CY1110358T1 - Υποκατεστημενα παραγωγα προπενυλ πιπεραζινης ως νεοι αναστολεις της αποακετυλασης ιστονης - Google Patents
Υποκατεστημενα παραγωγα προπενυλ πιπεραζινης ως νεοι αναστολεις της αποακετυλασης ιστονηςInfo
- Publication number
- CY1110358T1 CY1110358T1 CY20091100839T CY091100839T CY1110358T1 CY 1110358 T1 CY1110358 T1 CY 1110358T1 CY 20091100839 T CY20091100839 T CY 20091100839T CY 091100839 T CY091100839 T CY 091100839T CY 1110358 T1 CY1110358 T1 CY 1110358T1
- Authority
- CY
- Cyprus
- Prior art keywords
- hysteron
- removal
- piperazine derivatives
- substituted propenyl
- new suspensions
- Prior art date
Links
- QWLWFCBWJIJQAY-UHFFFAOYSA-N 1-prop-1-enylpiperazine Chemical class CC=CN1CCNCC1 QWLWFCBWJIJQAY-UHFFFAOYSA-N 0.000 title 1
- 239000000725 suspension Substances 0.000 title 1
- 102000003964 Histone deacetylase Human genes 0.000 abstract 1
- 108090000353 Histone deacetylase Proteins 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 230000002255 enzymatic effect Effects 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
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
-
- 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
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- 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
- C07D239/52—Two oxygen atoms
- C07D239/54—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
-
- 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
- C07D403/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Dermatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
Αυτή η εφεύρεση περιλαμβάνει τις νέες ενώσεις του τύπου (I) όπου τα R1, R2, R3, R4 και Χ έχουν καθορισμένες σημασίες, οι οποίες έχουν ενζυματική δράση αναστολής αποακετυλάσης ιστόνης· την παρασκευή τους, συνθέσεις που τις περιέχουν και τη χρήση τους ως φάρμακο.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04077171 | 2004-07-28 | ||
| US59235704P | 2004-07-29 | 2004-07-29 | |
| EP05777776A EP1776358B1 (en) | 2004-07-28 | 2005-07-25 | Substituted propenyl piperazine derivatives as novel inhibitors of histone deacetylase |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CY1110358T1 true CY1110358T1 (el) | 2015-04-29 |
Family
ID=39294123
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CY20091100839T CY1110358T1 (el) | 2004-07-28 | 2009-08-06 | Υποκατεστημενα παραγωγα προπενυλ πιπεραζινης ως νεοι αναστολεις της αποακετυλασης ιστονης |
Country Status (25)
| Country | Link |
|---|---|
| EP (1) | EP1776358B1 (el) |
| JP (1) | JP5279268B2 (el) |
| KR (1) | KR101282833B1 (el) |
| CN (1) | CN1993356B (el) |
| AR (1) | AR050189A1 (el) |
| AT (1) | ATE432274T1 (el) |
| AU (1) | AU2005266311B2 (el) |
| BR (1) | BRPI0513891B8 (el) |
| CA (1) | CA2572971C (el) |
| CY (1) | CY1110358T1 (el) |
| DE (1) | DE602005014646D1 (el) |
| DK (1) | DK1776358T3 (el) |
| EA (1) | EA011932B1 (el) |
| ES (1) | ES2327253T3 (el) |
| HR (1) | HRP20090439T1 (el) |
| IL (1) | IL180961A0 (el) |
| MX (1) | MX2007001119A (el) |
| MY (1) | MY142831A (el) |
| NO (1) | NO20071117L (el) |
| NZ (1) | NZ552758A (el) |
| PL (1) | PL1776358T3 (el) |
| PT (1) | PT1776358E (el) |
| SI (1) | SI1776358T1 (el) |
| TW (1) | TWI394752B (el) |
| WO (1) | WO2006010749A2 (el) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2003218736B2 (en) | 2002-03-13 | 2009-01-08 | Janssen Pharmaceutica N.V. | New inhibitors of histone deacetylase |
| US7767679B2 (en) | 2002-03-13 | 2010-08-03 | Janssen Pharmaceutica N.V. | Sulfonylamino-derivatives as novel inhibitors of histone deacetylase |
| KR20040093692A (ko) | 2002-03-13 | 2004-11-08 | 얀센 파마슈티카 엔.브이. | 히스톤 디아세틸라제의 신규한 저해제로서의 피페라지닐-,피페리디닐- 및 모르폴리닐-유도체 |
| KR101261305B1 (ko) | 2004-07-28 | 2013-05-08 | 얀센 파마슈티카 엔.브이. | 히스톤 디아세틸라제의 신규한 저해제로의 치환된 인돌릴알킬 아미노 유도체 |
| DK1885710T3 (en) | 2005-05-18 | 2015-11-23 | Janssen Pharmaceutica Nv | SUBSTITUTED AMINOPROPENYLPIPERIDINE OR MORPHOLINE DERIVATIVES AS UNKNOWN INHIBITORS OF HISTONDEACETYLASE |
| WO2007049262A1 (en) * | 2005-10-27 | 2007-05-03 | Berand Limited | Methods and compositions for the promotion of neuronal growth and the treatment of asociality and affective disorders |
