ME02123B - Antagonisti trpv1 i njihova upotreba - Google Patents
Antagonisti trpv1 i njihova upotrebaInfo
- Publication number
- ME02123B ME02123B MEP-2014-674A MEP67414A ME02123B ME 02123 B ME02123 B ME 02123B ME P67414 A MEP67414 A ME P67414A ME 02123 B ME02123 B ME 02123B
- Authority
- ME
- Montenegro
- Prior art keywords
- compound according
- alkyl
- ocf3
- och3
- pharmaceutically acceptable
- Prior art date
Links
- 101150016206 Trpv1 gene Proteins 0.000 title claims 3
- 239000005557 antagonist Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims 20
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 11
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 8
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 8
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 8
- 150000003839 salts Chemical class 0.000 claims 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
- -1 -OCH7CH3 Chemical group 0.000 claims 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 3
- 229910052799 carbon Inorganic materials 0.000 claims 3
- 125000001475 halogen functional group Chemical group 0.000 claims 3
- 102000003566 TRPV1 Human genes 0.000 claims 2
- 208000025865 Ulcer Diseases 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 125000001072 heteroaryl group Chemical group 0.000 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 230000002265 prevention Effects 0.000 claims 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- 231100000397 ulcer Toxicity 0.000 claims 2
- 101100240516 Caenorhabditis elegans nhr-10 gene Proteins 0.000 claims 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical group OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 125000006371 dihalo methyl group Chemical group 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 238000000338 in vitro Methods 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/02—Heterocyclic 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 two hetero rings
- C07D401/04—Heterocyclic 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 two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/10—Drugs for disorders of the urinary system of the bladder
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P23/00—Anaesthetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic 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
- C07D213/02—Heterocyclic 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
- C07D213/04—Heterocyclic 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
- C07D213/60—Heterocyclic 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
- C07D213/61—Halogen atoms or nitro radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic 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
- C07D213/02—Heterocyclic 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
- C07D213/04—Heterocyclic 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
- C07D213/60—Heterocyclic 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
- C07D213/72—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic 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
- C07D213/02—Heterocyclic 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
- C07D213/04—Heterocyclic 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
- C07D213/60—Heterocyclic 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
- C07D213/72—Nitrogen atoms
- C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/02—Heterocyclic 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 two hetero rings
- C07D401/12—Heterocyclic 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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/14—Heterocyclic 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic 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
- C07D405/14—Heterocyclic 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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic 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
- C07D407/14—Heterocyclic 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Urology & Nephrology (AREA)
- Pain & Pain Management (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Rheumatology (AREA)
- Anesthesiology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Hydrogenated Pyridines (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Claims (20)
1. Jedinjenje formule III: ili njegova farmaceutski prihvatljiva so, gde X je 0, S, N-CN, N-OH ili N-OR10; W je N ili C; isprekidana linija označava prisustvo ili odsustvo veze, i kada isprekidana linija označava prisustvo veze ili W je N, tada R4 nije prisutan, inače R4 je -H, -OH, -OCF3, -halo, -(C1-C6)alkil, -CH2OH, -CH2CI, -CH2Br, -CH2I, -CH2F, -CH(halo)2,-CF3, -OR10, -SR10, -COOH, -COOR10, -C(O)R10, -C(0)H, -OC(O)R10, -OC(O)NHR10, -NHC(0)R13, -CON(R13)2, -S(O)2R10, ili -NO2; R10 je -(C1-C4)alkil; svaki R13 je nezavisno: -H, -(C1-C4)alkil, -(C1-C4)alkenil, -(C1-C4)alkinil, ili -fenil; svaki R3 je nezavisno: (a) -H ili (C1-C6)alkil; ili (b) dve R3 grupe zajedno obrazuju (C2-C6)most, koji je nesupstituisan ili supstituisan sa 1, 2 ili 3 nezavisno izabrane R8 grupe, a most opciono sadrži -FIC=CH- u okviru (C2-C6) mosta; ili (c) dve R3 grupe zajedno obrazuju -CH2N(Ra)-CH2- most, most; ili most; Ra je izabran od -H, -(C1-C6)alkil, -(C3-C8)cikloalkil, -CH2-C(0)-RC, -(CH2)-C(0)-0RC, -(CH2)-C(0)-N(RC)2, -(CH2)2-0-Rc, -(CH2)2-S(0)2-N(Rc)2, ili -(CH2)2-N(Rc)S(0)2-Rc; Rbje izabran od: (a) -H, -(C1-C6)alkil, -(C3-C8)cikloakil, -(3- do 7-člani)heterocikl, -N(RC)2, -N(Rc)-(C3-C8)cikloalkil, ili -N(Rc)-(3- do 7-člani)heterocikl; ili (b) -fenil, -(5- ili 6-člani)heteroaril, -N(Rc)-fenil ili -N(Rc)-(5-do 10-člani)heteroaril, od kojih je svaki nesupstituisan ili supstituisan sa 1, 2 ili 3 nezavisno izabrane R7 grupe; svaki Rc je nezavisno izabran od -H ili -(C1-C4)alkil; m je ceo broj 0, 1, ili 2, gde Ar, je: R1 je -Cl, -F ili -CF3; gde Ar, je R14 je -H, -Cl, -F, -Br, -CF3, -OCF3, -(C1-C6)alkil, -SO2CF3, -SO2(C1-C6)alkil, -OCH3, -OCH2CH3, ili -OCH(CH3)2, i poželjno -CF3, -OCF3, -Cl, ili -F; R14 je -H, -Cl, -F, Br, -CH3, -CH2CH3, -OCH3, -OCH(CH3)2, ili -OCH2CH3; i svaki R8 i R9 je nezavisno -H, -Cl, -Br, -F, -CH3, -OCH3, -OCH7CH3, -CF3, -OCF3, izo-propil, ili terc-butil.
