MX2016007719A - Derivados de nicotinamida dialquil(oxido)-?4-sulfanilideno como inhibidores de cinasa. - Google Patents

Derivados de nicotinamida dialquil(oxido)-?4-sulfanilideno como inhibidores de cinasa.

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Publication number
MX2016007719A
MX2016007719A MX2016007719A MX2016007719A MX2016007719A MX 2016007719 A MX2016007719 A MX 2016007719A MX 2016007719 A MX2016007719 A MX 2016007719A MX 2016007719 A MX2016007719 A MX 2016007719A MX 2016007719 A MX2016007719 A MX 2016007719A
Authority
MX
Mexico
Prior art keywords
sulfanylidene
oxido
kinase inhibitors
nicotinamide derivatives
substituted dialkyl
Prior art date
Application number
MX2016007719A
Other languages
English (en)
Inventor
Boral Sougato
Wang Shimiao
Malone Thomas
Wurster Julie
Shen Jie
Robinson Michael
Original Assignee
Allergan Inc
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 Allergan Inc filed Critical Allergan Inc
Publication of MX2016007719A publication Critical patent/MX2016007719A/es

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    • AHUMAN NECESSITIES
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    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/443Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with oxygen as a ring hetero atom
    • AHUMAN NECESSITIES
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    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen 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
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81Amides; Imides
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    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • 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
    • C07D413/12Heterocyclic 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 chain containing hetero atoms as chain links

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  • Plural Heterocyclic Compounds (AREA)

Abstract

La presente invención se refiere a moléculas orgánicas que pueden de modular la transducción de señales de la tirosina cinasas para regular, modular y / o inhibir la proliferación celular anormal.
MX2016007719A 2013-12-12 2014-12-10 Derivados de nicotinamida dialquil(oxido)-?4-sulfanilideno como inhibidores de cinasa. MX2016007719A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201361915172P 2013-12-12 2013-12-12
PCT/US2014/069589 WO2015089210A1 (en) 2013-12-12 2014-12-10 Substituted dialkyl(oxido)-λ4-sulfanylidene nicotinamide derivatives as kinase inhibitors

Publications (1)

Publication Number Publication Date
MX2016007719A true MX2016007719A (es) 2017-01-18

Family

ID=52293208

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2016007719A MX2016007719A (es) 2013-12-12 2014-12-10 Derivados de nicotinamida dialquil(oxido)-?4-sulfanilideno como inhibidores de cinasa.

Country Status (13)

Country Link
US (1) US9266869B2 (es)
EP (2) EP3753935A1 (es)
JP (1) JP6531101B2 (es)
KR (1) KR20160096174A (es)
CN (1) CN105916850B (es)
AU (1) AU2014362381B2 (es)
BR (1) BR112016013544A8 (es)
CA (1) CA2933483A1 (es)
ES (1) ES2838448T3 (es)
IL (2) IL245918B (es)
MX (1) MX2016007719A (es)
RU (1) RU2711749C2 (es)
WO (1) WO2015089210A1 (es)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108456163A (zh) 2017-02-20 2018-08-28 中国科学院上海药物研究所 含邻氨基杂芳环炔基的化合物及其制备方法和用途
CN111662227B (zh) * 2019-03-06 2022-07-05 中国科学院上海药物研究所 邻氨基吡啶炔类化合物及其制备方法和用途

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10349423A1 (de) * 2003-10-16 2005-06-16 Schering Ag Sulfoximinsubstituierte Parimidine als CDK- und/oder VEGF-Inhibitoren, deren Herstellung und Verwendung als Arzneimittel
WO2005108370A1 (ja) * 2004-04-16 2005-11-17 Ajinomoto Co., Inc. ベンゼン化合物
US8143410B2 (en) * 2006-11-16 2012-03-27 Allergan, Inc. Kinase inhibitors
BRPI0718895A2 (pt) * 2006-11-16 2013-12-10 Allergan Inc Composto de sulfoximina e uso do referido composto
US8558002B2 (en) * 2006-11-16 2013-10-15 Allergan, Inc. Sulfoximines as kinase inhibitors

Also Published As

Publication number Publication date
JP2016540002A (ja) 2016-12-22
AU2014362381B2 (en) 2019-04-18
AU2014362381A1 (en) 2016-07-07
IL245918A0 (en) 2016-08-02
CN105916850A (zh) 2016-08-31
ES2838448T3 (es) 2021-07-02
BR112016013544A2 (es) 2017-08-08
EP3080105B1 (en) 2020-09-02
US20150166521A1 (en) 2015-06-18
KR20160096174A (ko) 2016-08-12
IL274874A (en) 2020-07-30
CA2933483A1 (en) 2015-06-18
BR112016013544A8 (pt) 2020-05-19
JP6531101B2 (ja) 2019-06-12
US9266869B2 (en) 2016-02-23
EP3753935A1 (en) 2020-12-23
RU2711749C2 (ru) 2020-01-21
IL245918B (en) 2020-06-30
WO2015089210A1 (en) 2015-06-18
CN105916850B (zh) 2020-03-20
EP3080105A1 (en) 2016-10-19

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