HRP20191339T1 - Novi anelirani fenoksiacetamidi - Google Patents

Novi anelirani fenoksiacetamidi Download PDF

Info

Publication number
HRP20191339T1
HRP20191339T1 HRP20191339TT HRP20191339T HRP20191339T1 HR P20191339 T1 HRP20191339 T1 HR P20191339T1 HR P20191339T T HRP20191339T T HR P20191339TT HR P20191339 T HRP20191339 T HR P20191339T HR P20191339 T1 HRP20191339 T1 HR P20191339T1
Authority
HR
Croatia
Prior art keywords
pharmaceutically acceptable
compound
acceptable salt
accordance
inhibitors
Prior art date
Application number
HRP20191339TT
Other languages
English (en)
Inventor
Armin Heckel
Dieter Hamprecht
Joerg Kley
Dieter Wiedenmayer
Original Assignee
Boehringer Ingelheim International Gmbh
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 Boehringer Ingelheim International Gmbh filed Critical Boehringer Ingelheim International Gmbh
Publication of HRP20191339T1 publication Critical patent/HRP20191339T1/hr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/14Heterocyclic 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 three or more hetero 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/4965Non-condensed pyrazines
    • A61K31/497Non-condensed pyrazines containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • 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
    • A61P11/02Nasal agents, e.g. decongestants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C53/00Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
    • C07C53/15Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen containing halogen
    • C07C53/16Halogenated acetic acids
    • C07C53/18Halogenated acetic acids containing fluorine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D407/00Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/14Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/645Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
    • C07F9/6503Five-membered rings
    • C07F9/6506Five-membered rings having the nitrogen atoms in positions 1 and 3
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/645Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
    • C07F9/6509Six-membered rings
    • C07F9/650952Six-membered rings having the nitrogen atoms in the positions 1 and 4
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6558Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
    • C07F9/65583Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system each of the hetero rings containing nitrogen as ring hetero atom

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Pulmonology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Epidemiology (AREA)
  • Immunology (AREA)
  • Otolaryngology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Claims (24)

1. Spoj, naznačen time, da je predstavljen formulom (I), u kojoj R1 i R2 su neovisno odabrani od etila, 2-hidroksietila, 2tetrahidrofuranilmetila i 4-tetrahidropiranilmetila; R3 je odabran od dijela skupine NRaRb, pri čemu su Ra i Rb neovisno odabrani od vodika, C1-C4-alkila i 1-(2-etoksietil)piperidin-4-ila, gdje C1-C4-alkil može nositi 1 ili 2 supstituenta odabrana od hidroksila, amino, C1-C4-alkilamino, di-C1-C4-alkilamino, (dimetilfosfinoil)metoksi, 4-(dimetilfosfinoil)fenila, 6-metil-3-hidroksi-piridin-2-ila i oksianiona od 6-metil-3-hidroksi-piridin-2-ila, uz uvjet da je najmanje jedan od Ra i Rb različit od vodika, ili pri čemu Ra i Rb zajedno s dušikom na kojega su priključeni, tvore heterociklički dio skupine odabrane od piperidina i 1oksotiomorfolinila, gdje heterociklički dio skupine može nositi 1 ili 2 supstituenta odabrana od NH2; i Z-je odabran od klorida, bromida, jodida, hidroksida, vodikovog sulfata, sulfata, nitrata, fosfata, formata, acetata, trifluoroacetata, fumarata, citrata, tartrata, oksalata, sukcinata, mandelata, metansulfonata i ptoluensulfonata, ili Z- može biti odsutan ako Ra ili Rb je C1-C4-alkil i nosi oksianion od 6metil-3-hidroksi-piridin-2-ila; ili njegova farmaceutski prihvatljiva sol.
2. Spoj u skladu sa zahtjevom 1 ili njegova farmaceutski prihvatljiva sol, naznačen time, da najmanje jedan od R1 i R2 je etil.
3. Spoj u skladu sa zahtjevom 2 ili njegova farmaceutski prihvatljiva sol, naznačen time, da oba dva R1 i R2 su etil.
4. Spoj u skladu s bilo kojim od zahtjeva 1 do 3 ili njegova farmaceutski prihvatljiva sol, naznačen time, da Z- je odabran od klorida, formata, i trifluoroacetata.
5. Spoj u skladu s bilo kojim od zahtjeva 1 do 4 ili njegova farmaceutski prihvatljiva sol, naznačen time, da R3 je odabran od sljedećih:
6. Spoj u skladu sa zahtjevom 1 ili njegova farmaceutski prihvatljiva sol, naznačen time, da je odabran iz skupine koja se sastoji od sljedećih:
7. Spoj u skladu s bilo kojim od zahtjeva 1 do 6, naznačen time, da je
8. Postupak sintetiziranja farmaceutski prihvatljive soli od spojeva u skladu sa zahtjevom 7, naznačen time, da izvorni spoj koji sadrži kationsku skupinu, reagira putem konvencionalnih kemijskih postupaka.
9. Postupak sintetiziranja farmaceutski prihvatljive soli od spojeva u skladu sa zahtjevom 8, naznačen time, da izvorni spoj koji sadrži kationsku skupinu, reagira s dovoljnom količinom prikladne baze ili kiseline u vodi ili u organskom razrjeđivaču.
10. Farmaceutski prihvatljiva sol, naznačena time, da je ona od izvornog spoja za spoj (1.02) u skladu sa zahtjevom 7.
11. Farmaceutski prihvatljiva sol, naznačena time, da je ona od izvornog spoja za spoj (2.03) u skladu sa zahtjevom 7.
12. Farmaceutski prihvatljiva sol, naznačena time, da je ona od izvornog spoja za spoj (2.04) u skladu sa zahtjevom 7.
13. Farmaceutski prihvatljiva sol, naznačena time, da je ona od izvornog spoja za spoj (2.05) u skladu sa zahtjevom 7.
14. Farmaceutski prihvatljiva sol, naznačena time, da je ona od izvornog spoja za spoj (2.06) u skladu sa zahtjevom 7.
15. Farmaceutski prihvatljiva sol, naznačena time, da je ona od izvornog spoja za spoj (1.03) u skladu sa zahtjevom 7.
16. Farmaceutski prihvatljiva sol, naznačena time, da je ona od izvornog spoja za spoj (1.1) u skladu sa zahtjevom 7.
17. Farmaceutski prihvatljiva sol, naznačena time, da je ona od izvornog spoja za spoj (2.01) u skladu sa zahtjevom 7.
18. Farmaceutski prihvatljiva sol, naznačena time, da je ona od izvornog spoja za spoj (2.07) u skladu sa zahtjevom 7.
19. Farmaceutski prihvatljiva sol, naznačena time, da je ona od izvornog spoja za spoj (2.02) u skladu sa zahtjevom 7.
20. Spoj u skladu s jednim ili više od zahtjeva 1 do 19 ili njegova farmaceutski prihvatljiva sol, naznačen time, da se upotrebljava kao lijek.
21. Spoj u skladu s jednim ili više od zahtjeva 1 do 19 ili njegova farmaceutski prihvatljiva sol, naznačen time, da se upotrebljava u liječenju bolesti odabrane između respiratornih bolesti ili poremećaja i alergijskih bolesti dišnih puteva.
22. Spoj u skladu s jednim ili više od zahtjeva 1 do 19 ili njegova farmaceutski prihvatljiva sol, naznačen time, da se upotrebljava u liječenju bolesti odabrane između kroničnog bronhitisa, akutnog bronhitisa, bronhitisa prouzročenog bakterijskom ili virusnom infekcijom ili gljivično ili infekcijom helmintima, alergijski bronhitis, toksični bronhitis, kronični opstrukcijski bronhitis (COPD), astma, dječja astma, bronhiektaza, alergijski alveolitis, alergijski ili nealergijski rinitis, kronični sinusitis, idiopatska plućna fibroza, cistična fibroza ili mukoviscidoza, deficijencija alfa-1-antitripsina, kašalj, plućni emfizem, intersticijske plućne bolesti, alveolitis, hiperreaktivni dišni putevi, nosni polipi, plućni edem, pneumonitis različitog podrijetla, i suhe oči.
23. Farmaceutski pripravak, naznačen time, da obuhvaća najmanje jedan spoj u skladu s jednim ili više od zahtjeva 1 do 19 ili njegovu farmaceutski prihvatljivu sol i farmaceutski prihvatljiv nosač.
24. Lijekovita kombinacija, naznačena time, da ona sadrži, osim jednog ili više spojeva u skladu s jednim ili više od zahtjeva 1 do 19 ili njegove farmaceutski prihvatljive soli, kao dodatne djelatne tvari, jedan ili više spojeva odabranih između kategorija dodatnih ENaC-inhibitora, betamimetika, antikolinergika, kortikosteroida, PDE4-inhibitora, LTD4-antagonista, EGFR-inhibitora, agonista dopamina, H1-antihistamina, PAF-antagonista, inhibitora MAP-kinaze, MPR4-inhibitora, iNOS-inhibitora, SYK-inhibitora, korekcijska sredstva za transmembranski regulator cistične fibroze (CFTR) i CFTR potencijacijska sredstva ili njihove dvostruke ili trostruke kombinacije.
HRP20191339TT 2015-08-20 2019-07-24 Novi anelirani fenoksiacetamidi HRP20191339T1 (hr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
PCT/EP2015/069152 WO2017028927A1 (en) 2015-08-20 2015-08-20 Novel annelated phenoxyacetamides
EP15760394.5A EP3298022B1 (en) 2015-08-20 2015-08-20 Novel annelated phenoxyacetamides