2. Jedinjenje prema zahtevu 1, gde X=0.
3. Jedinjenje prema bilo kom od patentnih zahteva 1 do 2, gde R4 je halo, poželjno F.
4. Jedinjenje prema bilo kom od patentnih zahteva, gde R1 je halo, poželjno Cl ili F, ili CF3.
5. Jedinjenje prema bilo kom od patentnih zahteva 1 do 4, gde W je C i isprekidana linija nije prisutna.
6. Jedinjenje prema bilo kom od patentnih zahteva 1 do 4, gde W je C i isprekidana linija je dvostruka veza.
7. Jedinjenje prema bilo kom od patentnih zahteva 1 do 4, gde W je N, R4 nije prisutan i isprekidana linija nije prisutna.
8. Jedinjenje prema bilo kom od prethodnih zahteva, gde je m=0.
9. Jedinjenje prema bilo kom od patentnih zahteva 1 do 7, gde m=l i poželjno R3 je (C1-C6)alkil i još poželjnije -CH3 ili -CH7CH3.
10. Jedinjenje prema bilo kom od patentnih zahteva 1 do 9, gde Ar7 je izabran od
11. Jedinjenje prema bilo kom od patentnih zahteva 1 do 10, gde Ar2 je a) ili b) gde je R14 izabran od -H, -Cl, -F, -Br, -CF3, -OCF3, -(Ca-C6)alkil, -SO2CF3, -SO2(C1-C6)alkil, -OCFI3, -OCH2CFI3, -OCH(CH3)2, a poželjno je -CF3, -OCF3, -Cl, ili -F; ili c) gde je R14 izabran od -H, -Cl, -F, -Br, -OCF3, -CH3, -CH7CH3, -OCH3, -OCH7CH3, -OCH(CH3)7, i poželjno je -OCF3, -OCH3, -OCH7CH3, -Cl, ili -F; ili d) gde je R14 izabran od -H, -Cl, -F, -Br, -OCF3, -CH3j -CH7CH3, -OCH3, -OCH7CH3, -OCH(CH3)7, i poželjno je -OCF3, -OCH3, -OCH2CH3, -Cl, ili -F; ili e) ili f) gde svaki R8 i R9 su nezavisno -H, -Cl, -Br, -F, -CH3, -OCH3, -OCH7CH3, -CF3, -OCF3, izo-propil, ili terc-butil.
12. Jedinjenje prema bilo kom od patentnih zahteva 1 do 11, gde hiralni ugljenikov atom Q grupe ima (S)-konfiguraciju: ili gde hiralni ugljenikov atom Q grupe ima (R)-konfiguraciju:
13. Jedinjenje prema zahtevu 1 koje ima formulu ili njegova farmaceutski prihvatljiva so.
14. Jedinjenje prema patentnom zahtevu 1, koje ima formulu ili njegova farmaceutski prihvatljiva so.
15. Jedinjenje prema bilo kom od prethodnih patentnih zahteva, gde je farmaceutski prihvatljiva so fumaratna so.
16. Kompozicija koja sadrži jedinjenje prema bilo kod od patentnih zahteva 1 do 15 ili njegovu farmaceutski prihvatljivu so i farmaceutski prihvatljiv nosač ili ekscipijent.
17. In-vitro postupak inhibicije funkcije TRPV1 u ćeliji koji obuhvata dovođenje u kontakt ćelije koja je u stanju da eksprimuje TRPV1 sa efikasnom količinom jedinjenja prema bilo kom od patentnih zahteva 1 do 15 ili njegove farmaceutski prihvatljive soli.
18. Upotreba jedinjenja prema bilo kom od patentnih zahteva 1 do 15 ili njegove farmaceutski prihvatljive soli u proizvodnji leka za lečenje ili prevenciju bola, čira, IBD ili IBS kod životinje.
19. Jedinjenje prema bilo kom od patentnih zahteva 1 do 15 za upotrebu kao lek.
20. Jedinjenje prema bilo kom od zahteva 1 do 15 za primenu u lečenju ili prevenciji bola, UI, čira, IBD ili IBS kod životinje.
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US92666107P | 2007-04-27 | 2007-04-27 | |
| US93003607P | 2007-05-11 | 2007-05-11 | |
| US93700307P | 2007-06-21 | 2007-06-21 | |
| US96240907P | 2007-07-27 | 2007-07-27 | |
| PCT/IB2008/001069 WO2008132600A2 (en) | 2007-04-27 | 2008-04-25 | Trpv1 antagonists and uses thereof |
| EP08737573.9A EP2142529B1 (en) | 2007-04-27 | 2008-04-25 | Trpv1 antagonists and uses thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ME02123B true ME02123B (me) | 2014-08-29 |
Family
ID=39688846
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MEP-2014-674A ME02123B (me) | 2007-04-27 | 2008-04-25 | Antagonisti trpv1 i njihova upotreba |
Country Status (27)
| Country | Link |
|---|---|
| US (8) | US20090170867A1 (me) |
| EP (3) | EP2604598B1 (me) |
| JP (2) | JP5462784B2 (me) |
| KR (2) | KR20100005725A (me) |
| CN (1) | CN101932570B (me) |
| AR (1) | AR066146A1 (me) |
| AU (1) | AU2008243874B2 (me) |
| BR (1) | BRPI0809795A2 (me) |
| CA (3) | CA2685266C (me) |
| CO (1) | CO6241153A2 (me) |
| CY (1) | CY1115262T1 (me) |
| DK (1) | DK2142529T3 (me) |
| ES (2) | ES2571533T3 (me) |
| HR (1) | HRP20140279T1 (me) |
| IL (2) | IL201688A (me) |
| ME (1) | ME02123B (me) |
| MX (1) | MX2009011600A (me) |
| MY (1) | MY148657A (me) |
| NZ (1) | NZ580266A (me) |
| PE (2) | PE20130325A1 (me) |
| PH (1) | PH12013500848A1 (me) |
| PL (1) | PL2142529T3 (me) |
| PT (1) | PT2142529E (me) |
| RS (1) | RS53212B (me) |
| TW (1) | TWI362930B (me) |
| UY (1) | UY31050A1 (me) |
| WO (1) | WO2008132600A2 (me) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100891887B1 (ko) | 2001-01-29 | 2009-04-03 | 시오노기세이야쿠가부시키가이샤 | 5-메틸-1-페닐-2-(1h)-피리돈을 활성 성분으로서 함유하는의약 제제 |
