HRP20070577T4 - Derivati kinazolinona koji se mogu upotrijebiti kao antagonisti vaniloida - Google Patents
Derivati kinazolinona koji se mogu upotrijebiti kao antagonisti vaniloida Download PDFInfo
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- HRP20070577T4 HRP20070577T4 HR20070577T HRP20070577T HRP20070577T4 HR P20070577 T4 HRP20070577 T4 HR P20070577T4 HR 20070577 T HR20070577 T HR 20070577T HR P20070577 T HRP20070577 T HR P20070577T HR P20070577 T4 HRP20070577 T4 HR P20070577T4
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- quinazolinone
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- AVRPFRMDMNDIDH-UHFFFAOYSA-N 1h-quinazolin-2-one Chemical class C1=CC=CC2=NC(O)=NC=C21 AVRPFRMDMNDIDH-UHFFFAOYSA-N 0.000 title 1
- 239000005557 antagonist Substances 0.000 title 1
- -1 quinazolinone compound Chemical class 0.000 claims abstract 4
- 150000003839 salts Chemical group 0.000 claims abstract 3
- 150000001875 compounds Chemical class 0.000 claims 4
- 102000011040 TRPV Cation Channels Human genes 0.000 claims 2
- 108010062740 TRPV Cation Channels Proteins 0.000 claims 2
- 230000004913 activation Effects 0.000 claims 2
- 230000006806 disease prevention Effects 0.000 claims 2
- 239000008177 pharmaceutical agent Substances 0.000 claims 2
- OJVMSICJWQFIOS-UHFFFAOYSA-N 3-(4-chlorophenyl)-7-hydroxy-2-propan-2-ylquinazolin-4-one Chemical compound CC(C)C1=NC2=CC(O)=CC=C2C(=O)N1C1=CC=C(Cl)C=C1 OJVMSICJWQFIOS-UHFFFAOYSA-N 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 229940079593 drug Drugs 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 239000008024 pharmaceutical diluent Substances 0.000 claims 1
- 239000002253 acid Substances 0.000 abstract 1
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- 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
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- 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
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- 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
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
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- C07D—HETEROCYCLIC COMPOUNDS
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- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
- C07D239/88—Oxygen atoms
- C07D239/91—Oxygen atoms with aryl or aralkyl radicals attached in position 2 or 3
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Abstract
Kinazolinonski spoj u slobodnom obliku ili u obliku soli, naznačen time, da je odabran od: 3-(4-klorofenil)-7-hidroksi-2-izopropil-3H-kinazolin-4-onPatent sadrži još 6 patentnih zahtjeva.
Claims (7)
1. Kinazolinonski spoj u slobodnom obliku ili u obliku soli, naznačen time, da je odabran od:
3-(4-klorofenil)-7-hidroksi-2-izopropil-3H-kinazolin-4-on
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2. Spoj prema zahtjevu 1, naznačen time, da ima sljedeću formulu
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3. Spoj prema zahtjevu 1, naznačen time, da ima sljedeću formulu
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4. Spoj prema zahtjevu 1, naznačen time, da ima sljedeću formulu
[image]
5. Uporaba kinazolinonskog spoja koji je određen u bilo kojem zahtjevu 1 do 4, naznačena time, da je za proizvodnju lijeka za liječenje ili prevenciju bolesti ili stanja, u kojima igra ulogu aktiviranje vaniloid receptora ili ima utjecaja na njih.
6. Kinazolinonski spoj koji je određen u bilo kojem zahtjevu 1 do 4, naznačen time, da se koristi kao farmaceutsko srestvo za liječenje ili prevenciju bolesti ili stanja, u kojima igra ulogu aktiviranje vaniloid receptora ili ima utjecaja na njih.
7. Farmaceutski sastav, naznačen time, da sadrži spoj prema bilo kojem zahtjevu 1 do 4 u spoju s farmaceutskim nosačem ili razrjeđivačima te opcijski u kombinaciji s drugim farmaceutskim sredstvom.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0412769.2A GB0412769D0 (en) | 2004-06-08 | 2004-06-08 | Organic compounds |
PCT/EP2005/006253 WO2005120510A1 (en) | 2004-06-08 | 2005-06-08 | Quinazolinone derivatives useful as vanilloid antagonists |
Publications (2)
Publication Number | Publication Date |
---|---|
HRP20070577T3 HRP20070577T3 (hr) | 2008-08-31 |
HRP20070577T4 true HRP20070577T4 (hr) | 2011-10-31 |
Family
ID=32696854
