HRP20230745T3 - Spojevi morfina - Google Patents

Spojevi morfina

Info

Publication number
HRP20230745T3
HRP20230745T3 HRP20230745TT HRP20230745T HRP20230745T3 HR P20230745 T3 HRP20230745 T3 HR P20230745T3 HR P20230745T T HRP20230745T T HR P20230745TT HR P20230745 T HRP20230745 T HR P20230745T HR P20230745 T3 HRP20230745 T3 HR P20230745T3
Authority
HR
Croatia
Prior art keywords
diseases
compound
formula
disorders
hbr salt
Prior art date
Application number
HRP20230745TT
Other languages
English (en)
Inventor
Roger Tung
Original Assignee
Sun Pharmaceutical Industries, 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 Sun Pharmaceutical Industries, Inc. filed Critical Sun Pharmaceutical Industries, Inc.
Publication of HRP20230745T3 publication Critical patent/HRP20230745T3/hr

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/195Carboxylic acids, e.g. valproic acid having an amino group
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/26Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving oxidoreductase
    • C12Q1/28Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving oxidoreductase involving peroxidase
    • 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4709Non-condensed quinolines and containing further heterocyclic rings
    • 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/485Morphinan derivatives, e.g. morphine, codeine
    • 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/49Cinchonan derivatives, e.g. quinine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/14Antitussive agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B59/00Introduction of isotopes of elements into organic compounds ; Labelled organic compounds per se
    • C07B59/002Heterocyclic compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D221/00Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
    • C07D221/02Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
    • C07D221/22Bridged ring systems
    • C07D221/28Morphinans
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/08Bridged systems
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/483Physical analysis of biological material
    • G01N33/487Physical analysis of biological material of liquid biological material
    • G01N33/49Blood
    • G01N33/491Blood by separating the blood components
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/483Physical analysis of biological material
    • G01N33/487Physical analysis of biological material of liquid biological material
    • G01N33/493Physical analysis of biological material of liquid biological material urine

Claims (15)

1. Sol HBr spoja formule (I): [image] pri čemu je faktor izotopskog obogaćivanja za svaki naznačeni atom deuterija najmanje 6000.
2. Sol HBr spoja formule (I) prema zahtjevu 1, naznačena time što je izotopski faktor obogaćivanja za svaki naznačeni atom deuterija najmanje 6333.3.
3. Sol HBr spoja formule (I) prema zahtjevu 1, naznačena time što je izotopski faktor obogaćivanja za svaki naznačeni atom deuterija najmanje 6466.7.
4. Sol HBr spoja formule (I) prema bilo kojem od zahtjeva 1-3, naznačena time što je bilo koji atom koji nije označen kao deuterij prisutan u svojoj prirodnoj izotopskoj zastupljenosti.
5. Farmaceutski pripravak koji sadrži sol HBr spoja formule (I) prema bilo kojem od zahtjeva 1-4 i farmaceutski prihvatljiv nosač.
6. Sol HBr spoja formule (I) prema bilo kojem od zahtjeva 1-4, ili farmaceutski pripravak prema zahtjevu 5, za uporabu u liječenju bolesti ili stanja odabranog između emocionalne labilnosti; pseudobulbarnog afekta; autizama; neurološkog poremećaja; neurodegenerativne bolesti; ozljede mozga; tegoba ili poremećaja svijesti; kardiovaskularne bolesti; glaukoma; tardivne diskinezije; dijabetičke neuropatije; retinopatske bolesti; bolesti ili poremećaja uzrokovanih apoptozom induciranom homocisteinom; bolesti ili poremećaja uzrokovanih povišenim razinama homocisteina; kronične boli; neizlječive boli; neuropatske boli; simpatički posredovane boli; boli povezane s gastrointestinalnom disfunkcijom; epileptičkih napadaja; zujanja u ušima; seksualne disfunkcije; nepopustljivog kašlja; dermatitisa; poremećaja ovisnosti; Rettovog sindroma (RTT); poremećaja glasa zbog nekontroliranih grčeva mišića grkljana; neurotoksičnosti metotreksata; i umora uzrokovanog rakom.
7. Sol HBr spoja formule (I) prema bilo kojem od zahtjeva 1-4, ili farmaceutski pripravak prema zahtjevu 5, za uporabu u liječenju neuropatske boli.
8. Sol HBr spoja formule (I) prema bilo kojem od zahtjeva 1-4, ili farmaceutski pripravak prema zahtjevu 5, za uporabu u liječenju pseudobulbarnog afekta.
9. Farmaceutski pripravak prema zahtjevu 5, nadalje sadrži drugo terapeutsko sredstvo korisno u liječenju ili prevenciji bolesti ili stanja odabranog između emocionalne labilnosti; pseudobulbarnog afekta; autizama; neurološkog poremećaja; neurodegenerativne bolesti; ozljede mozga; tegoba ili poremećaja svijesti; kardiovaskularne bolesti; glaukoma; tardivne diskinezije; dijabetičke neuropatije; retinopatske bolesti; bolesti ili poremećaja uzrokovanih apoptozom induciranom homocisteinom; bolesti ili poremećaja uzrokovanih povišenim razinama homocisteina; kronične boli; neizlječive boli; neuropatske boli; simpatički posredovane boli; boli povezane s gastrointestinalnom disfunkcijom; epileptičkih napadaja; zujanja u ušima; seksualne disfunkcije; nepopustljivog kašlja; dermatitisa; poremećaja ovisnosti; Rettovog sindroma (RTT); poremećaja glasa zbog nekontroliranih grčeva mišića grkljana; neurotoksičnosti metotreksata; i umora uzrokovanog rakom.
10. Farmaceutski pripravak prema zahtjevu 9, naznačen time što je drugo terapeutsko sredstvo odabrano između kinidina, kinidin sulfata, oksikodona, i gabapentina.
11. Farmaceutski pripravak prema zahtjevu 10, koji sadrži 10-60 mg soli HBr spoja formule (I) prema bilo kojem od zahtjeva 1-4, i 2.5-30 mg kinidina.
12. Odvojeni oblici doziranja: (i) sol HBr spoja formule (I) prema bilo kojem od zahtjeva 1-4, ili farmaceutski pripravak prema zahtjevu 5; i (ii) drugo terapeutsko sredstvo korisno u liječenju ili prevenciji bolesti ili stanja odabranog između emocionalne labilnosti; pseudobulbarnog afekta; autizama; neurološkog poremećaja; neurodegenerativne bolesti; ozljede mozga; tegoba ili poremećaja svijesti; kardiovaskularne bolesti; glaukoma; tardivne diskinezije; dijabetičke neuropatije; retinopatske bolesti; bolesti ili poremećaja uzrokovanih apoptozom induciranom homocisteinom; bolesti ili poremećaja uzrokovanih povišenim razinama homocisteina; kronične boli; neizlječive boli; neuropatske boli; simpatički posredovane boli; boli povezane s gastrointestinalnom disfunkcijom; epileptičkih napadaja; zujanja u ušima; seksualne disfunkcije; nepopustljivog kašlja; dermatitisa; poremećaja ovisnosti; Rettovog sindroma (RTT); poremećaja glasa zbog nekontroliranih grčeva mišića grkljana; neurotoksičnosti metotreksata; i umora uzrokovanog rakom, pri čemu su navedena sol HBr spoja formule (I), ili navedeni farmaceutski pripravak, i navedeno drugo terapeutsko sredstvo međusobno povezani.
13. Odvojeni oblici doziranja prema zahtjevu 12, naznačeni time što je navedeno drugo terapeutsko sredstvo odabrano između kinidina, kinidin sulfata, oksikodona, i gabapentina.
14. Odvojeni oblici doziranja prema zahtjevu 12, koji sadrže 10-60 mg soli HBr spoja formule (I) i 2.5-30 mg kinidina.
15. Paket koji sadrži odvojene oblike doziranja prema bilo kojem od zahtjeva 12-14.
HRP20230745TT 2007-05-01 2008-04-30 Spojevi morfina HRP20230745T3 (hr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US91513007P 2007-05-01 2007-05-01
US91666207P 2007-05-08 2007-05-08
US97604407P 2007-09-28 2007-09-28
EP20200633.4A EP3825306B8 (en) 2007-05-01 2008-04-30 Morphinan compounds