| DK2142529T3 (da) | 2007-04-27 | 2014-02-10 | Purdue Pharma Lp | Trpv1-antagonister og anvendelser deraf |
| US8703962B2 (en) * | 2008-10-24 | 2014-04-22 | Purdue Pharma L.P. | Monocyclic compounds and their use as TRPV1 ligands |
| US8759362B2 (en) * | 2008-10-24 | 2014-06-24 | Purdue Pharma L.P. | Bicycloheteroaryl compounds and their use as TRPV1 ligands |
| US8546388B2 (en) * | 2008-10-24 | 2013-10-01 | Purdue Pharma L.P. | Heterocyclic TRPV1 receptor ligands |
| LT2445502T (lt) | 2009-06-25 | 2017-09-25 | Alkermes Pharma Ireland Limited | Heterocikliniai junginiai, skirti neurologinių ir fiziologinių susirgimų gydymui |
| CA2797708C (en) | 2010-05-04 | 2016-08-16 | Alkermes Pharma Ireland Limited | Process for synthesizing oxidized lactam compounds |
| CN107898791A (zh) | 2010-06-03 | 2018-04-13 | 药品循环有限责任公司 | 布鲁顿酪氨酸激酶(btk)抑制剂的应用 |
| WO2011162409A1 (en) * | 2010-06-22 | 2011-12-29 | Shionogi & Co., Ltd. | Compounds having trpv1 antagonistic activity and uses thereof |
| AU2011270701B2 (en) | 2010-06-24 | 2015-05-14 | Alkermes Pharma Ireland Limited | Prodrugs of NH-acidic compounds: ester, carbonate, carbamate and phosphonate derivatives |
| JP5872585B2 (ja) | 2010-12-22 | 2016-03-01 | パーデュー、ファーマ、リミテッド、パートナーシップ | リン置換キノキサリンタイプピペリジン化合物とその使用 |
| WO2012158844A1 (en) | 2011-05-17 | 2012-11-22 | Shionogi & Co., Ltd. | Heterocyclic compounds |
| HRP20170507T1 (hr) * | 2011-06-22 | 2017-06-02 | Purdue Pharma Lp | Trpv1 antagonisti uključujući dihidroksi supstituente i njihove uporabe |
| US9394293B2 (en) | 2011-08-10 | 2016-07-19 | Purdue Pharma L.P. | TRPV1 antagonists including dihydroxy substituent and uses thereof |
| KR20130032847A (ko) * | 2011-09-23 | 2013-04-02 | 주식회사유한양행 | 이미드를 포함하는 벤조싸이아졸 유도체 또는 그의 염 및 이를 포함하는 약학 조성물 |
| JO3754B1 (ar) | 2012-06-04 | 2021-01-31 | Pharmacyclics Llc | أشكال كريستالين لمثبط أنزيم كيناز تيروسين بروتون |
| CN104704129A (zh) | 2012-07-24 | 2015-06-10 | 药品循环公司 | 与对布鲁顿酪氨酸激酶(btk)抑制剂的抗性相关的突变 |
| JP6249517B2 (ja) * | 2012-11-08 | 2017-12-20 | 花王株式会社 | 体感温度低減用外用剤 |
| EP2774919A1 (en) * | 2013-03-06 | 2014-09-10 | Pharmeste S.R.L. In Liquidazione | Novel sulfonamide TRPA1 receptor antagonists |
| EP3049082B1 (en) * | 2013-09-24 | 2019-05-22 | Purdue Pharma L.P. | Treatment of burn pain by trpv1 modulators |
| JP6308881B2 (ja) * | 2014-06-11 | 2018-04-11 | 保土谷化学工業株式会社 | 電荷制御剤およびそれを用いたトナー |
| IL315294A (en) | 2015-03-03 | 2024-10-01 | Pharmacyclics Llc | Pharmaceutical formulations of bruton's tyrosine kinase inhibitor |
| CA2937365C (en) | 2016-03-29 | 2018-09-18 | F. Hoffmann-La Roche Ag | Granulate formulation of 5-methyl-1-phenyl-2-(1h)-pyridone and method of making the same |
| CN113292485B (zh) * | 2021-06-08 | 2023-10-27 | 河南大学 | 苄基哌嗪脲类trpv1拮抗和mor激动双靶点药物及制备方法和应用 |
| CN120513091A (zh) | 2022-10-31 | 2025-08-19 | 盐野义制药株式会社 | 作为trpv1拮抗剂的吡啶衍生物的用途 |
Family Cites Families (149)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3536809A (en) | 1969-02-17 | 1970-10-27 | Alza Corp | Medication method |
| US3598123A (en) * | 1969-04-01 | 1971-08-10 | Alza Corp | Bandage for administering drugs |
| US3845770A (en) * | 1972-06-05 | 1974-11-05 | Alza Corp | Osmatic dispensing device for releasing beneficial agent |
| US3916899A (en) | 1973-04-25 | 1975-11-04 | Alza Corp | Osmotic dispensing device with maximum and minimum sizes for the passageway |
| US4008719A (en) | 1976-02-02 | 1977-02-22 | Alza Corporation | Osmotic system having laminar arrangement for programming delivery of active agent |
| US4409229A (en) | 1977-12-02 | 1983-10-11 | Hoechst-Roussel Pharmaceuticals, Inc. | Antidepressive and tranquilizing substituted 1,3-dihydrospiro[benzo(c)thiophene]s |
| IE58110B1 (en) | 1984-10-30 | 1993-07-14 | Elan Corp Plc | Controlled release powder and process for its preparation |
| DE3440141A1 (de) | 1984-11-02 | 1986-05-07 | Heiner Dipl.-Chem. Dr. 8000 München Eckert | Verwendung von kohlensaeure-bis-trichlormethylester als proreagens fuer phosgen |
| JPH0680054B2 (ja) | 1985-06-19 | 1994-10-12 | 吉富製薬株式会社 | ピペリジン誘導体 |
| JPS6289679U (me) | 1985-11-22 | 1987-06-08 | ||
| US4797419A (en) * | 1986-11-03 | 1989-01-10 | Warner-Lambert Company | Method of treating the symptoms of senile cognitive decline employing di- or trisubstituted urea cholinergic agents |
| US4866197A (en) | 1987-12-23 | 1989-09-12 | American Home Products Corporation | Production of N-((2-alkoxy-6-methoxy-5-(trifluoromethyl)-1-naphthalenyl)carbonyl)-N-methylglycine esters |
| US5073543A (en) | 1988-07-21 | 1991-12-17 | G. D. Searle & Co. | Controlled release formulations of trophic factors in ganglioside-lipsome vehicle |
| DE3905364A1 (de) * | 1989-02-22 | 1990-08-23 | Hoechst Ag | Substituierte pyrimidin-derivate, verfahren zu ihrer herstellung und ihre verwendung als tool |
| IT1229203B (it) * | 1989-03-22 | 1991-07-25 | Bioresearch Spa | Impiego di acido 5 metiltetraidrofolico, di acido 5 formiltetraidrofolico e dei loro sali farmaceuticamente accettabili per la preparazione di composizioni farmaceutiche in forma a rilascio controllato attive nella terapia dei disturbi mentali organici e composizioni farmaceutiche relative. |
| US5120548A (en) * | 1989-11-07 | 1992-06-09 | Merck & Co., Inc. | Swelling modulated polymeric drug delivery device |
| US5733566A (en) | 1990-05-15 | 1998-03-31 | Alkermes Controlled Therapeutics Inc. Ii | Controlled release of antiparasitic agents in animals |
| PT97888B (pt) * | 1990-06-07 | 1998-12-31 | Zeneca Ltd | Processo para a preparacao de compostos heterociclicos derivados de indol e de composicoes farmaceuticas que os contem |
| US5698155A (en) * | 1991-05-31 | 1997-12-16 | Gs Technologies, Inc. | Method for the manufacture of pharmaceutical cellulose capsules |
| US5580578A (en) * | 1992-01-27 | 1996-12-03 | Euro-Celtique, S.A. | Controlled release formulations coated with aqueous dispersions of acrylic polymers |
| JP3191429B2 (ja) | 1992-09-02 | 2001-07-23 | 富士通テン株式会社 | 電子機器の挿排装置 |
| US5728704A (en) * | 1992-09-28 | 1998-03-17 | Pfizer Inc. | Substituted pyridmidines for control of diabetic complications |
| DE4234295A1 (de) * | 1992-10-12 | 1994-04-14 | Thomae Gmbh Dr K | Carbonsäurederivate, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung |
| US5591767A (en) * | 1993-01-25 | 1997-01-07 | Pharmetrix Corporation | Liquid reservoir transdermal patch for the administration of ketorolac |
| DE4302051A1 (de) | 1993-01-26 | 1994-07-28 | Thomae Gmbh Dr K | 5-gliedrige Heterocyclen, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Arzneimittel |
| IT1270594B (it) * | 1994-07-07 | 1997-05-07 | Recordati Chem Pharm | Composizione farmaceutica a rilascio controllato di moguisteina in sospensione liquida |
| DE19514313A1 (de) * | 1994-08-03 | 1996-02-08 | Bayer Ag | Benzoxazolyl- und Benzothiazolyloxazolidinone |
| DE69635048T2 (de) | 1995-06-12 | 2006-02-16 | G.D. Searle & Co. | Mittel, enthaltend einen cyclooxygenase-2 inhibitor und einen 5-lipoxygenase inhibitor |
| RU2167865C2 (ru) * | 1995-09-07 | 2001-05-27 | Ф. Хоффманн-Ля Рош Аг | Производные пиперидина, способ их получения, фармацевтическая композиция на их основе и промежуточные вещества |
| EP0861075A1 (en) * | 1995-11-13 | 1998-09-02 | Albany Medical College | Analgesic compounds and uses thereof |
| FR2744448B1 (fr) | 1996-02-02 | 1998-04-24 | Pf Medicament | Nouvelles piperidines derivees d'aryl piperazine, ainsi que leur procede de preparation, les compositions pharmaceutiques et leur utilisation comme medicaments |
| US5891889A (en) | 1996-04-03 | 1999-04-06 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| JP2001519766A (ja) | 1996-04-03 | 2001-10-23 | メルク エンド カンパニー インコーポレーテッド | ファルネシルタンパク質トランスフェラーゼの阻害剤 |
| US5948786A (en) * | 1996-04-12 | 1999-09-07 | Sumitomo Pharmaceuticals Company, Limited | Piperidinylpyrimidine derivatives |
| US5854245A (en) * | 1996-06-28 | 1998-12-29 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
| US5990107A (en) * | 1996-06-28 | 1999-11-23 | Merck & Co., Inc. | Fibrinogen receptor antagonist prodrugs |
| US5798360A (en) * | 1996-08-01 | 1998-08-25 | Isis Pharmaceuticals, Inc. | N-(aminoalkyl)- and/or N-(amidoalkyl)- dinitrogen heterocyclic compositions |
| FR2758328B1 (fr) | 1997-01-15 | 1999-04-02 | Pf Medicament | Nouvelles amines aromatiques derivees d'amines cycliques utiles comme medicaments |
| FR2758327B1 (fr) | 1997-01-15 | 1999-04-02 | Pf Medicament | Nouvelles arylpiperazines derivees de piperidine |
| AU742391B2 (en) * | 1997-08-20 | 2002-01-03 | Regents Of The University Of California, The | Nucleic acid sequences encoding capsaicin receptor and capsaicin receptor-related polypeptides and uses thereof |
| JPH11199573A (ja) | 1998-01-07 | 1999-07-27 | Yamanouchi Pharmaceut Co Ltd | 5ht3受容体作動薬及び新規ベンゾチアゾール誘導体 |
| TR200002182T2 (tr) * | 1998-01-27 | 2000-12-21 | Aventis Pharmaceuticals Products Inc. | İkame edilmiş aksozaherosayklil faktör xa inhibitörleri |
| EP0943683A1 (en) * | 1998-03-10 | 1999-09-22 | Smithkline Beecham Plc | Human vanilloid receptor homologue Vanilrep1 |
| EP1087962A4 (en) | 1998-06-19 | 2001-10-04 | Lilly Co Eli | PRODUCTION OF HETEROARYL COMPOUNDS |
| WO2000001688A1 (en) | 1998-07-02 | 2000-01-13 | Sankyo Company, Limited | Five-membered heteroaryl compounds |
| ES2300151T3 (es) * | 1998-09-22 | 2008-06-01 | Astellas Pharma Inc. | Derivados de cianofenilo. |
| WO2000042852A1 (en) | 1999-01-25 | 2000-07-27 | Smithkline Beecham Corporation | Compounds and methods |
| GB9907097D0 (en) * | 1999-03-26 | 1999-05-19 | Novartis Ag | Organic compounds |
| AP2005003199A0 (en) | 1999-04-01 | 2005-03-31 | Pfizer Prod Inc | Aminopyrimidines as sorbitol dehydrogenase inhibitors |
| EP1183238A1 (en) | 1999-05-17 | 2002-03-06 | Eli Lilly And Company | Metabotropic glutamate receptor antagonists |
| GB9912411D0 (en) * | 1999-05-28 | 1999-07-28 | Pfizer Ltd | Compounds useful in therapy |
| DE19934799B4 (de) * | 1999-07-28 | 2008-01-24 | Az Electronic Materials (Germany) Gmbh | Chiral-smektische Flüssigkristallmischung und ihre Verwendung in Aktivmatrix-Displays mit hohen Kontrastwerten |
| US7343017B2 (en) * | 1999-08-26 | 2008-03-11 | American Technology Corporation | System for playback of pre-encoded signals through a parametric loudspeaker system |
| WO2001017965A2 (en) | 1999-09-07 | 2001-03-15 | Syngenta Participations Ag | Cyanopiperidines as pesticides |
| US6887870B1 (en) | 1999-10-12 | 2005-05-03 | Bristol-Myers Squibb Company | Heterocyclic sodium/proton exchange inhibitors and method |
| JP2003521543A (ja) * | 2000-02-07 | 2003-07-15 | アボット ゲーエムベーハー ウント カンパニー カーゲー | 2−ベンゾチアゾリル尿素誘導体およびそのプロテインキナーゼ阻害剤としての使用 |
| AU2001255600A1 (en) | 2000-04-25 | 2001-11-07 | Pharmacia Corporation | Regioselective synthesis of 3,4-di(carbocyclyl or heterocyclyl)thiophenes |
| AU8181701A (en) * | 2000-06-21 | 2002-01-02 | Hoffmann La Roche | Benzothiazole derivatives |
| AR028782A1 (es) * | 2000-07-05 | 2003-05-21 | Taisho Pharmaceutical Co Ltd | Derivados heterociclicos tetrahidropiridino o piperidino |
| WO2002006196A1 (en) * | 2000-07-13 | 2002-01-24 | Merck Patent Gmbh | Chiral compounds i |
| JP2004525071A (ja) * | 2000-07-20 | 2004-08-19 | ニューロジェン コーポレイション | カプサイシン受容体リガンド |
| IL154927A0 (en) * | 2000-10-18 | 2003-10-31 | Pfizer Prod Inc | Combination of statins and sorbitol dehydrogenase inhibitors |
| BR0115783A (pt) * | 2000-11-30 | 2003-09-16 | Pfizer Prod Inc | Combinação de agonistas de gaba e inibidores de sorbitol desidrogenase |
| AU2002222644A1 (en) | 2000-12-15 | 2002-06-24 | Japan Science And Technology Corporation | Arylbis (perfluoroalkylsulfonyl) methane, metal salt of the same, and processes for producing these |
| US7193113B2 (en) * | 2000-12-15 | 2007-03-20 | Japan Science And Technology Corporation | Arylbis(perfluoroalkylsulfonyl) methane and metallic salt thereof, and methods for producing the same |
| US20030232996A1 (en) | 2001-04-20 | 2003-12-18 | Brown David L | Regioselective synthesis of 3,4-di{(carboclyl or heterocyclyl)thiophenes |
| CA2446380A1 (en) | 2001-05-08 | 2002-11-14 | Yale University | Proteomimetic compounds and methods |
| US20040038982A1 (en) * | 2001-07-13 | 2004-02-26 | Bondinell William E. | Compounds and methods |
| JP2003095951A (ja) | 2001-09-25 | 2003-04-03 | Sumitomo Pharmaceut Co Ltd | 慢性関節リウマチ治療剤 |
| WO2003029199A1 (en) * | 2001-09-28 | 2003-04-10 | Takeda Chemical Industries, Ltd. | Benzene derivatives, process for preparing the same and use thereof |
| CA2470612A1 (en) | 2001-12-19 | 2003-07-03 | Merck & Co., Inc. | Heteroaryl substituted imidazole modulators of metabotropic glutamate receptor-5 |
| US7390813B1 (en) * | 2001-12-21 | 2008-06-24 | Xenon Pharmaceuticals Inc. | Pyridylpiperazines and aminonicotinamides and their use as therapeutic agents |
| US20050119251A1 (en) * | 2001-12-21 | 2005-06-02 | Jian-Min Fu | Nicotinamide derivatives and their use as therapeutic agents |
| JP2003192673A (ja) | 2001-12-27 | 2003-07-09 | Bayer Ag | ピペラジンカルボキシアミド誘導体 |
| WO2003066595A2 (en) * | 2002-02-01 | 2003-08-14 | Euro-Celtique S.A. | 2 - piperazine - pyridines useful for treating pain |
| ES2316777T3 (es) * | 2002-02-15 | 2009-04-16 | Glaxo Group Limited | Moduladores de receptores vainilloides. |
| US6974818B2 (en) * | 2002-03-01 | 2005-12-13 | Euro-Celtique S.A. | 1,2,5-thiadiazol-3-YL-piperazine therapeutic agents useful for treating pain |
| DE60326436D1 (en) * | 2002-03-13 | 2009-04-16 | Janssen Pharmaceutica Nv | Aminoderivate als histone-deacetylase-inhibitoren |
| GB0209715D0 (en) * | 2002-04-27 | 2002-06-05 | Astrazeneca Ab | Chemical compounds |
| CN1150176C (zh) * | 2002-05-22 | 2004-05-19 | 上海医药工业研究院 | 芳烷酮哌嗪衍生物及其应用 |
| WO2003099266A2 (en) * | 2002-05-23 | 2003-12-04 | Abbott Laboratories | Acetamides and benzamides that are useful in treating sexual dysfunction |
| DK1522314T3 (da) * | 2002-06-26 | 2014-05-26 | Ono Pharmaceutical Co | Midler for sygdomme forårsaget af vaskulær sammentrækning eller udvidelse |
| PT1556354E (pt) * | 2002-06-28 | 2008-04-17 | Euro Celtique Sa | Derivados de piperazina úteis como agentes terapêuticos para o tratamento da dor |
| EP1388538B1 (en) | 2002-07-09 | 2010-09-01 | Merck Patent GmbH | Polymerisation Initiator |
| US7262194B2 (en) * | 2002-07-26 | 2007-08-28 | Euro-Celtique S.A. | Therapeutic agents useful for treating pain |
| AU2003256922A1 (en) | 2002-07-31 | 2004-02-16 | Smithkline Beecham Corporation | Substituted heterocyclic compounds as modulators of the ccr5 receptor |
| US7157462B2 (en) * | 2002-09-24 | 2007-01-02 | Euro-Celtique S.A. | Therapeutic agents useful for treating pain |
| AU2003271064B2 (en) | 2002-09-27 | 2010-06-17 | Dainippon Sumitomo Pharma Co., Ltd. | Novel adenine compound and use thereof |
| EP1551811A1 (en) * | 2002-10-17 | 2005-07-13 | Amgen Inc. | Benzimidazole derivatives and their use as vanilloid receptor ligands |
| US7582635B2 (en) | 2002-12-24 | 2009-09-01 | Purdue Pharma, L.P. | Therapeutic agents useful for treating pain |
| US7223788B2 (en) | 2003-02-14 | 2007-05-29 | Sanofi-Aventis Deutschland Gmbh | Substituted N-aryl heterocycles, process for their preparation and their use as medicaments |
| DE10311065A1 (de) * | 2003-03-13 | 2004-09-23 | Abbott Gmbh & Co. Kg | Pyrimidin-2-on-Verbindungen und ihre therapeutische Verwendung |
| WO2004103954A1 (ja) * | 2003-05-20 | 2004-12-02 | Ajinomoto Co., Inc. | アミド誘導体 |
| MY142655A (en) | 2003-06-12 | 2010-12-15 | Euro Celtique Sa | Therapeutic agents useful for treating pain |
| US7129235B2 (en) * | 2003-07-11 | 2006-10-31 | Abbott Laboratories | Amides useful for treating pain |
| US20050009841A1 (en) * | 2003-07-11 | 2005-01-13 | Zheng Guo Zhu | Novel amides useful for treating pain |
| EP1867644B1 (en) | 2003-07-24 | 2009-05-20 | Euro-Celtique S.A. | Heteroaryl-tetrahydropiperidyl compounds useful for treating or preventing pain |
| AU2004259357B2 (en) | 2003-07-24 | 2010-02-18 | Euro-Celtique S.A. | Piperidine compounds and pharmaceutical compositions containing them |
| SI1867644T1 (sl) | 2003-07-24 | 2009-10-31 | Euro Celtique Sa | Heteroaril-tetrahidropiperidilne spojine, koristne za zdravljenje ali preprečevanje bolečine |
| MXPA06001202A (es) * | 2003-07-29 | 2006-08-31 | Xenon Pharmaceuticals Inc | Derivados piridilo y su uso como agentes terapeuticos. |
| US7754711B2 (en) * | 2003-07-30 | 2010-07-13 | Xenon Pharmaceuticals Inc. | Pyridazine derivatives and their use as therapeutic agents |
| CN1829701A (zh) * | 2003-07-30 | 2006-09-06 | 泽农医药公司 | 哌嗪衍生物和它们作为治疗剂的用途 |
| EP1648874B1 (en) * | 2003-07-30 | 2011-10-05 | Xenon Pharmaceuticals Inc. | Piperazine derivatives and their use as therapeutic agents |
| US7759348B2 (en) * | 2003-07-30 | 2010-07-20 | Xenon Pharmaceuticals Inc. | Pyridazine derivatives and their use as therapeutic agents |
| KR20060036106A (ko) * | 2003-07-30 | 2006-04-27 | 제논 파마슈티칼스 인크. | 피리딜 유도체 및 그의 치료제로서의 용도 |
| CN101712653A (zh) * | 2003-07-30 | 2010-05-26 | 泽农医药公司 | 哒嗪衍生物和它们作为治疗剂的用途 |
| JP4866610B2 (ja) * | 2003-08-18 | 2012-02-01 | 富士フイルムファインケミカルズ株式会社 | ピリジルテトラヒドロピリジン類およびピリジルピペリジン類 |
| WO2005037284A1 (en) | 2003-10-15 | 2005-04-28 | Pfizer Products Inc. | Sorbitol dehydrogenase inhibitor and hypertensive agent combinations |
| US20050130974A1 (en) * | 2003-10-17 | 2005-06-16 | Rigel Pharmaceuticals, Inc. | Benzothiazole compositions and their use as ubiquitin ligase inhibitors |
| GB0325287D0 (en) | 2003-10-29 | 2003-12-03 | Merck Sharp & Dohme | Therapeutic agents |
| MY145822A (en) * | 2004-08-13 | 2012-04-30 | Neurogen Corp | Substituted biaryl piperazinyl-pyridine analogues |
| DE102004039789A1 (de) * | 2004-08-16 | 2006-03-02 | Sanofi-Aventis Deutschland Gmbh | Arylsubstituierte polycyclische Amine, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| EP1827438B2 (en) * | 2004-09-20 | 2014-12-10 | Xenon Pharmaceuticals Inc. | Piperazin derivatives for inhibiting human stearoyl-coa-desaturase |
| CA2580857A1 (en) * | 2004-09-20 | 2006-09-28 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as stearoyl-coa desaturase inhibitors |
| CA2580762A1 (en) * | 2004-09-20 | 2006-03-30 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as therapeutic agents |
| EP1807085B1 (en) * | 2004-09-20 | 2013-08-21 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as stearoyl-coa desaturase inhibitors |