| HRP20090459T1 (hr) | 2006-01-19 | 2009-09-30 | Janssen Pharmaceutica N.V. | Aminofenil derivati kao novi inhibitori histonskih deacetilaza |
| CN101370790B (zh) | 2006-01-19 | 2015-10-21 | 詹森药业有限公司 | 作为组蛋白去乙酰化酶抑制剂的吡啶和嘧啶衍生物 |
| EP1979327A1 (en) * | 2006-01-19 | 2008-10-15 | Janssen Pharmaceutica, N.V. | Pyridine and pyrimidine derivatives as inhibitors of histone deacetylase |
| CA2635015C (en) | 2006-01-19 | 2014-06-03 | Janssen Pharmaceutica N.V. | Substituted indolyl-alkyl-amino-derivatives as inhibitors of histone deacetylase |
| EP1839656A1 (en) * | 2006-03-31 | 2007-10-03 | TopoTarget Germany AG | Use of valproic acid for the topical treatment of mild to moderate acne vulgaris |
| CA2703718A1 (en) * | 2007-11-02 | 2009-05-07 | Tammy Mallais | Inhibitors of histone deacetylase |
| CN101723896B (zh) * | 2009-11-03 | 2012-10-31 | 山东大学 | 酪氨酸衍生物类组蛋白去乙酰化酶抑制剂及其应用 |
| WO2012117421A1 (en) | 2011-03-02 | 2012-09-07 | Orchid Research Laboratories Ltd | Histone deacetylase inhibitors |
| KR101419836B1 (ko) * | 2012-05-10 | 2014-07-16 | 서울대학교산학협력단 | Δ5-2-옥소피페라진 유도체를 포함하는 중간엽 줄기세포의 연골세포로의 분화 유도용 조성물 |
| KR101586045B1 (ko) | 2013-07-30 | 2016-01-15 | 충북대학교 산학협력단 | 신규 페닐티아졸 기반 히드록삼산 및 이를 유효성분으로 포함하는 항암용 조성물 |
| KR102132078B1 (ko) | 2018-09-20 | 2020-07-08 | 원광대학교산학협력단 | 방향족 화합물, 아민 및 친핵체를 이용한 3가지 성분 반응으로 1-에틸-4-페닐피페라진 유도체를 제조하는 방법 |
| KR102730905B1 (ko) | 2022-05-03 | 2024-11-15 | 충북대학교 산학협력단 | 신규한 n-히드록시프로펜아미드 화합물 및 이를 유효성분으로 포함하는 암 예방 또는 치료용 약학적 조성물 |
| KR102870919B1 (ko) | 2022-05-03 | 2025-10-20 | 충북대학교 산학협력단 | 신규한 n-히드록시프로펜아미드 화합물 및 이를 유효성분으로 포함하는 암 예방 또는 치료용 약학적 조성물 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PH17194A (en) * | 1980-03-06 | 1984-06-19 | Otsuka Pharma Co Ltd | Novel carbostyril derivatives,and pharmaceutical composition containing the same |
| AU2003218736B2 (en) * | 2002-03-13 | 2009-01-08 | Janssen Pharmaceutica N.V. | New inhibitors of histone deacetylase |
| KR20040093692A (ko) * | 2002-03-13 | 2004-11-08 | 얀센 파마슈티카 엔.브이. | 히스톤 디아세틸라제의 신규한 저해제로서의 피페라지닐-,피페리디닐- 및 모르폴리닐-유도체 |
| NZ536116A (en) * | 2002-04-03 | 2007-01-26 | Topotarget Uk Ltd | Carbamic acid compounds comprising a piperazine linkage as HDAC inhibitors |
-
2005
- 2005-07-25 PL PL05777776T patent/PL1776358T3/pl unknown
- 2005-07-25 AT AT05777776T patent/ATE432274T1/de active
- 2005-07-25 SI SI200530748T patent/SI1776358T1/sl unknown
- 2005-07-25 KR KR1020077001641A patent/KR101282833B1/ko not_active Expired - Lifetime
- 2005-07-25 DK DK05777776T patent/DK1776358T3/da active
- 2005-07-25 PT PT05777776T patent/PT1776358E/pt unknown
- 2005-07-25 NZ NZ552758A patent/NZ552758A/en not_active IP Right Cessation
- 2005-07-25 DE DE602005014646T patent/DE602005014646D1/de not_active Expired - Lifetime
- 2005-07-25 MX MX2007001119A patent/MX2007001119A/es active IP Right Grant
- 2005-07-25 JP JP2007523072A patent/JP5279268B2/ja not_active Expired - Lifetime
- 2005-07-25 BR BRPI0513891A patent/BRPI0513891B8/pt active IP Right Grant
- 2005-07-25 EP EP05777776A patent/EP1776358B1/en not_active Expired - Lifetime
- 2005-07-25 CN CN2005800254878A patent/CN1993356B/zh not_active Expired - Lifetime
- 2005-07-25 CA CA2572971A patent/CA2572971C/en not_active Expired - Lifetime
- 2005-07-25 EA EA200700143A patent/EA011932B1/ru unknown
- 2005-07-25 AU AU2005266311A patent/AU2005266311B2/en not_active Expired
- 2005-07-25 ES ES05777776T patent/ES2327253T3/es not_active Expired - Lifetime
- 2005-07-25 HR HR20090439T patent/HRP20090439T1/hr unknown
- 2005-07-25 WO PCT/EP2005/053611 patent/WO2006010749A2/en not_active Ceased
- 2005-07-27 TW TW094125340A patent/TWI394752B/zh not_active IP Right Cessation
- 2005-07-28 AR ARP050103145A patent/AR050189A1/es active IP Right Grant
- 2005-07-28 MY MYPI20053492A patent/MY142831A/en unknown
-
2007
- 2007-01-25 IL IL180961A patent/IL180961A0/en active IP Right Grant
- 2007-02-27 NO NO20071117A patent/NO20071117L/no not_active Application Discontinuation
-
2009
- 2009-08-06 CY CY20091100839T patent/CY1110358T1/el unknown
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