AP3337A - Aminoalcohol substituted 2,3-dihydroimidazo[1,2-C]quinazoline derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesis - Google Patents
Aminoalcohol substituted 2,3-dihydroimidazo[1,2-C]quinazoline derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesisInfo
- Publication number
- AP3337A AP3337A AP2013006921A AP2013006921A AP3337A AP 3337 A AP3337 A AP 3337A AP 2013006921 A AP2013006921 A AP 2013006921A AP 2013006921 A AP2013006921 A AP 2013006921A AP 3337 A AP3337 A AP 3337A
- Authority
- AP
- ARIPO
- Prior art keywords
- dihydroimidazo
- angiogenesis
- diseases associated
- proliferative disorders
- derivatives useful
- Prior art date
Links
Classifications
-
- 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
-
- 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
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5386—1,4-Oxazines, e.g. morpholine spiro-condensed or forming part of bridged ring systems
-
- 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
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/541—Non-condensed thiazines containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- 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
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/08—Bridged systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US41255610P | 2010-11-11 | 2010-11-11 | |
PCT/EP2011/069637 WO2012062748A1 (en) | 2010-11-11 | 2011-11-08 | Aminoalcohol substituted 2,3-dihydroimidazo[1,2-c]quinazoline derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesis |
Publications (2)
Publication Number | Publication Date |
---|---|
AP2013006921A0 AP2013006921A0 (en) | 2013-06-30 |
AP3337A true AP3337A (en) | 2015-07-31 |
Family
ID=44999756
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AP2013006921A AP3337A (en) | 2010-11-11 | 2011-11-08 | Aminoalcohol substituted 2,3-dihydroimidazo[1,2-C]quinazoline derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesis |
Country Status (31)
Country | Link |
---|---|
US (2) | US8895549B2 (ja) |
EP (1) | EP2638045B1 (ja) |
JP (1) | JP6196156B2 (ja) |
KR (1) | KR20140003436A (ja) |
CN (1) | CN102906094B (ja) |
AP (1) | AP3337A (ja) |
AR (1) | AR083842A1 (ja) |
AU (1) | AU2011328192B2 (ja) |
BR (1) | BR112013011634A2 (ja) |
CA (1) | CA2817317C (ja) |
CL (1) | CL2013001295A1 (ja) |
CO (1) | CO6761350A2 (ja) |
CR (1) | CR20130213A (ja) |
CU (1) | CU20130069A7 (ja) |
DO (1) | DOP2013000105A (ja) |
EA (1) | EA024406B1 (ja) |
EC (1) | ECSP13012618A (ja) |
GT (1) | GT201300121A (ja) |
HK (1) | HK1180685A1 (ja) |
IL (1) | IL226066A0 (ja) |
MA (1) | MA34655B1 (ja) |
MX (1) | MX2013005305A (ja) |
MY (1) | MY164730A (ja) |
NZ (1) | NZ610018A (ja) |
PE (1) | PE20140411A1 (ja) |
SG (1) | SG190100A1 (ja) |
TW (1) | TW201305170A (ja) |
UA (1) | UA113280C2 (ja) |
UY (1) | UY33719A (ja) |
WO (1) | WO2012062748A1 (ja) |
ZA (1) | ZA201304244B (ja) |
Families Citing this family (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2646012T3 (es) * | 2010-11-11 | 2017-12-11 | Bayer Intellectual Property Gmbh | 2,3-Dihidroimidazo[1,2-c]quinazolinas sustituidas con alcoxi |