| US20060116368A1 (en) * | 2004-11-29 | 2006-06-01 | Calvo Raul R | 4-Piperidinecarboxamide modulators of vanilloid VR1 receptor |
| GT200600046A (es) * | 2005-02-09 | 2006-09-25 | Terapia de combinacion | |
| ES2400287T3 (es) * | 2005-03-14 | 2013-04-08 | High Point Pharmaceuticals, Llc | Derivados de benzazol, composiciones y procedimientos de uso como inhibidores de beta-secretasa |
| DE102005014904A1 (de) | 2005-03-26 | 2007-02-01 | Abbott Gmbh & Co. Kg | Substituierte Oxindol-Derivate, diese enthaltende Arzneimittel und deren Verwendung |
| FR2884516B1 (fr) | 2005-04-15 | 2007-06-22 | Cerep Sa | Antagonistes npy, preparation et utilisations |
| US8193206B2 (en) | 2005-06-14 | 2012-06-05 | Taigen Biotechnology Co., Ltd. | Pyrimidine compounds |
| JP4324221B2 (ja) | 2005-08-26 | 2009-09-02 | 株式会社医薬分子設計研究所 | Pparアゴニスト活性を有する誘導体 |
| AU2006296004B2 (en) | 2005-09-27 | 2011-11-17 | Shionogi & Co., Ltd. | Sulfonamide derivative having PGD2 receptor antagonistic activity |
| US20070155707A1 (en) * | 2005-12-29 | 2007-07-05 | Kadmus Pharmaceuticals, Inc. | Ionizable inhibitors of fatty acid amide hydrolase |
| ATE460404T1 (de) | 2006-01-18 | 2010-03-15 | Siena Biotech Spa | Modulatoren von alpha7-nikotin-acetylcholin- rezeptoren und therapeutische anwendungen davon |
| EP2562168B1 (en) * | 2006-02-28 | 2014-04-16 | Dart Neuroscience (Cayman) Ltd | Therapeutic piperazines as pde4 inhibitors |
| WO2007103719A2 (en) * | 2006-03-03 | 2007-09-13 | Incyte Corporation | MODULATORS OF 11-β HYDROXYL STEROID DEHYDROGENASE TYPE 1, PHARMACEUTICAL COMPOSITIONS THEREOF, AND METHODS OF USING THE SAME |
| TW200815426A (en) * | 2006-06-28 | 2008-04-01 | Astrazeneca Ab | New pyridine analogues II 333 |
| WO2008005368A2 (en) * | 2006-06-30 | 2008-01-10 | Abbott Laboratories | Piperazines as p2x7 antagonists |
| WO2008013622A2 (en) | 2006-07-27 | 2008-01-31 | E. I. Du Pont De Nemours And Company | Fungicidal azocyclic amides |
| US20080182851A1 (en) * | 2006-11-20 | 2008-07-31 | Glenmark Pharmaceuticals S.A. | Acetylene derivatives as stearoyl coa desaturase inhibitors |
| DE102006060598A1 (de) * | 2006-12-21 | 2008-06-26 | Merck Patent Gmbh | Tetrahydrobenzoisoxazole |
| EP2139869A2 (en) * | 2007-04-13 | 2010-01-06 | SuperGen, Inc. | Axl kinase inhibitors useful for the treatment of cancer or hyperproliferative disorders |
| WO2008133973A1 (en) * | 2007-04-27 | 2008-11-06 | Purdue Pharma L.P. | Therapeutic agents useful for treating pain |
| DK2142529T3 (da) * | 2007-04-27 | 2014-02-10 | Purdue Pharma Lp | Trpv1-antagonister og anvendelser deraf |
| WO2008147864A2 (en) | 2007-05-22 | 2008-12-04 | Xenon Pharmaceuticals Inc. | Methods of using piperazine compounds in treating sodium channel-mediated diseases or conditions |
| US8058299B2 (en) * | 2007-05-22 | 2011-11-15 | Via Pharmaceuticals, Inc. | Diacylglycerol acyltransferase inhibitors |
| AU2008287542C1 (en) | 2007-06-01 | 2015-01-22 | The Trustees Of Princeton University | Treatment of viral infections by modulation of host cell metabolic pathways |
| EP2167074A2 (en) | 2007-06-13 | 2010-03-31 | NorthEastern University | Antibiotic compounds |
| JP2010531360A (ja) | 2007-06-28 | 2010-09-24 | インターベット インターナショナル ベー. フェー. | Cb1拮抗剤としてのピペラジンの使用 |
| KR20100045983A (ko) | 2007-06-29 | 2010-05-04 | 에모리 유니버시티 | 신경보호를 위한 nmda 수용체 길항물질 |
| US7998982B2 (en) * | 2007-08-09 | 2011-08-16 | Abbott Laboratories | Amide derivatives as TRPV1 antagonists |
| US7994174B2 (en) * | 2007-09-19 | 2011-08-09 | Vertex Pharmaceuticals Incorporated | Pyridyl sulfonamides as modulators of ion channels |
| US8138168B1 (en) | 2007-09-26 | 2012-03-20 | Takeda Pharmaceutical Company Limited | Renin inhibitors |
| ES2428326T3 (es) | 2007-10-04 | 2013-11-07 | Merck Sharp & Dohme Corp. | Derivados de aril sulfona sustituida como bloqueadores de canales de calcio |
| WO2009076512A1 (en) | 2007-12-11 | 2009-06-18 | Epix Delaware, Inc. | Carboxamidξ compounds and their use as chemokine receptor agonists |
| JP2009249346A (ja) | 2008-04-08 | 2009-10-29 | Fujifilm Corp | ピリジン骨格を有する血液脳関門透過性化合物 |
| CN102105465B (zh) | 2008-07-21 | 2015-03-11 | 普渡制药公司 | 取代的喹喔啉型桥连哌啶化合物及其用途 |
-
2008
- 2008-04-25 DK DK08737573.9T patent/DK2142529T3/da active
- 2008-04-25 BR BRPI0809795-0A2A patent/BRPI0809795A2/pt not_active Application Discontinuation
- 2008-04-25 AR ARP080101756A patent/AR066146A1/es not_active Application Discontinuation
- 2008-04-25 US US12/110,089 patent/US20090170867A1/en not_active Abandoned
