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TN2009000287A1 - Cyclized derivatives as eg-5inhibitors - Google Patents

Cyclized derivatives as eg-5inhibitors

Info

Publication number
TN2009000287A1
TN2009000287A1 TNP2009000287A TN2009000287A TN2009000287A1 TN 2009000287 A1 TN2009000287 A1 TN 2009000287A1 TN P2009000287 A TNP2009000287 A TN P2009000287A TN 2009000287 A TN2009000287 A TN 2009000287A TN 2009000287 A1 TN2009000287 A1 TN 2009000287A1
Authority
TN
Tunisia
Prior art keywords
compounds
pharmaceutically acceptable
cyclized derivatives
cyclized
derivatives
Prior art date
Application number
TNP2009000287A
Other languages
English (en)
Inventor
Rustum Boyce
Eric Martin
Weibo Wang
Hong Yang
Paul A Barsanti
Original Assignee
Novartis Ag
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.)
Filing date
Publication date
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of TN2009000287A1 publication Critical patent/TN2009000287A1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic 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
    • C07D403/06Heterocyclic 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 carbon chain containing only aliphatic carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/42Oxazoles
    • A61K31/422Oxazoles not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/06Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Hematology (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
TNP2009000287A 2007-01-05 2009-07-03 Cyclized derivatives as eg-5inhibitors TN2009000287A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US88374007P 2007-01-05 2007-01-05
PCT/US2008/050149 WO2008086122A2 (fr) 2007-01-05 2008-01-03 Dérivés cyclisés en tant qu'inhibiteurs d'eg-5

Publications (1)

Publication Number Publication Date
TN2009000287A1 true TN2009000287A1 (en) 2010-12-31

Family

ID=39577804

Family Applications (1)

Application Number Title Priority Date Filing Date
TNP2009000287A TN2009000287A1 (en) 2007-01-05 2009-07-03 Cyclized derivatives as eg-5inhibitors

Country Status (30)

