SI3091011T1 - Modulatorji transporterjev ATP-vezavnih kaset - Google Patents
Modulatorji transporterjev ATP-vezavnih kaset Download PDFInfo
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- SI3091011T1 SI3091011T1 SI200732005T SI200732005T SI3091011T1 SI 3091011 T1 SI3091011 T1 SI 3091011T1 SI 200732005 T SI200732005 T SI 200732005T SI 200732005 T SI200732005 T SI 200732005T SI 3091011 T1 SI3091011 T1 SI 3091011T1
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Claims (10)
- Modulatorji transporteijev ATP-vezavnih kaset Patentni zahtevki1. Spojina s formulo Ud:ali njena farmacevtsko sprejemljiva sol; kjer obe skupini R2, skupaj z atomi na katere sta pripeti, tvorita skupino izbrano izmed:» kjer je R’3 neodvisno izbran izmed naslednjih: -H, -CH3, -CH2CH3, -C(0)CH3, -CH2CH20H, -C(0)0CH3,»»· ** * · »·· · t · ·«in, kjer je vsak R3 neodvisno izbran izmed -H, -CH3, -CH20H, -CH2CH3,-CH2CH20H, -CH2CH2CH3, -NH2, halo, -OCH3, -CN, -CF3, -C(0)0CH2CH3,-S(0)2CH3, -CH2NH2, -C(0)NH2,
- 2. Spojina po zahtevku 1, kjer obe skupini R2, skupaj z atomi na katere sta pripeti tvorita skupino, kije:
- 3. Spojina po zahtevku 1, kjer R’3 predstavlja
- 4. Spojina po zahtevku 1, kjer je v enem primeru R3 predstavlja halo.
- 5. Spojina po zahtevku 1, kjer je v enem primeru R3 predstavlja
- 6. Spojina po zahtevku 1, kjer je vsak R3 neodvisno izbran izmed halo in
- 7. Farmacevtski sestavek, ki vsebuje spojino po kateremkoli zahtevku od 1 do 6 in farmacevtsko sprejemljiv nosilec, adjuvans ali vehikel.
- 8. Farmacevtski sestavek po zahtevku 7, kjer sestavek nadalje vsebuje enega ali več dodatnih terapevtskih sredstev.
- 9. Spojina po kateremkoli zahtevku od 1 do 6 ali farmacevtski sestavek po zahtevku 7 ali zahtevku 8, za uporabo v postopku zdravljenja ali zmanjšanja resnosti bolezni v pacientu, kjer je omenjena bolezen izbrana iz skupine, ki vsebuje naslednje bolezni:cistična fibroza, dedni emfizem, dedna hemokromatoza, pomanjkanje koagulacije in fibrinolize, kot je pomanjkanje proteina C, dedni angioedem tipa 1, pomanjkanje procesiranja lipidov, kot je družinska hiperholesterolemija, hilomikronemija tipa 1, abetalipoproteinemija, bolezni lizosomskega shranjevanja, kot je bolezen I-celice/pseudo- Hurler, mukopolisaharidoze, Sandhof/Tay-Sachs, Crigler-Najjar tipa II, poliendokrinopatija/hiperinzulemija, diabetes mellitus, Laronova pritlikavost, pomanjkanje mileoperoksidaze, primarni hipoparatiroidizem, melanom, glikanoza CDG tipa 1, prirojen hipertiroidizem, osteogeneza imperfecta, dedna hipofibrinogenemija, pomanjkanje ACT, diabetes insipidus (Dl), Dl nevrofize, neprogenski Dl, Charcot-Marie Tooth-ov sindrom, Perlizaeus-Merzbacher-jeva bolezen, nevrodegenerativne bolezni kot je Alzheimerjeva bolezen, Parkinsonova bolezen, amiotrofična lateralna skleroza, progresivna supranukleama paraliza, Pickova bolezen, več poliglutaminskih nevroloških motenj kot je Huntingtonova, spinocerebelama ataksija tipa I, mišična atrofija hrbtenice in bulbarja, dentatorubralna-palidoluisianska in miotonična distrofija, kot tudi spongiformna encefalopatija, kot je dedna Creutzfeldt-Jakob-ova bolezen (zaradi napake pri procesiranju prionskega proteina), Fabry-eva bolezen, Straussler-Scheinker-jev sindrom, COPD, bolezen suhih oči ali Sjogrenova bolezen, kjer postopek obsega korak administriranja omenjenemu pacientu učinkovite količine spojine po kateremkoli zahtevku od 1 do 6 ali farmacevtskega sestavka po zahtevku 7 ali po zahtevku 8.
- 10. Spojina ali farmacevtski sestavek za uporabo po zahtevku 9, kjer je omenjena bolezen cistična fibroza.
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