UA113280C2 (xx) * | 2010-11-11 | 2017-01-10 | АМІНОСПИРТЗАМІЩЕНІ ПОХІДНІ 2,3-ДИГІДРОІМІДАЗО$1,2-c]ХІНАЗОЛІНУ, ПРИДАТНІ ДЛЯ ЛІКУВАННЯ ГІПЕРПРОЛІФЕРАТИВНИХ ПОРУШЕНЬ І ЗАХВОРЮВАНЬ, ПОВ'ЯЗАНИХ З АНГІОГЕНЕЗОМ | |
CN103370320B (zh) * | 2010-11-11 | 2016-04-27 | 拜耳知识产权有限责任公司 | 芳基氨基醇取代的2,3-二氢咪唑并[1,2-c]喹啉 |
JO3733B1 (ar) | 2011-04-05 | 2021-01-31 | Bayer Ip Gmbh | استخدام 3,2-دايهيدروايميدازو[1, 2 -c]كوينازولينات مستبدلة |
EP2508525A1 (en) | 2011-04-05 | 2012-10-10 | Bayer Pharma Aktiengesellschaft | Substituted 2,3-dihydroimidazo[1,2-c]quinazoline salts |
CN103214489B (zh) * | 2013-02-25 | 2016-10-26 | 中国人民解放军第二军医大学 | 一类具有抗肿瘤活性的多靶点激酶抑制剂及其制备方法 |
PE20151780A1 (es) * | 2013-04-08 | 2015-12-20 | Bayer Pharma AG | Uso de 2 - 3 dihidroimidazo[ 1,2- c] quinazolinas sustituidas |
CN105934256B (zh) | 2013-12-03 | 2019-12-27 | 拜耳制药股份公司 | Pi3k-抑制剂的组合产品 |
EP3077003A1 (en) | 2013-12-03 | 2016-10-12 | Bayer Pharma Aktiengesellschaft | Combination of pi3k-inhibitors |
WO2015082376A2 (en) | 2013-12-03 | 2015-06-11 | Bayer Pharma Aktiengesellschaft | Use of pi3k-inhibitors |
WO2016071382A1 (en) * | 2014-11-07 | 2016-05-12 | Bayer Pharma Aktiengesellschaft | Synthesis of pi3k inhibitor and salts thereof |
WO2016071380A1 (en) * | 2014-11-07 | 2016-05-12 | Bayer Pharma Aktiengesellschaft | Synthesis of pi3k inhibitor and salts thereof |
WO2016087490A1 (en) * | 2014-12-03 | 2016-06-09 | Bayer Pharma Aktiengesellschaft | Combination of pi3k-inhibitors |
WO2016087488A1 (en) * | 2014-12-03 | 2016-06-09 | Bayer Pharma Aktiengesellschaft | Administration regime for aminoalcohol substituted 2,3-dihydroimidazo[1,2-c]quinazoline derivatives |
AU2016349632A1 (en) | 2015-11-07 | 2018-05-24 | Multivir Inc. | Compositions comprising tumor suppressor gene therapy and immune checkpoint blockade for the treatment of cancer |
JP2019532922A (ja) | 2016-09-23 | 2019-11-14 | バイエル ファーマ アクチエンゲゼルシャフト | Pi3k−阻害剤の組み合わせ |
WO2018111902A1 (en) | 2016-12-12 | 2018-06-21 | Multivir Inc. | Methods and compositions comprising viral gene therapy and an immune checkpoint inhibitor for treatment and prevention of cancer and infectious diseases |
WO2018215282A1 (en) | 2017-05-26 | 2018-11-29 | Bayer Pharma Aktiengesellschaft | Combination of bub1 and pi3k inhibitors |
CA3068324A1 (en) | 2017-06-28 | 2019-01-03 | Bayer Consumer Care Ag | Combination of a pi3k-inhibitor with an androgen receptor antagonist |
KR20200135986A (ko) | 2018-03-19 | 2020-12-04 | 멀티비르 인코포레이티드 | 종양 억제인자 유전자 치료 및 cd122/cd132 작용제를 포함하는 암 치료를 위한 방법 및 조성물 |
CN108383849B (zh) * | 2018-04-26 | 2020-11-06 | 浙江大学 | 咪唑并喹唑啉衍生物及其在抗肿瘤抗炎中的应用 |
BR112021016960A2 (pt) * | 2019-03-07 | 2021-11-23 | BioNTech SE | Processo para a preparação de uma imidazoquinolina substituída |
WO2021074227A1 (en) * | 2019-10-15 | 2021-04-22 | Bayer Aktiengesellschaft | 2-methyl-aza-quinazolines |
WO2021113644A1 (en) | 2019-12-05 | 2021-06-10 | Multivir Inc. | Combinations comprising a cd8+ t cell enhancer, an immune checkpoint inhibitor and radiotherapy for targeted and abscopal effects for the treatment of cancer |