Country Link
US (3) US7820646B2 (fr)
EP (1) EP2106399A2 (fr)
JP (1) JP2010515687A (fr)
KR (1) KR20090097210A (fr)
CN (1) CN101622247A (fr)
AR (1) AR064760A1 (fr)
AU (1) AU2008205169B2 (fr)
BR (1) BRPI0806264A2 (fr)
CA (1) CA2674318A1 (fr)
CL (1) CL2008000029A1 (fr)
CO (1) CO6561828A2 (fr)
CR (1) CR10879A (fr)
DO (1) DOP2009000169A (fr)
EA (1) EA200900924A1 (fr)
EC (1) ECSP099485A (fr)
GE (1) GEP20125415B (fr)
GT (1) GT200900192A (fr)
HN (1) HN2009001262A (fr)
MA (1) MA31080B1 (fr)
MX (1) MX2009007260A (fr)
NI (1) NI200900134A (fr)
NZ (1) NZ577727A (fr)
PE (1) PE20081850A1 (fr)
SM (1) SMP200900065B (fr)
SV (1) SV2009003325A (fr)
TN (1) TN2009000287A1 (fr)
TW (1) TW200836722A (fr)
UA (1) UA97821C2 (fr)
WO (1) WO2008086122A2 (fr)
ZA (1) ZA200904175B (fr)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8252832B2 (en) 2007-12-14 2012-08-28 Novartis Ag Kinesin inhibitors as cancer therapeutics
MX2012011910A (es) 2010-04-15 2012-11-29 Novartis Ag Compuestos de triazol como inhibidores de ksp.
WO2011128388A2 (fr) * 2010-04-15 2011-10-20 Novartis Ag Composés d'oxazole et de thiazole comme inhibiteurs de ksp
EP2390247A1 (fr) * 2010-05-26 2011-11-30 Netherlands Organisation for Scientific Research (Advanced Chemical Technologies for Sustainability) Préparation de caprolactone, caprolactam, 2,5-tétrahydrofuranne diméthanol, 1,6-héxanediol ou 1,2,6-hexanetriol à partir de 5-hydroxymethyl-2-furfuraldehyde
GB201113538D0 (en) 2011-08-04 2011-09-21 Karobio Ab Novel estrogen receptor ligands
US9498540B2 (en) 2013-03-15 2016-11-22 Novartis Ag Cell proliferation inhibitors and conjugates thereof
CN105451773A (zh) * 2013-03-15 2016-03-30 诺华股份有限公司 细胞增殖抑制剂及其缀合物
KR102329024B1 (ko) * 2013-12-23 2021-11-19 바이엘 파마 악티엔게젤샤프트 키네신 스핀들 단백질(ksp)과의 항체 약물 접합체 (adcs)
JP6971858B2 (ja) * 2015-06-22 2021-11-24 バイエル ファーマ アクチエンゲゼルシャフト 酵素開裂性基を有する抗体薬物複合体(adc)および抗体プロドラッグ複合体(apdc)
CN105330657B (zh) * 2015-12-08 2019-05-21 华润双鹤药业股份有限公司 5-氯-2-[5-(r)-甲基-1,4-二氮杂环庚烷-1-]苯并恶唑的制备方法
CN105367506B (zh) * 2015-12-08 2021-02-05 华润双鹤药业股份有限公司 手性高哌嗪环的制备方法
EP3919518A1 (fr) 2016-06-15 2021-12-08 Bayer Pharma Aktiengesellschaft Conjugués anticorps-médicament spécifiques (adc) avec inhibiteurs de ksp et des anticorps anti-cd123
CN110072556B (zh) 2016-12-21 2023-05-02 拜耳制药股份公司 具有ksp抑制剂的特异性抗体药物缀合物(adc)
IL291308B2 (en) 2016-12-21 2024-07-01 Bayer Pharma AG Antibody drug conjugates (adcs) having enzymatically cleavable groups
EP3806908A1 (fr) 2018-06-18 2021-04-21 Bayer Aktiengesellschaft Conjugués liant-principe actif inhibant cxcr5 comprenant des éléments de liaison pouvant être fragmentés de manière enzymatique et présentant un profil d'action amélioré
CN119859151A (zh) * 2023-10-19 2025-04-22 北京振东光明药物研究院有限公司 从白土苓中分离得到的生物碱类化合物及其制备方法和应用