Publications (1)

Publication Number Publication Date
HRP20191339T1 true HRP20191339T1 (hr) 2020-02-21

Family

ID=54065852

Family Applications (1)

Application Number Title Priority Date Filing Date
HRP20191339TT HRP20191339T1 (hr) 2015-08-20 2019-07-24 Novi anelirani fenoksiacetamidi

Country Status (27)

Country Link
EP (1) EP3298022B1 (hr)
JP (1) JP6620171B2 (hr)
KR (1) KR20180044333A (hr)
CN (1) CN108200769B (hr)
AU (1) AU2015406100B2 (hr)
BR (1) BR112018001035A2 (hr)
CA (1) CA2996087A1 (hr)
CO (1) CO2018001700A2 (hr)
CY (1) CY1122077T1 (hr)
DK (1) DK3298022T3 (hr)
EA (1) EA035738B1 (hr)
ES (1) ES2739893T3 (hr)
HR (1) HRP20191339T1 (hr)
HU (1) HUE046014T2 (hr)
IL (1) IL257136B (hr)
LT (1) LT3298022T (hr)
ME (1) ME03534B (hr)
MX (1) MX370598B (hr)
MY (1) MY194711A (hr)
PH (1) PH12018500378B1 (hr)
PL (1) PL3298022T3 (hr)
PT (1) PT3298022T (hr)
RS (1) RS59169B1 (hr)
SA (1) SA518390920B1 (hr)
SI (1) SI3298022T1 (hr)
UA (1) UA121414C2 (hr)
WO (1) WO2017028927A1 (hr)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB201610854D0 (en) 2016-06-21 2016-08-03 Entpr Therapeutics Ltd Compounds
GB201619694D0 (en) 2016-11-22 2017-01-04 Entpr Therapeutics Ltd Compounds
GB201717051D0 (en) 2017-10-17 2017-11-29 Enterprise Therapeutics Ltd Compounds
GB201808093D0 (en) 2018-05-18 2018-07-04 Enterprise Therapeutics Ltd Compounds
CN116438200A (zh) 2020-09-10 2023-07-14 普雷西里克斯公司 针对fap的抗体片段
WO2023203135A1 (en) 2022-04-22 2023-10-26 Precirix N.V. Improved radiolabelled antibody
WO2023213801A1 (en) 2022-05-02 2023-11-09 Precirix N.V. Pre-targeting

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011079087A1 (en) * 2009-12-23 2011-06-30 Glaxo Group Limited Enac blockers
JP6461134B2 (ja) * 2013-07-15 2019-01-30 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 新規ベンゾイミダゾリウム化合物
JP6461948B2 (ja) * 2013-07-15 2019-01-30 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 新規5−置換ベンゾイミダゾリウム化合物
WO2015007517A1 (en) * 2013-07-15 2015-01-22 Boehringer Ingelheim International Gmbh Novel tetra- and pentasubstituted benzimidazolium compounds