WO2021260443A1 (en) | 2020-06-24 | 2021-12-30 | Bayer Aktiengesellschaft | Combinations of 2,3-dihydroimidazo[1,2-c]quinazolines |
CN115572256A (zh) * | 2021-06-21 | 2023-01-06 | 武汉睿健医药科技有限公司 | Oct4高选择性活化剂 |
CN113512040B (zh) * | 2021-08-25 | 2023-10-13 | 河南牧业经济学院 | 一种血根碱仿生化合物及其制备方法 |
WO2023205680A1 (en) * | 2022-04-20 | 2023-10-26 | Synnovation Therapeutics, Inc. | PI3Kα INHIBITORS |
WO2023230262A1 (en) * | 2022-05-26 | 2023-11-30 | Synnovation Therapeutics, Inc. | Tricyclic compounds as pi3kalpha inhibitors |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004029055A1 (en) * | 2002-09-30 | 2004-04-08 | Bayer Pharmaceuticals Corporation | Fused azole-pyrimidine derivatives |
WO2008070150A1 (en) * | 2006-12-05 | 2008-06-12 | Bayer Schering Pharma Aktiengesellschaft | Substituted 2,3-dihydroimidazo[1,2-c]quinazoline derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesis |
WO2010034414A1 (en) * | 2008-09-24 | 2010-04-01 | Bayer Schering Pharma Aktiengesellschaft | Use of substituted 2,3-dihydroimidazo[1,2-c]quinazolines for the treatment of myeloma |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5023252A (en) | 1985-12-04 | 1991-06-11 | Conrex Pharmaceutical Corporation | Transdermal and trans-membrane delivery of drugs |
US5011472A (en) | 1988-09-06 | 1991-04-30 | Brown University Research Foundation | Implantable delivery system for biological factors |
GB9400680D0 (en) | 1994-01-14 | 1994-03-09 | Sandoz Ltd | Improvements in or relating to organic compounds |
US5792766A (en) | 1996-03-13 | 1998-08-11 | Neurogen Corporation | Imidazo 1,5-c! quinazolines; a new class of GABA brain receptor ligands |
US8318752B2 (en) | 2003-09-19 | 2012-11-27 | Astrazeneca Ab | 4-(3-chloro-2-fluoroanilino)-7-methoxy-6-{[1-(N-methylcarbamoyl-methyl)piperidin-4-yl]oxy}quinazoline, its pharmaceutically acceptable salts, and pharmaceutical compositions comprising the same |
RU2412942C2 (ru) * | 2003-10-03 | 2011-02-27 | 3М Инновейтив Пропертиз Компани | Оксизамещенные имидазохинолины, способные модулировать биосинтез цитокинов |
US7842701B2 (en) * | 2004-02-19 | 2010-11-30 | Takeda Pharmaceutical Company Limited | Pyrazoloquinolone derivative and use thereof |
ES2394971T3 (es) | 2006-08-03 | 2013-02-07 | Rottapharm S.P.A. | Derivados de quinolinas y 6-1H-imidazo-quinazolina, agentes antiinflamatorios y analgésicos potentes nuevos |
GB2454549B (en) * | 2007-09-25 | 2009-09-23 | Medical & Pharm Ind Tech & Dev | Uses of 2-[piperidinyl]methyl-2,3-dihydroimidazo[1,2-c]quinazolin-5(6H)-one for providing an anti-allergic effect and histamine H1 receptor antagonism effect |
CA2728376C (en) | 2008-06-20 | 2015-05-12 | Rottapharm S.P.A. | 6-1h-imidazo-quinazoline and quinolines derivatives/mao inhibitors for treating depression |
EA020703B9 (ru) | 2008-06-26 | 2015-12-30 | Ле Лаборатуар Сервье | Пиразолохиназолины |
MX2012012064A (es) | 2010-04-16 | 2012-12-17 | Bayer Ip Gmbh | Combinaciones que contienen 2,3-dihidroimidazo[1,2-c]quinazolina sustituida. |
UA113280C2 (xx) * | 2010-11-11 | 2017-01-10 | АМІНОСПИРТЗАМІЩЕНІ ПОХІДНІ 2,3-ДИГІДРОІМІДАЗО$1,2-c]ХІНАЗОЛІНУ, ПРИДАТНІ ДЛЯ ЛІКУВАННЯ ГІПЕРПРОЛІФЕРАТИВНИХ ПОРУШЕНЬ І ЗАХВОРЮВАНЬ, ПОВ'ЯЗАНИХ З АНГІОГЕНЕЗОМ | |
