MX2016010411A - Compuestos agonistas de gpr142. - Google Patents

Compuestos agonistas de gpr142.

Info

Publication number
MX2016010411A
MX2016010411A MX2016010411A MX2016010411A MX2016010411A MX 2016010411 A MX2016010411 A MX 2016010411A MX 2016010411 A MX2016010411 A MX 2016010411A MX 2016010411 A MX2016010411 A MX 2016010411A MX 2016010411 A MX2016010411 A MX 2016010411A
Authority
MX
Mexico
Prior art keywords
agonist compounds
group
gpr142 agonist
gpr142
ch2chf2
Prior art date
Application number
MX2016010411A
Other languages
English (en)
Inventor
Ma Tianwei
Emily ZENG Mi
Long Hu Zhi
Zhu LIU Lian
Zhou Jingye
Original Assignee
Lilly Co Eli
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 Lilly Co Eli filed Critical Lilly Co Eli
Publication of MX2016010411A publication Critical patent/MX2016010411A/es

Links

Classifications

    • 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
    • A61K31/41Heterocyclic 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
    • A61K31/41641,3-Diazoles
    • A61K31/4174Arylalkylimidazoles, e.g. oxymetazolin, naphazoline, miconazole
    • 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
    • A61K31/41Heterocyclic 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
    • A61K31/41641,3-Diazoles
    • A61K31/41781,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
    • 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
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00Drugs for disorders of the endocrine system
    • A61P5/48Drugs for disorders of the endocrine system of the pancreatic hormones
    • A61P5/50Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/88Nitrogen atoms, e.g. allantoin
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2121/00Preparations for use in therapy

Abstract

La presente invención se refiere a compuestos de la fórmula (ver Fórmula) en donde R se selecciona a partir del grupo que consiste de CH3, CH(CH3)2, CH2CN, CH2CHF2, CH2CF3, (ver Fórmula) CH2CH2OCH3 y CH2C(O)OCH(CH3)2; R1 se selecciona a partir del grupo que consiste de CF3, OCF3 y CI; R2 se selecciona a partir del grupo que consiste de H y F; o una sal del mismo farmacéuticamente aceptable.
MX2016010411A 2014-02-14 2015-01-22 Compuestos agonistas de gpr142. MX2016010411A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
PCT/CN2014/072083 WO2015120610A1 (en) 2014-02-14 2014-02-14 Gpr142 agonist compound
PCT/CN2015/071286 WO2015120768A1 (en) 2014-02-14 2015-01-22 Gpr142 agonist compounds

Publications (1)

Publication Number Publication Date
MX2016010411A true MX2016010411A (es) 2016-10-17

Family

ID=53799520

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2016010411A MX2016010411A (es) 2014-02-14 2015-01-22 Compuestos agonistas de gpr142.

Country Status (10)

Country Link
US (1) US9861613B2 (es)
EP (1) EP3105207B1 (es)
JP (1) JP6298172B2 (es)
CN (1) CN106170478B (es)
AU (1) AU2015218135B2 (es)
CA (1) CA2935109A1 (es)
EA (1) EA201691265A1 (es)
ES (1) ES2693545T3 (es)
MX (1) MX2016010411A (es)
WO (2) WO2015120610A1 (es)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016138631A1 (en) 2015-03-03 2016-09-09 Eli Lilly And Company Imidazo benzamide compounds
WO2018014337A1 (en) * 2016-07-22 2018-01-25 Eli Lilly And Company 3-Chloro-N- [ (1R, 3S) -3- [5- (3, 5-dimethylimidazol-4-yl) -4H-1, 2, 4-triazol-3-yl] cyclohexyl] -N-methyl-benzamide
JP7391055B2 (ja) 2018-07-04 2023-12-04 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング Gpr142アゴニストとしてのトリアゾールベンズアミド誘導体

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ548208A (en) * 2004-02-12 2010-09-30 Transtech Pharma Inc Substituted azole derivatives, compositions, and methods of use
US20070032475A1 (en) * 2005-04-15 2007-02-08 Ye Xiaocong M Novel compounds useful for bradykinin B1 receptor antagonism
US7754717B2 (en) 2005-08-15 2010-07-13 Amgen Inc. Bis-aryl amide compounds and methods of use
US20090270394A1 (en) * 2008-04-28 2009-10-29 Galemmo Jr Robert Cyclylamine derivatives as calcium channel blockers
US8188098B2 (en) * 2008-05-19 2012-05-29 Hoffmann-La Roche Inc. GPR119 receptor agonists
WO2010101247A1 (ja) * 2009-03-05 2010-09-10 塩野義製薬株式会社 Npy y5受容体拮抗作用を有するシクロヘキサン誘導体
AR079170A1 (es) * 2009-12-10 2011-12-28 Lilly Co Eli Compuesto de ciclopropil-benzamida-imidazo-benzazepina inhibidor de diacil-glicerol aciltransferasa, sal del mismo, composicion farmaceutica que lo comprende, su uso para preparar un medicamento util para el tratamiento de obesidad o para mejorar la sensibilidad a insulina y compuesto intermedio par

Also Published As

Publication number Publication date
CA2935109A1 (en) 2015-08-20
EP3105207A4 (en) 2017-06-21
EP3105207A1 (en) 2016-12-21
WO2015120610A1 (en) 2015-08-20
EP3105207B1 (en) 2018-08-22
ES2693545T3 (es) 2018-12-12
EA201691265A1 (ru) 2016-11-30
AU2015218135B2 (en) 2017-06-08
JP6298172B2 (ja) 2018-03-20
CN106170478B (zh) 2019-04-09
US9861613B2 (en) 2018-01-09
JP2017505797A (ja) 2017-02-23
CN106170478A (zh) 2016-11-30
AU2015218135A1 (en) 2016-07-14
WO2015120768A1 (en) 2015-08-20
US20170165234A1 (en) 2017-06-15

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MX2016010411A (es) Compuestos agonistas de gpr142.