HRP20161742T1 - Soli i polimorfi od 8-fluoro-2-{4-[(metilamino)metil]fenil}-1,3,4,5-tetrahidro-6h-azepino[5,4,3-cd]indol-6-ona - Google Patents
Soli i polimorfi od 8-fluoro-2-{4-[(metilamino)metil]fenil}-1,3,4,5-tetrahidro-6h-azepino[5,4,3-cd]indol-6-ona Download PDFInfo
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- HRP20161742T1 HRP20161742T1 HRP20161742TT HRP20161742T HRP20161742T1 HR P20161742 T1 HRP20161742 T1 HR P20161742T1 HR P20161742T T HRP20161742T T HR P20161742TT HR P20161742 T HRP20161742 T HR P20161742T HR P20161742 T1 HRP20161742 T1 HR P20161742T1
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- 150000003839 salts Chemical class 0.000 title claims 47
- HMABYWSNWIZPAG-UHFFFAOYSA-N rucaparib Chemical compound C1=CC(CNC)=CC=C1C(N1)=C2CCNC(=O)C3=C2C1=CC(F)=C3 HMABYWSNWIZPAG-UHFFFAOYSA-N 0.000 title claims 4
- 238000000634 powder X-ray diffraction Methods 0.000 claims 8
- 238000000371 solid-state nuclear magnetic resonance spectroscopy Methods 0.000 claims 8
- 238000001228 spectrum Methods 0.000 claims 8
- 239000000126 substance Substances 0.000 claims 8
- 238000000034 method Methods 0.000 claims 5
- 239000008194 pharmaceutical composition Substances 0.000 claims 5
- 241000124008 Mammalia Species 0.000 claims 4
- MIOPJNTWMNEORI-UHFFFAOYSA-N camphorsulfonic acid Chemical class C1CC2(CS(O)(=O)=O)C(=O)CC1C2(C)C MIOPJNTWMNEORI-UHFFFAOYSA-N 0.000 claims 3
- 206010028980 Neoplasm Diseases 0.000 claims 2
- 201000011510 cancer Diseases 0.000 claims 2
- 102000012338 Poly(ADP-ribose) Polymerases Human genes 0.000 claims 1
- 108010061844 Poly(ADP-ribose) Polymerases Proteins 0.000 claims 1
- 229920000776 Poly(Adenosine diphosphate-ribose) polymerase Polymers 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 150000002688 maleic acid derivatives Chemical class 0.000 claims 1
- 230000001404 mediated effect Effects 0.000 claims 1
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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- C07C309/01—Sulfonic acids
- C07C309/02—Sulfonic acids having sulfo groups bound to acyclic carbon atoms
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Claims (27)
1. Kamsilat-sol, naznačena time, da je od 8-fluoro-2-{4-[(metilamino)metil]fenil}-1,3,4,5-tetrahidro-6H-azepino[5,4,3-cd]indol-6-ona.
2. Sol prema zahtjevu 1, naznačena time, da sol je kristalna.
3. Sol prema zahtjevu 1, naznačena time, da je to kristalna bezvodna sol.
4. Sol prema bilo kojem od zahtjeva 1 do 3, naznačena time, da kamsilat je S-kamsilat.
5. Sol prema bilo kojem od zahtjeva 1 do 3, naznačena time, da kamsilat je R-kamsilat.
6. Sol prema bilo kojem od zahtjeva 1 do 5, naznačena time, da sol ima uzorak difrakcije praha X-zraka koji sadrži jednu ili više ili tri ili više ili tri vršne vrijednosti s difrakcijskim kutevima (2θ) odabranima iz skupine koja se sastoji od 12,2 ± 0,2, 14,8 ± 0,2 i 22,4 ± 0,2, pri čemu se navedeni uzorak rendgenske difrakcije praha dobiva uporabom bakar-K-α1-X-zraka valne duljine od 1,5406 Angstroma.
7. Sol prema bilo kojem od zahtjeva 1 do 6, naznačena time, da sol ima kruto stanje NMR spektra koje sadrži jedan ili više 13C-kemijskih pomaka odabranih iz skupine koja se sastoji od 213,4 ± 0,2, 171,8 ± 0,2 i 17,3 ± 0,2 ppm.
