|
US7230000B1
(en)
|
1999-10-27 |
2007-06-12 |
Cytokinetics, Incorporated |
Methods and compositions utilizing quinazolinones
|
|
US6545004B1
(en)
|
1999-10-27 |
2003-04-08 |
Cytokinetics, Inc. |
Methods and compositions utilizing quinazolinones
|
|
US7009049B2
(en)
|
2002-02-15 |
2006-03-07 |
Cytokinetics, Inc. |
Syntheses of quinazolinones
|
|
JP4664597B2
(ja)
|
2002-04-17 |
2011-04-06 |
サイトキネティクス・インコーポレーテッド |
化合物、組成物および方法
|
|
AU2003270015A1
(en)
|
2002-05-09 |
2003-12-02 |
Cytokinetics, Inc. |
Compounds, compositions, and methods
|
|
US7166595B2
(en)
*
|
2002-05-09 |
2007-01-23 |
Cytokinetics, Inc. |
Compounds, methods and compositions
|
|
WO2003103575A2
(en)
|
2002-05-23 |
2003-12-18 |
Cytokinetics, Inc. |
Compounds, compositions, and methods
|
|
CA2489367A1
(en)
|
2002-06-14 |
2003-12-24 |
Cytokinetics, Inc. |
Compounds, compositions, and methods
|
|
ATE423110T1
(de)
|
2002-07-17 |
2009-03-15 |
Cytokinetics Inc |
Verbindungen, zusammensetzungen und verfahren zur behandlung von zellulären proliferativen erkrankungen
|
|
WO2004009036A2
(en)
|
2002-07-23 |
2004-01-29 |
Cytokinetics, Inc. |
Compounds compositions and methods
|
|
WO2004034972A2
(en)
|
2002-09-30 |
2004-04-29 |
Cytokinetics, Inc. |
Compounds, compositions, and methods
|
|
AU2003300031A1
(en)
*
|
2002-10-11 |
2004-05-04 |
Cytokinetics, Inc. |
Compounds, compositions, and methods
|
|
WO2004055008A1
(en)
*
|
2002-12-13 |
2004-07-01 |
Smithkline Beecham Corporation |
Compounds, compositions and methods
|
|
AR050920A1
(es)
*
|
2003-03-07 |
2006-12-06 |
Astrazeneca Ab |
Enantiomeros de heterociclos fusionados seleccionados y usos de los mismos
|
|
PT1601673E
(pt)
*
|
2003-03-07 |
2009-07-29 |
Astrazeneca Ab |
Heterociclos fundidos e suas utilizações
|
|
CA2533889A1
(en)
*
|
2003-08-15 |
2005-03-03 |
Merck & Co., Inc. |
Mitotic kinesin inhibitors
|
|
EP1692112A4
(de)
|
2003-12-08 |
2008-09-24 |
Cytokinetics Inc |
Verbindungen, zusammensetzungen und verfahren
|
|
ATE419249T1
(de)
*
|
2004-04-06 |
2009-01-15 |
Novartis Vaccines & Diagnostic |
Inhibitoren von mitotischem kinesin
|
|
DE602005008953D1
(de)
|
2004-05-21 |
2008-09-25 |
Novartis Vaccines & Diagnostic |
Substituierte chinolinderivate als inhibitoren von mitotischem kinesin
|
|
MXPA06014909A
(es)
|
2004-06-18 |
2007-02-28 |
Chiron Corp |
Derivados de n-(1-(1-bencil -4-fenil-1h -imidazol -2-il)-2, 2-dimetilpropil) benzamida y compuestos relacionados como inhibidores de proteina de huso de cinesina (ksp) para el tratamiento del cancer.
|
|
US20070287703A1
(en)
*
|
2004-07-22 |
2007-12-13 |
Astrazeneca Ab |
Fused Pyrimidones Useful in the Treatment and the Prevention of Cancer
|
|
CN101027309B
(zh)
*
|
2004-08-18 |
2010-10-27 |
阿斯利康(瑞典)有限公司 |
所选择的稠合嘧啶酮的对映体和在治疗和预防癌症中的用途
|
|
US20060041128A1
(en)
*
|
2004-08-18 |
2006-02-23 |
Astrazeneca Ab |
Selected fused heterocyclics and uses thereof
|
|
EP1807399A2
(de)
|
2004-10-19 |
2007-07-18 |
Novartis Vaccines and Diagnostics, Inc. |
Indol- und benzimidazolderivate
|
|
JP2008528448A
(ja)
*
|
2005-01-03 |
2008-07-31 |
ザ リージェンツ オブ ザ ユニバーシティ オブ ミシガン |
新規化合物に関連する組成物および方法、ならびにその標的
|
|
JP4545196B2
(ja)
*
|
2005-01-19 |
2010-09-15 |
メルク・シャープ・エンド・ドーム・コーポレイション |
有糸分裂キネシン阻害剤
|
|
ATE550019T1
(de)
|
2005-05-17 |
2012-04-15 |
Merck Sharp & Dohme |
Cis-4-ä(4-chlorophenyl)sulfonylü-4-(2,5- difluorophenyl)cyclohexanepropansäure zur behandlug von krebs
|
|
PE20070335A1
(es)
|
2005-08-30 |
2007-04-21 |
Novartis Ag |
Benzimidazoles sustituidos y metodos para su preparacion
|
|
EA200801414A1
(ru)
*
|
2005-11-22 |
2008-10-30 |
Смитклайн Бичам Корпорейшн |
Кальцилитические соединения
|
|
GB0603041D0
(en)
|
2006-02-15 |
2006-03-29 |
Angeletti P Ist Richerche Bio |
Therapeutic compounds
|
|
KR101464385B1
(ko)
|
2006-04-19 |
2014-11-21 |
노파르티스 아게 |
6-o-치환된 벤즈옥사졸 및 벤조티아졸 화합물, 및 csf-1r 신호전달의 억제 방법
|
|
SG172685A1
(en)
|
2006-06-28 |
2011-07-28 |
Amgen Inc |
Glycine transporter-1 inhibitors
|
|
US8063050B2
(en)
|
2006-07-06 |
2011-11-22 |
Array Biopharma Inc. |
Hydroxylated and methoxylated pyrimidyl cyclopentanes as AKT protein kinase inhibitors
|
|
UA95641C2
(xx)
*
|
2006-07-06 |
2011-08-25 |
Эррей Биофарма Инк. |
Гідроксильовані піримідильні циклопентани як інгібітори акт протеїнкінази$гидроксилированные пиримидильные циклопентаны как ингибиторы акт протеинкиназы
|
|
RU2481336C2
(ru)
*
|
2006-07-06 |
2013-05-10 |
Эррэй Биофарма Инк. |
Циклопента(d)пиримидины в качестве ингибиторов протеинкиназ акт
|
|
AU2007300627B2
(en)
|
2006-09-22 |
2012-02-16 |
Merck Sharp & Dohme Corp. |
Method of treatment using fatty acid synthesis inhibitors
|
|
US20110218176A1
(en)
|
2006-11-01 |
2011-09-08 |
Barbara Brooke Jennings-Spring |
Compounds, methods, and treatments for abnormal signaling pathways for prenatal and postnatal development
|
|
MX2009005071A
(es)
|
2006-11-13 |
2009-05-25 |
Novartis Ag |
Compuestos de pirazol y triazol sustituidos como inhibidores de ksp.
|
|
EP2441768A1
(de)
*
|
2006-11-13 |
2012-04-18 |
Eli Lilly & Co. |
Thienopyrimidinone zur Behandlung von Entzündungserkrankungen und Karzinomen
|
|
GEP20125415B
(en)
|
2007-01-05 |
2012-03-12 |
Novartis Ag |
Imidazole derivatives as kinesin spindle protein inhibitors (eg-5)
|
|
BRPI0806245B1
(pt)
|
2007-01-10 |
2022-01-25 |
Msd Italia S.R.L. |
Compostos de fórmula i e seus usos
|
|
CN101679266B
(zh)
|
2007-03-01 |
2015-05-06 |
诺华股份有限公司 |
Pim激酶抑制剂及其应用方法
|
|
AU2008254425A1
(en)
|
2007-05-21 |
2008-11-27 |
Novartis Ag |
CSF-1R inhibitors, compositions, and methods of use
|
|
WO2009002495A1
(en)
|
2007-06-27 |
2008-12-31 |
Merck & Co., Inc. |
4-carboxybenzylamino derivatives as histone deacetylase inhibitors
|
|
EP2413932A4
(de)
|
2009-04-01 |
2012-09-19 |
Merck Sharp & Dohme |
Hemmer der akt-aktivität
|
|
EP2448938B9
(de)
|
2009-06-29 |
2015-06-10 |
Incyte Corporation |
Pyrimidinone als pi3k-hemmer
|
|
CA2777043C
(en)
|
2009-10-14 |
2015-12-15 |
Schering Corporation |
Substituted piperidines that increase p53 activity and the uses thereof
|
|
WO2011075643A1
(en)
|
2009-12-18 |
2011-06-23 |
Incyte Corporation |
Substituted heteroaryl fused derivatives as pi3k inhibitors
|
|
EP2558463A1
(de)
|
2010-04-14 |
2013-02-20 |
Incyte Corporation |
Kondensierte derivate als i3-hemmer
|
|
US9062055B2
(en)
|
2010-06-21 |
2015-06-23 |
Incyte Corporation |
Fused pyrrole derivatives as PI3K inhibitors
|
|
EP2584903B1
(de)
|
2010-06-24 |
2018-10-24 |
Merck Sharp & Dohme Corp. |
Neue heterozyklische verbindungen als erk-hemmer
|
|
CN103068980B
(zh)
|
2010-08-02 |
2017-04-05 |
瑟纳治疗公司 |
使用短干扰核酸(siNA)的RNA干扰介导的联蛋白(钙粘蛋白关联蛋白质),β1(CTNNB1)基因表达的抑制
|
|
RU2745848C2
(ru)
|
2010-08-17 |
2021-04-01 |
Сирна Терапьютикс, Инк. |
ОПОСРЕДУЕМОЕ РНК-ИНТЕРФЕРЕНЦИЕЙ ИНГИБИРОВАНИЕ ЭКСПРЕССИИ ГЕНОВ ВИРУСА ГЕПАТИТА B (HBV) С ПРИМЕНЕНИЕМ МАЛОЙ ИНТЕРФЕРИРУЮЩЕЙ НУКЛЕИНОВОЙ КИСЛОТЫ (миНК)
|
|
US8883801B2
(en)
|
2010-08-23 |
2014-11-11 |
Merck Sharp & Dohme Corp. |
Substituted pyrazolo[1,5-a]pyrimidines as mTOR inhibitors
|
|
EP2613782B1
(de)
|
2010-09-01 |
2016-11-02 |
Merck Sharp & Dohme Corp. |
Indazolderivate als erk-hemmer
|
|
WO2012058210A1
(en)
|
2010-10-29 |
2012-05-03 |
Merck Sharp & Dohme Corp. |
RNA INTERFERENCE MEDIATED INHIBITION OF GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACIDS (siNA)
|
|
EP2455456A1
(de)
|
2010-11-22 |
2012-05-23 |
Institut Curie |
Verwendung von Kinesininhibitoren bei der Behandlung von HIV-Infektion und Verfahren zu deren Abtastung
|
|
JP5961187B2
(ja)
|
2010-12-20 |
2016-08-02 |
インサイト・ホールディングス・コーポレイションIncyte Holdings Corporation |
Pi3k阻害剤としてのn−(1−(置換フェニル)エチル)−9h−プリン−6−アミン
|
|
WO2012087772A1
(en)
|
2010-12-21 |
2012-06-28 |
Schering Corporation |
Indazole derivatives useful as erk inhibitors
|
|
US9108984B2
(en)
|
2011-03-14 |
2015-08-18 |
Incyte Corporation |
Substituted diamino-pyrimidine and diamino-pyridine derivatives as PI3K inhibitors
|
|
US9126948B2
(en)
|
2011-03-25 |
2015-09-08 |
Incyte Holdings Corporation |
Pyrimidine-4,6-diamine derivatives as PI3K inhibitors
|
|
TR201815685T4
(tr)
|
2011-04-01 |
2018-11-21 |
Genentech Inc |
Kanser tedavisi için akt ve mek inhibe edici bileşiklerin kombinasyonları.
|
|
FI2694072T4
(fi)
|
2011-04-01 |
2024-09-30 |
Genentech Inc |
Akt-inhibiittoriyhdisteen ja abirateronin yhdistelmä käytettäväksi terapeuttisissa hoidoissa
|
|
WO2012143879A1
(en)
|
2011-04-21 |
2012-10-26 |
Piramal Healthcare Limited |
A crystalline form of a salt of a morpholino sulfonyl indole derivative and a process for its preparation
|
|
US9227982B2
(en)
|
2011-07-13 |
2016-01-05 |
Novartis Ag |
4-oxo-3,5,7,8-tetrahydro-4H-pyrano[4,3-d]pyrminidinyl compounds for use as tankyrase inhibitors
|
|
US9181266B2
(en)
|
2011-07-13 |
2015-11-10 |
Novartis Ag |
2-piperidin-1-yl-acetamide compounds for use as tankyrase inhibitors
|
|
CA2841932A1
(en)
|
2011-07-13 |
2013-01-17 |
Novartis Ag |
4 - piperidinyl compounds for use as tankyrase inhibitors
|
|
MX389479B
(es)
|
2011-09-02 |
2025-03-20 |
Incyte Holdings Corp |
Heterociclilaminas como inhibidores de fosfoinositida 3-cinasas (pi3k)
|
|
EP2770987B1
(de)
|
2011-10-27 |
2018-04-04 |
Merck Sharp & Dohme Corp. |
Neue verbindungen als erk-hemmer
|
|
AR090548A1
(es)
|
2012-04-02 |
2014-11-19 |
Incyte Corp |
Azaheterociclobencilaminas biciclicas como inhibidores de pi3k
|
|
US8940742B2
(en)
|
2012-04-10 |
2015-01-27 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
|
EP3919620A1
(de)
|
2012-05-02 |
2021-12-08 |
Sirna Therapeutics, Inc. |
Zusammensetzungen mit kurzer interferierender nukleinsäure (sina)
|
|
CA2882950A1
(en)
|
2012-09-28 |
2014-04-03 |
Merck Sharp & Dohme Corp. |
Novel compounds that are erk inhibitors
|
|
SMT201700595T1
(it)
|
2012-11-28 |
2018-03-08 |
Merck Sharp & Dohme |
Composizioni e metodi per trattare il cancro
|
|
WO2014100065A1
(en)
|
2012-12-20 |
2014-06-26 |
Merck Sharp & Dohme Corp. |
Substituted imidazopyridines as hdm2 inhibitors
|
|
WO2014120748A1
(en)
|
2013-01-30 |
2014-08-07 |
Merck Sharp & Dohme Corp. |
2,6,7,8 substituted purines as hdm2 inhibitors
|
|
WO2015034925A1
(en)
|
2013-09-03 |
2015-03-12 |
Moderna Therapeutics, Inc. |
Circular polynucleotides
|
|
EP3964507A1
(de)
|
2013-10-04 |
2022-03-09 |
Infinity Pharmaceuticals, Inc. |
Heterocyclische verbindungen und verwendungen davon
|
|
WO2015051241A1
(en)
|
2013-10-04 |
2015-04-09 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
|
CN106456628A
(zh)
|
2014-03-19 |
2017-02-22 |
无限药品股份有限公司 |
用于治疗PI3K‑γ介导的障碍的杂环化合物
|
|
US10077277B2
(en)
|
2014-06-11 |
2018-09-18 |
Incyte Corporation |
Bicyclic heteroarylaminoalkyl phenyl derivatives as PI3K inhibitors
|
|
JO3589B1
(ar)
|
2014-08-06 |
2020-07-05 |
Novartis Ag |
مثبطات كيناز البروتين c وطرق استخداماتها
|
|
WO2016054491A1
(en)
|
2014-10-03 |
2016-04-07 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
|
SG10201912302VA
(en)
|
2015-02-27 |
2020-02-27 |
Incyte Corp |
Salts of pi3k inhibitor and processes for their preparation
|
|
WO2016183060A1
(en)
|
2015-05-11 |
2016-11-17 |
Incyte Corporation |
Process for the synthesis of a phosphoinositide 3-kinase inhibitor
|
|
US9988401B2
(en)
|
2015-05-11 |
2018-06-05 |
Incyte Corporation |
Crystalline forms of a PI3K inhibitor
|
|
CN114230571B
(zh)
|
2015-09-14 |
2025-07-08 |
无限药品股份有限公司 |
异喹啉酮的固体形式、其制备方法、包含其的组合物及其使用方法
|
|
WO2017161116A1
(en)
|
2016-03-17 |
2017-09-21 |
Infinity Pharmaceuticals, Inc. |
Isotopologues of isoquinolinone and quinazolinone compounds and uses thereof as pi3k kinase inhibitors
|
|
US10919914B2
(en)
|
2016-06-08 |
2021-02-16 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
|
JOP20190055A1
(ar)
|
2016-09-26 |
2019-03-24 |
Merck Sharp & Dohme |
أجسام مضادة ضد cd27
|
|
US10975084B2
(en)
|
2016-10-12 |
2021-04-13 |
Merck Sharp & Dohme Corp. |
KDM5 inhibitors
|
|
JP7160833B2
(ja)
|
2017-04-13 |
2022-10-25 |
サイロパ ビー.ブイ. |
抗sirpアルファ抗体
|
|
WO2019094312A1
(en)
|
2017-11-08 |
2019-05-16 |
Merck Sharp & Dohme Corp. |
Prmt5 inhibitors
|
|
EP3706742B1
(de)
|
2017-11-08 |
2023-03-15 |
Merck Sharp & Dohme LLC |
Prmt5-inhibitoren
|
|
WO2019148412A1
(en)
|
2018-02-01 |
2019-08-08 |
Merck Sharp & Dohme Corp. |
Anti-pd-1/lag3 bispecific antibodies
|
|
IL278889B2
(en)
|
2018-06-01 |
2025-11-01 |
Incyte Corp |
Dosing regimen for the treatment of pi3k related disorders
|
|
JP7336277B2
(ja)
|
2018-07-05 |
2023-08-31 |
キヤノン株式会社 |
有機el素子及びこれを用いた表示装置、撮像装置、通信機器、照明装置、灯具、移動体
|
|
WO2020033282A1
(en)
|
2018-08-07 |
2020-02-13 |
Merck Sharp & Dohme Corp. |
Prmt5 inhibitors
|
|
WO2020033285A1
(en)
|
2018-08-07 |
2020-02-13 |
Merck Sharp & Dohme Corp. |
Prmt5 inhibitors
|
|
EP3833667B1
(de)
|
2018-08-07 |
2024-03-13 |
Merck Sharp & Dohme LLC |
Prmt5-inhibitoren
|
|
CA3108388A1
(en)
|
2018-08-07 |
2020-02-13 |
Merck Sharp & Dohme Corp. |
Prmt5 inhibitors
|
|
EP4076459B1
(de)
|
2019-12-17 |
2026-04-29 |
Merck Sharp & Dohme LLC |
Prmt5-inhibitoren
|
|
ES3074517T3
(en)
|
2019-12-17 |
2026-07-21 |
Merck Sharp & Dohme Llc |
4-(3,4-dihydroisoquinolin-2(1h)-yl)-3-hydroxypiperidine derivatives as prmt5 inhibitors for the treatment of cancer and sickle cell disease
|
|
ES3022307T3
(en)
|
2019-12-17 |
2025-05-28 |
Merck Sharp & Dohme Llc |
Prmt5 inhibitors
|
|
EP4076460B1
(de)
|
2019-12-17 |
2026-01-21 |
Merck Sharp & Dohme LLC |
1,4-dihydro-2h-spiro[isoquinoline-3,4'-piperidin]-derivate als prmt5 inhibitoren zur behandlung von krebs
|
|
DE212025000115U1
(de)
|
2024-07-30 |
2026-06-18 |
Sairopa B.V. |
Anti-SIRP Alpha-Antikörperformulierungen und ihre Verwendung
|