CN103370320B (zh) * | 2010-11-11 | 2016-04-27 | 拜耳知识产权有限责任公司 | 芳基氨基醇取代的2,3-二氢咪唑并[1,2-c]喹啉 |
ES2646012T3 (es) * | 2010-11-11 | 2017-12-11 | Bayer Intellectual Property Gmbh | 2,3-Dihidroimidazo[1,2-c]quinazolinas sustituidas con alcoxi |
-
2011
- 2011-08-11 UA UAA201307179A patent/UA113280C2/uk unknown
- 2011-11-08 KR KR1020137014882A patent/KR20140003436A/ko not_active Application Discontinuation
- 2011-11-08 AP AP2013006921A patent/AP3337A/xx active
- 2011-11-08 NZ NZ610018A patent/NZ610018A/en not_active IP Right Cessation
- 2011-11-08 AU AU2011328192A patent/AU2011328192B2/en not_active Ceased
- 2011-11-08 PE PE2013001051A patent/PE20140411A1/es not_active Application Discontinuation
- 2011-11-08 CA CA2817317A patent/CA2817317C/en active Active
- 2011-11-08 US US13/885,122 patent/US8895549B2/en active Active
- 2011-11-08 WO PCT/EP2011/069637 patent/WO2012062748A1/en active Application Filing
- 2011-11-08 SG SG2013033634A patent/SG190100A1/en unknown
- 2011-11-08 CN CN201180023122.7A patent/CN102906094B/zh active Active
- 2011-11-08 JP JP2013538163A patent/JP6196156B2/ja active Active
- 2011-11-08 MY MYPI2013700753A patent/MY164730A/en unknown
- 2011-11-08 MX MX2013005305A patent/MX2013005305A/es unknown
- 2011-11-08 EA EA201300556A patent/EA024406B1/ru not_active IP Right Cessation
- 2011-11-08 BR BR112013011634A patent/BR112013011634A2/pt not_active IP Right Cessation
- 2011-11-08 EP EP11784978.6A patent/EP2638045B1/en active Active
- 2011-11-10 UY UY0001033719A patent/UY33719A/es not_active Application Discontinuation
- 2011-11-11 TW TW100141328A patent/TW201305170A/zh unknown
- 2011-11-11 AR ARP110104216A patent/AR083842A1/es unknown
-
2013
- 2013-04-30 IL IL226066A patent/IL226066A0/en unknown
- 2013-05-09 MA MA35889A patent/MA34655B1/fr unknown
- 2013-05-10 CO CO13117697A patent/CO6761350A2/es not_active Application Discontinuation
- 2013-05-10 CL CL2013001295A patent/CL2013001295A1/es unknown
- 2013-05-10 EC ECSP13012618 patent/ECSP13012618A/es unknown
- 2013-05-10 DO DO2013000105A patent/DOP2013000105A/es unknown
- 2013-05-10 GT GT201300121A patent/GT201300121A/es unknown
- 2013-05-10 CU CU2013000069A patent/CU20130069A7/es unknown
- 2013-05-10 CR CR20130213A patent/CR20130213A/es unknown
- 2013-06-10 ZA ZA2013/04244A patent/ZA201304244B/en unknown
- 2013-07-10 HK HK13108062.1A patent/HK1180685A1/zh not_active IP Right Cessation
-
2014
- 2014-11-25 US US14/553,280 patent/US9902727B2/en active Active
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004029055A1 (en) * | 2002-09-30 | 2004-04-08 | Bayer Pharmaceuticals Corporation | Fused azole-pyrimidine derivatives |
WO2008070150A1 (en) * | 2006-12-05 | 2008-06-12 | Bayer Schering Pharma Aktiengesellschaft | Substituted 2,3-dihydroimidazo[1,2-c]quinazoline derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesis |
WO2010034414A1 (en) * | 2008-09-24 | 2010-04-01 | Bayer Schering Pharma Aktiengesellschaft | Use of substituted 2,3-dihydroimidazo[1,2-c]quinazolines for the treatment of myeloma |
Also Published As
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