Family Cites Families (75)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2550959C3 (de) 1975-11-13 1980-12-04 Hoechst Ag, 6000 Frankfurt Tetrazolyl-imidazole und Tetrazolyl--benzimidazole, Verfahren zu deren Herstellung und diese enthaltende Arzneimittel
US4235871A (en) 1978-02-24 1980-11-25 Papahadjopoulos Demetrios P Method of encapsulating biologically active materials in lipid vesicles
US4501728A (en) 1983-01-06 1985-02-26 Technology Unlimited, Inc. Masking of liposomes from RES recognition
GB2157285B (en) 1984-04-11 1987-10-28 Erba Farmitalia 1h, 7h-pyrazolo1, 5-a pyrimidine-7-one derivatives and process for their preparation
US5023252A (en) 1985-12-04 1991-06-11 Conrex Pharmaceutical Corporation Transdermal and trans-membrane delivery of drugs
US4837028A (en) 1986-12-24 1989-06-06 Liposome Technology, Inc. Liposomes with enhanced circulation time
US5011472A (en) 1988-09-06 1991-04-30 Brown University Research Foundation Implantable delivery system for biological factors
US5859012A (en) * 1996-04-03 1999-01-12 Merck & Co., Inc. Inhibitors of farnesyl-protein transferase
WO1998027108A2 (fr) 1996-12-16 1998-06-25 Fujisawa Pharmaceutical Co., Ltd. Nouveaux composes amide
US6117940A (en) 1997-10-17 2000-09-12 Mjalli; Adnan M. M. Amino-ketone solid support templates
US6172087B1 (en) 1998-06-03 2001-01-09 Gpi Nil Holding, Inc. N-oxide of heterocyclic ester, amide, thioester, or ketone hair growth compositions and uses
CA2369549A1 (fr) 1999-04-02 2000-10-12 Robert W. Desimone Derives d'aminoalkyle-imidazole condenses aryles et heteroaryles et leur utilisation comme antidiabetiques
US6271241B1 (en) 1999-04-02 2001-08-07 Neurogen Corporation Cycloalkyl and aryl fused aminoalkyl-imidazole derivatives: modulators and GLP-1 receptors
US7291641B2 (en) 1999-10-11 2007-11-06 Societe De Conseils De Recherches Et D'applications Scientifiques (S.C.R.A.S.) Derivatives of heterocycles with 5 members, their preparation and their use as medicaments
US20040132788A1 (en) 1999-10-11 2004-07-08 Chabrier De Lassauniere Pierre-Etienne Derivatives of heterocycles with 5 members, their preparation and their use as medicaments
TWI292316B (en) 1999-10-11 2008-01-11 Sod Conseils Rech Applic Pharmaceutical composition of thiazole derivatives intended to inhibit mao and/or lipidic peroxidation and/or to act as modulators of sodium channels and the use thereof
US6545004B1 (en) 1999-10-27 2003-04-08 Cytokinetics, Inc. Methods and compositions utilizing quinazolinones
DE60028227T2 (de) 1999-10-27 2007-03-29 Cytokinetics, Inc., South San Francisco Chinazolinone benutzende verfahren und zusammenstellungen
AU2001227812A1 (en) 2000-05-02 2001-11-12 Advanced Syntech, Llc A Kentucky Limited Liability Corporation A novel solid support template for preparation of highly functionalized heterocycle compounds
US6951948B2 (en) 2000-06-05 2005-10-04 Ortho-Mcneil Pharmaceutical, Inc. Method for synthesis of substituted azole libraries
US6683191B2 (en) 2000-06-05 2004-01-27 Ortho-Mcneil Pharmaceuticals, Inc. Method for synthesis of substituted azole libraries
NZ523774A (en) 2000-08-01 2004-09-24 Sod Conseils Rech Applic Imidazolyl derivatives
WO2002028839A1 (fr) 2000-10-06 2002-04-11 Neurogen Corporation Derives de benzimidazole et d'indole en tant que modulateurs des recepteurs de la corticoliberine
WO2002046168A1 (fr) 2000-12-07 2002-06-13 Astrazeneca Ab Composes therapeutiques de benzimidazole
EA007538B1 (ru) 2000-12-11 2006-10-27 Туларик Инк. Антагонисты cxcr3
EP1360180A1 (fr) 2001-01-19 2003-11-12 Cytokinetics, Inc. Inhibiteurs de la kinesine a base de phenothiazine
US20040132830A1 (en) 2001-01-19 2004-07-08 Finer Jeffrey T Triphenylmethane kinesin inhibitors
WO2003039460A2 (fr) 2001-11-07 2003-05-15 Merck & Co., Inc. Inhibiteurs de la kinesine mitotique
WO2003043995A1 (fr) 2001-11-20 2003-05-30 Cytokinetics, Inc. Procede de racemisation de quinazolinones chirales
ES2291543T3 (es) 2001-12-06 2008-03-01 MERCK & CO., INC. Inhibicion de kinesina mitotica.
DE60232994D1 (de) 2001-12-06 2009-08-27 Merck & Co Inc Inhibitoren von mitotischem kinesin
AU2002351183B2 (en) 2001-12-06 2008-05-08 Merck Sharp & Dohme Corp. Mitotic kinesin inhibitors
WO2003049678A2 (fr) 2001-12-06 2003-06-19 Merck & Co., Inc. Inhibiteurs mitotiques de la kinesine
US7244723B2 (en) 2001-12-06 2007-07-17 Merck & Co., Inc. Substituted furopyrimidinones as a mitotic kinesin inhibitors
