SK9122003A3 - Tetrahydropyridine derivatives, their preparation and their use as cell proliferation inhibitors - Google Patents

Tetrahydropyridine derivatives, their preparation and their use as cell proliferation inhibitors Download PDF

Info

Publication number: SK9122003A3
Authority: SK; Slovakia
Prior art keywords: dihydro; isoquinolin; group; formula; compound
Prior art date: 2000-12-23

Application number

SK912-2003A

Other languages

English (en)

Slovak (sk)

Inventor

Guy Georges

Adelbert Grossmann

Olaf Mundigl

Der Saal Wolfgang Von

Tim Sattelkau

Original Assignee

Hoffmann La Roche

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2000-12-23

Filing date

2001-12-21

Publication date

2004-02-03

2001-12-21 Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche

2004-02-03 Publication of SK9122003A3 publication Critical patent/SK9122003A3/sk

Links

230000004663 cell proliferation Effects 0.000 title claims description 7
238000002360 preparation method Methods 0.000 title claims description 7
239000003112 inhibitor Substances 0.000 title claims description 5
VSWICNJIUPRZIK-UHFFFAOYSA-N 2-piperideine Chemical class C1CNC=CC1 VSWICNJIUPRZIK-UHFFFAOYSA-N 0.000 title description 16
150000001875 compounds Chemical class 0.000 claims abstract description 51
238000000034 method Methods 0.000 claims abstract description 19
239000008194 pharmaceutical composition Substances 0.000 claims abstract description 4
230000008569 process Effects 0.000 claims abstract description 4
-1 amino- Chemical class 0.000 claims description 41
125000000217 alkyl group Chemical group 0.000 claims description 19
125000001424 substituent group Chemical group 0.000 claims description 17
150000003839 salts Chemical class 0.000 claims description 14
239000000203 mixture Substances 0.000 claims description 12
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 10
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 10
125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 8
102000003964 Histone deacetylase Human genes 0.000 claims description 8
108090000353 Histone deacetylase Proteins 0.000 claims description 8
125000004432 carbon atom Chemical group C* 0.000 claims description 8
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 8
125000006239 protecting group Chemical group 0.000 claims description 8
125000003282 alkyl amino group Chemical group 0.000 claims description 7
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 6
125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 6
239000000460 chlorine Substances 0.000 claims description 6
229910052801 chlorine Inorganic materials 0.000 claims description 6
125000005843 halogen group Chemical group 0.000 claims description 6
230000002401 inhibitory effect Effects 0.000 claims description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
125000005236 alkanoylamino group Chemical group 0.000 claims description 5
125000005530 alkylenedioxy group Chemical group 0.000 claims description 5
HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims description 4
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UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
239000003814 drug Substances 0.000 claims description 4
229910052736 halogen Inorganic materials 0.000 claims description 4
150000002367 halogens Chemical class 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
125000001041 indolyl group Chemical group 0.000 claims description 4
RGUVUPQQFXCJFC-UHFFFAOYSA-N n-hydroxyoctanamide Chemical compound CCCCCCCC(=O)NO RGUVUPQQFXCJFC-UHFFFAOYSA-N 0.000 claims description 4
229910052760 oxygen Inorganic materials 0.000 claims description 4
239000001301 oxygen Substances 0.000 claims description 4
229910052717 sulfur Inorganic materials 0.000 claims description 4
125000004434 sulfur atom Chemical group 0.000 claims description 4
NIDFZDATJZQXTB-UHFFFAOYSA-N 8-(3,4-dihydro-1h-isoquinolin-2-yl)-n-hydroxyoctanamide Chemical compound C1=CC=C2CN(CCCCCCCC(=O)NO)CCC2=C1 NIDFZDATJZQXTB-UHFFFAOYSA-N 0.000 claims description 3
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125000002009 alkene group Chemical group 0.000 claims description 3
229910052731 fluorine Inorganic materials 0.000 claims description 3
239000011737 fluorine Substances 0.000 claims description 3
238000007327 hydrogenolysis reaction Methods 0.000 claims description 3
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 3
WSOCEYYLZHIVEI-UHFFFAOYSA-N 8-(6,7-diethoxy-3,4-dihydro-1h-isoquinolin-2-yl)-n-hydroxyoctanamide Chemical compound C1CN(CCCCCCCC(=O)NO)CC2=C1C=C(OCC)C(OCC)=C2 WSOCEYYLZHIVEI-UHFFFAOYSA-N 0.000 claims description 2
CNUTXVMVZXKCPJ-UHFFFAOYSA-N 8-(6,7-dimethoxy-1-phenyl-3,4-dihydro-1h-isoquinolin-2-yl)-n-hydroxyoctanamide Chemical compound C1=2C=C(OC)C(OC)=CC=2CCN(CCCCCCCC(=O)NO)C1C1=CC=CC=C1 CNUTXVMVZXKCPJ-UHFFFAOYSA-N 0.000 claims description 2
GWBJXKKKWGIYMG-UHFFFAOYSA-N 8-(6,7-dimethoxy-1-propan-2-yl-3,4-dihydro-1h-isoquinolin-2-yl)-n-hydroxyoctanamide Chemical compound C1CN(CCCCCCCC(=O)NO)C(C(C)C)C2=C1C=C(OC)C(OC)=C2 GWBJXKKKWGIYMG-UHFFFAOYSA-N 0.000 claims description 2
MIIOZNKTWSSHFH-UHFFFAOYSA-N 8-(6,7-dimethoxy-3-methyl-3,4-dihydro-1h-isoquinolin-2-yl)-n-hydroxyoctanamide Chemical compound C1C(C)N(CCCCCCCC(=O)NO)CC2=C1C=C(OC)C(OC)=C2 MIIOZNKTWSSHFH-UHFFFAOYSA-N 0.000 claims description 2
239000004480 active ingredient Substances 0.000 claims description 2
125000003118 aryl group Chemical group 0.000 claims description 2
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RZIWVBYJMFCTQG-UHFFFAOYSA-N 8-(6,7-dimethoxy-3,4-dihydro-1h-isoquinolin-2-yl)-n-hydroxyoctanamide Chemical compound C1CN(CCCCCCCC(=O)NO)CC2=C1C=C(OC)C(OC)=C2 RZIWVBYJMFCTQG-UHFFFAOYSA-N 0.000 claims 1
125000002947 alkylene group Chemical group 0.000 claims 1
125000005237 alkyleneamino group Chemical group 0.000 claims 1
230000000694 effects Effects 0.000 abstract description 5
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230000035755 proliferation Effects 0.000 abstract 1
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239000002585 base Substances 0.000 description 10
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
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DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 6
241000124008 Mammalia Species 0.000 description 6
SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 6
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
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UWYZHKAOTLEWKK-UHFFFAOYSA-N 1,2,3,4-tetrahydroisoquinoline Chemical group C1=CC=C2CNCCC2=C1 UWYZHKAOTLEWKK-UHFFFAOYSA-N 0.000 description 4
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235000013024 sodium fluoride Nutrition 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
239000008174 sterile solution Substances 0.000 description 1
210000002784 stomach Anatomy 0.000 description 1
201000000498 stomach carcinoma Diseases 0.000 description 1
238000007920 subcutaneous administration Methods 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
239000000758 substrate Substances 0.000 description 1
229960001603 tamoxifen Drugs 0.000 description 1
RCINICONZNJXQF-MZXODVADSA-N taxol Chemical compound O([C@@H]1[C@@]2(C[C@@H](C(C)=C(C2(C)C)[C@H](C([C@]2(C)[C@@H](O)C[C@H]3OC[C@]3([C@H]21)OC(C)=O)=O)OC(=O)C)OC(=O)[C@H](O)[C@@H](NC(=O)C=1C=CC=CC=1)C=1C=CC=CC=1)O)C(=O)C1=CC=CC=C1 RCINICONZNJXQF-MZXODVADSA-N 0.000 description 1
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
ZXLDQJLIBNPEFJ-UHFFFAOYSA-N tetrahydro-beta-carboline Natural products C1CNC(C)C2=C1C1=CC=C(OC)C=C1N2 ZXLDQJLIBNPEFJ-UHFFFAOYSA-N 0.000 description 1
229940124597 therapeutic agent Drugs 0.000 description 1
238000002560 therapeutic procedure Methods 0.000 description 1
238000004809 thin layer chromatography Methods 0.000 description 1
210000001519 tissue Anatomy 0.000 description 1
238000011200 topical administration Methods 0.000 description 1
229940044693 topoisomerase inhibitor Drugs 0.000 description 1
230000002103 transcriptional effect Effects 0.000 description 1
230000009466 transformation Effects 0.000 description 1
229960000575 trastuzumab Drugs 0.000 description 1
210000003932 urinary bladder Anatomy 0.000 description 1
229960003048 vinblastine Drugs 0.000 description 1
JXLYSJRDGCGARV-XQKSVPLYSA-N vincaleukoblastine Chemical compound C([C@@H](C[C@]1(C(=O)OC)C=2C(=CC3=C([C@]45[C@H]([C@@]([C@H](OC(C)=O)[C@]6(CC)C=CCN([C@H]56)CC4)(O)C(=O)OC)N3C)C=2)OC)C[C@@](C2)(O)CC)N2CCC2=C1NC1=CC=CC=C21 JXLYSJRDGCGARV-XQKSVPLYSA-N 0.000 description 1
238000005406 washing Methods 0.000 description 1
238000010626 work up procedure Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—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
- 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
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
- 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
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/02—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
- C07D217/04—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines with hydrocarbon or substituted hydrocarbon radicals attached to the ring nitrogen atom

