PL390769A1 - Analog cytozyny, sposób otrzymywania analogu cytozyny, inhibitor DNA metylotransferazy 1, sposób inhibowania metylacji DNA, zastosowanie analogu w leczeniu chorób związanych z odstępstwami od normy metylacji DNA - Google Patents
Analog cytozyny, sposób otrzymywania analogu cytozyny, inhibitor DNA metylotransferazy 1, sposób inhibowania metylacji DNA, zastosowanie analogu w leczeniu chorób związanych z odstępstwami od normy metylacji DNAInfo
- Publication number
- PL390769A1 PL390769A1 PL390769A PL39076910A PL390769A1 PL 390769 A1 PL390769 A1 PL 390769A1 PL 390769 A PL390769 A PL 390769A PL 39076910 A PL39076910 A PL 39076910A PL 390769 A1 PL390769 A1 PL 390769A1
- Authority
- PL
- Poland
- Prior art keywords
- dna methylation
- cytosine analogue
- analog
- treatment
- dna
- Prior art date
Links
- 230000007067 DNA methylation Effects 0.000 title abstract 6
- OPTASPLRGRRNAP-UHFFFAOYSA-N cytosine Chemical class NC=1C=CNC(=O)N=1 OPTASPLRGRRNAP-UHFFFAOYSA-N 0.000 title abstract 5
- 238000000034 method Methods 0.000 title abstract 5
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title abstract 4
- 201000010099 disease Diseases 0.000 title abstract 3
- 102100036279 DNA (cytosine-5)-methyltransferase 1 Human genes 0.000 title abstract 2
- 101000931098 Homo sapiens DNA (cytosine-5)-methyltransferase 1 Proteins 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 230000005764 inhibitory process Effects 0.000 title 1
- 230000005856 abnormality Effects 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/06—Pyrimidine radicals
- C07H19/073—Pyrimidine radicals with 2-deoxyribosyl as the saccharide radical
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
-
- 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
- C07D401/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
- C07D405/02—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 two hetero rings
- C07D405/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Saccharide Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Przedmiotem wynalazku jest analog cytozyny, sposób otrzymywania analogu cytozyny, inhibitor DNA metylotransferazy 1, sposób inhibowania metylacji DNA, zastosowanie analogu w leczeniu chorób związanych z odstępstwami od normy metylacji DNA. Bardziej szczegółowo wynalazek dotyczy różnych pochodnych cytozyny, a także sposobu otrzymywania mono- i wielo-1,4,5 i 6 podstawionych cytozyny. Ogólnie rozwiązanie dotyczy stworzenia efektywnych modulatorów metylacji DNA, które mogłyby być wykorzystywane przy przeciwdziałaniu oraz leczeniu chorób związanych z zaburzeniami poziomu metylacji DNA.
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL390769A PL229581B1 (pl) | 2010-03-19 | 2010-03-19 | Analog cytozyny i jego zastosowanie w leczeniu chorób związanych z zaburzeniami metylacji DNA |
| EP11716084.6A EP2556081B1 (en) | 2010-03-19 | 2011-03-17 | A cytosine analogue, a method of preparation of a cytosine analogue, a dna methyltransferase 1 inhibitor, a method for dna methylation inhibition, the use of the analogue in the treatment of diseases associated with deviations from normal dna methylation |
| US13/576,709 US9040490B2 (en) | 2010-03-19 | 2011-03-17 | Cytosine analogue, a method of preparation of a cytosine analogue, a DNA methyltransferase 1 inhibitor, a method for DNA methylation inhibition, the use of the analogue in the treatment of diseases associated with deviations from normal DNA methylation |
| PCT/PL2011/000032 WO2011115513A2 (en) | 2010-03-19 | 2011-03-17 | A cytosine analogue, a method of preparation of a cytosine analogue, a dna methyltransferase 1 inhibitor, a method for dna methylation inhibition, the use of the analogue in the treatment of diseases associated with deviations from normal dna methylation |
| JP2013500020A JP2013522289A (ja) | 2010-03-19 | 2011-03-17 | シトシン類似体、シトシン類似体の調製方法、dnaメチルトランスフェラーゼ1阻害剤、dnaメチル化の阻害方法、正常なdnaメチル化からの逸脱と関連する疾患の治療における類似体の使用 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL390769A PL229581B1 (pl) | 2010-03-19 | 2010-03-19 | Analog cytozyny i jego zastosowanie w leczeniu chorób związanych z zaburzeniami metylacji DNA |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| PL390769A1 true PL390769A1 (pl) | 2011-09-26 |
| PL229581B1 PL229581B1 (pl) | 2018-08-31 |
Family
ID=44168248