8. Sol prema bilo kojem od zahtjeva 1 do 7, naznačena time, da sol ima kruto stanje NMR spektra koje sadrži jedan ili više 19F-kemijskih pomaka odabranih iz skupine koja se sastoji od -118,9 ± 0,2 i -119,7 ppm ± 0,2.
9. Sol prema bilo kojem od zahtjeva 1 do 8, naznačena time, da sol ima uzorak difrakcije praha X-zraka koji sadrži jednu ili više ili tri ili više ili tri vršne vrijednosti s difrakcijskim kutevima (2θ) odabranima iz skupine koja se sastoji od 12,2 ± 0,2, 14,8 ± 0,2 i 22,4 ± 0,2, koji se dobiva uporabom bakar-K-α1-X-zraka valne duljine od 1,5406 Angstroma; gdje kruto stanje NMR spektra sadrži jedan ili više ili dva ili više ili tri 13C-kemijska pomaka odabrana iz skupine koja se sastoji od 213,4 ± 0,2, 171,8 ± 0,2 i 17,3 ± 0,2 ppm; i kruto stanje NMR spektra sadrži jedan ili više ili dva 19F-kemijska pomaka odabrana iz skupine koja se sastoji od -118,9 ± 0,2 i -119,7 ppm ± 0,2.
10. Sol prema bilo kojem od zahtjeva 1 do 9, naznačena time, da sol je bitno čisti polimorf od polimorfa S-kamsilat-oblik A.
11. Sol prema bilo kojem od zahtjeva 1 do 3, naznačena time, da sol je bitno čisti polimorf od polimorfa S-kamsilat-oblik B ili je bitno čisti polimorf od polimorfa S-kamsilat-oblik C.
12. Maleat-sol, naznačena time, da je od 8-fluoro-2-{4-[(metilamino)metil]fenil}-1,3,4,5-tetrahidro-6H-azepino[5,4,3-cd]indol-6-ona.
13. Sol prema zahtjevu 12, naznačena time, da sol je kristalna.
14. Sol prema zahtjevu 12, naznačena time, da sol je kristalna bezvodna sol.
15. Sol prema bilo kojem od zahtjeva 12 do 14, naznačena time, da sol ima uzorak difrakcije praha X-zraka koji sadrži vršne vrijednosti s difrakcijskim kutevima (2θ) od 6,0 ± 0,2, 20,3 ± 0,2 i 21,7 ± 0,2, pri čemu se navedeni uzorak rendgenske difrakcije praha dobiva uporabom bakar-K-α1-X-zraka valne duljine od 1,5406 Angstroma.
16. Sol prema bilo kojem od zahtjeva 12 do 15, naznačena time, da sol je bitno čisti polimorf od polimorfa maleat-oblik A.
17. Sol prema bilo kojem od zahtjeva 12 do 14, naznačena time, da sol ima uzorak difrakcije praha X-zraka koji sadrži vršne vrijednosti s difrakcijskim kutevima (2θ) od 7,5 ± 0,2, 11,3 ± 0,2 i 24,3 ± 0,2, pri čemu se navedeni uzorak rendgenske difrakcije praha dobiva uporabom bakar-K-α1-X-zraka valne duljine od 1,5406 Angstroma.
18. Sol prema bilo kojem od zahtjeva 12 do 14 i 17, naznačena time, da sol ima kruto stanje NMR spektra koje sadrži jedan ili više 13C-kemijskih pomaka odabranih iz skupine koja se sastoji od 171,3 ± 0,2, 112,4 ± 0,2 i 43,8 ± 0,2 ppm.
19. Sol prema bilo kojem od zahtjeva 12 do 14 i 17 do 18, naznačena time, da sol ima kruto stanje NMR spektra koje sadrži 19F-kemijski pomak na -123,1 ppm ± 0,2.
20. Sol prema bilo kojem od zahtjeva 12 do 14 i 17 do 19, naznačena time, da sol ima uzorak difrakcije praha X-zraka koji sadrži jednu ili više ili dvije ili više ili tri vršne vrijednosti s difrakcijskim kutevima (2θ) odabranima iz skupine koja se sastoji od 7,5 ± 0,2, 11,3 ± 0,2 i 24,3 ± 0,2, koji se dobiva uporabom bakar-K-α1-X-zraka valne duljine od 1,5406 Angstroma; gdje kruto stanje NMR spektra sadrži jedan ili više ili dva ili više ili tri 13C-kemijska pomaka odabrana iz skupine koja se sastoji od 171,3 ± 0,2, 112,4 ± 0,2 i 43,8 ± 0,2 ppm; i kruto stanje NMR spektra sadrži 19F-kemijski pomak na -123,1 ± 0,2 ppm.
