BRPI0708644A2 - compostos de pró-fármaco de anilina de pirrolotriazina úteis como inibidores de cinase - Google Patents

compostos de pró-fármaco de anilina de pirrolotriazina úteis como inibidores de cinase Download PDF

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Publication number
BRPI0708644A2
BRPI0708644A2 BRPI0708644-0A BRPI0708644A BRPI0708644A2 BR PI0708644 A2 BRPI0708644 A2 BR PI0708644A2 BR PI0708644 A BRPI0708644 A BR PI0708644A BR PI0708644 A2 BRPI0708644 A2 BR PI0708644A2
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formula
optionally substituted
original document
document page
see original
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BRPI0708644-0A
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English (en)
Portuguese (pt)
Inventor
Liu Chunjian
Leftheris Katherina
M. Vrudhula Vivekananda
Lin James
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Bristol-Myers Squibb Company
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Publication of BRPI0708644A2 publication Critical patent/BRPI0708644A2/pt

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
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    • 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
    • A61K31/53Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
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  • Immunology (AREA)
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  • Dermatology (AREA)
  • Tropical Medicine & Parasitology (AREA)
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BRPI0708644-0A 2006-03-07 2007-03-05 compostos de pró-fármaco de anilina de pirrolotriazina úteis como inibidores de cinase BRPI0708644A2 (pt)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US77985106P 2006-03-07 2006-03-07
US60/779,851 2006-03-07
PCT/US2007/063250 WO2007103839A2 (en) 2006-03-07 2007-03-05 Pyrrolotriazine aniline prodrug compounds useful as kinase inhibitors

Publications (1)

Publication Number Publication Date
BRPI0708644A2 true BRPI0708644A2 (pt) 2011-06-07

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ID=38475749

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI0708644-0A BRPI0708644A2 (pt) 2006-03-07 2007-03-05 compostos de pró-fármaco de anilina de pirrolotriazina úteis como inibidores de cinase

Country Status (17)

Country Link
US (2) US7572795B2 (enExample)
EP (1) EP2001886A2 (enExample)
JP (1) JP2009535295A (enExample)
KR (1) KR20080107408A (enExample)
CN (1) CN101395158A (enExample)
AR (1) AR059778A1 (enExample)
AU (1) AU2007223342A1 (enExample)
BR (1) BRPI0708644A2 (enExample)
CA (1) CA2645031A1 (enExample)
EA (1) EA200801945A1 (enExample)
IL (1) IL193653A0 (enExample)
MX (1) MX2008011136A (enExample)
NO (1) NO20083717L (enExample)
PE (1) PE20080139A1 (enExample)
TW (1) TW200804390A (enExample)
WO (1) WO2007103839A2 (enExample)
ZA (1) ZA200807459B (enExample)

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WO2009158450A1 (en) * 2008-06-25 2009-12-30 Bristol-Myers Squibb Company Crystalline forms of ((((4-((5-(cyclopropylcarbamoyl)-2-methylphenyl)amino)-5-methylpyrrolo[2,1-f][1,2,4]triazin-6-yl)carbonyl)(propyl)carbamoyl)oxy)methyl (4-(phosphonooxy)phenyl)acetate, preparation and use thereof
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TW201035100A (en) 2008-12-19 2010-10-01 Cephalon Inc Pyrrolotriazines as ALK and JAK2 inhibitors
AU2010266040B2 (en) * 2009-06-25 2015-01-15 Alkermes Pharma Ireland Limited Prodrugs of NH-acidic compounds
CN102596921B (zh) * 2009-09-29 2015-04-29 葛兰素集团有限公司 新化合物
JP5752691B2 (ja) 2009-09-29 2015-07-22 グラクソ グループ リミテッドGlaxo Group Limited 新規化合物
CN102918045A (zh) 2010-03-31 2013-02-06 百时美施贵宝公司 作为蛋白激酶抑制剂的取代的吡咯并三嗪
WO2012031057A1 (en) 2010-09-01 2012-03-08 Bristol-Myers Squibb Company Bms- 582949 for the treatment of resistant rheumatic disease
CN102153558B (zh) * 2011-02-23 2012-11-21 扬州永济医药新技术有限公司 多靶点抗肿瘤抑制剂2-氨吡咯-三嗪的衍生物及其合成方法
US8901305B2 (en) * 2012-07-31 2014-12-02 Bristol-Myers Squibb Company Aryl lactam kinase inhibitors
AU2013305684B2 (en) 2012-08-22 2016-11-24 Xenoport, Inc. Oral dosage forms of methyl hydrogen fumarate and prodrugs thereof
US9050345B2 (en) 2013-03-11 2015-06-09 Bristol-Myers Squibb Company Pyrrolotriazines as potassium ion channel inhibitors
WO2014160633A1 (en) 2013-03-24 2014-10-02 Xenoport, Inc. Pharmaceutical compositions of dimethyl fumarate
US9302977B2 (en) 2013-06-07 2016-04-05 Xenoport, Inc. Method of making monomethyl fumarate
WO2014205392A1 (en) 2013-06-21 2014-12-24 Xenoport, Inc. Cocrystals of dimethyl fumarate
WO2015035184A1 (en) 2013-09-06 2015-03-12 Xenoport, Inc. Crystalline forms of (n,n-diethylcarbamoyl)methyl methyl (2e)but-2-ene-1,4-dioate, methods of synthesis and use
US9999672B2 (en) 2014-03-24 2018-06-19 Xenoport, Inc. Pharmaceutical compositions of fumaric acid esters
MA41136A (fr) * 2014-12-09 2017-10-17 Bayer Pharma AG Composés pour le traitement d'un cancer
WO2017070135A1 (en) * 2015-10-20 2017-04-27 Bristol-Myers Squibb Company Prodrugs of 2-(4-(3-((4-amino-7-cyano-imidazo[2,1-f][1,2,4]triazin-2-yl)amino)phenyl)piperaz in-1-yl)propanamide derivatives as ck2 inhibitors for the treatment of cancer
NZ747259A (en) * 2016-04-04 2022-11-25 Chemocentryx Inc Soluble c5ar antagonists
PT3691620T (pt) 2017-10-05 2022-10-06 Fulcrum Therapeutics Inc Os inibidores da quinase p38 reduzem a expressão de dux4 e genes a jusante para o tratamento de fshd
US10342786B2 (en) 2017-10-05 2019-07-09 Fulcrum Therapeutics, Inc. P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD
AU2019230014B2 (en) 2018-03-05 2024-11-28 Alkermes Pharma Ireland Limited Aripiprazole dosing strategy
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