WO2008154905A3 - Modifications of the histone deacetylase inhibitor suberoylanilide hydroxamic acid - Google Patents
Modifications of the histone deacetylase inhibitor suberoylanilide hydroxamic acid Download PDFInfo
- Publication number
- WO2008154905A3 WO2008154905A3 PCT/DE2008/000993 DE2008000993W WO2008154905A3 WO 2008154905 A3 WO2008154905 A3 WO 2008154905A3 DE 2008000993 W DE2008000993 W DE 2008000993W WO 2008154905 A3 WO2008154905 A3 WO 2008154905A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- histone deacetylase
- modifications
- hydroxamic acid
- deacetylase inhibitor
- suberoylanilide hydroxamic
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic 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
- C07D213/02—Heterocyclic 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
- C07D213/04—Heterocyclic 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
- C07D213/60—Heterocyclic 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
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/64—One oxygen atom attached in position 2 or 6
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C259/00—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups
- C07C259/04—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids
- C07C259/06—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids having carbon atoms of hydroxamic groups bound to hydrogen atoms or to acyclic carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
The application relates to compounds of general formula (I) Ar-[CH2]m-Z1-N(Z2-R2)-Z3-[C(O)]r-[CH2]n-Y1-[C(O)]s-Y2-R1, in which the variables can take the values specified in the application. In particularly preferred individual compounds of formula (I), -Z1-N(Z2-R2)-Z3-[C(O)]r- forms an -O-NH-C(O)- or -NH-O-C(O)- group. Said compounds (I) are suitable as medicaments for the treatment of cancer diseases. The effect thereof is due to histone deacetylase inhibition.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE112008002230T DE112008002230A5 (en) | 2007-06-16 | 2008-06-16 | New pharmaceuticals, process for their preparation and their use in medical therapy |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102007028198.8 | 2007-06-16 | ||
DE102007028198A DE102007028198A1 (en) | 2007-06-16 | 2007-06-16 | New alkyl-ketone compounds are histone deacetylase inhibitors, useful to treat e.g. cancer, hematologic or solid tumors, non-Hodgkins tumors, T-cell lymphoma, type I diabetes or Hashimoto's thyroiditis, and to modulate e.g. cell cycle |
DE102007037372 | 2007-08-06 | ||
DE102007037372.6 | 2007-08-06 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2008154905A2 WO2008154905A2 (en) | 2008-12-24 |
WO2008154905A3 true WO2008154905A3 (en) | 2009-08-27 |
Family
ID=39944377
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/DE2008/000993 WO2008154905A2 (en) | 2007-06-16 | 2008-06-16 | Modifications of the histone deacetylase inhibitor suberoylanilide hydroxamic acid |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE112008002230A5 (en) |
WO (1) | WO2008154905A2 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102009019852A1 (en) | 2009-05-06 | 2010-11-11 | Schebo Biotech Ag | New polymer compound comprising amine structural elements, useful as synthetic resins, coatings, foams, liquid crystals, adhesives, paints, varnishes, composite materials, in cosmetics, and in polymer electronics |
CN107522654B (en) * | 2016-06-21 | 2020-09-01 | 中国人民解放军军事医学科学院毒物药物研究所 | Novel alpha-aminoamide derivatives and medicinal use thereof |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4018294B1 (en) * | 1962-01-30 | 1965-08-18 | ||