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL390769A PL229581B1 (pl) | 2010-03-19 | 2010-03-19 | Analog cytozyny i jego zastosowanie w leczeniu chorób związanych z zaburzeniami metylacji DNA |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US9040490B2 (pl) |
| EP (1) | EP2556081B1 (pl) |
| JP (1) | JP2013522289A (pl) |
| PL (1) | PL229581B1 (pl) |
| WO (1) | WO2011115513A2 (pl) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014039860A2 (en) * | 2012-09-07 | 2014-03-13 | University Of Louisville Research Foundation, Inc. | Compositions and methods for modulating dnmt1 inhibitor activity |
| US11504369B2 (en) | 2019-03-22 | 2022-11-22 | President And Trustees Of Bates College | Cytosine-based TET enzyme inhibitors |
| WO2020197541A1 (en) * | 2019-03-22 | 2020-10-01 | President And Trustees Of Bates College | Cytosine-based tet enzyme inhibitors |
| CN116284188B (zh) * | 2023-02-07 | 2024-07-26 | 南开大学 | 一种dna甲基转移酶dnmt1的双底物抑制剂及其应用 |
| PL450139A1 (pl) * | 2024-10-25 | 2026-04-27 | Instytut Chemii Bioorganicznej Polskiej Akademii Nauk | 4-N-furfurylocytozyna i kompozycja ją zawierająca do zastosowań medycznych |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7250416B2 (en) | 2005-03-11 | 2007-07-31 | Supergen, Inc. | Azacytosine analogs and derivatives |
| US7790746B2 (en) | 2007-10-12 | 2010-09-07 | Supergen, Inc. | Quinoline derivatives for modulating DNA methylation |
| PL216370B1 (pl) * | 2007-11-25 | 2014-03-31 | Inst Chemii Bioorg Pan | Sposób otrzymywania 4-N-furfurylocytozyny, kompozycja antystarzeniowa oraz zastosowanie 4-N-furfurylocytozyny do wytwarzania kompozycji antystarzeniowej |
-
2010
- 2010-03-19 PL PL390769A patent/PL229581B1/pl unknown
-
2011
- 2011-03-17 EP EP11716084.6A patent/EP2556081B1/en active Active
- 2011-03-17 JP JP2013500020A patent/JP2013522289A/ja not_active Withdrawn
- 2011-03-17 WO PCT/PL2011/000032 patent/WO2011115513A2/en not_active Ceased
- 2011-03-17 US US13/576,709 patent/US9040490B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| WO2011115513A3 (en) | 2012-02-23 |
| WO2011115513A9 (en) | 2012-05-03 |
| US9040490B2 (en) | 2015-05-26 |
| EP2556081B1 (en) | 2021-06-16 |
| WO2011115513A2 (en) | 2011-09-22 |
| EP2556081A2 (en) | 2013-02-13 |
| PL229581B1 (pl) | 2018-08-31 |
| JP2013522289A (ja) | 2013-06-13 |
| US20120322755A1 (en) | 2012-12-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| IN2014DN09134A (pl) | ||
| UA115983C2 (uk) | Інгібітори днк-пк | |
| MY171577A (en) | 2',4'-difluoro-2'-methyl substituted nucleoside derivatives as inhibitors of hcv rna replication | |
| MX2009013353A (es) | Compuestos activadores de telomerasa y metodos para su uso. | |
| SG10201909545XA (en) | Bile acid derivatives as fxr/tgr5 agonists and methods of use thereof | |
| MX365294B (es) | Inhibidores de proteína cinasa dependiente de adn. | |
| TW201613875A (en) | EGFR inhibitors, their preparation and their use thereof | |
| SG179418A1 (en) | Inhibitors of the hedgehog pathway | |
| WO2014028600A3 (en) | 3-AMINOCYCLOALKYL COMPOUNDS AS RORgammaT INHIBITORS AND USES THEREOF | |
| MX2011007750A (es) | Composiciones y metodos para inhibicion de la ruta jak. | |
| IN2015DN01156A (pl) | ||
| MX2013004329A (es) | 6-amino-nicotinamidas sustituidas como moduladores de kcnq2/3. | |
| MX2013004491A (es) | Boronatos como inhibidores de arginasa. | |
| MX2009008531A (es) | Cetonas de heterociclilo que contienen nitrogeno y su uso como inhibidores de c-met. | |
| MA33838B1 (fr) | Forme amorphe et cristalline de l'hémitartrate de genz 112638 au titre d'inhibiteur de la glucosylcéramide synthétase | |
| MX2011013032A (es) | Inhibidores de fosfatidilinositol 3-cinasa. | |
| MX2017004618A (es) | Inhibidores de la biosintesis de sulfato de heparano para el tratamiento de enfermedades. | |
| MX336711B (es) | Inhibidores de catecol o-metil transferasa y su uso en el tratamiento de transtornos psicoticos. | |
| MX2020009397A (es) | Composiciones y metodos para inhibicion de la via jak. | |
| MY186547A (en) | 4?-fluoro-2?-methyl substituted nucleoside derivatives | |
| PH12013500644A1 (en) | Co-crystals and salts of ccr3-inhibitors | |
| MX337849B (es) | Composiciones y metodos para inhibicion de la via jak. | |
| PH12017501043A1 (en) | 2-amino-5,5-difluoro-6-(fluoromethyl)-6-phenyl-3,4,5,6-tetrahydropyridines as bace1 inhibitors | |
| IN2015DN01151A (pl) | ||
| MX2015010876A (es) | Estra-1,3,5(10),16-tetraeno-3-carboxamidas para la inhibicion de la 17b-hidroxiesteroide deshidrogenasa (akr1 c3). |