Landscapes

Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Veterinary Medicine (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
General Chemical & Material Sciences (AREA)
Pharmacology & Pharmacy (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
Chemical Kinetics & Catalysis (AREA)
Public Health (AREA)
Medicinal Chemistry (AREA)
Engineering & Computer Science (AREA)
Bioinformatics & Cheminformatics (AREA)
Hematology (AREA)
Oncology (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Other In-Based Heterocyclic Compounds (AREA)

SK912-2003A 2000-12-23 2001-12-21 Tetrahydropyridine derivatives, their preparation and their use as cell proliferation inhibitors SK9122003A3 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
EP00128487		2000-12-23
PCT/EP2001/015390 WO2002051842A1 (fr)	2000-12-23	2001-12-21	Derives de tetrahydropyridine, leur preparation et leur utilisation en tant qu'inhibiteurs de proliferation cellulaire

Publications (1)

Publication Number	Publication Date
SK9122003A3 true SK9122003A3 (en)	2004-02-03

Family

ID=8170814

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK912-2003A SK9122003A3 (en)	2000-12-23	2001-12-21	Tetrahydropyridine derivatives, their preparation and their use as cell proliferation inhibitors

Country Status (27)

Country	Link
US (1)	US6800638B2 (fr)
EP (1)	EP1353921B1 (fr)
JP (1)	JP2004516325A (fr)
KR (1)	KR100836545B1 (fr)
CN (1)	CN1213046C (fr)
AR (1)	AR035513A1 (fr)
AT (1)	ATE323700T1 (fr)
AU (1)	AU2002226397B2 (fr)
BG (1)	BG107935A (fr)
BR (1)	BR0116402A (fr)
CA (1)	CA2431471A1 (fr)
CZ (1)	CZ20031940A3 (fr)
DE (1)	DE60118975T2 (fr)
EC (1)	ECSP034664A (fr)
ES (1)	ES2261519T3 (fr)
HU (1)	HUP0400554A2 (fr)
IL (1)	IL156131A0 (fr)
MA (1)	MA26976A1 (fr)
MX (1)	MXPA03005713A (fr)
NO (1)	NO20032830L (fr)
NZ (1)	NZ526189A (fr)
PL (1)	PL365531A1 (fr)
RU (1)	RU2276140C2 (fr)
SK (1)	SK9122003A3 (fr)
WO (1)	WO2002051842A1 (fr)
YU (1)	YU48803A (fr)
ZA (1)	ZA200304264B (fr)

