NO20062516L - Pyridinforbindelser som inhibitorer av dipeptidylreptidase IV - Google Patents

Pyridinforbindelser som inhibitorer av dipeptidylreptidase IV

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Publication number
NO20062516L
NO20062516L NO20062516A NO20062516A NO20062516L NO 20062516 L NO20062516 L NO 20062516L NO 20062516 A NO20062516 A NO 20062516A NO 20062516 A NO20062516 A NO 20062516A NO 20062516 L NO20062516 L NO 20062516L
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Norway
Prior art keywords
group
optionally substituted
chain hydrocarbon
divalent chain
hydrocarbon group
Prior art date
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NO20062516A
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English (en)
Inventor
Satoru Oi
Nobuhiro Suzuki
Hironobu Maezaki
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Takeda Pharmaceutical
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Application filed by Takeda Pharmaceutical filed Critical Takeda Pharmaceutical
Publication of NO20062516L publication Critical patent/NO20062516L/no

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    • 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
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4406Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 3, e.g. zimeldine
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Abstract

En forbindelse representert ved formelen, hvori R og R er like eller forskjellige og hver er en eventuelt substituert hydrokarbongruppe eller en eventuelt substituert hyd-roksygruppe; R3 er en eventuelt substituert aromatisk gruppe; R4 er en eventuelt substituert aminogruppe; L er en divalent kjede hydrokarbongruppe; Q er en binding eller en divalent kjede hydrokarbongruppe; og X er et hydrogenatom, en cyanogruppe, en ni-trogruppe, en acylgruppe, en substituert hydroksygruppe, en eventuelt substituert tiolgruppe, en eventuelt substituert aminogruppe, eller en eventuelt substituert cyklisk gruppe; forutsatt at når X er en etoksykarbonylgruppe, da er Q en divalent kjede hydrokarbongruppe. Forbindelsen har en peptidaseinhiberingsaktivitet, er anvendelig som et middel for profylakse eller behandling av diabetes og lignende, og har overlegen effektivitet, virkningsvarighet, spesifisitet, lavere toksisitet og lignende.
NO20062516A 2003-10-31 2006-05-31 Pyridinforbindelser som inhibitorer av dipeptidylreptidase IV NO20062516L (no)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP2003373776 2003-10-31
JP2004030491 2004-02-06
JP2004165977 2004-06-03
PCT/JP2004/016457 WO2005042488A1 (en) 2003-10-31 2004-10-29 Pyridine compounds as inhibitors of dipeptidyl peptidase iv

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NO20062516L true NO20062516L (no) 2006-07-25

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US (1) US20070037807A1 (no)
EP (1) EP1678138A1 (no)
KR (2) KR100858259B1 (no)
AR (1) AR046819A1 (no)
AU (1) AU2004285807A1 (no)
BR (1) BRPI0415960A (no)
CA (1) CA2543529A1 (no)
CO (1) CO5690607A2 (no)
IL (1) IL174608A0 (no)
MX (1) MXPA06003979A (no)
NO (1) NO20062516L (no)
NZ (1) NZ546787A (no)
PE (1) PE20050444A1 (no)
TW (1) TW200523252A (no)
WO (1) WO2005042488A1 (no)

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