ME02695B - Hinazolinoni kao inhibitori humane fosfatidilonozitol 3- delta kinaze - Google Patents
Hinazolinoni kao inhibitori humane fosfatidilonozitol 3- delta kinazeInfo
- Publication number
- ME02695B ME02695B MEP-2016-284A MEP28416A ME02695B ME 02695 B ME02695 B ME 02695B ME P28416 A MEP28416 A ME P28416A ME 02695 B ME02695 B ME 02695B
- Authority
- ME
- Montenegro
- Prior art keywords
- pharmaceutically acceptable
- acceptable salt
- salt
- quinazolinones
- inhibitors
- Prior art date
Links
- AVRPFRMDMNDIDH-UHFFFAOYSA-N 1h-quinazolin-2-one Chemical class C1=CC=CC2=NC(O)=NC=C21 AVRPFRMDMNDIDH-UHFFFAOYSA-N 0.000 title 1
- 108091007960 PI3Ks Proteins 0.000 title 1
- 102000003993 Phosphatidylinositol 3-kinases Human genes 0.000 title 1
- 108090000430 Phosphatidylinositol 3-kinases Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 150000003839 salts Chemical class 0.000 claims 13
- QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical group N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 claims 6
- 150000001875 compounds Chemical class 0.000 claims 5
- 239000008194 pharmaceutical composition Substances 0.000 claims 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 125000002467 phosphate group Chemical class [H]OP(=O)(O[H])O[*] 0.000 claims 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
- C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/28—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- 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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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/16—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two nitrogen atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Diabetes (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Communicable Diseases (AREA)
- Neurosurgery (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Dermatology (AREA)
- Urology & Nephrology (AREA)
- Pain & Pain Management (AREA)
- Ophthalmology & Optometry (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Epidemiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Biochemistry (AREA)
- Emergency Medicine (AREA)
- Obesity (AREA)
- Gastroenterology & Hepatology (AREA)
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Claims (12)
1. Farmaceutski prihvatljiva so jedinjenja: pri čemu je farmaceutski prihvatljiva so izabrana iz grupe koja se sastoji od hidrohloridne, hidrobromidne, hidrojodidne i fosfatne soli.
2. Farmaceutski prihvatljiva so prema patentnom zahtevu 1 pri čemu je farmaceutski prihvatljiva so, hidrohloridna so.
3. Farmaceutski prihvatljiva so prema patentnom zahtevu 1 pri čemu jedinjenje jeste S-enantiomer.
4. Farmaceutski prihvatljiva so prema patentnom zahtevu 1 pri čemu je jedinjenje a farmaceutski prihvatljiva so je hidrohloridna so.
5. Farmaceutska kompozicija koja obuhvata farmaceutski prihvatljivu so iz patentnog zahteva 1 i najmanje jedan farmaceutski prihvatljiv ekscipijent.
6. Farmaceutska kompozicija prema patentnom zahtevu 5, pri čemu je farmaceutski prihvatljiva so, hidrohloridna so.
7. Farmaceutska kompozicija iz patentnog zahteva 5, pri čemu je jedinjenje S-enantiomer.
8. Farmaceutska kompozicija prema patentnom zahtevu 7, pri čemu je farmaceutski prihvatljiva so, hidrohloridna so.
9. Komplet koji sadrži farmaceutski prihvatljivu so prema patentnom zahtevu 1.
10. Komplet prema patentnom zahtevu 9, pri čemu je farmaceutski prihvatljiva so, hidrohloridna so.
11. Komplet prema patentnom zahtevu 9 pri čemu je jedinjenje S-enantiomer.
12. Komplet prema patentnom zahtevu 11, pri čemu je farmaceutski prihvatljiva so , hidrohloridna so. 3
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US57078404P | 2004-05-13 | 2004-05-13 | |
| EP13150110.8A EP2612862B1 (en) | 2004-05-13 | 2005-05-12 | Quinazolinones as inhibitors of human phosphatidylinositol 3-kinase delta |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ME02695B true ME02695B (me) | 2017-10-20 |
Family
ID=34969603
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MEP-2016-297A ME02688B (me) | 2004-05-13 | 2005-05-12 | Hinazolinoni kao inhibitori humane fosfatidilinozitol 3 - kinaze delta |
| MEP-2016-284A ME02695B (me) | 2004-05-13 | 2005-05-12 | Hinazolinoni kao inhibitori humane fosfatidilonozitol 3- delta kinaze |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MEP-2016-297A ME02688B (me) | 2004-05-13 | 2005-05-12 | Hinazolinoni kao inhibitori humane fosfatidilinozitol 3 - kinaze delta |
Country Status (23)
| Country | Link |
|---|---|
| US (14) | USRE44638E1 (me) |
| EP (4) | EP1761540B1 (me) |
| JP (1) | JP2007537291A (me) |
| CN (2) | CN102229609A (me) |
| AU (2) | AU2005245875C1 (me) |
| BE (1) | BE2017C002I2 (me) |
| CA (1) | CA2566609C (me) |
| CY (3) | CY2016046I2 (me) |
| DK (2) | DK2612862T3 (me) |
| ES (3) | ES2873875T3 (me) |
| FR (1) | FR17C1007I2 (me) |
| HR (2) | HRP20161751T1 (me) |
| HU (3) | HUE030950T2 (me) |
| IL (4) | IL179176A (me) |
| LT (3) | LT1761540T (me) |
| LU (1) | LUC00005I2 (me) |
| ME (2) | ME02688B (me) |
| NL (1) | NL300867I2 (me) |
| PL (3) | PL2612862T3 (me) |
| PT (3) | PT3153514T (me) |
| RS (2) | RS55546B1 (me) |
| SI (2) | SI2612862T1 (me) |
| WO (2) | WO2005113556A1 (me) |
Families Citing this family (429)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6667300B2 (en) | 2000-04-25 | 2003-12-23 | Icos Corporation | Inhibitors of human phosphatidylinositol 3-kinase delta |
| US20050043239A1 (en) * | 2003-08-14 | 2005-02-24 | Jason Douangpanya | Methods of inhibiting immune responses stimulated by an endogenous factor |
| WO2005112935A1 (en) * | 2004-05-13 | 2005-12-01 | Vanderbilt University | Phosphoinositide 3-kinase delta selective inhibitors for inhibiting angiogenesis |
| EP1761540B1 (en) | 2004-05-13 | 2016-09-28 | Icos Corporation | Quinazolinones as inhibitors of human phosphatidylinositol 3-kinase delta |
| EP1831225A2 (en) | 2004-11-19 | 2007-09-12 | The Regents of the University of California | Anti-inflammatory pyrazolopyrimidines |
| WO2006089106A2 (en) * | 2005-02-17 | 2006-08-24 | Icos Corporation | Phosphoinositide 3-kinase inhibitors for inhibiting leukocyte accumulation |
| GB2431156A (en) * | 2005-10-11 | 2007-04-18 | Piramed Ltd | 1-cyclyl-3-substituted- -benzenes and -azines as inhibitors of phosphatidylinositol 3-kinase |
| EA200870409A1 (ru) | 2006-04-04 | 2009-04-28 | Дзе Риджентс Оф Дзе Юниверсити Оф Калифорния | Антагонисты киназы pi3 |
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