | 2009-12-29 | Hoffmann-La Roche Inc. | Hydroxamates, their manufacture and use as pharmaceutical agents |
US7642275B2 (en) | 2004-12-16 | 2010-01-05 | Takeda San Diego, Inc. | Histone deacetylase inhibitors |
EP1896436A2 (en) | 2005-05-11 | 2008-03-12 | Takeda San Diego, Inc. | Histone deacetylase inhibitors |
US7569600B2 (en) | 2005-05-13 | 2009-08-04 | Virochem Pharma Inc. | Compounds and methods for the treatment of prevention of Flavivirus infections |
US7732475B2 (en) | 2005-07-14 | 2010-06-08 | Takeda San Diego, Inc. | Histone deacetylase inhibitors |
GB0518237D0 (en) * | 2005-09-07 | 2005-10-19 | Angeletti P Ist Richerche Bio | Therapeutic compounds |
GB0522130D0 (en) * | 2005-10-31 | 2005-12-07 | Angeletti P Ist Richerche Bio | Therapeutic compounds |
GB0603041D0 (en) * | 2006-02-15 | 2006-03-29 | Angeletti P Ist Richerche Bio | Therapeutic compounds |
ES2423219T3 (es) | 2006-11-15 | 2013-09-18 | Vertex Pharmaceuticals (Canada) Incorporated | Análogos de tiofeno para el tratamiento o prevención de infecciones por flavivirus |
AR074797A1 (es) * | 2008-10-10 | 2011-02-16 | Japan Tobacco Inc | Compuesto de fluoreno , composiciones farmaceuticas , inhibidores de pdhk y pdhk2 , metodos de tratamiento , usos de los mismos y kit comercial |
US8546588B2 (en) * | 2010-02-26 | 2013-10-01 | Millennium Pharmaceuticals, Inc. | Substituted hydroxamic acids and uses thereof |
US20110212969A1 (en) * | 2010-02-26 | 2011-09-01 | Millennium Pharmaceuticals, Inc. | Substituted hydroxamic acids and uses thereof |
WO2012019772A1 (en) * | 2010-08-12 | 2012-02-16 | Institut De Recherche Pour Le Developpement (I.R.D) | Method for treating protozoan parasitic diseases |
US20140107166A1 (en) * | 2011-02-14 | 2014-04-17 | Dana-Farber Cancer Institute, Inc. | Histone deacetylase inhibitors and methods of use thereof |
AU2012319188B2 (en) | 2011-10-03 | 2016-11-24 | Sloan-Kettering Institute For Cancer Research | Novel molecules that selectively inhibit histone deacetylase 6 relative to histone deacetylase 1 |
EP2975028B1 (en) | 2013-03-15 | 2018-02-21 | Japan Tobacco, Inc. | Pyrazole-amide compound and medicinal uses therefor |
CN103159646B (zh) * | 2013-03-19 | 2014-10-22 | 广东药学院 | 一种异羟肟酸类化合物及其制备方法和应用 |
CA2933907A1 (en) | 2013-12-23 | 2015-07-02 | The Trustees Of Columbia University In The City Of New York | Selective hdac6 inhibitors |
US12084472B2 (en) | 2015-12-18 | 2024-09-10 | Ardelyx, Inc. | Substituted 4-phenyl pyridine compounds as non-systemic TGR5 agonists |
TW202246215A (zh) | 2015-12-18 | 2022-12-01 | 美商亞德利克斯公司 | 作為非全身tgr5促效劑之經取代之4-苯基吡啶化合物 |
MX2019001228A (es) | 2016-07-29 | 2019-06-03 | Japan Tobacco Inc | Metodo de produccion del compuesto de pirazol-amida. |
CN116120300B (zh) * | 2023-02-21 | 2024-10-15 | 贵州大学 | 一种含异羟肟酸片段的嘧啶类化合物其制备方法和应用 |
Family Cites Families (52)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE661226A (fr) | 1965-03-17 | 1965-09-17 | Acides arylacethydroxamiques, amides correspondants et procedes de preparation. | |
NL6406688A (es) * | 1964-06-05 | 1965-12-06 | ||
GB1200886A (en) * | 1966-09-23 | 1970-08-05 | Allen & Hanburys Ltd | Phenylaminoethanol derivatives |
NL7614113A (nl) | 1976-12-18 | 1978-06-20 | Akzo Nv | Hydroxamzuren. |
US4173652A (en) * | 1976-12-18 | 1979-11-06 | Akzona Incorporated | Pharmaceutical hydroxamic acid compositions and uses thereof |
JPS5436229A (en) | 1977-08-25 | 1979-03-16 | Hokuriku Pharmaceutical | Substituted acetohydroxam derivative |
JPS57145838A (en) | 1981-03-05 | 1982-09-09 | Hodogaya Chem Co Ltd | P-benzyloxybenzoic acid derivative and herbicide containing the same |
JPS57149254A (en) | 1981-03-10 | 1982-09-14 | Hodogaya Chem Co Ltd | M-benzyloxybenzamide derivative and herbicide containing the same |
GB8320702D0 (en) | 1983-08-01 | 1983-09-01 | Wellcome Found | Chemotherapeutic agents |
US4769461A (en) * | 1986-09-16 | 1988-09-06 | American Home Products Corporation | Quinolinyl benzene hydroxamic acids as anti-inflammatory/antiallergic agents |
GB8728051D0 (en) | 1987-12-01 | 1988-01-06 | Leo Pharm Prod Ltd | Chemical compounds |
JPH01216961A (ja) | 1988-02-25 | 1989-08-30 | Takeda Chem Ind Ltd | 12−リポキシゲネース阻害剤 |
DE3903989A1 (de) * | 1989-02-10 | 1990-09-20 | Basf Ag | Diphenylheteroalkylderivate, ihre herstellung und daraus hergestellte arzneimittel und kosmetika |
US5091533A (en) | 1990-03-12 | 1992-02-25 | Merck Frosst Canada, Inc. | 5-hydroxy-2,3-dihydrobenzofuran analogs as leukotriene biosynthesis inhibitors |
JPH04217950A (ja) | 1990-03-28 | 1992-08-07 | Asahi Chem Ind Co Ltd | ヒドロキサム酸誘導体および酵素阻害剤ならびに抗潰瘍剤 |
JPH03291264A (ja) | 1990-04-06 | 1991-12-20 | Japan Tobacco Inc | ジメチルアニリン誘導体、その製造方法及びそれを有効成分として含有するガン細胞分化誘導検査試薬及び制癌剤 |
JPH04187666A (ja) | 1990-11-20 | 1992-07-06 | Asahi Chem Ind Co Ltd | シクロヘキサンカルボン酸アミド誘導体及び酵素阻害剤ならびに抗潰瘍剤 |
US5369108A (en) * | 1991-10-04 | 1994-11-29 | Sloan-Kettering Institute For Cancer Research | Potent inducers of terminal differentiation and methods of use thereof |
US5700811A (en) * | 1991-10-04 | 1997-12-23 | Sloan-Kettering Institute For Cancer Research | Potent inducers of terminal differentiation and method of use thereof |
EP0544166A3 (en) * | 1991-11-26 | 1993-11-03 | Hoffmann La Roche | Cephalosporinderivatives |
EP0651772B1 (en) | 1992-07-16 | 1998-10-14 | The Dow Chemical Company | Thiodiphenol copolycarbonates and their use as components of multilayered polymeric reflective bodies |
US5783593A (en) | 1993-11-04 | 1998-07-21 | Abbott Laboratories | Inhibitors of squalene synthetase and protein farnesyltransferase |
US5776983A (en) * | 1993-12-21 | 1998-07-07 | Bristol-Myers Squibb Company | Catecholamine surrogates useful as β3 agonists |
US6008257A (en) * | 1994-01-28 | 1999-12-28 | Bayer Aktiengesellschaft | Hydroxamic-acid derivatives, method of preparing them and their use as fungicides |
GB9420557D0 (en) | 1994-10-12 | 1994-11-30 | Zeneca Ltd | Aromatic compounds |
CA2217707A1 (en) | 1995-04-10 | 1996-10-17 | Fujisawa Pharmaceutial Co., Ltd. | Indole derivatives as cgmp-pde inhibitors |
ATE212632T1 (de) | 1995-09-08 | 2002-02-15 | Univ Princeton | Nicht-klassische antifolate |
WO1997012903A1 (en) | 1995-10-04 | 1997-04-10 | Warner-Lambert Company | Compounds, compositions and methods for inhibiting the binding of proteins containing an sh2 domain to cognate phosphorylated proteins |
FR2746098B1 (fr) | 1996-03-14 | 1998-04-30 | Composes propynyl biaromatiques | |
AUPO118896A0 (en) | 1996-07-23 | 1996-08-15 | Fujisawa Pharmaceutical Co., Ltd. | New use |
EP0915832B1 (en) | 1996-08-05 | 2002-10-02 | Prolinx, Inc. | Boronic compound complexing reagents and highly stable complexes |
US6174905B1 (en) | 1996-09-30 | 2001-01-16 | Mitsui Chemicals, Inc. | Cell differentiation inducer |
JPH10114654A (ja) | 1996-10-09 | 1998-05-06 | Fujisawa Pharmaceut Co Ltd | 新規用途 |
WO1998016514A1 (en) | 1996-10-16 | 1998-04-23 | American Cyanamid Company | Ortho-sulfonamido bicyclic heteroaryl hydroxamic acids as matrix metalloproteinase and tace inhibitors |
US6392010B1 (en) * | 1996-12-19 | 2002-05-21 | Aventis Pharmaceuticals Inc. | Process for the solid phase synthesis of aldehyde, ketone, oxime, amine, hydroxamic acid and αβ-unsaturated carboxylic acid and aldehyde compounds |
JPH10182583A (ja) | 1996-12-25 | 1998-07-07 | Mitsui Chem Inc | 新規ヒドロキサム酸誘導体 |
ATE292622T1 (de) | 1997-01-22 | 2005-04-15 | Aventis Pharma Inc | Substituierte beta-thiocarbonsäuren |
TR199902095T2 (xx) | 1997-02-27 | 1999-12-21 | American Cyanamid Company | Matris metalloproteinaz �nleyicileri olarak amidler |
US6696449B2 (en) | 1997-03-04 | 2004-02-24 | Pharmacia Corporation | Sulfonyl aryl hydroxamates and their use as matrix metalloprotease inhibitors |
JPH10259176A (ja) | 1997-03-17 | 1998-09-29 | Japan Tobacco Inc | 血管新生阻害作用を有する新規アミド誘導体及びその用途 |
JPH10287634A (ja) | 1997-04-11 | 1998-10-27 | Otsuka Pharmaceut Co Ltd | ベンゼン誘導体 |
ES2174450T3 (es) | 1997-06-17 | 2002-11-01 | Schering Corp | Derivados de benzo(5,6)ciclohepta(1,2-b)piridina como inhibidores de la farnesil-protein-transferasa. |
AU749132B2 (en) | 1997-08-28 | 2002-06-20 | Biovitrum Ab | Inhibitors of protein tyrosine phosphatase |
WO1999012884A1 (fr) | 1997-09-09 | 1999-03-18 | Shionogi & Co., Ltd. | Derives d'acide benzoique a substitution en 4 et cancerostatiques renfermant ces derives comme ingredient actif |
CN1138760C (zh) | 1997-10-06 | 2004-02-18 | 惠氏控股公司 | 作为基质金属蛋白酶和tace抑制剂的邻亚磺酰氨基二环杂芳基异羟肟酸的制备和用途 |
KR100669836B1 (ko) | 1997-10-15 | 2007-01-18 | 와이어쓰 | 신규한 아릴옥시-알킬-디알킬아민 및 이의 제조 방법 |
EP1054858A1 (en) | 1998-02-19 | 2000-11-29 | American Cyanamid Company | N-hydroxy-2-(alkyl, aryl, or heteroaryl sulfanyl, sulfinyl or sulfonyl)-3-substituted-alkyl, aryl or heteroarylamides as matrix metalloproteinase inhibitors |
EP0960882A1 (en) * | 1998-05-19 | 1999-12-01 | Hoechst Marion Roussel Deutschland GmbH | Thienyl substituted acylguanidines as inhibitors of bone resorption and vitronectin receptor antagonists |
PT1233958E (pt) | 1999-11-23 | 2011-09-20 | Methylgene Inc | Inibidores de histona desacetilase |
EP1280764B1 (en) | 2000-03-24 | 2010-11-24 | Methylgene, Inc. | Inhibitors of histone deacetylase |
US6784173B2 (en) * | 2001-06-15 | 2004-08-31 | Hoffmann-La Roche Inc. | Aromatic dicarboxylic acid derivatives |
WO2003055479A1 (en) * | 2001-12-21 | 2003-07-10 | Consejo Superior De Investigaciones Cientificas | Compounds and their therapeutic use related to the phosphorylating activity of the enzyme gsk-3 |
-
2003
- 2003-12-10 TW TW092134881A patent/TW200418825A/zh unknown
- 2003-12-10 US US10/732,633 patent/US7098241B2/en not_active Expired - Fee Related
- 2003-12-11 PA PA20038592101A patent/PA8592101A1/es unknown
- 2003-12-11 PE PE2003001262A patent/PE20040913A1/es not_active Application Discontinuation
- 2003-12-12 CL CL200302611A patent/CL2003002611A1/es unknown
- 2003-12-12 AR ARP030104605A patent/AR042459A1/es unknown
- 2003-12-12 GT GT200300285A patent/GT200300285A/es unknown
- 2003-12-15 KR KR1020057011170A patent/KR100781929B1/ko not_active Expired - Fee Related
- 2003-12-15 EP EP03789278A patent/EP1575933A1/en not_active Withdrawn
- 2003-12-15 CA CA002507629A patent/CA2507629A1/en not_active Abandoned
- 2003-12-15 WO PCT/EP2003/014235 patent/WO2004054999A1/en active Application Filing
- 2003-12-15 CN CNB2003801059568A patent/CN100391954C/zh not_active Expired - Fee Related
- 2003-12-15 RU RU2005122447/04A patent/RU2348625C2/ru not_active IP Right Cessation
- 2003-12-15 PL PL377696A patent/PL377696A1/pl not_active Application Discontinuation
- 2003-12-15 JP JP2004560408A patent/JP2006513181A/ja not_active Ceased
- 2003-12-15 BR BR0317348-8A patent/BR0317348A/pt not_active IP Right Cessation
- 2003-12-15 AU AU2003293882A patent/AU2003293882A1/en not_active Abandoned
- 2003-12-15 UY UY28127A patent/UY28127A1/es not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
GT200300285A (es) | 2004-07-14 |
CN100391954C (zh) | 2008-06-04 |
AU2003293882A1 (en) | 2004-07-09 |
PA8592101A1 (es) | 2004-11-02 |
WO2004054999A1 (en) | 2004-07-01 |
CA2507629A1 (en) | 2004-07-01 |
UY28127A1 (es) | 2004-06-30 |
AR042459A1 (es) | 2005-06-22 |
TW200418825A (en) | 2004-10-01 |
CL2003002611A1 (es) | 2005-01-14 |
RU2348625C2 (ru) | 2009-03-10 |
JP2006513181A (ja) | 2006-04-20 |
US7098241B2 (en) | 2006-08-29 |
CN1726204A (zh) | 2006-01-25 |
PL377696A1 (pl) | 2006-02-06 |
BR0317348A (pt) | 2005-11-16 |
US20040122079A1 (en) | 2004-06-24 |
KR100781929B1 (ko) | 2007-12-04 |
RU2005122447A (ru) | 2006-05-27 |
EP1575933A1 (en) | 2005-09-21 |
KR20050089157A (ko) | 2005-09-07 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
PE20040913A1 (es) | Enantiomeros (r) y (s) de derivados del acido tiofeno hidroxamico como inhibidores de desacetilasa histona (hdac) | |
PE20050142A1 (es) | 2-hidroxi-3-diaminoalcanos de benzamida | |
PE20091523A1 (es) | Derivados de tiazol como inhibidores de la enzima fosfatidilinositol 3-cinasa (pi3k) | |