Publications (1)

Publication Number Publication Date
HRP20230745T3 true HRP20230745T3 (hr) 2023-10-27

Family

ID=51894365

Family Applications (5)

Application Number Title Priority Date Filing Date
HRP20230745TT HRP20230745T3 (hr) 2007-05-01 2008-04-30 Spojevi morfina
HRP20140903AT HRP20140903T1 (hr) 2007-05-01 2014-09-22 Morfinski spojevi
HRP20150809TT HRP20150809T1 (hr) 2007-05-01 2015-07-24 Spojevi morfinana
HRP20150848TT HRP20150848T1 (hr) 2007-05-01 2015-08-10 Morfinski spojevi
HRP20160521TT HRP20160521T8 (hr) 2007-05-01 2016-05-16 Morfinski spojevi

Family Applications After (4)

Application Number Title Priority Date Filing Date
HRP20140903AT HRP20140903T1 (hr) 2007-05-01 2014-09-22 Morfinski spojevi
HRP20150809TT HRP20150809T1 (hr) 2007-05-01 2015-07-24 Spojevi morfinana
HRP20150848TT HRP20150848T1 (hr) 2007-05-01 2015-08-10 Morfinski spojevi
HRP20160521TT HRP20160521T8 (hr) 2007-05-01 2016-05-16 Morfinski spojevi

Country Status (15)

Country Link
US (6) US9314440B2 (hr)
EP (5) EP3093290B1 (hr)
BR (1) BRPI0811478B8 (hr)
CA (3) CA2945581C (hr)
CY (1) CY1117826T1 (hr)
DK (4) DK2522668T3 (hr)
ES (5) ES2577477T3 (hr)
FI (1) FI3825306T3 (hr)
HK (5) HK1178154A1 (hr)
HR (5) HRP20230745T3 (hr)
HU (3) HUE063526T2 (hr)
LT (1) LT3825306T (hr)
PL (3) PL2792662T3 (hr)
PT (5) PT2792662T (hr)
SI (2) SI3825306T1 (hr)

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JP6525419B2 (ja) 2015-01-15 2019-06-05 株式会社半導体エネルギー研究所 二次電池

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