Families Citing this family (34)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6706686B2 (en)	2001-09-27	2004-03-16	The Regents Of The University Of Colorado	Inhibition of histone deacetylase as a treatment for cardiac hypertrophy
CA2463552C (fr)	2001-10-16	2011-05-17	Sloan-Kettering Institute For Cancer Research	Traitement des maladies neurodegeneratives et du cancer du cerveau
WO2003083323A1 (fr)	2002-04-01	2003-10-09	Ranko Rakanovic	Élément élastique en caoutchouc
US7154002B1 (en)	2002-10-08	2006-12-26	Takeda San Diego, Inc.	Histone deacetylase inhibitors
US7250514B1 (en)	2002-10-21	2007-07-31	Takeda San Diego, Inc.	Histone deacetylase inhibitors
AU2003900608A0 (en) *	2003-02-11	2003-02-27	Fujisawa Pharmaceutical Co., Ltd.	Hdac inhibitor
JP2006520796A (ja)	2003-03-17	2006-09-14	タケダサンディエゴインコーポレイテッド	ヒストンデアセチラーゼインヒビター
WO2004113336A1 (fr) *	2003-06-16	2004-12-29	Chroma Therapeutics Limited	Derives de carboline et de betacarboline inhibiteurs de l'enzyme hdac
EP1694329A4 (fr) *	2003-11-26	2009-06-03	Aton Pharma Inc	Derives d'acide hydroxamique a base d'acide diamine et iminodiacetique
US20050159470A1 (en) *	2003-12-19	2005-07-21	Syrrx, Inc.	Histone deacetylase inhibitors
WO2005066151A2 (fr) *	2003-12-19	2005-07-21	Takeda San Diego, Inc.	Inhibiteurs d'histone desacetylase
WO2006066133A2 (fr) *	2004-12-16	2006-06-22	Takeda San Diego, Inc.	Inhibiteurs d'histone desacetylase
US7772245B2 (en)	2005-02-14	2010-08-10	Miikana Therapeutics, Inc.	Inhibitors of histone deacetylase
GB0509223D0 (en)	2005-05-05	2005-06-15	Chroma Therapeutics Ltd	Enzyme inhibitors
US7642253B2 (en) *	2005-05-11	2010-01-05	Takeda San Diego, Inc.	Histone deacetylase inhibitors
KR20080032188A (ko) *	2005-07-14	2008-04-14	다케다 샌디에고, 인코포레이티드	히스톤 탈아세틸화 효소 억제제
EP2258359A3 (fr)	2005-08-26	2011-04-06	Braincells, Inc.	Neurogenèse par modulation des récepteurs muscariniques avec sabcomeline
JP2009506069A (ja)	2005-08-26	2009-02-12	ブレインセルス，インコーポレイティド	ムスカリン性受容体調節による神経発生
JP2009512711A (ja)	2005-10-21	2009-03-26	ブレインセルス，インコーポレイティド	Ｐｄｅ阻害による神経新生の調節
EP2314289A1 (fr)	2005-10-31	2011-04-27	Braincells, Inc.	Modulation de la neurogenese dont la médiation est assurée par récepteur gaba
EP1976835A2 (fr) *	2006-01-13	2008-10-08	Takeda San Diego, Inc.	Inhibiteurs des histone desacetylases
US20100216734A1 (en)	2006-03-08	2010-08-26	Braincells, Inc.	Modulation of neurogenesis by nootropic agents
CA2651862A1 (fr)	2006-05-09	2007-11-22	Braincells, Inc.	Neurogenese induite par le recepteur 5ht
AU2007249399A1 (en)	2006-05-09	2007-11-22	Braincells, Inc.	Neurogenesis by modulating angiotensin
WO2008030651A1 (fr)	2006-09-08	2008-03-13	Braincells, Inc.	Combinaisons contenant un dérivé de 4-acylaminopyridine
US20100184806A1 (en)	2006-09-19	2010-07-22	Braincells, Inc.	Modulation of neurogenesis by ppar agents
TWI425945B (zh) *	2007-05-28	2014-02-11	Seldar Pharma Inc	四氫異喹啉－１－酮衍生物或其鹽
US20100216805A1 (en)	2009-02-25	2010-08-26	Braincells, Inc.	Modulation of neurogenesis using d-cycloserine combinations
CA2768466C (fr) *	2009-07-22	2018-08-14	The Board Of Trustees Of The University Of Illinois	Inhibiteurs de hdac et procedes therapeutiques les utilisant
CN102153549B (zh) *	2010-12-14	2012-11-14	华东理工大学	γ咔啉化合物、制备方法和用途
PL2991982T3 (pl)	2013-04-29	2019-03-29	Chong Kun Dang Pharmaceutical Corp.	Nowe związki dla selektywnych inhibitorów deacetylazy histonowej i zawierające je kompozycja farmaceutyczna
WO2015051035A1 (fr)	2013-10-01	2015-04-09	The J. David Gladstone Institutes	Compositions, systèmes et procédés pour le criblage de médicament de bruit d'expression génétique et leurs utilisations
CN108084178B (zh) *	2018-01-04	2020-09-01	济南大学	一类含有四氢-β-咔碄结构的异羟肟酸类化合物的用途
CN108558653A (zh) *	2018-05-14	2018-09-21	湖南华腾制药有限公司	赛乐西帕中间体及赛乐西帕的制备方法