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HR20070577T HRP20070577T4 (hr) | 2004-06-08 | 2007-12-20 | Derivati kinazolinona koji se mogu upotrijebiti kao antagonisti vaniloida |
Country Status (30)
Country | Link |
---|---|
US (4) | US7960399B2 (hr) |
EP (1) | EP1755606B2 (hr) |
JP (2) | JP4703650B2 (hr) |
KR (2) | KR101018607B1 (hr) |
CN (1) | CN1956721B (hr) |
AT (1) | ATE376833T1 (hr) |
AU (2) | AU2005251476C1 (hr) |
BR (1) | BRPI0511933B8 (hr) |
CA (1) | CA2567821C (hr) |
CY (1) | CY1107846T1 (hr) |
DE (1) | DE602005003128T3 (hr) |
DK (1) | DK1755606T4 (hr) |
EC (2) | ECSP067067A (hr) |
ES (1) | ES2293584T5 (hr) |
GB (1) | GB0412769D0 (hr) |
HK (1) | HK1105577A1 (hr) |
HR (1) | HRP20070577T4 (hr) |
IL (1) | IL179532A (hr) |
MA (1) | MA28685B1 (hr) |
MX (1) | MXPA06014249A (hr) |
NO (1) | NO338181B1 (hr) |
NZ (1) | NZ551630A (hr) |
PL (1) | PL1755606T5 (hr) |
PT (1) | PT1755606E (hr) |
RU (2) | RU2449995C2 (hr) |
SG (1) | SG153811A1 (hr) |
SI (1) | SI1755606T2 (hr) |
TN (1) | TNSN06405A1 (hr) |
WO (1) | WO2005120510A1 (hr) |
ZA (1) | ZA200609634B (hr) |
Families Citing this family (25)
Publication number | Priority date | Publication date | Assignee | Title |
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GB0412769D0 (en) | 2004-06-08 | 2004-07-07 | Novartis Ag | Organic compounds |
GB0525068D0 (en) | 2005-12-08 | 2006-01-18 | Novartis Ag | Organic compounds |
CN101506210A (zh) | 2006-08-23 | 2009-08-12 | 神经能质公司 | 2-苯氧基嘧啶酮类似物 |
WO2008066664A2 (en) * | 2006-11-06 | 2008-06-05 | Neurogen Corporation | Cis-cyclohexyl substituted pyrimidinone derivatives |
EP2178562B1 (en) | 2007-07-18 | 2017-08-23 | Novartis AG | Synergistic combinations of vr-1 antagonists and cox-2 inhibitors |
US8915362B2 (en) | 2008-10-08 | 2014-12-23 | Ultimed, Inc. | Sharps container |
US8349852B2 (en) | 2009-01-13 | 2013-01-08 | Novartis Ag | Quinazolinone derivatives useful as vanilloid antagonists |
AR080055A1 (es) | 2010-02-01 | 2012-03-07 | Novartis Ag | Derivados de pirazolo-[5,1-b]-oxazol como antagonistas de los receptores de crf -1 |
AR080056A1 (es) | 2010-02-01 | 2012-03-07 | Novartis Ag | Derivados de ciclohexil-amida como antagonistas de los receptores de crf |
EP2531490B1 (en) | 2010-02-02 | 2014-10-15 | Novartis AG | Cyclohexyl amide derivatives as crf receptor antagonists |
US8546416B2 (en) | 2011-05-27 | 2013-10-01 | Novartis Ag | 3-spirocyclic piperidine derivatives as ghrelin receptor agonists |
EP2852591A1 (en) | 2012-05-03 | 2015-04-01 | Novartis AG | L-malate salt of 2, 7 - diaza - spiro [4.5]dec- 7 - yle derivatives and crystalline forms thereof as ghrelin receptor agonists |
JP2016510749A (ja) | 2013-03-05 | 2016-04-11 | ユニヴァーシティー オブ ノートル ダム デュ ラック | キナゾリノン抗生物質 |
US10016425B2 (en) | 2016-11-03 | 2018-07-10 | King Saud University | Anti-ulcerative colitis compound |
EP3873903B1 (en) | 2018-10-31 | 2024-01-24 | Gilead Sciences, Inc. | Substituted 6-azabenzimidazole compounds as hpk1 inhibitors |
US11071730B2 (en) | 2018-10-31 | 2021-07-27 | Gilead Sciences, Inc. | Substituted 6-azabenzimidazole compounds |
CA3130038A1 (en) * | 2019-02-15 | 2020-08-20 | Novartis Ag | Methods for treating ocular surface pain |
EP4431497A1 (en) | 2019-02-15 | 2024-09-18 | Bausch + Lomb Ireland Limited | Crystalline forms of 4-(7-hydroxy-2-isopropyl-4-oxo-4h-quinazolin-3-yl)-benzonitrile and formulations thereof |
JP6994061B2 (ja) | 2019-02-15 | 2022-01-14 | ノバルティス アーゲー | 4-(7-ヒドロキシ-2-イソプロピル-4-オキソ-4h-キナゾリン-3-イル)-ベンゾニトリルの製剤 |
WO2020237025A1 (en) | 2019-05-23 | 2020-11-26 | Gilead Sciences, Inc. | Substituted exo-methylene-oxindoles which are hpk1/map4k1 inhibitors |
RU2755206C1 (ru) | 2020-05-20 | 2021-09-14 | Федеральное государственное бюджетное учреждение науки Тихоокеанский институт биоорганической химии им. Г.Б. Елякова Дальневосточного отделения Российской академии наук (ТИБОХ ДВО РАН) | Средство пролонгированного анальгетического действия и лекарственный препарат на его основе |
CN116419918A (zh) | 2020-08-06 | 2023-07-11 | 诺华股份有限公司 | 4-(7-羟基-2-异丙基-4-氧代-4h-喹唑啉-3-基)-苄腈的结晶形式及其配制品 |
WO2022105792A1 (zh) * | 2020-11-17 | 2022-05-27 | 苏州晶云药物科技股份有限公司 | 一种喹唑啉酮衍生物的新晶型及其制备方法 |
UY39681A (es) | 2021-03-26 | 2022-10-31 | Novartis Ag | Derivados de ciclobutilo 1,3–sustituidos y sus usos |
WO2024062389A1 (en) | 2022-09-21 | 2024-03-28 | Bausch + Lomb Ireland Limited | Crystalline polymorph forms of a trpv1 antagonist and formulations thereof |
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