BRPI0920112A2 - derivados de anilinopirimidina substituídos com sulfoximina como inibidores cdk, sua produção e uso como medicamento. - Google Patents

derivados de anilinopirimidina substituídos com sulfoximina como inibidores cdk, sua produção e uso como medicamento.

Info

Publication number
BRPI0920112A2
BRPI0920112A2 BRPI0920112A BRPI0920112A BRPI0920112A2 BR PI0920112 A2 BRPI0920112 A2 BR PI0920112A2 BR PI0920112 A BRPI0920112 A BR PI0920112A BR PI0920112 A BRPI0920112 A BR PI0920112A BR PI0920112 A2 BRPI0920112 A2 BR PI0920112A2
Authority
BR
Brazil
Prior art keywords
medicament
production
cdk inhibitors
anilinopyrimidine derivatives
sulfoximine substituted
Prior art date
Application number
BRPI0920112A
Other languages
English (en)
Inventor
Gerhard Siemeister
Julia Schulze
Philip Lienau
Rolf Jautelat
Ulrich Lücking
Original Assignee
Bayer Schering Pharma Akltiengesellschaft
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 Bayer Schering Pharma Akltiengesellschaft filed Critical Bayer Schering Pharma Akltiengesellschaft
Publication of BRPI0920112A2 publication Critical patent/BRPI0920112A2/pt

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/47One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
    • 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
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
BRPI0920112A 2008-10-21 2009-10-09 derivados de anilinopirimidina substituídos com sulfoximina como inibidores cdk, sua produção e uso como medicamento. BRPI0920112A2 (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP08167113A EP2179991A1 (de) 2008-10-21 2008-10-21 Sulfoximinsubstituierte Anilino-Pyrimidinderivate als CDK-Inhibitoren, deren Herstellung und Verwendung als Arzneimittel
PCT/EP2009/007247 WO2010046035A1 (de) 2008-10-21 2009-10-09 Sulfoximinsubstituierte anilinopyrimidinderative als cdk-inhibitoren, deren herstellung und verwendung als arzeinmittel

Publications (1)

Publication Number Publication Date
BRPI0920112A2 true BRPI0920112A2 (pt) 2015-12-22

Family

ID=40282208

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI0920112A BRPI0920112A2 (pt) 2008-10-21 2009-10-09 derivados de anilinopirimidina substituídos com sulfoximina como inibidores cdk, sua produção e uso como medicamento.

Country Status (38)