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
HU196758B (en) *	1986-05-21	1989-01-30	Gyogyszerkutato Intezet	Process for production of 3-hidroxi-methil-quinolines and medical compositions containing them
WO1990002119A1 (fr) *	1988-08-18	1990-03-08	Banyu Pharmaceutical Co., Ltd.	Derives de 1,2,3,4-tetrahydro-isoquinoline
US5369108A (en) *	1991-10-04	1994-11-29	Sloan-Kettering Institute For Cancer Research	Potent inducers of terminal differentiation and methods of use thereof
US6429212B1 (en) *	1996-08-16	2002-08-06	Ishihara Sangyo Kaisha Ltd.	Medicinal composition
WO1998015525A1 (fr)	1996-10-07	1998-04-16	Sumitomo Pharmaceuticals Co., Ltd.	Acides hydroxamiques
AUPO721997A0 (en) *	1997-06-06	1997-07-03	Queensland Institute Of Medical Research, The	Anticancer compounds
US6465468B1 (en) *	1999-03-22	2002-10-15	Darwin Discovery Limited	Hydroxamic and carboxylic acid derivatives

2001
- 2001-12-06 AR ARP010105675A patent/AR035513A1/es not_active Application Discontinuation
- 2001-12-21 WO PCT/EP2001/015390 patent/WO2002051842A1/fr not_active Ceased
- 2001-12-21 ES ES01995721T patent/ES2261519T3/es not_active Expired - Lifetime
- 2001-12-21 US US10/451,757 patent/US6800638B2/en not_active Expired - Fee Related
- 2001-12-21 CZ CZ20031940A patent/CZ20031940A3/cs unknown
- 2001-12-21 HU HU0400554A patent/HUP0400554A2/hu unknown
- 2001-12-21 MX MXPA03005713A patent/MXPA03005713A/es active IP Right Grant
- 2001-12-21 NZ NZ526189A patent/NZ526189A/en unknown
- 2001-12-21 YU YU48803A patent/YU48803A/sh unknown
- 2001-12-21 CA CA002431471A patent/CA2431471A1/fr not_active Abandoned
- 2001-12-21 PL PL01365531A patent/PL365531A1/xx not_active Application Discontinuation
- 2001-12-21 AT AT01995721T patent/ATE323700T1/de not_active IP Right Cessation
- 2001-12-21 RU RU2003122190/04A patent/RU2276140C2/ru active
- 2001-12-21 KR KR1020037008028A patent/KR100836545B1/ko not_active Expired - Fee Related
- 2001-12-21 IL IL15613101A patent/IL156131A0/xx unknown
- 2001-12-21 EP EP01995721A patent/EP1353921B1/fr not_active Expired - Lifetime
- 2001-12-21 SK SK912-2003A patent/SK9122003A3/sk unknown
- 2001-12-21 JP JP2002552937A patent/JP2004516325A/ja not_active Ceased