- 2008-04-25 EP EP12198526.1A patent/EP2604598B1/en active Active
- 2008-04-25 JP JP2010504895A patent/JP5462784B2/ja active Active
- 2008-04-25 NZ NZ580266A patent/NZ580266A/en unknown
- 2008-04-25 US US12/110,212 patent/US20090176796A1/en not_active Abandoned
- 2008-04-25 CN CN200880013834.9A patent/CN101932570B/zh active Active
- 2008-04-25 WO PCT/IB2008/001069 patent/WO2008132600A2/en not_active Ceased
- 2008-04-25 MX MX2009011600A patent/MX2009011600A/es active IP Right Grant
- 2008-04-25 ES ES12198526T patent/ES2571533T3/es active Active
- 2008-04-25 ES ES08737573.9T patent/ES2453947T3/es active Active
- 2008-04-25 PE PE2012002000A patent/PE20130325A1/es active IP Right Grant
- 2008-04-25 PE PE2008000707A patent/PE20090422A1/es active IP Right Grant
- 2008-04-25 CA CA2685266A patent/CA2685266C/en active Active
- 2008-04-25 KR KR1020097024875A patent/KR20100005725A/ko not_active Ceased
- 2008-04-25 CA CA2756791A patent/CA2756791C/en active Active
- 2008-04-25 CA CA2833209A patent/CA2833209C/en active Active
- 2008-04-25 ME MEP-2014-674A patent/ME02123B/me unknown
- 2008-04-25 AU AU2008243874A patent/AU2008243874B2/en active Active
- 2008-04-25 TW TW097115334A patent/TWI362930B/zh not_active IP Right Cessation
- 2008-04-25 RS RS20140128A patent/RS53212B/sr unknown
- 2008-04-25 PT PT87375739T patent/PT2142529E/pt unknown
- 2008-04-25 US US12/110,155 patent/US8476277B2/en active Active
- 2008-04-25 EP EP13155157.4A patent/EP2604599A1/en not_active Withdrawn
- 2008-04-25 UY UY31050A patent/UY31050A1/es not_active Application Discontinuation
- 2008-04-25 HR HRP20140279AT patent/HRP20140279T1/hr unknown
- 2008-04-25 PL PL08737573T patent/PL2142529T3/pl unknown
- 2008-04-25 EP EP08737573.9A patent/EP2142529B1/en active Active
- 2008-04-25 KR KR1020127031094A patent/KR20130004524A/ko not_active Ceased
- 2008-04-25 MY MYPI20094480A patent/MY148657A/en unknown
-
2009
- 2009-10-22 IL IL201688A patent/IL201688A/en active IP Right Grant
- 2009-11-17 CO CO09130337A patent/CO6241153A2/es active IP Right Grant
-
2012
- 2012-02-14 US US13/396,450 patent/US8575199B2/en active Active
-
2013
- 2013-03-28 US US13/852,913 patent/US8889690B2/en active Active
- 2013-04-02 IL IL225521A patent/IL225521A0/en unknown
- 2013-04-26 PH PH12013500848A patent/PH12013500848A1/en unknown
- 2013-07-29 JP JP2013156236A patent/JP2014015465A/ja active Pending
-
2014
- 2014-03-24 CY CY20141100230T patent/CY1115262T1/el unknown
- 2014-09-26 US US14/498,724 patent/US9365563B2/en active Active
-
2016
- 2016-06-10 US US15/179,612 patent/US9878991B2/en active Active
-
2018
- 2018-01-08 US US15/864,750 patent/US10584110B2/en active Active
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ME02123B (me) | Antagonisti trpv1 i njihova upotreba | |
| JP2014015465A5 (me) | ||
| RU2019114954A (ru) | Способы применения индазол-3-карбоксамидов и их применение в качестве ингибиторов сигнального пути wnt/в-катенина | |
| SI3057943T1 (en) | Pyrimidine FGFR4 Inhibitors | |
| RU2014149076A (ru) | Применение простых эфиров циклогексанола, обладающих антимикробными свойствами | |
| AR045389A1 (es) | Inhibidores del c-kit con estructura de pirazolil-amidil-benzoimidazolilo n-sustituido | |
| MY158316A (en) | Cyclic carbodiimide compound | |
| JP2012523457A5 (me) | ||
| CA2690953A1 (en) | Benzimidazole derivatives | |
| HRP20110621T1 (hr) | SPOJEVI PIRIDO[2,3-d]PIRIMIDINONA I NJIHOVA UPOTREBA KAO INHIBITORI PI3 | |
| SG166791A1 (en) | Novel macrocyclic inhibitors of hepatitis c virus replication | |
| EA201070215A1 (ru) | Композиции, содержащие полифенол | |
| JP2015500843A5 (me) | ||
| EA201001682A1 (ru) | Производные фенил- и бензодиоксинилзамещенных индазолов | |
| RU2014114466A (ru) | ИНДАЗОЛ-3-КАРБОКСАМИДЫ И ИХ ПРИМЕНЕНИЕ В КАЧЕСТВЕ ИНГИБИТОРОВ СИГНАЛЬНОГО ПУТИ WNT/β-КАТЕНИНА | |
| NZ585370A (en) | Viral polymerase inhibitors | |
| TW200510353A (en) | Alpha substituted carboxylic acids as PPAR modulators | |
| JPWO2021069705A5 (me) | ||
| WO2009134616A3 (en) | Novel inhibitors of hepatitis c virus replication | |
| RU2013138372A (ru) | Производные азетидина, применяемые для лечения метаболических и воспалительных заболеваний | |
| JP2013542980A5 (me) | ||
| JP2018522112A5 (me) | ||
| AR079108A1 (es) | Metodos para el tratamiento del virus de la hepatitis c con compuestos de oxoacetamida | |
| DE602004017894D1 (de) | Biphenylderivate, die sich als rar-rezeptor-aktivierende liganden eignen, verfahren zu deren herstellung und deren verwendung in der humanmedizin und in kosmetika | |
| ATE478054T1 (de) | Benzimidazolderivate |