CA2472470A1 (fr) 2002-01-10 2003-07-24 Neurogen Corporation Ligands recepteurs de l'hormone de concentration de la melanine: analogues de benzoimidazole substitue
CA2475879A1 (fr) 2002-02-15 2003-08-28 Cytokinetics, Inc. Synthesis de quinazolinones
ATE448207T1 (de) 2002-03-08 2009-11-15 Merck & Co Inc Mitotische kinesin-hemmer
DE10211770A1 (de) 2002-03-14 2003-10-02 Boehringer Ingelheim Pharma Neue substituierte Piperidine, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung
US7026312B2 (en) 2002-03-14 2006-04-11 Boehringer Ingelheim Pharma Gmbh & Co. Kg Substituted piperidines, pharmaceutical compositions containing these compounds, their use and processes for the preparation thereof
CN100381437C (zh) 2002-04-17 2008-04-16 赛特凯恩蒂克公司 化合物、组合物和方法
GB0209995D0 (en) 2002-05-01 2002-06-12 Merck Sharp & Dohme Therapeutic agents
CA2485093A1 (fr) 2002-05-02 2003-11-13 Neurogen Corporation Derives d'imidazole substitues: ligands du recepteur gaba<sb>a</sb>
WO2004041809A2 (fr) 2002-05-08 2004-05-21 Neurogen Corporation Imidazolylmethyl pyridine substituee et derives de pyrazine: les ligands des recepteurs gabaa
US7214800B2 (en) 2002-05-09 2007-05-08 Cytokinetics, Inc. Compounds, compositions, and methods
KR20050036911A (ko) 2002-05-09 2005-04-20 싸이토키네틱스, 인코포레이티드 화합물들, 방법 및 조성물
EP1507534A4 (fr) 2002-05-10 2006-11-08 Cytokinetics Inc Composes, compositions et procedes
WO2003097643A1 (fr) 2002-05-17 2003-11-27 Neurogen Corporation Derives d'imidazole a cycles fusionnes se fixant aux recepteurs gabaa, ligands des recepteurs gabaa
CA2483627A1 (fr) * 2002-05-23 2003-12-04 Merck & Co., Inc. Inhibiteurs de kinesine mitotique
JP2005536475A (ja) 2002-05-23 2005-12-02 サイトキネティクス・インコーポレーテッド 化合物、組成物、および方法
CA2489367A1 (fr) 2002-06-14 2003-12-24 Cytokinetics, Inc. Composes, compositions et procedes
DE60329756D1 (de) 2002-06-14 2009-12-03 Merck & Co Inc Mitotische kinesin-hemmer
CA2486215A1 (fr) 2002-06-14 2003-12-24 Merck & Co., Inc. Inhibiteurs de kinesine mitotique
US20060134767A1 (en) 2002-07-08 2006-06-22 Buser-Doepner Carolyn A Mitotic kinesin binding site
EP1539727B1 (fr) 2002-07-17 2009-02-18 Cytokinetics, Inc. Composes, compositions et methodes pour le traitement des maladies proliferatives cellulaires
WO2004009036A2 (fr) 2002-07-23 2004-01-29 Cytokinetics, Inc. Composes, compositions et procedes
US20040048853A1 (en) 2002-08-21 2004-03-11 Gustave Bergnes Compounds, compositions, and methods
JP2005539062A (ja) 2002-09-13 2005-12-22 サイトキネティクス・インコーポレーテッド 化合物、組成物および方法
CN100579579C (zh) 2002-10-01 2010-01-13 诺华疫苗和诊断公司 抗癌及抗感染性疾病组合物及其使用方法
ATE335732T1 (de) 2002-11-08 2006-09-15 Neurogen Corp 4-imidazol-1-ylmethylpyrimidinderivate als liganden für gabaa-rezeptoren
WO2004055008A1 (fr) * 2002-12-13 2004-07-01 Smithkline Beecham Corporation Composes, compositions et methodes
JP2006515886A (ja) 2003-01-17 2006-06-08 サイトキネティクス・インコーポレーテッド 化合物、組成物、および方法
WO2004071448A2 (fr) 2003-02-12 2004-08-26 Transtech Pharma Inc. Derives d'azole substitues comme agents therapeutiques
JP2007500213A (ja) 2003-05-07 2007-01-11 サイトキネティクス・インコーポレーテッド 化合物、組成物および方法
JP2007500746A (ja) 2003-05-15 2007-01-18 サイトキネティクス・インコーポレーテッド 化合物、組成物および方法
CA2528771A1 (fr) 2003-06-20 2004-12-29 Chiron Corporation Composes de pyridino[1,2-a]pyrimidin-4-one servant d'agents anticancereux
EP1682534A2 (fr) * 2003-11-03 2006-07-26 Cytokinetics, Inc. Derives de pyrimidin-4-one, compositions et methodes
NZ548208A (en) 2004-02-12 2010-09-30 Transtech Pharma Inc Substituted azole derivatives, compositions, and methods of use
AU2005233576A1 (en) 2004-04-06 2005-10-27 Novartis Vaccines And Diagnostics, Inc. Mitotic kinesin inhibitors
US20080132549A1 (en) 2004-04-14 2008-06-05 Pfizer Inc. Sulphur-Linked Imidazone Compounds for the Treatment of Hiv/Aids
US7618981B2 (en) 2004-05-06 2009-11-17 Cytokinetics, Inc. Imidazopyridinyl-benzamide anti-cancer agents
ES2311992T3 (es) 2004-05-21 2009-02-16 Novartis Vaccines And Diagnostics, Inc. Derivados de quinolina sustituida com,o inhibidores de cinesina mitotica.
TW200612958A (en) * 2004-06-18 2006-05-01 Chiron Corp Substituted imidazole derivatives
CA2584979A1 (fr) 2004-10-19 2006-05-11 Novartis Vaccines And Diagnostics, Inc. Derives d'indole et de benzimidazole
MY147188A (en) 2005-08-09 2012-11-14 Novartis Ag Substituted imidazole compounds as ksp inhibitors
KR20090081020A (ko) 2006-11-13 2009-07-27 노파르티스 아게 Ksp 억제제로서의 치환된 피라졸 및 트리아졸 화합물

