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SMAP200900065A - Derivati ciclizzati come inibitori di eg-5 - Google Patents

Derivati ciclizzati come inibitori di eg-5

Info

Publication number
SMAP200900065A
SMAP200900065A SM200900065T SM200900065T SMAP200900065A SM AP200900065 A SMAP200900065 A SM AP200900065A SM 200900065 T SM200900065 T SM 200900065T SM 200900065 T SM200900065 T SM 200900065T SM AP200900065 A SMAP200900065 A SM AP200900065A
Authority
SM
San Marino
Prior art keywords
inhibitors
cyclized derivatives
cyclized
derivatives
Prior art date
Application number
SM200900065T
Other languages
English (en)
Other versions
SMP200900065B (it
Inventor
Paul A Barsanti
Weibo Wang
Hong Yang
Rustum Boyce
Eric Martin
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 SMAP200900065A publication Critical patent/SMAP200900065A/it
Publication of SMP200900065B publication Critical patent/SMP200900065B/it

Links

Classifications

    • 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
    • C07D403/06—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 carbon chain containing only aliphatic carbon atoms
    • 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
    • A61K31/41—Heterocyclic 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
    • A61K31/42—Oxazoles
    • A61K31/422—Oxazoles not condensed and containing further heterocyclic rings
    • 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
    • A61P35/00—Antineoplastic agents
    • A61P35/04—Antineoplastic agents specific for metastasis
    • 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
    • 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
    • C07D413/02—Heterocyclic 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
    • C07D413/06—Heterocyclic 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)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Hematology (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (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)
SM200900065T 2007-01-05 2009-07-23 Derivati ciclizzati come inibitori di EG-5. SMP200900065B (it)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US88374007P 2007-01-05 2007-01-05
PCT/US2008/050149 WO2008086122A2 (en) 2007-01-05 2008-01-03 Imidazole derivatives as kinesin spindle protein inhibitors (eg-5)

Publications (2)

Publication Number Publication Date
SMAP200900065A true SMAP200900065A (it) 2009-09-07
SMP200900065B SMP200900065B (it) 2010-09-10

Family

ID=39577804

Family Applications (1)

Application Number Title Priority Date Filing Date
SM200900065T SMP200900065B (it) 2007-01-05 2009-07-23 Derivati ciclizzati come inibitori di EG-5.

Country Status (30)

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

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
US8748626B2 (en) * 2010-04-15 2014-06-10 Novartis Ag Oxazole and thiazole compounds as KSP inhibitors
AR080893A1 (es) 2010-04-15 2012-05-16 Novartis Ag Compuestos de triazol como inhibidores de ksp
EP2390247A1 (en) * 2010-05-26 2011-11-30 Netherlands Organisation for Scientific Research (Advanced Chemical Technologies for Sustainability) Preparation of caprolactone, caprolactam, 2,5-tetrahydrofuran dimethanol, 1,6-hexanediol or 1,2,6-hexanetriol from 5-hydroxymethyl-2-furfuraldehyde
GB201113538D0 (en) 2011-08-04 2011-09-21 Karobio Ab Novel estrogen receptor ligands
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
US9498540B2 (en) 2013-03-15 2016-11-22 Novartis Ag Cell proliferation inhibitors and conjugates thereof
CA2934617A1 (en) * 2013-12-23 2015-07-02 Bayer Pharma Aktiengesellschaft Antibody drug conjugates (adcs) with kinesin spindle protein (ksp)
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
CN109310781B (zh) 2016-06-15 2024-06-18 拜耳制药股份公司 具有ksp抑制剂和抗-cd123-抗体的特异性抗体-药物-缀合物(adc)
WO2018114804A1 (de) 2016-12-21 2018-06-28 Bayer Pharma Aktiengesellschaft Spezifische antikörper-wirkstoff-konjugate (adcs) mit ksp-inhibitoren
US11660351B2 (en) 2016-12-21 2023-05-30 Bayer Aktiengesellschaft Antibody drug conjugates (ADCs) having enzymatically cleavable groups
MX2020013832A (es) 2018-06-18 2021-03-25 Bayer Ag Conjugados de ligante/agente activo dirigidos contra cxcr5 que tienen enlazadores escindibles enzimaticamente y un perfil de actividad mejorado.
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

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Also Published As

Publication number Publication date
ECSP099485A (es) 2009-08-28
HN2009001262A (es) 2012-01-09
ZA200904175B (en) 2010-04-28
US20110003791A1 (en) 2011-01-06
NZ577727A (en) 2012-03-30
CA2674318A1 (en) 2008-07-17
CR10879A (es) 2009-08-05
GT200900192A (es) 2010-06-24
WO2008086122A2 (en) 2008-07-17
US20080207589A1 (en) 2008-08-28
CO6561828A2 (es) 2012-11-15
NI200900134A (es) 2010-07-05
PE20081850A1 (es) 2009-02-05
SMP200900065B (it) 2010-09-10
MA31080B1 (fr) 2010-01-04
US7820646B2 (en) 2010-10-26
TW200836722A (en) 2008-09-16
CN101622247A (zh) 2010-01-06
BRPI0806264A2 (pt) 2011-08-30
UA97821C2 (en) 2012-03-26
AR064760A1 (es) 2009-04-22
TN2009000287A1 (en) 2010-12-31
US20120189623A1 (en) 2012-07-26
AU2008205169A1 (en) 2008-07-17
WO2008086122A3 (en) 2008-10-16
EA200900924A1 (ru) 2009-12-30
SV2009003325A (es) 2011-08-09
KR20090097210A (ko) 2009-09-15
MX2009007260A (es) 2009-07-10
DOP2009000169A (es) 2009-08-31
GEP20125415B (en) 2012-03-12
CL2008000029A1 (es) 2008-04-04
JP2010515687A (ja) 2010-05-13
EP2106399A2 (en) 2009-10-07
AU2008205169B2 (en) 2012-02-02

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