CY1119218T1 - Αναστολεις διυδροπυριδοφθαλαζινονης της πολυμερασης της πολυαδενοσφωσφορικης ριβοζης (parp) - Google Patents
Αναστολεις διυδροπυριδοφθαλαζινονης της πολυμερασης της πολυαδενοσφωσφορικης ριβοζης (parp)Info
- Publication number
- CY1119218T1 CY1119218T1 CY20171100578T CY171100578T CY1119218T1 CY 1119218 T1 CY1119218 T1 CY 1119218T1 CY 20171100578 T CY20171100578 T CY 20171100578T CY 171100578 T CY171100578 T CY 171100578T CY 1119218 T1 CY1119218 T1 CY 1119218T1
- Authority
- CY
- Cyprus
- Prior art keywords
- polymadene
- phosphorosis
- diahydrodyphythrophalazinone
- parp
- polymerase
- Prior art date
Links
- 239000000725 suspension Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 1
Classifications
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- 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
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
-
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- A61K31/28—Compounds containing heavy metals
- A61K31/282—Platinum compounds
-
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
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- 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
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- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- C07D—HETEROCYCLIC COMPOUNDS
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- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/06—Peri-condensed systems
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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- A61N2005/1092—Details
- A61N2005/1098—Enhancing the effect of the particle by an injected agent or implanted device
Abstract
Η εφεύρεση παρέχει μια ένωση του τύπου:
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US8668708P | 2008-08-06 | 2008-08-06 | |
US15103609P | 2009-02-09 | 2009-02-09 | |
US17308809P | 2009-04-27 | 2009-04-27 | |
EP09805360.6A EP2326650B9 (en) | 2008-08-06 | 2009-07-27 | Dihydropyridophthalazinone inhibitors of poly(adp-ribose)polymerase (parp) |
Publications (1)
Publication Number | Publication Date |
---|---|
CY1119218T1 true CY1119218T1 (el) | 2018-02-14 |
Family
ID=41129519
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CY20141100240T CY1115022T1 (el) | 2008-08-06 | 2014-03-28 | Αναστολεις πολυ (adp-ριβοζης)πολυμερασης (parp) του τυπου διυδροπυριδοφθαλαζινονης |
CY20171100578T CY1119218T1 (el) | 2008-08-06 | 2017-05-31 | Αναστολεις διυδροπυριδοφθαλαζινονης της πολυμερασης της πολυαδενοσφωσφορικης ριβοζης (parp) |
CY2019044C CY2019044I1 (el) | 2008-08-06 | 2019-11-28 | Αναστολεις διυδροπυριδοφθαλαζινονης της πολυμερασης της πολυαδενοσφωσφορικης ριβοζης (parp) |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CY20141100240T CY1115022T1 (el) | 2008-08-06 | 2014-03-28 | Αναστολεις πολυ (adp-ριβοζης)πολυμερασης (parp) του τυπου διυδροπυριδοφθαλαζινονης |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CY2019044C CY2019044I1 (el) | 2008-08-06 | 2019-11-28 | Αναστολεις διυδροπυριδοφθαλαζινονης της πολυμερασης της πολυαδενοσφωσφορικης ριβοζης (parp) |
Country Status (31)
Country | Link |
---|---|
US (7) | US8012976B2 (el) |
EP (3) | EP2767537B1 (el) |
JP (3) | JP5984389B2 (el) |
KR (1) | KR101846029B1 (el) |
CN (3) | CN103896942A (el) |
AR (1) | AR072970A1 (el) |
AU (1) | AU2009279944B2 (el) |
BR (1) | BRPI0917119B1 (el) |
CA (1) | CA2732797C (el) |
CY (3) | CY1115022T1 (el) |
DK (2) | DK2326650T3 (el) |
ES (2) | ES2625817T3 (el) |
FR (1) | FR19C1071I2 (el) |
GB (1) | GB2462361A (el) |
HK (2) | HK1157755A1 (el) |
HR (1) | HRP20170982T1 (el) |
HU (2) | HUE035295T2 (el) |
IL (1) | IL211070A (el) |
LT (2) | LT2767537T (el) |
LU (1) | LUC00140I2 (el) |
MX (1) | MX2011001328A (el) |
NL (1) | NL301021I2 (el) |
NO (1) | NO2019042I1 (el) |
NZ (1) | NZ591166A (el) |
PL (2) | PL2767537T3 (el) |
PT (2) | PT2326650E (el) |
SG (2) | SG193842A1 (el) |
SI (2) | SI2767537T1 (el) |
TW (2) | TWI448464B (el) |
WO (1) | WO2010017055A2 (el) |
ZA (1) | ZA201100897B (el) |
Families Citing this family (65)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PT2326650E (pt) | 2008-08-06 | 2014-05-06 | Biomarin Pharm Inc | Inibidores de di-hidropiridoftalazinona de poli(adpribose) polimerase (parp) |
RU2016141566A (ru) | 2008-12-19 | 2018-12-20 | Вертекс Фармасьютикалз Инкорпорейтед | Производные пиразина, используемые в качестве ингибиторов киназы atr |