US3262978A (en) * | 1963-06-19 | 1966-07-26 | Colgate Palmolive Co | O-arylamino-and-aralkyl-amino-alkylhydroxyl-amines |
WO2001070675A2 (en) * | 2000-03-24 | 2001-09-27 | Methylgene, Inc. | Inhibitors of histone deacetylase |
-
2008
- 2008-06-16 WO PCT/DE2008/000993 patent/WO2008154905A2/en active Application Filing
- 2008-06-16 DE DE112008002230T patent/DE112008002230A5/en not_active Ceased
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4018294B1 (en) * | 1962-01-30 | 1965-08-18 | ||
US3262978A (en) * | 1963-06-19 | 1966-07-26 | Colgate Palmolive Co | O-arylamino-and-aralkyl-amino-alkylhydroxyl-amines |
WO2001070675A2 (en) * | 2000-03-24 | 2001-09-27 | Methylgene, Inc. | Inhibitors of histone deacetylase |
Non-Patent Citations (27)
Title |
---|
"Org. Synth. Coll. Vol. IV", 1963 * |
"SMALL MOLECULE INHIBITORS OF HISTONE DEACETYLASE", EXPERT OPIN. THER. PATENTS, vol. 12, no. 6, 1 January 2002 (2002-01-01), pages 943 - 947, XP001120539, ISSN: 1354-3776 * |
BIOORG. MED. CHEM., vol. 15, no. 1, 1 January 2007 (2007-01-01), pages 63 - 76 * |
CHEM. COMMUN., vol. 3, 1992, pages 274 - 275 * |
CHEMTECH, vol. 10, 1958, pages 693 - 698 * |
DATABASE BEILSTEIN [online] BEILSTEIN INSTITUTE FOR ORGANIC CHEMISTRY, FRANKFURT-MAIN, DE; Database accession no. 2721683, 2722080, 2723874, 272628 (BRNs) * |
DATABASE BEILSTEIN [online] BEILSTEIN INSTITUTE FOR ORGANIC CHEMISTRY, FRANKFURT-MAIN, DE; XP002504399, Database accession no. 2205846 (BRN) * |
DATABASE BEILSTEIN [online] BEILSTEIN INSTITUTE FOR ORGANIC CHEMISTRY, FRANKFURT-MAIN, DE; XP002504400, Database accession no. 2205845 (BRN) * |
DATABASE BEILSTEIN [online] BEILSTEIN INSTITUTE FOR ORGANIC CHEMISTRY, FRANKFURT-MAIN, DE; XP002504401, Database accession no. 5332703 (BRN) * |
DATABASE BEILSTEIN [online] BEILSTEIN INSTITUTE FOR ORGANIC CHEMISTRY, FRANKFURT-MAIN, DE; XP002504402, Database accession no. 129470 (BRN) * |
DATABASE BEILSTEIN [online] BEILSTEIN INSTITUTE FOR ORGANIC CHEMISTRY, FRANKFURT-MAIN, DE; XP002504403, Database accession no. 7874189 BRN) * |
DATABASE BEILSTEIN [online] BEILSTEIN INSTITUTE FOR ORGANIC CHEMISTRY, FRANKFURT-MAIN, DE; XP002504404, Database accession no. 2751837 (BRN) * |
DATABASE BEILSTEIN [online] BEILSTEIN INSTITUTE FOR ORGANIC CHEMISTRY, FRANKFURT-MAIN, DE; XP002504405, Database accession no. 2837833, 2840716, 2837818, 2840833 (BRN's) * |
DATABASE BEILSTEIN [online] BEILSTEIN INSTITUTE FOR ORGANIC CHEMISTRY, FRANKFURT-MAIN, DE; XP002504406, Database accession no. 3955418, 3955977, 4030972, 4030992 (BRNs) * |
DATABASE BEILSTEIN [online] BEILSTEIN INSTITUTE FOR ORGANIC CHEMISTRY, FRANKFURT-MAIN, DE; XP002504407, Database accession no. 6986422 (BRN) * |
DATABASE BEILSTEIN [online] BEILSTEIN INSTITUTE FOR ORGANIC CHEMISTRY, FRANKFURT-MAIN, DE; XP002504408, Database accession no. 10541154, 10550489, 10544261, 10554562 (BRN's) * |
DATABASE BEILSTEIN [online] BEILSTEIN INSTITUTE FOR ORGANIC CHEMISTRY, FRANKFURT-MAIN, DE; XP002504409, Database accession no. 2982944 (BRN) * |
DATABASE BEILSTEIN [online] BEILSTEIN INSTITUTE FOR ORGANIC CHEMISTRY, FRANKFURT-MAIN, DE; XP002504410, Database accession no. 7379654 (BRN) * |
FARMACO, vol. 42, no. 10, 1987, pages 697 - 708 * |
INDIAN J. CHEM., vol. 34, no. 2, 1995, pages 102 - 106 * |
J. CHEM. SOC., PERKIN TRANS. 1, 1975, pages 825 - 830 * |
J. CHEM. SOC., PERKIN TRANS. 2, 1980, pages 1 - 3 * |
J. PHARM. SCI., vol. 61, 1972, pages 1739 - 1745 * |
KELLY ET AL.: "HISTONE DEACETYLASE INHIBITORS: FROM TARGET TO CLINICAL TRIALS", EXPERT OPIN. INVESTIG. DRUGS, vol. 11, no. 12, 1 December 2002 (2002-12-01), pages 1695 - 1713, XP001202636, ISSN: 1354-3784 * |
