PT2612862T - Quinazolinonas como inibidores de fosfatidilinositol 3-quinase delta humana - Google Patents

Quinazolinonas como inibidores de fosfatidilinositol 3-quinase delta humana Download PDF

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Publication number
PT2612862T
PT2612862T PT131501108T PT13150110T PT2612862T PT 2612862 T PT2612862 T PT 2612862T PT 131501108 T PT131501108 T PT 131501108T PT 13150110 T PT13150110 T PT 13150110T PT 2612862 T PT2612862 T PT 2612862T
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PT
Portugal
Prior art keywords
compound
shown below
acid
compounds
pi3k5
Prior art date
Application number
PT131501108T
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English (en)
Portuguese (pt)
Inventor
Treiberg Jennifer
A Kesicki Edward
W Fowler Kerry
Huang Danwen
Chee Ooi Hua
Ruan Fuqiang
Deep Puri Kamal
R Oliver Amy
Original Assignee
Icos Corp
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=34969603&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PT2612862(T) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Icos Corp filed Critical Icos Corp
Publication of PT2612862T publication Critical patent/PT2612862T/pt

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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
    • 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
    • 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
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    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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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
    • 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
    • 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
    • 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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  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
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  • Diabetes (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Rheumatology (AREA)
  • Endocrinology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Urology & Nephrology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Dermatology (AREA)
  • Pain & Pain Management (AREA)
  • Ophthalmology & Optometry (AREA)
  • Biomedical Technology (AREA)
  • Communicable Diseases (AREA)
  • Epidemiology (AREA)
  • Cardiology (AREA)
  • Emergency Medicine (AREA)
  • Biochemistry (AREA)
  • Vascular Medicine (AREA)
  • Obesity (AREA)
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PT131501108T 2004-05-13 2005-05-12 Quinazolinonas como inibidores de fosfatidilinositol 3-quinase delta humana PT2612862T (pt)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US57078404P 2004-05-13 2004-05-13

Publications (1)

Publication Number Publication Date
PT2612862T true PT2612862T (pt) 2016-12-15

Family

ID=34969603

Family Applications (3)

Application Number Title Priority Date Filing Date
PT131501108T PT2612862T (pt) 2004-05-13 2005-05-12 Quinazolinonas como inibidores de fosfatidilinositol 3-quinase delta humana
PT57521221T PT1761540T (pt) 2004-05-13 2005-05-12 Quinazolinonas como inibidores de fosfatidilinositol-3-cinase delta humana
PT161852132T PT3153514T (pt) 2004-05-13 2005-05-12 Quinazolinonas como inibidoras da fosfatidilinositol 3-quinase delta humana

Family Applications After (2)

Application Number Title Priority Date Filing Date
PT57521221T PT1761540T (pt) 2004-05-13 2005-05-12 Quinazolinonas como inibidores de fosfatidilinositol-3-cinase delta humana
PT161852132T PT3153514T (pt) 2004-05-13 2005-05-12 Quinazolinonas como inibidoras da fosfatidilinositol 3-quinase delta humana

Country Status (23)

Country Link
US (14) US7932260B2 (cg-RX-API-DMAC10.html)
EP (4) EP2612862B1 (cg-RX-API-DMAC10.html)
JP (1) JP2007537291A (cg-RX-API-DMAC10.html)
CN (2) CN102229609A (cg-RX-API-DMAC10.html)
AU (2) AU2005245875C1 (cg-RX-API-DMAC10.html)
BE (1) BE2017C002I2 (cg-RX-API-DMAC10.html)
CA (1) CA2566609C (cg-RX-API-DMAC10.html)
CY (3) CY2016046I2 (cg-RX-API-DMAC10.html)
DK (2) DK2612862T3 (cg-RX-API-DMAC10.html)
ES (3) ES2873875T3 (cg-RX-API-DMAC10.html)
FR (1) FR17C1007I2 (cg-RX-API-DMAC10.html)
HR (2) HRP20161751T1 (cg-RX-API-DMAC10.html)
HU (3) HUE030839T2 (cg-RX-API-DMAC10.html)
IL (4) IL179176A (cg-RX-API-DMAC10.html)
LT (3) LT2612862T (cg-RX-API-DMAC10.html)
LU (1) LUC00005I2 (cg-RX-API-DMAC10.html)
ME (2) ME02695B (cg-RX-API-DMAC10.html)
NL (1) NL300867I2 (cg-RX-API-DMAC10.html)
PL (3) PL2612862T3 (cg-RX-API-DMAC10.html)
PT (3) PT2612862T (cg-RX-API-DMAC10.html)
RS (2) RS55551B1 (cg-RX-API-DMAC10.html)
SI (2) SI2612862T1 (cg-RX-API-DMAC10.html)
WO (2) WO2005113556A1 (cg-RX-API-DMAC10.html)

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US20050043239A1 (en) * 2003-08-14 2005-02-24 Jason Douangpanya Methods of inhibiting immune responses stimulated by an endogenous factor
LT2612862T (lt) 2004-05-13 2017-01-25 Icos Corporation Chinazolinonai kaip žmogaus fosfatidilinozitol-3-kinazės delta inhibitoriai
EP1750714A1 (en) * 2004-05-13 2007-02-14 Vanderbilt University Phosphoinositide 3-kinase delta selective inhibitors for inhibiting angiogenesis
US9512125B2 (en) 2004-11-19 2016-12-06 The Regents Of The University Of California Substituted pyrazolo[3.4-D] pyrimidines as anti-inflammatory agents
US20080287469A1 (en) * 2005-02-17 2008-11-20 Diacovo Thomas G 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
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WO2009002553A1 (en) * 2007-06-25 2008-12-31 Prolexys Pharmaceuticals, Inc. Methods of treating multiple myeloma and resistant cancers
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SG185996A1 (en) * 2007-11-13 2012-12-28 Icos Corp Inhibitors of human phosphatidyl-inositol 3-kinase delta
AU2014203687B2 (en) * 2008-01-04 2016-04-14 Intellikine Llc Certain chemical entities, compositions and methods
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BRPI0906473A8 (pt) * 2008-01-04 2016-02-10 Intellikine Inc Certas entidades químicas, composições e métodos
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WO2009114870A2 (en) * 2008-03-14 2009-09-17 Intellikine, Inc. Kinase inhibitors and methods of use
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US20110105457A1 (en) * 2008-04-18 2011-05-05 Shionogi & Co., Ltd. Heterocyclic compound having inhibitory activity on pi3k
CA2722326A1 (en) 2008-04-24 2009-10-29 Incyte Corporation Macrocyclic compounds and their use as kinase inhibitors
US20110224223A1 (en) * 2008-07-08 2011-09-15 The Regents Of The University Of California, A California Corporation MTOR Modulators and Uses Thereof
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