HRP20070542T3 - Sulfonamide derivatives for the treatment of diseases - Google Patents
Sulfonamide derivatives for the treatment of diseasesInfo
- Publication number
- HRP20070542T3 HRP20070542T3 HR20070542T HRP20070542T HRP20070542T3 HR P20070542 T3 HRP20070542 T3 HR P20070542T3 HR 20070542 T HR20070542 T HR 20070542T HR P20070542 T HRP20070542 T HR P20070542T HR P20070542 T3 HRP20070542 T3 HR P20070542T3
- Authority
- HR
- Croatia
- Prior art keywords
- group
- alkyl
- optionally substituted
- halogen
- diseases
- Prior art date
Links
- 201000010099 disease Diseases 0.000 title 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title 1
- 229940124530 sulfonamide Drugs 0.000 title 1
- 150000003456 sulfonamides Chemical class 0.000 title 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 5
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- VMWNQDUVQKEIOC-CYBMUJFWSA-N apomorphine Chemical compound C([C@H]1N(C)CC2)C3=CC=C(O)C(O)=C3C3=C1C2=CC=C3 VMWNQDUVQKEIOC-CYBMUJFWSA-N 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 230000000155 isotopic effect Effects 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/02—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
- C07D217/06—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines with the ring nitrogen atom acylated by carboxylic or carbonic acids, or with sulfur or nitrogen analogues thereof, e.g. carbamates
-
- 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
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/18—Sulfonamides
-
- 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
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/352—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline
-
- 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
- A61K31/495—Heterocyclic 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
- A61K31/52—Purines, e.g. adenine
- A61K31/522—Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C311/08—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyrrole Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Spoj opće formule (1): gdje (CH2)n-C(=O)Q1 skupina zauzima meta ili para položaj, a R1 i R2 se neovisno jedan o drugome odabiru između H i C1-C4 alkila, n jest 0, 1 ili 2 i Q1 se odabire između: i skupine *-NR8-Q2-A, gdje p jest 1 ili 2, Q2 jest C1-C4 alkilen opcijski supstituiran s OH, R8 jest H ili C1-C4 alkil i A jest piridil opcijski supstituiran s OH, C3-C7 cikloalkil opcijski supstituiran sOH ili pak skupinagdje R3, R4, R5, R6 i R7 jesu istovjetni ili su pak različiti, te se odabiru iz grupe koju tvore H, C1-C4 alkil, OR9, SR9, halogen,CN, CF3, OCF3, COOR9, SO2NR9R10, CONR9R10, NR9R10, NHCOR10 i fenil opcijski supstituiran s 1 do 3 skupine odabrane između OR9, halogena i C1-C4 alkila; gdje R9 i R10 jesu istovjetni ili su pak različiti, te se odabiru između H ili C1-C4 alkila i * predstavlja mjesto vezanja na karbonilnu skupinu; gdje je Q1 skupina supstituirana s barem jednom OH skupinom; ili, gdje je to potrebno, njegove farmaceutski prihvatljive soli i/ili izomeri, tautomeri,solvati ili izotopne varijante. Patent sadrži još32 patentna zahtjeva.Compound of general formula (1): where (CH2)n-C(=O)Q1 group occupies the meta or para position, and R1 and R2 are independently selected from H and C1-C4 alkyl, n is 0, 1 or 2 and Q1 is selected from: and the group *-NR8-Q2-A, where p is 1 or 2, Q2 is C1-C4 alkylene optionally substituted with OH, R8 is H or C1-C4 alkyl and A is pyridyl optionally substituted with OH, C3-C7 cycloalkyl optionally substituted with OH or a group where R3, R4, R5, R6 and R7 are the same or different, and are selected from the group formed by H, C1-C4 alkyl, OR9, SR9, halogen, CN, CF3, OCF3, COOR9, SO2NR9R10, CONR9R10, NR9R10, NHCOR10 and phenyl optionally substituted with 1 to 3 groups selected from OR9, halogen and C1-C4 alkyl; where R9 and R10 are the same or different, and are chosen from H or C1-C4 alkyl and * represents the point of attachment to the carbonyl group; where the Q1 group is substituted with at least one OH group; or, where appropriate, its pharmaceutically acceptable salts and/or isomers, tautomers, solvates or isotopic variants. The patent contains another 32 patent claims.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP04290169 | 2004-01-22 | ||
GB0406387A GB0406387D0 (en) | 2004-03-22 | 2004-03-22 | Sulfonamide derivatives for the treatment of diseases |
US60026004P | 2004-08-09 | 2004-08-09 | |
PCT/IB2005/000086 WO2005080313A2 (en) | 2004-01-22 | 2005-01-12 | Sulfonamide derivatives for the treatment of diseases |
Publications (1)
Publication Number | Publication Date |
---|---|
HRP20070542T3 true HRP20070542T3 (en) | 2008-02-29 |
Family
ID=34890770
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HR20070542T HRP20070542T3 (en) | 2004-01-22 | 2007-11-28 | Sulfonamide derivatives for the treatment of diseases |
Country Status (7)
Country | Link |
---|---|
CR (1) | CR9838A (en) |
CY (1) | CY1107107T1 (en) |
EC (1) | ECSP066700A (en) |
HK (1) | HK1096379A1 (en) |
HR (1) | HRP20070542T3 (en) |
IL (1) | IL176564A (en) |
MA (1) | MA28302A1 (en) |
-
2006
- 2006-06-26 IL IL176564A patent/IL176564A/en not_active IP Right Cessation
- 2006-07-13 EC EC2006006700A patent/ECSP066700A/en unknown
- 2006-07-21 MA MA29201A patent/MA28302A1/en unknown
-
2007
- 2007-03-30 HK HK07103436.9A patent/HK1096379A1/en not_active IP Right Cessation
- 2007-11-28 HR HR20070542T patent/HRP20070542T3/en unknown
- 2007-12-20 CY CY20071101628T patent/CY1107107T1/en unknown
-
2008
- 2008-03-27 CR CR9838A patent/CR9838A/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
HK1096379A1 (en) | 2007-06-01 |
CY1107107T1 (en) | 2012-10-24 |
IL176564A (en) | 2011-11-30 |
CR9838A (en) | 2008-04-21 |
MA28302A1 (en) | 2006-11-01 |
IL176564A0 (en) | 2006-10-31 |
ECSP066700A (en) | 2006-10-31 |
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