Country Link
US (1) US8735412B2 (pt)
EP (2) EP2179991A1 (pt)
JP (1) JP5564054B2 (pt)
KR (1) KR20110069115A (pt)
CN (1) CN102197029B (pt)
AR (1) AR074053A1 (pt)
AU (1) AU2009306733C1 (pt)
BR (1) BRPI0920112A2 (pt)
CA (1) CA2739739C (pt)
CO (1) CO6361926A2 (pt)
CR (1) CR20110210A (pt)
CU (1) CU24052B1 (pt)
CY (1) CY1115590T1 (pt)
DK (1) DK2350026T3 (pt)
DO (1) DOP2011000107A (pt)
EA (1) EA019230B1 (pt)
EC (1) ECSP11010992A (pt)
ES (1) ES2499028T3 (pt)
HN (1) HN2011001019A (pt)
HR (1) HRP20140830T1 (pt)
IL (1) IL211713A (pt)
MA (1) MA32723B1 (pt)
MX (1) MX2011004238A (pt)
MY (1) MY155230A (pt)
NZ (1) NZ592314A (pt)
PA (1) PA8846201A1 (pt)
PE (1) PE20110546A1 (pt)
PL (1) PL2350026T3 (pt)
PT (1) PT2350026E (pt)
RS (1) RS53523B1 (pt)
SA (1) SA109300632B1 (pt)
SI (1) SI2350026T1 (pt)
TN (1) TN2011000199A1 (pt)
TW (2) TWI458716B (pt)
UA (1) UA103500C2 (pt)
UY (1) UY32190A (pt)
WO (1) WO2010046035A1 (pt)
ZA (1) ZA201103727B (pt)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8933227B2 (en) 2009-08-14 2015-01-13 Boehringer Ingelheim International Gmbh Selective synthesis of functionalized pyrimidines
WO2011018517A1 (en) 2009-08-14 2011-02-17 Boehringer Ingelheim International Gmbh Regioselective preparation of 2-amino-5-trifluoromethylpyrimidine derivatives
DE102010014426A1 (de) * 2010-04-01 2011-10-06 Bayer Schering Pharma Aktiengesellschaft Verwendung neuer pan-CDK-Inhibitoren zur Behandlung von Tumoren
DE102010014427A1 (de) 2010-04-01 2011-10-06 Bayer Schering Pharma Aktiengesellschaft Kombinationen neuer pan-CDK-Inhibitoren zur Behandlung von Tumoren
DE102010046720A1 (de) * 2010-09-23 2012-03-29 Bayer Schering Pharma Aktiengesellschaft Verfahren zur Herstellung von pan-CDK-Inhibitoren der Formel (l), sowie Intermediate der Herstellung
TWI555737B (zh) 2011-05-24 2016-11-01 拜耳知識產權公司 含有硫醯亞胺基團之4-芳基-n-苯基-1,3,5-三氮雜苯-2-胺
DE102011080991A1 (de) 2011-08-16 2013-02-21 Bayer Pharma AG Verwendung von CCNE2 als Stratifikationsmarker bei der Behandlung von Brusttumoren mit neuen pan-CDK-Inhibitoren
DE102011080992A1 (de) * 2011-08-16 2013-02-21 Bayer Pharma AG Verwendung von MAD2L2 als Stratifikationsmarker bei der Behandlung von Brusttumoren mit neuen pan-CDK-Inhibitoren
JP5976814B2 (ja) 2011-09-16 2016-08-24 バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH スルホキシイミン基を含有する二置換5−フルオロピリミジン誘導体
WO2013139734A1 (de) * 2012-03-21 2013-09-26 Bayer Intellectual Property Gmbh Verwendung von (rs)-s-cyclopropyl-s-(4-{[4-{[(1r, 2r)-2-hydroxy-1-methylpropyl]oxy}-5-(trifluormethyl)pyrimidin-2-yl]amino}phenyl)sulfoximid zur behandlung spezifischer tumore
CA2964696C (en) * 2014-10-16 2022-09-06 Bayer Pharma Aktiengesellschaft Fluorinated benzofuranyl-pyrimidine derivatives containing a sulfoximine group
EP3849537B1 (en) 2018-09-10 2024-10-23 Mirati Therapeutics, Inc. Combination therapies
US12441707B2 (en) 2019-12-30 2025-10-14 Tyra Biosciences, Inc. Indazole compounds

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4029650A1 (de) 1990-09-19 1992-03-26 Hoechst Ag 2-anilino-pyrimidine, verfahren zu ihrer herstellung, sie enthaltene mittel und ihre verwendung als fungizide
EP1017394B1 (en) 1997-07-12 2005-12-07 Cancer Research Technology Limited Cyclin dependent kinase inhibiting purine derivatives
US6440965B1 (en) 1997-10-15 2002-08-27 Krenitsky Pharmaceuticals, Inc. Substituted pyrimidine derivatives, their preparation and their use in the treatment of neurodegenerative or neurological disorders of the central nervous system
US6632820B1 (en) 1998-08-29 2003-10-14 Astrazeneca Ab Pyrimidine compounds
GB9828511D0 (en) 1998-12-24 1999-02-17 Zeneca Ltd Chemical compounds
GB9919778D0 (en) 1999-08-21 1999-10-27 Zeneca Ltd Chemical compounds
GB0016877D0 (en) 2000-07-11 2000-08-30 Astrazeneca Ab Chemical compounds
BR0209774A (pt) 2001-05-29 2004-06-01 Schering Ag Pirimidinas inibidoras de cdk, sua preparação e aplicação como medicamento
EP1483260A1 (de) * 2002-03-11 2004-12-08 Schering Aktiengesellschaft Cdk inhibitorische 2-heteroaryl-pyrimidine, deren herstellung und verwendung als arzneimittel
JP2006508997A (ja) 2002-11-28 2006-03-16 シエーリング アクチエンゲゼルシャフト Chk−、Pdk−およびAkt−阻害性ピリミジン、それらの製造および薬剤としての使用
DE10349423A1 (de) 2003-10-16 2005-06-16 Schering Ag Sulfoximinsubstituierte Parimidine als CDK- und/oder VEGF-Inhibitoren, deren Herstellung und Verwendung als Arzneimittel
EP1794134A1 (de) * 2004-09-29 2007-06-13 Bayer Schering Pharma Aktiengesellschaft Substituierte 2-anilinopyrimidine als zellzyklus -kinase oder rezeptortyrosin-kinase inhibitoren, deren herstellung und verwendung als arzneimittel
DE102005062742A1 (de) 2005-12-22 2007-06-28 Bayer Schering Pharma Ag Sulfoximin substituierte Pyrimidine, Verfahren zu deren Herstellung und ihre Verwendung als Arzneimittel
DE102006027156A1 (de) 2006-06-08 2007-12-13 Bayer Schering Pharma Ag Sulfimide als Proteinkinaseinhibitoren
EP2179992A1 (de) * 2008-10-21 2010-04-28 Bayer Schering Pharma Aktiengesellschaft Sulfonsubstituierte Anlinopyrimidinderivative als CDK-Inhibitoren, deren Herstellung und Verwendung als Arzneimittel