Also Published As

Publication number Publication date
HN2009001262A (es) 2012-01-09
JP2010515687A (ja) 2010-05-13
EP2106399A2 (fr) 2009-10-07
US20120189623A1 (en) 2012-07-26
CA2674318A1 (fr) 2008-07-17
WO2008086122A2 (fr) 2008-07-17
KR20090097210A (ko) 2009-09-15
CR10879A (es) 2009-08-05
DOP2009000169A (es) 2009-08-31
ZA200904175B (en) 2010-04-28
PE20081850A1 (es) 2009-02-05
CO6561828A2 (es) 2012-11-15
AU2008205169B2 (en) 2012-02-02
GT200900192A (es) 2010-06-24
US20080207589A1 (en) 2008-08-28
TW200836722A (en) 2008-09-16
MX2009007260A (es) 2009-07-10
MA31080B1 (fr) 2010-01-04
SMAP200900065A (it) 2009-09-07
SMP200900065B (it) 2010-09-10
ECSP099485A (es) 2009-08-28
CN101622247A (zh) 2010-01-06
AU2008205169A1 (en) 2008-07-17
EA200900924A1 (ru) 2009-12-30
WO2008086122A3 (fr) 2008-10-16
US20110003791A1 (en) 2011-01-06
AR064760A1 (es) 2009-04-22
SV2009003325A (es) 2011-08-09
US7820646B2 (en) 2010-10-26
NI200900134A (es) 2010-07-05
GEP20125415B (en) 2012-03-12
UA97821C2 (en) 2012-03-26
CL2008000029A1 (es) 2008-04-04
NZ577727A (en) 2012-03-30
BRPI0806264A2 (pt) 2011-08-30

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