AU2011212928B2 (en) | 2010-02-03 | 2016-06-23 | Medivation Technologies Llc | Dihydropyridophthalazinone inhibitors of poly(ADP-ribose) polymerase (PARP) for use in treatment of diseases associated with a PTEN deficiency |
US20110190266A1 (en) * | 2010-02-04 | 2011-08-04 | Daniel Chu | 5,6,6a,7,8,9-HEXAHYDRO-2H-PYRIDOPHTHALAZINONE INHIBITORS OF POLY(ADP-RIBOSE)POLYMERASE (PARP) |
HUE030794T2 (en) * | 2010-02-08 | 2017-06-28 | Medivation Technologies Inc | Synthesis Processes of Dihydro-Pyrido-Phthalazinone Derivatives |
WO2011130661A1 (en) * | 2010-04-16 | 2011-10-20 | Biomarin Pharmaceutical Inc. | Methods of using dihydropyridophthalazinone inhibitors of poly (adp-ribose)polymerase (parp) |
MX2012013081A (es) | 2010-05-12 | 2013-05-09 | Vertex Pharma | Compuestos utiles como inhibidores de cinasa atr. |
RU2598606C3 (ru) * | 2010-10-21 | 2021-12-20 | МЕДИВЭЙШН ТЕКНОЛОДЖИЗ ЭлЭлСи | Кристаллическая тозилатная соль (8s,9r)-5-фтор-8-(4-фторфенил)-9-(1-метил-1н-1,2,4-триазол-5-ил)-8-9-дигидро-2н-пиридо[4,3,2-de]фталазин-3(7н)-она |
WO2012166151A1 (en) * | 2011-06-03 | 2012-12-06 | Biomarin Pharmaceutical Inc. | Use of dihydropyridophthalazinone inhibitors of poly (adp-ribose) polymerase (parp) in the treatment of myelodysplastic syndrome (mds) and acute myeloid leukaemia (aml) |
WO2013028495A1 (en) * | 2011-08-19 | 2013-02-28 | Biomarin Pharmaceutical Inc. | Dihydropyridophthalazinone inhibitors of poly (adp-ribose) polymerase (parp) for the treatment of multiple myeloma |
BR112014007721B1 (pt) * | 2011-09-30 | 2022-11-01 | Vertex Pharmaceuticals Incorporated | Processos para preparar compostos úteis como inibidores de atr quinase |
MX2014003785A (es) | 2011-09-30 | 2014-07-24 | Vertex Phamaceuticals Inc | Tratamiento del cancer de pancreas y del cancer de pulmon de celulas no pequeñas con inhibidores de atr. |
AU2011384859B2 (en) * | 2011-12-31 | 2016-03-17 | Beigene, Ltd. | Fused tetra or penta-cyclic pyridophthalazinones as PARP inhibitors |
EP2797921B1 (en) | 2011-12-31 | 2017-09-06 | BeiGene, Ltd. | Fused tetra or penta-cyclic dihydrodiazepinocarbazolones as parp inhibitors |
CN110711188A (zh) | 2012-01-20 | 2020-01-21 | 德玛公司 | 经取代的己糖醇类用于治疗恶性肿瘤的用途 |
CA2869309C (en) | 2012-04-05 | 2021-02-09 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of atr kinase and combination therapies thereof |
US8999632B2 (en) | 2012-10-04 | 2015-04-07 | Vertex Pharmaceuticals Incorporated | Method for measuring ATR inhibition mediated increases in DNA damage |
JP6223995B2 (ja) | 2012-11-08 | 2017-11-01 | 日本化薬株式会社 | カンプトテシン類と抗癌効果増強剤の結合した高分子化合物及びその用途 |
CN105492008B (zh) * | 2013-03-13 | 2020-11-27 | 福马治疗股份有限公司 | 用于抑制fasn的化合物及组合物 |
KR20160104612A (ko) | 2013-07-26 | 2016-09-05 | 업데이트 파마 인코포레이트 | 비산트렌의 치료 효과 개선용 조성물 |
US20160280691A1 (en) | 2013-11-07 | 2016-09-29 | Biomarin Pharmaceutical Inc. | Triazole intermediates useful in the synthesis of protected n-alkyltriazolecarbaldehydes |
CN103772395B (zh) * | 2014-01-23 | 2016-05-11 | 中国药科大学 | 一类具有parp抑制活性的化合物、其制备方法及用途 |
WO2015154064A2 (en) | 2014-04-04 | 2015-10-08 | Del Mar Pharmaceuticals | Use of dianhydrogalactitol and analogs or derivatives thereof to treat non-small-cell carcinoma of the lung and ovarian cancer |
PT3157566T (pt) | 2014-06-17 | 2019-07-11 | Vertex Pharma | Método para tratamento de cancro utilizando uma combinação de inibidores chk1 e atr |
EP3174855B1 (en) | 2014-07-31 | 2023-05-10 | Medivation Technologies LLC | Coformer salts of (2s,3s)-methyl 7-fluoro-2-(4-fluorophenyl)-3-(1-methyl-1h-1,2,4-triazol-5-yl)-4-oxo-1,2,3,4-tetrahydroquinoline-5-carboxylate and methods of preparing them |
CN109121418A (zh) | 2015-03-02 | 2019-01-01 | 西奈健康*** | 同源重组因子 |
WO2017003723A1 (en) | 2015-07-01 | 2017-01-05 | Crinetics Pharmaceuticals, Inc. | Somatostatin modulators and uses thereof |
NZ739876A (en) | 2015-08-25 | 2022-09-30 | Beigene Ltd | Process for preparing parp inhibitor, crystalline forms, and uses thereof |
AU2016331955B2 (en) | 2015-09-30 | 2022-07-21 | Vertex Pharmaceuticals Incorporated | Method for treating cancer using a combination of DNA damaging agents and ATR inhibitors |
US9708319B1 (en) * | 2016-06-13 | 2017-07-18 | Yong Xu | Synthesis of PARP inhibitor talazoparib |
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