Also Published As

Publication number Publication date
PE20110546A1 (es) 2011-08-12
AR074053A1 (es) 2010-12-22
CA2739739C (en) 2016-12-20
EP2179991A1 (de) 2010-04-28
EA201100623A1 (ru) 2011-12-30
RS53523B1 (sr) 2015-02-27
SA109300632B1 (ar) 2013-07-04
CA2739739A1 (en) 2010-04-29
CU20110088A7 (es) 2011-12-28
MY155230A (en) 2015-09-30
HN2011001019A (es) 2013-07-01
JP5564054B2 (ja) 2014-07-30
TW201444803A (zh) 2014-12-01
CY1115590T1 (el) 2017-01-04
HRP20140830T1 (hr) 2014-11-21
TW201020237A (en) 2010-06-01
MX2011004238A (es) 2011-05-23
CN102197029A (zh) 2011-09-21
AU2009306733A1 (en) 2010-04-29
US8735412B2 (en) 2014-05-27
PT2350026E (pt) 2014-09-12
IL211713A0 (en) 2011-06-30
AU2009306733C1 (en) 2016-07-14
ES2499028T3 (es) 2014-09-26
ECSP11010992A (es) 2011-05-31
CO6361926A2 (es) 2012-01-20
WO2010046035A1 (de) 2010-04-29
CU24052B1 (es) 2014-12-26
TWI458716B (zh) 2014-11-01
CN102197029B (zh) 2014-05-14
EP2350026B1 (de) 2014-06-18
AU2009306733B2 (en) 2015-11-12
TN2011000199A1 (en) 2012-12-17
TWI496774B (zh) 2015-08-21
US20110294838A1 (en) 2011-12-01
DK2350026T3 (da) 2014-09-15
UA103500C2 (uk) 2013-10-25
ZA201103727B (en) 2014-11-26
PL2350026T3 (pl) 2014-11-28
KR20110069115A (ko) 2011-06-22
IL211713A (en) 2015-04-30
UY32190A (es) 2010-05-31
EA019230B1 (ru) 2014-02-28
SI2350026T1 (sl) 2014-10-30
PA8846201A1 (es) 2010-05-26
CR20110210A (es) 2011-06-08
NZ592314A (en) 2013-02-22
EP2350026A1 (de) 2011-08-03
JP2012506391A (ja) 2012-03-15
MA32723B1 (fr) 2011-10-02
DOP2011000107A (es) 2011-05-15

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Legal Events

Date Code Title Description
B25D Requested change of name of applicant approved

Owner name: BAYER PHARMA AKTIENGESELLSCHAFT (DE)

B25A Requested transfer of rights approved

Owner name: BAYER INTELLECTUAL PROPERTY GMBH (DE)

B08F Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette]
B08K Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette]