AR042668A1 - Derivados de fosfonoxi quinazolinas y su uso farmaceutico - Google Patents
Derivados de fosfonoxi quinazolinas y su uso farmaceuticoInfo
- Publication number
- AR042668A1 AR042668A1 ARP030104824A ARP030104824A AR042668A1 AR 042668 A1 AR042668 A1 AR 042668A1 AR P030104824 A ARP030104824 A AR P030104824A AR P030104824 A ARP030104824 A AR P030104824A AR 042668 A1 AR042668 A1 AR 042668A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- phosphonooxy
- substituted
- halo
- hydrogen
- Prior art date
Links
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 12
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 abstract 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 9
- 229910052757 nitrogen Inorganic materials 0.000 abstract 9
- 229910052739 hydrogen Inorganic materials 0.000 abstract 8
- 239000001257 hydrogen Substances 0.000 abstract 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 8
- 125000005843 halogen group Chemical group 0.000 abstract 7
- 229910052799 carbon Inorganic materials 0.000 abstract 5
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 5
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 4
- 229920006395 saturated elastomer Polymers 0.000 abstract 4
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 3
- 125000001475 halogen functional group Chemical group 0.000 abstract 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 1
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 abstract 1
- 125000006163 5-membered heteroaryl group Chemical group 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 abstract 1
- 230000001028 anti-proliverative effect Effects 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 150000001721 carbon Chemical group 0.000 abstract 1
- 230000001413 cellular effect Effects 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 abstract 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 1
- 125000004446 heteroarylalkyl group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 125000002294 quinazolinyl group Chemical class N1=C(N=CC2=CC=CC=C12)* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 238000002560 therapeutic procedure Methods 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6509—Six-membered rings
- C07F9/6512—Six-membered rings having the nitrogen atoms in positions 1 and 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6558—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
- C07F9/65583—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system each of the hetero rings containing nitrogen as ring hetero atom
-
- 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
- A61K31/66—Phosphorus compounds
- A61K31/661—Phosphorus acids or esters thereof not having P—C bonds, e.g. fosfosal, dichlorvos, malathion or mevinphos
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6558—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Derivados de quinazolina, según composiciones que los contienen, procesos para su preparación, y su uso en terapia como antiproliferativo celular. Reivindicación 1: Un compuesto de fórmula (1), en la cual A es heteroarilo de 5 miembros que contiene un átomo de nitrógeno y opcionalmente contiene uno o dos átomos más de nitrógeno; X es O, S, S(O), S(O)2 o NR14; m es 0,1, 2 ó 3; Z es un grupo seleccionado de -NR1R2, fosfonooxi, cicloalquilo C3-6 (sustituido con fosfonooxi o alquilo C1-4 (sustituido con fosfonooxi)) y un anillo de 4 a 7 miembros unido por un átomo de carbono que contiene un átomo de nitrógeno y que opcionalmente contiene otro átomo de nitrógeno, anillo que puede ser saturado, parcialmente saturado o no saturado, en el cual el anillo está sustituido en carbono o nitrógeno con fosfonooxi o alquilo C1-4 (sustituido con fosfonooxi) y en el cual el anillo se sustituye además, de manera opcional, en el carbono o nitrógeno, con 1, 2 ó 3 grupos halo o alquilo C1-4; R1 es -COR8, -CONR8R9 o alquilo C1-6 (sustituido con fosfonooxi y además de manera opcional sustituido con 1 ó 2 grupos halo o metoxi); R2 es hidrógeno, -COR10, -CONR10R11, alquilo C1-6 (sustituido opcionalmente con 1, 2 ó 3 grupos halo o alcoxi C1-4 o -S(O)pR11 (donde p es 0, 1 ó 2) o fosfonooxi), alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-6 y cicloalquil(C3-6)-alquilo(C1-4); o R1 y R2 junto con el nitrógeno al cual se encuentran unidos forman un anillo de 4 a 7 miembros que contiene opcionalmente otro átomo de nitrógeno, que puede ser saturado, parcialmente saturado o no saturado, en el cual el anillo está sustituido en carbono o nitrógeno con un grupo seleccionado de fosfonooxi y alquilo C1-4 (sustituido con fosfonooxi o -NR8R9) y donde el anillo está sustituido además de manera opcional en el carbono o nitrógeno con 1, 1 ó 3 grupos halo o alquilo C1-4; R3 es hidrógeno, halo, ciano, nitro, alcoxi C1-6, alquilo C1-6, -OR12, -CHR12R13, -OC(O)R12, -C(O)R12, -NR12C(O)R13, -C(O)NR12R13, -NR12SO2R13 o -NR12R13; R4 es hidrógeno o un grupo seleccionado de alquilo C1-4, heteroarilo, heteroarilalquilo C1-4, arilo y arilalquilo C1-4, grupo que está sustituido de manera opcional con 1, 2 ó 3 sustituyentes seleccionados de halo, metilo, etilo, ciclopropilo y etinilo; R5 se selecciona de hidrógeno, alquilo C1-4, alquenilo C2-4, alquinilo C2-4, cicloalquilo C3-6 y cicloalquil C1-4; R6 y R7 son independientemente hidrógeno, halo, alquilo C1-4, cicloalquilo C3-6, hidroxi y alcoxi C1-4; R8 es alquilo C1-4 sustituido con fosfonooxi y además está sustituido opcionalmente con 1 ó 2 grupos halo o metoxi; R9 es hidrógeno o alquilo C1-4; R10 es hidrógeno o alquilo C1-4 (sustituido de manera opcional con halo, alcoxi C1-4, S(O)q (donde q es 0, 1 ó 2) o fosfonooxi); R11, R12, R13 y R14 son independientemente hidrógeno, alquilo C1-4 o heterociclilo; o una sal aceptable para uso farmacéutico del mismo.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP02293238 | 2002-12-24 | ||
EP03291315 | 2003-06-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR042668A1 true AR042668A1 (es) | 2005-06-29 |
Family
ID=32683824
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP030104824A AR042668A1 (es) | 2002-12-24 | 2003-12-23 | Derivados de fosfonoxi quinazolinas y su uso farmaceutico |
ARP070102117A AR057753A2 (es) | 2002-12-24 | 2007-05-16 | Derivados de quinazolina, proceso para su preparacion y composiciones farmaceuticas que los contienen |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP070102117A AR057753A2 (es) | 2002-12-24 | 2007-05-16 | Derivados de quinazolina, proceso para su preparacion y composiciones farmaceuticas que los contienen |
Country Status (30)
Country | Link |
---|---|
US (4) | US7528121B2 (es) |
EP (2) | EP1847539B1 (es) |
JP (3) | JP4422102B2 (es) |
KR (1) | KR101010299B1 (es) |
AR (2) | AR042668A1 (es) |
AT (2) | ATE438644T1 (es) |
AU (1) | AU2003290313B2 (es) |
BR (1) | BRPI0317717B8 (es) |
CA (1) | CA2511613C (es) |
CL (1) | CL2003002731A1 (es) |
CY (2) | CY1107775T1 (es) |
DE (2) | DE60315892T2 (es) |
DK (2) | DK1847539T3 (es) |
ES (2) | ES2290529T3 (es) |
HK (2) | HK1080481A1 (es) |
IL (2) | IL169112A (es) |
IS (2) | IS2504B (es) |
MX (1) | MXPA05006918A (es) |
MY (2) | MY136174A (es) |
NO (2) | NO335193B1 (es) |
NZ (1) | NZ540698A (es) |
PL (2) | PL223998B1 (es) |
PT (2) | PT1847539E (es) |
RU (3) | RU2350611C1 (es) |
SA (1) | SA04240504B1 (es) |
SI (2) | SI1847539T1 (es) |
TW (2) | TWI336327B (es) |
UA (1) | UA83814C2 (es) |
UY (1) | UY28149A1 (es) |
WO (1) | WO2004058781A1 (es) |
Families Citing this family (49)
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JP4498741B2 (ja) * | 2001-12-24 | 2010-07-07 | アストラゼネカ アクチボラグ | オーロラキナーゼ阻害剤としての置換キナゾリン誘導体 |
JP2006516138A (ja) * | 2002-12-24 | 2006-06-22 | アストラゼネカ アクチボラグ | キナゾリン化合物 |
CA2511613C (en) | 2002-12-24 | 2012-10-02 | Astrazeneca Ab | Phosphonooxy quinazoline derivatives and their pharmaceutical use |
BRPI0409427A (pt) | 2003-04-16 | 2006-04-18 | Astrazeneca Ab | composto, uso do mesmo, composição farmacêutica, método de tratamento de um humano sofrendo de uma doença hiperproliferativa, e, processo para a preparação de um composto ou de um sal, éster ou pró-droga farmaceuticamente aceitáveis do mesmo |
ATE534649T1 (de) * | 2003-05-15 | 2011-12-15 | Arqule Inc | Imidazothiazole und imidazoxazolderivative als inhibitoren von p38 |
US20060135541A1 (en) * | 2003-06-02 | 2006-06-22 | Astrazeneca Ab | (3-((Quinazolin-4-yl) amino)-1h-pyrazol-1-yl)acetamide derivatives and related compounds as aurora kinase inhibitors for the treatment of proliferative diseases such as cancer |
WO2006040520A1 (en) * | 2004-10-12 | 2006-04-20 | Astrazeneca Ab | Quinazoline derivatives |
US20090036474A1 (en) * | 2004-10-12 | 2009-02-05 | Patrick Ple | Quinazoline derivatives for use against cancer |
DE602005023333D1 (de) | 2004-10-15 | 2010-10-14 | Takeda Pharmaceutical | Kinaseinhibitoren |
JP2008517064A (ja) * | 2004-10-19 | 2008-05-22 | アークル インコーポレイテッド | P38mapキナーゼのイミダゾオキサゾールおよびイミダゾチアゾール阻害剤の合成 |
US8119655B2 (en) | 2005-10-07 | 2012-02-21 | Takeda Pharmaceutical Company Limited | Kinase inhibitors |
UY30183A1 (es) | 2006-03-02 | 2007-10-31 | Astrazeneca Ab | Derivados de quinolina |
US7501430B2 (en) * | 2006-04-17 | 2009-03-10 | Arqule, Inc. | RAF inhibitors and their uses |
GB0609621D0 (en) * | 2006-05-16 | 2006-06-21 | Astrazeneca Ab | Novel co-crystal |
GB0609617D0 (en) | 2006-05-16 | 2006-06-21 | Astrazeneca Ab | Process & intermediate |
GB0609619D0 (en) * | 2006-05-16 | 2006-06-21 | Astrazeneca Ab | Combination |
SG158147A1 (en) | 2006-10-09 | 2010-01-29 | Takeda Pharmaceutical | Kinase inhibitors |
US20110136766A1 (en) * | 2008-03-04 | 2011-06-09 | Vitae Pharmaceuticals, Inc. | Aurora kinase inhibitors |
US20110033461A1 (en) * | 2008-03-12 | 2011-02-10 | Vladimir Ratushny | Combination Therapy for the Treatment of Cancer |
US8138194B2 (en) | 2008-04-30 | 2012-03-20 | National Health Research Institutes | Fused bicyclic pyrimidine compounds as aurora kinase inhibitors |
BRPI0914936A2 (pt) * | 2008-07-03 | 2015-10-20 | Merck Patent Gmbh | naftiridininonas como inibidores de aurora quinase |
BRPI0921862A2 (pt) * | 2008-12-05 | 2015-12-29 | Arqule Inc | inibidores de raf e seus usos |
WO2010068861A1 (en) | 2008-12-11 | 2010-06-17 | Axcentua Pharmaceutucals Ab | Crystalline forms of genistein |
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MX2011006725A (es) | 2008-12-22 | 2011-09-15 | Millennium Pharm Inc | Combinacion de inhibidores de aurora cinasa y anticuerpos anti-cd20. |
ES2609578T3 (es) | 2011-03-04 | 2017-04-21 | Glaxosmithkline Intellectual Property Development Limited | Amino-quinolinas como inhibidores de quinasa |
TWI547494B (zh) | 2011-08-18 | 2016-09-01 | 葛蘭素史克智慧財產發展有限公司 | 作為激酶抑制劑之胺基喹唑啉類 |
AR092529A1 (es) | 2012-09-13 | 2015-04-22 | Glaxosmithkline Llc | Compuesto de aminoquinazolina, composicion farmaceutica que lo comprende y uso de dicho compuesto para la preparacion de un medicamento |
TW201425307A (zh) | 2012-09-13 | 2014-07-01 | Glaxosmithkline Llc | 作為激酶抑制劑之胺基-喹啉類 |
EP2956138B1 (en) | 2013-02-15 | 2022-06-22 | Kala Pharmaceuticals, Inc. | Therapeutic compounds and uses thereof |
EP3763710A1 (en) | 2013-02-20 | 2021-01-13 | Kala Pharmaceuticals, Inc. | Therapeutic compounds and uses thereof |
US9688688B2 (en) | 2013-02-20 | 2017-06-27 | Kala Pharmaceuticals, Inc. | Crystalline forms of 4-((4-((4-fluoro-2-methyl-1H-indol-5-yl)oxy)-6-methoxyquinazolin-7-yl)oxy)-1-(2-oxa-7-azaspiro[3.5]nonan-7-yl)butan-1-one and uses thereof |
JP6301374B2 (ja) * | 2013-02-21 | 2018-03-28 | グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited | キナーゼ阻害剤としてのキナゾリン類 |
DK3311845T3 (da) | 2013-09-16 | 2020-04-06 | Astrazeneca Ab | Terapeutiske polymernanopartikler og fremgangsmåder til fremstilling og anvendelse heraf |
CN106061261B (zh) | 2013-11-01 | 2018-04-24 | 卡拉制药公司 | 治疗化合物的结晶形式及其用途 |
US9890173B2 (en) | 2013-11-01 | 2018-02-13 | Kala Pharmaceuticals, Inc. | Crystalline forms of therapeutic compounds and uses thereof |
JP6525474B2 (ja) | 2013-12-06 | 2019-06-05 | ミレニアム ファーマシューティカルズ, インコーポレイテッドMillennium Pharmaceuticals, Inc. | オーロラキナーゼ阻害剤と抗cd30抗体の併用 |
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MX2019002629A (es) | 2016-09-08 | 2019-10-07 | Kala Pharmaceuticals Inc | Formas cristalinas de compuestos terapéuticos y usos de los mismos. |
EP4327882A3 (en) | 2017-09-08 | 2024-05-15 | The Board of Trustees of the Leland Stanford Junior University | Enpp1 inhibitors and their use for the treatment of cancer |
WO2019195658A1 (en) | 2018-04-05 | 2019-10-10 | Dana-Farber Cancer Institute, Inc. | Sting levels as a biomarker for cancer immunotherapy |
WO2020049208A1 (es) | 2018-09-09 | 2020-03-12 | Fundacio Privada Institut De Recerca De La Sida - Caixa | Aurora cinasa como diana para tratar, prevenir o curar una infección por vih o sida |
WO2021041532A1 (en) | 2019-08-26 | 2021-03-04 | Dana-Farber Cancer Institute, Inc. | Use of heparin to promote type 1 interferon signaling |
US20210161897A1 (en) | 2019-11-12 | 2021-06-03 | Astrazeneca Ab | Epidermal growth factor receptor tyrosine kinase inhibitors for the treatment of cancer |
CN112939948B (zh) * | 2019-12-11 | 2022-05-17 | 苏州美诺医药科技有限公司 | 新型含喹唑啉类化合物及其中间体与应用 |
WO2021260582A1 (en) | 2020-06-24 | 2021-12-30 | Astrazeneca Uk Limited | Combination of antibody-drug conjugate and aurora b inhibitor |
WO2022192139A1 (en) | 2021-03-10 | 2022-09-15 | Astrazeneca Ab | Aurora kinase b inhibitors for use for treating cancer |
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