21. Sol prema bilo kojem od zahtjeva 12 do 14 i 17 do 20, naznačena time, da sol je bitno čisti polimorf od polimorfa maleat-oblik B.
22. Farmaceutski sastav, naznačen time, da obuhvaća sol prema bilo kojem od zahtjeva 1 do 21.
23. Sol prema bilo kojem od zahtjeva 1 do 21, i farmaceutski sastav prema zahtjevu 22, naznačen/a time, da se upotrebljava u postupku liječenja bolesnih stanja kod sisavaca koja su posredovana putem djelovanja poli(ADP-riboza)-polimeraza, pri čemu postupak obuhvaća primjenu terapeutski učinkovite količine navedene soli ili navedenog farmaceutskog sastava, na sisavcu kojemu je to potrebno.
24. Sol prema bilo kojem od zahtjeva 1 do 21, i farmaceutski sastav prema zahtjevu 22, naznačen/a time, da se upotrebljava u postupku liječenja raka kod sisavaca, pri čemu postupak obuhvaća primjenu terapeutski učinkovite količine navedene soli ili navedenog farmaceutskog sastava, na sisavcu kojemu je to potrebno.
25. Uporaba soli prema bilo kojem od zahtjeva 1 do 21, naznačena time, da je za proizvodnju lijeka za liječenje raka.
26. Postupak, naznačen time, da se koristi za proizvodnju soli prema bilo kojem od zahtjeva 1 do 21.
27. Postupak prema zahtjevu 26, naznačen time, da sol je polimorfna sol i bitno je oslobođena od ostalih polimorfnih oblika od 8-fluoro-2-{4-[(metilamino)metil]fenil}-1,3,4,5-tetrahidro-6H-azepino[5,4,3-cd]indol-6-ona.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US30427710P | 2010-02-12 | 2010-02-12 | |
PCT/IB2011/050571 WO2011098971A1 (en) | 2010-02-12 | 2011-02-10 | Salts and polymorphs of 8-fluoro-2-{4-[(methylamino}methyl]phenyl}-1,3,4,5-tetrahydro-6h-azepino[5,4,3-cd]indol-6-one |
EP11708094.5A EP2534153B1 (en) | 2010-02-12 | 2011-02-10 | Salts and polymorphs of 8-fluoro-2-{4-[(methylamino}methyl]phenyl}-1,3,4,5-tetrahydro-6h-azepino[5,4,3-cd]indol-6-one |
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HRP20161742T1 true HRP20161742T1 (hr) | 2017-02-24 |
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HRP20161742TT HRP20161742T1 (hr) | 2010-02-12 | 2016-12-19 | Soli i polimorfi od 8-fluoro-2-{4-[(metilamino)metil]fenil}-1,3,4,5-tetrahidro-6h-azepino[5,4,3-cd]indol-6-ona |
HRP20191944TT HRP20191944T1 (hr) | 2010-02-12 | 2019-10-25 | Soli i polimorfi od 8-fluoro-2-{4-[(metilamino)metil]fenil}-1,3,4,5-tetrahidro-6h-azepino[5,4,3-cd]indol-6-ona |
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HRP20191944TT HRP20191944T1 (hr) | 2010-02-12 | 2019-10-25 | Soli i polimorfi od 8-fluoro-2-{4-[(metilamino)metil]fenil}-1,3,4,5-tetrahidro-6h-azepino[5,4,3-cd]indol-6-ona |
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US (5) | US8754072B2 (hr) |
EP (4) | EP2534153B1 (hr) |
JP (6) | JP5745283B2 (hr) |
KR (2) | KR102108226B1 (hr) |
CN (2) | CN102884066B (hr) |
AR (2) | AR080164A1 (hr) |
AU (1) | AU2011213944B2 (hr) |
CA (2) | CA3024216C (hr) |