ROCZNIKI CHEMII, vol. 41, 1967, pages 493 * |
STERNSON ET AL.: "Synthesis of 7200 Small Molecules Based on a Substructural Analysis of the Histone Deacetylase Inhibitors Trichostatin and Trapoxin", ORGANIC LETTERS, AMERICAN CHEMICAL SOCIETY, COLUMBUS, OH; US, vol. 3, no. 26, 1 January 2001 (2001-01-01), pages 4239 - 4242, XP002220922, ISSN: 1523-7060 * |
SYNLETT, vol. 3, 1998, pages 301 - 303 * |
Also Published As
Publication number | Publication date |
---|---|
WO2008154905A2 (en) | 2008-12-24 |
DE112008002230A5 (en) | 2010-05-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
IL203448A (en) | Azabiphenylaminobenzoic acid derivatives for use in the treatment or prevention of a pathological condition or disease susceptible to amelioration by inhibition of dhodh and pharmaceutical compositions comprising them | |
WO2010009139A3 (en) | Imidazolylpyrimidine compounds as hdac and / or cdk inhibitors | |
WO2012016186A8 (en) | Macrocyclic kinase inhibitors and uses thereof | |
MA32604B1 (en) | ORGANIC COMPOUNDS | |
EA201001669A1 (en) | SUBSTITUTED PYRIMIDIN-5-CARBOXAMIDES 281 | |
WO2011058474A8 (en) | N1-pyrazolospiroketone acetyl-coa carboxylase inhibitors | |
EA200802223A1 (en) | 1,5-DIPHENYLPYRAZOLES II AS HSP90 INHIBITORS | |
WO2008106128A3 (en) | CYCLIC UREA AND CARBAMATE INHIBITORS OF 11β -HYDROXYSTEROID DEHYDROGENASE 1 | |
WO2009039397A3 (en) | Substituted amides, methods of making, use thereof for the treatment of diseases such as cancer | |
TN2012000413A1 (en) | Pyrrolopyrimidine compounds as inhibitors of cdk4/6 | |
WO2012116290A3 (en) | Neuroactive 17(20)-z-vinylcyano-substituted steroids, prodrugs thereof, and methods of treatment using same | |
CL2012001056A1 (en) | Substituted chromenone derived compounds, inhibitors of pi 3 kinase enzymes; pharmaceutical composition; and use in the treatment or prevention of cell proliferation disorders, such as tumors, inflammatory and fibrotic diseases, asthma, insulin-dependent diabetes, among others. | |
MX2010002353A (en) | Heterocyclic amides useful for the treatment of cancer and psoriasis. | |
WO2008086188A3 (en) | Thiophene carboxamides as factor xa inhibitors | |
TW200833663A (en) | Therapeutic agents | |
EP2639229A3 (en) | Thiazole Derivative and use thereof as VAP-1 Inhibitor | |
EA024702B8 (en) | Novel immunomodulator and anti inflammatory compounds | |
WO2009080705A3 (en) | Bis-thiazole derivatives, process for their preparation and their use as medicaments | |
WO2008054698A3 (en) | Spiropiperidine beta-secretase inhibitors for the treatment of alzheimer's disease | |
TN2010000038A1 (en) | Organic compounds | |
WO2009030952A3 (en) | Phenylcarboxamide derivatives as inhibitors and effectors of the hedgehog pathway | |
WO2013061004A8 (en) | Novel disubstituted 3,4-diamino-3-cyclobutene-1,2-dione compounds for use in the treatment of chemokine-mediated diseases | |
WO2006063294A3 (en) | Novel inhibitors of histone deacetylase for the treatment of disease | |
WO2010107807A3 (en) | Compounds for treating inflammation and pain | |
MX340577B (en) | Phosphoinositide 3-kinase inhibitor with a zinc binding moiety. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 08758190 Country of ref document: EP Kind code of ref document: A2 |
|
REF | Corresponds to |
Ref document number: 112008002230 Country of ref document: DE Date of ref document: 20100520 Kind code of ref document: P |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 08758190 Country of ref document: EP Kind code of ref document: A2 |