PE20121509A1 (es) | Compuestos de triazolopiridinas como inhibidores de quinasa mps-1 | |
AR048642A1 (es) | Compuestos de metil-aril o heteroaril-amida sustituida utiles como antagonistas del receptor de prostaglandinas e2; composiciones farmaceuticas que los contienen y su uso en la fabricacion de un medicamento | |
AR043823A1 (es) | Compuestos derivados de oxima, su preparacion y elaboracion de medicamentos que los contienen | |
AR044856A1 (es) | Acidos biariloximetilarenocarboxilicos; procedimientos para su preparacion; composiciones farmaceuticas que los contienen y su uso en la fabricacion de medicamentos. | |
BRPI0517461A (pt) | compostos farmacêuticos | |
BRPI0407695A (pt) | compostos, processo para a preparação de um composto, composições farmacêuticas que compreendem o composto, utilização dos compostos e processo de tratamento para diabetes do tipo 2 | |
AR054560A1 (es) | Espiropiperidina como inhibidores de beta-secretasa para el tratamiento de la enfermedad de alzheimer | |
PT83310B (pt) | Processo para a preparacao de derivados de indol heterociclicamente substituiods, de produtos intermediarios para a sua preparacao e de composicoes farmaceuticas que os contem | |
PE20050525A1 (es) | Derivados de pirazol sustituido y compuestos relacionados como antagonistas del receptor de bradiquinina b1 | |
ES2190396T3 (es) | Nuevos compuestos amino-triazoles, su procedimiento de preparacion y las composiciones farmaceuticas que los contienen. | |
NO20075623L (no) | Benzodioksan- og benzodioksolanderivater og deres anvendelse | |
PE20121474A1 (es) | Nuevos compuestos de espiropiperidina | |
AR072793A1 (es) | Compuestos de aril isoxazol con actividades antitumorales | |
RS53523B1 (en) | ANILINE-PYRIMIDINE DERIVATIVES WITH SUBSTITUTED SULFOXIMIN AS CDK INHIBITORS, THEIR PRODUCTION AND USE AS MEDICINES | |
EA202191968A1 (ru) | Новые замещенные производные сульфонилмочевины | |
PE20040768A1 (es) | Derivados de arilen-(2-amino-fenil)-carboxamida como inhibidores de la histona desacetilasa (hdac) | |
EA200600878A1 (ru) | Производные феноксиуксусных кислот, применимые в качестве двойных агонистов активируемого пероксисомным пролифератором рецептора ( ppar ) | |
PE20080191A1 (es) | Compuestos heterociclicos apropiados para tratar trastornos que responden a la modulacion del receptor de serotonina 5ht6 | |
ATE396189T1 (de) | Cyanopyrrolhaltige cyclische carbamat- und thiocarbamatbiaryle und verfahren zu deren herstellung | |
AR013004A1 (es) | Derivados de aminospiropiperidina quinazolina, composicion farmaceutica, uso de dichos derivados en la preparacion de medicamentos, proceso para lapreparacion de dichos derivados y compuestos intermediarios para su exclusivo uso en dicho proceso. | |
PE20060869A1 (es) | Sulfonamido-macrociclos y sus sales como inhibidores de tie2 y composiciones farmaceuticas que comprenden estos compuestos | |
UY25249A1 (es) | Procedimiento de sintesis de pirrol amidas |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FC | Refusal |