CY (3) | CY1118319T1 (hr) |
DK (2) | DK2534153T3 (hr) |
ES (2) | ES2607806T3 (hr) |
HK (1) | HK1176617A1 (hr) |
HR (2) | HRP20161742T1 (hr) |
HU (3) | HUE030969T2 (hr) |
IL (1) | IL220921B (hr) |
LT (3) | LT2534153T (hr) |
LU (1) | LUC00093I2 (hr) |
MX (1) | MX343383B (hr) |
NL (1) | NL300958I2 (hr) |
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Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011098971A1 (en) | 2010-02-12 | 2011-08-18 | Pfizer Inc. | Salts and polymorphs of 8-fluoro-2-{4-[(methylamino}methyl]phenyl}-1,3,4,5-tetrahydro-6h-azepino[5,4,3-cd]indol-6-one |
TW201516636A (zh) * | 2013-10-22 | 2015-05-01 | Hon Hai Prec Ind Co Ltd | 電子裝置及其供電方法 |
WO2016028689A1 (en) | 2014-08-22 | 2016-02-25 | Clovis Oncology, Inc. | High dosage strength tablets of rucaparib |
CN109415323A (zh) | 2016-05-16 | 2019-03-01 | 普尔玛根治疗(哮喘)有限公司 | 喹啉衍生物的结晶 |
DE102016218772A1 (de) * | 2016-09-28 | 2018-03-29 | Bruker Biospin Gmbh | Verbesserte Temperierung eines NMR-MAS-Rotors |
WO2018140377A1 (en) | 2017-01-24 | 2018-08-02 | Assia Chemical Industries Ltd. | Solid state forms of rucaparib and of rucaparib salts |
CN109651377B (zh) * | 2017-10-12 | 2020-10-20 | 成都海创药业有限公司 | 一种治疗癌症的化合物及其用途 |
CA3080657A1 (en) * | 2017-11-03 | 2019-05-09 | Sandoz Ag | Crystalline salt of a tricyclic poly(adp-ribose) polymerase inhibitor |
WO2019115000A1 (en) * | 2017-12-15 | 2019-06-20 | Advitech Advisory And Technologies Sa | Process for the preparation of rucaparib and novel synthesis intermediates |
WO2019130229A1 (en) | 2017-12-28 | 2019-07-04 | Mylan Laboratories Ltd | Methods and intermediates for preparing rucaparib |
CN111989137A (zh) | 2018-01-05 | 2020-11-24 | 赛博克萨1公司 | 用于治疗涉及酸性或缺氧性患病组织的疾病的化合物、组合物和方法 |
US10442813B2 (en) | 2018-01-30 | 2019-10-15 | RK Pharma Solutions LLC | Polymorphs of rucaparib camsylate and methods of making same |
WO2019207596A1 (en) | 2018-04-25 | 2019-10-31 | Mylan Laboratories Limited | Novel crystalline forms of rucaparib (s)-camsylate salt and rucaparib free base |
WO2019207498A1 (en) * | 2018-04-25 | 2019-10-31 | Biophore India Pharmaceuticals Pvt. Ltd | Solid forms of 8-fluoro-2-{4-[(methylamino)methyl] phenyl}-1,3,4,5-tetrahydro-6h-azepino[5,4,3-cd] indol-6-one ((1s,4r)-7,7dimethyl-2-oxobicyclo [2.2.1] hept-1-yl) methanesulfonic acid salt (rucaparib camsylate) and the prerparation thereof |
CN108743557A (zh) * | 2018-06-27 | 2018-11-06 | 李莉 | 一种磷酸瑞卡帕布软胶囊及其制备方法 |
CN109111454A (zh) * | 2018-08-01 | 2019-01-01 | 宁波金未生物科技有限公司 | 一种瑞卡帕布s-樟脑磺酸盐 |
CN111217818A (zh) * | 2018-11-27 | 2020-06-02 | 台耀化学股份有限公司 | 芦卡帕尼樟脑磺酸盐的结晶、及制备三环化合物、芦卡帕尼及其樟脑磺酸盐结晶的方法 |
WO2020113500A1 (zh) * | 2018-12-06 | 2020-06-11 | 上海诚妙医药科技有限公司 | 芦卡帕利樟脑磺酸盐的新晶型和制备方法及其用途 |
PE20220563A1 (es) | 2019-07-10 | 2022-04-13 | Cybrexa 2 Inc | Conjugados peptidicos de citotoxinas como terapeuticos |
CR20220057A (es) | 2019-07-10 | 2022-07-19 | Cybrexa 3 Inc | Conjugados peptídicos de agentes dirigidos a microtúbulos como terapéuticos |
CN111004244A (zh) * | 2019-12-27 | 2020-04-14 | 重庆市碚圣医药科技股份有限公司 | 一种瑞卡帕布樟脑磺酸盐的合成方法 |
EP4100125A1 (en) | 2020-02-03 | 2022-12-14 | Sandoz AG | Polymorph of rucaparib mesylate |
AU2021260109A1 (en) * | 2020-04-24 | 2022-12-15 | Astrazeneca Ab | Pharmaceutical formulations |
IL297537A (en) | 2020-04-28 | 2022-12-01 | Rhizen Pharmaceuticals Ag | New compounds useful as poly (adp-ribose) polymerase (parp) inhibitors |
CN116113406A (zh) | 2020-07-10 | 2023-05-12 | 密歇根大学董事会 | Gas41抑制剂及其使用方法 |
WO2022015557A1 (en) | 2020-07-14 | 2022-01-20 | Assia Chemical Industries Ltd | Solid state forms of rucaparib salts |
WO2022090938A1 (en) | 2020-10-31 | 2022-05-05 | Rhizen Pharmaceuticals Ag | Phthalazinone derivatives useful as parp inhibitors |
AU2022255809A1 (en) | 2021-04-08 | 2023-10-26 | Incozen Therapeutics Pvt. Ltd. | Inhibitors of poly(adp-ribose) polymerase |
WO2023137060A1 (en) | 2022-01-11 | 2023-07-20 | Assia Chemical Industries Ltd. | Solid state forms of rucaparib tosylate |
WO2023152754A1 (en) * | 2022-02-08 | 2023-08-17 | Sawant, Mohit Manikrao | Crystalline form of rosuvastatin allyl ester |
Family Cites Families (80)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4489011A (en) | 1983-05-16 | 1984-12-18 | Merrell Dow Pharmaceuticals Inc. | Hypoglycemic N-(2-substituted-3-dialkylamino-2-propenylidene)-N-alkylalkanaminium camsylate salts |
GB8607683D0 (en) | 1986-03-27 | 1986-04-30 | Ici Plc | Anti-tumor agents |
GB8608335D0 (en) | 1986-04-04 | 1986-05-08 | Pfizer Ltd | Pharmaceutically acceptable salts |
GB8827305D0 (en) | 1988-11-23 | 1988-12-29 | British Bio Technology | Compounds |
DE4125292A1 (de) * | 1991-07-31 | 1993-02-04 | Kali Chemie Pharma Gmbh | 6-oxo-azepinoindol-verbindungen sowie verfahren und zwischenprodukte zu ihrer herstellung und diese verbindungen enthaltende arzneimittel |
US5587458A (en) | 1991-10-07 | 1996-12-24 | Aronex Pharmaceuticals, Inc. | Anti-erbB-2 antibodies, combinations thereof, and therapeutic and diagnostic uses thereof |
AU675929B2 (en) | 1992-02-06 | 1997-02-27 | Curis, Inc. | Biosynthetic binding protein for cancer marker |
US6177401B1 (en) | 1992-11-13 | 2001-01-23 | Max-Planck-Gesellschaft Zur Forderung Der Wissenschaften | Use of organic compounds for the inhibition of Flk-1 mediated vasculogenesis and angiogenesis |
US5455258A (en) | 1993-01-06 | 1995-10-03 | Ciba-Geigy Corporation | Arylsulfonamido-substituted hydroxamic acids |
IL112248A0 (en) | 1994-01-25 | 1995-03-30 | Warner Lambert Co | Tricyclic heteroaromatic compounds and pharmaceutical compositions containing them |
US5863949A (en) | 1995-03-08 | 1999-01-26 | Pfizer Inc | Arylsulfonylamino hydroxamic acid derivatives |
CA2218503C (en) | 1995-04-20 | 2001-07-24 | Pfizer Inc. | Arylsulfonyl hydroxamic acid derivatives |
US5747498A (en) | 1996-05-28 | 1998-05-05 | Pfizer Inc. | Alkynyl and azido-substituted 4-anilinoquinazolines |
US5880141A (en) | 1995-06-07 | 1999-03-09 | Sugen, Inc. | Benzylidene-Z-indoline compounds for the treatment of disease |
GB9520822D0 (en) | 1995-10-11 | 1995-12-13 | Wellcome Found | Therapeutically active compounds |
GB9624482D0 (en) | 1995-12-18 | 1997-01-15 | Zeneca Phaema S A | Chemical compounds |
ATE225343T1 (de) | 1995-12-20 | 2002-10-15 | Hoffmann La Roche | Matrix-metalloprotease inhibitoren |
JP4464466B2 (ja) | 1996-03-05 | 2010-05-19 | アストラゼネカ・ユーケイ・リミテッド | 4―アニリノキナゾリン誘導体 |
JP3195756B2 (ja) | 1996-07-04 | 2001-08-06 | 公子 吉水 | 潤滑補助体 |
EP0818442A3 (en) | 1996-07-12 | 1998-12-30 | Pfizer Inc. | Cyclic sulphone derivatives as inhibitors of metalloproteinases and of the production of tumour necrosis factor |
TR199900048T2 (xx) | 1996-07-13 | 1999-04-21 | Glaxo Group Limited | Protein tirozin kinaz inhibit�rleri olarak bisiklik heteroaromatik bile�ikler |
ES2186908T3 (es) | 1996-07-13 | 2003-05-16 | Glaxo Group Ltd | Compuestos heterociciclos condensados como inhibidores de pproteina-tirosina-quinasas. |
HRP970371A2 (en) | 1996-07-13 | 1998-08-31 | Kathryn Jane Smith | Heterocyclic compounds |
HUP9903014A3 (en) | 1996-07-18 | 2000-08-28 | Pfizer | Phosphinate derivatives having matrix metalloprotease inhibitor effect and medicaments containing the same |
US6153609A (en) | 1996-08-23 | 2000-11-28 | Pfizer Inc | Arylsulfonylamino hydroxamic acid derivatives |
ID18494A (id) | 1996-10-02 | 1998-04-16 | Novartis Ag | Turunan pirazola leburan dan proses pembuatannya |
CA2277100C (en) | 1997-01-06 | 2005-11-22 | Pfizer Inc. | Cyclic sulfone derivatives |
TR199901849T2 (xx) | 1997-02-03 | 2000-02-21 | Pfizer Products Inc. | Arils�lfonilamino hidroksamik asit t�revleri. |
CA2279863A1 (en) | 1997-02-07 | 1998-08-13 | Pfizer Inc. | N-hydroxy-beta-sulfonyl-propionamide derivatives and their use as inhibitors of matrix metalloproteinases |
NZ336836A (en) | 1997-02-11 | 2001-02-23 | Pfizer | Arylsulfonyl hydroxamic acid derivatives suitable for a broad range of medicinal treatments |
CA2289102A1 (en) | 1997-05-07 | 1998-11-12 | Sugen, Inc. | 2-indolinone derivatives as modulators of protein kinase activity |
JP2002501532A (ja) | 1997-05-30 | 2002-01-15 | メルク エンド カンパニー インコーポレーテッド | 新規血管形成阻害薬 |
US5835420A (en) | 1997-06-27 | 1998-11-10 | Aplus Flash Technology, Inc. | Node-precise voltage regulation for a MOS memory system |
ATE263147T1 (de) | 1997-08-08 | 2004-04-15 | Pfizer Prod Inc | Derivate von aryloxyarylsulfonylamino hydroxyaminsäuren |
ATE368665T1 (de) | 1997-08-22 | 2007-08-15 | Astrazeneca Ab | Oxindolylchinazolinderivate als angiogenesehemmer |
EP1017682A4 (en) | 1997-09-26 | 2000-11-08 | Merck & Co Inc | NEW ANGIOGENESIS INHIBITORS |
CN1280580A (zh) | 1997-11-11 | 2001-01-17 | 辉瑞产品公司 | 用作抗癌药的噻吩并嘧啶和噻吩并吡啶衍生物 |
GB9725782D0 (en) | 1997-12-05 | 1998-02-04 | Pfizer Ltd | Therapeutic agents |
GB9800575D0 (en) | 1998-01-12 | 1998-03-11 | Glaxo Group Ltd | Heterocyclic compounds |
GB9800569D0 (en) | 1998-01-12 | 1998-03-11 | Glaxo Group Ltd | Heterocyclic compounds |
GB9801690D0 (en) | 1998-01-27 | 1998-03-25 | Pfizer Ltd | Therapeutic agents |
JP4462654B2 (ja) | 1998-03-26 | 2010-05-12 | ソニー株式会社 | 映像素材選択装置及び映像素材選択方法 |
PA8469501A1 (es) | 1998-04-10 | 2000-09-29 | Pfizer Prod Inc | Hidroxamidas del acido (4-arilsulfonilamino)-tetrahidropiran-4-carboxilico |
PA8469401A1 (es) | 1998-04-10 | 2000-05-24 | Pfizer Prod Inc | Derivados biciclicos del acido hidroxamico |
HUP0103617A2 (hu) | 1998-05-29 | 2002-02-28 | Sugen, Inc. | Protein kinázt gátló, pirrolilcsoporttal helyettesített 2-indolszármazékok, e vegyületeket tartalmazó gyógyászati készítmények, valamint e vegyületek alkalmazása |
UA60365C2 (uk) | 1998-06-04 | 2003-10-15 | Пфайзер Продактс Інк. | Похідні ізотіазолу, спосіб їх одержання, фармацевтична композиція та спосіб лікування гіперпроліферативного захворювання у ссавця |
DK1004578T3 (da) | 1998-11-05 | 2004-06-28 | Pfizer Prod Inc | 5-oxo-pyrrolidin-2-carboxylsyrehydroxamidderivater |
EP1140182A2 (en) | 1998-12-23 | 2001-10-10 | G.D. Searle & Co. | Use of a matrix metalloproteinase inhibitor together with an antineoplastic agent, optionally also together with radiation, in the treatment of neoplasia |
US6649645B1 (en) | 1998-12-23 | 2003-11-18 | Pharmacia Corporation | Combination therapy of radiation and a COX-2 inhibitor for treatment of neoplasia |
EP1140936B1 (en) | 1999-01-11 | 2004-03-17 | Agouron Pharmaceuticals, Inc. | Tricyclic inhibitors of poly(adp-ribose) polymerases |
KR100452491B1 (ko) | 2001-03-29 | 2004-10-12 | 한미약품 주식회사 | 신규한 결정형 암로디핀 캠실레이트 염 및 그의 제조방법 |
KR20040011751A (ko) | 2002-07-30 | 2004-02-11 | 씨제이 주식회사 | 암로디핀의 유기산염 |
AU2003283743A1 (en) | 2002-12-19 | 2004-07-14 | Pfizer Products Inc. | Complexes of E-2-Methoxy-N-(3-{4-[3-methyl-4-(6-methyl-pyridin-3-yloxy)-phenylamino]-quinazolin-6-yl}-allyl)-acetamide, their method of production, and use |
MXPA05010563A (es) * | 2003-03-31 | 2005-11-23 | Pfizer | Sales de los inhibidores triciclicos de las poli(adp-ribosa) polimerasas. |
CA2533332C (en) | 2003-07-25 | 2012-01-10 | Cancer Research Technology Limited | Therapeutic compounds |
BRPI0515255A (pt) * | 2004-09-22 | 2008-07-15 | Pfizer | método para preparar inibidores de poli(adp-ribose) polimerases |
KR20070046183A (ko) * | 2004-09-22 | 2007-05-02 | 화이자 인코포레이티드 | 폴리(에이디피-리보오스) 폴리머라제 저해제를 포함하는치료 배합물 |
WO2006033007A2 (en) | 2004-09-22 | 2006-03-30 | Pfizer Inc. | Polymorphic and amorphous forms of the phosphate salt of 8-fluoro-2-{4-[(methylamino)methyl]phenyl}-1,3,4,5-tetrahydro-6h-azepino[5,4,3-cd]indol-6-one |
CN101384264B (zh) * | 2004-09-22 | 2012-03-14 | 辉瑞大药厂 | 含有聚(adp-核糖)聚合酶抑制剂的治疗组合物 |
GB0502509D0 (en) | 2005-02-07 | 2005-03-16 | Pfizer Ltd | Novel salt form of a dopamine agonist |
MX2007010233A (es) * | 2005-02-23 | 2007-11-07 | Teva Pharma | Formulaciones de rasagilina de uniformidad de contenido mejorada. |
WO2008005036A1 (en) * | 2006-07-05 | 2008-01-10 | Teva Pharmaceutical Industries Ltd. | Pharmaceutical compositions of memantine |
KR100843401B1 (ko) | 2006-12-04 | 2008-07-04 | 씨제이제일제당 (주) | 결정성 s-(-)-암로디핀 캠실레이트 무수물 및 이의제조방법 |
PL2091910T3 (pl) * | 2006-12-06 | 2015-02-27 | Conatus Pharmaceuticals Inc | Postacie krystaliczne kwasu (3S)-3-[N-(N’-(2-tert-butylofenylo)oksamylo)alaninylo]amino-5-(2’,3’,5’,6’-tetrafluorofenoksy)-4-oksopentanowego |
WO2008114114A2 (en) * | 2007-03-16 | 2008-09-25 | Pfizer Products Inc. | Poly(adp-ribose) polymerases inhibitor for treating ophthalmic condition |
EP2065385A1 (en) | 2007-11-28 | 2009-06-03 | Laboratorios SALVAT, S.A. | Stable crystalline salt of (R)-3-fluorophenyl-3,4,5-trifluorobenzylcarbamic acid 1-azabiciyclo [2.2.2]oct-3-yl ester |
US20110053997A1 (en) * | 2007-12-05 | 2011-03-03 | Alexander Beliaev | Salts and Crystal Forms |
KR20090060674A (ko) | 2007-12-10 | 2009-06-15 | 씨제이제일제당 (주) | 결정형의 지프라시돈 술폰산염, 그 제조방법, 및 그것를포함하는 약제학적 조성물 |
CN106008460B (zh) | 2008-01-08 | 2022-08-12 | 默沙东公司 | 2-{4-[(3s)-哌啶-3-基]苯基}-2h-吲唑-7-羧酰胺的药学可接受的盐 |
BRPI1006813A2 (pt) | 2009-01-17 | 2016-04-12 | Boomerang Systems Inc | sistema de armazenamento automático e veículo de transporte |
WO2011098971A1 (en) * | 2010-02-12 | 2011-08-18 | Pfizer Inc. | Salts and polymorphs of 8-fluoro-2-{4-[(methylamino}methyl]phenyl}-1,3,4,5-tetrahydro-6h-azepino[5,4,3-cd]indol-6-one |
CN103930931A (zh) | 2011-09-23 | 2014-07-16 | 金泰克斯公司 | 用于后视镜显示的***和方法 |
WO2013099476A1 (ja) | 2011-12-26 | 2013-07-04 | ウィンテックポリマー株式会社 | ポリブチレンテレフタレート樹脂ペレット、及び当該ポリブチレンテレフタレート樹脂ペレットの製造方法 |
US9384339B2 (en) | 2012-01-13 | 2016-07-05 | Telecommunication Systems, Inc. | Authenticating cloud computing enabling secure services |
US9672526B2 (en) | 2012-03-13 | 2017-06-06 | American Express Travel Related Services Company, Inc. | Systems and methods for tailoring marketing |
KR101984831B1 (ko) | 2013-01-31 | 2019-05-31 | 삼성전자 주식회사 | 반도체 패키지 및 그 제조 방법 |
CN103309115B (zh) | 2013-05-30 | 2016-03-23 | 京东方科技集团股份有限公司 | 彩色电泳显示面板及其制造方法、显示装置 |
US9501163B2 (en) | 2014-05-06 | 2016-11-22 | Symbol Technologies, Llc | Apparatus and method for activating a trigger mechanism |
US10884952B2 (en) | 2016-09-30 | 2021-01-05 | Intel Corporation | Enforcing memory operand types using protection keys |
JP6943759B2 (ja) | 2017-12-28 | 2021-10-06 | 株式会社東海理化電機製作所 | シフト装置 |
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- 2019-12-26 JP JP2019235421A patent/JP2020050671A/ja not_active Withdrawn
-
2021
- 2021-05-06 JP JP2021078485A patent/JP2021107460A/ja active Pending
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