- 2001-12-21 BR BR0116402-3A patent/BR0116402A/pt not_active IP Right Cessation
- 2001-12-21 AU AU2002226397A patent/AU2002226397B2/en not_active Ceased
- 2001-12-21 CN CNB018212050A patent/CN1213046C/zh not_active Expired - Fee Related
- 2001-12-21 DE DE60118975T patent/DE60118975T2/de not_active Expired - Fee Related
2003
- 2003-05-30 ZA ZA200304264A patent/ZA200304264B/en unknown
- 2003-06-20 MA MA27207A patent/MA26976A1/fr unknown
- 2003-06-20 NO NO20032830A patent/NO20032830L/no not_active Application Discontinuation
- 2003-06-22 EC EC2003004664A patent/ECSP034664A/es unknown
- 2003-06-23 BG BG107935A patent/BG107935A/bg unknown

Also Published As

Publication number	Publication date
CA2431471A1 (fr)	2002-07-04
ECSP034664A (es)	2003-07-25
NO20032830D0 (no)	2003-06-20
US20040053960A1 (en)	2004-03-18
EP1353921A1 (fr)	2003-10-22
CN1213046C (zh)	2005-08-03
KR20030063424A (ko)	2003-07-28
ES2261519T3 (es)	2006-11-16
BR0116402A (pt)	2003-11-11
AU2002226397B2 (en)	2006-10-05
RU2003122190A (ru)	2005-02-27
AR035513A1 (es)	2004-06-02
PL365531A1 (en)	2005-01-10
ATE323700T1 (de)	2006-05-15
CN1483033A (zh)	2004-03-17
YU48803A (sh)	2006-05-25
DE60118975T2 (de)	2006-12-21
RU2276140C2 (ru)	2006-05-10
WO2002051842A1 (fr)	2002-07-04
IL156131A0 (en)	2003-12-23
NO20032830L (no)	2003-08-04
CZ20031940A3 (cs)	2003-10-15
US6800638B2 (en)	2004-10-05
ZA200304264B (en)	2004-08-30
NZ526189A (en)	2004-10-29
MXPA03005713A (es)	2003-10-06
BG107935A (bg)	2004-08-31
EP1353921B1 (fr)	2006-04-19
MA26976A1 (fr)	2004-12-20
JP2004516325A (ja)	2004-06-03
DE60118975D1 (de)	2006-05-24
KR100836545B1 (ko)	2008-06-10
HUP0400554A2 (hu)	2004-06-28

Publication	Publication Date	Title
SK9122003A3 (en)	2004-02-03	Tetrahydropyridine derivatives, their preparation and their use as cell proliferation inhibitors
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AU2002226397A1 (en)	2003-01-23	Tetrahydropyridine derivatives, their preparation and their use as cell proliferation inhibitors
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CN103373986B (zh)	2016-10-05	克里唑替尼前药及其制备方法与用途
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AU687414B2 (en)	1998-02-26	Piperidinyl substituted methanoanthracenes as D1/D2-antagonists and 5HT2-serotanin-antagonists