Also Published As

Publication number Publication date
MX370598B (es) 2019-12-18
EA035738B1 (ru) 2020-08-03
DK3298022T3 (da) 2019-08-26
SA518390920B1 (ar) 2021-12-14
PT3298022T (pt) 2019-09-26
CN108200769B (zh) 2021-07-27
BR112018001035A2 (pt) 2018-12-04
UA121414C2 (uk) 2020-05-25
AU2015406100A1 (en) 2018-02-01
CO2018001700A2 (es) 2018-05-21
PH12018500378A1 (en) 2018-08-29
SI3298022T1 (sl) 2019-08-30
EP3298022B1 (en) 2019-06-05
CA2996087A1 (en) 2017-02-23
JP2018522841A (ja) 2018-08-16
EP3298022A1 (en) 2018-03-28
PH12018500378B1 (en) 2018-08-29
RS59169B1 (sr) 2019-10-31
IL257136A (en) 2018-03-29
EA201890534A1 (ru) 2018-09-28
CN108200769A (zh) 2018-06-22
ME03534B (me) 2020-04-20
MY194711A (en) 2022-12-15
JP6620171B2 (ja) 2019-12-11
HUE046014T2 (hu) 2020-01-28
WO2017028927A1 (en) 2017-02-23
IL257136B (en) 2022-02-01
LT3298022T (lt) 2019-09-25
MX2018001945A (es) 2018-06-19
KR20180044333A (ko) 2018-05-02
PL3298022T3 (pl) 2019-12-31
AU2015406100B2 (en) 2020-04-23
CY1122077T1 (el) 2020-11-25
NZ738967A (en) 2021-09-24
ES2739893T3 (es) 2020-02-04

Similar Documents

Publication Publication Date Title
HRP20191339T1 (hr) Novi anelirani fenoksiacetamidi
HRP20171614T1 (hr) Heterociklički spojevi, lijekovi koji sadrže te spojeve, njihova primjena i postupci za njihovu proizvodnju
JP2016534088A5 (hr)
JP2018529657A5 (hr)
ES2292988T3 (es) Derivados de nicotinamida utiles como inhibidores de pde4.
JP2016532677A5 (hr)
NO20082000L (no) Pyrimidinamidforbindelser som PGDS-inhibitorer
MY154895A (en) Pyrimidine hydrazide compounds as pgds inhibitors
MX2009000999A (es) Derivados de quinuclidina como antagonistas de m3.
JP2014534222A5 (hr)
PT1252157E (pt) Carboxamidas de pirimidina uteis como inibidores de isozimas pde4
TW200616967A (en) Novel indazole carboxamides and their use
NO20051540L (no) 2,5-dioksoimidazolidin-4-yl acetamider og analoger som inhibitorer av metalloproteinas MMP12
TW200708513A (en) Novel crystalline forms of tiotropium bromide
ECSP14013173A (es) 3,5-diamino-6-cloro-n-(n-(4-(4-(2-(hexil(2,3,4,5,6-pentahidroxihexil)amino)etoxi)fenil)butil) carbamimidoil)pirazina-2-carboxamida
CY1114804T1 (el) Νεες ενωσεις 951: ενα διφαινυλοξυπροπανοϊκο οξυ ως ρυθμιστης crth2 και ενδιαμεσες ενωσεις
JP2011509284A5 (hr)
PE20070081A1 (es) Derivados de 2,6-quinolinilo y preparaciones que los comprenden
PE20081779A1 (es) Derivados de nicotinamida
MX2009010270A (es) Indol carboxamidas como inhibidores de quinasas ikappa2.
AR078552A1 (es) Derivados de feniloxadiazol como agentes inhibidores de las pgds
HRP20120869T1 (hr) Spirocikliäśki heterocikli, lijekovi koji sadrže te spojeve, njihova uporaba te postupak njihove proizvodnje
TW200307545A (en) Nicotinamide derivatives and a tiotropium salt in combination for the treatment of diseases
NO20080457L (no) Kjemiske forbindelser
NO20081480L (no) Kombinasjon av forbindelser som kan brukes ved behandling av respiratoriske sykdommer, spesielt kronisk obstruktiv pulmonaer sykdom (COPD) og astma