BRPI0921392A2 - inibidores quinase com perfil de segurança cyp aperfeiçoado - Google Patents

inibidores quinase com perfil de segurança cyp aperfeiçoado

Info

Publication number
BRPI0921392A2
BRPI0921392A2 BRPI0921392A BRPI0921392A BRPI0921392A2 BR PI0921392 A2 BRPI0921392 A2 BR PI0921392A2 BR PI0921392 A BRPI0921392 A BR PI0921392A BR PI0921392 A BRPI0921392 A BR PI0921392A BR PI0921392 A2 BRPI0921392 A2 BR PI0921392A2
Authority
BR
Brazil
Prior art keywords
cypase
inhibitors
safety profile
improved cyp
cyp
Prior art date
Application number
BRPI0921392A
Other languages
English (en)
Inventor
Michael L Curtin
Michael R Michaelides
Robin R Frey
Original Assignee
Abbott Lab
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 Abbott Lab filed Critical Abbott Lab
Publication of BRPI0921392A2 publication Critical patent/BRPI0921392A2/pt

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04—Ortho-condensed systems
    • 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
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4365—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system having sulfur as a ring hetero atom, e.g. ticlopidine
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D333/30—Hetero atoms other than halogen
    • C07D333/36—Nitrogen atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
BRPI0921392A 2008-12-05 2009-12-04 inibidores quinase com perfil de segurança cyp aperfeiçoado BRPI0921392A2 (pt)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US12028108P 2008-12-05 2008-12-05
US22376009P 2009-07-08 2009-07-08
PCT/US2009/066725 WO2010065825A2 (en) 2008-12-05 2009-12-04 Kinase inhibitors with improved cyp safety profile

Publications (1)

Publication Number Publication Date
BRPI0921392A2 true BRPI0921392A2 (pt) 2016-04-26

Family

ID=41559043

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI0921392A BRPI0921392A2 (pt) 2008-12-05 2009-12-04 inibidores quinase com perfil de segurança cyp aperfeiçoado

Country Status (25)

Country Link
US (2) US20100144783A1 (pt)
EP (1) EP2373662B1 (pt)
JP (1) JP5588458B2 (pt)
KR (1) KR101639642B1 (pt)
CN (1) CN102239171B (pt)
AR (1) AR074481A1 (pt)
AU (1) AU2009322270B2 (pt)
BR (1) BRPI0921392A2 (pt)
CA (1) CA2743592A1 (pt)
CL (1) CL2011001312A1 (pt)
CO (1) CO6382131A2 (pt)
DO (1) DOP2011000153A (pt)
EC (1) ECSP11011172A (pt)
ES (1) ES2524966T3 (pt)
IL (1) IL212716A (pt)
MX (1) MX2011005943A (pt)
MY (1) MY179042A (pt)
NZ (1) NZ592714A (pt)
PA (1) PA8852401A1 (pt)
PE (1) PE20110830A1 (pt)
RU (2) RU2480472C2 (pt)
TW (2) TWI441827B (pt)
UA (1) UA103351C2 (pt)
UY (1) UY32291A (pt)
WO (1) WO2010065825A2 (pt)

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KR20130109092A (ko) * 2010-06-09 2013-10-07 아보트 러보러터리즈 키나제 억제제를 함유하는 고체 분산물
US8911725B2 (en) 2010-06-23 2014-12-16 University Of Central Florida Research Foundation, Inc. Co-targeting of aurora A kinase and LIM kinase 1 for cancer therapy
WO2013012909A1 (en) 2011-07-20 2013-01-24 Abbott Laboratories Kinase inhibitor with improved aqueous solubility
AU2012352112A1 (en) 2011-12-14 2014-06-12 Abbvie Inc. Compositions containing kinase inhibitors
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US20170197980A1 (en) * 2014-06-25 2017-07-13 Abbvie Inc. N-(4-phenyl)-n'-(3-fluorophenyl)urea docusate
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AU2020291464A1 (en) * 2019-06-12 2022-02-03 Vanderbilt University Amino acid transport inhibitors and the uses thereof
US12624049B2 (en) 2020-05-11 2026-05-12 University Health Network Salt and crystal forms of 4-amino-5-(6-(4-methylpiperazin-1-yl)-1H-benzo[d]imidazol-z-yl)thieno[2.3-b]pyridin-6(7H)-one

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Also Published As

Publication number Publication date
PE20110830A1 (es) 2011-12-14
IL212716A (en) 2013-10-31
MY179042A (en) 2020-10-26
US8722890B2 (en) 2014-05-13
IL212716A0 (en) 2011-07-31
AR074481A1 (es) 2011-01-19
TW201431862A (zh) 2014-08-16
PA8852401A1 (es) 2010-07-27
MX2011005943A (es) 2011-06-27
DOP2011000153A (es) 2011-06-30
EP2373662B1 (en) 2014-09-24
KR101639642B1 (ko) 2016-07-14
US20100144783A1 (en) 2010-06-10
CO6382131A2 (es) 2012-02-15
CA2743592A1 (en) 2010-06-10
UY32291A (es) 2010-07-30
CN102239171B (zh) 2014-06-11
WO2010065825A3 (en) 2010-08-26
AU2009322270A1 (en) 2011-07-14
RU2480472C2 (ru) 2013-04-27
UA103351C2 (uk) 2013-10-10
CL2011001312A1 (es) 2011-10-07
TW201026706A (en) 2010-07-16
EP2373662A2 (en) 2011-10-12
US20120309783A1 (en) 2012-12-06
HK1159628A1 (en) 2012-08-03
JP5588458B2 (ja) 2014-09-10
CN102239171A (zh) 2011-11-09
RU2012156958A (ru) 2014-06-27
TWI441827B (zh) 2014-06-21
WO2010065825A2 (en) 2010-06-10
TWI500621B (zh) 2015-09-21
ECSP11011172A (es) 2011-08-31
ES2524966T3 (es) 2014-12-16
AU2009322270B2 (en) 2014-12-18
JP2012511016A (ja) 2012-05-17
RU2011127451A (ru) 2013-01-10
KR20110091577A (ko) 2011-08-11
NZ592714A (en) 2013-03-28

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Legal Events

Date Code Title Description
B25C Requirement related to requested transfer of rights

Owner name: ABBOTT LABORATORIES (US)

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]
B25B Requested transfer of rights rejected

Owner name: ABBOTT LABORATORIES (US)

B25B Requested transfer of rights rejected

Owner name: ABBOTT LABORATORIES (US)